Batteries, electronic devices and vehicles

Abstract

Provided is a battery that suppresses a decrease in discharge capacity retention rate in a charge-discharge cycle test. The battery comprises a positive electrode and a negative electrode. When the positive electrode of the battery is used as the positive electrode of a test battery of which the negative electrode comprises a lithium metal, and a test is conducted in which a charge-discharge cycle is repeated 50 times using the test battery and the discharge capacity of the test battery is measured at each cycle, the value of the discharge capacity measured at the 50th cycle is greater than or equal to 90% and less than 100% of the maximum value of the discharge capacity from the total of 50 cycles. In each charge-discharge cycle, the test battery is charged at a constant current at a charge rate of 1 C (1 C = 200 mA / g) under a 25°C environment or a 45°C environment until the test battery reaches a voltage of 4.6 V, is charged at a constant voltage of 4.6 V until the charge rate reaches 0.1 C, and is then discharged at a constant current at a discharge rate of 1 C until the test battery reaches a voltage of 2.5 V.

Description

[Technical Field]

[0001] One embodiment of the present invention relates to a battery, an electronic device, and a vehicle. Another embodiment of the present invention relates to an object, a method, or a manufacturing method. Another embodiment of the present invention relates to a process, a machine, a manufacture, or a composition of matter. Another embodiment of the present invention relates to a semiconductor device, a display device, a light-emitting device, a power storage device, a lighting device, or an electronic device, or a manufacturing method thereof.

[0002] In this specification, "battery" includes a secondary battery. In addition, in this specification, "power storage device" includes a stationary device having the function of a battery, such as a home storage battery. In addition, in this specification, "electronic device" refers to all devices that have a battery, including, for example, an electro-optical device that has a battery or an information terminal device that has a battery. [Background technology]

[0003] In recent years, there has been active development of various types of batteries, including lithium-ion secondary batteries, lithium-ion capacitors, air batteries, and all-solid-state batteries. Demand for high-power, high-capacity lithium-ion secondary batteries (also referred to as lithium-ion batteries) has expanded rapidly in line with the development of the semiconductor industry, and they have become indispensable in today's information society as a rechargeable energy source.

[0004] In particular, there is a high demand for secondary batteries for mobile electronic devices that have a large discharge capacity per weight and excellent cycle characteristics. To meet these demands, there has been active research into improving the positive electrode active material of the positive electrode of secondary batteries (for example, Patent Documents 1 to 3). Research is also being conducted on the crystalline structure of positive electrode active materials (Non-Patent Documents 1 to 3).

[0005] X-ray diffraction (XRD) is one of the techniques used to analyze the crystalline structure of positive electrode active materials. XRD data can be analyzed using the Inorganic Crystal Structure Database (ICSD) introduced in Non-Patent Document 4. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] Japanese Patent Application Publication No. 2019-179758 [Patent Document 2] WO2020 / 026078 Brochure [Patent Document 3] Japanese Patent Publication No. 2020-140954 [Non-patent literature]

[0007] [Non-Patent Document 1] Toyoki Okumura et al, “Correlation of lithium ion distribution and X-ray absorption near-edge structure in O3-and O2-lithium cobalt oxides from first-principle calculation”, Journal of Materials Chemistry, 2012, 22, p. 17340-17348 [Non-patent document 2] Motohashi, T. et al, “Electronic phase diagram of the layered cobalt oxide system LixCoO▲2▼(0.0≦x≦1.0)”, Physical Review B, 80(16);165114 [Non-patent document 3] Zhaohui Chen et al, “Staging Phase Transitions in LixCoO▲2▼”, Journal of The Electrochemical Society, 2002, 149(12)A1604-A1609 [Non-patent document 4] Belsky, A. et al., “New developments in the Inorganic Crystal Structure Database (ICSD): accessibility in support of materials research and design”, Acta Cryst., (2002) B58 364-369. Summary of the Invention [Problem to be solved by the invention]

[0008] Lithium ion secondary batteries and positive electrode active materials used therein still have room for improvement in various aspects, such as charge / discharge capacity, cycle characteristics, reliability, safety, and cost.

[0009] An object of the present invention is to provide a positive electrode active material or composite oxide that, when used in a lithium ion secondary battery, suppresses a decrease in charge / discharge capacity during charge / discharge cycles. Another object is to provide a positive electrode active material or composite oxide that is resistant to collapse of its crystal structure even after repeated charge / discharge. Another object is to provide a positive electrode active material or composite oxide that has a large charge / discharge capacity. Another object is to provide a secondary battery that is safe or highly reliable.

[0010] Another object of the present invention is to provide a positive electrode active material, a composite oxide, a secondary battery, or a manufacturing method thereof.

[0011] Note that the description of these problems does not preclude the existence of other problems. Note that one embodiment of the present invention does not necessarily solve all of these problems. Note that problems other than these can be extracted from the description of the specification, drawings, and claims. [Means for solving the problem]

[0012] One aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 200 mA / g to a voltage of 4.6 V in a 25°C environment or a 45°C environment, followed by constant voltage charging at a voltage of 4.6 V until the charging current becomes 20 mA / g, and then discharged at a constant current of 200 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0013] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is subjected to a test in which the test battery is charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) until the voltage reaches 4.6 V in a 25°C environment or a 45°C environment, and then is charged at a constant voltage until the charge rate reaches 0.05 C at a voltage of 4.6 V, and then is discharged at a constant current at a discharge rate of 0.5 C until the voltage reaches 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0014] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 100 mA / g to a voltage of 4.6 V in a 25°C environment or a 45°C environment, followed by constant voltage charging at a voltage of 4.6 V until the charging current becomes 10 mA / g, and then discharged at a constant current of 100 mA / g to a voltage of 2.5 V, repeating this charge / discharge cycle 50 times, and measuring the discharge capacity for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0015] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 200 mA / g to a voltage of 4.65 V in an environment of 25°C, then charged at a constant voltage of 4.65 V until the charging current becomes 20 mA / g, and then discharged at a constant current of 200 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0016] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is subjected to a test in which the test battery is charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) until the voltage reaches 4.65 V in an environment of 25°C, then charged at a constant voltage until the charge rate reaches 0.05 C at a voltage of 4.65 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reaches 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0017] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 100 mA / g to a voltage of 4.65 V in an environment of 25°C, then charged at a constant voltage of 4.65 V until the charging current becomes 10 mA / g, and then discharged at a constant current of 100 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0018] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 200 mA / g to a voltage of 4.7 V in an environment of 25°C, then charged at a constant voltage of 4.7 V until the charging current becomes 20 mA / g, and then discharged at a constant current of 200 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0019] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is subjected to a test in which the test battery is charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) until the voltage reaches 4.7 V in an environment of 25°C, then charged at a constant voltage until the charge rate reaches 0.05 C at a voltage of 4.7 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reaches 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0020] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 100 mA / g to a voltage of 4.7 V in an environment of 25°C, then charged at a constant voltage of 4.7 V until the charging current becomes 10 mA / g, and then discharged at a constant current of 100 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0021] In the present invention, when a test battery is subjected to 50 repeated charge / discharge cycles in a 25°C environment and a 45°C environment and the discharge capacity is measured for each cycle, it is preferable that the discharge capacity measured at the 50th cycle be 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0022] In the present invention, it is preferable that the value of the discharge capacity measured at the 50th cycle is 95% or more of the maximum value of the discharge capacity over all 50 cycles.

[0023] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is subjected to a test in which the test battery is charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) until the voltage reaches 4.65 V in an environment of 25°C, then charged at a constant voltage until the charge rate reaches 0.05 C at a voltage of 4.65 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reaches 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 85% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0024] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 100 mA / g to a voltage of 4.65 V in an environment of 25°C, then charged at a constant voltage of 4.65 V until the charging current becomes 10 mA / g, and then discharged at a constant current of 100 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 85% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0025] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is subjected to a test in which the test battery is charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) until the voltage reaches 4.7 V in an environment of 25°C, then charged at a constant voltage until the charge rate reaches 0.05 C at a voltage of 4.7 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reaches 2.5 V, repeating this charge and discharge cycle 50 times, and measuring the discharge capacity for each cycle. The discharge capacity measured in the 50th cycle is 80% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0026] Another aspect of the present invention is a battery having a positive electrode and a negative electrode, in which the positive electrode of the battery is used as the positive electrode of a test battery whose negative electrode is made of lithium metal, and the test battery is charged at a constant current of 100 mA / g to a voltage of 4.7 V in an environment of 25°C, then charged at a constant voltage of 4.7 V until the charging current becomes 10 mA / g, and then discharged at a constant current of 100 mA / g to a voltage of 2.5 V. This charge-discharge cycle is repeated 50 times, and the discharge capacity is measured for each cycle. The discharge capacity measured in the 50th cycle is 80% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

[0027] In the present invention, the test battery is preferably a coin-type half cell.

[0028] In the present invention, the positive electrode preferably contains a layered rock salt type positive electrode active material.

[0029] In the present invention, the positive electrode active material preferably contains lithium cobalt oxide.

[0030] The present invention also provides an electronic device or a vehicle equipped with the above battery. [Effects of the Invention]

[0031] The present invention can provide a positive electrode active material or composite oxide that, when used in a lithium ion secondary battery, suppresses a decrease in charge / discharge capacity during charge / discharge cycles. Alternatively, it can provide a positive electrode active material or composite oxide that is resistant to collapse of its crystal structure even after repeated charge / discharge cycles. Alternatively, it can provide a positive electrode active material or composite oxide that has a large charge / discharge capacity. Alternatively, it can provide a secondary battery that is highly safe and reliable.

[0032] The present invention also provides a positive electrode active material, a secondary battery, or a method for producing the same.

[0033] Note that the description of these effects does not preclude the existence of other effects. Note that one embodiment of the present invention does not necessarily have all of these effects. Note that effects other than these will become apparent from the description in the specification, drawings, claims, etc., and it is possible to extract other effects from the description in the specification, drawings, claims, etc. [Brief explanation of the drawings]

[0034] 1A to 1C are diagrams illustrating a method for producing a positive electrode active material. FIG. 2 is a diagram illustrating a method for producing a positive electrode active material. 3A to 3C are diagrams illustrating a method for producing a positive electrode active material. FIG. 4A is a cross-sectional view of the positive electrode active material, and FIGS. 4B1 to 4C2 are partial cross-sectional views of the positive electrode active material. 5A and 5B are cross-sectional views of the positive electrode active material, and FIGS. 5C1 and 5C2 are partial cross-sectional views of the positive electrode active material. FIG. 6 is a cross-sectional view of the positive electrode active material. FIG. 7 is a cross-sectional view of the positive electrode active material. FIG. 8 is a diagram illustrating the depth of charge and the crystal structure of the positive electrode active material. FIG. 9 shows the XRD pattern calculated from the crystal structure. FIG. 10 is a diagram illustrating the state of charge and the crystal structure of the positive electrode active material of the comparative example. FIG. 11 shows the XRD pattern calculated from the crystal structure. 12A and 12B are diagrams showing XRD patterns calculated from the crystal structure. 13A to 13C show the lattice constants calculated from XRD. 14A to 14C show the lattice constants calculated from XRD. Figure 15 is an example of a TEM image in which the crystal orientations are roughly consistent. Figure 16A is an example of a STEM image in which the crystal orientations are roughly consistent, Figure 16B is an FFT of a region of the rock-salt-type crystal RS, and Figure 16C is an FFT of a region of the layered rock-salt-type crystal LRS. 17A and 17B are cross-sectional views of an active material layer in which a graphene compound is used as the conductive agent. 18A and 18B are diagrams illustrating an example of a secondary battery. 19A to 19C are diagrams illustrating an example of a secondary battery. 20A and 20B are diagrams illustrating an example of a secondary battery. 21A to 21C are diagrams illustrating a coin-type secondary battery. 22A to 22D are diagrams illustrating a cylindrical secondary battery. 23A and 23B are diagrams illustrating an example of a secondary battery. 24A to 24D are diagrams illustrating an example of a secondary battery. 25A and 25B are diagrams illustrating an example of a secondary battery. FIG. 26 is a diagram illustrating an example of a secondary battery. 27A to 27C are diagrams illustrating a laminated secondary battery. 28A and 28B are diagrams illustrating a laminated secondary battery. FIG. 29 is a diagram showing the appearance of a secondary battery. FIG. 30 is a diagram showing the appearance of a secondary battery. 31A to 31C are diagrams illustrating a method for manufacturing a secondary battery. 32A to 32H are diagrams illustrating an example of an electronic device. 33A to 33C are diagrams illustrating an example of an electronic device. FIG. 34 is a diagram illustrating an example of an electronic device. 35A to 35D are diagrams illustrating an example of an electronic device. 36A to 36C are diagrams showing an example of an electronic device. 37A to 37C are diagrams illustrating an example of a vehicle. 38A and 38B are graphs showing cycle characteristics. 39A and 39B are graphs showing cycle characteristics. 40A and 40B are graphs showing cycle characteristics. FIG. 41 is a graph showing cycle characteristics. 42A and 42B are diagrams showing charge and discharge curves. 43A and 43B are diagrams showing charge and discharge curves. 44A and 44B are diagrams showing charge and discharge curves. 45A and 45B are graphs showing cycle characteristics. 46A and 46B are graphs showing cycle characteristics. 47A and 47B are graphs showing cycle characteristics. FIG. 48 is a diagram showing the discharge capacity retention rate relative to the maximum discharge capacity. FIG. 49 is a diagram showing the discharge capacity retention rate relative to the maximum discharge capacity. 50A and 50B are diagrams showing charge and discharge curves. 51A and 51B are diagrams showing charge and discharge curves. 52A and 52B are diagrams showing charge and discharge curves. 53A and 53B are diagrams showing rate characteristics. 54A and 54B are diagrams showing rate characteristics. 55A and 55B are diagrams showing rate characteristics. 56A and 56B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. 57A and 57B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. FIG. 58 is a diagram showing the relationship between the measured temperature and the charge / discharge voltage. 59A and 59B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. 60A and 60B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. FIG. 61 is a diagram showing the relationship between the measured temperature and the charge / discharge voltage. 62A and 62B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. 63A and 63B are diagrams showing the relationship between the measured temperature and the charge / discharge voltage. FIG. 64 is a diagram showing the relationship between the measured temperature and the charge / discharge voltage. 65A and 65B are diagrams showing charging curves versus measured temperatures. 66A and 66B are diagrams showing charging curves versus measured temperatures. FIG. 67 shows a charging curve versus the measured temperature. 68A and 68B are diagrams showing charging curves versus measured temperatures. 69A and 69B are diagrams showing charge curves versus measured temperatures. FIG. 70 shows a charging curve versus the measured temperature. 71A and 71B are diagrams showing charge curves versus measured temperatures. 72A and 72B are diagrams showing charging curves versus measured temperatures. FIG. 73 shows a charging curve versus the measured temperature. FIG. 74 is a graph showing the discharge capacity retention rate versus the measurement temperature. FIG. 75 is a diagram showing the state of charge versus the measured temperature. FIG. 76 is a conceptual diagram showing the relationship between the depth of charge and the crystal structure. FIG. 77 is a conceptual diagram showing the change in the crystalline phase inside the active material particles as the charge-discharge cycle progresses. FIG. 78 shows the cycle characteristics, maximum discharge capacity, and discharge capacity retention rate of a full cell. FIG. 79 shows the cycle characteristics and maximum discharge capacity of a full cell. FIG. 80 shows the cycle characteristics, maximum discharge capacity, and discharge capacity retention rate of a full cell. FIG. 81 shows the cycle characteristics and maximum discharge capacity of a full cell. 82A and 82B are diagrams showing discharge curves versus measurement temperature. 83A and 83B are diagrams showing discharge curves versus measurement temperature. FIG. 84 is a diagram showing the relationship between discharge capacity and measurement temperature. 85A and 85B are diagrams showing the relationship between the gravimetric energy density and the measured temperature. FIG. 86 is a diagram showing the relationship between the gravimetric energy density and the measurement temperature. FIG. 87 is a diagram showing a discharge curve versus measurement temperature. FIG. 88 is a diagram showing a discharge curve versus measurement temperature. 89A and 89B are diagrams showing the relationship between discharge capacity and rate. 90A and 90B are diagrams showing discharge curves with respect to rate. 91A and 91B are diagrams showing the relationship between discharge capacity and rate. 92A and 92B are graphs showing the relationship between gravimetric energy density and rate. 93A and 93B are diagrams showing the relationship between gravimetric energy density and rate. 94A and 94B are graphs showing discharge curves with respect to rate. FIG. 95 is a diagram showing a discharge curve. DETAILED DESCRIPTION OF THE INVENTION

[0035] Hereinafter, examples of embodiments of the present invention will be described with reference to the drawings, etc. However, the present invention should not be construed as being limited to the following examples. The embodiments of the present invention can be modified within the scope of the spirit of the present invention.

[0036] In this specification and the like, crystal planes and crystal directions are expressed using Miller indices. Individual planes indicating crystal planes are expressed using ( ). In crystallography, crystal planes, crystal directions, and space groups are expressed by adding a superscript bar to the number, but in this specification and the like, due to formatting restrictions, the number may be expressed by adding a - (minus sign) before it instead of adding a bar above it.

[0037] In this specification, the theoretical capacity of a positive electrode active material refers to the amount of electricity when all of the intercalable lithium contained in the positive electrode active material is deintercalated. For example, the theoretical capacity of LiCoO2 is 274 mAh / g, the theoretical capacity of LiNiO2 is 274 mAh / g, and the theoretical capacity of LiMn2O4 is 148 mAh / g.

[0038] In this specification and the like, the depth of charge is used as an index in which 0 is defined as when all intercalable and deintercalable lithium has been intercalated, and 1 is defined as when all intercalable and deintercalable lithium contained in the positive electrode active material has been deintercalated.

[0039] In this specification, the depth of charge is a value that indicates the amount of capacity that has been charged based on the theoretical capacity of the positive electrode active material, in other words, the amount of lithium that has been released from the positive electrode. For example, lithium cobalt oxide (LiCoO2) and lithium nickel-cobalt-manganese oxide (LiNi x Co y Mn z In the case of a positive electrode active material with a layered rock salt structure such as O2 (x+y+z=1), based on the theoretical capacity of 274 mAh / g, a charge depth of 0 refers to a state in which no Li has been released from the positive electrode active material, a charge depth of 0.5 refers to a state in which lithium equivalent to 137 mAh / g has been released from the positive electrode, and a charge depth of 0.8 refers to a state in which lithium equivalent to 219.2 mAh / g has been released from the positive electrode.

[0040] In this specification, Li x The value of x in CoO2 can be used as an indicator of how much lithium remains in the positive electrode active material and can be inserted and removed. Co is replaced by a transition metal M that is oxidized and reduced as lithium is inserted and removed, and Li x It can also be written as MO2. x can be calculated by (theoretical capacity - charge capacity) / theoretical capacity. Note that when calculating x, charge capacity can be read as discharge capacity. For example, when a secondary battery using LiCoO2 as the positive electrode active material is charged at 219.2 mAh / g, x = 0.2. The state of x = 0.2 can be said to be the same as the state where the depth of charge is 0.8. A small x in LixCoO2 means, for example, that it is 0.1 <x≦0.24をいう。

[0041] It is preferable to measure the charge capacity used to calculate x under conditions where there is little or no influence of short circuit and / or decomposition of the electrolyte. For example, data from a secondary battery that has experienced a sudden change in capacity that is considered to be due to a short circuit should not be used to calculate x. The same applies when using discharge capacity to calculate x.

[0042] The positive electrode active material is difficult to absorb lithium beyond the stoichiometric ratio, and when lithium stops absorbing, the voltage of the secondary battery drops sharply. This is the end of discharge for the secondary battery. When discharge is complete, lithium cobalt oxide is in a state where no lithium can be absorbed, and x can be considered to be 1 in LixCoO2. In lithium-ion secondary batteries that use lithium cobalt oxide as the positive electrode, discharge is said to be complete when the voltage drops below 2.5 V (lithium counter electrode) at a current of 100 mA / g.

[0043] (Embodiment 1) In this embodiment, a method for manufacturing a positive electrode active material, which is one embodiment of the present invention, will be described.

[0044] <<Method 1 for preparing positive electrode active material>> <Step S11> In step S11 shown in FIG. 1A, a lithium source (referred to as Li source in the drawing) and a transition metal source (referred to as M source in the drawing) are prepared as starting materials (also referred to as starting raw materials) for the lithium material and the transition metal material, respectively.

[0045] The lithium source is preferably a compound containing lithium, such as lithium carbonate, lithium hydroxide, lithium nitrate, or lithium fluoride. The lithium source is preferably of high purity, and for example, a material with a purity of 99.99% or higher may be used.

[0046] The transition metal can be selected from elements in Groups 3 to 11 of the periodic table, and for example, at least one of manganese, cobalt, and nickel is used. The transition metal may be only cobalt, only nickel, two elements (cobalt and manganese), two elements (cobalt and nickel), or three elements (cobalt, manganese, and nickel). When only cobalt is used, the positive electrode active material obtained by this preparation method has lithium cobalt oxide (also referred to as LCO). When three elements (cobalt, manganese, and nickel) are used, the positive electrode active material obtained has lithium nickel-cobalt-manganese oxide (also referred to as NCM).

[0047] When two or more transition metal sources are used, the two or more transition metal sources are preferably prepared in a ratio (mixing ratio) that allows the two or more transition metal sources to form a layered rock salt type crystal structure.

[0048] As the transition metal source, it is preferable to use a compound containing the above transition metal, and for example, an oxide or hydroxide of the metal exemplified as the above transition metal can be used. As a cobalt source, cobalt oxide or cobalt hydroxide can be used. As a manganese source, manganese oxide or manganese hydroxide can be used. As a nickel source, nickel oxide or nickel hydroxide can be used. As an aluminum source, aluminum oxide or aluminum hydroxide can be used.

[0049] The transition metal source preferably has a high purity, for example, a material with a purity of 3N (99.9%) or higher, preferably 4N (99.99%) or higher, more preferably 4N (99.995%) or higher, and even more preferably 5N (99.999%) or higher. By using a high-purity material, impurities in the positive electrode active material can be controlled. As a result, the capacity and / or reliability of the secondary battery can be increased.

[0050] In addition, it is preferable that the transition metal source has high crystallinity, for example, single crystal grains. The crystallinity of the transition metal source can be evaluated using TEM (Transmission Electron Microscope) images, STEM (Scanning Transmission Electron Microscope) images, HAADF-STEM (High-Angle Annular Dark Field Scanning TEM) images, ABF-STEM (Annular Bright-Field Scanning Transmission Electron Microscope) images, or X-ray diffraction (XRD), electron diffraction, neutron diffraction, etc. Note that the above-mentioned crystallinity evaluation techniques can be applied not only to the evaluation of the crystallinity of the transition metal source, but also to the evaluation of the crystallinity of the positive electrode active material, etc.

[0051] <Step S12> Next, in step S12 shown in FIG. 1A, the lithium source and the transition metal source are pulverized and mixed to prepare a mixed material (also referred to as a mixture). The pulverization and mixing can be performed by either a dry or wet method. The wet method is preferred because it allows for finer pulverization. When using the wet method, a solvent is prepared. Examples of solvents that can be used include ketones such as acetone, alcohols such as ethanol and isopropanol, ether, dioxane, acetonitrile, and N-methyl-2-pyrrolidone (NMP). It is more preferable to use an aprotic solvent that is less likely to react with lithium. In this embodiment, dehydrated acetone or super-dehydrated acetone with a purity of 99.5% or higher is used. It is preferable to mix the lithium source and the transition metal source in super-dehydrated acetone with a purity of 99.5% or higher, with a water content reduced to 10 ppm or less, and then pulverize and mix them. Using dehydrated acetone or super-dehydrated acetone with the above purity can reduce impurities that may be mixed into the mixed material.

[0052] A ball mill, a bead mill, or the like can be used as a means for mixing, etc. When using a ball mill, alumina balls or zirconia balls are preferably used as the grinding media. Zirconia balls are preferred because they emit less impurities. Furthermore, when using a ball mill, a bead mill, or the like, the peripheral speed should be set to 100 mm / s or more and 2000 mm / s or less to suppress contamination from the grinding media. For example, mixing should be performed at a peripheral speed of 838 mm / s (rotation speed 400 rpm, ball mill diameter 40 mm).

[0053] <Step S13> Next, in step S13 shown in FIG. 1A, the mixed material is heated. The heating temperature is preferably 800°C to 1100°C, more preferably 900°C to 1000°C, and even more preferably about 950°C. If the temperature is too low, the decomposition and melting of the lithium source and transition metal source may be insufficient. On the other hand, if the temperature is too high, defects may occur due to lithium evaporation or sublimation from the lithium source and / or excessive reduction of the metal used as the transition metal source. For example, when cobalt is used as the transition metal, such defects may be oxygen defects induced by excessive reduction of cobalt from trivalent to divalent.

[0054] The heating time is preferably from 1 hour to 100 hours, more preferably from 2 hours to 20 hours.

[0055] The temperature rise rate depends on the heating temperature reached, but should be between 80°C / h and 250°C / h. For example, if heating at 1000°C for 10 hours, the temperature should be raised at 200°C / h.

[0056] Heating is preferably carried out in an atmosphere with little moisture, such as dry air, for example, an atmosphere with a dew point of -50°C or less, more preferably an atmosphere with a dew point of -80°C or less. In this embodiment, heating is carried out in an atmosphere with a dew point of -93°C. In addition, to suppress impurities that may be mixed into the mixed material, the concentrations of impurities such as CH4, CO, CO2, and H2 in the heating atmosphere should each be 5 ppb (parts per billion) or less.

[0057] An oxygen-containing atmosphere is preferred as the heating atmosphere. For example, there is a method of continuously introducing dry air into the reaction chamber (also referred to as the heating chamber). In this case, the flow rate of the dry air is preferably 10 L / min. The method of continuously supplying oxygen, such as dry air, into the reaction chamber and having the oxygen flow through the reaction chamber is called flow.

[0058] When the heating atmosphere is an oxygen-containing atmosphere, it is also possible to prevent oxygen from being supplied to the reaction chamber. For example, the reaction chamber may be depressurized and then filled with oxygen to prevent the oxygen from entering or leaving the reaction chamber, which is called purging. For example, the reaction chamber may be depressurized to -970 hPa on a differential pressure gauge and then filled with oxygen to 50 hPa.

[0059] After heating, the material can be cooled naturally, but it is preferable that the time required to cool the material from the specified temperature to room temperature is between 10 and 50 hours. However, cooling to room temperature is not always necessary, as long as the material is cooled to a temperature acceptable for the next step.

[0060] The container used for heating is preferably an aluminum oxide (hereinafter referred to as alumina) crucible or sheath. Alumina crucibles are made of a material that does not easily release impurities. In this embodiment, an alumina crucible with a purity of 99.9% is used. It is preferable to heat the crucible with a lid on, as this can prevent the material from volatilizing or sublimating.

[0061] The heating in this step may be performed using a rotary kiln or a roller hearth kiln. Heating in a rotary kiln may be either a continuous or batch type, and in either type, the material can be heated while being stirred.

[0062] After heating, the material may be crushed and sieved as necessary. When recovering the heated material, it may be transferred from the crucible to a mortar and then recovered. An alumina mortar is preferably used as the mortar. An alumina mortar is a material that does not easily release impurities. Specifically, an alumina mortar with a purity of 90% or more, preferably 99% or more, is used. Note that heating conditions equivalent to those of step S13 can be applied to heating steps other than step S13, which will be described later.

[0063] <Step S14> Through the above steps, LiMO2 (composite oxide or composite oxide containing a transition metal) can be obtained in step S14 shown in FIG. 1A. Although expressed as LiMO2, the composite oxide only needs to have the crystal structure of a lithium composite oxide, and its composition is not strictly limited to Li:M:O=1:1:2. When cobalt is used as the transition metal, it is called a composite oxide containing cobalt and expressed as LiCoO2. The composition is not strictly limited to Li:Co:O=1:1:2.

[0064] Although the composite oxide is produced by the solid phase method in steps S11 to S14, the composite oxide may also be produced by a coprecipitation method or a hydrothermal method.

[0065] <Step S15> Next, in step S15 shown in FIG. 1A, the composite oxide is heated. Because this is the first heating of the composite oxide, the heating in step S15 is sometimes called initial heating. After initial heating, the surface of the composite oxide becomes smooth. A smooth surface refers to a state in which there are few irregularities, the composite oxide is rounded overall, and the corners are also rounded. Furthermore, a state in which there is little foreign matter adhering to the surface is called smooth. Foreign matter is thought to be a cause of irregularities, so it is preferable that it does not adhere to the surface of the composite oxide.

[0066] The initial heating is carried out after the composite oxide is completed. As described above, the initial heating makes the surface smooth, and furthermore, deterioration after charge and discharge can be suppressed.

[0067] In this initial heating, it is not necessary to prepare a lithium compound source, an additive element source, or a fluxing agent.

[0068] The initial heating is performed before step S31 described below, and may be called preheating or pretreatment.

[0069] The lithium source and / or transition metal source prepared in step S11 or the like may contain impurities. The composite oxide completed in step S14 may contain these impurities. It is possible to reduce these impurities by initial heating.

[0070] The heating conditions for the initial heating may be any conditions that result in a smooth surface of the composite oxide. For example, the heating conditions may be selected from those described in step S13. Regarding the heating conditions, the heating temperature for the initial heating may be lower than the temperature for step S13 in order to maintain the crystalline structure of the composite oxide in step S14. Furthermore, the heating time for the initial heating may be shorter than the heating time for step S13 in order to maintain the crystalline structure of the composite oxide in step S14. For example, the heating conditions for the initial heating may be a temperature of 700°C to 1000°C for 2 hours or more.

[0071] The heating in step S13 may cause a temperature difference between the surface and interior of the composite oxide in step S14. This temperature difference may induce a contraction difference. It is thought that the temperature difference causes a difference in fluidity between the surface and interior, resulting in a contraction difference. The energy associated with the contraction difference causes an internal stress difference in the composite oxide. The internal stress difference is also called strain, and this energy is sometimes called strain energy. The internal stress is removed by the initial heating in step S15; in other words, the strain energy is homogenized by the initial heating in step S15. When the strain energy is homogenized, the strain in the composite oxide is alleviated. Therefore, the surface of the composite oxide may become smoother after step S15. This is also referred to as the surface being improved by step S15. In other words, it is thought that the contraction difference that occurred in the composite oxide is alleviated after step S15, resulting in a smoother surface of the composite oxide.

[0072] Furthermore, the shrinkage difference may cause microscopic misalignment, such as crystal misalignment, in the composite oxide in step S14. Initial heating is recommended to reduce this misalignment. After initial heating, it is possible to equalize the misalignment of the composite oxide. When the misalignment is equalized, the surface of the composite oxide may become smooth. This is also referred to as the alignment of crystal grains. In other words, it is believed that after step S15, the misalignment of crystals and other components in the composite oxide is alleviated, resulting in a smoother surface of the composite oxide.

[0073] When a composite oxide with a smooth surface is used as a positive electrode active material, deterioration during charge and discharge in a secondary battery is reduced, and cracking of the positive electrode active material can be suppressed.

[0074] A smooth surface of a complex oxide can be said to have a surface roughness of 10 nm or less when the surface roughness information of a cross section of the complex oxide is quantified from measurement data. The cross section is, for example, a cross section obtained during STEM observation.

[0075] Note that a pre-synthesized composite oxide may be used in step S14. In this case, steps S11 to S13 can be omitted. By performing step S15 on a pre-synthesized composite oxide, a composite oxide with a smooth surface can be obtained.

[0076] It is possible that the lithium in the composite oxide is reduced by the initial heating. The reduced lithium may make it easier for the additive elements, which will be explained in the next step S20, to enter the composite oxide.

[0077] <Step S20> The additive element X may be added to a composite oxide having a smooth surface, as long as it can form a layered rock salt type crystal structure. Adding the additive element X to a composite oxide having a smooth surface allows the additive element X to be added evenly. Therefore, it is preferable to add the additive element X after the initial heating. The step of adding the additive element X will be described with reference to FIG. 1B and FIG. 1C.

[0078] <Step S21> 1B, an additive element source (X source) to be added to the composite oxide is prepared. A lithium source may be prepared together with the additive element source (X source).

[0079] The additive element X can be one or more selected from nickel, cobalt, magnesium, calcium, chlorine, fluorine, aluminum, manganese, titanium, zirconium, yttrium, vanadium, iron, chromium, niobium, lanthanum, hafnium, zinc, silicon, sulfur, phosphorus, boron, and arsenic. The additive element X can also be one or more selected from bromine and beryllium. However, since bromine and beryllium are toxic to living organisms, it is more preferable to use the additive element X described above.

[0080] When magnesium is selected as the additive element X, the additive element source (X source) can be called a magnesium source. As the magnesium source, magnesium fluoride, magnesium oxide, magnesium hydroxide, magnesium carbonate, etc. can be used. Furthermore, a plurality of the above-mentioned magnesium sources may be used.

[0081] When fluorine is selected as the additive element X, the additive element source (X source) can be called a fluorine source. Examples of the fluorine source that can be used include lithium fluoride, magnesium fluoride, aluminum fluoride, titanium fluoride, cobalt fluoride, nickel fluoride, zirconium fluoride, vanadium fluoride, manganese fluoride, iron fluoride, chromium fluoride, niobium fluoride, zinc fluoride, calcium fluoride, sodium fluoride, potassium fluoride, barium fluoride, cerium fluoride, lanthanum fluoride, and sodium aluminum hexafluoride. Among these, lithium fluoride is preferred because it has a relatively low melting point of 848°C and is easily melted in the heating step described below.

[0082] Magnesium fluoride can be used as both a fluorine source and a magnesium source, and lithium fluoride can be used as a lithium source. Another lithium source that can be used in step S21 is lithium carbonate.

[0083] The fluorine source may be a gas, such as fluorine, carbon fluoride, sulfur fluoride, or oxygen fluoride (including those written as OF, OF, OF, OF, OF, OF, or OF), which may be mixed into the atmosphere during the heating step described below. A plurality of the above-mentioned fluorine sources may also be used.

[0084] In this embodiment, lithium fluoride (LiF) is prepared as the fluorine source, and magnesium fluoride (MgF2) is prepared as both the fluorine source and the magnesium source. The melting point is most effectively lowered when lithium fluoride and magnesium fluoride are mixed in a molar ratio of approximately LiF:MgF2 = 65:35. On the other hand, if the amount of lithium fluoride is too high, there is a concern that the lithium content will be excessive, resulting in poor cycle performance. Therefore, the molar ratio of lithium fluoride to magnesium fluoride is preferably LiF:MgF2 = x:1 (0≦x≦1.9), more preferably LiF:MgF2 = x:1 (0.1≦x≦0.5), and even more preferably LiF:MgF2 = x:1 (x = 0.33 or thereabouts). In this specification, "nearby" refers to a value greater than 0.9 times but less than 1.1 times the value.

[0085] <Step S22> 1B, the magnesium source and the fluorine source are pulverized and mixed. This step can be performed under pulverization and mixing conditions selected from those described in step S12.

[0086] If necessary, a heating step may be performed after step S22. The heating step can be performed under heating conditions selected from those described in step S13. The heating time is preferably 2 hours or more, and the heating temperature is preferably 800°C or higher and 1100°C or lower.

[0087] <Step S23> 1B, the pulverized and mixed materials are collected to obtain an additive element source (X source). The additive element source (X source) shown in step S23 contains multiple starting materials and can be called a mixture.

[0088] The particle size of the mixture is preferably a median diameter (D50) of 600 nm to 20 μm, more preferably 1 μm to 10 μm. Even when a single material is used as the additive element source (X source), the median diameter (D50) is preferably 600 nm to 20 μm, more preferably 1 μm to 10 μm.

[0089] Such a finely pulverized mixture (including cases where the additive element X is a single type) can be easily adhered to the surface of the composite oxide particles when mixed with the composite oxide in a subsequent process. Having the mixture adhered uniformly to the surface of the composite oxide is preferable because it facilitates uniform distribution or diffusion of the additive element X (typically fluorine and magnesium) in the surface layer of the composite oxide upon heating. The region where fluorine and magnesium are distributed can also be referred to as the surface layer of the composite oxide. If there is a region in the surface layer that does not contain fluorine or magnesium, it may be difficult to obtain the O3'-type crystal structure described below in the charged state. While fluorine has been used in the explanation, fluorine can also be chlorine, and the term "halogen" can be used to refer to both.

[0090] <Step S21> A step different from that shown in FIG. 1B will be described with reference to FIG. 1C. In step S21 shown in FIG. 1C, four types of additive element sources (X sources) to be added to the composite oxide are prepared. That is, the types of additive element sources shown in FIG. 1C are different from those shown in FIG. 1B. A lithium source may be prepared together with the additive element sources (X sources).

[0091] Four additive element sources (X sources) are prepared: a magnesium source (Mg source), a fluorine source (F source), a nickel source (Ni source), and an aluminum source (Al source). The magnesium source and the fluorine source can be selected from the compounds described in FIG. 1B. Nickel oxide or nickel hydroxide can be used as the nickel source. Aluminum oxide or aluminum hydroxide can be used as the aluminum source.

[0092] <Step S22> and <Step S23> Next, steps S22 and S23 shown in FIG. 1C are similar to the steps described in FIG. 1B.

[0093] <Step S31> 1A, the composite oxide is mixed with an additive element source (X source). The number of atoms A of the transition metal in the composite oxide containing lithium, the transition metal, and oxygen is M and the number of magnesium atoms A in the added element X. Mg The ratio of A M :A Mg = 100:y (0.1 ≦ y ≦ 6), and A M :A Mg It is more preferable that y=100:y (0.3≦y≦3).

[0094] The mixing conditions in step S31 are preferably milder than those in step S12 so as not to destroy the composite oxide particles in step S14. For example, the mixing conditions are preferably lower in rotation speed or shorter in time than in step S12. It can also be said that dry mixing provides milder conditions than wet mixing. For example, a ball mill or a bead mill can be used for mixing. When using a ball mill, it is preferable to use zirconia balls as the grinding media.

[0095] In this embodiment, dry mixing is performed in a ball mill using zirconia balls with a diameter of 1 mm at 150 rpm for 1 hour in a dry room with a dew point of -100°C or higher and -10°C or lower.

[0096] <Step S32> 1A, the mixed materials are collected to obtain a mixture 903. When collecting the materials, they may be crushed and then sieved, if necessary.

[0097] In this embodiment, a method is described in which lithium fluoride as a fluorine source and magnesium fluoride as a magnesium source are added to the composite oxide after initial heating. However, the present invention is not limited to the above method. In step S11, that is, at the stage of the starting materials for the composite oxide, a magnesium source, a fluorine source, etc. can be added to the lithium source and transition metal source (M source). Then, heating is performed in step S13 to obtain LiMO2 doped with magnesium and fluorine. In this case, there is no need to separate the steps S11 to S14 from the steps S21 to S23. This method can be said to be simple and highly productive.

[0098] Alternatively, lithium cobalt oxide to which magnesium and fluorine have been added may be used. If lithium cobalt oxide to which magnesium and fluorine have been added is used, steps S11 to S32 and step S20 can be omitted. This method is simple and has high productivity.

[0099] Alternatively, a magnesium source and a fluorine source may be further added to lithium cobalt oxide to which magnesium and fluorine have been added in advance according to step S20 shown in FIG. 1B, or a magnesium source, a fluorine source, a nickel source, and an aluminum source may be further added according to step S20 shown in FIG. 1C.

[0100] <Step S33> 1A, the mixture 903 is heated under heating conditions selected from those described in step S13. The heating time is preferably 2 hours or more.

[0101] Here, a supplementary note about the heating temperature will be provided. The lower limit of the heating temperature in step S33 must be equal to or higher than the temperature at which the reaction between the composite oxide (LiMO2) and the additive element source proceeds. The temperature at which the reaction proceeds may be any temperature at which mutual diffusion of elements contained in LiMO2 and the additive element source occurs, and may be lower than the melting temperature of these materials. An oxide will be used as an example for explanation, and the melting temperature T m It is known that solid-phase diffusion occurs when the temperature is 0.757 times the normal temperature (Tammann's law). Therefore, the heating temperature in step S33 should be 500° C. or higher.

[0102] Of course, the reaction proceeds more easily at a temperature equal to or higher than the temperature at which at least a portion of mixture 903 melts. For example, when LiF and MgF2 are used as the additive element source (X source), the eutectic point of LiF and MgF2 is around 742°C, so the lower limit of the heating temperature in step S33 is preferably set to 742°C or higher.

[0103] Furthermore, a mixture 903 obtained by mixing so as to achieve a molar ratio of LiCoO2:LiF:MgF2=100:0.33:1 exhibits an endothermic peak at around 830°C in differential scanning calorimetry (DSC measurement). Therefore, the lower limit of the heating temperature is more preferably 830°C or higher.

[0104] A higher heating temperature is preferable because the reaction proceeds more easily, the heating time is shorter, and productivity is higher.

[0105] The upper limit of the heating temperature is below the decomposition temperature of LiMO2 (the decomposition temperature of LiCoO2 is 1130°C). At temperatures close to the decomposition temperature, there is a concern that LiMO2 may decompose, albeit in a small amount. Therefore, a temperature of 1000°C or less is more preferable, a temperature of 950°C or less is even more preferable, and a temperature of 900°C or less is even more preferable.

[0106] Considering these, the heating temperature in step S33 is preferably 500°C to 1130°C, more preferably 500°C to 1000°C, even more preferably 500°C to 950°C, and even more preferably 500°C to 900°C. Also, it is preferably 742°C to 1130°C, more preferably 742°C to 1000°C, even more preferably 742°C to 950°C, and even more preferably 742°C to 900°C. Also, it is preferably 800°C to 1100°C, or 830°C to 1130°C, more preferably 830°C to 1000°C, even more preferably 830°C to 950°C, and even more preferably 830°C to 900°C. The heating temperature in step S33 is preferably lower than that in step S13.

[0107] Furthermore, when the mixture 903 is heated, it is preferable to control the partial pressure of fluorine or fluoride resulting from the fluorine source or the like within an appropriate range.

[0108] In the fabrication method described in this embodiment, some materials, such as LiF, a fluorine source, may function as a flux. This function allows the heating temperature in step S33 to be lower than the decomposition temperature of the composite oxide (LiMO), for example, to a temperature between 742°C and 950°C, allowing magnesium and other additive elements to be distributed in the surface layer, resulting in the fabrication of a positive electrode active material with excellent characteristics.

[0109] However, because LiF has a lower specific gravity in its gaseous state than oxygen, it may volatilize or sublime upon heating. This volatilization or sublimation reduces the amount of LiF in the mixture 903, weakening its function as a flux. Therefore, it is necessary to heat the mixture while suppressing the volatilization or sublimation of LiF. Even if LiF is not used as a fluorine source, the Li on the LiMO2 surface may react with the F fluorine source, producing LiF, which may then volatilize or sublime. Therefore, even if a fluoride with a higher melting point than LiF is used, it is still necessary to suppress the volatilization or sublimation.

[0110] Therefore, it is preferable to heat the mixture 903 in an atmosphere containing LiF, that is, to heat the mixture 903 in a state where the partial pressure of LiF is high in the heating furnace. By heating in this manner, it is possible to suppress the volatilization or sublimation of LiF in the mixture 903.

[0111] The heating in this step is preferably performed so as not to cause adhesion of particles of the mixture 903. If the particles of the mixture 903 adhere to each other during heating, the contact area with oxygen in the atmosphere will decrease and the route along which the additive element X (for example, fluorine) diffuses will be blocked, which may result in poor distribution of the additive element X (for example, magnesium and fluorine) in the surface layer.

[0112] It is also believed that uniform distribution of the additive element X (e.g., fluorine) in the surface layer portion results in a smooth positive electrode active material with few irregularities. Therefore, in order to maintain or further smooth the surface after the heating in step S15 in this process, it is better for the particles of mixture 903 not to stick together.

[0113] Furthermore, when heating in a rotary kiln is applied in step S33, it is preferable to heat the kiln (also referred to as a furnace) while controlling the flow rate of the oxygen-containing atmosphere. For example, it is preferable to reduce the flow rate of the oxygen-containing atmosphere, or to first purge the atmosphere and then not supply oxygen after introducing the oxygen atmosphere into the kiln. Supplying oxygen and letting it flow through the atmosphere may cause the fluorine source to evaporate or sublimate, which is undesirable in terms of maintaining surface smoothness.

[0114] When heating by a roller hearth kiln is applied in step S33, mixture 903 can be heated in an atmosphere containing LiF by placing a lid on a container containing mixture 903, for example.

[0115] Regarding the heating time, the heating time varies depending on conditions such as the heating temperature, the size of the LiMO2 particles in step S14, and the composition. When the particles are small, a lower temperature or a shorter time may be preferable than when the particles are large.

[0116] When the median diameter (D50) of the composite oxide (LiMO2) in step S14 of FIG. 1A is about 12 μm, the heating temperature is preferably, for example, 600° C. or higher and 950° C. or lower. The heating time is preferably, for example, 3 hours or higher, more preferably 10 hours or higher, and even more preferably 60 hours or higher. The temperature-lowering time after heating is preferably, for example, 10 hours or higher and 50 hours or lower.

[0117] On the other hand, when the median diameter (D50) of the composite oxide (LiMO2) in step S14 is about 5 μm, the heating temperature is preferably, for example, 600°C or higher and 950°C or lower. The heating time is preferably, for example, 1 hour or higher and 10 hours or lower, and more preferably about 2 hours. The temperature reduction time after heating is preferably, for example, 10 hours or higher and 50 hours or lower.

[0118] <Step S34> Next, in step S34 shown in FIG. 1A, the heated material is recovered and crushed as necessary to obtain the positive electrode active material 100. At this time, it is preferable to further sieve the recovered particles. Through the above steps, the positive electrode active material 100 according to one embodiment of the present invention can be produced. The positive electrode active material according to one embodiment of the present invention has a smooth surface.

[0119] <<Method 2 for preparing positive electrode active material>> Next, a method for carrying out the present invention, which is different from the positive electrode active material preparation method 1, will be described.

[0120] In FIG. 2, steps S11 to S15 are carried out in the same manner as in FIG. 1A to prepare a composite oxide (LiMO2) with a smooth surface.

[0121] <Step S20a> As described above, the additive element X may be added to the composite oxide within a range that allows the composite oxide to have a layered rock-salt type crystal structure. In the present production method 2, however, a step of adding the additive element X in two or more batches as additive elements X1 and X2 will be described with reference to FIG. 3A as well.

[0122] <Step S21> In step S21 shown in FIG. 3A, a first additive element source is prepared. The first additive element source can be selected from the additive elements X described in step S21 shown in FIG. 1B. For example, one or more selected from magnesium, fluorine, and calcium can be suitably used as the additive element X1. FIG. 3A illustrates an example in which a magnesium source (Mg source) and a fluorine source (F source) are used as the additive element X1.

[0123] Steps S21 to S23 shown in Fig. 3A can be performed under the same conditions as steps S21 to S23 shown in Fig. 1B, as a result of which an additive element source (X1 source) can be obtained in step S23.

[0124] Furthermore, steps S31 to S33 shown in FIG. 2 can be performed in the same manner as steps S31 to S33 shown in FIG. 1A.

[0125] <Step S34a> Next, in step S33, the heated material is recovered to produce a composite oxide containing the additive element X1. To distinguish it from the composite oxide in step S14, the composite oxide in this step may be referred to as the second composite oxide by adding an ordinal number.

[0126] <Step S40> 2, a second additive element source (X2 source) is added. This will be described with reference to FIGS. 3B and 3C.

[0127] <Step S41> In step S41 shown in FIG. 3B, a second additive element source is prepared. The second additive element source can be selected from the additive elements X described in step S21 shown in FIG. 1B and is preferably different from the additive element X1. For example, the additive element X2 can be one or more selected from nickel, titanium, boron, zirconium, and aluminum. FIG. 3B illustrates an example in which nickel and aluminum are used as the additive element X2.

[0128] Steps S41 to S43 shown in Fig. 3B can be performed under the same conditions as steps S21 to S23 shown in Fig. 1B, as a result of which an additive element source (X2 source) can be obtained in step S43.

[0129] 3C shows a modified example of the steps described with reference to FIG. 3B. In step S41 shown in FIG. 3C, a nickel source (Ni source) and an aluminum source (Al source) are prepared, and in step S42a, they are independently pulverized. As a result, in step S43, a plurality of second additive element sources (X2 sources) are prepared. The steps in FIG. 3C differ from those in FIG. 3B in that the additive element X2 is independently pulverized in step S42a.

[0130] <Steps S51 to S54> 2 can be performed under the same conditions as steps S31 to S34 shown in FIG. 1A. The conditions for step S53, which is a heating step, can be a lower temperature and a shorter time than those for step S33. Through the above steps, in step S54, a positive electrode active material 100 according to one embodiment of the present invention can be produced.

[0131] 2 and 3, in the preparation method 2, the additive element X is introduced into the composite oxide separately as a first additive element X1 and a second additive element X2. By introducing the elements separately, the depth profile of each additive element X can be changed. For example, it is possible to profile the first additive element X1 so that its concentration is higher in the surface layer portion than in the interior, and profile the second additive element X2 so that its concentration is higher in the interior than in the surface layer portion.

[0132] In this production method 2 as well, a positive electrode active material with a smooth surface can be obtained after the initial heating.

[0133] In the preparation methods 1 and 2 described in this embodiment, the initial heating is performed on the composite oxide. Therefore, the initial heating is preferably performed under conditions that are lower than the heating temperature required to obtain the composite oxide and shorter than the heating time required to obtain the composite oxide. When an additional element X is added to the composite oxide, it is preferable to perform the addition step after the initial heating. This addition step can be performed in two or more steps. Following this order of steps is preferable because the smoothness of the surface obtained by the initial heating is maintained.

[0134] In this embodiment, when the composite oxide contains cobalt as a transition metal, it can be read as a composite oxide containing cobalt.

[0135] In this embodiment, the composite oxide before containing the additive element may be referred to as a first composite oxide, and the composite oxide containing the additive element may be referred to as a second composite oxide to distinguish them.

[0136] In the present embodiment, the obtained positive electrode active material may be referred to as a composite oxide. When distinguished as above, the positive electrode active material may be referred to as a second composite oxide.

[0137] This embodiment can be used in combination with other embodiments.

[0138] (Embodiment 2) In this embodiment, a positive electrode active material of one embodiment of the present invention will be described with reference to FIGS.

[0139] Fig. 4A is a cross-sectional view of a positive electrode active material 100 according to one embodiment of the present invention. Enlarged views of the vicinity of AB in Fig. 4A are shown in Fig. 4B1 and Fig. 4B2. Enlarged views of the vicinity of CD in Fig. 4A are shown in Fig. 4C1 and Fig. 4C2.

[0140] 4A to 4C2, the positive electrode active material 100 has a surface layer portion 100a and an interior portion 100b. In these figures, the boundary between the surface layer portion 100a and the interior portion 100b is indicated by a dashed line. Also, in Fig. 4A, a portion of the crystal grain boundary is indicated by a dashed line.

[0141] In this specification, the surface layer 100a of the positive electrode active material 100 refers to, for example, a region within 50 nm from the surface toward the interior, more preferably within 35 nm from the surface toward the interior, even more preferably within 20 nm from the surface toward the interior, and most preferably within 10 nm from the surface toward the interior. Surfaces formed by cracks may also be referred to as the surface. The surface layer 100a may also be referred to as the near-surface, near-surface region, or shell. The region deeper than the surface layer 100a of the positive electrode active material is referred to as the interior 100b. The interior 100b may also be referred to as the interior region or core.

[0142] The surface layer 100a preferably has a higher concentration of the additive element X than the inner portion 100b. The additive element X preferably has a concentration gradient. When there are multiple additive elements X, it is preferable that the positions of the peak tops showing the maximum concentrations differ depending on the additive element X.

[0143] For example, a case where the additional element Xa and the additional element Xb are included will be described. The additional element Xa preferably has a concentration gradient that increases from the interior 100b toward the surface, as shown by the gradation in FIG. 4B1. Examples of the additional element Xa that preferably has such a concentration gradient include magnesium, fluorine, titanium, silicon, phosphorus, boron, and calcium.

[0144] The additional element Xb, which is different from the additional element Xa, preferably has a concentration gradient as shown by the gradation in FIG. 4B2, and the peak top showing the maximum concentration is located in a region deeper than that shown in FIG. 4B1. The peak top of the additional element Xb may be located in the surface layer portion 100a or may be deeper than the surface layer portion 100a. In other words, the additional element Xb preferably has a peak top in a region other than the outermost surface side. For example, the additional element Xb preferably has a peak top in a region 5 nm to 30 nm from the surface toward the interior. Examples of the additional element Xb that preferably have such a concentration gradient include aluminum and manganese.

[0145] Furthermore, it is preferable that the crystal structure continuously changes from the interior 100b toward the surface due to the concentration gradient of the added element as described above.

[0146] The positive electrode active material 100 contains lithium, a transition metal M, oxygen, and an additive element X. The positive electrode active material 100 may be said to be a composite oxide represented by LiMO2 to which the additive element X has been added. However, the positive electrode active material of one embodiment of the present invention is only required to have the crystal structure of a lithium composite oxide represented by LiMO2, and its composition is not strictly limited to Li:M:O=1:1:2. Furthermore, a positive electrode active material to which the additive element X has been added may also be referred to as a composite oxide or a lithium composite oxide.

[0147] The transition metal M contained in the positive electrode active material 100 is preferably a metal that can form a layered rock-salt composite oxide belonging to the space group R-3m with lithium. For example, at least one of manganese, cobalt, and nickel can be used. That is, the transition metal M contained in the positive electrode active material 100 may be cobalt alone, nickel alone, a combination of cobalt and manganese, or a combination of cobalt and nickel, or three of cobalt, manganese, and nickel. That is, the positive electrode active material 100 may contain a composite oxide containing lithium and the transition metal M, such as lithium cobalt oxide, lithium nickel oxide, lithium cobalt oxide in which some of the cobalt is substituted with manganese, lithium cobalt oxide in which some of the cobalt is substituted with nickel, or nickel-manganese-lithium cobalt oxide.

[0148] In particular, using 75 atomic % or more, preferably 90 atomic % or more, and more preferably 95 atomic % or more of cobalt as the transition metal M in the positive electrode active material 100 has many advantages, such as relatively easy synthesis and handling, and excellent cycle characteristics. Furthermore, containing nickel in addition to the cobalt in the above range as the transition metal M can sometimes suppress the deviation of the layered structure consisting of cobalt and oxygen octahedra. This is preferable because it can sometimes make the crystal structure more stable, especially in the charged state at high temperatures.

[0149] The transition metal M does not necessarily have to contain manganese. By making the cathode active material 100 substantially manganese-free, the above-mentioned advantages of relatively easy synthesis and handling, and excellent cycle characteristics, may be enhanced. The weight of manganese contained in the cathode active material 100 is preferably, for example, 600 ppm or less, more preferably 100 ppm or less. The weight of manganese can be analyzed, for example, using glow discharge mass spectrometry (GD-MS).

[0150] On the other hand, when nickel is used as the transition metal M in the positive electrode active material 100 at 33 atomic % or more, preferably at 60 atomic % or more, and more preferably at 80 atomic % or more, the raw material may be cheaper than when cobalt is used in large amounts, and the charge / discharge capacity per weight may increase, which is preferable.

[0151] The transition metal M does not necessarily have to contain nickel.

[0152] The additive element X contained in the positive electrode active material 100 is preferably at least one of magnesium, fluorine, aluminum, titanium, zirconium, vanadium, iron, chromium, niobium, cobalt, arsenic, zinc, silicon, sulfur, phosphorus, and boron. These additive elements X may further stabilize the crystalline structure of the positive electrode active material 100, as described below. Specifically, the positive electrode active material 100 may include lithium cobalt oxide doped with magnesium and fluorine, lithium cobalt oxide doped with magnesium, fluorine, and titanium, lithium nickel-cobalt oxide doped with magnesium and fluorine, lithium cobalt-aluminate doped with magnesium and fluorine, nickel-cobalt-aluminate doped with magnesium and fluorine, nickel-cobalt-aluminate doped with magnesium and fluorine, and nickel-manganese-cobalt oxide doped with magnesium and fluorine. In this specification and the like, the additive element X may be referred to as a mixture, a part of a raw material, an impurity element, or the like.

[0153] The additional element X does not necessarily have to include magnesium, fluorine, aluminum, titanium, zirconium, vanadium, iron, chromium, niobium, cobalt, arsenic, zinc, silicon, sulfur, phosphorus, or boron.

[0154] In the positive electrode active material 100 according to one embodiment of the present invention, the surface layer 100a having a high concentration of the additive element X, i.e., the outer periphery of the particle, reinforces the positive electrode active material 100 so that the layered structure consisting of the transition metal M and oxygen octahedra is not destroyed even when lithium is released from the positive electrode active material 100 upon charging.

[0155] Furthermore, it is preferable that the concentration gradient of the additive element X be the same throughout the entire surface layer portion 100a. It can be said that it is preferable that the reinforcement resulting from the high concentration of the additive element is uniformly present in the surface layer portion 100a. Even if a portion of the surface layer portion 100a is reinforced, if there is a portion without reinforcement, stress may be concentrated in the unreinforced portion. If stress is concentrated in a portion of the particle, defects such as cracks may occur, which may lead to breakage of the positive electrode active material and a decrease in charge / discharge capacity.

[0156] In this specification, "homogeneous" refers to the phenomenon in which a certain element (e.g., A) is distributed with similar characteristics in a specific region in a solid composed of multiple elements (e.g., A, B, C). It is sufficient that the concentration of the element in each specific region is substantially the same. For example, it is sufficient that the difference in element concentration between each specific region is within 10%. Examples of specific regions include a surface layer, a surface, a convex portion, a concave portion, and an interior.

[0157] However, the additive element does not necessarily have to have the same concentration gradient throughout the entire surface layer portion 100a of the positive electrode active material 100. For example, an example of the distribution of additive element Xa near the CD in FIG. 4A is shown in FIG. 4C1, and an example of the distribution of additive element Xb near the CD in FIG. 4C2.

[0158] Here, the area near the CD has an R-3m layered rock-salt crystal structure, and the surface is (001) oriented. The (001)-oriented surface (sometimes referred to as the (001) plane) shown in FIGS. 4C1 and 4C2 may have a different distribution of additive elements than the other planes shown in FIGS. 4B1 and 4B2. For example, the distribution of additive element Xa in the (001) plane and the surface layer 100a including this plane shown in FIG. 4C1 may be shallower than the other planes shown in FIG. 4B1. Alternatively, the concentration of additive element Xa in the (001) plane and the surface layer 100a including this plane shown in FIG. 4C1 may be lower than the other planes shown in FIG. 4B1. Alternatively, the concentration of additive element Xa in the (001) plane and the surface layer 100a including this plane shown in FIG. 4C1 may be below the lower detection limit. Furthermore, for example, the distribution of the additional element Xb in the (001) plane and the surface layer portion 100a including the plane shown in Fig. 4C2 may be shallower than that in the other planes shown in Fig. 4B2. Alternatively, the concentration of the additional element Xb in the (001) plane and the surface layer portion 100a including the plane shown in Fig. 4C2 may be lower than that in the other planes shown in Fig. 4B2. Alternatively, the concentration of the additional element Xb in the (001) plane and the surface layer portion 100a including the plane shown in Fig. 4C2 may be below the lower detection limit.

[0159] In the layered rock-salt crystal structure of R-3m, cations are arranged parallel to the (001) plane. This is because the layered rock-salt crystal structure of R-3m is composed of MO2 layers consisting of transition metal M and oxygen octahedra, and lithium layers, stacked alternately parallel to the (001) plane. Therefore, the diffusion path for lithium ions also exists parallel to the (001) plane.

[0160] The MO2 layer, which is composed of a transition metal M and an oxygen octahedron, is relatively stable, so the (001) plane is a stable plane and no diffusion path for lithium ions is exposed on the (001) plane.

[0161] On the other hand, the diffusion paths of lithium ions are exposed on surfaces other than the (001) plane as shown in Figures 4B1 and 4B2. Therefore, the surfaces other than the (001) plane and the surface layer portion 100a including these surfaces are important regions for maintaining the diffusion paths of lithium ions, but at the same time, they are also regions from which lithium ions are first desorbed and therefore prone to instability. Therefore, reinforcing the surfaces other than the (001) plane and the surface layer portion 100a including these surfaces is extremely important for maintaining the crystal structure of the entire positive electrode active material 100.

[0162] Therefore, in the positive electrode active material 100 according to another embodiment of the present invention, it is important that the distribution of the additional element X in the surface other than the (001) plane and in the surface layer portion 100a including the surface is as shown in Fig. 4B1 or 4B2. On the other hand, in the (001) plane and in the surface layer portion 100a including the (001) plane as shown in Fig. 4C1 and 4C2, the concentration of the additional element may be low or no additional element may be present, as described above.

[0163] In the manufacturing method shown in the previous embodiment, in which high-purity LiMO2 is manufactured, and then the additive element X is mixed therein and heated, the additive element X spreads mainly through the diffusion path of lithium ions, and therefore the distribution of the additive element X in the surface other than the (001) plane and in the surface layer portion 100a including the surface can be easily controlled to a preferred range.

[0164] Furthermore, in the fabrication method that involves initial heating, it is expected that lithium atoms in the surface layer will be desorbed from LiMO2 by the initial heating, which is thought to make it easier to distribute magnesium atoms and other additive elements X in high concentrations in the surface layer.

[0165] Furthermore, while the surface of the positive electrode active material 100 is preferably smooth and minimally uneven, this need not necessarily be the case for the entire surface of the positive electrode active material 100. Composite oxides having an R-3m layered rock salt crystal structure are prone to slippage on planes parallel to the (001) plane, such as the plane where lithium is arranged. When the (001) plane is horizontal, as shown in FIG. 5A, horizontal slippage may occur as indicated by the arrows in FIG. 5B, resulting in deformation, as a result of a pressing process or other process. Pressing may be performed multiple times. The pressing pressure is 100 kN / m to 300 kN / m, preferably 150 kN / m to 250 kN / m, and more preferably 190 kN / m to 230 kN / m. When pressing is performed multiple times, the pressing pressure for the second press is 5 to 8 times, preferably 6 to 7 times, the pressing pressure for the first press.

[0166] In this case, the surface newly formed as a result of the slip and its surface layer 100a may be free of the additional element, or the concentration may be below the detection limit. EF in FIG. 5B is an example of the surface newly formed as a result of the slip and its surface layer 100a. Enlarged views of the vicinity of EF are shown in FIGS. 5C1 and 5C2. Unlike FIGS. 4B1 to 4C2, FIGS. 5C1 and 5C2 do not have a gradation indicating the concentration gradient of the additional element Xa and the additional element Xb.

[0167] However, since slippage tends to occur parallel to the (001) plane, the newly generated surface becomes the (001) plane, and this plane is included in the surface layer portion 100a. Since the (001) plane does not expose the diffusion path of lithium ions and is relatively stable, there is almost no problem even if the added element X does not exist or its concentration is below the detection limit.

[0168] As mentioned above, in a composite oxide with a composition of LiMO2 and a layered rock-salt crystal structure of R-3m, cations are arranged parallel to the (001) plane. Furthermore, in an HAADF-STEM image, the transition metal M, which has the highest atomic number in LiMO2, exhibits the highest brightness. Therefore, in an HAADF-STEM image, the arrangement of bright atoms can be considered to be the arrangement of transition metal M atoms. The repetition of this bright arrangement can be called crystal fringes or lattice fringes. Furthermore, when the crystal structure is a layered rock-salt R-3m structure, the crystal fringes or lattice fringes can be considered to be parallel to the (001) plane.

[0169] The positive electrode active material 100 may have recesses, cracks, dents, or V-shaped cross sections. These are defects, and repeated charge and discharge may cause the defects to leach out the transition metal M, collapse the crystalline structure, crack the positive electrode active material 100, or cause oxygen desorption. However, if a buried portion 102 (FIG. 7) such as that shown in FIG. 4A is present to fill these defects, the leach out of the transition metal M can be suppressed. The buried portion 102 preferably contains an additive element X. The buried portion 102 allows the positive electrode active material 100 to have excellent reliability and cycle characteristics.

[0170] The positive electrode active material 100 may also have protrusions 103 (FIG. 7) as regions where the additional element X is unevenly distributed.

[0171] As described above, an excessive amount of the additive element X contained in the positive electrode active material 100 may adversely affect the insertion and desorption of lithium. Furthermore, when the positive electrode active material 100 is used in a secondary battery, this may result in an increase in internal resistance and a decrease in charge / discharge capacity. On the other hand, an insufficient amount of the additive element X may not be distributed throughout the entire surface layer portion 100a, and the effect of suppressing deterioration of the crystal structure may be insufficient. Thus, the additive element X needs to be present at an appropriate concentration in the positive electrode active material 100, but adjusting this concentration is not easy.

[0172] Therefore, if the positive electrode active material 100 has a region where the additive element X is unevenly distributed, for example, in the surface layer portion 100a, an appropriate concentration of the additive element can be achieved in the interior portion 100b. This makes it possible to suppress an increase in internal resistance and a decrease in charge / discharge capacity when the positive electrode active material 100 is used as a secondary battery. The ability to suppress an increase in internal resistance of a secondary battery is an extremely desirable characteristic, particularly in charge / discharge at high rates, for example, at 2C (1C is defined as 200 mA / g) or higher.

[0173] Furthermore, in the positive electrode active material 100 having a region where the additive element X is unevenly distributed, an appropriate concentration of the additive element can be achieved in the interior 100b, and therefore, mixing of an excess amount of the additive element to some extent is permitted in the manufacturing process, which is preferable because it widens the margin in production.

[0174] In this specification and the like, uneven distribution refers to the concentration of an element in a certain region being different from that in other regions, and may also be referred to as segregation, precipitation, non-uniformity, bias, or the mixture of areas with high concentration and areas with low concentration.

[0175] Magnesium, one of the additive elements X, is divalent and is more stable at the lithium site than at the transition metal site in the layered rock-salt crystal structure, and therefore more likely to enter the lithium site. The presence of magnesium at an appropriate concentration at the lithium site in the surface layer portion 100a facilitates the maintenance of the layered rock-salt crystal structure. Furthermore, the presence of magnesium can suppress the desorption of oxygen around the magnesium at high depths of charge. The presence of magnesium is also expected to increase the density of the positive electrode active material. At an appropriate concentration, magnesium is preferable because it does not adversely affect the intercalation and deintercalation of lithium during charge and discharge. However, excessive magnesium may adversely affect the intercalation and deintercalation of lithium. Therefore, as described below, it is preferable that the concentration of the transition metal M in the surface layer portion 100a is higher than that of magnesium.

[0176] Aluminum, one of the additive elements X, is trivalent and can exist at the transition metal site in the layered rock salt crystal structure. Aluminum can suppress the elution of surrounding cobalt. Furthermore, because aluminum has a strong bond with oxygen, it can suppress the desorption of oxygen from around the aluminum. Therefore, if aluminum is included as the additive element X, it is possible to obtain a positive electrode active material 100 whose crystal structure is resistant to collapse even after repeated charge and discharge.

[0177] Fluorine is a monovalent anion, and when some of the oxygen in the surface layer 100a is replaced by fluorine, the lithium desorption energy decreases. This is because the valence of the cobalt ion changes with lithium desorption, from trivalent to tetravalent in the absence of fluorine, and from divalent to trivalent in the presence of fluorine, resulting in a difference in redox potential. Therefore, when some of the oxygen in the surface layer 100a of the positive electrode active material 100 is replaced by fluorine, it can be said that desorption and insertion of lithium ions near the fluorine easily occurs. Therefore, when used in a secondary battery, charge / discharge characteristics, rate characteristics, etc. are improved, which is preferable.

[0178] Titanium oxide is known to have superhydrophilic properties. Therefore, by using a cathode active material 100 having titanium oxide in the surface layer portion 100a, it is possible that the cathode active material 100 has good wettability with highly polar solvents. When used in a secondary battery, this improves the contact at the interface between the cathode active material 100 and a highly polar electrolyte, which may prevent an increase in internal resistance.

[0179] As the charging voltage of a secondary battery increases, the voltage of the positive electrode generally increases. The positive electrode active material of one embodiment of the present invention has a stable crystal structure even at high voltages. The stable crystal structure of the positive electrode active material in a charged state can suppress a decrease in charge / discharge capacity due to repeated charge / discharge.

[0180] Furthermore, a short circuit in a secondary battery not only causes problems in the charging and / or discharging operations of the secondary battery, but may also lead to heat generation and fire. To achieve a safe secondary battery, it is preferable that the short circuit current be suppressed even at a high charging voltage. The positive electrode active material 100 of one embodiment of the present invention suppresses the short circuit current even at a high charging voltage. Therefore, a secondary battery that achieves both high charge / discharge capacity and safety can be obtained.

[0181] The concentration gradient of the added element X can be evaluated using, for example, energy dispersive X-ray spectroscopy (EDX), electron probe microanalysis (EPMA), etc. Among EDX measurements, EDX area analysis is performed by scanning an area and evaluating the area two-dimensionally. EDX line analysis is performed by scanning a line and evaluating the distribution of atomic concentration within the positive electrode active material particles. Furthermore, data extracted from a linear area of ​​EDX area analysis is sometimes called line analysis. Measurement of a certain area without scanning is called point analysis.

[0182] EDX area analysis (e.g., element mapping) can quantitatively analyze the concentration of the additional element X in the surface layer portion 100a, the interior 100b, the grain boundary 101, and the vicinity thereof of the positive electrode active material 100. Furthermore, EDX line analysis can analyze the concentration distribution and maximum value of the additional element X.

[0183] When EDX analysis is performed on the positive electrode active material 100 having magnesium as the added element X, the maximum peak of the magnesium concentration in the surface layer portion 100a is preferably present at a depth of up to 3 nm from the surface toward the center of the positive electrode active material 100, more preferably at a depth of up to 1 nm, and even more preferably at a depth of up to 0.5 nm.

[0184] Furthermore, in the positive electrode active material 100 having magnesium and fluorine as the added element X, the distribution of fluorine preferably overlaps with the distribution of magnesium. Therefore, when EDX analysis is performed, the maximum peak of the fluorine concentration in the surface layer 100a is preferably present within a depth of 3 nm from the surface toward the center of the positive electrode active material 100, more preferably within a depth of 1 nm, and even more preferably within a depth of 0.5 nm.

[0185] It should be noted that not all of the additive elements X need have the same concentration distribution. For example, when the positive electrode active material 100 contains aluminum as the additive element X, it is preferable that the distribution be slightly different from that of magnesium and fluorine, as described above. For example, when EDX analysis is performed, it is preferable that the maximum peak of the magnesium concentration is closer to the surface than the maximum peak of the aluminum concentration in the surface layer portion 100a. For example, the maximum peak of the aluminum concentration is preferably present at a depth of 0.5 nm to 50 nm from the surface of the positive electrode active material 100, more preferably at a depth of 5 nm to 30 nm. Alternatively, it is preferably present at a depth of 0.5 nm to 30 nm. Alternatively, it is preferably present at a depth of 5 nm to 50 nm.

[0186] Furthermore, when the positive electrode active material 100 is subjected to linear or area analysis, the ratio of the number of atoms of the additive element X to the transition metal M in the surface layer portion 100a (X / M) is preferably 0.05 to 1.00. Furthermore, when the additive element is titanium, the ratio of the number of atoms of titanium to the transition metal M (Ti / M) is preferably 0.05 to 0.4, more preferably 0.1 to 0.3. Furthermore, when the additive element is magnesium, the ratio of the number of atoms of magnesium to the transition metal M (Mg / M) is preferably 0.4 to 1.5, more preferably 0.45 to 1.00. Furthermore, when the additive element is fluorine, the ratio of the number of atoms of fluorine to the transition metal M (F / M) is preferably 0.05 to 1.5, more preferably 0.3 to 1.00.

[0187] The surface of the positive electrode active material 100 based on the EDX analysis results can be estimated, for example, as follows: For an element that is uniformly present in the interior 100b of the positive electrode active material 100, such as oxygen or a transition metal M such as cobalt, the surface is defined as the point where the amount detected in the interior 100b is half that of the amount detected in the interior 100b.

[0188] Since the positive electrode active material 100 is a composite oxide, it is preferable to estimate the surface using the detected amount of oxygen. Specifically, first, the average oxygen concentration O ave At this time, oxygen O, which is thought to be due to chemisorption or background, is found in the area that can be clearly determined to be outside the surface. background If O is detected, the measurement background The average oxygen concentration is calculated by subtracting ave This average value O ave Half the value of, that is, 1 / 2O ave The measurement point showing the measurement value closest to this can be assumed to be the surface of the positive electrode active material.

[0189] The surface can also be estimated using the transition metal M contained in the positive electrode active material 100. For example, if 95% or more of the transition metal M is cobalt, the surface can be estimated in the same manner as above using the detected amount of cobalt. Alternatively, the surface can be estimated in the same manner using the sum of the detected amounts of multiple transition metals M. The detected amount of transition metal M is suitable for estimating the surface because it is less susceptible to the influence of chemical adsorption.

[0190] Furthermore, when the positive electrode active material 100 is subjected to linear or area analysis, the ratio (X / M) of the number of atoms of the additive element X to the transition metal M in the vicinity of the grain boundary 101 is preferably 0.020 or more and 0.50 or less. It is further preferably 0.025 or more and 0.30 or less. It is further preferably 0.030 or more and 0.20 or less. It is also preferably 0.020 or more and 0.30 or less. It is also preferably 0.020 or more and 0.20 or less. It is also preferably 0.025 or more and 0.50 or less. It is also preferably 0.025 or more and 0.20 or less. It is also preferably 0.030 or more and 0.50 or less. It is also preferably 0.030 or more and 0.30 or less.

[0191] For example, when the additive element X is magnesium and the transition metal M is cobalt, the ratio of the number of magnesium atoms to the number of cobalt atoms (Mg / Co) is preferably 0.020 or more and 0.50 or less. It is even more preferably 0.025 or more and 0.30 or less. It is even more preferably 0.030 or more and 0.20 or less. Or it is preferably 0.020 or more and 0.30 or less. Or it is preferably 0.020 or more and 0.20 or less. Or it is preferably 0.025 or more and 0.50 or less. Or it is preferably 0.025 or more and 0.20 or less. Or it is preferably 0.030 or more and 0.50 or less. Or it is preferably 0.030 or more and 0.30 or less.

[0192] In addition, progressive defects (also called pits) may occur in the positive electrode active material 100 when it is charged at 4.5 V or higher, or when it is charged and discharged at high temperatures (45°C or higher). Furthermore, defects such as fissures (also called cracks) may occur due to the expansion and contraction of the positive electrode active material during charging and discharging. Figure 6 shows a schematic cross-sectional view of a positive electrode active material 51. In the positive electrode active material 51, pits 54 and 58 are depicted as holes, but their openings are not circular but have a deep, groove-like shape. The source of the pits may be point defects. Furthermore, it is believed that the crystal structure of LCO collapses near the pits, resulting in a crystal structure different from that of the layered rock salt structure. The collapse of the crystal structure may inhibit the diffusion and release of lithium ions, which are carrier ions, and pits are thought to be a cause of deterioration in cycle characteristics. Cracks 57 are also shown in the positive electrode active material 51. Crystal planes 55 are crystal planes parallel to the cation arrangement, and the positive electrode active material 51 may have recesses 52. Regions 53 and 56 indicate regions where the additive element is present, and region 53 is positioned so as to fill at least recess 52 .

[0193] The positive electrode active materials of lithium-ion secondary batteries are typically LCO and NMC (lithium nickel-manganese-cobalt oxide), which can also be considered composite oxides containing multiple metal elements (e.g., cobalt, nickel, etc.). At least one of these positive electrode active materials may contain defects, and these defects may change before and after charging and discharging. When used in secondary batteries, positive electrode active materials may be chemically or electrochemically corroded by the surrounding environmental substances (e.g., electrolyte), or may even deteriorate. This deterioration does not occur uniformly on the surface of the positive electrode active material, but rather occurs in localized areas. Repeated charging and discharging of the secondary battery can lead to deep defects extending from the surface to the interior.

[0194] The phenomenon in which defects progress and form holes in the positive electrode active material can be called pitting corrosion, and holes generated by pitting corrosion are shown as pits 54 and 58 in FIG.

[0195] In this specification, cracks and pits are different. Immediately after the preparation of the positive electrode active material, cracks may be present but pits are not. Pits can be described as holes formed by the loss of several layers of cobalt and oxygen due to charging and discharging under conditions of high depth of charge, such as high voltage conditions of 4.5 V or higher or high temperature (45°C or higher), or as locations where cobalt has dissolved. Cracks refer to new surfaces formed by the application of physical pressure or fissures caused by the grain boundaries 101 in Figure 4A. Cracks can also occur due to the expansion and contraction of the positive electrode active material caused by charging and discharging. Pits can also occur from cracks and / or cavities within the positive electrode active material.

[0196] The positive electrode active material 100 may have a coating (sometimes referred to as a coating portion) on at least a portion of the surface. An example of the positive electrode active material 100 having a coating 104 is shown in FIG.

[0197] The coating 104 is preferably formed, for example, by the deposition of decomposition products of the electrolyte solution during charge and discharge. In particular, when repeated charging to a high depth of charge is performed, the presence of a coating derived from the electrolyte solution on the surface of the positive electrode active material 100 is expected to improve charge-discharge cycle characteristics. This is due to reasons such as suppressing an increase in impedance on the surface of the positive electrode active material or suppressing the elution of the transition metal M. The coating 104 preferably contains, for example, carbon, oxygen, and fluorine. Furthermore, a high-quality coating is easily obtained when lithium bis(oxalato)borate (LiBOB) and / or SUN (suberonitrile) is used as the electrolyte. Therefore, a coating 104 containing at least one of boron, nitrogen, sulfur, and fluorine may be a high-quality coating and is therefore preferred. Furthermore, the coating 104 does not have to cover the entire positive electrode active material 100.

[0198] <Crystal structure> Materials with a layered rock-salt crystal structure, such as lithium cobalt oxide (LiCoO2), are known to have high discharge capacity and are excellent as positive electrode active materials for secondary batteries. An example of a material with a layered rock-salt crystal structure is the composite oxide represented by LiMO2.

[0199] It is known that the strength of the Jahn-Teller effect in transition metal compounds varies depending on the number of electrons in the d orbital of the transition metal.

[0200] In compounds containing nickel, distortion may occur due to the Jahn-Teller effect. Therefore, when LiNiO2 is charged and discharged to a high depth of charge, there is a concern that the crystal structure may collapse due to distortion. In LiCoO2, the influence of the Jahn-Teller effect is suggested to be small, and the resistance to high depth of charge may be better, so using cobalt as a transition metal is preferable.

[0201] The crystal structure of the positive electrode active material will be described with reference to Figures 8 to 12. Figures 8 to 12 describe the case where cobalt is used as the transition metal M contained in the positive electrode active material.

[0202] <Conventional positive electrode active materials> The positive electrode active material shown in FIG. 10 is lithium cobalt oxide (LiCoO2) to which fluorine and magnesium are not added using the manufacturing method described below. As described in Non-Patent Documents 1 and 2, the crystal structure of lithium cobalt oxide changes. x This shows how the crystal structure of lithium cobalt oxide changes depending on the x in CoO2.

[0203] Figure 10 shows R-3m(O3) and Li x The crystal structure of lithium cobalt oxide with x=1 in CoO2 is shown. x When x = 1 in CoO2, lithium cobalt oxide corresponds to a depth of charge of 0 (discharged state). In this crystal structure, there are three CoO2 layers in the unit cell, with lithium located between the CoO2 layers. Lithium also occupies octahedral sites with six oxygen atoms coordinated. For this reason, this crystal structure is sometimes called an O3-type crystal structure. Note that a CoO2 layer is defined as a structure in which octahedral structures with six oxygen atoms coordinated to cobalt are connected in a plane with edge sharing. This is sometimes called a layer consisting of octahedra of cobalt and oxygen.

[0204] In addition, conventional lithium cobalt oxide is known to have a crystal structure that belongs to the monoclinic space group P2 / m, where the symmetry of lithium increases when x = 0.5. This structure has one CoO2 layer in the unit cell. Therefore, it is sometimes called O1 type or monoclinic O1 type. In Figure 10, P2 / m (monoclinic O1) is added to indicate Li x This shows the crystal structure of lithium cobalt oxide in CoO2 when x=0.5.

[0205] When x = 0, the positive electrode active material has a crystal structure of the trigonal space group P-3m1, and there is also one CoO2 layer in the unit cell. Therefore, this crystal structure is sometimes called O1 type or trigonal O1 type. In addition, the trigonal structure is sometimes converted to a complex hexagonal lattice and called hexagonal O1 type. In Figure 10, P-3m1 (trigonal O1) is added, and Li x This shows the crystal structure of lithium cobalt oxide in CoO2 when x=0.

[0206] Furthermore, conventional lithium cobalt oxide when x is about 0.12 has a crystal structure of the space group R-3m. x When x = 0.12 in CoO2, lithium cobalt oxide corresponds to a charge depth of about 0.8, which is about 80% in percentage terms. This structure can be said to be a structure in which a trigonal O1-type CoO2 structure and an R-3m(O3)-type LiCoO2 structure are alternately stacked. For this reason, this crystal structure is sometimes called an H1-3-type crystal structure. In Figure 10, R-3m(H1-3) is added to indicate Li x This shows the crystal structure of lithium cobalt oxide in CoO2 when x = 0.12. Note that, because actual lithium insertion and desorption can be uneven, the H1-3 crystal structure is experimentally observed from approximately x = 0.25. In reality, the H1-3 crystal structure has twice the number of cobalt atoms per unit cell as other structures. However, in Figure 10 and elsewhere in this specification, to facilitate comparison with other crystal structures, the c-axis of the H1-3 crystal structure is shown as half the unit cell.

[0207] As an example, as described in Non-Patent Document 3, the coordinates of cobalt and oxygen in the unit cell of the H1-3 type crystal structure can be expressed as Co(0, 0, 0.42150±0.00016), O1(0, 0, 0.27671±0.00045), and O2(0, 0, 0.11535±0.00045). O1 and O2 are each oxygen atoms. Thus, the H1-3 type crystal structure is expressed by a unit cell using one cobalt atom and two oxygen atoms. On the other hand, as described below, the O3' type crystal structure of one embodiment of the present invention is preferably expressed by a unit cell using one cobalt atom and one oxygen atom. This indicates that the symmetry between cobalt and oxygen differs between the O3' type structure and the H1-3 type structure, and the O3' type structure changes less from the O3 type structure than the H1-3 type structure. The unit cell that is more preferably used to represent the crystal structure of the positive electrode active material may be selected, for example, so that the GOF (goodness of fit) value is smaller in Rietveld analysis of the XRD pattern.

[0208] The charging voltage is 4.6V (vs Li / Li) based on the redox potential of lithium metal. + ) or Li x When conventional lithium cobalt oxide is repeatedly charged so that x in CoO2 becomes 0.24 or less (this corresponds to a deep charge where the depth of charge becomes 0.8 or more) and then discharged, the crystal structure changes repeatedly (i.e., a non-equilibrium phase change) between the H1-3 type crystal structure and the R-3m(O3) structure in the discharged state.

[0209] However, these two crystal structures have a large deviation in the CoO2 layers. As shown by the dotted lines and arrows in Figure 10, in the H1-3 type crystal structure, the CoO2 layers are significantly deviated from the R-3m(O3) structure. Such dynamic structural changes can adversely affect the stability of the crystal structure.

[0210] Furthermore, the difference in volume between these two crystal structures is large: when compared per the same number of cobalt atoms, the difference in volume between the H1-3 crystal structure and the discharged O3 crystal structure is more than 3.0%, typically more than 3.9%.

[0211] In addition, the H1-3 type crystal structure has a structure in which the CoO2 layers are continuous, but a structure in which the CoO2 layers are continuous also has P-3m1 (trigonal O1), and is therefore likely to be unstable.

[0212] Therefore, when the charge / discharge cycle is repeated to increase the depth of charge or to reduce x to 0.24 or less, the crystalline structure of lithium cobalt oxide breaks down. This break in the crystalline structure causes a deterioration in cycle performance. This is because the number of sites where lithium can exist stably decreases and it becomes difficult for lithium to be inserted and extracted.

[0213] <Positive Electrode Active Material of One Embodiment of the Present Invention> <Crystal structure> The positive electrode active material 100 according to one embodiment of the present invention can reduce the displacement of the CoO layer during repeated charge and discharge cycles that increase the depth of charge. x The change in the crystal structure between the state where x in CoO2 is 1 and the state where x is 0.24 or less is smaller than that of conventional positive electrode active materials. More specifically, the deviation of the CoO2 layer between the discharged state where x is 1 and the charged state where x is 0.24 or less can be reduced. Furthermore, the change in volume compared per cobalt atom can be reduced. Therefore, the positive electrode active material 100 of one embodiment of the present invention is less likely to collapse in crystal structure even when repeatedly charged and discharged so that x is 0.24 or less, and excellent cycle characteristics can be achieved. Furthermore, the positive electrode active material 100 of one embodiment of the present invention is less likely to collapse in crystal structure even when repeatedly charged and discharged so that x is 0.24 or less. x When x in CoO2 is 0.24 or less, the positive electrode active material can have a more stable crystal structure than conventional positive electrode active materials. x When x in CoO2 is kept at 0.24 or less, short circuits in the secondary battery may be less likely to occur, which is preferable because the safety of the secondary battery is further improved in such cases.

[0214] Li x The crystal structure of the interior 100b of the positive electrode active material 100 when x in CoO2 is approximately 1 and 0.2 is shown in Figure 8. The interior 100b occupies the majority of the volume of the positive electrode active material 100 and is the part that contributes greatly to charge and discharge, so it can be said that this is the part where displacement of the CoO2 layer and changes in volume are most problematic.

[0215] The positive electrode active material 100 is a composite oxide containing lithium, cobalt as the transition metal M, and oxygen. In addition to the above, the inner portion 100b preferably contains magnesium as an additive element, and more preferably contains nickel in addition to cobalt as the transition metal M. The surface layer portion 100a preferably contains fluorine as an additive element, and more preferably contains aluminum and / or nickel. Details of the surface layer portion 100a will be described later.

[0216] In FIG. 8, when x = 1, the cathode active material 100 has the same R-3m(O3) crystal structure as conventional lithium cobalt oxide. Meanwhile, when fully charged, the interior 100b of the cathode active material 100 typically has a crystal structure different from the H1-3 crystal structure when x is 0.24 or less, e.g., approximately 0.2 or 0.12. When x = approximately 0.2, the cathode active material 100 of one embodiment of the present invention has a trigonal space group R-3m, with ions such as cobalt and magnesium occupying six oxygen coordination positions. This structure has the same symmetry as the O3 CoO2 layer. Therefore, this structure is referred to herein as the O3' crystal structure and is shown in FIG. 8 with the R-3m(O3') designation. In both the O3 and O3' crystal structures, magnesium is preferably present in a dilute form between the CoO2 layers, i.e., at the lithium sites. It is also preferable that fluorine is present randomly and dilutely at the oxygen sites.

[0217] In the O3'-type crystal structure, a light element such as lithium may occupy the oxygen tetracoordination position.

[0218] In addition, in O3' of FIG. 8, lithium is shown to exist at all lithium sites with a probability of 1 / 5, but the positive electrode active material 100 of one embodiment of the present invention is not limited to this. It may exist unevenly at some lithium sites. For example, Li belonging to the space group P2 / m 0.5 As with CoO2, lithium may be present at some of the ordered lithium sites. The distribution of lithium can be analyzed, for example, by neutron diffraction.

[0219] It can also be said that the O3' type crystal structure is similar to the CdCl2 type crystal structure, although it has random lithium between the layers. This CdCl2 type-like crystal structure was observed when lithium nickel oxide was charged to a charge depth of 0.94 (Li 0.06 The crystal structure is similar to that of lithium cobaltate (NiO2), but it is known that pure lithium cobaltate or layered rock salt-type positive electrode active materials containing a large amount of cobalt do not usually adopt this crystal structure.

[0220] In the cathode active material 100 according to one embodiment of the present invention, the change in the crystal structure when a large amount of lithium is desorbed is suppressed more than in conventional cathode active materials. For example, as shown by the dotted line in Figure 8, there is almost no displacement of the CoO layers in these crystal structures.

[0221] More specifically, the cathode active material 100 of one embodiment of the present invention has a highly stable crystal structure even when a large amount of lithium is desorbed. For example, in conventional cathode active materials, there exists a region of charge voltages where the R-3m(O3) crystal structure can be maintained even at charge voltages where the H1-3 crystal structure is obtained, for example, at a voltage of about 4.6 V relative to the potential of lithium metal. Furthermore, there exists a region where the O3' crystal structure can be obtained even at higher charge voltages, for example, at voltages of 4.65 V or higher and 4.7 V or lower relative to the potential of lithium metal. Furthermore, the H1-3 crystal may not be observed until the charge voltage is further increased. Furthermore, even at lower charge voltages (for example, at a charge voltage of 4.5 V or higher but lower than 4.6 V relative to the potential of lithium metal), the cathode active material 100 of one embodiment of the present invention may be able to obtain the O3' crystal structure.

[0222] Therefore, in the positive electrode active material 100 of one embodiment of the present invention, the crystal structure is not easily broken even when charge and discharge are repeated in such a way that a large amount of lithium is released.

[0223] The space group of a crystal structure is identified by XRD, electron diffraction, neutron diffraction, etc. Therefore, in this specification and the like, "belonging to a certain space group" or "being a certain space group" can be rephrased as "identified with a certain space group."

[0224] Note that when graphite is used as the negative electrode active material in a secondary battery, the voltage of the secondary battery is lower than the above-mentioned value by the potential of the graphite. The potential of graphite is approximately 0.05 V to 0.2 V relative to the potential of lithium metal. Therefore, even when the voltage of a secondary battery using graphite as the negative electrode active material is 4.3 V or higher and 4.5 V or lower, the positive electrode active material 100 of one embodiment of the present invention can maintain the R-3m(O3) crystal structure. Furthermore, even when the charge voltage is higher, for example, when the voltage of the secondary battery is higher than 4.5 V and lower than 4.6 V, the positive electrode active material 100 of one embodiment of the present invention can also adopt the O3'-type crystal structure. Furthermore, even when the charge voltage is lower, for example, when the voltage of the secondary battery is 4.2 V or higher but lower than 4.3 V, the positive electrode active material 100 of one embodiment of the present invention can adopt the O3'-type crystal structure.

[0225] The O3' type crystal structure can be expressed by the coordinates of cobalt and oxygen in the unit cell being Co(0,0,0.5), O(0,0,x), with the range of 0.20≦x≦0.25. The lattice constant of the unit cell is 2.797×10 -1 ≦a≦2.837×10 -1 (nm) is preferred, 2.807 × 10 -1 ≦a≦2.827×10 -1 (nm) is more preferable, and typically a=2.817×10 -1 (nm). The c-axis is 13.681×10 -1 ≦c≦13.881×10 -1 (nm) is preferred, 13.751 × 10 -1 ≦c≦13.811×10 -1 (nm) is more preferable, and typically c=13.781×10-1 (nm).

[0226] An additive element, such as magnesium, randomly and dilutely present between the CoO2 layers, i.e., at the lithium sites, has the effect of suppressing the displacement of the CoO2 layers at high depths of charge. Therefore, the presence of magnesium between the CoO2 layers tends to result in an O3'-type crystal structure. Therefore, it is preferable that magnesium be distributed throughout the positive electrode active material 100 of one embodiment of the present invention. Furthermore, to distribute magnesium throughout the positive electrode active material 100, it is preferable to perform heat treatment during the process of preparing the positive electrode active material 100 of one embodiment of the present invention.

[0227] However, if the heat treatment temperature is too high, cation mixing occurs, increasing the possibility that added elements, such as magnesium, will enter the cobalt site. Magnesium present in the cobalt site will not be effective in maintaining the R-3m structure when a large amount of lithium is released. Furthermore, if the heat treatment temperature is too high, there are concerns that adverse effects such as cobalt being reduced to divalent and lithium evaporating may occur.

[0228] Therefore, it is preferable to add a fluorine compound to the lithium cobalt oxide before the heat treatment for distributing the magnesium. Adding the fluorine compound lowers the melting point of the lithium cobalt oxide. Lowering the melting point makes it easier to distribute the magnesium throughout the positive electrode active material 100 at a temperature where cation mixing is unlikely to occur. Furthermore, the presence of the fluorine compound is expected to improve corrosion resistance against hydrofluoric acid produced by decomposition of the electrolyte.

[0229] Furthermore, by performing the initial heating described above, the distribution of added elements such as magnesium and aluminum can be improved. Therefore, even when the charging voltage is higher, for example, between 4.6 V and 4.8 V, and a large amount of lithium is desorbed, the H1-3 type crystal structure does not occur, and a crystal structure in which the displacement of the CoO2 layer is suppressed may be maintained. Although this crystal structure has the same symmetry as the O3' type crystal structure, the lattice constant differs from that of the O3' type crystal structure. Therefore, this structure is referred to as the O3" type crystal structure in this specification. The O3" type can also be said to be a crystal structure similar to the CdCl2 type crystal structure.

[0230] Note that increasing the magnesium concentration above the desired value may reduce the effect on stabilizing the crystal structure. This is thought to be because magnesium occupies not only the lithium site but also the cobalt site. The number of magnesium atoms in the cathode active material 100 of one embodiment of the present invention is preferably 0.001 to 0.1 times the number of atoms of the transition metal M, more preferably more than 0.01 to less than 0.04, and even more preferably approximately 0.02 times. Alternatively, the number is preferably 0.001 to 0.04 times. Alternatively, the number is preferably 0.01 to 0.1 times. The magnesium concentration shown here may be a value obtained by performing elemental analysis of the entire cathode active material 100 using, for example, inductively coupled plasma mass spectrometry (ICP-MS), or may be based on the value of the raw material composition during the production process of the cathode active material.

[0231] The transition metals M, including nickel, and aluminum are preferably present at the cobalt site, but may be partially present at the lithium site. Magnesium is preferably present at the lithium site. Oxygen may be partially substituted with fluorine.

[0232] As the magnesium concentration of the positive electrode active material of one embodiment of the present invention increases, the charge / discharge capacity of the positive electrode active material may decrease. For example, this may be due to magnesium entering the lithium site, reducing the amount of lithium contributing to charge / discharge. Excess magnesium may also produce magnesium compounds that do not contribute to charge / discharge. By including nickel in addition to magnesium in the positive electrode active material of one embodiment of the present invention, the charge / discharge capacity per weight and per volume may be increased. Furthermore, by including aluminum in addition to magnesium in the positive electrode active material of one embodiment of the present invention, the charge / discharge capacity per weight and per volume may be increased. Furthermore, by including nickel and aluminum in addition to magnesium in the positive electrode active material of one embodiment of the present invention, the charge / discharge capacity per weight and per volume may be increased.

[0233] Hereinafter, the concentrations of elements such as magnesium and metal Z contained in the positive electrode active material of one embodiment of the present invention will be expressed in terms of the number of atoms.

[0234] The number of nickel atoms in the positive electrode active material 100 of one embodiment of the present invention is preferably more than 0% but not more than 7.5% of the number of cobalt atoms, preferably 0.05% to 4%, preferably 0.1% to 2%, and more preferably 0.2% to 1%. Alternatively, it is preferably more than 0% but not more than 4%. Alternatively, it is preferably more than 0% but not more than 2%. Alternatively, it is preferably 0.05% to 7.5%. Alternatively, it is preferably 0.05% to 2%. Alternatively, it is preferably 0.1% to 7.5%. Alternatively, it is preferably 0.1% to 4%. The nickel concentration shown here may be a value obtained by performing elemental analysis of the entire positive electrode active material 100 using, for example, GD-MS, ICP-MS, or the like, or may be based on the value of the composition of raw materials in the process of producing the positive electrode active material 100.

[0235] Nickel contained at the above concentration is easily dissolved uniformly throughout the positive electrode active material 100, thereby contributing to the stabilization of the crystalline structure, particularly in the inner portion 100b. Furthermore, the presence of divalent nickel in the inner portion 100b may allow divalent additive elements, such as magnesium, present randomly and dilutely at lithium sites nearby to be more stable. This can suppress the elution of magnesium even after charge / discharge cycles that result in the desorption of a large amount of lithium. This can improve the charge / discharge cycle characteristics. Thus, combining the effects of nickel in the inner portion 100b and the effects of magnesium, aluminum, titanium, fluorine, etc. in the surface portion 100a is extremely effective in stabilizing the crystalline structure when a large amount of lithium is desorbed.

[0236] The number of aluminum atoms in the positive electrode active material of one embodiment of the present invention is preferably 0.05% to 4% of the number of cobalt atoms, preferably 0.1% to 2% and more preferably 0.3% to 1.5%. Alternatively, 0.05% to 2% is preferred. Alternatively, 0.1% to 4% is preferred. The aluminum concentration shown here may be a value obtained by performing elemental analysis of the entire positive electrode active material 100 using, for example, GD-MS, ICP-MS, or the like, or may be based on the value of the composition of raw materials in the process of producing the positive electrode active material 100.

[0237] The positive electrode active material 100 of one embodiment of the present invention preferably further contains phosphorus as an additional element, and more preferably contains a compound containing phosphorus and oxygen.

[0238] When the positive electrode active material 100 of one embodiment of the present invention contains a compound containing phosphorus, short-circuiting of the secondary battery can be suppressed in some cases when a large amount of lithium is kept in a deintercalated state.

[0239] When the positive electrode active material 100 of one embodiment of the present invention contains phosphorus, the hydrogen fluoride generated by decomposition of the electrolyte solution may react with the phosphorus, resulting in a decrease in the concentration of hydrogen fluoride in the electrolyte solution.

[0240] When the electrolyte contains LiPF6, hydrogen fluoride may be generated by hydrolysis. Hydrogen fluoride may also be generated by the reaction of polyvinylidene fluoride (PVDF), which is used as a component of the positive electrode, with alkali. By reducing the hydrogen fluoride concentration in the electrolyte, corrosion of the current collector and / or peeling of the coating 104 may be suppressed. Furthermore, a decrease in adhesion due to gelation and / or insolubilization of PVDF may be suppressed.

[0241] When the positive electrode active material of one embodiment of the present invention contains phosphorus in addition to magnesium, the stability is extremely high even when a large amount of lithium is deintercalated. When phosphorus is contained, the number of phosphorus atoms is preferably 1% to 20% of the number of cobalt atoms, more preferably 2% to 10%, and even more preferably 3% to 8%. Alternatively, 1% to 10% is preferred. Alternatively, 1% to 8% is preferred. Alternatively, 2% to 20% is preferred. Alternatively, 2% to 8% is preferred. Alternatively, 3% to 20% is preferred. Alternatively, 3% to 10% is preferred. In addition, the number of magnesium atoms is preferably 0.1% to 10% of the number of cobalt atoms, more preferably 0.5% to 5%, and more preferably 0.7% to 4%. Alternatively, 0.1% to 5% is preferred. Alternatively, 0.1% to 4% is preferred. Alternatively, 0.5% to 10% is preferred. Alternatively, 0.5% to 4% is preferred. Alternatively, 0.7% to 10% is preferred. The phosphorus and magnesium concentrations shown here may be values ​​obtained by performing elemental analysis of the entire cathode active material 100 using, for example, ICP-MS or the like, or may be based on values ​​obtained by mixing raw materials in the process of producing the cathode active material 100.

[0242] The positive electrode active material 100 may have cracks. The presence of phosphorus, more specifically, a compound containing phosphorus and oxygen, in the interior or recess of the positive electrode active material 100 having the cracks on the surface, for example, in the embedded portion 102, may inhibit the progression of the cracks.

[0243] ≪Surface layer≫ Magnesium is preferably distributed throughout the cathode active material 100 of one embodiment of the present invention. In addition, the magnesium concentration in the surface layer 100a is preferably higher than the average throughout the cathode active material 100. Alternatively, the magnesium concentration in the surface layer 100a is preferably higher than the concentration in the interior 100b. For example, the magnesium concentration in the surface layer 100a measured by XPS (X-ray photoelectron spectroscopy) or the like is preferably higher than the average magnesium concentration throughout the cathode active material 100 measured by ICP-MS or the like. Alternatively, the magnesium concentration in the surface layer 100a measured by EDX (energy dispersive X-ray spectroscopy) area analysis or the like is preferably higher than the magnesium concentration in the interior 100b.

[0244] Furthermore, when the cathode active material 100 of one embodiment of the present invention contains an additional element X, the concentration of the additional element X in the surface layer portion 100a is preferably higher than the average concentration throughout the cathode active material 100. Alternatively, the concentration of the additional element X in the surface layer portion 100a is preferably higher than the average concentration throughout the cathode active material 100, as measured by XPS or the like. For example, the concentration of an element other than cobalt in the surface layer portion 100a is preferably higher than the average concentration of the element throughout the cathode active material 100, as measured by ICP-MS or the like. Alternatively, the concentration of an element other than cobalt in the surface layer portion 100a is preferably higher than the average concentration of the element other than cobalt in the interior 100b, as measured by EDX area analysis or the like.

[0245] Unlike the inner portion 100b, which maintains its crystalline structure, the surface portion 100a is in a state where bonds are broken, and since lithium is released from the surface during charging, the surface portion 100a is more likely to have a lower lithium concentration than the inner portion 100b. As a result, this portion is more likely to become unstable and its crystalline structure to collapse. If the magnesium concentration in the surface portion 100a is high, changes in the crystalline structure can be more effectively suppressed. Furthermore, if the magnesium concentration in the surface portion 100a is high, it can be expected that corrosion resistance to hydrofluoric acid produced by decomposition of the electrolyte will be improved.

[0246] Furthermore, the fluorine concentration in the surface layer portion 100a of the cathode active material 100 according to one embodiment of the present invention is preferably higher than the average concentration in the entire cathode active material 100. Alternatively, the fluorine concentration in the surface layer portion 100a is preferably higher than the concentration in the interior portion 100b. The presence of fluorine in the surface layer portion 100a, which is the region in contact with the electrolyte, can effectively improve corrosion resistance to hydrofluoric acid.

[0247] As described above, the surface portion 100a of the cathode active material 100 according to one embodiment of the present invention preferably has a different composition from the interior portion 100b, i.e., a higher concentration of additive elements, such as magnesium and fluorine, than the interior portion 100b. Furthermore, the composition preferably has a stable crystal structure at room temperature (25°C). Therefore, the surface portion 100a may have a different crystal structure from the interior portion 100b. For example, at least a portion of the surface portion 100a of the cathode active material 100 according to one embodiment of the present invention may have a rock-salt crystal structure. Furthermore, when the surface portion 100a and the interior portion 100b have different crystal structures, it is preferable that the crystal orientations of the surface portion 100a and the interior portion 100b roughly match.

[0248] The anions in layered rock salt crystals and rock salt crystals have a cubic close-packed structure (face-centered cubic lattice structure). It is estimated that the anions in O3' crystals also have a cubic close-packed structure.

[0249] In this specification, if the anions have a structure in which three layers are stacked with a skew, such as ABCABC, it is called a cubic close-packed structure. Therefore, the anions do not necessarily have to be in a cubic lattice. At the same time, because real crystals always have defects, analytical results may not always be consistent with theory. For example, in an electron diffraction pattern or an FFT (fast Fourier transform) pattern such as a TEM image, spots may appear at positions slightly different from the theoretical positions. For example, if the orientation from the theoretical positions is 5 degrees or less, or 2.5 degrees or less, it can be said to have a cubic close-packed structure.

[0250] When layered rock salt crystals come into contact with each other, there are crystal faces where the cubic close-packed structures formed by anions are oriented in the same direction.

[0251] Alternatively, it can be explained as follows: Anions on the (111) plane of the cubic crystal structure have a triangular arrangement. Layered rocksalt has a space group of R-3m and a rhombohedral structure, but to make the structure easier to understand, it is generally expressed as a compound hexagonal lattice, while the (0001) plane of the layered rocksalt has a hexagonal lattice. The triangular lattice on the cubic (111) plane has the same atomic arrangement as the hexagonal lattice on the (0001) plane of the layered rocksalt. The compatibility of the two lattices can be said to be the alignment of the cubic close-packed structure.

[0252] However, the space group of the layered rock salt type crystal and the O3' type crystal is R-3m, which is different from the space group of the rock salt type crystal, and therefore the Miller indices of the crystal planes that satisfy the above conditions are different between the layered rock salt type crystal and the O3' type crystal and the rock salt type crystal. In this specification, when the orientations of the cubic close-packed structures formed by anions in the layered rock salt type crystal, the O3' type crystal, and the rock salt type crystal are aligned, it may be said that the crystal orientations are approximately the same.

[0253] The fact that the crystal orientations of the two regions roughly match can be determined from TEM images, STEM images, HAADF-STEM images, ABF-STEM images, electron diffraction patterns, FFT patterns of TEM images, etc. XRD, electron diffraction, neutron diffraction, etc. can also be used as materials for determination.

[0254] An example of a TEM image in which the orientation of the layered rock salt-type crystals LRS and RS roughly coincides is shown in Figure 15. Images that reflect the crystal structure can be obtained from TEM, STEM, HAADF-STEM, ABF-STEM, etc.

[0255] For example, in high-resolution TEM images, contrast originating from crystal planes can be observed. When an electron beam is incident perpendicular to the c-axis of a layered rock-salt type composite hexagonal lattice, for example, due to the diffraction and interference of the electron beam, the contrast originating from the (0003) plane is observed as a repetition of bright bands (bright strips) and dark bands (dark strips). Therefore, a repetition of bright and dark lines is observed in the TEM image, and the bright lines (for example, the L shown in Figure 15)RS and L LRS If the angle between the dark lines is 5 degrees or less, or 2.5 degrees or less, it can be determined that the crystal planes are roughly aligned, i.e., that the crystal orientations are roughly aligned. Similarly, if the angle between the dark lines is 5 degrees or less, or 2.5 degrees or less, it can be determined that the crystal orientations are roughly aligned.

[0256] Furthermore, HAADF-STEM images exhibit contrast dependent on atomic number, with elements with higher atomic numbers appearing brighter. For example, in the case of layered rock-salt lithium cobaltate, which belongs to the space group R-3m, cobalt (atomic number 27) has the highest atomic number, so the electron beam is strongly scattered at the cobalt atoms, resulting in the arrangement of the cobalt atoms being observed as bright lines or an array of highly luminous dots. Therefore, when lithium cobaltate with a layered rock-salt crystal structure is observed perpendicular to the c-axis, the arrangement of the cobalt atoms perpendicular to the c-axis is observed as bright lines or an array of highly luminous dots, while the arrangements of lithium and oxygen atoms are observed as dark lines or low-luminance regions. The same is true when lithium cobaltate contains fluorine (atomic number 9) and magnesium (atomic number 12) as additive elements.

[0257] Therefore, in an HAADF-STEM image, if repeated bright and dark lines are observed in two regions with different crystal structures and the angle between the bright lines is 5 degrees or less or 2.5 degrees or less, it can be determined that the atomic arrangements are roughly the same, i.e., that the crystal orientations are roughly the same. Similarly, if the angle between the dark lines is 5 degrees or less or 2.5 degrees or less, it can also be determined that the crystal orientations are roughly the same.

[0258] Elements with smaller atomic numbers appear brighter in ABF-STEM, but like HAADF-STEM, contrast is obtained according to atomic number, making it possible to determine crystal orientation in the same way as with HAADF-STEM images.

[0259] Figure 16A shows an example of a STEM image in which the orientations of the layered rock-salt-type crystal LRS and the rock-salt-type crystal RS roughly coincide. Figure 16B shows an FFT of the region of the rock-salt-type crystal RS, and Figure 16C shows an FFT of the region of the layered rock-salt-type crystal LRS. The left side of Figures 16B and 16C shows the composition, JCPDS card number, and the d-value and angle calculated from these. The right side shows the measured values. The spot marked with O is the zeroth-order diffraction.

[0260] The spot marked A in Figure 16B is due to the 11-1 reflection of the cubic crystal. The spot marked A in Figure 16C is due to the 0003 reflection of the layered rock salt type. From Figures 16B and 16C, it can be seen that the orientation of the 11-1 reflection of the cubic crystal and the orientation of the 0003 reflection of the layered rock salt type roughly coincide. In other words, it can be seen that the line passing through AO in Figure 16B is roughly parallel to the line passing through AO in Figure 16C. Here, "roughly coincident" and "roughly parallel" mean that the angle is 5 degrees or less, or 2.5 degrees or less.

[0261] In this way, FFT and electron diffraction showed that when the orientation of the layered rock salt crystal and the rock salt crystal roughly matched, the layered rock salt crystal <0003> In some cases, the orientation of the reciprocal lattice points roughly coincides with the <11-1> orientation of the rock salt type. In this case, it is preferable that these reciprocal lattice points are spot-like, that is, not continuous with other reciprocal lattice points. Spot-like reciprocal lattice points that are not continuous with other reciprocal lattice points indicate high crystallinity.

[0262] Furthermore, even if the orientation of the 11-1 reflection of the cubic crystal and the orientation of the 0003 reflection of the layered rock salt crystal are roughly the same as described above, depending on the incident orientation of the electron beam, spots not originating from the 0003 reflection of the layered rock salt crystal may be observed in a reciprocal lattice space different from the orientation of the 0003 reflection of the layered rock salt crystal. For example, the spot marked B in Figure 16C originates from the 1014 reflection of the layered rock salt crystal. This spot may be observed at an angle of 52° to 56° (i.e., ∠AOB is 52° to 56°) from the orientation of the reciprocal lattice point originating from the 0003 reflection of the layered rock salt crystal (A in Figure 16C), and at a location where d is 0.19 nm to 0.21 nm. Note that this index is merely an example and does not necessarily have to be identical. For example, a reciprocal lattice point equivalent to 0003 and 1014 may also be used.

[0263] Similarly, spots not originating from the 11-1 reflection of the cubic crystal may be observed in a reciprocal lattice space other than the orientation where the 11-1 reflection of the cubic crystal is observed. For example, the spot marked B in Figure 16B is originating from the 200 reflection of the cubic crystal. This is because a diffraction spot may be observed at an angle of 54° to 56° (i.e., ∠AOB is 54° to 56°) from the orientation of the reflection (A in Figure 16B) originating from the 11-1 reflection of the cubic crystal. Note that this index is just an example and does not necessarily have to be the same. For example, a reciprocal lattice point equivalent to 11-1 and 200 may also be used.

[0264] It is known that layered rock-salt cathode active materials, such as lithium cobalt oxide, tend to exhibit the (0003) plane and its equivalents, as well as the (10-14) plane and its equivalents, as crystal planes. Therefore, by carefully observing the shape of the cathode active material using an SEM or similar, it is possible to thin-section the observation sample using an FIB or similar technique so that the electron beam is [12-10] incident in a TEM or similar technique, making it easier to observe the (0003) plane. When determining whether the crystal orientation is consistent, it is preferable to thin-section the layered rock-salt cathode active material so that the (0003) plane can be easily observed.

[0265] However, if the surface layer 100a is composed of only MgO or only a solid solution of MgO and CoO(II), it becomes difficult to insert and extract lithium. Therefore, the surface layer 100a must contain at least cobalt, and in a discharged state, it must also contain lithium, providing a path for lithium insertion and extraction. It is also preferable that the concentration of cobalt be higher than that of magnesium.

[0266] The additional element X is preferably located in the surface layer portion 100a of the positive electrode active material 100 of one embodiment of the present invention. For example, the positive electrode active material 100 of one embodiment of the present invention may be covered with a coating 104 containing the additional element X.

[0267] ≪Grain boundary≫ In addition to the above-described distribution, the additive element contained in the positive electrode active material 100 of one embodiment of the present invention preferably has a part segregated at and near the crystal grain boundary 101 as shown in FIG. 4A.

[0268] More specifically, the magnesium concentration at and near the grain boundaries 101 of the positive electrode active material 100 is preferably higher than that in other regions of the interior 100b. Also, the fluorine concentration at and near the grain boundaries 101 is preferably higher than that in other regions of the interior 100b.

[0269] The grain boundary 101 is a type of planar defect. Therefore, like the grain surface, it is prone to instability and changes in the crystal structure are likely to occur. Therefore, if the magnesium concentration at and near the grain boundary 101 is high, changes in the crystal structure can be more effectively suppressed.

[0270] Furthermore, when the magnesium concentration and fluorine concentration are high at and near the grain boundary 101, even if cracks occur along the grain boundary 101 in the positive electrode active material 100 of one embodiment of the present invention, the magnesium concentration and fluorine concentration are high near the surface where the cracks occur. Therefore, the corrosion resistance to hydrofluoric acid can be improved even in the positive electrode active material after the cracks occur.

[0271] In this specification and the like, the vicinity of the grain boundary 101 refers to a region up to about 10 nm from the grain boundary. The grain boundary 101 refers to a surface where there is a change in the atomic arrangement, and can be observed with an electron microscope. Specifically, the vicinity of the grain boundary 101 refers to a location where the angle between repeated bright and dark lines in an electron microscope image exceeds 5 degrees, or a location where the crystal structure can no longer be observed.

[0272] ≪Particle size≫ If the particle size of the positive electrode active material 100 of one embodiment of the present invention is too large, problems such as difficulty in diffusing lithium and excessive roughness of the surface of the active material layer when applied to a current collector may occur. On the other hand, if the particle size is too small, problems such as difficulty in supporting the active material layer when applied to a current collector and excessive reaction with the electrolyte may occur. Therefore, the median diameter (D50) is preferably 1 μm or more and 100 μm or less, more preferably 2 μm or more and 40 μm or less, and even more preferably 5 μm or more and 30 μm or less. Alternatively, 1 μm or more and 40 μm or less is preferable. Alternatively, 1 μm or more and 30 μm or less is preferable. Alternatively, 2 μm or more and 100 μm or less is preferable. Alternatively, 2 μm or more and 30 μm or less is preferable. Alternatively, 5 μm or more and 100 μm or less is preferable. Alternatively, 5 μm or more and 40 μm or less is preferable.

[0273] <Analysis method> Whether a certain cathode active material is the cathode active material 100 of one embodiment of the present invention that exhibits an O3'-type crystal structure when a large amount of lithium is released can be determined by analyzing a cathode having a cathode active material from which a large amount of lithium has been released using XRD, electron diffraction, neutron diffraction, electron spin resonance (ESR), nuclear magnetic resonance (NMR), etc. XRD is particularly preferred because it can analyze the symmetry of transition metals such as cobalt contained in the cathode active material with high resolution, it can compare the level of crystallinity and the orientation of the crystals, it can analyze the periodic distortion of the lattice and the crystallite size, and it can obtain sufficient accuracy even when measuring a cathode obtained by disassembling a secondary battery.

[0274] As described above, the cathode active material 100 of one embodiment of the present invention is characterized by minimal change in crystal structure between the discharged state and the state where a large amount of lithium is released. Materials in which 50 wt% or more of a crystal structure exhibiting a large change in the discharged state when a large amount of lithium is released is present in the discharged state are undesirable because they cannot withstand charge / discharge cycles that result in the release of a large amount of lithium. It should be noted that the desired crystal structure may not be achieved simply by adding an additive element X. For example, even if both materials share the commonality of being lithium cobalt oxide containing magnesium and fluorine, there are cases in which the O3'-type crystal structure accounts for 60 wt% or more when a large amount of lithium is released, and cases in which the H1-3-type crystal structure accounts for 50 wt% or more. Furthermore, at a certain voltage, the O3'-type crystal structure may be nearly 100 wt%, and further increasing the voltage may result in the H1-3-type crystal structure. Therefore, crystal structure analysis, such as XRD, is required to determine whether a material is the cathode active material 100 of one embodiment of the present invention.

[0275] However, when positive electrode active materials are in a discharged or de-lithiated state, their crystal structure may change when exposed to air. For example, they may change from an O3'-type crystal structure to an H1-3-type crystal structure. Therefore, it is recommended that all samples be handled in an inert atmosphere such as an argon atmosphere.

[0276] ≪Charging method≫ High-voltage charging for determining whether a certain composite oxide is the positive electrode active material 100 of one embodiment of the present invention can be performed, for example, by preparing a coin cell (CR2032 type, diameter 20 mm, height 3.2 mm) with a lithium counter electrode and charging it.

[0277] More specifically, the positive electrode may be prepared by coating a positive electrode current collector made of aluminum foil with a slurry containing a positive electrode active material, a conductive agent, and a binder.

[0278] Lithium metal can be used for the counter electrode (negative electrode). When a material other than lithium metal is used for the counter electrode, the potential of the secondary battery and the potential of the positive electrode are different. Unless otherwise specified, the voltage and potential in this specification refer to the potential of the positive electrode (V vs. Li / Li) when lithium metal is used for the counter electrode. + )

[0279] The electrolyte used in the electrolytic solution is 1 mol / L lithium hexafluorophosphate (LiPF6), and the electrolytic solution can be a mixture of ethylene carbonate (EC) and diethyl carbonate (DEC) in a volume ratio of 3:7, with 2 wt% vinylene carbonate (VC).

[0280] The separator can be a 25 μm thick porous polypropylene film.

[0281] The positive electrode can and the negative electrode can may be made of stainless steel (SUS).

[0282] The coin cell fabricated under the above conditions was charged at a constant current of 0.5C at a given voltage (e.g., 4.6V, 4.65V, 4.7V, 4.75V, or 4.8V), and then charged at a constant voltage of 0.01C until the current reached 0.01C. Note that 1C is the current required for discharging from a charged state for one hour. A small current is desirable for observing the phase change of the positive electrode active material. For example, 1C = 137mA / g or 1C = 200mA / g can be used. When a coin cell is assembled as a test battery, if the coin cell contains 10mg of positive electrode active material, charging at a 0.5C charge rate corresponds to charging at 0.685mA when 1C = 137mA / g, and to charging at 1mA when 1C = 200mA / g. The temperature is 25°C or 45°C. After charging in this manner, the coin cell is disassembled in an argon-filled glove box and the positive electrode is removed, yielding a positive electrode active material with a large amount of lithium desorbed. When performing various analyses, it is preferable to seal the cell in an argon-filled container to prevent reactions with external components. For example, XRD can be performed by sealing the cell in an argon-filled container.

[0283] <XRD> The XRD measurement apparatus and conditions are not particularly limited. For example, the measurement can be performed using the following apparatus and conditions. XRD equipment: Bruker AXS, D8 ADVANCE X-ray source:CuKα ray Output: 40kV, 40mA Slit type: Div.Slit, 0.5° Detector: LynxEye Scan method: 2θ / θ continuous scan Measurement range (2θ): 15° to 90° Step width (2θ): 0.01° setting Counting time: 1 second / step Sample stage rotation: 15 rpm

[0284] If the measurement sample is a powder, it can be set by placing it in a glass sample holder, or by sprinkling the sample on a greased silicone anti-reflective plate, etc. If the measurement sample is a positive electrode, the positive electrode can be attached to the substrate with double-sided tape, and the positive electrode active material layer can be set to match the measurement surface required by the device.

[0285] The ideal powder XRD patterns calculated from the O3'-type crystal structure and the H1-3-type crystal structure model using CuKα1 radiation are shown in Figures 9, 11, 12A, and 12B. For comparison, Li x The ideal XRD patterns calculated from the crystal structures of LiCoO2(O3) where x = 1 in CoO2 and CoO2(O1) where x = 0 are also shown. Figures 12A and 12B show the XRD patterns of the O3'-type crystal structure and the H1-3-type crystal structure side by side. Figure 12A shows an enlarged view of the 2θ range from 18° to 21°, while Figure 12B shows an enlarged view of the 2θ range from 42° to 46°. The LiCoO2(O3) and CoO2(O1) patterns were created using Reflex Powder Diffraction, a module of Materials Studio (BIOVIA), from crystal structure information obtained from the ICSD (Inorganic Crystal Structure Database) (see Non-Patent Document 4). The 2θ range was 15° to 75°, with a step size of 0.01 and a wavelength of λ1 = 1.540562 × 10. -10 m and λ2 were not set, and the monochromator was set to single. The pattern of the H1-3 type crystal structure was similarly created from the crystal structure information described in Non-Patent Document 3. The pattern of the O3' type crystal structure was created by estimating the crystal structure from the XRD pattern of the positive electrode active material of one embodiment of the present invention, fitting it using TOPAS ver. 3 (crystal structure analysis software manufactured by Bruker), and creating an XRD pattern in the same way as the others.

[0286] As shown in Figures 9 and 12, the O3'-type crystal structure exhibits diffraction peaks at 2θ = 19.30 ± 0.20° (19.10° to 19.50°) and 2θ = 45.55 ± 0.10° (45.45° to 45.65°). More specifically, sharp diffraction peaks appear at 2θ = 19.30 ± 0.10° (19.20° to 19.40°) and 2θ = 45.55 ± 0.05° (45.50° to 45.60°). However, as shown in Figures 11 and 12, the H1-3-type crystal structure and CoO2(P-3m1, O1) do not exhibit peaks at these positions. Therefore, the appearance of peaks at 2θ=19.30±0.20° and 2θ=45.55±0.10° at a high state of charge can be said to be a characteristic of the positive electrode active material 100 of one embodiment of the present invention.

[0287] This means that the positions at which XRD diffraction peaks appear are close between the crystal structures with x = 1 and x ≦ 0.24. More specifically, the difference in the positions at which two or more, preferably three or more, of the main diffraction peaks of both structures appear is 2θ = 0.7 or less, more preferably 2θ = 0.5 or less.

[0288] Although not shown, in the O3' type crystal structure, diffraction peaks appear at 2θ = 19.47 ± 0.10° (19.37° to 19.57°) and 2θ = 45.62 ± 0.05° (45.57° to 45.67°). In the H1-3 type crystal structure and CoO2 (P-3m1, O1), no peaks appear at these positions. Therefore, it is difficult to determine the Li x The appearance of peaks at 2θ=19.47±0.10° and 2θ=45.62±0.05° when x in CoO2 is small can be said to be a characteristic of the positive electrode active material 100 of one embodiment of the present invention that is produced after initial heating.

[0289] The positive electrode active material 100 according to one embodiment of the present invention is Li xWhen x in CoO2 is small, the particles have an O3'-type crystal structure, but not all of the particles need to have an O3'-type crystal structure. They may contain other crystal structures, or some may be amorphous. However, when Rietveld analysis is performed on the XRD pattern, the O3'-type crystal structure is preferably 50 wt% or more, more preferably 60 wt% or more, and even more preferably 66 wt% or more. If the O3'-type crystal structure is 50 wt% or more, more preferably 60 wt% or more, and even more preferably 66 wt% or more, the positive electrode active material can have sufficiently excellent cycle characteristics.

[0290] Furthermore, even after 100 or more charge / discharge cycles from the start of measurement, when Rietveld analysis is performed, the O3' type crystal structure is preferably 35 wt% or more, more preferably 40 wt% or more, and even more preferably 43 wt% or more.

[0291] Furthermore, the sharpness of diffraction peaks in an XRD pattern indicates the degree of crystallinity. Therefore, it is preferable that each diffraction peak after charging is sharp, i.e., the half-width, e.g., the full width at half maximum, is narrow. The half-width varies depending on the XRD measurement conditions or the value of 2θ, even for peaks arising from the same crystalline phase. Under the measurement conditions described above, for peaks observed between 2θ = 43° and 46°, the half-width is preferably 0.2° or less, more preferably 0.15° or less, and even more preferably 0.12° or less. Note that not all peaks necessarily meet this requirement. If some peaks meet this requirement, it can be said that the crystallinity of that crystalline phase is high. Such high crystallinity contributes to the stabilization of the crystal structure after charging.

[0292] In addition, the crystallite size of the O3'-type crystal structure of the positive electrode active material particles is reduced to only about 1 / 10 of that of LiCoO2(O3) in the discharged state. xWhen x in CoO2 is small, a clear peak of the O3'-type crystal structure can be confirmed. On the other hand, in simple LiCoO2, even if a part of it can adopt a structure similar to the O3'-type crystal structure, the crystallite size becomes small and the peak becomes broad and small. The crystallite size can be determined from the half-width of the XRD peak.

[0293] As described above, the positive electrode active material of one embodiment of the present invention preferably has a small influence of the Jahn-Teller effect. The positive electrode active material of one embodiment of the present invention preferably has a layered rock salt crystal structure and contains cobalt as a transition metal. Furthermore, the positive electrode active material of one embodiment of the present invention may contain the aforementioned metal Z in addition to cobalt, as long as the influence of the Jahn-Teller effect is small.

[0294] Using XRD analysis, we consider the range of lattice constants in the positive electrode active material where the influence of the Jahn-Teller effect is small.

[0295] FIG. 13 shows the results of calculating the a-axis and c-axis lattice constants using XRD for a positive electrode active material according to one embodiment of the present invention, which has a layered rock-salt crystal structure and contains cobalt and nickel. FIG. 13A shows the a-axis result, and FIG. 13B shows the c-axis result. Note that the XRD patterns used for these calculations are for powder after synthesis of the positive electrode active material, but before incorporation into the positive electrode. The nickel concentration on the horizontal axis indicates the nickel concentration when the sum of the number of cobalt and nickel atoms is taken as 100%. The positive electrode active material was prepared according to the preparation method shown in FIG. 2, except that an aluminum source was not used. The nickel concentration indicates the nickel concentration when the sum of the number of cobalt and nickel atoms in the positive electrode active material is taken as 100%.

[0296] FIG. 14 shows the results of estimating the a-axis and c-axis lattice constants using XRD for a positive electrode active material according to one embodiment of the present invention, which has a layered rock-salt crystal structure and contains cobalt and manganese. FIG. 14A shows the a-axis result, and FIG. 14B shows the c-axis result. Note that the lattice constants shown in FIG. 14 were obtained by XRD measurement of the powder after synthesis of the positive electrode active material and before incorporation into the positive electrode. The manganese concentration on the horizontal axis represents the manganese concentration when the sum of the number of cobalt and manganese atoms is set to 100%. The positive electrode active material was prepared according to the preparation method shown in FIG. 2, except that a manganese source was used instead of the nickel source and no aluminum source was used. The manganese concentration represents the manganese concentration when the sum of the number of cobalt and manganese atoms in step S21 is set to 100%.

[0297] Figure 13C shows the value obtained by dividing the a-axis lattice constant by the c-axis lattice constant (a-axis / c-axis) for the positive electrode active materials whose lattice constant results are shown in Figures 13A and 13B. Figure 14C shows the value obtained by dividing the a-axis lattice constant by the c-axis lattice constant (a-axis / c-axis) for the positive electrode active materials whose lattice constant results are shown in Figures 14A and 14B.

[0298] Figure 13C shows that the a-axis / c-axis tends to change significantly at nickel concentrations of 5% and 7.5%, with the a-axis distortion increasing at 7.5% nickel. This distortion may be Jahn-Teller distortion. This suggests that excellent cathode active materials with small Jahn-Teller distortion can be obtained at nickel concentrations below 7.5%.

[0299] Next, Figure 14A suggests that when the manganese concentration is 5% or more, the behavior of the change in lattice constant is different and does not follow Vegard's law. Therefore, it is suggested that when the manganese concentration is 5% or more, the crystal structure is different. Therefore, the manganese concentration is preferably, for example, 4% or less.

[0300] The above ranges of nickel concentration and manganese concentration do not necessarily apply to the surface layer portion 100a, that is, the surface layer portion 100a may have concentrations higher than the above ranges.

[0301] From the above, a preferable range of the lattice constant was considered, and it was found that in the positive electrode active material of one embodiment of the present invention, the layered rock-salt crystal structure of the particles of the positive electrode active material in a state where no charge / discharge is performed or in a discharged state, which can be estimated from the XRD pattern, has an a-axis lattice constant of 2.814 × 10 -10 m, 2.817×10 -10 m and the c-axis lattice constant is 14.05×10 -10 m, 14.07 × 10 -10 It has been found that it is preferable that the value be smaller than m. The state in which no charge or discharge is performed may be, for example, the state of powder before the positive electrode of a secondary battery is produced.

[0302] Alternatively, in the layered rock-salt crystal structure of the particles of the positive electrode active material in a state where no charge or discharge is performed or in a discharged state, it is preferable that the value obtained by dividing the lattice constant of the a-axis by the lattice constant of the c-axis (a-axis / c-axis) is greater than 0.20000 and smaller than 0.20049.

[0303] Alternatively, when XRD analysis is performed on the layered rock salt crystal structure of particles of a positive electrode active material in a state where no charge or discharge is performed or in a discharged state, a first peak may be observed at 2θ of 18.50° or more and 19.30° or less, and a second peak may be observed at 2θ of 38.00° or more and 38.80° or less.

[0304] The peaks appearing in the powder XRD pattern reflect the crystalline structure of the interior 100b of the positive electrode active material 100, which occupies most of the volume of the positive electrode active material 100. The crystalline structure of the surface layer 100a, the grain boundaries 101, etc. can be analyzed by electron beam diffraction of a cross section of the positive electrode active material 100, or the like.

[0305] <Charging curve and dQ / dV curve> The positive electrode active material 100 of one embodiment of the present invention may exhibit a characteristic voltage change during charging. The voltage change can be read from a dQ / dV vs. V curve obtained by differentiating (dQ / dV) the capacity (Q) of the charging curve with respect to the voltage (V). For example, it is believed that a non-equilibrium phase change occurs around the peak in the dQ / dV vs. V curve, resulting in a significant change in the crystal structure. Note that in this specification and elsewhere, a non-equilibrium phase change refers to a phenomenon that causes a non-linear change in a physical quantity.

[0306] The positive electrode active material 100 according to one embodiment of the present invention may have a broad peak near 4.55 V in its dQ / dV curve. The peak near 4.55 V reflects the voltage change that occurs during the phase change from the O3-type crystal structure to the O3'-type crystal structure. Therefore, a broader peak is considered to indicate a more gradual change in the crystal structure than a sharp peak. A gradual change in the crystal structure to the O3'-type is preferable because it reduces the effects of shifting the CoO2 layers and volume changes.

[0307] More specifically, when the maximum value appearing between 4.5 V and 4.6 V in the dQ / dV curve of the charging curve is defined as the first peak, it is considered sufficiently broad and is preferable that the half-width of the first peak be 0.10 V or more. In this specification, the half-width of the first peak is defined as the sum of the average value HWHM1 between the first peak and the first minimum when the minimum value appearing between 4.3 V and 4.5 V is defined as the first minimum, and the average value HWHM2 between the first peak and the second minimum when the minimum value appearing between 4.6 V and 4.8 V is defined as the second minimum.

[0308] <Discharge curve and dQ / dV curve> Furthermore, when the positive electrode active material 100 of one embodiment of the present invention is charged at a high voltage and then discharged at a low rate of, for example, 0.2 C or less, a characteristic voltage change may occur near the end of discharge. This change can be clearly confirmed by the presence of at least one peak in the dQ / dV ratio calculated from the discharge curve, which is lower than the peak that appears around 3.9 V and falls within the range up to 3.5 V.

[0309] XPS XPS can analyze the region from the surface to a depth of about 2 to 8 nm (usually 5 nm or less). It can quantitatively analyze the concentration of each element in the surface layer 100a up to the depth range. Furthermore, narrow scan analysis can analyze the bonding state of elements. The quantitative accuracy of XPS is often about ±1 atomic %, and the lower detection limit is about 1 atomic %, depending on the element.

[0310] When XPS analysis is performed on the positive electrode active material 100 of one embodiment of the present invention, the number of atoms of a certain additive element X is preferably 1.6 to 6.0 times, and more preferably 1.8 to less than 4.0 times, the number of atoms of the transition metal M. For example, when the positive electrode active material 100 contains magnesium as the additive element X and the transition metal M is cobalt, the number of magnesium atoms is preferably 1.6 to 6.0 times, and more preferably 1.8 to less than 4.0 times, the number of cobalt atoms. Furthermore, the number of atoms of a halogen such as fluorine is preferably 0.2 to 6.0 times, and more preferably 1.2 to 4.0 times, the number of atoms of the transition metal M.

[0311] When performing XPS analysis, for example, monochromated aluminum can be used as the X-ray source. The take-off angle can be set to, for example, 45°. Measurement can be performed using the following equipment and conditions, for example. Measurement equipment: PHI Quantera II X-ray source: Monochromated Al (1486.6 eV) Detection area: 100 μmφ Detection depth: Approximately 4 to 5 nm (take-off angle 45°) Measurement spectrum: Wide scan, narrow scan for each detected element

[0312] Furthermore, when the positive electrode active material 100 of one embodiment of the present invention is analyzed by XPS, the peak showing the bond energy between fluorine and other elements is preferably equal to or greater than 682 eV and less than 685 eV, and more preferably about 684.3 eV. This value is different from both the bond energy of lithium fluoride (685 eV) and the bond energy of magnesium fluoride (686 eV). In other words, when the positive electrode active material 100 of one embodiment of the present invention contains fluorine, the bond is preferably other than that of lithium fluoride or magnesium fluoride.

[0313] Furthermore, when the positive electrode active material 100 of one embodiment of the present invention is subjected to XPS analysis, the peak showing the bond energy between magnesium and other elements is preferably equal to or greater than 1302 eV and less than 1304 eV, and more preferably about 1303 eV. This value is different from the bond energy of magnesium fluoride, 1305 eV, and is close to the bond energy of magnesium oxide. In other words, when the positive electrode active material 100 of one embodiment of the present invention contains magnesium, the bond is preferably other than that of magnesium fluoride.

[0314] The concentration of the additional element X, such as magnesium and aluminum, which is preferably present in large amounts in the surface layer portion 100a, measured by XPS or the like is preferably higher than the concentration measured by ICP-MS or GD-MS or the like.

[0315] When a cross section of the sample is exposed by processing and analyzed using TEM-EDX, the magnesium and aluminum concentrations in the surface layer 100a are preferably higher than the concentrations in the interior 100b. For example, in TEM-EDX analysis, the magnesium concentration preferably decays to 60% or less of the peak at a point 1 nm deep from the peak top. It is also preferable that the magnesium concentration decays to 30% or less of the peak at a point 2 nm deep from the peak top. Processing can be performed using, for example, a focused ion beam (FIB).

[0316] In XPS (X-ray photoelectron spectroscopy) analysis, the number of magnesium atoms is preferably 0.4 to 1.5 times the number of cobalt atoms, while in ICP-MS analysis, the ratio of the number of magnesium atoms to the number of cobalt atoms, Mg / Co, is preferably 0.001 to 0.06.

[0317] On the other hand, it is preferable that nickel contained in the transition metal M is not unevenly distributed in the surface layer portion 100a but is distributed throughout the positive electrode active material 100. However, this does not apply when there is a region where the additive element X is unevenly distributed as described above.

[0318] ESR As described above, the positive electrode active material of one embodiment of the present invention preferably contains cobalt and nickel as the transition metal M and magnesium as the additional element. 3+ Ni 2+ and some Li + Mg 2+ It is preferably substituted with Li + Mg 2+ With the replacement of Ni 2+ is reduced to Ni 3+ In addition, some Li + Mg 2+ is replaced by Mg 2+ Nearby Co 3+ is reduced to Co 2+ In addition, some Co 3+ Mg 2+ is replaced by Mg 2+ Nearby Co 3+ is oxidized to Co 4+ This may occur.

[0319] Therefore, the positive electrode active material according to one embodiment of the present invention is Ni 2+ , Ni 3+ , Co 2+ and Co 4+ It is preferable that the positive electrode active material contains at least one of the following: 2+ , Ni 3+ , Co2+ and Co 4+ The spin density due to one or more of the following is 2.0×10 17 spins / g or more 1.0×10 21 It is preferable that the positive electrode active material has the above-mentioned spin density, because the crystal structure is stable especially in the charged state. 2+ , Ni 3+ , Co 2+ and Co 4+ The spin density may be reduced due to one or more of the above.

[0320] The spin density in the positive electrode active material can be analyzed, for example, by using electron spin resonance (ESR).

[0321] EPMA EPMA (Electron Probe Microanalysis) allows for quantitative analysis of elements. Area analysis allows for the distribution of each element.

[0322] EPMA analyzes the region from the surface to a depth of about 1 μm. Therefore, the concentration of each element may differ from the measurement results obtained using other analytical methods. For example, when performing a surface analysis of the positive electrode active material 100, the concentration of the added element X present in the surface layer may be lower than the result obtained by XPS. Also, the concentration of the added element X present in the surface layer may be higher than the result obtained by ICP-MS or the value obtained from the raw material composition during the production process of the positive electrode active material.

[0323] When EPMA surface analysis is performed on a cross section of the cathode active material 100 according to one embodiment of the present invention, the concentration of the additive element X preferably has a concentration gradient that increases from the interior toward the surface. More specifically, as shown in FIG. 4C1, magnesium, fluorine, titanium, and silicon preferably have concentration gradients that increase from the interior toward the surface of the cathode active material 100. Furthermore, as shown in FIG. 4C2, aluminum preferably has a concentration peak in a region deeper than the concentration peaks of the above elements. The aluminum concentration peak may be present in the surface or may be deeper than the surface.

[0324] The surface and surface layer of the positive electrode active material of one embodiment of the present invention are assumed to be free of carbonates, hydroxyl groups, and the like that are chemically adsorbed after the preparation of the positive electrode active material. They are also assumed to be free of electrolyte, binder, conductive agent, and compounds derived therefrom that adhere to the surface of the positive electrode active material. Therefore, when quantitatively analyzing the elements contained in the positive electrode active material, corrections may be made to exclude carbon, hydrogen, excess oxygen, excess fluorine, and the like that can be detected by surface analysis such as XPS and EPMA. For example, XPS can separate the types of bonds in the analysis, and corrections may be made to exclude C—F bonds derived from the binder.

[0325] Furthermore, before subjecting the sample to various analyses, the sample of the positive electrode active material and the positive electrode active material layer may be washed to remove the electrolyte, binder, conductive agent, or compounds derived therefrom adhering to the surface of the positive electrode active material. At this time, lithium may dissolve in the solvent used for washing, but even in this case, the added element X is unlikely to dissolve, and therefore the atomic ratio of the added element X is not affected.

[0326] <Surface roughness and specific surface area> The positive electrode active material 100 according to one embodiment of the present invention preferably has a smooth surface with few irregularities. A smooth surface with few irregularities is one factor indicating that the distribution of the additive elements in the surface layer portion 100a is good.

[0327] Whether the surface is smooth and has few irregularities can be determined from, for example, a cross-sectional SEM image or cross-sectional TEM image of the positive electrode active material 100, the specific surface area of ​​the positive electrode active material 100, or the like.

[0328] For example, the surface smoothness can be quantified from a cross-sectional SEM image of the positive electrode active material 100 as follows.

[0329] First, the cathode active material 100 is processed using FIB or the like to expose its cross section. At this time, it is preferable to cover the cathode active material 100 with a protective film, protective material, or the like. Next, an SEM image of the interface between the protective film or the like and the cathode active material 100 is taken. The SEM image is subjected to noise processing using image processing software. For example, Gaussian blurring (σ=2) is performed, followed by binarization. The interface is then extracted using image processing software. The interface line between the protective film or the like and the cathode active material 100 is selected using an automatic selection tool or the like, and the data is extracted to a spreadsheet or the like. Using the functions of the spreadsheet or the like, correction is performed from a regression curve (quadratic regression), and parameters for calculating roughness are obtained from the data after slope correction. The root mean square (RMS) surface roughness is calculated by calculating the standard deviation. This surface roughness is the surface roughness within at least 400 nm of the outer periphery of the cathode active material particles.

[0330] On the particle surfaces of the positive electrode active material 100 of this embodiment, the root mean square (RMS) surface roughness, which is an index of roughness, is preferably less than 3 nm, more preferably less than 1 nm, and even more preferably less than 0.5 nm.

[0331] The image processing software used for noise processing, boundary extraction, etc. is not particularly limited, but for example, "ImageJ" can be used. Similarly, the spreadsheet software is not particularly limited, but for example, Microsoft Office Excel can be used.

[0332] For example, the actual specific surface area A measured by the gas adsorption method using the constant volume method R and the ideal specific surface area A iThe smoothness of the surface of the positive electrode active material 100 can also be quantified from the ratio of the surface roughness to the surface smoothness.

[0333] Ideal specific surface area A i is calculated assuming that all particles have the same diameter as the median diameter (D50), the same weight, and an ideal spherical shape.

[0334] The median diameter (D50) can be measured by a particle size distribution analyzer using a laser diffraction / scattering method, etc. The specific surface area can be measured by a specific surface area measuring device using a gas adsorption method based on a constant volume method, for example.

[0335] The positive electrode active material 100 according to one embodiment of the present invention has an ideal specific surface area A calculated from the median diameter (D50). i and the actual specific surface area A R Ratio A R / A i is preferably 2.1 or less.

[0336] Alternatively, the surface smoothness can be quantified from a cross-sectional SEM image of the positive electrode active material 100 by the following method.

[0337] First, a surface SEM image of the positive electrode active material 100 is obtained. At this time, a conductive coating may be applied as a pretreatment for observation. The observation surface is preferably perpendicular to the electron beam. When comparing multiple samples, the measurement conditions and observation area should be the same.

[0338] Next, using image processing software (such as "ImageJ"), the above SEM image is converted to, for example, an 8-bit image (called a grayscale image). Grayscale images contain luminance (brightness information). For example, in an 8-bit grayscale image, luminance can be expressed in 2 to the power of 8 = 256 levels. Dark areas have lower levels of gradation, and bright areas have higher levels of gradation. Changes in luminance can be quantified by relating them to the number of levels of gradation. This number is called the grayscale value. By obtaining the grayscale value, it is possible to evaluate the unevenness of the positive electrode active material numerically.

[0339] Furthermore, it is possible to display the brightness change of the target area as a histogram. A histogram is a three-dimensional representation of the gradation distribution in the target area, and is also called a brightness histogram. Obtaining a brightness histogram makes it possible to visually evaluate the unevenness of the positive electrode active material in an easy-to-understand manner.

[0340] In the positive electrode active material 100 of one embodiment of the present invention, the difference between the maximum and minimum values ​​of the grayscale value is preferably 120 or less, more preferably 115 or less, and even more preferably 70 or more and 115 or less. The standard deviation of the grayscale value is preferably 11 or less, more preferably 8 or less, and even more preferably 4 or more and 8 or less.

[0341] This embodiment can be used in combination with other embodiments.

[0342] (Embodiment 3) In this embodiment, an example of a secondary battery of one embodiment of the present invention will be described with reference to FIGS.

[0343] <Configuration example 1 of secondary battery> The following description will be given taking as an example a secondary battery in which a positive electrode, a negative electrode, and an electrolyte are enclosed in an exterior body.

[0344] [Positive electrode] The positive electrode includes a positive electrode active material layer and a positive electrode current collector. The positive electrode active material layer includes a positive electrode active material and may include a conductive agent and a binder. The positive electrode active material is formed by the method described in the above embodiment.

[0345] The positive electrode active material described in the above embodiment may be mixed with another positive electrode active material.

[0346] Examples of other cathode active materials include composite oxides having an olivine-type crystal structure, a layered rock salt-type crystal structure, or a spinel-type crystal structure. Examples of such compounds include LiFePO4, LiFeO2, LiNiO2, LiMn2O4, V2O5, Cr2O5, MnO2, and the like.

[0347] In addition, as another cathode active material, it is preferable to mix a lithium-containing material having a spinel-type crystal structure containing manganese such as LiMn2O4 with lithium nickelate (LiNiO2 or LiNi 1-x M x O2 (0 < x < 1) (M = Co, Al, etc.)). By adopting such a configuration, the characteristics of the secondary battery can be improved.

[0348] In addition, as another cathode active material, a lithium manganese composite oxide represented by the composition formula Li a Mn b M c O d can be used. Here, the element M is preferably a metal element selected from those other than lithium and manganese, or silicon or phosphorus, and more preferably nickel. When measuring the entire lithium manganese composite oxide, it is preferable to satisfy 0 < a / (b + c) < 2, c > 0, and 0.26 ≦ (b + c) / d < 0.5 during discharge. The composition of metals, silicon, phosphorus, etc. in the entire lithium manganese composite oxide can be measured using, for example, ICP-MS (inductively coupled plasma mass spectrometer). The oxygen composition of the entire lithium manganese composite oxide can be measured using, for example, EDX. It can also be obtained by using valence evaluation of melting gas analysis and XAFS (X-ray absorption fine structure) analysis in combination with ICP-MS analysis. The lithium manganese composite oxide refers to an oxide containing at least lithium and manganese, and may contain at least one element selected from the group consisting of chromium, cobalt, aluminum, nickel, iron, magnesium, molybdenum, zinc, indium, gallium, copper, titanium, niobium, silicon, and phosphorus.

[0349] As an example, a cross-sectional configuration example in which graphene or a graphene compound is used as the conductive agent in the active material layer 200 will be described below.

[0350] 17A shows a vertical cross-sectional view of active material layer 200. Active material layer 200 includes granular positive electrode active material 100, graphene or a graphene compound 201 as a conductive agent, and a binder (not shown).

[0351] In this specification and the like, graphene compounds 201 include multilayer graphene, multigraphene, graphene oxide, multilayer graphene oxide, multi-graphene oxide, reduced graphene oxide, reduced multilayer graphene oxide, reduced multi-graphene oxide, graphene quantum dots, and the like. Graphene compounds contain carbon, have a shape such as a plate or sheet, and have a two-dimensional structure formed by six-membered carbon rings. The two-dimensional structure formed by six-membered carbon rings may also be called a carbon sheet. Graphene compounds may have functional groups. Furthermore, graphene compounds preferably have a curved shape. Furthermore, graphene compounds may be rolled up to resemble carbon nanofibers.

[0352] In this specification and the like, graphene oxide refers to a material that contains carbon and oxygen, has a sheet shape, and has a functional group, in particular, an epoxy group, a carboxy group, or a hydroxy group.

[0353] In this specification, reduced graphene oxide refers to a material containing carbon and oxygen, having a sheet-like shape, and having a two-dimensional structure formed by six-membered carbon rings. It may also be called a carbon sheet. Although a single sheet of reduced graphene oxide can function, multiple sheets may also be stacked. Reduced graphene oxide preferably has a portion where the carbon concentration is greater than 80 atomic % and the oxygen concentration is between 2 atomic % and 15 atomic %. By achieving these carbon and oxygen concentrations, reduced graphene oxide can function as a highly conductive material even in small amounts. Furthermore, reduced graphene oxide preferably has an intensity ratio G / D between the G band and the D band in a Raman spectrum of 1 or more. Reduced graphene oxide with such an intensity ratio can function as a highly conductive material even in small amounts.

[0354] Graphene compounds may have excellent electrical properties, such as high conductivity, and excellent physical properties, such as high flexibility and high mechanical strength. Graphene compounds may also have a sheet-like shape. Graphene compounds may have curved surfaces, enabling surface contact with low contact resistance. Even thin graphene compounds may have very high conductivity, allowing a small amount of graphene to efficiently form a conductive path within an active material layer. Therefore, using a graphene compound as a conductive agent can increase the contact area between the active material and the conductive agent. The graphene compound preferably covers 80% or more of the active material. It is preferable that the graphene compound clings to at least a portion of the active material particles. It is also preferable that the graphene compound overlaps at least a portion of the active material particles. It is also preferable that the shape of the graphene compound matches at least a portion of the shape of the active material particles. The shape of the active material particles refers to, for example, the unevenness of a single active material particle or the unevenness formed by multiple active material particles. It is also preferable that the graphene compound surrounds at least a portion of the active material particles. The graphene compound may also have holes.

[0355] When using active material particles with a small particle size, for example, 1 μm or less, the specific surface area of ​​the active material particles is large, and more conductive paths connecting the active material particles are required. In such cases, it is preferable to use a graphene compound, which can efficiently form conductive paths even in a small amount.

[0356] Because of the properties described above, graphene compounds are particularly effective as conductive agents for secondary batteries that require rapid charging and rapid discharging. For example, rapid charging and rapid discharging characteristics may be required for secondary batteries for two-wheeled or four-wheeled vehicles and secondary batteries for drones. Rapid charging and rapid discharging may also be referred to as high-rate charging and high-rate discharging. For example, rapid charging and rapid discharging refer to charging and discharging at 1C, 2C, or 5C or higher.

[0357] 17B , in a longitudinal cross section of active material layer 200, sheet-like graphene or graphene compound 201 is dispersed approximately uniformly within active material layer 200. In FIG. 17B , graphene or graphene compound 201 is schematically represented by a thick line, but in reality, it is a thin film having a thickness corresponding to a single layer or multiple layers of carbon molecules. The plurality of graphene or graphene compound 201 is formed so as to partially cover the plurality of granular positive electrode active material 100 or to be attached to the surfaces of the plurality of granular positive electrode active material 100, and thus is in surface contact with one another.

[0358] Here, a mesh-like graphene compound sheet (hereinafter referred to as a graphene compound net or graphene net) can be formed by bonding multiple graphenes or graphene compounds together. When an active material is covered with a graphene net, the graphene net can also function as a binder that bonds the active materials together. Therefore, the amount of binder can be reduced or can be eliminated, thereby improving the ratio of active material to the electrode volume and electrode weight. In other words, the charge / discharge capacity of a secondary battery can be increased.

[0359] Here, it is preferable to use graphene oxide as the graphene or graphene compound 201, mix it with an active material to form a layer that will become the active material layer 200, and then reduce it. That is, the completed active material layer preferably has reduced graphene oxide. By using graphene oxide, which has extremely high dispersibility in a polar solvent, to form the graphene or graphene compound 201, it is possible to substantially uniformly disperse the graphene or graphene compound 201 inside the active material layer 200. The solvent is volatilized and removed from the dispersion medium containing the uniformly dispersed graphene oxide, and the graphene oxide is reduced. Therefore, the graphene or graphene compound 201 remaining in the active material layer 200 partially overlaps and is dispersed to such an extent that it is in surface contact with each other, thereby forming a three-dimensional conductive path. Note that the reduction of the graphene oxide may be performed, for example, by heat treatment or using a reducing agent.

[0360] Therefore, unlike a granular conductive agent such as acetylene black that makes point contact with the active material, graphene or the graphene compound 201 enables surface contact with low contact resistance, and therefore can improve the electrical conductivity between the granular positive electrode active material 100 and the graphene or the graphene compound 201 with a smaller amount than that of a typical conductive agent. This allows the ratio of the positive electrode active material 100 in the active material layer 200 to be increased, thereby increasing the discharge capacity of the secondary battery.

[0361] Furthermore, by using a spray dryer in advance, a graphene compound, which is a conductive agent, can be formed as a coating that covers the entire active material, and further a conductive path can be formed between the active material particles by the graphene compound.

[0362] Furthermore, a material used in forming the graphene compound may be mixed with the graphene compound and used in the active material layer 200. For example, particles used as a catalyst in forming the graphene compound may be mixed with the graphene compound. Examples of catalysts used in forming the graphene compound include silicon oxide (SiO2, SiO x(x<2)), aluminum oxide, iron, nickel, ruthenium, iridium, platinum, copper, germanium, etc. The particles preferably have a median diameter (D50) of 1 μm or less, more preferably 100 nm or less.

[0363] [Binder] As the binder, it is preferable to use a rubber material such as styrene-butadiene rubber (SBR), styrene-isoprene-styrene rubber, acrylonitrile-butadiene rubber, butadiene rubber, ethylene-propylene-diene copolymer, etc. Also, fluororubber can be used as the binder.

[0364] Furthermore, it is preferable to use, for example, a water-soluble polymer as the binder. Examples of the water-soluble polymer that can be used include polysaccharides. Examples of the polysaccharide that can be used include one or more of cellulose derivatives such as carboxymethyl cellulose (CMC), methyl cellulose, ethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, and regenerated cellulose, and starch. It is even more preferable to use these water-soluble polymers in combination with the above-mentioned rubber material.

[0365] Alternatively, it is preferable to use materials such as polystyrene, polymethyl acrylate, polymethyl methacrylate (polymethyl methacrylate, PMMA), sodium polyacrylate, polyvinyl alcohol (PVA), polyethylene oxide (PEO), polypropylene oxide, polyimide, polyvinyl chloride, polytetrafluoroethylene, polyethylene, polypropylene, polyisobutylene, polyethylene terephthalate, nylon, polyvinylidene fluoride (PVDF), polyacrylonitrile (PAN), ethylene propylene diene polymer, polyvinyl acetate, and nitrocellulose as the binder.

[0366] The binder may be used in combination with two or more of the above.

[0367] For example, a material with a particularly excellent viscosity adjusting effect may be used in combination with other materials. For example, elastic materials, typically rubber materials, have excellent adhesive strength and / or elasticity, but may have difficulty adjusting the viscosity when mixed with a solvent. In such cases, it is preferable to mix them with a material with a particularly excellent viscosity adjusting effect. For example, a water-soluble polymer may be used as a material with a particularly excellent viscosity adjusting effect. Furthermore, as water-soluble polymers with a particularly excellent viscosity adjusting effect, the above-mentioned polysaccharides, such as carboxymethyl cellulose (CMC), methyl cellulose, ethyl cellulose, hydroxypropyl cellulose, and diacetyl cellulose, cellulose derivatives such as regenerated cellulose, and starch may be used.

[0368] In addition, the solubility of cellulose derivatives such as carboxymethyl cellulose can be increased by converting them into salts such as sodium and ammonium salts of carboxymethyl cellulose, making them more effective as viscosity adjusters. Higher solubility can also improve dispersibility with the active material and other components when preparing electrode slurry. In this specification, the cellulose and cellulose derivatives used as electrode binders also include their salts.

[0369] Water-soluble polymers stabilize viscosity by dissolving in water, and they also allow active materials and other materials combined as binders, such as styrene-butadiene rubber, to be stably dispersed in aqueous solutions. Furthermore, their functional groups are expected to facilitate stable adsorption to the surface of active materials. Furthermore, many cellulose derivatives, such as carboxymethyl cellulose, contain functional groups, such as hydroxyl and carboxyl groups, and these functional groups are expected to interact with each other and widely cover the surface of active materials.

[0370] When the binder covering or contacting the surface of the active material forms a film, it is expected to function as a passive film and have the effect of suppressing decomposition of the electrolyte. Here, the passive film is a film with no electrical conductivity or a film with extremely low electrical conductivity. For example, when a passive film is formed on the surface of the active material, it can suppress decomposition of the electrolyte at the battery reaction potential. Furthermore, it is more desirable that the passive film suppresses electrical conductivity while still allowing lithium ions to conduct.

[0371] [Positive electrode current collector] The positive electrode current collector can be made of a highly conductive material, such as a metal such as stainless steel, gold, platinum, aluminum, or titanium, or an alloy thereof. It is preferable that the material used for the positive electrode current collector does not dissolve at the potential of the positive electrode. Aluminum alloys containing elements that improve heat resistance, such as silicon, titanium, neodymium, scandium, or molybdenum, can also be used. The positive electrode current collector may also be made of a metal element that reacts with silicon to form a silicide. Examples of metal elements that react with silicon to form a silicide include zirconium, titanium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, and nickel. The positive electrode current collector can be in the form of a foil, plate, sheet, mesh, punched metal, expanded metal, or the like. It is preferable that the positive electrode current collector have a thickness of 5 μm to 30 μm.

[0372] A positive electrode can be obtained by applying a slurry containing the positive electrode active material, the binder, a solvent, a conductive agent, and the like to a positive electrode current collector and pressing the applied slurry. NMP can be used as the solvent. A press is used for the press, and the slurry is heated by setting the temperature of the first and second rolls of the press to 80°C to 150°C, preferably 100°C to 130°C. Higher roll temperatures can increase electrode density. However, the temperature should be below the melting point of the binder. For example, the melting point of PVDF used as the binder is 158°C to 160°C. The pressing pressure is 100kN / m to 300kN / m, preferably 150kN / m to 250kN / m, and more preferably 190kN / m to 230kN / m. When pressing is performed multiple times, the pressing pressure for the second press is 5 to 8 times, preferably 6 to 7 times, the pressing pressure for the first press.

[0373] [Negative electrode] The negative electrode includes a negative electrode active material layer and a negative electrode current collector. The negative electrode active material layer may also include a conductive agent and a binder.

[0374] [Negative electrode active material] As the negative electrode active material, for example, an alloy-based material and / or a carbon-based material can be used.

[0375] The negative electrode active material can be an element capable of undergoing charge-discharge reactions through alloying and dealloying reactions with lithium. For example, materials containing at least one of silicon, tin, gallium, aluminum, germanium, lead, antimony, bismuth, silver, zinc, cadmium, and indium can be used. These elements have a higher charge-discharge capacity than carbon, and silicon, in particular, has a high theoretical capacity of 4200 mAh / g. For this reason, silicon is preferred as the negative electrode active material. Compounds containing these elements can also be used. Examples include SiO, Mg2Si, Mg2Ge, SnO, SnO2, Mg2Sn, SnS2, V2Sn3, FeSn2, CoSn2, Ni3Sn2, Cu6Sn5, Ag3Sn, Ag3Sb, Ni2MnSb, CeSb3, LaSn3, La3Co2Sn7, CoSb3, InSb, and SbSn. Here, elements that can undergo charge-discharge reactions by alloying / dealloying reactions with lithium, and compounds containing such elements, are sometimes called alloy-based materials.

[0376] In this specification and the like, SiO refers to, for example, silicon monoxide. Alternatively, SiO refers to SiO x Here, x preferably has a value close to 1. For example, x is preferably 0.2 or more and 1.5 or less, more preferably 0.3 or more and 1.2 or less, or preferably 0.2 or more and 1.2 or less, or preferably 0.3 or more and 1.5 or less.

[0377] Examples of carbonaceous materials that can be used include graphite, easily graphitizable carbon (soft carbon), non-graphitizable carbon (hard carbon), carbon nanotubes, graphene, and carbon black.

[0378] Examples of graphite include artificial graphite and natural graphite. Examples of artificial graphite include mesocarbon microbeads (MCMB), coke-based artificial graphite, and pitch-based artificial graphite. Here, spherical graphite having a spherical shape can be used as the artificial graphite. For example, MCMB may have a spherical shape and is preferred. Furthermore, it is relatively easy to reduce the surface area of ​​MCMB, and this may be preferred. Examples of natural graphite include flake graphite and spherical natural graphite.

[0379] When lithium ions are inserted into graphite (when lithium-graphite intercalation compounds are formed), graphite exhibits a low potential similar to that of metallic lithium (0.05 V to 0.3 V vs. Li / Li + ) This allows lithium-ion secondary batteries to exhibit high operating voltages. Furthermore, graphite is preferred because it has advantages such as a relatively high charge / discharge capacity per unit volume, relatively little volume expansion, low cost, and higher safety compared to lithium metal.

[0380] In addition, titanium dioxide (TiO2), lithium titanium oxide (Li4Ti5O 12 ), lithium-graphite intercalation compound (Li x C6), niobium pentoxide (Nb2O5), tungsten oxide (WO2), molybdenum oxide (MoO2), and other oxides can be used.

[0381] In addition, the negative electrode active material is a composite nitride of lithium and transition metals, Li3N-type. 3-x M x N (M=Co, Ni, Cu) can be used. For example, Li 2.6 Co 0.4 N3 has a large charge / discharge capacity (900mAh / g, 1890mAh / cm 3 ) and is preferred.

[0382] When a composite nitride of lithium and a transition metal is used, lithium ions are contained in the negative electrode active material, and therefore it can be preferably combined with a material that does not contain lithium ions, such as V2O5 or Cr3O8, as the positive electrode active material. Even when a material containing lithium ions is used as the positive electrode active material, the composite nitride of lithium and a transition metal can be used as the negative electrode active material by first desorbing the lithium ions contained in the positive electrode active material.

[0383] In addition, materials that undergo a conversion reaction can also be used as the negative electrode active material. For example, transition metal oxides that do not form alloys with lithium, such as cobalt oxide (CoO), nickel oxide (NiO), and iron oxide (FeO), can be used as the negative electrode active material. Materials that undergo a conversion reaction include oxides such as Fe2O3, CuO, Cu2O, RuO2, and Cr2O3, and CoS 0.89 It also occurs with sulfides such as NiS and CuS, nitrides such as Zn3N2, Cu3N and Ge3N4, phosphides such as NiP2, FeP2 and CoP3, and fluorides such as FeF3 and BiF3.

[0384] The conductive agent and binder that can be contained in the negative electrode active material layer can be the same materials as the conductive agent and binder that can be contained in the positive electrode active material layer.

[0385] [Negative electrode current collector] The negative electrode current collector may be made of the same material as the positive electrode current collector, but it is preferable that the negative electrode current collector be made of a material that does not alloy with carrier ions such as lithium.

[0386] A negative electrode can be obtained by applying a slurry containing the negative electrode active material, the binder, a solvent, a conductive agent, and the like to a negative electrode current collector and pressing the coating. NMP can be used as the solvent. A press is used for the press processing, and the slurry is heated by setting the temperature of the first and second rolls of the press to 80°C to 150°C, preferably 100°C to 130°C. Higher roll temperatures can increase electrode density. However, the temperature should be below the melting point of the binder. For example, the melting point of PVDF used as the binder is 158°C to 160°C. The pressing pressure is 100 kN / m to 300 kN / m, preferably 150 kN / m to 250 kN / m, and more preferably 190 kN / m to 230 kN / m. When pressing is performed multiple times, the pressing pressure for the second press is 5 to 8 times, preferably 6 to 7 times, the pressing pressure for the first press.

[0387] [Electrolyte] The electrolytic solution contains a solvent and an electrolyte. The solvent for the electrolytic solution is preferably an aprotic organic solvent, such as ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate, chloroethylene carbonate, vinylene carbonate, γ-butyrolactone, γ-valerolactone, dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), methyl formate, methyl acetate, ethyl acetate, methyl propionate, ethyl propionate, propyl propionate, methyl butyrate, 1,3-dioxane, 1,4-dioxane, dimethoxyethane (DME), dimethyl sulfoxide, diethyl ether, methyl diglyme, acetonitrile, benzonitrile, tetrahydrofuran, sulfolane, or sultone, or any combination and ratio of two or more of these.

[0388] Furthermore, by using one or more flame-retardant and non-volatile ionic liquids (room-temperature molten salts) as the solvent for the electrolyte, it is possible to prevent the secondary battery from exploding and / or catching fire even if the internal temperature rises due to an internal short circuit or overcharging of the secondary battery. Ionic liquids are composed of cations and anions, including organic cations and anions. Examples of organic cations used in the electrolyte include aliphatic onium cations such as quaternary ammonium cations, tertiary sulfonium cations, and quaternary phosphonium cations, and aromatic cations such as imidazolium cations and pyridinium cations. Examples of anions used in the electrolyte include monovalent amide anions, monovalent methide anions, fluorosulfonate anions, perfluoroalkylsulfonate anions, tetrafluoroborate anions, perfluoroalkylborate anions, hexafluorophosphate anions, and perfluoroalkylphosphate anions.

[0389] Examples of the electrolyte to be dissolved in the solvent include LiPF6, LiClO4, LiAsF6, LiBF4, LiAlCl4, LiSCN, LiBr, LiI, Li2SO4, and Li2B 10 Cl 10 , Li2B 12 Cl 12 Lithium salts such as LiCF3SO3, LiC4F9SO3, LiC(CF3SO2)3, LiC(C2F5SO2)3, LiN(FSO2)2, LiN(CF3SO2)2, LiN(C4F9SO2)(CF3SO2), LiN(C2F5SO2)2 can be used alone or in any combination and ratio of two or more of these.

[0390] The electrolyte used in the secondary battery is preferably a highly purified electrolyte with a low content of granular dust or elements other than the constituent elements of the electrolyte (hereinafter simply referred to as "impurities"). Specifically, the weight ratio of impurities to the electrolyte is preferably 1% or less, preferably 0.1% or less, and more preferably 0.01% or less.

[0391] The electrolyte may also contain additives such as vinylene carbonate (VC), propane sultone (PS), tert-butylbenzene (TBB), fluoroethylene carbonate (FEC), lithium bis(oxalato)borate (LiBOB), or dinitrile compounds such as succinonitrile and adiponitrile. The concentration of the additive may be, for example, 0.1 wt% to 5 wt% of the total solvent. VC or LiBOB is particularly preferred because it easily forms a good coating.

[0392] Alternatively, a polymer gel electrolyte may be used in which a polymer is swollen with an electrolytic solution.

[0393] The use of a polymer gel electrolyte improves safety against leakage, etc. It also enables the secondary battery to be made thinner and lighter.

[0394] Examples of polymers that can be gelled include silicone gel, acrylic gel, acrylonitrile gel, polyethylene oxide gel, polypropylene oxide gel, and fluorine-based polymer gel.

[0395] Examples of polymers that can be used include polymers having a polyalkylene oxide structure such as polyethylene oxide (PEO), PVDF, polyacrylonitrile, and copolymers containing these. For example, PVDF-HFP, a copolymer of PVDF and hexafluoropropylene (HFP), can be used. The polymer formed may also have a porous shape.

[0396] In addition, instead of an electrolyte solution, a solid electrolyte containing an inorganic material such as a sulfide or oxide, or a polymer material such as a polyethylene oxide (PEO) can be used. When a solid electrolyte is used, the installation of a separator and / or spacer is unnecessary. Furthermore, since the entire battery can be solidified, the risk of leakage is eliminated, dramatically improving safety.

[0397] [Exterior body] The exterior body of the secondary battery can be made of a metal material such as aluminum and / or a resin material. Alternatively, a film-like exterior body can be used. Examples of films that can be used include a three-layer structure in which a thin, flexible metal film made of aluminum, stainless steel, copper, nickel, or the like is provided on a film made of a material such as polyethylene, polypropylene, polycarbonate, ionomer, or polyamide, and an insulating synthetic resin film made of polyamide resin, polyester resin, or the like is further provided on the thin metal film as the outer surface of the exterior body.

[0398] <Configuration example 2 of secondary battery> As an example of the configuration of a secondary battery, the configuration of a secondary battery using a solid electrolyte layer will be described below.

[0399] As shown in FIG. 18A, a secondary battery 400 according to one embodiment of the present invention includes a positive electrode 410, a solid electrolyte layer 420, and a negative electrode 430.

[0400] The positive electrode 410 includes a positive electrode current collector 413 and a positive electrode active material layer 414. The positive electrode active material layer 414 includes a positive electrode active material 411 and a solid electrolyte 421. The positive electrode active material 411 is formed using the positive electrode active material formed by the method described in the above embodiment. The positive electrode active material layer 414 may include a conductive agent and a binder.

[0401] Solid electrolyte layer 420 has solid electrolyte 421. Solid electrolyte layer 420 is located between positive electrode 410 and negative electrode 430, and is a region that has neither positive electrode active material 411 nor negative electrode active material 431.

[0402] The negative electrode 430 includes a negative electrode current collector 433 and a negative electrode active material layer 434. The negative electrode active material layer 434 includes a negative electrode active material 431 and a solid electrolyte 421. The negative electrode active material layer 434 may also include a conductive agent and a binder. When metallic lithium is used for the negative electrode 430, the negative electrode 430 may not include the solid electrolyte 421, as shown in FIG. 18B . Using metallic lithium for the negative electrode 430 is preferable because it can improve the energy density of the secondary battery 400.

[0403] As solid electrolyte 421 included in solid electrolyte layer 420, for example, a sulfide-based solid electrolyte, an oxide-based solid electrolyte, a halide-based solid electrolyte, or the like can be used.

[0404] Sulfide-based solid electrolytes include thiolithium-based (Li 10 GeP2S 12 , Li 3.25 Ge 0.25 P 0.75 S4, etc.), sulfide glasses (70Li2S·30P2S5, 30Li2S·26B2S3·44LiI, 63Li2S·36SiS2·1Li3PO4, 57Li2S·38SiS2·5Li4SiO4, 50Li2S·50GeS2, etc.), sulfide crystallized glasses (Li7P3S 11 , Li 3.25 P 0.95 Sulfide-based solid electrolytes have the advantages of being highly conductive, being able to be synthesized at low temperatures, and being relatively soft, which makes it easy to maintain conductive paths even after charging and discharging.

[0405] Oxide-based solid electrolytes include materials with a perovskite crystal structure (La 2 / 3-x Li 3x TiO3, etc.), materials with NASICON-type crystal structure (Li 1+x Al x Ti 2-x (PO4)3, etc.), materials with garnet-type crystal structure (Li7La3Zr2O 12 etc.), materials with LISICON-type crystal structure (Li 14 ZnGeO 16 etc.), LLZO(Li7La3Zr2O 12 ), oxide glass (Li3PO4-Li4SiO4, 50Li4SiO4·50Li3BO3, etc.), oxide glass-ceramics (Li 1.07 Al 0.69 Ti 1.46 (PO4)3, Li 1.5 Al 0.5 Ge 1.5 Oxide-based solid electrolytes have the advantage of being stable in the atmosphere.

[0406] Halide-based solid electrolytes include LiAlCl4, Li3InBr6, LiF, LiCl, LiBr, LiI, etc. In addition, composite materials in which these halide-based solid electrolytes are filled in the pores of porous aluminum oxide and / or porous silica can also be used as solid electrolytes.

[0407] Also, different solid electrolytes may be mixed and used.

[0408] Among them, Li 1+x Al x Ti 2-x (PO4)3 (0 < x < 1) (hereinafter referred to as LATP) contains aluminum and titanium, which are elements that the positive electrode active material used in the secondary battery 400 of one aspect of the present invention may have. Therefore, a synergistic effect can be expected for improving the cycle characteristics, which is preferable. In addition, an improvement in productivity due to reduction of processes can also be expected. In this specification and the like, the NASICON-type crystal structure refers to a compound represented by M2(XO4)3 (M: transition metal, X: S, P, As, Mo, W, etc.), which has a structure in which MO6 octahedra and XO4 tetrahedra share vertices and are three-dimensionally arranged.

[0409] 〔Shape of the exterior body and the secondary battery〕 For the exterior body of the secondary battery 400 of one aspect of the present invention, various materials and shapes can be used, but it preferably has a function of pressing the positive electrode, the solid electrolyte layer, and the negative electrode.

[0410] For example, FIG. 19 is an example of a cell for evaluating the materials of an all-solid-state battery.

[0411] 19A is a cross-sectional schematic diagram of the evaluation cell, which has a lower member 761, an upper member 762, and a fixing screw or wing nut 764 that fixes them together, and electrode plate 753 is pressed to fix the evaluation material by rotating a holding screw 763. An insulator 766 is provided between lower member 761 and upper member 762, which are made of stainless steel. An O-ring 765 is also provided between upper member 762 and holding screw 763 to provide a tight seal.

[0412] The evaluation material is placed on electrode plate 751, surrounded by insulating tube 752, and pressed from above by electrode plate 753. An enlarged perspective view of the evaluation material and its surroundings is shown in Figure 19B.

[0413] The evaluation material is an example of a laminate of a positive electrode 750a, a solid electrolyte layer 750b, and a negative electrode 750c, and its cross-sectional view is shown in Figure 19C. Note that the same reference numerals are used for the same parts in Figures 19A, 19B, and 19C.

[0414] The electrode plate 751 and lower member 761, which are electrically connected to the positive electrode 750a, can be said to correspond to a positive electrode terminal. The electrode plate 753 and upper member 762, which are electrically connected to the negative electrode 750c, can be said to correspond to a negative electrode terminal. Electrical resistance and the like can be measured by applying pressure to the evaluation material via the electrode plate 751 and the electrode plate 753.

[0415] The secondary battery of one embodiment of the present invention preferably uses an airtight package for its exterior. For example, a ceramic package and / or a resin package can be used. The exterior is preferably sealed in a sealed atmosphere, such as a glove box, while blocking external air.

[0416] Fig. 20A shows a perspective view of a secondary battery of one embodiment of the present invention, which has an exterior body and a shape different from those in Fig. 19. The secondary battery in Fig. 20A has external electrodes 771 and 772 and is sealed in an exterior body having multiple package members.

[0417] An example of a cross section taken along the dashed line in Figure 20A is shown in Figure 20B. A laminate including positive electrode 750a, solid electrolyte layer 750b, and negative electrode 750c is enclosed and sealed within package member 770a, which is a flat plate with electrode layer 773a provided thereon, frame-shaped package member 770b, and package member 770c, which is a flat plate with electrode layer 773b provided thereon. Package members 770a, 770b, and 770c can be made of an insulating material, such as a resin material and / or a ceramic material.

[0418] The external electrode 771 is electrically connected to the positive electrode 750a via the electrode layer 773a and functions as a positive electrode terminal, while the external electrode 772 is electrically connected to the negative electrode 750c via the electrode layer 773b and functions as a negative electrode terminal.

[0419] This embodiment mode can be implemented in appropriate combination with other embodiment modes.

[0420] (Fourth embodiment) In this embodiment, an example of the shape of a secondary battery having the positive electrode described in the previous embodiment will be described. The description in the previous embodiment can be referred to for materials used in the secondary battery described in this embodiment.

[0421] <Coin-type secondary battery> First, an example of a coin-type secondary battery will be described. Figure 21A is an external view of a coin-type (single-layer flat) secondary battery, and Figure 21B is a cross-sectional view thereof.

[0422] In a coin-type secondary battery 300, a positive electrode can 301, which also serves as a positive electrode terminal, and a negative electrode can 302, which also serves as a negative electrode terminal, are insulated and sealed by a gasket 303 made of polypropylene or the like. The positive electrode 304 is formed by a positive electrode current collector 305 and a positive electrode active material layer 306 provided in contact with the positive electrode current collector. The negative electrode 307 is formed by a negative electrode current collector 308 and a negative electrode active material layer 309 provided in contact with the negative electrode current collector.

[0423] It is to be noted that the positive electrode 304 and the negative electrode 307 used in the coin-type secondary battery 300 each only need to have an active material layer formed on one side.

[0424] Positive electrode can 301 and negative electrode can 302 can be made of metals such as nickel, aluminum, titanium, or alloys thereof and / or alloys of these with other metals (e.g., stainless steel) that are corrosion-resistant to the electrolyte. Furthermore, to prevent corrosion by the electrolyte, it is preferable to coat them with nickel and / or aluminum. Positive electrode can 301 is electrically connected to positive electrode 304, and negative electrode can 302 is electrically connected to negative electrode 307.

[0425] These negative electrode 307, positive electrode 304, and separator 310 are impregnated with an electrolyte, and as shown in FIG. 21B, the positive electrode 304, separator 310, negative electrode 307, and negative electrode can 302 are stacked in this order with the positive electrode can 301 facing downwards, and the positive electrode can 301 and the negative electrode can 302 are crimped together via a gasket 303 to produce a coin-type secondary battery 300.

[0426] By using the positive electrode active material described in the above embodiment for the positive electrode 304, the coin-type secondary battery 300 can have high charge / discharge capacity and excellent cycle characteristics.

[0427] Here, we will explain the current flow during charging of a secondary battery using Figure 21C. When a lithium-based secondary battery is considered as a closed circuit, the movement of lithium ions and the flow of current are in the same direction. In lithium-based secondary batteries, the anode (positive electrode) and cathode (negative electrode) are interchanged during charging and discharging, and the oxidation and reduction reactions are alternated. Therefore, the electrode with the higher reaction potential is called the positive electrode, and the electrode with the lower reaction potential is called the negative electrode. Therefore, in this specification, the positive electrode will be called the "positive electrode" or "+ electrode (plus electrode)," and the negative electrode will be called the "negative electrode" or "- electrode (minus electrode)," regardless of whether the battery is being charged or discharged, whether a reverse pulse current is being applied, or whether a charging current is being applied. Using the terms anode (positive electrode) and cathode (negative electrode), which are related to oxidation and reduction reactions, may lead to confusion because their roles are reversed during charging and discharging. Therefore, the terms anode (positive electrode) and cathode (negative electrode) will not be used in this specification. If the terms anode and cathode are used, it should be clearly stated whether they are used during charging or discharging, and whether they correspond to the positive or negative pole.

[0428] A charger is connected to the two terminals shown in Fig. 21C to charge the secondary battery 300. As the charging of the secondary battery 300 progresses, the potential difference between the electrodes increases.

[0429] <Cylindrical secondary battery> Next, an example of a cylindrical secondary battery will be described with reference to Fig. 22. Fig. 22A shows an external view of a cylindrical secondary battery 600. Fig. 22B is a schematic diagram showing a cross section of the cylindrical secondary battery 600. As shown in Fig. 22B, the cylindrical secondary battery 600 has a positive electrode cap (battery lid) 601 on the top surface, and a battery can (external can) 602 on the side and bottom surfaces. The positive electrode cap 601 and the battery can (external can) 602 are insulated by a gasket (insulating packing) 610.

[0430] A battery element is provided inside a hollow cylindrical battery can 602, in which a strip-shaped positive electrode 604 and a negative electrode 606 are wound with a separator 605 sandwiched between them. Although not shown, the battery element is wound around a center pin. One end of the battery can 602 is closed and the other end is open. The battery can 602 can be made of a metal such as nickel, aluminum, or titanium that is corrosion-resistant to the electrolyte, or an alloy of these metals and / or alloys of these metals with other metals (e.g., stainless steel). To prevent corrosion by the electrolyte, the battery can 602 is preferably coated with nickel and / or aluminum. Inside the battery can 602, the wound battery element, in which the positive electrode, negative electrode, and separator are wound, is sandwiched between a pair of opposing insulating plates 608 and 609. A nonaqueous electrolyte (not shown) is poured into the battery can 602, in which the battery element is provided. The nonaqueous electrolyte may be the same as that used in coin-type secondary batteries.

[0431] Because the positive and negative electrodes used in cylindrical storage batteries are wound, it is preferable to form active materials on both sides of the current collector. A positive electrode terminal (positive electrode current collector lead) 603 is connected to the positive electrode 604, and a negative electrode terminal (negative electrode current collector lead) 607 is connected to the negative electrode 606. Both the positive electrode terminal 603 and the negative electrode terminal 607 can be made of a metal material such as aluminum. The positive electrode terminal 603 is resistance-welded to a safety valve mechanism 612, and the negative electrode terminal 607 is resistance-welded to the bottom of the battery can 602. The safety valve mechanism 612 is electrically connected to the positive electrode cap 601 via a PTC (Positive Temperature Coefficient) element 611. The safety valve mechanism 612 cuts off the electrical connection between the positive electrode cap 601 and the positive electrode 604 when the internal pressure of the battery exceeds a predetermined threshold. The PTC element 611 is a thermosensitive resistor whose resistance increases as the temperature rises, and the increased resistance limits the amount of current to prevent abnormal heat generation. Barium titanate (BaTiO3) based semiconductor ceramics or the like can be used for the PTC element.

[0432] 22C , a module 615 may be configured by sandwiching a plurality of secondary batteries 600 between conductive plates 613 and 614. The plurality of secondary batteries 600 may be connected in parallel, in series, or in parallel and then in series. By configuring a module 615 having a plurality of secondary batteries 600, a large amount of power can be extracted.

[0433] FIG. 22D is a top view of module 615. For clarity, conductive plate 613 is shown with dotted lines. As shown in FIG. 22D, module 615 may have conductors 616 that electrically connect multiple secondary batteries 600. A conductive plate can be superimposed on the conductors 616. Furthermore, a temperature control device 617 may be provided between multiple secondary batteries 600. When a secondary battery 600 overheats, it can be cooled by the temperature control device 617, and when a secondary battery 600 is too cold, it can be heated by the temperature control device 617. This makes the performance of module 615 less susceptible to the influence of the outside air temperature. It is preferable that the heat medium in temperature control device 617 is insulating and non-flammable.

[0434] By using the positive electrode active material described in the above embodiment for the positive electrode 604, the cylindrical secondary battery 600 can have high charge / discharge capacity and excellent cycle characteristics.

[0435] [Separator] The secondary battery preferably has a separator. Examples of the separator include paper, nonwoven fabric, glass fiber, ceramics, and synthetic fibers such as nylon (polyamide), vinylon (polyvinyl alcohol fiber), polyester, acrylic, polyolefin, and polyurethane. The separator is preferably envelope-shaped and disposed so as to encase either the positive electrode or the negative electrode.

[0436] The separator may have a multilayer structure. For example, an organic film such as polypropylene or polyethylene may be coated with a ceramic material, a fluorine-based material, a polyamide material, or a mixture of these. Examples of ceramic materials include aluminum oxide particles and silicon oxide particles. Examples of fluorine-based materials include PVDF and polytetrafluoroethylene. Examples of polyamide materials include nylon and aramid (meta-aramid and para-aramid).

[0437] Coating with ceramic materials improves oxidation resistance, suppressing separator degradation during high-voltage charging and discharging and improving the reliability of secondary batteries. Coating with fluorine-based materials also improves adhesion between the separator and electrodes, improving output characteristics. Coating with polyamide materials, especially aramid, improves heat resistance, improving the safety of secondary batteries.

[0438] For example, both sides of a polypropylene film may be coated with a mixed material of aluminum oxide and aramid, or the surface of the polypropylene film that comes into contact with the positive electrode may be coated with a mixed material of aluminum oxide and aramid, and the surface that comes into contact with the negative electrode may be coated with a fluorine-based material.

[0439] When a separator with a multilayer structure is used, the safety of the secondary battery can be maintained even if the overall thickness of the separator is thin, and therefore the charge / discharge capacity per volume of the secondary battery can be increased.

[0440] <Example of secondary battery structure> Another structural example of the secondary battery will be described with reference to FIGS.

[0441] 23A and 23B are diagrams showing the appearance of a battery pack. The battery pack has a secondary battery 913 and a circuit board 900. The secondary battery 913 is connected to an antenna 914 via the circuit board 900. A label 910 is attached to the secondary battery 913. Furthermore, as shown in FIG. 23B, the secondary battery 913 is connected to terminals 951 and 952. The circuit board 900 is fixed with a sticker 915.

[0442] The circuit board 900 has a terminal 911 and a circuit 912. The terminal 911 is connected to a terminal 951, a terminal 952, an antenna 914, and the circuit 912. Note that a plurality of terminals 911 may be provided, and each of the plurality of terminals 911 may be used as a control signal input terminal, a power supply terminal, or the like.

[0443] The circuit 912 may be provided on the back surface of the circuit board 900. The antenna 914 is not limited to a coil shape and may be, for example, a wire or plate shape. Also, a planar antenna, an aperture antenna, a traveling wave antenna, an EH antenna, a magnetic field antenna, a dielectric antenna, or the like may be used. Alternatively, the antenna 914 may be a flat conductor. This flat conductor can function as one of the conductors for electric field coupling. In other words, the antenna 914 may function as one of the two conductors of a capacitor. This allows power to be exchanged not only by electromagnetic fields and magnetic fields but also by electric fields.

[0444] The battery pack has a layer 916 between the antenna 914 and the secondary battery 913. The layer 916 has a function of, for example, shielding an electromagnetic field generated by the secondary battery 913. The layer 916 can be made of, for example, a magnetic material.

[0445] The structure of the battery pack is not limited to that shown in FIG.

[0446] For example, as shown in Figures 24A and 24B, an antenna may be provided on each of a pair of opposing surfaces of secondary battery 913 shown in Figures 23A and 23B. Figure 24A is an external view showing one of the pair of surfaces, and Figure 24B is an external view showing the other of the pair of surfaces. Note that, in the secondary battery shown in Figures 24A and 24B, the same parts as those in the secondary battery shown in Figures 23A and 23B can be described as appropriate, and therefore will not be described here.

[0447] 24A, an antenna 914 is provided on one of a pair of surfaces of a secondary battery 913 with a layer 916 sandwiched therebetween, and as shown in Fig. 24B, an antenna 918 is provided on the other of the pair of surfaces of the secondary battery 913 with a layer 917 sandwiched therebetween. The layer 917 has a function of, for example, being able to shield the electromagnetic field caused by the secondary battery 913. The layer 917 can be made of, for example, a magnetic material.

[0448] The above structure allows the sizes of both antenna 914 and antenna 918 to be increased. Antenna 918 has a function of, for example, performing data communication with an external device. For example, an antenna having a shape applicable to antenna 914 can be used for antenna 918. As a communication method between the secondary battery and other devices via antenna 918, a response method that can be used between the secondary battery and other devices, such as NFC (near field wireless communication), can be used.

[0449] Alternatively, as shown in Fig. 24C, a display device 920 may be provided on the secondary battery 913 shown in Fig. 23A and Fig. 23B. The display device 920 is electrically connected to the terminal 911. Note that the label 910 does not need to be provided on the portion where the display device 920 is provided. Note that the description of the same parts of the secondary battery shown in Fig. 24C as those of the secondary battery shown in Fig. 23A and Fig. 23B can be used as appropriate, and therefore will not be repeated here.

[0450] The display device 920 may display, for example, an image indicating whether charging is in progress or an image indicating the amount of stored power. For example, electronic paper, a liquid crystal display device, an electroluminescence (EL) display device, or the like can be used as the display device 920. For example, by using electronic paper, the power consumption of the display device 920 can be reduced.

[0451] Alternatively, as shown in Fig. 24D, a sensor 921 may be provided in the secondary battery 913 shown in Fig. 23A and 23B. The sensor 921 is electrically connected to the terminal 911 via a terminal 922. Note that, in the secondary battery shown in Fig. 24D, the same parts as those in the secondary battery shown in Fig. 23A and 23B can be described as appropriate, and therefore the description thereof will be omitted here.

[0452] The sensor 921 may have a function of measuring, for example, displacement, position, speed, acceleration, angular velocity, rotation speed, distance, light, liquid, magnetism, temperature, chemical substance, sound, time, hardness, electric field, current, voltage, power, radiation, flow rate, humidity, gradient, vibration, odor, or infrared ray. By providing the sensor 921, for example, data indicating the environment in which the secondary battery is placed (such as temperature) can be detected and stored in the memory in the circuit 912.

[0453] Furthermore, an example of the structure of the secondary battery 913 will be described with reference to FIGS.

[0454] A secondary battery 913 shown in Fig. 25A has a wound body 950 in which terminals 951 and 952 are provided inside a housing 930. The wound body 950 is impregnated with an electrolyte inside the housing 930. The terminal 952 contacts the housing 930, and the terminal 951 is not in contact with the housing 930 by using an insulating material or the like. Note that in Fig. 25A, for convenience, the housing 930 is shown separated, but in reality, the wound body 950 is covered by the housing 930, and the terminals 951 and 952 extend outside the housing 930. The housing 930 can be made of a metal material (such as aluminum) or a resin material.

[0455] 25B, the housing 930 shown in Fig. 25A may be formed from a plurality of materials. For example, the secondary battery 913 shown in Fig. 25B has housings 930a and 930b bonded together, and a wound body 950 is provided in the area surrounded by housings 930a and 930b.

[0456] The housing 930a can be made of an insulating material such as organic resin. In particular, by using a material such as organic resin on the surface on which the antenna is formed, it is possible to prevent the secondary battery 913 from blocking the electric field. Note that if the electric field blocking by the housing 930a is small, an antenna such as the antenna 914 may be provided inside the housing 930a. The housing 930b can be made of, for example, a metal material.

[0457] 26 shows the structure of the wound body 950. The wound body 950 has a negative electrode 931, a positive electrode 932, and a separator 933. The wound body 950 is a wound body in which the negative electrode 931 and the positive electrode 932 are stacked on top of each other with the separator 933 sandwiched therebetween, and the laminated sheet is wound. Note that a plurality of layers of the negative electrode 931, the positive electrode 932, and the separator 933 may be stacked.

[0458] 23 via one of terminal 951 and terminal 952. The positive electrode 932 is connected to terminal 911 shown in FIG.

[0459] By using the positive electrode active material described in the above embodiment for the positive electrode 932, the secondary battery 913 can have high charge / discharge capacity and excellent cycle characteristics.

[0460] <Laminated secondary battery> Next, examples of laminated secondary batteries will be described with reference to Figures 27 to 31. If a laminated secondary battery has a flexible configuration, and is mounted in an electronic device having at least a flexible portion, the secondary battery can also be bent in accordance with deformation of the electronic device.

[0461] A laminated secondary battery 980 will be described using Fig. 27. The laminated secondary battery 980 has a wound body 993 shown in Fig. 27A. The wound body 993 has a negative electrode 994, a positive electrode 995, and a separator 996. Similar to the wound body 950 described in Fig. 26, the wound body 993 is formed by stacking the negative electrode 994 and the positive electrode 995 on top of each other with the separator 996 sandwiched therebetween, and winding the laminated sheet.

[0462] The number of layers of the negative electrode 994, the positive electrode 995, and the separator 996 may be appropriately designed depending on the required charge / discharge capacity and element volume. The negative electrode 994 is connected to a negative electrode current collector (not shown) via one of the lead electrodes 997 and 998, and the positive electrode 995 is connected to a positive electrode current collector (not shown) via the other of the lead electrodes 997 and 998.

[0463] 27B, a film 981 serving as an exterior body and a film 982 having a recess are bonded together by thermocompression or the like to form a space, and the above-described wound body 993 is stored in the space, thereby producing a secondary battery 980 as shown in Fig. 27C. The wound body 993 has lead electrodes 997 and 998, and is impregnated with an electrolyte solution between the film 981 and the film 982 having a recess.

[0464] For example, a metal material such as aluminum and / or a resin material can be used for film 981 and film 982 having recesses. If a resin material is used as the material for film 981 and film 982 having recesses, film 981 and film 982 having recesses can be deformed when an external force is applied, and a flexible storage battery can be produced.

[0465] Although an example using two films is shown in FIGS. 27B and 27C, a space may be formed by folding one film, and the wound body 993 described above may be housed in that space.

[0466] By using the positive electrode active material described in the above embodiment for the positive electrode 995, the secondary battery 980 can have high charge / discharge capacity and excellent cycle characteristics.

[0467] Furthermore, although Figure 27 describes an example of a secondary battery 980 having a wound body in a space formed by a film that serves as an outer casing, it may also be a secondary battery having multiple rectangular positive electrodes, separators, and negative electrodes in a space formed by a film that serves as an outer casing, as shown in Figure 28, for example.

[0468] 28A includes a positive electrode 503 having a positive electrode current collector 501 and a positive electrode active material layer 502, a negative electrode 506 having a negative electrode current collector 504 and a negative electrode active material layer 505, a separator 507, an electrolyte 508, and an exterior body 509. The separator 507 is disposed between the positive electrode 503 and the negative electrode 506 provided in the exterior body 509. The exterior body 509 is filled with the electrolyte 508. The electrolyte solution described in Embodiment 3 can be used as the electrolyte 508.

[0469] 28A , positive electrode current collector 501 and negative electrode current collector 504 also serve as terminals for electrical contact with the outside. Therefore, positive electrode current collector 501 and negative electrode current collector 504 may be arranged so as to be partially exposed to the outside from outer casing 509. Alternatively, positive electrode current collector 501 and negative electrode current collector 504 may not be exposed to the outside from outer casing 509, and lead electrodes may be used to ultrasonically bond positive electrode current collector 501 or negative electrode current collector 504 to expose the lead electrodes to the outside.

[0470] In the laminated secondary battery 500, the exterior body 509 may be a three-layer laminate film having a highly flexible thin metal film made of aluminum, stainless steel, copper, nickel, or the like provided on a film made of a material such as polyethylene, polypropylene, polycarbonate, ionomer, or polyamide, and further having an insulating synthetic resin film made of polyamide-based resin, polyester-based resin, or the like provided on the thin metal film as the outer surface of the exterior body.

[0471] 28B shows an example of the cross-sectional structure of laminated secondary battery 500. For simplicity, Fig. 28A shows an example configured with two current collectors, but in reality, as shown in Fig. 28B, it is configured with multiple electrode layers.

[0472] In FIG. 28B, the number of electrode layers is 16 as an example. Note that even if the number of electrode layers is 16, the secondary battery 500 remains flexible. FIG. 28B shows a structure with a total of 16 layers, including 8 layers of negative electrode current collectors 504 and 8 layers of positive electrode current collectors 501. Note that FIG. 28B also shows a cross section of the negative electrode lead-out portion, in which 8 layers of negative electrode current collectors 504 are ultrasonically bonded. Of course, the number of electrode layers is not limited to 16 and may be more or less. When the number of electrode layers is large, a secondary battery with a larger charge / discharge capacity can be obtained. Furthermore, when the number of electrode layers is small, a secondary battery can be made thinner and have excellent flexibility.

[0473] 29 and 30 show an example of an external view of a laminated secondary battery 500. Figures 29 and 30 show a positive electrode 503, a negative electrode 506, a separator 507, an outer casing 509, a positive electrode lead electrode 510, and a negative electrode lead electrode 511.

[0474] FIG. 31A shows the appearance of a positive electrode 503 and a negative electrode 506. The positive electrode 503 has a positive electrode current collector 501, and a positive electrode active material layer 502 is formed on the surface of the positive electrode current collector 501. The positive electrode 503 also has a region where the positive electrode current collector 501 is partially exposed (hereinafter referred to as a tab region). The negative electrode 506 has a negative electrode current collector 504, and a negative electrode active material layer 505 is formed on the surface of the negative electrode current collector 504. The negative electrode 506 also has a region where the negative electrode current collector 504 is partially exposed, i.e., a tab region. The area and shape of the tab regions of the positive electrode and negative electrode are not limited to the example shown in FIG. 31A.

[0475] <Method for manufacturing laminated secondary batteries> Here, an example of a method for producing the laminated secondary battery whose external view is shown in FIG. 29 will be described with reference to FIGS. 31B and 31C.

[0476] First, the negative electrode 506, separator 507, and positive electrode 503 are stacked. FIG. 31B shows the stacked negative electrode 506, separator 507, and positive electrode 503. Here, an example is shown in which five pairs of negative electrodes and four pairs of positive electrodes are used. Next, the tab regions of the positive electrodes 503 are joined together, and a positive electrode lead electrode 510 is joined to the tab region of the outermost positive electrode. For example, ultrasonic welding or the like may be used for joining. Similarly, the tab regions of the negative electrode 506 are joined together, and a negative electrode lead electrode 511 is joined to the tab region of the outermost negative electrode.

[0477] Next, negative electrode 506 , separator 507 and positive electrode 503 are placed on exterior body 509 .

[0478] Next, as shown in Fig. 31C, exterior body 509 is folded at the portion indicated by the dashed line. Thereafter, the outer periphery of exterior body 509 is joined. For the joining, for example, thermocompression bonding or the like may be used. At this time, an area (hereinafter referred to as an inlet) that is not joined is provided in a part (or one side) of exterior body 509 so that electrolyte 508 can be introduced later.

[0479] Next, electrolyte 508 (not shown) is introduced into the inside of exterior body 509 through an inlet provided in exterior body 509. The introduction of electrolyte 508 is preferably carried out under a reduced pressure atmosphere or an inert atmosphere. Finally, the inlet is joined. In this manner, laminated secondary battery 500 can be produced.

[0480] By using the positive electrode active material described in the above embodiment for the positive electrode 503, the secondary battery 500 can have high charge / discharge capacity and excellent cycle characteristics.

[0481] In an all-solid-state battery, applying a predetermined pressure in the stacking direction of the stacked positive and negative electrodes can maintain good contact at the internal interfaces. Applying a predetermined pressure in the stacking direction of the positive and negative electrodes can suppress expansion in the stacking direction due to charging and discharging of the all-solid-state battery, thereby improving the reliability of the all-solid-state battery.

[0482] This embodiment mode can be implemented in appropriate combination with other embodiment modes.

[0483] (Embodiment 5) In this embodiment, an example in which a secondary battery according to one embodiment of the present invention is mounted on an electronic device will be described.

[0484] 32A to 32G show examples of electronic devices incorporating the bendable secondary battery described in the previous embodiment. Examples of electronic devices that use the bendable secondary battery include television devices (also called televisions or television receivers), computer monitors, digital cameras, digital video cameras, digital photo frames, mobile phones (also called mobile phones or mobile phone devices), portable game machines, personal digital assistants, audio playback devices, and large game machines such as pachinko machines.

[0485] Furthermore, a secondary battery having a flexible shape can be incorporated along the curved surfaces of the inner or outer walls of houses, buildings, etc., and the interior or exterior of automobiles.

[0486] 32A illustrates an example of a mobile phone. The mobile phone 7400 includes a display portion 7402 built into a housing 7401, operation buttons 7403, an external connection port 7404, a speaker 7405, a microphone 7406, and the like. Note that the mobile phone 7400 includes a secondary battery 7407. By using the secondary battery of one embodiment of the present invention as the secondary battery 7407, a lightweight mobile phone with a long life can be provided.

[0487] FIG. 32B shows the mobile phone 7400 in a bent state. When the mobile phone 7400 is deformed by an external force and bent as a whole, the secondary battery 7407 installed inside is also bent. FIG. 32C shows the state of the bent secondary battery 7407 at that time. The secondary battery 7407 is a thin storage battery. The secondary battery 7407 is fixed in a bent state. The secondary battery 7407 has a lead electrode electrically connected to the current collector. For example, the current collector is copper foil, and a portion of the current collector is alloyed with gallium to improve adhesion with the active material layer in contact with the current collector, resulting in a configuration with high reliability when the secondary battery 7407 is bent.

[0488] FIG. 32D shows an example of a bangle-type display device. The portable display device 7100 includes a housing 7101, a display unit 7102, operation buttons 7103, and a secondary battery 7104. FIG. 32E shows a bent secondary battery 7104. When the secondary battery 7104 is worn on a user's arm in a bent state, the housing deforms, causing a change in the curvature of part or the entire secondary battery 7104. Note that the degree of curvature at any point on the curve, expressed as the radius of the corresponding circle, is called the radius of curvature, and the reciprocal of the radius of curvature is called the curvature. Specifically, part or the entire main surface of the housing or the secondary battery 7104 changes when the radius of curvature is in the range of 40 mm to 150 mm. High reliability can be maintained when the radius of curvature of the main surface of the secondary battery 7104 is in the range of 40 mm to 150 mm. By using the secondary battery of one embodiment of the present invention as the secondary battery 7104, a lightweight and long-life portable display device can be provided.

[0489] 32F shows an example of a wristwatch-type portable information terminal 7200. The portable information terminal 7200 includes a housing 7201, a display portion 7202, a band 7203, a buckle 7204, operation buttons 7205, an input / output terminal 7206, and the like.

[0490] The portable information terminal 7200 can execute various applications such as mobile phone calls, e-mail, document browsing and creation, music playback, internet communication, and computer games.

[0491] The display surface of the display portion 7202 is curved, and a display can be performed along the curved display surface. The display portion 7202 is also provided with a touch sensor, and can be operated by touching the screen with a finger or a stylus. For example, an application can be started by touching an icon 7207 displayed on the display portion 7202.

[0492] The operation button 7205 can be provided with various functions, such as time setting, power on / off operation, wireless communication on / off operation, silent mode activation / deactivation, power saving mode activation / deactivation, etc. For example, the functions of the operation button 7205 can be freely set by an operating system incorporated in the mobile information terminal 7200.

[0493] The mobile information terminal 7200 is also capable of performing standardized short-range wireless communication. For example, hands-free conversation is possible by communicating with a wirelessly enabled headset.

[0494] The portable information terminal 7200 also includes an input / output terminal 7206, and can directly exchange data with another information terminal via a connector. Charging can also be performed via the input / output terminal 7206. Note that charging may be performed by wireless power supply without using the input / output terminal 7206.

[0495] The display portion 7202 of the mobile information terminal 7200 includes the secondary battery of one embodiment of the present invention. By using the secondary battery of one embodiment of the present invention, a lightweight mobile information terminal with a long life can be provided. For example, the secondary battery 7104 shown in FIG. 32E can be installed in a curved state inside the housing 7201 or in a bendable state inside the band 7203.

[0496] The portable information terminal 7200 preferably has a sensor, such as a fingerprint sensor, a pulse sensor, a body temperature sensor, a touch sensor, a pressure sensor, an acceleration sensor, or the like.

[0497] 32G illustrates an example of an armband-type display device. The display device 7300 includes a display portion 7304 and the secondary battery of one embodiment of the present invention. The display device 7300 can also be provided with a touch sensor in the display portion 7304 and can function as a portable information terminal.

[0498] The display surface of the display portion 7304 is curved, and display can be performed along the curved display surface. The display state of the display device 7300 can be changed by short-range wireless communication according to a communication standard.

[0499] The display device 7300 also includes an input / output terminal, allowing direct data exchange with other information terminals via a connector. Charging can also be performed via the input / output terminal. Note that charging may also be performed by wireless power supply without using the input / output terminal.

[0500] By using the secondary battery of one embodiment of the present invention as the secondary battery included in the display device 7300, a lightweight display device with a long lifetime can be provided.

[0501] An example in which the secondary battery having good cycle characteristics shown in the above embodiment is mounted in an electronic device will be described with reference to FIGS. 32H, 33, and 34. FIG.

[0502] By using a secondary battery of one embodiment of the present invention as a secondary battery in daily electronic devices, products that are lightweight and have a long life can be provided. For example, daily electronic devices include electric toothbrushes, electric shavers, and electric beauty devices. For secondary batteries in these products, a stick-shaped secondary battery that is easy for users to hold, small, lightweight, and has a large charge / discharge capacity is desired.

[0503] FIG. 32H is a perspective view of a device also known as a tobacco-containing smoking device (electronic cigarette). In FIG. 32H, electronic cigarette 7500 includes atomizer 7501 including a heating element, secondary battery 7504 that supplies power to the atomizer, and cartridge 7502 including a liquid supply bottle, a sensor, and the like. To enhance safety, a protection circuit that prevents overcharging and / or over-discharging of secondary battery 7504 may be electrically connected to secondary battery 7504. Secondary battery 7504 shown in FIG. 32H has external terminals that allow connection to a charging device. Because secondary battery 7504 is the tip portion when held, it is desirable that its total length be short and its weight be light. The secondary battery of one embodiment of the present invention has a high charge / discharge capacity and favorable cycle characteristics, making it possible to provide a compact and lightweight electronic cigarette 7500 that can be used for a long period of time.

[0504] Next, an example of a foldable tablet terminal is shown in Figures 33A and 33B. The tablet terminal 9600 shown in Figures 33A and 33B includes a housing 9630a, a housing 9630b, a movable portion 9640 connecting the housings 9630a and 9630b, a display portion 9631 having display portions 9631a and 9631b, switches 9625 to 9627, a fastener 9629, and an operation switch 9628. A flexible panel can be used for the display portion 9631 to provide a tablet terminal with a larger display area. Figure 33A shows the tablet terminal 9600 in an open state, and Figure 33B shows the tablet terminal 9600 in a closed state.

[0505] The tablet terminal 9600 also includes a power storage unit 9635 inside the housing 9630a and the housing 9630b. The power storage unit 9635 passes through the movable portion 9640 and is provided across the housing 9630a and the housing 9630b.

[0506] The entire or part of the display portion 9631 can be a touch panel area, and data can be input by touching an image including an icon, text, an input form, etc. displayed in the area. For example, keyboard buttons may be displayed on the entire surface of the display portion 9631a on the housing 9630a side, and information such as text and images may be displayed on the display portion 9631b on the housing 9630b side.

[0507] A keyboard may be displayed on the display portion 9631b of the housing 9630b, and information such as text and images may be displayed on the display portion 9631a of the housing 9630a. A keyboard display switch button of a touch panel may be displayed on the display portion 9631, and the keyboard may be displayed on the display portion 9631 by touching the button with a finger or a stylus.

[0508] In addition, touch input can be simultaneously performed on the touch panel area of ​​the display portion 9631a on the housing 9630a side and the touch panel area of ​​the display portion 9631b on the housing 9630b side.

[0509] The switches 9625 to 9627 may be interfaces capable of switching various functions in addition to interfaces for operating the tablet terminal 9600. For example, at least one of the switches 9625 to 9627 may function as a switch for turning the tablet terminal 9600 on and off. For example, at least one of the switches 9625 to 9627 may have a function for switching the display orientation, such as portrait or landscape, or a function for switching between monochrome and color display. For example, at least one of the switches 9625 to 9627 may have a function for adjusting the brightness of the display unit 9631. The brightness of the display unit 9631 can be optimized depending on the amount of external light detected by an optical sensor built into the tablet terminal 9600 during use. The tablet terminal may also have built-in not only an optical sensor but also other detection devices, such as a gyroscope, an acceleration sensor, or other sensors for detecting tilt.

[0510] 33A shows an example in which the display areas of the display portion 9631a on the housing 9630a side and the display portion 9631b on the housing 9630b side are substantially the same, the display areas of the display portion 9631a and the display portion 9631b are not particularly limited, and the sizes of one and the other may be different, and the display qualities may also be different. For example, one may be a display panel that can display at a higher resolution than the other.

[0511] 33B shows a tablet terminal 9600 folded in half, and the tablet terminal 9600 includes a housing 9630, a solar cell 9633, and a charge / discharge control circuit 9634 including a DC-DC converter 9636. In addition, a secondary battery according to one embodiment of the present invention is used as a power storage unit 9635.

[0512] As described above, the tablet terminal 9600 can be folded in half, and therefore, can be folded so that the housing 9630a and the housing 9630b overlap each other when not in use. By folding, the display portion 9631 can be protected, thereby improving durability of the tablet terminal 9600. Furthermore, the power storage unit 9635 using the secondary battery of one embodiment of the present invention has high charge / discharge capacity and favorable cycle characteristics; therefore, the tablet terminal 9600 can be used for a long period of time.

[0513] In addition, the tablet terminal 9600 shown in Figures 33A and 33B can have functions such as displaying various information (still images, videos, text images, etc.), displaying a calendar, date or time on the display unit, a touch input function for touch inputting or editing information displayed on the display unit, and controlling processing using various software (programs).

[0514] A solar cell 9633 attached to the surface of the tablet terminal 9600 can supply power to a touch panel, a display unit, a video signal processor, or the like. The solar cell 9633 can be provided on one or both sides of the housing 9630, and can be configured to efficiently charge the power storage unit 9635. Use of a lithium-ion battery as the power storage unit 9635 has the advantage of enabling miniaturization.

[0515] The configuration and operation of the charge / discharge control circuit 9634 shown in Fig. 33B will be described with reference to a block diagram in Fig. 33C. Fig. 33C shows a solar cell 9633, a power storage unit 9635, a DC-DC converter 9636, a converter 9637, switches SW1 to SW3, and a display unit 9631. The power storage unit 9635, the DC-DC converter 9636, the converter 9637, and the switches SW1 to SW3 correspond to the charge / discharge control circuit 9634 shown in Fig. 33B.

[0516] First, an example of operation when power is generated by the solar cell 9633 using external light will be described. The power generated by the solar cell is stepped up or down by a DC-DC converter 9636 to a voltage for charging a power storage unit 9635. When power from the solar cell 9633 is used to operate the display unit 9631, a switch SW1 is turned on, and the converter 9637 steps up or steps down the voltage to a voltage required for the display unit 9631. When no display is to be performed on the display unit 9631, SW1 is turned off and SW2 is turned on to charge the power storage unit 9635.

[0517] Note that the solar cell 9633 is shown as an example of a power generating means, but is not particularly limited thereto, and the power storage unit 9635 may be charged by other power generating means such as a piezoelectric element (piezo element) and a thermoelectric conversion element (Peltier element). For example, a contactless power transmission module that transmits and receives power wirelessly (contactlessly) for charging may be combined with other charging means.

[0518] FIG. 34 illustrates an example of another electronic device. In FIG. 34, a display device 8000 is an example of an electronic device using a secondary battery 8004 according to one embodiment of the present invention. Specifically, the display device 8000 corresponds to a display device for receiving TV broadcasts and includes a housing 8001, a display portion 8002, a speaker portion 8003, a secondary battery 8004, and the like. The secondary battery 8004 according to one embodiment of the present invention is provided inside the housing 8001. The display device 8000 can receive power from a commercial power source or can use power stored in the secondary battery 8004. Therefore, even when power cannot be supplied from the commercial power source due to a power outage or the like, the display device 8000 can be used by using the secondary battery 8004 according to one embodiment of the present invention as an uninterruptible power source.

[0519] The display unit 8002 can be a liquid crystal display device, a light-emitting device having a light-emitting element such as an organic EL element in each pixel, an electrophoretic display device, a semiconductor display device such as a DMD (Digital Micromirror Device), a PDP (Plasma Display Panel), or an FED (Field Emission Display).

[0520] The display device includes all display devices for displaying information, such as those for receiving TV broadcasts, those for personal computers, and those for displaying advertisements.

[0521] 34 , a stationary lighting device 8100 is an example of an electronic device using a secondary battery 8103 according to one embodiment of the present invention. Specifically, the lighting device 8100 includes a housing 8101, a light source 8102, a secondary battery 8103, and the like. Although FIG. 34 illustrates the case where the secondary battery 8103 is provided inside a ceiling 8104 on which the housing 8101 and the light source 8102 are installed, the secondary battery 8103 may be provided inside the housing 8101. The lighting device 8100 can receive power from a commercial power source or can use power stored in the secondary battery 8103. Therefore, even when power cannot be supplied from the commercial power source due to a power outage or the like, the lighting device 8100 can be used by using the secondary battery 8103 according to one embodiment of the present invention as an uninterruptible power supply.

[0522] Note that although Figure 34 illustrates an example of a stationary lighting device 8100 provided on a ceiling 8104, the secondary battery of one embodiment of the present invention can also be used in a stationary lighting device provided in a place other than the ceiling 8104, such as a side wall 8105, a floor 8106, or a window 8107, or can also be used in a tabletop lighting device.

[0523] Furthermore, an artificial light source that artificially obtains light using electric power can be used as the light source 8102. Specifically, examples of the artificial light source include discharge lamps such as incandescent lamps and fluorescent lamps, and light-emitting elements such as LEDs and organic EL elements.

[0524] In FIG. 34 , an air conditioner including an indoor unit 8200 and an outdoor unit 8204 is an example of an electronic device using a secondary battery 8203 of one embodiment of the present invention. Specifically, the indoor unit 8200 includes a housing 8201, an air outlet 8202, a secondary battery 8203, and the like. Although FIG. 34 illustrates the case where the secondary battery 8203 is provided in the indoor unit 8200, the secondary battery 8203 may be provided in the outdoor unit 8204. Alternatively, the secondary battery 8203 may be provided in both the indoor unit 8200 and the outdoor unit 8204. The air conditioner can receive power from a commercial power source or can use power stored in the secondary battery 8203. In particular, when the secondary battery 8203 is provided in both the indoor unit 8200 and the outdoor unit 8204, the air conditioner can be used by using the secondary battery 8203 of one embodiment of the present invention as an uninterruptible power supply even when power cannot be supplied from a commercial power source due to a power outage or the like.

[0525] Note that although FIG. 34 illustrates an example of a separate-type air conditioner including an indoor unit and an outdoor unit, a secondary battery according to one embodiment of the present invention can also be used in an integrated air conditioner that has the functions of both the indoor unit and the outdoor unit in a single housing.

[0526] 34 , an electric refrigerator-freezer 8300 is an example of an electronic device using a secondary battery 8304 of one embodiment of the present invention. Specifically, the electric refrigerator-freezer 8300 includes a housing 8301, a refrigerator door 8302, a freezer door 8303, a secondary battery 8304, and the like. In FIG. 34 , the secondary battery 8304 is provided inside the housing 8301. The electric refrigerator-freezer 8300 can receive power from a commercial power source or can use power stored in the secondary battery 8304. Therefore, even when power cannot be supplied from the commercial power source due to a power outage or the like, the electric refrigerator-freezer 8300 can be used by using the secondary battery 8304 of one embodiment of the present invention as an uninterruptible power source.

[0527] Among the electronic devices described above, electronic devices such as microwave ovens and other high-frequency heating devices and electric rice cookers require a large amount of power for a short period of time. Therefore, by using a secondary battery according to one embodiment of the present invention as an auxiliary power source for supplementing the power that cannot be supplied by the commercial power source, it is possible to prevent the breaker of the commercial power source from tripping when the electronic device is in use.

[0528] Furthermore, by storing power in the secondary battery during times when electronic devices are not in use, particularly during times when the ratio of the amount of power actually used to the total amount of power that can be supplied by the commercial power supplier (referred to as the power usage rate) is low, it is possible to prevent the power usage rate from increasing outside of these times. For example, in the case of electric refrigerator-freezer 8300, power is stored in secondary battery 8304 during the night when the temperature is low and refrigerator door 8302 and freezer door 8303 are not opened or closed. Then, during the day when the temperature rises and refrigerator door 8302 and freezer door 8303 are opened and closed, secondary battery 8304 is used as an auxiliary power source, thereby making it possible to keep the daytime power usage rate low.

[0529] According to one embodiment of the present invention, the cycle characteristics of the secondary battery can be improved, and the reliability can be improved. Furthermore, according to one embodiment of the present invention, a secondary battery with high charge / discharge capacity can be obtained, thereby improving the characteristics of the secondary battery, and thus the secondary battery itself can be made smaller and lighter. Therefore, by incorporating the secondary battery according to one embodiment of the present invention in the electronic device described in this embodiment, the electronic device can have a longer life and be lighter.

[0530] This embodiment mode can be implemented in appropriate combination with other embodiment modes.

[0531] (Embodiment 6) In this embodiment, examples of electronic devices using the secondary battery described in the above embodiment will be described with reference to FIGS. 35A to 36C.

[0532] Figure 35A shows an example of a wearable device. The wearable device uses a secondary battery as a power source. Furthermore, in order to improve splash-proof, water-resistant, or dust-proof performance when used at home or outdoors, there is a demand for a wearable device that can be charged wirelessly as well as via a wired connection with an exposed connector.

[0533] For example, a secondary battery according to one embodiment of the present invention can be mounted on an eyeglasses-type device 4000 as shown in FIG. 35A . The eyeglasses-type device 4000 includes a frame 4000a and a display unit 4000b. Mounting a secondary battery on temples of the curved frame 4000a makes it possible to provide an eyeglasses-type device 4000 that is lightweight, has a good weight balance, and has a long continuous use time. The inclusion of a secondary battery according to one embodiment of the present invention makes it possible to realize a configuration that can accommodate space savings associated with a smaller housing.

[0534] Furthermore, the secondary battery according to one embodiment of the present invention can be mounted on a headset device 4001. The headset device 4001 includes at least a microphone unit 4001a, a flexible pipe 4001b, and an earphone unit 4001c. The secondary battery can be provided in the flexible pipe 4001b and / or the earphone unit 4001c. By providing the secondary battery according to one embodiment of the present invention, a configuration that can accommodate space saving due to a smaller housing can be realized.

[0535] Furthermore, the secondary battery according to one embodiment of the present invention can be mounted on a device 4002 that can be directly attached to the body. A secondary battery 4002b can be provided in a thin housing 4002a of the device 4002. By providing the secondary battery according to one embodiment of the present invention, a space-saving configuration can be realized that accompanies a miniaturized housing.

[0536] Furthermore, the secondary battery according to one embodiment of the present invention can be mounted on a device 4003 that can be attached to clothing. A secondary battery 4003b can be provided in a thin housing 4003a of the device 4003. By providing the secondary battery according to one embodiment of the present invention, a space-saving configuration can be realized that accompanies a miniaturized housing.

[0537] Furthermore, the secondary battery of one embodiment of the present invention can be mounted on the belt-type device 4006. The belt-type device 4006 has a belt portion 4006a and a wireless power receiving portion 4006b, and the secondary battery can be mounted inside the belt portion 4006a. By including the secondary battery of one embodiment of the present invention, a configuration that can accommodate space saving due to miniaturization of the housing can be realized.

[0538] Furthermore, the secondary battery of one embodiment of the present invention can be mounted on the wristwatch device 4005. The wristwatch device 4005 has a display portion 4005a and a belt portion 4005b, and the secondary battery can be provided on the display portion 4005a or the belt portion 4005b. By providing the secondary battery of one embodiment of the present invention, a space-saving configuration can be realized that accompanies a miniaturized housing.

[0539] The display unit 4005a can display not only the time but also various other information such as incoming emails and phone calls.

[0540] Furthermore, since the wristwatch device 4005 is a wearable device that is worn directly on the wrist, it may be equipped with sensors that measure the user's pulse, blood pressure, etc. Data on the user's exercise volume and health can be accumulated to manage the user's health.

[0541] FIG. 35B shows a perspective view of the wristwatch type device 4005 removed from the wrist.

[0542] 35C shows a side view of the display portion 4005a. FIG. 35C shows that a secondary battery 913 is built in the display portion 4005a. The secondary battery 913 is the secondary battery described in Embodiment 4. The secondary battery 913 is provided at a position overlapping with the display portion 4005a, and is small and lightweight.

[0543] 35D shows an example of a wireless earphone. Here, the wireless earphone is shown with a pair of main bodies 4100a and 4100b, but this does not necessarily have to be a pair.

[0544] The main bodies 4100a and 4100b each have a driver unit 4101, an antenna 4102, and a secondary battery 4103. They may also have a display unit 4104. They also preferably have a substrate on which a circuit such as a wireless IC is mounted, a charging terminal, and the like. They may also have a microphone.

[0545] The case 4110 has a secondary battery 4111. It also preferably has a board on which circuits such as a wireless IC and a charge control IC are mounted, and a charging terminal. It may also have a display unit, buttons, etc.

[0546] The main units 4100a and 4100b can wirelessly communicate with other electronic devices such as smartphones. This allows sound data and the like sent from other electronic devices to be played back on the main units 4100a and 4100b. If the main units 4100a and 4100b have microphones, they can send sounds picked up by the microphones to the other electronic devices, and the sound data after processing by the electronic devices can be sent back to the main units 4100a and 4100b for playback. This allows them to be used as, for example, translation devices.

[0547] Furthermore, the secondary battery 4111 in the case 4100 can charge the secondary battery 4103 in the main body 4100b. The coin-type secondary battery, the cylindrical secondary battery, or the like described in the previous embodiments can be used as the secondary battery 4111 and the secondary battery 4103. A secondary battery using the positive electrode active material 100 obtained in Embodiment 1 for its positive electrode has high energy density, and by using the secondary battery 4103 and the secondary battery 4111, a configuration that can accommodate space saving associated with miniaturization of wireless earphones can be realized.

[0548] 36A shows an example of a cleaning robot. The cleaning robot 6300 includes a display unit 6302 arranged on the top surface of a housing 6301, a plurality of cameras 6303 arranged on the side surface, a brush 6304, an operation button 6305, a secondary battery 6306, various sensors, and the like. Although not shown, the cleaning robot 6300 is provided with tires, a suction port, and the like. The cleaning robot 6300 can move by itself, detect dust 6310, and suck the dust from a suction port arranged on the bottom surface.

[0549] For example, the cleaning robot 6300 can analyze an image captured by the camera 6303 to determine whether or not there is an obstacle such as a wall, furniture, or a step. Furthermore, when an object that may become entangled in the brush 6304, such as a wire, is detected through image analysis, the cleaning robot 6300 can stop rotation of the brush 6304. The cleaning robot 6300 includes a secondary battery 6306 according to one embodiment of the present invention and a semiconductor device or an electronic component therein. By using the secondary battery 6306 according to one embodiment of the present invention in the cleaning robot 6300, the cleaning robot 6300 can be a highly reliable electronic device with a long operating time.

[0550] Fig. 36B shows an example of a robot. A robot 6400 shown in Fig. 36B includes a secondary battery 6409, an illuminance sensor 6401, a microphone 6402, an upper camera 6403, a speaker 6404, a display unit 6405, a lower camera 6406, an obstacle sensor 6407, a movement mechanism 6408, a computing device, etc.

[0551] The microphone 6402 has a function of detecting the user's speaking voice, environmental sounds, etc. The speaker 6404 has a function of emitting sound. The robot 6400 can communicate with the user using the microphone 6402 and the speaker 6404.

[0552] The display unit 6405 has a function of displaying various information. The robot 6400 can display information desired by the user on the display unit 6405. The display unit 6405 may be equipped with a touch panel. The display unit 6405 may also be a detachable information terminal, which can be installed in a fixed position on the robot 6400 to enable charging and data transfer.

[0553] The upper camera 6403 and the lower camera 6406 have the function of capturing images of the surroundings of the robot 6400. In addition, the obstacle sensor 6407 can detect the presence or absence of obstacles in the direction of travel when the robot 6400 moves forward using the movement mechanism 6408. The robot 6400 can recognize the surrounding environment and move safely using the upper camera 6403, the lower camera 6406, and the obstacle sensor 6407.

[0554] The robot 6400 includes a secondary battery 6409 according to one embodiment of the present invention and a semiconductor device or an electronic component inside the robot 6400. By using the secondary battery according to one embodiment of the present invention in the robot 6400, the robot 6400 can be a highly reliable electronic device with a long operating time.

[0555] Fig. 36C shows an example of an aircraft. Aircraft 6500 shown in Fig. 36C has propeller 6501, camera 6502, secondary battery 6503, etc., and has the function of flying autonomously.

[0556] For example, image data captured by the camera 6502 is stored in the electronic component 6504. The electronic component 6504 can analyze the image data and detect the presence or absence of an obstacle when moving. Furthermore, the electronic component 6504 can estimate the remaining battery charge from a change in the storage capacity of the secondary battery 6503. The flying object 6500 includes the secondary battery 6503 according to one embodiment of the present invention therein. By using the secondary battery according to one embodiment of the present invention in the flying object 6500, the flying object 6500 can be an electronic device with a long operating time and high reliability.

[0557] This embodiment mode can be implemented in appropriate combination with other embodiment modes.

[0558] (Embodiment 7) In this embodiment, an example in which a secondary battery according to one embodiment of the present invention is mounted on a vehicle will be described.

[0559] By installing secondary batteries in vehicles, next-generation clean energy vehicles such as hybrid vehicles (HVs), electric vehicles (EVs), and plug-in hybrid vehicles (PHVs) can be realized.

[0560] FIG. 37 illustrates a vehicle using a secondary battery according to one embodiment of the present invention. An automobile 8400 illustrated in FIG. 37A is an electric automobile using an electric motor as a power source for traveling. Alternatively, it is a hybrid automobile that can appropriately select and use an electric motor or an engine as a power source for traveling. By using one embodiment of the present invention, a vehicle with a long cruising distance can be realized. Furthermore, the automobile 8400 includes a secondary battery. The secondary battery may be arranged in the form of secondary battery modules shown in FIGS. 22C and 22D on the floor of the vehicle. Alternatively, a battery pack combining a plurality of secondary batteries as shown in FIG. 25 may be installed on the floor of the vehicle. The secondary battery not only drives the electric motor 8406 but also supplies power to light-emitting devices such as a headlight 8401 and a room light (not shown).

[0561] The secondary battery can also supply power to display devices such as a speedometer and a tachometer included in the automobile 8400. The secondary battery can also supply power to semiconductor devices such as a navigation system included in the automobile 8400.

[0562] The automobile 8500 shown in FIG. 37B can charge its secondary battery by receiving power from an external charging facility using a plug-in method and / or a wireless power supply method. FIG. 37B shows a state in which a secondary battery 8024 mounted on the automobile 8500 is being charged via a cable 8022 from a ground-mounted charging device 8021. The charging method and connector specifications may be determined as appropriate using a predetermined method such as CHAdeMO (registered trademark) or Combo. The charging device 8021 may be a charging station installed in a commercial facility or a household power source. For example, plug-in technology can be used to charge the secondary battery 8024 mounted on the automobile 8500 using external power supply. Charging can be performed by converting AC power to DC power using a conversion device such as an AC-DC converter.

[0563] Furthermore, although not shown, a power receiving device can be mounted on a vehicle and power can be supplied contactlessly from a ground-based power transmitting device for charging. In the case of this contactless power supply method, by incorporating a power transmitting device into the road and / or exterior wall, charging can be performed not only while the vehicle is stopped but also while it is moving. This contactless power supply method can also be used to transmit and receive power between vehicles. Furthermore, solar cells can be installed on the exterior of the vehicle, and secondary batteries can be charged while the vehicle is stopped and / or moving. Electromagnetic induction and / or magnetic resonance methods can be used for such contactless power supply.

[0564] 37C shows an example of a two-wheeled vehicle using the secondary battery of one embodiment of the present invention. A scooter 8600 shown in FIG. 37C includes a secondary battery 8602, a side mirror 8601, and a turn signal light 8603. The secondary battery 8602 can supply electricity to the turn signal light 8603.

[0565] 37C, the secondary battery 8602 can be stored in the under-seat storage 8604. Even if the under-seat storage 8604 is small, the secondary battery 8602 can be stored in the under-seat storage 8604. The secondary battery 8602 is removable, and when charging, the secondary battery 8602 can be carried indoors, charged, and stored before riding.

[0566] According to one aspect of the present invention, the cycle characteristics of the secondary battery are improved, and the charge / discharge capacity of the secondary battery can be increased. Therefore, the secondary battery itself can be made smaller and lighter. Reducing the size and weight of the secondary battery itself contributes to reducing the weight of the vehicle, thereby improving the cruising range. Furthermore, the secondary battery mounted on the vehicle can also be used as a power supply source for purposes other than the vehicle. In this case, for example, it is possible to avoid using a commercial power source during peak power demand periods. Avoiding the use of a commercial power source during peak power demand periods can contribute to energy conservation and the reduction of carbon dioxide emissions. Furthermore, good cycle characteristics allow the secondary battery to be used for a long period of time, thereby reducing the amount of rare metals used, such as cobalt.

[0567] This embodiment mode can be implemented in appropriate combination with other embodiment modes. [Example]

[0568] In this example, a positive electrode active material 100 according to one embodiment of the present invention was fabricated, and its battery characteristics were measured.

[0569] <Preparation of positive electrode active material> The sample produced in this example will be described with reference to the production method shown in FIGS.

[0570] As LiMO2 in step S14 of Figure 2, commercially available lithium cobalt oxide (Cellseed C-10N, manufactured by Nippon Chemical Industry Co., Ltd.) containing cobalt as the transition metal M and no additive elements was prepared. For the heating in step S15, this lithium cobalt oxide was placed in a crucible, covered, and heated in a muffle furnace at 850 °C for 2 hours. This heating corresponds to the initial heating. After an oxygen atmosphere was created in the muffle furnace, oxygen was not supplied (this is referred to as O2 purging). It is possible that impurities were removed from LCO after the initial heating.

[0571] According to steps S21 and S41 shown in FIGS. 3A and 3B, Mg, F, Ni, and Al were prepared as additive elements, and Mg and F, and Ni and Al were added separately. According to step S21 shown in FIG. 3A, LiF was prepared as the F source, and MgF2 was prepared as the Mg source. LiF:MgF2 was weighed out so that the molar ratio was 1:3. Next, LiF and MgF2 were mixed in ultra-dehydrated acetone, and stirred at a rotation speed of 400 rpm for 12 hours to obtain the additive element source X. A Then, the powder was sieved through a sieve with 300 μm openings to obtain additive element source X with a uniform median diameter (D50). A obtained.

[0572] Next, the additive element source X A The transition metal M, that is, cobalt, was weighed out so that it was 1 at% of the cobalt, and mixed with the LCO after initial heating in a dry state. The mixture was stirred at a rotation speed of 150 rpm for 1 hour. This is the additive element source X A The stirring conditions are gentler than those used to obtain the LCO, and are preferably conditions under which the LCO does not break down. Finally, the mixture was sieved through a sieve with 300 μm openings to obtain a mixture A with a uniform median diameter (D50).

[0573] Next, mixture A was heated. The heating conditions were 900°C and 20 hours. During heating, a lid was placed on the crucible containing mixture A, and the mixture was heated in a muffle furnace. The inside of the muffle furnace was filled with oxygen, and then purged with O2. By heating, an LCO containing Mg and F (referred to as composite oxide A) was obtained.

[0574] Next, the additive element source X is added to the composite oxide A. B According to step S41 shown in FIG. 3B, nickel hydroxide was prepared as the Ni source, and aluminum hydroxide was prepared as the Al source. The nickel hydroxide was weighed out so that it was 0.5 at% of the transition metal M, i.e., cobalt, and the aluminum hydroxide was weighed out so that it was 0.5 at% of the transition metal M, i.e., cobalt, and then mixed with the composite oxide A in a dry state. The mixture was stirred at a rotation speed of 150 rpm for 1 hour. This was because the additive element source X A The stirring conditions are gentler than those used to obtain the composite oxide A. The stirring conditions are preferably such that the obtained composite oxide A does not crumble. Finally, the mixture was sieved through a sieve with 300 μm openings to obtain a mixture B with a uniform particle size.

[0575] Next, mixture B was heated. The heating conditions were 850°C and 10 hours. During heating, a lid was placed on the crucible containing mixture B, and the mixture was heated in a muffle furnace. The muffle furnace was filled with an oxygen atmosphere, and then purged with O2. By heating, an LCO (referred to as composite oxide B) containing Mg, F, Ni, and Al was obtained. A positive electrode active material was thus prepared.

[0576] Next, the resulting positive electrode active material (LCO), acetylene black (AB) as a conductive agent, and polyvinylidene fluoride (PVDF) as a binder were mixed at 1500 rpm in a ratio of LCO:AB:PVDF = 95:3:2 (wt%) to prepare a slurry. NMP was used as the solvent for the slurry, and the slurry was applied to an aluminum current collector, after which the solvent was evaporated. After the solvent was evaporated, the slurry on the current collector was pressed.

[0577] As for the pressing conditions, Sample 1-1 was pressed at 210 kN / m, and Sample 1-2 was pressed at 210 kN / m and then at 1467 kN / m. For both Sample 1-1 and Sample 1-2, the temperature of the rolls of the pressing machine was set to 120°C. The amount of positive electrode active material carried per unit area of ​​the positive electrodes of Sample 1-1 and Sample 1-2 was about 7 mg / cm. 2In this way, the positive electrode was completed. The preparation conditions for Sample 1-1 and Sample 1-2 are shown in Table 1.

[0578] [Table 1]

[0579] Table 2 shows the electrode density, packing ratio, and porosity for Sample 1-1 and Sample 1-2, respectively.

[0580] [Table 2]

[0581] The electrode density was calculated by dividing the weight of the active material layer (corresponding to the positive electrode active material, conductive agent, and binder) excluding the current collector from the positive electrode by the volume of the active material layer x 100. The packing ratio was calculated by dividing the electrode density by the true density of the mixture x 100. The true densities of the materials were 5.05 g / cc for LiCoO2, 1.95 g / cc for AB used as the conductive agent, and 1.78 g / cc for PVDF used as the binder. The porosity was calculated by (1 - packing ratio) x 100.

[0582] As shown in Table 2, when Sample 1-1 and Sample 1-2 are compared, it can be seen that Sample 1-1 has a higher porosity than Sample 1-2.

[0583] Two positive electrodes, Sample 1-1 and Sample 1-2, were used to assemble half-cells as test batteries. Lithium metal was used as the negative electrode, or counter electrode. A separator was placed between the positive electrode, Sample 1-1, and the negative electrode, respectively, and the battery was housed in a housing along with an electrolyte. Polypropylene was used for the separator. The electrolyte was a mixture of ethylene carbonate (EC) and diethyl carbonate (DEC) in a volume ratio of 3:7, with 2 wt% vinylene carbonate (VC) added as an additive. The electrolyte used in the battery was 1 mol / L lithium hexafluorophosphate (LiPF6). Because the battery was housed in a coin-shaped housing, it is sometimes called a coin-shaped half-cell.

[0584] In this way, a coin-shaped half cell was formed, and a charge-discharge cycle test was performed using a charge-discharge measurement system (TOSCAT-3100) manufactured by Toyo Systems Co., Ltd. The charge-discharge cycle test using a half cell, that is, cycle characteristic evaluation, allows us to understand the performance of the positive electrode alone.

[0585] The rate of charge-discharge cycle test conditions is explained below. The rate at which a battery is discharged is called the discharge rate, which is the relative ratio of the discharge current to the battery capacity and is expressed in units of C. For a battery with a rated capacity of X (Ah), the current equivalent to 1C is X (A). Discharging at a current of 2X (A) is said to have been discharged at 2C, and discharging at a current of X / 2 (A) is said to have been discharged at 0.5C. The rate at which a battery is charged is called the charge rate. Similarly to the charge rate, charging at a current of 2X (A) is said to have been charged at 2C, and charging at a current of X / 2 (A) is said to have been charged at 0.5C. The charge rate and discharge rate are collectively referred to as the charge-discharge rate.

[0586] <Charge / discharge cycle test conditions: charge / discharge rate 1C> A charge-discharge cycle test was conducted at a charge-discharge rate of 1 C. Specifically, the battery was charged at a constant current of 1 C (1 C = 200 mA / g) in a thermostatic chamber maintained at 25°C or 45°C (referred to as a 25°C or 45°C environment) until a voltage of 4.60 V (referred to as 4.6 V) was reached, followed by constant voltage charging at a voltage of 4.6 V until a charge rate of 0.1 C was reached, and then constant current discharging was performed at a discharge rate of 1 C until a voltage of 2.5 V was reached. A rest period of 5 to 15 minutes may be provided between charge and discharge, and a rest period of 10 minutes was provided in this example.

[0587] Another test was conducted under different upper limit voltage conditions. Specifically, the battery was charged at a constant current of 1C (1C = 200mA / g) at 25°C or 45°C until the voltage reached 4.65V, then further charged at a constant voltage of 4.65V until the charge rate reached 0.1C, and then discharged at a constant current of 1C until the voltage reached 2.5V. A 10-minute rest period was provided between the charge and discharge.

[0588] Another test was conducted under different upper limit voltage conditions. Specifically, the battery was charged at a constant current of 1 C (1 C = 200 mA / g) at 25°C or 45°C until the voltage reached 4.70 V (referred to as 4.7 V)....

Claims

1. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was subjected to a test in which the test battery was charged at a constant current at a charge rate of 1 C (1 C = 200 mA / g) in a 25°C environment or a 45°C environment until the voltage reached 4.6 V, then was charged at a constant voltage until the charge rate reached 0.1 C at a voltage of 4.6 V, and then was discharged at a constant current at a discharge rate of 1 C until the voltage reached 2.5 V. This charge / discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

2. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 200 mA / g in a 25°C environment or a 45°C environment until the voltage reached 4.6 V, then charged at a constant voltage of 4.6 V until the charging current reached 20 mA / g, and then discharged at a constant current of 200 mA / g until the voltage reached 2.5 V. This charge-discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

3. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) in a 25°C or 45°C environment until the voltage reached 4.6 V, then charged at a constant voltage until the charge rate reached 0.05 C at a voltage of 4.6 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reached 2.5 V. This charge / discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

4. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 100 mA / g in a 25°C environment or a 45°C environment until the voltage reached 4.6 V, then charged at a constant voltage of 4.6 V until the charging current reached 10 mA / g, and then discharged at a constant current of 100 mA / g until the voltage reached 2.5 V. This charge-discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle satisfies 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

5. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was subjected to a test in which the test battery was charged at a constant current at a charge rate of 1 C (1 C = 200 mA / g) in a 25°C environment until the voltage reached 4.65 V, then charged at a constant voltage until the charge rate reached 0.1 C at a voltage of 4.65 V, and then discharged at a constant current at a discharge rate of 1 C until the voltage reached 2.5 V. This test was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

6. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 200 mA / g in a 25°C environment until the voltage reached 4.65 V, then charged at a constant voltage of 4.65 V until the charging current reached 20 mA / g, and then discharged at a constant current of 200 mA / g until the voltage reached 2.5 V. This charge / discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

7. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was subjected to a test in which the test battery was charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) in a 25°C environment until the voltage reached 4.65 V, then charged at a constant voltage until the charge rate reached 0.05 C at a voltage of 4.65 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reached 2.5 V. This test was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

8. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 100 mA / g in a 25°C environment until the voltage reached 4.65 V, then charged at a constant voltage of 4.65 V until the charging current reached 10 mA / g, and then discharged at a constant current of 100 mA / g until the voltage reached 2.5 V. This charge / discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle satisfies 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

9. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was subjected to a test in which the test battery was charged at a constant current at a charge rate of 1 C (1 C = 200 mA / g) in a 25°C environment until the voltage reached 4.7 V, then charged at a constant voltage until the charge rate reached 0.1 C at a voltage of 4.7 V, and then discharged at a constant current at a discharge rate of 1 C until the voltage reached 2.5 V. This test was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

10. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 200 mA / g in a 25°C environment until the voltage reached 4.7 V, then charged at a constant voltage of 4.7 V until the charging current reached 20 mA / g, and then discharged at a constant current of 200 mA / g until the voltage reached 2.5 V. This charge-discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

11. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was subjected to a test in which the test battery was charged at a constant current at a charge rate of 0.5 C (1 C = 200 mA / g) in a 25°C environment until the voltage reached 4.7 V, then charged at a constant voltage until the charge rate reached 0.05 C at a voltage of 4.7 V, and then discharged at a constant current at a discharge rate of 0.5 C until the voltage reached 2.5 V. This test was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle is 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

12. A battery having a positive electrode and a negative electrode, The positive electrode was used as the positive electrode of a test battery having a negative electrode made of lithium metal, The test battery was charged at a constant current of 100 mA / g in a 25°C environment until the voltage reached 4.7 V, then charged at a constant voltage of 4.7 V until the charging current reached 10 mA / g, and then discharged at a constant current of 100 mA / g until the voltage reached 2.5 V. This charge / discharge cycle was repeated 50 times, and the discharge capacity was measured for each cycle. A battery in which the discharge capacity measured at the 50th cycle satisfies 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

13. In any one of claims 1 to 4, When the test battery is placed in the 25°C environment and the 45°C environment, the discharge capacity measured at the 50th cycle satisfies 90% or more and less than 100% of the maximum discharge capacity over all 50 cycles.

14. 14. The battery according to claim 1, wherein the discharge capacity measured at the 50th cycle is 95% or more of the maximum discharge capacity measured over all 50 cycles.

15. 15. The battery according to claim 1, wherein the test battery is a coin-type half cell.

16. In any one of claims 1 to 15, The test battery has an electrolyte, the electrolyte including a solvent having ethylene carbonate and diethyl carbonate, an additive having vinylene carbonate, and a lithium salt having lithium hexafluorophosphate.

17. 17. The battery according to claim 1, wherein the positive electrode comprises a layered rock salt type positive electrode active material.

18. 20. The battery of claim 17, wherein the positive electrode active material comprises lithium cobalt oxide.

19. An electronic device equipped with the battery according to any one of claims 1 to 18.

20. A vehicle equipped with the battery according to any one of claims 1 to 18.

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