Positive electrode plate and non-aqueous electrolyte secondary battery

Abstract

To provide a positive electrode plate which can attain a high charge capacity and an excellent thermal stability at the same time.SOLUTION: The positive electrode plate includes: a first active material as a lithium transition metal composite oxide; and a second active material as a lithium transition metal composite oxide, the average particle diameter (D50) of the second active material being smaller than that of the first active material. The particle size of the second active material is 800 nm or larger. The ratio (Li / M) of the amount by mole of lithium (Li) in the first active material and the total amount by mole of the transition metal (M) is 1.05 or more, and the ratio (Li / M) of the amount by mole of lithium (Li) in the second active material and the total amount by mole of the transition metal (M) is 1.04 or less.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a positive electrode plate and a non-aqueous electrolyte secondary battery. [Background technology]

[0002] It is known that in non-aqueous electrolyte secondary batteries such as lithium ion secondary batteries, a lithium transition metal composite oxide, which is a composite oxide of lithium and a transition metal, is used as the positive electrode active material contained in the active material layer of the positive electrode plate.Patent Documents 1 to 3 disclose that a positive electrode plate using two or more types of lithium transition metal composite oxides with different particle sizes, etc., can improve capacity, output, etc. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Special Publication No. 2021-518049 [Patent Document 2] Japanese Patent Application Laid-Open No. 2011-113825 [Patent Document 3] International Publication No. 2021 / 065162 Summary of the Invention [Problem to be solved by the invention]

[0004] In non-aqueous electrolyte secondary batteries, increasing the charge capacity can sometimes result in a decrease in thermal stability, so there is a demand for non-aqueous electrolyte secondary batteries that combine high charge capacity with excellent thermal stability.

[0005] An object of the present disclosure is to provide a positive electrode plate that can achieve both high charge capacity and excellent thermal stability, and a nonaqueous electrolyte secondary battery including the same. [Means for solving the problem]

[0006] [1] A battery comprising a first active material that is a lithium transition metal composite oxide and a second active material that has a smaller average particle diameter (D50) than the first active material and is also a lithium transition metal composite oxide, The crystallite size of the second active material is 800 nm or more, the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the first active material is 1.05 or more; a ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the second active material is 1.04 or less;

[0007] [2] The positive electrode plate according to [1], wherein the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the first active material is 1.12 or less.

[0008] [3] The positive electrode plate according to [1] or [2], wherein the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the second active material is 0.98 or more.

[0009] [4] The positive electrode plate according to any one of [1] to [3], wherein the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the second active material is 1.01 or more.

[0010] [5] The positive electrode plate according to any one of [1] to [4], wherein the mass ratio of the first active material to the second active material (first active material / second active material) is 5 / 5 or more and 8 / 2 or less.

[0011] [6] The positive electrode plate according to any one of [1] to [5], wherein the first active material has an average particle diameter (D50) of 12 μm or more and 20 μm or less.

[0012] [7] The positive electrode plate according to any one of [1] to [6], wherein the second active material has an average particle diameter (D50) of 2 μm or more and 8 μm or less.

[0013] [8] The positive electrode plate according to any one of [1] to [7], wherein the first active material and the second active material each contain 80 mol % or more of nickel (Ni) relative to the total amount of transition metals.

[0014] [9] The positive electrode plate according to any one of [1] to [8], wherein the second active material is at least one of a single particle and a secondary particle formed by aggregation of three or less primary particles.

[0015]

[10] An electrode assembly including the positive electrode plate, the negative electrode plate, and a separator interposed between the positive electrode plate and the negative electrode plate according to any one of [1] to [9]; and an electrolyte solution. [Effects of the Invention]

[0016] The positive electrode plate of the present disclosure can provide a nonaqueous electrolyte secondary battery that can achieve both high charge capacity and excellent thermal stability. [Brief explanation of the drawings]

[0017] [Figure 1] 1 is a graph plotting the charge capacity when a test cell (r1) having a positive electrode plate (r1) formed using a first active material is charged, and the percentage of the capacity at a potential of 4.1 V vs. Li / Li+ or higher, against the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the first active material. [Figure 2] 1 is a graph plotting the charge capacity when a test cell (r2) having a positive electrode plate (r2) formed using a second active material is charged, and the percentage of the capacity at a potential of 4.1 V vs. Li / Li+ or higher, against the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the second active material. DETAILED DESCRIPTION OF THE INVENTION

[0018] (positive electrode plate) The positive electrode plate of this embodiment can be used in a non-aqueous electrolyte secondary battery (hereinafter also referred to as a "secondary battery"). The positive electrode plate includes a first active material that is a lithium transition metal composite oxide, and a second active material that is also a lithium transition metal composite oxide and has a smaller average particle diameter (D50) than the first active material. The crystallite size of the second active material is 800 nm or more.

[0019] The lithium transition metal composite oxide is an oxide containing lithium and a transition metal. The transition metal contained in the lithium transition metal composite oxide can be one or more selected from the group consisting of nickel (Ni), manganese (Mn), cobalt (Co), aluminum (Al), and titanium (Ti), preferably one or more selected from the group consisting of Ni, Mn, Co, and Al, and more preferably one or more selected from the group consisting of Ni, Mn, and Co. The transition metal preferably includes Ni, Mn, and Co, and may include Ni, Mn, Co, and Al.

[0020] The first active material and the second active material each independently contain Ni in an amount of preferably 80 mol % or more, more preferably 80 mol % to 98 mol %, or alternatively 81 mol % to 95 mol %, or alternatively 82 mol % to 90 mol % relative to the total amount of transition metals. By using a first active material and a second active material having Ni contents within the above ranges, it is possible to increase the capacity of the secondary battery.

[0021] The ratio (Li / M) of the number of moles of Li to the total number of moles of transition metals (M) in the first active material is 1.05 or more, may be 1.07 or more, or may be 1.09 or more. The ratio (Li / M) in the first active material is preferably 1.05 or more and 1.12 or less, may be 1.05 or more and 1.10 or less, may be 1.07 or more and 1.10 or less, or may be 1.07 or more and 1.09 or less.

[0022] The ratio (Li / M) of the number of moles of Li to the total number of moles of transition metals (M) in the second active material is 1.04 or less, and may be 1.03 or less, or 1.02 or less. The ratio (Li / M) in the second active material is preferably 0.98 to 1.04 or less, and may be 1.00 to 1.04 or less, more preferably 1.01 to 1.04 or less, or may be 1.02 to 1.03 or less. The compositions of the first active material and the second active material (lithium transition metal composite oxide) can be determined by high-frequency inductively coupled plasma (ICP) optical emission spectroscopy.

[0023] As will be described in the manufacturing example of the examples below, when the ratio (Li / M) in the first active material is less than 1.05, the total capacity when a test cell (r1) having a positive electrode plate (r1) formed using the first active material is charged is 4.1 V vs. Li / Li + The ratio of the capacity at potentials above this level increases (Fig. 1 and Table 1). On the other hand, when the ratio (Li / M) in the first active material is 1.05 or higher, the ratio of the capacity converges and the change tends to become smaller (Fig. 1 and Table 1). When the test cell (r1) was charged at 4.1 V vs. Li / Li + It is believed that an increase in the capacity ratio at these potentials reduces the structural stability of the lithium transition metal composite oxide constituting the first active material, making the lithium transition metal composite oxide more susceptible to phase transition. As a result, it is presumed that the potential of the secondary battery increases more easily during charging, and the capacity ratio at these potentials increases. The capacity ratio is an index representing the thermal stability of the test cell (r1), and the smaller the capacity ratio, the better the thermal stability. Therefore, it can be said that whether the ratio (Li / M) of the first active material is 1.05 or higher has a significant impact on the thermal stability of the secondary battery.

[0024] In contrast, when the ratio (Li / M) in the second active material is 1.04 or less, the charge capacity per unit mass of the second active material can be increased when a test cell (r2) having a positive electrode plate (r2) formed using the second active material is charged (see the manufacturing example in the Examples described below, FIG. 2, and Table 2). On the other hand, when the ratio (Li / M) in the second active material exceeds 1.04, the charge capacity tends to decrease significantly (FIG. 2 and Table 2). From this, it can be said that whether the ratio (Li / M) of the second active material is 1.04 or less has a significant effect on the charge capacity of the secondary battery.

[0025] Therefore, by obtaining a positive electrode plate using a first active material having the above ratio (Li / M) of 1.05 or more and a second active material having the above ratio (Li / M) of 1.04 or less, it becomes easier to obtain a secondary battery that combines excellent thermal stability with a high charging capacity.

[0026] When a lithium transition metal composite oxide having a Ni content of 80 mol % or more relative to the total amount of the above-mentioned transition metals is used as the first active material and the second active material, the capacity of the secondary battery can be increased, but the resistance of the positive electrode plate is reduced, which makes it easier for the potential of the secondary battery to increase and the thermal stability to decrease. Therefore, from the viewpoint of achieving both excellent thermal stability and high charge capacity, it is preferable to use a lithium transition metal composite oxide having a ratio (Li / M) within the above range, especially when using first and second active materials with a high Ni content among the transition metals.

[0027] The crystallite size of the second active material may be 800 nm or more, 850 nm or more, or 900 nm or more. The crystallite size of the second active material may be 800 nm or more to 2000 nm or less, 800 nm or more to 1500 nm or less, 850 nm or more to 1200 nm or less, or 900 nm or more to 1100 nm or less. The crystallite size of the second active material is the size of the crystallite contained in a single particle when the second active material is a single particle, and is the size of the crystallite contained in a primary particle that constitutes the secondary particle when the second active material is a secondary particle. The crystallite size can be measured by X-ray diffraction. When the crystallite size of the second active material is within the above range, the storage durability of the secondary battery can be improved. Even when a second active material having the above crystallite size is used in the positive electrode plate, a lithium transition metal composite oxide having a ratio (Li / M) within the above range is used as the first particle and the second particle. Therefore, by using the positive electrode plate, a secondary battery that combines excellent thermal stability with a high charge capacity can be obtained.

[0028] The average particle diameter (D50) of the first active material (hereinafter also referred to as "D50") is not particularly limited as long as it is larger than the D50 of the second active material. The D50 of the first active material is preferably 12 μm or more and 20 μm or less, and may be 14 μm or more and 19 μm or less, or 15 μm or more and 18 μm or less. When the D50 of the first active material is within the above range, a secondary battery that combines excellent thermal stability and high charge capacity can be easily obtained. When the first active material is a secondary particle, the D50 of the first active material is based on the particle diameter of the secondary particle. In this specification, the average particle diameter (D50) is the particle diameter at which the cumulative frequency of the smaller particle diameters in the volume-based particle size distribution becomes 50%. The volume-based particle size distribution can be measured using a laser diffraction particle size analyzer.

[0029] The D50 of the second active material is not particularly limited as long as it is smaller than the D50 of the first active material. The D50 of the second active material is preferably 2 μm or more and 8 μm or less, and may be 2 μm or more and 6 μm or less, or may be 4 μm or more and 6 μm or less. When the D50 of the second active material is within the above range, a secondary battery that combines excellent thermal stability and high charge capacity is easily obtained. The D50 of the second active material is based on the particle diameter of the single particle when the second active material is a single particle, and is based on the particle diameter of the secondary particle when the second active material is a secondary particle.

[0030] The first active material is preferably a secondary particle (aggregated particle) formed by aggregation of primary particles, and the number of primary particles contained in the secondary particle is, for example, 100 or more. When both the first active material and the second active material are secondary particles, the number of primary particles contained in one first active material is preferably greater than the number of primary particles contained in one second active material.

[0031] The second active material is preferably at least one of a single particle and a secondary particle formed by an aggregation of up to three primary particles, and may be at least one of a single particle and a secondary particle formed by an aggregation of two primary particles. The second active material may contain a single particle and a secondary particle formed by an aggregation of up to three primary particles. This makes it easier to obtain a secondary battery that combines excellent thermal stability with a high charge capacity. The particle size of the single particle or primary particle constituting the second active material may be 0.7 μm or more, 0.8 μm or more, or 1 μm or more, for example, 0.7 μm to 8 μm or less, or 0.8 μm to 6 μm or less.

[0032] The mass ratio (first active material / second active material) of the first active material to the second active material contained in the positive electrode plate is preferably 5 / 5 or more and 8 / 2 or less, and may be 5 / 5 or more and 7 / 3 or less, or may be 6 / 4 or more and 7 / 3 or less. When the mass ratio (first active material / second active material) is within the above range, the filling efficiency of the first active material and the second active material in the positive electrode plate can be improved, and the output and capacity of the secondary battery can be improved.

[0033] The positive electrode plate may have an active material layer including a first active material and a second active material, and the active material layer may be formed on a positive electrode current collector. The positive electrode current collector is a metal foil made of an aluminum material such as aluminum or an aluminum alloy. The positive electrode plate may have a tab made of an aluminum material.

[0034] In addition to the first active material and the second active material, the active material layer may contain other positive electrode active materials, and may also contain a conductive material, a binder, etc. Of the total amount of positive electrode active material contained in the active material layer, the content of the first active material and the second active material is preferably from 95% to 100% by mass, more preferably from 95% to 99% by mass, and may be from 96% to 98% by mass.

[0035] The conductive material may be, for example, a carbon material. The carbon material may be, for example, one or more selected from the group consisting of fibrous carbon, carbon black (acetylene black, ketjen black, etc.), coke, and activated carbon. The fibrous carbon may be, for example, carbon nanotubes (CNTs). The CNTs may be single-walled carbon nanotubes (SWCNTs) or multi-walled carbon nanotubes such as double-walled carbon tubes (DWCNTs).

[0036] The binder may be, for example, one or more selected from the group consisting of styrene butadiene rubber (SBR), polyvinylidene fluoride (PVdF), and polytetrafluoroethylene (PTFE).

[0037] The positive electrode plate can be manufactured, for example, by forming an active material layer containing a first active material and a second active material on a positive electrode current collector. The active material layer can be formed by applying a slurry containing the first active material and the second active material to the positive electrode current collector, drying it, and compressing it. The slurry can further contain a conductive material, a binder, and a solvent such as N-methyl-2-pyrrolidone (NMP).

[0038] (Nonaqueous electrolyte secondary battery) The secondary battery may include an electrode assembly having the above-described positive electrode plate, negative electrode plate, and separator interposed between the positive electrode plate and the negative electrode plate, and an electrolyte solution. The secondary battery may further include a battery case that houses the electrode assembly and the electrolyte solution.

[0039] The electrode body may be a laminated electrode body composed of a laminate in which a positive electrode plate, a negative electrode plate, and a separator are stacked, or may be a wound electrode body in which the laminate is wound. The laminated electrode body may have a quadrangular shape in plan view, preferably a square or rectangular shape, more preferably a rectangular shape. The wound electrode body may be a flat wound electrode body that is pressed after winding the laminate.

[0040] The negative electrode plate may include a negative electrode current collector and a negative electrode active material layer formed on the negative electrode current collector. The negative electrode current collector may be a metal foil made of a copper material such as copper or a copper alloy. The negative electrode active material layer includes a negative electrode active material and may further include one or both of a conductive material and a binder.

[0041] Examples of negative electrode active materials include carbon-based active materials containing carbon (C) atoms, such as graphite; and metal-based active materials containing metal elements, such as simple metals or metal oxides containing elements selected from the group consisting of silicon (Si), tin (Sn), antimony (Sb), bismuth (Bi), titanium (Ti), and germanium (Ge). Examples of conductive materials include carbon materials such as fibrous carbon, carbon black (e.g., acetylene black, ketjen black), coke, and activated carbon. Examples of fibrous carbon include those described above. Examples of binders include cellulose-based binders such as carboxymethyl cellulose (CMC), and styrene-butadiene rubber (SBR).

[0042] The separator may be a porous sheet (film, nonwoven fabric, etc.) made of a resin such as polyethylene, polypropylene, polyester, cellulose, or polyamide. The porous sheet may have a single-layer structure or a multi-layer structure of two or more layers. The separator may have a functional layer on the surface of the porous sheet. The functional layer may be at least one of a heat-resistant layer and an adhesive layer for adhering to the positive electrode plate and the negative electrode plate.

[0043] Examples of the electrolyte include non-aqueous electrolytes, such as those containing a supporting salt in a non-aqueous solvent such as an organic solvent. Examples of non-aqueous solvents include ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), and diethyl carbonate (DEC). The electrolyte may contain one or more of these non-aqueous solvents. Examples of supporting salts include lithium perchlorate (LiClO), lithium hexafluorophosphate (LiPF), and lithium fluoroborate (LiBF). The electrolyte may contain one or more of these supporting salts. The electrolyte may further contain additives such as vinylene carbonate (VC), vinylethylene carbonate (VEC), and fluoroethylene carbonate.

[0044] The battery case is preferably made of metal, and can be formed using, for example, aluminum, an aluminum alloy, iron, or an iron alloy. [Example]

[0045] Hereinafter, the present disclosure will be described more specifically with reference to examples and comparative examples.

[0046] [Analysis of the Compositions of the First Active Material and the Second Active Material] The compositions of the first and second active materials were analyzed by high-frequency inductively coupled plasma (ICP) optical emission spectroscopy.

[0047] [Measurement of average particle diameter (D50) of first active material and second active material] The average particle diameters (D50) of the first active material and the second active material were measured using a laser diffraction particle size distribution measuring device ("Mastersizer-3000", manufactured by Malvern Panalytical).

[0048] [Crystallite size measurement] The crystallite size of the second active material was calculated from the peak intensity of the (104) plane using an X-ray diffractometer ("SmartLab", manufactured by Rigaku).

[0049] [Production Example 1] (Preparation of First Active Material) Ni 0.80 Co 0.05 Mn 0.15 A transition metal compound represented by (OH)2 was mixed with LiOH and fired to obtain a first active material which was a lithium transition metal composite oxide, had a ratio (Li / M) of the number of moles of Li to the total number of moles of transition metals (M) of 1.05, and had an average particle diameter (D50) of 17.2 μm.

[0050] The NiCoMn composite hydroxide and the lithium compound were mixed and fired at 700 to 1000°C to obtain first active materials that were lithium transition metal composite oxides and had ratios (Li / M) of the number of moles of Li to the total number of moles of transition metals (M) of 1.03, 1.07, 1.09, and 1.12. The average particle diameters of these first active materials were in the range of 12 μm to 20 μm.

[0051] (Preparation of positive electrode plate (r1)) Using the first active material having the ratio (Li / M) obtained above, a positive electrode plate (r1) was fabricated in the following manner. First, 97.5 parts by mass of the first active material, 1.5 parts by mass of carbon black as a conductive material, and 1.0 parts by mass of polyvinylidene fluoride (PVdF) as a binder were mixed, and an appropriate amount of N-methyl-2-pyrrolidone (NMP) was added to obtain a slurry. The slurry was applied to an aluminum foil serving as a positive electrode current collector, dried, and rolled to a predetermined thickness using a rolling roller. As a result, a density of 3.30 g / cm was obtained on the aluminum foil. 3The positive electrode active material layer was formed on the positive electrode sheet (r1) to obtain a raw positive electrode sheet (r1). The raw positive electrode sheet (r1) was cut to a predetermined size, and an aluminum tab was attached to obtain a positive electrode sheet (r1).

[0052] (Preparation of Electrolyte) An electrolyte solution was prepared by adding lithium hexafluorophosphate (LiPF6) as a supporting salt to a mixed solvent prepared by mixing ethylene carbonate (EC) and ethyl methyl carbonate (EMC) as a non-aqueous solvent in a volume ratio of 30:70, so that the concentration per 1 L of the mixed solvent was 1 mol / L, and adding vinylene carbonate (VC) so that the content was 0.3 mass% relative to the total mass of the mixed solvent.

[0053] (Preparation of test cell (r1)) Using each of the positive electrode plates (r1) obtained above, a test cell (r1) was prepared according to the following procedure. The positive electrode plate (r1) and a lithium metal plate as a counter electrode of the positive electrode plate (r1) were stacked via a polyolefin separator to obtain a stacked electrode body. The stacked electrode body was housed in a battery case made of an aluminum laminate sheet, and the electrolyte solution prepared above was poured into it. The opening was then sealed to obtain a test cell (r1).

[0054] Each test cell (r1) was placed under a temperature condition of 25°C and a current density of 0.2 mA / cm 2 So, 4.3V vs. Li / Li + The battery was charged at a constant current until the potential reached 4.3V vs. Li / Li. + At a potential of 0.04 mA / cm 2 The charge capacity per unit mass of the first active material was measured by constant voltage charging until the current density reached 4.1 V vs. Li / Li relative to the total capacity of the test cell (r1) during charging of the test cell (r1). + The capacity ratios at the above potentials were calculated, and the results are shown in Figure 1 and Table 1.

[0055] FIG. 1 is a plot of the results shown in Table 1, and shows the charge capacity [mAh / g] and the charge capacity at 4.1 V vs. Li / Li when a test cell (r1) having a positive electrode plate (r1) formed using the first active material was charged. + 1 and Table 1, when the ratio (Li / M) of the first active material is less than 1.05, the overall capacity when the test cell (r1) is charged is 4.1V vs. Li / Li. + It can be seen that the proportion of capacitance increases at potentials above this level.

[0056] [Table 1]

[0057] [Production Example 2] (Production of second active material) Ni 0.83 Co 0.12 Mn 0.05 A second active material was obtained by mixing a transition metal compound represented by (OH)2 with LiOH and calcining the mixture, which was a lithium transition metal composite oxide with a ratio of the number of moles of Li to the total number of moles of transition metals (M) (Li / M) of 1.01. The second active material had an average particle size (D50) of 5.9 μm and a crystallite size of 965 nm.

[0058] The NiCoMn composite hydroxide and the lithium compound were mixed and fired at 700 to 1000°C to obtain second active materials that were lithium transition metal composite oxides and had ratios (Li / M) of the number of moles of Li to the total number of moles of transition metals (M) of 0.98, 1.00, 1.04, 1.07, and 1.10. The average particle diameters of these second active materials were in the range of 2 μm to 8 μm, and the crystallite sizes were in the range of 800 nm or more.

[0059] (Preparation of positive electrode plate (r2)) A positive electrode plate (r2) was obtained by the same procedure as described for the production of the positive electrode plate (r1), except that the second active material was used instead of the first active material.

[0060] (Preparation of test cell (r2)) A test cell (r2) was obtained by the same procedure as described for the production of the test cell (r1), except that the positive electrode plate (r2) was used instead of the positive electrode plate (r1).

[0061] For the test cell (r2), constant current charging and low voltage charging were performed in the same manner as for the test cell (r1), and the charge capacity [mAh / g] per unit mass of the second active material was measured. Also, the ratio of the capacity at a potential of 4.1 V vs. Li / Li + to the total capacity of the test cell (r2) during charging of the test cell (r2) was calculated. The results are shown in Figure 2 and Table 2.

[0062] Figure 2 is a plot of the results shown in Table 2, and shows the charge capacity [mAh / g] and the ratio [%] of the capacity at a potential of 4.1 V vs. Li / Li + or higher when charging the test cell (r2) having the positive electrode plate (r2) formed using the second active material, plotted against the ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metal (M) in the second active material. From the graph shown in Figure 2 and Table 2, it can be seen that when the above ratio (Li / M) of the first active material exceeds 1.04, the charge capacity when charging the test cell (r2) significantly decreases.

[0063]

Table 2

[0064] [Examples 1 to 3, Comparative Examples 1 to 3] (Production of positive electrode plate) A positive electrode active material in which the first active material and the second active material having the ratio (Li / M) shown in Table 3 were mixed at a ratio of first active material:second active material = 6:4 (mass ratio) was prepared. A positive electrode plate was obtained by the same procedure as described for the production of the positive electrode plate (r1), except that the positive electrode active material was used instead of the first active material.

[0065] (Fabrication of non-aqueous electrolyte secondary battery) A non-aqueous electrolyte secondary battery was obtained in the same manner as described for producing the test cell (r1), except that the positive electrode plate (r1) obtained above was used instead of the positive electrode plate (r1).

[0066] The non-aqueous electrolyte secondary battery was subjected to constant current charging and low voltage charging in the same manner as the test cell (r1), and the charge capacity per unit mass of the positive electrode active material [mAh / g] was measured. + The capacity ratios at these potentials were calculated, and the results are shown in Table 3.

[0067] [Table 3]

[0068] As shown in Table 2, a positive electrode plate using a positive electrode active material containing a first active material having a ratio (Li / M) of 1.05 or more and a second active material having a ratio (Li / M) of 1.04 or less can produce a nonaqueous electrolyte secondary battery that achieves both high charging capacity and excellent thermal stability.

[0069] [Evaluation of filling] The first active material having the above ratio (Li / M) of 1.05 and the second active material having the above ratio (Li / M) of 1.01 were mixed in the mass ratio shown in Table 4, and the density was measured when pressed under a pressure of 200 Pa. The results are shown in Table 4.

[0070] [Table 4]

[0071] As shown in Table 4, when the mass ratio of the first particles to the second particles is in the range of 5 / 5 or more and 8 / 2 or less, the density is 3.40 g / cm 3 It can be seen that the above can be achieved and good filling properties can be obtained.

Claims

1. a first active material that is a lithium transition metal composite oxide; and a second active material that is a lithium transition metal composite oxide and has a smaller average particle diameter (D50) than the first active material, The crystallite size of the second active material is 800 nm or more, a ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the first active material is 1.05 or more and 1.12 or less; a ratio (Li / M) of the number of moles of lithium (Li) to the total number of moles of transition metals (M) in the second active material is 1.01 or more and 1.04 or less; The positive electrode plate, wherein the first active material and the second active material each contain 80 mol % or more of nickel (Ni) with respect to the total amount of transition metals.

2. A positive electrode plate as described in claim 1, wherein the first active material and the second active material, which are the lithium transition metal composite oxides, each independently further contain, as the transition metal (M), one or more selected from the group consisting of Mn (manganese), cobalt (Co), aluminum (Al), and titanium (Ti).

3. The positive electrode plate according to claim 1 , wherein a mass ratio of the first active material to the second active material (first active material / second active material) is 5 / 5 or more and 8 / 2 or less.

4. The positive electrode plate according to claim 1 , wherein the first active material has an average particle diameter (D50) of 12 μm or more and 20 μm or less.

5. The positive electrode plate according to claim 1 , wherein the second active material has an average particle diameter (D50) of 2 μm or more and 8 μm or less.

6. The positive electrode plate according to claim 1 , wherein the second active material is at least one of a single particle and a secondary particle formed by aggregation of three or less primary particles.

7. An electrode assembly including the positive electrode plate, the negative electrode plate, and a separator interposed between the positive electrode plate and the negative electrode plate according to any one of claims 1 to 6; and an electrolyte solution.

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