Negative Electrode Plate and its Application

Description

TECHNICAL FIELD

[0001] The present invention relates to a negative electrode plate, and in particular to a negative electrode plate, an electrochemical energy storage apparatus and an electronic apparatus comprising the negative electrode plate, belonging to the field of battery technologies.BACKGROUND

[0002] Lithium-ion batteries are widely used electrochemical energy storage apparatuses, and may provide continuous and stable power. Currently, graphite is a negative electrode active material used in commercial lithium batteries, which is widely used at low price. As a negative electrode active material, graphite has lithium intercalation potential close to 0V (lithium metal potential), and thus lithium dendrites easily occur. The occurrence of lithium dendrites causes a risk of thermal runaway. In addition, with continuous charging and discharging of a battery, cell thickness increases continuously. In order to cope with the increase of the cell thickness, an electronic device needs to reserve a thickness expansion space in advance, which is not good for portability of the electronic device, and also reduces volumetric energy density of the electronic device. In addition, a theoretical capacity of graphite is 372 mAh / g, with an obvious upper limit of capacity, and thus further increase of volumetric energy density is limited.

[0003] JP6303278B2, CN108963254B and CN103633306A have also studied carbon materials used in negative electrodes of lithium secondary batteries.SUMMARY

[0004] The invention is as defined in claims 1 to 12.

[0005] Disclosed is a negative electrode plate (not explicitly claimed), lithium dendrites not easily occur for the negative electrode plate, and the negative electrode plate has a significantly low thickness expansion rate after cycling. In addition, the negative electrode plate helps significantly improve energy density of a lithium-ion battery.

[0006] The present invention provides an electrochemical energy storage apparatus, and the electrochemical energy storage apparatus includes the negative electrode plate. Therefore, the electrochemical energy storage apparatus not only has good energy density, but also has an advantage of low expansion after long-term cycle.

[0007] The present invention further provides an electronic apparatus, and the electronic apparatus includes the electrochemical energy storage apparatus. Therefore, the electronic apparatus has a long endurance time and high customer satisfaction.

[0008] The present invention provides an electrochemical energy storage apparatus. The electrochemical energy storage apparatus comprises a negative electrode plate and a positive electrode plate; the negative electrode plate includes a current collector and a negative electrode active layer disposed on at least one function surface of the current collector, and a negative electrode active material of the negative electrode active layer includes a first amorphous carbon material; and an interlayer spacing d002 of the first amorphous carbon material is greater than 0.34 nm, and an average pore diameter of pores of the first amorphous carbon material ranges from 2 nm to 20 nm; and the positive electrode plate includes a positive electrode current collector and a positive electrode active layer disposed on at least one function surface of the positive electrode current collector, a thickness ratio of the negative electrode active layer to the positive electrode active layer ranges from 0.93:1 to 1.68:1.

[0009] The negative electrode active material of the negative electrode plate in the present invention includes the first amorphous carbon material, and the first amorphous carbon material has a relatively large interlayer spacing and a special average pore diameter of pores. Therefore, very small thickness expansion of the negative electrode plate is caused by intercalation and deintercalation of lithium ions, and may be almost ignored. In addition, the first amorphous carbon material has a relatively high capacity per gram, may meet a relatively high energy density, and a design of a volumetric energy density of ED 800 Wh / L. Furthermore, using the first amorphous carbon material having a high lithium intercalation potential as a negative electrode active material may reduce a risk of lithium deintercalation of the negative electrode plate.

[0010] In an implementation, the first amorphous carbon material has a capacity per gram of not less than 470 mAh / g.

[0011] In an implementation, a average particle size d 1 of the first amorphous carbon material ranges from 3 µm to 15 µm; and / or a specific surface area of the first amorphous carbon material ranges from 2.8 m 2< / g to 19 m 2< / g; and / or a Raman spectrum Id / Ig peak ratio of the first amorphous carbon material is greater than 1.0 (not explicitly claimed) ; and / or an X-ray diffraction pattern of the first amorphous carbon material includes a diffraction peak with 20 being less than 26 degrees, and an intensity of the diffraction peak is less than 20000 (not explicitly claimed) ; and / or, a full width at half maximum of the diffraction peak is greater than 1.2 degrees.

[0012] In an implementation, the negative electrode active material further includes a second amorphous carbon material, where the second amorphous carbon material is in a shape of spherical particles.

[0013] A average particle size d 2 of the spherical particles ranges from 0.2 µm to 4 µm.

[0014] In an implementation, a specific surface area of the second amorphous carbon material ranges from 2 m 2< / g to 23 m 2< / g.

[0015] In an implementation, the negative electrode active material includes a first mixture of the first amorphous carbon material and the second amorphous carbon material.

[0016] In an implementation, a mass percentage of the second amorphous carbon material in the first mixture is not less than 3%.

[0017] In an implementation, the negative electrode active layer includes a first amorphous carbon layer and a second amorphous carbon layer that are stacked, where the first amorphous carbon layer includes the first amorphous carbon material, and the second amorphous carbon layer includes the second amorphous carbon material.

[0018] In an implementation, the negative electrode active layer includes the first amorphous carbon layer close to the current collector and the second amorphous carbon layer away from the current collector.

[0019] In an implementation, a thickness H 1 of the first amorphous carbon layer and a thickness H 2 of the second amorphous carbon layer satisfy the following relationship: 0.3 H 1 + H 2 ≥ H 2 ≥ D 2 where D 2 denotes a maximum particle size of the second amorphous carbon material.

[0020] In an implementation, the negative electrode active material includes a second mixture of the first amorphous carbon material and a graphite material.

[0021] In an implementation, a ratio of a average particle size d 3 of the graphite material to a average particle size d 1 of the first amorphous carbon material ranges from 0.95:1 to 8.3:1.

[0022] In an implementation, a mass percentage of the first amorphous carbon material in the second mixture is not less than 28%.

[0023] In an implementation, the negative electrode active layer includes a first amorphous carbon layer and a graphite layer that are stacked, where the first amorphous carbon layer includes a first amorphous carbon material and the graphite layer includes a graphite material.

[0024] In an implementation, a thickness H 1 of the first amorphous carbon layer and a thickness H 3 of the graphite layer satisfy the following relationship: H 1 + H 3 − 0.39 D 3 ≥ H 1 ≥ 0.63 D 1 where D 1 denotes a maximum particle size of the first amorphous carbon material, and D 3 denotes a maximum particle size of the graphite material.

[0025] In an implementation, the negative electrode active layer includes graphite layer close to the current collector and the first amorphous carbon layer away from the current collector.

[0026] In an implementation, the graphite material includes graphite particles and / or graphite core-shell particles, and the graphite core-shell particles are constituted by a core formed by graphite and a shell covering at least part of a surface of the core.

[0027] In an implementation, the negative electrode active material includes a third mixture of the first amorphous carbon material and a silicon-based material.

[0028] In an implementation, a mass percentage of the silicon-based material in the third mixture ranges from 0.3% to 20%.

[0029] In an implementation, the negative electrode active layer includes a first amorphous carbon layer and a silicon-based active layer that are stacked, the first amorphous carbon layer includes the first amorphous carbon material, and the silicon-based active layer includes the silicon-based material.

[0030] In an implementation, a thickness H 1 of the first amorphous carbon layer and a thickness H 4 of the silicon-based active layer satisfy the following relationship: H 4 ≤ 0.2 H 1 + H 4 .

[0031] In an implementation, the silicon-based material is selected from at least one of a silicon material, a silicon oxide material, and a silicon-carbon composite material.

[0032] In an implementation, a unit thickness capacity of the negative electrode plate ranges from 26.9 mAh / µm to 123 mAh / µm.

[0033] The electrochemical energy storage apparatus of the present invention includes the negative electrode plate, and therefore has good safety performance and energy density.

[0034] The present invention further provides an electronic apparatus, and the electronic apparatus includes the electrochemical energy storage apparatus.

[0035] The electronic apparatus in the present invention includes the electrochemical energy storage apparatus, which not only has a good endurance capability, but also has characteristics of a lower thickness and a lighter weight. Therefore, on the basis of meeting usage requirements of a conventional electronic product, the electronic apparatus may also meet requirements of a next-generation wearable device.BRIEF DESCRIPTION OF THE DRAWINGS

[0036] FIG. 1 is an SEM graph of a first amorphous carbon material in Example 1. FIG. 2 is an XRD pattern of a first amorphous carbon material in Example 1. FIG. 3 is a Raman pattern of a first amorphous carbon material in Example 1. FIG. 4 is a BJH pore size distribution graph of a first amorphous carbon material in Example 1. FIG. 5 is an SEM pattern of a first amorphous carbon material in Example 2. FIG. 6 is an XRD pattern of a first amorphous carbon material in Example 2. FIG. 7 is a Raman pattern of a first amorphous carbon material in Example 2. FIG. 8 is a BJH pore size distribution graph of a first amorphous carbon material in Example 2. FIG. 9 is an SEM pattern of a first amorphous carbon material in Example 3. FIG. 10 is an XRD pattern of a first amorphous carbon material in Example 3. FIG. 11 is a Raman pattern of a first amorphous carbon material in Example 3. FIG. 12 is a BJH pore size distribution graph of a first amorphous carbon material in Example 3. DETAILED DESCRIPTIONS OF THE EMBODIMENTS

[0037] To make the objectives, technical solutions, and advantages of the present invention clearer, the following clearly describes the technical solutions in the embodiments of the present invention with reference to the embodiments of the present invention. Apparently, the described embodiments are some but not all of the embodiments of the present invention.

[0038] Disclosed is a negative electrode plate (not explicitly claimed). The negative electrode plate includes a current collector and a negative electrode active layer disposed on at least one function surface of the current collector, and a negative electrode active material of the negative electrode active layer includes a first amorphous carbon material. An interlayer spacing d002 of the first amorphous carbon material is greater than 0.34 nm, and an average pore diameter of pores of the first amorphous carbon material ranges from 2 nm to 20 nm.

[0039] The "average pore diameter of pores" in the present invention is defined as a average pore size of pores on a surface and inside of an amorphous carbon material.

[0040] The negative electrode plate in the present invention includes a negative electrode current collector and a negative electrode active layer disposed on at least one function surface of the current collector, where the function surface refers to the largest and opposite surfaces, for the negative electrode active layer to be coated, of the current collector. The negative electrode active layer may be disposed on one or two function surfaces of the current collector. A thickness of the negative electrode active layer is not limited in the present invention, for example, may range from 40 µm to 120 µm, for example, 43 µm, 59 µm, 65.1 µm, 69.6 µm, 81.2 µm, and 113.6 µm.

[0041] The negative electrode active material of the negative electrode active layer includes a first amorphous carbon material. Since the first amorphous carbon material has a special interlayer spacing d002 and a special average pore diameter of pores, relatively large pores exist inside the first amorphous carbon material. During long-term charging and discharging, an inner space of the first amorphous carbon material helps buffer expansion of an electrochemical energy storage apparatus, reducing thickness expansion of the electrochemical energy storage apparatus caused during long-term disclosure, and improving safety performance. Specifically, after the negative electrode plate is cycled for 50 T, the negative electrode plate has a thickness change rate of less than 5% in the condition of being fully charged.

[0042] In addition, the first amorphous carbon material has performance of suppressing expansion, so as to avoid the current approach of improving safety performance of the electrochemical energy storage apparatus by reserving an expansion space for the electrochemical energy storage apparatus, thereby helping further improve volumetric energy density of the electrochemical energy storage apparatus.

[0043] It is worth emphasizing that the first amorphous carbon material not only can suppress expansion of the electrochemical energy storage apparatus, but also has an advantage of improving energy density of the electrochemical energy storage apparatus.

[0044] The first amorphous carbon material is a carbon material having a disordered structure of a graphite layer. Generally, an amorphous carbon material has a high capacity per gram, and has no theoretical upper limit for the capacity per gram.

[0045] The first amorphous carbon material is a small-sized graphite layered structure exhibiting disordered arrangement and a porous structure. Specifically, an interlayer spacing d002 of greater than 0.34 nm and an average pore diameter of 2-20 nm of pores makes the first amorphous carbon material have high capacity performance. The capacity of an amorphous carbon material higher than that of graphite mainly originates from a highly disordered structure, and this structure provides a large number of lithium storage sites. In addition, pores of the amorphous carbon material itself may help increase lithium storage sites.

[0046] Therefore, the negative electrode plate of the present invention not only helps improve the energy density of the electrochemical energy storage apparatus, but also can effectively improve performance of suppressing expansion of thickness of the electrochemical energy storage apparatus.

[0047] In addition, since the amorphous carbon material in the negative electrode plate of the present invention has a relatively high lithium intercalation potential, precipitation of lithium dendrites can be effectively suppressed, and a negative impact of lithium dendrites on cycle performance and safety performance of the electrochemical energy storage apparatus is also avoided.

[0048] In a specific implementation, a first amorphous carbon material in the present invention has a capacity per gram of not less than 470 mAh / g.

[0049] Further, a average particle size d 1 of the first amorphous carbon material in the negative electrode plate of the present invention ranges from 3 µm to 15 µm. The larger the average particle size d 1 of the first amorphous carbon material, the smaller a specific surface area of the first amorphous carbon material, which is not good for conduction and intercalation of lithium ions. However, if the average particle size d 1 is too small, the specific surface area of the first amorphous carbon material may be significantly increased, a contact area between an electrolytic solution and the first amorphous carbon material is increased, and a large amount of the electrolytic solution is consumed, thereby reducing the cycle performance of the electrochemical energy storage apparatus. Therefore, in the present invention, the average particle size d 1 of the first amorphous carbon material ranges from 3 µm to 15 µm, and may further range from 5 µm to 12 µm. Specifically, in a process of preparing the negative electrode plate, the first amorphous carbon material with a average particle size d 1 ranging from 3 µm to 15 µm may be selected by using a laser particle size analyzer. After the electrochemical energy storage apparatus is assembled, the foregoing average particle size of the first amorphous carbon material may also be measured by a focused ion beam-3D scanning electron microscopy (FIB-SEM).

[0050] Further, the specific surface area of the first amorphous carbon material in the negative electrode plate of the present invention ranges from 2.8 m 2< / g to 19 m 2< / g. The specific surface area will not suppress intercalation and transmission capability of lithium ions, so that fast charging performance of the electrochemical energy storage apparatus is improved, and the electrochemical energy storage apparatus can have sufficient electrolyte in a long-term cycle process, thereby further improving cycle performance of the electrochemical energy storage apparatus by further maintaining the transmission capability of lithium ions.

[0051] According to the research of the present invention, a Raman spectrum Id / Ig peak ratio of the first amorphous carbon material in the present invention is greater than 1.0; and an X-ray diffraction pattern includes a diffraction peak with 20 being less than 26 degrees, where an intensity of the diffraction peak is less than 20000, and further a full width at half maximum of the diffraction peak is greater than 1.2 degrees. For example, 20 of the diffraction peak is 25.48 degrees, 23.23 degrees or 22.58 degrees; and peak intensity of the diffraction peak may be, for example, 8000, 9000, or 18000.

[0052] The first amorphous carbon material in the negative electrode plate of the present invention may be obtained by performing a carbonization process on an asphaltene base material, a biomass raw material, or a polymer raw material.

[0053] The negative electrode active material of the negative electrode plate of the negative electrode active layer of the present invention includes the foregoing first amorphous carbon material. Therefore, with a significant lithium intercalation capacity, the negative electrode plate is not easy to precipitate lithium dendrites and has a low thickness expansion rate during cycling.

[0054] As mentioned above, in the present invention, in addition to the first amorphous carbon material, the negative electrode active material of the negative electrode active layer of the negative electrode plate may also include another negative electrode active material.

[0055] In an implementation, the negative electrode active material of the negative electrode active layer further includes a second amorphous carbon material, where the second amorphous carbon material is in a shape of spherical particles, and a average particle size d 2 of the spherical particles ranges from 0.2 µm to 4 µm. Specifically, in the process of preparing the negative electrode plate, the second amorphous carbon material with a average particle size d 2 ranging from 0.2 µm to 4 µm may be selected by using a laser particle size analyzer. After the electrochemical energy storage apparatus is assembled, the foregoing average particle size of the second amorphous carbon material may also be measured by a focused ion beam-3D scanning electron microscopy (FIB-SEM).

[0056] Specifically, macroscopic representation of the second amorphous carbon material may be a powdery material formed by particles having a spherical structure with a average particle size d 2 ranging from 0.2 µm to 4 µm. According to the research of the present invention, a Raman (Raman) spectrum Id / Ig peak ratio of the second amorphous carbon material (or referred to as a spherical carbon material) ranges from 0.5 to 1.5. In the result of the X-ray diffraction (XRD) analysis, a peak position of the diffraction peak is less than 26.5 degrees, so that the second amorphous carbon material is a carbon-based active substance having a low temperature. Compared with an amorphous carbon material with irregular morphologies, particles of the second amorphous carbon material have a spherical structure with a small particle size (the average particle size d 2 ranges from 0.2 µm to 4 µm), and have a large number of end surfaces, which facilitates de-intercalation / transmission of lithium ions; therefore, the second amorphous carbon material has good low-temperature dynamic performance, and specifically, a lower limit voltage during low-temperature discharge is high.

[0057] Further, a specific surface area of the second amorphous carbon material ranges from 2 m 2< / g to 23 m 2< / g, which helps further improve low-temperature performance of the electrochemical energy storage apparatus. Further, the specific surface area of the second amorphous carbon material ranges from 4 m 2< / g to 15 m 2< / g.

[0058] Therefore, when the negative electrode active material in the negative electrode plate of the present invention includes both the first amorphous carbon material and the second amorphous carbon material, a lithium-ion battery has high energy density and a low expansion rate, and also has relatively good low-temperature dynamic performance, so that electrical performance of the lithium-ion battery is better, which helps further expand an disclosure range of the lithium-ion battery.

[0059] Specific forms of the first amorphous carbon material and the second amorphous carbon material in the negative electrode plate are not limited in the present invention. For example, the negative electrode active material in the negative electrode active layer includes a first mixture of the first amorphous carbon material and the second amorphous carbon material. Further, a mass percentage of the second amorphous carbon material in the first mixture is not less than 3%.

[0060] Alternatively, the negative electrode active layer includes a first amorphous carbon layer and a second amorphous carbon layer that are stacked, where the first amorphous carbon layer includes the first amorphous carbon material, and the second amorphous carbon layer includes the second amorphous carbon material.

[0061] Further, when the negative electrode active layer includes the first amorphous carbon layer and the second amorphous carbon layer that are stacked, the first amorphous carbon layer is located between a function surface of the current collector and the second amorphous carbon layer.

[0062] Further, a thickness H 1 of the first amorphous carbon layer and a thickness H 2 of the second amorphous carbon layer satisfy the following relationship: 0.3 H 1 + H 2 ≥ H 2 ≥ D 2 where D 2 denotes a maximum particle size of the second amorphous carbon material.

[0063] D 2 may be obtained through detection by using a laser particle size analyzer. Herein, the thickness H 1 of the first amorphous carbon layer and the thickness H 2 of the second amorphous carbon layer mean thickness of the first amorphous carbon layer and thickness of the second amorphous carbon layer on one function surface, respectively.

[0064] The inventors find that when H 1 and H 2 satisfy the foregoing relationship, the electrochemical energy storage apparatus has both good low-temperature performance and low thickness expansion rate.

[0065] In another implementation, the negative electrode active material further includes a graphite material.

[0066] It can be understood that, since the first amorphous carbon material has a special average pore diameter of pores and an interlayer spacing d002, relatively large pores exist inside the first amorphous carbon material. During long-term charging and discharging, when the graphite material in the negative electrode plate expands, the pores inside the first amorphous carbon material may provide a space for the expansion of the graphite material, thereby greatly suppressing expansion of the electrochemical energy storage apparatus caused by expansion of the negative electrode active layer.

[0067] The first amorphous carbon material not only can provide an expansion space for the graphite material, but also can avoid excessive expansion of the graphite material to some extent. Structural stability of the graphite material is maintained, so that ability of lithium ions to be intercalated into graphite is ensured, and a precipitation probability of lithium dendrites in a graphite layer material is reduced, further ensuring cycle performance and safety performance of the electrochemical energy storage apparatus.

[0068] Specific forms of the first amorphous carbon material and the graphite material in the negative electrode plate are not limited in the present invention. For example, the negative electrode active material in the negative electrode active layer includes a second mixture of the first amorphous carbon material and the graphite material.

[0069] Further, a ratio of a average particle size d 3 of the graphite material to a average particle size d 1 of the first amorphous carbon material in the second mixture ranges from 0.95:1 to 8.3:1. Specifically, a high specific surface area of the graphite material facilitates infiltration of the electrolyte, thereby ensuring efficient transmission of lithium ions, and further avoiding precipitation of lithium dendrites in the graphite material. As mentioned above, d 3 may be measured by using a laser particle size analyzer or a focused ion beam-3D scanning electron microscopy (FIB-SEM).

[0070] The inventors find that when a ratio of a mass of the first amorphous carbon material to a sum of masses of the first amorphous carbon material and the graphite material is no less than 28%, the negative electrode plate has better performance in improving energy density and suppressing expansion of thickness of the electrochemical energy storage apparatus, and especially can reduce the expansion of the thickness more significantly.

[0071] Alternatively, the negative electrode active layer includes a first amorphous carbon layer and a graphite layer that are stacked, where the first amorphous carbon layer includes a first amorphous carbon material and the graphite layer includes a graphite material.

[0072] Further, a thickness H 1 of the first amorphous carbon layer and a thickness H 3 of the graphite layer satisfy the following relationship: H 1 + H 3 − 0.39 D 3 ≥ H 1 ≥ 0.63 D 1 where D 1 denotes a maximum particle size of the first amorphous carbon material, and D 3 denotes a maximum particle size of the graphite material. The inventors find that when the maximum particle size D 1 of the first amorphous carbon material, the maximum particle size D 3 of the graphite material, the thickness H 1 of the first amorphous carbon layer, and the thickness H 3 of the graphite layer have the foregoing matching relationship, an expansion rate of the negative electrode plate is further reduced.

[0073] It should be noted that both D 1 and D 3 may be measured and obtained by using a laser particle size analyzer.

[0074] In a preferred implementation, the graphite layer is located between a current collector and an amorphous carbon layer, facilitating further suppression of expansion of the graphite layer by the first amorphous carbon layer.

[0075] The graphite material in the negative electrode plate of the present invention may be a conventional graphite-based negative electrode active material in the field, or may be constituted by a core formed by graphite and a shell covering at least part of a surface of the core. The graphite material of the core-shell structure may be prepared according to a conventional method in the art, for example, by using a carbon coating method.

[0076] Comparatively, using the graphite material having the foregoing core-shell structure as the negative electrode active material facilitates cooperation with the first amorphous carbon material, and an effect of improving energy density of the electrochemical energy storage apparatus and suppressing thickness expansion can be improved. In some preferred implementations, the shell of the graphite material of the foregoing core-shell structure includes an amorphous carbon material, specifically, the graphite material of the core-shell structure may be a structure in which graphite is used as a core and an amorphous carbon material is used as a shell. It should be noted that, the amorphous carbon material in the shell material may be the first amorphous carbon material mentioned in the present invention, or may be another amorphous carbon material.

[0077] In another implementation, the negative electrode active material further includes a silicon-based material. During long-term charging and discharging of the electrochemical energy storage apparatus, the special interlayer spacing and pore size of the first amorphous carbon material provide a buffer for expansion of the silicon-based material in the negative electrode plate, so that thickness expansion of the electrochemical energy storage apparatus due to the expansion of the silicon-based material can be reduced to some extent. Moreover, the first amorphous carbon material has a higher hardness relative to the silicon-based material, so that stress of the silicon-based material is affected, and a probability of excessive expansion of the silicon-based material is reduced. In addition to being able to alleviate the expansion of the silicon-based material, an internal space of the amorphous carbon material having special pores and interlayer spacing in the negative electrode plate of the present invention also helps buffer expansion of the electrochemical energy storage apparatus and reduce thickness expansion of the electrochemical energy storage apparatus caused due to long-term application.

[0078] The first amorphous carbon material is capable of relieving the expansion of the silicon-based material so as to promote efficient development of the feature of high energy density of the silicon-based material. In addition, the first amorphous carbon material also helps resolve a problem that internal resistance of a lithium-ion battery is too low due to conductivity of the silicon-based material, thereby improving rate performance of the lithium-ion battery to some extent.

[0079] Specific forms of the first amorphous carbon material and the silicon-based material in the negative electrode plate are not limited in the present invention. For example, the negative electrode active material in the negative electrode active layer includes a third mixture of the first amorphous carbon material and the silicon-based material. Further, the inventors find that when a mass percentage of the silicon-based material in the third mixture ranges from 0.3% to 20%, thermodynamic performance of the electrochemical energy storage apparatus is further improved, for example, the electrochemical energy storage apparatus has better energy density and performance of suppressing expansion.

[0080] Alternatively, the negative electrode active layer includes a first amorphous carbon layer and a silicon-based active layer that are stacked, the first amorphous carbon layer includes the first amorphous carbon material, and the silicon-based active layer includes the silicon-based material. The first amorphous carbon layer and the silicon-based active layer may be stacked in a manner that the first amorphous carbon layer is close to the current collector and the silicon-based active layer is away from the current collector, or that the first amorphous carbon layer is away from the current collector and the silicon-based active layer is close to the current collector. Preferably, when the first amorphous carbon layer is away from the current collector and the silicon-based active layer is close to the current collector, the energy density of the electrochemical energy storage apparatus is improved and expansion is suppressed.

[0081] Further, when the negative electrode active layer includes a first amorphous carbon layer and a silicon-based active layer that are stacked, the thickness H 1 of the first amorphous carbon layer and a thickness H 4 of the silicon-based active layer satisfy the following relationship: H 4 ≤ 0.2 H 1 + H 4

[0082] In the present invention, the silicon-based material is selected from at least one of a silicon material, a silicon oxide material, and a silicon-carbon composite material.

[0083] A porosity of the negative electrode plate in the present invention ranges from 35% to 49%. Specifically, the porosity means a porosity of the negative electrode active layer of the negative electrode plate. The inventors find that when the porosity of the negative electrode plate is in the range, rapid infiltration of the electrolyte is facilitated, cycle performance of the lithium-ion battery is improved, and discharge performance with high capacity and high rate is always achieved. However, when the porosity is too high, it means that an amount the negative electrode active material in the negative electrode active layer is too small, so that the energy density of the lithium-ion battery may be adversely affected.

[0084] Specifically, a compacted density of the negative electrode plate in the present invention may be controlled to range from 1.02 g / cm 3< to 1.7 g / cm 3< , so that volumetric energy density of the electrochemical energy storage apparatus is further optimized. Further, a surface density of the negative electrode plate in the present invention ranges from 3.25 g / cm 2< to 13.25g / cm 2< .

[0085] In the negative electrode plate of the present invention, the negative electrode active layer includes a conductive agent and a binder in addition to the negative electrode active material. The conductive agent may be selected from at least one of superconducting carbon black, acetylene black, ketjen black, carbon fiber, and graphene; and the binder may be selected from at least one of carboxymethyl cellulose (CMC), styrene-butadiene rubber (SBR), polyvinyl chloride, carboxylated polyvinyl chloride, polyvinyl fluoride, polymer containing ethylene oxide, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, polyamideimide, polyvinyl alcohol, sodium polyacrylate.

[0086] In some implementations, the negative electrode active layer includes 95-99% negative electrode active material, 0.1-2.3%% conductive agent, and 0.5-3.7% binder according to mass percentage.

[0087] A aspect of the present invention provides a electrochemical energy storage apparatus, and the electrochemical energy storage apparatus includes the foregoing negative electrode plate. The electrochemical energy storage apparatus of the present invention includes the foregoing negative electrode plate, so that energy density, safety performance, and fast charging performance are good.

[0088] Further, when the negative electrode active material of the negative electrode active layer in the negative electrode plate includes a second mixture of a first amorphous carbon material and a graphite material, a unit thickness capacity of the negative electrode plate in an electrochemical energy storage apparatus ranges from 26.9 mAh / µm to 123 mAh / µm. Specifically, the unit thickness capacity of the negative electrode plate is a ratio of an actual capacity of the electrochemical energy storage apparatus to a thickness of the negative electrode active layer of the negative electrode plate in the electrochemical energy storage apparatus. For example, when the electrochemical energy storage apparatus is a lithium-ion battery, the unit thickness capacity of the negative electrode plate is a ratio of an actual capacity of the lithium-ion battery to a thickness of a negative electrode active layer of a negative electrode plate in the lithium-ion battery.

[0089] The electrochemical energy storage apparatus further includes a positive electrode plate, and the positive electrode plate includes a positive electrode current collector and a positive electrode active layer disposed on at least one function surface of the positive electrode current collector. The function surface refers to the largest and opposite surfaces, for the positive electrode active layer to be coated, of the current collector. The positive electrode active layer generally includes a positive electrode active material, a conductive agent, and a binder. The positive electrode active material may be selected from at least one of lithium cobalt oxide, lithium manganate, lithium nickel oxide, lithium nickel cobalt manganese, lithium iron phosphate, lithium manganese iron phosphate, lithium vanadium phosphate, lithium vanadyl phosphate, a lithium-rich manganese-based material, and lithium nickel cobalt aluminate. Lithium nickel cobalt manganate (NCM) may include, for example, at least one of NCM 111, NCM 523, NCM 532, NCM 622, and NCM 811; the conductive agent may be selected from at least one of acetylene black (AB), conductive carbon black (Super-P), ketjen black (KB), carbon nanotube (CNT), and graphene; and the binder may be selected from at least one of polyvinylidene fluoride (PVDF), sodium carboxymethyl cellulose (CMC-Na), and sodium alginate (SA).

[0090] Further, a thickness ratio of the negative electrode active layer to the positive electrode active layer ranges from 0.93:1 to 1.68:1. Specifically, the thickness ratio means a thickness ratio at zero electrical state. In the foregoing range, the negative electrode plate can provide more lithium intercalation sites to intercalate lithium ions from the positive electrode plate, thereby further facilitating suppression of formation of lithium dendrites, and ensuring cycle performance and safety performance of the electrochemical energy storage apparatus. Herein, the thickness of the negative electrode active layer means thickness of the negative electrode active layer on a function surface of the negative electrode current collector, and the thickness of the positive electrode active layer means thickness of the positive electrode active layer on a function surface of the positive electrode current collector.

[0091] The electrochemical energy storage apparatus in the present invention further includes a separator located between the positive electrode plate and the negative electrode plate for separating the positive electrode plate and the negative electrode plate.

[0092] In some embodiments, the separator includes a substrate and a coating layer on at least one surface of the substrate, a thickness of the substrate ranges from 3 µm to 22µm, and a thickness of the coating layer ranges from 0 µm to 10 µm (when the thickness of the coating layer is 0, the separator is an uncoated separator; when the thickness of the coating layer is not 0, the separator is a coated separator). The substrate may include at least one of a polyethylene (PE) film, a polypropylene (PP) film, and a composite film composed of the PP film and the PE film. The composite film is, for example, a composite film composed of the PP film, the PE film, and the PP film in sequence (PP / PE / PP composite film for short). The coating layer may include a glue coating layer on a surface of the substrate and a ceramic coating layer on a surface of the glue coating layer. A raw material of the glue coating layer may be a binder, a raw material of the ceramic coating may include ceramic particles and a binder, and the ceramic particles may include, but are not limited to, alumina.

[0093] The electrochemical energy storage apparatus in the present invention further includes an electrolyte, and a common electrolyte may be employed in the present invention. For example, the electrolyte may include a non-aqueous electrolyte, and a raw material of the non-aqueous electrolyte may include a non-aqueous solvent, a lithium salt, and an additive. The non-aqueous solvent includes at least one of ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, ethyl acetate, ethyl propionate, propyl propionate, and propyl acetate. The lithium salt includes at least one of lithium hexafluorophosphate, lithium bis(fluorosulfonyl)imide, lithium difluoro oxalate borate, lithium bis(trifluoromethanesulfonyl)imide, and lithium bis(oxalate)borate. The additive includes at least one of ethylene sulphite, lithium bis(oxalate)borate, ethylene sulfate, tris(trimethylsilyl) borate, 1,3-propene sultone, 1,3-propane sultone, vinylethylene carbonate, ethylene sulfite ethylidene, lithium difluorophosphate, lithium difluorobisoxalate phosphate, lithium tetrafluoro(oxalato)phosphate, lithium borophosphate, and ethyl 3-methoxypropionate.

[0094] For example, the electrochemical energy storage apparatus in the present invention may be a lithium-ion battery. The lithium-ion battery of the present invention may be prepared according to a conventional method in the art. For example, a positive electrode plate, a separator, and a negative electrode plate may be stacked in sequence, and wound (or laminated) to form a battery cell, and then a battery is manufactured after processes such as packaging, baking of the battery cell, electrolyte filling (that is, injection of an electrolyte), hot pressing, and formation, and these steps / processes are all conventional operations in the art and will not be described again.

[0095] In addition, the lithium-ion battery in the present invention further includes a pre-lithiation layer. For example, the pre-lithiation layer may be provided on a surface, close to the separator, of the negative electrode plate. The composition of the pre-lithiation layer is consistent with that common in the art, and details are not described in the present invention.

[0096] A aspect of the present invention provides an electronic apparatus, and the electronic apparatus includes the electrochemical energy storage apparatus in the former aspect. The electrochemical energy storage apparatus provides energy for driving the electronic apparatus. A specific type of the electronic apparatus is not limited in the present invention, and the electronic apparatus may be any electronic apparatus capable of operating based on a supply of electric power output by the electrochemical energy storage apparatus. For example, the electronic apparatus may be a mobile phone, an unmanned aerial vehicle, an electric vehicle, or the like.

[0097] The negative electrode plate and the lithium-ion battery according to the present invention will be described below in detail through specific examples.Example 1-Example 4

[0098] The negative electrode plate in the examples includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and a negative electrode active material in the negative electrode active layer is a first amorphous carbon material.

[0099] Other related parameters of the negative electrode plate are shown in Table 1. In Example 1 and Example 4, a same first amorphous carbon material was used.

[0100] FIG. 1 is an SEM graph of the first amorphous carbon material in Example 1. It may be learned from FIG. 1 that the first amorphous carbon material exhibits a random structure.

[0101] FIG. 2 is an XRD pattern of the first amorphous carbon material in Example 1, and the XRD detection was performed by using a Bruker D8 x-ray diffractometer. It may be learned from FIG. 2 that, 20 of a diffraction peak of the first amorphous carbon material is 22.58 degrees, and an intensity of the diffraction peak is 3049, with a peak width at half height of 13.6. FIG. 3 is a Raman pattern of the first amorphous carbon material in Example 1, and the Raman detection was performed by using an InVia Reflex Raman spectrometer. It may be learned from FIG. 3 that, an Id / Ig peak ratio of the first amorphous carbon material is 1.09. FIG. 4 is a BJH pore size distribution graph of the first amorphous carbon material in Example 1. It may be learned from FIG. 4 that, a average particle size of pores of the first amorphous carbon material is 12.57 nm.

[0102] FIG. 5 is an SEM pattern of the first amorphous carbon material in Example 2. FIG. 6 is an XRD pattern of the first amorphous carbon material in Example 2, and the XRD detection was performed by using a Bruker D8 x-ray diffractometer. It may be learned from FIG. 6 that, 20 of a diffraction peak of the first amorphous carbon material is 25.47 degrees, and an intensity of the diffraction peak is 7567, with a peak width at half height of 5.33. FIG. 7 is a Raman pattern of the first amorphous carbon material in Example 2, and the Raman detection was performed by using an InVia Reflex Raman spectrometer. It may be learned from FIG. 7 that, an Id / Ig peak ratio of the first amorphous carbon material is 1.05. FIG. 8 is a BJH pore size distribution graph of the first amorphous carbon material in Example 2.

[0103] FIG. 9 is an SEM pattern of the first amorphous carbon material in Example 3. FIG. 10 is an XRD pattern of the first amorphous carbon material in Example 3, and the XRD detection was performed by using a Bruker D8 x-ray diffractometer. It may be learned from FIG. 10 that, 20 of a diffraction peak of the first amorphous carbon material is 25.22 degrees, and an intensity of the diffraction peak is 8826, with a peak width at half height of 4.47. FIG. 11 is a Raman pattern of the first amorphous carbon material in Example 3, and the Raman detection was performed by using an In Via Reflex Raman spectrometer. It may be learned from FIG. 11 that, an Id / Ig peak ratio of the first amorphous carbon material is 1.04. FIG. 12 is a BJH pore size distribution graph of the first amorphous carbon material in Example 3.Comparative Example 1

[0104] A negative electrode plate in this comparative example includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and a negative electrode active material in the negative electrode active layer is a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1.

[0105] In Examples 1 to 4 and Comparative Example 1, the negative electrode active layer includes 97% negative electrode active material (a first amorphous carbon material or a low-capacity amorphous carbon material), 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage. Table 1Negative electrode active layerThickness of negative electrode active layer (µm)First amorphous carbon materialInterlayer spacing d002 (nm)Average pore diameter of pores (nm)d 1 (µm)BET (m 2< / g)Capacity per gram (mAh / g)Example 169.60.38312.578.43.9560Example 2750.3494.44.32.9520Example 3790.3454.95.32.3480Example 4870.38312.578.43.9560Comparative Example 1125.10.3381.87.31.25286 Example 1a-Example 7a

[0106] The negative electrode plate in the foregoing examples includes a copper foil and a negative electrode active layer on two function surfaces of the copper foil (with a thickness of 5 µm), and a negative electrode active material in the negative electrode active layer is a first mixture of a first amorphous carbon material (with a mass of M 1 ) and a second amorphous carbon material (with a mass of M 2 ). Other related parameters of the negative electrode plate are shown in Table 1-a.

[0107] Negative electrode active layers of the negative electrode plates in Examples 1a-Example 5a have a same mass.Comparative Example 1a

[0108] The negative electrode plate in this comparative example differs from those in the foregoing examples in that the first amorphous carbon material is replaced with a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-a. Table 1-aNegative electrode plateNegative electrode active layerM 2 / (M 2 +M 1 ) (%)First amorphous carbon materialSecond amorphous carbon materialInterlayer spacing d002 (nm)Average pore diameter of pores (nm)d 1 (µm)BET (m 2< / g)Capacity per gram (mAh / g)d 2 (µm)BET (m 2< / g)Example 1a2%Example 12.38.34Example 2a5%Example 12.38.34Example 3a10%Example 12.38.34Example 4a15%Example 12.38.34Example 5a30%Example 12.38.34Example 6a10%Example 22.38.34Example 7a10%Example 32.38.34Comparative Example 1a10%Comparative Example 12.38.34 Example 1b-Example 10b

[0109] The negative electrode plate in the examples includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and the negative electrode active layer includes a first amorphous carbon layer and a second amorphous carbon layer that are sequentially away from the current collector.

[0110] A negative electrode active material in the first amorphous carbon layer is a first amorphous carbon material, and a negative electrode active material in the second amorphous carbon layer is a second amorphous carbon material.

[0111] Other related parameters of the negative electrode plate are shown in Table 1-b.

[0112] Examples 8b and 9b are substantially identical to Example 1b except that the second amorphous carbon material is replaced.Comparative Example 1b

[0113] A negative electrode active layer of the negative electrode plate in the comparative example is only a first amorphous carbon layer. Other related parameters of the negative electrode plate are shown in Table 1-b.Comparative Example 2b

[0114] A negative electrode plate in this comparative example is substantially identical to that in Example 1b, and a difference lies in that the first amorphous carbon material in Example 1b is replaced with a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-b.

[0115] In Example 1b-Example 10b and Comparative Examples, the first amorphous carbon layer includes 97% negative electrode active material (a first amorphous carbon material), 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage. The second amorphous carbon material includes 97% negative electrode active material (a second amorphous carbon material), 0.5% superconducting carbon black, 1.5% SBR, and 1% CMC according to mass percentage. A compacted density of the negative electrode plate in each example is 1 g / cm 3< . Table 1-bFirst amorphous carbon layerSecond amorphous carbon layerThickness H 1 (µm)First amorphous carbon materialThickness H 2 (µm)Second amorphous carbon materialSourced 2 (µm)BET (m 2< / g)D 2 (µm)Example 1b63.07Example 111.132.38.349.5Example 2b60.64Example 115.162.38.349.5Example 3b55.58Example 123.822.38.349.5Example 4b65.43Example 17.072.38.349.5Example 5b52.73Example 124.172.38.349.5Example 6b65.45Example 211.552.38.349.5Example 7b67.75Example 311.952.38.349.5Example 8b63.07Example 111.131.58.349.5Example 9b63.07Example 111.1339.24.3Example 10b43.26Example 118.542.38.349.5Comparative Example 1b69.6Example 1\\Comparative Example 2b102.94Comparative Example 118.162.38.349.5 Examples 1c-Example 13c, and Example 15c-Example 18c

[0116] The negative electrode plate in the examples includes a copper foil and a negative electrode active layer on two function surfaces of the copper foil (with a thickness of 5 µm), a negative electrode active material in the negative electrode active layer is a second mixture of a graphite material (graphite is a core-shell structured graphite material of a core) and a first amorphous carbon material, and a mass percentage of the first amorphous carbon material in the mixture is W.

[0117] Other related parameters of the negative electrode plate are shown in Table 1-c. Negative electrode active layers of the negative electrode plates in Example 1c-Example 9c have a same mass. Example 12c is substantially the same as Example 5c except that the graphite material is replaced. Example 13c is substantially the same as Example 10c except that the graphite material is replaced.Example 14c

[0118] Example 14c is substantially the same as Example 5c, except that the core-shell graphite material is replaced with ordinary pure graphite particles. Other related parameters of the negative electrode plate are shown in Table 1-c.Comparative Example 1c

[0119] A negative electrode active material of the negative electrode active layer in this comparative example is only a graphite material. Other related parameters of the negative electrode plate are shown in Table 1-c.Comparative Example 2c

[0120] A negative electrode plate in this comparative example is substantially identical to that in Example 5c, and a difference lies in that the amorphous carbon material in Example 5c is replaced with a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-c.

[0121] In Examples 1c-18c and Comparative Examples, the negative electrode active layer includes 97% negative electrode active material, 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage. Table 1-cNegative electrode active layerThickness (µm)W (%)First amorphous carbon materialGraphite materialSourced 3 (µm)Example 1c69.490Example 112.7Example 2c68.880Example 112.7Example 3c67.370Example 112.7Example 4c67.860Example 112.7Example 5c66.950Example 112.7Example 6c68.140Example 112.7Example 7c63.730Example 112.7Example 8c64.320Example 112.7Example 9c64.810Example 112.7Example 10c69.650Example 212.7Example 11c73.850Example 312.7Example 12c66.950Example 17.2Example 13c69.650Example 238.0Example 14c66.950Example 111.1Example 15c77.850Example 112.7Example 16c66.950Example 112.7Example 17c189.750Example 112.7Example 18c39.750Example 112.7Comparative Example 1c62.60 / 12.7Comparative Example 2c66.950Comparative Example 112.7 Example 1d-Example 11d, Example 14d, and Example 15d

[0122] The negative electrode plate in the examples includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and the negative electrode active layer includes a graphite layer and a first amorphous carbon layer that are sequentially away from the current collector. A negative electrode active material in the graphite layer is a core-shell structured graphite material with graphite as a core and the first amorphous carbon material as a shell. A negative electrode active material in the first amorphous carbon layer is the first amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-d.Example 12d

[0123] The negative electrode plate in the example includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and the negative electrode active layer includes a graphite layer and a first amorphous carbon layer that are sequentially away from the current collector. A negative electrode active material in the graphite layer is common graphite particles. A negative electrode active material in the first amorphous carbon layer is the first amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-d.Example 13d

[0124] A negative electrode plate in this example is substantially identical to that in Example 4d, and a difference lies in that a negative electrode active layer in this example includes a first amorphous carbon layer and a graphite layer that are sequentially away from the current collector. Other related parameters of the negative electrode plate are shown in Table 1-d.Comparative Example 1d

[0125] A negative electrode active layer in this comparative example only includes a graphite layer. Other related parameters of the negative electrode plate are shown in Table 1-d.Comparative Example 2d

[0126] A negative electrode plate in this comparative example is substantially identical to that in Example 1d, and a difference lies in that the first amorphous carbon material (including a shell in a core-shell structured graphite material and a first amorphous carbon material in the first amorphous carbon layer) in Example 1b is replaced with a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-d.

[0127] In Example 1d-Example 15d and Comparative Examples, the first amorphous carbon layer includes 97% first amorphous carbon material, 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage. The graphite layer includes 97% graphite material, 0.5% conductive agent, 1.5 binder, and 1% CMC by mass percentage. Table 1-dNegative electrode active layerFirst amorphous carbon layerGraphite layerCompacted density (g / cm 3< )Thickness H 1 (µm)Amorphous carbon materialThickness H 3 (µm)Graphite materialSourceD 1 (µm)d 3 (µm)D 3 (µm)Example 1d13.38Example 11253.5212.7321.45Example 2d20.07Example 11246.8312.7321.35Example 3d26.76Example 11240.1412.7321.30Example 4d33.45Example 11233.4512.7321.25Example 5d40.14Example 11226.7612.7321.21Example 6d6.69Example 11260.2112.7321.54Example 7d56Example 11210.912.7321.06Example 8d36.2Example 11236.212.7321.23Example 9d43.98Example 11229.3212.7321.26Example 10d34.4Example 21434.412.7321.3Example 11d34.7Example 316.134.712.7321.35Example 12d33.45Example 11233.4511.1281.25Example 13d33.45Example 11233.4512.7321.25Example 14d38.9Example 11238.912.7321.28Example 15d29.9Example 11229.912.7321.1Comparative Example 1\\\66.912.7321.75Comparative Example 244.7Comparative Example 117.844.712.7321.35 Example 1e-Example 10e, Example 14e, and Example 15e

[0128] The negative electrode plate in Example 1e-Example 10e, Example 14e, and Example 15e includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 5 µm), and a negative electrode active material in the negative electrode active layer is a third mixture of a silicon-based material (with a mass of M 4 ) and a first amorphous carbon material (with a mass of M 1 ). Mixtures in Example 1e-Example 10e have a same mass. Other related parameters of the negative electrode plate are shown in Table 1-1e.Example 11e-Example 13e

[0129] The negative electrode plate in the examples includes a copper foil and a negative electrode active layer located on two function surfaces of the copper foil (with a thickness of 6 µm), and the negative electrode active layer includes a silicon-based active layer (with a thickness of H 4 ) and a first amorphous carbon layer (with a thickness of H 1 ) that are sequentially away from the current collector. A negative electrode active material in the first amorphous carbon layer is a first amorphous carbon material, and a negative electrode active material in the silicon-based active layer is a silicon-based material. Other related parameters of the negative electrode plate are shown in Table 1-2e.Comparative Example 1e

[0130] A negative electrode plate in this comparative example is substantially identical to that in Example 1e, and a difference lies in that the amorphous carbon material in Example 1e is replaced with a low-capacity amorphous carbon material. Other related parameters of the negative electrode plate are shown in Table 1-1e.

[0131] In Examples 1e-10e, Example 14e, Example 15e, and Comparative Examples, the negative electrode active layer includes 97% negative electrode active material, 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage.

[0132] In Example 11e-Example 13e, the first amorphous carbon layer includes 97% negative electrode active material, 1.5% SBR, 0.5% superconducting carbon black, and 1% CMC according to mass percentage. The silicon-based active layer includes 97% silicon-based material, 0.5% conductive carbon black, 1.5% SBR binder, and 1% CMC according to mass percentage. Table 1-1eNegative electrode active layer (mixture of a first amorphous carbon material and a silicon-based material)Thickness (µm)First amorphous carbon materialSilicon-based materialSource(µm)(µm)ComponentM 2 / (M 2 +M 4 )(%)Example 1e68.5Example 18.922SiO1Example 2e66.3Example 18.922SiO3Example 3e63.2Example 18.922SiO6Example 4e57.9Example 18.922SiO12Example 5e50.2Example 18.922SiO23Example 6e69.5Example 18.922SiO0.1Example 7e66.3Example 11231.2SiO3Example 8e68.7Example 17.920SiC3Example 9e71Example 28.922SiO3Example 10e79.6Example 38.922SiO3Example 14e95.4Example 38.922SiO3Example 15e38.6Example 18.922SiO3Comparative Example 1e129.3Comparative Example 18.922SiO3 Table 1-2e Negative electrode active layer (first amorphous carbon layer and silicon-based active layer that are stacked)Thickness (µm)first amorphous carbon layerSilicon-based active layerFirst amorphous carbon materialThickness H 1 (µm)Silicon-based materialThickness H 4 (µm)Sourced 4 (µm)D 4 (µm)ComponentExample 11e64.3Example 162.38.922SiO2Example 12e63.2Example 179.48.922SiO3.8Example 13e38.65Example 127.108.922SiO11.55

[0133] Specific detection methods for each parameter in the foregoing tables are as follows. 1. Interlayer spacing Tested with XRD by using a Brooke D8 x-ray diffractometer, and calculated by using the Bragg equation 2d sinθ = nλ. 2. Average pore diameter of pores Tested by using the BET N 2 gas adsorption method. 3. average particle sizes d 1 , d 2 , d 3 , and d 4 measured by using an FIB-SEM system. 4. Specific surface area BET Tested by using TriStar 3020, Micromeritics, USA. 5. Thicknesses H 1 , H 2 , H 3 , and H 4 Active layer thicknesses of electrode plates are measured by using a spiral micrometer. 6. Maximum particle sizes D 1 , D 2 , D 3 , and D 4 measured by using a laser particle size analyzer. 7. Capacity per gram measured by using a button battery. Test Example 1

[0134] The negative electrode plate in each of Examples 1-4 and Comparative Example 1, a positive electrode plate, and a separator were stacked in sequence, then wound to form a battery cell, and then lithium-ion batteries 1 to 6, where the lithium-ion batteries 5 and 6 are not within the scope of the present invention, were obtained after processes such as packaging, baking of the battery cell, electrolyte filling, hot pressing, and formation. The positive electrode plate includes an aluminum foil and a positive electrode active layer located on two function surfaces of the aluminum foil (with a thickness of 9 µm), and the positive electrode active layer includes 98.4% lithium cobalt oxide, 0.5% PVDF, and 1.1% Super-P according to mass percentage. Related parameters of the lithium-ion batteries are shown in Table 2.

[0135] The following parameters of the lithium-ion batteries 1 to 6 were measured, and the results are shown in Table 2. The detection methods are as follows.1. -20°C discharge capacity retention rate

[0136] A lithium-ion battery is left at -20°C, and is charged and discharged in a cyclic manner by using a current of 0.7 C in a charging and discharging voltage range of 4.48-3V; an initial capacity is recorded as Q, and a capacity after 50 cycles is Q 2 ; and a capacity retention rate of the battery circulating at a low temperature is calculated from the following formula: Capacity retention rate % = Q 2 / Q × 1002. Volumetric energy density

[0137]

[0138] A capacity discharged when a battery cell is discharged to 3V at a current of 0.2C after the battery cell is charged to a cell upper limit voltage (4.48V) at a constant current of 0.5C and a constant voltage at room temperature is the initial capacity.3. Cell expansion rate

[0139] An initial thickness of a battery cell is measured by using PPG, and a cell thickness after 50T cycles is measured by using PPG after 50T cycles of charging at 1.2C and discharging at 0.5C at 25°C. Table 2Lithium-ion batteryNegative electrode platePositive electrode plate-20°C discharge capacity retention rate (%)Volumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Thickness of positive electrode active layer (µm)1Example 169.65072.26812.481.012Example 2755072.12783.181.033Example 3795071.32762.31.044Example 4875071.01724.191.025Example 169.677.271.17680.471.06Comparative Example 1125.15070.63584.991.06 Test Example 1a

[0140] Lithium-ion batteries 1a-8a, where the lithium-ion battery 8a is not within the scope of the present invention, were obtained after the negative electrode plates in foregoing Examples 1a-7a and Comparative Example 1a are assembled respectively according to the method in Test Example 1. The -20°C discharge capacity retention rate, the volumetric energy density, and the cell expansion rate of the lithium-ion batteries 1a-8a were measured according to the foregoing methods, and the results are shown in Table 2-a. Table 2-aLithium-ion batteryNegative electrode platePositive electrode plate-20°C discharge capacity retention rate (%)Volumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Thickness of positive electrode active layer (µm)1aExample 1a70.25072.84809.291.032aExample 2a71.15072.95804.331.033aExample 3a72.65073.11795.931.024aExample 4a74.25074.42787.351.015aExample 5a79.45076.21760.450.986aExample 6a77.85072.96768.431.027aExample 7a83.85072.98738.951.038aComparative Example 1a134.25070.11559.361.04 Test Example 1b

[0141] Lithium-ion batteries 1b-14b, where the lithium-ion batteries 11b, 13b and 14b are not within the scope of the present invention, were obtained after the negative electrode plates in foregoing Examples 1b-10b and Comparative Examples 1b and 2b are assembled respectively according to the method in Test Example 1. Related parameters of the lithium-ion batteries are shown in Table 2-b.

[0142] The following parameters of the lithium-ion batteries 1b-14b were measured, and the results are shown in Table 2-b. The detection methods are the same as those mentioned above. Table 2-bLithium-ion batteryNegative electrode platePositive electrode plate-20°C discharge capacity retention rate (%)Volumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Thickness of positive electrode active layer (µm)1bExample 1b74.25076.15808.111.032bExample 2b75.85076.98799.780.983bExample 3b79.45078.18791.20.964bExample 4b72.55074.04809.371.025bExample 5b76.95078.93787.071.046bExample 6b775075.08776.361.027bExample 7b79.75075.05762.911.018bExample 8b74.25077.20791.21.039bExample 9b74.25075.04791.21.0310bExample 3b79.445.174.68770.371.0111bExample 10b61.867.075.64771.11.0312bExample 10b61.85075.81784.21.0213bComparative Example 1b69.65072.26812.481.0114bComparative Example 2b121.15072.13597.061.03

[0143] It may be learned from Table 2-b that: 1. Compared with Comparative Example 1b and Comparative Example 2b, the negative electrode plate in the examples of the present invention can not only help improve low-temperature cycle performance of the lithium-ion battery, but also improve the volumetric energy density of the lithium-ion battery and effectively suppress expansion of the lithium-ion battery during cycling.

[0144] Comparative Example 2b is used as an example. When the negative electrode plate does not contain the first amorphous carbon material in the present invention, even if the negative electrode activity has higher thickness (that is, more negative electrode active materials are contained), the volumetric energy density of the lithium-ion battery cannot meet the requirements of the volumetric energy density of the lithium-ion battery in the present invention;

[0145] 2. Compared with Example 4b and Example 5b, when the thickness H 1 of the first amorphous carbon layer and the thickness H 2 of the second amorphous carbon layer satisfy a specific relationship, the lithium-ion battery has both good low-temperature cycle performance and good volumetric energy density.Test Example 1c

[0146] Lithium-ion batteries 1c-21c, where the lithium-ion batteries 15c, 16c, 20c and 21c are not within the scope of the present invention, were obtained after the negative electrode plates in foregoing Examples 1c-18c and Comparative Examples 1c and 2c are assembled respectively according to the method in Test Example 1. Parameters of the lithium-ion batteries are shown in Table 2-c.

[0147] The volumetric energy density, cell expansion rate, and unit thickness capacity of the lithium-ion batteries 1c-21c were measured according to the foregoing methods. The unit thickness capacity was calculated as initial capacity of the lithium-ion battery / thickness of the negative electrode active layer. The results are shown in Table 2-c. Table 2-cLithium -ion batteryNegative electrode platePositive electrode plateVolumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Compacted density (mg / cm 3< )Surface density (mg / cm 2< )Unit thickness capacity (mAh / µm)Positive electrode active layer thickness (µm)1cExample 1c69.41.027.2972.0450802.051.22cExample 2c68.81.17.5772.8850817.071.383cExample 3c67.31.177.8774.2950820.591.74cExample 4c67.81.218.273.7450823.062.755cExample 5c66.91.288.5674.7350828.473.476cExample 6c68.11.349.1273.450821.43.417cExample 7c63.71.59.5578.4950810.274.058cExample 8c64.31.5710.0377.7650806.495.239cExample 9c64.81.6310.5677.1650803.565.2810cExample 10c69.61.339.1571.8350812.313.6711cExample 11c73.81.249.1567.7550789.013.2512cExample 12c66.91.288.5674.7350828.475.4413cExample 13c69.61.339.1571.8350812.314.2314cExample 14c66.91.288.5674.7350828.473.4715cExample 15c77.81.18.5664.2645.3786.475.4116cExample 16c66.91.438.5674.772.8784.775.4317cExample 17c189.71.041919.7626.36113.8809.765.6518cExample 18c39.71.45.56125.831.5795.95.6320cComparative Example 1c62.61.7611.4578.6150776.15.721cComparative Example 2c66.91.3512.1985.250670.693.48

[0148] It may be learned from Table 2-c that: 1. Compared with Comparative Examples 1c and 2c, the negative electrode plate in the examples of the present invention not only helps improve the volumetric energy density of the lithium-ion battery, but also effectively suppress expansion of the lithium-ion battery during cycling. 2. Compared with Examples 8c and 9c, when the mass of the first amorphous carbon material in the negative electrode active layer is not less than 28% of the total mass of the first amorphous carbon material and the graphite material, the energy density of the lithium-ion battery is higher, and the expansion rate is also significantly reduced. In addition, it may also be found from Example 1c that, when the proportion of the first amorphous carbon material is too high, compaction of the amorphous carbon material is relatively low, resulting in a relatively low energy density of the lithium-ion battery. 3. Compared with Examples 12c and 13c, when the ratio of the average particle size of the graphite material to the volume-based particle size of the first amorphous carbon material ranges from 0.95:1 to 8.3:1, the compacted density of the negative electrode active layer is improved, so that the lithium-ion battery can have a higher energy density. 4. Compared with Examples 15c and 16c, when the thickness ratio of the negative electrode active layer in the negative electrode plate of the present invention to the positive electrode active layer in the lithium-ion battery is within a specific range, the energy density of the lithium-ion battery is further improved. 5. Compared with Examples 17c and 18c, when the unit thickness capacity of the lithium-ion battery in the present invention ranges from 26.9 mAh / µm to 123 mAh / µm, both the energy density and the expansion rate of the lithium-ion battery can be improved in some extent. Test Example 1d

[0149] Lithium-ion batteries 1d-17d, where the lithium-ion batteries 15d, 16d and 17d are not within the scope of the present invention, were obtained after the negative electrode plates in foregoing Examples 1d-15d and Comparative Examples 1d and 2d are assembled respectively according to the method in Test Example 1. Related parameters of the lithium-ion batteries are shown in Table 2-d. The volumetric energy density and the cell expansion rate of the lithium-ion batteries 1d-17d were measured according to the foregoing methods, and the results are shown in Table 2-d. Table 2-dLithium -ion batteryNegative electrode platePositive electrode plateVolumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Thickness of positive electrode active layer (µm)1dExample 1d66.950822.513.792dExample 2d66.950813.532.153dExample 3d66.950817.011.794dExample 4d66.950819.081.745dExample 5d66.950823.061.786dExample 6d66.950826.045.327dExample 7d66.950817.295.148dExample 8d72.450821.571.739dExample 9d73.350823.91.7410dExample 10d68.850817.011.8511dExample 11d69.450813.531.8212dExample 12d66.950818.11.7413dExample 13d66.950818.35.0214dExample 14d77.845.3792.231.8915dExample 15d59.865.1784.771.7516dComparative Example 1d66.950778.15.717dComparative Example 2d89.450685.81.85

[0150] It may be learned from Table 2-d that: 1. Compared with Comparative Examples 1d and 2d, the negative electrode plate in the examples of the present invention helps improve the volumetric energy density of the lithium-ion battery, and effectively suppress expansion of the lithium-ion battery during cycling. 2. Compared with Examples 6d and 7d, when the thickness H 1 of the first amorphous carbon layer, the thickness H 2 of the graphite layer, the maximum particle size D 1 of the first amorphous carbon material, and the maximum particle size D 2 of the graphite material satisfy (H 1 + H 2 ) - 0.39D 2 ≥ H 1 ≥ 0.63D 1 , expansion of the lithium-ion battery during cycling may be obviously suppressed. 3. Compared with Examples 14d and 15d, when the thickness ratio of the negative electrode active layer in the negative electrode plate of the present invention to the positive electrode active layer in the lithium-ion battery is within a specific range, the energy density of the lithium-ion battery is further improved. Test Example 1e

[0151] Lithium-ion batteries 1d-16e, where the lithium-ion batteries 14e, 15e and 16e are not within the scope of the present invention, were obtained after the negative electrode plates in foregoing Examples 1d-15e and Comparative Example 1e are assembled respectively according to the method in Test Example 1. Related parameters of the lithium-ion batteries are shown in Table 2-e. The volumetric energy density and the cell expansion rate of the lithium-ion batteries 1e-16e were measured according to the foregoing methods, and the results are shown in Table 2-e. Table 2-eLithium-ion batteryNegative electrode platePositive electrode plateVolumetric energy density (Wh / L)Cell expansion rate (%)SourceThickness of negative electrode active layer (µm)Thickness of positive electrode active layer (µm)1eExample 1e68.550819.071.312eExample 2e66.350831.932.463eExample 3e63.250850.423.984eExample 4e57.950884.914.525eExample 5e50.250890.355.786eExample 6e69.550813.141.017eExample 7e66.350817.542.478eExample 8e68.750831.932.369eExample 9e7150804.92.4110eExample 10e79.650759.242.3711eExample 11e64.350832.032.1812eExample 12e63.250850.613.2513eExample 13e38.6550890.35.6414eExample 14e95.450688.031.2515eExample 15e38.650883.25.4516eComparative Example 1e129.350572.842.51

[0152] It may be learned from Table 2-e that: Compared with Comparative Example 1e, the negative electrode plate in the examples of the present invention not only helps improve the volumetric energy density of the lithium-ion battery, but also can effectively suppress expansion of the lithium-ion battery during cycling.

Claims

1. An electrochemical energy storage apparatus, characterized in that the electrochemical energy storage apparatus comprises a negative electrode plate and a positive electrode plate; the negative electrode plate comprises a current collector and a negative electrode active layer disposed on at least one function surface of the current collector, and a negative electrode active material of the negative electrode active layer comprises a first amorphous carbon material; an interlayer spacing d002 of the first amorphous carbon material is greater than 0.34 nm, and an average pore diameter of pores of the first amorphous carbon material ranges from 2 nm to 20 nm; and the positive electrode plate includes a positive electrode current collector and a positive electrode active layer disposed on at least one function surface of the positive electrode current collector, a thickness ratio of the negative electrode active layer to the positive electrode active layer ranges from 0.93:1 to 1.68:1.

2. The electrochemical energy storage apparatus according to claim 1, characterized in that capacity per gram of the first amorphous carbon material is not less than 470 mAh / g; and / or a average particle size d1 of the first amorphous carbon material ranges from 3µm to 15 µm; and / or a specific surface area of the first amorphous carbon material ranges from 2.8 m2 / g to 19 m2 / g; and / or an X-ray diffraction pattern of the first amorphous carbon material comprises a diffraction peak with 2θ being less than 26 degrees, and a full width at half maximum of the diffraction peak is greater than 1.2 degrees.

3. The electrochemical energy storage apparatus according to claim 1 or 2, characterized in that the negative electrode active material further comprises a second amorphous carbon material, and the second amorphous carbon material is in a shape of spherical particles; preferably, a average particle size d2 of the spherical particles ranges from 0.2 µm to 4 µm; preferably, a specific surface area of the second amorphous carbon material ranges from 2 m2 / g to 23 m2 / g.

4. The electrochemical energy storage apparatus according to claim 3, characterized in that the negative electrode active material comprises a first mixture of the first amorphous carbon material and the second amorphous carbon material; preferably, a mass percentage of the second amorphous carbon material in the first mixture is not less than 3%.

5. The electrochemical energy storage apparatus according to claim 3 or 4, characterized in that the negative electrode active layer comprises a first amorphous carbon layer and a second amorphous carbon layer that are stacked, the first amorphous carbon layer comprises the first amorphous carbon material, and the second amorphous carbon layer comprises the second amorphous carbon material; preferably, the negative electrode active layer comprises the first amorphous carbon layer close to the current collector and the second amorphous carbon layer away from the current collector; preferably, a thickness H1 of the first amorphous carbon layer and a thickness H2 of the second amorphous carbon layer satisfy the following relationship: 0.3 H 1 + H 2 ≥ H 2 ≥ D 2 wherein D2 denotes a maximum particle size of the second amorphous carbon material.

6. The electrochemical energy storage apparatus according to claim 1 or 2, characterized in that the negative electrode active material comprises a second mixture of the first amorphous carbon material and a graphite material; preferably, a ratio of a average particle size d3 of the graphite material to a average particle size d1 of the first amorphous carbon material ranges from 0.95:1 to 8.3:1; preferably, a mass percentage of the first amorphous carbon material in the second mixture is not less than 28%.

7. The electrochemical energy storage apparatus according to any one of claims 1, 2 and 6, characterized in that the negative electrode active layer comprises a first amorphous carbon layer and a graphite layer that are stacked, the first amorphous carbon layer comprises the first amorphous carbon material, and the graphite layer comprises a graphite material; preferably, a thickness H1 of the first amorphous carbon layer and a thickness H3 of the graphite layer satisfy the following relationship: H 1 + H 3 − 0.39 D 3 ≥ H 1 ≥ 0.63 D 1 wherein D1 denotes a maximum particle size of the first amorphous carbon material, and D3 denotes a maximum particle size of the graphite material.

8. The electrochemical energy storage apparatus according to any one of claims 1, 2, 6 and 7, characterized in that the negative electrode active layer comprises the graphite layer close to the current collector and the first amorphous carbon layer away from the current collector; preferably, the graphite material comprises graphite particles and / or graphite core-shell particles, and the graphite core-shell particles are constituted by a core formed by graphite and a shell covering at least part of a surface of the core.

9. The electrochemical energy storage apparatus according to claim 1 or 2, characterized in that the negative electrode active material comprises a third mixture of the first amorphous carbon material and a silicon-based material; preferably, a mass percentage of the silicon-based material in the third mixture ranges from 0.3% to 20%.

10. The electrochemical energy storage apparatus according to any one of claims 1, 2 and 9, characterized in that the negative electrode active layer comprises a first amorphous carbon layer and a silicon-based active layer that are stacked, the first amorphous carbon layer comprises the first amorphous carbon material, and the silicon-based active layer comprises the silicon-based material; preferably, a thickness H1 of the first amorphous carbon layer and a thickness H4 of the silicon-based active layer satisfy the following relationship: H 4 ≤ 0.2 H 1 + H 4 ; preferably, the silicon-based material is selected from at least one of a silicon material, a silicon oxide material, and a silicon-carbon composite material.

11. The electrochemical energy storage apparatus according to claim 6, characterized in that a unit thickness capacity of the negative electrode plate ranges from 26.9 mAh / µm to 123 mAh / µm.

12. An electronic apparatus, characterized in that the electronic apparatus comprises the electrochemical energy storage apparatus according to any one of claims 1 to 11.