Patent Application
20230231144
This application relates to the field of electronic technologies, and in particular, to an electrode plate, an electrochemical apparatus, and an electronic apparatus.
At present, to ensure processing and safety performance of an electrode plate, a primer coating layer is generally added between a current collector and an active material layer. Although adding a primer coating layer can significantly increase a bonding force between the electrode plate and the current collector, volumetric energy density of an electrochemical apparatus (for example, a lithium-ion battery) is decreased. How electric performance of an electrochemical apparatus is improved and volumetric energy density of the electrochemical apparatus is ensured is a problem to be resolved.
This application adds a primer coating layer to a specific region, which improves electric performance and safety performance of an electrochemical apparatus, while minimizing influence on volumetric energy density of the electrochemical apparatus.
An embodiment of this application provides an electrode plate, including: a current collector, including, in a width direction, a first edge region, a second edge region, and a middle region located between the first edge region and the second edge region; a first coating layer, including a first portion and a second portion disposed on the first edge region and the second edge region respectively; and a second coating layer, where part of the second coating layer is disposed on the middle region, another part of the second coating layer is disposed on the first coating layer, and the second coating layer includes an active material; where there is a first bonding force between the first portion and the first edge region, there is a second bonding force between the second portion and the second edge region, there is a third bonding force between the second coating layer and the middle region, and the first bonding force and the second bonding force are both greater than the third bonding force.
In some embodiments, the first portion has a width d1, the second portion has a width d2, and the second coating layer has a width D, where 1% ≤ d1/D≤ 20%, and 1% ≤ d2/D ≤ 20%.
In some embodiments, the first bonding force and the second bonding force are both 2 to 5 times the third bonding force; and/or the first bonding force and the second bonding force are both greater than 10 N/m.
In some embodiments, a thickness of the first coating layer is h, and a thickness of the second coating layer is H, where 0.5 µm < h < 8 µm, and 20 µm < H < 200 µm.
In some embodiments, the first coating layer includes a first conductive agent and a first binder, where the first conductive agent includes at least one of conductive carbon black, carbon nanotubes, conductive graphite, graphene, acetylene black, or carbon nanofibers, and the first binder includes at least one of polyvinylidene fluoride, vinylidene fluoride-fluorinated olefin copolymer, polyvinylpyrrolidone, polyacrylonitrile, poly(methyl acrylate), polytetrafluoroethylene, sodium carboxymethyl cellulose, styrene-butadiene rubber, polyurethane, fluorinated rubber, or polyvinyl alcohol; where a mass percentage of the first conductive agent is 30%-80%, and a mass percentage of the first binder is 20%-70%.
In some embodiments, in a length direction of the current collector, the first portion and/or the second portion is discontinuously coated, a percentage of a total coating length of the first portion to a coating length of the second coating layer is greater than 80%, and a percentage of a total coating length of the second portion to the length of the second coating layer is greater than 80%. In some embodiments, at least part of the current collector is etched.
In some embodiments, the first edge region and the second edge region are etched, and roughness of the first edge region and roughness of the second edge region are both 2 to 4 times roughness of the middle region.
Another embodiment of this application provides an electrochemical apparatus, including a positive electrode plate, a negative electrode plate, and a separator disposed between the positive electrode plate and the negative electrode plate, where the positive electrode plate and/or the negative electrode plate is the electrode plate according to any one of the foregoing embodiments.
An embodiment of this application further provides an electronic apparatus, including the foregoing electrochemical apparatus.
In this application, the coating layer with a different bonding force is disposed on the edge regions of the current collector, such that the bonding force between the coating layer and the current collector is greater than the bonding force between the active material coating layer and the current collector, which prevents the current collector from peeling off during cycling of the electrochemical apparatus, and improves the electric performance and safety performance of the electrochemical apparatus. In addition, the coating layer is disposed on only the edge regions of the current collector, minimizing the influence on the volumetric energy density of the electrochemical apparatus.
The following embodiments may allow persons skilled in the art to understand this application more comprehensively, and impose no limitation on this application in any manner.
As shown in
In some embodiments, the electrode plate further includes a second coating layer 3, where part of the second coating layer 3 is disposed on the middle region 6, another part of the second coating layer 3 is disposed on the first coating layer 2, and the second coating layer 3 includes an active material. In some embodiments, there is a first bonding force between the first portion 7 and the first edge region 4, there is a second bonding force between the second portion 8 and the second edge region 5, there is a third bonding force between the second coating layer 3 and the middle region 6, and the first bonding force and the second bonding force are both greater than the third bonding force. In this embodiment of this application, the first coating layer 2 is disposed on the first edge region 4 and the second edge region 5 of the current collector 1, such that the bonding force between the first coating layer 2 and the current collector 1 is greater than the bonding force between the second coating layer 3 and the middle region 6, which prevents peeling between the current collector 1 and the second coating layer 3 during cycling of an electrochemical apparatus, and improves electric performance and safety performance of the electrochemical apparatus. In addition, the coating layer is disposed on only the first edge region 4 and the second edge region 5 of the current collector 1, minimizing influence on volumetric energy density of the electrochemical apparatus.
In some embodiments, the first portion 7 has a width d1, the second portion 8 has a width d2, and the second coating layer 3 has a width D, where 1% ≤ d1/D ≤ 20%, and 1% ≤ d2/D ≤ 20%. If the width of the first portion 7 or the second portion 8 is excessively small, for example, lower than 1% of the width of the second coating layer 3, the first coating layer 2 has a limited effect on increasing the bonding force between the second coating layer 3 and the current collector 1. Generally, because a binder contained in the second coating layer is limited, the bonding force between the second coating layer and the current collector is correspondingly limited. If no first coating layer is disposed between the current collector and the second coating layer, expansion and contraction of the second coating layer during cycling easily causes peeling between the second coating layer and the current collector. Disposing the first coating layer and increasing the binder contained in the first coating layer increase the bonding force between the second coating layer and the current collector, thereby preventing the peeling between the second coating layer and the current collector. If the width of the first portion or the second portion is excessively large, for example, higher than 20% of the width of the second coating layer, the volumetric energy density of the electrochemical apparatus is adversely affected. In some embodiments, to further reduce the influence on the volumetric energy density of the electrochemical apparatus while still achieving a great bonding force between the first coating layer and the current collector, 1% ≤ d1/D ≤ 10%, and 1% ≤ d2/D ≤ 10%.
In some embodiments, the first bonding force and the second bonding force are both 2 to 5 times the third bonding force. In some embodiments, the first bonding force and the second bonding force are both greater than 10 N/m. In this way, the bonding force between the second coating layer and the current collector can be well increased.
In some embodiments, a thickness of the first coating layer 2 is h, and a thickness of the second coating layer 3 is H, where 0.5 µm < h < 8 µm, and 20 µm < H < 200 µm.The thickness H of the second coating layer is a thickness of the second coating layer 3 on the middle region 6, or a total thickness of the first portion 7 of the first coating layer 2 on the first edge region 4 and the second coating layer 3, or a total thickness of the second portion 8 of the first coating layer 2 on the second edge region 5 and the second coating layer 3. If the thickness of the first coating layer is excessively small, for example, less than 0.5 µm, there is a limited effect on increasing the bonding force between the second coating layer and the current collector. If the thickness of the first coating layer is excessively large, the volumetric energy density of the electrochemical apparatus is adversely affected. If the thickness of the second coating layer is excessively small, the active material per unit area is excessively few, which affects the volumetric energy density of the electrochemical apparatus. If the thickness of the second coating layer is excessively large, a migration path for intercalation and deintercalation of lithium ions close to the second coating layer of the current collector is excessively long, which affects efficiency of intercalation and deintercalation of the lithium ions.
In some embodiments, the first coating layer 2 includes a first conductive agent and a first binder. In some embodiments, the first conductive agent includes at least one of conductive carbon black, carbon nanotubes, conductive graphite, graphene, acetylene black, or carbon nanofibers. In some embodiments, the first binder includes at least one of polyvinylidene fluoride, vinylidene fluoride-fluorinated olefin copolymer, polyvinylpyrrolidone, polyacrylonitrile, poly(methyl acrylate), polytetrafluoroethylene, sodium carboxymethyl cellulose, styrene-butadiene rubber, polyurethane, fluorinated rubber, or polyvinyl alcohol. In some embodiments, a mass percentage of the first conductive agent in the first coating layer is 30%-80%, and a mass percentage of the first binder is 20%-70%. If the mass percentage of the first conductive agent is excessively small, conductive performance of the first coating layer is adversely affected. If the mass percentage of the first conductive agent is excessively large, the mass percentage of the first binder is excessively small, which affects bonding performance of the first coating layer.
It should be understood that in
As shown in
As shown in
In some embodiments, at least part or all of the current collector 1 is etched. The current collector 1 being etched can correspondingly increase roughness of the current collector, thereby increasing the bonding force between the current collector and the first coating layer or the second coating layer. In some embodiments, the first edge region and the second edge region are etched, and roughness of the first edge region 4 and roughness of the second edge region 5 are both 2 to 4 times roughness of the middle region 6. The first edge region 4 and the second edge region 5 being etched further increases the bonding force between the current collector 1 and the first coating layer 2. In some embodiments, etching may be performed at a region of the first coating layer where the current collector is disposed. In some embodiments, etching is mainly performed by browning or blackening, or certainly may be performed in other suitable manners. In some embodiments, roughness of an etched region of the current collector is 2 to 4 times roughness of a region not etched. In some embodiments, the roughness of the region not etched is less than 2 µm.
It should be understood that the electrode plate of this application may be a positive electrode plate or a negative electrode plate. As shown in
In some embodiments, a positive electrode current collector of the positive electrode plate 12 may be aluminum (Al) foil, or certainly may be another positive electrode current collector commonly used in the art. In some embodiments, a thickness of the positive electrode current collector may be 1 µm-200 µm.
In some embodiments, when the electrode plate is the positive electrode plate 12, the active material of the second coating layer 3 may include at least one of lithium cobalt oxide, lithium manganate oxide, lithium iron phosphate, lithium nickel cobalt manganate, lithium nickel cobalt aluminate, or lithium nickel manganate. In some embodiments, the second coating layer 3 further includes a binder and a conductive agent. In some embodiments, the binder in the second coating layer 3 may include at least one of polyvinylidene fluoride, vinylidene fluoride-hexafluoropropylene copolymer, styrene-acrylate copolymer, styrene-butadiene copolymer, polyamide, polyacrylonitrile, polyacrylic ester, polyacrylic acid, polyacrylic salt, sodium carboxymethyl cellulose, polyvinyl acetate, polyvinylpyrrolidone, polyvinylether, polymethyl methacrylate, polytetrafluoroethylene, or polyhexafluoropropylene. In some embodiments, the conductive agent in the second coating layer 3 may include at least one of conductive carbon black, Ketjen black, laminated graphite, graphene, carbon nanotubes, or carbon fibers. In some embodiments, a mass ratio of the positive electrode active material, the conductive agent, and the binder in the second coating layer 3 may be 91-99:0.5-3:0.5-6. It should be understood that the foregoing descriptions are merely examples, and any other suitable material, thickness, and mass ratio may be used for the positive electrode active substance layer.
In some embodiments, a negative electrode current collector of the negative electrode plate 13 may be at least one of copper foil, nickel foil, or carbon-based current collector, or certainly may be another negative electrode current collector commonly used in the art. In some embodiments, a thickness of the negative electrode current collector may be 1 µm-200 µm.
In some embodiments, when the electrode plate is the negative electrode plate 13, the active material of the second coating layer 3 may include at least one of artificial graphite, natural graphite, hard carbon, meso-carbon microbeads, silicon alloy, tin alloy, or pure silicon. In some embodiments, the second coating layer 3 may further include a conductive agent and a binder. The conductive agent in the second coating layer 3 may include at least one of conductive carbon black, Ketjen black, laminated graphite, graphene, carbon nanotubes, or carbon fibers. In some embodiments, the binder in the second coating layer 3 may include at least one of carboxymethyl cellulose (CMC), polyacrylic acid, polyvinyl pyrrolidone, polyaniline, polyimide, polyamide-imide, polysiloxane, styrene-butadiene rubber, epoxy resin, polyester resin, urethane resin, or polyfluorene. It should be understood that the materials disclosed above are merely examples, and any other suitable material may be used for the second coating layer 3 of the negative electrode active material layer. In some embodiments, a mass ratio of the negative electrode active material, the conductive agent, and the binder in the second coating layer 3 may be 91-99:0-3:1-6. It should be understood that the foregoing description is merely an example, and any other suitable mass ratio may be used.
In some embodiments, the separator 11 includes at least one of polyethylene, polypropylene, polyvinylidene fluoride, polyethylene terephthalate, polyimide, or aramid. For example, polyethylene includes at least one of high-density polyethylene, low-density polyethylene, or ultra-high-molecular-weight polyethylene. Especially, polyethylene and polypropylene have a good effect on preventing short circuits and can improve stability of a battery through a shutdown effect. In some embodiments, a thickness of the separator is approximately 5 µm-20 µm.
In some embodiments, a surface of the separator may further include a porous layer. The porous layer is disposed on at least one surface of the separator, and includes inorganic particles and a binder, where the inorganic particles are selected from at least one of aluminum oxide (Al2O3), silicon oxide (SiO2), magnesium oxide (MgO), titanium oxide (TiO2), hafnium oxide (HfO2), stannic oxide (SnO2), cerium dioxide (CeO2), nickel oxide (NiO), zinc oxide (ZnO), calcium oxide (CaO), zirconium oxide (ZrO2), yttrium oxide (Y2O3), silicon carbide (SiC), boehmite, aluminum hydroxide, magnesium hydroxide, calcium hydroxide, or barium sulfate. In some embodiments, pores of the separator have a diameter range of approximately 0.01 µm-1 µm. The binder of the porous layer is selected from at least one of polyvinylidene fluoride, vinylidene fluoride-hexafluoropropylene copolymer, polyamide, polyacrylonitrile, polyacrylic ester, polyacrylic acid, polyacrylic salt, sodium carboxymethyl cellulose, polyvinylpyrrolidone, polyvinyl ether, polymethyl methacrylate, polytetrafluoroethylene, or polyhexafluoropropylene. The porous layer on the surface of the separator can improve heat resistance, oxidation resistance, and electrolyte infiltration performance of the separator, and enhance adhesion between the separator and the electrode plate.
In some embodiments of this application, an electrode assembly of the electrochemical apparatus is a wound electrode assembly or a laminated electrode assembly.
In some embodiments, the electrochemical apparatus includes a lithium-ion battery, but this application is not limited thereto. In some embodiments, the electrochemical apparatus may further include an electrolyte. The electrolyte may be one or more of a gel electrolyte, a solid electrolyte, and an electrolyte solution, and the electrolyte solution includes a lithium salt and a non-aqueous solvent. The lithium salt is selected from one or more of LiPF6, LiBF4, LiAsF6, LiClO4, LiB(C6H5)4, LiCH3SO3, LiCF3SO3, LiN(SO2CF3)2, LiC(SO2CF3)3, LiSiF6, LiBOB, or lithium difluoro borate. For example, LiPF6 is selected as the lithium salt because it can provide a high ionic conductivity and improve cycling characteristics.
The non-aqueous solvent may be selected from a carbonate compound, a carboxylate compound, an ether compound, another organic solvent, or a combination thereof.
The carbonate compound may be selected from a linear carbonate compound, a cyclic carbonate compound, a fluorocarbonate compound, or a combination thereof.
The linear carbonate compound may be selected from diethyl carbonate (DEC), dimethyl carbonate (DMC), dipropyl carbonate (DPC), methyl propyl carbonate (MPC), ethyl propyl carbonate (EPC), methyl ethyl carbonate (MEC), and a combination thereof. The cyclic carbonate compound may be selected from ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), vinyl ethylene carbonate (VEC), or a combination thereof. The fluorocarbonate compound may be selected from fluoroethylene carbonate (FEC), 1,2-difluoroethylene carbonate, 1,1-difluoroethylene carbonate, 1,1,2-trifluoroethylene carbonate, 1,1,2,2-tetrafluoroethylene carbonate, 1-fluoro-2-methylethylene carbonate, 1-fluoro-1-methylethylene carbonate, 1,2-difluoro-1-methylethylene carbonate, 1,1,2-trifluoro-2-methylethylene carbonate, trifluoromethylethylene carbonate, or a combination thereof.
The carboxylate compound may be selected from methyl acetate, ethyl acetate, n-propyl acetate, tert-butyl acetate, methyl propionate, ethyl propionate, propyl propionate, y-butyrolactone, decanolide, valerolactone, mevalonolactone, caprolactone, methyl formate, or a combination thereof.
The ether compound may be selected from dibutyl ether, tetraglyme, diglyme, 1,2-dimethoxyethane, 1,2-diethoxyethane, ethoxymethoxy ethane, 2-methyltetrahydrofuran, tetrahydrofuran, or a combination thereof.
The another organic solvent may be selected from dimethyl sulfoxide, 1,2-dioxolane, sulfolane, methyl sulfolane, 1,3-dimethyl-2-imidazolidinone, N-methyl-2-pyrrolidone, formamide, dimethylformamide, acetonitrile, trimethyl phosphate, triethyl phosphate, trioctyl phosphate, phosphate ester, or a combination thereof.
In some embodiments of this application, a lithium-ion battery is used as an example. A positive electrode plate, a separator, and a negative electrode plate are wound or stacked in sequence to form an electrode assembly, and the electrode assembly is then packaged in, for example, an aluminum-plastic film, followed by electrolyte injection, formation, and packaging, to prepare a lithium-ion battery. Then, a performance test is performed on the prepared lithium-ion battery.
Persons skilled in the art will understand that the preparation method of the electrochemical apparatus (for example, the lithium-ion battery) described above is merely an example. Without departing from the content disclosed in this application, other methods commonly used in the art may be used.
An embodiment of this application further provides an electronic apparatus including the foregoing electrochemical apparatus. The electronic apparatus in the embodiments of this application is not particularly limited, and may be any known electronic apparatus used in the prior art. In some embodiments, the electronic apparatus may include but is not limited to a notebook computer, a pen-input computer, a mobile computer, an electronic book player, a portable telephone, a portable fax machine, a portable copier, a portable printer, a stereo headset, a video recorder, a liquid crystal television, a portable cleaner, a portable CD player, a mini-disc, a transceiver, an electronic notebook, a calculator, a storage card, a portable recorder, a radio, a standby power source, a motor, an automobile, a motorcycle, a motor bicycle, a bicycle, a lighting appliance, a toy, a game console, a clock, an electric tool, a flash lamp, a camera, a large household battery, or a lithium-ion capacitor.
Some specific examples and comparative examples are listed below to better illustrate this application. Lithium-ion batteries are used as examples.
Preparation of positive electrode plate: A positive electrode active material lithium cobalt oxide, a conductive agent conductive carbon black, and a binder polyvinylidene fluoride (PVDF) were dissolved in an N-methylpyrrolidone (NMP) solution at a mass ratio of 97.6: 1.1: 1.3, to form a positive electrode slurry. Aluminum foil was used as a positive electrode current collector. The positive electrode slurry was applied onto the positive electrode current collector with a coating thickness of 50 µm, followed by drying, cold pressing, and cutting, to obtain a positive electrode plate.
Preparation of negative electrode plate: A first binder polyvinylidene fluoride and a first conductive agent conductive carbon black were dissolved in an N-methylpyrrolidone (NMP) solution at a mass ratio of 60:40, to form a first coating layer slurry. Copper foil with a thickness of 10 µm and a width of 80 mm was used as a negative electrode current collector. The first coating layer slurry was applied onto edge positions of the negative electrode current collector with a coating width of 5 mm and a thickness of 2 µm on two edge positions, followed by drying, to obtain a first coating layer.
A negative electrode active material artificial graphite and a binder styrene-butadiene rubber were dissolved in deionized water at a mass ratio of 98:2, to form a second coating layer slurry. The second coating layer slurry was applied onto the negative electrode current collector and the first coating layer, followed by drying and cold pressing, to obtain a negative electrode active material layer with a thickness of 60 µm. After cutting, a negative electrode plate was obtained.
Preparation of separator: Polyethylene (PE) with a thickness of 8 µm was used as a separator substrate, a 2 µm aluminum oxide ceramic layer was applied on two sides of the separator substrate, and finally, 2.5 mg of binder polyvinylidene fluoride (PVDF) was applied on the two sides coated with the ceramic layers, followed by drying.
Preparation of electrolyte: In an environment with a water content less than 10 ppm, lithium hexafluorophosphate and a non-aqueous organic solvent (ethylene carbonate (EC):dimethyl carbonate (DMC) = 40:60 by mass) were mixed at a mass ratio of 8:92, to prepare an electrolyte.
Preparation of lithium-ion battery: The positive electrode plate, the separator, and the negative electrode plate were stacked in sequence, such that the separator was sandwiched between the positive electrode plate and the negative electrode plate for separation, and the stack was wound to obtain an electrode assembly. The electrode assembly was put in an outer packaging aluminum-plastic film, and was dehydrated at 80° C. Then, the foregoing electrolyte was injected and packaging was performed, followed by processes such as formation, degassing, and trimming, to obtain a lithium-ion battery.
For other examples and comparative examples, parameters were changed based on steps in Example 1. In Example 5, the two edge regions of the negative electrode current collector coated with the first portion and the second portion were etched, roughness of the etched edge regions was 3 µm, and roughness of other regions not etched was 1 µm . Specific changed parameters are shown in the table below.
The following describes test methods for various parameters in this application.
Test method for volumetric energy density:
The lithium-ion battery was placed in a 25° C. thermostat and left standing for 30 minutes, such that the lithium-ion battery reached a constant temperature. The lithium-ion battery having reached a constant temperature was charged to a voltage of 4.4 V at a constant current of 0.5 C, then charged to a current of 0.05 C at a constant voltage of 4.4 V, and discharged to a voltage of 3.0 V at 0.5 C. A discharge capacity was recorded.
Heavy impact test of lithium-ion battery:
At 25° C., the lithium-ion battery was charged to a voltage of 4.4 V at a constant current of 0.5 C, and then charged to a current of 0.05 C at a constant voltage of 4.4 V The UL 1642 test standard was used. With a heavy hammer with a mass of 9.8 kg, a diameter of 15.8 mm, a falling height of 61 ± 2.5 cm, and a falling direction being parallel to the longitudinal direction of the separator, the lithium-ion battery was subj ected to the impact test, and a lithium-ion battery that did not explode, catch fire, or smoke was recorded as passing the impact test. Ten lithium-ion batteries were tested in each group, and the pass rate of the heavy impact test of the lithium-ion batteries was calculated (if four lithium-ion batteries passed the heavy impact test, the pass rate was represented as 4/10).
Table 1 shows the parameters and test results in the examples and comparative examples.
It can be learned from comparison between Example 1 and Comparative Example 1 that the first coating layer is applied on only two edge regions of the current collector, such that the bonding force between the first coating layer and the current collector is greater than the bonding force between the second coating layer and the middle region of the current collector. Because the bonding force between the second coating layer and the current collector is weak, peeling between the active substance coating layer and the current collector is likely to occur during impact, increasing the pass rate of the impact test of the lithium-ion batteries from 4/10 to 8/10. In addition, because the coating region of the first coating layer is decreased, the thickness of the electrode assembly of the lithium-ion battery becomes smaller, and the volumetric energy density of the lithium-ion battery is increased by 1%. It can be learned from Examples 2 to 5 that adjusting the width of the first coating layer can achieve increases in the energy density and the pass rate of the impact test. However, increasing the coating width causes a smaller energy density increase rate. It can be learned from comparison between Example 5 and Example 1 that etching the edge regions of the current collector coated with the first coating layer can increase the bonding force between the first coating layer and the current collector, thereby increasing the pass rate of the impact test of the lithium-ion batteries to 9/10.
It can be learned from comparison among Example 1 and Examples 6 to 8 that the thickness of the first coating layer is increased to enhance the bonding force between the first coating layer and the current collector. Generally, if the second coating layer has a specific thickness, the first coating layer has an optimal thickness value. If the first coating layer has a relatively small thickness, a coating status cannot be ensured well and the bonding force between the first coating layer and the current collector is limited. However, an excessively large thickness causes excessive pressure on the second coating layer active substance on the edge regions, affecting extractable capacity to some extent. Adjusting the thickness of the first coating layer has small influence on the impact test, and the pass rates can reach 8/10, but the volumetric energy density increase rate becomes smaller as the thickness of the first coating layer increases.
It can be learned from comparison among Example 1 and Examples 9 to 11 that for different thicknesses of the second coating layers, the increases in the energy density and the pass rate of the impact test can be achieved by adjusting the thickness. However, after the thickness of the electrode plate is increased, the first coating layer limits the increase in the overall energy density, with the increase being reduced from 1% to 0.5%. In addition, there is small influence on the pass rate of the impact test.
It can be learned from comparison among Example 1 and Examples 12 to 14 that adjusting the percentage of the binder in the first coating layer can enhance the bonding force between the edge of the first coating layer and the current collector. In specific cases, if the energy density increase rates are the same, the increase of 1% can be achieved for all the first coating layers in these examples. When the percentage of the bonding force is low, for example, lower than 20%, the bonding force between the first coating layer and the current collector is excessively weak, leading to an adverse effect on the thickness of the electrode plate, causing loss of part of the volumetric energy density, with the energy density increase rate being reduced to less than 0.8%. Because the bonding force between the second coating layer and the current collector is not changed, the influence on the pass rate of the impact test is small, and the pass rate of 8/10 can be ensured.
It can be learned from comparison between Example 15 and Comparative Example 1 that the bonding force between the first coating layer and the current collector being greater than the bonding force between the second coating layer and the middle region of the current collector increases the pass rate of the impact test of the lithium-ion batteries from 4/10 to 8/10. In addition, the discontinuous coating is applied to the first coating layer, and the width ratio of the first coating layer and the second coating layer is decreased, which increase the volumetric energy density of the lithium-ion battery by 1.3%.
The foregoing descriptions are merely preferred examples of this application and explanations of the technical principles used. Persons skilled in the art should understand that the scope of disclosure involved in this application is not limited to the technical solutions formed by the specific combination of the foregoing technical features, and should also cover other technical solutions formed by any combination of the foregoing technical features or their equivalent features, for example, the technical solution formed by replacement between the foregoing features and technical features having similar functions disclosed in this application.
This application is a continuation application of International Application No. PCT/CN2020/112470, filed on Aug. 31, 2020, the contents of which are incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2020/112470 | Aug 2020 | WO |
| Child | 18175824 | US |
