The present disclosure relates to the field of lithium-ion battery technologies, and in particular to an electrode plate, a method for preparing the same and a lithium-ion battery.
With the advent of the 5G era, lithium-ion batteries have become increasingly important. The lithium-ion batteries are currently developing in a direction of high energy density and high fast charging rate. Currently, a connection position of a tab is adjusted from the edge of an electrode plate to the middle position of a side of the electrode plate, to reduce impedance of a lithium-ion battery.
However, when the position of the tab is changed, current density around the tab is increased, and with cycle of the lithium-ion battery, lithium ions are precipitated, resulting in deterioration of cycling performance of the lithium-ion battery. Therefore, increasing attention has been paid to how to resolve problems of deterioration of cycling performance of a lithium-ion battery caused by such a tab connection manner.
The present disclosure provides an electrode plate to resolve problems of deterioration of cycling performance of a lithium-ion battery caused by such a tab connection manner.
According to a first aspect of the present disclosure, an electrode plate is provided. The electrode plate includes a current collector, a first active layer, and a second active layer. The first active layer is disposed on a surface of the current collector and provided with a first groove, and the second active layer is divided into a first portion disposed in the first groove and a second portion disposed on a surface, away from the current collector, of the first active layer. The first portion is provided with a second groove, a tab is disposed at the second groove and is electrically connected to the current collector, and a thickness of the first portion of the second active layer is less than a total thickness of the first active layer and the second portion of the second active layer.
According to a second aspect of the present disclosure, a lithium-ion battery is provided, and the lithium-ion battery includes any one of the foregoing electrode plates.
The present disclosure provides an electrode plate, and a person skilled in the art, on the basis of the electrode plate provided in the present disclosure, may prepare a lithium-ion battery in combination with the conventional technology. The lithium-ion battery provided in the present disclosure has good cycling performance.
Embodiments of the present application have at least the following advantages.
1. According to the electrode plate provided in the present disclosure, the thickness of the portion of the active layer near the tab is reduced, avoiding a charging risk at a connection position of the tab to a specific extent and improving cycling performance of a lithium-ion battery.
2. The electrode plate provided in the present disclosure is applicable to both a positive electrode plate and a negative electrode plate.
3. When the electrode plate is a positive electrode plate, the electrode plate structure provided in the present disclosure may be used to avoid problems that the tab cannot be connected to the middle position of the side surface of the current collector due to presence of the high-viscosity substance in the first active layer.
4. The lithium-ion battery provided in the present disclosure has good cycling performance.
To make the objectives, technical solutions, and advantages of the present disclosure clearer, the following clearly describes the technical solutions in embodiments of the present disclosure with reference to the embodiments of the present disclosure. Apparently, the described embodiments are merely some but not all of the embodiments of the present disclosure. All other embodiments obtained by a person of ordinary skill in the art based on the embodiments of the present disclosure without creative efforts shall fall within the protection scope of the present disclosure.
Currently, an electrode plate used in the conventional technology generally includes a current collector and an active layer disposed on a surface of the current collector, and a groove is formed in the middle of a side of the active layer. The groove is connected to a tab in a corresponding region on the current collector. In order to resolve the problem of deterioration of cycling performance of a lithium-ion battery caused by such a tab connection manner, a thickness of a portion of the active layer around the tab is reduced in the present disclosure. Specifically,
In an embodiment, in order to further improve cycling performance of a lithium-ion battery, a thickness of the first active layer should be appropriately reduced, that is, a thickness of the second active layer is greater than a thickness of the first active layer. In addition, since being disposed in the first groove, the first portion of the second active layer is subjected to less force in a subsequent electrode plate rolling process, thus causing a difference in thicknesses of the first portion and the second portion of the second active layer. Specifically, the thickness of the first portion of the second active layer is greater than the thickness of the second portion.
According to the electrode plate structure shown in
It may be appreciated that an intersection of the diagonal lines of a vertical projected region of the second groove on the current collector is used as the center, and the center of the vertical projection region of the second groove on the current collector is located within the first groove.
Further referring to
An area ratio of the first groove to the second groove on a cross section in a length direction has a greater impact on performance of a lithium-ion battery. Specifically, a vertical projected area of the second groove on the current collector ranges from 1% to 50% of a vertical projected area of the first groove on the current collector. In a specific preparation process, a person skilled in the art may determine widths of the first groove and the second groove, and adjust the area ratio of the first groove and the second groove by adjusting length ranges thereof.
In order to improve fast charging performance of a lithium-ion battery, when the electrode plate is a negative electrode plate, an average particle size of an active substance in the second active layer ranges from 5 μm to 20 μm and a degree of graphitization of the active substance in the second active layer ranges from 90% to 98%.
The electrode plate provided in the present disclosure is also applicable to a positive electrode plate, and when the electrode plate is a positive electrode plate, a material of the first active layer generally uses a high-viscosity substance to improve safety performance of a lithium-ion battery. However, because viscosity of the high-viscosity substance is high, during cleaning of a region where the first groove is located in the first active layer, the high-viscosity substance cannot be thoroughly cleaned, and thus there is the high-viscosity substance residue in a corresponding region of the first groove, affecting connection between the tab and the current collector and causing the tab to fail to be connected to the middle position of a side surface of the current collector. Therefore, use of the electrode plate structure provided in the present disclosure may effectively avoid the problems that the tab cannot be connected to the middle position of the side surface of the current collector due to presence of the high-viscosity substance in the first active layer, that is, the first active layer uses the high-viscosity substance, and subsequently only the second active layer needs to be cleaned without cleaning the first active layer. Specifically, the high-viscosity substance refers to a binder in an active layer material having a molecular weight ranging from 800000 to 2000000, and a mass of the binder ranges from 3% to 40% of a total mass of the first active layer.
In addition, the thickness of the first active layer and the second active layer in the electrode plate has a great impact on performance of a lithium-ion battery. The inventors of the present application found through research that, when a thickness ratio of the first active layer increases, cycling performance of a lithium-ion battery decreases moderately. Therefore, the thickness of the first active layer ranges from 5% to 80% of the total thickness of the first active layer and the second portion of the second active layer.
When the electrode plate is a positive electrode plate, the thickness of the first active layer should be appropriately reduced. For example,
On the basis of the electrode plate structure provided in the present disclosure, a person skilled in the art may prepare an electrode plate in combination with an existing electrode plate preparation method. Specifically, first active layer slurry and second active layer slurry are prepared first. Next, the prepared first active layer slurry is coated on a surface of a current collector, and blank coating is performed on a region corresponding to the first groove to obtain a first active layer provided with a first groove, and then the second active layer slurry is coated according to a conventional electrode plate coating process. Part of the second active layer slurry is filled in the first groove under the action of gravity to obtain a first portion of a second active layer, and a second portion of the second active layer is obtained based on the remaining part of the second active layer slurry. Finally, an active layer located in part of the first portion in the first groove is cleaned to obtain a second groove, and a tab is disposed in the second groove and electrically connected to the current collector, to obtain the electrode plate.
A person skilled in the art may select materials of the positive electrode plate and the negative electrode plate in combination with the conventional technology. For example, when the electrode plate is a positive electrode plate, the current collector may be aluminum foil, and a positive electrode active substance includes at least one of lithium cobalt oxide, lithium manganate, lithium nickelate, lithium nickel cobalt manganate, lithium iron phosphate, lithium iron manganese phosphate, lithium vanadium phosphate, lithium vanadyl phosphate, a lithium-rich manganese-based material, and lithium nickel cobalt aluminate.
When the electrode plate is a negative electrode plate, the current collector may be copper foil, and a negative electrode active material includes at least one of artificial graphite, natural graphite, and modified graphite.
The positive electrode plate and the negative electrode plate use a same binder and a same conductive agent. Specifically, the binder may be made of at least one of polyvinylidene fluoride (PVDF), a vinylidene fluoride-hexafluoropropylene copolymer, polyamide, polyacrylonitrile, polyacrylate, polyacrylic acid, polyacrylate, polyvinyl pyrrolidone, polyvinyl ether, polymethyl methacrylate, polytetrafluoroethylene, polyhexafluoropropylene, and styrene-butadiene rubber (SBR). The conductive agent may be made of at least one of conductive carbon black, a carbon nanotube, conductive graphite, and graphene. The negative electrode plate may further include a thickener, and the thickener may be made of sodium carboxymethyl cellulose.
It may be appreciated that the second groove is used to dispose the tab, so that the width of the second groove is less than the width of the first groove in a width direction of the current collector.
In an actual preparing process, in order to facilitate connection between the tab and the current collector, the vertical projected area of the second groove on the current collector may be increased, so that the vertical projected area of the second groove on the current collector is larger than an area of a tab connection region on the current collector.
Further, a width of the second groove is 1 to 2 times a width of the tab connection region, and a length of the second groove is 1 to 2 times a length of the tab connection region.
In conclusion, according to the electrode plate provided in the present disclosure, a thickness of the portion of an active layer around the tab is reduced, avoiding a charging risk at a connection position of the tab to a specific extent and improving cycling performance of a lithium-ion battery.
Embodiment 1
An electrode plate provided in this embodiment is a positive electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is aluminum foil, with a width of 79 mm.
A first groove has a width of 79 mm and a length of 15 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 10 μm, and a thickness of a second active layer is 80 μm.
A material used for the first active layer is a high-viscosity substance including lithium cobaltate, conductive carbon, and polyvinylidene fluoride. A molecular mass of the polyvinylidene fluoride is 800000, and a mass of the polyvinylidene fluoride is 20% of a total mass of the first active layer.
Embodiment 2
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 50 μm, and a thickness of a second active layer is 50 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 15 μm and a degree of graphitization of 94%.
Embodiment 3
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 30 μm, and a thickness of a second active layer is 70 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 15 μm and a degree of graphitization of 94%.
Embodiment 4
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 40 μm, and a thickness of a second active layer is 60 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 15 μm and a degree of graphitization of 94%.
Embodiment 5
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 50 μm, and a thickness of a second active layer is 50 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 10 μm and a degree of graphitization of 92%.
Embodiment 6
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 50 μm, and a thickness of a second active layer is 50 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 10 μm and a degree of graphitization of 95%.
Embodiment 7
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 50 μm, and a thickness of a second active layer is 50 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 15 μm and a degree of graphitization of 92%.
Embodiment 8
An electrode plate provided in this embodiment is a negative electrode plate. A front view of a structure of the electrode plate is shown in
A current collector is copper foil, with a width of 81 mm.
A first groove has a width of 81 mm and a length of 50 mm.
A second groove has a width of 25 mm and a length of 10 mm.
A thickness of a first active layer is 50 μm, and a thickness of a second active layer is 50 μm.
An active substance used for the second active layer is graphite, and the graphite has an average particle size of 15 μm and a degree of graphitization of 95%.
Comparative Embodiment 1
An electrode plate provided in this comparative embodiment is a positive electrode plate including a current collector and an active layer disposed on a surface of the current collector, and a tab is connected to the outermost edge side of the current collector.
The current collector is aluminum foil, with a width of 79 mm.
A thickness of the active layer is 90 μm.
Comparative Embodiment 2
An electrode plate provided in the present comparative embodiment is a negative electrode plate including a current collector, a first active layer and a second active layer, and the first active layer and the second active layer are disposed on a surface of the current collector. A groove is disposed at a middle position of a side surface of each of the first active layer and the second active layer, and a tab is connected to the current collector in the groove.
The current collector is copper foil, with a width of 81 mm.
A groove has a width of 25 mm and a length of 10 mm.
A total thickness of the first active layer and the second active layer is 100 μm.
On the basis of the electrode plates provided in Embodiments 1 to 8 and Comparative Embodiments 1 and 2 of the present disclosure, a lithium-ion battery was prepared with a negative electrode plate/positive electrode plate having a same structure, a separator and an electrolyte. For example, a positive electrode plate is provided in Embodiment 1 and Comparative Embodiment 1, and thus a structure of the corresponding negative electrode plate is the same as that of the positive electrode plate. A negative electrode plate is provided in Embodiments 2 to 8 and Comparative Embodiment 2, and thus a structure of the corresponding positive electrode plate is the same as that of the negative electrode plate. In addition, cycling performance of the lithium-ion battery was tested.
The positive electrode material is purchased from XTC New Energy Materials (Xiamen) Co., Ltd., the negative electrode material is purchased from Shanghai Shanshan Technology Co., Ltd., the separator is purchased from Dongguan Advanced Electronic Technology Co., Ltd., and the electrolyte is purchased from Shenzhen Capchem Technology Co., Ltd.
Method for testing performance of the lithium-ion battery is as follows
The lithium-ion batteries prepared on the basis of Embodiment 1 and Comparative Embodiment 1 were subjected to a charge/discharge cycle test of 2 C/0.7 C at 25° C. and cycle retentions (%) were calculated. A cell surface temperature was monitored with a temperature sensor, and a difference between a maximum temperature value and an initial temperature value was recorded as a temperature rise (° C.) for each lithium-ion battery. The test results are shown in Table 1.
The lithium-ion batteries prepared on the basis of Embodiments 2 to 8 and Comparative Embodiment 2 were subjected to a charge/discharge cycle test of 2 C/0.7 C at 25° C./10° C. and cycle retentions (%) were calculated, respectively. The test results are shown in Table 2.
As can be learned from Table 1 and Table 2, the lithium-ion batteries provided in Embodiments 1-8 all have good cycling performance. According to the data provided in Embodiments 2 to 4, as a ratio of a thickness of a first active layer to a total thickness of an active layer is increased, performance of a lithium-ion battery is moderately degraded, so that the thickness of the first active layer should be under controlled. According to the data provided in Embodiments 5 to 8, in a negative electrode plate, as an average particle size and a degree of graphitization of a negative electrode active substance in a second active layer are increased, a cycle retention of a lithium-ion battery is decreased.
Finally, it should be noted that the foregoing embodiments are merely intended to describe the technical solutions of the present disclosure, but not intended to constitute any limitation. Although the present disclosure is described in detail with reference to the foregoing embodiments, persons of ordinary skill in the art should understand that they may still make modifications to the technical solutions described in the foregoing embodiments or make equivalent replacements to some or all technical features thereof; and these modifications or replacements do not make the essence of the corresponding technical solution depart from the scope of the technical solutions of the embodiments of the present disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202011628654.0 | Dec 2020 | CN | national |
This application is a continuation application of International Application No. PCT/CN2021/142831, filed on Dec. 30, 2021, which claims priority to Chinese Patent Application No. 202011628654.0, filed with the China National Intellectual Property Administration on Dec. 30, 2020 and entitled “ELECTRODE PLATE AND LITHIUM-ION BATTERY”. Both of the aforementioned applications are hereby incorporated by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2021/142831 | Dec 2021 | US |
| Child | 18146308 | US |