Lithium-supplement layer and its negative electrode sheet, lithium ion battery and device

Abstract

The application relates to the field of lithium ion battery technology and, more particularly, relates to a lithium-supplement layer and its negative electrode sheet, a lithium ion battery and a device. The lithium-supplement layer is formed by connecting a transition layer, an oxide layer and a surface layer in sequence, the surface layer contains an appropriate amount of an organic material and a filling substance, which can reduce a winding temperature of the negative electrode sheet, the oxide layer substance in the lithium-supplement layer is used to provide an additional lithium source, after injection, the lithium source can be continuously supplemented during the cycle process to improve the activity of a lithium layer, at the same time, the filling substance contained in the surface layer can effectively play a role of restraining the expansion of an active substance, and improve the battery cycle performance.

Claims

1. A lithium-supplement negative electrode sheet, comprising: a current collector; a diaphragm, located on the current collector and comprising an active substance, an adhesive and a conductive agent; and a lithium-supplement layer comprising: a transition layer on the diaphragm, wherein the transition layer is one or more selected from Li.sub.2O, Li.sub.xC, and Li.sub.x1Si.sub.y, wherein, 0<x≤2, 0<x1≤4.4, 0≤y2; an oxide layer on the transition layer, wherein the oxide layer is a lithium source selected from the group consisting of Li metal, Li.sub.2O, LiF, LiOH, Li.sub.3N, Li.sub.2CO.sub.3, or any combinations thereof; and a surface layer on the oxide layer, wherein the surface layer contains an organic material and a filling substance, the organic material is one or more selected from stearic acid, 12-hydroxystearic acid, fatty acid metal salt, polyglycol, polyhydrocarbon cyclopentane, polyisobutyl methacrylate, phosphate ester, paraffin, polyurea, poly a-olefins, alkyl naphthalene, and polydimethylsiloxane, and the filling substance is one or more selected from graphite, graphene, aluminum oxide, sodium hydroxide, lithium hydroxide, calcium hydroxide and molybdenum disulfide.

2. The lithium-supplement negative electrode sheet according to claim 1, wherein, based on a quality of the surface layer, a content of the organic material is 10%-97%; a content of the filling substance is 3%-90%.

3. The lithium-supplement negative electrode sheet according to claim 1, wherein, a thickness of the surface layer is 0.1 μm-15 μm.

4. The lithium-supplement negative electrode sheet according to claim 1, wherein, a thickness of the transition layer is 0.01 μm-1 μm.

5. The lithium-supplement negative electrode sheet according to claim 1, wherein, a thickness of the oxide layer is 0.5 μm-20 μm.

6. A lithium-supplement lithium ion battery, comprising: the lithium-supplement negative electrode sheet according to claim 1; a positive electrode sheet; an electrolyte and a separator.

7. A device comprising: the lithium ion battery according to claim 6.

8. The lithium-supplement negative electrode sheet according to claim 2, wherein, based on the quality of the surface layer, the content of the organic material is 20%-80%.

9. The lithium-supplement negative electrode sheet according to claim 2, wherein, based on the quality of the surface layer, the content of the filling substance is 20%-80%.

10. The lithium-supplement negative electrode sheet according to claim 3, wherein, the thickness of the surface layer is 1 μm-8 μm.

11. The lithium-supplement negative electrode sheet according to claim 4, wherein, the thickness of the transition layer is 0.05 μm-0.7 μm.

12. The lithium-supplement negative electrode sheet according to claim 5, wherein, the thickness of the oxide layer is 0.8 m-10 m.

13. The lithium-supplement negative electrode sheet according to claim 1, wherein, the surface layer is a layered covering.

14. The lithium-supplement negative electrode sheet according to claim 1, wherein, the surface layer is a dotted covering.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) In order to illustrate more clearly the technical solutions of the embodiments of the present application, the drawings that need to be used in the embodiments of the present application will be briefly introduced in the following, obviously, the drawings described below are only some examples of the present application, and other drawings can be obtained by those skilled in the art without creative work.

(2) FIG. 1 is a schematic diagram of an electrode sheet of a layered covering lithium-supplement layer of a specific embodiment;

(3) FIG. 2 is a schematic diagram of an electrode sheet of a dotted covering lithium-supplement layer of a specific embodiment;

(4) FIG. 3 is a scanning electron micrograph (SEM) of a lithium-supplement cross section of an electrode sheet after formation of lithium ion cell containing the lithium-supplement layer of a specific embodiment;

(5) FIG. 4 is a schematic diagram of a lithium ion battery of a specific embodiment;

(6) FIG. 5 is a schematic diagram of a battery module of a specific embodiment;

(7) FIG. 6 is a schematic diagram of a battery pack of a specific embodiment;

(8) FIG. 7 is an exploded view of FIG. 6;

(9) FIG. 8 is a schematic diagram of a device using a lithium ion battery as a power of a specific embodiment;

DESCRIPTION OF EMBODIMENTS

(10) In order to make the purpose, technical solutions and advantages of the embodiments of the present application clearer, the technical solutions of the embodiments of the present application will be described clearly and completely in conjunction with the drawings in the embodiments of the present application, obviously, the described embodiments are part of the embodiments of this application, rather than all of the embodiments. Based on the embodiments in the present application, all other embodiments obtained by those skilled in the art without creative work all fall within the protection scope of the present application.

(11) The lithium-supplement layer, the lithium-supplement negative electrode sheet, and the lithium ion battery and device of the present application will be described in detail below.

(12) Firstly, the lithium-supplement layer of the first aspect of the present application is described, which includes a transition layer, an oxide layer and a surface layer connected in sequence, wherein, the surface layer is a layered covering or a dotted covering, and the surface layer contains an organic material and a filling substance. Generally, “connected” here can be understood as overlapped along the thickness direction.

(13) The transition layer in the lithium-supplement layer is a side reactant between the active substance and the lithium-supplement layer, which can be regarded as an inorganic SEI film additionally generated in the lithium-supplement electrode sheet, and can play a role of protecting the SEI film formed by the active substance itself, and can effectively solve the problem that the lithium ions in the electrolyte would be consumed due to expansion and cracking of active substance during the cycle process.

(14) The main components of the oxide layer are lithium metal and lithium metal oxides, nitrides and hydroxide. The oxide layer is used to provide an additional lithium source, after injection, the lithium source can be continuously supplemented during the cycle process to improve the battery cycle performance. The oxide layer substance can also provide a part of substance that is used to form a transition layer, which is, additionally forming a layer of inorganic SEI film to improve the battery cycle performance. The oxide layer substance can form a dense or sparse isolation layer on the surface of the electrode sheet, to further improve the problem that the winding temperature of the lithium-supplement electrode sheet would be increased due to the reaction between the lithium foil and the air/active substance.

(15) The organic material in the surface layer mainly uses alcohols, esters and fatty acids. And the main roles of the organic material lie in: as a carrier of the filling substance to form a slurry coated on the surface of the lithium foil, as a film-forming substance of the surface layer of the lithium-supplement layer, so that the surface layer can form a film or evenly distributed on the surface of the transition layer and the oxide layer of the lithium-supplement layer. The filling substance in the lithium-supplement layer can be used to improve the deterioration of the cell internal resistance caused by the side reaction between the organic material and the electrolyte. The filling substance can form a network structure or a film-forming structure with the organic material, which can solve the expansion problem of the electrode sheet during the cycle process of active substance. The distribution form of the surface layer on the oxide layer can be uniformly layered covering or dotted covering.

(16) Optionally, the organic material is one or more selected from stearic acid, 12-hydroxystearic acid, fatty acid metal salt, polyglycol, polyhydrocarbon cyclopentane, polyisobutyl methacrylate, phosphate ester, paraffin, polyurea, poly α-olefins, alkyl naphthalene and polydimethylsiloxane, the filling substance is one or more selected from graphite, graphene, aluminum oxide, sodium hydroxide, lithium hydroxide, calcium hydroxide and molybdenum disulfide.

(17) Optionally, the transition layer is selected from an Li oxide or an embedded compound of lithium, for example, one or more selected from Li.sub.2O, LixC, and Li.sub.x1Si.sub.y, where 0<x≤2, 0<x1≤4.4, 0<y≤2. If choosing embedded silicide of lithium, it may generally be Li.sub.x1Si, x1 may be 4.4, 3.75, 3.25, 2.33, etc. More optionally, the oxide layer is one or more selected from Li metal, Li.sub.2O, LiF, LiOH, Li.sub.3N, and Li.sub.2CO.sub.3.

(18) Furthermore, a content and ratio of the organic material and filling substance in the surface layer of the lithium-supplement layer have a certain influence on the performance of the electrode sheet and lithium ion battery. When the proportion of the organic material in the surface layer is high, although it is helpful to form the isolation layer on the surface of the lithium-supplement layer, thereby lowering the winding temperature of the lithium-supplement electrode sheet, and improving the activity of the lithium-supplement layer, however, a very high proportion of organic materials may cause: a, the isolation layer formed by the lithium-supplement layer is too dense, which affects the lithium ion transmission efficiency, resulting in an increase of the battery internal resistance, affecting the battery performance; b, the lithium-supplement layer contains alcohols and other materials, if the proportion of organic materials is too high, side products is easily to be formed by reaction with the electrolyte, and affecting the battery performance; c. filling substance is too little, and cannot play a role of restraining the expansion of the active substance during the cycle process, thereby affecting the battery performance.

(19) Optionally, based on a quality of the surface layer, the content of the organic material is 10%-97%, optionally 20%-80%; the content of the filling substance is 3%-90%, optionally 20%-80%.

(20) When the proportions of the organic material and filling substance in the surface layer of the lithium-supplement layer are the same, the thickness of the surface layer is too small, for example, the thickness of the surface layer is 0 μm-0.1 μm, although it may also have a certain isolation effect, however, this surface layer cannot form an effective isolation layer on the surface of the lithium-supplement layer, and resulting in an increase of the reaction area between the lithium layer and the air, which accelerates the reaction, the temperature during winding process of lithium-supplement electrode sheet exceeds the standard, causing production safety risks. At the same time, an over high temperature of the electrode sheet will reduce the activity of the lithium layer, a part of lithium layers will form dead lithium under high temperature conditions, and cannot be used to provide capacity, resulting in a significant impact on electrical performance, and reducing cycle performance. On the other hand, when the thickness of the surface layer is too thick, for example, the thickness of the surface layer is greater than 15 μm, although the thick surface layer can form an excellent isolation layer to the air on the surface of the lithium-supplement layer, and effectively reducing the winding temperature of the lithium-supplement electrode sheet, however, the surface layer is too thick, which will directly affect the transmission efficiency of lithium ions, thus, the obtained cell internal resistance increases, and its cycle performance decreases. When the thickness of the surface layer of the lithium-supplement layer is in the range of 0.1 μm-15 μm, the surface layer can form an isolation layer between the lithium-supplement layer and the air, at the same time, the transmission efficiency of lithium ions cannot be significantly affected, and as the winding temperature of the lithium-supplement electrode sheet is controllable, the activity of the lithium-supplement layer can be guaranteed to provide capacity, and to improve the performance of the lithium ion battery.

(21) Optionally, the thickness of the surface layer is 0.1 μm-15 μm, optionally 1 μm-8 μm.

(22) The transition layer is too thin, that is, the inorganic SEI film formed on the lithium-supplement electrode sheet is too thin, although the performance of the electrode sheet can be improved to a certain extent, it cannot really play a protection role for the expansion of the active substance layer itself, and the improvement of the cell performance is not obvious. However, the transition layer is too thick, although it can play a good protection role for the expansion of active substance layer, it may affect the direct transmission efficiency of lithium ions in the positive and negative electrode sheets, further affects the battery performance.

(23) Optionally, the thickness of the transition layer is 0.01 μm-1 μm, optionally, 0.05 μm-0.7 μm.

(24) The inventor further studied and found that if the thickness of the oxide layer is too thin, that is, under the same amount of lithium-supplement, the lithium layer is pressed to the thinnest, and can be considered that most of the lithium layer is directly pressed into the active substance layer, under this circumstance, the active substance of the electrode sheet reacts violently with the substance in the lithium-supplement layer, the heat generated is more obvious, and the winding temperature of the electrode sheet increases greatly, which affects the safety of manufacturing, at the same time, the increase of winding temperature of the electrode sheet directly affects the activity of the oxide layer substance, and affects the battery cycle performance. On the contrary, if the thickness of the oxide layer is too thick, that is, under the same amount of lithium-supplement, the lithium layer rarely contacts with the active substance on the surface of the electrode sheet, under this circumstance, due to the oxide layer of the lithium-supplement layer rarely reacts with the active substance, the winding temperature of the lithium-supplement electrode sheet decreases; at the same time, due to the thickness of the oxide layer is too thick, it will directly affect the efficiency of the oxide layer of the lithium-supplement layer embedded into the active substance, even under the circumstance of liquid injection, due to the ions channels and electron channels between the oxide layer and the active substance layer are too few (the contact area between the oxide layer and the active substance layer is small), and the contact area between the oxide layer and the active substance layer is small, causing the thickness of the transition layer in the lithium-supplement layer is difficult to achieve an optimal window, thereby, affecting the battery cycle performance to a certain extent.

(25) Optionally, the thickness of the oxide layer is 0.5 μm-20 μm, optionally, 0.8 μm-10 μm.

(26) Secondly, a lithium-supplement negative electrode sheet of the second aspect of the present application is described, which includes: a current collector; a diaphragm, located on the current collector and including an active substance, an adhesive, and a conductive agent; and the lithium-supplement layer described in the first aspect of the present application, where, the transition layer in the lithium-supplement layer is connected with the diaphragm.

(27) A third aspect of the present application proposes a lithium-supplement lithium ion battery, which includes: the negative electrode sheet described in the second aspect of the present application, a positive electrode sheet, an electrolyte, and a separator.

(28) The present application has no particular limitation on the shape of the lithium ion battery, which may be cylindrical, square, or any other shapes. FIG. 4 is an example of a lithium ion battery 5 with a square structure.

(29) In some embodiments, lithium ion battery may be assembled into a battery module, and the number of lithium ion batteries contained in the battery module may be multiple, and the specific number may be adjusted according to the application and capacity of the battery module.

(30) FIG. 5 is an example of a battery module 4. Referring to FIG. 5, in the battery module 4, a plurality of lithium ion batteries 5 may be arranged in sequence along the length direction of the battery module 4. Of course, also it is possible to arrange them in any other arbitrary manner. Furthermore, a plurality of lithium ion batteries 5 may be secured by fasteners.

(31) Optionally, battery module 4 may further include a housing with an accommodation space, and a plurality of lithium ion batteries 5 are accommodated in the accommodation space.

(32) In some embodiments, the above battery modules can also be assembled into a battery pack, and the number of battery modules contained in the battery pack can be adjusted according to the application and capacity of the battery pack.

(33) FIG. 6 and FIG. 7 are illustrated as examples of battery packs 1. Referring to FIG. 6 and FIG. 7, the battery pack 1 may include a battery box and a plurality of battery modules 4 that are installed in the battery box. The battery box includes an upper case 2 and a lower case 3, the upper case 2 can be covered on the lower case 3, and forming an enclosed space for accommodating the battery module 4. A plurality of battery modules 4 can be arranged in the battery box in any other arbitrary manner.

(34) A fourth aspect of the present application provides a device, the device includes the lithium ion battery of the third aspect of the present application. The lithium ion battery provides power to the device, and may also serve as an energy storage unit of the device. The device may be, but not limited to, mobile equipment (such as mobile phone, notebook computer, etc.), electric vehicles (such as pure electric vehicle, hybrid electric vehicle, plug-in hybrid electric vehicle, electric bicycle, electric scooter, electric golf balls vehicle, electric truck, etc.), electric train, ship and satellite, energy storage system, etc.

(35) The device may select a lithium ion cell (Cell), a battery module (Module), or a battery pack (Pack) according to its usage requirement.

(36) FIG. 8 is an example of a device. The device is a pure electric vehicle, a hybrid electric vehicle, or a plug-in hybrid electric vehicle, etc. In order to meet the requirement of the device for high power and high energy density of lithium ion battery, a battery pack or a battery module may be used.

(37) As another example, the device may be a mobile phone, a tablet computer, a notebook computer, etc. The device usually requires lightness and thinness, which may use a lithium ion battery as a power.

(38) In order to explain the technical content, structural feature, achieved purpose and effects of the technical solution in detail, the following is a detailed description with reference to specific embodiments and drawings. It should be understood that these embodiments are only used to illustrate the present application and are not intended to limit the scope of the present application.

(39) The battery of examples 1-28 and comparative examples 1-4 are prepared according to the following methods.

(40) (1) Manufacturing Method of the Negative Electrode Sheet Containing the Lithium-Supplement Layer

(41) Referring to FIG. 1, the lithium foil band with a thickness of 5000 μm is rolled by two rolling rollers to obtain ultra-thin lithium foil bands with different thicknesses, and then the ultra-thin lithium foil bands with different thicknesses in accordance with the parameters in Table 1 and the electrode sheet coated with the active substance are rolled by two calendering rollers, and the ultra-thin lithium foil bands with different thicknesses are adhered to the surface of the electrode sheet by rolling, thereby transition layers with different thickness are obtained. Then, uniformly coating the surface of the electrode sheet with ultra-thin lithium foil bands adhered thereto with oxide layer (comparative example 2 without oxide layer) and surface layer (comparative example 1 without surface layer) in sequence according to the parameters shown in Table 1, and weight of the lithium-supplement layer is 10 mg/1540.25 mm.sup.2 single-sided active substance surface, so double-sided active substance surface is 20 mg/1540.25 mm.sup.2.

(42) (2) Manufacturing Method of the Positive Electrode Sheet

(43) Mixing the positive electrode active material LiNi.sub.1/3Co.sub.1/3Mn.sub.1/3O.sub.2, conductive agent Super-P, adhesive PVDF together according to the mass ratio of 94:3:3, adding the solvent NMP, and stirring under the action of a vacuum stirrer until the system is uniform, a positive electrode slurry is obtained; uniformly coating the positive electrode slurry on the two surfaces of the positive electrode current collector aluminum foil, after drying at room temperature, transferred to an oven for further drying, then subjected to cold pressing and slitting, a positive electrode sheet is obtained.

(44) (3) Preparation of the Electrolyte

(45) Mixing ethylene carbonate (EC) and ethyl methyl carbonate (EMC) together at a volume ratio of 3:7 to obtain an organic solvent, and then dissolving the fully dried LiPF.sub.6 in the mixed organic solvent to prepare an electrolyte with a concentration of 1 mol/L.

(46) (4) Preparation of a Separator Film

(47) Selecting the PE/PP/PE three-layer porous polymer film as the separator film.

(48) (5) Preparation of the Lithium Ion Battery

(49) Stacking the above positive electrode sheet, separator film, and negative electrode sheet containing lithium-supplement layer in order, so that the separator film is between the positive and negative electrode sheets and plays a role of isolation, and then winding to obtain a bare cell; placing the bare cell in the outer packaging shell, after drying, injecting the electrolyte, and subjected to vacuum packaging, standing, forming, shaping and other processes, a lithium ion battery is obtained.

(50) Then, the test method of the temperature of the lithium-supplement electrode sheet and the test methods of the internal resistance and cycle performance of the lithium ion battery are illustrated.

(51) (1) Temperature test of electrode sheet, winding the lithium-supplement electrode sheet with a 6-inch reel for 1000 m, inserting a temperature sensing line at the winding position of 500 m to test the temperature of electrode sheet, the temperature measuring instrument is: thermometer: SKF TKDT 10, the temperature specification is ≤60° C.

(52) (2) Battery internal resistance test: that is, AC resistance, AC internal resistance equipment: Itech company IT5100 series battery internal resistance tester, test method: adding a fixed frequency 1 KHz and a fixed current 50 mA on the test cell, sampling the voltage, and calculating the resistance value by the rectifier instrument.

(53) (3) Cycle test: using lithium ion charge and discharge equipment: Xinwei mobile power product special tester (6V4A) repeatedly charges and discharges the battery until the capacity decay rate reaches 80%, the above cell capacity is 4.2 Ah, charge and discharge of the cell repeatedly using 1 C current rate (that is, the current is 4.2 Ah), charging the cell to a voltage of 4.2V at a current rate of 1 C, and then discharging the cell to a voltage of 2.5V at a current rate of 1 C, recording the charge and discharge as one cycle; when the cell capacity decays to 3.36 Ah, stopping the test, and recording the repeated times of charge and discharge, that is, the data of cycle performance of the cell, and the qualified number of cycle times is ≥700 times.

(54) The relevant parameters of the lithium-supplement layers provided by examples 1-28 and comparative examples 1-4 are shown in Table 1, and the performance test results of the lithium ion batteries prepared by examples 1-28 and comparative examples 1-4 are shown in Table 2.

(55) TABLE-US-00001 TABLE 1 relevant parameters of the lithium-supplement layers provided by examples 1-28 and comparative examples 1-4 the the the the thickness thickness thickness thickness surface layer of of of of the content the content surface Lithium transition oxide organic of organic filling of filling layer/ foil/ Transition layer/ oxide layer/ sample material material substance substance μm μm layer μm layer μm example stearic  4% graphene 96% 4 4 Li.sub.2O 1 Li.sub.2O 2 1 acid example stearic 10% graphene 90% 4 4 Li.sub.2O 1 Li.sub.2O 2 2 acid example stearic 20% graphene 80% 4 4 Li.sub.2O 1 Li.sub.2O 2 3 acid example stearic 50% graphene 50% 4 4 Li.sub.2O 1 Li.sub.2O 2 4 acid example stearic 80% graphene 20% 4 4 Li.sub.2O 1 Li.sub.2O 2 5 acid example stearic 97% graphene  3% 4 4 Li.sub.2O 1 Li.sub.2O 2 6 acid example 12- 20% graphene 80% 4 4 Li.sub.2O 1 Li.sub.2O 2 7 Hydroxy- stearic acid example polyglycol 20% graphene 80% 4 4 Li.sub.2O 1 Li.sub.2O 2 8 example phosphate 20% graphene 80% 4 4 Li.sub.2O 1 Li.sub.2O 2 9 example polyisobutyl 20% graphene 80% 4 4 Li.sub.2O 1 Li.sub.2O 2 10 methacrylate example stearic 80% sodium 20% 4 4 Li.sub.2O 1 Li.sub.2O 2 11 acid hydroxide example stearic 80% aluminum 20% 4 4 Li.sub.2O 1 Li.sub.2O 2 12 acid oxide example stearic 80% molybdenum 20% 4 4 Li.sub.2O 1 Li.sub.2O 2 13 acid disulfide example stearic 80% graphene 20% 4 4 Li.sub.2C 1 LiOH 2 14 acid example stearic 80% graphene 20% 4 4 Li.sub.2C 1 Li.sub.3N 2 15 acid example stearic 80% graphene 20% 4 4 Li.sub.2C 1 Li 2 16 acid example stearic 80% graphene 20% 0.1 4 Li.sub.2O 1 Li.sub.2O 2 17 acid example stearic 80% graphene 20% 1 4 Li.sub.2O 1 Li.sub.2O 2 18 acid example stearic 80% graphene 20% 5 4 Li.sub.2O 1 Li.sub.2O 2 19 acid example stearic 80% graphene 20% 8 4 Li.sub.2O 1 Li.sub.2O 2 20 acid example stearic 80% graphene 20% 4 2 Li.sub.2O 0.01 Li.sub.2O 2 21 acid example stearic 80% graphene 20% 4 2.5 Li.sub.2O 0.05 Li.sub.2O 2 22 acid example stearic 80% graphene 20% 4 3 Li.sub.2O 0.7 Li.sub.2O 2 23 acid example stearic 80% graphene 20% 4 2 Li.sub.2O 1 Li.sub.2O 0.5 24 acid example stearic 80% graphene 20% 4 2.5 Li.sub.2O 1 Li.sub.2O 0.8 25 acid example stearic 80% graphene 20% 4 7 Li.sub.2O 1 Li.sub.2O 5 26 acid example stearic 80% graphene 20% 4 12 Li.sub.2O 1 Li.sub.2O 10 27 acid example stearic 80% graphene 20% 4 24 Li.sub.2O 1 Li.sub.2O 20 28 acid comparative / / / / / 4 Li.sub.2O 1 Li.sub.2O 2 example 1 comparative stearic 80% graphene 20% 4 / / / / / example acid 2 comparative stearic 100%  / / 4 4 Li.sub.2O 1 Li.sub.2O 2 example acid 3 comparative / / graphene 100%  4 4 Li.sub.2O 1 Li.sub.2O 2 example 4

(56) TABLE-US-00002 TABLE 2 battery heating temperature, internal resistance and cycle performance test results provided by examples 1-28 and comparative examples 1-4 heating temperature of electrode sheet internal resistance cycle performance sample (° C.) (mOHM) (circle) example 1 45 5.64 700 example 2 43 5.68 725 example 3 41 5.71 730 example 4 41 5.75 730 example 5 39 5.80 725 example 6 37 5.91 710 example 7 40 5.75 735 example 8 41 5.90 720 example 9 42 5.77 725 example 10 40 5.71 740 example 11 40 5.84 715 example 12 39 5.78 725 example 13 39 5.82 730 example 14 38 5.76 740 example 15 39 5.84 715 example 16 41 5.78 725 example 17 44 5.68 720 example 18 43 5.72 740 example 19 41 5.81 720 example 20 36 5.96 705 example 21 41 5.78 720 example 22 40 5.75 730 example 23 38 5.85 710 example 24 45 5.71 705 example 25 44 5.73 715 example 26 42 5.82 725 example 27 38 5.89 705 example 28 34 5.96 700 comparative 101 5.60 600 example 1 comparative 21 5.80 420 example 2 comparative 37 6.10 650 example 3 comparative 45 5.64 660 example 4

(57) From the data in Table 1 and Table 2, it can be seen that there is no surface layer in lithium-supplement layer (comparative example 1), that is, a conventional lithium-supplement layer, which includes a transition layer and an oxide layer. Since there is no surface layer to block the oxidation layer substance in the lithium-supplement layer from continuing to react with the air, the reaction is an exothermic reaction, resulting in production safety problems such as an over high temperature of the lithium-supplement electrode sheet during the winding process, at the same time, the over high temperature of the electrode sheet which will directly affect the activity of the lithium layer, and ultimately affect the electrical performance. There is a surface layer in the lithium-supplement layer (example 5), which forms an isolation layer between lithium-supplement layer and air, at the same time, it will not significantly affect the transmission efficiency of lithium ions; furthermore, due to the winding temperature of the lithium-supplement electrode sheet is controllable, the activity of the lithium-supplement layer can be guaranteed to provide capacity and improve the performance of the lithium ion battery.

(58) Similarly, from the data in Table 1 and Table 2, it can be seen that the lithium-supplement layer only has a surface layer (comparative example 2), that is, there is no transition layer and oxide layer, that is, there is no lithium layer for providing capacity on the surface of the electrode sheet, and cannot provide additional lithium ions during the cycle process, thereby affecting the cycle electrical performance of the lithium ion battery; the phenomenon that the transition layer/oxide layer reacting with air and active substance is not exist, and the winding temperature of the electrode sheet is not increased.

(59) By observing the data of comparative examples 1-4 and examples 1-6 in Table 1 and Table 2, it can be seen that the ratio relationship between the organic material and the filling substance has a certain influence on the battery performance.

(60) When the proportion of organic material in a coating is too small (the proportion of filling substance is too large), for example, the ratio of organic material to filling substance is 0:100 (comparative example 4), this will cause the following adverse effects: a. organic material is too little or there is no organic material, which is a challenge for slurry processing, too much filling substance is more difficult to be completely dissolved/suspended in the organic material, and it is difficult to form a slurry; b. too much filling substance, especially graphite-based filling substance, during charge and discharge process, a part of the lithium ions on the positive electrode will be embedded in the graphite-based filling substance in the surface layer of the lithium-supplement layer, which directly leads to the reduction of lithium ions that can be used for cycle, which ultimately affects the battery performance. When the proportion of organic material of surface layer in the lithium-supplement layer is too high, although it may be helpful for the surface layer to form an isolation layer on the surface of the lithium-supplement layer, thereby lowering the winding temperature of the lithium-supplement electrode sheet, and improving the activity of the lithium layer; however, if the proportion of the organic material is too high and it will cause: a. the isolation layer formed on the surface layer is too dense, which affects the lithium ion transmission efficiency, resulting in an increase of the battery internal resistance and affecting the battery performance; b. the surface layer contains organic material such as alcohols, if the proportion of organic materials is too high, it is easy to react with the electrolyte to form side products, thereby increasing the battery internal resistance and affecting battery performance; c. too little filling substance cannot play a role of restraining the expansion of the active substance during the cycle process, thereby affecting battery performance. When the content of the organic material in the surface layer of the lithium-supplement layer is 10%-97%, it is more conducive to ensure that the coating provides the isolation layer, reducing the winding temperature of the lithium-supplement electrode sheet, and improving the activity of the lithium layer, at the same time, the filling substance can effectively restrain the expansion of the active substance, and ultimately improve the battery performance.

(61) From the data in Table 1 and Table 2, it can be seen that the functions and types of organic materials in the surface layer of the lithium-supplement layer. Example 5, examples 7-10 mainly use alcohols, esters and fatty acids organic materials, the main roles are: as a carrier of the filling substance to form a slurry coated on the surface of the lithium-supplement layer, as film-forming substance of the surface layer of lithium-supplement layer, so that the surface layer can form a film or evenly distributed on the surface of the transition layer and the oxide layer of the lithium-supplement layer.

(62) From the data of example 5 and examples 11-13 in Table 1 and Table 2, it can be seen the function of filling substance in the surface layer of the lithium-supplement layer, the filling substance can be used to improve the deterioration of the cell internal resistance caused by the side reaction between the organic material and the electrolyte; the filling substance can form a network structure or a film-forming structure with the organic material, which can solve the expansion problem of the electrode sheet during the cycle process of the active substance.

(63) From example 5 and examples 14-16 in Table 1 and Table 2, it can be seen that the main function of the oxide layer is: the oxide layer substance in the lithium-supplement layer is used to provide an additional lithium source, after injection, the lithium source can be continuously supplemented during the cycle process to improve the battery cycle performance, the oxide layer substance can provide a part of the substance for forming the transition layer, that is, an layer of inorganic SEI film is additionally formed to improve the battery cycle performance, the oxide layer substance may form a dense (Li.sub.2O) or sparse (Li.sub.3N) isolation layer on the surface of the electrode sheet, to further improve the problem that the winding temperature of electrode sheet of the lithium-supplement layer would be increased due to the reaction between the lithium layer and the air/active substance.

(64) From example 5 and examples 17-20 in Table 1 and Table 2, it can be seen that: the thickness of the coating is thicker, the cell internal resistance is greater, while during the cycle process, as the lithium ion transmission efficiency becomes worse, the cycle performance will be significantly affected. When the thickness of the surface layer of the lithium-supplement layer is in the range of 0.1 μm-15 μm, the surface layer can form an isolation layer between the lithium-supplement layer and the air, at the same time, it will not significantly affect the transmission efficiency of lithium ions, due to the winding temperature of the lithium-supplement electrode sheet is controllable, the activity of the lithium-supplement layer can be guaranteed to provide capacity, and to improve the performance of the lithium ion battery.

(65) From example 5 and examples 17-20 in Table 1 and Table 2, it can be seen that: under the same proportion of the organic material and the filling substance in the surface layer of the lithium-supplement layer: that is, when the proportions of organic material and the filling substance are the same, if the thickness of the surface layer is too small, for example, when the thickness of the surface layer is 0 μm-0.1 μm, the effective isolation layer cannot be formed on the surface of the lithium-supplement layer, resulting in an increase of the reaction area between the lithium layer and the air, which accelerates the reaction, the temperature during the winding process of the lithium-supplement electrode sheet exceeds the standard, causing production safety risks. At the same time, an over high temperature of the electrode sheet will reduce the activity of the lithium layer, a part of lithium layers will form dead lithium under high temperature condition, and cannot be used to provide capacity, resulting in a significant impact on electrical performance and reducing cycle performance.

(66) When the thickness of the surface layer of the lithium-supplement layer is too thick, for example, the thickness of the surface layer is greater than 15 μm, since the thick surface layer can form an isolation layer to the air on the surface of the lithium-supplement layer, so that the winding temperature of the lithium-supplement electrode sheet decreases, however, if the surface layer is too thick, it will directly affect the transmission efficiency of lithium ions, it is obvious to see that: the thickness of the coating is thicker, the cell internal resistance is greater, while during the cycle process, as the lithium ion transmission efficiency becomes worse, the cycle performance will be significantly affected.

(67) When the thickness of the surface layer of the lithium-supplement layer is in the range of 0.1p m-15p m, the surface layer can form an isolation layer between the lithium-supplement layer and the air, at the same time, it will not significantly affect the transmission efficiency of lithium ions, due to the winding temperature of the lithium-supplement electrode sheet is controllable, the activity of the lithium-supplement layer can be guaranteed to provide capacity, and to improve the performance of the lithium ion battery.

(68) From comparative example 2, example 5 and examples 21-23 in Table 1 and Table 2, it can be seen that: the transition layer is too thin (<10 nm), the formed inorganic SEI film is too thin, cannot play a protection role for the expansion of the active substance layer itself, and the improvement of the electrical performance is not obvious, if the transition layer is too thick, it may directly affect the direct transmission efficiency of lithium ions in the positive and negative electrode sheets, further affects the battery performance.

(69) From comparative example 2, example 5 and examples 24-28 in Table 1 and Table 2, it can be seen that: the thickness of the oxide layer is too thin (<0.5 μm), that is, under the same amount of lithium-supplement, the lithium layer is pressed to the thinnest, it can be considered that most of the lithium layer is directly pressed into the active substance layer, under this circumstance, the active substance of the electrode sheet reacts violently with the substance in the lithium-supplement layer, the heating generated is more obvious, and the winding temperature of the electrode sheet increases greatly, and affects the safety of manufacturing; at the same time, the high winding temperature of the electrode sheet directly affects the activity of the oxide layer substance, and affects the battery cycle performance. If the thickness of the oxide layer is too thick (>20 μm), that is, under the same amount of lithium-supplement, the lithium layer rarely contacts with the active substance on the surface of the electrode sheet, under this circumstance, since the oxide layer of the lithium-supplement layer rarely reacts with the active substance, and winding temperature of the lithium-supplement electrode sheet decreases; at the same time, since the thickness of the oxide layer is too thick, it will directly affect the efficiency of the oxide layer of the lithium-supplement layer embedded into the active substance, even under the circumstance of liquid injection, since the ion channels and electron channels between the oxide layer and the active substance layer are too few (the contact area between the oxide layer and the active substance layer is small), thereby affecting the battery cycle performance in a certain extent. If the thickness of oxide layer is too thick, and the contact area between the oxide layer and the active substance layer is small, leading to the thickness of the transition layer in the lithium-supplement layer is difficult to achieve an optimal window, which also affects the battery cycle performance.

(70) In addition, referring to FIG. 2, the present application also provides a schematic diagram of dotted covering lithium-supplement layer, the manufacturing method of the electrode sheet is similar to the manufacturing method of the negative electrode sheet containing lithium-supplementary layer of examples 1-28 and comparative examples 1-4, except that when the surface layer is coated, uniform dot dip coating is used to make the surface layer appear dotted covering on the oxide layer.

(71) Referring to FIG. 3, the figure shows a scanning electron micrograph (SEM) of a lithium-supplement cross section of an electrode sheet after formation of lithium ion cell containing the lithium-supplement layer of the present application. The electron micrograph is the micro-morphology of the electrode sheet that after formation of the lithium ion cell produced in example 22, and it can be seen that, there is a transition layer on the upper surface of the active substance layer, through composition analysis, the main layer of the transition layer is Li.sub.2O; the upper surface of the transition layer is an oxide layer, and the surface layer (organic+inorganic particles) shows dotted covering on the oxide layer; the thickness of the oxide layer is about 2 μm, and the thickness of the surface layer is about 4 μm.

(72) It should be noted that, although the above examples have been described herein, it is not intended to limit the patent protection scope of this application. Therefore, based on the innovative ideas of this application, changes and modifications to the examples described herein, or the equivalent structure or equivalent process transformation made by the description and drawings of this application, directly or indirectly apply the above technical solutions to other related technical fields, all are included in the scope of patent protection of this application.