CN116154176A

CN116154176A - Secondary battery and device

Info

Publication number: CN116154176A
Application number: CN202310429686.5A
Authority: CN
Inventors: 李思远
Original assignee: Weilai Battery Technology Anhui Co ltd
Current assignee: Weilai Battery Technology Anhui Co ltd
Priority date: 2023-04-18
Filing date: 2023-04-18
Publication date: 2023-05-23
Anticipated expiration: 2043-04-18
Also published as: CN116154176B

Abstract

The present application relates to a secondary battery and an apparatus. The secondary battery of the application comprises a positive electrode, a negative electrode and an electrolyte, wherein the electrolyte comprises a fluorine-containing additive and a sulfur-containing additive; the positive electrode comprises a negative electrode active material layer and a solid electrolyte interface film positioned on the surface of the negative electrode active material layer, wherein the solid electrolyte interface film is tested by adopting an X-ray photoelectron spectrometer, the mass percentage of fluorine element in the solid electrolyte interface film is R percent, and the mass percentage of sulfur element is S percent, wherein S is more than or equal to 0.01 and less than or equal to 0.15R and less than or equal to 2. The secondary battery effectively improves the first coulombic efficiency, the cycle performance at high temperature, the storage performance and the safety performance by controlling the contents of sulfur element and fluorine element in the solid electrolyte interface film (SEI film) formed on the surface of the anode active material layer.

Description

Secondary battery and device

Technical Field

The present application relates to the field of energy storage. In particular, the present application relates to a secondary battery and an apparatus.

Background

Because the energy density of the existing commercial lithium ion battery is difficult to exceed 300 Wh/kg due to the restriction of the theoretical specific capacity of the anode and cathode materials, the application of the lithium ion battery in the fields of pure electric vehicles, aerospace, 5G and the like is greatly limited. Therefore, development of a next-generation high specific energy battery system and a high capacity electrode material to meet the development needs of the future society has been urgent.

Silicon has a theoretical specific capacity up to 4200 mAh/g (Li4.4Si) which is more than 10 times that of graphite, and has a moderate electrode potential (0.3V vs Li/Li+) and extremely rich crust reserves, and is considered as one of the most potential negative electrode materials. However, during cycling, significant volume changes occur in the silicon material itself, thereby accelerating mechanical cracking and loss of electrical contact to the silicon electrode and the formation of "dead silicon". In addition, a negative electrode interface passivation film SEI formed on the surface of a silicon material by using an electrolyte commonly used in industry is loose and porous, and continuous decomposition of the electrolyte cannot be prevented, so that the problems of low coulomb efficiency, rapid capacity decay, short cycle life and the like of a battery are caused.

Disclosure of Invention

In view of the shortcomings of the prior art, the present application provides a secondary battery and related apparatus. The secondary battery effectively improves the first coulombic efficiency, the cycle performance at high temperature, the storage performance and the safety performance by controlling the contents of sulfur element and fluorine element in the solid electrolyte interface film (SEI film) formed on the surface of the anode active material layer.

A first aspect of the present application provides a secondary battery comprising a positive electrode, a negative electrode, and an electrolyte, wherein the electrolyte comprises a fluorine-containing additive and a sulfur-containing additive; the anode comprises an anode active material layer and a solid electrolyte interface film positioned on the surface of the anode active material layer, wherein the solid electrolyte interface film is tested by an X-ray photoelectron spectrometer, the mass percentage of fluorine element in the solid electrolyte interface film is R percent, and the mass percentage of sulfur element is S percent, wherein S is more than or equal to 0.01 and less than or equal to 0.15R and less than or equal to 2.

A second aspect of the present application provides an apparatus comprising the secondary battery of the first aspect.

The beneficial effects of this application are: the secondary battery provided by the application has the advantages that the contents of sulfur and fluorine in the solid electrolyte interface film (SEI film) formed on the surface of the anode active material layer are controlled, so that the SEI film is more compact and stable, the electrolyte and the anode active material can be effectively inhibited from being contacted and continuously subjected to side reaction, the electrolyte is consumed, and the cycle life of the secondary battery is prolonged. Meanwhile, sulfur-containing compounds (such as Li2S, lithium alkylsulfinate RSO2Li and the like) and fluorine-containing compounds (such as LiF, lixPOyFz and the like) in the SEI have good synergistic effect, and can effectively relieve the negative effects of low coulomb efficiency, quick electrolyte consumption and the like caused by the volume effect of the silicon negative electrode in the circulation process. Based on the above improvement, the secondary battery of the present application has high first coulombic efficiency while having excellent cycle performance, storage performance, and safety performance at high temperatures.

Detailed Description

For simplicity, this application discloses only a few numerical ranges specifically. However, any lower limit may be combined with any upper limit to form a range not explicitly recited; and any lower limit may be combined with any other lower limit to form a range not explicitly recited, and any upper limit may be combined with any other upper limit to form a range not explicitly recited. Furthermore, each separately disclosed point or individual value may itself be combined as a lower limit or upper limit with any other point or individual value or with other lower limit or upper limit to form a range not explicitly recited.

Unless otherwise indicated, terms used in the present application have well-known meanings commonly understood by those skilled in the art. Unless otherwise indicated, the numerical values of the parameters set forth in this application may be measured by various measurement methods commonly used in the art (e.g., may be tested according to the methods set forth in the examples of this application).

The list of items to which the term "at least one of," "at least one of," or other similar terms are connected may mean any combination of the listed items. For example, if items a and B are listed, the phrase "at least one of a and B" means only a; only B; or A and B. In another example, if items A, B and C are listed, then the phrase "at least one of A, B and C" means only a; or only B; only C; a and B (excluding C); a and C (excluding B); b and C (excluding A); or A, B and C. Item a may comprise a single component or multiple components. Item B may comprise a single component or multiple components. Item C may comprise a single component or multiple components.

The term "C1-C6 alkyl" includes, but is not limited to: methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, cyclobutyl, n-pentyl, isopentyl, neopentyl, cyclopentyl, methylcyclopentyl, n-hexyl, isohexyl, cyclohexyl and the like.

The term "C1-C6 alkylene" includes, but is not limited to: methylene, ethylene, n-propylene, isopropylene, cyclopropylene, n-butylene, isobutylene, sec-butylene, tert-butylene, cyclobutylene, n-pentylene, isopentylene, neopentylene, cyclopentylene, methylcyclopentylene, n-hexylene, isohexylene, cyclohexylene.

The term "C2-C6 alkenylene" includes, but is not limited to: ethenylene, n-propenylene, isopropenylene, n-but-2-enyl, but-3-enyl, n-hex-3-enyl, and the like.

The present application is further described below in conjunction with the detailed description. It should be understood that these specific embodiments are presented by way of example only and are not intended to limit the scope of the present application.

1. Secondary battery

The secondary battery comprises a positive electrode, a negative electrode and an electrolyte, wherein the electrolyte comprises a fluorine-containing additive and a sulfur-containing additive; the anode comprises an anode active material layer and a solid electrolyte interface film positioned on the surface of the anode active material layer, wherein the solid electrolyte interface film is tested by an X-ray photoelectron spectrometer, the mass percentage of fluorine element in the solid electrolyte interface film is R percent, and the mass percentage of sulfur element is S percent, wherein S is more than or equal to 0.01 and less than or equal to 0.15R and less than or equal to 2.

Fluorine element, especially LiF, in the SEI film of the solid electrolyte of the negative electrode can effectively inhibit the reduction decomposition of electrolyte on the surface of the electrode under low voltage, reduce gas production, and sulfur element can improve the high-temperature stability of the SEI film, thereby being beneficial to improving the high-temperature storage performance and the high-temperature cycle performance of the negative electrode; however, since fluorine and sulfur are poor conductors of lithium ions and electrons, their contents are large, which affects the dynamic properties of the electrode and thus the electrochemical properties of the battery. By controlling the contents of sulfur and fluorine in the above range, on one hand, the SEI film is more compact and stable, can effectively inhibit continuous side reaction and consumption of electrolyte due to contact of the electrolyte with the anode active material, further prolongs the cycle life of the secondary battery, and can avoid the problems of pulverization of the anode active material, especially a silicon anode, and gas production due to reduction reaction of carbonate electrolyte at high temperature; on the other hand, the sulfur-containing compound and the fluorine-containing compound in the SEI film have good synergistic effect, so that the dynamic property of lithium ion transmission at an interface can be improved, and the performance of the secondary battery is greatly improved.

In some embodiments, S-0.15R is 0.05, 0.1, 0.3, 0.5, 0.7, 0.9, 1.0, 1.03, 1.05, 1.07, 1.09, 1.1, 1.13, 1.15, 1.17, 1.19, 1.2, 1.23, 1.25, 1.27, 1.29, 1.30, 1.33, 1.35, 1.37, 1.4, 1.43, 1.45, 1.47, 1.5, 1.53, 1.55, 1.57, 1.6, 1.63, 1.65, 1.67, 1.7, 1.73, 1.75, 1.77, or any value therebetween. In some embodiments, 1.ltoreq.S-0.15 R.ltoreq.1.8.

In some embodiments, 3.ltoreq.R.ltoreq.10. In some embodiments, R is 3, 3.5, 4, 4.5, 5, 5.3, 5.5, 5.7, 5.9, 6, 6.3, 6.5, 6.7, 6.9, 7.0, 7.3, 7.5, 7.7, 7.9, 8, 8.3, 8.5, 8.7, 8.9, 9, 9.5, or any value therebetween. In some embodiments, 6.ltoreq.R.ltoreq.10.

In some embodiments, 0.ltoreq.S.ltoreq.5. In some embodiments, S is 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.3, 1.5, 1.7, 2.0, 2.3, 2.5, 3.7, 3.0, 3.5, 4.0, 4.5, or any value therebetween. In some embodiments, 2.ltoreq.S.ltoreq.5.

In some embodiments, the porosity of the negative electrode is T, wherein 0<2 SR-T.ltoreq.20. When the 2SR-T value is too large, the porosity of the positive electrode is correspondingly smaller, the capacity of absorbing electrolyte of the positive electrode is reduced, the electrolyte is difficult to infiltrate, and the polarization of the secondary battery is increased in the circulating process, so that the circulating performance of the secondary battery is affected. When the 2SR-T value is too small, the porosity of the positive electrode is correspondingly too large, the conductivity of the electrode is also reduced, the utilization rate of the secondary battery is reduced, and the electrochemical performance and the energy density of the secondary battery are affected. In some embodiments, 2SR-T is 0.5, 1, 2, 3, 4, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 10.5, 11, 11.5, 12, 12.5, 13, 13.5, 14, 14.5, 15, 16, 17, 18, 19 or any value therebetween. In some embodiments, 5.ltoreq.2 SR-T.ltoreq.15.

In some embodiments, the porosity of the negative electrode is T.ltoreq.T.ltoreq.50. In some embodiments, T is 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49 or any value therebetween. In some embodiments, 30.ltoreq.T.ltoreq.40. In other embodiments, 34.ltoreq.T.ltoreq.38. In the present application, the porosity of the negative electrode can be adjusted according to the selected active material characteristics by means conventional in the art, such as controlling the pole piece rolling pressure, rolling temperature, rolling speed.

In some embodiments, the fluorine-containing additive includes at least one of a fluorocarbonate, a fluorophosphate, a fluorocyclotriphosphazene, a fluoroether, and a fluorine-containing lithium salt. The fluorine-containing additive can improve the composition and structure of the interfacial film to more effectively exert the above effects, thereby further improving the cycle performance and storage performance of the secondary battery.

In some embodiments, the fluorine-containing additive comprises at least one of the fluorocarbonate compounds represented by formula I-1,

in the formula I-1, R2, R3 and R4 are independently selected from hydrogen atom, fluorine atom, C1-C6 alkyl or fluorinated C1-C6 alkyl, at least one of R1, R2, R3 and R4 is fluorine atom or fluorinated C1-C6 alkyl, Q1 is absent or Q1 is selected from C1-C6 alkylene.

In the present application, the fluoro-substituted C1-C6 alkyl group is selected from fluoromethyl, fluoroethyl, fluoro-n-propyl, fluoroisopropyl, fluoro-n-butyl, fluoroisobutyl, fluoro-t-butyl, fluoro-n-pentyl, fluoroisopentyl or fluoro-n-hexyl, wherein fluoro represents that at least one hydrogen atom in the C1-C6 alkyl group is replaced by a fluorine atom. In some embodiments, the fluorinated C1-C6 alkyl is selected from the group consisting of monofluoromethyl, difluoromethyl, trifluoromethyl, monofluoroethyl, difluoroethyl, trifluoroethyl, pentafluoroethyl, or hexafluoroisopropyl.

In some embodiments, in formula I-1, R2, R3, R4 are independently selected from a hydrogen atom, a fluorine atom, a C1-C4 alkyl group, or a fluorinated C1-C4 alkyl group, at least one of R1, R2, R3, R4 is a fluorine atom, and Q1 is absent or selected from a methylene group or an ethylene group.

In some embodiments, in formula I-1, R2, R3, R4 are independently selected from a hydrogen atom, a fluorine atom, a methyl group, an ethyl group, a trifluoromethyl group, a 2, 2-trifluoroethyl group, at least one of R1, R2, R3, R4 is a fluorine atom, Q1 is absent or Q1 is selected from a methylene group or an ethylene group.

In some embodiments, the fluorine-containing additive includes at least one of fluoroethylene carbonate (FEC), difluoroethylene carbonate (DFEC), and trifluoropropylene carbonate (TFPC).

In some embodiments, the fluorine-containing additive comprises at least one of the fluorocarbonate compounds represented by formula I-2,

in the formula I-2, R5 and R6 are the same or different and are independently selected from C1-C6 alkyl or fluorinated C1-C6 alkyl, and at least one of R5 and R6 is fluorinated C1-C6 alkyl.

In some embodiments, in formula I-2, R5 and R6 are the same or different and are independently selected from C1-C4 alkyl or fluorinated C1-C4 alkyl, and at least one of R5 and R6 is fluorinated C1-C4 alkyl.

In some embodiments, in formula I-2, R5 and R6 are the same or different and are independently selected from methyl, ethyl, n-propyl, isopropyl, trifluoromethyl or 2, 2-trifluoroethyl, and at least one of R5 and R6 is trifluoromethyl or 2, 2-trifluoroethyl.

In some embodiments, the fluorine-containing additive includes at least one of 2, 2-trifluoroethyl carbonate (MTFEC) and 2, 2-diethyl trifluorocarbonate (ETFEC).

In some embodiments, the fluorine-containing additive comprises a fluorophosphate compound of formula IIAt least one of the above-mentioned materials,

in the formula II, R7, R8 and R9 are independently selected from C1-C6 alkyl or fluorinated C1-C6 alkyl, and at least one of R7, R8 and R9 is fluorinated C1-C6 alkyl.

In some embodiments, in formula II, R7, R8, R9 are independently selected from C1-C4 alkyl or fluoro C1-C4 alkyl, and at least one of R7, R8, R9 is fluoro C1-C4 alkyl.

In some embodiments, in formula II, R7, R8, R9 are independently selected from methyl, ethyl, n-propyl, isopropyl, trifluoromethyl, or 2, 2-trifluoroethyl, and at least one of R7, R8, R9 is trifluoromethyl or 2, 2-trifluoroethyl.

In some embodiments, the fluorophosphate comprises at least one of tris (2, 2-trifluoroethyl) phosphate (TFEP), bis (2, 2-trifluoroethyl) methylphosphonate, and bis (2, 2-trifluoroethyl) ethylphosphate.

In some embodiments, the fluorine-containing additive comprises at least one of the fluorocyclotriphosphazene compounds represented by formula III,

in the formula III, R10 is selected from C1-C6 alkyl or fluorinated C1-C6 alkyl, R11, R12, R13, R14 and R15 are independently selected from hydrogen atom, fluorine atom, C1-C6 alkyl or fluorinated C1-C6 alkyl, and at least one of R11, R12, R13, R14 and R15 is fluorine atom or fluorinated C1-C6 alkyl.

In some embodiments, in formula III, R10 is selected from C1-C4 alkyl or fluoro C1-C4 alkyl, R11, R12, R13, R14, R15 are independently selected from fluorine atoms, C1-C4 alkyl or fluoro C1-C4 alkyl, and at least one of R11, R12, R13, R14, R15 is a fluorine atom or fluoro C1-C6 alkyl.

In some embodiments, in formula III, R10 is selected from methyl, ethyl, n-propyl, isopropyl, trifluoromethyl, or 2, 2-trifluoroethyl, R11, R12, R13, R14, R15 are independently selected from fluorine atoms or fluorinated C1-C4 alkyl groups, and at least one of R11, R12, R13, R14, R15 is a fluorine atom.

In some embodiments, the fluorine-containing additive includes at least one of methoxy pentafluoroethylene triphosphazene, trifluoromethoxy pentafluoroethylene triphosphazene, ethoxy pentafluoroethylene triphosphazene (PFPN), and 2, 2-trifluoroethoxy pentafluoroethylene Triphosphazene (TFPN).

In some embodiments, the fluorine-containing additive comprises at least one of the fluoroether compounds represented by formula IV,

in formula IV, Q2 is selected from C1-C6 alkylene, Q3 is absent or Q3 is selected from C1-C6 alkylene.

In some embodiments, Q2 is selected from C1-C4 alkylene, Q3 is absent or Q3 is selected from C1-C4 alkylene.

In some embodiments of the present invention, in some embodiments, the fluorine-containing additive comprises 1, 2-tetrafluoroethyl-2, 3-tetrafluoropropyl ether (D2) 1, 2-tetrafluoroethyl-2, 2-trifluoroethyl ether 1, 2-tetrafluoroethyl-2, 2-trifluoroethyl ether.

In some embodiments, the fluorine-containing lithium salt includes at least one of lithium difluorophosphate, lithium fluoride, and lithium bisoxalato difluorophosphate.

In some embodiments, the sulfur-containing additive comprises at least one of a sulfonate, a sulfate, and a sulfite. The sulfur-containing additive can improve the composition and structure of the interfacial film to more effectively exert the above effects, thereby further improving the cycle performance and storage performance of the secondary battery.

In some embodiments, the sulfur-containing additive comprises at least one sulfonate represented by formula V-1,

in formula V-1, Q4 and Q5 are independently selected from C1-C6 alkylene.

In some embodiments, Q4 and Q5 are independently selected from C1-C4 alkylene, such as methylene or ethylene. In some embodiments, the sulfur-containing additive includes at least one of Methylene Methylsulfonate (MMDS) and ethylene ethyldisulfonate.

In some embodiments, the sulfur-containing additive comprises at least one sulfonate represented by formula V-2,

in the formula V-2, R16, R17, R18 and R19 are independently selected from hydrogen atoms or C1-C6 alkyl groups, Q6 is absent or Q6 is selected from C1-C6 alkylene groups and C2-C6 alkenylene groups.

In some embodiments, in formula V-2, R16, R17, R18, R19 are independently selected from a hydrogen atom or a C1-C4 alkyl group, Q6 is absent or Q6 is selected from a C1-C4 alkylene group, a C2-C4 alkenylene group.

In some embodiments, the sulfur-containing additive includes at least one of 1, 3-propane sultone (1, 3-PS), 1-propylene-1, 3-sultone (PST), and 1, 4-butane sultone (1, 4-BS).

In some embodiments, the sulfur-containing additive comprises at least one of the sulfate compounds of formula VI,

in the formula VI, R20, R21, R22 and R23 are independently selected from hydrogen atoms or C1-C6 alkyl groups, Q7 is absent or Q7 is selected from C1-C6 alkylene groups.

In some embodiments, in formula VI, R20, R21, R22, R23 are independently selected from a hydrogen atom or a C1-C4 alkyl group, and Q7 is absent or selected from a C1-C4 alkylene group.

In some embodiments, in formula VI, R20, R21, R22, R23 are independently selected from a hydrogen atom, methyl, ethyl, n-propyl, or isopropyl, and Q7 is absent.

In some embodiments, the sulfur-containing additive includes at least one of vinyl sulfate (DTD), 4-methyl ethylene sulfate (PCS), 4-ethyl ethylene sulfate (PES), 4-propyl ethylene sulfate (PEGLST), and propylene sulfate (TS).

In some embodiments, the sulfur-containing additive comprises at least one of the sulfites of formula VII-1,

formula VII-1, formula VII-1 wherein R24, R25, R26, R27 are independently selected from hydrogen atom or C1-C6 alkyl, Q8 is absent or Q8 is selected from C1-C6 alkylene.

In some embodiments, in formula VII-1, R24, R25, R26, R27 are independently selected from a hydrogen atom or a C1-C4 alkyl group, Q8 is absent or Q8 is selected from a C1-C4 alkylene group.

In some embodiments, the sulfur-containing additive is ethylene sulfite (DTO).

In some embodiments, the sulfur-containing additive comprises at least one of the sulfites of formula VII-2,

formula VII-2, wherein R28 and R29 are independently selected from C1-C6 alkyl.

In some embodiments, in formula VII-2, R28 and R29 are independently selected from C1-C4 alkyl. In some embodiments, the sulfur-containing additive comprises at least one of dimethyl sulfite (DMS) and diethyl sulfite (DES).

In some embodiments, the fluorine-containing additive is present in an amount of 0.5% to 10% by mass based on the mass of the electrolyte. In some embodiments, the fluorine-containing additive is present in an amount of 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, 6%, 7%, 8%, 9% by mass or any value therebetween. In some embodiments, the fluorine-containing additive is present in an amount of 1% to 5% by mass.

In some embodiments, the sulfur-containing additive is present in an amount of 0.05% to 5% by mass. In some embodiments, the sulfur-containing additive is present in an amount of 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1.0%, 1.5%, 2.0%, 2.5%, 3.0%, 3.5%, 4.0%, 4.5% by mass, or any value therebetween. In some embodiments, the sulfur-containing additive is present in an amount of 0.1% to 3% by mass.

In some embodiments, the electrolyte further comprises other additives including at least one of cyclic carbonates containing carbon-carbon double bonds, phosphates containing silane groups, borates containing silane groups, nitriles, and pyridinium propane sulfonate. In some embodiments, the other additive is selected from at least one of Vinylene Carbonate (VC), ethylene carbonate, tris (trimethylsilane) phosphate, tris (trimethylsilane) borate, succinonitrile, adiponitrile, glutaronitrile, and hexanetrinitrile.

In some embodiments, the other additive is present in an amount of 0.05% to 10% by mass based on the mass of the electrolyte. In some embodiments, the other additive is present in an amount of 0.5%, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, 6%, 7%, 8%, 9% by mass or any value therebetween. In some embodiments, the other additive is present in an amount of 0.1% to 5% by mass.

In some embodiments, the electrolyte further comprises an electrolyte lithium salt selected from at least one of lithium hexafluorophosphate (LiPF 6), lithium tetrafluoroborate (LiBF 4), lithium trifluorosulfonyl (LiTf), lithium bis (fluorosulfonyl) imide (LiFSI), (trifluoromethylsulfonyl) (perfluorobutylsulfonyl) imide (LiFNFSI), lithium bis (trifluoromethylsulfonyl) imide (LiTFSI), lithium bis (pentafluoroethanesulfonate) imide (LiBETI), lithium bis (oxalato) borate (LiBOB), lithium bis (fluoromalonic acid) borate (LiBFMB), lithium 4, 5-dicyano-2- (trifluoromethyl) imidazole) (liti), and lithium difluorooxalato borate (lifdiob).

In some embodiments, the electrolyte further comprises a solvent. In some embodiments, the solvent comprises at least one of a chain carbonate, a cyclic carbonate, and a carboxylate.

In some embodiments, the chain carbonate is selected from at least one of dimethyl carbonate, diethyl carbonate, dipropyl carbonate, methylethyl carbonate, methylpropyl carbonate, ethylpropyl carbonate, and fluoro chain carbonate. In some embodiments, the cyclic carbonate comprises at least one of ethylene carbonate, propylene carbonate, and butylene carbonate. In some embodiments, the carboxylic acid ester is selected from at least one of methyl formate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate, gamma-butyrolactone, and a fluorocarboxylic acid ester.

In some embodiments, the anode active material layer includes an anode active material including a silicon-based material, or a mixture of a silicon-based material and at least one material selected from a carbon-based material, a tin-based material, a phosphorus-based material, and metallic lithium.

In some embodiments, the silicon-based material includes at least one of silicon, a silicon alloy, a silicon oxygen compound, and a silicon carbon compound. In some embodiments, the carbon-based material comprises at least one of graphite, soft carbon, hard carbon, carbon nanotubes, and graphene. In some embodiments, the tin-based material includes at least one of tin, tin oxide, and tin alloy. In some embodiments, the phosphorus-based material includes phosphorus and/or a phosphorus complex.

In some embodiments, the mass content z% of the silicon-based material, based on the mass of the anode active material, satisfies: z is more than or equal to 10 and less than or equal to 100. In some embodiments, z is 11, 13, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or any value therebetween.

In some embodiments, the anode active material layer further includes a binder and a conductive agent. In some embodiments, the binder includes, but is not limited to: polyvinyl alcohol, hydroxypropyl cellulose, diacetyl cellulose, polyvinyl chloride, carboxylated polyvinyl chloride, polyvinyl fluoride, an ethyleneoxy-containing polymer, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, styrene-butadiene rubber, acrylated styrene-butadiene rubber, epoxy resin, nylon, or the like.

In some embodiments, the conductive agent includes, but is not limited to: carbon-based materials, metal-based materials, conductive polymers, and mixtures thereof. In some embodiments, the carbon-based material is selected from natural graphite, synthetic graphite, carbon black, acetylene black, ketjen black, carbon fiber, or any combination thereof. In some embodiments, the metal-based material is selected from metal powder, metal fiber, copper, nickel, aluminum, or silver. In some embodiments, the conductive polymer is a polyphenylene derivative.

In some embodiments, the negative electrode further comprises a negative electrode current collector comprising: copper foil, nickel foil, stainless steel foil, titanium foil, nickel foam, copper foam, a polymer substrate coated with a conductive metal, or any combination thereof.

In some embodiments, the positive electrode includes a positive electrode active material layer including a positive electrode active material including at least one of a nickel-cobalt-based ternary material and a phosphate-based material.

In some embodiments, the nickel-cobalt ternary material includes at least one of LiNimConA (1-m-n) O2 materials, A is selected from at least one of manganese, aluminum, magnesium, chromium, calcium, zirconium, molybdenum, silver, or niobium, 0.5.ltoreq.m.ltoreq.1, 0.ltoreq.n.ltoreq.0.5, and m+n.ltoreq.1.

In some embodiments, m is 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, or a range consisting of any two of these values. In some embodiments, n is 0.05, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, or a range consisting of any two of these values.

In some embodiments, the nickel cobalt-based ternary material includes at least one of NCA, NCM111, NCM523, NCM622, NCM811, ni90, ni92, or Ni 95.

In some embodiments, the phosphate-based material includes at least one of LiMnkB (1-k) PO4, wherein 0.ltoreq.k.ltoreq.1, and the B element is selected from at least one of iron, cobalt, magnesium, calcium, zinc, chromium, or lead. In some embodiments, k is 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, or a range of any two of these values. In some embodiments, the phosphate-based material includes at least one of lithium iron phosphate, limn0.6fe0.4po4, or limn0.8fe0.2po4.

In some embodiments, the positive electrode active material includes at least one of lithium nickel oxide, lithium nickel cobalt aluminum oxide, lithium nickel cobalt manganese oxide, lithium nickel manganese cobalt magnesium oxide, lithium manganese oxide, lithium nickel manganese oxide, lithium iron phosphate, and lithium manganese iron phosphate.

In some embodiments, the positive electrode active material layer further includes a binder, and optionally includes a conductive material. The binder enhances the bonding of the positive electrode active material particles to each other and also enhances the bonding of the positive electrode active material to the current collector.

In some embodiments, the binder includes, but is not limited to: polyvinyl alcohol, hydroxypropyl cellulose, diacetyl cellulose, polyvinyl chloride, carboxylated polyvinyl chloride, polyvinyl fluoride, an ethyleneoxy-containing polymer, polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, styrene-butadiene rubber, acrylated styrene-butadiene rubber, epoxy resin, nylon, or the like.

In some embodiments, the conductive material includes, but is not limited to: carbon-based materials, metal-based materials, conductive polymers, and mixtures thereof. In some embodiments, the carbon-based material is selected from natural graphite, synthetic graphite, carbon black, acetylene black, ketjen black, carbon fiber, or any combination thereof. In some embodiments, the metal-based material is selected from metal powder, metal fiber, copper, nickel, aluminum, or silver. In some embodiments, the conductive polymer is a polyphenylene derivative.

In some embodiments, the positive electrode further includes a positive electrode current collector, which may be a metal foil or a composite current collector. For example, aluminum foil may be used. The composite current collector may be formed by forming a metal material (copper, copper alloy, nickel alloy, titanium alloy, silver alloy, or the like) on a polymer substrate.

In some embodiments, a separator is provided between the positive and negative electrodes to prevent shorting. The materials and shape of the release film that can be used in the embodiments of the present application are not particularly limited, and can be any of the techniques disclosed in the prior art. In some embodiments, the separator comprises a polymer or inorganic, etc., formed from a material that is stable to the electrolyte of the present application.

For example, the release film may include a substrate layer and a surface treatment layer. The substrate layer is a non-woven fabric, a film or a composite film with a porous structure, and the material of the substrate layer comprises at least one of polyethylene, polypropylene, polyethylene terephthalate or polyimide. Specifically, a polypropylene porous membrane, a polyethylene porous membrane, a polypropylene nonwoven fabric, a polyethylene nonwoven fabric or a polypropylene-polyethylene-polypropylene porous composite membrane can be selected.

The surface treatment layer is provided on at least one surface of the base material layer, and the surface treatment layer may be a polymer layer or an inorganic layer, or may be a layer formed by mixing a polymer and an inorganic substance.

The inorganic layer includes inorganic particles including at least one of aluminum oxide, silicon oxide, magnesium oxide, titanium oxide, hafnium oxide, tin oxide, cerium oxide, nickel oxide, zinc oxide, calcium oxide, zirconium oxide, yttrium oxide, silicon carbide, boehmite, aluminum hydroxide, magnesium hydroxide, calcium hydroxide, or barium sulfate, and a binder. The binder comprises at least one of polyvinylidene fluoride, copolymer of vinylidene fluoride-hexafluoropropylene, polyamide, polyacrylonitrile, polyacrylate, polyacrylic acid, polyacrylate, polyvinylpyrrolidone, polyvinyl ether, polymethyl methacrylate, polytetrafluoroethylene or polyhexafluoropropylene.

The polymer layer contains a polymer, and the material of the polymer comprises at least one of polyamide, polyacrylonitrile, acrylic polymer, polyacrylic acid, polyacrylate, polyvinylpyrrolidone, polyvinyl ether, polyvinylidene fluoride or poly (vinylidene fluoride-hexafluoropropylene).

In some embodiments, the method of manufacturing the secondary battery includes providing an electrode assembly, injecting a liquid, packaging, and forming. In some embodiments, the temperature of the formation is 40 ℃ to 50 ℃, e.g., 41 ℃, 42 ℃, 43 ℃, 44 ℃, 45 ℃, 46 ℃, 47 ℃, 48 ℃, or 49 ℃.

In some embodiments, the forming comprises: charging to 4.25V at a current of 0.05C under a condition of a temperature of 40-50 deg.C, for example 45 deg.C, and a pressure of 150-250 kgf, for example 210kgf, standing for 60 min, then charging to 4.25V at 0.1C, and then discharging to 3.0V at 0.2C.

In some embodiments, the secondary battery is a lithium secondary battery or a sodium secondary battery. In some embodiments, lithium secondary batteries include, but are not limited to: lithium metal secondary batteries, lithium ion secondary batteries, lithium polymer secondary batteries, or lithium ion polymer secondary batteries.

In some embodiments, the secondary battery may include an outer package, which may be a hard shell, such as a hard plastic shell, an aluminum shell, a steel shell, or the like. The exterior package of the secondary battery may also be a pouch type pouch, for example. The soft bag can be made of one or more of polypropylene (PP), polybutylene terephthalate (PBT), polybutylene succinate (PBS), etc.

In some embodiments, the shape of the secondary battery is not particularly limited, and may be cylindrical, square, or any other shape.

In some embodiments, the present application also provides a battery module. The battery module includes the secondary battery described above. The battery module of the present application employs the above-described secondary battery, and thus has at least the same advantages as the secondary battery. The number of secondary batteries contained in the battery module of the present application may be plural, and the specific number may be adjusted according to the application and capacity of the battery module.

In some embodiments, the present application also provides a battery pack including the above battery module. The number of battery modules included in the battery pack may be adjusted according to the application and capacity of the battery pack.

2. Device and method for controlling the same

The present application also provides an apparatus comprising at least one of the above secondary battery, battery module or battery pack.

In some embodiments, the apparatus includes, but is not limited to: electric vehicles, hybrid electric vehicles, plug-in hybrid electric vehicles, electric storage systems, and the like. In order to meet the high power and high energy density requirements of the device for the secondary battery, a battery pack or a battery module may be employed.

In other embodiments, the device may be a cell phone, tablet, notebook, or the like. The device is generally required to be light and thin, and a secondary battery can be used as a power source.

Examples and comparative examples

Example 1

The preparation method of the positive electrode comprises the following steps: the positive electrode active material LiNi0.9Co0.05Mn0.05O2, the conductive agent carbon nano tube/acetylene black and the binder polyvinylidene fluoride PVDF are mixed according to the weight ratio of LiNi0.9Co0.05Mn0.05O2: CNT/Super-P: pvdf=95: 2.0/1.0: and 2, fully homogenizing in an N-methyl pyrrolidone NMP solvent system, coating on a 12 mu m thick aluminum-coated current collector, and drying and rolling to obtain the positive electrode plate.

The preparation method of the negative electrode comprises the following steps: silicon (SiOx, x is more than or equal to 0.5 and less than or equal to 1.5) -graphite compound, conductive agent acetylene black, binder styrene butadiene rubber SBR, thickener sodium carboxymethyl cellulose CMCNa and polyacrylic acid PAA according to the weight ratio of 96:2:1.5:1: and 0.5, fully homogenizing in deionized water, coating the surface of an 8-mu m thick copper current collector, and drying, rolling and slitting to obtain the negative electrode plate, wherein the porosity of the negative electrode plate is 36.3%.

A diaphragm: adopts a PP/PE/PP three-layer composite diaphragm.

Preparing an electrolyte: lithium salt LiPF6 and solvent EC/DEC/emc=25/20/55 were uniformly mixed in a glove box filled with argon (H2O < 0.1ppm, O2 < 0.1 ppm) in a certain ratio to prepare a solution of 1M, and finally the sulfur-containing compound additive (0.5 wt% based on the total mass of the electrolyte) and the fluorine-containing compound additive (2.0 wt% based on the total mass of the electrolyte) in table 1 were added and uniformly stirred to obtain the lithium ion battery electrolyte of example 1.

Preparation of a lithium ion battery: sequentially stacking the prepared positive pole piece, the diaphragm and the negative pole piece, enabling the diaphragm to be positioned between the positive pole piece and the negative pole piece, and winding to obtain a bare cell; the bare cell is placed in an aluminum plastic film outer package, the prepared lithium ion battery electrolyte is injected after the bare cell is fully dried, the battery is placed at 45 ℃ for 48 hours and is formed by high-temperature clamping (the formation condition is that the temperature is 45 ℃, the pressure is 210kgf, the current is charged to 4.25V for 60 minutes at 0.05C, then the current is charged to 4.25V at 0.1C, then the current is discharged to 3.0V at 0.2C, and the process is repeated for three times), and after secondary sealing, the conventional capacity division is carried out.

Examples 2 to 12 and comparative examples 1 to 9

Examples 2 to 12 and comparative examples 1 to 19 were carried out by adjusting the kinds and contents of additives in the electrolyte, formation conditions, porosity of the negative electrode sheet (wherein the porosity is achieved by adjusting the negative electrode roll pressing load during the preparation), and the like on the basis of example 1, and specific adjustment measures and detailed data are shown in table 1.

TABLE 1

Test method

1. Pole piece porosity determination

The porosity is measured by a mercury porosimeter, and is specifically as follows: the dried pole piece samples were slit into strips of a certain size and the apparent volume of the pole piece coating was determined using a ten-thousandth ruler, apparent volume = sample coating thickness x sample length x sample width. The pole piece is then vacuum degassed and wound in a sample cell, the sample volume must be ensured to be 40-70% of the effective volume of the sample tube, so as to ensure measurement accuracy, and then the pore volume of the sample, i.e. the volume of mercury pressed into the sample, is measured using a mercury porosimeter, then the porosity = pore volume/apparent volume.

2. Cycle capacity retention test

And (3) charging the lithium ion battery to 4.25V under the constant current and constant pressure of 1C at 25 ℃, and discharging to 2.5V under the constant current and constant pressure of 1C. After 500 cycles of charge and discharge, the capacity retention after 500 cycles at 25℃was calculated according to the following formula: the discharge capacity after 500 th cycle/the discharge capacity after first cycle is multiplied by 100%.

And (3) charging the lithium ion battery to 4.25V under the constant current and constant pressure of 1C at 45 ℃, and discharging to 2.5V under the constant current and constant pressure of 1C. After 400 cycles of charge and discharge, the capacity retention after 400 cycles at 45℃was calculated according to the following formula: the discharge capacity after 400 th cycle/the discharge capacity after first cycle is multiplied by 100%.

And (3) charging the lithium ion battery to 4.25V under the constant current and constant pressure of 1C at 60 ℃, and discharging to 2.5V under the constant current and constant pressure of 1C. After 200 cycles of charge and discharge, the capacity retention after the 200 th cycle at 60℃was calculated according to the following formula: the discharge capacity after the 200 th cycle/the discharge capacity after the first cycle is multiplied by 100%.

Storage thickness Change Rate at 3.45 ℃

The cell was discharged to 3.0V at 25 ℃ at 0.5C, charged to 0.05C at constant voltage at 0.5C to 4.45V, and measured using a PPG pouch cell thickness gauge, at which time the thickness of the cell was noted as a. The battery was placed in an oven and stored for 30 days at a constant voltage of 4.45V at 45 ℃ for 30 days, the subsequent record after 30 days of testing was b, the calculation formula for the thickness expansion ratio: (b-a)/a.times.100%.

4. First coulombic efficiency test

The prepared lithium ion secondary battery was charged to 4.2V at a constant current of 1C rate at 25C, then charged at a constant voltage until the current was less than 0.05C, and the initial charge capacity was recorded. After standing for 5 minutes, the initial discharge capacity was again recorded by discharging to 2.5V at 1C magnification. First coulombic efficiency performance test of lithium ion secondary battery = initial discharge capacity/initial charge capacity x 100%.

5. XPS test

Discharging the lithium ion battery to 2.5V under the current of 0.1C, and detaching the lithium ion battery in a glove box filled with argon to obtain the electrode plate. Cutting the obtained electrode plate into a test sample with the size of 8 mm multiplied by 8 mm, soaking and cleaning for half an hour by using a low-boiling point dimethyl carbonate DMC solvent, sticking the test sample on a sample table of XPS after the test sample is completely dried, enabling the surface of the negative electrode active material layer, which is far away from a current collector, to face upwards, and measuring under the condition of not being exposed to the atmosphere. The specific test conditions and steps are as follows:

single crystal spectral alkα radiation was used, as for the X-ray points, 1000X 1750 μm ellipse forms with outputs of 10 KV and 22 mA were used, 284.8eV was used for neutral carbon C1s, and as for data processing such as peak differentiation, 3-point smoothing, peak area measurement, background subtraction and peak synthesis were used to calculate atoms for each component.

Test results

TABLE 2

While certain exemplary embodiments of the present application have been illustrated and described, the present application is not limited to the disclosed embodiments. Rather, one of ordinary skill in the art will recognize that certain modifications and changes may be made to the described embodiments without departing from the spirit and scope of the present application, as described in the appended claims.

Claims

1. A secondary battery includes a positive electrode, a negative electrode, and an electrolyte, wherein,

the electrolyte comprises a fluorine-containing additive and a sulfur-containing additive;

the anode comprises an anode active material layer and a solid electrolyte interface film positioned on the surface of the anode active material layer, wherein the solid electrolyte interface film is tested by an X-ray photoelectron spectrometer, the mass percentage of fluorine element in the solid electrolyte interface film is R percent, and the mass percentage of sulfur element is S percent, wherein S is more than or equal to 0.01 and less than or equal to 0.15R and less than or equal to 2.

2. The secondary battery according to claim 1, wherein 1.ltoreq.S-0.15 R.ltoreq.1.8.

3. The secondary battery according to claim 1 or 2, wherein 3.ltoreq.r.ltoreq.10, and/or 0.ltoreq.s.ltoreq.5.

4. The secondary battery according to claim 1 or 2, wherein 6.ltoreq.r.ltoreq.10, and/or 2.ltoreq.s.ltoreq.5.

5. The secondary battery according to claim 1 or 2, wherein the porosity of the negative electrode is t%, wherein 0<2sr-T is equal to or less than 20.

6. The secondary battery according to claim 5, wherein 20.ltoreq.T.ltoreq.50.

7. The secondary battery according to claim 6, wherein 30.ltoreq.T.ltoreq.40.

8. The secondary battery according to claim 1 or 2, wherein the fluorine-containing additive includes at least one of a fluorocarbonate, a fluorophosphate, a fluorocyclotriphosphazene, a fluoroether, and a fluorine-containing lithium salt.

9. The secondary battery according to claim 8, wherein the fluorine-containing additive satisfies at least one of the following conditions (i) to (iv):

(i) The fluorine-containing additive comprises at least one of compounds shown in a formula I-1 and a formula I-2,

formula I-1, ">

Formula I-2

In the formula I-1, R ₁ 、R ₂ 、R ₃ 、R ₄ Independently selected from hydrogen atom, fluorine atom, C1-C6 alkyl or fluoro C1-C6 alkyl, R ₁ 、R ₂ 、R ₃ 、R ₄ At least one of them being a fluorine atom or a fluorinated C1-C6 alkyl group, Q ₁ Absence or Q ₁ Selected from C1-C6 alkylene; in the formula I-2, R ₅ And R is ₆ Identical or different, are independently selected from C1-C6 alkyl or fluoro C1-C6 alkyl, and R ₅ And R is ₆ At least one of them is a fluorinated C1-C6 alkyl group;

(ii) The fluorophosphate comprises at least one of the compounds represented by formula II,

II (II)

In formula II, R ₇ 、R ₈ 、R ₉ Independently selected from C1-C6 alkyl or fluorineSubstituted by C1-C6 alkyl, and R ₇ 、R ₈ 、R ₉ At least one of them is a fluorinated C1-C6 alkyl group;

(iii) The fluorocyclotriphosphazene comprises at least one of the compounds of formula III,

formula III

In formula III, R ₁₀ Selected from C1-C6 alkyl or fluoro C1-C6 alkyl, R ₁₁ 、R ₁₂ 、R ₁₃ 、R ₁₄ 、R ₁₅ Independently selected from hydrogen atom, fluorine atom, C1-C6 alkyl or fluorinated C1-C6 alkyl, and R ₁₁ 、R ₁₂ 、R ₁₃ 、R ₁₄ 、R ₁₅ At least one of them is a fluorine atom or a fluorinated C1-C6 alkyl group;

(iv) The fluoroether comprises at least one of the compounds represented by formula IV,

IV (IV)

In formula IV, Q ₂ Selected from C1-C6 alkylene, Q ₃ Absence or Q ₃ Selected from C1-C6 alkylene;

(v) The fluorine-containing lithium salt comprises at least one of lithium difluorophosphate, lithium fluoride and lithium difluorophosphate bisoxalate.

10. The secondary battery according to claim 8, wherein the fluorine-containing additive satisfies at least one of the following conditions (vi) to (ix):

(vi) The fluorocarbonate comprises at least one of fluoroethylene carbonate, difluoroethylene carbonate, propylene trifluorocarbonate, 2-trifluoroethyl carbonate and 2, 2-diethyl trifluorocarbonate;

(vii) The fluorophosphate includes at least one of tris (2, 2-trifluoroethyl) phosphate, bis (2, 2-trifluoroethyl) methylphosphonate and bis (2, 2-trifluoroethyl) ethylphosphonate;

(viii) The fluorocyclotriphosphazene comprises at least one of methoxy pentafluoroetriphosphazene, trifluoromethoxy pentafluoroetriphosphazene, ethoxy pentafluoroetriphosphazene and 2, 2-trifluoroethoxy pentafluoroetriphosphazene;

(ix) The fluoroether comprises 1, 2-tetrafluoroethyl-2, 3-tetrafluoropropyl ether 1, 2-tetrafluoroethyl-2, 2-trifluoroethyl ether 1, 2-tetrafluoroethyl-2, 3-tetrafluoropropyl ether and at least one of 1, 3-hexafluoroisopropyl methyl ether.

11. The secondary battery according to claim 1 or 2, wherein the sulfur-containing additive includes at least one of a sulfonate, a sulfate, and a sulfite.

12. The secondary battery according to claim 11, wherein the sulfur-containing additive satisfies at least one of the following conditions (x) to (xii):

(x) The sulfonate comprises at least one of formula V-1 and formula V-2,

formula V-1, -, I>

V-2

In formula V-1, Q ₄ And Q ₅ Independently selected from C1-C6 alkylene, of formula V-2, R ₁₆ 、R ₁₇ 、R ₁₈ 、R ₁₉ Independently selected from hydrogen atom or C1-C6 alkyl, Q ₆ Absence or Q ₆ Selected from C1-C6 alkylene, C2-C6 alkenylene;

(xi) The sulfate comprises at least one of the compounds of formula VI,

VI (VI)

In formula VI, R ₂₀ 、R ₂₁ 、R ₂₂ 、R ₂₃ Independently selected from hydrogen atom or C1-C6 alkyl, Q ₇ Absence or Q ₇ Selected from C1-C6 alkylene;

(xii) The sulfite comprises at least one of the formulas VII-1 and VII-2,

formula VII-1, -/->

Formula VII-2

In formula VII-1, R ₂₄ 、R ₂₅ 、R ₂₆ 、R ₂₇ Independently selected from hydrogen atom or C1-C6 alkyl, Q ₈ Absence or Q ₈ Selected from C1-C6 alkylene, of formula VII-2, R ₂₈ And R is ₂₉ Independently selected from C1-C6 alkyl.

13. The secondary battery according to claim 11, wherein the sulfur-containing additive satisfies at least one of the following conditions (xiii) to (xv):

(xiii) The sulfonate comprises at least one of methyl methylene disulfonate, ethyl ethylene disulfonate, methyl propylene disulfonate, 1, 3-propane sultone, 1-propylene-1, 3-sultone and 1, 4-butane sultone;

(xiv) The sulfate comprises at least one of vinyl sulfate, 4-methyl ethylene sulfate, 4-ethyl ethylene sulfate, 4-propyl ethylene sulfate and propylene sulfate;

(xv) The sulfite includes at least one of ethylene sulfite, dimethyl sulfite and diethyl sulfite.

14. The secondary battery according to claim 1 or 2, wherein the fluorine-containing additive is contained in an amount of 0.5% to 10% by mass based on the mass of the electrolyte; and/or

The mass content of the sulfur-containing additive is 0.05% -5%.

15. The secondary battery according to claim 14, wherein the fluorine-containing additive is contained in an amount of 1% to 5% by mass based on the mass of the electrolyte; and/or

The mass content of the sulfur-containing additive is 0.1% -3%.

16. The secondary battery according to claim 1 or 2, wherein the electrolyte further comprises other additives including at least one of cyclic carbonates containing carbon-carbon double bonds, phosphates containing silane groups, borates containing silane groups, nitriles and pyridinium propane sulfonate,

The mass content of the other additives is 0.05% -10% based on the mass of the electrolyte.

17. The secondary battery according to claim 16, wherein the other additive is selected from at least one of vinylene carbonate, ethylene carbonate, tris (trimethylsilane) phosphate, tris (trimethylsilane) borate, succinonitrile, adiponitrile, glutaronitrile and hexanetrinitrile; and/or

The mass content of the other additives is 0.1% -5% based on the mass of the electrolyte.

18. The secondary battery according to claim 1 or 2, wherein the anode includes an anode active material layer including an anode active material including a silicon-based material, or a mixture of a silicon-based material and at least one material selected from a carbon-based material, a tin-based material, a phosphorus-based material, and metallic lithium; and/or

The positive electrode includes a positive electrode active material layer including a positive electrode active material including at least one of a nickel-cobalt-based ternary material and a phosphate-based material.

19. The secondary battery of claim 18, wherein the silicon-based material comprises at least one of silicon, a silicon alloy, a silicon oxygen compound, and a silicon carbon compound, the carbon-based material comprises at least one of graphite, soft carbon, hard carbon, carbon nanotubes, and graphene, the tin-based material comprises at least one of tin, tin oxide, and a tin alloy, and the phosphorus-based material comprises phosphorus and/or a phosphorus-carbon composite; and/or

The nickel-cobalt ternary material comprises LiNi _m Co _n A _(1-m-n) O ₂ At least one of the materials, A is selected from at least one of manganese, aluminum, magnesium, chromium, calcium, zirconium, molybdenum, silver or niobium, m is more than or equal to 0.5 and less than or equal to 1, n is more than or equal to 0 and less than or equal to 0.5, and m+n is more than or equal to 1; and/or

The phosphate-based material comprises LiMn _k B _(1-k) PO ₄ Wherein k is more than or equal to 0 and less than or equal to 1, and the B element is selected from at least one of iron, cobalt, magnesium, calcium, zinc, chromium or lead.

20. The secondary battery according to claim 18, wherein the positive electrode active material includes at least one of lithium nickel oxide, lithium nickel cobalt aluminum oxide, lithium nickel cobalt manganese oxide, lithium nickel manganese cobalt magnesium oxide, lithium manganese oxide, lithium nickel manganese oxide, lithium iron phosphate, and lithium manganese iron phosphate; and/or

Based on the mass of the anode active material, the mass content z% of the silicon-based material satisfies: z is more than or equal to 10 and less than or equal to 100.

21. An apparatus comprising the secondary battery according to any one of claims 1 to 20.