WO2021083074A1 - 一种固液电池 - Google Patents

一种固液电池 Download PDF

Info

Publication number
WO2021083074A1
WO2021083074A1 PCT/CN2020/123624 CN2020123624W WO2021083074A1 WO 2021083074 A1 WO2021083074 A1 WO 2021083074A1 CN 2020123624 W CN2020123624 W CN 2020123624W WO 2021083074 A1 WO2021083074 A1 WO 2021083074A1
Authority
WO
WIPO (PCT)
Prior art keywords
solid
electrolyte
positive electrode
negative electrode
liquid battery
Prior art date
Application number
PCT/CN2020/123624
Other languages
English (en)
French (fr)
Inventor
许晓雄
崔言明
张秩华
黄园桥
Original Assignee
浙江锋锂新能源科技有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 浙江锋锂新能源科技有限公司 filed Critical 浙江锋锂新能源科技有限公司
Priority to JP2021555870A priority Critical patent/JP7418464B2/ja
Priority to CA3133860A priority patent/CA3133860C/en
Priority to US17/604,528 priority patent/US20220200047A1/en
Priority to AU2020377021A priority patent/AU2020377021B2/en
Priority to EP20882107.4A priority patent/EP3930066A1/en
Priority to KR1020217028781A priority patent/KR20210129098A/ko
Publication of WO2021083074A1 publication Critical patent/WO2021083074A1/zh

Links

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562—Solid materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0565—Polymeric materials, e.g. gel-type or solid-type
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0567—Liquid materials characterised by the additives
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0568—Liquid materials characterised by the solutes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0569—Liquid materials characterised by the solvents
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/134—Electrodes based on metals, Si or alloys
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/381—Alkaline or alkaline earth metals elements
    • H01M4/382—Lithium
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/027—Negative electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/028—Positive electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
    • H01M2300/0028—Organic electrolyte characterised by the solvent
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
    • H01M2300/0045—Room temperature molten salts comprising at least one organic ion
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0048—Molten electrolytes used at high temperature
    • H01M2300/0051—Carbonates
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0068—Solid electrolytes inorganic
    • H01M2300/0071—Oxides
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0085—Immobilising or gelification of electrolyte
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the invention relates to the field of lithium batteries, in particular to a new type of solid-liquid battery.
  • ether electrolytes There are three types of electrolytes currently used in batteries, ether electrolytes, ester electrolytes and solid electrolytes.
  • the cycle performance of lithium negative electrodes in ether electrolytes is much higher than that of ester electrolytes and lithium metal in ether electrolytes.
  • the coulombic efficiency can be as high as 99.9%, which is very beneficial to the cycle life of lithium metal as a negative electrode.
  • the positive electrode In order to obtain high energy density, the positive electrode needs to be charged to 4.2V or even above 5V.
  • the voltage resistance of the ether electrolyte is poor, generally only stable at about 4.0V (vsLi+/Li), and severe decomposition will occur at higher voltages. , Resulting in battery flatulence, etc. affect the cycle performance of the full battery.
  • the ester electrolyte is used, although the withstand voltage is relatively high, the coulombic efficiency for lithium metal is mostly below 60%, and the cycle life of lithium metal is severely limited. If all solid electrolytes are used, the high strength of the solid electrolyte can effectively prevent the dendritic short circuit of the lithium metal negative electrode and improve the safety of the battery. On the one hand, the higher density of the solid electrolyte will reduce the energy density of the battery. The poor compatibility of the solid-solid interface of the positive electrode will increase the complexity of the battery process.
  • the purpose of the present invention is to provide a new type of lithium metal negative high-voltage positive solid-liquid battery, which not only has high coulombic efficiency, but also has good cycle performance.
  • a solid-liquid battery comprising a positive electrode and a negative electrode, the negative electrode is made of lithium metal, a solid electrolyte is arranged between the positive electrode and the negative electrode, and the An ester electrolyte is filled between the solid electrolyte and the positive electrode, and an ether electrolyte is filled between the solid electrolyte and the negative electrode.
  • the ether electrolyte is filled between the lithium metal and the solid electrolyte, which is beneficial to improve the cycle life of the lithium metal;
  • the ester electrolyte is filled between the positive electrode and the solid electrolyte. It has high voltage resistance, which helps to increase the choice of positive electrode, especially the material with high potential voltage can be used as the positive electrode, which is beneficial to increase the energy density of the battery;
  • the amount of solid electrolyte used can be reduced, and the quality of the battery can be improved.
  • the solid-liquid interface with better compatibility can be used instead of the solid-solid interface to reduce Battery interface impedance;
  • the presence of solid electrolyte can completely block the influence of metal ions (nickel ions or manganese ions) eluted from the electrolyte of high nickel ternary or manganese-based lithium-rich positive electrode materials to the surface of lithium metal on the performance of the negative electrode.
  • the battery has a higher cycle life and energy density.
  • the positive electrode includes one of high nickel ternary or manganese-based lithium-rich positive electrode materials.
  • the high-nickel ternary and manganese-based rich lithium have a higher voltage, and can form a higher potential difference with the lithium metal material, which is beneficial to increase the energy density of the battery.
  • the ester electrolyte includes carbonate, lithium salt and additive one, and the mass ratio of the three is (4-7):(2-5):1.
  • the carbonate is one of ethyl methyl carbonate, dimethyl carbonate, and ethylene carbonate.
  • the lithium salt is LiBOB (lithium dioxalate borate), LiODFB (lithium difluorooxalate), LiFSI (lithium bisfluorosulfonimide), and LiTFSI (potassium bistrifluoromethanesulfonimide) ).
  • the additive one is a mixture of cyclohexylbenzene and ( ⁇ -chloromethyl) phosphate, and the molar ratio of the two is 1:1.
  • the ether electrolyte contains fluoroether, lithium salt and additive two, and the mass ratio of the three is (3-6):(3-6):1.
  • the fluoroether is methyl nonafluoro n-butyl ether, 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether and octafluoro A kind of pentyl-tetrafluoroethyl ether.
  • methyl nonafluoron-butyl ether, 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether and octafluoropentyl-tetrafluoroethyl ether Base ethers have good oxidation resistance, and have good stability at high voltages around 4.4v, and can reduce the viscosity of the electrolyte, which is conducive to the infiltration of the electrolyte and the performance of the battery capacity, and also helps the electrolyte Flame retardant.
  • the second additive is one of fluoroethylene carbonate, trifluoroethylene carbonate, and trifluoroethyl acrylate.
  • the mixed use of fluoroether and fluoroester on the one hand, it will not increase the viscosity of the solution, has good stability, strong resistance to electrochemical oxidation, high dielectric constant, can fully dissolve organics, and has a wide application temperature range. , Also has high lightning and high safety, these compounds make the battery have excellent voltage resistance and charge-discharge cycle performance.
  • fluorine-substituted cyclic carbonates of fluoroethylene carbonate, trifluoroethylene carbonate and trifluoroethyl acrylate are selected. Under low temperature conditions, the reduction potential of fluorocarbonate is slightly higher than that of EC. Additives It is easy to co-reduced with the solvent to introduce CF-containing groups into the SEI film, which reduces the surface energy of the SEI film and facilitates Li+ diffusion in the SEI film.
  • the metal lithium surface of the negative electrode has a layer of lithium nitride.
  • lithium nitride as a protective layer can effectively isolate the direct contact between metallic lithium and electrolyte, thereby avoiding the reaction between the two during battery charging and discharging to produce SEI film, which in turn affects solid-state batteries Normal use.
  • Cyclohexylbenzene and ( ⁇ -chloromethyl) phosphate are used as additive one, which can play a protective role when the lithium ion battery system is overcharged and reduce the probability of burning or even explosion of the lithium battery;
  • a method for preparing a solid-liquid battery with a lithium metal negative electrode and a high-voltage positive electrode includes the following steps:
  • Step 1 Coat lithium metal on the copper foil, and then place the copper foil with lithium metal in a nitrogen atmosphere for 7 hours to form lithium nitride on the surface of the lithium metal.
  • the temperature of the nitrogen is 45°C and the flow rate is 4m/s, finally get the negative pole piece;
  • Step 2 Add LiNi 0.8 Co 0.1 Mn 0.1 O 2 material, conductive carbon black and polyoxyethylene-polyvinylidene fluoride in a mass ratio of 90:4:6 into tetrahydrofuran and mix thoroughly to obtain a solid content of 0.5g/ L's positive electrode slurry;
  • Step 3 Coat the positive electrode slurry evenly on the aluminum foil with a coating thickness of 25 ⁇ m, and dry it at a temperature of 110°C ⁇ 150°C until the water content is less than 100ppm, and then after rolling and cutting, The positive pole piece is prepared;
  • Step 4 Melt and mix lithium lanthanum zirconium oxide, polyvinylidene fluoride, and bistrifluoromethanesulfonic acid imine at a mass ratio of 90:5:5, and then coat them on both sides of the PP film, and on both sides The coating thickness is 2.5 ⁇ m; after cooling, solidification and cutting, a solid electrolyte is obtained;
  • Step 5 Lay the positive pole piece and the negative pole piece on both sides of the solid electrolyte, and then fill the ether electrolyte between the positive pole piece and the solid electrolyte, and fill the ester electrolysis between the negative pole piece and the solid electrolyte Liquid to obtain battery cells;
  • Step 6 Pack the battery cores, and the finished solid-liquid battery must be packed.
  • the ether electrolyte is mixed with ethyl methyl carbonate, LiBOB and additive one in a mass ratio of 4:2:1, and the additive one is mixed with cyclohexylbenzene and ( ⁇ -chloromethyl) phosphate, and the two The molar ratio is 1:1.
  • the ester electrolyte is mixed with methyl nonafluoro-n-butyl ether, LiDFOB and fluoroethylene carbonate in a mass ratio of 3:3:1.
  • a method for preparing a lithium metal negative high-voltage positive solid-liquid battery The difference from the first embodiment is that the positive electrode slurry in step two is composed of LiNi 0.5 Mn 1.5 O 4 , conductive carbon black and polyoxyethylene-polyvinylidene fluoride. Ethylene is added to the mixture in a mass ratio of 45:2:3, and the solid content is 0.5g/L.
  • a method for preparing a solid-liquid battery with a lithium metal negative electrode and a high-voltage positive electrode is that the ether electrolyte is mixed with dimethyl carbonate, LiFSI and additive one in a mass ratio of 7:5:1 , Ester electrolyte is made of 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether, LiTFSI and trifluoroethylene carbonate in a mass ratio of 6:6:1 mixing.
  • a new type of lithium metal anode high-voltage anode solid-liquid battery preparation method The difference from Example 1 is that the ether electrolyte is made of ethylene carbonate, LiODFB and additives at a mass ratio of 5:3:1. Mixing, the ester electrolyte is mixed with octafluoropentyl-tetrafluoroethyl ether, LiBOB and trifluoroethyl acrylate in a mass ratio of 4:4:1.
  • a method for preparing a solid-liquid battery with a lithium metal negative high-voltage positive electrode The difference from the first embodiment is that the ether electrolyte is mixed with dimethyl carbonate, LiTFSI and additive one in a mass ratio of 4:5:1 , Ester electrolyte is made of 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether, LiFSI and fluoroethylene carbonate in a mass ratio of 4:4:1 mixing.
  • a method for preparing a solid-liquid battery with a lithium metal negative electrode and a high-voltage positive electrode is different from the first embodiment only in that the solid electrolyte chemical formula is a pure inorganic ceramic sheet of Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12.
  • the only difference from the first embodiment is that the surface of the lithium metal is not treated in a nitrogen atmosphere.
  • the only difference from the first embodiment is that the first additive only contains cyclohexylbenzene.
  • the only difference from the first embodiment is that the first additive only contains ( ⁇ -chloromethyl) phosphate.
  • the voltage is 4.3V (the positive electrode is LiNi 0.8 Co).
  • the charging ends at 0.1 Mn 0.1 O 2 ) or 5V (LiNi 0.8 Co 0.1 Mn 0.1 O 2 as the positive electrode).
  • the same discharge is performed at a current of 0.05C, and the discharge ends when the voltage is 3.0V. In this way, the Coulomb efficiency and discharge capacity of the battery are obtained, and the impedance is characterized by testing the battery EIS.
  • the specific ether electrolyte is filled between the lithium metal and the solid electrolyte, which is beneficial to improve the cycle life of the lithium metal; on the other hand, the positive electrode and the solid electrolyte
  • the electrolyte is filled with a specific ester electrolyte, which has high withstand voltage performance, which helps to increase the selection space of the positive electrode, especially the material with high potential voltage can be used as the positive electrode, which is beneficial to increase the energy of the battery Density;
  • the solid-liquid interface with better compatibility is also used to replace the solid-solid interface, reducing the battery interface impedance, and ultimately making the battery Obtain higher cycle life, energy density, and overcharge resistance.

Abstract

一种固液电池，包括正极和负极，所述负极由金属锂制成，所述正极和负极之间设置有固体电解质，且所述固体电解质与正极之间填充有酯类电解液，所述固体电解质与负极之间填充有醚类电解液。一方面在锂金属和固体电解质之间填充醚类电解液，这样有利于提高了锂金属的循环寿命；另一方面在正极和固体电解质之间填充酯类电解液，有利于提高了正极的选择空间，进而提高电池的能量密度；另外，通过填充电解液，这样可以降低固体电解质使用量，在保证利用固体电解质提高安全性的基础上，降低电池界面阻抗；再者，固体电解质的存在可以阻挡电解质溶出的金属离子迁移到金属锂表面后对负极性能的影响。

Description

一种固液电池 技术领域
本发明涉及锂电池领域，特别涉及一种新型固液电池。
背景技术
目前用于电池的电解质有三大类，醚类电解液与酯类电解液以及固态电解质，其中锂负极在醚类电解液中的循环性能远高于酯类电解液，醚类电解液的锂金属库伦效率可高达99.9％以上，非常有利于锂金属作为负极的循环寿命。而为了获得高能量密度，正极需要充电到4.2V甚至5V以上，然而醚类电解液的耐压性能较差，一般仅在4.0V(vsLi+/Li)左右稳定，较高电压下会发生严重分解，导致电池胀气等影响全电池循环性能。
而若采用酯类电解液虽然耐压较高，但对锂金属的库伦效率大多在60％以下，锂金属的循环寿命严重限制。若全部采用固体电解质，固体电解质的高强度可以有效防止锂金属负极的枝晶短路，提高电池安全性，但一方面固体电解质的密度较高，会降低电池的能量密度，而且固体电解质与负极或者正极的固固界面相容性差，会增加电池工艺复杂性。
因此，在本领域中仍需对采用固体电解质的电池进行改进。
发明内容
针对本领域中存在的前述问题，本发明的目的是提供一种新型的锂金属负极高电压正极的固液电池，其既具有较高的库伦效率，又具有良好的循环性能。
本发明的上述发明目的是通过以下技术方案得以实现的：一种固液电池，包括正极和负极，所述负极由金属锂制成，所述正极和负极之间设置有固体电解质，且所述固体电解质与正极之间填充有酯类电解液，所述固体电解质与负极之间填充有醚类电解液。
通过采用上述技术方案，一方面在锂金属和固体电解质之间填充醚类电解液，这样有利于提高了锂金属的循环寿命；另一方面在正极和固体电解质之间填充酯类电解液，其具有较高的耐压性能，从而有利于提高了正极的选择空间，尤其是可采用高电势电压的材料来作为正极，从而有利于提高电池的能量密度；
另外，通过填充电解液，这样可以降低固体电解质使用量，提高电池质量，在保证利用固体电解质提高安全性的基础上，还利用相容性更好的固-液界面替代固-固界面，降低电池界面阻抗；再者，固体电解质的存在可以完全阻挡高镍三元或者锰基富锂正极材料的电解质溶出的金属离子(镍离子或者锰离子)迁移到金属锂表面后对负极性能的影响，最终使得电池获得较高的循环寿命与能量密度。
在一些实施方案中，所述正极包括高镍三元或者锰基富锂正极材料中的一种。
通过采用上述技术方案，高镍三元和锰基富锂具有较高的电压，其与锂金属材料能够组成较高的电势差，这样有利于提高电池的能量密度。
在一些实施方案中，所述酯类电解液包括碳酸酯、锂盐和添加剂一，三者的质量比为(4～7)∶(2～5)∶1。在另一些实施方案中，所述碳酸酯为碳酸甲乙酯、碳酸二甲酯和碳酸乙烯酯中的一种。
通过采用上述技术方案，其有效地保证电池的各项性能都能够长时间良好的运行。
在一些实施方案中，所述锂盐为LiBOB(二草酸硼酸锂)、LiODFB(二氟草酸硼酸锂)、LiFSI(双氟磺酰亚胺锂)和LiTFSI(双三氟甲烷磺酰亚胺钾)中的一种。在另一些实施方案中，所述添加剂一为环已基苯和(β-氯甲基)磷酸酯混合物，且两者的摩尔比为1∶1。
通过采用上述技术方案，当锂离子电池体系过充电时，环已基苯和(β-氯甲基)磷酸酯协同作用，能够有效地抑制正极活性物质结构发生不可逆变化及电解液发生氧化分解反应，从而降低了负极发生过多的锂沉积。进而，也有利于避免负极材料结构的破坏，而在短时间内电池内部产生大量气体并放出大量的热量，使得电池的内压和温度迅速上升，而引发电解液的燃烧甚至电池的爆炸等安全隐患的发生。
在一些实施方案中，所述醚类电解液包含有氟代醚、锂盐和添加剂二，三者的质量比为(3～6)∶(3～6)∶1。
在一些实施方案中，所述氟代醚为甲基九氟正丁基醚、1，1，2，2-四氟乙基-2，2，3，3-四氟 丙基醚和八氟戊基-四氟乙基醚的一种。
通过采用上述技术方案，甲基九氟正丁基醚、1，1，2，2-四氟乙基-2，2，3，3-四氟丙基醚和八氟戊基-四氟乙基醚均具有良好的耐氧化性，且在高电压4.4v左右具有较好的稳定性，并且能够降低电解液的粘度，有利于电解液的浸润和电池容量的发挥，还有助于电解液的阻燃。
在一些实施方案中，所述添加剂二为氟代碳酸乙烯酯、三氟乙烯碳酸酯和三氟乙基丙烯酸酯中的一种。
通过采用上述技术方案，将氟代醚和氟酯进行混合使用，一方面不会增加溶液黏度，稳定性好，抗电化学氧化性强，介电常数高，能充分溶解有机物并且应用温度范围宽，还具有高闪电和高安全性，这些化合物使电池具有优异的耐电压性及充放电循环性能。
而且选用氟代碳酸乙烯酯、三氟乙烯碳酸酯和三氟乙基丙烯酸酯的氟取代的环状碳酸酯，在低温条件下，氟类碳酸酯的还原电位略高于EC的还原电位，添加剂就容易与溶剂共同还原而在SEI膜中引入含有C-F的基团，降低SEI膜的表面能，有利于Li+在SEI膜中扩散。
在一些实施方案中，所述负极的金属锂表面带有一层氮化锂。
通过采用上述技术方案，将氮化锂作为保护层，能够有效地隔绝金属锂和电解液的直接接触，从而避免了两者之间在电池充放电过程中发生反应生产SEI膜，进而影响固态电池的正常使用。
综上所述，本发明的有益技术效果为：
1、在负极锂金属和固体电解质之间填充醚类电解液，在正极和固体电解质之间填充酯类电解液，这样在延长锂金属的循环寿命的同时，也有利于提高电池的能量密度；
2、选用环已基苯和(β-氯甲基)磷酸酯作为添加剂一，这样可以在锂离子电池体系过充电时，起到保护作用，降低锂电池发生燃烧甚至爆炸概率；
3、选用氟代碳酸酯和氟代醚进行共同使用，一方面可使电池具有优异的耐电压性及充放电循环性能，另一方面降低SEI膜的表面能，有利于Li +在SEI膜中扩散。
具体实施方式
实施例一
一种锂金属负极高电压正极的固液电池的制备方法，包括如下步骤：
步骤一、将锂金属涂敷在铜箔上，然后将带有锂金属的铜箔置于氮气气氛中7小时，以便在锂金属表面形成氮化锂，其中氮气的温度为45℃，流速为4m/s，最终获得负极极片；
步骤二、将LiNi 0.8Co 0.1Mn 0.1O 2材料、导电炭黑和聚氧化乙烯-聚偏氟乙烯以质量比为90∶4∶6加入于四氢呋喃中充分混合，制得固含量为0.5g/L的正极浆料；
步骤三、将正极浆料均匀涂敷于铝箔上，且涂敷厚度为25μm，并在温度为110℃～150℃下进行干燥，直至含水量小于100ppm，之后再经辊压及裁切后，制得正极极片；
步骤四、将锂镧锆氧、聚偏氟乙烯和双三氟甲烷磺酸亚胺以质量比为90∶5∶5进行熔融混合均匀，然后涂敷于PP膜的两侧，且两侧的涂敷厚度均为2.5μm；待冷却固化裁切后，得到固体电解质；
步骤五、将正极极片和负极极片分别叠放于固体电解质的两侧，之后向正极极片和固体电解质之间填充醚类电解液，向负极极片和固体电解质之间填充酯类电解液，得到电池芯；
步骤六、将电池芯进行包装，得打成品的固液电池。
其中，醚类电解液由碳酸甲乙酯、LiBOB和添加剂一以质量比为4∶2∶1进行混合，并且添加剂一由环已基苯和(β-氯甲基)磷酸酯混合，且两者的摩尔比为1∶1。而酯类电解液由甲基九氟正丁基醚、LiDFOB和氟代碳酸乙烯酯以质量比为3∶3∶1进行混合。
实施例二
一种锂金属负极高电压正极的固液电池的制备方法，与实施例一的区别仅在于，步骤二的正极浆料由LiNi 0.5Mn 1.5O 4、导电炭黑和聚氧化乙烯-聚偏氟乙烯以质量比为45∶2∶3加入于中混合得到，其固含量为0.5g/L。
实施例三
一种锂金属负极高电压正极的固液电池的制备方法，与实施例一的区别仅在于，醚类电解液由碳酸二甲酯、LiFSI和添加剂一以质量比为7∶5∶1进行混合，酯类电解液由1，1，2，2-四氟乙基-2，2，3，3-四氟丙基醚、LiTFSI和三氟乙烯碳酸酯以质量比为6∶6∶1进行混合。
实施例四
一种新型的锂金属负极高电压正极的固液电池的制备方法，与实施例一的区别仅在于，醚类电解液由碳酸乙烯酯、LiODFB和添加剂一以质量比为5∶3∶1进行混合，酯类电解液由八氟戊基-四氟乙基醚、LiBOB和三氟乙基丙烯酸酯以质量比为4∶4∶1进行混合。
实施例五
一种锂金属负极高电压正极的固液电池的制备方法，与实施例一的区别仅在于，醚类电解液由碳酸二甲酯、LiTFSI和添加剂一以质量比为4∶5∶1进行混合，酯类电解液由1，1，2，2-四氟乙基-2，2，3，3-四氟丙基醚、LiFSI和氟代碳酸乙烯酯以质量比为4∶4∶1进行混合。
实施例六
一种锂金属负极高电压正极的固液电池的制备方法，与实施例一的区别仅在于，固体电解质化学式为Li 6.4La 3Zr 1.4Ta 0.6O 12的纯无机陶瓷片。
对比例一
与实施例一的区别仅在于，锂金属表面未在氮气气氛中进行处理。
对比例二
与实施例一的区别仅在于，添加剂一仅含有环已基苯。
对比例三
与实施例一的区别仅在于，添加剂一仅含有(β-氯甲基)磷酸酯。
对比例四
与实施例一的区别仅在于，酯类电解液未添加氟代碳酸乙烯酯(添加剂二)。
对比例五
与实施例二的区别仅在于，无酯类电解液。
对比例六
与实施例二的区别仅在于，无醚类电解液。
[使用测试]
以LiNi 0.5Mn 1.5O 4或LiNi 0.8Co 0.1Mn 0.1O 2三元材料作为正极匹配组合体组装，使用金属锂作为负极，再在正负极上配置不锈钢集流体，并在集流体上附加引线。最后使用绝缘套，将绝缘外筒内部与外部气体气氛隔断密闭，由此制作了测试电池。对测试电池进行试运行。
[阻抗和循环性能测试]
将电池置于25℃恒温条件下，以相对于电池的理论容量为0.05C(20h，以正极计算，1C＝1mA)的电流值进行恒流充电，在电压为4.3V(正极为LiNi 0.8Co 0.1Mn 0.1O 2)或5V(正极为LiNi 0.8Co 0.1Mn 0.1O 2)时结束充电。接着，同样以0.05C倍率的电流放电，在电压为3.0V时结束放电。以此获得电池的库伦效率和放电容量，另通过测试电池EIS表征阻抗。
从第二周循环开始，以0.2C进行200次充放电循环，计算器容量保持率越高代表循环性能越好。
测试结果如表一所示：
表一
Figure PCTCN2020123624-appb-000001
Figure PCTCN2020123624-appb-000002
从上述电池测试结果可以发现，相较于对比例，一方面在锂金属和固体电解质之间填充特定的醚类电解液，这样有利于提高了锂金属的循环寿命；另一方面在正极和固体电解质之间填充特定的酯类电解液，其具有较高的耐压性能，从而有利于提高了正极的选择空间，尤其是可采用高电势电压的材料来作为正极，从而有利于提高电池的能量密度；另外，通过填充耐高温电解液添加剂，在保证利用固体电解质提高安全性的基础上，还利用相容性更好的固-液界面替代固-固界面，降低电池界面阻抗，最终使得电池获得较高的循环寿命、能量密度、以及耐过充性能。
本具体实施例仅仅是对本发明的解释，其并不是对本发明的限制，本领域技术人员在阅读完本说明书后可以根据需要对本实施例做出没有创造性贡献的修改，但只要在本发明的权利要求范围内都受到专利法的保护。

Claims (10)

  1. 一种固液电池，包括正极和负极，所述负极由金属锂制成，其特征在于：所述正极和负极之间设置有固体电解质，且所述固体电解质与正极之间填充有酯类电解液，所述固体电解质与负极之间填充有醚类电解液。
  2. 根据权利要求1所述的一种固液电池，其特征在于：所述正极包括高镍三元或者锰基富锂正极材料中的一种。
  3. 根据权利要求1所述的一种固液电池，其特征在于：所述酯类电解液包括碳酸酯、锂盐和添加剂一，三者的质量比为(4～7)∶(2～5)∶1。
  4. 根据权利要求3所述的一种固液电池，其特征在于：所述碳酸酯为碳酸甲乙酯、碳酸二甲酯和碳酸乙烯酯中的一种。
  5. 根据权利要求3所述的一种固液电池，其特征在于：所述锂盐为LiBOB、LiODFB、LiFSI和LiTFSI中的一种。
  6. 根据权利要求3所述的一种固液电池，其特征在于：所述添加剂一为环己基苯和(β-氯甲基)磷酸酯混合物，且两者的摩尔比为1∶1。
  7. 根据权利要求1所述的一种固液电池，其特征在于：所述醚类电解液包含有氟代醚、锂盐和添加剂二，三者的质量比为(3～6)∶(3～6)∶1。
  8. 根据权利要求7所述的一种固液电池，其特征在于：所述氟代醚为甲基九氟正丁基醚、1，1，2，2-四氟乙基-2，2，3，3-四氟丙基醚和八氟戊基-四氟乙基醚的一种。
  9. 根据权利要求7所述的一种固液电池，其特征在于：所述添加剂二为氟代碳酸乙烯酯、三氟乙烯碳酸酯和三氟乙基丙烯酸酯中的一种。
  10. 根据权利要求1所述的一种固液电池，其特征在于：所述负极的金属锂表面带有一层氮化锂。
PCT/CN2020/123624 2019-10-28 2020-10-26 一种固液电池 WO2021083074A1 (zh)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2021555870A JP7418464B2 (ja) 2019-10-28 2020-10-26 固体・液体電池
CA3133860A CA3133860C (en) 2019-10-28 2020-10-26 A solid-liquid battery comprising a lithium negative electrode and electrolyte solutions
US17/604,528 US20220200047A1 (en) 2019-10-28 2020-10-26 Solid-liquid battery
AU2020377021A AU2020377021B2 (en) 2019-10-28 2020-10-26 Solid-liquid battery
EP20882107.4A EP3930066A1 (en) 2019-10-28 2020-10-26 Solid-liquid battery
KR1020217028781A KR20210129098A (ko) 2019-10-28 2020-10-26 고액 전지

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201911035198.6A CN110931843B (zh) 2019-10-28 2019-10-28 一种新型的锂金属负极高电压正极的固液电池
CN201911035198.6 2019-10-28

Publications (1)

Publication Number Publication Date
WO2021083074A1 true WO2021083074A1 (zh) 2021-05-06

Family

ID=69849675

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2020/123624 WO2021083074A1 (zh) 2019-10-28 2020-10-26 一种固液电池

Country Status (8)

Country Link
US (1) US20220200047A1 (zh)
EP (1) EP3930066A1 (zh)
JP (1) JP7418464B2 (zh)
KR (1) KR20210129098A (zh)
CN (1) CN110931843B (zh)
AU (1) AU2020377021B2 (zh)
CA (1) CA3133860C (zh)
WO (1) WO2021083074A1 (zh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110931843B (zh) * 2019-10-28 2021-11-19 浙江锋锂新能源科技有限公司 一种新型的锂金属负极高电压正极的固液电池
EP4325618A1 (en) * 2021-12-08 2024-02-21 LG Energy Solution, Ltd. Method for preparing polymer solid electrolyte and polymer solid electrolyte prepared thereby
CN114583294B (zh) * 2022-02-21 2024-04-30 浙江锋锂新能源科技有限公司 固液混合电解质界面添加剂组合、锂金属电池及制备方法
CN114914539A (zh) * 2022-06-28 2022-08-16 肇庆小鹏汽车有限公司 固态/半固体电解质及其制备方法和应用
CN117229447B (zh) * 2023-11-16 2024-02-06 华中科技大学 聚合物固态电解质的制备方法、固态电解质及固态电池

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103531840A (zh) * 2013-11-01 2014-01-22 中国科学院上海硅酸盐研究所 一种双电解质体系锂硫电池及其制备方法
CN104054210A (zh) * 2012-01-20 2014-09-17 株式会社丰田自动织机 二次电池
WO2018159950A1 (ko) * 2017-03-03 2018-09-07 주식회사 엘지화학 리튬 이차전지
CN109155427A (zh) * 2016-09-30 2019-01-04 株式会社Lg化学 锂二次电池
CN110931843A (zh) * 2019-10-28 2020-03-27 浙江锋锂新能源科技有限公司 一种新型的锂金属负极高电压正极的固液电池

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5848545B2 (ja) * 2011-08-08 2016-01-27 三星エスディアイ株式会社Ｓａｍｓｕｎｇ ＳＤＩ Ｃｏ．，Ｌｔｄ． 二次電池用セパレータ層及び二次電池
JP5447578B2 (ja) * 2012-04-27 2014-03-19 株式会社豊田自動織機 固体電解質及び二次電池
CN105190969B (zh) * 2013-03-15 2019-01-18 赛昂能源有限公司 用于电极的保护结构
CN103456991B (zh) * 2013-09-02 2015-07-15 宁德时代新能源科技有限公司 锂离子电池及其凝胶电解质以及其制备方法
JP2015109235A (ja) * 2013-12-05 2015-06-11 三星エスディアイ株式会社Ｓａｍｓｕｎｇ ＳＤＩ Ｃｏ．，Ｌｔｄ． リチウムイオン（Ｌｉｔｈｉｕｍｉｏｎ）二次電池
KR101984719B1 (ko) * 2014-10-23 2019-05-31 주식회사 엘지화학 다층구조의 리튬금속 전극 및 이의 제조방법

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104054210A (zh) * 2012-01-20 2014-09-17 株式会社丰田自动织机 二次电池
CN103531840A (zh) * 2013-11-01 2014-01-22 中国科学院上海硅酸盐研究所 一种双电解质体系锂硫电池及其制备方法
CN109155427A (zh) * 2016-09-30 2019-01-04 株式会社Lg化学 锂二次电池
WO2018159950A1 (ko) * 2017-03-03 2018-09-07 주식회사 엘지화학 리튬 이차전지
CN110931843A (zh) * 2019-10-28 2020-03-27 浙江锋锂新能源科技有限公司 一种新型的锂金属负极高电压正极的固液电池

Also Published As

Publication number Publication date
KR20210129098A (ko) 2021-10-27
EP3930066A1 (en) 2021-12-29
US20220200047A1 (en) 2022-06-23
JP2022525234A (ja) 2022-05-11
AU2020377021B2 (en) 2023-01-12
AU2020377021A1 (en) 2021-10-07
CA3133860A1 (en) 2021-05-06
JP7418464B2 (ja) 2024-01-19
CA3133860C (en) 2023-08-08
CN110931843B (zh) 2021-11-19
CN110931843A (zh) 2020-03-27

Similar Documents

Publication Publication Date Title
CN113644317B (zh) 一种锂离子电池
WO2021083074A1 (zh) 一种固液电池
EP3699997B1 (en) Lithium secondary battery electrolyte and lithium secondary battery comprising the same
CN109119685A (zh) 电解液及锂离子电池
CN111697266B (zh) 电解液和包括其的电化学装置及电子装置
US11031630B2 (en) Electrolyte and electrochemical device
CN112467209A (zh) 一种高低温性能兼顾的高电压锂离子电池
WO2017185703A1 (zh) 一种高温锂离子电池电解液及其制备方法和高温锂离子电池
CN112635835B (zh) 高低温兼顾的非水电解液及锂离子电池
WO2022262230A1 (zh) 非水电解液及其二次电池
CN103579677A (zh) 一种电解液及含有该电解液的二次锂电池和电容器
TW201817072A (zh) 用於可充電式電池組之電解質溶液
CN113299996A (zh) 一种三元正极材料与负极硅氧-碳复合负极材料锂离子电池用非水电解液
CN109309245A (zh) 电解液及电化学储能装置
JP2005502179A (ja) 非水電解質
WO2023174185A1 (zh) 正极片及锂离子电池
CN109309249A (zh) 电解液及电化学储能装置
WO2023109259A1 (zh) 电解液添加剂、电解液以及包含其的锂离子二次电池
CN114497739B (zh) 一种锂二次电池电解液及其应用
CN110492177A (zh) 电池电解液用添加剂、锂离子电池电解液、锂离子电池
WO2023123841A1 (zh) 电解液添加剂和含有该添加剂的电解液及锂离子电池
CN111342134B (zh) 一种宽温域锂离子电池非水电解液及其制备方法
CN113764731A (zh) 二恶唑酮类化合物于电池电解液中的应用
CN113871715A (zh) 一种磷酸铁锂电池
CN108987803A (zh) 一种用于锂硫电池的锂金属负极成膜电解液及其添加剂

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20882107

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 20217028781

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2021555870

Country of ref document: JP

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 3133860

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 2020882107

Country of ref document: EP

Effective date: 20210921

ENP Entry into the national phase

Ref document number: 2020377021

Country of ref document: AU

Date of ref document: 20201026

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE