WO2021023265A1 - 一种电解液及其制备方法和锂离子电池 - Google Patents

一种电解液及其制备方法和锂离子电池 Download PDF

Info

Publication number
WO2021023265A1
WO2021023265A1 PCT/CN2020/107415 CN2020107415W WO2021023265A1 WO 2021023265 A1 WO2021023265 A1 WO 2021023265A1 CN 2020107415 W CN2020107415 W CN 2020107415W WO 2021023265 A1 WO2021023265 A1 WO 2021023265A1
Authority
WO
WIPO (PCT)
Prior art keywords
electrolyte
mass fraction
lithium
ion battery
lithium ion
Prior art date
Application number
PCT/CN2020/107415
Other languages
English (en)
French (fr)
Inventor
王海
李素丽
廖波
母英迪
李俊义
徐延铭
Original Assignee
珠海冠宇电池股份有限公司
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 珠海冠宇电池股份有限公司 filed Critical 珠海冠宇电池股份有限公司
Publication of WO2021023265A1 publication Critical patent/WO2021023265A1/zh
Priority to US17/590,957 priority Critical patent/US20220158242A1/en

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
    • H01M10/056—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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D327/10—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms two oxygen atoms and one sulfur atom, e.g. cyclic sulfates
    • 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
    • H01M10/052—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
    • H01M10/0568—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
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic 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

Definitions

  • the application relates to an electrolyte, a preparation method thereof, and a lithium ion battery, and belongs to the technical field of lithium ion batteries.
  • the current composition of lithium-ion batteries mainly includes a positive electrode, a negative electrode, a separator and an electrolyte.
  • the electrode material and the electrolyte will react on the surface of the electrode material to form a passivation layer covering the surface of the electrode material, which is often mentioned in the art as having the characteristics of a solid electrolyte
  • the interface film solid electronic interface, referred to as SEI film.
  • the SEI film has a very important influence on the performance of lithium ion batteries.
  • the SEI film can prevent further contact between the electrolyte and the electrode material, and inhibit side reactions of the electrolyte on the surface of the electrode material, which is beneficial to the improvement of the cycle performance of the lithium ion battery; on the other hand, the generation of the SEI film will also consume the electrolysis Part of the lithium ions in the liquid reduces the capacity of the lithium ion battery.
  • the present application provides an electrolyte, which can be used in a lithium ion battery to significantly improve the performance of the SEI film, thereby helping to improve the cycle performance and storage performance of the lithium ion battery.
  • the present application also provides a method for preparing an electrolyte, which is simple and easy to implement, and helps to safely and efficiently prepare an electrolyte that can improve the cycle performance and storage performance of the lithium ion battery.
  • the present application also provides a lithium ion battery containing the above electrolyte, so the lithium ion battery has excellent cycle performance and storage performance.
  • This application provides an electrolyte, which comprises the following components according to mass fraction: 10-20% of lithium salt and 0.2-7% of additive composition, the balance being solvent;
  • the additive composition includes a boron-containing lithium salt compound and a sulfur compound of formula 1,
  • R 1 and R 3 are each independently selected from hydrogen, halogen, substituted or unsubstituted alkyl
  • R 2 is selected from substituted or unsubstituted alkylene groups or directly bonded;
  • the mass fraction of the boron-containing lithium salt compound in the electrolyte is at least 0.1%.
  • the sulfur compound is specifically selected from at least one of the compounds represented by T1-T4:
  • the boron-containing lithium salt compound is selected from at least one of lithium bisfluorooxalate borate, lithium bisoxalate borate and lithium tetrafluoroborate.
  • the solvent includes at least one of ethylene carbonate and propylene carbonate.
  • This application also provides a method for preparing any one of the foregoing electrolytes, including:
  • the solvent, the lithium salt and the additive composition are mixed to obtain the electrolyte.
  • the application also provides a lithium ion battery, the electrolyte of the lithium ion battery is any one of the foregoing electrolytes.
  • the electrolyte provided by this application by adding a specific additive composition, can form a stable and firm SEI film on the surface of the electrode in preference to other components in the electrolyte, thereby effectively preventing the electrolyte from contacting the electrode and significantly improving lithium ion Cycle performance and storage performance of the battery;
  • the preparation method of the electrolyte provided in this application has simple process and strong operability, which is convenient for practical promotion and large-scale application;
  • the lithium ion battery provided by this application includes the aforementioned electrolyte, the lithium ion battery has excellent cycle performance and storage performance.
  • This application provides an electrolyte, which comprises the following components according to mass fraction: 10-20% of lithium salt and 0.2-7% of additive composition, the balance being solvent;
  • the additive composition includes a boron-containing lithium salt compound and the sulfur compound described in Formula 1,
  • R 1 and R 3 are each independently selected from hydrogen, halogen, substituted or unsubstituted alkyl
  • R 2 is selected from substituted or unsubstituted alkylene groups or directly bonded;
  • the mass fraction of the boron-containing lithium salt compound in the electrolyte is at least 0.1%.
  • the additive composition of the present application is a combination of a boron-containing lithium salt compound and the sulfur compound described in Formula 1.
  • the mass fraction of the additive composition in the electrolyte is 0.2-7%, and when the boron-containing lithium salt compound is in the When the mass fraction in the electrolyte is at least 0.1%, the performance of the SEI film formed on the electrode surface of the lithium ion battery during the first charge and discharge can be significantly improved, which can have a positive impact on the cycle performance and storage performance of the lithium ion battery.
  • the inventor analyzed the SEI film and believed that it may be that the additive composition can electrochemically react at a lower potential, which is superior to other components in the electrolyte to form a boron and sulfur element on the electrode surface.
  • the boron element is beneficial to reduce the mass transfer resistance of lithium ions
  • the sulfur element in the form of a polymer in the SEI film is beneficial to improve the strength of the SEI film.
  • lithium ions can pass through the SEI film with low resistance to complete the intercalation and deintercalation on the electrode, which is beneficial to improve the stability of intercalation and deintercalation of lithium and the dynamics of the electrode electrolyte interface. , Thereby significantly improving the performance of lithium-ion batteries, such as cycle life, self-discharge, rated rate, and battery temperature resistance.
  • the increase in the strength of the SEI film can prevent the SEI film from dissolving in the electrolyte, avoid the damage to the electrode material caused by the co-embedding of solvent molecules, and ensure the electrode's insulation performance against other particles or electrons, thereby further improving the electrode cycle Performance and storage performance.
  • R 1 and R 3 may be substituted or unsubstituted C 1 -C 5 linear alkyl groups, C 3 -C 5 branched chain alkyl groups, or C 3 -C 5 cycloalkyl groups, R 1 and R 3 can specifically be -CH 3 , -CH 2 CH 3 , -C(CH 3 ) 3 , -C(CH 3 ) 2 F, -CH 2 F, -CH 2 (C 6 H 6 ),- One of CH(C 6 H 6 )CH 2 CH 3 , -CH 2 CH 2 CH 2 CH 2 CH 3 , -CH 2 C(CH 3 ) 3 ; R 2 is selected from substituted or unsubstituted C 1- C 10 alkylene group, direct bond, R 2 can specifically be -CH 2 -, -CHF-, -CH 2 CHFCH 2 -, -CH 2 CH 2 -, -CH 2 CHFCH 2 -, -CH 2 C One of (CH 3 ) 2 CH
  • the sulfur compound represented by Formula 1 of the present application can be obtained commercially or by any feasible preparation method.
  • the mass fraction of the sulfur compound described in Formula 1 in the electrolyte can be controlled to be 0.1-5%.
  • the use of different lithium salts and/or solvents in the electrolyte, or even the use of different positive electrode materials, negative electrode materials or separators, will have an impact on the final performance of the lithium ion battery. Therefore, roughly speaking, when the mass fraction of sulfur compounds in the electrolyte is controlled at 0.1%-2%, the lithium ion battery can basically have excellent performance.
  • the mass fraction of the boron-containing lithium salt compound in the electrolyte is 0.1-2%, the compatibility with sulfur compounds is higher, which helps to further improve the cycle performance and storage performance of the lithium ion battery.
  • sulfur compound of the present application is specifically selected from at least one of the compounds represented by T1-T4:
  • the boron-containing lithium salt compound of the present application is selected from at least one of lithium bisfluorooxalate borate (LiODFB), lithium bisoxalate borate (LiBOB), and lithium tetrafluoroborate (LiBF 4 ).
  • LiODFB lithium bisfluorooxalate borate
  • LiBOB lithium bisoxalate borate
  • LiBF 4 lithium tetrafluoroborate
  • the boron-containing lithium salt compound is two or more of the above compounds, the application does not particularly limit the ratio between the compounds.
  • ethylene carbonate and propylene carbonate may assist the above additive composition to form SEI film on the electrode surface, which can accelerate the formation of SEI film by the additive composition prior to other components on the electrode surface, thereby increasing the sulfur in the SEI film.
  • the content of element and boron may assist the above additive composition to form SEI film on the electrode surface, which can accelerate the formation of SEI film by the additive composition prior to other components on the electrode surface, thereby increasing the sulfur in the SEI film.
  • the performance of the lithium ion battery can be further optimized.
  • the solvent includes one of ethylene carbonate or propylene carbonate
  • the mass fraction of ethylene carbonate or propylene carbonate in the electrolyte can be 10-50%
  • the solvent includes ethylene carbonate and carbonic acid Propylene ester
  • the total mass fraction of ethylene carbonate and propylene carbonate in the electrolyte can be 10-50%.
  • the electrolyte of the present application may also include one or more of other solvents commonly used in current lithium-ion battery electrolytes, such as: butylene carbonate, fluorocarbon Ethylene carbonate (FEC), dimethyl carbonate (DMC), diethyl carbonate (DEC), difluoroethylene carbonate (DFEC), dipropyl carbonate, ethyl methyl carbonate (EMC), ethyl acetate, Ethyl propionate, propyl acetate, propyl propionate, sulfolane, ⁇ -butyrolactone, etc.
  • FEC fluorocarbon Ethylene carbonate
  • DMC dimethyl carbonate
  • DEC diethyl carbonate
  • DFEC difluoroethylene carbonate
  • EMC ethyl methyl carbonate
  • EMC ethyl methyl carbonate
  • EMC ethyl methyl carbonate
  • EMC ethyl methyl carbonate
  • This application does not specifically limit the lithium salt in the electrolyte. It can be the electrolyte lithium salt commonly used in the current lithium ion electrolyte.
  • lithium hexafluorophosphate (LiPF 6 ) and lithium bis(fluorosulfonyl)imide (LiFSI) can be selected.
  • LiFSI lithium bis(fluorosulfonyl)imide
  • LiTFSI lithium bis(trifluoromethanesulfonate) imide
  • the application does not particularly limit the ratio between the compounds.
  • This application also provides a method for preparing any one of the above-mentioned electrolytes, including: mixing a solvent, a lithium salt, and an additive composition under an inert atmosphere to obtain the electrolyte.
  • lithium salt and additive composition can be added to the solvent, and after stirring, the electrolyte solution of the present application can be obtained.
  • the present application does not limit the order of adding the lithium salt and the additive composition, and the sulfur compound and the boron-containing lithium salt compound in the additive composition may be added together or separately before and after.
  • the preparation method of the electrolyte of the present application is easy to operate, and only needs to mix raw materials and stir to complete, so the preparation of the electrolyte can be completed with high efficiency and low cost.
  • the application also provides a lithium ion battery, the electrolyte of which is any one of the foregoing electrolytes.
  • the lithium ion battery of the present application also includes a positive electrode, a negative electrode, and a separator.
  • This application does not strictly limit the active material of the positive electrode. It can be the positive electrode active material commonly used in current lithium ion batteries, such as lithium cobaltate, lithium nickelate, lithium manganate, lithium manganate, nickel cobalt manganese ternary material, nickel At least one of cobalt-aluminum ternary materials, lithium iron phosphate (LFP), lithium nickel manganese oxide, lithium-rich manganese-based materials, and the like.
  • the positive electrode active material commonly used in current lithium ion batteries, such as lithium cobaltate, lithium nickelate, lithium manganate, lithium manganate, nickel cobalt manganese ternary material, nickel At least one of cobalt-aluminum ternary materials, lithium iron phosphate (LFP), lithium nickel manganese oxide, lithium-rich manganese-based materials, and the like.
  • the at least one positive electrode active material mentioned above, conductive carbon black, conductive graphite, and binder polyvinylidene fluoride can be dispersed in an appropriate amount of N-methylpyrrolidone at a mass ratio of 96:1:1:2.
  • NMP N-methylpyrrolidone
  • the present application does not strictly limit the active material of the negative electrode, and it may be the negative active material commonly used in current lithium ion batteries, such as at least one of artificial graphite, hard carbon, and soft carbon.
  • the above-mentioned at least one negative electrode active material can be combined with conductive carbon black, binder styrene butadiene rubber (SBR) and thickener sodium carboxymethyl cellulose (CMC) at a mass ratio of 96:1:1.5: 1.5 Disperse in an appropriate amount of deionized water solvent, fully stir and mix to form a uniform negative electrode slurry; uniformly coat the negative electrode slurry on the copper foil of the negative electrode current collector, and obtain a negative electrode sheet after drying, rolling and slitting.
  • SBR binder styrene butadiene rubber
  • CMC thickener sodium carboxymethyl cellulose
  • This application does not strictly limit the material selection of the separator. It can be the separator material commonly used in lithium ion batteries, such as polypropylene separator (PP), polyethylene separator (PE), polypropylene/polyethylene double-layer composite film ( PP/PE), polyimide electrospinning membrane (PI), polypropylene/polyethylene/polypropylene three-layer composite membrane (PP/PE/PP), cellulose non-woven membrane, ceramic-coated membrane One of them.
  • PP polypropylene separator
  • PE polyethylene separator
  • PP/PE polypropylene/polyethylene double-layer composite film
  • PI polyimide electrospinning membrane
  • PP/PE/PP polypropylene/polyethylene/polypropylene three-layer composite membrane
  • cellulose non-woven membrane ceramic-coated membrane One of them.
  • the positive electrode sheet, the separator and the negative electrode sheet are wound to obtain a bare cell, and the cell is packaged in a pre-punched aluminum plastic film bag. After the packaged battery is dried with moisture at 85°C, the electrolyte of the present application is injected into the dry battery, and the lithium ion battery is prepared after the battery is placed, formed, and sealed again.
  • the lithium ion battery of the present application includes the aforementioned electrolyte, it can form an SEI film with excellent performance on the electrode surface during the first charge and discharge, so that the lithium ion battery of the present application has excellent cycle performance and storage performance.
  • the mass fraction of the solvent in the electrolyte is 84.5%, wherein the mass fraction of ethylene carbonate and propylene carbonate in the electrolyte is 25.35%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%;
  • the sulfur compound shown in T1 accounts for 1% of the mass fraction of the electrolyte, and LiODFB accounts for 1% of the mass fraction of the electrolyte.
  • Example 1 The electrolyte in Example 1 is combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 1#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, except that the sulfur compound represented by T1 in the electrolyte of this embodiment accounts for 0.2% of the mass fraction of the electrolyte, and the solvent accounts for the mass fraction of the electrolyte. It is 85.3%, the mass fraction of LiPF 6 in the electrolyte is 13.5%, and the mass fraction of LiODFB in the electrolyte is 1.0%.
  • Example 2 The electrolyte in Example 2 is combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 2#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, except that the sulfur compound in the electrolyte of this embodiment is the sulfur compound shown in T2 and accounts for 0.5% of the mass fraction of the electrolyte.
  • the boron lithium salt compound is LiBOB, and the mass fraction of LiBOB in the electrolyte is 1%, the mass fraction of the solvent in the electrolyte is 85%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 3 The electrolyte in Example 3 is combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 3#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, except that the sulfur compound in the electrolyte of this embodiment is a sulfur compound shown in T3 and accounts for 2% of the mass fraction of the electrolyte.
  • the boron lithium salt compound is LiBF 4, and the mass fraction of LiBF 4 in the electrolyte is 0.5%, the mass fraction of the solvent in the electrolyte is 84%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 4 The electrolyte in Example 4 was combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 4#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, except that the lithium salt compound containing boron in the electrolyte of this embodiment is LiBF 4 and the mass fraction of LiBF 4 in the electrolyte is 2%, as shown by T1
  • the mass fraction of sulfur compounds in the electrolyte is 1%, the mass fraction of the solvent in the electrolyte is 83.5%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 5 The electrolyte in Example 5 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 5#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, except that the sulfur compound represented by T1 in the electrolyte of this embodiment accounts for 2% of the mass fraction of the electrolyte, and LiODFB accounts for the mass fraction of the electrolyte. It is 1%, the mass fraction of the solvent in the electrolyte is 83.5%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 6 The electrolyte in Example 6 was combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 6#.
  • the preparation method of the electrolyte of this example is the same as that of Example 1, except that the sulfur compound shown in T1 in the electrolyte of this example accounts for 4% of the mass fraction of the electrolyte, and LiODFB accounts for the mass fraction of the electrolyte. It is 1%, the mass fraction of the solvent in the electrolyte is 81.5%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 7 The electrolyte in Example 7 was combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 7#.
  • the preparation method of the electrolyte of this embodiment is the same as that of embodiment 1, the only difference is that the mass fraction of LiODFB in the electrolyte of this embodiment is 2.5%, and the sulfur compound shown in T1 accounts for the mass fraction of the electrolyte. It is 1%, the mass fraction of the solvent in the electrolyte is 83%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • Example 8 The electrolyte in Example 8 was combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 8#.
  • Example 9 The electrolyte in Example 9 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 9#.
  • the preparation method of the electrolyte of this example is the same as that of example 1, except that in the electrolyte of this example, the solvent contains ethylene carbonate (EC), propylene carbonate (PC), and diethyl carbonate (DEC).
  • EC ethylene carbonate
  • PC propylene carbonate
  • DEC diethyl carbonate
  • PP propyl propionate
  • ethylene carbonate and propylene carbonate account for 8.45% of the electrolyte.
  • Example 10 The electrolyte in Example 10 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 10#.
  • the preparation method of the electrolyte of this example is the same as that of example 1, except that in the electrolyte of this example, the solvent contains ethylene carbonate (EC), propylene carbonate (PC), and diethyl carbonate (DEC).
  • EC ethylene carbonate
  • PC propylene carbonate
  • DEC diethyl carbonate
  • PP propyl propionate
  • PP mass fraction of the solvent in the electrolyte
  • Example 11 The electrolyte in Example 11 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 11#.
  • the preparation method of the electrolyte of this example is the same as that of example 1, except that the lithium salt in the electrolyte of this example is LiPF 6 and LiTFSI, and the mass fractions of LiPF 6 and LiTFSI in the electrolyte are 10% and 10% respectively.
  • the sulfur compound shown by T1 accounts for 0.5% of the mass fraction of the electrolyte
  • the boron-containing lithium salt compound is LiBOB
  • the mass fraction of LiBOB accounts for 1% of the electrolyte.
  • Example 12 The electrolyte in Example 12 is combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 12#.
  • the preparation method of the electrolyte of this example is the same as that of example 1, except that the lithium salt in the electrolyte of this example is LiPF 6 and LiFSI, and the mass fractions of LiPF 6 and LiFSI in the electrolyte are 10% and 10% respectively. 5%, the sulfur compound shown in T1 accounts for 1% of the electrolyte, and LiODFB accounts for 1% of the electrolyte.
  • Example 13 The electrolyte in Example 13 is combined with lithium cobalt oxide positive electrode sheet, separator and artificial graphite negative electrode to assemble lithium ion battery 13#.
  • the preparation method of the electrolyte of this comparative example is the same as that of Example 1. The only difference is that the additive in the electrolyte of this comparative example is only the compound shown in T1, and the compound shown in T1 accounts for 1% of the mass fraction of the electrolyte.
  • the mass fraction of the solvent in the electrolyte is 85.5%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • the electrolyte in Comparative Example 1 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 14#.
  • the preparation method of the electrolyte of this comparative example is the same as that of Example 1. The only difference is that the additive in the electrolyte of this comparative example is only LiODFB, and the mass fraction of LiODFB in the electrolyte is 1%, and the mass fraction of the solvent in the electrolyte is 85.5%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • the electrolyte in Comparative Example 2 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 15#.
  • the preparation method of the electrolyte of this comparative example is the same as that of Example 1. The only difference is that LiODFB in the electrolyte of this comparative example accounts for 0.01% of the mass fraction of the electrolyte, and the sulfur compound shown in T1 accounts for the mass fraction of the electrolyte. It is 1%, the mass fraction of the solvent in the electrolyte is 85.49%, and the mass fraction of LiPF 6 in the electrolyte is 13.5%.
  • the electrolyte in Comparative Example 3 was combined with a lithium cobalt oxide positive electrode sheet, a separator and an artificial graphite negative electrode to assemble a lithium ion battery 16#.
  • the lithium ion battery 1-16# was tested at room temperature with a charge-discharge rate of 0.5C for 3 cycles of charge and discharge, and then charged to a full charge at a rate of 0.5C, and the highest discharge capacity Q and the first 3 cycles of 0.5C were recorded respectively Battery thickness T.
  • Battery thickness T Store the fully charged battery at 60°C for 30 days, record the battery thickness T0 and 0.5C discharge capacity Q1 after 30 days, then charge and discharge the battery 3 times at a rate of 0.5C at room temperature, and record the highest of the 3 cycles Discharge capacity Q2, calculate the thickness change rate, capacity retention rate and capacity recovery rate of the battery during high temperature storage. The results are shown in Table 1.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Electrochemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Secondary Cells (AREA)

Abstract

一种电解液及其制备方法和锂离子电池，电解液按照质量分数包括以下组分：锂盐10-20％以及添加剂组合物0.2-7％，余量为溶剂；其中，所述添加剂组合物包括含硼锂盐化合物和式1所述的硫类化合物，式1中，R 1和R 3各自独立的选自氢、卤素、取代或未取代的烷基；R 2选自取代或为取代的亚烷基或者直接键合；所述含硼锂盐化合物在所述电解液中的质量分数至少为0.1％。所述电解液能够显著改善SEI膜的性能，从而有利于提高锂离子电池的循环性能和存储性能。

Description

一种电解液及其制备方法和锂离子电池
本申请要求于2019年8月6日提交中国专利局、申请号为201910722002.4、申请名称为“一种电解液及其制备方法和锂离子电池”的中国专利申请的优先权，其全部内容通过引用结合在本申请中。
技术领域
本申请涉及一种电解液及其制备方法和锂离子电池，属于锂离子电池技术领域。
背景技术
近年来，锂离子电池作为一种二次电池得到了快速的发展以及广泛的应用。目前锂离子电池的组成主要包括正极、负极、隔膜以及电解液。其中，在锂离子电池首次充放电过程中，电极材料与电解液会在电极材料的表面发生反应,形成一层覆盖于电极材料表面的钝化层，即本领域经常提及的具有固体电解质特征的界面膜(solid electrolyte interface，简称：SEI膜)。
SEI膜对锂离子电池的性能具有十分重要的影响。一方面，SEI膜能够阻止电解液与电极材料的进一步接触，抑制电解液在电极材料表面发生副反应，从而有利于锂离子电池循环性能的提高；另一方面，SEI膜的生成也会消耗电解液中的部分锂离子，从而降低了锂离子电池的电容量。
因此，如何在电极表面形成具有优异性能的SEI膜以显著优化锂离子电池的工作性能，是本领域亟待解决的技术问题。
发明内容
针对上述缺陷，本申请提供一种电解液，将该电解液用于锂离子电池中，能够显著改善SEI膜的性能，从而有利于提高锂离子电池的循环性能和存储性能。
本申请还提供一种电解液的制备方法，该方法工艺简便易实施，有助于 安全、高效的制备能够提高锂离子电池的循环性能和存储性能的电解液。
本申请还提供一种锂离子电池，含有上述电解液，因此该锂离子电池具有优异的循环性能和存储性能。
本申请提供一种电解液，按照质量分数包括以下组分：锂盐10-20％以及添加剂组合物0.2-7％，余量为溶剂；
其中，所述添加剂组合物包括含硼锂盐化合物和式1的硫类化合物，
Figure PCTCN2020107415-appb-000001
R 1和R 3各自独立的选自氢、卤素、取代或未取代的烷基；
R 2选自取代或未取代的亚烷基或者直接键合；
所述含硼锂盐化合物在所述电解液中的质量分数至少为0.1％。
如上所述的电解液，其中，所述硫类化合物在所述电解液中的质量分数为0.1-5％。
如上所述的电解液，其中，所述硫类合物在所述电解液中的质量分数为0.1-2％。
如上所述的电解液，其中，所述含硼锂盐化合物在所述电解液中的质量分数为0.1-2％。
如上所述的电解液，其中，所述硫类化合物具体选自T1-T4所示化合物中的至少一种：
Figure PCTCN2020107415-appb-000002
Figure PCTCN2020107415-appb-000003
如上所述的电解液，其中，所述含硼锂盐化合物选自双氟草酸硼酸锂、双草酸硼酸锂和四氟硼酸锂中的至少一种。
如上所述的电解液，其中，所述溶剂至少包括碳酸乙烯酯和碳酸丙烯酯中的一种。
如上所述的电解液，其中，所述碳酸乙烯酯和/或碳酸丙烯酯在所述电解液中的质量分数为10-50％。
本申请还提供一种上述任一所述的电解液的制备方法，包括：
在惰性气氛下，将溶剂、锂盐以及添加剂组合物混合，得到所述电解液。
本申请还提供一种锂离子电池，所述锂离子电池的电解液为上述任一所述的电解液。
本申请的实施，至少具有以下优势：
1、本申请提供的电解液，通过加入特定的添加剂组合物，能够优先于电解液中其他组分在电极表面形成稳定坚固的SEI膜，从而有效阻止电解液与电极的接触，显著提高锂离子电池的循环性能和存储性能；
2、本申请提供的电解液的制备方法工艺简单、可操作性强，便于实际推广和大规模应用；
3、本申请提供的锂离子电池，由于包括了本申请前述的电解液，因此该锂离子电池的具有优异的循环性能和存储性能。
具体实施方式
为使本申请实施例的目的、技术方案和优点更加清楚，下面将对本申请实施例中的技术方案进行清楚、完整地描述，显然，所描述的实施例是本申请一部分实施例，而不是全部的实施例。基于本申请中的实施例，本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例，都属于本申请保护的范围。
本申请提供一种电解液，按照质量分数包括以下组分：锂盐10-20％以及添加剂组合物0.2-7％，余量为溶剂；
其中，所述添加剂组合物包括含硼锂盐化合物和式1所述的硫类化合物，
Figure PCTCN2020107415-appb-000004
R 1和R 3各自独立的选自氢、卤素、取代或未取代的烷基；
R 2选自取代或未取代的亚烷基或者直接键合；
所述含硼锂盐化合物在所述电解液中的质量分数至少为0.1％。
本申请的添加剂组合物为含硼锂盐化合物和式1所述的硫类化合物的组合，添加剂组合物在电解液中的质量分数为0.2-7％，且当含硼锂盐化合物在所述电解液中的质量分数至少为0.1％时，能够显著提升锂离子电池首次充放电时在电极表面形成的SEI膜的性能，从而能够对锂离子电池的循环性能和存储性能产生积极的影响。发明人基于此现象对SEI膜进行分析，认为可能是：添加剂组合物能够在较低的电位发生电化学反应，从而优于电解液中的其他组分在电极表面形成具有硼元素和硫元素的SEI膜，其中，硼元素有利于降低锂离子的传质阻抗，硫元素以聚合物的形式存在于SEI膜中有利于提高SEI膜的强度。
因此，锂离子电池在充放电过程中，锂离子能够以较低的阻力通过SEI膜而完成在电极上的极嵌脱过，因此有利于提升嵌脱锂以及电极电解液界面动力学的稳定性，从而对锂离子电池的性能，如循环寿命、自放电、额定速率以及电池的耐温性能等产生显著的提升作用。而SEI膜强度的提高能够避免SEI膜在电解液中发生溶解，避免因溶剂分子共嵌入对电极材料造成的破坏，又能够保证电极对其他粒子或电子的绝缘性能，从而进一步提高了电极的循环性能和存储性能。
式1中，R 1和R 3可以是取代或未取代的C 1-C 5的直链烷基，C 3-C 5的支链烷基，或者C 3-C 5的环烷基，R 1和R 3具体可以是-CH 3、-CH 2CH 3、-C(CH 3) 3、-C(CH 3) 2F、-CH 2F、-CH 2(C 6H 6)、-CH(C 6H 6)CH 2CH 3、 -CH 2CH 2CH 2CH 2CH 3、-CH 2C(CH 3) 3中的一种；R 2选自取代或未取代的C 1－C 10的亚烷基、直接键合，R 2具体可以是-CH 2-、-CHF-、-CH 2CHFCH 2-、-CH 2CH 2-、-CH 2CHFCH 2-、-CH 2C(CH 3) 2CH 2-中的一种，其中，直接键合是指两个五元环直接键结，并不通过任何取代基连接。
本申请式1所示的硫类化合物可以通过商购或者任何可行的制备方法获得。
进一步地，可以控制式1所述的硫类化合物在电解液中的质量分数为0.1-5％。研究表明，随着硫类化合物的用量在一定范围内增加，锂离子电池的存储性能和循环性能都具有较为优异的表现。当然，对于电解液中使用不同的锂盐和/或溶剂，甚至采用不同的正极材料、负极材料或隔膜，对于锂离子电池的最终性能都会产生影响。因此大致而言，当将电解液中硫类化合物的质量分数控制在0.1％-2％，可基本使锂离子电池具有优异的表现。
此外，当含硼锂盐化合物在电解液中的质量分数为0.1-2％时，与硫类化合物的适配性更高，有助于进一步提升锂离子电池的循环性能和存储性能。
进一步地，本申请的硫类化合物具体选自T1-T4所示化合物中的至少一种：
Figure PCTCN2020107415-appb-000005
本申请的含硼锂盐化合物选自双氟草酸硼酸锂(LiODFB)、双草酸硼酸锂(LiBOB)和四氟硼酸锂(LiBF 4)中的至少一种。当然，若含硼锂盐化合物为上述化合物中的两种或以上，本申请不特别限定各化合物之间的 比例。
在发明人研究的过程中发现，当电解液中的溶剂至少包括碳酸乙烯酯和碳酸丙烯酯的一种时，有助于进一步优化锂离子电池的循环性能和存储性能。发明人推测，可能是碳酸乙烯酯和碳酸丙烯酯对上述添加剂组合物在电极表面形成SEI膜具有辅助作用，能够加快添加剂组合物在电极表面优先其他组分形成SEI膜，从而提高SEI膜中硫元素与硼元素的含量。
进一步的，当碳酸乙烯酯和/或碳酸丙烯酯在所述电解液中的质量分数为10-50％时，能够进一步优化锂离子电池的性能。
也就是说，若溶剂中包括碳酸乙烯酯或碳酸丙烯酯的一种，则碳酸乙烯酯或碳酸丙烯酯在电解液中的质量分数可以为10-50％；若溶剂中包括碳酸乙烯酯和碳酸丙烯酯，则碳酸乙烯酯和碳酸丙烯酯的总量在电解液中的质量分数可以为10-50％。
本申请的电解液除了包括碳酸乙烯酯和/或碳酸丙烯酯之外，还可以包括目前锂离子电池电解液中常用的其他溶剂中的一种或多种，例如：碳酸丁烯酯、氟代碳酸乙烯酯(FEC)、碳酸二甲酯(DMC)、碳酸二乙酯(DEC)、二氟代碳酸乙烯酯(DFEC)、碳酸二丙酯、碳酸甲乙酯(EMC)、乙酸乙酯、丙酸乙酯、乙酸丙酯、丙酸丙酯、环丁砜、γ-丁内酯等。当然，若电解液的溶剂包括上述化合物中的两种或更多种，本申请不特别限定各化合物之间的比例。
本申请对于电解液中的锂盐不做特别限定，可以是目前锂离子电解液中所常用的电解质锂盐，比如可以选择六氟磷酸锂(LiPF 6)、双(氟磺酰)亚胺锂(LiFSI)、双(三氟甲基磺酸酰)亚氨锂(LiTFSI)中的一种或多种。当然，若电解液的锂盐包括上述化合物中的两种或更多种，本申请不特别限定各化合物之间的比例。
本申请还提供一种上述任一所述的电解液的制备方法，包括：在惰性气氛下，将溶剂、锂盐以及添加剂组合物混合，得到所述电解液。
具体可以在充满氩气的手套箱(水分＜1ppm，氧气＜1ppm)中进行性。
在制备过程中，可以向溶剂中加入锂盐和添加剂组合物，搅拌后，得到本申请的电解液。其中，本申请不限制锂盐和添加剂组合物的加入顺序，并且添加剂组合物中的硫类化合物和含硼锂盐化合物可以一起加入，也可 以分开前后加入。
本申请的电解液的制备方法操作简便，只需要混合原料并进行搅拌即可完成，因此能够以高效率、低成本完成电解液的制备。
本申请还提供一种锂离子电池，该锂离子电池的电解液为前述任一所述的电解液。
能够想到的是，本申请的锂离子电池除了上述电解液外，还包括正极、负极以及隔膜。
本申请并不严格限定正极的活性材料，可以是目前锂离子电池中所常用的正极活性材料，比如钴酸锂、镍酸锂、锰酸锂、锰酸锂、镍钴锰三元材料、镍钴铝三元材料、磷酸铁锂(LFP)、镍锰酸锂、富锂锰基材料、等中的至少一种。
具体在操作时，可以将上述至少一种正极活性材料与导电碳黑、导电石墨和粘结剂聚偏二氟乙烯按质量比96:1:1:2分散在适量的N-甲基吡咯烷酮(NMP)溶剂中，充分搅拌混合形成均匀的正极浆料；将正极浆料均匀涂覆在正极集流体铝箔上，经过烘干、辊压和分切，得到正极片。
本申请并不严格限定负极的活性材料，可以是目前锂离子电池中所常用的负极活性材料，比如人造石墨、硬炭、软炭等中的至少一种。
具体在操作时，可以将上述至少一种负极活性材料与导电碳黑、粘结剂丁苯橡胶(SBR)和增稠剂羧甲基纤维素钠(CMC)按质量比96:1:1.5:1.5分散在适量的去离子水溶剂中，充分搅拌混合形成均匀的负极浆料；将负极浆料均匀涂覆在负极集流体铜箔上，经过烘干、辊压和分切，得到负极片。
本申请并不严格限定隔膜的材料选择，可以是目前锂离子电池中所常用的隔膜材料，比如为聚丙烯隔膜(PP)、聚乙烯隔膜(PE)、聚丙烯/聚乙烯双层复合膜(PP/PE)、聚酰亚胺静电纺丝隔膜(PI)、聚丙烯/聚乙烯/聚丙烯三层复合膜(PP/PE/PP)、纤维素无纺布隔膜、带陶瓷涂层的隔膜中的一种。
在制备锂离子电池时，将正极片、隔膜和负极片进行卷绕得到裸电芯，并将电芯封装到预先冲压成型的铝塑膜袋中。封装好的电池经过85℃烘干水分后，将本申请的电解液注入到干燥的电池中，电池经过搁置、化成和二次封口后完成锂离子电池的制备。
本申请的锂离子电池，由于包括了前述的电解液，因此在首次充放电时能够在电极表面形成性能极佳的SEI膜，使本申请的锂离子电池具有优异的循环性能和存储性能。
以下，通过具体实施例对本申请的电解液及其制备方法和锂离子电池进行详细的介绍。
实施例1
本实施例的电解液按照下述方法制备得到：
在充满氩气的手套箱(水分＜1ppm，氧分＜1ppm)中，将碳酸乙烯酯(EC)、碳酸丙烯酯(PC)、碳酸二乙酯(DEC)和丙酸丙酯(PP)以15:15:15:55质量比混合均匀，在混合溶液中缓慢加入LiPF 6，搅拌至其完全溶解,再依次加入T1所示的硫类化合物和LiODFB，得到实施例1的电解液。
本实施例的电解液中，溶剂占电解液的质量分数为84.5％，其中，碳酸乙烯酯与碳酸丙烯酯占电解液的质量分数为25.35％，LiPF 6占电解液的质量分数为13.5％；T1所示的硫类化合物占电解液的质量分数为1％，LiODFB占电解液的质量分数为1％。
将实施例1中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池1#。
实施例2
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中T1所示的硫类化合物占电解液的质量分数为0.2％，溶剂占电解液的质量分数为85.3％，LiPF 6占电解液的质量分数为13.5％，LiODFB占电解液的质量分数为1.0％。
将实施例2中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池2#。
实施例3
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施 例电解液中的硫类化合物为T2所示的硫类化合物且占电解液的质量分数为0.5％，含硼锂盐化合物为LiBOB且LiBOB占电解液的质量分数为1％，溶剂占电解液的质量分数为85％，LiPF 6占电解液的质量分数为13.5％。
将实施例3中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池3#。
实施例4
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中的硫类化合物为T3所示的硫类化合物且占电解液的质量分数为2％，含硼锂盐化合物为LiBF 4且LiBF 4占电解液的质量分数为0.5％，溶剂占电解液的质量分数为84％，LiPF 6占电解液的质量分数为13.5％。
将实施例4中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池4#。
实施例5
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中含硼锂盐化合物为LiBF 4且LiBF 4占电解液的质量分数为2％，T1所示的硫类化合物占电解液的质量分数为1％，溶剂占电解液的质量分数为83.5％，LiPF 6占电解液的质量分数为13.5％。
将实施例5中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池5#。
实施例6
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中T1所示的硫类化合物占电解液的质量分数为2％，LiODFB占电解液的质量分数为1％，溶剂占电解液的质量分数为83.5％，LiPF 6占电解液的质量分数为13.5％。
将实施例6中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池6#。
实施例7
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中T1所示的硫类化合物占电解液的质量分数为4％，LiODFB占电解液的质量分数为1％，溶剂占电解液的质量分数为81.5％，LiPF 6占电解液的质量分数为13.5％。
将实施例7中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池7#。
实施例8
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中LiODFB占电解液的质量分数为2.5％，T1所示的硫类化合物占电解液的质量分数为1％，溶剂占电解液的质量分数为83％，LiPF 6占电解液的质量分数为13.5％。
将实施例8中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池8#。
实施例9
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中溶剂为DEC:PP＝50:50，且电解液中不含有EC和PC。
将实施例9中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池9#。
实施例10
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中，溶剂中碳酸乙烯酯(EC)、碳酸丙烯酯(PC)、碳酸二乙酯(DEC)和丙酸丙酯(PP)的质量比为5:5:50:40，且溶剂占电解液的质量分数为84.5％，其中，碳酸乙烯酯与碳酸丙烯酯占电解液的质量分数为8.45％
将实施例10中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池10#。
实施例11
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中，溶剂中碳酸乙烯酯(EC)、碳酸丙烯酯(PC)、碳酸二乙酯(DEC)和丙酸丙酯(PP)的质量比为30:30:30:10，且溶剂占电解液的质量分数为84.5％，其中，碳酸乙烯酯与碳酸丙烯酯占电解液的质量分数为50.7％
将实施例11中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池11#。
实施例12
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中锂盐为LiPF 6和LiTFSI，且LiPF 6和LiTFSI分别占电解液的质量分数为10％和5％，T1所示的硫类化合物占电解液的质量分数为0.5％，含硼锂盐化合物为LiBOB，且LiBOB占电解液的质量分数为1％。
将实施例12中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池12#。
实施例13
本实施例的电解液的制备方法与实施例1相同，唯一不同的是，本实施例电解液中锂盐为LiPF 6和LiFSI，且LiPF 6和LiFSI分别占电解液的质量分数为10％和5％，T1所示的硫类化合物占电解液的质量分数为1％，LiODFB占电解液的质量分数为1％。
将实施例13中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池13#。
对比例1
本对比例的电解液制备方法与实施例1相同，唯一不同的是，本对比例电解液中的添加剂只有T1所示的化合物，且T1所示的化合物占电解液的质量分数为1％，溶剂占电解液的质量分数为85.5％，LiPF 6占电解液的质量分数为13.5％。
将对比例1中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成 锂离子电池14#。
对比例2
本对比例的电解液制备方法与实施例1相同，唯一不同的是，本对比例电解液中的添加剂只有LiODFB，且LiODFB占电解液的质量分数为1％，溶剂占电解液的质量分数为85.5％，LiPF 6占电解液的质量分数为13.5％。
将对比例2中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池15#。
对比例3
本对比例的电解液制备方法与实施例1相同，唯一不同的是，本对比例电解液中的LiODFB占电解液的质量分数为0.01％，T1所示的硫类化合物占电解液的质量分数为1％，溶剂占电解液的质量分数为85.49％，LiPF 6占电解液的质量分数为13.5％。
将对比例3中的电解液搭配钴酸锂正极片、隔膜及人造石墨负极组装成锂离子电池16#。
对上述锂离子电池1-16#进行电化学性能测试，具体如下所述：
1、常温循环实验
将锂离子电池1-16#置于(25±2)℃环境中，电池按照1C恒流充电4.45V截止电流为0.02C，电池充满电后搁置5min，再以1C恒流放电至截止电压3.0V，记录前3次循环的最高放电容量为初始容量Q，当循环达到200次时，记录锂离子电池的最后一次的放电容量Q1，并按照下述公式计算常温循环200次后的容量保持率，结果见表1。
Figure PCTCN2020107415-appb-000006
2、高温存储实验
将锂离子电池1-16#在室温下以0.5C的充放电倍率进行3次充放电循环测试，然后0.5C倍率充到满电状态，分别记录前3次0.5C循环的最高放电容量Q和电池厚度T。将满电状态的电池在60℃下存储30天，记录 30天后的电池厚度T0和0.5C放电容量Q1，然后将电池在室温下以0.5C的倍率充放3次，记录3次循环的最高放电容量Q2，计算得到电池高温存储的厚度变化率、容量保持率和容量恢复率，结果见表1。
Figure PCTCN2020107415-appb-000007
Figure PCTCN2020107415-appb-000008
Figure PCTCN2020107415-appb-000009
表1
Figure PCTCN2020107415-appb-000010
通过表1可知：本申请实施例通过在锂离子电池的电解液中加入特定的添加剂组合物，可显著地提高锂离子电池的循环性能和存储性能。
最后应说明的是：以上各实施例仅用以说明本申请的技术方案，而非 对其限制；尽管参照前述各实施例对本申请进行了详细的说明，本领域的普通技术人员应当理解：其依然可以对前述各实施例所记载的技术方案进行修改，或者对其中部分或者全部技术特征进行等同替换；而这些修改或者替换，并不使相应技术方案的本质脱离本申请各实施例技术方案的范围。

Claims (10)

  1. 一种电解液，其中，按照质量分数包括以下组分：锂盐10-20％以及添加剂组合物0.2-7％，余量为溶剂；
    其中，所述添加剂组合物包括含硼锂盐化合物和式1的硫类化合物，
    Figure PCTCN2020107415-appb-100001
    R 1和R 3各自独立的选自氢、卤素、取代或未取代的烷基；
    R 2选自取代或未取代的亚烷基或者直接键合；
    所述含硼锂盐化合物在所述电解液中的质量分数至少为0.1％。
  2. 根据权利要求1所述的电解液，其中，所述硫类化合物在所述电解液中的质量分数为0.1-5％。
  3. 根据权利要求1所述的电解液，其中，所述硫类合物在所述电解液中的质量分数为0.1-2％。
  4. 根据权利要求1-3任一所述的电解液，其中，所述含硼锂盐化合物在所述电解液中的质量分数为0.1-2％。
  5. 根据权利要求1-4任一所述的电解液，其中，所述硫类化合物具体选自T1-T4所示化合物中的至少一种：
    Figure PCTCN2020107415-appb-100002
  6. 根据权利要求1-4任一所述的电解液，其中，所述含硼锂盐化合物 选自双氟草酸硼酸锂、双草酸硼酸锂和四氟硼酸锂中的至少一种。
  7. 根据权利要求1-4任一所述的电解液，其中，所述溶剂至少包括碳酸乙烯酯和碳酸丙烯酯中的一种。
  8. 根据权利要求7所述的电解液，其中，所述碳酸乙烯酯和/或碳酸丙烯酯在所述电解液中的质量分数为10-50％。
  9. 一种权利要求1-8任一项所述电解液的制备方法，其中，包括：
    在惰性气氛下，将溶剂、锂盐以及添加剂组合物混合，得到所述电解液。
  10. 一种锂离子电池，其中，所述锂离子电池的电解液为权利要求1-8任一项所述的电解液。
PCT/CN2020/107415 2019-08-06 2020-08-06 一种电解液及其制备方法和锂离子电池 WO2021023265A1 (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US17/590,957 US20220158242A1 (en) 2019-08-06 2022-02-02 Electrolyte and preparation method thereof and lithium ion battery

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201910722002.4A CN112349958B (zh) 2019-08-06 2019-08-06 一种电解液及其制备方法和锂离子电池
CN201910722002.4 2019-08-06

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/590,957 Continuation US20220158242A1 (en) 2019-08-06 2022-02-02 Electrolyte and preparation method thereof and lithium ion battery

Publications (1)

Publication Number Publication Date
WO2021023265A1 true WO2021023265A1 (zh) 2021-02-11

Family

ID=74367117

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2020/107415 WO2021023265A1 (zh) 2019-08-06 2020-08-06 一种电解液及其制备方法和锂离子电池

Country Status (3)

Country Link
US (1) US20220158242A1 (zh)
CN (1) CN112349958B (zh)
WO (1) WO2021023265A1 (zh)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20230046273A (ko) * 2021-09-27 2023-04-05 컨템포러리 엠퍼렉스 테크놀로지 씨오., 리미티드 이차 전지, 전지 모듈, 전지 팩 및 전기 장치

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103208653A (zh) * 2013-03-21 2013-07-17 东莞新能源科技有限公司 一种镍基阴极锂离子电池用电解液及锂离子电池
CN105810998A (zh) * 2016-04-06 2016-07-27 宁德新能源科技有限公司 一种电解液以及包括该电解液的锂离子电池
CN106905291A (zh) * 2015-12-22 2017-06-30 天津鑫源广泰新材料科技有限公司 一种3，3—联二硫酸乙烯酯的生产方法
CN109148950A (zh) * 2017-06-15 2019-01-04 宁德时代新能源科技股份有限公司 一种电解液及电池

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1891700A (zh) * 2005-07-01 2007-01-10 北京大学 卤代环状亚硫酸酯及一种电解液、锂电池和锂硫电池
KR20130119842A (ko) * 2010-06-04 2013-11-01 우베 고산 가부시키가이샤 비수 전해액 및 그것을 이용한 전기 화학 소자
JP6911655B2 (ja) * 2016-09-16 2021-07-28 株式会社Ｇｓユアサ 蓄電素子用非水電解質、非水電解質蓄電素子、及び非水電解質蓄電素子の製造方法
CN110998957B (zh) * 2017-08-24 2023-03-24 三井化学株式会社 电池用非水电解液及锂二次电池
JP2019075320A (ja) * 2017-10-18 2019-05-16 日立化成株式会社 リチウムイオン二次電池
CN109273765A (zh) * 2018-09-20 2019-01-25 合肥国轩高科动力能源有限公司 一种电池电解液、制备方法及含有该电解液的硅负极电池

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103208653A (zh) * 2013-03-21 2013-07-17 东莞新能源科技有限公司 一种镍基阴极锂离子电池用电解液及锂离子电池
CN106905291A (zh) * 2015-12-22 2017-06-30 天津鑫源广泰新材料科技有限公司 一种3，3—联二硫酸乙烯酯的生产方法
CN105810998A (zh) * 2016-04-06 2016-07-27 宁德新能源科技有限公司 一种电解液以及包括该电解液的锂离子电池
CN109148950A (zh) * 2017-06-15 2019-01-04 宁德时代新能源科技股份有限公司 一种电解液及电池

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
LEE SANG HYUN, SUKEON YOON, EUI-HYUNG HWANG, YOUNG-GIL KWON, YOUNG-GI LEE, KUK YOUNG CHO: "[4, 4′-bi(1, 3, 2-dioxathiolane)] 2, 2′-dioxide: A novel cathode additive for high-voltage performance in lithium ion batteries", JOURNAL OF POWER SOURCES, pages 112 - 118, XP055778283 *

Also Published As

Publication number Publication date
CN112349958B (zh) 2022-02-11
CN112349958A (zh) 2021-02-09
US20220158242A1 (en) 2022-05-19

Similar Documents

Publication Publication Date Title
JP7159459B2 (ja) リチウムイオン二次電池
JP7196364B2 (ja) 二次電池及び当該二次電池を含む電池モジュール、電池パック並びに装置
WO2020063371A1 (zh) 正极极片及锂离子二次电池
CN109728340B (zh) 锂离子电池
WO2016110123A1 (zh) 一种非水电解液及锂离子二次电池
CN114597493A (zh) 一种锂离子电池及其电解液
CN111525190B (zh) 电解液及锂离子电池
CN112635835B (zh) 高低温兼顾的非水电解液及锂离子电池
WO2023040687A1 (zh) 一种电解液、包含该电解液的电化学装置和电子装置
WO2020043151A1 (zh) 正极极片、其制备方法及锂离子二次电池
CN111883839A (zh) 高压电解液及基于其的锂离子电池
WO2023087213A1 (zh) 一种电池包及其用电装置
CN109687026B (zh) 一种高压三元锂离子电池电解液及含该电解液的锂离子电池
WO2021047405A1 (zh) 一种电解液及包含该电解液的锂金属电池、电池模块、电池包和装置
WO2021180021A1 (zh) 一种电解液及其制备方法和应用
WO2023070988A1 (zh) 电化学装置和包含其的电子装置
CN109119599B (zh) 一种二次电池及其制备方法
CN112928328A (zh) 一种含有硅烷基磺酰胺化合物的锂离子电池电解液和锂离子二次电池
US20230026621A1 (en) Secondary battery
WO2021023265A1 (zh) 一种电解液及其制备方法和锂离子电池
CN109802176B (zh) 电解液和含有电解液的锂离子电池
CN112467213B (zh) 电解液和使用了其的锂离子电池
JP7389245B2 (ja) 二次電池及び該二次電池を備える装置
CN114497746A (zh) 一种电池
CN112349957A (zh) 一种电解液及其制备方法和锂离子电池

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: 20850335

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 20850335

Country of ref document: EP

Kind code of ref document: A1

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205A DATED 12.08.2022).

122 Ep: pct application non-entry in european phase

Ref document number: 20850335

Country of ref document: EP

Kind code of ref document: A1