CN110854435A - Lithium battery electrolyte and lithium battery - Google Patents

Lithium battery electrolyte and lithium battery Download PDF

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CN110854435A
CN110854435A CN201911161849.6A CN201911161849A CN110854435A CN 110854435 A CN110854435 A CN 110854435A CN 201911161849 A CN201911161849 A CN 201911161849A CN 110854435 A CN110854435 A CN 110854435A
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electrolyte
carbonate
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additive
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CN110854435B (en
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沈丽明
吴月
陈淑青
李敏
方耀国
田秀君
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Sichuan Lingpai New Energy Technology Co ltd
Suzhou Lingpai New Energy Technology Co ltd
Hunan Lingpai New Energy Technology Co Ltd
Hunan Lead Power Dazhi Technology Inc
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Lingpa New Energy Technology Shanghai Co Ltd
Shanxi Konos New Energy Technology Co Ltd
Hunan Xinminya New Energy Technology Co Ltd
Sichuan Xinminya Battery Technology Co Ltd
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/056Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564Accumulators 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
    • H01M10/0566Liquid materials
    • H01M10/0567Liquid materials characterised by the additives
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00Electrolytes
    • H01M2300/0017Non-aqueous electrolytes
    • H01M2300/0025Organic electrolyte
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

The application belongs to the technical field of lithium ion batteries, and particularly relates to a lithium battery electrolyte and a lithium battery. The electrolyte comprises an organic solvent, a lithium salt and a first additive, wherein the first additive comprises a silane compound, and the silane compound is selected from at least one of compounds shown in a structural formula (1):
Figure DDA0002284544500000011
wherein, X is selected from one of P ═ O, P and B, and Y is selected from substituted or unsubstituted C1~10Alkyl, substituted or unsubstituted C1~10Alkoxy, substituted or unsubstituted C2~10Alkenyl, substituted or unsubstituted C2~10Alkenyloxy, substituted or unsubstituted C2~10Alkynyl, substituted or unsubstituted C2~10Alkynyloxy, C ═ O functional group, O ═ S ═ O functional group; n is taken from any of 1, 2 or 3. For silicon in the first additiveThe structure of the alkyl compound is optimized, and a functional group with good film forming capability is introduced into the structure, so that the film forming capability can be improved while the impedance of the electrolyte is optimized, and the performance of the battery is improved.

Description

Lithium battery electrolyte and lithium battery
Technical Field
The application belongs to the technical field of lithium ion batteries, and particularly relates to a lithium battery electrolyte and a lithium battery.
Background
Nowadays, with the expansion of market demand of electronic products and the development of power and energy storage devices, power type lithium ion batteries are beginning to be applied to electric tools and electric vehicles, so that the requirements of people on lithium ion batteries are also continuously improved, and it is urgent to develop lithium ion batteries with lower internal resistance and higher dynamics. The electrolyte is one of the core components of the lithium ion battery, and the optimization and improvement of the electrolyte are more and more paid attention by people. At present, the effective method is to reduce the dosage of the film forming additive in the electrolyte based on the existing components, but the storage and the cycle performance of the battery cell are influenced; or resistance-reducing additives, but such additives generally do not have good film-forming ability and need to be used in combination with other film-forming additives, and thus the overall resistance-reducing performance is not satisfactory.
Moreover, the electrolyte widely used in the current lithium ion battery still has many defects, especially under high energy density, the performance of the lithium ion battery is poor, such as larger direct current impedance and poor cycle performance. Therefore, there is a need to develop a new electrolyte for lithium battery and lithium battery, which can effectively reduce impedance and improve battery performance.
Disclosure of Invention
The application provides a lithium battery electrolyte and a lithium battery, which can improve the film forming capacity while optimizing the impedance of the electrolyte, thereby improving the performance of the battery.
One aspect of the present application provides a lithium battery electrolyte including an organic solvent, a lithium salt, and a first additive, wherein the first additive includes a silane compound selected from at least one of compounds represented by structural formula (1):
Figure BDA0002284544490000021
wherein, X is selected from one of P ═ O, P and B, and Y is selected from substituted or unsubstituted C1~10Alkyl, substituted or unsubstituted C1~10Alkoxy, substituted or unsubstituted C2~10Alkenyl, substituted or unsubstituted C2~10Alkenyloxy, substituted or unsubstituted C2~10Alkynyl, substituted or unsubstituted C2~10Alkynyloxy, C ═ O functional group, O ═ S ═ O functional group; part or all of the hydrogen on the Y can be respectively replaced by halogen, nitro, cyano, carboxyl and C1~6Alkyl radical, C2~6Alkenyl substitution; n is taken from any of 1, 2 or 3.
In some embodiments herein, the silane compound is selected from at least one of the following compounds:
Figure BDA0002284544490000022
Figure BDA0002284544490000023
Figure BDA0002284544490000031
in some embodiments of the present application, the electrolyte further comprises a second additive, the second additive comprising at least one of vinylene carbonate, 1, 3-propane sultone, vinyl vinylene carbonate, 1, 3-propene sultone, and vinyl sulfate.
In some embodiments of the present application, the second additive is contained in the electrolyte in an amount of 0.01% to 20% by mass.
In some embodiments of the present application, the silane compound is contained in the electrolyte in an amount of 0.01 to 10% by mass.
In some embodiments of the present application, the organic solvent includes cyclic carbonates and chain carbonates.
In some embodiments of the present application, the cyclic carbonate is selected from at least one of propylene carbonate, ethylene carbonate; the chain carbonate is at least one selected from dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, methyl propyl carbonate, ethyl acetate and propyl acetate.
In some embodiments of the present application, the lithium salt is LiPF6、LiBF4、LiBOB、LiODFB、LiFSI、LiPO2F2One or more of (a).
In some embodiments of the present application, the lithium salt is LiPF6The concentration is 0.8 to 1.5 mol/L.
Another aspect of the present application further provides a lithium battery, including a positive electrode, a negative electrode and an electrolyte, where the electrolyte is the above-mentioned electrolyte.
According to the lithium battery electrolyte and the lithium battery, the structure of the silane compound in the first additive is optimized, and the functional group with good film forming capability is introduced into the structure, so that the film forming capability can be improved while the impedance of the electrolyte is optimized, and the performance of the battery is improved.
Detailed Description
The following description is presented to enable any person skilled in the art to make and use the present disclosure, and is provided in the context of a particular application and its requirements. Various local modifications to the disclosed embodiments will be readily apparent to those skilled in the art, and the general principles defined herein may be applied to other embodiments and applications without departing from the spirit and scope of the present disclosure. Thus, the present disclosure is not to be limited to the embodiments shown, but is to be accorded the widest scope consistent with the claims.
The technical solution of the present invention will be described in detail with reference to examples.
Research shows that in the first charge and discharge process of the liquid lithium ion battery, the electrode material and the electrolyte react on a solid-liquid interface to form a passivation layer covering the surface of the electrode material. This passivation layer is an interfacial layer, which is characterized by a solid electrolyte, is an electronic insulator but is a good conductor of lithium ions, and lithium ions can freely intercalate and deintercalate through the passivation layer, so this passivation film is called a "solid electrolyte interface film" (SEI film for short).
The formation of the SEI film has a crucial influence on the performance of the electrode material. On one hand, the formation of the SEI film consumes part of lithium ions, so that the irreversible capacity of the first charge and discharge is increased, and the charge and discharge efficiency of the electrode material is reduced; on the other hand, the SEI film has organic solvent insolubility and can stably exist in an organic electrolyte solution, and solvent molecules cannot pass through the passivation film, so that co-embedding of the solvent molecules can be effectively prevented, damage to an electrode material due to the co-embedding of the solvent molecules is avoided, and the cycle performance and the service life of the electrode are greatly improved. Therefore, developing a lithium battery electrolyte with lower impedance and higher film forming capability becomes a hot spot of lithium battery research. Through intensive research, the inventors of the present application find a functional additive for an electrolyte of a lithium battery, which can improve the film forming ability while optimizing the impedance of the electrolyte, thereby improving the electrochemical performance of the lithium battery.
The embodiment of the application provides a lithium battery electrolyte, which comprises an organic solvent, a lithium salt and a first additive, wherein the first additive comprises a silane compound, and the silane compound is selected from at least one of compounds shown in a structural formula (1):
Figure BDA0002284544490000051
wherein, X is selected from one of P ═ O, P and B, and Y is selected from substituted or unsubstituted C1~10Alkyl, substituted or unsubstituted C1~10Alkoxy, substituted or unsubstituted C2~10Alkenyl, substituted or unsubstituted C2~10Alkenyloxy, substituted or unsubstituted C2~10Alkynyl, substituted or unsubstituted C2~10Alkynyloxy, C ═ O functional group, O ═ S ═ O functional group; some or all of the hydrogens on the Y may be replaced by halogen, nitro, cyano, carboxyl, C1~6Alkyl radical, C2~6Alkenyl substitution; n is taken from any of 1, 2 or 3.
The conventional silane compound has trimethylsilyl group, so that the effect of reducing the impedance is better, but the silane compound is not an excellent film forming additive and cannot improve the film forming capability of the electrolyte, so that the silane compound has no obvious improvement effect on the high-temperature performance of the battery. The present application is optimized for the structure of silane compounds, in which a substituted or unsubstituted C is introduced1~10Alkyl, substituted or unsubstituted C1~10Alkoxy, substituted or unsubstituted C2~10Alkenyl, substituted or unsubstituted C2~10Alkenyloxy, substituted or unsubstituted C2~10Alkynyl, substituted or unsubstituted C2~10And a functional group having a good film forming ability, such as an alkynyloxy group, a C ═ O functional group, an O ═ S ═ O functional group, and the like, so that the first additive including the silane compound can optimize the resistance and simultaneously improve the film forming ability of the electrolyte, thereby improving the high-temperature performance of the battery. Among them, the group represented by Y has a function of improving the film forming ability of the electrolyte, and the trimethylsilyl group has a function of reducing the impedance of the electrolyte.
In some embodiments of the present application, n may be 1, 2, or 3. The group represented by Y has a function of improving the film forming ability of the electrolyte, and in the structural formula (1), the larger the value of n indicates that the larger the proportion of the group represented by Y in the silane compound is, the stronger the film forming ability of the electrolyte is, and thus, specifically, the value of n can be selected according to the desired electrolyte property.
In some embodiments herein, the silane compound is selected from at least one of the following compounds:
Figure BDA0002284544490000061
Figure BDA0002284544490000062
Figure BDA0002284544490000071
in some embodiments of the present application, the silane compound is contained in the electrolyte in an amount of 0.01% to 10% by mass, for example, 1%, 3%, 5%, 7%, 9%, etc.
In some embodiments of the present application, the silane compound is contained in the electrolyte in an amount of 0.5% to 3% by mass, such as 0.5%, 1%, 3%, and the like.
In some embodiments of the present application, the electrolyte further comprises a second additive, the second additive comprising at least one of vinylene carbonate, 1, 3-propane sultone, vinyl vinylene carbonate, 1, 3-propene sultone, and vinyl sulfate. Besides the silane compound, the electrolyte can be matched with the second additive, and the second additive can play a role in assisting film formation and further optimize the performance of the electrolyte.
In some embodiments of the present application, the second additive is present in the electrolyte in an amount of 0.01% to 20% by mass, for example, 1%, 5%, 10%, 15%, 20%, etc.
In some embodiments of the present application, the second additive is present in the electrolyte in an amount of 0.2% to 5% by mass, for example, 1%, 2%, 3%, 4%, 5%, etc.
In some embodiments of the present application, the organic solvent includes cyclic carbonates and chain carbonates. The organic solvent is an important component of the electrolyte, and has a large influence on the properties of the electrolyte, such as thermal stability, conductivity and viscosity. In particular, different combinations of organic solvents may be selected depending on the desired properties.
In some embodiments of the present application, the concentration ratio of the cyclic carbonate to the chain carbonate may be between 10: 70 and 40: 60 by mass percent. The mass percentage concentration is preferably between 25: 75 and 35: 65, and the electrochemical performance of the electrolyte is improved.
In some embodiments of the present application, the cyclic carbonate is selected from at least one of propylene carbonate, ethylene carbonate; the chain carbonate is at least one selected from dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, methyl propyl carbonate, ethyl acetate and propyl acetate.
In some embodiments of the present application, the organic solvent consists of ethylene carbonate, ethyl methyl carbonate.
In some embodiments of the present application, the organic solvent consists of ethylene carbonate, ethyl methyl carbonate, diethyl carbonate.
In some embodiments of the present application, the organic solvent consists of ethylene carbonate, dimethyl carbonate, ethyl methyl carbonate.
In some embodiments of the present application, the lithium salt is LiPF6、LiBF4、LiBOB、LiODFB、LiFSI、LiPO2F2One or more of (a). In a lithium battery, a lithium salt is mainly used to supply lithium ions, making the basic operation of the lithium battery possible.
In some embodiments of the present application, the lithium salt is LiPF6The concentration is 0.8 to 1.5mol/L, for example, 0.8mol/L, 1mol/L, 1.2mol/L, etc. Increasing the concentration of lithium hexafluorophosphate can increase the density of the ionophore, which is helpful for increasing the interface reaction frequency, but when the concentration is too high, the phenomena of obvious reduction of ion conductivity and viscosity increase are caused, the overall resistance of the battery is increased, and the mobility of lithium ions is reduced.
Example 1
Uniformly mixing organic solvents ethylene carbonate and methyl ethyl carbonate according to the mass ratio of 30: 70, and slowly adding 1mol/L lithium salt LiPF into the organic solvents6Then, a silane compound represented by the structural formula (2) in an amount of 0.5% by weight of the total mass of the electrolyte and vinylene carbonate in an amount of 0.5% by weight were added to prepare an electrolyte 1.
Example 2
Uniformly mixing organic solvents ethylene carbonate and methyl ethyl carbonate according to the mass ratio of 30: 70, and slowly adding 1mol/L lithium salt LiPO into the organic solvents2F2Then, a silane compound represented by the structural formula (2) in an amount of 1% by mass of the total electrolyte and vinylene carbonate in an amount of 0.5% by mass of the total electrolyte are added to prepare an electrolyte 2.
Example 3
Uniformly mixing organic solvent ethylene carbonate and methyl ethyl carbonate according to the mass ratio of 30: 70, slowly adding 1mol/L lithium salt LiBOB into the organic solvent, and then adding a silane compound shown in a structural formula (2) accounting for 3% of the total mass of the electrolyte and vinylene carbonate accounting for 0.5% of the total mass of the electrolyte to prepare the electrolyte 3.
Example 4
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 40: 30: 20, and slowly adding 0.8mol/L lithium salt LiPO into the organic solvents2F2And then adding a silane compound represented by a structural formula (3) accounting for 0.5% of the total mass of the electrolyte and LiFSI accounting for 1% of the total mass of the electrolyte to prepare the electrolyte 4.
Example 5
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 40: 30: 20, and slowly adding 0.8mol/L lithium salt Li PF into the organic solvents6And then adding a silane compound represented by a structural formula (3) accounting for 1% of the total mass of the electrolyte and LiFSI accounting for 1% of the total mass of the electrolyte to prepare the electrolyte 5.
Example 6
Uniformly mixing organic solvents of ethylene carbonate, ethyl methyl carbonate and diethyl carbonate according to the mass ratio of 40: 30: 20, slowly adding 0.8mol/L lithium salt LiBOB into the organic solvents, and then adding a silane compound which is 3% of the total mass of the electrolyte and is shown in a structural formula (3) and 1% of LiFSI to prepare the electrolyte 6.
Example 7
Uniformly mixing organic solvents of ethylene carbonate, ethyl methyl carbonate and diethyl carbonate according to the mass ratio of 30: 50: 20, slowly adding 1.2mol/L lithium salt LiBOB into the organic solvents, and then adding a silane compound shown in a structural formula (4) accounting for 0.5% of the total mass of the electrolyte and 1, 3-propylene sultone according to the proportion of 1% to prepare the electrolyte 7.
Example 8
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 30: 50: 20, and slowly adding 1.2mol/L lithium salt LiPF into the organic solvents6And then adding a silane compound represented by a structural formula (4) accounting for 1% of the total mass of the electrolyte and 1, 3-propylene sultone accounting for 1% of the total mass of the electrolyte to prepare an electrolyte 8.
Example 9
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 30: 50: 20, and slowly adding 1.2mol/L lithium salt LiPF into the organic solvents6And then adding a silane compound represented by a structural formula (4) accounting for 3% of the total mass of the electrolyte and 1, 3-propylene sultone accounting for 1% of the total mass of the electrolyte to prepare an electrolyte 9.
Comparative example 1
Uniformly mixing organic solvents ethylene carbonate and methyl ethyl carbonate according to the mass ratio of 30: 70, and slowly adding 1mol/L lithium salt LiPF into the organic solvents6Then vinylene carbonate accounting for 0.5 percent of the total mass of the electrolyte is added to prepare the electrolyte 10.
Comparative example 2
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 40: 30: 20, and slowly adding the mixture into the reactorAdding 0.8mol/L lithium salt LiPF into organic solvent6And then adding LiFSI accounting for 1% of the total mass of the electrolyte to prepare the electrolyte 11.
Comparative example 3
Uniformly mixing organic solvents of ethylene carbonate, methyl ethyl carbonate and diethyl carbonate according to the mass ratio of 30: 50: 20, and slowly adding 1.2mol/L lithium salt LiPO into the organic solvents2F2Then adding 1, 3-propylene sultone accounting for 1 percent of the total mass of the electrolyte to prepare the electrolyte 12.
According to the lithium battery electrolyte, the structure of the silane compound in the first additive is optimized, and the functional group with good film forming capability is introduced into the structure, so that the film forming capability can be improved while the impedance of the electrolyte is optimized, and the battery performance is improved.
The embodiment of the application also provides a lithium battery, which comprises a positive electrode, a negative electrode and electrolyte, wherein the electrolyte is any one of the electrolytes described in the embodiments of the application.
In some embodiments of the present application, the method of preparing the positive electrode is: in a homogenizing device, N-methyl pyrrolidone is used as a solvent, lithium cobalt oxide, acetylene black and polyvinylidene fluoride are uniformly mixed according to the mass ratio of 96: 2 to form anode slurry, the anode slurry is coated on an aluminum foil of 12 microns, and an anode sheet is obtained after drying and cold pressing.
In some embodiments of the present application, the method of preparing the negative electrode is: in a homogenizing device, deionized water is used as a solvent, artificial graphite, acetylene black, styrene butadiene rubber and sodium carboxymethylcellulose are uniformly mixed according to the mass ratio of 94.5: 2: 1 to form negative electrode slurry, the negative electrode slurry is coated on a copper foil of 8 microns, and the negative electrode sheet is obtained after drying and cold pressing.
In some embodiments of the present application, a method of making the battery comprises: stacking the positive plate, the PE isolating film and the negative plate in sequence to enable the PE isolating film to be positioned between the positive plate and the negative plate to play an isolating role, and then winding to obtain a bare cell; and placing the bare cell in an aluminum-plastic film shell, injecting the prepared electrolyte into the dried battery, and performing vacuum packaging, standing, formation, shaping and other processes to complete the preparation of the lithium ion battery.
The inventors also performed several experiments to test the performance of the lithium ion batteries described in the examples of the present application. The cell used for the test was made as described above.
Test 1: cycle test at ambient temperature 25 deg.C
And (3) respectively placing the prepared batteries at the normal temperature of 25 ℃, charging to 4.2V at a constant current and a constant voltage of 1C, then discharging to 3V at a constant current of 1C, performing charge-discharge cycle test, circulating for 300 times, and recording cycle data.
And (3) testing 2: high temperature 45 ℃ cycle test
And (3) respectively placing the prepared batteries at the normal temperature of 45 ℃, charging to 4.2V at a constant current and a constant voltage of 1C, then discharging to 3V at a constant current of 1C, performing charge-discharge cycle test, circulating for 300 times, and recording cycle data.
Table 1 shows the charge-discharge cycle test results of the batteries using different electrolytes.
TABLE 1
Figure BDA0002284544490000121
Referring to table 1, the test results of the battery 1, the battery 2, the battery 3 and the comparative battery 1 are compared to show that the electrolyte using the silane compound as an additive can improve the capacity retention rate of the battery at 25 ℃ and 45 ℃, i.e., improve the cycle characteristics of the battery.
According to the lithium battery provided by the application, the structure of the silane compound in the first additive is optimized, and the functional group with good film forming capability is introduced into the structure, so that the film forming capability can be improved while the impedance of the electrolyte is optimized, and the performance of the battery is improved.
In conclusion, upon reading the present detailed disclosure, those skilled in the art will appreciate that the foregoing detailed disclosure can be presented by way of example only, and not limitation. Those skilled in the art will appreciate that the present application is intended to cover various reasonable variations, adaptations, and modifications of the embodiments described herein, although not explicitly described herein. Such alterations, improvements, and modifications are intended to be suggested by this disclosure, and are within the spirit and scope of the exemplary embodiments of this disclosure.
It is to be understood that the term "and/or" as used herein in this embodiment includes any and all combinations of one or more of the associated listed items. It will be further understood that the terms "comprises," "comprising," "includes" and/or "including," when used herein, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
It will be further understood that, although the terms first, second, third, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another. Thus, a first element in some embodiments may be termed a second element in other embodiments without departing from the teachings of the present invention. The same reference numerals or the same reference identifiers denote the same elements throughout the specification.

Claims (10)

1. A lithium battery electrolyte comprising an organic solvent, a lithium salt and a first additive, wherein the first additive comprises a silane compound selected from at least one of compounds represented by structural formula (1):
wherein, X is selected from one of P ═ O, P and B, and Y is selected from substitutionOr unsubstituted C1~10Alkyl, substituted or unsubstituted C1~10Alkoxy, substituted or unsubstituted C2~10Alkenyl, substituted or unsubstituted C2~10Alkenyloxy, substituted or unsubstituted C2~10Alkynyl, substituted or unsubstituted C2~10Alkynyloxy, C ═ O functional group, O ═ S ═ O functional group; part or all of the hydrogen on the Y can be respectively replaced by halogen, nitro, cyano, carboxyl and C1~6Alkyl radical, C2~6Alkenyl substitution; n is taken from any of 1, 2 or 3.
2. The electrolyte of claim 1, wherein the silane compound is selected from at least one of the following compounds:
Figure FDA0002284544480000012
Figure FDA0002284544480000013
3. the electrolyte of claim 1, further comprising a second additive comprising at least one of vinylene carbonate, 1, 3-propane sultone, vinyl vinylene carbonate, 1, 3-propene sultone, and vinyl sulfate.
4. The electrolyte of claim 3, wherein the second additive is present in the electrolyte in an amount of 0.01% to 20% by weight.
5. The electrolyte according to claim 1, wherein the silane compound is contained in the electrolyte in an amount of 0.01 to 10% by mass.
6. The electrolyte of claim 1, wherein the organic solvent comprises cyclic carbonates and chain carbonates.
7. The electrolyte as claimed in claim 6, wherein the cyclic carbonate is at least one selected from the group consisting of propylene carbonate and ethylene carbonate; the chain carbonate is at least one selected from dimethyl carbonate, diethyl carbonate, methyl ethyl carbonate, methyl propyl carbonate, ethyl acetate and propyl acetate.
8. The electrolyte of claim 1, wherein the lithium salt is LiPF6、LiBF4、LiBOB、LiODFB、LiFSI、LiPO2F2One or more of (a).
9. The electrolyte of claim 8, wherein the lithium salt is LiPF6The concentration is 0.8 to 1.5 mol/L.
10. A lithium battery comprising a positive electrode, a negative electrode and an electrolyte, characterized in that the electrolyte is the electrolyte of any one of claims 1 to 9.
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