CN111725563A - Lithium ion battery non-aqueous electrolyte and lithium ion battery - Google Patents

Lithium ion battery non-aqueous electrolyte and lithium ion battery Download PDF

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CN111725563A
CN111725563A CN201910203026.9A CN201910203026A CN111725563A CN 111725563 A CN111725563 A CN 111725563A CN 201910203026 A CN201910203026 A CN 201910203026A CN 111725563 A CN111725563 A CN 111725563A
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lithium ion
ion battery
carbonate
nonaqueous electrolyte
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CN111725563B (en
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康媛媛
曹宗泽
刘中波
唐希武
曹朝伟
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Novolyte Battery Materials Suzhou Co Ltd
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    • 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
    • H01M10/052—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
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
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    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
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    • Y02E60/10—Energy storage using batteries

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Abstract

In order to overcome the problem that the cycle performance and the high-temperature storage performance of the lithium ion battery in the prior art are not ideal under the high-pressure state, the invention provides a lithium ion battery non-aqueous electrolyte, which comprises a compound shown in a structural formula 1,

Description

Lithium ion battery non-aqueous electrolyte and lithium ion battery
Technical Field
The invention relates to the technical field of lithium ion batteries, in particular to a lithium ion battery non-aqueous electrolyte and a lithium ion battery using the same.
Background
Lithium ion batteries have been developed in the field of portable electronic products due to their high operating voltage, high safety, long life, no memory effect, and the like. With the development of new energy automobiles, the lithium ion battery has a huge application prospect in a power supply system for the new energy automobiles.
In a nonaqueous electrolyte lithium ion battery, a nonaqueous electrolyte is a key factor affecting high and low temperature performance of the battery, and particularly, an additive in the nonaqueous electrolyte is particularly important for exerting the high and low temperature performance of the battery. During the initial charging process of the lithium ion battery, lithium ions in the battery anode material are extracted and are inserted into the carbon cathode through electrolyte. Due to its high reactivity, the electrolyte reacts on the carbon negative electrode surface to produce Li2CO3、Li2O, LiOH, thereby forming a passivation film on the surface of the negative electrode, the passivation film being referred to as a solid electrolyte interface film (SEI). The SEI film formed during the initial charging process not only prevents the electrolyte from further decomposing on the surface of the carbon negative electrode, but also acts as a lithium ion tunnel, allowing only lithium ions to pass through. Therefore, the SEI film determines the performance of the lithium ion battery.
In order to improve various performances of the lithium ion battery, many researchers add different negative electrode film-forming additives (such as vinylene carbonate, fluoroethylene carbonate and ethylene carbonate) to the electrolyte to improve the quality of the SEI film, thereby improving various performances of the battery. For example, the prior art proposes to add a fluoroalkyl vinyl carbonate substance to the electrolyte, but the lithium ion battery added with the substance has insufficient cycle performance and high-temperature storage performance under a high-pressure state.
Disclosure of Invention
The invention aims to solve the technical problem that the cycle performance and the high-temperature storage performance of a lithium ion battery in a high-pressure state are not ideal in the prior art, and provides a lithium ion battery non-aqueous electrolyte.
The technical scheme adopted by the invention for solving the technical problems is as follows:
provides a lithium ion battery non-aqueous electrolyte, which comprises a compound shown in a structural formula 1,
Figure BDA0001998065730000021
wherein, X group is selected from one or more of S, Si and N or carbon-containing group containing unsaturated bond, R group is selected from hydrogen, halogen atom or group containing 1-4 carbon atoms; m is an integer of 0 to 10.
The non-aqueous electrolyte solution of the lithium ion battery contains the compound shown in the formula 1, and the inventor finds that the cyclic carbonate in the compound shown in the formula 1 is connected with a heteroatom-containing structural group or an unsaturated bond-containing carbon-containing group X through an ether bond directly connected to the cyclic carbonate, so that the X group in the compound is more favorably broken and detached, free radicals formed after breakage can be further polymerized, a more stable solid electrolyte membrane is formed at a positive electrode and a negative electrode, and the solid electrolyte membrane can inhibit further decomposition of a solvent and simultaneously effectively reduce impedance. Therefore, the lithium ion battery non-aqueous electrolyte has excellent high-temperature performance and low-temperature performance.
Preferably, m is an integer of 1 to 4.
Preferably, the S-containing group is selected from one of sulfonate, sulfate and sulfite; the Si-containing group is selected from siloxane groups; the N-containing group is selected from one of cyano and amino; the carbon-containing group containing unsaturated bonds is selected from one of carbonyl, alkenyl and alkynyl.
Preferably, the group containing 1 to 4 carbon atoms is selected from cyano, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl.
Preferably, R is selected from a hydrogen atom, a fluorine atom, a cyano group, a methyl group, an ethyl group, a propyl group, an ethenyl group, an propenyl group, a propynyl group, a fluoroethenyl group, a fluoroethynyl group, a fluoropropenyl group, and a fluoropropynyl group.
Preferably, the content of the compound represented by the structural formula 1 is 0.01 to 5% with respect to the total mass of the lithium ion battery nonaqueous electrolyte.
Preferably, the compound represented by the structural formula 1 is selected from and not limited to the following compounds 1 to 10:
Figure BDA0001998065730000022
Figure BDA0001998065730000031
preferably, the lithium ion battery non-aqueous electrolyte further comprises one or more of vinylene carbonate, ethylene carbonate and fluoroethylene carbonate;
and the lithium ion battery non-aqueous electrolyte also selectively comprises one or more than two of 1, 3-propane sultone, 1, 4-butane sultone and 1, 3-propene sultone.
Preferably, the lithium ion battery non-aqueous electrolyte further comprises a lithium salt and a non-aqueous organic solvent;
the lithium salt is selected from LiPF6、LiBF4、LiBOB、LiF2PO2、LiDFOB、LiSbF6、LiAsF6、LiN(SO2CF3)2、LiN(SO2C2F5)2、LiC(SO2CF3)3Or LiN (SO)2F)2One or more than two of the above;
the non-aqueous organic solvent is a mixture of cyclic carbonate and chain carbonate, the cyclic carbonate is selected from one or more of ethylene carbonate, propylene carbonate or butylene carbonate, and the chain carbonate is selected from one or more of dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate or propyl methyl carbonate.
Meanwhile, the invention also provides a lithium ion battery which comprises a positive electrode, a negative electrode, a diaphragm arranged between the positive electrode and the negative electrode, and the lithium ion battery non-aqueous electrolyte.
Preferably, the active material of the positive electrode is selected from LiCoO2、LiNiO2、LiMn2O4、LiCo1-yMyO2、LiNi1- yMyO2、LiMn2-yMyO4And LiNixCoyMnzM1-x-y-zO2Wherein M is selected from one or more of Fe, Co, Ni, Mn, Mg, Cu, Zn, Al, Sn, B, Ga, Cr, Sr, V and Ti, y is more than or equal to 0 and less than or equal to 1, x is more than or equal to 0 and less than or equal to 1, z is more than or equal to 0 and less than or equal to 1, and x + y + z is less than or equal to 1.
As another aspect of the present invention, the active material of the positive electrode is selected from LiFe1-xMxPO4, wherein M is selected from one or more of Mn, Mg, Co, Ni, Cu, Zn, Al, Sn, B, Ga, Cr, Sr, V or Ti, and x is more than or equal to 0 and less than 1.
Detailed Description
In order to make the technical problems, technical solutions and advantageous effects solved by the present invention more apparent, the present invention is further described in detail below with reference to the following embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.
The lithium ion battery non-aqueous electrolyte provided by the invention comprises a compound shown in a structural formula 1,
Figure BDA0001998065730000041
wherein, X group is selected from one or more of S, Si and N or carbon-containing group containing unsaturated bond, R group is selected from hydrogen, halogen atom or group containing 1-4 carbon atoms; m is an integer of 0 to 10.
The lithium ion battery non-aqueous electrolyte contains the compound shown in the structural formula 1, and the compound 1 has an obvious positive electrode protection effect, can effectively inhibit the structure of a positive electrode material from being damaged, and also inhibits the catalytic decomposition reaction of metal ions on the electrolyte and the damage effect on a negative electrode passivation film. In the full-electricity storage process, the side reaction between the anode material and the electrolyte under high voltage can be effectively reduced, so that the storage performance of the lithium ion battery under high voltage is improved. Meanwhile, the negative electrode has a good film forming effect and has little influence on film impedance, so that the stability of the negative electrode in the recycling process is improved, and the cycle performance is improved.
The preparation method of the compound shown in the structural formula 1 is known by those skilled in the art of organic synthesis according to the structure of the compound, and for example, 2- (1, 2-dihydroxy-ethoxy-ethyl methyl) sulfate or 2- (1, 2-dihydroxy-ethoxy-ethyl) sulfate or 1- (2-trimethylsiloxy-ethoxy) -1, 2-ethanediol or 3- (1, 2-dihydroxy-ethoxy) -propionitrile and carbon dioxide are subjected to esterification reaction under high pressure to form a ring, and then the compound is obtained by recrystallization or column chromatography purification. The synthetic route is exemplified as follows:
Figure BDA0001998065730000051
preferably, m is an integer from 1 to 4, more preferably 2.
Preferably, the S-containing group is selected from one of sulfonate, sulfate and sulfite; the Si-containing group is selected from siloxane groups; the N-containing group is selected from one of cyano and amino; the carbon-containing group containing unsaturated bonds is selected from one of carbonyl, alkenyl and alkynyl.
Preferably, R is selected from hydrogen, halogen atoms or groups containing 1 to 4 carbon atoms.
In the case where R is selected from a group containing carbon atoms, it is advantageous to control the number of carbon atoms to 4 or less (including 4), preferably 4 or less. Controlling the number of carbon atoms to 4 or less can reduce the impedance of the battery and achieve both high-temperature performance and low-temperature performance. If a carbon atom-containing group having 5 or more carbon atoms is selected as the substituent, the resistance of the battery is rather increased, and the high-temperature performance and the low-temperature performance of the battery are adversely affected, so that the carbon atom-containing group having 5 or more carbon atoms is not selected as the substituent in the present invention. In the present invention, alternative groups having 1 to 4 carbon atoms are preferably cyano, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl. Preferably, R is selected from a hydrogen atom, a fluorine atom, a cyano group, a methyl group, an ethyl group, a propyl group, an ethenyl group, an propenyl group, a propynyl group, a fluoroethenyl group, a fluoroethynyl group, a fluoropropenyl group, and a fluoropropynyl group.
Preferably, the content of the compound represented by the structural formula 1 is 0.01 to 5% with respect to the total mass of the lithium ion battery nonaqueous electrolyte.
Controlling the content of the compound represented by formula 1 in the nonaqueous electrolytic solution has a favorable effect on further optimization of high-pressure performance, high-temperature performance and low-temperature performance. In a preferred embodiment of the present invention, the content of the compound represented by structural formula 1 is 0.01% to 5% with respect to the total mass of the nonaqueous electrolytic solution for lithium ion batteries. When the content is less than 0.01%, it is not favorable to sufficiently form a passivation film on the surface of the negative electrode, thereby being unfavorable to sufficiently improve the high-temperature and low-temperature performance of the nonaqueous electrolyte battery, and when the content exceeds 5.0%, a thicker passivation film is formed on the surface of the negative electrode, but the internal resistance of the battery is increased, thereby reducing the performance of the battery. Research shows that the content of the compound shown in the structural formula 1 is less than 0.01% or more than 5% of the total mass of the non-aqueous electrolyte of the lithium ion battery, and compared with the content of the compound in the range of 0.01-5%, the high-temperature performance and the low-temperature performance of the lithium ion battery are reduced to different degrees, which indicates that the content of the compound shown in the structural formula 1 in the non-aqueous electrolyte is positively controlled.
Preferably, the compound represented by the structural formula 1 is selected from and not limited to the following compounds 1 to 10:
Figure BDA0001998065730000061
Figure BDA0001998065730000071
preferably, the lithium ion battery nonaqueous electrolyte further comprises one or more of vinylene carbonate, ethylene carbonate and fluoroethylene carbonate.
Preferably, the lithium ion battery nonaqueous electrolyte further selectively comprises one or more than two of 1, 3-propane sultone, 1, 4-butane sultone and 1, 3-propylene sultone.
The additives can form a more stable SEI film on the surface of the graphite negative electrode, so that the cycle performance of the lithium ion battery is remarkably improved. These additives may be added in an amount generally added in the art, for example, 0.01% to 5%, preferably 0.1% to 3%, more preferably 0.5% to 2% with respect to the total mass of the electrolyte.
It has been found that the compound represented by formula 1 of the present invention, used in combination with the above-mentioned additive, can achieve superior effects to those achieved when they are used alone, and it is presumed that there is a synergistic effect between them, i.e., the compound represented by formula 1 and the above-mentioned additive cooperate to improve the cycle performance, high-temperature storage and/or low-temperature performance of the battery in a high-pressure state.
Preferably, the lithium ion battery nonaqueous electrolyte further comprises a lithium salt and a nonaqueous organic solvent.
The lithium salt is selected from LiPF6、LiBF4、LiBOB、LiDFOB、LiF2PO2、LiSbF6、LiAsF6、LiN(SO2CF3)2、LiN(SO2C2F5)2、LiC(SO2CF3)3Or LiN (SO)2F)2One or more than two of them. The lithium salt is preferably LiPF6Or LiPF6And other lithium salts.
The non-aqueous organic solvent is a mixture of cyclic carbonate and chain carbonate, the cyclic carbonate is selected from one or more of ethylene carbonate, propylene carbonate or butylene carbonate, and the chain carbonate is selected from one or more of dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate or propyl methyl carbonate. The mixed solution of the cyclic carbonate organic solvent with high dielectric constant and the chain carbonate organic solvent with low viscosity is used as the solvent of the lithium ion battery electrolyte, so that the mixed solution of the organic solvent has high ionic conductivity, high dielectric constant and low viscosity.
Meanwhile, the invention also provides a lithium ion battery which comprises a positive electrode, a negative electrode, a diaphragm arranged between the positive electrode and the negative electrode, and the lithium ion battery non-aqueous electrolyte.
Preferably, the active material of the positive electrode is selected from LiCoO2、LiNiO2、LiMn2O4、LiCo1-yMyO2、LiNi1- yMyO2、LiMn2-yMyO4And LiNixCoyMnzM1-x-y-zO2Wherein M is selected from one or more of Fe, Co, Ni, Mn, Mg, Cu, Zn, Al, Sn, B, Ga, Cr, Sr, V and Ti, y is more than or equal to 0 and less than or equal to 1, x is more than or equal to 0 and less than or equal to 1, z is more than or equal to 0 and less than or equal to 1, and x + y + z is less than or equal to 1.
As another aspect of the present invention, the active material of the positive electrode is selected from LiFe1-xMxPO4, wherein M is selected from one or more of Mn, Mg, Co, Ni, Cu, Zn, Al, Sn, B, Ga, Cr, Sr, V or Ti, and x is more than or equal to 0 and less than 1.
The present invention will be further illustrated by the following examples.
Example 1
This example is for explaining a lithium ion battery nonaqueous electrolytic solution and a lithium ion battery disclosed in the present invention.
1) Preparation of the electrolyte
Ethylene Carbonate (EC), diethyl carbonate (DEC) and Ethyl Methyl Carbonate (EMC) were mixed in a mass ratio of EC: DEC: EMC ═ 1:1:1, and then lithium hexafluorophosphate (LiPF) was added6) To a molar concentration of 1mol/L, 1% by mass of compound 1 based on the total mass of the electrolyte was added (note: here compound 1 is compound 1 in table 1, the same as in the examples below).
2) Preparation of Positive plate
A positive electrode active material lithium nickel cobalt manganese oxide LiNi was mixed in a mass ratio of 93:4:30.5Co0.2Mn0.3O2Conductive carbon black Super-P and a binder polyvinylidene fluoride (PVDF), and then dispersed in N-methyl-2-pyrrolidone (NMP) to obtain a positive electrode slurry. Uniformly coating the slurry on two sides of an aluminum foil, drying, rolling and vacuum drying, and welding an aluminum outgoing line by using an ultrasonic welding machine to obtain a positive plate and a polar plateThe thickness of (D) is within the range of 120-150 μm.
3) Preparation of negative plate
Mixing artificial graphite serving as a negative electrode active material, conductive carbon black Super-P, Styrene Butadiene Rubber (SBR) serving as a binder and carboxymethyl cellulose (CMC) according to a mass ratio of 94:1:2.5:2.5, and dispersing the materials in deionized water to obtain negative electrode slurry. Coating the slurry on two sides of the copper foil, drying, rolling and vacuum drying, and welding a nickel outgoing line by using an ultrasonic welding machine to obtain a negative plate, wherein the thickness of the negative plate is 120-150 mu m.
4) Preparation of cell
And placing three layers of isolating films with the thickness of 20 mu m between the positive plate and the negative plate, then winding the sandwich structure consisting of the positive plate, the negative plate and the diaphragm, flattening the wound body, then placing the wound body into an aluminum foil packaging bag, and baking for 48h at 75 ℃ in vacuum to obtain the battery cell to be injected with liquid.
5) Liquid injection and formation of battery core
And (3) in a glove box with the dew point controlled below-40 ℃, injecting the prepared electrolyte into the battery cell, carrying out vacuum packaging, and standing for 24 hours.
Then the first charge is normalized according to the following steps: charging at 0.05C for 180min, charging at 0.2C to 3.95V, vacuum sealing for the second time, further charging at 0.2C to 4.2V, standing at room temperature for 24hr, and discharging at 0.2C to 3.0V.
6) High temperature cycle performance test
Placing the battery in a constant-temperature oven at 45 ℃, charging to 4.5V by a current of 1C at a constant current, then charging at a constant voltage until the current is reduced to 0.02C, then discharging to 3.0V by the current of 1C at a constant current, so cycling, recording the discharge capacity of the 1 st circle and the discharge capacity of the last circle, and calculating the capacity retention rate of high-temperature cycling according to the following formula:
capacity retention rate ═ last round of discharge capacity/1 st round of discharge capacity × (100)%
7) High temperature storage Performance test
And (3) charging the formed battery to 4.2V at constant current and constant voltage of 1C at normal temperature, measuring the initial discharge capacity and the initial battery thickness of the battery, then storing the battery for 30 days at 60 ℃, discharging the battery to 3V at 1C, and measuring the retention capacity and recovery capacity of the battery and the thickness of the battery after storage. The calculation formula is as follows:
battery capacity retention (%) — retention capacity/initial capacity × 100%;
battery capacity recovery (%) — recovery capacity/initial capacity × 100%;
thickness expansion (%) (battery thickness after storage-initial battery thickness)/initial battery thickness × 100%.
8) Low temperature Performance test
At 25 ℃, the formed battery is charged to 4.2V by using a 1C constant current and constant voltage, then discharged to 3.0V by using a 1C constant current, and the discharge capacity is recorded. And then charging to 4.2V at constant current and constant voltage of 1C, standing for 12h in an environment at the temperature of minus 20 ℃, discharging to 3.0V at constant current of 0.2C, and recording the discharge capacity.
A low-temperature discharge efficiency value of-20 ℃ was 0.2C discharge capacity (-20 ℃) per 1C discharge capacity (25 ℃) x 100%.
Example 2
As shown in Table 1, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 2, except that 1% of the compound 1 is replaced with 1% of the compound 4 in the preparation of the electrolyte, which is the same as that of example 1.
Example 3
As shown in Table 1, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 2, except that 1% of the compound 1 is replaced with 1% of the compound 6 in the preparation of the electrolyte, which is the same as that of example 1.
Example 4
As shown in Table 1, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 2, except that 1% of the compound 1 is replaced with 1% of the compound 9 in the preparation of the electrolyte, which is the same as that of example 1.
Example 5
As shown in Table 1, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 2, except that 1% of the compound 1 is replaced with 1% of the compound 10 in the preparation of the electrolyte, which is the same as that of example 1.
Comparative example 1
As shown in Table 1, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 2, which is the same as example 1 except that 1% of the compound 1 is not added in the preparation of the electrolyte.
Comparative example 2
As shown in Table 2, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 3, except that 1% of the compound 1 is replaced by 1% of FEC in the preparation of the electrolyte, which is the same as that of example 1.
Comparative example 3
As shown in Table 2, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 3, except that 1% of the compound 1 is replaced with 1% of PS in the preparation of the electrolyte, which is the same as that of example 1.
Comparative example 4
As shown in table 2, the data of the high temperature performance and the low temperature performance obtained by the test are shown in table 3, except that 1% of compound 1 is replaced with 1% of trimethylsulfolane in the preparation of the electrolyte, which is the same as example 1.
TABLE 1
Examples/comparative examples Compound shown in structural formula 1 and content thereof Additive and content
Example 1 1: 1% of compound
Example 2 The compound is 4: 1%
Example 3 The compound is 6: 1%
Example 4 The compound is 9: 1%
Example 5 The compound is 10: 1%
Comparative example 1 - -
Comparative example 2 - FEC:1％
Comparative example 3 - PS:1％
Comparative example 4 - 1 percent of trimethyl sulfolane
TABLE 2
Figure BDA0001998065730000111
The results in table 2 show that adding 1% of compound 1, compound 4, compound 6, or compound 10 to the nonaqueous electrolytic solution can significantly improve the high-temperature performance and the low-temperature performance of the lithium ion battery, compared to adding no additive or adding a conventional additive. The lithium ion battery containing the electrolyte for the lithium ion battery has 75% or more of excellent low-temperature discharge efficiency and 80% or more of excellent cycle and high-temperature storage efficiency under a high-pressure state; furthermore, it was confirmed that the increase rate of the thickness of the battery was significantly low (2 to 7%) when the battery was maintained at a high temperature for a long time.
Example 6
As shown in Table 3, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 4, except that 1% of the compound 1 is changed to 0.1% of the compound 1 in the preparation of the electrolyte, which is the same as that of example 3.
Example 7
As shown in Table 3, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 4, except that 1% of the compound 1 was changed to 2% of the compound 1 in the preparation of the electrolyte, which is the same as that of example 3.
Example 8
As shown in Table 3, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 4, except that 1% of the compound 1 was changed to 3% of the compound 1 in the preparation of the electrolyte, which is the same as that of example 3.
Example 9
As shown in Table 3, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 4, except that 1% of the compound 1 was changed to 5% of the compound 1 in the preparation of the electrolyte, which is the same as that of example 3.
TABLE 3
Examples/comparative examples Compound shown in structural formula 1 and content thereof
Example 6 Compound 1: 0.1 percent of
Example 7 Compound 1:2 percent of
Example 8 Compound 1: 3 percent of
Example 9 Compound 1: 5 percent of
TABLE 4
Figure BDA0001998065730000121
Example 10
As shown in Table 5, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 6, except that 1% of FEC is additionally added in the preparation of the electrolyte, which is the same as that of example 3.
Example 11
As shown in Table 5, the data of the high temperature performance and the low temperature performance obtained by the test are shown in Table 6, except that 1% of PS is additionally added in the preparation of the electrolyte solution, which is the same as that of example 3.
Example 12
As shown in table 5, the data of the high temperature performance and the low temperature performance obtained by the test are shown in table 6, which is the same as example 3 except that 1% of trimethylsulfolane is additionally added in the preparation of the electrolyte.
TABLE 5
Figure BDA0001998065730000131
TABLE 6
Figure BDA0001998065730000132
The results show that the high-temperature performance and the low-temperature performance can be further improved by adding an additive (FEC, PS or trimethylsulfolane) to the compound represented by the structural formula 1 of the present invention. Or, the compound shown in the formula 1 of the invention is further added on the basis of the existing additive (FEC, PS or trimethyl sulfolane), so that the high-temperature performance and the low-temperature performance can be further improved.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents and improvements made within the spirit and principle of the present invention are intended to be included within the scope of the present invention.

Claims (10)

1. A lithium ion battery non-aqueous electrolyte is characterized by comprising a compound shown as a structural formula 1,
Figure FDA0001998065720000011
wherein, X group is selected from one or more of S, Si and N or carbon-containing group containing unsaturated bond, R group is selected from hydrogen, halogen atom or group containing 1-4 carbon atoms; m is an integer of 0 to 10.
2. The nonaqueous electrolyte solution for lithium ion batteries according to claim 1, wherein m is an integer of 1 to 4.
3. The nonaqueous electrolyte solution for the lithium ion battery of claim 1, wherein the S-containing group is selected from one of sulfonate, sulfate and sulfite; the Si-containing group is selected from siloxane groups; the N-containing group is selected from one of cyano and amino; the carbon-containing group containing unsaturated bonds is selected from one of carbonyl, alkenyl and alkynyl.
4. The nonaqueous electrolyte solution for a lithium ion battery according to any one of claims 1 to 3, wherein the group having 1 to 4 carbon atoms is selected from a cyano group, an alkyl group, an alkenyl group, an alkynyl group, a halogenated alkyl group, a halogenated alkenyl group, and a halogenated alkynyl group.
5. The nonaqueous electrolyte solution for lithium ion batteries according to claim 4, wherein R is selected from a hydrogen atom, a fluorine atom, a methyl group, an ethyl group, a propyl group, a cyano group, an ethenyl group, an propenyl group, a propynyl group, a fluoroethenyl group, a fluoroethynyl group, a fluoropropenyl group, and a fluoropropynyl group.
6. The nonaqueous electrolyte solution for lithium ion batteries according to claim 1, wherein the content of the compound represented by the formula 1 is 0.01 to 5% based on the total mass of the nonaqueous electrolyte solution for lithium ion batteries.
7. The nonaqueous electrolyte solution for a lithium ion battery according to any one of claims 1 to 3 and 5, wherein the compound represented by the structural formula 1 is selected from the following compounds 1 to 10:
Figure FDA0001998065720000021
8. the nonaqueous electrolyte solution for lithium ion batteries according to any one of claims 1 to 5, further comprising one or more of vinylene carbonate, ethylene carbonate, and fluoroethylene carbonate;
and the lithium ion battery non-aqueous electrolyte also selectively comprises one or more than two of 1, 3-propane sultone, 1, 4-butane sultone and 1, 3-propene sultone.
9. The nonaqueous electrolyte solution for lithium ion batteries according to claim 1, wherein the nonaqueous electrolyte solution for lithium ion batteries comprises a lithium salt and a nonaqueous organic solvent;
the lithium salt is selected from LiPF6、LiBF4、LiBOB、LiDFOB、LiF2PO2、LiSbF6、LiAsF6、LiN(SO2CF3)2、LiN(SO2C2F5)2、LiC(SO2CF3)3Or LiN (SO)2F)2One or more than two of the above;
the non-aqueous organic solvent is a mixture of cyclic carbonate and chain carbonate, the cyclic carbonate is selected from one or more of ethylene carbonate, propylene carbonate or butylene carbonate, and the chain carbonate is selected from one or more of dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate or propyl methyl carbonate.
10. A lithium ion battery comprising a positive electrode, a negative electrode, and a separator interposed between the positive electrode and the negative electrode, characterized by further comprising the lithium ion battery nonaqueous electrolytic solution of any one of claims 1 to 9.
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