CN109935891B - Lithium cobaltate digital lithium ion battery with high and low temperature consideration - Google Patents

Lithium cobaltate digital lithium ion battery with high and low temperature consideration Download PDF

Info

Publication number
CN109935891B
CN109935891B CN201910277718.8A CN201910277718A CN109935891B CN 109935891 B CN109935891 B CN 109935891B CN 201910277718 A CN201910277718 A CN 201910277718A CN 109935891 B CN109935891 B CN 109935891B
Authority
CN
China
Prior art keywords
ion battery
lithium ion
low temperature
lithium cobaltate
digital
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
CN201910277718.8A
Other languages
Chinese (zh)
Other versions
CN109935891A (en
Inventor
王海
刘春洋
曾家江
李素丽
李俊义
徐延铭
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhuhai Cosmx Battery Co Ltd
Original Assignee
Zhuhai Cosmx Battery Co Ltd
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 Zhuhai Cosmx Battery Co Ltd filed Critical Zhuhai Cosmx Battery Co Ltd
Priority to CN201910277718.8A priority Critical patent/CN109935891B/en
Publication of CN109935891A publication Critical patent/CN109935891A/en
Application granted granted Critical
Publication of CN109935891B publication Critical patent/CN109935891B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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

A lithium cobaltate digital lithium ion battery with high and low temperature consideration belongs to the technical field of lithium ion batteries. The invention aims to solve the problem that the impedance and high-low temperature performance of the existing lithium ion battery are not ideal, and the lithium cobaltate digital lithium ion battery comprises a lithium cobaltate anode, a high-capacity artificial graphite cathode and a non-aqueous electrolyte, wherein the lithium cobaltate anode is subjected to doping coating treatment; the non-aqueous electrolyte is an organic compound dissolved in a solvent containing cyclic carbonate and chain carbonate, the organic compound is a sultone compound and a polynitrile compound, and the sultone compound accounts for 3.0-10% of the mass fraction of the electrolyte. The electrolyte containing high content of the sulfonate compound does not influence the performance exertion of the anode and cathode materials, so that the lithium ion battery has very excellent high-temperature performance and low-temperature performance.

Description

Lithium cobaltate digital lithium ion battery with high and low temperature consideration
Technical Field
The invention belongs to the technical field of lithium ion batteries, and particularly relates to a lithium cobaltate digital lithium ion battery with high and low temperature consideration.
Background
Since commercialization, lithium ion batteries have been widely used in the digital fields such as notebooks and mobile phones because of their high specific energy and good cycle performance. With the wide application of lithium ion batteries, the usage environment of the lithium ion batteries also tends to be diversified, and consumers expect that the lithium ion batteries have excellent performance under high and low temperature conditions. For example: in areas with relatively low temperature, the notebook computer can also work normally, and the lithium ion battery is required to have good low-temperature discharge performance. In areas with higher temperatures, it is expected that high temperatures do not have an obvious effect on the life of lithium ion batteries, and lithium ion batteries are required to have good high-temperature cycle performance.
The performance of lithium ion batteries is closely related to the positive electrode material, negative electrode material and electrolyte material in the batteries. U.S. Pat. No. 6,6033809 discloses a nonaqueous electrolytic solution containing 1, 3-propane sultone (whose content by mass in the electrolytic solution is 4%) which is capable of improving the cycle performance of a battery. U.S. patent application No. US9742033 discloses a nonaqueous electrolytic solution combining 1, 3-propanesultone and adiponitrile (the mass percentage content of the two substances in the electrolytic solution is less than or equal to 3%), which can improve the cycle performance and high-temperature storage performance of a lithium ion battery. However, if the mass percentage of the sultone compound and the polynitrile compound in the electrolyte is more than or equal to 3%, a compact SEI film is formed on the surface of the negative electrode material, and the probability of oxidation on the surface of the positive electrode material is increased, so that the impedance of the lithium ion battery is increased rapidly, and the low-temperature discharge performance of the lithium ion battery is obviously reduced. Therefore, how to obtain the digital lithium ion battery with high and low temperature performance through the synergistic effect of the anode material, the cathode material and the electrolyte is very important.
Disclosure of Invention
The invention aims to solve the problem that the impedance and high-low temperature performance of the existing lithium ion battery are not ideal, and provides a lithium cobaltate digital lithium ion battery with high and low temperature compatibility.
In order to achieve the purpose, the technical scheme adopted by the invention is as follows:
a lithium cobaltate digital lithium ion battery with high and low temperature consideration comprises a lithium cobaltate positive electrode, an artificial graphite negative electrode with gram capacity more than or equal to 355mAh/g and a non-aqueous electrolyte, wherein the lithium cobaltate positive electrode is subjected to doping coating treatment; the non-aqueous electrolyte is an organic compound dissolved in a solvent containing cyclic carbonate and chain carbonate, the organic compound is a sultone compound and a polynitrile compound, and the sultone compound accounts for 3.0-10% of the mass fraction of the electrolyte.
Furthermore, the chemical formula of the lithium cobaltate positive electrode is LixCo1-yMeyO2Wherein x is more than or equal to 0.95 and less than or equal to 1.05, y is more than 0 and less than or equal to 0.1, and Me is Mz1Nz2Wherein, z1+ z2 is more than 0 and less than or equal to 1, and M and N elements are one or more of Al, Mg, Ti, Zr, Co, Ni, Mn, Y, La or Sr.
Compared with the prior art, the invention has the beneficial effects that: the invention provides a lithium cobaltate positive electrode material with stable structure and excellent high and low temperature performance, a negative electrode material with good dynamic performance and small cyclic expansion and an electrolyte with excellent high temperature performance. Due to the synergistic effect of the anode material and the cathode material, the high-content sulfonate compound in the electrolyte forms a low-impedance SEI film at the cathode, and meanwhile, the high-content sulfonate compound cannot be oxidized on the surface of the anode material, so that the performance of the anode material and the cathode material cannot be influenced by the high-content sulfonate compound electrolyte, and the lithium ion battery has very excellent high-temperature performance and low-temperature performance.
Detailed Description
The technical solutions of the present invention are further described below with reference to the following examples, but the present invention is not limited thereto, and any modifications or equivalent substitutions may be made to the technical solutions of the present invention without departing from the spirit and scope of the technical solutions of the present invention.
The first embodiment is as follows: the embodiment describes a lithium cobaltate digital lithium ion battery with high and low temperature compatibility, which comprises a lithium cobaltate positive electrode, an artificial graphite negative electrode with gram capacity of more than or equal to 355mAh/g and a non-aqueous electrolyte, wherein the lithium cobaltate positive electrode is subjected to doping coating treatment; the non-aqueous electrolyte is an organic compound dissolved in a solvent containing cyclic carbonate and chain carbonate, the organic compound is a sultone compound and a polynitrile compound, and the sultone compound accounts for 3.0-10% of the mass fraction of the electrolyte. The doping and coating treatment of the lithium cobaltate positive electrode specifically comprises the following steps: firstly, carrying out high-temperature doping sintering treatment at 1000-1100 ℃, and then carrying out secondary high-temperature coating modification treatment at 800-1000 ℃ to synthesize the material.
Research shows that when the content of the sultone compound in the electrolyte is higher than 3%, the sultone compound can obviously improve the high-temperature storage performance and the high-temperature cycle performance of the lithium ion battery. But the SEI formed on the negative electrode has larger impedance, and meanwhile, the sultone compound is oxidized on the surface of the lithium cobaltate positive electrode, so that the impedance performance of the lithium ion battery is further improved.
The second embodiment is as follows: in a specific embodiment, the lithium cobaltate digital lithium ion battery with both high and low temperature includes a polynitrile compound selected from succinonitrile, adiponitrile, 1, 3, 6-hexanetricarbonitrile, glutaronitrile or octanedinitrile. The polynitrile compound can form a protective film on the surface of the lithium cobaltate anode, and the high-temperature performance of the lithium ion battery is remarkably improved.
The third concrete implementation mode: in the lithium cobaltate digital lithium ion battery with both high temperature and low temperature, the mass fraction of the polynitrile compound in the electrolyte is 0.1-10%.
The fourth concrete implementation mode: in the lithium cobaltate digital lithium ion battery with both high temperature and low temperature, the polynitrile compound accounts for 1-5% of the electrolyte by mass.
The fifth concrete implementation mode: in a specific embodiment, the sultone compound is one or a mixture of 1, 3-propane sultone, 1, 4-butane sultone or 1, 3-propene sultone.
The sixth specific implementation mode: in the lithium cobaltate digital lithium ion battery with both high temperature and low temperature, the sultone compound accounts for 3.1-6% of the electrolyte by mass.
The seventh embodiment: in the lithium cobaltate digital lithium ion battery with both high temperature and low temperature, the artificial graphite cathode is a material mixed by secondary particles and single particles, and the graphitization degree is 92.5% -95%.
The specific implementation mode is eight: in the lithium cobaltate digital lithium ion battery compatible with high temperature and low temperature, the specific surface area (BET) of the material mixed by the secondary particles and the single particles is less than or equal to 2m2/g。
The specific implementation method nine: in the lithium cobaltate digital lithium ion battery compatible with high and low temperatures, the average particle size D50 of the mixed material of the secondary particles and the single particles is 10 to 16 μm.
The artificial graphite with the grain diameter between D50 and 10 to 16 can well balance the capacity and the dynamic performance of the material, ensure the high capacity of the negative electrode and simultaneously meet the requirement of sufficient charge-discharge multiplying power. BET is controlled at 2m2The surface modification of the material is mainly controlled within/g, and the side reaction of the cathode and the electrolyte is reduced.
The detailed implementation mode is ten: in the lithium cobaltate digital lithium ion battery according to the seventh embodiment, the secondary particles are mixed with the single particles, the secondary particles are formed by bonding the single graphite particles through heating treatment of asphalt at a temperature higher than 500 ℃, and the raw material is needle coke.
The concrete implementation mode eleven: in the lithium cobaltate digital lithium ion battery according to the seventh embodiment, the single particle of the material in which the secondary particle and the single particle are mixed is prepared by graphitizing needle coke or petroleum coke as a raw material.
The specific implementation mode twelve: in the lithium cobaltate digital lithium ion battery compatible with high temperature and low temperature, the mass mixing ratio of the secondary particles and the single particles is 20-80%, so that good dynamic performance and low cyclic expansion characteristic can be ensured.
The high-capacity graphite negative electrode material provided by the invention has good dynamic performance, lower cyclic expansion characteristic and excellent high and low temperature performance; meanwhile, the impedance of an SEI film formed on the surface of the high-content sulfonate compound in the electrolyte is very low, so that the low-temperature performance of the battery can be prevented from being deteriorated by the high-content sulfonate compound.
The specific implementation mode is thirteen: in the lithium cobaltate digital lithium ion battery with high and low temperature compatibility, the chemical formula of the lithium cobaltate positive electrode is LixCo1-yMeyO2Wherein x is more than or equal to 0.95 and less than or equal to 1.05, y is more than 0 and less than or equal to 0.1, and Me is Mz1Nz2Wherein, z1+ z2 is more than 0 and less than or equal to 1, and M and N elements are one or more of Al, Mg, Ti, Zr, Co, Ni, Mn, Y, La or Sr.
The specific implementation mode is fourteen: in the thirteenth embodiment, y is greater than 0 and less than or equal to 0.05, z is greater than 0 and less than or equal to 0.1 and less than or equal to 0.5, and z is greater than 0 and less than or equal to 0.2 and less than or equal to 0.5.
The concrete implementation mode is fifteen: in a thirteenth or fourteenth embodiment, the lithium cobaltate digital lithium ion battery with high and low temperature compatibility is characterized in that the lithium cobaltate material is LiCo0.985Al0.009Mg0.004Ti0.002O2、LiCo0.9915Al0.004Mg0.002Ti0.0015O2And LiCo0.995Al0.003Mg0.001Ti0.001O2One kind of (1).
The doped and coated lithium cobaltate material is assembled into a button cell, the charge-discharge capacity is 0.1C, the discharge capacity is 182-195 mAh/g (3.0-4.5V), and the full cell discharge 0.2C capacity exertion formed by the lithium cobaltate material, the electrolyte and the negative electrode is 169-195 mAh/g (the charge cut-off voltage is 4.4-4.5V). The lithium cobaltate positive electrode material provided by the invention has a stable structure and good high-low temperature performance, and can inhibit the oxidation of high-content sulfonate compounds in the electrolyte on the surface of the lithium cobaltate positive electrode material, so that the impedance of the battery is further reduced.
Example 1
(1) Preparing an electrolyte: in an argon atmosphere glove box with a water content of <10ppm, Ethylene Carbonate (EC), diethyl carbonate (DEC), Propylene Carbonate (PC) were mixed according to 30: 65: 5 to obtain a non-aqueous solvent, and then adding 4% of 1, 3-propane sultone, 2% of adiponitrile and 13% of lithium hexafluorophosphate into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
(2) Preparing a positive plate: lithium cobaltate (molecular formula LiCo) doped and coated with positive electrode active material0.985Al0.009Mg0.004Ti0.002O2) Acetylene black as a conductive agent and polyvinylidene fluoride (PVDF) as a binder in a weight ratio of 96: 2: 2 in N-methyl pyrrolidone (NMP) solvent, fully stirring and mixing to form uniform anode slurry, coating the slurry on an anode current collector Al foil, drying and cold pressing to obtain the anode sheet. The drying and cold pressing are the prior art. The solid content of the cathode slurry is in the range conventionally employed in the art.
(3) Preparing a negative plate: mixing a negative active material artificial graphite (the particle size D50: 13 +/-1 mu m, the graphitization degree 94 +/-0.5 percent, and secondary particles and single particles, wherein the mass percentage of the secondary particles is 50 percent), a conductive agent acetylene black, a binder Styrene Butadiene Rubber (SBR), and a thickener sodium carboxymethyl cellulose (CMC) according to the weight ratio of 95: 2: 2: and (2) fully stirring and mixing the mixture in a deionized water solvent according to the mass ratio of 1 to form uniform negative electrode slurry, coating the slurry on a negative electrode current collector Cu foil, drying and cold-pressing to obtain the negative electrode plate. The drying and cold pressing are the prior art. The solid content of the negative electrode slurry is in the conventional range adopted in the field.
(4) And (3) isolation film: a PE porous polymer film is used as a separation film.
(5) Preparing a lithium ion battery: and stacking the positive plate, the isolating film and the negative plate in sequence to enable the isolating film to be positioned between the positive plate and the negative plate to play an isolating role, then winding to obtain a bare cell, placing the bare cell in an outer packaging foil, injecting the prepared electrolyte into the dried battery, and carrying out vacuum packaging, standing, formation, shaping and other processes to obtain the lithium ion battery. The procedures of vacuum packaging, standing, formation, shaping and the like are the prior art.
Example 2
This example differs from example 1 in that: according to the preparation of the electrolyte, 5% of 1, 3-propane sultone, 1% of succinonitrile and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Example 3
This example differs from example 1 in that: preparation of electrolyte solution 3.1% of 1, 3-propane sultone, 0.5% of 1, 3, 6-hexanetricarbonitrile, 1% of octanedionitrile and 13% of lithium hexafluorophosphate were added to the mixed solution based on the total mass of the electrolyte solution to obtain an electrolyte solution.
Example 4
This example differs from example 1 in that: preparation of the electrolyte, 4% of 1, 3-propane sultone, 0.5% of 1, 4-butane sultone, 2% of adiponitrile and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Example 5
This example differs from example 1 in that: according to the preparation of the electrolyte, 5% of 1, 3-propane sultone, 0.5% of 1, 3-propylene sultone, 2% of adiponitrile, 0.5% of succinonitrile and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Example 6
This example differs from example 1 in that: according to the preparation of the electrolyte, 6% of 1, 3-propane sultone, 2% of adiponitrile, 0.5% of succinonitrile and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Example 7
This example differs from example 1 in that: according to the preparation of the electrolyte, 4% of 1, 3-propane sultone, 2% of adiponitrile, 2% of succinonitrile and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Example 8
This example differs from example 1 in that: preparation of electrolyte solution according to the total mass of the electrolyte solution, 3.5% of 1, 3-propane sultone, 2% of adiponitrile, 2% of succinonitrile, 1% of suberonitrile and 13% of lithium hexafluorophosphate are added into the mixed solution to obtain the electrolyte solution.
Example 9
This example differs from example 1 in that: preparing a positive plate: the molecular formula of the positive active material lithium cobaltate is LiCo0.9915Al0.004Mg0.002Ti0.0015O2
Example 10
This example differs from example 1 in that: preparing a positive plate: the positive electrode active material lithium cobaltate is LiCo0.995Al0.003Mg0.001Ti0.001O2
Example 11
This example differs from example 1 in that: preparing a negative plate: the negative electrode active material was artificial graphite (particle size D50: 14. + -. 1 μm, graphitization degree 94. + -. 0.5% secondary particles mixed with single particles, wherein the secondary particles accounted for 60% by mass).
Example 12
This example differs from example 1 in that: preparing a negative plate: the negative electrode active material was artificial graphite (particle size D50: 13. + -. 1 μm, graphitization degree 94. + -. 0.5% secondary particles mixed with single particles, wherein the secondary particles accounted for 40% by mass).
Comparative example 1
This comparative example differs from example 1 in that: the preparation of the electrolyte is that 2 percent of 1, 3-propane sultone, 2 percent of adiponitrile and 13 percent of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Comparative example 2
This comparative example differs from example 1 in that: according to the preparation of the electrolyte, 4% of 1, 3-propane sultone and 13% of lithium hexafluorophosphate are added into the mixed solution according to the total mass of the electrolyte to obtain the electrolyte.
Comparative example 3
This comparative example differs from example 1 in that: preparing a positive plate: the positive electrode active material is an active material lithium cobaltate which is not coated by doping.
Comparative example 4
This comparative example differs from example 1 in that: preparing a negative plate: the negative active material was artificial graphite (particle diameter D50: 13. + -. 1 μm, graphitization degree 94. + -. 0.5% pure secondary particle).
Comparative example 5
This comparative example differs from example 1 in that: preparing a negative plate: the negative electrode active material was artificial graphite (particle diameter D50: 18 ± 1 μm, graphitization degree 94 ± 0.5% pure secondary particle), BET: 2.8.
-10 ℃ low temperature discharge experiment:
the batteries obtained in examples 1 to 12 and comparative examples 1 to 5 were subjected to a charge-discharge cycle test 5 times at a charge-discharge rate of 1C and a charge-discharge cutoff voltage of 3.0V to 4.5V at room temperature, and then charged to a full charge state at a rate of 1C. Record 1C capacity Q separately1. The battery in a full-charge state is kept stand for 4 hours at the temperature of minus 10 ℃, then the battery is placed for 3.0V at the temperature of minus 10 ℃ at the multiplying power of 0.4C, the discharge capacity Q is recorded, the capacity retention rate is obtained through calculation, and the recording results are shown in table 1.
The calculation formula used therein is as follows:
Figure BDA0002020599140000061
-20 ℃ low temperature discharge experiment:
the batteries obtained in examples 1 to 12 and comparative examples 1 to 5 were subjected to a charge-discharge cycle test 5 times at a charge-discharge rate of 1C and a charge-discharge cutoff voltage of 3.0V to 4.5V at room temperature, and then charged to a full charge state at a rate of 1C. Record 1C capacity Q separately1. The battery in a full-charge state is kept stand for 4 hours at the temperature of minus 20 ℃, then the battery is placed for 3.0V at the temperature of minus 20 ℃ at the multiplying power of 0.25C, the discharge capacity Q is recorded, the capacity retention rate is obtained through calculation, and the recording results are shown in table 1.
The calculation formula used therein is as follows:
Figure BDA0002020599140000071
-30 ℃ low temperature discharge experiment:
the batteries obtained in examples 1 to 12 and comparative examples 1 to 5 were subjected to a charge-discharge cycle test at room temperature for 5 times at a charge-discharge rate of 1C and a charge-discharge cutoff voltage of 3.0V to 4.5V, and then charged to full charge at a rate of 1CStatus. Record 1C capacity Q separately1. The battery in a full-charge state is kept stand for 4h at the temperature of minus 30 ℃, then the battery is placed for 3.0V at the temperature of minus 30 ℃ at the multiplying power of 0.15C, the discharge capacity Q is recorded, the capacity retention rate is obtained through calculation, and the recording results are shown in table 1.
The calculation formula used therein is as follows:
Figure BDA0002020599140000072
45 ℃ cycle test:
the batteries obtained in examples 1 to 12 and comparative examples 1 to 5 were subjected to charge-discharge cycles 500 times at 45 ℃ at a charge-discharge rate of 1C/1C and a charge-discharge cutoff voltage of 3.0V to 4.5V, the cycle discharge capacity was recorded and divided by the discharge capacity of the 1 st cycle to obtain a capacity retention ratio, the thickness of the battery after the recording cycle was divided by the thickness of the battery before the cycle to obtain a thickness change ratio, and the recording results are shown in Table 1.
TABLE 1 comparison of experimental results for examples and comparative examples
Figure BDA0002020599140000073
Figure BDA0002020599140000081
As can be seen from table 1: the storage and cycle performance of the lithium ion battery using the electrolyte is obviously improved. The above embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above embodiments, and any other changes, modifications, substitutions, combinations and simplifications which do not depart from the spirit and principle of the present invention should be construed as equivalents thereof, and all such changes, modifications, substitutions, combinations and simplifications are intended to be included in the scope of the present invention.

Claims (13)

1. A lithium cobaltate digital lithium ion battery with high and low temperature consideration is characterized in that: the lithium ion battery comprises a lithium cobaltate anode, an artificial graphite cathode with gram capacity of more than or equal to 355mAh/g and a non-aqueous electrolyte, wherein the lithium cobaltate anode is subjected to doping coating treatment; the non-aqueous electrolyte is an organic compound dissolved in a solvent containing cyclic carbonate and chain carbonate, the organic compound is a sultone compound and a polynitrile compound, and the sultone compound accounts for 3.0-10% of the mass fraction of the electrolyte; the artificial graphite cathode is a material mixed by secondary particles and single particles, and the graphitization degree of the artificial graphite cathode is 92.5% -95%; the average particle size D50 of the mixed material of the secondary particles and the single particles is 10-16 mu m.
2. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the polynitrile compound is one or more of succinonitrile, adiponitrile, 1, 3, 6-hexanetrinitrile, glutaronitrile or suberonitrile.
3. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the mass fraction of the polynitrile compound in the electrolyte is 0.1-10%.
4. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 3, characterized in that: the mass fraction of the polynitrile compound in the electrolyte is 1-5%.
5. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the sultone compound is one or a mixture of more of 1, 3-propane sultone, 1, 4-butane sultone or 1, 3-propene sultone.
6. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the mass fraction of the sultone compound in the electrolyte is 3.1-6%.
7.The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the specific surface area of the material mixed by the secondary particles and the single particles is less than or equal to 2m2/g。
8. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the secondary particles are mixed with single particles, the secondary particles are formed by bonding single graphite particles through heating treatment of asphalt at the temperature higher than 500 ℃, and the raw material is needle coke.
9. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the single particle of the material mixed by the secondary particle and the single particle is prepared by taking needle coke or petroleum coke as a raw material and carrying out graphitization treatment.
10. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the mass mixing proportion of the secondary particles and the single particles is 20-80%.
11. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 1, characterized in that: the chemical formula of the lithium cobaltate anode is LixCo1-yMeyO2Wherein x is more than or equal to 0.95 and less than or equal to 1.05, y is more than 0 and less than or equal to 0.1, and Me is Mz1Nz2Wherein, z1+ z2 is more than 0 and less than or equal to 1, and M and N elements are one or more of Al, Mg, Ti, Zr, Co, Ni, Mn, Y, La or Sr.
12. The high-low temperature compatible lithium cobaltate digital lithium ion battery according to claim 11, characterized in that: y is more than 0 and less than or equal to 0.05, z1 is more than 0 and less than or equal to 0.5, and z2 is more than 0 and less than or equal to 0.5.
13. The high-low temperature compatible lithium cobaltate digital lithium according to claim 11 or 12An ion battery, characterized in that: the lithium cobaltate material is LiCo0.985Al0.009Mg0.004Ti0.002O2、LiCo0.9915Al0.004Mg0.002Ti0.0015O2And LiCo0.995Al0.003Mg0.001Ti0.001O2One kind of (1).
CN201910277718.8A 2019-04-08 2019-04-08 Lithium cobaltate digital lithium ion battery with high and low temperature consideration Active CN109935891B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910277718.8A CN109935891B (en) 2019-04-08 2019-04-08 Lithium cobaltate digital lithium ion battery with high and low temperature consideration

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910277718.8A CN109935891B (en) 2019-04-08 2019-04-08 Lithium cobaltate digital lithium ion battery with high and low temperature consideration

Publications (2)

Publication Number Publication Date
CN109935891A CN109935891A (en) 2019-06-25
CN109935891B true CN109935891B (en) 2021-10-29

Family

ID=66989458

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910277718.8A Active CN109935891B (en) 2019-04-08 2019-04-08 Lithium cobaltate digital lithium ion battery with high and low temperature consideration

Country Status (1)

Country Link
CN (1) CN109935891B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112467209A (en) * 2019-09-09 2021-03-09 珠海冠宇电池股份有限公司 High-voltage lithium ion battery with high and low temperature performance
CN114566710A (en) * 2022-02-23 2022-05-31 珠海市赛纬电子材料股份有限公司 Lithium ion battery non-aqueous electrolyte for quick charging and lithium ion battery
CN117751470A (en) * 2022-03-28 2024-03-22 宁德新能源科技有限公司 Electrochemical device and electronic device comprising same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101305484A (en) * 2005-12-20 2008-11-12 松下电器产业株式会社 Nonaqueous electrolyte secondary battery
CN102779976A (en) * 2011-10-10 2012-11-14 北大先行科技产业有限公司 Preparation method of cathode material of LCO (lithium cobaltate)-based lithium ion battery
CN104241627A (en) * 2014-09-11 2014-12-24 北大先行科技产业有限公司 Lithium cobaltate for positive electrode of lithium ion battery and preparation method of lithium cobaltate for positive electrode of lithium ion battery
CN104659366A (en) * 2014-12-30 2015-05-27 东莞市凯金新能源科技有限公司 Preparation method of anode material for power lithium ion battery
CN107871854A (en) * 2016-09-27 2018-04-03 宁波杉杉新材料科技有限公司 A kind of preparation method of graphite negative material of lithium ion battery second particle
CN109346772A (en) * 2018-09-26 2019-02-15 东莞市杉杉电池材料有限公司 A kind of non-aqueous electrolyte for lithium ion cell and lithium ion battery

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101569976B1 (en) * 2012-02-29 2015-11-17 신코베덴키 가부시키가이샤 Lithium ion battery
CN103325991B (en) * 2013-05-31 2017-11-07 余玉英 A kind of full temperature range lithium ion battery

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101305484A (en) * 2005-12-20 2008-11-12 松下电器产业株式会社 Nonaqueous electrolyte secondary battery
CN102779976A (en) * 2011-10-10 2012-11-14 北大先行科技产业有限公司 Preparation method of cathode material of LCO (lithium cobaltate)-based lithium ion battery
CN104241627A (en) * 2014-09-11 2014-12-24 北大先行科技产业有限公司 Lithium cobaltate for positive electrode of lithium ion battery and preparation method of lithium cobaltate for positive electrode of lithium ion battery
CN104659366A (en) * 2014-12-30 2015-05-27 东莞市凯金新能源科技有限公司 Preparation method of anode material for power lithium ion battery
CN107871854A (en) * 2016-09-27 2018-04-03 宁波杉杉新材料科技有限公司 A kind of preparation method of graphite negative material of lithium ion battery second particle
CN109346772A (en) * 2018-09-26 2019-02-15 东莞市杉杉电池材料有限公司 A kind of non-aqueous electrolyte for lithium ion cell and lithium ion battery

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
The Roles of Sulfur-Containing Additives and TheirWorking;Zeli Wu等;《Journal of The Electrochemical Society》;20180828;第165卷(第11期);第A2792-A2800 *
⽯石墨墨形貌对锂离⼦子电池倍率性能的影响;容亮斌等;《电池》;20180430;第48卷(第2期);第113-116页 *

Also Published As

Publication number Publication date
CN109935891A (en) 2019-06-25

Similar Documents

Publication Publication Date Title
KR101546251B1 (en) Electrolyte for electrochemical device and the electrochemical device thereof
EP4220754A1 (en) Lithium metal negative electrode plate, electrochemical apparatus, and electronic device
CN112151764A (en) Electrode plate and preparation method and application thereof
CN111883839B (en) High-voltage electrolyte and lithium ion battery based on same
CN111525191B (en) Electrolyte and electrochemical device
EP4220759A1 (en) Lithium metal negative electrode plate, electrochemical apparatus, and electronic device
US20210249650A1 (en) Negative electrode sheet and secondary battery
CN113906606B (en) Electrolyte, electrochemical device, and electronic device
CN109935891B (en) Lithium cobaltate digital lithium ion battery with high and low temperature consideration
WO2017185703A1 (en) High-temperature lithium-ion battery electrolyte solution and preparation method therefor and high-temperature lithium-ion battery
CN112614703B (en) Negative electrode material of ionic capacitor and preparation method and application thereof
CN110797574A (en) Non-aqueous electrolyte for lithium ion battery and lithium ion battery thereof
WO2024007142A1 (en) Negative electrode plate, secondary battery, battery module, battery pack and electric device
CN109390629B (en) Electrolyte and battery
JP2011249293A (en) Lithium transition metal compound and its manufacturing method, and lithium ion battery
CN114039097A (en) Lithium ion battery
CN115411346A (en) Lithium ion battery and electrochemical device comprising same
CN109494348B (en) Negative pole piece and secondary battery
CN111740162A (en) Electrolyte solution, electrochemical device including the same, and electronic device
WO2023206342A1 (en) Secondary battery and battery module, battery pack and electric device comprising same
CN115275166A (en) Long-life graphite composite material and preparation method thereof
WO2022140952A1 (en) Silicon-carbon composite particle, negative electrode active material and negative electrode containing same, electrochemical device, and electronic device
CN108987803B (en) Lithium metal negative electrode film-forming electrolyte for lithium-sulfur battery and additive thereof
CN114097108A (en) Cathode material, preparation method thereof, electrochemical device and electronic device
CN112368872A (en) Electrolyte and electrochemical device

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
CB02 Change of applicant information

Address after: 519180 No. 209 Pearl Peak Avenue, Jingan Town, Doumen District, Zhuhai City, Guangdong Province

Applicant after: Zhuhai Guanyu Battery Co., Ltd

Address before: 519180 No. 209 Pearl Peak Avenue, Jingan Town, Doumen District, Zhuhai City, Guangdong Province

Applicant before: ZHUHAI COSLIGHT BATTERY Co.,Ltd.

CB02 Change of applicant information
GR01 Patent grant
GR01 Patent grant