CN111370687A - Preparation method of lithium ion battery - Google Patents

Preparation method of lithium ion battery Download PDF

Info

Publication number
CN111370687A
CN111370687A CN202010201085.5A CN202010201085A CN111370687A CN 111370687 A CN111370687 A CN 111370687A CN 202010201085 A CN202010201085 A CN 202010201085A CN 111370687 A CN111370687 A CN 111370687A
Authority
CN
China
Prior art keywords
active material
slurry
positive electrode
negative electrode
electrode active
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.)
Granted
Application number
CN202010201085.5A
Other languages
Chinese (zh)
Other versions
CN111370687B (en
Inventor
谈益
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.)
Jiangsu Zhongyi Hechuang Intelligent Technology Co.,Ltd.
Original Assignee
谈益
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 谈益 filed Critical 谈益
Priority to CN202010201085.5A priority Critical patent/CN111370687B/en
Publication of CN111370687A publication Critical patent/CN111370687A/en
Application granted granted Critical
Publication of CN111370687B publication Critical patent/CN111370687B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • H01M10/058Construction or manufacture
    • 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
    • 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
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/04Processes of manufacture in general
    • H01M4/0402Methods of deposition of the material
    • H01M4/0404Methods of deposition of the material by coating on electrode collectors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/13Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139Processes of manufacture
    • H01M4/1391Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/13Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/139Processes of manufacture
    • H01M4/1393Processes of manufacture of electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • 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
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Landscapes

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

Abstract

The invention provides a preparation method of a lithium ion battery, wherein the lithium ion battery comprises a positive electrode and a negative electrode, and an active substance of the positive electrode is LiNi0.35Co0.25Mn0.4O2Wherein D10 is 1.3-1.4 μm, D50 is 2.4-2.5 μm, and D90 is 3.3-3.4 μm; the negative active material is natural graphite, wherein D10 is 1.8-1.9 μm, D50 is 3.1-3.2 μm, and D90 is 4.2-4.3 μm; the preparation method comprises the steps of screening the positive active substance, wherein the aperture of the screen is 2-2.2 mu m, and obtaining a first positive active substance and a second positive active substance; then mixing the first positive electrode active substance and the second positive electrode active substance according to different mass ratios to obtain a first positive electrode slurry and a second positive electrode slurry, and sequentially coating the first positive electrode slurry and the second positive electrode slurry on a current collector and drying to obtain the positive electrode; mixing a first negative electrode active substance and a second negative electrode active substance to obtain a first negative electrode slurry and a second negative electrode slurry, and sequentially coating the first negative electrode slurry and the second negative electrode slurry on a current collector and drying to obtain the negative electrode; the preparation method also comprises the steps of assembling the anode, the diaphragm and the cathode into a battery, injecting liquid and forming to obtain the battery.

Description

Preparation method of lithium ion battery
Technical Field
The invention relates to a preparation method of a lithium ion battery.
Background
The lithium ion battery has the advantages of high voltage, high specific energy, light weight, small volume, small self-discharge, long service life and the like, is one of the battery systems with the best comprehensive performance at present, and is widely applied to high-energy portable electronic equipment. In the civil field, lithium ion batteries are rapidly expanding from the 3C field (mobile electronic devices, smart phones, notebook computers, and the like) to the energy transportation field, including electric vehicles, power grid peak shaving, solar energy, wind power station power storage, and the like. The nickel-cobalt-manganese ternary positive electrode material is used as an important lithium ion battery positive electrode material, and compared with lithium cobaltate, lithium nickelate and lithium manganate, the nickel-cobalt-manganese ternary positive electrode material has wide attention in academic circles and industrial circles due to the advantages of good cycle performance, large discharge capacity, good thermal stability, low cost, relatively stable structure and the like.
Disclosure of Invention
The invention provides a preparation method of a lithium ion battery, wherein the lithium ion battery comprises a positive electrode and a negative electrode, and an active substance of the positive electrode is LiNi0.35Co0.25Mn0.4O2Wherein D10 is 1.3-1.4 μm, D50 is 2.4-2.5 μm, and D90 is 3.3-3.4 μm; the negative active material is natural graphite, wherein D10 is 1.8-1.9 μm, D50 is 3.1-3.2 μm, and D90 is 4.2-4.3 μm; the preparation method comprises the steps of screening the positive active substance, wherein the aperture of the screen is 2-2.2 mu m, and obtaining a first positive active substance and a second positive active substance; then mixing the first positive electrode active substance and the second positive electrode active substance according to different mass ratios to obtain a first positive electrode slurry and a second positive electrode slurry, and sequentially coating the first positive electrode slurry and the second positive electrode slurry on a current collector and drying to obtain the positive electrode; sieving the negative electrode active material, wherein the mesh diameter is 3.4-3.6 μm to obtain a first negative electrode active material and a second negative electrodeAn active substance; then mixing the first negative electrode active substance and the second negative electrode active substance according to different mass ratios to obtain a first negative electrode slurry and a second negative electrode slurry, and sequentially coating the first negative electrode active substance and the second negative electrode active substance on a current collector and drying to obtain the negative electrode; the preparation method also comprises the steps of assembling the anode, the diaphragm and the cathode into a battery, injecting liquid and forming to obtain the battery.
The specific scheme is as follows:
a preparation method of a lithium ion battery comprises a positive electrode and a negative electrode, wherein the positive electrode active material is LiNi0.35Co0.25Mn0.4O2Wherein D10 is 1.3-1.4 μm, D50 is 2.4-2.5 μm, and D90 is 3.3-3.4 μm; the negative active material is natural graphite, wherein D10 is 1.8-1.9 μm, D50 is 3.1-3.2 μm, and D90 is 4.2-4.3 μm; the preparation method comprises the following steps:
1) sieving the positive active material, wherein the aperture of the sieve is 2-2.2 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 3.4-3.6 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry, wherein the solid content of the slurry is 60-65%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
4) preparing a second positive electrode active material slurry, wherein the solid content of the slurry is 50-55%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
5) preparing a first negative electrode active material slurry, wherein the solid content of the slurry is 60-65%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
6) preparing a second negative electrode active material slurry, wherein the solid content of the slurry is 50-55%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 70:30-85: 15; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurries to be 50-52% so as to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 15:85-30: 70; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurries to be 50-52% so as to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 8:2 to 9: 1; adding a solvent into the first negative electrode active material slurry and the second negative electrode active material slurry to adjust the solid content of the slurry to be 50-52% to obtain first negative electrode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 50-52% to serve as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode;
12) and laminating the anode, the diaphragm and the cathode, filling the laminated anode, diaphragm and cathode into a battery shell, injecting liquid and forming to obtain the battery.
Further, the coating thickness ratio of the first positive electrode slurry to the second positive electrode slurry is 6:4-7: 3; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 6:4-7: 3.
Further, the electrolyte comprises ethyl carbonate and propyl carbonate as organic solvents, and vinylene carbonate and trimethyl phosphate as additives.
Further, the volume ratio of the ethyl carbonate to the propyl carbonate is 2:1-1: 2.
Further, the content of the vinylene carbonate is 2.5-3 times of that of the trimethyl phosphate.
Further, the content of the vinylene carbonate is 2.8 times of that of the trimethyl phosphate.
Further, the formation process comprises constant voltage formation in a voltage range of 3.35-3.4V.
Further, the positive electrode of the lithium ion battery is prepared by the method.
The invention has the following beneficial effects:
1) against LiNi0.35Co0.25Mn0.4O2In a battery system including a positive electrode and a graphite negative electrode, researchers have developed a specific electrode structure by limiting LiNi0.35Co0.25Mn0.4O2The particle size ranges of the positive electrode active material layer and the graphite active material layer, so that the active material layer with a specific structure is designed, the stability of the electrode active material layer can be effectively improved, and the cycle life of the battery can be prolonged.
2) Through numerous experiments, researchers find that the combination of vinylene carbonate and trimethyl phosphate can effectively improve the cycle performance of the lithium manganate battery, and the specific mechanism is not clear, but experimental data show that when two additives are used together, the cycle performance of the battery is remarkably improved and is obviously higher than that of a single-addition mode;
3) the other invention point of the invention is that the constant voltage formation under the specific voltage can effectively improve the cycle performance of the battery, and the principle of the invention is probably that the additive of the invention can make the SEI formation speed more stable under the voltage.
Detailed Description
The present invention will be described in more detail below with reference to specific examples, but the scope of the present invention is not limited to these examples.
The positive electrode active material is LiNi0.35Co0.25Mn0.4O2(ii) a The negative active material is natural graphite; the particle size distribution of the positive and negative electrodes is shown in table 1; the solvent of the electrolyte is PC + EC with the volume ratio of 1: 1; the electrolyte salt is lithium hexafluorophosphate with the concentration of 1mol/L, and the additives are vinylene carbonate and trimethyl phosphate, wherein the content of trimethyl phosphate is 1 volume percent, and the content of vinylene carbonate is 2.8 volume percent. The positive electrode solvent is NMP, the positive electrode binder is PVDF, the negative electrode solvent is deionized water, the negative electrode binder is SBR, and the conductive agent is acetylene black.
TABLE 1
Figure BDA0002419404220000041
Example 1
1) Sieving the positive active material, wherein the aperture of the sieve is 2 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 3.4 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry having a solid content of 60%, wherein the active material: adhesive: the conductive agent is 100:4: 4;
4) preparing a second positive electrode active material slurry having a solid content of 50%, wherein the active material: adhesive: the conductive agent is 100:4: 4;
5) preparing a first negative electrode active material slurry having a solid content of 60%, wherein the active material: adhesive: the conductive agent is 100:4: 4;
6) preparing a second negative electrode active material slurry having a solid content of 50%, wherein the active material: adhesive: the conductive agent is 100:4: 4;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 70: 30; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 50% so as to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 15: 85; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 50% so as to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 8: 2; adding a solvent to adjust the solid content of the slurry to 50% to obtain a first cathode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 50% to serve as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode; wherein the thickness of the positive electrode active material layer and the negative electrode active material layer is 50 μm on one side, and the coating thickness ratio of the first positive electrode slurry to the second positive electrode slurry is 6: 4; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 7: 3;
12) stacking the positive electrode, the separator and the negative electrode, and filling the stacked positive electrode, separator and negative electrode into a battery shell;
13) injecting liquid;
14) charging to 3.38V at 0.05C, and then charging at constant voltage until the charging current is less than 0.01C; and then charging to 4.2V at a constant current of 0.1C, and then charging and discharging for 3 times at a constant current of 0.2C from 4.2V to 2.7V to obtain the battery.
Example 2
1) Sieving the positive active material, wherein the aperture of the sieve is 2.2 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 3.6 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry having a solid content of 65%, wherein the active material: adhesive: the conductive agent is 100:6: 6;
4) preparing a second positive electrode active material slurry having a solid content of 55%, wherein the active material: adhesive: the conductive agent is 100:6: 6;
5) preparing a first negative electrode active material slurry having a solid content of 65%, wherein the active material: adhesive: the conductive agent is 100:6: 6;
6) preparing a second negative electrode active material slurry having a solid content of 55%, wherein the active material: adhesive: the conductive agent is 100:6: 6;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 85: 15; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 52% to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 30: 70; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 52% to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 9: 1; adding a solvent to adjust the solid content of the slurry to 52% to obtain first negative electrode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 52 percent, and taking the slurry as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode; wherein the thickness of the positive electrode active material layer and the negative electrode active material layer is 50 μm on one side, and the coating thickness ratio of the first positive electrode slurry to the second positive electrode slurry is 6: 4; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 7: 3;
12) stacking the positive electrode, the separator and the negative electrode, and filling the stacked positive electrode, separator and negative electrode into a battery shell;
13) injecting liquid;
14) charging to 3.38V at 0.05C, and then charging at constant voltage until the charging current is less than 0.01C; and then charging to 4.2V at a constant current of 0.1C, and then charging and discharging for 3 times at a constant current of 0.2C from 4.2V to 2.7V to obtain the battery.
Example 3
1) Sieving the positive active material, wherein the aperture of the sieve is 2.2 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 3.5 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry having a solid content of 62%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
4) preparing a second positive electrode active material slurry having a solid content of 52%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
5) preparing a first negative electrode active material slurry having a solid content of 62%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
6) preparing a second negative electrode active material slurry having a solid content of 52%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 80: 30; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 51% so as to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 20: 80; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 51% so as to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 8: 2; adding a solvent into the first negative electrode active material slurry and the second negative electrode active material slurry to adjust the solid content of the slurry to 51% to obtain a first negative electrode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 51 percent, and taking the slurry as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode; wherein the thickness of the positive electrode active material layer and the negative electrode active material layer is 50 μm on one side, and the coating thickness ratio of the first positive electrode slurry to the second positive electrode slurry is 6: 4; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 7: 3;
12) stacking the positive electrode, the separator and the negative electrode, and filling the stacked positive electrode, separator and negative electrode into a battery shell;
13) injecting liquid;
14) charging to 3.38V at 0.05C, and then charging at constant voltage until the charging current is less than 0.01C; and then charging to 4.2V at a constant current of 0.1C, and then charging and discharging for 3 times at a constant current of 0.2C from 4.2V to 2.7V to obtain the battery.
Comparative example 1
1) Sieving the positive active material, wherein the aperture of the sieve is 3 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 2 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry having a solid content of 62%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
4) preparing a second positive electrode active material slurry having a solid content of 52%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
5) preparing a first negative electrode active material slurry having a solid content of 62%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
6) preparing a second negative electrode active material slurry having a solid content of 52%, wherein the active material: adhesive: the conductive agent is 100:5: 5;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 80: 30; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 51% so as to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 20: 80; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurry to 51% so as to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 8: 2; adding a solvent into the first negative electrode active material slurry and the second negative electrode active material slurry to adjust the solid content of the slurry to 51% to obtain a first negative electrode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 51 percent, and taking the slurry as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode; wherein the thickness of the positive electrode active material layer and the negative electrode active material layer is 50 μm on one side, and the coating thickness ratio of the first positive electrode slurry to the second positive electrode slurry is 6: 4; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 7: 3;
12) stacking the positive electrode, the separator and the negative electrode, and filling the stacked positive electrode, separator and negative electrode into a battery shell;
13) injecting liquid;
14) charging to 3.38V at 0.05C, and then charging at constant voltage until the charging current is less than 0.01C; and then charging to 4.2V at a constant current of 0.1C, and then charging and discharging for 3 times at a constant current of 0.2C from 4.2V to 2.7V to obtain the battery.
Comparative example 2
1) Preparing positive electrode slurry, wherein the solid content of the slurry is 52%, and the content of active substances: adhesive: the conductive agent is 100:5: 5;
2) preparing a negative electrode slurry, wherein the solid content of the slurry is 52%, and the active material: adhesive: the conductive agent is 100:5: 5;
3) coating anode slurry on an anode current collector, and drying to obtain the anode; coating negative electrode slurry on a negative electrode current collector, and drying to obtain the negative electrode; wherein the thickness of the positive electrode active material layer and the negative electrode active material layer is 50 μm on one side;
4) stacking the positive electrode, the separator and the negative electrode, and filling the stacked positive electrode, separator and negative electrode into a battery shell;
5) injecting liquid;
6) charging to 3.38V at 0.05C, and then charging at constant voltage until the charging current is less than 0.01C; and then charging to 4.2V at a constant current of 0.1C, and then charging and discharging for 3 times at a constant current of 0.2C from 4.2V to 2.7V to obtain the battery.
Comparative example 3
The electrolyte contained no additive, and the other processes were the same as in example 3.
Comparative example 4
The electrolyte contained no vinylene carbonate, and the other processes were the same as in example 3.
Comparative example 5
The electrolyte contained no trimethyl phosphate, and the other processes were the same as in example 3.
Comparative example 6
The electrolyte contained vinylene carbonate and trimethyl phosphate, wherein the trimethyl phosphate content was 2 vol% and the vinylene carbonate content was 2.8 vol%, and the other processes were the same as in example 3.
Comparative example 7
After the liquid injection in the step 13, the battery is charged to 4.2V at a constant current of 0.1C, and then charged and discharged for 3 times at a constant current of 0.2C from 4.2V to 2.7V, so that the battery is obtained, the constant voltage formation of 3.38V is omitted, and other processes are the same as those in the embodiment 3.
Test and results
The batteries of examples 1-3 and comparative examples 1-7 were cycled 200 times at a rate of 0.5C, and the capacity retention rates of the batteries were recorded. The results are shown in table 2, and it can be seen from table 2 that the aperture range of the mesh, the structural arrangement of the electrodes, and the selection of additives, and the constant voltage formation of a specific voltage range all have great influence on the cycle performance of the battery.
TABLE 2
Figure BDA0002419404220000091
Figure BDA0002419404220000101
While the present invention has been described in detail with reference to the preferred embodiments, it should be understood that the above description should not be taken as limiting the invention.

Claims (8)

1. A preparation method of a lithium ion battery comprises a positive electrode and a negative electrode, wherein an active substance of the positive electrode is LiNi0.35Co0.25Mn0.4O2Wherein D10 is 1.3-1.4 μm, D50 is 2.4-2.5 μm, and D90 is 3.3-3.4 μm; the negative active material is natural graphite, wherein D10 is 1.8-1.9 μm, D50 is 3.1-3.2 μm, and D90 is 4.2-4.3 μm; the preparation method comprises the following steps:
1) sieving the positive active material, wherein the aperture of the sieve is 2-2.2 mu m, collecting the material on the sieve to obtain a first positive active material, and collecting the material under the sieve to obtain a second positive active material;
2) sieving the negative electrode active material, wherein the aperture of the sieve is 3.4-3.6 mu m, collecting the material on the sieve to obtain a first negative electrode active material, and collecting the material under the sieve to obtain a second negative electrode active material;
3) preparing a first positive electrode active material slurry, wherein the solid content of the slurry is 60-65%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
4) preparing a second positive electrode active material slurry, wherein the solid content of the slurry is 50-55%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
5) preparing a first negative electrode active material slurry, wherein the solid content of the slurry is 60-65%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
6) preparing a second negative electrode active material slurry, wherein the solid content of the slurry is 50-55%, and the active material: adhesive: the conductive agent is 100:4-6: 4-6;
7) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 70:30-85: 15; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurries to be 50-52% so as to obtain a first positive electrode slurry;
8) according to the first positive electrode active material: mixing the second positive electrode active material at a ratio of 15:85-30: 70; adding a solvent into the first positive electrode active material slurry and the second positive electrode active material slurry to adjust the solid content of the slurries to be 50-52% so as to obtain a first positive electrode slurry;
9) according to the first negative electrode active material: mixing the second negative electrode active material at a ratio of 8:2 to 9: 1; adding a solvent into the first negative electrode active material slurry and the second negative electrode active material slurry to adjust the solid content of the slurry to be 50-52% to obtain first negative electrode slurry;
10) adding a solvent into the second active material slurry to adjust the solid content of the slurry to be 50-52% to serve as second negative electrode slurry;
11) sequentially coating first positive electrode slurry and second positive electrode slurry on a positive electrode current collector, and drying to obtain the positive electrode; sequentially coating first negative electrode slurry and second negative electrode slurry on a negative electrode current collector, and drying to obtain a negative electrode;
12) and laminating the anode, the diaphragm and the cathode, filling the laminated anode, diaphragm and cathode into a battery shell, injecting liquid and forming to obtain the battery.
2. The production method according to the preceding claim, wherein the coating thickness ratio of the first positive electrode paste to the second positive electrode paste is 6:4 to 7: 3; the coating thickness ratio of the first negative electrode slurry to the second negative electrode slurry is 6:4-7: 3.
3. The method according to the preceding claim, wherein the electrolyte comprises ethyl carbonate and propyl carbonate as organic solvents and vinylene carbonate and trimethyl phosphate as additives.
4. The process according to the preceding claim, wherein the volume ratio of ethyl carbonate to propyl carbonate is from 2:1 to 1: 2.
5. The method according to the preceding claim, wherein the vinylene carbonate content is 2.5-3 times higher than the trimethyl phosphate content.
6. The method according to the preceding claim, wherein the vinylene carbonate content is 2.8 times higher than the trimethyl phosphate content.
7. The method of claim, wherein the formation process comprises a constant voltage formation within a voltage range of 3.35-3.4V.
8. A lithium ion battery, the positive electrode being prepared by the method of any one of claims 1 to 7.
CN202010201085.5A 2020-03-20 2020-03-20 Preparation method of lithium ion battery Active CN111370687B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010201085.5A CN111370687B (en) 2020-03-20 2020-03-20 Preparation method of lithium ion battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010201085.5A CN111370687B (en) 2020-03-20 2020-03-20 Preparation method of lithium ion battery

Publications (2)

Publication Number Publication Date
CN111370687A true CN111370687A (en) 2020-07-03
CN111370687B CN111370687B (en) 2021-11-30

Family

ID=71210519

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010201085.5A Active CN111370687B (en) 2020-03-20 2020-03-20 Preparation method of lithium ion battery

Country Status (1)

Country Link
CN (1) CN111370687B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113690412A (en) * 2021-06-16 2021-11-23 浙江锂威能源科技有限公司 Active slurry, preparation method thereof, positive plate and lithium ion battery

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101826634A (en) * 2010-05-17 2010-09-08 江西省福斯特新能源有限公司 Lithium ion battery and manufacturing method thereof
CN103762379A (en) * 2014-01-28 2014-04-30 泉州劲鑫电子有限公司 High-capacity lithium ion battery and production process thereof
CN104466171A (en) * 2014-12-13 2015-03-25 西安瑟福能源科技有限公司 Lithium ion battery for emergency start
CN107046131A (en) * 2017-04-06 2017-08-15 桑顿新能源科技有限公司 A kind of LiFePO4 system lithium ion battery and preparation method
CN109687013A (en) * 2018-12-27 2019-04-26 江西省汇亿新能源有限公司 A kind of high magnification, high safety, long-life ferric phosphate lithium cell and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101826634A (en) * 2010-05-17 2010-09-08 江西省福斯特新能源有限公司 Lithium ion battery and manufacturing method thereof
CN103762379A (en) * 2014-01-28 2014-04-30 泉州劲鑫电子有限公司 High-capacity lithium ion battery and production process thereof
CN104466171A (en) * 2014-12-13 2015-03-25 西安瑟福能源科技有限公司 Lithium ion battery for emergency start
CN107046131A (en) * 2017-04-06 2017-08-15 桑顿新能源科技有限公司 A kind of LiFePO4 system lithium ion battery and preparation method
CN109687013A (en) * 2018-12-27 2019-04-26 江西省汇亿新能源有限公司 A kind of high magnification, high safety, long-life ferric phosphate lithium cell and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113690412A (en) * 2021-06-16 2021-11-23 浙江锂威能源科技有限公司 Active slurry, preparation method thereof, positive plate and lithium ion battery

Also Published As

Publication number Publication date
CN111370687B (en) 2021-11-30

Similar Documents

Publication Publication Date Title
EP2660904B1 (en) Method for preparing graphene-like doped positive electrode material of lithium-ion battery
CN111193071A (en) Electrolyte of high-voltage quick-charging lithium ion battery and lithium ion battery
US20180366720A1 (en) Positive active material and lithium-ion secondary battery
US20230282836A1 (en) Lithium metal negative electrode plate, electrochemical apparatus, and electronic device
CN103779572A (en) Lithium ion battery cathode additive and preparation method thereof, lithium ion battery cathode piece and lithium ion battery
CN102082259A (en) Lithium secondary battery electrodes and production method thereof
EP4220759A1 (en) Lithium metal negative electrode plate, electrochemical apparatus, and electronic device
CN102082290A (en) High-voltage high-energy-density lithium ion battery and manufacturing method thereof
CN103594735B (en) A kind of preparation method of lithium titanate lithium ion battery
CN111293365B (en) Preparation method of lithium manganate battery
JP2003297353A (en) Negative electrode for secondary battery, secondary battery using such negative electrode, and manufacturing method for negative electrode
WO2018059180A1 (en) High-power, high-energy chemical power supply and preparation method therefor
CN101587952A (en) Compound lithium cobaltate cathode material, preparing method and application thereof
CN103035948A (en) Non-carbonate based novel electrolyte solution system used for spinel lithium titanate energy storage type lithium ion secondary battery
US11437623B2 (en) Secondary battery and apparatus contained the secondary battery
CN111370687B (en) Preparation method of lithium ion battery
CN111313085B (en) Preparation method of lithium ion battery anode
CN110611117A (en) Lithium ion battery and positive pole piece
CN115207335A (en) Low-temperature chargeable and dischargeable lithium ion battery cathode material and lithium ion battery
CN103855400A (en) Lithium silicate ferrous/graphene composite and its preparation method and application
CN103022447B (en) The preparation method of serondary lithium battery negative pole Sn-Co-C composite material and serondary lithium battery
CN111600012A (en) Cobalt-free lithium-rich manganese-based positive electrode material, composite positive electrode piece and lithium ion battery
CN111554895A (en) Solid polymer lithium ion battery anode and preparation method and application thereof
CN111293366A (en) Preparation method of lithium ion battery with lithium iron phosphate anode
CN114864868B (en) Preparation method and application of high-voltage multilayer solid composite electrode

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
CB03 Change of inventor or designer information

Inventor after: Xu Hao

Inventor after: Tan Yi

Inventor before: Tan Yi

CB03 Change of inventor or designer information
TA01 Transfer of patent application right

Effective date of registration: 20211101

Address after: 225400 talent science and Technology Plaza, Taixing high tech Industrial Development Zone, Taizhou City, Jiangsu Province

Applicant after: Jiangsu Zhongyi Hechuang Intelligent Technology Co.,Ltd.

Address before: 224700 Room 401, building 44, xiyuanxin village, Jianhu County, Yancheng City, Jiangsu Province

Applicant before: Tan Yi

TA01 Transfer of patent application right
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A preparation method for lithium-ion batteries

Effective date of registration: 20230331

Granted publication date: 20211130

Pledgee: Bank of Nanjing Co.,Ltd. Taizhou Branch

Pledgor: Jiangsu Zhongyi Hechuang Intelligent Technology Co.,Ltd.

Registration number: Y2023320000175

PE01 Entry into force of the registration of the contract for pledge of patent right