CN109962211A - A kind of preparation method of lithium ion battery - Google Patents

A kind of preparation method of lithium ion battery Download PDF

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Publication number
CN109962211A
CN109962211A CN201910233984.0A CN201910233984A CN109962211A CN 109962211 A CN109962211 A CN 109962211A CN 201910233984 A CN201910233984 A CN 201910233984A CN 109962211 A CN109962211 A CN 109962211A
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active layer
lithium ion
ion battery
negative electrode
positive
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赵亚
张芳芳
刘桐桐
杨冬生
翟博
刘俊军
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Zhejiang Hengyuan New Energy Technology Co Ltd
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Zhejiang Hengyuan New Energy Technology Co Ltd
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0061Electro-spinning characterised by the electro-spinning apparatus
    • D01D5/0069Electro-spinning characterised by the electro-spinning apparatus characterised by the spinning section, e.g. capillary tube, protrusion or pin
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0061Electro-spinning characterised by the electro-spinning apparatus
    • D01D5/0076Electro-spinning characterised by the electro-spinning apparatus characterised by the collecting device, e.g. drum, wheel, endless belt, plate or grid
    • D01D5/0084Coating by electro-spinning, i.e. the electro-spun fibres are not removed from the collecting device but remain integral with it, e.g. coating of prostheses
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0061Electro-spinning characterised by the electro-spinning apparatus
    • D01D5/0092Electro-spinning characterised by the electro-spinning apparatus characterised by the electrical field, e.g. combined with a magnetic fields, using biased or alternating fields
    • 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
    • H01M10/058Construction or manufacture
    • 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/403Manufacturing processes of separators, membranes or diaphragms
    • 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

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Textile Engineering (AREA)
  • Materials Engineering (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

The present invention relates to a kind of preparation methods of lithium ion battery, belong to battery technology field.In order to solve the problems, such as that the existing poor synchronization internal resistance of cell is big, a kind of preparation method of lithium ion battery is provided, including anode sizing agent and negative electrode slurry are transferred to respectively in corresponding positive syringe and cathode syringe, by anode sizing agent and negative electrode slurry, synchronous electrostatic spinning is coated in the two opposite side surfaces of diaphragm respectively, after drying, positive-active layer and negative electrode active layer are respectively formed in the two opposite side surfaces of diaphragm;Plus plate current-collecting body and negative current collector are respectively corresponded into positive-active layer and negative electrode active layer carries out hot-rolling pressure and is compounded in surface, corresponding lithium ion battery is made using cross cutting and following process.The present invention can reduce the internal resistance of cell, improve the battery chemistries impact of performance.With simple process, easily operated advantage.

Description

A kind of preparation method of lithium ion battery
Technical field
The present invention relates to a kind of preparation methods of lithium ion battery, belong to battery technology field.
Background technique
Lithium ion battery is a kind of novel Green Chemistry power supply, is had compared with traditional nickel-cadmium cell, nickel-metal hydride battery The advantage that voltage is high, the service life is long, energy density is big.From after nineteen ninety Sony Corporation of Japan release first generation lithium ion battery, it Various portable devices have been rapidly developed and be widely used in, the neck such as 3C Product, power device, energy storage device is related to Domain.Due to flourishing for new-energy automobile, while the demand to power battery is increasing, to its energy and high rate performance More stringent requirements are proposed, and high-energy and high power lithium battery have become the focus on research direction of battery industry.
Complete lithium ion battery is mainly made of anode, cathode, diaphragm, electrolyte and battery case.Electrode mainly leads to It crosses in collection liquid surface coating slurry, drying, compacting, finally obtains positive/negative pole piece.It needs in assembly cell process by diaphragm It is aligned between positive/negative pole piece, finally obtains battery core component by lamination or winding process.It is numerous that the technique assembles battery process It is trivial, especially in assembling process, needs to realize being aligned and well contacting for electrode slice and diaphragm, avoid the burr in die cutting process Bring internal short-circuit, the degree of automation is limited, at high cost;Different procedure calls mutually restrict in traditional technology, lead to battery Consistency is poor.Further, since the interfacial structure of positive/negative pole piece and diaphragm is more complex, the internal resistance of cell is larger, leads to the electricity of battery Chemical property performance is restricted, meanwhile, existing processing is all to be processed by substep to positive and negative pole material layer, and there are differences The restriction for walking processing, influences battery performance.
Summary of the invention
The present invention is directed to the above defect existing in the prior art, provides a kind of preparation method of lithium ion battery, solves The technical issues of be how to realize that synchronism is good and the interfacial resistance of battery can be reduced to reduce the performance of the internal resistance of cell.
The purpose of the present invention is be achieved through the following technical solutions: a kind of preparation method of lithium ion battery, this method The following steps are included:
A, anode sizing agent and negative electrode slurry are transferred to respectively in corresponding positive syringe and cathode syringe, it will be positive Synchronous electrostatic spinning is coated in the two opposite side surfaces of diaphragm respectively for slurry and negative electrode slurry, after dry, opposite the two of diaphragm Positive-active layer and negative electrode active layer are respectively formed on a side;
B, plus plate current-collecting body and negative current collector are respectively corresponded into positive-active layer and negative electrode active layer carries out hot-rolling pressure again It closes on surface, corresponding lithium ion battery is made using cross cutting and following process.
Anode sizing agent and cathode data are coated in the both side surface of diaphragm respectively by synchronous electrostatic spinning processing, Can make to form uniform coating by electrostatic spinning, can be formed between diaphragm it is closer cover effect, make shape At positive-active layer and the formation of negative electrode active layer and diaphragm to connect solution closer, to effectively reduce positive electrode active materials and cathode Active material realizes the effect for reducing the internal resistance of battery with the interfacial resistance between diaphragm;And positive and negative electrode coating is due to using quiet Electrospun processing is capable of forming complicated staggered multi-cellular structure, is equivalent to netted structure and morphology, helps to reduce Polarization phenomena during electrode electro Chemical alleviate the defect of volume expansion, make the chemical stability for improving battery on the whole. Meanwhile electrospinning coating processing is used by synchronous, the production time is shortened, the mutual shadow between different processes is avoided It rings, synchronous processing formation improves battery with two side terminals, keeps battery performance more stable, and technical process is simple, is conducive to reality Border application.
In the preparation method of above-mentioned lithium ion battery, preferably, the condition of synchronous electrostatic spinning described in step A Are as follows:
The voltage is set as 20~25kV, and spinning flow velocity is 0.6~0.8mL/h, and receiving distance is 15~25cm;And The metal needle diameter of the anode syringe and cathode syringe is 0.5~0.6mm.Make the granularity of the spinning to be formed and Uniformity is more superior, and the active layer to be formed can be made to have the effect of preferable high-energy density.
In the preparation method of above-mentioned lithium ion battery, preferably, the surface density of the positive-active layer be 10~ 30mg/cm2, the surface density of the negative electrode active layer is 5~20mg/cm2.It handles to be more advantageous to by using electrostatic spinning to be formed Higher surface density makes that preferable capacity ratio can be reached between positive and negative electrode, and the energy for being conducive to improve lithium ion battery is close Degree.
In the preparation method of above-mentioned lithium ion battery, preferably, the positive reversible capacity of the lithium ion battery with The ratio between cathode reversible capacity is 1:1~1:1.3.The specific energy that lithium ion battery can be effectively improved makes further to improve The multiplying power and energy density of lithium ion battery.
In the preparation method of above-mentioned lithium ion battery, preferably, positive-active layer and negative electrode active described in step A The thickness of the coating of layer is 50~200 μm.It can guarantee that there is preferable battery performance.
In the preparation method of above-mentioned lithium ion battery, preferably, the temperature of hot-rolling pressure described in step B be 20~ 100 DEG C, and the pressure of the hot-rolling pressure is 10~1000N/cm2.Purpose is to be compounded in corresponding collector preferably Surface reduces the contact resistance between collector and active coating, is conducive to the performance of material property.
In the preparation method of above-mentioned lithium ion battery, preferably, the anode sizing agent includes positive electrode active materials, leads The mixed slurry of electric agent and binder;The negative electrode slurry includes the mixed slurry of negative electrode active material, conductive agent and binder. It further include having other solvent compositions such as organic solvent in slurry, solvent here can be NMP, dimethylformamide or acetone Etc..
In the preparation method of above-mentioned lithium ion battery, preferably, plus plate current-collecting body described in step B be selected from aluminium foil or Aluminium net;The negative current collector is selected from copper foil or copper mesh.It is easy to get with raw material, advantage at low cost.
In the preparation method of above-mentioned lithium ion battery, preferably, diaphragm described in step A is selected from PP film, PE film, double Layer PP/PE film, bilayer PP/PP film or three layers of PP/PE/PP film, the surface that the diaphragm is located at positive-active layer side are coated with pottery Ceramic material layer.The wetting property for being conducive to improve the heat resistance of diaphragm by the surface coated ceramic material layer in diaphragm, makes more The effective performance for guaranteeing battery.
In conclusion compared with prior art, the present invention having the advantage that
1. by making the positive-active layer surface coated in diaphragm directly synchronous with negative electrode active layer, when shortening production Between, so that anode and cathode active materials and diaphragm is formed closer composite construction characteristic, reduce the interfacial resistance between them, It realizes and reduces the internal resistance of cell, improve battery performance effect.
2. the positive and negative electrode active layer to be formed can be made to have compactness good and stablize by using synchronous electrostatic spinning processing Property high advantage, and there is the advantages of simple process, Yi Li is operated.
Specific embodiment
Below by specific embodiment, the technical solutions of the present invention will be further described, but the present invention is simultaneously It is not limited to these embodiments.
This lithium ion battery passes through is transferred to corresponding anode note for the anode sizing agent being uniformly mixed and negative electrode slurry respectively In emitter and cathode syringe, by anode sizing agent and negative electrode slurry, synchronous electrostatic spinning is coated in opposite two sides of diaphragm respectively Face is respectively formed positive-active layer and negative electrode active layer in the two opposite side surfaces of diaphragm after dry;Again by plus plate current-collecting body and Negative current collector respectively corresponds positive-active layer and negative electrode active layer carries out hot-rolling pressure and is compounded in surface, preferably makes the temperature of hot-rolling pressure Degree is 20~100 DEG C, and the pressure of hot-rolling pressure is 10~1000N/cm2;Optimum condition is that the temperature of hot-rolling pressure is 80 DEG C, and heat The pressure of roll-in is 120N/cm2;Corresponding lithium ion battery is made using cross cutting and following process, following process here It such as include winding, tab welding, assembling, vacuum bakeout, fluid injection, chemical conversion, sealing, the obtained lithium ion battery of full capacity test.This In by synchronous electrospinning process will just, pole slurry is synchronous is coated in corresponding diaphragm both side surface, be capable of forming well Composite effect makes to effectively reduce interfacial resistance and polarization phenomena.Specifically, the lithium ion battery that this method obtains includes electricity Core, general lithium ion battery all have shell and electrolyte, and battery core is arranged inside the shell, it is often more important that, this battery core include every Film, a side surface of diaphragm passes through synchronous electrostatic spinning and is coated with positive-active layer, and coats in another side surface of diaphragm There is negative electrode active layer, plus plate current-collecting body is compounded on the outside of positive-active layer, is compounded with negative pole currect collecting on the outside of negative electrode active layer Body.Battery core can be conventional takeup type or stacked design feature.Here electrostatic spinning operation is synchronized, can be avoided use The difference of different process processing restricts the defect for causing battery performance to decline.
Further scheme can make 10~30mg/cm of surface density of positive-active layer2, the face of negative electrode active layer Density is 5~20mg/cm2.Can also make the ratio between positive reversible capacity and cathode reversible capacity of lithium ion battery is 1:1~1: 1.3.The performance for being conducive to positive electrode active materials capacity improves the cycle life of battery.Preferably make positive-active layer and cathode living The thickness of property layer is at 50~200 μm.
Further scheme can also make diaphragm be selected from PP film, PE film, bilayer PP/PE film, bilayer PP/PP film or three Layer PP/PE/PP film, the surface that the diaphragm is located at positive-active layer side are coated with ceramic material layer, improve the heat resistance of diaphragm And wellability.The corresponding anode sizing agent of positive-active layer may include positive conductive additive, positive electrode binder, positive solvent, The mass ratio of positive coating slurry each component is positive electrode active materials: positive conductive additive: positive electrode binder: positive solvent 10~100:1 of mass ratio~20:1~20:5~100.The corresponding negative electrode slurry of negative electrode active layer may include negative conductive addition Agent, negative electrode binder, cathode solvent, the mass ratio of the component of cathode coating slurry are negative electrode active material: negative conductive addition Agent: negative electrode binder: 10~100:1 of mass ratio~20:1~20:5~100 of cathode solvent.Further, preferably make anode Slurry uses nickel-cobalt-manganese ternary material: Super-P: carbon nanotube: the mass ratio of PVDF:NMP is 96:1.5:1:1.5:54;It is negative Pole slurry uses graphite: Super-P:CMC:SBR: the mass ratio of deionized water improves the stability of battery for 95:2:1:2:72 With the performance of circulation volume conservation rate.The electrolyte of battery is using conventional, it is preferred to use the solute of electrolyte be lithium Salt, concentration are 0.7~2M, and solute is selected from LiPF6、LiBF6、LiAsF6、LiClF6, any one in LiBOB;Electrolyte it is molten Agent includes carbonic ester and esters, wherein carbonic ester is selected from ethylene carbonate, propene carbonate, dimethyl carbonate, carbonic acid diethyl At least one of ester, methyl ethyl carbonate and methyl propyl carbonate, esters are selected from gamma-butyrolacton, methyl formate, Ethyl formate, second At least one of sour methyl esters, ethyl acetate and ethyl butyrate;It can also make the quality of carbonic ester and esters solvent in electrolyte Than for 1:2~3:1.Specific manufacture craft explanation is carried out to lithium ion battery of the invention below.
Embodiment 1
It is nickel-cobalt-manganese ternary material: Super-P: carbon nanotube that anode sizing agent in the present embodiment is prepared in mass ratio: The ratio of PVDF:NMP=96:1.5:1:1.5:54 is prepared;It is graphite: Super-P: carbon that negative electrode slurry is prepared in mass ratio Nanotube: the ratio of PVDF:NMP=95:2:1:2:72 is prepared.The ratio between reversible capacity and the reversible capacity of cathode of anode For 1:1.17.Above-mentioned anode sizing agent is respectively transferred to the two of synchronous electrostatic spinning apparatus with negative electrode slurry respectively after mixing evenly In a syringe, electrostatic spinning processing is synchronized on two opposite sides of diaphragm, wherein diaphragm is using wherein side Anode sizing agent is coated on the membrane surface for having nano ceramic material side by the double-deck PP/PE film of coating nano ceramic material, Meanwhile negative electrode slurry being coated on opposite another side surface of diaphragm, wherein the condition of corresponding electrostatic spinning processing Are as follows: voltage is set as 20kV, and spinning flow velocity is 0.6mL/h, and receiving distance is 20cm;And the positive syringe and cathode are infused The metal needle diameter of emitter is 0.50mm;After electrostatic spinning, obtain being respectively formed anode on the surface of diaphragm two sides Active layer and negative electrode active layer, wherein making the surface density 19mg/cm of positive-active layer2, the surface density of negative electrode active layer is 8mg/cm2;Dry 120min is then transferred in vacuum oven at 95 DEG C;Aluminium foil and copper foil are respectively corresponded into positive-active Layer and negative electrode active layer carry out hot-rolling pressure, in temperature 60 C and pressure 400N/cm2Under carry out compacting make to be compounded in corresponding activity Layer surface;It is tested using cross cutting, winding, tab welding, assembling, vacuum bakeout, fluid injection, chemical conversion, sealing, full capacity and phase is made The lithium ion battery answered.Here the shape of battery can be the structures such as cylindrical, rectangular or special-shaped.Use concentration for 1M The electrolyte of LiPF6-EC/DEC (1:1).Battery capacity retention ratio after 100 circulations is 99%, and battery DC internal resistance is 0.45mΩ.Compared to conventional design, battery capacity improves 10.5% under 1C.
Embodiment 2
It is nickel-cobalt-manganese ternary material: Super-P: carbon nanotube that anode sizing agent in the present embodiment is prepared in mass ratio: The ratio of PVDF:NMP=96:1.5:1:1.5:54 is prepared;It is graphite: Super-P: carbon that negative electrode slurry is prepared in mass ratio Nanotube: the ratio of PVDF:NMP=95:2:1:2:72 is prepared.The ratio between reversible capacity and the reversible capacity of cathode of anode For 1:1.2.Above-mentioned anode sizing agent is respectively transferred to the two of synchronous electrostatic spinning apparatus with negative electrode slurry respectively after mixing evenly In a syringe, electrostatic spinning processing is synchronized on two opposite sides of diaphragm, wherein diaphragm is using wherein side Anode sizing agent is coated on the PP film membrane surface for having nano ceramic material side, together by the PP film of coating nano ceramic material When, negative electrode slurry is coated on PP film every on another side surface of diaphragm, wherein the condition of corresponding electrostatic spinning processing are as follows: Voltage is set as 20kV, and spinning flow velocity is 0.6mL/h, and receiving distance is 20cm;And positive syringe and cathode syringe Metal needle diameter is 0.51mm;After electrostatic spinning, obtain being respectively formed positive-active layer on the surface of diaphragm two sides With negative electrode active layer, wherein making the surface density 30mg/cm of positive-active layer2, the surface density of negative electrode active layer is 14mg/cm2; Dry 120min is then transferred in vacuum oven at 90 DEG C;Aluminium foil and copper foil are respectively corresponded into positive-active layer and cathode Active layer carries out hot-rolling pressure, in 80 DEG C of temperature and pressure 1000N/cm2Under carry out compacting and make to be compounded in corresponding active layer surface; Corresponding lithium is made using cross cutting, winding, tab welding, assembling, vacuum bakeout, fluid injection, chemical conversion, sealing, full capacity test Ion battery.Use concentration for the electrolyte of 1M LiPF6-EC/DEC (1:1).Battery capacity retention ratio after 100 circulations It is 99%, battery DC internal resistance is 0.38m Ω.Compared to conventional design, battery capacity improves 12.4% under 1C.
Embodiment 3
It is nickel-cobalt-manganese ternary material: Super-P: carbon nanotube that anode sizing agent in the present embodiment is prepared in mass ratio: The ratio of PVDF:NMP=96:1.5:1:1.5:54 is prepared;It is graphite: Super-P: carbon that negative electrode slurry is prepared in mass ratio Nanotube: the ratio of PVDF:NMP=95:2:1:2:72 is prepared.The ratio between reversible capacity and the reversible capacity of cathode of anode For 1:1.3.Above-mentioned anode sizing agent is respectively transferred to the two of synchronous electrostatic spinning apparatus with negative electrode slurry respectively after mixing evenly In a syringe, electrostatic spinning processing is synchronized on two opposite sides of diaphragm, wherein diaphragm is using wherein side Anode sizing agent is coated on the PP film membrane surface for having nano ceramic material side, together by the PP film of coating nano ceramic material When, negative electrode slurry is coated on PP film every on another side surface of diaphragm, wherein the condition of corresponding electrostatic spinning processing are as follows: Voltage is set as 25kV, and spinning flow velocity is 0.8mL/h, and receiving distance is 25cm;And the positive syringe and cathode are injected The metal needle diameter of device is 0.6mm;After electrostatic spinning, obtain being respectively formed positive-active on the surface of diaphragm two sides Layer and negative electrode active layer, wherein the thickness of the coating of positive-active layer and negative electrode active layer is 10 μm, and makes positive-active layer Surface density be 30mg/cm2, the surface density of negative electrode active layer is 20mg/cm2;It is then transferred in vacuum oven at 95 DEG C Dry 120min;Aluminium foil and copper foil are respectively corresponded into positive-active layer and negative electrode active layer and carry out hot-rolling pressure, in 20 DEG C of temperature and Pressure 10N/cm2Under carry out compacting and make to be compounded in corresponding active layer surface;Using cross cutting, winding, tab welding, assembling, Corresponding lithium ion battery is made in vacuum bakeout, fluid injection, chemical conversion, sealing, full capacity test.Use concentration for 1M LiPF6-EC/ The electrolyte of DEC (1:1).Battery capacity retention ratio after 100 circulations is 98.5%, and battery DC internal resistance is 0.43m Ω. Compared to conventional design, battery capacity improves 10.4% under 1C.
Comparative example 1
It is nickel-cobalt-manganese ternary material: Super-P: carbon nanotube that anode sizing agent in this comparative example is prepared in mass ratio: The ratio of PVDF:NMP=96:1.5:1:1.5:54 is prepared;It is graphite: Super-P: carbon that negative electrode slurry is prepared in mass ratio Nanotube: the ratio of PVDF:NMP=95:2:1:2:72 is prepared.The ratio between reversible capacity and the reversible capacity of cathode of anode For 1:1.17.The positive/negative slurry stirred evenly is passed through method of electrostatic spinning respectively, and coated in aluminium foil and copper foil surface, (diaphragm is adopted Nano ceramic material is coated with the membrane surface of the double-deck PP/PE film of coating nano ceramic material, positive side), it obtains The surface density of the positive-active layer of plus plate current-collecting body aluminium foil surface is 19mg/cm2, the negative electrode active layer on negative current collector surface Surface density is 8mg/cm2;Then it is compacted, makes to improve in positive-active layer between particle and between collector by roll-in Contact, then, using cross cutting, winding, vacuum drying, tab welding, assembling, vacuum bakeout, fluid injection, chemical conversion, sealing, Quan Rong Lithium ion battery is manufactured experimently to obtain in measurement.Vacuum drying condition is dry 120min at 95 DEG C;Anode pole piece and cathode pole piece roll-in item Part is normal moderate pressure 400N/cm2.Other process parameter is the same as embodiment 1.Use concentration for 1M LiPF6-EC/DEC's (1:1) Electrolyte.Battery capacity retention ratio after 100 circulations is 93%, and battery DC internal resistance is 0.8m Ω.
It can be seen that from above-described embodiment and comparative example and be respectively coated on positive and negative electrode afflux compared to by positive and negative electrode slurry For on the surface of body, the present invention is coated in diaphragm by what synchronous electrostatic spinning made anode sizing agent and negative electrode slurry Direct Uniform Opposite sides surface form corresponding positive and negative electrode active layer, can make battery have better capacity retention ratio and battery it is straight Flow the small effect of internal resistance.
Specific embodiment described in the present invention only illustrate the spirit of the present invention by way of example.The neck of technology belonging to the present invention The technical staff in domain can make various modifications or additions to the described embodiments or replace by a similar method In generation, however, it does not deviate from the spirit of the invention or beyond the scope of the appended claims.
It is skilled to this field although present invention has been described in detail and some specific embodiments have been cited For technical staff, as long as it is obvious for can making various changes or correct without departing from the spirit and scope of the present invention.

Claims (9)

1. a kind of preparation method of lithium ion battery, which is characterized in that method includes the following steps:
A, anode sizing agent and negative electrode slurry are transferred to respectively in corresponding positive syringe and cathode syringe, by anode sizing agent Synchronous electrostatic spinning is coated in the two opposite side surfaces of diaphragm respectively with negative electrode slurry, after dry, in opposite two sides of diaphragm Positive-active layer and negative electrode active layer are respectively formed on face;
B, plus plate current-collecting body and negative current collector are respectively corresponded into positive-active layer and negative electrode active layer carries out hot-rolling pressure and is compounded in Corresponding lithium ion battery is made using cross cutting and following process in surface.
2. the preparation method of lithium ion battery according to claim 1, which is characterized in that synchronous Static Spinning described in step A The condition of silk are as follows:
The voltage is set as 20~25kV, and spinning flow velocity is 0.6~0.8mL/h, and receiving distance is 15~25cm;And it is described The metal needle diameter of positive syringe and cathode syringe is 0.5~0.6mm.
3. the preparation method of lithium ion battery according to claim 1, which is characterized in that positive-active layer described in step A Surface density be 10~30mg/cm2, the surface density of the negative electrode active layer is 5~20mg/cm2
4. the preparation method of lithium ion battery according to claim 3, which is characterized in that the anode of the lithium ion battery can Inverse the ratio between capacity and cathode reversible capacity are 1:1~1:1.3.
5. the preparation method of lithium ion battery described in -4 any one according to claim 1, which is characterized in that described in step A The thickness of the coating of positive-active layer and negative electrode active layer is 50~200 μm.
6. the preparation method of lithium ion battery described in -4 any one according to claim 1, which is characterized in that described in step B The temperature of hot-rolling pressure is 20~100 DEG C, and the pressure of the hot-rolling pressure is 10~1000N/cm2
7. the preparation method of lithium ion battery according to claim 1, which is characterized in that the anode sizing agent includes that anode is living The mixed slurry of property material, conductive agent and binder;The negative electrode slurry includes negative electrode active material, conductive agent and binder Mixed slurry.
8. the preparation method of lithium ion battery according to claim 1, which is characterized in that plus plate current-collecting body described in step B Selected from aluminium foil or aluminium net;The negative current collector is selected from copper foil or copper mesh.
9. the preparation method of lithium ion battery according to claim 1, which is characterized in that diaphragm described in step A is selected from PP Film, PE film, bilayer PP/PE film, bilayer PP/PP film or three layers of PP/PE/PP film, the diaphragm are located at the table of positive-active layer side Face is coated with ceramic material layer.
CN201910233984.0A 2019-03-26 2019-03-26 A kind of preparation method of lithium ion battery Pending CN109962211A (en)

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CN112542569A (en) * 2020-12-04 2021-03-23 宁德新能源科技有限公司 Electrode assembly, electrochemical device comprising same and electronic device
CN114512631A (en) * 2022-02-22 2022-05-17 上海兰钧新能源科技有限公司 Lithium ion battery composite pole piece and preparation method thereof
CN115117365A (en) * 2022-07-27 2022-09-27 湖北亿纬动力有限公司 Carbon-coated current collector and preparation method and application thereof

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CN106549185A (en) * 2015-09-17 2017-03-29 中国科学院金属研究所 A kind of lithium ion battery with integral structure and preparation method thereof
CN108448034A (en) * 2018-02-05 2018-08-24 合肥国轩高科动力能源有限公司 A kind of Low ESR lithium battery diaphragm and preparation method thereof
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CN106549185A (en) * 2015-09-17 2017-03-29 中国科学院金属研究所 A kind of lithium ion battery with integral structure and preparation method thereof
CN108448034A (en) * 2018-02-05 2018-08-24 合肥国轩高科动力能源有限公司 A kind of Low ESR lithium battery diaphragm and preparation method thereof
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CN112542569A (en) * 2020-12-04 2021-03-23 宁德新能源科技有限公司 Electrode assembly, electrochemical device comprising same and electronic device
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