CN107768589A - A kind of high safety type lithium ion battery with high energy density - Google Patents

A kind of high safety type lithium ion battery with high energy density Download PDF

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Publication number
CN107768589A
CN107768589A CN201610668167.4A CN201610668167A CN107768589A CN 107768589 A CN107768589 A CN 107768589A CN 201610668167 A CN201610668167 A CN 201610668167A CN 107768589 A CN107768589 A CN 107768589A
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battery
lithium ion
energy density
ion battery
safety type
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CN201610668167.4A
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彭波
吕豪杰
殷月辉
袁园
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Wanxiang Group Corp
Wanxiang A123 Systems Asia Co Ltd
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Wanxiang Group Corp
Wanxiang A123 Systems Asia Co Ltd
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/50Current conducting connections for cells or batteries
    • H01M50/572Means for preventing undesired use or discharge
    • 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
    • H01M10/42Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/4235Safety or regulating additives or arrangements in electrodes, separators or electrolyte
    • 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
    • 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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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Secondary Cells (AREA)

Abstract

The present invention relates to a kind of high safety type lithium ion battery with high energy density, the battery includes positive pole, negative pole, barrier film, electrolyte, lug and shell, positive pole and negative pole are separated with barrier film, winding or lamination form battery core, lug is respectively welded on both positive and negative polarity pole piece, battery core is encapsulated into battery case to inject electrolyte and seal and obtains battery, with LiFePO4, LiMn2O4, cobalt acid lithium, nickel cobalt aluminium or the main material that nickel-cobalt-manganese ternary material is positive active material, the indium oxide coated with CNT, polyaniline, graphene, poly styrene sulfonate and binding agent are positive active material auxiliary material, the lug of positive pole and negative pole is coated with PTC coatings.One layer of PTC coating is coated with lithium battery pole ear opening position so that battery just can realize open circuit at the initial stage of thermal runaway by the protection of PTC coatings, so as to control the further generation of thermal runaway, it is therefore prevented that the unsafe condition such as battery catches fire blast.

Description

A kind of high safety type lithium ion battery with high energy density
Technical field
The present invention relates to field of lithium ion battery, especially a kind of effectively control battery thermal runaway, cell safety is greatly improved Property with improve battery performance high safety type lithium ion battery with high energy density.
Background technology
The dual-pressure deficient from environmental pollution and petroleum resources has greatly promoted the development of electric automobile.Lithium ion Battery turns into the emphasis that Vehicular dynamic battery is researched and developed because of significant advantages such as, good cycles higher than energy.However, constantly occur Safety hazards seriously hinder the commercial applications of Large Copacity and high power lithium ion cell.Lithium ion battery security Accident inducement is a lot, overcharge, short circuit, extruding, vibration, collision etc., but in terms of the mechanism of generation, nothing more than voltage it is out of control and Both thermal runaways.On the one hand, due to use organic solution electrolyte, unlike aqueous electrolyte can reversible decomposition answer Close, thus irreversible oxidation decomposition easily occurs in overcharging state, produce imflammable gas and release big calorimetric, cause battery Internal temperature and pressure steeply rise, and trigger thermal runaway even to explode.On the other hand, because inside battery has many possible hairs Raw exothermic reaction, inside battery temperature rise will be caused if there is inside and outside short circuit phenomenon during use.Once internal temperature When degree rises to 120 DEG C, carbon anode surface passivating film (i.e. SEI films) is decomposed unavoidably, loses the high activity of passivating film protection Vigorous reaction occurs between organic electrolyte for embedding Li-C Electrode, a large amount of imflammable gas and heat is released, so as to cause electricity The danger such as burning occur inside pond.It finally can also show as thermal runaway it can be seen that voltage is out of control and then make battery produce danger Danger, so the key point for solving lithium battery safety problem is exactly to prevent thermal runaway.
PTC:Positive Temperature Coefficient positive temperature coefficients
Prevent the scheme of lithium ion battery thermal runaway from mainly having at present:(1) the subsidiary PTC-element outside battery pack, works as battery pack When temperature is increased to the Curie temperature of PTC-element, PTC-element internal resistance increases rapidly, and battery pack temperature is prevented so as to cut off electric current Further rise;(2) using the refractory coating barrier film (or electrode) of inorganic oxide ceramic (such as aluminum oxide) modification, although heat-resisting Coating can effectively prevent the internal short-circuit because caused by temperature rise causes diaphragm retracts;(3) PTC electrodes are coated and electrode Between collector and active material, so perceiving inside battery at any time, caused temperature becomes due to excessively stream or internal short-circuit Change, reduce or block the electric current passed through.
Three kinds of schemes mentioned above have the defects of respective, are respectively:(1) PTC-element energy subsidiary outside battery pack Enough monitoring the thermal runaway caused by abuse condition such as overcharge due to external short circuit, but because it is away from electrode and electrolyte liquor interface, it is right Inside battery thermal runaway can not play timely monitoring and inhibitory action;(2) inorganic oxide ceramic (such as aluminum oxide) modification Refractory coating barrier film (or electrode), although refractory coating can be prevented effectively in because caused by temperature rise causes diaphragm retracts Portion's short circuit, but to other side reactions and external short circuit caused by the overheat, overcharge etc. caused by thermal runaway it is helpless; (3) although PTC coatings can play certain protective effect to thermal runaway outwardly and inwardly, PTC coatings add collection Contact impedance between fluid and active material, the high rate performance of battery is had a great influence, and PTC coatings can reduce battery Energy density, in addition such one layer of coating also virtually increase the complexity of manufacturing process.
The content of the invention
It is an object of the invention to can not take into account outside in control lithium battery thermal runaway technology to solve prior art With a kind of effectively control battery thermal runaway is provided the defects of internal thermal runaway, battery security is greatly improved and raising is cell performance The high safety type lithium ion battery with high energy density of energy.
To achieve these goals, the present invention uses following technical scheme:
A kind of high safety type lithium ion battery with high energy density, the battery include positive pole, negative pole, barrier film, electrolyte, lug with And shell, positive pole and negative pole are separated with barrier film, winding or lamination form battery core, and lug is respectively welded at both positive and negative polarity pole piece On, battery core is encapsulated into injection electrolyte in battery case and sealing obtains battery, with LiFePO4, LiMn2O4, cobalt acid lithium, nickel Cobalt aluminium or the main material that nickel-cobalt-manganese ternary material is positive active material, with the indium oxide, polyaniline, graphite of CNT cladding Alkene, poly styrene sulfonate and binding agent are positive active material auxiliary material, and the lug of positive pole and negative pole is coated with PTC coatings. In the technical program, one layer of PTC coating is coated with lithium battery pole ear opening position so that battery thermal runaway initial stage with regard to energy Open circuit is realized by the protection of PTC coatings, so as to control the further generation of thermal runaway, it is therefore prevented that the danger such as battery catches fire blast Dangerous situation.
Preferably, the mass ratio of main material and auxiliary material is 3-5:1, the parts by weight of various components are in auxiliary material:50- 60 parts of polyanilines, 30-35 parts graphene oxide, 40-50 parts poly styrene sulfonate, 10-15 parts binding agent and 40-45 part nanometers The indium oxide of carbon pipe cladding.In the technical program, polyaniline, graphene oxide, poly styrene sulfonate and CNT bag Auxiliary material of the indium oxide covered as positive active material, there is very high conductance, high mechanical properties and corrosion resistance, can The electronic conduction ability of positive active material is improved,.Therefore polyaniline, graphene oxide, poly styrene sulfonate and nano-sized carbon Auxiliary material of the indium oxide of pipe cladding as positive active material, can improve battery performance, and and can improves corrosion resistance, extends The life-span of lithium ion battery.
Preferably, the preparation method of the indium oxide of CNT cladding is:Indium oxide is dissolved in into diethylene glycol (DEG) to be reacted System, sodium hydroxide is then slowly added into, 140-160 DEG C is warming up in 2-2.5h after stirring 1-3h, is cooled down after reacting 1-3h; Centrifuge obtained sediment and use volume ratio 1 successively:2 ethanol washs with methyl acetate mixed solution, acetone, deionized water, very Sky is dried to obtain base core nano indium oxide;Then by the nano oxidized chlorine ultrasonic disperse of base core in absolute ethyl alcohol, add to contain and receive The ethanol solution of rice carbon pipe, is added dropwise concentrated ammonia liquor, stirring reaction 1-1.5h at 85-95 DEG C, the sediment being centrifugally separating to obtain Washed successively with absolute ethyl alcohol, deionized water, crushed after roasting and obtain CNT cladding nano indium oxide.
Preferably, the temperature of roasting is 600-750 DEG C, time 2-5h, it is 10-100nm to be crushed to particle diameter.
Preferably, negative material is graphite-like, silicon materials class or alloy anode class material.
Preferably, barrier film is the nonwoven that polyethylene, polypropylene, polyimides or surface are coated with nano ceramic material Cloth.In the technical program, using the good heat endurance of nano ceramic material and mechanical feature, lithium ion battery is improved Security performance, while nano ceramic material cost is relatively low.
Preferably, the preparation method of non-woven fabrics of the surface coated with nano ceramic material is:Using plasma spraying skill Nano ceramic material is injected in nonwoven surface by art.
Preferably, PTC coatings are made up of the raw material of following parts by weight:60-90 part PTC matrix materials, 5-20 parts are disperseed Agent and 5-20 part binding agents.
Preferably, PTC matrix materials are BaTiO3、V2O3Or BaPbO3;Dispersant be Triton X-100, Polyethylene glycol oxide or polyacrylic acid, binding agent are Kynoar, polyvinylidene fluoride -co- hexafluoropropene, gather inclined 1,1- It is difluoroethylene -co- trichloro ethylene, polymethyl methacrylate, polyacrylonitrile, polyvinylpyrrolidone, polyvinyl acetate, poly- Ethylene-co-vinyl acetate, PEO, cellulose acetate, cellulose acetate-butyrate, cellulose-acetate propionate, cyanoethyl Amylopectin, cyanoethyl polyvinylalcohol, cyanethyl cellulose, cyanoethyl sucrose, amylopectin, carboxymethyl cellulose one kind or two The mixture of the kind above.
Adhesive gelatin is made preferably, binding agent is dissolved in solvent, then by PTC matrix materials, dispersant, viscous Knot agent glue is mixed into coating paste, and 30-45min is stirred by ultrasonic under 65-85 DEG C, 55-65KHz, by obtained coating On positive pole and negative lug, vacuum drying obtains slurry dual coating.
The beneficial effects of the invention are as follows:
1) when short circuit (including outwardly and inwardly short-circuit) or super-charge super-discharge occur for battery, electric current that battery pole ear position passes through Maximum, the caloric value of lug position is also maximum, is passed through so can timely and effectively be controlled in lug position increase PTC coatings The thermal runaway that outwardly and inwardly reason is introduced, prevents inside battery from further reacting, and prevents the unsafe conditions such as blast on fire from occurring;
2) more simple and easy, complex operation degree reduction, saving are coated on pole piece relatively in lug opening position coating PTC coatings Manufacturing cost;
3) it is much smaller than in influence of the lug opening position coating PTC coatings for battery energy density on pole piece and coats PTC coatings.
Embodiment
Below by specific embodiment, technical scheme is described in further detail.It should be appreciated that this hair Bright implementation is not limited to the following examples, and any formal accommodation and/or change made to the present invention will all fall Enter the scope of the present invention.
In the present invention, if not refering in particular to, all parts, percentage are unit of weight, used equipment and raw material etc. It is commercially available or commonly used in the art.Method in following embodiments, it is the normal of this area unless otherwise instructed Rule method.
Embodiment 1
It is prepared by positive plate:Nickel-cobalt-manganese ternary material is chosen as positive electrode main material, with the indium oxide of CNT cladding, is gathered Aniline, graphene, poly styrene sulfonate and binding agent are the mass ratio of positive active material auxiliary material, main material and auxiliary material For 3:1, the parts by weight of various components are in auxiliary material:50 parts of polyanilines, 30 parts of graphene oxides, 40 parts of polystyrolsulfon acids The indium oxide of salt, 10 parts of binding agents and 40 parts of CNT claddings.By positive electrode active materials: conductive agent: binding agent=18: 1: 1 Part by weight blended anode slurry, uniformly coated on positive pole base flow body aluminium foil.Rolled after drying with roller, so Anode pole piece is made in cutting afterwards.Wherein, the preparation method of the indium oxide of CNT cladding is:Indium oxide is dissolved in into diethylene glycol (DEG) to obtain To reaction system, sodium hydroxide is then slowly added into, 140 DEG C are warming up in 2h after stirring 1h, is cooled down after reacting 1h;Centrifuge The sediment arrived uses volume ratio 1 successively:2 ethanol washs with methyl acetate mixed solution, acetone, deionized water, vacuum drying Obtain base core nano indium oxide;Then by the nano oxidized chlorine ultrasonic disperse of base core in absolute ethyl alcohol, addition contains CNT Ethanol solution, concentrated ammonia liquor is added dropwise, stirring reaction 1h at 85 DEG C, the sediment being centrifugally separating to obtain is successively with anhydrous second Alcohol, deionized water washing, crushed after roasting and obtain CNT cladding nano indium oxide, the temperature of roasting is 600 DEG C, and the time is 2h, it is 10-100nm to be crushed to particle diameter.
It is prepared by negative plate:From graphite material as negative electrode active material, according to active material:Conductive agent:Binding agent= 95:1:4 ratio is mixed to get cathode size with aqueous solvent, uniformly coated on negative pole base flow body copper foil.With stone roller after drying Press is rolled, and cathode pole piece is made in then cutting.
Barrier film prepares:Choose commercial PE barrier films.
Electrolyte prepares:Choose commercial LiPF6It is dissolved in the electrolyte of organic solution.
Lug prepares:Lithium ion cell positive ear is chosen, the lug material is aluminium, and binding agent is dissolved in into organic solvent is made Adhesive gelatin, the binding agent are Kynoar, and organic solvent is 1-METHYLPYRROLIDONE (NMP), binding agent with it is organic molten The part by weight of agent is 1:19.Dispersant and PTC matrix materials are added in adhesive gelatin, stirring forms PTC slurries, should PTC matrix materials are BaTiO3, dispersant is Triton X-100, matrix material, dispersant, the parts by weight of binding agent Number is respectively 90 parts, and 5 parts, 5 parts, be coated in anode ear surface by above-mentioned PTC slurries, coating thickness is 5 μm of one side, then The lug of the coating containing PTC is made in vacuum drying.
It is prepared by battery:Battery core is made in above-mentioned positive/negative plate and barrier film by way of lamination, and lug is welded, then encapsulates In aluminum plastic film, electrolyte, sealing are injected, chemical conversion obtains battery.
Embodiment 2
It is prepared by positive plate:Nickel cobalt aluminium is chosen as positive electrode main material, with the indium oxide, polyaniline, stone of CNT cladding Black alkene, poly styrene sulfonate and binding agent are positive active material auxiliary material, and the mass ratio of main material and auxiliary material is 4:1, The parts by weight of various components are in auxiliary material:55 parts of polyanilines, 32 parts of graphene oxides, 45 parts of poly styrene sulfonates, 12 parts The indium oxide of binding agent and 43 parts of CNT claddings.By positive electrode active materials: conductive agent: binding agent=89: 6: 4 weight ratio Example blended anode slurry, uniformly coated on positive pole base flow body aluminium foil.Rolled after drying with roller, then cutting system Into anode pole piece.Wherein, the preparation method of the indium oxide of CNT cladding is:Indium oxide is dissolved in diethylene glycol (DEG) and obtains reactant System, sodium hydroxide is then slowly added into, 150 DEG C are warming up in 2.5h after stirring 2h, is cooled down after reacting 2h;Centrifugation obtains heavy Starch uses volume ratio 1 successively:2 ethanol washs with methyl acetate mixed solution, acetone, deionized water, and vacuum drying obtains base Core nano indium oxide;Then the nano oxidized chlorine ultrasonic disperse of base core is added containing the anhydrous of CNT in absolute ethyl alcohol Ethanol solution, concentrated ammonia liquor is added dropwise, stirring reaction 1.5h at 90 DEG C, the sediment being centrifugally separating to obtain successively with absolute ethyl alcohol, go Ion water washing, crushed after roasting and obtain CNT cladding nano indium oxide, the temperature of roasting is 700 DEG C, time 3h, powder It is 10-100nm to be broken to particle diameter.
It is prepared by negative plate:From lithium titanate as negative electrode active material, according to active material:Conductive agent:Binding agent=95: 1:4 ratio is mixed to get cathode size with aqueous solvent, uniformly coated on negative pole base flow body copper foil.Roller is used after drying Rolled, cathode pole piece is made in then cutting.
Barrier film prepares:It is barrier film to choose non-woven fabrics of the surface coated with nano ceramic material, and surface is coated with nano ceramics The preparation method of the non-woven fabrics of material is:Nano ceramic material is injected in by nonwoven surface using plasma spraying technology.
Electrolyte prepares:Choose commercial LiPF6It is dissolved in the electrolyte of organic solution.
Lug prepares:Lithium ionic cell cathode ear pole is chosen, the lug material is aluminium, and binding agent is dissolved in into organic solvent system Into adhesive gelatin, the binding agent is polyvinylidene fluoride -co- trichloro ethylene, and organic solvent is 1-METHYLPYRROLIDONE (NMP), the part by weight of binding agent and organic solvent is 1:20.Dispersant and PTC matrix materials are added to adhesive gelatin In, stirring forms PTC slurries, and the PTC matrix materials are V2O3, dispersant is polyethylene glycol oxide, matrix material, dispersant, is bonded The parts by weight of agent are respectively 60 parts, 20 parts, 20 parts;It is to be coated in anode ear surface, coating thickness by above-mentioned PTC slurries 5 μm of one side, then it is dried in vacuo the lug that the coating containing PTC is made.
It is prepared by battery:Battery core is made in above-mentioned positive/negative plate and barrier film by way of lamination, and lug is welded, then encapsulates In aluminum plastic film, electrolyte, sealing are injected, chemical conversion obtains battery.
Embodiment 3
It is prepared by positive plate:LiMn2O4 is chosen as positive electrode main material, with the indium oxide, polyaniline, stone of CNT cladding Black alkene, poly styrene sulfonate and binding agent are positive active material auxiliary material, and the mass ratio of main material and auxiliary material is 5:1, The parts by weight of various components are in auxiliary material:60 parts of polyanilines, 35 parts of graphene oxides, 50 parts of poly styrene sulfonates, 15 parts The indium oxide of binding agent and 45 parts of CNT claddings.By positive electrode active materials: conductive agent: binding agent=95: 2: 3 weight ratio Example blended anode slurry, uniformly coated on positive pole base flow body aluminium foil.Rolled after drying with roller, then cutting system Into anode pole piece.Wherein, the preparation method of the indium oxide of CNT cladding is:Indium oxide is dissolved in diethylene glycol (DEG) and obtains reactant System, sodium hydroxide is then slowly added into, 160 DEG C are warming up in 2.5h after stirring 3h, is cooled down after reacting 3h;Centrifugation obtains heavy Starch uses volume ratio 1 successively:2 ethanol washs with methyl acetate mixed solution, acetone, deionized water, and vacuum drying obtains base Core nano indium oxide;Then the nano oxidized chlorine ultrasonic disperse of base core is added containing the anhydrous of CNT in absolute ethyl alcohol Ethanol solution, concentrated ammonia liquor is added dropwise, stirring reaction 1.5h at 95 DEG C, the sediment being centrifugally separating to obtain successively with absolute ethyl alcohol, go Ion water washing, crushed after roasting and obtain CNT cladding nano indium oxide, the temperature of roasting is 750 DEG C, time 5h, powder It is 10-100nm to be broken to particle diameter.
It is prepared by negative plate:From graphite material as negative electrode active material, according to active material:Conductive agent:Binding agent= 95:1:4 ratio is mixed to get cathode size with aqueous solvent, uniformly coated on negative pole base flow body copper foil.With stone roller after drying Press is rolled, and cathode pole piece is made in then cutting.
Barrier film prepares:Choose polypropylene diaphragm.
Electrolyte prepares:Choose commercial LiPF6It is dissolved in the electrolyte of organic solution.
Lug prepares:It is aluminium to choose lithium ion cell positive ear and negative lug, lug material, binding agent is dissolved in organic Adhesive gelatin is made in solvent, and the binding agent is that the mixture quality ratio of Kynoar and carboxymethyl cellulose is 1:1, it is organic Solvent is 1-METHYLPYRROLIDONE (NMP), and the part by weight of binding agent and organic solvent is 3:97.By dispersant and PTC matrixes Material is added in adhesive gelatin, and stirring forms PTC slurries, and the PTC matrix materials are BaPbO3, dispersant is polypropylene Acid, matrix material, dispersant, the parts by weight of binding agent are respectively 70 parts, 15 parts, 15 parts;It is coating by above-mentioned PTC slurries On anode ear surface, coating thickness is 5 μm of one side, is then dried in vacuo the lug that the coating containing PTC is made.
It is prepared by battery:Battery core is made in above-mentioned positive/negative plate and barrier film by way of lamination, and lug is welded, then encapsulates In aluminum plastic film, electrolyte, sealing are injected, chemical conversion obtains battery.
After tested, the efficiency first of the battery reaches 98%, and energy density can reach 300Wh/kg.Significantly improve existing electricity The first effect and energy density in pond.And the battery can by overcharging, cross put, the safety test such as acupuncture and extruding, say the battery With extraordinary security performance.
It should be appreciated that to those skilled in the art, it can according to the above description be improved or be become Change, and all these modifications and variations should all belong to the protection domain of appended claims of the present invention.

Claims (10)

1. a kind of high safety type lithium ion battery with high energy density, the battery includes positive pole, negative pole, barrier film, electrolyte, lug And shell, positive pole and negative pole are separated with barrier film, winding or lamination form battery core, and lug is respectively welded at both positive and negative polarity pole piece On, battery core is encapsulated into injection electrolyte in battery case and sealing obtains battery, it is characterised in that with LiFePO4, mangaic acid Lithium, cobalt acid lithium, nickel cobalt aluminium or nickel-cobalt-manganese ternary material are the main material of positive active material, with the oxidation of CNT cladding Indium, polyaniline, graphene, poly styrene sulfonate and binding agent are positive active material auxiliary material, the lug of negative or positive electrode Coated with PTC coatings.
A kind of 2. high safety type lithium ion battery with high energy density according to claim 1, it is characterised in that main material with The mass ratio of auxiliary material is 3-5:1, the parts by weight of various components are in auxiliary material:50-60 parts polyaniline, 30-35 parts oxidation stone Black alkene, 40-50 parts poly styrene sulfonate, 10-15 parts binding agent and the indium oxide of 40-45 parts CNT cladding.
A kind of 3. high safety type lithium ion battery with high energy density according to claim 1 or 2, it is characterised in that nanometer The preparation method of indium oxide of carbon pipe cladding is:Indium oxide is dissolved in diethylene glycol (DEG) and obtains reaction system, is then slowly added into hydrogen-oxygen Change sodium, 140-160 DEG C is warming up in 2-2.5h after stirring 1-3h, is cooled down after reacting 1-3h;Centrifuge obtained sediment successively With volume ratio 1:2 ethanol washs with methyl acetate mixed solution, acetone, deionized water, and vacuum drying obtains base core nano oxygen Change indium;Then the nano oxidized chlorine ultrasonic disperse of base core is added into the ethanol solution containing CNT in absolute ethyl alcohol, Concentrated ammonia liquor is added dropwise, stirring reaction 1-1.5h at 85-95 DEG C, the sediment being centrifugally separating to obtain is successively with absolute ethyl alcohol, deionization Water washing, crushed after roasting and obtain CNT cladding nano indium oxide.
A kind of 4. high safety type lithium ion battery with high energy density according to claim 3, it is characterised in that the temperature of roasting Spend for 600-750 DEG C, time 2-5h, it is 10-100nm to be crushed to particle diameter.
A kind of 5. high safety type lithium ion battery with high energy density according to claim 1, it is characterised in that negative material For graphite-like, silicon materials class or alloy anode class material.
6. a kind of high safety type lithium ion battery with high energy density according to claim 1, it is characterised in that barrier film is poly- Ethene, polypropylene, polyimides or surface are coated with the non-woven fabrics of nano ceramic material.
7. a kind of high safety type lithium ion battery with high energy density according to claim 6, it is characterised in that surface coats The preparation method for having the non-woven fabrics of nano ceramic material is:Nano ceramic material is injected in by nonwoven using plasma spraying technology Cloth surface.
A kind of 8. high safety type lithium ion battery with high energy density according to claim 1, it is characterised in that PTC coatings It is made up of the raw material of following parts by weight:60-90 part PTC matrix materials, 5-20 parts dispersant and 5-20 part binding agents.
A kind of 9. high safety type lithium ion battery with high energy density according to claim 8, it is characterised in that PTC matrixes Material is BaTiO3、V2O3Or BaPbO3;Dispersant is Triton X-100, polyethylene glycol oxide or polyacrylic acid, is bonded Agent is Kynoar, polyvinylidene fluoride -co- hexafluoropropene, polyvinylidene fluoride -co- trichloro ethylene, poly- first Base methyl acrylate, polyacrylonitrile, polyvinylpyrrolidone, polyvinyl acetate, polyethylene -co- vinyl acetate, polycyclic oxygen Ethane, cellulose acetate, cellulose acetate-butyrate, cellulose-acetate propionate, cyanoethyl pullulan, cyanoethyl polyvinylalcohol, The one or more kinds of mixture of cyanethyl cellulose, cyanoethyl sucrose, amylopectin, carboxymethyl cellulose.
10. a kind of high safety type lithium ion battery with high energy density according to claim 8 or claim 9, it is characterised in that will be viscous Knot agent, which is dissolved in solvent, is made adhesive gelatin, and PTC matrix materials, dispersant, adhesive gelatin then are mixed into coating slurry Material, and is stirred by ultrasonic 30-45min under 65-85 DEG C, 55-65KHz, by obtained coating paste dual coating in positive pole or In negative lug, vacuum drying obtains.
CN201610668167.4A 2016-08-15 2016-08-15 A kind of high safety type lithium ion battery with high energy density Pending CN107768589A (en)

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110429241A (en) * 2019-08-29 2019-11-08 桑顿新能源科技(长沙)有限公司 Lithium battery anode and preparation method thereof and lithium battery, power supply system and electrical equipment
CN110429240A (en) * 2019-08-08 2019-11-08 宁德时代新能源科技股份有限公司 Positive pole piece and electrochemical device comprising same
CN110474114A (en) * 2019-08-08 2019-11-19 宁德时代新能源科技股份有限公司 A kind of electrochemical energy storage device
CN111326739A (en) * 2020-02-28 2020-06-23 浙江克能新能源科技有限公司 Soft-package lithium manganate battery and manufacturing method thereof
CN112234313A (en) * 2020-10-15 2021-01-15 江苏厚生新能源科技有限公司 Oxidation-resistant carbon nanotube coating diaphragm and preparation method thereof
CN112490586A (en) * 2020-12-14 2021-03-12 远景动力技术(江苏)有限公司 Composite diaphragm with thermal runaway prevention function and lithium ion battery
CN113394405A (en) * 2021-05-24 2021-09-14 西安交通大学 Preparation method of electrode coating for actively preventing thermal runaway of lithium ion battery
CN114497824A (en) * 2021-12-31 2022-05-13 北京卫蓝新能源科技有限公司 Self-adaptive temperature-limiting battery cell based on PTC material, battery system and PTC material
CN114899364A (en) * 2022-06-13 2022-08-12 蜂巢能源科技(无锡)有限公司 Negative pole piece and preparation method and application thereof
US11973196B2 (en) 2019-08-08 2024-04-30 Contemporary Amperex Technology Co., Limited Positive electrode plate, and electrochemical apparatus and device associated therewith
US12040455B2 (en) 2019-08-08 2024-07-16 Contemporary Amperex Technology Co., Limited Electrochemical energy storage apparatus and device

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101887960A (en) * 2010-07-13 2010-11-17 清华大学 Lithium ion battery pole ear and lithium ion battery with same
JP2012009284A (en) * 2010-06-24 2012-01-12 Fdk Corp Lithium-ion secondary battery
CN104201327A (en) * 2014-08-14 2014-12-10 中天储能科技有限公司 Pole piece of lithium-ion energy storing battery and preparation method thereof
CN104425795A (en) * 2013-09-10 2015-03-18 浙江万向亿能动力电池有限公司 High-energy and high-safety lithium ion power battery
CN105470523A (en) * 2015-01-16 2016-04-06 万向A一二三***有限公司 Lithium ion power battery with high safety performance

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012009284A (en) * 2010-06-24 2012-01-12 Fdk Corp Lithium-ion secondary battery
CN101887960A (en) * 2010-07-13 2010-11-17 清华大学 Lithium ion battery pole ear and lithium ion battery with same
CN104425795A (en) * 2013-09-10 2015-03-18 浙江万向亿能动力电池有限公司 High-energy and high-safety lithium ion power battery
CN104201327A (en) * 2014-08-14 2014-12-10 中天储能科技有限公司 Pole piece of lithium-ion energy storing battery and preparation method thereof
CN105470523A (en) * 2015-01-16 2016-04-06 万向A一二三***有限公司 Lithium ion power battery with high safety performance

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11894524B2 (en) 2019-08-08 2024-02-06 Contemporary Amperex Technology Co., Limited Positive electrode plate, and electrochemical apparatus and device associated therewith
CN110429240A (en) * 2019-08-08 2019-11-08 宁德时代新能源科技股份有限公司 Positive pole piece and electrochemical device comprising same
CN110474114A (en) * 2019-08-08 2019-11-19 宁德时代新能源科技股份有限公司 A kind of electrochemical energy storage device
US12040455B2 (en) 2019-08-08 2024-07-16 Contemporary Amperex Technology Co., Limited Electrochemical energy storage apparatus and device
US11973196B2 (en) 2019-08-08 2024-04-30 Contemporary Amperex Technology Co., Limited Positive electrode plate, and electrochemical apparatus and device associated therewith
CN110429241A (en) * 2019-08-29 2019-11-08 桑顿新能源科技(长沙)有限公司 Lithium battery anode and preparation method thereof and lithium battery, power supply system and electrical equipment
CN111326739A (en) * 2020-02-28 2020-06-23 浙江克能新能源科技有限公司 Soft-package lithium manganate battery and manufacturing method thereof
CN112234313A (en) * 2020-10-15 2021-01-15 江苏厚生新能源科技有限公司 Oxidation-resistant carbon nanotube coating diaphragm and preparation method thereof
CN112490586B (en) * 2020-12-14 2022-11-25 远景动力技术(江苏)有限公司 Composite diaphragm with thermal runaway prevention function and lithium ion battery
CN112490586A (en) * 2020-12-14 2021-03-12 远景动力技术(江苏)有限公司 Composite diaphragm with thermal runaway prevention function and lithium ion battery
CN113394405B (en) * 2021-05-24 2022-07-12 西安交通大学 Preparation method of electrode coating for actively preventing thermal runaway of lithium ion battery
CN113394405A (en) * 2021-05-24 2021-09-14 西安交通大学 Preparation method of electrode coating for actively preventing thermal runaway of lithium ion battery
CN114497824A (en) * 2021-12-31 2022-05-13 北京卫蓝新能源科技有限公司 Self-adaptive temperature-limiting battery cell based on PTC material, battery system and PTC material
CN114497824B (en) * 2021-12-31 2024-03-01 北京卫蓝新能源科技有限公司 Self-adaptive temperature-limiting battery cell based on PTC material, battery system and PTC material
CN114899364A (en) * 2022-06-13 2022-08-12 蜂巢能源科技(无锡)有限公司 Negative pole piece and preparation method and application thereof
CN114899364B (en) * 2022-06-13 2023-09-12 蜂巢能源科技(无锡)有限公司 Negative electrode plate and preparation method and application thereof

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