CN102403537A - Method for manufacturing lithium iron phosphate battery - Google Patents

Method for manufacturing lithium iron phosphate battery Download PDF

Info

Publication number
CN102403537A
CN102403537A CN2011103889682A CN201110388968A CN102403537A CN 102403537 A CN102403537 A CN 102403537A CN 2011103889682 A CN2011103889682 A CN 2011103889682A CN 201110388968 A CN201110388968 A CN 201110388968A CN 102403537 A CN102403537 A CN 102403537A
Authority
CN
China
Prior art keywords
phosphate battery
lithium iron
iron phosphate
specific area
battery
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.)
Pending
Application number
CN2011103889682A
Other languages
Chinese (zh)
Inventor
程传捷
杨丛利
邱小勇
许谦
张益明
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.)
Shuangdeng Science & Technology Development Academy Co Ltd Nanjing City
Original Assignee
Shuangdeng Science & Technology Development Academy Co Ltd Nanjing City
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 Shuangdeng Science & Technology Development Academy Co Ltd Nanjing City filed Critical Shuangdeng Science & Technology Development Academy Co Ltd Nanjing City
Priority to CN2011103889682A priority Critical patent/CN102403537A/en
Publication of CN102403537A publication Critical patent/CN102403537A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • 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

  • Battery Electrode And Active Subsutance (AREA)

Abstract

The method provides a method for manufacturing a lithium iron phosphate battery. The method comprises the following steps of: adding carbon substances with high specific surface areas when a positive electrode material and a negative electrode material are mixed, wherein the carbon substances is 1 to 15 percent based on the weight of the total electrode powder; stirring and mixing to obtain slurry; coating slurry on an aluminum foil and a copper foil; tabletting; assembling; injecting liquid; forming; and sealing to manufacture the lithium iron phosphate battery. The lithium iron phosphate battery has good charge-discharge performance, can be charged and discharged quickly, is long in cycle life and can meet using requirements of electrombiles and power for grid peak and valley adjustment.

Description

A kind of manufacture method of ion-lithium phosphate battery
Technical field
The present invention relates to the lithium ion battery production method, particularly a kind of manufacture method of ion-lithium phosphate battery with excellent fast charging and discharging performance, long circulation life.
Background technology
Environmental pollution, shortage of resources, oil crisis etc. force human cleaning, the regenerative resource used.Replace oil with electricity on the one hand, reduce municipal pollution, the development electric motor car is the task of top priority; The development and utilization new forms of energy are regulated the electrical network electricity using at the peak time on the other hand, effectively store and utilize the low ebb electric weight, and secondary cell especially large capacity version secondary cell then becomes electric motor car and the key that stores the valley electricity technology.
Lithium ion battery with monomer whose operating voltage height, high-energy-density density, have extended cycle life, advantages such as self-discharge rate is little, memory-less effect, environmental protection.Especially positive electrode uses the lithium ion battery of LiFePO4 (LiFePO4) made; Advantage such as good with its stability of material, that security performance is good, cost is low, have extended cycle life; Be more suitable for being made into great-capacity power battery, to be used in electric motor car and to store the valley electricity aspect.
Because the shortcoming of LiFePO4 (LiFePO4) material self, lithium ion is lower in LiFePO4 (LiFePO4) material granule diffusion inside speed, and the electron conduction of material is also relatively poor.Though now people adopt to the shortcoming of LiFePO 4 material mix, the surface coats, reduce method such as material particle size handles; But in the present ferric phosphate lithium cell manufacturing process; The most specific area of carbon substance conductance agent that is added during the both positive and negative polarity batch mixing is lower; Therefore, present ferric phosphate lithium cell is when the electrokinetic cell, and the performances such as cycle life when its cryogenic property, fast charging and discharging performance, fast charging and discharging still are difficult to the level that reaches higher.
Summary of the invention
The object of the present invention is to provide a kind of manufacture method of ferric phosphate lithium cell of the long circulation life with excellent fast charging and discharging performance.
Technical scheme of the present invention relates to the mixing of materials when anode and cathode slurry prepares in the ferric phosphate lithium cell making; By existing technological preparation both positive and negative polarity material, its improvements add total powder weight 1.0%~15% when being the both positive and negative polarity mixing of materials specific area is the carbon material of 80~5000 ㎡/g.
The above-mentioned high specific area carbon elemental substance that adds is the mixture of a kind of or several kinds of arbitrary proportions in active carbon, CNT, carbon fiber, Graphene, the conductive carbon black.
The present invention is when the both positive and negative polarity batch mixing; The carbon material that all adds high-specific surface area; Process slurry through mixing; Slurry is coated in respectively on aluminium foil and the Copper Foil, passes through compressing tablet, film-making, assembling, fluid injection then, change into, seal, promptly process the ferric phosphate lithium cell of long circulation life with excellent fast charging and discharging performance.Compressing tablet, film-making, assembling, fluid injection, the normal ferric phosphate lithium cell manufacture craft of process using such as change into, seal.
The present invention adds the latter made ferric phosphate lithium cell of high specific area carbon material and compares with common ferric phosphate lithium cell and have following two advantages in the both positive and negative polarity material:
(1) has excellent fast charging and discharging performance;
The carbon element material that adds high-specific surface area; To increase LiFePO4 (LiFePO4) positive electrode and the particle of negative material and the contact area of high surface area carbon elemental substance; Thereby strengthen the conductivity that is made into pole piece, make ferric phosphate lithium cell can realize the fast charging and discharging performance of 3C~20C.
(2) cycle life of ferric phosphate lithium cell in the time of can significantly improving fast charging and discharging.
The carbon element material that adds high-specific surface area; Strengthened the conductivity that is made into pole piece; Lithium ion reduces the possibility that Li dendrite forms in the pole piece surface time of staying when shortening fast charging and discharging, thereby improves the cycle life of ferric phosphate lithium cell when fast charging and discharging.
Embodiment
Instance 1: making can be carried out the long-life ferric phosphate lithium cell of 3~5 rate charge-discharges circulation.
When anodal batch mixing, add total powder (press common process and prepare, down together), 1% specific area of weight is 250m 2The CNT of/g and 2% specific area are 360m 2The mixture of/g Graphene; 1% specific area that when the negative pole batch mixing, adds total powder weight is 250m 2/ g CNT and 1.5% specific area are 100m 2The mixture of/g conductive carbon black; Process slurry through mixing, slurry is coated in respectively on aluminium foil and the Copper Foil, pass through conventional compressing tablet, film-making, assembling, fluid injection then, change into, seal promptly to process and to carry out 3~5 rate charge-discharge recycled phosphoric acid lithium iron batteries.Battery circulates after 2000 times when carrying out 3 rate charge-discharge loop tests, and the discharge capacity of battery still remains on more than 90% of initial capacity.
Instance 2: making can be carried out the long-life ferric phosphate lithium cell of 7~10 rate charge-discharges circulation.
3% specific area that when anodal batch mixing, adds total powder weight is 4000m 2The active carbon of/g and 2% specific area are 360m 2The mixture of/g Graphene; 1.5% specific area that when the negative pole batch mixing, adds total powder weight is 360m 2/ g Graphene and 2% specific area are 100m 2The mixture of/g conductive carbon black; Process slurry through mixing, slurry is coated in respectively on aluminium foil and the Copper Foil, pass through conventional compressing tablet, film-making, assembling, fluid injection then, change into, seal promptly to process and to carry out 7~10 rate charge-discharge recycled phosphoric acid lithium iron batteries.Battery circulates after 3000 times when carrying out 8 rate charge-discharge loop tests, and the discharge capacity of battery still remains on more than 88% of initial capacity.
Instance 3: making can be carried out the long-life ferric phosphate lithium cell of 13~15 rate charge-discharges circulation.
6% specific area that when anodal batch mixing, adds total powder weight is 4000m 2The active carbon of/g and 3% specific area are 360m 2The mixture of/g Graphene; 2.5% specific area that when the negative pole batch mixing, adds total powder weight is 360m 2/ g Graphene and 4% specific area are 250m 2The mixture of the CNT of/g; Process slurry through mixing, slurry is coated in respectively on aluminium foil and the Copper Foil, pass through conventional compressing tablet, film-making, assembling, fluid injection then, change into, seal promptly to process and to carry out 13~15 rate charge-discharge recycled phosphoric acid lithium iron batteries.Battery circulates after 3500 times when carrying out 13 rate charge-discharge loop tests, and the discharge capacity of battery still remains on more than 88% of initial capacity.
Instance 4: making can be carried out the long-life ferric phosphate lithium cell of 20~25 rate charge-discharges circulation.
10% specific area that when anodal batch mixing, adds total powder weight is 4000m 2The active carbon of/g and 5% specific area are 360m 2The mixture of/g Graphene; 3.5% specific area that when the negative pole batch mixing, adds total powder weight is 360m 2/ g Graphene and 6% specific area are 250m 2The mixture of the CNT of/g; Process slurry through mixing, slurry is coated in respectively on aluminium foil and the Copper Foil, pass through conventional compressing tablet, film-making, assembling, fluid injection then, change into, seal promptly to process and to carry out 13~15 rate charge-discharge recycled phosphoric acid lithium iron batteries.Battery circulates after 5000 times when carrying out 25 rate charge-discharge loop tests, and the discharge capacity of battery still remains on more than 91% of initial capacity.
Instance 5: making can be carried out the long-life ferric phosphate lithium cell of 15~25 rate charge-discharges circulation.
15% specific area that when anodal batch mixing, adds total powder weight is 360m 2/ g Graphene; 8% specific area that when the negative pole batch mixing, adds total powder weight is 3500m 2The active carbon of/g; Process slurry through mixing, slurry is coated in respectively on aluminium foil and the Copper Foil, pass through conventional compressing tablet, film-making, assembling, fluid injection then, change into, seal promptly to process and to carry out 15~25 rate charge-discharge recycled phosphoric acid lithium iron batteries.Battery circulates after 5000 times when carrying out 20 rate charge-discharge loop tests, and the discharge capacity of battery still remains on more than 90% of initial capacity.
The ferric phosphate lithium cell that a large amount of experiment proofs adopts the inventive method to process has excellent fast charging and discharging performance, and the cycle life of battery is also well a lot of than the ferric phosphate lithium cell cycle life that conventional method is made during fast charging and discharging.

Claims (2)

1. a manufacture method of ion-lithium phosphate battery comprises the both positive and negative polarity mixing of materials, and the specific area that adds total powder weight 1.0%~15% when it is characterized in that the both positive and negative polarity mixing of materials is the carbon material of 80~5000 ㎡/g.
2. by the described manufacture method of ion-lithium phosphate battery of claim 1, it is characterized in that said carbon material is the mixture of one or more arbitrary proportions in active carbon, CNT, carbon fiber, Graphene, the conductive carbon black.
CN2011103889682A 2011-11-30 2011-11-30 Method for manufacturing lithium iron phosphate battery Pending CN102403537A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011103889682A CN102403537A (en) 2011-11-30 2011-11-30 Method for manufacturing lithium iron phosphate battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011103889682A CN102403537A (en) 2011-11-30 2011-11-30 Method for manufacturing lithium iron phosphate battery

Publications (1)

Publication Number Publication Date
CN102403537A true CN102403537A (en) 2012-04-04

Family

ID=45885502

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011103889682A Pending CN102403537A (en) 2011-11-30 2011-11-30 Method for manufacturing lithium iron phosphate battery

Country Status (1)

Country Link
CN (1) CN102403537A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103050292A (en) * 2012-12-20 2013-04-17 上海奥威科技开发有限公司 High-power double-electric layer capacitor
CN106058252A (en) * 2016-08-17 2016-10-26 江苏金坛绿能新能源科技有限公司 Lithium ion battery cathode slurry and preparation method thereof
CN107256966A (en) * 2017-05-17 2017-10-17 常州第六元素材料科技股份有限公司 A kind of anode slice of lithium ion battery and preparation method thereof, lithium ion battery anode glue size and its method
RU2674167C2 (en) * 2014-12-23 2018-12-05 Нр Электрик Ко., Лтд. Method of switching passive section to connection to power system

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060166093A1 (en) * 2002-11-13 2006-07-27 Hydro-Quebec Electrode coated with a film obtained from an aqueous solution comprising a water-soluble binder, production method thereof and uses of same
CN101207204A (en) * 2006-12-22 2008-06-25 比亚迪股份有限公司 Lithium ion battery anode material and lithium ion battery and anode containing the material
CN101510625A (en) * 2009-03-26 2009-08-19 西安瑟福能源科技有限公司 Ultra-high magnification lithium ion battery
JP2009295465A (en) * 2008-06-06 2009-12-17 Iwate Univ Positive electrode active material for lithium secondary battery and manufacturing method

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060166093A1 (en) * 2002-11-13 2006-07-27 Hydro-Quebec Electrode coated with a film obtained from an aqueous solution comprising a water-soluble binder, production method thereof and uses of same
CN101207204A (en) * 2006-12-22 2008-06-25 比亚迪股份有限公司 Lithium ion battery anode material and lithium ion battery and anode containing the material
JP2009295465A (en) * 2008-06-06 2009-12-17 Iwate Univ Positive electrode active material for lithium secondary battery and manufacturing method
CN101510625A (en) * 2009-03-26 2009-08-19 西安瑟福能源科技有限公司 Ultra-high magnification lithium ion battery

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103050292A (en) * 2012-12-20 2013-04-17 上海奥威科技开发有限公司 High-power double-electric layer capacitor
RU2674167C2 (en) * 2014-12-23 2018-12-05 Нр Электрик Ко., Лтд. Method of switching passive section to connection to power system
CN106058252A (en) * 2016-08-17 2016-10-26 江苏金坛绿能新能源科技有限公司 Lithium ion battery cathode slurry and preparation method thereof
CN107256966A (en) * 2017-05-17 2017-10-17 常州第六元素材料科技股份有限公司 A kind of anode slice of lithium ion battery and preparation method thereof, lithium ion battery anode glue size and its method

Similar Documents

Publication Publication Date Title
CN104779394A (en) Aqueous lithium (sodium) ion battery mixed negative material
CN102969548B (en) A kind of lithium-ion energy storage device and preparation method thereof
CN107742709A (en) A kind of lithium iron phosphate battery anode active material and its preparation and application
Zhang et al. Effect of slurry preparation and dispersion on electrochemical performances of LiFePO 4 composite electrode
CN102768901A (en) Long-life capacitance battery
CN101221853A (en) Semi-solid state or full-solid state water system super capacitor
CN101764263A (en) Super lead carbon battery with active carbon negative electrode and preparation method thereof
CN106025194A (en) Black-phosphorus-based composite negative electrode material and preparing method thereof
CN106654154A (en) Water-based ion battery plate manufacturing process
CN101567469A (en) Power polymer lithium ion battery and fabricating process thereof
CN107086128B (en) A kind of mixed type electrochmical power source device electrode and preparation method thereof
CN106384855A (en) Recovery method of waste lithium iron phosphate positive electrode material
CN101262056A (en) A water solution chargeable lithium ion battery
CN105355849A (en) Lithium battery cathode additive, lithium ion battery, preparation method and uses thereof
CN212907803U (en) Lithium ion battery with high-rate charge and discharge
CN105742695A (en) Lithium-ion battery and preparation method thereof
CN108172744B (en) Sb for lithium-sulfur battery diaphragm2Se3Method for preparing composite material
CN108807912B (en) C @ SnOx(x=0,1,2)Preparation and application of @ C mesoporous nano hollow sphere structure
CN102263280A (en) Flow aqueous chargeable alkali metal ion battery
CN101262076A (en) A water solution chargeable lithium battery
CN102403537A (en) Method for manufacturing lithium iron phosphate battery
CN109802107A (en) A kind of preparation method of sodium-ion battery polyene-based composite negative pole material
CN101894686A (en) Super capacitor battery
Lang et al. High‐performance porous lead/graphite composite electrode for bipolar lead‐acid batteries
CN109244531A (en) A kind of high purity copper matrix graphite alkene composite lithium ion cell and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20120404