CN102299371B - Lithium ion power cell and preparation method of lithium ion power cell - Google Patents

Lithium ion power cell and preparation method of lithium ion power cell Download PDF

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Publication number
CN102299371B
CN102299371B CN201110231029.7A CN201110231029A CN102299371B CN 102299371 B CN102299371 B CN 102299371B CN 201110231029 A CN201110231029 A CN 201110231029A CN 102299371 B CN102299371 B CN 102299371B
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lithium
battery
power cell
lithium ion
bakings
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CN102299371A (en
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李宝玉
王保
刘兴福
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ZHUHAI LIYUAN NEW ENERGY TECHNOLOGY Co Ltd
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ZHUHAI LIYUAN NEW ENERGY TECHNOLOGY Co Ltd
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    • 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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Abstract

The invention discloses a lithium ion power cell and a preparation method of the lithium ion power cell. A negative material is made from the following raw materials of: by weight, 83-94% of lithium titanate, 2-10% of an adhesive and 3-10% of a conductive agent; a positive material is made from the following raw materials of: by weight, 82-93% of lithium manganate, 1-10% of the adhesive and 4-12% of the conductive agent. The lithium ion power cell provided by the invention has advantages of low cost, large capacity, long cycle life and good safety performance, and can be applied in many fields, such as hybrid electric vehicles, military goods with high property requirements and the like. The preparation method provided by the invention is simple. As water is used as a solvent instead of using NMP as the solvent during the electrode manufacturing process, there exists no pollution as well as dangerous accidents such as explosion or combustion, the zero discharge of pollutants is realized, and simultaneously the complexity of the cell processing technology is reduced.

Description

The preparation method of a kind of lithium-ion-power cell and lithium-ion-power cell
Technical field
The present invention relates to the preparation method of a kind of lithium-ion-power cell and lithium-ion-power cell.
Background technology
World energy sources and Environmental Protection Situation day are becoming tight, and battery is more and more subject to people's favor as new forms of energy.Lithium ion battery is because its energy density is high, and volume is light, and weight is little, environment friendly and pollution-free, becomes the main direction of new forms of energy development.Along with the fast development of electric automobile, space technology, national defense industry and electric energy storing system etc., having higher requirement in the aspects such as specific capacity to secondary cell, cycle life, fail safe, improves the chemical property of battery and can start with from aspects such as electrode materials.
Traditional lithium ion battery is invariably using graphite as negative material main active substances.Comparative maturity of formula using graphite as negative electrode active material.Graphite is the lithium-ion battery system of negative pole, also has self intrinsic defect.As easily " analysing lithium " of overtension, cause fail safe hidden danger, current commercial lithium ion battery negative material is all embedding lithium material with carbon element mostly.The diaphragm that negative material surface forms, recycling in process because continual chemical reaction and crystal formation change, also at the cyclicity and the electrical property that constantly affect battery.And finally cause hydraulic performance decline and cell decay.Meanwhile, also there is the common imbedding problem of electrolyte in graphite electrode, and this also will affect the cyclical stability of electrode.
Lithium titanate anode material is lithium titanate with spinel structure superfines, is the lithium secondary battery cathode material of a kind of high-performance, high magnification type.LTO is 1.55V with respect to the current potential of lithium electrode, and theoretical specific capacity is 175mAh/g, actual specific capacity 150-160 mAh/g, and concentrate on land regions, there is good cycle performance and good charge and discharge platform.Embed or deviate from process at Li, crystal formation does not change, change in volume is less than 1%, therefore be called as " zero strain material ", this is significant, can avoid in charge and discharge cycles because the flexible back and forth of electrode material causes structural damage, thus cycle performance and the useful life of improving electrode, having reduced with cycle-index and increased and bring specific capacity significantly to decay, is (Li 4ti 5o 12) there is the cycle performance better than carbon negative pole.There is not electrolyte imbedding problem altogether in lithium titanate, can be due to the unstable cycle life that affects of SEI.Lithium titanate anode material has stable physics and chemistry character, does not react with electrolyte, has outstanding stability in use and fail safe.At 25 DEG C, Li 4ti 5o 12chemical diffusion coefficient be 2 × 10 -8cm 2/ s, makes a call to an order of magnitude than the diffusion coefficient in carbon negative pole material, and high diffusion coefficient makes this negative material can quick, many cycle charge-discharges.Lithium titanate material electromotive force, than the height of pure metal lithium, is difficult for producing lithium dendrite arm, for the safety that ensures lithium battery provides the foundation.Be considered to thoroughly to solve the fail safe of lithium battery.
Positive electrode is also an important component part of lithium-ion-power cell, has mainly adopted cobalt acid lithium (LiCoO at first by the positive electrode of Sony industrialization 2), and now because cobalt resource is more and more deficienter, its price is also more and more higher, its thermal stability is poor simultaneously, environment is also had to larger destruction, therefore, increasing researcher and engineering staff have turned one's attention to other positive electrode, and the positive electrode that lithium-ion-power cell receives much concern also has LiNiO 2, LiMn 2o 4, LiFePO4 etc., LiNiO 2capacity is larger, more difficult but preparation is got up, and obtain purer material and be difficult to, and its security performance is bad; LiMn 2o 4price is relatively cheap, and security performance is also better, but its cycle performance is poor, and capacity is not high, and high-temperature behavior is not good simultaneously, LiFePO 4not containing noble element, raw material cheapness, resource is greatly abundant, but, with LiFePO 4for the voltage of the battery of positive active material lower.
The current potential of LiMn2O4 is higher, and LiMn2O4 has the overall merits such as price is low, current potential is high, environmental friendliness, security performance height simultaneously, is subject to increasing people and pays close attention to.
While making electrode slurry, conventional adhesive is PVDF, and conventional solvent is NMP, but, use the problem of NMP to be: environmental pollution is large, and NMP belongs to inflammable and explosive article, making in the process of electrode slurry, should be noted that in time NMP ventilation is distributed and removed, in addition, because NMP can absorb water, and then affect the bond properties of adhesive, therefore, in the process of making electrode, must control the moisture content of NMP, therefore, it is complicated that technique can become.
Summary of the invention
The object of this invention is to provide a kind of lithium-ion-power cell and preparation method thereof.
The technical solution used in the present invention is:
A kind of lithium-ion-power cell, negative material is made up of the raw material of following mass percent: the conductive agent of the lithium titanate of 83-94%, the adhesive of 2-10%, 3-10%, positive electrode is made up of the raw material of following mass percent: the conductive agent of the LiMn2O4 of 82-93%, the adhesive of 1-10%, 4-12%.
Described adhesive is at least one in LA132, LA133, LA135.
Described conductive agent is at least one in SP, superconduction carbon black, electrically conductive graphite, carbon nano-tube.
A preparation method for lithium-ion-power cell, comprises the following steps:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, stir, obtain anode sizing agent, anode sizing agent is coated on aluminium foil, under vacuum environment, 80-120 DEG C of baking, after 5-12 hour, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, stir, obtain cathode size, cathode size is coated on aluminium foil, under vacuum environment, 80-120 DEG C of baking, after 5-12 hour, roll-in, cuts into negative plate;
3) respectively by positive plate, negative plate under vacuum environment, 60 ~ 120 DEG C baking 12 ~ 24 hours after, positive plate, barrier film, negative plate are laminated into battery core together, insert in battery container, become semi-finished product battery;
4) by semi-finished product battery under vacuum environment, 60 ~ 90 DEG C baking 48 ~ 96 hours after, fluid injection, change into, partial volume, obtain a kind of lithium-ion-power cell.
The vacuum pressure of described vacuum environment is-0.08 ~-0.10 MPa.
The invention has the beneficial effects as follows: 1. lithium-ion-power cell cost of the present invention is lower, and capacity is larger, has extended cycle life, and security performance is good, can be applicable to a lot of fields, as hybrid-electric car, the militaria of high performance requirements etc.; 2. manufacture method of the present invention is simple; 3. owing to not using NMP making in the process of electrode, and water is cooked solvent, therefore, can not produce pollution, also there will not be the perils such as blast or burning, and zero emission has reduced the complex manufacturing technology degree of battery simultaneously.
Brief description of the drawings
Fig. 1 is the discharge curve of lithium-ion-power cell of the present invention.
Fig. 2 is the charging curve of lithium-ion-power cell of the present invention.
Fig. 3 is the discharge curve of lithium-ion-power cell of the present invention.
Fig. 4 is the charging curve of lithium-ion-power cell of the present invention.
Fig. 5 is the cyclic curve figure of lithium-ion-power cell of the present invention.
Embodiment
Further illustrate the present invention below in conjunction with specific embodiment:
embodiment 1:
A kind of formula table 1 composed as follows of lithium ion power cell cathode pole piece material:
A kind of formula table 2 composed as follows of lithium ion power battery cathode pole piece material:
Barrier film is: the single-layer septum of PP material
Electrolyte is: 1.2mol/L LiPF 6solution, solvent composition is EC:DMC:EMC=1:1:1
Shell is plastic casing
Concrete preparation method is as follows:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain anode sizing agent, anode sizing agent is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 80 DEG C of bakings after 12 hours, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain cathode size, cathode size is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 80 DEG C of bakings after 12 hours, roll-in, cuts into negative plate;
3) respectively the 60 DEG C of bakings under-0.08MPa of positive plate, negative plate, after 24 hours, are laminated into battery core together by positive plate, barrier film, negative plate, insert in plastic casing, become semi-finished product battery;
4) by the 60 DEG C of bakings after 96 hours under-0.08MPa of semi-finished product battery, fluid injection, change into, partial volume becomes 120Ah battery.After tested, as shown in Figure 1,0.5C charging curve as shown in Figure 2 for the 0.5C discharge curve of gained battery.
embodiment 2:
A kind of formula table 3 composed as follows of lithium ion power cell cathode pole piece material:
A kind of formula table 4 composed as follows of lithium ion power battery cathode pole piece material:
Barrier film is: the single-layer septum of PP material
Electrolyte is: 1.2mol/L LiPF 6solution, solvent composition is EC:DMC:EMC=1:1:1
Shell is plastic casing
Concrete preparation method is as follows:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain anode sizing agent, anode sizing agent is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 100 DEG C of bakings after 10 hours, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain cathode size, cathode size is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 100 DEG C of bakings after 10 hours, roll-in, cuts into negative plate;
3) respectively the 120 DEG C of bakings under-0.10MPa of positive plate, negative plate, after 12 hours, are laminated into battery core together by positive plate, barrier film, negative plate, insert in plastic casing, become semi-finished product battery;
4) by the 90 DEG C of bakings after 48 hours under-0.10MPa of semi-finished product battery, fluid injection, change into, partial volume becomes 120Ah battery.After tested, as shown in Figure 3,0.5C charging curve as shown in Figure 4 for the 0.5C discharge curve of gained battery.
embodiment 3:
A kind of formula table 5 composed as follows of lithium ion power cell cathode pole piece material:
A kind of formula table 6 composed as follows of lithium ion power battery cathode pole piece material:
Barrier film is: the single-layer septum of PP material
Electrolyte is: 1.2mol/L LiPF 6solution, solvent composition is EC:DMC:EMC=1:1:1
Shell is plastic casing
Concrete preparation method is as follows:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain anode sizing agent, anode sizing agent is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 120 DEG C of bakings after 5 hours, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain cathode size, cathode size is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 120 DEG C of bakings after 5 hours, roll-in, cuts into negative plate;
3) respectively the 120 DEG C of bakings under-0.10MPa of positive plate, negative plate, after 12 hours, are laminated into battery core together by positive plate, barrier film, negative plate, insert in plastic casing, become semi-finished product battery;
4) by the 90 DEG C of bakings after 48 hours under-0.10MPa of semi-finished product battery, fluid injection, change into, partial volume becomes 120Ah battery.The 1C cyclic curve of gained battery as shown in Figure 5.
embodiment 4:
A kind of formula table 7 composed as follows of lithium ion power cell cathode pole piece material:
A kind of formula table 8 composed as follows of lithium ion power battery cathode pole piece material:
Barrier film is: the single-layer septum of PP material
Electrolyte is: 1.2mol/L LiPF 6solution, solvent composition is EC:DMC:EMC=1:1:1
Shell is plastic casing
Concrete preparation method is as follows:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain anode sizing agent, anode sizing agent is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 120 DEG C of bakings after 5 hours, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain cathode size, cathode size is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 120 DEG C of bakings after 5 hours, roll-in, cuts into negative plate;
3) respectively the 100 DEG C of bakings under-0.09MPa of positive plate, negative plate, after 16 hours, are laminated into battery core together by positive plate, barrier film, negative plate, insert in plastic casing, become semi-finished product battery;
4) by the 80 DEG C of bakings after 72 hours under-0.09MPa of semi-finished product battery, fluid injection, change into, partial volume becomes 120Ah battery.

Claims (1)

1. a lithium-ion-power cell, it is characterized in that: negative material is made up of the raw material of following mass percent: 83% lithium titanate, 10% adhesive LA132,7% electrically conductive graphite, positive electrode is made up of the raw material of following mass percent: 82% LiMn2O4,6% adhesive LA132,12% conductive agent SP; Barrier film is: the single-layer septum of PP material, electrolyte is: 1.2mol/L LiPF 6solution, solvent composition is EC: DMC: EMC=1:1:1; The preparation method of this battery is:
1) making of positive plate: add positive electrode by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain anode sizing agent, anode sizing agent is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 80 DEG C of bakings after 12 hours, roll-in, cuts into positive plate;
2) making of negative plate: add negative material by formula ratio, be dissolved in water, even by double star power mixer high-speed stirred, eliminate bubble, iron filings, obtain cathode size, cathode size is uniformly coated on aluminium foil through automatical feeding system, coating machine, under vacuum environment, 80 DEG C of bakings after 12 hours, roll-in, cuts into negative plate;
3) respectively the 60 DEG C of bakings under-0.08MPa of positive plate, negative plate, after 24 hours, are laminated into battery core together by positive plate, barrier film, negative plate, insert in plastic casing, become semi-finished product battery;
4) by the 60 DEG C of bakings after 96 hours under-0.08MPa of semi-finished product battery, fluid injection, change into, partial volume becomes 120Ah battery.
CN201110231029.7A 2011-08-12 2011-08-12 Lithium ion power cell and preparation method of lithium ion power cell Expired - Fee Related CN102299371B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100546076C (en) * 2007-12-27 2009-09-30 南京工业大学 Method for synthesizing nano-scale lithium ion power battery cathode material by micro-reactor spontaneous combustion method
CN101582522A (en) * 2009-06-23 2009-11-18 珠海市鹏辉电池有限公司 High rate charge-discharge power lithium battery
CN101964428B (en) * 2010-08-05 2013-02-20 深圳市贝特瑞新能源材料股份有限公司 Preparation method of lamellar lithium manganese battery
CN101958428B (en) * 2010-09-15 2013-11-13 东莞新能源科技有限公司 Lithium ion secondary battery

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