CN100459277C - Dynamic electrolyte for lithium ion battery - Google Patents

Dynamic electrolyte for lithium ion battery Download PDF

Info

Publication number
CN100459277C
CN100459277C CNB2006101222620A CN200610122262A CN100459277C CN 100459277 C CN100459277 C CN 100459277C CN B2006101222620 A CNB2006101222620 A CN B2006101222620A CN 200610122262 A CN200610122262 A CN 200610122262A CN 100459277 C CN100459277 C CN 100459277C
Authority
CN
China
Prior art keywords
content
percentage
electrolyte
carbonate
lithium ion
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.)
Active
Application number
CNB2006101222620A
Other languages
Chinese (zh)
Other versions
CN1925206A (en
Inventor
刘建生
左晓希
贺云鹏
周莉
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.)
Guangzhou Tinci Materials Technology Co Ltd
Original Assignee
Guangzhou Tinci Materials Technology Co Ltd
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 Guangzhou Tinci Materials Technology Co Ltd filed Critical Guangzhou Tinci Materials Technology Co Ltd
Priority to CNB2006101222620A priority Critical patent/CN100459277C/en
Publication of CN1925206A publication Critical patent/CN1925206A/en
Application granted granted Critical
Publication of CN100459277C publication Critical patent/CN100459277C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

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

Abstract

This invention relates to dynamic lithium ion battery electrolyte and to one safe dynamic high capacity lithium ion electrolyte and discloses the following components: w/w carbonic acid esters agent composed of vinylene carbonate less than 40 percentage; propylene carbonate less than 20 percentage; methyl propionate less than 40 percentage; propylene carbonate less than 40 percentage; lithium salt 10-16 percentage to prevent additive agent phenylcyclohexyl, p-methyl peroxide, phthalandione or fluoride content less than 12 percentage or combustion inhibitor less than 10 percentage and film addictive agent less than 5 percentage.

Description

A kind of power-type lithium ion battery electrolyte
Technical field
The present invention relates to the electrolyte that lithium ion battery is used, specifically a kind of safe power type high-capacity lithium ion cell electrolyte.
Background technology
Lithium ion battery has operating voltage height, specific energy height, has extended cycle life, with characteristics such as environmental friendliness and memory-less effect, obtained development rapidly, be widely used on the portable electronics.What conventional liquid lithium ionic cell used is the lithium salt solution of organic carbonate, has easy-to-leak liquid and incendive potential safety hazard, and overcharge blast easily when battery is abused, and this has had a strong impact on the development of lithium ion battery to the power type direction.
Solve the simple of lithium ion battery safety problem and valid approach is a development all solid state lithium ion battery, because all solid state lithium ion battery room temperature and poor performance at low temperatures now have a lot of technology to remain to be broken through.Polymer gel attitude lithium ion battery also can be alleviated the safety problem of liquid lithium ionic cell to a certain extent, but its big shortcoming of polarization when having poor performance at low temperatures, big electric current equally.
(in<5Ah) the lithium ion battery, the content of electrolyte is fewer, and battery can comparatively fast distribute at the time heat that produces of short circuit, generally situation about can not blast in low capacity; Under the state of overcharging, because the input of external electric energy is arranged, battery can cause blast by persistent fever, if in electrolyte, add anti-overcharge additive such as biphenyl, cyclohexyl benzene etc., polymerization takes place under a certain current potential, open circuit in inside battery formation, battery is in a safe condition, can improve or solve the safety problem that overcharges of battery.Yet the ambient temperature that power-type lithium ion battery uses is than higher (40~90 ℃) and capacity height, and the heat of battery moment generation can not get in time distributing during short circuit, and the temperature meeting of battery sharply raises, and the interior voltage rise height of battery explodes, burns thereby produce.If in electrolyte, add fire retardant and anti-overcharge additive simultaneously, just can prevent the short circuit of battery or the safety problem when overcharging.But the affiliation that adds of these two kinds of additives influences battery capacity and useful life.
Summary of the invention
The purpose of this invention is to provide a kind of novel power-type lithium ion battery electrolyte, its amount by selecting carbonate solvent to add, and functional additive, when keeping this lithium-ion electrolyte cell high-capacity, improve high-temperature behavior, solve the safety problem of battery, make battery have the good life-span that recycles.
The technology of the present invention solution is that electrolyte is made up of following various materials, and content of material is represented to account for the heavy w/w of total liquid:
A, carbonate solvent main component comprise that ethylene carbonate content is not more than 40%, and the propylene carbonate ester content is not more than 20%, and carbonic acid first propyl ester content is not more than 40%, and dipropyl carbonate content is not more than 40% mixed liquor;
B, contain lithium salts 10~16%;
C, anti-overcharge additive comprise cyclohexyl benzene, terephthaldehyde's ether, and one or more in the fluoro thing of perhaps 1,2-dimethoxy benzene, or above material, content is not more than 12%;
D, fire retardant comprise tributyl phosphate, the trifluoromethyl phosphate, or 2,2, one or more in the 2-trifluoroethyl phosphate, content is not more than 10%;
E, film for additive comprise halogenated ethylene carbonate, halo propene carbonate, vinylene carbonate, vinylethylene carbonate, 1,3-sulfonic acid propiolactone, 1,4-sulfonic acid butyrolactone, ethylene sulfite, or in the propylene sulfite one or more, content is not more than 6%.
More than carbonate solvent of the present invention comprise gamma-butyrolacton 0~40%, dimethyl carbonate 0~15%, methyl ethyl carbonate 0~40%, diethyl carbonate 0~50%, carbonic acid first isopropyl ester 0~40%.
More than lithium salts of the present invention be selected from LiPF 6, LiBOB, LiSO 3CF 3, LiBF 4, LiAsF 6, Li (CF 3SO 2) 2N, LiC (CF 3SO 2) 3In one or more, addition is 11~13%.
Its addition of anti-overcharge additive of the present invention is 6~8%.
More than fire retardant of the present invention comprise trimethyl phosphate, triethyl phosphate, triphenyl phosphate, tributyl phosphate, trifluoromethyl phosphate, or 2,2, one or more in the 2-trifluoroethyl phosphate, its addition is 5~8%.
Film for additive addition of the present invention is 2~4%.
The high boiling dicyandiamide solution of employing of the present invention makes electrolyte highly stable under hot conditions, and decomposition reaction does not take place, and can not produce higher vapour pressure at inside battery.In electrolyte, add phosphate flame retardant, the phosphate of preferably fluoridizing, both can improve lithium salts thermal stability in the electrolyte, improve the security performance of battery when thermal shock, battery is burnt at the Shi Buhui of accident blast, because the phosphate viscosity of fluoridizing is lower, can not influence battery performance simultaneously.Another aspect that improves the electrolyte security performance is to use anti-overcharge additive in electrolyte, guarantees the safety of battery under the state of overcharging.The use of these additives in the capacity and the useful life that can influence battery in varying degrees, therefore adds film for additive in electrolyte, at the preferential passivation protection film that forms good thermal stability in the both positive and negative polarity surface of battery.The present invention to the selection of dicyandiamide solution and above three class functional additives with and the amount that adds, thereby improve the various aspects of performance of power-type lithium ion battery, obtained good effect.
The invention has the advantages that and improve high-temperature behavior when keeping this lithium-ion electrolyte cell high-capacity, solve the safety problem of battery, make battery have the good life-span that recycles.
Description of drawings
Fig. 1 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 1;
Fig. 2 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 2;
Fig. 3 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 3;
Fig. 4 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 4;
Fig. 5 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 5;
Fig. 6 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 6;
Fig. 7 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 7;
Fig. 8 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 8;
Fig. 9 is the figure line of the high temperature circulation discharge capacity of two batteries among the embodiment 9;
Figure 10 is the figure line of the high temperature circulation discharge capacity of two batteries in the Comparative Examples 2;
Figure 11 is the figure line of the high temperature circulation discharge capacity of two batteries in the Comparative Examples 2.
Embodiment
Embodiment 1
With the ethylene carbonate of carbonate solvent, propene carbonate, carbonic acid first propyl ester, dipropyl carbonate by account for total liquid heavy 26.43%, 11.32%, 12.94%, 24.81%, mix, in this solvent, add 12.5% LiPF then 6, average mark adds for three times, each 1.5~2.0 hours time intervals that add, fully shake up after the adding, the back adds the vinylene carbonate 1.0% and the propylene sulfite 2.0% of film for additive, anti-overcharge additive cyclohexyl benzene 7.0%, fire retardant trifluoromethyl phosphate 2.0%.The process for preparation of whole electrolyte is all operated in glove box, and glove box is an ar gas environment, and the temperature in the case is controlled in 25 ℃, and moisture is below 1ppm.
This electrolyte is injected in the battery, tests.
The battery that uses is:
Anodal preparation: active material LiCoO 2Content 94%, carbon black 3.0%, binding agent PVDF3.0%, aluminium foil are collector.Pole piece width 9.0cm, thickness 130 μ m.
The negative pole preparation: the content 90.0% of active material MCMB, the content 10.0% of binding agent PVDF, Copper Foil are collector, the wide 9.2cm of pole piece, thickness 158 μ m.
Barrier film is PE/PP/PE three strata compound films.The design capacity of battery is 10Ah.
Detection method:
Gained electrolyte is respectively annotated ten batteries, and after battery changed into, six batteries of detection computations are irreversible capacity first on average, wherein four batteries carry out 3C5V and overcharge, four are carried out 1C10V and overcharge, and four are carried out short-circuit test, in addition two batteries in 70 ℃ of environment with the 1C cycle charge-discharge.
Electrolyte prepares the multiplying power discharging characteristic detecting method of battery behind the battery:
1, with 1C electric current constant voltage charge to 4.2V, cut-off current is 20mA;
2, leave standstill 10 minutes, use secondary cell Performance Detection cabinet to detect battery capacity;
3, with the 1C current discharge to 3.0V;
4, leave standstill 10 minutes, use secondary cell Performance Detection cabinet to detect battery capacity.
Battery circulation discharge detection method: recycle the 1st to the 4th step of battery multiplying power discharging characteristic detecting method.
With the moisture in the coulomb Ka Shi method mensuration electrolyte, the acidity in the acid base titration test electrolyte, measure the conductivity of electrolyte with DJS-307 type electric conductivity instrument.
Embodiment 2-7
With embodiment 1, just each content of material is adjusted as shown in table 1 belowly, and do embodiment 1 described various tests with regard to the electrolyte of each embodiment gained.
Embodiment 8
With embodiment 1, just the cyclohexyl benzene with anti-overcharge additive changes terephthaldehyde's ether into, change the trifluoromethyl phosphate of fire retardant into 2,2,2-trifluoroethyl phosphate changes the vinylethylene carbonate in the film for additive into 1,3-sulfonic acid propiolactone, propylene sulfite changes ethylene sulfite into, LiPF 6Change Li (CF into 3SO 2) 2N also does embodiment 1 described various tests with regard to the electrolyte of gained.
Embodiment 9
With embodiment 1, just the cyclohexyl benzene with anti-overcharge additive changes adjacent benzene fluorine dimethyl ether into, change the trifluoromethyl phosphate of fire retardant into tributyl phosphate, and change vinylethylene carbonate in the film for additive and propylene sulfite into the chloroethylene carbonate ester, LiPF 6Change LiC (CF into 3SO 2) 3, and do embodiment 1 described various tests with regard to the electrolyte of gained.
Comparative Examples 1
Solvent ethylene carbonate, methyl ethyl carbonate, diethyl carbonate are mixed by mass ratio at 23.13%: 23.13%: 30.84%, and the back adds 12.9% LiPF 6, average mark three times adds, each 1.5~2.0 hours time intervals that add, stir, and the back adds 2.0% vinylene carbonate, 4.0% biphenyl, 4.0% cyclohexyl benzene, and does embodiment 1 described various tests with regard to the electrolyte of gained.
Comparative Examples 2
Solvent ethylene carbonate, dimethyl carbonate, diethyl carbonate are mixed by mass ratio at 23.55%: 23.55%: 31.4%, and the back adds 12.5% LiPF 6, average mark three times adds, each 1.5~2.0 hours time intervals that add, stir, add at last 2.0% vinylene carbonate, 7.0% 2,2,2-trifluoroethyl phosphate, and do embodiment 1 described various tests with regard to the electrolyte of gained.
Table 2 is the on average irreversible capacity loss first of battery in each example
Example 1 2 3 4 5 6 7 8 9 Contrast 1 Contrast 2
Irreversible capacity loss (%) 12.9 12.8 13.2 13.0 12.8 13.0 13.1 12.8 12.9 12.9 12.6
Table 3 is the experimental result that overcharges of battery in each example
Example 3C5V 1C10V
1 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
2 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
3 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
4 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
5 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
6 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
7 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
8 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
9 Do not explode, do not smolder, not on fire Do not explode, do not smolder, not on fire
Contrast
1 Do not explode, do not smolder, not on fire 2 blasts are smoldered for 2
Contrast 2 Battery explosion is smoldered, and is not on fire Battery explosion is smoldered, and 1 on fire
The short circuit experiment result of battery in each example of table 3
Example Phenomenon Example Phenomenon
1 Do not explode, do not smolder, not on fire 7 Do not explode, do not smolder, not on fire
2 Do not explode, do not smolder, not on fire 8 Do not explode, do not smolder, not on fire
3 Do not explode, do not smolder, not on fire 9 Do not explode, do not smolder, not on fire
4 Do not explode, do not smolder, not on fire Contrast 1 3 blasts, on fire
5 Do not explode, do not smolder, not on fire Contrast 2 4 blasts are smoldered, and are not on fire
6 Do not explode, do not smolder, not on fire

Claims (2)

1, a kind of power-type lithium ion battery electrolyte is characterized in that electrolyte is made up of following various materials, and content of material is represented to account for the heavy w/w of total liquid:
A, carbonate solvent main component comprise that ethylene carbonate content is 26.43~40%, and the propylene carbonate ester content is not more than 20%, and carbonic acid first propyl ester content is not more than 40%, and dipropyl carbonate content is not more than 40% mixed liquor;
B, contain lithium salts 10~16%;
C, anti-overcharge additive main component comprise that cyclohexyl benzene, terephthaldehyde's ether or adjacent benzene fluorine dimethyl ether content are 6~12%;
D, fire retardant main component comprise tributyl phosphate, trifluoromethyl phosphate or 2,2,2-trifluoroethyl phosphate, and content is not more than 10%;
E, film for additive main component are halogenated ethylene carbonate, and content is 4~6%.
2, a kind of power-type lithium ion battery electrolyte according to claim 1 is characterized in that lithium salts is selected from LiPF 6, LiBOB, LiSO 3CF 3, LiBF 4, LiAsF 6, Li (CF 3SO 2) 2N, LiC (CF 3SO 2) 3In one or more, addition is 11~13%.
CNB2006101222620A 2006-09-20 2006-09-20 Dynamic electrolyte for lithium ion battery Active CN100459277C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2006101222620A CN100459277C (en) 2006-09-20 2006-09-20 Dynamic electrolyte for lithium ion battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2006101222620A CN100459277C (en) 2006-09-20 2006-09-20 Dynamic electrolyte for lithium ion battery

Publications (2)

Publication Number Publication Date
CN1925206A CN1925206A (en) 2007-03-07
CN100459277C true CN100459277C (en) 2009-02-04

Family

ID=37817743

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2006101222620A Active CN100459277C (en) 2006-09-20 2006-09-20 Dynamic electrolyte for lithium ion battery

Country Status (1)

Country Link
CN (1) CN100459277C (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101079504B (en) * 2007-05-10 2010-05-26 武汉大学 An electrolyte of efficient low-poison and combustion-resisting lithium cell and its lithium cell
CN101079505B (en) * 2007-05-11 2010-05-26 武汉大学 Combustion-resisting electrolyte of lithium secondary cell and its lithium cell
EP2526578B1 (en) * 2007-08-16 2015-09-30 LG Chem, Ltd. Non-aqueous electrolyte lithium secondary battery
CN101593851B (en) * 2008-05-29 2012-05-23 比亚迪股份有限公司 Additive composition, electrolyte containing same and lithium ion secondary battery
CN101640288B (en) * 2008-07-30 2012-03-07 比亚迪股份有限公司 Lithium-ion battery electrolyte and lithium-ion battery containing same
CN102460817A (en) * 2009-06-22 2012-05-16 日立车辆能源株式会社 Lithium-ion secondary battery
CN101807720B (en) * 2010-03-31 2012-08-15 张家港市国泰华荣化工新材料有限公司 Flame-retardant electrolyte solution and application thereof
CN101826635A (en) * 2010-04-09 2010-09-08 广州天赐高新材料股份有限公司 Polymer electrolyte for lithium battery and manufacturing method of battery thereof
CN102237551B (en) * 2010-04-30 2014-04-02 比亚迪股份有限公司 Non-aqueous electrolyte, preparation method thereof and battery adopting electrolyte
CN101867065B (en) * 2010-06-21 2013-07-10 张家港市国泰华荣化工新材料有限公司 Flame-retardant electrolyte solution and application thereof
CN102544601A (en) * 2010-12-17 2012-07-04 上海空间电源研究所 Composite non-electrolyte additive for improving high-temperature safety performance of battery
CN102315484A (en) * 2011-08-30 2012-01-11 珠海汉格能源科技有限公司 Overcharge resistant electrolyte of polymer lithium ion battery
CN102496738A (en) * 2011-12-31 2012-06-13 天津力神电池股份有限公司 Non-aqueous electrolyte capable of improving safety performance of battery
CN102544581A (en) * 2012-02-26 2012-07-04 河北工业大学 Flame-retardant electrolyte for lithium iron phosphate power cell
CN102832408B (en) * 2012-09-18 2015-04-08 广州天赐高新材料股份有限公司 Electrolyte with high flame retardation performance and electrochemical performance and lithium ion battery
CN106340671B (en) * 2015-07-08 2018-10-26 宁德时代新能源科技股份有限公司 Lithium ion battery and electrolyte thereof
CN108242568A (en) * 2016-12-26 2018-07-03 宁德时代新能源科技股份有限公司 Electrolyte solution and secondary battery

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000012080A (en) * 1998-06-19 2000-01-14 Mitsui Chemicals Inc Nonaqueous electrolyte for secondary battery and nonaqueous electrolyte secondary battery
CN1411619A (en) * 2001-01-04 2003-04-16 三菱化学株式会社 Nonaqueous electrolytic liquid and lithium secondary battery employing same
CN1430306A (en) * 2001-12-28 2003-07-16 三井化学株式会社 Nonaqueous electrolyte and lithium secondary battery using the electrolyte
CN1770541A (en) * 2003-10-31 2006-05-10 三星Sdi株式会社 Electrolyte for rechargeable lithium battery and rechargeable lithium battery comprising same
CN1825675A (en) * 2005-02-24 2006-08-30 三洋电机株式会社 Non-aqueous electrolyte secondary battery

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000012080A (en) * 1998-06-19 2000-01-14 Mitsui Chemicals Inc Nonaqueous electrolyte for secondary battery and nonaqueous electrolyte secondary battery
CN1411619A (en) * 2001-01-04 2003-04-16 三菱化学株式会社 Nonaqueous electrolytic liquid and lithium secondary battery employing same
CN1430306A (en) * 2001-12-28 2003-07-16 三井化学株式会社 Nonaqueous electrolyte and lithium secondary battery using the electrolyte
CN1770541A (en) * 2003-10-31 2006-05-10 三星Sdi株式会社 Electrolyte for rechargeable lithium battery and rechargeable lithium battery comprising same
CN1825675A (en) * 2005-02-24 2006-08-30 三洋电机株式会社 Non-aqueous electrolyte secondary battery

Also Published As

Publication number Publication date
CN1925206A (en) 2007-03-07

Similar Documents

Publication Publication Date Title
CN100459277C (en) Dynamic electrolyte for lithium ion battery
Zhang et al. Tris (2, 2, 2-trifluoroethyl) phosphite as a co-solvent for nonflammable electrolytes in Li-ion batteries
CN100438198C (en) Mixed additive and electrolyte and lithium ion secondary battery containing same
CN102522590B (en) Non-aqueous organic electrolyte, lithium ion secondary battery containing non-aqueous organic electrolyte, preparation method of lithium ion secondary battery and terminal communication equipment
US20020110739A1 (en) Non-flammable electrolytes
CN102610859B (en) Non-aqueous electrolyte for lithium manganate power battery
CN103996874B (en) High temperature safety non-aqueous electrolyte for lithium ion cell
CN106450461A (en) Lithium secondary battery overcharge protection electrolyte and lithium secondary battery
CN103633368B (en) Flame-retardant additive used for electrolyte and flame-retardant lithium ion battery electrolyte
CN111146502B (en) Composite flame-retardant electrolyte and lithium ion battery
CN109524715B (en) Additive for lithium ion battery electrolyte, electrolyte and lithium ion battery
US20170294677A1 (en) Fluorine-Substituted Propylene Carbonate-Based Electrolytic Solution and Lithium-Ion Battery
CN100449852C (en) A mixed additive agent and electrolyte of lithium ion secondary battery synthesized with this mixed additive agent
CN105702950A (en) Special safety lithium-ion battery for new energy vehicle
CN103762384A (en) Safe non-aqueous electrolyte for battery
US6455200B1 (en) Flame-retardant additive for li-ion batteries
CN103682442A (en) Non-aqueous electrolyte and application thereof
CN101453036A (en) Non-aqueous electrolytic solution for lithium ion secondary battery and manufacturing method thereof
CN101017919A (en) Phosphor-included additive for the lithium ion battery electrolyte
CN106025354A (en) High-temperature and high-safety non-water electrolyte
CN102237551B (en) Non-aqueous electrolyte, preparation method thereof and battery adopting electrolyte
Zhai et al. Customized design of electrolytes for high-safety and high-energy-density lithium batteries
CN113745659A (en) Composite high-safety electrolyte and lithium ion battery
CN104241685B (en) A kind of anti-overcharge lithium-ion battery electrolytes
Sun et al. Ninth International Conference on Engineering Failure Analysis A review of mitigation strategies for Li-ion battery thermal runaway

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right

Effective date of registration: 20091113

Pledge (preservation): Pledge

PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20101227

Granted publication date: 20090204

Pledgee: China Merchants Bank, Limited by Share Ltd, Guangzhou surplus Plaza Branch

Pledgor: Guangzhou heaven sent high-tech materials Limited by Share Ltd|Guangzhou heaven sent silicone Technology Co.,Ltd.

Registration number: 2009440000644

PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20101227

Granted publication date: 20090204

Pledgee: China Merchants Bank, Limited by Share Ltd, Guangzhou surplus Plaza Branch

Pledgor: Guangzhou heaven sent high-tech materials Limited by Share Ltd|Guangzhou heaven sent silicone Technology Co.,Ltd.

Registration number: 2009440000644

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

Denomination of invention: Dynamic electrolyte for lithium ion battery

Effective date of registration: 20091113

Granted publication date: 20090204

Pledgee: China Merchants Bank, Limited by Share Ltd, Guangzhou surplus Plaza Branch

Pledgor: Guangzhou Tianci High-Tech Material Co., Ltd.

Registration number: 2009440000644

PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20101227

Granted publication date: 20090204

Pledgee: China Merchants Bank, Limited by Share Ltd, Guangzhou surplus Plaza Branch

Pledgor: Guangzhou heaven sent high-tech materials Limited by Share Ltd|Guangzhou heaven sent silicone Technology Co.,Ltd.

Registration number: 2009440000644

PLDC Enforcement, change and cancellation of contracts on pledge of patent right or utility model