CN109216770A - 一种非水锂离子电池电解液及使用该电解液的锂离子电池 - Google Patents
一种非水锂离子电池电解液及使用该电解液的锂离子电池 Download PDFInfo
- Publication number
- CN109216770A CN109216770A CN201811320790.6A CN201811320790A CN109216770A CN 109216770 A CN109216770 A CN 109216770A CN 201811320790 A CN201811320790 A CN 201811320790A CN 109216770 A CN109216770 A CN 109216770A
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- Prior art keywords
- lithium ion
- ion battery
- electrolyte
- compound
- phosphine
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Links
- 239000003792 electrolyte Substances 0.000 title claims abstract description 92
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 229910001416 lithium ion Inorganic materials 0.000 title claims abstract description 69
- -1 phosphine compound Chemical class 0.000 claims abstract description 49
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims abstract description 20
- 239000000654 additive Substances 0.000 claims abstract description 10
- 230000000996 additive effect Effects 0.000 claims abstract description 10
- 229910003002 lithium salt Inorganic materials 0.000 claims abstract description 6
- 159000000002 lithium salts Chemical class 0.000 claims abstract description 6
- LRMLWYXJORUTBG-UHFFFAOYSA-N dimethylphosphorylmethane Chemical compound CP(C)(C)=O LRMLWYXJORUTBG-UHFFFAOYSA-N 0.000 claims description 14
- VEWLDLAARDMXSB-UHFFFAOYSA-N ethenyl sulfate;hydron Chemical compound OS(=O)(=O)OC=C VEWLDLAARDMXSB-UHFFFAOYSA-N 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- AOUFNFSQKTZWRG-UHFFFAOYSA-N 1-diphenylphosphoryl-2,3-difluorobenzene Chemical compound FC1=C(C=CC=C1F)P(C1=CC=CC=C1)(C1=CC=CC=C1)=O AOUFNFSQKTZWRG-UHFFFAOYSA-N 0.000 claims description 3
- FYXPKOPFEGFWHG-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-phenylphosphoryl]phenol Chemical class C1=CC(O)=CC=C1P(=O)(C=1C=CC(O)=CC=1)C1=CC=CC=C1 FYXPKOPFEGFWHG-UHFFFAOYSA-N 0.000 claims description 3
- DFVANUYVZDJAHN-UHFFFAOYSA-N CCC[PH2]=O Chemical class CCC[PH2]=O DFVANUYVZDJAHN-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 150000001345 alkine derivatives Chemical class 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 150000005840 aryl radicals Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 239000004305 biphenyl Substances 0.000 claims description 3
- 235000010290 biphenyl Nutrition 0.000 claims description 3
- 125000006267 biphenyl group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 230000005611 electricity Effects 0.000 claims description 3
- 150000002168 ethanoic acid esters Chemical class 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 2
- YYQLNLDMILHCQP-UHFFFAOYSA-N [PH3]=O.C1=CC=CC=C1C1=CC=CC=C1 Chemical compound [PH3]=O.C1=CC=CC=C1C1=CC=CC=C1 YYQLNLDMILHCQP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 230000001681 protective effect Effects 0.000 abstract description 7
- 239000008151 electrolyte solution Substances 0.000 abstract description 6
- 238000007599 discharging Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract description 2
- 239000013538 functional additive Substances 0.000 abstract 1
- 239000011356 non-aqueous organic solvent Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 50
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 6
- 229910052744 lithium Inorganic materials 0.000 description 6
- 150000001875 compounds Chemical group 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 description 3
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- DIMZOVQGUDDSHG-UHFFFAOYSA-N ethene;sulfuric acid Chemical group C=C.OS(O)(=O)=O DIMZOVQGUDDSHG-UHFFFAOYSA-N 0.000 description 3
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- JAVBBFXUGDCHLZ-UHFFFAOYSA-N 1-$l^{1}-oxidanylpropane Chemical compound CCC[O] JAVBBFXUGDCHLZ-UHFFFAOYSA-N 0.000 description 1
- OLLUAZWXLAKWNC-UHFFFAOYSA-N 1-diphenylphosphoryl-3,5-bis(trifluoromethyl)benzene Chemical class FC(F)(F)C1=CC(C(F)(F)F)=CC(P(=O)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 OLLUAZWXLAKWNC-UHFFFAOYSA-N 0.000 description 1
- 241001269238 Data Species 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- BKIWAQYWKUFSRE-UHFFFAOYSA-N prop-1-ene;sulfuric acid Chemical group CC=C.OS(O)(=O)=O BKIWAQYWKUFSRE-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0567—Liquid materials characterised by the additives
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0017—Non-aqueous electrolytes
- H01M2300/0025—Organic electrolyte
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Inorganic Chemistry (AREA)
- Secondary Cells (AREA)
Abstract
Description
Claims (6)
Priority Applications (1)
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CN201811320790.6A CN109216770A (zh) | 2018-11-07 | 2018-11-07 | 一种非水锂离子电池电解液及使用该电解液的锂离子电池 |
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CN201811320790.6A CN109216770A (zh) | 2018-11-07 | 2018-11-07 | 一种非水锂离子电池电解液及使用该电解液的锂离子电池 |
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CN201811320790.6A Pending CN109216770A (zh) | 2018-11-07 | 2018-11-07 | 一种非水锂离子电池电解液及使用该电解液的锂离子电池 |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110429337A (zh) * | 2019-08-01 | 2019-11-08 | 中国科学院过程工程研究所 | 一种有机磷化合物的用途、锂离子电池电解液及锂离子电池 |
CN110994029A (zh) * | 2019-12-27 | 2020-04-10 | 北京理工大学 | 一种用于锂离子电池的含有三苯基膦类添加剂的砜基高电压电解液 |
CN111342134A (zh) * | 2020-03-13 | 2020-06-26 | 河南电池研究院有限公司 | 一种宽温域锂离子电池非水电解液及其制备方法 |
CN111834661A (zh) * | 2019-04-18 | 2020-10-27 | 张家港市国泰华荣化工新材料有限公司 | 一种非水电解液及二次电池 |
CN112448033A (zh) * | 2019-09-05 | 2021-03-05 | 杉杉新材料(衢州)有限公司 | 高电压锂离子电池电解液及长循环寿命高电压锂离子电池 |
CN112928327A (zh) * | 2019-12-06 | 2021-06-08 | 宁德国泰华荣新材料有限公司 | 一种二次电池 |
CN113661589A (zh) * | 2019-04-10 | 2021-11-16 | 株式会社村田制作所 | 锂离子二次电池 |
CN115332630A (zh) * | 2022-10-12 | 2022-11-11 | 广州天赐高新材料股份有限公司 | 非水电解液及二次电池 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20160031212A (ko) * | 2014-09-12 | 2016-03-22 | 에스케이이노베이션 주식회사 | 리튬 이차전지 전해액 및 이를 포함하는 리튬 이차전지 |
CN105789697A (zh) * | 2014-12-22 | 2016-07-20 | 宁德时代新能源科技股份有限公司 | 非水电解液及使用该非水电解液的锂离子电池 |
-
2018
- 2018-11-07 CN CN201811320790.6A patent/CN109216770A/zh active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20160031212A (ko) * | 2014-09-12 | 2016-03-22 | 에스케이이노베이션 주식회사 | 리튬 이차전지 전해액 및 이를 포함하는 리튬 이차전지 |
CN105789697A (zh) * | 2014-12-22 | 2016-07-20 | 宁德时代新能源科技股份有限公司 | 非水电解液及使用该非水电解液的锂离子电池 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113661589A (zh) * | 2019-04-10 | 2021-11-16 | 株式会社村田制作所 | 锂离子二次电池 |
CN113661589B (zh) * | 2019-04-10 | 2024-07-26 | 株式会社村田制作所 | 锂离子二次电池 |
CN111834661A (zh) * | 2019-04-18 | 2020-10-27 | 张家港市国泰华荣化工新材料有限公司 | 一种非水电解液及二次电池 |
CN110429337A (zh) * | 2019-08-01 | 2019-11-08 | 中国科学院过程工程研究所 | 一种有机磷化合物的用途、锂离子电池电解液及锂离子电池 |
CN112448033A (zh) * | 2019-09-05 | 2021-03-05 | 杉杉新材料(衢州)有限公司 | 高电压锂离子电池电解液及长循环寿命高电压锂离子电池 |
CN112928327A (zh) * | 2019-12-06 | 2021-06-08 | 宁德国泰华荣新材料有限公司 | 一种二次电池 |
CN110994029A (zh) * | 2019-12-27 | 2020-04-10 | 北京理工大学 | 一种用于锂离子电池的含有三苯基膦类添加剂的砜基高电压电解液 |
CN111342134A (zh) * | 2020-03-13 | 2020-06-26 | 河南电池研究院有限公司 | 一种宽温域锂离子电池非水电解液及其制备方法 |
CN111342134B (zh) * | 2020-03-13 | 2022-09-13 | 河南电池研究院有限公司 | 一种宽温域锂离子电池非水电解液及其制备方法 |
CN115332630A (zh) * | 2022-10-12 | 2022-11-11 | 广州天赐高新材料股份有限公司 | 非水电解液及二次电池 |
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