CN105609318B - The preparation method and the pre- embedding lithium cathode sheet of gained of a kind of pre- embedding lithium cathode sheet - Google Patents
The preparation method and the pre- embedding lithium cathode sheet of gained of a kind of pre- embedding lithium cathode sheet Download PDFInfo
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- CN105609318B CN105609318B CN201610009533.5A CN201610009533A CN105609318B CN 105609318 B CN105609318 B CN 105609318B CN 201610009533 A CN201610009533 A CN 201610009533A CN 105609318 B CN105609318 B CN 105609318B
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- 229910052744 lithium Inorganic materials 0.000 title claims abstract description 108
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 title claims abstract description 103
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- 239000011149 active material Substances 0.000 claims abstract description 23
- 229910003002 lithium salt Inorganic materials 0.000 claims abstract description 22
- 159000000002 lithium salts Chemical class 0.000 claims abstract description 22
- 230000005518 electrochemistry Effects 0.000 claims abstract description 20
- 239000005486 organic electrolyte Substances 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims description 28
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 19
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
- 239000003960 organic solvent Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 239000002033 PVDF binder Substances 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 5
- 229910001290 LiPF6 Inorganic materials 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- QSZMZKBZAYQGRS-UHFFFAOYSA-N lithium;bis(trifluoromethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F QSZMZKBZAYQGRS-UHFFFAOYSA-N 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 4
- 239000006258 conductive agent Substances 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 3
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 claims description 3
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 claims description 3
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical group COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 3
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 3
- 229910001220 stainless steel Inorganic materials 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 229910013188 LiBOB Inorganic materials 0.000 claims description 2
- 229910000552 LiCF3SO3 Inorganic materials 0.000 claims description 2
- 229910010941 LiFSI Inorganic materials 0.000 claims description 2
- 229910052493 LiFePO4 Inorganic materials 0.000 claims description 2
- 229910013164 LiN(FSO2)2 Inorganic materials 0.000 claims description 2
- 229910013406 LiN(SO2CF3)2 Inorganic materials 0.000 claims description 2
- 229910013426 LiN(SO2F)2 Inorganic materials 0.000 claims description 2
- 229910002097 Lithium manganese(III,IV) oxide Inorganic materials 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- DJZIBVUGARDLOC-UHFFFAOYSA-N [Ni]=O.[Co]=O.[Li] Chemical compound [Ni]=O.[Co]=O.[Li] DJZIBVUGARDLOC-UHFFFAOYSA-N 0.000 claims description 2
- 239000006230 acetylene black Substances 0.000 claims description 2
- 230000001680 brushing effect Effects 0.000 claims description 2
- 239000002041 carbon nanotube Substances 0.000 claims description 2
- 229910021393 carbon nanotube Inorganic materials 0.000 claims description 2
- SIXOAUAWLZKQKX-UHFFFAOYSA-N carbonic acid;prop-1-ene Chemical compound CC=C.OC(O)=O SIXOAUAWLZKQKX-UHFFFAOYSA-N 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 150000004862 dioxolanes Chemical class 0.000 claims description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 2
- 239000004816 latex Substances 0.000 claims description 2
- 229920000126 latex Polymers 0.000 claims description 2
- 229910003473 lithium bis(trifluoromethanesulfonyl)imide Inorganic materials 0.000 claims description 2
- 229910001540 lithium hexafluoroarsenate(V) Inorganic materials 0.000 claims description 2
- NMHMDUCCVHOJQI-UHFFFAOYSA-N lithium molybdate Chemical compound [Li+].[Li+].[O-][Mo]([O-])(=O)=O NMHMDUCCVHOJQI-UHFFFAOYSA-N 0.000 claims description 2
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 claims description 2
- 229910001486 lithium perchlorate Inorganic materials 0.000 claims description 2
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 claims description 2
- ACFSQHQYDZIPRL-UHFFFAOYSA-N lithium;bis(1,1,2,2,2-pentafluoroethylsulfonyl)azanide Chemical compound [Li+].FC(F)(F)C(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)C(F)(F)F ACFSQHQYDZIPRL-UHFFFAOYSA-N 0.000 claims description 2
- VDVLPSWVDYJFRW-UHFFFAOYSA-N lithium;bis(fluorosulfonyl)azanide Chemical compound [Li+].FS(=O)(=O)[N-]S(F)(=O)=O VDVLPSWVDYJFRW-UHFFFAOYSA-N 0.000 claims description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910001453 nickel ion Inorganic materials 0.000 claims description 2
- 238000004544 sputter deposition Methods 0.000 claims description 2
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- QXZUUHYBWMWJHK-UHFFFAOYSA-N [Co].[Ni] Chemical compound [Co].[Ni] QXZUUHYBWMWJHK-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- UFLFSNVZQRNKOX-UHFFFAOYSA-N carbonic acid;ethenyl acetate Chemical compound OC(O)=O.CC(=O)OC=C UFLFSNVZQRNKOX-UHFFFAOYSA-N 0.000 claims 1
- 238000005868 electrolysis reaction Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 20
- 229910001416 lithium ion Inorganic materials 0.000 description 20
- 239000003990 capacitor Substances 0.000 description 15
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 7
- 238000005253 cladding Methods 0.000 description 6
- 239000002134 carbon nanofiber Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000003575 carbonaceous material Substances 0.000 description 3
- 239000011889 copper foil Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- -1 polytetrafluoroethylene Polymers 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 229910021384 soft carbon Inorganic materials 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 230000002687 intercalation Effects 0.000 description 2
- 238000009830 intercalation Methods 0.000 description 2
- 230000002427 irreversible effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000007773 negative electrode material Substances 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 229910015645 LiMn Inorganic materials 0.000 description 1
- 229910013716 LiNi Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910010252 TiO3 Inorganic materials 0.000 description 1
- 230000004308 accommodation Effects 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910021385 hard carbon Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000006138 lithiation reaction Methods 0.000 description 1
- OVAQODDUFGFVPR-UHFFFAOYSA-N lithium cobalt(2+) dioxido(dioxo)manganese Chemical compound [Li+].[Mn](=O)(=O)([O-])[O-].[Co+2] OVAQODDUFGFVPR-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002931 mesocarbon microbead Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 125000001979 organolithium group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/50—Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
- H01G11/86—Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
- H01M4/0404—Methods of deposition of the material by coating on electrode collectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0438—Processes of manufacture in general by electrochemical processing
-
- 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
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
The invention discloses a kind of preparation method of pre- embedding lithium cathode sheet, include the following steps:(1), active material admixture containing lithium salt is attached on porous collector by Physical and forms active material layer, obtain the negative plate through the pre- embedding lithium of physics;(2), the negative plate through the pre- embedding lithium of physics obtained by step (1) is inserted into progress constant current charge-discharge processing in organic electrolyte containing lithium salt, obtains the negative plate through the pre- embedding lithium of electrochemistry.The present invention is combined by the pre- embedding lithium of the pre- embedding lithium of physics and electrochemistry, makes up the microcosmic embedding lithium inhomogeneities by the pre- embedding lithium of physics, it is long to solve the problems, such as that the pre- embedding lithium of electrochemistry depth takes.
Description
Technical field
Preparation method and the negative plate that is obtained by this method the present invention relates to a kind of pre- embedding lithium cathode sheet, belong to storage
Can devices field.
Background technology
Can the energy storage device of industrialized production mainly include lithium ion battery (LIB) and double layer capacitor (EDLC, that is, surpass
Level capacitor), achieve and be widely applied.Lithium ion battery has the advantages that energy density is high, and there is service life is short, work(
The low density shortcoming of rate, ultracapacitor have the advantages that output power, have extended cycle life, and ask there are energy density is low
Topic.
Lithium-ion capacitor (LIC) uses lithium ion battery and double layer capacitor mixed structure, and cathode uses activated carbon,
Anode is using materials such as graphite.Have the height output, long-life characteristics and lithium ion battery high-energy-density of double layer capacitor concurrently
Characteristic.
Whether lithium ion battery or lithium-ion capacitor, are directed to the pre- embedding lithium of anode.And pre- embedding lithium is equally two
The core technology of person.All there is irreversible embedding lithium in varying degrees during first charge-discharge in most of embedding lithium electrodes.Together
When, in lithium-ion capacitor the behavior also result in the anion with same molar in the irreversible suction in positive-active surface
It is attached.Body ion concentration decrease to some degree in electrolyte can be caused, and further results in the reduction of capacitance, most
The charge-discharge characteristic of lithium-ion capacitor can be seriously affected eventually.Therefore, a degree of pre- embedding lithium is carried out to anode, on the one hand may be used
To solve the above problems, on the other hand anode current potential can be made significantly to decline, so as to improve energy density and service life cycle.
The pre-embedding lithium method illustrated in patent CN101138058B, is using lithium metal as lithium source, uses the gold with through hole
Category paper tinsel is collector, and lithium metal is placed in anode relative position, utilizes the electrical potential difference between them to discharge by short circuit manner, from
And realize pre- embedding lithium.But cause preparation process will, it is necessary to strictly control the content of water and oxygen due to the active very high of lithium
Ask harsh;Multicellular metal foil is used at the same time, adds manufacture cost;In addition, short circuit manner is not easily-controllable, the inequality of embedding lithium can be caused
Even property.
Lithium piece is connected with anode at -30 DEG C~60 DEG C in patent CN103915262A, discharge 1h~60h.Lithium piece meeting
It is slowly dissolve into electrolyte and forms lithium ion, so as to is embedded into anode.This method uses lithium piece, adds operating environment
It is required that and lithium piece there is certain danger in itself, and pretreatment time is long.By positive and negative anodes in patent CN104681311A
It is connected on charge-discharge test instrument, once to be discharged after once charging for a circulation, 100 times repeatedly, reaches pre- embedding lithium
Method, this two kinds time-consuming, and the uniformity of embedding lithium is not good enough.
The pre- embedding lithium of electrochemistry can be very good to realize the uniform pre- embedding lithium of both macro and micro aspect, but shortcoming is to take long,
One layer of SEI film is inevitably produced on anode using the pre- embedding lithium of electrochemistry, this not only slow down the insertion of lithium with it is embedding go out
Speed, and increase the internal resistance of storing up electricity device.Shi Zhiqiang seminars (J.Zhang, H.Wu, J.Wang, J.Shi, Z.Shi,
Pre-lithiation design and lithium ion intercalation plateaus utilization of
mesocarbon microbeads anode for lithium-ion capacitor,Electrochimica Acta,182
(2015) 156-164) research is found in initial cycle, the formation of the oxidation peak surface SEI films of 1.2V.Tsinghua University Yuan Mei Rongs
Deng (M.Yuan, W.Liu, Y.Zhu, Y.Xu, Electrochemical Performance of Pre-Lithiated
Graphite as Negative Electrode in Lithium Ion Capacitors,Russian Journal of
Electrochemistry, 50 (2014) 1050-1057) research shows lithium-ion capacitor in the pre- embedding lithium 8h of 10C up to optimal
Effect.(T.S.Ong, H.Yang, Lithium Intercalation into the Mechanically Milled such as T.S.Ong
Natural Graphite-Electrochemical and Kinetic Characterization, 149 (2002) 1-8) grind
Study carefully and show in pre- embedding lithium technology, good granularity and crystallinity can be kept by being ground using disordered carbon under oxygen atmosphere.
Active material layer table is coated on after being mixed in patent CN104409224A with stabilized lithium metal and binding agent
Face, is arranged at negative electrode active material layer surface in patent CN104392846A with the mixture of lithium powder and lithium salts.The two methods,
It is the 3rd electrode similar to lithium layer, and equally used lithium metal due to being coated with two layers on same collector.
Patent CN104157463A describes a kind of new method of the pre- embedding lithium of anode, under protective atmosphere, by lithium powder with having
Machine catalyst, which is dissolved in organic solvent, obtains organolithium solution;Under protective atmosphere, by the solution spraying or brush to anode half
Finished surface.Patent CN102385991A forms lithium film in membrane surface by vacuum vapor deposition, makes lithium film and anode
Relatively, it is embedded into advance in anode with the lithium ion in lithium film.The two methods are complicated, and the amount of pre- embedding lithium is few.
Describe what is sprayed by coating machine coating or screen process press brush plating or flush coater in patent CN103021675A
Mode plates one layer of prelithiation slurry on negative electrode active material layer surface.This method forms prelithiation by brush plating or spraying method
Layer, method is simple, but equally exists the problem of pre- lithium-inserting amount is few.
In above physics pre-embedding lithium method, it can be very good to realize profound and macroscopically homogeneous pre- embedding lithium, still
Have a problem that to be exactly to be unable to reach microcosmic uniform mixing.
The content of the invention
The technical problem to be solved by the invention is to provide a kind of method of the pre- embedding lithium of anode, by the pre- embedding lithium of physics and
The pre- embedding lithium of electrochemistry combines, and makes up the microcosmic embedding lithium inhomogeneities by the pre- embedding lithium of physics, solves the pre- embedding lithium consumption of electrochemistry depth
When long problem.
To solve above technical problem, the invention discloses a kind of preparation method of pre- embedding lithium cathode sheet, including following step
Suddenly:
(1), active material admixture containing lithium salt is attached on porous collector by Physical and forms activity
Material layer, obtains the negative plate through the pre- embedding lithium of physics;
(2), the negative plate through the pre- embedding lithium of physics obtained by step (1) is inserted with carrying out perseverance in organic electrolyte containing lithium salt
Charge and discharge electric treatment is flowed, obtains the negative plate through the pre- embedding lithium of electrochemistry;
Further, step (1) described Physical includes any one in sputtering, coating, spraying or brushing.
Further, step (1) active material admixture containing lithium salt by mass percentage by representing as follows
Component is mixed to get:Active material 75%-85%, conductive agent 10%-20% and binding agent 5%-10%;The active material by
Obtained after the following component mixing represented by mass percentage under oxygen atmosphere through being fully ground:Disordered carbon 50%-70%,
Lithium salts 30%-50%;When using coating, spraying or the Physical brushed, organic solvent used is to include dimethyl carbonate
(DMC), diethyl carbonate (DEC), propene carbonate (PC), ethylene carbonate (EC), methyl ethyl carbonate (EMC), 1- fluoro carbon
Sour vinyl esters, 1- (trifluoromethyl) carboxylic acid vinyl ester, gamma-butyrolacton, acetonitrile, dimethoxy-ethane, tetrahydrofuran, dioxy
Penta ring, dichloromethane or sulfolane, one kind in 1-methyl-2-pyrrolidinone (NMP) or any two or more mixture;It is described
Ginding process includes:Mechanical attrition method, mechanical rod milling method (stainless steel bar), agate polishing etc.;The disordered carbon is unordered hard
Any one of matter carbon or unordered soft carbon;
Step (2) described organic electrolyte is lithium salts and the mixed liquor of organic solvent, and lithium salt scope is 1.0mol/L
~1.5mol/L.
Further, lithium salts used in step (1) for cobalt acid lithium, lithium titanate, lithium molybdate, tungstate lithium, LiMn2O4, lithium nickelate,
One kind or any two or more mixture in LiFePO4, lithium nickel cobalt dioxide, nickel ion doped or nickle cobalt lithium manganate.
Further, step (1) described collector uses copper, nickel or stainless steel, its thickness is 10 μm -50 μm, the porosity
For 30-70%;Step (1) the active material layer thickness is 30 μm -100 μm.
Further, step (1) described conductive agent is gas-phase growth of carbon fibre (VGCF), acetylene black, conductive carbon black
(Super P), graphitized carbon fibre or one kind in carbon nanotubes or any two or more mixture.
Further, the binding agent is polytetrafluoroethylene (PTFE) (PTFE), polyvinylidene fluoride (PVDF), acrylic acid, polyoxy
Change ethene, carboxymethylcellulose sodium (CMS), butadiene-styrene rubber (SBR), hydroxypropyl methyl cellulose, carboxylic styrene butadiene latex or poly- second
One kind or any two or more mixture in enol.
Further, the lithium salts in step (2) described organic electrolyte is LiClO4、LiPF6、LiAsF6、LiBF4、
LiCF3SO3、LiBOB、LiBFX、LiN(C2F5SO2)2、LiN(CF3SO2)2、LiN(FSO2)2、LiTFSI(LiN(SO2CF3)2)、
LiFSI(LiN(SO2F)2) one kind or any two or more mixture;
Organic solvent used in step (2) described organic electrolyte is dimethyl carbonate (DMC), diethyl carbonate (DEC), carbon
Acid propylene ester (PC), ethylene carbonate (EC), methyl ethyl carbonate (EMC), 1- fluoro carboxylic acid vinyl ester, 1- (trifluoromethyl) carbon
Sour vinyl esters, gamma-butyrolacton, acetonitrile, dimethoxy-ethane, tetrahydrofuran, dioxolanes, dichloromethane or sulfolane, N-
One kind or any two or more mixture in methyl pyrrolidone (NMP).
Further, the multiplying power scope of the constant current charge-discharge described in step (2) is 8C~12C, voltage range for 1.5V~
3.8V, discharge and recharge time are 6~10h.
The invention also discloses a kind of pre- embedding lithium cathode sheet being prepared according to preceding method.
Beneficial effects of the present invention are as follows:
The method that the present invention is combined using the pre- embedding lithium of the pre- embedding lithium of physics and electrochemistry, makes up by the microcosmic of the pre- embedding lithium of physics
Embedding lithium inhomogeneities, it is long to solve the problems, such as that the pre- embedding lithium of electrochemistry depth takes.
The present invention makes anode using physics pre-embedding lithium method, is applicable to lithium ion battery, lithium-ion capacitor, unordered
Carbon material is fully ground with lithium salts under oxygen atmosphere, this can not only realize that unordered carbon material and lithium salts are abundant macroscopically
Mixing, and can also ensure that unordered carbon material has the specific surface area of certain crystallinity and bigger, make the pre- embedding lithium of electrochemistry
In can suppress SEI films and formed.
The present invention carries out anode using electrochemistry pre-embedding lithium method the pre- embedding lithium of microcosmic point, suitable voltage range
Selection can reduce because of the part internal resistance that SEI films are formed and produce, and provide pre- embedding lithium to avoid the formation of SEI films
Speed.
The present invention carries out anode using electrochemistry pre-embedding lithium method the pre- embedding lithium of microcosmic point, the choosing of its pre- embedding lithium time
The cycle performance that the pre- embedding lithium of electrochemistry can be made by taking is in preferable states, improves the efficiency of the pre- embedding lithium of electrochemistry.
The present invention pre-embedding lithium method, can not only realize lithium depth insertion, but also can also realize lithium macroscopic view and
The insertion of microcosmic point.
Embodiment
With reference to embodiment, present disclosure is more specifically illustrated.The implementation of the present invention is not limited to following reality
Example is applied, the accommodation in any form made to the present invention or change all should be within the scope of the present invention.
Embodiment 1
(1) cladding process prepares lithium-ion capacitor anode
The unordered hard carbon and 40% Li of mass fraction 60%2TiO3Through mechanical ball grinding machine under oxygen atmosphere after mixing
Active material admixture containing lithium salt is obtained after being fully ground.
The active material of mass fraction 80%, 10% VGCF, 10% PVDF are stirred into 12h in appropriate NMP.
It is coated to using cladding process on the copper foil of 50% porosity, is then transferred into constant temperature 8h in 85 DEG C of vacuum drying chambers,
And a vacuum was taken out every two hours, obtains being attached with the negative plate through the pre- embedding lithium of physics of active material layer.
(2) the pre- embedding lithium of electrochemistry
The negative plate for preparing and not being compacted is put into the organic electrolyte of 1.5mol/L, wherein solute is
LiPF6, organic solvent EC:EMC volume ratio=3:7, constant current charge and discharge is carried out in 1.5V~3.8V voltage ranges with 10C multiplying powers
Electric 8h, checks lithium-inserting amount capacity retention ratio with the end of first.
Embodiment 2
(1) cladding process prepares lithium-ion capacitor anode
The unordered soft carbon and 50% LiMn of mass fraction 50%2O4Through mechanical ball grinding machine under oxygen atmosphere after mixing
Active material is obtained after being fully ground, obtains being attached with the negative plate through the pre- embedding lithium of physics of active material layer.
The active material of mass fraction 75%, 15% VGCF, 10% PVDF are stirred into 12h in appropriate NMP.
It is coated to using cladding process on the copper foil of 30% porosity, is then transferred into constant temperature 8h in 85 DEG C of vacuum drying chambers,
And took out a vacuum every two hours.
(2) the pre- embedding lithium of electrochemistry
The negative plate for preparing and not being compacted is put into the organic electrolyte of 1.2mol/L, wherein solute is
LiPF6, organic solvent EC:EMC volume ratio=3:7, constant current charge and discharge is carried out in 1.5V~3.8V voltage ranges with 8C multiplying powers
Electric 6h, checks lithium-inserting amount capacity retention ratio with the end of first.
Embodiment 3
(1) cladding process prepares lithium-ion capacitor anode
The unordered soft carbon and 30% LiNi of mass fraction 70%1/3Co1/3Mn1/3O2Passed through after mixing under oxygen atmosphere
Mechanical ball grinding machine obtains active material after being fully ground.
The active material of mass fraction 85%, 10% VGCF, 5% PVDF are stirred into 12h in appropriate NMP.
It is coated to using cladding process on the copper foil of 70% porosity, is then transferred into constant temperature 8h in 85 DEG C of vacuum drying chambers,
And a vacuum was taken out every two hours, obtains being attached with the negative plate through the pre- embedding lithium of physics of active material layer.
(2) the pre- embedding lithium of electrochemistry
The negative plate for preparing and not being compacted is put into the organic electrolyte of 1.5mol/L, wherein solute is
LiPF6, organic solvent EC:EMC volume ratio=3:7, constant current charge and discharge is carried out in 1.5V~3.8V voltage ranges with 12C multiplying powers
Electric 10h, checks lithium-inserting amount capacity retention ratio with the end of first.
In above example:
Charging and discharging currents | The discharge and recharge time | Lithium-inserting amount first | Capacity retention ratio | |
Embodiment 1 | 10C | 8h | 243mAh/g | 99.1% |
Embodiment 2 | 8C | 6h | 200.5mAh/g | 98.6% |
Embodiment 3 | 12C | 10h | 275.9mAh/g | 98.2% |
Claims (9)
1. a kind of preparation method of pre- embedding lithium cathode sheet, it is characterised in that this method comprises the following steps:
(1), active material admixture containing lithium salt be attached on porous collector by Physical form active material
Layer, obtains the negative plate through the pre- embedding lithium of physics;
(2), by step(1)Negative plate of the gained through the pre- embedding lithium of physics inserts progress constant current charge and discharge in organic electrolyte containing lithium salt
Electric treatment, obtains the negative plate through the pre- embedding lithium of electrochemistry,
Step(1)The active material admixture containing lithium salt is mixed to get by the following component represented by mass percentage:
Active material 75%-85%, conductive agent 10%-20% and binding agent 5%-10%;The active material by mass percentage by being represented
Following component mixing after obtained under oxygen atmosphere through being fully ground:Disordered carbon 50%-70%, lithium salts 30%-50%;
Step(2)The organic electrolyte for lithium salts and organic solvent mixed liquor, lithium salt scope for 1.0mol/L ~
1.5mol/L。
2. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(1)The Physical bag
Include any one in sputtering, spraying or brushing.
3. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(1)Lithium salts used is cobalt
Sour lithium, lithium titanate, lithium molybdate, tungstate lithium, LiMn2O4, lithium nickelate, LiFePO4, lithium nickel cobalt dioxide, nickel ion doped or nickel cobalt mangaic acid
One kind or any two or more mixture in lithium.
4. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(1)The collector is adopted
With copper, nickel or stainless steel, its thickness is 10 μm -50 μm, porosity 30-70%;Step(1)The active material layer thickness is
30μm-100μm。
5. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(1)The conductive agent is
One kind or any two or more in gas-phase growth of carbon fibre, acetylene black, conductive carbon black, graphitized carbon fibre or carbon nanotubes
Mixture.
6. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:The binding agent is polytetrafluoroethyl-ne
Alkene, polyvinylidene fluoride, acrylic acid, polyethylene glycol oxide, carboxymethylcellulose sodium, butadiene-styrene rubber, hydroxypropyl methyl cellulose, carboxylic
One kind or any two or more mixture in base butadiene-styrene latex or polyvinyl alcohol.
7. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(2)The organic electrolysis
Lithium salts in liquid is LiClO4、LiPF6、LiAsF6、LiBF4、LiCF3SO3、LiBOB、LiBFX、LiN(C2F5SO2)2、LiN
(CF3SO2)2、LiN(FSO2)2、LiTFSI(LiN(SO2CF3)2)、LiFSI(LiN(SO2F)2) one kind or any two or more
Mixture;
Step(2)Organic solvent used in the organic electrolyte is dimethyl carbonate, diethyl carbonate, propene carbonate, carbonic acid
Vinyl acetate, methyl ethyl carbonate, 1- fluoro carboxylic acid vinyl ester, 1- (trifluoromethyl) carboxylic acid vinyl ester, gamma-butyrolacton, acetonitrile,
One kind or any in dimethoxy-ethane, tetrahydrofuran, dioxolanes, dichloromethane or sulfolane, 1-methyl-2-pyrrolidinone
Two or more mixtures.
8. the preparation method of pre- embedding lithium cathode sheet according to claim 1, it is characterised in that:Step(2)The constant current is filled
The multiplying power scope of electric discharge is 8C ~ 12C, and voltage range is 1.5V ~ 3.8V, and the discharge and recharge time is 6 ~ 10h.
A kind of 9. pre- embedding lithium cathode sheet being prepared according to claim 1-8 any one claim the methods.
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