Solid electrolyte composition, electrode sheet for battery using the same, all solid state secondary battery, and method for manufacturing electrode sheet for battery and all solid state secondary battery
US-2017301950-A1 · Oct 19, 2017 · US
US11631839B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11631839-B2 |
| Application number | US-201816312812-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 22, 2018 |
| Priority date | Mar 22, 2017 |
| Publication date | Apr 18, 2023 |
| Grant date | Apr 18, 2023 |
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An electrode for a solid state battery is provided. The electrode active material layer of the electrode shows improved mechanical properties, such as elasticity or rigidity, of the electrode layer through the crosslinking of a binder resin. Thus, it is possible to inhibit or reduce the effect of swelling and/or shrinking of the electrode active material during charging/discharging. Therefore, the interfacial adhesion between the electrode active material layer and an electrolyte layer and the interfacial adhesion between the electrode active material layer and a current collector are maintained to a high level to provide a solid state battery having excellent cycle characteristics.
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What is claimed is: 1. A method for manufacturing an electrode, comprising the following sequential steps (S 10 )-(S 40 ) of: (S 10 ) preparing a slurry for forming an electrode layer comprising an electrode active material, a binder resin, a crosslinking initiator, an inorganic solid electrolyte and a solvent; (S 20 ) applying the slurry for forming an electrode layer to the surface of a current collector, followed by drying, to form an electrode layer (a); (S 30 ) pressing the electrode layer (a) to form an electrode layer (a′); and (S 40 ) warming the electrode layer (a′) to form an electrode layer (a″), wherein the drying in step (S 20 ) is carried out at room temperature where no crosslinking is initiated, and step (S 40 ) is carried out at a temperature range of 45° C.−150° C. where crosslinking of the electrode layer (a″) is initiated and performed; wherein the binder resin comprises a rubber-based binder resin; wherein the crosslinking initiator is an organic peroxide-based crosslinking initiator which is at least one selected from the group consisting of dicumyl peroxide (DCP), di(2-ethylhexyl)peroxydicarbonate, di(4-t-butylcyclohexyl)peroxydicarbonate, di-secbutylperoxydicarbonate, t-butylperoxyneodecanoate, t-hexylperoxy pivalate, t-butylperoxy pivalate, dilauroyl peroxide, di-n-octanoyl peroxide, 1,1,3,3,-tetramethylbutylperoxy-2-ethylhexanoate, di(4-methylbenzoyl) peroxide, dibenzoyl peroxide, t-butylperoxyisobutyrate and 1,1-di(t-hexylperoxy)cyclohexane; wherein the inorganic solid electrolyte comprises a sulfide-based solid electrolyte; wherein the solvent in step (S 10 ) is a nonpolar solvent; and wherein the solvent in step (S 10 ) excludes polar solvents. 2. The method for manufacturing an electrode according to claim 1 , wherein the slurry further comprises a conductive material. 3. The method for manufacturing an electrode according to claim 1 , wherein the organic peroxide-based crosslinking initiator is at least dicumyl peroxide (DCP). 4. The method for manufacturing an electrode according to claim 1 , wherein step (S 40 ) is carried out under vacuum. 5. An electrode for a solid state battery obtained by the method as defined in claim 1 , which comprises the current collector and the electrode layer (a″) formed on at least one surface of the current collector, wherein the electrode layer (a″) comprises the electrode active material, the inorganic solid electrolyte and the binder resin, the electrode active material particles and the inorganic solid electrolyte particles in the electrode layer are fixed and integrated through surface-surface binding and point-point binding by the binder resin, and the binder resin is further crosslinked. 6. The electrode for a solid state battery according to claim 5 , wherein the rubber-based binder resin comprises at least one selected from the group consisting of natural rubber, butyl rubber, bromobutyl rubber, chlorobutyl rubber, styrene isoperene rubber, styrene-ethylene-butyrene-styrene rubber, acrylonitrile-butadiene-styrene rubber, polybutadiene rubber, nitrile butadiene rubber, styrene butadiene rubber, styrene butadiene styrene (SBS) rubber, ethylene propylene diene monomer (EPDM) rubber and hydrogenated nitrile butadiene rubber (HNBR). 7. The method for manufacturing an electrode according to claim 1 , wherein the nonpolar solvent is selected from the group consisting of pentane, cyclohexane, toluene, benzene, xylene, hexane, anisole, heptane, chloroform, diethyl ether and butyl butyrate, and mixtures thereof. 8. The method for manufacturing an electrode according to claim 1 , wherein the nonpolar solvent is toluene, xylene, or a mixture thereof. 9. The method for manufacturing an electrode according to claim 1 , wherein the rubber based binder resin comprises at least one selected from the group consisting of natural rubber, butyl rubber, bromobutyl rubber, chlorobutyl rubber, styrene isoperene rubber, styrene-ethylene-butyrenestyrene rubber, acrylonitrile-butadiene-styrene rubber, polybutadiene rubber, nitrile butadiene rubber, styrene butadiene rubber, styrene butadiene styrene (SBS) rubber, ethylene propylene diene monomer (EPDM) rubber and hydrogenated nitrile butadiene rubber (HNBR). 10. The method for manufacturing an electrode according to claim 1 , wherein the rubber based binder resin comprises at least one selected from the group consisting of vinylidene fluorideco-hexafluoropropylene, styrene butadiene rubber and mixtures thereof. 11. The method for manufacturing an electrode according to claim 1 , wherein the sulfide based solid electrolyte is selected from the group consisting of lithium sulfide, silicon sulfide, germanium sulfide and boron sulfide. 12. The method for manufacturing an electrode according to claim 1 , wherein the sulfide based solid electrolyte is selected from the group consisting of Li 2 S—P 2 S 5 , Li 3.833 Sn 0.833 AS 0.166 S 4 , Li 4 SnS 4 , Li 3.25 Ge 0.25 P 0.75 S 4 , B 2 S 3 —Li 2 S, xLi 2 S-(100-x)P 2 S 5 (x=70-80), Li 2 S—SiS 2 —Li 3 N, Li 2 S—P 2 S 5 —LiI, Li 2 S—SiS 2 —LiI, Li 2 S—B 2 S 3 —LiI, Li 3 N, LISICON, LIPON (Li 3+y PO 4−x N x ), Thio-LISICON (Li 3.25 Ge 0.25 P 0.75 S 4 ), and Li 2 O—Al 2 O 3 —TiO 2 —P 2 O 5 (LATP).
Energy storage using batteries · CPC title
Processes of manufacture · CPC title
Binders · CPC title
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
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