Method for manufacturing non-aqueous secondary battery electrode
US-2024332484-A1 · Oct 3, 2024 · US
US2018175366A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018175366-A1 |
| Application number | US-201615738863-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 27, 2016 |
| Priority date | Jun 26, 2015 |
| Publication date | Jun 21, 2018 |
| Grant date | — |
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A method of making an electrode for an electrochemical cell includes the step of providing an electrode composite comprising from 70-98% active material, from 0-10% conductive material additives, and from 2-20% polymer binder, based on the total weight of the electrode composite. The electrode composite is mixed and then compressed the electrode composite into an electrode composite sheet. The electrode composite sheet is applied to a current collector with pressure to form an electrode, wherein the electrode possesses positive characteristics for adhesion according to ASTM standard test D3359-09e2, entitled Standard Test Methods for Measuring Adhesion by Tape Test, and wherein the electrode composite sheet and the electrode possess positive characteristics for flexibility according to the Mandrel Test. The binder can be a single nonfluoropolymer binder. Dry process electrodes are also disclosed.
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We claim: 1 . A method of making an electrode for an electrochemical cell, comprising the steps of: providing an electrode composite comprising from 70-98% active material, from 0-10% conductive material additives, and from 2-20% polymer binder, based on the total weight of the electrode composite; mixing the electrode composite; compressing the electrode composite into an electrode composite sheet; applying the electrode composite sheet to a current collector with pressure to form an electrode, wherein the electrode possesses positive characteristics for adhesion according to ASTM standard test D3359-09e2, entitled Standard Test Methods for Measuring Adhesion by Tape Test, and wherein the electrode composite sheet and the electrode possess positive characteristics for flexibility according to the Mandrel Test. 2 . The method of claim 1 , wherein the binder is a single nonfluoropolymer binder. 3 . The method of claim 1 , wherein the active material comprises at least 80% by weight of the electrode composite. 4 . The method of claim 1 , wherein the active material is a positive electrode active material comprising at least one selected from the group consisting of LiCoO 2 , LiNi 1/3 Co 1/3 Mn 1/3 O 2 , LiNi 0.8 Co 0.15 Al 0.05 O 2 , Li 1+x Ni 1/3 Co 1/3 Mn 1/3 O 2 , where 0<x<0.8, LiMn 2 O 4 , LiFePO 4 , Li 2 Mn 2 O 4 , LiNiCoAlO 2 , LiNi y Co x M z O, where M=Mn, Al, Sn, In, Ga or Ti and 0.15<x<0.5, 0.5<y<0.8 and 0<z<0.15, Li[Li (1−2y)/3 Ni y Mn (2−y)/3 ]O 2 , Li[Li (1−y)/3 Co y Mn (2−2y)/3 ]O 2 and Li[Ni y Co 1−2y Mn y ]O 2 , 0<y<0.5, LiNiCoO 2 .MnO 2 , lithium rich compounds Li 1+y (Ni 1/3 Co 1/3 Mn 1/3 ) 1−y O 2 , where y=x/(2+x) and x=0-0.33, and xLi 2 MnO 3 (1−x)Li(NiCoMn)O 2 and Li (1+y) (Ni 0.5 Co 0.2 Mn 0.3 ) 1−y O 2 , where y=x/(2+x) and x=0-0.33, and LiMPO 4 , where M is at least one selected from the group consisting of V, Cr, Mn, Fe, Co, and Ni. 5 . The method of claim 1 , wherein the active material is an anode active material comprising at least one selected from the group consisting of carbon, hard carbon, soft carbon, synthetic graphite, natural graphite, mesophase carbon microbeads, SnO 2 , SnO, TiO 2 , Li 4 Ti 5 O 12 , LiTi 2 O 4 , SiO 2 and silicon. 6 . The method of claim 1 , wherein the conductive material additive comprises at least one selected from the group consisting of carbon black, acetylene black, carbon nanotube, carbon nanofiber, carbon fibers, coke, high surface area carbon, graphite, metal particles, and conducting polymer. 7 . The method of claim 1 , wherein the binder material is a soft polymer comprising at least one selected from the group consisting of acrylic-based soft polymers, isobutylene-based soft polymers, diene-based soft polymers, silicon-containing soft polymers, olefin-based soft polymers, vinyl-based soft polymers, epoxy-based soft polymers, fluorine-containing soft polymers, natural rubbers, polypeptides, proteins, polyester-based thermoplastic elastomers, vinyl chloride-based thermoplastic elastomers, and polyamide-based thermoplastic elastomers. 8 . The method of claim 1 , wherein the binder material is a soft polymer comprising at least one selected from the group consisting of homopolymers or copolymers of acrylic acid or methacrylic acid derivatives, polybutyl acrylate, polybutyl methacrylate, polyhydroxyethyl methacrylate, polyacrylamide, polyacrylonitrile, butyl acrylate-styrene copolymers, butyl acrylate-acrylonitrile copolymers, butyl acrylate-acrylonitrile-glycidyl methacrylate copolymers, polyisobutylene, isobutylene-isoprene rubber, isobutylene-styrene copolymers, polybutadiene, polyisoprene, butadiene-styrene random copolymers, isoprene-styrene random copolymers, acrylonitrile-butadiene copolymers, acrylonitrile-butadiene-styrene copolymers, butadiene-styrene-block copolymers, styrene-butadiene-styrene-block copolymers, isoprene-styrene-block copolymers, styrene-isoprene-styrene-block copolymers, dimethylpolysiloxane, diphenylpolysiloxane, dihydroxypolysiloxane, liquid polyethylene, polypropylene, poly-1-butene, ethylene-α-olefin copolymers, propylene-α-olefin copolymers, ethylene-propylene-diene copolymers (EPDM), ethylene-propylene-styrene copolymers, polyvinyl alcohol, polyvinyl acetate, polyvinyl stearate, vinyl acetate-styrene copolymers, polyethylene oxide, polypropylene oxide, epichlorohydrin rubbers, vinylidene fluoride-based rubbers, tetrafluoroethylene-propylene rubbers, poly(2-methoxyethoxyethoxyethylene), styrene butadiene rubber (SBR), butadiene-acrylonitrile, rubber (NBR), hydrogenated NBR (HNBR), epichlorhydrin rubber (CHR) and acrylate rubber (ACM). 9 . The method of claim 1 , wherein the binder material comprises asoft polymer comprising at least one selected from the group consisting of soft polymers having a crosslinked structure, and soft polymers having a functional group in the range of about 3-12% by weight of the soft polymer, wherein the functional group is at least one selected from the group consisting of an unsaturated group, a carboxyl group, a hydroxy group, an amino group, and an epoxy group. 10 . The method of claim 1 , wherein the mixing step comprises at least one selected from the group consisting of rubber kneading, two roll milling, tumbling mixing, air jet mixing, mixture grinding, high-shear mixing, V-blender mixing, mixing by a screw-driven mass mixer, double-cone mixing, drum mixing, conical mixing, two-dimensional mixing, double Z-arm blending, ball-milling, and fluidized-bed blending. 11 . The method of claim 1 , wherein the mixing step further comprises the step of providing a solvent and mixing the solvent with the binder at a binder to solvent ratio of from 100:1 to 1:100 by weight, and adding the active material particles and carbonaceous conductors to binder solution in a ratio of from 10:1 to 1:5, by weight. 12 . The method of claim 11 , wherein the solvent comprises at least one selected from the group consisting of a hydrocarbon, ketone, naphtha, acetate, acrylonitrile, toluene, xylene, alcohol, or esters. 13 . The method of claim 1 , wherein said electrode composite sheet has a thickness of less than 200 microns. 14 . The method of claim 1 , wherein said electrode composite sheet has a thickness of from 50-150 microns. 15 . The method of claim 1 , wherein the electrode composite sheet comprises less than 50% solvent, by weight of the electrode composite sheet. 16 . The method of claim 1 , wherein the binder material comprises at least two binder materials. 17 . The method of claim 1 , further comprising the step of forming a binder coating of a Li ion transporting material on the surface of the active materials. 18 . The method of claim 17 , wherein the binder materials comprise at least one selected from the group consisting of homopolymers and copolymers of polyvinylidenefluoride (PVDF), polyolefinic materials with electron withdrawing substituents, and water soluble binders. 19 . The method of claim 17 , wherein the binders comprise at least one selected from the group consisting of copolymers of vinylidene fluoride and hexafluoropropylene, poly(methyl methacrylate) (PMMA), polyacrylic acids, polyacrylronitrile (PAN), polyvinyl chloride (PVC), poly vinylalcohols (PVA), polyvinyl pyrrolidone, polyethylene oxides (PEO), polyethylene glycols, polyacrylamide (PAAm), poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, polyactic acid (PLA), polyacrylic acid (PAA), polysuccinic acid, poly maleic acid and anhydride, poly furoic(pyromucic aci
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