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Power Your Innovations with a Breakthrough in Electrode Manufacturing
Introduction
Imagine a world where the production of high-performance electrodes is not only more efficient but also environmentally friendly. Our innovative dry process method for producing electrodes for electrochemical devices is designed to revolutionize the way batteries, capacitors, and other energy storage systems are manufactured. This method isn’t just an incremental improvement; it’s a leap forward that can redefine your product’s efficiency, sustainability, and cost-effectiveness.
The Challenge
Traditional methods of electrode production involve wet processes that require solvents, extensive drying times, and significant energy input. These methods can be cumbersome, costly, and harmful to the environment, making it difficult to meet the growing demand for sustainable and scalable energy solutions.
The Solution
Our dry process method eliminates the need for solvents, drastically reducing production time and energy consumption. This method not only speeds up manufacturing but also reduces the environmental impact, aligning your production with the growing demand for greener technologies. By licensing this technology, you can streamline your manufacturing process, lower costs, and enhance the sustainability of your products.
Why This Innovation Matters
- Efficiency and Cost Savings: By cutting out the need for solvents and reducing energy usage, this dry process method significantly lowers production costs. This makes it easier to scale up production and meet the increasing demand for advanced electrochemical devices.
- Environmental Sustainability: With no solvents to dispose of and less energy required, this method supports your commitment to sustainability. It helps reduce your carbon footprint while still delivering high-performance products.
- Superior Product Performance: The electrodes produced using this method exhibit exceptional electrochemical properties, ensuring that your devices will be at the cutting edge of performance and reliability.
The Opportunity
Licensing this technology means more than just adopting a new production method—it’s about embracing the future of energy storage innovation. This dry process method offers you the chance to lead in an industry that’s rapidly evolving, delivering products that are not only efficient and cost-effective but also aligned with the global push towards sustainability.
Seize the opportunity to transform your production process and elevate your product offerings. License this technology today and be a part of the energy revolution.
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.
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, said composite being devoid of polytetrafluoroethylene;
mixing the electrode composite, wherein the mixing step further comprises the step of providing a solvent for the binder and dissolving the binder in the solvent to provide a binder solution, and then adding the active material particles and conductive material additives to the binder solution in a ratio of from 10:1 to 1:5, by weight;
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 LiCoO2, LiNi1/3Co1/3Mn1/3O2, LiNi0.8Co0.15Al0.05O2, Li1+xNi1/3Co1/3Mn1/3O2, where 0<x<0.8, LiMn2O4, LiFePO4, Li2Mn2O4, LiNiCoAlO2, LiNiyCoxMzO, 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)/3NiyMn(2−y)/3]O2, Li[Li(1−y)/3CoyMn(2−2y)/3]O2 and Li[NiyCo1−2yMny]O2, 0<y<0.5, LiNiCoO2.MnO2, lithium rich compounds Li1+y(Ni1/3Co1/3Mn1/3)1−yO2, where y=x/(2+x) and x=0-0.33, and xLi2MnO3(1−x)Li(NiCoMn)O2 and Li(1+y)(Ni0.5Co0.2Mn0.3)1−yO2, where y=x/(2+x) and x=0-0.33, and LiMPO4, 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, SnO2, SnO, TiO2, Li4Ti5O12, LiTi2O4, SiO2 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, di methylpolysiloxane, 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 a polymer comprising at least one selected from the group consisting of polymers having a crosslinked structure, and polymers having a functional group in the range of about 3-12% by weight of the 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 solvent comprises at least one selected from the group consisting of a hydrocarbon, ketone, naphtha, acetate, acrylonitrile, toluene, xylene, alcohol, or esters.
12. The method of claim 1, wherein said electrode composite sheet has a thickness of less than 200 microns.
13. The method of claim 1, wherein said electrode composite sheet has a thickness of from 50-150 microns.
14. The method of claim 1, wherein the electrode composite sheet comprises less than 50% solvent, by weight of the electrode composite sheet.
15. The method of claim 1, wherein the binder material comprises at least two binder materials.
16. The method of claim 1, further comprising the step of forming a binder coating of a Li ion transporting binder material on the surface of the active materials.
17. The method of claim 16, wherein the Li ion transporting binder materials comprises 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.
18. The method of claim 16, wherein the Li ion transporting binder material comprises 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, polylactic acid (PLA), polyacrylic acid (PAA), polysuccinic acid, poly maleic acid and anhydride, poly furoic(pyromucic acid), poly fumaric acid, poly sorbic acid, poly linoleic acid, poly linolenic acid, poly glutamic acid, poly methacrylic acid, poly licanic acid, poly glycolic acid, polyaspartic acid, poly amic acid, poly formic acid, poly acetic acid, poly propionic acid, poly butyric acid, poly sebacic acid, acrylic acid-type water-soluble polymers, maleicanhydride-type water-soluble polymers, poly(N-vinyl amides), polyacrylamides, N-methylacrylamide, N-ethyl acrylamide, N,N-dimethyl acrylamide, and N,Ndiethylacrylamide, poly(hydroxy-ethyl methacrylate), polyesters, poly(ethyl oxazolines), poly(oxymethylene), poly(vinyl methyl ether), poly(styrene sulfonic acid), poly(ethylenesulfonic acid), poly(vinyl phosphoric) acid, poly(maleic acid), starch, cellulose, protein, polysaccharide, dextrans, tannin, lignin, polyethylene-polypropylene copolymer, copolymers of poly(acrylonitrile-co-acrylamide), co-polymer of polystyrenebutadiene rubber and poly(acrylonitrile-co-acrylamide), or mixtures or co-polymers thereof, carboxymethyl cellulose (CMC), poly vinylalcohols (PVA), polyacrylic acids (PAA), polystyrenebutadiene rubber (SBR), PEO, or co-polymers of polyacrylonitrile, polyethylene oxides (PEO) and polyacrylamide (PAAm), poly vinylalcohols (PVA) and polyacrylamide (PAAm), or PEO and polyacrylronitrile (PAN), or co-polymers or mixtures thereof.
19. The method of claim 16, wherein the Li ion transporting 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).
20. The method of claim 1, wherein the compressing step comprises passing the electrode composite through a pair of opposing rollers.
21. The method of claim 20, wherein the electrode composite sheet is passed through a plurality of pairs of rollers, the spacing between the rollers decreasing for each subsequent pair of rollers.
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Title
Dry process method for producing electrodes for electrochemical devices and electrodes for electrochemical devices
Inventor(s)
Jian-Ping Zheng, Qiang Wu
Assignee(s)
Florida State University Research Foundation Inc
Patent #
10923707
Patent Date
February 16, 2021