# US 11,908,592 B2 · Flexible electrode and fabrication method therefor > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 11,908,592 B2 - Document ID: US11908592B2 - Status: Granted - Kind: B2 - Application number: 17/165,273 - Filed: 2021-02-02 - Published: 2021-08-19 - Granted: 2024-02-20 - Earliest claimed: 2020-02-18 - Assignees: National Synchrotron Radiation Research Center - Applicants: National Synchrotron Radiation Research Center - Inventors: Wei-Tsung Chuang; Rong-Hao Guo; Ming-Jay Deng - Web page: https://patentgrep.com/patent/US11908592B2 ## CPC - H01B 1/124: {Intrinsically conductive polymers} - B29C 45/0001: {characterised by the choice of material} - B29C 45/17: Component parts, details or accessories; Auxiliary operations - C25D 7/0614: {Strips or foils} - H01B 1/08: oxides - H01B 1/122: {Ionic conductors} - B29K 2509/02: Ceramics - B29L 2031/3406: {Components, e.g. resistors} - C25D 5/56: of plastics - H01B: CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES (selection for magnetic properties H01F1/00; waveguides H01P {; printed circuits H05K}) - B29C: SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING (making preforms B29B11/00; making laminated products by combining previously unconnected layers which become one product whose layers will remain together B32B37/00 - B32B41/00) - C25D: PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR - B29K: INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR {MOULDS, } REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS - B29L: INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES ## Abstract A flexible electrode and a fabrication method therefor are provided. The flexible electrode is formed by mixing organic-soft-matrix with inorganic-hard-material. The inorganic-hard-material is composed of silicate lamellar blocks and electrochemically active materials. Each of the silicate lamellar blocks is formed by multiple stacked nano-scaled sheet-like silicate lamellae. The organic-soft-matrix includes conductive polymer and binder. The binder is water-soluble and ionically conductive. The flexible electrode has a floor-ramp like opened-perforated layer structure formed by hierarchically aggregated inorganic silicate lamellar blocks, and pores of the opened-perforated layer structure are filled with the organic-soft-matrix, so as to form a network channel structure having organic phase and inorganic phase interlaced with each other. The floor-ramp like opened-perforated layer structure composed of aggregated inorganic silicate lamellar blocks contributes to stiffness of the flexible electrode, and the conductive polymer and the binder in the organic-soft-matrix respectively form electron channels and ion channels in the flexible electrode. ## Claims ### Claim 1 A flexible electrode, comprising: an organic soft matrix comprising a conductive polymer and a binder, wherein the binder is water-soluble and ionically conductive; and an inorganic hard material comprising an opened-perforated layer structure formed by a plurality of aggregated silicate lamellar blocks, wherein the organic soft matrix is filled in open pores of the opened-perforated layer structure to form a three-dimensional network structure having an organic phase domain and an inorganic phase domain interlaced with each other, and each of the aggregated silicate lamellar blocks comprises a plurality of silicate lamellae, wherein the silicate lamellae are stacked face-to-face in a stacking direction parallel to a thickness direction of the organic soft matrix; wherein a content of the silicate lamellae ranges from 25 wt % to 35 wt %, a content of the binder ranges from 15 wt % to 25 wt %, and a content of the conductive polymer ranges from 45 wt % to 55 wt %. ### Claim 2 (depends on 1) The flexible electrode according to claim 1, wherein a first capacitively active material is adsorbed on a surface of at least a part of the silicate lamellae, wherein the first capacitively active material is transition metal ions. ### Claim 3 (depends on 2) The flexible electrode according to claim 2, wherein the first capacitively active material is selected from a group composed of transition metal nitrate, transition metal sulfate, transition metal acetate, transition metal chloride, and a combination thereof. ### Claim 4 (depends on 3) The flexible electrode according to claim 3, wherein the organic soft matrix further comprises a second capacitively active material, wherein the second capacitively active material is transition metal oxide particles. ### Claim 5 (depends on 4) The flexible electrode according to claim 4, wherein the second capacitively active material is selected from a group composed of manganese oxide particles, cobalt oxide particles, vanadium oxide particles, and a combination thereof. ### Claim 6 (depends on 1) The flexible electrode according to claim 1, wherein an average particle size of the silicate lamellae ranges from 100 nm to 400 nm. ### Claim 7 (depends on 1) The flexible electrode according to claim 1, wherein the binder is selected from a group composed of vinyl alcohol, polyethylene oxide, polyacrylamide, poly vinyl acetate, poly vinyl pyrrolidone, and a combination thereof. ### Claim 8 (depends on 1) The flexible electrode according to claim 1, wherein the organic soft matrix further comprises a second capacitively active material, wherein the second capacitively active material is transition metal oxide particles. ### Claim 9 (depends on 8) The flexible electrode according to claim 8, wherein the second capacitively active material is selected from a group composed of manganese oxide particles, cobalt oxide particles, vanadium oxide particles, and a combination thereof. ### Claim 10 (depends on 1) A fabrication method for the flexible electrode of claim 1, the method comprising: (a) providing the silicate lamellae, the binder, and the conductive polymer; (b) uniformly dispersing the silicate lamellae in water to form a suspension; (c) uniformly mixing the binder and the conductive polymer of step (a) with the suspension of step (b) to form a mixed solution, wherein a viscosity of the mixed solution ranges from 50 mPa·s to 500 mPa·s; and (d) injecting the mixed solution into a mold or applying the mixed solution on a template before drying. ### Claim 11 (depends on 10) The fabrication method for the flexible electrode according to claim 10, wherein before step (a), the method further comprises: immersing the silicate lamellae in a 1 M aqueous solution of a salt of a first capacitively active material; and passing the aqueous solution of the salt of the first capacitively active material in which the silicate lamellae are immersed through a screen or centrifuging the aqueous solution to obtain silicate lamellar blocks on which first capacitively active ions are adsorbed. ### Claim 12 (depends on 11) The fabrication method for the flexible electrode according to claim 11, wherein the salt of the first capacitively active material is a transition metal salt. ### Claim 13 (depends on 12) The fabrication method for the flexible electrode according to claim 12, wherein the first capacitively active material is selected from a group composed of transition metal nitrate, transition metal sulfate, transition metal acetate, transition metal chloride, and a combination thereof of. ### Claim 14 (depends on 13) The fabrication method for the flexible electrode according to claim 13, wherein after step (d), the method further comprises: adding a second capacitively active material to the binder through electroplating. ### Claim 15 (depends on 14) The fabrication method for the flexible electrode according to claim 14, wherein the second capacitively active material is selected from a group composed of manganese oxide, cobalt oxide, vanadium oxide, and a combination thereof. ### Claim 16 (depends on 11) The fabrication method for the flexible electrode according to claim 11, wherein the silicate lamellae are immersed in the aqueous solution of the salt of the first capacitively active material at a room temperature for more than 12 hours. ### Claim 17 (depends on 10) The fabrication method for the flexible electrode according to claim 10, wherein an average particle size of the silicate lamellae ranges from 100 nm to 400 nm. ### Claim 18 (depends on 10) The fabrication method for the flexible electrode according to claim 10, wherein the binder is selected from a group composed of vinyl alcohol, polyethylene oxide, polyacrylamide, poly vinyl acetate, poly vinyl pyrrolidone, and a combination thereof. ### Claim 19 (depends on 10) The fabrication method for the flexible electrode according to claim 10, wherein after step (d), the method further comprises: adding a second capacitively active material to the binder through electroplating. ### Claim 20 (depends on 19) The fabrication method for the flexible electrode according to claim 19, wherein the second capacitively active material is selected from a group composed of manganese oxide, cobalt oxide, vanadium oxide, and a combination thereof.