Filter-press photoelectrochemical water oxidation and co2 reduction cell
US-2018023203-A1 · Jan 25, 2018 · US
US2022127736A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022127736-A1 |
| Application number | US-201917295894-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 21, 2019 |
| Priority date | Nov 21, 2018 |
| Publication date | Apr 28, 2022 |
| Grant date | — |
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The present invention relates to an electrolysis device comprising an anode and a cathode, wherein the anode and the cathode each are an electrode comprising an electrically conductive support of which at least a part of the surface is covered by a metal deposit of copper, wherein the surface of the metal deposit is in an oxidized, sulfurated, selenated and/or tellurized form and the metal deposit has a specific surface area greater than or equal to 1 m 2 /g. The present invention relates also to a method for reducing CO 2 into hydrocarbons using an electrolysis device according to the invention. The method according to the invention comprises: a) providing an electrolysis device according to the invention; b) exposing the cathode of said electrolysis device to a CO 2 -containing aqueous catholyte solution; c) exposing the anode of said electrolysis device to an aqueous anolyte solution; and d) applying an electrical current between the anode and the cathode in order to reduce the carbon dioxide into hydrocarbons.
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1 . An electrolysis device comprising an anode and a cathode, wherein the anode and the cathode each are an electrode comprising an electrically conductive support of which at least a part of the surface is covered by a metal deposit of copper, wherein the metal deposit may comprise other metals than copper selected from iron, nickel, zinc, cobalt, manganese, titanium, gold, silver, lead, ruthenium, iridium and a mixture thereof, said other metals representing no more than 50% by weight of the metal deposit, wherein the surface of the metal deposit is in an oxidized form and the metal deposit has a specific surface area greater than or equal to 1 m 2 /g, the specific surface area being determined by the Brunauer, Emmett and Teller (BET) method. 2 . The electrolysis device according to claim 1 , wherein said other metals represent no more than 30% by weight of the metal deposit. 3 . The electrolysis device according to claim 1 , wherein the electrically conductive support comprises an electrically conductive material selected from a metal; a metal oxide; a metal sulphide; carbon; a semiconductor; and a mixture thereof. 4 . The electrolysis device according to claim 1 , wherein the metal deposit is dendritic. 5 . The electrolysis device according to claim 1 , wherein the metal deposit has a thickness comprised between 10 μm and 2 mm. 6 . The electrolysis device according to claim 1 , wherein the metal deposit has a specific surface area comprised between 1 m 2 /g and 500 m 2 /g. 7 . The electrolysis device according to claim 1 , wherein the metal deposit has a porous structure with an average pore size of between 10 μm and 500 μm, the average pore size being determined by means of photographs obtained by Scanning Electron Microscopy (SEM). 8 . The electrolysis device according to claim 1 , wherein the distance between the anode and the cathode is comprised between 15 and 0.1 cm. 9 . The electrolysis device according to claim 1 , comprising an anodic compartment and a cathodic compartment separated by a membrane. 10 . The electrolysis device according to claim 9 , wherein the anodic compartment and the cathodic compartment each comprise an inlet and an outlet intended to allow the circulation of an anolyte solution through the anodic compartment and a catholyte solution through the cathodic compartment respectively. 11 . The electrolysis device according to claim 10 , wherein the anodic compartment and the cathodic compartment each comprise a flow spacer linked to the inlet and to the outlet of the anodic or cathodic compartment respectively, the flow spacer being a system that guides the flow of the anolyte or catholyte solution from the inlet to the outlet of the anodic or cathodic compartment respectively. 12 . The electrolysis device according to claim 11 , wherein the flow spacer is separated from the anode or the cathode and from the membrane by a sealing ring. 13 . The electrolysis device according to claim 1 , coupled to a source of an electrical energy. 14 . A method for reducing carbon dioxide (CO 2 ) into hydrocarbons comprising the following steps: a) providing an electrolysis device according to claim 1 ; b) exposing the cathode of said electrolysis device to a CO 2 -containing aqueous catholyte solution; c) exposing the anode of said electrolysis device to an aqueous anolyte solution; and d) applying an electrical current between the anode and the cathode in order to reduce the carbon dioxide into hydrocarbons. 15 . The method according to claim 14 , wherein the catholyte solution comprises a salt of hydrogen carbonate, and wherein the anolyte solution comprises a salt of carbonate. 16 . The method according to claim 14 , wherein the electrical current applied between the anode and the cathode has a potential difference comprised between 10 and 1.5 V. 17 . The electrolysis device according to claim 3 , wherein the metal is copper, steel, aluminum, zinc or titanium; the metal oxide is Fluorine-doped Titanium Oxide (FTO) or Indium Tin Oxide (ITO); the metal sulphide is cadmium sulphide or zinc sulphide; the carbon is in the form of carbon felt, graphite, vitreous carbon, or boron-doped diamond; the semiconductor is silicon. 18 . The electrolysis device according to claim 1 , wherein the metal deposit has a specific surface area comprised between between 3 m 2 /g and 50 m 2 /g; a porous structure with an average pore size of between 30 μm and 70 μm, the average pore size being determined by means of photographs obtained by Scanning Electron Microscopy (SEM); and a thickness comprised between 70 μm and 300 μm. 19 . The electrolysis device according to claim 9 , wherein the membrane is an anion exchange membrane. 20 . The electrolysis device according to claim 13 , wherein the electrical energy is a photovoltaic panel or a wind turbine. 21 . The method according to claim 15 , wherein the salt of hydrogen carbonate is an alkali metal salt or a quaternary ammonium salt of hydrogen carbonate, and the salt of carbonate is an alkali metal salt or a quaternary ammonium salt of carbonate.
of metals or alloys not provided for in groups C25D11/04 - C25D11/32 · CPC title
Metal or alloy · CPC title
by heat-treatment · CPC title
Acyclic or carbocyclic hydrocarbons · CPC title
of copper · CPC title
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