An electrolyzer system includes an anticorrosive, conductive material including a first oxide having oxygen vacancies and a formula (Ia): MgTi.sub.2O.sub.5-δ (Ia), where δ is any number between 0 and 3 including a fractional part denoting the oxygen vacancies; and a second oxide having a formula (II): Ti.sub.aO.sub.b (II), where 1<=a<=20 and 1<=b<=30, optionally including a fractional part, the first and second oxides of formulas (Ia) and (II) forming a polycrystalline matrix within the electrolyzer system.

An object of the present invention is to provide an electrolysis technique such that the electrolysis performance is unlikely to be deteriorated, and excellent catalytic activity is retained stably over a long period of time even when electric power having a large output fluctuation, such as renewable energy, is used a power source, and this object is realized by an alkaline water electrolysis method, in which an electrolytic solution obtained by dispersing a catalyst containing a hybrid cobalt hydroxide nanosheet (Co-NS) being a composite of a metal hydroxide and an organic substance is supplied to an anode chamber and a cathode chamber that form an electrolytic cell, and the electrolytic solution is used for electrolysis in each chamber in common, and an alkaline water electrolysis anode.

Provided is a catalyst structure for electrochemical CO.sub.2 reduction. The catalyst structure includes carbon nanofibers doped with nitrogen (N), and copper (Cu) particles dispersed on the carbon nanofibers. At least portions of the carbon nanofibers at interfaces with the Cu particles may have a pyridinic-N structure.

The present invention provides an electrode for electrolysis in which a planarized metal substrate having a mesh structure such that the aspect ratio of an individual cross-section of a wire constituting the mesh structure is 120% or greater is used to increase the surface area of a coating layer, thereby increasing adhesion to a membrane and gas trap is reduced to reduce overvoltage.

The present invention relates to a photo-electrochemical device for production of a gas, liquid or solid using concentrated electromagnetic irradiation. The device comprises a photovoltaic component configured to generate charge carriers from the concentrated electromagnetic irradiation; and an electrochemical component configured to carry out electrolysis of a reactant. The photovoltaic component contacts the electrochemical component at a solid interface to form an integrated photo-electrochemical device; and further includes at least one reactant channel or a plurality of reactant channels extending between the photovoltaic component and the electrochemical component to transfer heat and the reactant from the photovoltaic component to the electrochemical component. The integrated photo-electrochemical device and auxiliary devices (such as concentrator, flow controllers) build a system which can flexibly react to changes in operating condition and guarantee best performance.

The present disclosure provides for and includes electrocatalytic devices and methods for the production of Dry Hydrogen Peroxide (DHP), a non-hydrated, gaseous form of hydrogen peroxide.

The present disclosure relates to a carbon dioxide capture device comprising a first reactor and a second reactor both of which show a (photo)anode containing or connected to oxygen evolution and/or carbon dioxide evolution catalyst(s) and a (photo)cathode containing or connected to an oxygen reduction catalyst, wherein the first reactor comprises an anion exchange membrane placed between the porous (photo)anode and porous (photo)cathode, and the second reactor comprises a proton exchange membrane placed between the porous (photo)anode and porous (photo)cathode. On the porous (photo)cathode side of the first reactor there is a fluid inlet able to carry carbon dioxide, air and water, and on the side of the porous (photo)cathode of the second reactor there is a fluid outlet able to carry carbon dioxide and water.

We provide a single-atom catalyst comprising nanostructures of a conductive material and a plurality of single-atom metal sites dispersed on the surface of each of the nanostructures. A method of manufacture of such catalyst is also provided. It relies on the electrodeposition or drop casting of the nanostructures of a conductive material on a substrate, followed by the adsorption and electrochemical reduction of complex ions comprising a single atom of each of one or more metal on the surface of the nanostructures.

We provide a single-atom catalyst comprising nanostructures of a conductive material and a plurality of single-atom metal sites dispersed on the surface of each of the nanostructures. A method of manufacture of such catalyst is also provided. It relies on the electrodeposition or drop casting of the nanostructures of a conductive material on a substrate, followed by the adsorption and electrochemical reduction of complex ions comprising a single atom of each of one or more metal on the surface of the nanostructures.

Processes for converting nitrate to ammonia are described. Nitrate is electrochemically converted in the presence of a catalyst to form a product comprising ammonia. The catalyst comprises cobalt on a support, where the support is in the form of a foil, mesh, cloth, gauze, sponge, and combinations thereof. The catalyst may alternatively comprise a cobalt in the form of a foil, mesh, cloth, gauze, sponge, and combinations thereof.