A clad porous metal substrate for use in a metal-supported electrochemical cell, wherein a metal support layer of defined porosity is clad on top and bottom sides with a layer containing a metal and/or a metal oxide. A metal-supported electrochemical half-cell and a metal-supported electrochemical cell are also described.

The presently disclosed subject matter relates to devices, systems, and methods for fabricating a solid polymer electrolyte electrode assembly are provided. One or more electrode for a solid polymer electrolyte electrode assembly includes a porous substrate configured as a liquid/gas diffusion layer and an ionomer-free catalyst coated on the substrate.

The presently disclosed subject matter relates to devices, systems, and methods for fabricating a solid polymer electrolyte electrode assembly are provided. One or more electrode for a solid polymer electrolyte electrode assembly includes a porous substrate configured as a liquid/gas diffusion layer and an ionomer-free catalyst coated on the substrate.

A wastewater to chemical fuel conversion device is provided that includes a housing having a first chamber and a second chamber, where the first chamber includes a bio-photoanode, where the second chamber includes a photocathode, where a backside of the bio-photoanode abuts a first side of a planatized fluorine doped tin oxide (FTO) glass, where a backside of the photocathode abuts a second side of the FTO glass, where a proton exchange membrane separates the first chamber from the second chamber, where the first chamber includes a wastewater input and a reclaimed water output, where the second chamber includes a solar light input and a H.sub.2 gas output, where the solar light input is disposed for solar light illumination of the first chamber and the second chamber.

A process for preparing a catalytic material of an electrode for electrochemical reduction reactions, said material comprising an active phase based on at least one group VIB metal and an electrically conductive support, which process is carried out according to at least the following steps:

a) bringing water into contact with said electrically conductive support,
b) bringing said wet support into contact with at least one metallic acid hydrate comprising at least one group VIB metal, of which the melting point of said metallic acid hydrate is between 20° C. and 100° C., the weight ratio of said metallic acid to said electrically conductive support being between 0.1 and 4,
c) heating, with stirring, to a temperature between the melting point of said metallic acid hydrate and 100° C.,
d) carrying out a sulfurization step at a temperature of between 100° C. and 600° C.

A process for preparing a catalytic material of an electrode for electrochemical reduction reactions, said material comprising an active phase based on at least one group VIB metal and an electrically conductive support, which process is carried out according to at least the following steps:

a) bringing water into contact with said electrically conductive support,
b) bringing said wet support into contact with at least one metallic acid hydrate comprising at least one group VIB metal, of which the melting point of said metallic acid hydrate is between 20° C. and 100° C., the weight ratio of said metallic acid to said electrically conductive support being between 0.1 and 4,
c) heating, with stirring, to a temperature between the melting point of said metallic acid hydrate and 100° C.,
d) carrying out a sulfurization step at a temperature of between 100° C. and 600° C.

An electrolysis electrode includes a conductive substrate, a catalyst layer and a tantalum oxide layer. The conductive substrate includes at least titanium. The catalyst layer is provided on the conductive substrate. The catalyst layer includes platinum and iridium oxide. The tantalum oxide layer is provided on the catalyst layer. In the electrolysis electrode, the catalyst layer is partially exposed.

This application relates to new process that utilizes electrodes that incorporate acids that facilitate upgrading of methane and other low molecular weight alkanes to higher order hydrocarbon molecules, such as paraffins, olefins, and aromatics, at temperatures less than 250° C. A primary focus of the invention includes methane conversion to ethylene. The first step of the process includes acid containing electrodes that facilitate the activation of the alkane in the anode layer of the electrochemical reactor. Subsequent steps include the separation of protons from produced longer chain hydrocarbons followed by subsequent electrochemical reduction of the protons to yield hydrogen at the cathode or protons combined with oxygen at the cathode to yield water. The reaction steps in the anode upgrade methane to higher order hydrocarbon products.

An electrochemical method includes performing anodic halogenation of Cu foils, performing subsequent oxide-formation in a KHCO.sub.3 electrolyte, and performing an electroreduction in neutral KHCO.sub.3 to generate a copper catalyst.

This invention is directed to a method of oxygenating hydrocarbons with molecular oxygen, O.sub.2, as oxidant under electrochemical reducing conditions, using polyoxometalate compounds containing copper such as Q.sub.10[Cu.sub.4(H.sub.2O).sub.2(B-α-PW.sub.9O.sub.34).sub.2] or Q.sub.13{[Cu(H.sub.2O)].sub.3[(A-α-PW.sub.9O.sub.34).sub.2(NO.sub.3).sup.−]} or solvates thereof as catalysts, wherein Q are each independently selected from alkali metal cations, alkaline earth metal cations, transition metal cations, NH.sub.4.sup.+, H.sup.+ or any combination thereof.