A glucose electrolysis apparatus for breaking down glucose and reducing osmolality of the blood includes a catheter having an anode located at a distal end of the catheter. A cathode is connected to the anode by a reduction wire located within the catheter. A mesh covers the anode to exclude molecules from the catheter. A power source is connected to the reduction wire to drive a reaction forward on the anode surface.

Proposed are a photoelectrochemical cell for producing hydrogen peroxide, a method of fabricating the same, and a method of producing hydrogen peroxide using the photoelectrochemical cell. The photoelectrochemical cell includes a photoanode including a photocatalyst, a cathode, and a solid polymer electrolyte layer disposed between the photoanode and the cathode and including a solid polymer electrolyte. The photoelectrochemical cell is for use in the production of hydrogen peroxide, and can produce hydrogen peroxide with electric energy generated from solar energy without requiring the supply of external electric energy.

The present disclosure generally relates to apparatuses, systems, and methods for separating a target species (e.g., CO.sub.2) from a gas mixture (e.g., gas stream) via an electrochemical process.

The present disclosure generally relates to apparatuses, systems, and methods for separating a target species (e.g., CO.sub.2) from a gas mixture (e.g., gas stream) via an electrochemical process.

In one aspect, the disclosure relates to catalysts for electrochemical water splitting, in particular catalysts useful for oxygen evolution at an anode in electrochemical water splitting. The disclosed catalysts compositions comprise a catalyst core component, a shell component, and optionally a catalyst outer component; wherein the catalyst core component comprises a composition having the chemical formula M.sub.xP.sub.y; where M is a transition metal; wherein x is a number from about 1 to about 20; wherein y is a number from about 1 to about 20; wherein the shell component comprises a conducting polymer; and wherein the catalyst outer component is a transition metal that is not the same as the transition metal M. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

A synthesis gas production system for producing CO and H.sub.2 by electrolyzing an aqueous solution containing CO.sub.2 includes: an electrolysis device including an anode chamber and a cathode chamber separated by a separator membrane; a cathode-side circulation line connected to the cathode chamber to circulate a cathode solution containing CO.sub.2; a catalyst supply device provided in the cathode-side circulation line to supply a CO production catalyst to the cathode solution; and a gas composition detection device configured to measure a ratio between CO and H.sub.2 in a production gas produced in the cathode chamber. At least one of control of a supply amount of the CO production catalyst by the catalyst supply device and control of a voltage applied between the anode and the cathode by the electrolysis device is performed to make a ratio of H.sub.2 to CO in the production gas be within a predetermined target range.

Methods, apparatuses, and systems related to electrochemical capture of Lewis acid gases from fluid mixtures are generally described. Certain embodiments are related to electrochemical methods involving selectively removing a first Lewis acid gas from a fluid mixture containing multiple types of Lewis acid gases (e.g., a first Lewis acid gas and a second Lewis acid gas). Certain embodiments are related to electrochemical systems comprising certain types of electroactive species having certain redox states in which the species is capable of binding a first Lewis acid gas but for which binding with a second Lewis acid gas is thermodynamically and/or kinetically unfavorable. The methods, apparatuses, and systems described herein may be useful in carbon capture and pollution mitigation applications.

The electrochemical carbon dioxide reduction reaction (CO.sub.2RR) provides opportunities to synthesize value-added products from this greenhouse gas in a sustainable manner. Efficient catalysts for this reaction are provided that selectively drive CO.sub.2 reduction over the thermodynamic and kinetically competitive hydrogen evolution reaction (HER) in organic or aqueous electrolytes. The catalysts are metal-polypyridyl coordination complexes of a redox non-innocent terpyridine-based pentapyridine ligand and a first-row transition metal. The metal-ligand cooperativity in [Fe(tpyPY2Me)].sup.2+ drives the electrochemical reduction of CO.sub.2 to CO at low overpotentials with high selectivity for CO.sub.2RR (>90%).

The present invention discloses a method for preparing an ultra-thin Ni—Fe-MOF nanosheet, which comprises the steps of dissolving an organic ligand in an organic solvent, dripping the resulting solution to an aqueous solution containing a nickel salt and an iron salt, mixing uniformly and reacting at 140-160° C. for 3-6 h to obtain the ultra-thin Ni—Fe-MOF nanosheet, wherein the organic ligand is terephthalic acid and/or disodium terephthalate, and the organic solvent is N,N-dimethylacetamide and/or N,N-dimethylformamide. The present invention discloses an ultra-thin Ni—Fe-MOF nanosheet, and use thereof. The preparation method does not require a surfactant, the surface of the product is neat and easy to be cleaned, and the large-scale synthesis of 2D ultra-thin MOF materials can be realized.

The present invention discloses a method for preparing an ultra-thin Ni—Fe-MOF nanosheet, which comprises the steps of dissolving an organic ligand in an organic solvent, dripping the resulting solution to an aqueous solution containing a nickel salt and an iron salt, mixing uniformly and reacting at 140-160° C. for 3-6 h to obtain the ultra-thin Ni—Fe-MOF nanosheet, wherein the organic ligand is terephthalic acid and/or disodium terephthalate, and the organic solvent is N,N-dimethylacetamide and/or N,N-dimethylformamide. The present invention discloses an ultra-thin Ni—Fe-MOF nanosheet, and use thereof. The preparation method does not require a surfactant, the surface of the product is neat and easy to be cleaned, and the large-scale synthesis of 2D ultra-thin MOF materials can be realized.