The present invention realizes industrially excellent effects such that when electric power having a large output fluctuation, such as renewable energy, is used as a power source, electrolysis performance is unlikely to be deteriorated and excellent catalytic activity is retained stably over a longer period of time, and in addition, the present invention provides a technique that enables forming a catalyst layer of an oxygen generation anode, which gives such excellent effects, with a more versatile materials and by a simple electrolysis method. Provided are an alkaline water electrolysis method including supplying an electrolyte obtained by dispersing a catalyst containing a hybrid nickel-iron hydroxide nanosheet (NiFe-ns) being a composite of a metal hydroxide and an organic substance to an anode chamber and a cathode chamber, and using the electrolyte for electrolysis in each chamber in common, an alkaline water electrolysis method including supplying an electrolyte obtained by dispersing a catalyst containing the NiFe-ns to an anode chamber and a cathode chamber, and performing electrolytic deposition of the NiFe-ns in the electrolytic cell during operation to electrolytically deposit the NiFe-ns on a surface of an electrically conductive substrate having a catalyst layer formed on a surface of an oxygen generation anode, thereby recovering and improving electrolysis performance, and an alkaline water electrolysis anode.

Disclosed is a method for manufacturing an electrode for alkaline water electrolysis, the method including: dissolving a metal salt in a solvent, followed by synthesis, to prepare a wet powder; performing an oxidative heat treatment on the wet powder; and performing a reductive heat treatment on the oxidatively heat treated powder.

Disclosed is a method for manufacturing an electrode for alkaline water electrolysis, the method including: dissolving a metal salt in a solvent, followed by synthesis, to prepare a wet powder; performing an oxidative heat treatment on the wet powder; and performing a reductive heat treatment on the oxidatively heat treated powder.

A catalytic system for CO.sub.2 capture and sequestration. The system includes a reduction cell for separating a carrier medium having an anode generating oxygen, a cathode generating hydrogen, and a CO precursor from the carrier medium. In addition, the system includes a power supply for providing electrical power to the anode and the cathode. An electrolysis process occurs where oxygen, hydrogen, CO precursors are produced. The anode and the cathode include a plurality of geometrical constructs to increase an active surface area of a catalytic surface of the anode and cathode to increase an efficiency of the electrolysis process. The geometrical constructs may include vias and pillars. In one embodiment, a capillary action is produced for CO.sub.2 sequestration across the catalytic surface having a plurality of vias.

A catalytic system for CO.sub.2 capture and sequestration. The system includes a reduction cell for separating a carrier medium having an anode generating oxygen, a cathode generating hydrogen, and a CO precursor from the carrier medium. In addition, the system includes a power supply for providing electrical power to the anode and the cathode. An electrolysis process occurs where oxygen, hydrogen, CO precursors are produced. The anode and the cathode include a plurality of geometrical constructs to increase an active surface area of a catalytic surface of the anode and cathode to increase an efficiency of the electrolysis process. The geometrical constructs may include vias and pillars. In one embodiment, a capillary action is produced for CO.sub.2 sequestration across the catalytic surface having a plurality of vias.

The application discloses an electrode having polarity capable of being reversed and use thereof. The electrode includes a substrate comprising a metal or an alloy thereof; an intermediate layer arranged on the substrate and comprising a platinum group metal and a platinum group metal oxide; and a catalytic layer arranged on the intermediate layer and comprising a mixed metal oxide. The electrode may be used as an electrode for electrolysis, electrodialysis or electroplating. The electrode can simultaneously meet the working environment requirements of the cathode and the anode, which improves the environmental tolerance and realizes the protection of the substrate; and can carry out polarity reversal to clean deposits on the surface of the electrode quickly and efficiently.

Electrochemical systems and methods for cleaving C—C bonds are disclosed. In performing the method, a reactant adsorption electrical potential, a C—C bond breaking electrical potential, and a desorption electrical potential are sequentially applied to an electrode pair contacting a composition initially containing a target chemical reactant, such as a polymer or alkane. As a result of performing the method, one or more desired chemical products, such as smaller alkane-containing molecules, are released from the electrode into the region between the electrode pairs. The method may be performed at ambient temperatures using renewable electricity.

A method for preparing hydrogen sulfide from sulfur dioxide by electrochemical reduction includes electrochemically reducing sulfur dioxide absorbed in an aqueous solution into gaseous hydrogen sulfide with a membrane electrode, resulting in efficient and selective conversion of the sulfur dioxide absorbed in the aqueous solution into the hydrogen sulfide to avoid a deactivation of a cathode due to colloidal sulfur produced on the cathode and adhesion onto a surface of the cathode, wherein the method is carried out at ambient temperature and normal pressure without addition of a reducing agent, having no waste salts produced, and is simple in operation, and is convenient for large-scale application.

A method for preparing hydrogen sulfide from sulfur dioxide by electrochemical reduction includes electrochemically reducing sulfur dioxide absorbed in an aqueous solution into gaseous hydrogen sulfide with a membrane electrode, resulting in efficient and selective conversion of the sulfur dioxide absorbed in the aqueous solution into the hydrogen sulfide to avoid a deactivation of a cathode due to colloidal sulfur produced on the cathode and adhesion onto a surface of the cathode, wherein the method is carried out at ambient temperature and normal pressure without addition of a reducing agent, having no waste salts produced, and is simple in operation, and is convenient for large-scale application.

Electrosynthesis of oxirane can include contacting a halide electrolyte with an anode and cathode respectively located in anodic and cathodic compartments; supplying olefin reactants into the electrolyte in the anodic compartment, such that the anode generates ethylene chlorohydrin; withdrawing a loaded anodic solution comprising ethylene halohydrin from the anodic compartment, and a loaded cathodic solution comprising OH.sup.- ions from the cathodic compartment; and mixing the loaded anodic solution with the loaded cathodic solution under conditions to react ethylene halohydrin with OH- to produce oxirane. The electrocatalyst can include iridium oxide on a titanium substrate, with the iridium oxide provided as nanoparticles on a titanium mesh, and the electrolyte can be aqueous KCl. The electrocatalyst can define an extended heterogenous:homogenous interface with halide ions acting as a reservoir for positive charges, thereby storing and redistributing positive charges to promote selective generation of ethylene halohydrins.