H01M4/8803

CATALYST
20220403535 · 2022-12-22 ·

A catalyst comprising a porous electrically conductive substrate (such as a foam, carbon fibre paper and carbon fibre cloth) and a porous metallic composite of amorphous NiMoP coating at least a portion of the surface or multiple surfaces of the substrate. The composite preferably forms a continuous layer which coats the surfaces and pores of the substrate. Also methods for preparing and using the catalyst, for example in electrolytic water splitting.

MATERIALS AND METHODS OF MANUFACTURE

An array includes a support substrate, surface structures protruding from a surface of the support substrate formed from or coated with a first material, a second material deposited on at least some of the surface structures such that the second material is in contact with the first material; and wherein the first material, the second material or the first and second material is conducting or semiconducting, and wherein the first and second material at least partially form a composite.

HIGH-STABILITY CATALYST FOR AN ELECTROCHEMICAL CELL

The present invention relates to a method for producing a catalyst for an electrochemical cell, wherein: a graphited porous carbon material is treated with an oxygen-containing plasma or an aqueous medium containing an oxidising agent, at least one noble metal compound is deposited on the treated carbon material, the impregnated carbon material is brought into contact with a reducing agent such that the noble metal compound is reduced to a metallic noble metal.

CATALYST INK COMPOSITIONS AND METHODS FOR FORMING HYDROGEN PUMPING PROTON EXCHANGE MEMBRANE ELECTROCHEMICAL CELL

A membrane electrode assembly (MEA) includes an ionically-conductive proton exchange membrane, an anode contacting a first side of the membrane and a cathode contacting a second side of the membrane and including third catalyst particles and a cathode GDL. The anode includes an anode gas diffusion layer (GDL), a first anode catalyst layer containing first catalyst particles, a hydrophobic polymer bonding agent, and a first ionomer bonding agent that lacks functional chains on a molecular backbone, and a second anode catalyst layer containing second catalyst particles and a second ionomer bonding agent that includes functional chains on a molecular backbone.

Titanium-based porous body and method of producing the same

To provide a titanium-based porous body that has high void fraction to ensure gas permeability and water permeability for practical use as an electrode and a filter, has a large specific surface area to ensure conductivity and sufficient reaction sites with a reaction solution or a reaction gas, thus showing excellent reaction efficiency, and contains less contaminants because of no organic substance used. A titanium-based porous body having a specific void fraction and a high specific surface area is obtained by filling an irregular-shaped titanium powder having an average particle size of 10 to 50 μm in a dry system without using any binder or the like into a thickness of 4.0×10.sup.−1 to 1.6 mm, and sintering the irregular-shaped titanium powder at 800 to 1100° C.

POROUS BODY AND FUEL CELL INCLUDING THE SAME

A porous body includes a framework having a three-dimensional network structure, the framework having a body including crystal grains including nickel and cobalt as constituent elements, the cobalt having a proportion in mass of 0.2 or more and 0.8 or less with respect to a total mass of the nickel and the cobalt, the crystal grains having a shorter grain diameter of 2 μm or more, as determined in a first observed image obtained by observing the body of the framework in cross section at a magnification of 200 times.

Method of manufacturing anode dual catalyst for fuel cell for preventing reverse voltage phenomenon and dual catalyst manufactured thereby

Disclosed are a method of manufacturing an anode dual catalyst for a fuel cell so as to prevent a reverse voltage phenomenon and a dual catalyst manufactured by the same. The method may include supporting effectively metal catalyst particles and oxide particles on a conductive support, and thus, a dual catalyst manufactured using the method may be suitably used for controlling a reverse voltage phenomenon that occurs at the anode.

METHOD FOR PRODUCING BATTERY, AND BATTERY
20220344629 · 2022-10-27 · ·

A small diameter roll is provided on the upstream side of a heating and sucking roll, an electrode slurry is applied by using a slot nozzle on the small diameter roll or an OFF roll, and an electrode is formed by instantaneously evaporating a solvent by the heating and sucking roll.

Dynamic piezocatalyst system

Methods are provided for tailoring multi-step chemical reactions having competing elementary steps using a strained catalyst. In various aspects, a layered piezo-catalytic system is provided, and may include a metal catalyst overlayer disposed on a piezo-electric substrate. The methods include applying a voltage bias to the piezo-electric substrate of the piezo-catalytic system resulting in a strained catalyst having an altered catalytic activity as a result of one or both of a compressive stress and tensile stress. The methods include exposing reagents for at least one step of the multi-step chemical reaction to the strained catalyst, and catalyzing the at least one step of the multi-step chemical reaction. In various aspects, the methods may include using an oscillating voltage bias applied to the piezo-electric substrate.

SUPPORTED METAL CATALYST, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING CARRIER

The present invention provides a supported metal catalyst with excellent effectiveness factor of active metal particles which are also free from deactivation by contacting with ionomer.

According to the present invention, provided is a supported metal catalyst, comprising a support that is a collective body of conductive particles; and dispersed active metal particles supported on the conductive particles, wherein the conductive particles include a plurality of pores, an average entrance pore diameter of the pores is 1 to 20 nm, a standard deviation of the average entrance pore diameter is equal to or less than 50% of the average entrance pore diameter, a number fraction of the active metal particles supported in a surface layer region of the conductive particles divided by the total number of the active metal particles is equal to or more than 50%, and the surface layer region is a region on a surface of the conductive particles or a region in the pores within a depth of 15 nm from the surface.