Disclosed is the synthesis of novel supported metal catalytic materials for electromagnetic radiation absorption and chemical catalysis especially in the presence of plasma used in the conversion of nitrogen from air and hydrogen from water to useful products such as nitric acid, hydrogen, ammonia and fertilizers. These materials can also generate plasma when subjected to microwave irradiation thus form the basis of catalytic plasma reactors. They can be used in chemical looping reactions because plasma generation under microwave irradiation in air results in the reduction of catalyst oxides and oxidation of nitrogen.

Disclosed are a photocatalyst and application thereof in environmentally friendly photocatalytic treatment of a power battery. The photocatalyst is obtained by loading Ag-TaON on a hollow glass microsphere, wherein a mass ratio of the Ag-TaON to the hollow glass microsphere is 1: 5 to 10. According to the invention, the Ag-TaON and the hollow glass microsphere are compounded, the hollow glass microsphere has better light permeability, which avoids mutual shielding between catalysts, such that the photocatalyst filled in a reactor is fully excited, which is capable of effectively improving a light utilization rate, thus improving the catalytic conversion efficiency of the photocatalyst.

A method consisting in depositing coating of a semiconductor such as TiO.sub.2 on the surface of a substrate of activated carbon in the form of grain or powder that acts by an advanced oxidation-reduction mechanism in environmental decontamination processes, by way of a heterogeneous electrocatalysis system applying an electrical potential having a magnitude equal to or greater than that of the bandgap energy of the semiconductor, which is 3.2 eV in the case of anatase TiO.sub.2, such that an electron rises from the valence band to the conduction band, leaving in its place holes, h+, with enough oxidative capacity to be able to oxidise H.sub.2O and form OH radicals.

A method for the manufacture of a catalyst comprising substrate particles having gold nanoparticles thereon, the method comprising providing a first solution comprising gold nanoparticles; providing a second solution comprising substrate particles having polyelectrolyte on the surface thereof; and combining the solutions to form substrate particles having gold nanoparticles thereon. A catalyst comprising substrate particles having gold nanoparticles thereon, wherein the gold nanoparticles comprise capping agent comprising polyelectrolyte. A catalyst as a component of a cigarette filter, an air conditioning unit, an exhaust, or a diesel exhaust.

Provided is an oxygen reduction catalyst having a high oxygen reduction performance. An oxygen reduction catalyst according to the present embodiment includes a transition metal oxide to which an oxygen defect is introduced, and a layer that is provided on the transition metal oxide and that contains an electron conductive substance. A method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition metal carbonitride as a starting material in an oxygen-containing mixed gas. In addition, a method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition-metal phthalocyanine and a carbon fiber powder as starting materials in an oxygen-containing mixed gas.

The present disclosure provides a catalyst product having particular three-dimensional plate-like shape and comprising catalyst nanoparticles and a method for manufacturing same. The present product may be useful in fuel cells or battery applications. In certain embodiments the present catalysts show good catalytic activity and durability even at low catalyst loads.

Catalyst comprising an Ir layer having an outer layer with a layer comprising Pt directly thereon, wherein the Ir layer has an average thickness in a range from 0.04 to 30 nanometers, wherein the layer comprising Pt has an average thickness in a range from 0.04 to 50 nanometers, and wherein the Pt and Ir are present in an atomic ratio in a range from 0.01:1 to 10:1. Catalysts described herein are useful, for example, in fuel cell membrane electrode assemblies.

Carbon dioxide can be converted into a higher energy product by contacting carbon dioxide with a polarized monocrystalline magnesium oxide producing at least in part carbon. Further a novel crystalline magnesium oxide carbon composite comprising crystalline magnesium oxide and crystalline carbon having graphene structure which are interwoven is provided.

A heterogeneous catalysis method for catalyzing the conversion of a first chemical species to a second chemical species includes varying a binding energy of the first chemical species, the second chemical species, or both over time and in the presence of a catalyst. Systems configured to catalyze the conversion of the first chemical species to the second chemical species by varying a binding energy of the first chemical species, the second chemical species, or both over time and in the presence of a catalyst include a sound wave generator, a pressure generator, a piezoelectric material, or a back gate device configured to facilitate the varying of the binding energy of the first chemical species, the second chemical species, or both.

The present disclosure provides a noble metal-transition metal-based nano-catalyst thin film and a preparation method thereof, belonging to the fields of energy development and pollutant emission reduction. Based on a micro-nano processing technology, a noble metal-transition metal-based nano-catalyst thin film is loaded on a semi-cylindrical pipe with an inner thread structure, and heat generated is quickly accumulated on an upper surface of the catalyst to establish a large temperature gradient. By the insulation and high roughness of an alumina carrier layer and the inner thread structure of the pipe, a catalyst loading area is maximized and dispersion of noble metal atoms is enhanced. A transition metal-transition metal oxide thin film protects a noble metal nano-catalyst by core-shell wrapping, and a transition metal oxide prevents catalyst deactivation caused by oxygen occupying too many metal active sites.