A catalyst for production of carboxylic acid ester, containing: catalyst particles containing at least one element selected from the group consisting of nickel, cobalt, palladium, lead, platinum, ruthenium, gold, silver, and copper; and a support supporting the catalyst particles, wherein the catalyst for production of carboxylic acid ester has half-width Wa of pore distribution of 10 nm or less, the half-width Wa being calculated using BJH method from an adsorption isotherm obtained by nitrogen adsorption.

A catalyst for production of carboxylic acid ester, containing: catalyst particles containing at least one element selected from the group consisting of nickel, cobalt, palladium, lead, platinum, ruthenium, gold, silver, and copper; and a support supporting the catalyst particles, wherein the catalyst for production of carboxylic acid ester has half-width Wa of pore distribution of 10 nm or less, the half-width Wa being calculated using BJH method from an adsorption isotherm obtained by nitrogen adsorption.

Present exemplary embodiments provide a nano-hybrid catalyst including: a two-dimensional platinum (Pt) nanodendrite sheet layer with a controlled crystal plane; and a NiFe layered double hydroxide nanosheet layer, in which the two-dimensional platinum (Pt) nanodendrite sheet layer with the controlled crystal plane and the NiFe layered double hydroxide nanosheet layer are alternately stacked, and a method for manufacturing the same.

An efficient photocatalyst nanocomposite comprising reduced graphene oxide, noble metal, and a metal oxide prepared by a one-step method that utilizes date seed extract as a reducing and nanoparticle determining size agent. The photocatalyst of the invention is a more effective sunlight photocatalyst than that prepared by traditional method in the photo decomposition of organic compounds in contaminated water.

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.

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.

Aspects described herein generally relate to bimetallic structures, syntheses thereof, and uses thereof. In an embodiment, a process for forming a bimetallic nanoframe is provided. The process includes forming a first bimetallic structure by reacting a first precursor comprising platinum (Pt) and a second precursor comprising a Group 8-11 metal (M.sup.2), wherein M.sup.2 is free of Pt; reacting a third precursor comprising Pt with the first bimetallic structure to form a second bimetallic structure, the second bimetallic structure having a higher molar ratio of Pt to Group 8-11 metal than the first bimetallic structure; and introducing the second bimetallic structure with an acid to form the bimetallic nanoframe, the bimetallic nanoframe having a higher molar ratio of Pt to Group 8-11 metal than that of the second bimetallic structure, the bimetallic nanoframe having the formula: (Pt).sub.a(M.sup.2).sub.b, wherein: a is the amount of Pt; b is the amount of M.sup.2.

Novel doped oxide and mixed-oxide materials having a metal homogenously dispersed in the form of isolated metal ions throughout the oxide lattice and methods for making the same.

The present disclosure provides perovskite catalytic materials and catalysts comprising platinum-group metals and perovskites. These catalysts may be used as oxygen storage materials with automotive applications, such as three-way catalysts. They are also useful for water or CO.sub.2 reduction, or thermochemical energy storage.

The present invention is generally directed to the production of low-carbon syngas from captured CO.sub.2 and renewable H.sub.2. The H.sub.2 is generated from water using an electrolyzer powered by renewable electricity, or from any other method of low-carbon H.sub.2 production. The improved catalysts use low-cost metals, they can be produced economically in commercial quantities, and they are chemically and physically stable up to 2,100° F. CO.sub.2 conversion is between 80% and 100% with CO selectivity of greater than 99%. The catalysts don't sinter or form coke when converting H.sub.2:CO.sub.2 mixtures to syngas in the operating ranges of 1,300-1,800° F., pressures of 75-450 psi, and space velocities of 2,000-100,000 hr.sup.−1. The catalysts are stable, exhibiting between 0 and 1% CO.sub.2 conversion decline per 1,000 hrs. The syngas can be used for the synthesis of low-carbon fuels and chemicals, or for the production of purified H.sub.2. The H.sub.2 can be used at the production site for the synthesis of low-carbon chemical products or compressed for transportation use.