A method for preparing a multi-component alloy catalyst on which a catalytic metal is supported includes preparing a carbon composite having a carbon support coated with a cationic polymer, supporting a catalytic metal containing at least two metal elements on the carbon composite to prepare an alloy catalyst precursor, and washing the alloy catalyst precursor to remove the cationic polymer.

Chiral polyvinylpyrrolidinone (CSPVP), complexes of CSPVP with a core species, such as a metallic nanocluster catalyst, and enantioselective oxidation reactions utilizing such complexes are disclosed. The CSPVP complexes can be used in asymmetric oxidation of diols, enantioselective oxidation of alkenes, and carbon-carbon bond forming reactions, for example. The CSPVP can also be complexed with biomolecules such as proteins, DNA, and RNA, and used as nanocarriers for siRNA or dsRNA delivery.

A method for producing a hydrofluoroolefin is provided. The formation of by-products of an over-reduced product having hydrogen added to a material chlorofluoroolefin and an over-reduced product having not only chlorine atoms but also fluorine atoms in the chlorofluoroolefin replaced with hydrogen atoms is suppressed in the method. The method includes reacting a specific chlorofluoroolefin with hydrogen in the presence of a catalyst supported on a carrier to obtain the hydrofluoroolefin. The catalyst is a catalyst composed of an alloy containing at least one platinum group element of palladium and platinum, and at least one second element of copper, gold, lithium, potassium, silver, zinc, tin, lead, and bismuth.

Zeolite catalysts and systems and methods for preparing and using zeolite catalysts having the CHA crystal structure are disclosed. The catalysts can be used to remove nitrogen oxides from a gaseous medium across a broad temperature range and exhibit hydrothermal stable at high reaction temperatures. The zeolite catalysts include a zeolite carrier having a silica to alumina ratio from about 15:1 to about 256:1 and a copper to alumina ratio from about 0.25:1 to about 1:1.

The present disclosure is directed to a system for treating an exhaust gas stream from an engine, which includes a diesel oxidation catalyst (DOC) located downstream of the engine and adapted for oxidation of hydrocarbons and carbon monoxide, an injector adapted for the addition of a reductant to the exhaust gas stream located downstream of the DOC, a catalyzed soot filter (CSF) located downstream of the injector, and a selective catalytic reduction component adapted for the oxidation of nitrogen oxides located downstream of the CSF. The CSF is adapted for oxidizing hydrocarbons and includes a selective oxidation catalyst composition on a filter with high selectivity ratio for hydrocarbon oxidation: ammonia oxidation (e.g., at least 0.6).

In embodiments a metal or metal alloy nanowires are assembled into a nanoporous membrane that can be used in methods for catalyzing various reactions under low pressures and achieving high flow rate of the reactions. In embodiments, the membranes of the disclosure can catalyze CuAAC reactions with high efficiency and minimum leaching of active Cu species.

A photocatalyst/alloy fine-particle dispersion containing two kinds of fine particles dispersed in an aqueous dispersion medium, (i) photocatalyst fine particles and (ii) alloy fine particles containing an antibacterial/antifungal metal, easily forms a photocatalyst/alloy fine-particle thin film of high transparency that exhibits antibacterial/antifungal properties regardless of the presence or absence of light irradiation.

A mixed metal oxide solid acid catalyst composition is disclosed which provides substantially improved conversion for hydrocarbon transformation reactions namely, alkylation and isomerization. The catalyst composition includes a sulfate ion, Platinum group metal and a mixed metal oxide support material bearing molecular formula:

x.sub.1ZrO.sub.2.x.sub.2Al.sub.2O.sub.3.x.sub.3Yb.sub.2O.sub.3.x.sub.4CuO

wherein the molar coefficients for individual metal oxides are as follows:
x1=55 to 7510.sup.2; x2=12 to 2510.sup.2; x3=1 to 610.sup.2 and x4=0.1 to 510.sup.2;

The concentration of the sulfate ion on the aforementioned catalyst support is between 5 to 17 wt % and that of Platinum group metal is 0.05 to 2.0 wt %.

In some aspects and embodiments, the present application provides a wide range of porous 1-D polymeric graphitic carbon-nitride materials that are atomically doped with binary metals in different morphologies. In some embodiments, the graphitic carbon-nitride materials can be prepared with high mass production from inexpensive and natural abundant precursors. In some embodiments, the materials were used successfully for the oxidation of CO to CO.sub.2 under ambient reaction temperature in addition to the reduction of CO.sub.2 into hydrocarbons. In some embodiments, the materials can be used for practical and large-scale gas conversion for household or industrial applications.

Disclosed herein are trimetallic PtAu-based nanocatalysts for electrochemical hydrogen production and screening methods thereof. Nanocatalysts are produced through a polymer pen lithography (PPL) technique, which enables large-scale fabrication of nanoparticle arrays with programmable specifications such as size, shape, and composition, providing a route to the high-throughput screening and discovery of new catalysts.