Single-Atom Alloy Formation via Reaction-Driven Catalyst Restructuring.

We demonstrate that single-atom alloy catalysts can be made by exposing physical mixtures of monometallic supported Cu and Pd catalysts to vinyl acetate (VA) synthesis reaction conditions. This reaction induces the formation of mobile clusters of metal diacetate species that drive extensive metal nanoparticle restructuring, leading to atomic dispersion of the precious metal, smaller nanoparticle sizes than the parent catalysts, and high activity and selectivity for both VA synthesis and ethanol dehydrogenation reactions. This approach is scalable and appears to be generalizable to other alloy catalysts.

Correction: One pot ligand exchange method for a highly stable Au-SBA-15 catalyst and its room temperature CO oxidation.

Correction for 'One pot ligand exchange method for a highly stable Au-SBA-15 catalyst and its room temperature CO oxidation' by Yogita Soni et al., Chem. Commun., 2018, DOI: 10.1039/c8cc06887a.

One pot ligand exchange method for a highly stable Au-SBA-15 catalyst and its room temperature CO oxidation.

A modified deposition precipitation (DP) method has been developed to address a fundamental issue of supporting well dispersed Au nanoparticles on silica. Ammonium chloride (NH4Cl) plays an important role in in situ modifying the gold precursor (HAuCl4·3H2O) solution allowing facile deposition of gold NPs in the channels of SBA-15. The Au-SBA-15 catalyst (2.8 wt%) synthesized by this procedure showed 100% conversion for CO oxidation at room temperature with excellent stability at room temperature and high temperature.