Abstract

Au–Pd colloidal NPs immobilised on ceria nanorods are highly active catalysts for selective oxidation.

Highlights

  • Since it was first reported by Haruta[1] and Hutchings,[2] the unique catalytic properties of supported gold nanoparticles (NPs) have been extensively studied over the past few decades

  • We have recently demonstrated that bimetallic Au–Pd NPs prepared by colloidal synthesis can be immobilised on titanate nanotubes to create a very active selective oxidation catalyst.[23]

  • The Brunauer–Emmett– Teller (BET) surface area, pore volume, and mean pore diameter of the as-synthesised Ti-NT and Ce-NRs are given in Table S1,† and are typical of powders composed of Ti-NTs and Ce-NRs

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Summary

Introduction

Since it was first reported by Haruta[1] and Hutchings,[2] the unique catalytic properties of supported gold nanoparticles (NPs) have been extensively studied over the past few decades. The catalytic activity of supported gold-based catalysts is highly influenced by the nature of the support and its physiochemical properties, the metal particle size, and the catalyst preparation method. It has been demonstrated that highly-dispersed Au NPs ≤ 5 nm in size typically exhibit the highest catalytic activity.[9,10] Au and Au–Pd NPs supported on Al2O3, SiO2 and carbon are active for selective

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