Abstract

Over the past three decades, supported gold nanoparticles have demonstrated outstanding properties and continue to attract the interest of the scientific community. Several books and comprehensive reviews as well as numerous papers cover a variety of fundamental and applied aspects specific to gold-based catalyst synthesis, characterization by different techniques, relationship among catalyst support features, electronic and structural properties of gold particles, and catalytic activity, reaction mechanism, and theoretical modeling. Among the Au-catalyzed reactions targeting environmental protection and sustainable energy applications, particular attention is paid to pure hydrogen production. The increasing demands for high-purity hydrogen for fuel cell systems caused a renewed interest in the water–gas shift reaction. This well-known industrial process provides an attractive way for hydrogen generation and additional increase of its concentration in the gas mixtures obtained by processes utilizing coal, petroleum, or biomass resources. An effective step for further elimination of CO traces from the reformate stream after water–gas shift unit is the preferential CO oxidation. Developing highly active, stable, and selective catalysts for these two reactions is of primary importance for efficient upgrading of hydrogen purity in fuel cell applications. This review aims to extend the existing knowledge and understanding of the properties of gold-based catalysts for H2 clean-up reactions. In particular, new approaches and strategies for design of high-performing and cost-effective formulations are addressed. Emphasis is placed on efforts to explore appropriate and economically viable supports with complex composition prepared by various synthesis procedures. Relevance of ceria application as a support for new-generation WGS catalysts is pointed out. The role of the nature of support in catalyst behavior and specifically the existence of an active gold–support interface is highlighted. Long-term stability and tolerance toward start-up/shutdown cycling are discussed. Very recent advances in catalyst design are described focusing on structured catalysts and microchannel reactors. The latest mechanistic aspects of the water–gas shift reaction and preferential CO oxidation over gold-based catalysts from density functional theory calculations are noted because of their essential role in discovering novel highly efficient catalysts.

Highlights

  • For over three decades, catalysis by gold continues to be a topic of special interest to stimulate research activities in discovering new properties and attractive applications of of gold-based catalysts

  • On dispersing catalytic active components over high surface area supports such as alumina, silica, etc., a successful strategy was demonstrated for achievement of higher surface-tobulk ratios, contributing to preparation of high-performing gold catalysts

  • New insights into water–gas shift (WGS) and preferential CO oxidation in hydrogen-rich gas stream (PROX) reaction mechanisms and the nature of active sites have been gained from theoretical studies and exploration of model catalysts

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Summary

Introduction

Catalysis by gold continues to be a topic of special interest to stimulate research activities in discovering new properties and attractive applications of of gold-based catalysts. The scientific community is already well aware about the catalytic power of supported gold nanoparticles. Haruta et al (1987) discovered an extremely high CO oxidation activity of gold nanoparticles supported on transition metal oxides at, or even below, room temperature. Hutchings revealed the catalytic potential of gold nanoparticles for hydrochlorination of acetylene to vinyl chloride (Hutchings, 1985). These groundbreaking works encouraged many scientists to be involved in the attractive research area of gold catalysts that opened up new opportunities for the catalysis community. Without any doubt, we can affirm that gold loses its nobility when occurring at the nanometer length scale. Corma and Garcia (2008) explained in a perfect way this phenomenon, describing “gold catalysis as a paradigmatic example of those properties that are only observed in nanoparticles and can disappear completely as the particle size grows into the micrometric scale.”

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