Abstract

Oxide reducibility is a central concept quantifying the role of the support in catalysis. While reducible oxides are often considered catalytically active, irreducible oxides are seen as inert supports. Enhancing the reducibility of irreducible oxides has, however, emerged as an effective way to increase their catalytic activity while retaining their inherent thermal stability. In this work, we focus on the prospect of using single metal atoms to increase the reducibility of a prototypical irreducible oxide, zirconia. Based on extensive self-consistent DFT+U calculations, we demonstrate that single metal atoms significantly improve and tune the surface reducibility of zirconia. Detailed analysis of the observed single atom induced reducibility allows us to attribute the enhanced reducibility to strong interactions between the metal atom and the electrons trapped in the vacancy and d–p orbital interactions between the metal atom and oxygen. This analysis enables transferring the obtained theoretical understanding to other irreducible oxides as well. The detailed understanding of how oxide reducibility can be tuned offers precise control over the catalytic properties of metal oxides.

Highlights

  • Metal oxides play a crucial role in heterogeneous catalysis, where they are considered as both catalysts and support materials,[1] but this division is artificial, as oxides often play multiple roles.[1]

  • We explored the influence of an adsorbed metal atom on the reduction energy by depositing single transition metal (TM) atoms one by one on both ideal and O-deficient m-ZrO2(1̅11)

  • As the focus of this study is in the comparison of the reducibility-enhancing properties of different single metal atoms rather than in identifying the most favorable adsorption site for each metal atom on m-ZrO2(1̅11), the other sites are only considered in selected cases

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Summary

Introduction

Metal oxides play a crucial role in heterogeneous catalysis, where they are considered as both catalysts and support materials,[1] but this division is artificial, as oxides often play multiple roles.[1]. Irreducible oxides are often considered as inert supports, while reducible oxides are thought to be more catalytically active.[6,8]

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