Investigating the impact of dynamic structural changes of Au/rutile catalysts on the catalytic activity of CO oxidation

Abstract

The surface properties of oxidic supports and their interaction with the supported metals play critical roles in governing the catalytic activities of oxide-supported metal catalysts. When metals are supported on reducible oxides, dynamic surface reconstruction phenomena, including strong metal–support interaction (SMSI) and oxygen vacancy formation, complicate the determination of the structural–functional relationship at the active sites. Here, we performed a systematic investigation of the dynamic behavior of Au nanocatalysts supported on flame-synthesized TiO₂, which takes predominantly a rutile phase, using CO oxidation above room temperature as a probe reaction. Our analysis conclusively elucidated a negative correlation between the catalytic activity of Au/TiO₂ and the oxygen vacancy at the Au/TiO₂ interface. Although the reversible formation and retracting of SMSI overlayers have been ubiquitously observed on Au/TiO₂ samples, the catalytic consequence of SMSI remains inconclusive. Density functional theory suggests that the electron transfer from TiO₂ to Au is correlated to the presence of the interfacial oxygen vacancies, retarding the catalytic activation of CO oxidation.

Keywords

CO oxidation / electronic metal–support interactions / flame-synthesis / metal–support interactions / oxygen vacancy / strong metal–support interaction

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2023 2023 The Authors. Carbon Energy published by Wenzhou University and John Wiley & Sons Australia, Ltd.