Factors in gold nanocatalysis: Oxidation of CO in the non-scalable size regime

Uzi Landman, Bokwon Yoon, Chun Zhang, Ueli Heiz, Matthias Arenz

Research output: Contribution to journalArticlepeer-review

182 Scopus citations

Abstract

Focusing on size-selected gold clusters consisting of up to 20 atoms, that is, in the size regime where properties cannot be obtained from those of the bulk material through scaling considerations, we discuss the current state of understanding pertaining to various factors that control the reactivity and catalytic activity of such nanostructures, using the CO oxidation reaction catalyzed by the gold nanoclusters adsorbed on MgO as a paradigm. These factors include the role of the metal-oxide support and its defects, the charge state of the cluster, structural fluxionality of the clusters, electronic size effects, the effect of an underlying metal support on the dimensionality, charging and chemical reactivity of gold nanoclusters adsorbed on the metal-supported metal-oxide, and the promotional effect of water. We show that through joined experimental and first-principles quantum mechanical calculations and simulations, a detailed picture of the reaction mechanism emerges.

Original languageEnglish
Pages (from-to)145-158
Number of pages14
JournalTopics in Catalysis
Volume44
Issue number1-2
DOIs
StatePublished - Jun 2007

Keywords

  • Activation barriers
  • Active sites
  • Amide
  • CO oxidation
  • Cu(110), amine oxide
  • Defects
  • Dimethylamine
  • First principle calculations
  • Humidity effects
  • Metal oxide films
  • Nanocatalysis
  • Non-scalable size regime
  • Pyridine
  • Reaction mechanisms
  • Size selected gold clusters
  • STM
  • Structural dynamic fluxionality
  • Surface
  • Tuning catalytic activity
  • XPS

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