4.8 Article

Evaluating differences in the active-site electronics of supported Au nanoparticle catalysts using Hammett and DFT studies

Journal

NATURE CHEMISTRY
Volume 10, Issue 3, Pages 268-274

Publisher

NATURE PORTFOLIO
DOI: 10.1038/nchem.2911

Keywords

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Funding

  1. US National Science Foundation (NSF) [CBET-1160217, CHE-1012395]
  2. NSF DMREF grant [1436206]
  3. NSF [ACI-1053575]
  4. Department of Energy, Office of Basic Energy Sciences, Chemical Sciences, Geosciences and Biosciences Division, Catalysis Sciences Program [DE-SC0016192]
  5. Robert A. Welch Foundation [W-0031]
  6. Direct For Education and Human Resources [1449785] Funding Source: National Science Foundation

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Supported metal catalysts, which are composed of metal nanoparticles dispersed on metal oxides or other high-surface-area materials, are ubiquitous in industrially catalysed reactions. Identifying and characterizing the catalytic active sites on these materials still remains a substantial challenge, even though it is required to guide rational design of practical heterogeneous catalysts. Metal-support interactions have an enormous impact on the chemistry of the catalytic active site and can determine the optimum support for a reaction; however, few direct probes of these interactions are available. Here we show how benzyl alcohol oxidation Hammett studies can be used to characterize differences in the catalytic activity of Au nanoparticles hosted on various metal-oxide supports. We combine reactivity analysis with density functional theory calculations to demonstrate that the slope of experimental Hammett plots is affected by electron donation from the underlying oxide support to the Au particles.

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