4.8 Article

CO Oxidation over AuPd(100) from Ultrahigh Vacuum to Near-Atmospheric Pressures: The Critical Role of Contiguous Pd Atoms

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 16, Pages 5734-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja9008437

Keywords

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Funding

  1. Department of Energy, Office of Basic Energy Sciences, Division of Chemical-Sciences, Geosciences, and Biosciences [DE-FG02-95ER-14511]
  2. Robert A. Welch Foundation

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It is demonstrated that gas-phase CO pressure higher than similar to 0.1 Torr is required to segregate a sufficient amount of Pd to the surface of a well-annealed AuPd(100) sample to form contiguous Pd sites. These contiguous sites are critical in dissociating O-2 for low-temperature CO oxidation, where CO chemisorbed on Au sites clearly participates in the reaction at temperatures below similar to 400 K. Measured reaction kinetics demonstrates that the higher reaction rate is achieved on a surface with higher coverages of contiguous Pd sites.

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