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

Gao, Feng, Wang, Yilin, Goodman, D. Wayne·2009·Journal of the American Chemical Society

Abstract

It is demonstrated that gas-phase CO pressure higher than approximately 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 approximately 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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Metadata

Authors
Gao, F., Wang, Y., & Goodman, D. W.
Venue
Journal of the American Chemical Society
Published
2009-04-02
Volume
131
Issue
16
Pages
5734-5735
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2087076159
Cited by
246
References
0
FWCI
7.50
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: CO Oxidation over AuPd(100) from Ultrahigh Vacuum to Near-Atmospheric Pressures: The Critical Role of Contiguous Pd Atoms. https://app.cochat.ai/papers/10.1021/ja9008437
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Gao, F., Wang, Y., & Goodman, D. W. (2009). CO Oxidation over AuPd(100) from Ultrahigh Vacuum to Near-Atmospheric Pressures: The Critical Role of Contiguous Pd Atoms. Journal of the American Chemical Society. https://doi.org/10.1021/ja9008437

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.