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- W2124670109 abstract "Pd–Au bimetallic catalysts have shown promising performance in numerous reactions that involve hydrogen. Fundamental studies of hydrogen interactions with Pd–Au surfaces could provide useful insights into the reaction mechanisms over Pd–Au catalysts, which may, in turn, guide future catalyst design. In this study, the interactions of hydrogen (i.e., adsorption, absorption, diffusion, and desorption) with Pd/Au(111) model surfaces were studied using temperature-programmed desorption (TPD) under ultrahigh-vacuum conditions. Our experimental results reveal Pd–Au bimetallic surfaces readily dissociate H2 and yet also weakly bind H adatoms, properties that could be beneficial for catalytic reactions involving hydrogen. The presence of contiguous Pd sites, characterized by reflection–absorption infrared spectroscopy using CO as a probe molecule (CO-RAIRS), was found to be vital for the dissociative adsorption of H2 at 77 K. The H adatom binds to Pd–Au alloy sites more strongly than to Au(111) but more weakly th..." @default.
- W2124670109 created "2016-06-24" @default.
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- W2124670109 creator A5072678129 @default.
- W2124670109 creator A5077813936 @default.
- W2124670109 date "2013-09-26" @default.
- W2124670109 modified "2023-10-18" @default.
- W2124670109 title "Hydrogen Adsorption and Absorption with Pd–Au Bimetallic Surfaces" @default.
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- W2124670109 doi "https://doi.org/10.1021/jp406736b" @default.
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