Au deposits on graphite: On the nature of high temperature desorption peaks in CO thermal desorption spectra |
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Authors: | T. Nowitzki C. Deiter K. Al-Shamery |
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Affiliation: | a Institut für Angewandte und Physikalische Chemie, Universität Bremen, Postfach 330440, D-28334 Bremen, Germany b Physikalische Chemie, Universität Oldenburg, Postfach 2503, D-25111 Oldenburg, Germany |
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Abstract: | Due to the discovery of Au as a catalyst for low temperature CO oxidation, the adsorption of CO on Au surfaces has attracted a lot of attention recently. On stepped and rough single crystal surfaces as well as on deposited particles two characteristic desorption states above 100 K have been observed via TPD. We have studied Au deposits on graphite in order to elucidate the nature of these desorption peaks in more detail. For this purpose, Au was deposited at 100 K and 300 K on HOPG as a weakly interacting support. In analogy to other supports, we obtain two desorption states (∼140 K and ∼170 K) whose relative intensities depend strongly on the deposition temperature with the high temperature peak being much more pronounced for the 100 K deposits. After annealing to 600 K, both states drastically lose intensity. XP spectra, on the other hand, show virtually no decrease of the Au 4f intensity as would be expected for desorption or significant changes of the particle morphologies. We conclude that both desorption peaks are defect-related and connected with under-coordinated Au atoms that are lost for the most part upon annealing. These sites could be located at the perimeter of dendritic islands or on small, defect-rich particles in addition to larger particles not adsorbing CO at 100 K. Preliminary STM results are in favour of the second interpretation. |
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Keywords: | Gold Graphite Carbon monoxide Scanning tunneling microscopy Temperature programmed desorption Photoelectron spectroscopy |
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