Oxidation of carbidic carbon on a rhodium surface |
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Authors: | S N Mikhailov L C A van den Oetelaar H H Brongersma R A van Santen |
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Affiliation: | (1) Schürt Institute of Catalysis, Eindhoven University of Technology, PO Box513, 5600 MB Eindhoven, The Netherlands |
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Abstract: | Different mechanisms of atomic carbon and oxygen recombination on a rhodium surface are studied with Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS). The kinetics of adsorbed carbidic carbon oxidation (carbon coverage
c 0.1–0.3 ML) by gas-phase oxygen that proceeds by a Langmuir-Hinshelwood reaction mechanism, provides the value of the activation energy for recombination (E
rec
t
170±20 kJ/mol).E
rec
t
depends slightly on the carbon coverage. An Eley-Rideal type of reaction was observed for adsorbed oxygen and atomic gas-phase carbon recombination which occurs in a dynamic regime. The low value found for the activation energy (near zero) is consistent with the mechanism that this exothermic reaction is too fast for energy dissipation into the substrate; the energy is mainly transferred into translational, vibrational and rotational energy of CO.On leave from A.F. Ioffe Institute, St. Petersburg, Russia. |
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Keywords: | kinetics carbon oxygen recombination rhodium surface characterisation XPS AES |
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