Nitric oxide reduction by CO ON Rh(111): Temperature programmed reaction |
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Authors: | T.W. Root L.D. Schmidt Galen B. Fisher |
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Affiliation: | Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, USA;Physical Chemistry Department, General Motors Research Laboratories, Warren, Michigan 48090, USA |
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Abstract: | The reaction of NO with CO on Rh(111) has been studied with temperature programmed reaction (TPR). Comparisons are made with the reaction of O2 with CO and the reaction of NO with H2. The rate-determining step for both CO oxidation reactions is CO(a) + O(a) → CO2(g). Repulsive interactions between adsorbed CO and adsorbed nitrogen atoms lead to desorption of CO in a peak at 415 K which is in the temperature range where the reaction between CO(a) and O(a) produces CO2(g). Thus the extent of reaction of CO(a) with NO(a) is less than that between CO(a) and O(a) due to the lower coverage of CO caused by adsorbed N atoms and NO. A similar repulsive interaction between NO(a) and H(a) suppresses the NO + H2 reaction. CO + NO reaction behavior on Rh(111) is compared to that observed on Pt(111). |
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