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In Situ controlled promotion of catalyst surfaces via NEMCA: the effect of Na on the Pt-catalyzed CO oxidation

Gentekakis Ioannis, Moggridge, G.D, Vayenas, Costas G, Lambert Richard M.

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URI: http://purl.tuc.gr/dl/dias/52AF71A8-1CEC-44B5-9E75-8B3D07050483
Year 1994
Type of Item Peer-Reviewed Journal Publication
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Bibliographic Citation I. V. Yentekakis, G. Moggridge, C. G. Vayenas and R. M. Lambert, "In Situ controlled promotion of catalyst surfaces via NEMCA: The effect of Na on the Pt-catalyzed CO oxidation", J. Catal., vol. 146, no. 1, pp. 292-305, Mar. 1994. doi:10.1016/0021-9517(94)90033-7 https://doi.org/10.1016/0021-9517(94)90033-7
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Summary

It was found that the catalytic activity of Pt for CO oxidation can be markedly and reversibly affected by depositing polycrystalline Pt films on β″-Al2O3, a Na+ conductor, and applying external potentials to supply or remove Na to or from the Pt catalyst surface. The change in the rate of CO oxidation is typically 103-105 times larger than the rate of supply or removal of Na. The use of the β″-Al2O3 solid electrolyte supports permits precise in situ control of the Na coverage on the Pt surface. Sodium coverages of 0.02 cause up to 600% steady-state increase in the rate of CO oxidation under CO-rich conditions. The promoting effect is due to enhanced oxygen chemisorption on the Pt surface. Higher (>0.06) Na coverages poison the rate severely and reversibly due to the formation of a CONaPt surface complex. Rate oscillations can be reversibly induced or stopped and their frequency can be controlled by controlling the catalyst potential VWR and average work function eφ.

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