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Local reaction environments and their properties for ethene deuterogenation on the surfaces of SMSI catalysts

DOI: 10.1039/f19888404337

Source and publish data:

Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases p. 4337 - 4346 (1988)

Update date:2022-08-10

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Authors:

Yoshitake, HideakiYoshitake, Hideaki

Asakura, KiyotakaAsakura, Kiyotaka

Iwasawa, YasuhiroIwasawa, Yasuhiro

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Article abstract of DOI:10.1039/f19888404337

Ethene deuterogenation and H2-D2 exchange reaction over Nb2O5-supported Rh and Ir catalysts have been investigated in relation to strong metal-support interaction (SMSI) phenomena.The activation energies for these reactions were considerably changed by high-temperature reduction of the catalyst in the case of Ir/Nb2O5, but were not modified in the case of Rh/Nb2O5.The change is ascribed to a reduction in the energy barrier for deuterium dissociation.The deuterium distribution in ethane formed during ethene deuterogenation was also investigated at various reaction temperatures and as a function of the reduction time of the catalyst.By studying the catalysts in their working state instead of by static adsorption measurements two kinds of active sites in different environments are suggested to exist on the surface of these catalysts in the SMSI states.One of the sites (site I) is on the bare metal surface and the other (site II) is on the perimeter of a migrating NbOx island.The surface isotropic ratio of hydrogen during ethene deuterogenation is different at sites I and II.Site I, on which D2 dissociates, acts as a deuterium supply for site II.A model for the deuterogenation of ethene on the SMSI catalysts is proposed.

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