The role of co-adsorbed metal atoms in the chemistry of methyl species on Pt(111) formed by the decomposition of dimethylmercury and dimethylzinc

John C Wenger, Darren J Oakes, Martin McCoustra, Michael A Chesters

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Abstract

The chemistry of methyl species resulting from the decomposition of dimethyhmercury (DMM) and dimethylzinc (DMZ) on Pt(111) in the range 300-400 K has been investigated by temperature programmed desorption (TPD) and Auger electron spectroscopy (AES). In each case at 300 K, dissociative adsorption of the precursor results in the formation of an adlayer of methylmetal (CH(3)M) moieties. These species are thermally stable to around 350 K before decomposing to yield mainly gaseous products, methane and hydrogen, and surface bound metal atoms. For DMM, subsequent heating to 400 K or direct dissociative adsorption at 400 K results in the formation of ethyiidyne species. Ethylidyne formation is not observed in the thermal chemistry of DMZ at temperatures below 400 K and only transiently in the chemistry at 400 K. Complementary TPD and AES data indicate that, for DMM, desorption of the mercury atoms produced by CH3Hg decomposition is the limiting factor in allowing the prevailing C-1 species to couple to form ethylidyne. In contrast, AES evidence indicates that zinc atoms remain on the surface to temperatures in excess of 750 K and hence prevent C-C coupling by blocking surface sites.
Original languageEnglish
Pages (from-to)81-92
Number of pages12
JournalSurface Science
Volume360
Issue number1-3
DOIs
Publication statusPublished - 10 Jul 1996

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