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Title: The chemistry of acetylene on the Ru(001)-p(2 times 2)O and Ru(001)-p(1 times 2)O surfaces

Journal Article · · Journal of the American Chemical Society; (USA)
DOI:https://doi.org/10.1021/ja00232a002· OSTI ID:5093748
; ;  [1]
  1. California Institute of Technology, Pasadena (USA)

The chemisorption and decomposition of acetylene on Ru(001) surfaces with ordered p(2{times}2) and p(1{times}2) overlayers of oxygen adatoms has been studied by using high-resolution electron energy loss spectroscopy and thermal desorption mass spectrometry. The chemisorbed acetylene species formed on these oxygen precovered surfaces are not significantly different from molecularly chemisorbed acetylene on clean Ru(001), although one of the two types of chemisorbed acetylene formed on the clean surface is not formed on Ru(001)-p(1{times}2)O. The preadsorption of oxygen reduces the saturation coverages of chemisorbed acetylene, which is approximately 0.39 on clean Ru(001), 0.31 on Ru(001)-p(2{times}2)O, and 0.09 on Ru(001)-p(1{times}2)O. As on clean Ru(001), the chemisorbed acetylene on the oxygen-precovered surfaces does not desorb upon annealing but rather decomposes between 200 and 350 K to produce a number of stable intermediates, including ethylidyne (CCH{sub 3}), acetylide (CCH), methylidyne (CH), and an sp{sup 2}-hybridized vinylidene (CCH{sub 2}) species. The vinylidene is formed in particularly large amounts on Ru(001)-p(2{times}2)O after annealing to 350 K and appears to be stabilized strongly by the presence of coadsorbed oxygen because it is formed not at all or in trivial amounts on clean Ru(001). The stability, formation, and decomposition of the various intermediates is discussed, and the results are compared with earlier work. The decomposition of all of these intermediates leads eventually to hydrogen desorption, which is complete on both oxygen-precovered surfaces by approximately 700 K. 26 refs., 7 figs., 2 tabs.

OSTI ID:
5093748
Journal Information:
Journal of the American Chemical Society; (USA), Vol. 110:24; ISSN 0002-7863
Country of Publication:
United States
Language:
English