Evolution of adsorbed species during C2H2 adsorption on Ni(111) in relation to their vibrational spectra

作者：J.C. Bertolini, J. Massardier, Gisèle Dalmai-Imelik · 发表于：Journal of the Chemical Society Faraday Transactions 1 Physical Chemistry in Condensed Phases · 年份：1978 · DOI：10.1039/f19787401720 · 被引用次数：56 · 研究领域：Advanced Chemical Physics Studies、Electron and X-Ray Spectroscopy Techniques、Surface Chemistry and Catalysis

Acetylene adsorption at room temperature on Ni (111) has been studied by low energy electron diffraction (l.e.e.d.), thermal desorption, work function changes and high resolution electron energy loss spectroscopy (h.r.e.l.s.). The existence of two adsorbed states has been demonstrated depending upon exposure.At low exposure, C2H2 is associatively adsorbed but a large rehybridization occurs, characterized by a carbon–carbon bond order close to 1.15. According to its hybridization state C2H2 should be adsorbed on a triangular site through two σ bonds and one π bond with nickel atoms.With increasing exposure, large modifications occur. In addition to self-hydrogenated species, benzene should be formed as shown by comparison of the vibrational spectra of adsorbed C2H2 and adsorbed C6H6. This conclusion is in agreement with the benzene formation as detected after contact between C2H2 and Ni/SiO2 catalysts with (111) exposed faces.