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Photoelectron diffraction study of a catalytically active overlayer: C2H2 on Pd{111}
Authors:C J Baddeley  A F Lee  R M Lambert  T Gie   el  O Schaff  V Fernandez  K -M Schindler  A Theobald  C J Hirschmugl  R Lindsay  A M Bradshaw and D P Woodruff
Institution:

a Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK

b Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4–6, 14195 Berlin-Dahlem, Germany

c Department of Physics, University of Warwick, Coventry CV4 7AL, UK

Abstract:A quantitative structure determination of a newly discovered (2×2) adsorption phase of acetylene chemisorbed on Pd{111} has been performed by scanned-energy mode photoelectron diffraction: this phase corresponds to the threshold coverage for the catalytic conversion of acetylene to benzene. The carbon atoms in the C2H2 molecule are located almost over bridge sites with a C–C bond length of 1.34+0.10 Å, the centre of the molecule being positioned almost over a hollow site. Of the two hollow sites the hcp site (directly above a second layer Pd atom) is favoured, particularly by a subset of the data most sensitive to this aspect of the structure, but the full analysis indicates that the fcc site (above a third layer Pd atom) cannot formally be excluded. The adsorption site adopted by acetylene in the higher coverage Image phase on Pd{111} is essentially identical. This is the dominant structure in the coverage regime which is catalytically active for the conversion of acetylene to benzene. The implications of these findings for acetylene coupling reactions over Pd{111} are discussed.
Keywords:Acetylene  Palladium  Gas adsorption  Catalysis  Single crystals  Electron diffraction  Chemisorption  Chemical bonds  Benzene  Photoelectron diffraction  Low index single crystals
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