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Photoelectron diffraction study of a catalytically active overlayer: C2H2 on Pd{111}

MPS-Authors
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Gießel,  Tatjana
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Schaff,  Oliver
Fritz Haber Institute, Max Planck Society;

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Fernandez,  V.
Fritz Haber Institute, Max Planck Society;

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Schindler,  Karl-Michael
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Theobald,  Andreas
Fritz Haber Institute, Max Planck Society;

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Hirschmugl,  C. J.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Lindsay,  Robert
Fritz Haber Institute, Max Planck Society;

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Bradshaw,  Alexander M.
Theory, Fritz Haber Institute, Max Planck Society;

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Citation

Baddeley, C., Lee, A., Lambert, R., Gießel, T., Schaff, O., Fernandez, V., et al. (1998). Photoelectron diffraction study of a catalytically active overlayer: C2H2 on Pd{111}. Surface Science, 400(1-3), 166-175. doi:10.1016/S0039-6028(97)00859-5.


Cite as: https://hdl.handle.net/21.11116/0000-0008-9D1F-6
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 (3x3)R30° 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.