Structural analysis of Pt(111)c(√3x5)rect.-CO using photoelectron diffraction

被引:4
|
作者
Nisbet, G.
Lamont, C. L. A. [1 ]
Polcik, M.
Terborg, R.
Sayago, D. I.
Hoeft, J. T.
Kittel, M.
Toomes, R. L.
Woodruff, D. P.
机构
[1] Univ Huddersfield, Dept Chem & Biol Sci, Huddersfield HD1 3DH, W Yorkshire, England
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[3] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
carbon monoxide; photoelectron diffraction; platinum; surface structure;
D O I
10.1016/j.susc.2006.12.073
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Core level shift scanned-energy mode photoelectron diffraction using the two distinct components of the C 1s emission has been used to determine the structure of the Pt(111)c(root 3 x 5)rect.-CO phase formed by 0.6 ML of adsorbed CO. The results confirm earlier assignments of these components to CO in atop and bridging sites, further confirm that the best structural model involves a 2:1 occupation ratio of these two sites, and provides quantitative structural parameter values. In particular the Pt-C chemisorption bondlengths for the atop and bridging sites are, respectively, 1.86 +/- 0.02 angstrom and 2.02 +/- 0.04 angstrom. These values are closely similar to those found in the 0.5 ML coverage c(4 x 2) phase, involving an atop:bridge occupation ratio of 1:1, obtained in earlier quantitative low energy electron diffraction studies. The results also indicate a clear tilt of the molecular axis of atop CO species in this compression phase, consistent with the finding of an earlier electron-stimulated desorption ion angular distribution investigation. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1296 / 1303
页数:8
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