The structure of oxygen on Cu(100) at low and high coverages

被引:73
作者
Kittel, M
Polcik, M
Terborg, R
Hoeft, JT
Baumgärtel, P
Bradshaw, AM
Toomes, RL
Kang, JH
Woodruff, DP [1 ]
Pascal, M
Lamont, CLA
Rotenberg, E
机构
[1] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[3] Univ Huddersfield, Dept Chem & Biol Sci, Ctr Appl Catalysis, Huddersfield HD1 3DH, W Yorkshire, England
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
基金
英国工程与自然科学研究理事会;
关键词
surface structure; morphology; roughness; and topography; surface relaxation and reconstruction; copper; oxygen; chemisorption; photoelectron diffraction;
D O I
10.1016/S0039-6028(00)00873-6
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
The local adsorption structure of oxygen on Cu(1 0 0) has been studied using O Is scanned-energy mode photoelectron diffraction. A detailed quantitative determination of the structure of the 0.5 ML (root2 x 2 root2)R45 degrees -O ordered phase confirms the missing-row character of this reconstruction and agrees well with earlier structural determinations of this phase by other methods, the adsorbed O atoms lying only approximately 0.1 Angstrom above the outermost Cu layer. At much lower coverages, the results indicate that the O atoms adopt unreconstructed hollow sites at a significantly larger O-Cu layer spacing, but with some form of local disorder. The best fit to these data is achieved with a two-site model involving O atoms at Cu-O layer spacings of 0.41 and 0.70 Angstrom in hollow sites: these two sites (also implied by an earlier electron-energy-loss study) are proposed to be associated with edge and centre positions in very small c(2 x 2) domains as seen in a recent scanning tunnelling microscopy investigation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:311 / 324
页数:14
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