On the structure and evolution of the buried S/Au interface in self-assembled monolayers: X-ray standing wave results

被引:156
作者
Fenter, P
Schreiber, F
Berman, L
Scoles, G
Eisenberger, P
Bedzyk, MJ
机构
[1] Argonne Natl Lab, Div Environm Res, Argonne, IL 60439 USA
[2] Brookhaven Natl Lab, Natl Synchrotron Light Source, Upton, NY 11973 USA
[3] Max Planck Inst Met Forsch, D-70569 Stuttgart, Germany
[4] Princeton Univ, Princeton Mat Inst, Princeton, NJ 08542 USA
[5] Columbia Univ, Lamont Doherty Earth Observ, New York, NY 10027 USA
[6] Northwestern Univ, Dept Mat Sci, Evanston, IL 60208 USA
关键词
decanethiol; gold; metal-organic interfaces; self-assembly; single crystal surfaces; surface structure; morphology; roughness; and topography; X-ray standing waves;
D O I
10.1016/S0039-6028(98)00428-2
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
We describe a structural study of the S/Au interface for decanethiol monolayers (C10) on a Au(111) surface using the technique of X-ray standing waves (XSWs). The XSW results for full-coverage monolayers are inconsistent with any model incorporating a single sulfur adsorption site, such as the widely assumed threefold hollow site on the Au(111) surface. Instead, the XSW results reveal two distinct sulfur head group sites, each with a distinct lateral and vertical location with respect to the underlying gold lattice. We discuss structural models that are consistent with these results. We have also studied the evolution of the structure versus coverage with XSW and X-ray photoelectron spectroscopy (XPS) and have determined that the local S/Au interface structure of the "lying down" striped phase at low coverages (0.27 ML, 1 ML=4.62 x 10(14) molecules cm(-2)) is indistinguishable from that of the "standing up" c(4 x 2) phase at saturation (1 ML). Some important implications concerning the structure acid growth of these monolayers are discussed. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:213 / 235
页数:23
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