Growth of ordered bithiophene layers on the p(2x1)O reconstructed Cu(110) surface

被引:22
作者
Koller, G [1 ]
Blyth, RIR [1 ]
Sardar, SA [1 ]
Netzer, FP [1 ]
Ramsey, MG [1 ]
机构
[1] Karl Franzens Univ Graz, Inst Expt Phys, A-8010 Graz, Austria
基金
奥地利科学基金会;
关键词
angle resolved photoemission; near edge extended X-ray absorption fine structure (NEXAFS); thermal desorption spectroscopy; self-assembly; copper; aromatics; low index single crystal surfaces;
D O I
10.1016/S0039-6028(03)00592-2
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
Submonolayer to multilayer coverages of bithiophene on the clean Cu(1 1 0) and the Cu(1 1 0)-p(2 x 1)O reconstructed surface have been investigated comparatively with thermal desorption spectroscopy, angle resolved ultraviolet photoemission spectroscopy (ARUPS) and near edge X-ray absorption fine structure spectroscopy. On the clean Cu(I 10) substrate the bithiophene monolayer is strongly bound via the pi-orbitals and flat lying. After the completion of the wetting layer, further growth occurs in islands with no evidence for a preferred molecular orientation or order. In contrast, on the oxygen reconstructed surface the wetting layer formed has a weaker interaction with the substrate and in this monolayer the molecular plane is tilted with respect to the surface. For the multilayer film on the Cu(1 1 0)-p(2 x 1)O reconstructed surface the ARUPS displays a distinct azimuthal anisotropy. This is suggested to arise from a template effect of the reconstruction. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 165
页数:11
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