共 6 条
Evolution of one-dimensional Cs chains on InAs(110) as determined by scanning-tunneling microscopy and core-level spectroscopy
被引:31
|作者:
Modesti, S
Falasca, A
Polentarutti, M
Betti, MG
De Renzi, V
Mariani, C
机构:
[1] Univ Modena, Dipartimento Fis, Ist Nazl Fis Mat, I-41100 Modena, Italy
[2] TASC Lab, Ist Nazl Fis Mat, I-34012 Trieste, Italy
[3] Univ Trieste, Dipartimento Fis, I-34127 Trieste, Italy
关键词:
alkali metals;
indium arsenide;
metal-semiconductor interfaces;
scanning tunneling microscopy;
surface structure;
morphology;
roughness;
and topography;
visible and ultraviolet photoelectron spectroscopy;
D O I:
10.1016/S0039-6028(99)01155-3
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 present a combined scanning tunneling microscopy and ultraviolet photoelectron spectroscopy investigation on the formation and evolution of one-dimensional (1D) Cs chains on the InAs(110) surface. At 40% of saturation coverage, the linear phase evolves into a two-dimensional (2D) cluster layer. Each Cs nanowire, several hundreds of angstroms long, is aligned along the [1(1) over bar 0] direction. The Cs chain phase presents different adsorption sites, as deduced by the Cs 5p core-level lineshape and STM. The coverage dependence of the mean interchain distance shows that the Cs nanowires repel each other in the [001] direction, even when they are about 50 Angstrom apart. A repulsive long-range dipole-like interaction influences the mesoscopic properties of the chain phase. The binding energy shift of the Cs core levels can be quantitatively explained, taking into account the Cs depolarization as a function of the chain-chain distance. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:133 / 142
页数:10
相关论文