Copper electrodeposition on alkanethiolate covered gold electrodes

被引:45
作者
Cavalleri, O
Bittner, AM [1 ]
Kind, H
Kern, K
机构
[1] Ecole Polytech Fed Lausanne, Inst Phys Expt, CH-1015 Lausanne, Switzerland
[2] Univ Zurich, Inst Phys, CH-8057 Zurich, Switzerland
来源
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS | 1999年 / 208卷
关键词
cyclic voltammetry; film growth; scanning tunnelling microscopy (STM); single crystal electrode; surface structure; thiols; X-ray photoelectron spectroscopy (XPS);
D O I
10.1524/zpch.1999.208.Part_1_2.107
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 have investigated the structure and thermal dynamics of alkanethiolate layers on Au(111) with variable temperature scanning tunnelling microscopy (STM), X-ray photoelectron spectroscopy (XPS) and voltammetry. The results build the basis for a study of electrodeposition of copper on alkanethiolate-covered Au(111). Electrodeposition has been studied as a function of the thiolate chain length, the deposition potential and the temperature. Time-resolved in situ STM and voltammetry, both at temperatures up to 345 K, and XPS of emersed samples showed that copper can - depending on the deposition potential - either form nanometer-sized islands or layers, both without destruction of the thiolate. We propose a mechanism where copper penetrates the thiolate layer The slow deposition rate is determined only by kinetic factors since Cu/Cu2+ exchange processes cannot operate. Finally we discuss the role of thiolates as preadsorbed surfactants.
引用
收藏
页码:107 / 136
页数:30
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