Morf Peter, Raimondi Fabio, Nothofer Heinz-Georg, Schnyder Bernhard, Yasuda Akio, Wessels Jurina M, Jung Thomas A
Laboratory for Micro and Nanotechnology, Paul Scherrer Institut, 5232 Villigen, Switzerland.
Langmuir. 2006 Jan 17;22(2):658-63. doi: 10.1021/la052952u.
Self-assembled monolayers have evolved into one of the best established self-assembly systems with high relevance in a scientific and applied context. So far, however, virtually exclusively thiol functional groups have been used for the investigation of fundamental processes on metal surfaces. In this paper, an alternative binding group, the dithiocarbamate (DTC) group, is re-visited. Complete SAM formation with new layer properties characteristically different from thiol SAMs is demonstrated for mono-functional acyclic and bifunctional cyclic dithiocarbamates on Au111 by X-ray photoelectron spectroscopy, cyclic voltammetry, and scanning tunneling microscopy. Furthermore, the chemical adsorption and voltammetric desorption reactions are quantitatively determined. The resonant bi-dentate structure of the DTC provides a characteristically different molecule-metal coupling compared to the thiols and makes the DTC an interesting system for molecular electronics.
自组装单分子层已发展成为在科学和应用领域中具有高度相关性的最成熟的自组装系统之一。然而,到目前为止,几乎仅使用硫醇官能团来研究金属表面的基本过程。在本文中,我们重新审视了一种替代的结合基团——二硫代氨基甲酸盐(DTC)基团。通过X射线光电子能谱、循环伏安法和扫描隧道显微镜,我们证明了单官能无环和双官能环状二硫代氨基甲酸盐在Au111上能够形成具有与硫醇自组装单分子层显著不同的新层性质的完整自组装单分子层。此外,还对化学吸附和伏安脱附反应进行了定量测定。与硫醇相比,DTC的共振双齿结构提供了一种显著不同的分子 - 金属耦合方式,这使得DTC成为分子电子学中一个有趣的系统。