Aix-Marseille Université, IM2NP, CNRS UMR 6242, Campus de Saint-Jérôme, Case 142, F-13397 Marseille Cedex 20, France.
Langmuir. 2011 Jan 18;27(2):627-9. doi: 10.1021/la103641w. Epub 2010 Dec 20.
We studied the coverage-dependent self-assembly of the flat-lying phase of ethylthiolate on Au(111). At low coverage, we observed the formation of short stripes of chiral Au-(SC(2)H(5))(2) complexes that arrange in a disordered phase. The latter grow partly at the expense of the native Au(111) surface reconstruction, which is fully lifted for a coverage of ∼0.60 ML. We found that the lift of the reconstruction and evaporation from step edges are competing adatom sources. Close to saturation coverage (0.70 to 0.75 ML), large, well-ordered domains with a (8 × √3)rectangular superstructure formed. Alternation of chirality was found in adjacent stripes as already reported for other short alkanethiolates. We suggest that, because of a simple geometrical consideration, the chirality should, on the contrary, be preserved in the stripe phase of longer alkanethiolates.
我们研究了在金(111)表面上伸展的乙基硫醇单层的覆盖率相关的自组装。在低覆盖率下,我们观察到短的手性金-(SC(2)H(5))(2) 配合物条纹的形成,这些条纹无序排列。后者的形成部分是牺牲了原生金(111)表面重构的结果,当覆盖率达到约 0.60 ML 时,表面重构完全被抬升。我们发现,重构的抬升和台阶边缘的蒸发是竞争的 adatoms 源。在接近饱和覆盖度(0.70 到 0.75 ML)时,形成了大的、有序的、具有(8 × √3)rectangular 超结构的畴。在相邻条纹中发现了手性的交替,这已经在其他短链烷硫醇中报道过。我们认为,由于一个简单的几何考虑,手性应该在较长链烷硫醇的条纹相中得到保持。