School of Physics and Astronomy, Cardiff University, Cardiff CF24 3AA, UK.
Langmuir. 2010 Jun 1;26(11):8174-9. doi: 10.1021/la9044754.
Using scanning tunnelling microscopy (STM), we have studied mixed self-assembled monolayers of linear alkanethiol molecules. Nonanedithiol (C9S2), nonanethiol (C9S), decanethiol (C10S), and dodecanethiol (C12S) were inserted into a self-assembled octanethiol (C8S) host matrix monolayer on an Au(111) surface using a two-step method. Quasi-one-dimensional double-row structures were found in the ordered, close-packed domains of the C8S matrix for each mixed monolayer system. These close-packed domains coexist with ordered striped phase domains (for C9S and C10S) or with a disordered phase (for C9S2 and C12S). Results from high-resolution images suggest that the double-rows are composed of inserted non-nearest-neighbor substitutional molecules, the ordering of which may be a result of locally induced surface stress.
我们使用扫描隧道显微镜(STM)研究了线性烷硫醇分子的混合自组装单层。在 Au(111)表面上,我们使用两步法将正九硫醇(C9S2)、正九硫醇(C9S)、正十硫醇(C10S)和正十二硫醇(C12S)插入到自组装的正八硫醇(C8S)主基质单层中。对于每个混合单层体系,在 C8S 基质的有序、密堆积区域中都发现了准一维双排结构。这些密堆积区域与有序条纹相域(对于 C9S 和 C10S)或无序相共存(对于 C9S2 和 C12S)。高分辨率图像的结果表明,双排由插入的非最近邻取代分子组成,其有序性可能是由局部诱导的表面应力引起的。