Mäkinen Antti J, Long James P, Watkins Neil J, Kafafi Zakya H
Naval Research Laboratory, 4555 Overlook Avenue S.W., Washington, D.C. 20375, USA.
J Phys Chem B. 2005 Mar 31;109(12):5790-5. doi: 10.1021/jp044921y.
We have investigated the initial stages of vacuum-deposited sexithiophene (alpha-6T) adlayer formation on Au(111) vicinal surfaces at room temperature. The in situ scanning tunneling microscopy (STM) and photoemission spectroscopy (PES) reveal a step edge-driven growth of alpha-6T on the Au(111) vicinal surfaces that first leads to the formation of an ordered monolayer, comprising two phases with the molecular major axes aligned along the step edges. The monolayer formation is then followed by the appearance of a single-phase 2D superstructure at a two-monolayer coverage. The results highlight the potential of using vicinal metal surfaces as templates for generating organized organic nanostructures over macroscopic areas for applications in organic electronics and moletronics.
我们研究了室温下在Au(111) 近邻表面上真空沉积六噻吩(α-6T)吸附层形成的初始阶段。原位扫描隧道显微镜(STM)和光电子能谱(PES)揭示了α-6T在Au(111) 近邻表面上由台阶边缘驱动的生长过程,该过程首先导致形成有序单层,其由两个相组成,分子长轴沿台阶边缘排列。然后在覆盖两层时出现单相二维超结构。这些结果突出了使用近邻金属表面作为模板在宏观区域生成有组织的有机纳米结构以应用于有机电子学和分子电子学的潜力。