Kang Hungu, Ito Eisuke, Hayashi Tomohiro, Hara Masahiko, Noh Jaegeun
J Nanosci Nanotechnol. 2016 Jun;16(6):6360-3. doi: 10.1166/jnn.2016.12115.
The surface structures of self-assembled monolayers (SAMs) formed by the adsorption of pentachlorobenzenethiol (PCBT) molecules on Au(111) as a function of solution concentration were examined by means of scanning tunneling microscopy (STM) to understand the effect of concentration on the formation of ordered domains. STM imaging revealed that PCBT SAMs formed in a 0.01 or 1 mM ethanol solution at room temperature for 20 min contained small ordered domains in the range of several to 20 nm2 and disordered phases, while PCBT SAMs formed in a 0.1 mM ethanol solution were composed of long-range ordered domains in the range of 20 to 50 nm2, which can be assigned as a (4 x √3)R45 degrees packing structure. Interestingly, the bright aggregated domains stacked by π-π interactions between PCBT rings were usually observed around boundary regions of ordered domains. In addition, X-ray photoelectron spectroscopy measurements revealed that ordered PCBT SAMs on Au(111) were formed via the chemical interactions between the sulfur atom of PCBT and gold surface. Our results obtained here will be very useful in understanding the formation and structure of PCBT SAMs on gold surfaces.
通过扫描隧道显微镜(STM)研究了五氯苯硫醇(PCBT)分子吸附在Au(111)上形成的自组装单分子层(SAMs)的表面结构随溶液浓度的变化,以了解浓度对有序域形成的影响。STM成像显示,在室温下于0.01或1 mM乙醇溶液中形成20分钟的PCBT SAMs包含几至20 nm2范围内的小有序域和无序相,而在0.1 mM乙醇溶液中形成的PCBT SAMs由20至50 nm2范围内的长程有序域组成,可以归为(4 x √3)R45°堆积结构。有趣的是,通常在有序域的边界区域周围观察到由PCBT环之间的π-π相互作用堆叠而成的明亮聚集域。此外,X射线光电子能谱测量表明,Au(111)上的有序PCBT SAMs是通过PCBT的硫原子与金表面之间的化学相互作用形成 的。我们在此获得的结果对于理解金表面上PCBT SAMs的形成和结构将非常有用。