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Phase Transition of Octaneselenolate Self-assembled Monolayers on Au(111) Studied by Scanning Tunneling Microscopy

机译:扫描隧道显微镜研究Au(111)上辛烯油酸酯自组装单分子膜的相变

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We investigated the surface structure and wetting behavior of octaneselenolate self-assembled monolayers (SAMs) on Au(111) formed in a 50 μM ethanol solution according to immersion time, using scanning tunneling microscopy (STM) and an automatic contact angle (CA) goniometer. Closely-packed, well-ordered alkanethiol SAMs would form as the immersion time increased; unexpectedly, however, we observed the structural transition of octaneselenolate SAMs from a molecular row phase with a long-range order to a disordered phase with a high density of vacancy islands (VIs). Molecularly resolved STM imaging revealed that the missing-row ordered phase of the SAMs could be assigned as a (6 × √3)R30° superlattice containing three molecules in the rectangular unit cell. In addition, CA measurements showed that the structural order and defect density of VIs are closely related to the wetting behaviors of octaneselenolate SAMs on gold. In this study, we clearly demonstrate that interactions between the headgroups and gold surfaces play an important role in determining the physical properties and surface structure of SAMs.
机译:我们使用扫描隧道显微镜(STM)和自动接触角(CA)测角仪研究了浸入时间为50μM的乙醇溶液中形成的Au(111)上的辛烯硒酸酯自组装单分子膜(SAMs)的表面结构和润湿行为。随着浸泡时间的增加,会形成密排,有序的链烷硫醇SAM。然而,出乎意料的是,我们观察到辛烯硒酸酯SAMs的结构从具有长程有序的分子行相转变为具有高空位岛(VIs)密度的无序相。分子分辨STM成像显示,SAM的缺失行有序相可以指定为在矩形晶胞中包含三个分子的(6×√3)R30°超晶格。此外,CA测量表明,VI的结构顺序和缺陷密度与辛硒烯酸盐SAM在金上的润湿行为密切相关。在这项研究中,我们清楚地表明,头基与金表面之间的相互作用在确定SAM的物理性质和表面结构方面起着重要作用。

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