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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Unexpected Formation of Dense Phases along with Temperature-Induced, Self-Assembled Terphenylthiolate Monolayers on Au(111)
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Unexpected Formation of Dense Phases along with Temperature-Induced, Self-Assembled Terphenylthiolate Monolayers on Au(111)

机译:在Au(111)上意外地形成致密相以及温度诱导的自组装三苯硫醇酯单分子层

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Self-assembled monolayers (SAMs) of terphenylthiol (TP0) prepared on Au(111) from ethanolic solution at room temperature and subsequently annealed at different temperatures of up to 473 K were investigated using scanning tunneling microscopy and infrared reflection absorption spectroscopy. Upon annealing, the TP0 adlayer formed a series of different structural phases with different molecular arrangements. Our results show that SAMs prepared at RT without annealing and SAMs annealed at 313 K exhibited the formation of a closely packed "alpha" structure where TP0 molecular axes are orientated almost upright. The formation of the alpha-phase was accompanied by the formation of a loosely packed phase (beta-phase). During annealing from 333 to 473 K, the results revealed the formation of different structural phases, namely, gamma, delta, epsilon, sigma, and phi. With the exception of the phi-phase, the phases were found to form loosely packed structures with the molecular axes largely tilted away from surface normal but do not form "flat-lying" phases. Surprisingly, upon annealing at 453 K, the SAMs exhibited a phase transition to a higher dense network of molecular structure (phi-phase) with almost upright standing molecules. An additional annealing at 463 K led to a significant increase in the size of the well-ordered domains of the phi-phase at the expense of their density. At the same time, a partial desorption of the TP0-SAMs was noticed to take place. The formation of a densely packed phase upon annealing and subsequently desorption of TP0 molecules from this state completely contradicts the behavior of n-alkanethiol and other oligophenylthiol SAMs, in which desorption occurs from lying-flat geometry. The phi-phase, which was the only one remaining on the surface, did not cover more than 30% of the gold surface area. A further increase of the annealing temperature to 473 K caused a substantial increase in the number of the desorbed molecules. Therefore, a remarkable reduction in both the size and density of the ordered domains of the phi-phase was observed. On the other hand, the annealing temperature was found to have a significant influence on both the appearance and the shape of the gold islands. Moreover, it has been found that the gold islands, regardless of their shapes, were always covered by standing-up, densely packed, and ordered phases such as the alpha- and phi-phases.
机译:使用扫描隧道显微镜和红外反射吸收光谱研究了在室温下从乙醇溶液在Au(111)上制备的三苯并硫醇(TP0)的自组装单分子层(SAMs),随后在高达473 K的不同温度下进行了退火。退火后,TP0附加层形成了一系列具有不同分子排列的不同结构相。我们的结果表明,在室温下制备的未退火的SAM和在313 K退火的SAM表现出紧密堆积的“α”结构的形成,其中TP0分子轴几乎直立。 α相的形成伴随着松散堆积相(β相)的形成。在从333 K到473 K的退火过程中,结果表明形成了不同的结构相,即γ,δ,ε,σ和phi。除phi相外,发现这些相形成了松散堆积的结构,分子轴大大偏离表面法线,但没有形成“平展”相。出人意料的是,在453 K退火时,SAM表现出相变,转变为具有几乎直立的分子的更高密度的分子结构网络(phi相)。在463 K处进行的额外退火导致φ相的有序畴的尺寸显着增加,但以其密度为代价。同时,注意到发生了TP0-SAM的部分解吸。在退火状态下形成紧密堆积的相,然后从该状态解吸TP0分子,这与正构烷硫醇和其他低聚苯硫醇SAM的行为完全矛盾,在这种情况下,解吸发生于平坦的几何形状。 phi相是表面上唯一残留的ph相,覆盖的金表面积不超过30%。退火温度进一步提高到473 K导致解吸分子的数量大大增加。因此,观察到phi相的有序域的大小和密度都显着减小。另一方面,发现退火温度对金岛的外观和形状都具有显着影响。此外,已经发现,无论其形状如何,金岛总是被直立,密堆积和有序相(例如α相和phi相)覆盖。

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