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Growth study of para-sexiphenyl on Ag(001): From single molecule to crystalline film

机译:对亚联苯在Ag(001)上的生长研究:从单分子到结晶膜

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In this work we investigate the formation of crystalline organic thin films for p-sexiphenyl (6P) on Ag(001) with a combination of STM, LEED, TPD, SFM, UPS, XRD and DFT. For weakly interacting van-der-Waals-dominated systems of small organic molecules on single crystalline metals we demonstrate the complex epitaxial evolution from sub-monolayer to bulk structure. In the delicate interplay between molecule-substrate and intermolecular interactions we identify the oligo-phenyl's flexibility of central importance for the film growth. We observe a change from a planar to a twisted molecular conformation and, accompanying, a molecular realignment during the formation of a dense monolayer as the result of enhanced 2-dimensional intermolecular interaction. A second molecular realignment occurs collectively for whole domains with the formation of 3-dimensional bilayer structures. Finally the bilayer acts as a template for the epitaxial growth of the molecular thin film, determining the azimuthal orientation and a single contact plane for the organic crystallites.
机译:在这项工作中,我们结合STM,LEED,TPD,SFM,UPS,XRD和DFT研究了在Ag(001)上对-对苯二酚(6P)的结晶有机薄膜的形成。对于单晶金属上小有机分子的弱相互作用的范德华支配体系,我们证明了从亚单层到整体结构的复杂外延演化。在分子-底物与分子间相互作用之间的微妙相互作用中,我们确定了低聚苯基对于薄膜生长至关重要的柔韧性。我们观察到从平面到扭曲的分子构象的变化,并伴随着由于增强的二维分子间相互作用而在致密的单分子层形成过程中的分子重新排列。随着3维双层结构的形成,整个结构域共同发生第二次分子重排。最终,双层充当分子薄膜外延生长的模板,确定方位取向和有机微晶的单接触面。

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