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Effect of Molecule-Substrate Interaction on Thin-Film Structures and Molecular Orientation of Pentacene on Silver and Gold

机译:分子-底物相互作用对银和金上并五苯薄膜结构和分子取向的影响

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摘要

Evaporated pentacene thin films with thicknesses from several nm to 150 nm on gold and silver substrates have been studied by ultraviolet photoelectron spectroscopy(UPS),near-edge X-ray absorption fine structure(NEXAFS),scanning tunneling microscopy(STM),and atomic force microscopy(AFM).It was found that pentacene thin-film structures,particularly their molecular orientations,are strongly influenced by the metal substrates.UPS measurements revealed a distinct change in the valence band structures of pentacene on Au compared to those on Ag,which is attributed to the different packing between adjacent molecules.Using NEXAFS,we observed 74+-5 deg and 46+-5 deg molecular tilt angles on Ag and Au,respectively,for all measured thicknesses.We propose that pentacene molecules stand up on the surface and form the"thin-film phase"structure on Ag.On Au,pentacene films grow in domains with molecules either lying flat or standing up on the substrate.Such a mixture of two crystalline phases leads to an average tilt angle of 46 deg for the whole film and the change in valence band structures.STM and distance-voltage(z-V)spectroscopy studies confirm the existence of two crystalline phases on Au with different conducting properties.z-V spectra on the low conducting phase clearly indicate its nature as"thin-film phase".
机译:通过紫外光电子能谱(UPS),近缘X射线吸收精细结构(NEXAFS),扫描隧道显微镜(STM)和原子研究了金和银衬底上厚度从几纳米到150纳米的并五苯薄膜的蒸发。力显微镜(AFM)。发现并五苯薄膜的结构,特别是其分子取向受到金属基底的强烈影响.UPS测量显示,与Ag相比,Au上并五苯的价带结构发生了明显变化,这归因于相邻分子之间的不同堆积。使用NEXAFS,我们在所有测得的厚度上均观察到了在Ag和Au上的74 + -5度和46 + -5度分子倾斜角。我们建议并五苯分子在在金上,并五苯薄膜在畴中生长,分子处于平坦或直立在基底上。这种两种晶相的混合物会导致在表面上形成并形成“薄膜相”结构。整个薄膜的平均倾斜角为46度,并且价带结构发生变化.STM和距离-电压(zV)光谱研究证实了在Au上存在两个具有不同导电特性的晶相。在低导电相上的zV光谱清楚地表明其性质为“薄膜相”。

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