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Confocal Raman Spectroscopy Of α-sexithiophene: From Bulk Crystals To Field-effect Transistors

机译:α-硒代噻吩的共聚焦拉曼光谱:从块状晶体到场效应晶体管

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摘要

We report confocal micro-Raman spectra of the organic semiconductor α-sexithiophene (T6) on bulk crystals and on thin films grown on technologically relevant substrates and devices. We show that the two polymorphs, which are Clearly identified by their lattice phonon spectra, may coexist as physical impurities of one inside the other in the same crystallite. Spatial distribution of the two phases is monitored by Raman phonon mapping of crystals grown upon different conditions. Raman microscopy has then been extended to T6 thin films grown on silicon oxide wafers. We identify the crystal phase in thin films whose thickness is just 18 nm. The most intense total-symmetric Raman vibration is still detectable for a two-monolayer thick film. Comparative analysis between micro-Raman and AFM of T6 thin films grown on field effect transistors shows that electrode-channel steps favour the nucleation and growth of T6 molecules on the substrate, at least below 50 nm.
机译:我们报告了有机半导体α-sexithiophene(T6)在体晶体上以及在与技术相关的衬底和设备上生长的薄膜上的共聚焦显微拉曼光谱。我们表明,这两种多晶型物可以通过它们的晶格声子光谱清楚地识别出来,并且可以作为同一晶体中另一个内部的物理杂质共存。通过在不同条件下生长的晶体的拉曼声子作图法可以监测两相的空间分布。拉曼显微镜随后被扩展到在氧化硅晶片上生长的T6薄膜。我们确定了厚度仅为18 nm的薄膜中的晶相。对于两层的厚膜,仍然可以检测到最强烈的总对称拉曼振动。在场效应晶体管上生长的T6薄膜的显微拉曼光谱和AFM之间的比较分析表明,电极通道步骤有利于衬底上T6分子的成核和生长,至少在50 nm以下。

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