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Scanning Angle Raman Spectroscopy of Poly(3-hexylthiophene)-Based Films on Indium Tin Oxide, Gold, and Sapphire Surfaces

机译:氧化铟锡,金和蓝宝石表面上基于聚(3-己基噻吩)的薄膜的扫描角拉曼光谱

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摘要

Interest in realizing conjugated polymer-based films with controlled morphology for efficient electronic devices, including photovoltaics, requires a parallel effort to characterize these films. Scanning angle (SA) Raman spectroscopy is applied to measure poly(3-hexylthiophene) (P3HT):phenyl—C61— butyric acid methyl ester (PCBM)-blend morphology on sapphire, gold, and indium tin oxide, interfaces, including functional organic photovoltaic devices, Nonresonant SA Raman spectra are collected in seconds with signal-to-noise ratios that exceed 80, which is possible due to the reproducible SA signal enhancement. Raman spectra are collected as the incident angle of the 785 nm excitation laser is precisely varied upon a prism/sample interface from approximately 35 to 70°. The width of the ~1447 cnT1 thiophene C=C stretch is sensitive to P3HT order, and polymer order varied depending on the underlying substrate. This demonstrates the importance of performing the spectroscopic measurements on substrates and configurations used in the functioning devices, which is not a common practice. The experimental measurements are modeled with calculations of the interfacial mean square electric field to determine the distance dependence of the SA Raman signal. SA Raman spectroscopy is a versatile method applicable whenever the chemical composition, structure, and thickness of interfacial polymer layers need to be simultaneously measured.
机译:为了实现包括光电器件在内的有效电子设备的具有可控形态的共轭聚合物基薄膜,人们需要做出平行努力来表征这些薄膜。扫描角(SA)拉曼光谱用于测量聚(3-己基噻吩)(P3HT):苯基-C61-丁酸甲酯(PCBM)-蓝宝石,金和铟锡氧化物混合界面的形态,包括功能性有机物光伏设备中,非共振SA拉曼光谱可在几秒钟内以超过80的信噪比收集,这是由于可再现的SA信号增强所致。随着785 nm激发激光的入射角在大约35至70°的棱镜/样品界面上精确变化,收集了拉曼光谱。 〜1447 cnT1噻吩C = C链的宽度对P3HT阶数敏感,聚合物阶数取决于下面的底物。这证明了在功能装置中使用的基板和配置上执行光谱测量的重要性,这是不常见的做法。用界面均方电场的计算对实验测量值进行建模,以确定SA拉曼信号的距离依赖性。 SA拉曼光谱法是一种通用方法,适用于需要同时测量界面聚合物层的化学组成,结构和厚度的情况。

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