Research Institute for Ubiquitous Energy Devices, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka, Japan.
J Phys Chem B. 2012 Jan 12;116(1):189-93. doi: 10.1021/jp207487z. Epub 2011 Dec 22.
Controlling the molecular orientation of the conjugated oligomer, α-sexithiophene (6T), is crucial to improve organic optoelectronic device performance. Most 6T molecules evaporated onto quartz and SiO(2)/Si substrates orient nearly perpendicular to the substrate. Here, we report the formation of oriented thin films of 6T on in-plane-oriented polythiophene (PT) films formed by the friction-transfer method. 6T was evaporated onto oriented PT films under vacuum. The films were investigated by polarized optical microscopy, polarized ultraviolet-visible light (UV-vis) absorption spectroscopy, and grazing incidence X-ray diffraction measurement (GIXD). In all spectra, larger absorbance derived from PT and 6T was observed, in parallel polarization to the friction direction, compared to that of orthogonal polarization. These results indicate that the 6T molecular axis is aligned in the friction direction (PT chain direction) of PT films. GIXD also confirmed that the 6T molecular axis was aligned parallel to the PT chain axis. In contrast, 6T molecules evaporated onto quartz and poly(ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)-coated silicon substrates aligned nearly perpendicular to the substrate. These results indicate that oriented PT films induce 6T orientation parallel to the PT chain direction.
控制共轭寡聚物α-六噻吩(6T)的分子取向对于改善有机光电设备的性能至关重要。大多数蒸发到石英和 SiO2/Si 衬底上的 6T 分子几乎垂直于衬底取向。在这里,我们报告了通过摩擦传递法形成的平面取向聚噻吩(PT)薄膜上 6T 的定向薄膜的形成。6T 在真空中蒸发到取向的 PT 薄膜上。通过偏振光学显微镜、偏振紫外可见(UV-vis)吸收光谱和掠入射 X 射线衍射测量(GIXD)研究了这些薄膜。在所有光谱中,与正交偏振相比,在平行于摩擦方向的偏振中观察到来自 PT 和 6T 的更大吸收。这些结果表明 6T 分子轴沿 PT 薄膜的摩擦方向(PT 链方向)排列。GIXD 还证实了 6T 分子轴与 PT 链轴平行排列。相比之下,蒸发到石英和聚(3,4-亚乙基二氧噻吩):聚(苯乙烯磺酸盐)(PEDOT:PSS)-涂覆硅衬底上的 6T 分子几乎垂直于衬底排列。这些结果表明,取向的 PT 薄膜诱导 6T 平行于 PT 链方向取向。