材料科学
噻吩
薄膜
吸收(声学)
衍射
沉积(地质)
纳米技术
结晶学
化学物理
光电子学
光学
有机化学
复合材料
化学
沉积物
古生物学
生物
物理
作者
Tim Hawly,Manuel Johnson,Andreas Späth,Hannah Nickles Jäkel,Mingjian Wu,Erdmann Spiecker,Benjamin Watts,Alexei Nefedov,R. Fink
标识
DOI:10.1021/acsami.2c00097
摘要
Crystalline organic semiconducting thin films from the benchmark molecule C8-BTBT-C8 were obtained using physical vapor deposition and various solution-based methods. Utilizing atomic force microscopy and X-ray spectromicroscopy, we illustrate the influence of the underlying growth mechanism and determine the highly preparation-dependent orientation of the thiophene backbone. We observe a continuous trend for crystalline C8-BTBT-C8 thin film domains to extend into the square millimeter-range under near-equilibrium growth conditions. For such well-defined systems, electron diffraction tomography allows us to precisely determine the unit cell directly after film deposition and to reveal an 8° molecular tilt angle with respect to the surface normal. This finding is in almost perfect accordance with the values derived from near-edge X-ray absorption fine structure linear dichroism. Within this work, we shine a light on both the successes and challenges connected to the realization of potent, thiophene-based semiconducting films, paving the way toward square centimeter-sized ultrathin organic crystals and their application in organic circuitry.
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