1] Fakultät für Physik and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität München, Geschwister-Scholl-Platz 1, 80539 München, Germany [2] Nanosystems Initiative Munich, Schellingstrasse 4, 80799 München, Germany.
1] Fakultät für Physik and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität München, Geschwister-Scholl-Platz 1, 80539 München, Germany [2] Neaspec GmbH, Bunsenstrasse 5, 82152 Martinsried, Germany.
Nat Commun. 2014 Jun 11;5:4101. doi: 10.1038/ncomms5101.
Controlling the domain size and degree of crystallization in organic films is highly important for electronic applications such as organic photovoltaics, but suitable nanoscale mapping is very difficult. Here we apply infrared-spectroscopic nano-imaging to directly determine the local crystallinity of organic thin films with 20-nm resolution. We find that state-of-the-art pentacene films (grown on SiO2 at elevated temperature) are structurally not homogeneous but exhibit two interpenetrating phases at sub-micrometre scale, documented by a shifted vibrational resonance. We observe bulk-phase nucleation of distinct ellipsoidal shape within the dominant pentacene thin-film phase and also further growth during storage. A faint topographical contrast as well as X-ray analysis corroborates our interpretation. As bulk-phase nucleation obstructs carrier percolation paths within the thin-film phase, hitherto uncontrolled structural inhomogeneity might have caused conflicting reports about pentacene carrier mobility. Infrared-spectroscopic nano-imaging of nanoscale polymorphism should have many applications ranging from organic nanocomposites to geologic minerals.
控制有机薄膜中的域大小和结晶度对于电子应用(如有机光伏)非常重要,但合适的纳米级映射非常困难。在这里,我们应用红外光谱纳米成像技术直接确定有机薄膜的局部结晶度,分辨率达到 20nm。我们发现,最先进的并五苯薄膜(在高温下生长在 SiO2 上)在结构上是不均匀的,而是在亚微米尺度上表现出两个相互渗透的相,这可以通过振动共振的移动来证明。我们观察到在主导的并五苯薄膜相中存在具有不同椭圆形状的体相成核,并且在存储过程中进一步生长。微弱的形貌对比以及 X 射线分析证实了我们的解释。由于体相成核阻碍了薄膜相中的载流子渗流路径,因此迄今为止不受控制的结构不均匀性可能导致了关于并五苯载流子迁移率的相互矛盾的报告。纳米级多态性的红外光谱纳米成像应该在从有机纳米复合材料到地质矿物的许多应用中具有应用前景。