Institut für Experimentelle und Angewandte Physik, Universität Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany.
Kekulé-Institut für Organische Chemie und Biochemie, Universität Bonn, Gerhard-Domagk-Straße 1, 53121, Bonn, Germany.
Nat Commun. 2017 Nov 21;8(1):1641. doi: 10.1038/s41467-017-01773-0.
The aggregation of conjugated polymers and electronic coupling of chromophores play a central role in the fundamental understanding of light and charge generation processes. Here we report that the predominant coupling in isolated aggregates of conjugated polymers can be switched reversibly between H-type and J-type coupling by partially swelling and drying the aggregates. Aggregation is identified by shifts in photoluminescence energy, changes in vibronic peak ratio, and photoluminescence lifetime. This experiment unravels the internal electronic structure of the aggregate and highlights the importance of the drying process in the final spectroscopic properties. The electronic coupling after drying is tuned between H-type and J-type by changing the side chains of the conjugated polymer, but can also be entirely suppressed. The types of electronic coupling correlate with chain morphology, which is quantified by excitation polarization spectroscopy and the efficiency of interchromophoric energy transfer that is revealed by the degree of single-photon emission.
共轭聚合物的聚集和发色团的电子耦合在对光和电荷产生过程的基本理解中起着核心作用。在这里,我们报告说,通过部分溶胀和干燥聚集物,可以将共轭聚合物孤立聚集物中的主要耦合可逆地从 H 型耦合切换到 J 型耦合。聚集通过荧光能量的位移、振子峰比的变化和荧光寿命来识别。该实验揭示了聚集物的内部电子结构,并强调了干燥过程对最终光谱性质的重要性。通过改变共轭聚合物的侧链,可以在 H 型和 J 型之间调节干燥后的电子耦合,但也可以完全抑制电子耦合。电子耦合的类型与链形态相关,通过激发偏振光谱和单光子发射的程度揭示的发色团间能量转移效率来定量。