Noda Hiroki, Chen Xian-Kai, Nakanotani Hajime, Hosokai Takuya, Miyajima Momoka, Notsuka Naoto, Kashima Yuuki, Brédas Jean-Luc, Adachi Chihaya
Center for Organic Photonics and Electronics Research, Kyushu University, Fukuoka, Japan.
JST, ERATO, Adachi Molecular Exciton Engineering Project, Kyushu University, Fukuoka, Japan.
Nat Mater. 2019 Oct;18(10):1084-1090. doi: 10.1038/s41563-019-0465-6. Epub 2019 Sep 2.
Spin-flip in purely organic molecular systems is often described as a forbidden process; however, it is commonly observed and utilized to harvest triplet excitons in a wide variety of organic material-based applications. Although the initial and final electronic states of spin-flip between the lowest singlet and lowest triplet excited state are self-evident, the exact process and the role of intermediate states through which spin-flip occurs are still far from being comprehensively determined. Here, via experimental photo-physical investigations in solution combined with first-principles quantum-mechanical calculations, we show that efficient spin-flip in multiple donor-acceptor charge-transfer-type organic molecular systems involves the critical role of an intermediate triplet excited state that corresponds to a partial molecular structure of the system. Our proposed mechanism unifies the understanding of the intersystem crossing mechanism in a wide variety of charge-transfer-type molecular systems, opening the way to greater control over spin-flip rates.
在纯有机分子体系中,自旋翻转通常被描述为一个禁阻过程;然而,它在多种基于有机材料的应用中普遍被观察到并用于捕获三重态激子。尽管最低单重态和最低三重态激发态之间自旋翻转的初始和最终电子态是显而易见的,但自旋翻转发生所经由的中间态的确切过程及其作用仍远未得到全面确定。在此,通过溶液中的实验光物理研究结合第一性原理量子力学计算,我们表明,多个供体-受体电荷转移型有机分子体系中的高效自旋翻转涉及一个对应于体系部分分子结构的中间三重态激发态的关键作用。我们提出的机制统一了对多种电荷转移型分子体系中系间窜越机制的理解,为更好地控制自旋翻转速率开辟了道路。