系统间交叉
化学物理
单重态
激发态
三重态
单重态裂变
激子
自旋(空气动力学)
自旋态
电荷(物理)
接受者
分子
化学
分子物理学
原子物理学
凝聚态物理
物理
量子力学
热力学
有机化学
作者
Hiroki Noda,Xiankai Chen,Hajime Nakanotani,Takuya Hosokai,Momoka Miyajima,Naoto Notsuka,Yuuki Kashima,Jean‐Luc Brédas,Chihaya Adachi
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2019-09-02
卷期号:18 (10): 1084-1090
被引量:351
标识
DOI:10.1038/s41563-019-0465-6
摘要
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.
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