系统间交叉
发色团
单重态裂变
分子内力
单重态
激子
化学物理
化学
内部转换
三重态
光化学
原子物理学
物理
电子
激发态
量子力学
立体化学
作者
Ekadashi Pradhan,Tao Zeng
标识
DOI:10.1021/acs.jpclett.3c03238
摘要
Singlet fission (SF) has the potential to play a key role in photovoltaics since it generates a larger number of longer-lived triplet excitons after photoabsorption. Intramolecular SF (iSF) is of special interest since it enables tuning of SF efficiency by adjusting interchromophore configuration through covalent interaction. However, as elaborated in the present work, iSF chromophores are doomed to dissatisfy one general thermodynamic criterion for all SF chromophores, intramolecular or not: E(T2) ≥ 2E(T1), and therefore, the fusion of two triplet excitons to one triplet exciton is thermodynamically favorable. In our nonadiabatic quantum dynamics simulation for a model iSF chromophore, this expected fusion does not occur, because of the inefficient intersystem crossing hidden under the cover of internal conversion of the triplet fusion. A reconciliation is achieved between the dissatisfaction of E(T2) ≥ 2E(T1) and the large tetraradical character for general iSF chromophores.
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