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共面苝二聚体上激发电子态的单线态裂变

Singlet Fission from Upper Excited Electronic States of Cofacial Perylene Dimer.

作者信息

Ni Wenjun, Gurzadyan Gagik G, Zhao Jianzhang, Che Yuanyuan, Li Xiaoxin, Sun Licheng

机构信息

State Key Laboratory of Fine Chemicals, Institute of Artificial Photosynthesis , Dalian University of Technology , 116024 Dalian , China.

State Key Laboratory of Fine Chemicals , Dalian University of Technology , 116024 Dalian , China.

出版信息

J Phys Chem Lett. 2019 May 16;10(10):2428-2433. doi: 10.1021/acs.jpclett.9b00717. Epub 2019 Apr 30.

Abstract

Singlet fission directly from the upper excited vibrational and electronic states of cofacial perylene dimers, bypassing the relaxed state S, was detected within 50 fs. This process competes well with vibrational cooling in S (4.7-7.0 ps) and S → S internal conversion (380 fs). The singlet fission has the energy threshold E = 3.06 eV. Other competitive relaxation processes are excimer and dimer cation formation on an ultrafast time scale. Excitation to higher energy levels (4.96 eV) leads to a higher efficiency of singlet fission.

摘要

在50飞秒内检测到了单重态裂变直接从并苯二聚体的上激发振动和电子态发生,绕过了弛豫态S。该过程与S态的振动冷却(4.7 - 7.0皮秒)和S→S内转换(380飞秒)竞争良好。单重态裂变的能量阈值E = 3.06电子伏特。其他竞争性弛豫过程是在超快时间尺度上形成准分子和二聚体阳离子。激发到更高能级(4.96电子伏特)会导致单重态裂变效率更高。

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