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喹啉二噻吩中的高产率超快分子内单线态激子裂变

High Yield Ultrafast Intramolecular Singlet Exciton Fission in a Quinoidal Bithiophene.

作者信息

Varnavski Oleg, Abeyasinghe Neranga, Aragó Juan, Serrano-Pérez Juan J, Ortí Enrique, López Navarrete Juan T, Takimiya Kazuo, Casanova David, Casado Juan, Goodson Theodore

机构信息

†Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.

‡Instituto de Ciencia Molecular, Universidad de Valencia, 46980 Paterna, Spain.

出版信息

J Phys Chem Lett. 2015 Apr 16;6(8):1375-84. doi: 10.1021/acs.jpclett.5b00198. Epub 2015 Apr 1.

Abstract

We report the process of singlet exciton fission with high-yield upon photoexcitation of a quinoidal thiophene molecule. Efficient ultrafast triplet photogeneration and its yield are determined by photoinduced triplet-triplet absorption, flash photolysis triplet lifetime measurements, as well as by femtosecond time-resolved transient absorption and fluorescence methods. These experiments show that optically excited quinoidal bithiophene molecule undergoes ultrafast formation of the triplet-like state with the lifetime ∼57 μs. CASPT2 and RAS-SF calculations have been performed to support the experimental findings. To date, high singlet fission rates have been reported for crystalline and polycrystalline materials, whereas for covalently linked dimers and small oligomers it was found to be relatively small. In this contribution, we show an unprecedented quantum yield of intramolecular singlet exciton fission of ∼180% for a quinoidal bithiophene system.

摘要

我们报道了在对醌式噻吩分子进行光激发时高产率的单线态激子裂变过程。高效的超快三线态光生及其产率通过光致三线态-三线态吸收、闪光光解三线态寿命测量以及飞秒时间分辨瞬态吸收和荧光方法来确定。这些实验表明,光激发的醌式联噻吩分子会经历超快的类三线态状态形成,其寿命约为57微秒。已进行CASPT2和RAS-SF计算以支持实验结果。迄今为止,已报道晶体和多晶材料具有高单线态裂变率,而对于共价连接的二聚体和小寡聚物,发现其单线态裂变率相对较小。在本论文中,我们展示了醌式联噻吩体系分子内单线态激子裂变前所未有的约180%的量子产率。

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