| Literature DB >> 26263138 |
Oleg Varnavski1, Neranga Abeyasinghe1, Juan Aragó2, Juan J Serrano-Pérez2, Enrique Ortí2, Juan T López Navarrete3, Kazuo Takimiya4, David Casanova5,6,7, Juan Casado3, Theodore Goodson1.
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.Entities:
Keywords: Intramolecular; Organic photovoltaics; Quinoidal Oligothiophenes; Singlet exciton fission; Ultrafast spectroscopy
Year: 2015 PMID: 26263138 DOI: 10.1021/acs.jpclett.5b00198
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475