| Literature DB >> 33332757 |
David Rais1, Petr Toman1, Jiří Pfleger1, Udit Acharya1,2, Yadu R Panthi1,2, Miroslav Menšík1, Alexander Zhigunov3, Muhammed A Thottappali1,2, Martin Vala4, Aneta Marková4, Stanislav Stříteský4, Martin Weiter4, Martin Cigánek4, Jozef Krajčovič4, Karel Pauk5, Aleš Imramovský5, Alexandr Zaykov6,7, Josef Michl6,8.
Abstract
The singlet fission (SF) process discovered in bis(thienyl)diketopyrrolopyrroles (TDPPs) can boost their potential for photovoltaics (PV). The crystal structures of TDPP analogs carrying n-hexyl, n-butyl, or 2-(adamant-1-yl)ethyl substituents are similar, but contain increasingly slipped stacked neighbor molecules. The observed SF rate constants, kSF , (7±4), (9±3) and (5.6±1.9) ns-1 for thin films of the three compounds, respectively, are roughly equal, but the triplet quantum yields vary strongly: (120±40), (160±40) and (70±16), respectively. The recent molecular pair model reproduces the near equality of all three kSF at the crystal geometries and identifies all possible pair arrangements in which SF is predicted to be faster, by up to two orders of magnitude. However, it is also clear that the presently non-existent ability to predict the rates of processes competing with SF is pivotal for providing a guide for efforts to optimize the materials for PV.Entities:
Keywords: optical spectroscopy; photophysics; singlet fission; thin films; triplet excitons
Year: 2020 PMID: 33332757 DOI: 10.1002/cplu.202000623
Source DB: PubMed Journal: Chempluschem ISSN: 2192-6506 Impact factor: 2.863