| Literature DB >> 31729139 |
Long Wang1,2, Shuming Bai3, Yishi Wu1, Yanping Liu1, Jiannian Yao1,4, Hongbing Fu1,4.
Abstract
Singlet fission (SF) holds the potential to boost the maximum power conversion efficiency of photovoltaic devices. Internal conversion (IC) has been considered as one of the major competitive deactivation pathways to transform excitation energy into heat. Now, using time-resolved spectroscopy and theoretical calculation, it is demonstrated that, instead of a conventional IC pathway, an unexpected intramolecular singlet fission (iSF) process is responsible for excited state deactivation in isoindigo derivatives. The 1 TT state could form at ultrafast rate and nearly quantitatively in solution. In solid films, the slipped stacked intermolecular packing of a thiophene-functionalized derivative leads to efficient triplet pair separation, giving rise to an overall triplet yield of 181 %. This work not only enriches the pool of iSF-capable materials, but also contributes to a better understanding of the iSF mechanism, which could be relevant for designing new SF sensitizers.Entities:
Keywords: internal conversion; intramolecular singlet fission; isoindigo; photophysics; transient absorption spectroscopy
Year: 2019 PMID: 31729139 DOI: 10.1002/anie.201912202
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336