Issue 8, 2018

Tuning the singlet fission relevant energetic levels of quinoidal bithiophene compounds by means of backbone modifications and functional group introduction

Abstract

Efficient singlet fission (SF) has been obtained in quinoidal bithiophene, end-capped with dicyanomethylene groups (QBT). However, QBT suffers from low triplet state energy [E(T1)] because of its biradicaloid nature, which results in a great driving force for SF but also a large loss of energy during the SF process. This is not favorable for the application of SF in solar cells. Modifications to the molecular structure of QBT were performed to optimize the SF relevant excited state energy levels and its diradical character in the present study. This includes chalcogen replacement, the fusing of the heterocyclic ring between the two thiophene rings, and the introduction of side substituents. Detailed analysis focused on the correlation between the molecular structure of the QBT derivatives and their diradical character y0, bond length alternation (BLA), molecular orbitals, and SF relevant excited state energy levels. The results show that electron-donating substituents, particularly groups introduced at the inner β-positions of the thiophene ring, can increase E(T1) and reduce the energy loss of SF significantly under the premise of exothermic SF. These results would be beneficial to the development of new SF candidates for application in solar cells.

Graphical abstract: Tuning the singlet fission relevant energetic levels of quinoidal bithiophene compounds by means of backbone modifications and functional group introduction

Supplementary files

Article information

Article type
Paper
Submitted
12 Dec 2017
Accepted
23 Jan 2018
First published
23 Jan 2018

Phys. Chem. Chem. Phys., 2018,20, 5795-5802

Tuning the singlet fission relevant energetic levels of quinoidal bithiophene compounds by means of backbone modifications and functional group introduction

L. Shen, X. Wang, H. Liu and X. Li, Phys. Chem. Chem. Phys., 2018, 20, 5795 DOI: 10.1039/C7CP08313K

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