Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms13622
Title: Tuning the role of charge-transfer states in intramolecular singlet exciton fission through side-group engineering
Authors: Lukman, S
Chen, K
Hodgkiss, J.M
Turban, D.H.P
Hine, N.D.M
Dong, S 
Wu, J 
Greenham, N.C
Musser, A.J
Keywords: dimer
energy budget
geometry
optimization
photovoltaic system
physics
absorption
Article
chemical engineering
chemical structure
chromatophore
comparative study
dipole
electron transport
geometry
intramolecular singlet exciton fission
photoluminescence
solid state
synthesis
ultraviolet spectrophotometry
Issue Date: 2016
Publisher: Nature Publishing Group
Citation: Lukman, S, Chen, K, Hodgkiss, J.M, Turban, D.H.P, Hine, N.D.M, Dong, S, Wu, J, Greenham, N.C, Musser, A.J (2016). Tuning the role of charge-transfer states in intramolecular singlet exciton fission through side-group engineering. Nature Communications 7 : 13622. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms13622
Rights: Attribution 4.0 International
Abstract: Understanding the mechanism of singlet exciton fission, in which a singlet exciton separates into a pair of triplet excitons, is crucial to the development of new chromophores for efficient fission-sensitized solar cells. The challenge of controlling molecular packing and energy levels in the solid state precludes clear determination of the singlet fission pathway. Here, we circumvent this difficulty by utilizing covalent dimers of pentacene with two types of side groups. We report rapid and efficient intramolecular singlet fission in both molecules, in one case via a virtual charge-transfer state and in the other via a distinct charge-transfer intermediate. The singlet fission pathway is governed by the energy gap between singlet and charge-transfer states, which change dynamically with molecular geometry but are primarily set by the side group. These results clearly establish the role of charge-transfer states in singlet fission and highlight the importance of solubilizing groups to optimize excited-state photophysics. ©The Author(s) 2016.
Source Title: Nature Communications
URI: https://scholarbank.nus.edu.sg/handle/10635/179778
ISSN: 2041-1723
DOI: 10.1038/ncomms13622
Rights: Attribution 4.0 International
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