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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 |
Appears in Collections: | Elements Staff Publications |
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