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Controlling triplet-pair formation in acene-bridged trimers through locally excited–charge-transfer state mixing †

Abstract:
Singlet fission (SF) offers a pathway to surpass conventional efficiency limits in photovoltaics, yet how bridge–chromophore coupling governs locally excited/charge-transfer state (LE–CT) mixing and thereby the multiexciton yield remains elusive. We design three systems, TIPS-BT0, TIPS-TAT, and Encap-TAT, that progressively increase bridge–chromophore coupling. Steady-state spectroscopy and transient absorption reveal that TIPS-BT0 and TIPS-TAT undergo efficient SF, forming correlated triplet pairs (1TT) and, in TIPS-TAT, long-lived triplets. By contrast, Encap-TAT loses vibronic structure and relaxes ultrafast into a broad, red-shifted intramolecular exciplex-like (Ex) state. Quantum chemical analysis shows that the Ex state originates from strong hybridization between local excitations (LEs) and bridge–chromophore CT configurations, driven by large electron and hole transfer integrals and a small LE–CT energy gap. Such strong LE–CT hybridisation suppresses well-defined 1TT formation, favouring intramolecular Ex emission and enhancing photoluminescence quantum yield (≃80.5% vs. ≃38.5% for TIPS-TAT). These findings establish a unifying framework in which the balance between multiexciton generation and exciplex emission in acene-bridged trimers is governed by the degree of LE–CT mixing. Tuning bridge energetics and LE–CT offsets enables deliberate routing of excited-state pathways toward efficient triplet production or bright exciplex emission, providing actionable design rules for next-generation singlet-fission and optoelectronic architectures.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1039/d6sc00278a

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Role:
Author
ORCID:
0000-0003-3913-8851
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-2509-7641
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Role:
Author
ORCID:
0000-0002-6927-0969


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Funder identifier:
https://ror.org/01bj3aw27
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Funder identifier:
https://ror.org/03wnrjx87
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Funder identifier:
https://ror.org/05mmh0f86
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Funder identifier:
https://ror.org/00b6sbb32
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Funder identifier:
https://ror.org/001aqnf71


Publisher:
Royal Society of Chemistry
Journal:
Chemical Science More from this journal
Publication date:
2026-03-23
Acceptance date:
2026-03-09
DOI:
EISSN:
2041-6539
ISSN:
2041-6520


Language:
English
Keywords:
Pubs id:
2406721
Local pid:
pubs:2406721
Source identifiers:
3947872
Deposit date:
2026-04-21
ARK identifier:
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