Journal article
Intersystem crossing outcompetes triplet-pair separation from 1(TT) below 270 k in anthradithiophene films
- Abstract:
- Singlet fission (SF) and triplet–triplet annihilation (TTA) are processes which may be exploited to boost the efficiency of solar energy technology. Despite being studied since the late 1960s, the mechanism of singlet fission is still not fully understood. This is partly because the main technique used to study singlet fission, optical or visible/near-IR transient absorption spectroscopy, cannot distinguish between the strongly coupled triplet-pair state 1(TT), weakly interacting triplet pairs (T..T), and independent triplet states T1 +T1. To solve this problem, we combine transient optical spectroscopy performed as a function of magnetic field and transient electron spin resonance (ESR) spectroscopy to probe the different steps involved in the singlet fission mechanism. By using transient photoluminescence spectroscopy performed as a function of magnetic field to selectively probe the second step of singlet fission: T1⇌ (T..T), we show that in a well-studied model system, anthradithiophene (diF-TES-ADT), this step is highly temperature-dependent, even though the first step, 1S →1(TT), is not. Transient ESR measurements confirm the absence of singlet fission at temperatures between 40 and 250 K for this system, with clear signatures of triplets generated by intersystem crossing and evidence for decay by triplet–triplet annihilation, further supported by magnetic field effect measurements. We conclude that in polycrystalline diF-TES-ADT, intersystem crossing outcompetes triplet hopping at temperatures below 270 K, enabling direct intersystem crossing from the bound triplet pair 1(TT) to an independent triplet state T1 localized on a single chromophore. The generated triplets can re-encounter and decay through triplet–triplet annihilation.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 8.8MB, Terms of use)
-
- Publisher copy:
- 10.1021/jacs.5c00001
Authors
+ U.S. National Science Foundation
More from this funder
- Funder identifier:
- https://ror.org/021nxhr62
- Grant:
- DMR 2414541
+ Royal Society
More from this funder
- Funder identifier:
- https://ror.org/03wnrjx87
- Grant:
- URF\R1\201071
+ Engineering and Physical Sciences Research Council
More from this funder
- Funder identifier:
- https://ror.org/0439y7842
- Grant:
- EP/V034804/1
- EP/V055127/1
- EP/M028437/1
- EP/L022613
- EP/T012455
- EP/R042802
- Publisher:
- American Chemical Society
- Journal:
- Journal of the American Chemical Society More from this journal
- Volume:
- 147
- Issue:
- 32
- Pages:
- 28638−28650
- Publication date:
- 2025-07-30
- Acceptance date:
- 2025-06-09
- DOI:
- EISSN:
-
1520-5126
- ISSN:
-
0002-7863
- Language:
-
English
- Pubs id:
-
2257506
- Local pid:
-
pubs:2257506
- Deposit date:
-
2025-07-31
- ARK identifier:
Terms of use
- Copyright holder:
- Bu et al.
- Copyright date:
- 2025
- Rights statement:
- ©2025 The Authors. Published by American Chemical Society. This article is licensed under CC-BY 4.0.
- Licence:
- CC Attribution (CC BY)
If you are the owner of this record, you can report an update to it here: Report update to this record