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New insights into the design of conjugated polymers for intramolecular singlet fission

Journal Article · · Nature Communications
 [1];  [1];  [1];  [2];  [1];  [3];  [4];  [1];  [5]
  1. Wuhan Univ. of Technology (China). State Key Lab. of Advanced Technology for Materials Synthesis and Processing, School of Chemistry, Chemical Engineering and Life Science
  2. Brookhaven National Lab. (BNL), Upton, NY (United States). Center for Functional Nanomaterials (CFN)
  3. Peking Univ., Beijing (China). Beijing National Lab. for Molecular Sciences (BNLMS), Key Lab. of Bioorganic Chemistry and Molecular Engineering of Ministry of Education; Key Lab. of Polymer Chemistry and Physics of Ministry of Education; Center of Soft Matter Science and Engineering; College of Chemistry and Molecular Engineering
  4. Peking Univ., Beijing (China). Beijing National Lab. for Molecular Sciences (BNLMS), Key Lab. of Bioorganic Chemistry and Molecular Engineering of Ministry of Education; Key Lab. of Polymer Chemistry and Physics of Ministry of Education; Center of Soft Matter Science and Engineering; College of Chemistry and Molecular Engineering
  5. Wuhan Univ. of Technology (China). State Key Lab. of Advanced Technology for Materials Synthesis and Processing, School of Chemistry, Chemical Engineering and Life Science; Brookhaven National Lab. (BNL), Upton, NY (United States). Center for Functional Nanomaterials (CFN)

Singlet fission (SF), a multiple exciton generation process which generates two triplet excitons after the absorption of one photon, can potentially enable more efficient solar cell designs, by harvesting energy normally lost as heat. While low-bandgap conjugated polymers are the highly promising candidates for efficient SF-based solar cells, few polymer materials capable of SF have been reported because the SF process in polymer chains is poorly understood. Using transient spectroscopy, we demonstrate a new, highly efficient (triplet yield of 160~200%) isoindigo-based donor-acceptor polymer and show that the triplet pairs are directly emissive and exhibit a time dependent energy evolution. Importantly, aggregation in poor solvents and in films significantly lowers the singlet energy, suppressing triplet formation because the energy conservation criterion is no longer met. These results suggest a new design rule for developing intramolecular SF capable low-bandgap conjugated polymers whereby inter-chain interactions must be carefully engineered.

Research Organization:
Brookhaven National Laboratory (BNL), Upton, NY (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22); National Natural Science Foundation of China (NNSFC); Wuhan University of Technology
Grant/Contract Number:
SC0012704
OSTI ID:
1474070
Report Number(s):
BNL--209083-2018-JAAM
Journal Information:
Nature Communications, Journal Name: Nature Communications Journal Issue: 1 Vol. 9; ISSN 2041-1723
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English

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Cited By (9)

Two-electron transfer stabilized by excited-state aromatization journal November 2019
Revealing the Nature of Singlet Fission under the Veil of Internal Conversion journal December 2019
Revealing the Nature of Singlet Fission under the Veil of Internal Conversion journal January 2020
Efficient triplet pair separation from intramolecular singlet fission in dibenzopentalene derivatives journal May 2019
Enhancing the intermolecular singlet fission efficiency by controlling the self-assembly of amphipathic tetracene derivatives in aqueous solution journal January 2019
Morphology independent triplet formation in pentalene films: Singlet fission as the triplet formation mechanism journal September 2019
Vibronic fingerprint of singlet fission in hexacene journal August 2019
Heavy-atom effects on intramolecular singlet fission in a conjugated polymer journal July 2019
Lessons from intramolecular singlet fission with covalently bound chromophores journal January 2020

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