4.6 Article

Singlet Fission in Quaterrylenediimide Thin Films

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 124, Issue 5, Pages 2791-2798

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.9b10397

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-FG02-99ER14999]
  2. Ryan Fellowship
  3. Northwestern University International Institute for Nanotechnology
  4. National Science Foundation Graduate Research Fellowship Program [DGE-1324585]
  5. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF) [ECCS-1542205]
  6. State of Illinois
  7. International Institute for Nanotechnology (IIN)
  8. MRSEC program of the National Science Foundation at the Materials Research Center of Northwestern University [DMR-1720139]
  9. MRSEC program (NSF) at the Materials Research Center [DMR-1720139]
  10. Keck Foundation
  11. State of Illinois, through the IIN

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Singlet fission (SF) creates two triplet excitons following absorption of a photon by two electronically interacting chromophores. Quaterrylene-3,4:13,14-bis(dicarboximide) (QDI) is a strongly absorbing chromophore that readily fulfills the energetic requirements for SF, E(S-1) > 2E(T-1), and thus should undergo rapid and efficient SF. SF was studied in thin films of the QDI derivative N,N-bis(2,6-diisopropylphenyl)-QDI (ArQDI), which undergoes SF in <300 fs to form the correlated triplet pair state, (1)(T1T1), which dissociates with a (7.3 +/- 1.2 ns)(-1) rate constant. The observed triplet yield for a thin film that has been solvent-vapor annealed with CH2Cl2 is 135 +/- 20% instead of 200%, which is typically expected of chromophores that undergo ultrafast formation of the (1)(T1T1) state. The lower SF yield in ArQDI results from the failure of the (1)(T1T1) state to dissociate before returning to the ground state. In contrast to other molecules, like hexacene, which have low triplet energies, the SF rate in ArQDI is not limited by a multiphonon relaxation bottleneck, largely due to the fact that the S-T energy gap in the film is substantially smaller than that measured for monomeric ArQDI. The ability to maintain a favorable S-T energy gap in a film is a design consideration when chromophores are considered for use to enhance solar cell performance.

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