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Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response

Aldrich, Thomas J., Matta, Micaela, Zhu, Weigang, Swick, Steven M., Stern, Charlotte L., Schatz, George C., Facchetti, Antonio, Melkonyan, Ferdinand S., Marks, Tobin J.·2019·Journal of the American Chemical Society

Abstract

Indacenodithienothiophene (IDTT)-based postfullerene electron acceptors, such as ITIC (2,2′-[[6,6,12,12-tetrakis(4-hexylphenyl)-6,12-dihydrodithieno[2,3- d:2′,3′- d ′]-s-indaceno[1,2- b:5,6- b ′]dithiophene-2,8-diyl]-bis[methylidyne(3-oxo-1 H -indene-2,1(3 H )-diylidene)]]bis[propanedinitrile]), have become synonymous with high power conversion efficiencies (PCEs) in bulk heterojunction (BHJ) polymer solar cells (PSCs). Here we systematically investigate the influence of end-group fluorination density and positioning on the physicochemical properties, single-crystal packing, end-group redistribution propensity, and BHJ photovoltaic performance of a series of ITIC variants, ITIC- n F ( n = 0, 2, 3, 4, and 6). Increasing n from 0 → 6 contracts the optical bandgap, but only marginally lowers the LUMO for n > 4. This yields enhanced photovoltaic short-circuit current density and good open-circuit voltage, so that ITIC-6F achieves the highest PCE of the series, approaching 12% in blends with the PBDB-TF donor polymer. Single-crystal diffraction reveals that the ITIC- n F molecules cofacially interleave with ITIC-6F having the shortest π–π distance of 3.28 Å. This feature together with ZINDO-level computed intermolecular electronic coupling integrals as high as 57 meV, and B3LYP/DZP-level reorganization energies as low as 147 meV, rival or surpass the corresponding values for fullerenes, ITIC-0F, and ITIC-4F, and track a positive correlation between the ITIC- n F space-charge limited electron mobility and n . Finally, a heretofore unrecognized solution-phase redistribution process between the 2-(3-oxo-indan-1-ylidene)-malononitrile-derived end-groups (EGs) of IDTT-based NFAs, i.e., EG 1 -IDTT-EG 1 + EG 2 -IDTT-EG 2 ⇌ 2 EG 1 -IDTT-EG 2, with implications for the entire ITIC PSC field, is identified and mechanistically characterized, and the effects on PSC performance are assessed.

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Metadata

Authors
Aldrich, T. J., Matta, M., Zhu, W., Swick, S. M., Stern, C. L., Schatz, G. C., Facchetti, A., Melkonyan, F. S., & Marks, T. J.
Venue
Journal of the American Chemical Society
Published
2019-01-23
Volume
141
Issue
7
Pages
3274-3287
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2911935006
Cited by
428
References
69
FWCI
23.53
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response. https://app.cochat.ai/papers/10.1021/jacs.8b13653
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Aldrich, T. J., Matta, M., Zhu, W., Swick, S. M., Stern, C. L., Schatz, G. C., Facchetti, A., Melkonyan, F. S., & Marks, T. J. (2019). Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.8b13653

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