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Probing Interfacial Halogen-Bonding Effects with Halogenated Organic Dyes and a Lewis Base-Decorated Transition Metal-Based Redox Shuttle at a Metal Oxide Interface in Dye-Sensitized Solar Cells
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    Probing Interfacial Halogen-Bonding Effects with Halogenated Organic Dyes and a Lewis Base-Decorated Transition Metal-Based Redox Shuttle at a Metal Oxide Interface in Dye-Sensitized Solar Cells
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    The Journal of Physical Chemistry C

    Cite this: J. Phys. Chem. C 2021, 125, 32, 17647–17659
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    https://doi.org/10.1021/acs.jpcc.1c05051
    Published August 9, 2021
    Copyright © 2021 American Chemical Society

    Abstract

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    Metal-free bis-cyclopentadithiophene-based molecular sensitizers with varying halogens (Cl, Br, and I) installed at a terminal position in conjugation with the dye frontier molecular orbital π-system are studied in combination with two cobalt redox shuttles (RSs): with and without a nonmetal-coordinated nitrogen atom (pyrazine or pyridine) accessible to the halide-decorated dyes. This systematic study employs UV–vis absorption, cyclic voltammetry, density functional theory calculations, and nanosecond transient absorption spectroscopy to probe the influence of possible halogen-bonding between the dyes and the pyrazine-based RS on electron-transfer reactions and effects on dye-sensitized solar cell performances. The results of this study imply a possible halogen-bonding event occurring between the halogenated dyes and the halogen binding RS with substantial effects on electron-transfer reaction rates.

    Copyright © 2021 American Chemical Society

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    This article is cited by 14 publications.

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    The Journal of Physical Chemistry C

    Cite this: J. Phys. Chem. C 2021, 125, 32, 17647–17659
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.jpcc.1c05051
    Published August 9, 2021
    Copyright © 2021 American Chemical Society

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