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Issue 6, 2016
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Enhancement of dye regeneration kinetics in dichromophoric porphyrin–carbazole triphenylamine dyes influenced by more exposed radical cation orbitals

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Abstract

Reduction kinetics of oxidized dyes absorbed on semiconductor surfaces and immersed in redox active electrolytes has been mainly modeled based on the free energy difference between the oxidation potential of the dye and the redox potential of the electrolyte. Only a few mechanisms have been demonstrated to enhance the kinetics by other means. In this work, the rate constant of the reduction of oxidized porphyrin dye is enhanced by attaching non-conjugated carbazole triphenylamine moiety using iodine/triiodide and tris(2,2′-bispyridinium)cobalt II/III electrolytes. These results are obtained using transient absorption spectroscopy by selectively probing the regeneration kinetics at the porphyrin radical cation and the carbazole triphenylamine radical cation absorption wavelengths. The enhancement in the reduction kinetics is not attributed to changes in the driving force, but to the more exposed dye cation radical orbitals of the dichromophoric dye. The results are important for the development of high efficiency photo-electrochemical devices with minimalized energy loss at electron transfer interfaces.

Graphical abstract: Enhancement of dye regeneration kinetics in dichromophoric porphyrin–carbazole triphenylamine dyes influenced by more exposed radical cation orbitals

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Publication details

The article was received on 28 Jan 2016, accepted on 27 Feb 2016 and first published on 01 Mar 2016


Article type: Edge Article
DOI: 10.1039/C6SC00429F
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Chem. Sci., 2016,7, 3506-3516
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    Enhancement of dye regeneration kinetics in dichromophoric porphyrin–carbazole triphenylamine dyes influenced by more exposed radical cation orbitals

    L. Zhao, P. Wagner, J. E. Barnsley, T. M. Clarke, K. C. Gordon, S. Mori and A. J. Mozer, Chem. Sci., 2016, 7, 3506
    DOI: 10.1039/C6SC00429F

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