Abstract
The ability of Pt nanostructures to induce the splitting of the I-I bond in iodine (triiodide) molecules is explored here to enhance electron transfer in the iodine/iodide redox couple. Following the dispersal of Pt nanoparticles at 2% (weight) level, charge transport was accelerated in triiodide/iodide-containing 1,3-dialkylimidazolium roomerature ionic liquid. If both Pt nanoparticles and multi-walled carbon nanotubes were introduced into the ionic-liquid-based system, a solid-type (nonfluid) electrolyte was obtained. By using solid-state voltammetric (both sandwich-type and microelectrode-based) methodology, the apparent diffusion coefficients for charge transport increased to approximately 1×10-6 cm2s-1 upon the incorporation of the carbon-nanotube-supported iodine-modified Pt nanostructures. A dye-sensitized solar cell comprising TiO2 covered with a heteroleptic RuII-type sensitizer (dye) and the semisolid triiodide/iodide ionic liquid electrolyte admixed with carbon-nanotube-supported Pt nanostructures yielded somewhat higher power conversion efficiencies (up to 7.9% under standard reporting conditions) than those of the analogous Pt-free system.
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Rutkowska, I. A., Marszalek, M., Orlowska, J., Ozimek, W., Zakeeruddin, S. M., Kulesza, P. J., & Grätzel, M. (2015). Nanocomposite Semi-Solid Redox Ionic Liquid Electrolytes with Enhanced Charge-Transport Capabilities for Dye-Sensitized Solar Cells. ChemSusChem, 8(15), 2560–2568. https://doi.org/10.1002/cssc.201403475
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