Abstract
Cobalt based, outer-sphere, one-electron redox shuttles represents an exciting class of alternative electrolyte to be used in dye-sensitized solar cells. The flexibility of redox potential tuning by varying the substituents on peripheral organic ligands renders them the advantage of achieving higher photovoltage. However, higher recombination experienced in these systems by employing diffusion-limited cobalt species serves as a bottleneck which significantly limits attaining higher performance. The focus of the present contribution is to systematically investigate in detail the effect of structural variations and steric hindrance of organic triphenylamine dyes (TPAA4 and TPAA5) which differs in the number and nature of binding groups and peripheral hole accepting units on the recombination reactions and mass transport variations employing two different cobalt electrolytes, [Co3]3+/2+ and [Co(phen)3]3+/2+, having variable driving force for recombination. The detailed photovoltaic analysis provides us the i...
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