An atomistic picture of the regeneration process in dye sensitized solar cells

Abstract

A highly efficient mechanism for the regeneration of the cis-bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)-ruthenium(II) sensitizing dye (N3) by I^- in acetonitrile has been identified by using molecular dynamics simulation based on density functional theory. Barrier–free complex formation of the oxidized dye with both I^- and , and facile dissociation of and from the reduced dye are key steps in this process. In situ vibrational spectroscopy confirms the reversible binding of I₂ to the thiocyanate group. Additionally, simulations of the electrolyte near the interface suggest that acetonitrile is able to cover the (101) surface of anatase with a passivating layer that inhibits direct contact of the redox mediator with the oxide, and that the solvent structure specifically enhances the concentration of I^- at a distance which further favors rapid dye regeneration.