Anionic structure-dependent photoelectrochemical responses of dye-sensitized solar cells based on a binary ionic liquid electrolyte

Abstract

Room temperature ionic liquids (RTILs) have been used as electrolytes to investigate the anionic structure dependence of the photoelectrochemical responses of dye-sensitized solar cells (DSCs). A series of RTILs with a fixed cation structure coupling with various anion structures are employed, in which 1-methyl-3-propylimidazolium iodide (PMII) and I₂ are dissolved as redox couples. It is found that both the diffusivity of the electrolyte and the photovoltaic performance of the device show a strong dependence on the fluidity of the ionic liquids, which is primarily altered by the anion structure. Further insights into the structure-dependent physical properties of the employed RTILs are discussed in terms of the reported van der Waals radius, the atomic charge distribution over the anion backbones, the interaction energy of the anion and cation, together with the existence of ion-pairs and ion aggregates. Particularly, both the short-circuit photocurrent and open-circuit voltage exhibit obvious fluidity dependence. Electrochemical impedance and intensity-modulated photovoltage/photocurrent spectroscopy analysis further reveal that increasing the fluidity of the ionic liquid electrolytes could significantly decrease the diffusion resistance of I₃⁻ in the electrolyte, and retard the charge recombination between the injected electrons with triiodide in the high-viscous electrolyte, thus improving the electron diffusion length in the device, as well as the photovoltaic response. However, the variation of the electron diffusion coefficients is trivial primarily due to the effective charge screening of the high cation concentration.