Abstract

A stable surface treatment for the nanoporous TiO2 electrode of dye-sensitized solar cells (DSCs) has been developed via sol-gel processing of titanium(IV) isopropoxide (TiP), enabling controllable performance improvements, which has been hitherto unachievable. A systematic study of the electrode chemistry and morphology was performed to examine the mechanisms by which the treatment contributes to enhancement in DSC performance. The electrode exhibited a linear increase in mass with TiP concentration and a corresponding reduction in porosity. The increase in nanoparticle diameter resulted in the increase in surface area without altering the surface chemistry, leading to an increase in dye loading. Current–voltage characteristics and incident photon-to-electron conversion efficiencies (IPCE) were analyzed. A linear increase in the short-circuit photocurrent was measured with TiP concentration, increasing by 30 % for a 4 mM TiP treatment, which resulted in a corresponding efficiency gain of 23 %. This was found to primarily result from a controllable increase in the charge collection efficiency, via a 30 % faster electron transport time and a 19 % increase in the electron lifetime. The results elucidate the underlying physical mechanisms for improvement in DSC performance by surface treatment.

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