Abstract
Water-splitting dye-sensitized photoelectrochemical cells (WS-DSPECs) use visible light to split water using molecular sensitizers and water oxidation catalysts codeposited onto mesoporous TiO2 electrodes. Despite a high quantum yield of charge injection and low requirement for the catalytic turnover rate, the quantum yield of water splitting in WS-DSPECs is typically low (<1%). Here we examine the charge separation and recombination processes in WS-DSPECs photoanodes functionalized with varying amounts of IrO2 nanoparticle catalyst. Charge extraction and transient open-circuit voltage decay measurements provide insight into the relationship between light intensity, conduction band electron density, open-circuit photovoltage, and recombination time scale. We correlate these results with electrochemical impedance spectroscopy and present the first complete equivalent circuit model for a WS-DSPEC. The data show quantitatively that recombination of photoinjected electrons with oxidized sensitizer molecules a...
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