Photoelectrochemical (PEC) water splitting offers a sustainable route for solar-to-hydrogen conversion, yet its large-scale deployment is often hindered by energy-intensive and costly fabrication processes for semiconductor photoelectrodes. Electrodeposition provides an attractive alternative owing to its solution-based, low-temperature, and scalable nature; however, the relationship between electrochemical deposition parameters and photoelectrode functionality remains insufficiently understood. Herein, we systematically investigate system-level control in electrodeposition for photoelectrode synthesis using BiVO4 photoanodes and CuO/Cu2O photocathodes as model systems. By modulating deposition potential, current density, and electrical control modes, we elucidate how interfacial ion dynamics and growth kinetics govern film morphology, phase evolution, and PEC performance. DC electrodeposition establishes a baseline structure–performance relationship governed by precursor concentration and current density, while pulsed operation enables decoupling of nucleation and growth, leading to refined nanostructures and enhanced photocurrent responses. Further incorporation of reverse-pulsed potentials provides dynamic interfacial reset, enabling precise control over porosity and grain connectivity. The optimized BiVO4 photoanodes fabricated under tailored reverse-pulsed conditions exhibit improved photocurrent density compared to continuously deposited counterparts. The insights presented here provide practical guidelines for rationally engineering high-performance, scalable, and environmentally benign photoelectrodes for PEC water splitting.
Mi Gyoung Lee (Thu,) studied this question.