Direct water electrolysis was achieved with a novel, integrated, monolithic photoelectrochemical-photovoltaic design. This photoelectrochemical cell, which is voltage biased with an integrated photovoltaic device, splits water directly upon illumination; light is the only energy input. The hydrogen production efficiency of this system, based on the short-circuit current and the lower heating value of hydrogen, is 12.4 percent.
With an eye toward developing a photoelectrochemical system for water splitting using p-GaInP2, the electrochemical stability of p-GaInP2 was studied in 10 M KOH, 3 M H2504, and a phosphate buffer of pH 7. It was found that inthe dark, the p-GaInP2 electrode is susceptible to corrosion in all investigated solutions. Upon illumination, the anodic corrosion current increases. Under cathodic polarization in 10 M KOH, the p-GaInP2 electrode shows saturated photocurrent density, however the photocurrent slowly decreases with time due to the precipitation of an indium-enriched oxide. In 3 M H,S04, the anodic process can be inhibited under relatively low cathodic potentials, and stable photocurrents can be obtained. In neutral solution, p-GaInP2 is covered by a semi-insulating oxide film and the observed photocurrent densities are much lower than those in 10 M KOH and 3 M H2504.
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