Protection of inorganic semiconductors for sustained, efficient photoelectrochemical water oxidation

Abstract

Small-band-gap (E_g < 2 eV) semiconductors must be stabilized for use in integrated devices that convert solar energy into the bonding energy of a reduced fuel, specifically H_2(g) or a reduced-carbon species such as CH_3OH or CH_4. To sustainably and scalably complete the fuel cycle, electrons must be liberated through the oxidation of water to O_2(g). Strongly acidic or strongly alkaline electrolytes are needed to enable efficient and intrinsically safe operation of a full solar-driven water-splitting system. However, under water-oxidation conditions, the small-band-gap semiconductors required for efficient cell operation are unstable, either dissolving or forming insulating surface oxides. We describe herein recent progress in the protection of semiconductor photoanodes under such operational conditions. We specifically describe the properties of two protective overlayers, TiO_2/Ni and NiO_x, both of which have demonstrated the ability to protect otherwise unstable semiconductors for >100 h of continuous solar-driven water oxidation when in contact with a highly alkaline aqueous electrolyte (1.0 M KOH(aq)). The stabilization of various semiconductor photoanodes is reviewed in the context of the electronic characteristics and a mechanistic analysis of the TiO_2 films, along with a discussion of the optical, catalytic, and electronic nature of NiO_x films for stabilization of semiconductor photoanodes for water oxidation.