Photoelectrochemical Properties and Photostabilities of High Surface Area CuBi2O4 and Ag-Doped CuBi2O4 Photocathodes

Electrochemical synthesis methods were developed to produce CuBi2O4, a promising p-type oxide for use in solar water splitting, as high surface area electrodes with uniform coverage. These methods involved electrodepositing nanoporous Cu/Bi films with a Cu:Bi ratio of 1:2 from dimethyl sulfoxide or ethylene glycol solutions, and thermally oxidizing them to CuBi2O4 at 450 degrees C in air. Ag-doped CuBi2O4 electrodes were also prepared by adding a trace amount of Ag+ in the plating medium and codepositing Ag with the Cu/Bi films. In the Ag-doped CuBi2O4, Ag ions substitutionally replaced Bi3+ ions and increased the hole concentration in CuBi2O4. As a result, photocurrent enhancements for both O-2 reduction and water reduction were achieved. Furthermore, while undoped CuBi2O4 electrodes suffered from anodic photocorrosion during O-2 reduction due to poor hole transport, Ag-doped CuBiO4 effectively suppressed anodic photocorrosion. The flat-band potentials of CuBi2O4 and Ag-doped CuBi2O4 electrodes prepared in this study were found to be more positive than 1.3 V vs RHE in a 0.1 M NaOH solution (pH 12.8), which make these photocathodes highly attractive for use in solar hydrogen production. The optimized CuBi2O4/Ag-doped CuBi2O4 photocathode showed a photocurrent onset for water reduction at 1.1 V vs RHE, achieving a photovoltage higher than 1 V for water reduction. The thermodynamic feasibility of photoexcited electrons in the conduction band of CuBi2O4 to reduce water was also confirmed by detection of H-2 during photocurrent generation. This study provides new understanding for constructing improved CuBi2O4 photocathodes by systematically investigating photocorrosion as well as photoelectrochemical properties of high-quality CuBi2O4 and Ag-doped CuBi2O4 photoelectrodes for photoreduction of both O-2 and water.