Electrochemical synthesis methods were developed to produce CuBi 2 O 4 , 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 CuBi 2 O 4 at 450 °C in air. Ag-doped CuBi 2 O 4 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 CuBi 2 O 4 , Ag + ions substitutionally replaced Bi 3+ ions and increased the hole concentration in CuBi 2 O 4 . As a result, photocurrent enhancements for both O 2 reduction and water reduction were achieved. Furthermore, while undoped CuBi 2 O 4 electrodes suffered from anodic photocorrosion during O 2 reduction due to poor hole transport, Ag-doped CuBiO 4 effectively suppressed anodic photocorrosion. The flat-band potentials of CuBi 2 O 4 and Ag-doped CuBi 2 O 4 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 CuBi 2 O 4 /Ag-doped CuBi 2 O 4 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 CuBi 2 O 4 to reduce water was also confirmed by detection of H 2 during photocurrent generation. This study provides new understanding for constructing improved CuBi 2 O 4 photocathodes by systematically investigating photocorrosion as well as photoelectrochemical properties of high-quality CuBi 2 O 4 and Ag-doped CuBi 2 O 4 photoelectrodes for photoreduction of both O 2 and water.