WO 3 is a promising candidate for a photoanode material in an acidic electrolyte, in which it is more stable than most metal oxides, but kinetic limitations combined with the large driving force available in the WO 3 valence band for water oxidation make competing reactions such as the oxidation of the acid counterion a more favorable reaction. The incorporation of an oxygen evolving catalyst (OEC) on the WO 3 surface can improve the kinetics for water oxidation and increase the branching ratio for O 2 production. Ir-based OECs were attached to WO 3 photoanodes by a variety of methods including sintering from metal salts, sputtering, drop-casting of particles, and electrodeposition to analyze how attachment strategies can affect photoelectrochemical oxygen production at WO 3 photoanodes in 1 M H 2 SO 4 . High surface coverage of catalyst on the semiconductor was necessary to ensure that most minority-carrier holes contributed to water oxidation through an active catalyst site rather than a sidereaction through the WO 3 /electrolyte interface. Sputtering of IrO 2 layers on WO 3 did not detrimentally affect the energy-conversion behavior of the photoanode and improved the O 2 yield at 1.2 V vs. RHE from B0% for bare WO 3 to 50-70% for a thin, optically transparent catalyst layer to nearly 100% for thick, opaque catalyst layers. Measurements with a fast one-electron redox couple indicated ohmic behavior at the IrO 2 /WO 3 junction, which provided a shunt pathway for electrocatalytic IrO 2 behavior with the WO 3 photoanode under reverse bias. Although other OECs were tested, only IrO 2 displayed extended stability under the anodic operating conditions in acid as determined by XPS.