α-Fe2O3 is a very attractive photoanode for photoelectrochemical (PEC) water decomposition. However, its short diffusion length, poor conductivity, and fast charge-carrier recombination severely limit device efficiency. Here, coloading an Al2O3 passivation layer and a CoOx cocatalyst onto Ti-doped α-Fe2O3 was carried out to promote PEC water oxidation by improving charge separation and transfer at the electrode/electrolyte interface and inhibiting photocarrier recombination. The optimized Ti:Fe2O3/Al2O3/CoOx photoanode shows a large photocurrent density of 1.41 mA cm-2 at 1.23 V vs reversible hydrogen electrode, which is 47 times greater than that of a pristine Ti:Fe2O3 photoanode. The dual modifications with a combined passivation layer and cocatalyst on the photoanode verify a valuable way for solar energy conversion in PEC water oxidation.
Keywords: PEC water oxidation; cocatalyst; passivation layer; photoanode; α-Fe2O3.