Photo-driven electrochemical etching to construct porous structures with oxygen vacancies on ZnO photoanodes for efficient solar water splitting

Abstract

Fast charge separation and oxidation kinetics are the key issues for photoelectrochemical (PEC) water splitting. Herein, photo-driven electrochemical etching (PEE) was applied to modify the morphology and surface properties of ZnO photoanodes to improve PEC performance. By regulating the applied potential and treatment time, the PEE generated a lotus root like porous structure with a pore diameter of 20–30 nm and depth of about 300 nm, and produced a large amount (30.1 %) of oxygen vacancies (Ov) on ZnO photoanode. PEE treated-ZnO array demonstrated a charge separation efficiency of 87 %, and achieved 1.8 times larger photocurrent (1.26 mAcm−2 at 1.23 VRHE) with a cathodic shift of onset potential of 0.12 VRHE than pristine ZnO. The introduced Ov and the shortened charge transport distance of porous microstructures by PEE treatment improved the electrode/electrolyte interface charge transfer and water oxidation kinetics. DFT calculations indicate that the construction of oxygen defects on the catalyst surface can reduce the overpotential of oxygen evolution reaction (OER) and further promote the catalytic activity of OER. Moreover, electrode surface pore structure can be tailored by adjusting illumination parameters and electrolytes. This work illustrates a novel and effective approach to tunable photo-corrodible electrode materials for solar water splitting.