Schiff Base Complex Cocatalyst with Coordinatively Unsaturated Cobalt Sites for Photoelectrochemical Water Oxidation

Integrating inorganic oxygen evolution cocatalysts (OECs) with photoanodes is regarded as an available strategy to increase the photogenerated charge utilization for accelerated water oxidation kinetics. Nevertheless, most widely used transition metal (oxyhydr)oxides OECs suffer from inevitable charge recombination at photoanode/OECs interfaces and underabundant catalytic active sites. Herein, a cobalt-organic complex with microflower-like features (denoted as MF) was constructed by coordination of Schiff base ligands and Co2+ metal ions and then decorated on porous BiVO4 employed as photoanodes for photoelectrochemical (PEC) water oxidation. The as-synthesized BiVO4/MF photoanode achieves a photocurrent density of 4.38 mA cm(-2) and at 1.23 V-RHE in 0.5 M Na2SO4 electrolyte under simulated 1 sun illumination, over approximately 5.48 times larger than that of BiVO4 counterpart, and exhibits a 120 mV cathodic shift of onset potential with outstanding photostability. Systematic characterizations reveal that the improved PEC efficiency is mainly attributed to the well-designed coordinatively unsaturated Co2+ sites, which not only serve as powerful photohole extraction engines along reversed interfacial Co-O-Bi bonds to promote charge transfer across the BiVO4/complex interface but also act as reaction active centers by accelerating surface water oxidation kinetics. This work provides new insights for designing highly effective OECs for PEC water oxidation.

Automated summary

Integrating inorganic oxygen evolution cocatalysts with photoanodes is a viable strategy to increase the photogenerated charge utilization. In this study, a cobalt-organic complex was constructed and applied to the photoelectrochemical water oxidation. The synthesized photoanode exhibited high photocurrent density and excellent photostability.