Developing bifunctional electrocatalysts capable of efficiently driving the interconversion between oxygen and water molecules via oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is crucial for establishing renewable-driven energy infrastructure. A series of lead-free halide perovskites Cs2SnX6 (X = Cl, Br, I) is designed, along with their mixed halide derivatives Cs2SnClxBr6-x (where x = 2, 3, 4), to probe bifunctional OER/ORR activity. Measurements reveal the influence of halide ions on the morphology and unravel the unique halide-electronegativity-tunable electronic properties. Further, these materials are immobilized on carbon paper and utilized as anode, where Cs2SnCl6 and Cs2SnCl2Br4 displayed the best OER activity and appreciable Faradic efficiency. The photophysical properties of the perovskites lead to a distinct enhancement (≈0.24-0.72 mA cm-2) in the OER current response for Cs2SnCl6 and Cs2SnCl2Br4 under white-light irradiation. The perovskites maintain their structural and chemical integrity during the (photo)electrocatalysis, as demonstrated by in-depth post-electrolytic surface analysis. The electrocatalysts continue to demonstrate active ORR during the cathodic scan (onset potential of ≈0.6 V vs RHE); however, with minimal influence of photoirradiation. Overall, the Cs2SnX6-based perovskite electrocatalysts exhibit promising bidirectional OER/ORR activity with competitive catalytic efficiency and stability, suitable for developing sustainable devices for O2/H2O redox chemistry-mediated energy transduction applications.
Takhar et al. (Fri,) studied this question.