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The development of durable and efficient bifunctional electrocatalysts for the oxygen reduction (ORR) and oxygen evolution (OER) reactions is crucial for advancing rechargeable Zn-air batteries. In this work, an A-site-deficient triple perovskite oxide, La 1 Sr 1.5 Co 1.5 Fe 1.5 O 9-δ (LSCFO), was synthesized and applied as a bifunctional catalyst. The introduction of A-site deficiency generated oxygen vacancies and modified the electronic structure, thereby enhancing charge transfer and increasing the density of active sites. Rotating disk electrode (RDE) studies revealed excellent ORR (E 1/2 = 0.84 V) and OER (η 10 = 1.53 V) activity, with a narrow potential gap of 0.68 V. Density functional theory (DFT) calculations further confirmed that Sr incorporation tunes the electronic states of B-site cations, optimizes oxygen intermediate adsorption, and accounts for the improved OER kinetics. When integrated into a Zn-air battery, LSCFO-1:1.5 delivered 1.45 V open-circuit voltage, 108 mW cm −2 power density, and 810 mAh g Zn −1 capacity, while retaining excellent stability over 600 h of cycling. • A-site deficiency in triple perovskite oxides as a novel catalyst to enhance Zn-air battery performance. • Utilization of A-site-deficient triple perovskite as a bifunctional ORR/OER electrocatalyst. • Superior activity and stability in Zn-air batteries compared to conventional catalysts. • Systematic study of A-site deficiency and multi-element synergy on catalytic behavior. • Oxygen mobility analysis reveals its role in facilitating ORR and OER. • Highlights scalability and cost-effectiveness for potential commercialization in next-generation Zn-air batteries.
Ali et al. (Wed,) studied this question.