Improving Electrocatalytic Activity and Durability of Cobalt‐Free Bismuth Ferrite‐Based Perovskite Oxygen Electrode for Reversible Solid Oxide Cells

作者：Ning Sun, Guangjun Zhang, Jiancheng Wang, Guozhu Zheng, Hui Xu, Yating Zhang, Lang Xu, Fangjun Jin, Ting Chen, Shaorong Wang · 发表于：Advanced Functional Materials · 年份：2025 · DOI：10.1002/adfm.202509535 · 被引用次数：9 · 研究领域：Advancements in Solid Oxide Fuel Cells、Advanced battery technologies research、Perovskite Materials and Applications

Abstract High electrocatalytic activity and robust thermal/chemical stability in oxygen electrode materials are critical properties for achieving high‐performance and long‐lifespan reversible solid oxide cells (RSOCs). Herein, a series of rare‐earth element‐substituted perovskite compounds Bi 0.8− x Ln x Ca 0.2 FeO 3− δ (Ln = La, Pr, and Nd) are explored as potential oxygen electrode materials. Particular attention is devoted to investigating their crystalline structure, oxygen exchange capabilities, electrocatalytic activity, and chemical durability. The density functional theory results indicate that praseodymium doping induces an increase in oxygen vacancies and reduces the adsorption energy of CO 2 , which helps to enhance electrochemical performance and durability. Electrochemical investigations reveal that the cell employing Bi 0.7 Pr 0.1 Ca 0.2 FeO 3− δ (BPCF) as oxygen electrode material achieves a peak power density of 1.278 W cm −2 and an electrolysis current density of 1.19 A cm −2 (1.3 V) at 800°C, outperforming most previously reported oxygen electrode materials. Moreover, the praseodymium‐doped BPCF oxygen electrode exhibits significantly enhanced resistance to CO 2 . This work presents an efficient approach for designing highly active and stable oxygen electrodes for RSOCs.