摘要
Advancing clean energy technologies demands efficient and durable electrode catalysts for solid oxide cells (SOCs). Despite their exceptional catalytic properties, Pt-based materials face critical challenges in high-temperature applications owing to particle agglomeration and cost constraints. Here, we demonstrate a rational design strategy utilizing controlled in situ exsolution to create strongly anchored PtSn nanoalloys on oxygen-deficient PrBaMn 1.8 Pt 0.1 Sn 0.1 O 5+ δ (L-PBMPtSn) perovskite oxide. Through precise compositional engineering and structural control, we achieved a uniform dispersion of PtSn nanoparticles with unique socket-like interfaces that prevent agglomeration while maintaining high catalytic accessibility. The optimized electrode demonstrates remarkable bifunctional performance, achieving a current density of 1.6 A cm −2 at 1.8 V for CO 2 electrolysis and a maximum power density of 316 mW cm −2 for fuel cell operation at 800 °C. More significantly, the electrode exhibits exceptional stability with only 9.6% performance degradation over 100 h of operation, which is a substantial improvement over conventional electrodes. Our findings establish a new paradigm for designing high-performance SOC electrodes through the controlled exsolution of precious metal alloys, offering broader implications for catalyst design in high-temperature electrochemical systems. Graphical abstract
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