Lee Jinsil, Park Jinhong, Kim Taeyun, Choi Soomin, Kim Seong Kyun, Yoon Kyung Joong, Joo Jong Hoon
Department of Environment and Energy Engineering, Gwangju Institute of Science and Technology, 123, Cheomdangwagi-ro, Buk-gu, Gwangju, 61005, Republic of Korea.
Research Center for Innovative Energy and Carbon Optimized Synthesis for Chemicals (Inn-ECOSysChem), Gwangju Institute of Science and Technology, 123 Cheomdangwagi-ro, Buk-gu, Gwangju, 61005, Republic of Korea.
Small. 2025 Sep;21(38):e06595. doi: 10.1002/smll.202506595. Epub 2025 Aug 14.
Surface modification via nanocatalyst infiltration has emerged as an effective strategy for enhancing the performance and lifespan of high-temperature electrochemical devices, addressing the limitations of conventional perovskite-based air electrodes. Although surface modification has been widely adopted, how infiltration simultaneously enhances electrochemical activity and durability remains unclear. Herein, the effect of SmSrCoO (SSC) infiltration into LaSrCoFeO (LSCF) electrodes is systematically investigated using dense model systems, which enable for detailed analysis of surface phenomena and accurate quantification of electrochemical processes. The SSC coating significantly enhanced the oxygen surface-exchange kinetics while concurrently suppressing cation segregation and phase decomposition under the solid oxide fuel cell (SOFC) operating conditions. This improvement is attributed to the reduced electrode polarization via the catalytic promotion of surface reactions, which lowers the surface potential and mitigates instability in the LSCF backbone. These findings are consistently validated in full-cell configurations, confirming that infiltration not only improved performance but also suppressed Cr poisoning and phase decomposition. This study offers new insights into the dual role of infiltration in enhancing both the catalytic activity and structural stability, establishing design principles for durable, high-performance SOFC electrodes.
通过纳米催化剂渗透进行表面改性已成为提高高温电化学装置性能和寿命的有效策略,解决了传统钙钛矿基空气电极的局限性。尽管表面改性已被广泛采用,但渗透如何同时提高电化学活性和耐久性仍不清楚。在此,使用致密模型系统系统地研究了SmSrCoO(SSC)渗透到LaSrCoFeO(LSCF)电极中的效果,该系统能够详细分析表面现象并准确量化电化学过程。在固体氧化物燃料电池(SOFC)运行条件下,SSC涂层显著增强了氧表面交换动力学,同时抑制了阳离子偏析和相分解。这种改进归因于通过催化促进表面反应降低了电极极化,从而降低了表面电位并减轻了LSCF骨架中的不稳定性。这些发现在全电池配置中得到了一致验证,证实渗透不仅提高了性能,还抑制了Cr中毒和相分解。本研究为渗透在增强催化活性和结构稳定性方面的双重作用提供了新的见解,确立了耐用、高性能SOFC电极的设计原则。