Improving cathode electrocatalysis via Co-substitution-driven interstitial transport for proton-conducting solid oxide fuel cells

被引:0
作者
Hu, Jiani [1 ]
Ma, Lei [1 ]
Jiang, Wang [1 ]
Xie, Zhangjin [1 ]
Wu, Fang [1 ]
Hou, Jie [1 ]
机构
[1] Univ South China, Hengyang 421001, Peoples R China
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2025年 / 319卷
基金
中国国家自然科学基金;
关键词
Proton conducting solid oxide fuel cells; Interstitial oxygen species; Proton migration; Ionic transport; CERAMIC FUEL; SYSTEM LA2-XSRXNIO4+DELTA; COMPOSITE CATHODE; PERFORMANCE; SPECTROSCOPY; DESIGN; STATE;
D O I
10.1016/j.mseb.2025.118372
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Strategic engineering of B-site coordination environment in K2NiF4-type oxides presents a rational pathway to optimize electrocatalytic functionality. Herein, Co substitution in La1.2Sr0.8NiO4+delta (LSNO) induces structural reorganization that accommodates excess interstitial oxygen species, enabling dual enhancement of ionic transport with 30-fold enhanced oxygen diffusion and 3.5-11.1-fold improved proton migration. The NiOBaZr0.1Ce0.7Y0.2O3-delta|BaZr0.1Ce0.7Y0.2O3-delta|La1.2Sr0.8Ni0.5Co0.5O4+delta (LSNCO) cell demonstrates exceptional electrochemical performance with the power density of 1698 mW cm- 2 and polarization resistance of 0.056 Omega cm2 at 700 degrees C, outperforming both LSNO counterpart and reported Ln2NiO4-based cathodes. The synergistic integration of exceptional power generation, optimized interfacial polarization, and excellent operational stability establishes LSNCO as a benchmark cathode material for proton conducting solid oxide fuel cells. This study systematically validates a Co-mediated B-site coordination engineering strategy in K2NiF4-type lattices, providing a generalized framework for designing high electrocatalytically active electrodes with coupled ionic transport channels.
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页数:7
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