阴极
材料科学
电解质
陶瓷
化学工程
氧化物
电化学
质子
极化(电化学)
分析化学(期刊)
无机化学
电极
复合材料
物理化学
色谱法
化学
冶金
量子力学
物理
工程类
作者
Chenghao Yang,Jin Li,Shiming Hu,Jian Pu,Bo Chi
标识
DOI:10.1016/j.ceramint.2023.09.166
摘要
The application of cobalt-based perovskite cathode materials in proton-conducting SOFCs (H–SOFCs) is challenged by their high thermal expansion coefficient (TEC). To address interface degradation/separation between the cobalt-based perovskite cathode and the proton-conducting electrolyte, we design and prepare the high-entropy perovskite oxide (HEPO) BaCo0.2Zn0.2Ga0.2Zr0.2Y0.2O3-δ (BCX) as the cathode for proton-conducting SOFCs (H–SOFCs). BCX demonstrates remarkable performance and stability in the oxygen reduction reaction, validated through structural analysis and electrochemical characterizations. The TEC of BCX is as low as 12.75 × 10-6 K−1 compared to the 18.69 × 10-6 K−1 of the un-doped BaCoO3-δ (BC). The polarization resistance of BCX cathode about 0.69 Ω cm2 is realized at 600 °C, much lower than that for pristine BC cathode (1.27 Ω cm2). Cell with BCX cathode exhibits remarkable long-term stability without detectable degradation over 100 h.
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