材料科学
合金
阳极
复合材料
氧化物
Boosting(机器学习)
固体氧化物燃料电池
燃料电池
冶金
化学工程
电极
计算机科学
机器学习
工程类
物理化学
化学
作者
Yan Yi,Xiuan Xi,Lingui Huang,Бо Лю,Yuanfeng Liao,Jianwen Liu,Jun Long,Jiujun Zhang,Xian‐Zhu Fu,Jing‐Li Luo
标识
DOI:10.1002/adfm.202412486
摘要
Abstract Sr 2 Fe 1.5 Mo 0.5 O 6‐δ (SFM) perovskite oxide is one of the most promising materials for solid oxide fuel cells (SOFCs) anode. However, the low catalytic activity is a major roadblock that obstructs its practical applications. Although in situ exsolution of B‐site metals is demonstrated as a promising approach to enhancing its performance, it can easily induce the co‐segregation of A‐site Sr, which seriously deteriorates the performance stability. In this work, the A‐site Sr element in SFM is partially replaced by Pr, while B‐site Mo is partially replaced by Ni. The in situ co‐exsolution of both FeNi alloy and PrO x nanoparticles on the reduced Pr 0.8 Sr 1.2 Fe 1.5 Mo 0.3 Ni 0.2 O 6‐δ (R‐PSFMN) perovskite is successfully achieved. It is found that the peak power densities (P max ) of the single cell using R‐PSFMN as the anode reaches as high as 2.29, 1.60, 1.07, and 0.67 W cm − 2 in H 2 atmosphere at the operating temperatures of 850, 800, 750 and 700 °C, respectively. Furthermore, it also exhibits excellent performance stability and anticoke properties when using ethane as fuel. The impregnation experiment further corroborates that the improved performance and stability are partly attributable to the contribution of PrO x nanoparticles, presenting a promising approach to enhance the electrochemical performance of SOFC perovskite anodes.
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