钙钛矿(结构)
材料科学
氧化物
离子电导率
电解质
氧气
热重分析
正交晶系
固体氧化物燃料电池
热膨胀
快离子导体
化学工程
无机化学
离子键合
热稳定性
晶体结构
结晶学
物理化学
化学
离子
电极
冶金
有机化学
工程类
作者
Bryce G. Mullens,Frederick P. Marlton,Caleb J. Bennett,Matilde Saura-Múzquiz,Maria K. Nicholas,Helen E. A. Brand,Brendan J. Kennedy
出处
期刊:APL Materials
[American Institute of Physics]
日期:2024-12-01
卷期号:12 (12)
被引量:2
摘要
The efficient operation of solid oxide fuel cells for renewable energy generation requires solid electrolytes with high ionic conductivity, thermal stability, and chemical durability. Metal oxide perovskites of the form ABO3 are promising candidates, especially when doped with cations that incorporate interstitial oxygen or oxygen vacancies to enhance ionic conductivity. However, doping can lead to complex and poorly understood crystallographic structures. In this study, we investigate the effects of Fe3+ doping on the orthorhombic Pbnm CaTiO3 perovskite, forming Ca(Ti0.8Fe0.2)O3−δ, and demonstrate the complexity of its phase transitions at operational temperatures. Using synchrotron X-ray diffraction and thermogravimetric analysis, we show that this material undergoes significant oxygen uptake at elevated temperatures, leading to an irreversible expansion of the unit cell and changes in polyhedral coordination upon cooling. These structural modifications are attributed to the partial oxidation of Fe3+ to Fe4+, providing insight into the inconsistencies observed in previous studies of oxygen-deficient perovskites. Our findings highlight the critical role of thermal history and oxygen availability in determining the structural stability and long-term performance of perovskite-based solid electrolytes in solid oxide fuel cells.
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