氧气
空位缺陷
焓
钙钛矿(结构)
离子键合
化学物理
材料科学
原子间势
热力学
金属
离子电导率
化学
混合焓
熵(时间箭头)
电阻率和电导率
电导率
凝聚态物理
格子(音乐)
离子半径
过渡金属
物理化学
无机化学
热的
作者
Arron R. Potter,Yifan Wang,Kiran Hamkins,Dongjae Kong,Yuzhe Li,Jian Qin,Xiaolin Zheng
标识
DOI:10.1038/s41467-026-70835-z
摘要
High-entropy perovskite oxides have emerged as promising electrode materials for solid oxide electrolyzers. However, their compositional complexity makes the formation of oxygen vacancies, which influence properties such as oxygen ionic conductivity and thermal expansion, challenging to predict. Here, we experimentally measure changes in oxygen vacancy concentration for fourteen perovskite oxides with high and low-entropy A-site compositions, finding a dependence on cation size variance in addition to divalent cation fraction. Atomistic simulations using a machine-learned universal interatomic potential reveal cation size mismatches broaden a distribution of vacancy formation energies, shown through statistical thermodynamics to shift bulk formation thermodynamics. Treating oxygen vacancies statistically enables accurate predictions of oxygen vacancy formation compared to traditional models. Practically, increasing the size variance between A-site cations reduces the temperature sensitivity of oxygen vacancy concentrations, making it key for tuning critical properties. More broadly, this study demonstrates statistical treatment of oxygen vacancies is essential for understanding high-entropy perovskite oxides.
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