过电位
材料科学
电化学
氧化物
电极
氧气
原位
析氧
化学工程
电化学电池
无机化学
钙钛矿(结构)
固体氧化物燃料电池
表征(材料科学)
分析化学(期刊)
空位缺陷
化学物理
电位滴定法
催化作用
电极电位
下降(电信)
克拉克电极
电化学能量转换
分压
交换电流密度
固溶体
参比电极
作者
Taeyun Kim,J. H. Lee,Heejun Yang,Ji Haeng Yu,J. M. Serra,Jong Hoon Joo
摘要
ABSTRACT Solid oxide electrochemical cells (SOCs) employ mixed ionic–electronic conducting (MIEC) perovskite electrodes, where electrochemical performance is dictated by the oxygen surface exchange coefficient ( k ) and the concentration of oxygen vacancies (δ). Conventional methods evaluate k and δ separately and under conditions that do not reflect their coupled behavior during operation, offering only a partial picture of the underlying processes. Here we report an in situ methodology that simultaneously resolves k and δ under realistic SOC operating conditions, using a dense bulk electrode integrated with a solid electrolyte. An applied overpotential induces an abrupt drop in the oxygen chemical potential gradient, enabling direct analysis of defect chemistry and surface reaction kinetics. The extracted values are consistent with those obtained from established characterization methods, validating the accuracy of the approach. Beyond fundamental characterization, the platform captures dynamic evolutions in defect chemistry and reaction kinetics, providing mechanistic insights into electrode degradation.
科研通智能强力驱动
Strongly Powered by AbleSci AI