电解质
交换电流密度
材料科学
聚合物
极化(电化学)
相间
电阻抗
电流密度
介电谱
锂(药物)
电化学
放松(心理学)
高氯酸锂
分析化学(期刊)
动力学
化学工程
电荷密度
聚乙烯
电极
电流(流体)
电化学动力学
快离子导体
化学物理
聚合物电解质
磁滞
循环伏安法
作者
Katrin Geng,Bryce A. Tappan,Stefano Passerini,Yang Shao‐Horn,Dominic Bresser
标识
DOI:10.1002/advs.202514492
摘要
While interfacial processes can dominate the internal resistance in solid-state batteries, the (electro-)chemical reactions occurring at the lithium│polymer interface are complex and dynamic upon cycling. A central factor for evaluating such reactions is the exchange current density j0 that characterizes the kinetics of the interfacial charge transfer. However, its determination is challenging due to superimposed impedance contributions from the solid electrolyte interphase and interfacial charge transfer reactions. Moreover, different methodologies for determining j0 can lead to different j0 values. Herein, a carefully validated method to determine j0 for polymer electrolytes is reported, using the example of polyethylene oxide-based systems, by combining electrochemical impedance spectroscopy, Bayesian inference analysis, and distribution of relaxation times analysis. These impedance-based methodologies are validated via the determination of j0 using DC polarization measurements that are fit to a modified Butler-Volmer model, enabling the reliable determination of j0 for polymer electrolytes and, thus, the analysis of the interfacial processes and reactions occurring in such systems.
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