锂(药物)
离子
插层(化学)
碳酸丙烯酯
循环伏安法
介电谱
电化学
阶跃势薛定谔方程的解
速率决定步骤
分析化学(期刊)
化学
电极
无机化学
物理化学
有机化学
内分泌学
医学
催化作用
作者
Sergey Yu. Vassiliev,Vyacheslav V. Sentyurin,Eduard E. Levin,Victoria A. Nikitina
标识
DOI:10.1016/j.electacta.2019.02.043
摘要
The elucidation of the reaction rate-determining step nature in intercalation processes is essential for the development of approaches for the precise control of rate-limiting factors. In this work, we explore the kinetic patterns of lithium-ion intercalation into two model cathode materials (LiCoO2 and LiMn2O4) and develop criteria for distinguishing between Butler-Volmer slow charge transfer and slow chemical steps. A numerical model for the rate-limiting ion desolvation step is developed and the predictions of the model are compared with the experimental voltammetric and electrochemical impedance spectroscopy data. We show that slow desolvation step results in essential changes in the shape of both cyclic voltammetry and impedance responses with the kinetic resistance vs. potential dependencies being highly informative for the reaction rate control diagnostics. The consideration of the intercalation kinetics in four solvents (water, propylene carbonate, acetonitrile and dimethyl sulfoxide) allows concluding on the influence of the resistivity of surface layer/electrode material interface on the reaction slow step nature.
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