电子转移
动力学
循环伏安法
线性扫描伏安法
伏安法
阳极
电化学
化学
电解质
马库斯理论
电极
电化学动力学
分析化学(期刊)
材料科学
锂(药物)
反应速率常数
物理化学
有机化学
物理
内分泌学
医学
量子力学
作者
David Boyle,Xian Kong,Allen Pei,Paul E. Rudnicki,Feifei Shi,William Huang,Zhenan Bao,Jian Qin,Yi Cui
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-02-03
卷期号:5 (3): 701-709
被引量:126
标识
DOI:10.1021/acsenergylett.0c00031
摘要
Fully understanding the mechanism of lithium metal deposition is critical for the development of rechargeable lithium battery anodes. The heterogeneous electron transfer kinetics are an important aspect of lithium electrodeposition, but they have been difficult to measure and understand. Here, we use transient voltammetry with ultramicroelectrodes to explicitly investigate the electron transfer kinetics of lithium electrodeposition. The results deviate from the Butler–Volmer model of electrode kinetics; instead, a Marcus model accurately describes the electron transfer. Measuring the kinetics in a series of electrolytes shows the mechanism of lithium deposition under electron transfer control is consistent with the general framework of Marcus theory. Comparison of the transient voltammetry results to electrochemical impedance spectra provides a strategy for understanding how the interplay of the electron transfer and mass transport resistances affect the morphology of lithium.
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