石墨
电解质
锂(药物)
电镀(地质)
电化学
电极
阳极
材料科学
化学工程
无机化学
化学
冶金
地质学
工程类
内分泌学
物理化学
医学
地球物理学
作者
Eric J. McShane,Andrew M. Colclasure,David E. Brown,Zachary M. Konz,Kandler Smith,Bryan D. McCloskey
出处
期刊:Meeting abstracts
日期:2020-11-23
卷期号:MA2020-02 (3): 542-542
标识
DOI:10.1149/ma2020-023542mtgabs
摘要
Lithium plating on graphite anodes currently limits the fast charging performance of lithium-ion batteries because plated Li is prone to become electronically isolated from the electrode (referred to as 'inactive Li') or react with electrolyte, both of which contribute to rapid cell capacity fade. To understand the onset and extent of these detrimental processes, it is critical to quantify these sources of capacity loss. In this work, we demonstrate a titration technique to quantify both inactive Li and solid electrolyte interphase (SEI) species (solid carbonates and lithium acetylide, Li 2 C 2 ) that remain on the graphite electrode after fast charging. We additionally compare electrochemical modeling results with our experimental data to determine the Li plating exchange current density (10 A/m 2 ) and stripping efficiency (65%) of plated Li metal on graphite. Our techniques lay the groundwork for benchmarking proposed Li plating detection techniques and provide an avenue to pursue more comprehensive studies of Li plating on graphite surfaces.
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