电解质
扩散
化学物理
相间
锂(药物)
化学工程
电子
离子
化学
材料科学
电极
纳米技术
热力学
物理化学
物理
医学
遗传学
有机化学
量子力学
生物
内分泌学
工程类
作者
Fabian Single,Arnulf Latz,Birger Horstmann
出处
期刊:Chemsuschem
[Wiley]
日期:2018-04-17
卷期号:11 (12): 1950-1955
被引量:78
标识
DOI:10.1002/cssc.201800077
摘要
Continued growth of the solid-electrolyte interphase (SEI) is the major reason for capacity fade in modern lithium-ion batteries. This growth is made possible by a yet unidentified transport mechanism that limits the passivating ability of the SEI towards electrolyte reduction. We, for the first time, differentiate the proposed mechanisms by analyzing their dependence on the electrode potential. Our calculations are compared to recent experimental capacity-fade data. We show that the potential dependence of SEI growth facilitated by solvent diffusion, electron conduction, or electron tunneling qualitatively disagrees with the experimental observations. Only diffusion of Li interstitials results in a potential dependence matching the experiments. Therefore, we identify the diffusion of neutral radicals, such as Li interstitials, as the cause of long-term SEI growth.
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