溶剂化
电解质
相间
化学
化学物理
离子
锂(药物)
极地的
作文(语言)
隐溶剂化
密度泛函理论
化学工程
无机化学
计算化学
物理化学
电极
有机化学
物理
哲学
内分泌学
工程类
生物
医学
遗传学
语言学
天文
作者
Solomon T. Oyakhire,Sheng-Lun Liao,Sanzeeda Baig Shuchi,Mun Sek Kim,Sang Cheol Kim,Zhiao Yu,Rafael A. Vilá,Paul E. Rudnicki,Yi Cui,Stacey F. Bent
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-08-11
卷期号:23 (16): 7524-7531
被引量:4
标识
DOI:10.1021/acs.nanolett.3c02037
摘要
The composition of the solid electrolyte interphase (SEI) plays an important role in controlling Li-electrolyte reactions, but the underlying cause of SEI composition differences between electrolytes remains unclear. Many studies correlate SEI composition with the bulk solvation of Li ions in the electrolyte, but this correlation does not fully capture the interfacial phenomenon of SEI formation. Here, we provide a direct connection between SEI composition and Li-ion solvation by forming SEIs using polar substrates that modify interfacial solvation structures. We circumvent the deposition of Li metal by forming the SEI above Li+/Li redox potential. Using theory, we show that an increase in the probability density of anions near a polar substrate increases anion incorporation within the SEI, providing a direct correlation between interfacial solvation and SEI composition. Finally, we use this concept to form stable anion-rich SEIs, resulting in high performance lithium metal batteries.
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