电解质
锂(药物)
阳极
离子
电池(电)
金属锂
纳米技术
材料科学
离子电导率
锂离子电池
离子键合
工程物理
商业化
化学
计算机科学
电极
物理
功率(物理)
物理化学
热力学
医学
有机化学
政治学
法学
内分泌学
作者
Benjamin P. Williams,Haochuan Zhang,Yu Mu,James R. Wilkes,Haden Wikar,Dunwei Wang
标识
DOI:10.1021/acs.jpcc.2c03215
摘要
The unsurpassed energy density of lithium metal batteries (LMBs) offers a promising route to meet increasing clean energy demand. Nonetheless, their instability creates critical safety and performance concerns that prevent their effective implementation. Careful design of the solid-electrolyte interphase (SEI) that passivates the lithium metal anode could allow for stable, efficient cycling, unlocking the commercialization of LMBs. However, the complexity of the SEI, both formed in situ through electrolyte decomposition and fabricated ex situ, introduces significant ambiguity. Here, we present several mechanisms that define ionic transport through the SEI, grounded in studies that concretely relate structure to ionic conductivity. We build on these mechanisms with examples of their application in real battery systems. Overall, we seek to lay a foundation of structure–property relationships that will guide the rational design of stable SEIs that efficiently transport Li + ions.
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