锚固
电解质
钝化
化学
锂(药物)
化学工程
相间
碳酸乙烯酯
无机化学
吡啶
材料科学
图层(电子)
阳极
电极
金属
有机化学
物理化学
内分泌学
结构工程
遗传学
生物
医学
工程类
作者
Tianhong Zhou,Yan Zhao,Mario El Kazzi,Jang Wook Choi,Ali Coşkun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-04-07
卷期号:6 (5): 1711-1718
被引量:59
标识
DOI:10.1021/acsenergylett.1c00274
摘要
The lithium (Li) metal anode is considered to be a promising candidate for next-generation batteries but is impeded by Li dendrites and the resulting poor reversibility. Here, we introduce monoquat salts with an ability to anchor onto the Li metal surface through pyridine moieties as electrolyte additives. We systematically varied both the number and the spatial arrangement of anchoring units along with the number of positive charges bearing PF6 counteranions to probe their impact on Li metal protection. A high surface concentration of PF6 counteranions and their immediate reaction with the deposited Li facilitate the in situ formation and homogeneous distribution of LiF in the surface passivation layer. Our results revealed that the monoquat dication, through stable pyridine-based anchoring, formed an ionically conductive and dense solid electrolyte interphase layer and showed superior cycling performance in both ether-based and carbonate-based electrolytes, thus clearly demonstrating the importance of the anchoring strategy for Li metal surface protection.
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