扫描电子显微镜
枝晶(数学)
材料科学
电池(电)
聚合物
碳化物
阴极
化学工程
锂(药物)
聚焦离子束
纳米技术
分析化学(期刊)
复合材料
离子
化学
有机化学
物理化学
工程类
内分泌学
物理
功率(物理)
医学
量子力学
色谱法
数学
几何学
作者
Maryam Golozar,Pierre Hovington,Andrea Paolella,Stéphanie Bessette,Marin Lagacé,Patrick Bouchard,Hendrix Demers,Raynald Gauvin,Karim Zaghib
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-11-21
卷期号:18 (12): 7583-7589
被引量:97
标识
DOI:10.1021/acs.nanolett.8b03148
摘要
Li metal batteries suffer from dendrite formation which causes short circuit of the battery. Therefore, it is important to understand the chemical composition and growth mechanism of dendrites that limit battery efficiency and cycle life. In this study, in situ scanning electron microscopy was employed to monitor the cycling behavior of all-solid Li metal batteries with LiFePO4 cathodes. Chemical analyses of the dendrites were conducted using a windowless energy dispersive spectroscopy detector, which showed that the dendrites are not metallic lithium as universally recognized. Our results revealed the carbide nature of the dendrites with a hollow morphology and hardness greater than that of pure lithium. These carbide-based dendrites were able to perforate through the polymer, which was confirmed by milling the polymer using focused ion beam. It was also shown that applying pressure on the battery can suppress growth of the dendrites.
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