材料科学
阳极
锂(药物)
阴极
电解质
镓
合金
化学工程
金属
容量损失
电极
电化学
枝晶(数学)
冶金
物理化学
医学
化学
几何学
数学
工程类
内分泌学
作者
Ying Zhou,Jiaming Zhang,Kai Zhao,Yue Ma,Hongzhou Zhang,Dawei Song,Xixi Shi,Lianqi Zhang,Yi Ding
标识
DOI:10.1016/j.ensm.2021.04.042
摘要
Lithium (Li) metal has been considered as an ideal anode for high-energy density rechargeable batteries. However, it faces huge obstacles toward practical application due to the growth of Li dendrites and the uncontrollable side reactions with electrolyte. Here, we demonstrate a novel gallium-lithium alloy based dual-protection interface layer for Li metal by a facile in-situ ion-exchange reaction that possesses long service life for effectively alleviating the extra consumption of active Li as well as homogenizing the Li deposition. Such dual-protected feature is attributed to its outstanding stability, excellent Li affinity and favorable charge transfer kinetics. By means of in-situ visualization electrodeposition studies, the modified Li metal (GaLi-Li) anode can effectively suppress the Li dendrite even under a high deposition capacity of 7 mAh cm−2. Moreover, the GaLi-Li based symmetric cell achieves excellent cycling stability for over 1500 cycles at a high current density of 5 mA cm−2. Pairing the GaLi-Li anodes with LiFePO4 and LiNi0.8Co0.1Mn0.1O2 cathodes, the cells also realize better long-term cycling stability with higher discharge capacity than that of the bare Li. Our strategy offers a practical way to realize highly stable and safety Li metal batteries.
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