电解质
材料科学
枝晶(数学)
硫化物
阳极
化学工程
锂(药物)
快离子导体
无机化学
电极
冶金
化学
物理化学
内分泌学
工程类
医学
数学
几何学
作者
Ruochen Xu,Fudong Han,Xiao Ji,Xiulin Fan,J.P. Tu,Chunsheng Wang
出处
期刊:Nano Energy
[Elsevier]
日期:2018-11-01
卷期号:53: 958-966
被引量:249
标识
DOI:10.1016/j.nanoen.2018.09.061
摘要
All-solid-state lithium batteries (ASSLIBs) employing sulfide solid electrolyte hold high promise to replace traditional liquid-electrolyte LIBs due to their high safety and energy density. However, Li dendritic growth in sulfide electrolyte limits the realization of the high energy of ASSLIBs. In this work, we use LiF (or LiI) layer at the interface between Li and sulfide electrolyte and penetrated HFE (or I solution) inside of sulfide electrolyte to suppress the Li dendrite growth. Due to the higher interface energy of LiF/Li than that of LiI/Li, LiF interlayer show much higher capability than LiI in suppressing the Li dendrite. Even if the Li dendrite breaks through LiF (or LiI) interlayer, the Li dendrites will be consumed by coated/penetrated HEF (or I) forming LiF (or LiI) thus preventing Li dendrite growth. A LiNbO3 @LiCoO2/Li7P3S11/Li ASSLIB employing HFE coated/infiltrated Li7P3S11 glass-ceramic as electrolyte, and LiF coated Li metal as anode shows a high reversible discharge capacity of 118.9 mAh g−1 at 0.1 mA cm−2 and retains 96.8 mAh g−1 after 100 cycles. The designed solid electrolyte interphase between Li and solid electrolyte that has a high interface energy to Li provides new opportunity to commercialize the Li metal batteries.
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