电解质
离子电导率
电导率
材料科学
阳极
快离子导体
硫化物
化学工程
兴奋剂
无机化学
相容性(地球化学)
电化学窗口
化学
电极
冶金
复合材料
物理化学
光电子学
工程类
作者
Zhi-Kai Huang,Zhi‐Hao Yan,Dingding Zhu,Xuedong Zhang,Shuaiyu He,Jianyu Huang,Guobao Xu
标识
DOI:10.1016/j.jallcom.2023.172334
摘要
Despite lithium-argyrodite electrolytes have attracted great attention due to the high ionic conductivity and relatively lower cost, their applications are hindered by the inferior air stability and poor Li compatibility. Herein, we report a Sn/I co-doping the Li6PS5Cl strategy to overcome above obstacles. The optimized LPSC-0.05SnI4 exhibits high ionic conductivity of 3.9×10-3 S cm-1 at room temperature, and improved air stability. More importantly, an in situ formed LiI-rich interface on the lithium anode is introduced through the LPSC-0.05SnI4. As a result, the Li/LPSC-0.05SnI4/Li symmetric batteries deliver high critical current density of 1.45 mA cm-2 and a remarkable steady Li plating/stripping performance over 6000 h at 0.1 mA cm-2. The assembled LNO@NMC811/LPSC-0.05SnI4/Li all-solid-state batteries display prominent capacity and cycling stability. This work provides a practical and effective method for designing versatile and high-performance sulfide-based solid electrolytes.
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