A kinetically stable anode interface for Li3YCl6-based all-solid-state lithium batteries

被引:62
作者
Ji, Weixiao [1 ]
Zheng, Dong [1 ]
Zhang, Xiaoxiao [1 ]
Ding, Tianyao [1 ]
Qu, Deyang [1 ]
机构
[1] Univ Wisconsin, Dept Mech Engn, Milwaukee, WI 53211 USA
关键词
ELECTROLYTES; STABILITY; COMPATIBILITY; PERFORMANCE;
D O I
10.1039/d1ta03042f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite their excellent ionic conductivity and electrochemical oxidative stability, the emerging halide-based solid electrolytes suffer from inherent instability toward Li metal anodes. A thick and resistive interface can be formed by continuous reaction between halide electrolytes and Li anodes, leading to high impedance, low coulombic efficiency, and even short circuit of solid-state cells. Here, we report a thin argyrodite (Li6PS5Cl) protection layer to avoid the direct physical contact of the Li anode with Li3YCl6, a representative halide electrolyte. Li6PS5Cl is kinetically stable towards lithium and can also form a good hetero-contact with Li3YCl6. Highly stable Li plating/stripping cycling of a symmetric cell with a steady overpotential of 100 mV after 1000 h was demonstrated, compared to severe overpotential build-up to reach 1500 mV after 60 h of the control group. Besides, the LiNi0.8Co0.1Mn0.1O2/Li full solid-state cell displayed a high initial coulombic efficiency of >87% and a stable lifetime of over 100 cycles. The facile protection of Li6PS5Cl provides a universal way to prevent unfavorable interaction at the anode interface and realize high performance all-solid-state Li-metal batteries.
引用
收藏
页码:15012 / 15018
页数:7
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