In situ thermally polymerized solid composite electrolytes with a broad electrochemical window for all-solid-state lithium metal batteries

被引:76
作者
Li, Zhuo [1 ]
Xie, Hui-Xin [1 ]
Zhang, Xing-Yan [1 ]
Guo, Xin [1 ]
机构
[1] Huazhong Univ Sci & Technol, State Key Lab Mat Proc & Die Mould Technol, Lab Solid State Ion, Sch Mat Sci & Engn, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
LI-ION CONDUCTORS; INTERFACIAL RESISTANCE; HYBRID ELECTROLYTES; ANODE; TEMPERATURE; STABILITY; CHEMISTRY; NETWORK;
D O I
10.1039/c9ta09969g
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
Solid composite electrolytes are prepared by polymerizing a liquid precursor containing Li6.25Ga0.25La3Zr2O12 (Ga-LLZO) nanoparticles. The composite electrolyte shows an ionic conductivity of 1.8 x 10(-4) S cm(-1) and a Li-ion transference number of 0.58 at 30 degrees C. Moreover, polymerized composite electrolytes (PCEs) are electrochemically stable up to 6.5 V versus Li/Li+ at room temperature. Li/PCEs/Li symmetric cells maintain stable cycling for more than 1000 h at 0.5 mA cm(-2), and the dendrite formation is effectively inhibited, showing compatibility with lithium anodes. Using in situ polymerization, PCEs retain conformal interfacial contacts with all electrodes, and the interfacial resistance of solid-state batteries is decreased by half. Coupled with LiNi0.6Co0.2Mn0.2O2 (NCM622) and LiNi0.85Co0.05Al0.1O2 (NCA) cathodes, solid-state Li metal batteries with PCEs exhibit good cycling performances, including superior specific capacity, high coulombic efficiency and a long cycle lifetime at room temperature. This work offers an approach to meet both the bulk and interfacial requirements of solid-state Li metal batteries and extends the applications of solid composite electrolytes to high-voltage cathodes.
引用
收藏
页码:3892 / 3900
页数:9
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