Lithium-Salt-Containing Ionic Liquid-Incorporated Li-Al-Layered Double Hydroxide-Based Solid Electrolyte with High-Performance and Safety in Solid-State Lithium Batteries

被引:22
作者
Wu, Zhijun [1 ]
Xie, Zhengkun [1 ]
Wang, Jing [1 ]
Yu, Tao [1 ]
Wang, Zhongde [2 ]
Hao, Xiaogang [2 ]
Abudula, Abuliti [1 ]
Guan, Guoqing [3 ]
机构
[1] Hirosaki Univ, Grad Sch Sci & Technol, Hirosaki, Aomori 0368560, Japan
[2] Taiyuan Univ Technol, Dept Chem Engn, Taiyuan 030024, Peoples R China
[3] Hirosaki Univ, Inst Reg Innovat IRI, Energy Convers Engn Lab, Aomori 0300813, Japan
关键词
ionic conductivity; lithium ion transfer number; memory effect; electrochemical stability; interface resistance; METAL-ORGANIC FRAMEWORK; MECHANOCHEMICAL SYNTHESIS; POLYMER ELECTROLYTES; TEMPERATURE; LI7LA3ZR2O12; LDH; CONDUCTIVITY; RESISTANCE; STABILITY; MEMBRANE;
D O I
10.1021/acssuschemeng.0c02362
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state lithium batteries are highly promising for energy storage applications because of their high energy density and good safety. Herein, a novel solid electrolyte based on ionic-liquid- impregnated Li-Al layered double hydroxides (Li-IL@Li-Al LDH) is reported. Since the Li+ ions can be inserted into the vacant octahedral sites of the Li-Al LDH and the related anions intercalated into the interlayer for the charge balance, which can facilitate the transport of Li+ ions and avoid the interference of anions, the Li-IL@Li-Al LDH solid electrolyte with the optimized Li-IL/Li-Al LDH wight ratio of 2:1 exhibits a high ionic conductivity of 1.04 X 10(-3) S. cm(-1) with a Li+ transfer number of 0.35 at 40 degrees C. Moreover, this solid electrolyte demonstrates excellent nonflammability, good lithium stability, high electrochemical stability, and low interface resistance with electrodes. The fabricated LiFePO4/Li-IL@Li-Al LDH (2.0:1)/Li battery displays outstanding cyclability and rate capability at 40 degrees C, indicating that the Li-IL@Li-Al LDH SE should have great potential for applications in the solid-state lithium batteries.
引用
收藏
页码:12378 / 12387
页数:10
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