High-Performance Garnet-Type Solid-State Lithium Metal Batteries Enabled by Scalable Elastic and Li+-Conducting Interlayer

被引:11
作者
Zheng, Chujun [1 ,2 ]
Lu, Yan [1 ,2 ]
Chang, Qiang [1 ,2 ]
Song, Zhen [3 ]
Xiu, Tongping [4 ]
Jin, Jun [1 ,2 ]
Badding, Michael E. [3 ]
Wen, Zhaoyin [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, CAS Key Lab Mat Energy Convers, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, 19 Yuquan Rd, Beijing 100049, Peoples R China
[3] Corning Inc, Corning, NY 14831 USA
[4] Corning Res Ctr China, 200 Jinsu Rd, Shanghai 201206, Peoples R China
[5] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
critical current density; garnet-type electrolytes; interfacial modification; lithium dendrites; lithium metal batteries; ELECTROLYTES; INTERFACES; DENDRITE; GROWTH; ENERGY; ANODE;
D O I
10.1002/adfm.202302729
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Promoting the interfacial Li+ transport and suppressing detrimental lithium dendrites are the main challenges for developing practical solid-state lithium metal batteries. In this respect, interface rationalizing to synergize the enhancement of ion transport and suppression of lithium dendrites is of paramount significance. Herein, a novel strategy is demonstrated to address those issues by a designed multifunctional composite interlayer. The photocrosslinkable polymer is introduced in a scalable elastic skeleton, which promotes the migration and diffusion of Li+. Moreover, adding perfluoropolyether in the interlayer benefits to regulating the formation of LiF-rich interface, sufficiently suppress the growth of lithium dendrites. Benefitting from the elasticity, high Li+ conductivity and the lithium dendrites suppression capability, the interlayer can significantly improve the interfacial performance of the solid electrolyte/lithium interface, thus leading to the greatly enhanced electrochemical performance of solid-state lithium metal batteries. A high critical current density of 3.6 mA cm(-2) and a long cycling life at 1.0 mA cm(-2) for >400 h are achieved for the symmetric cells. Besides, when used in a pouch-type full cell coupled with LiNi0.6Co0.2Mn0.2O2 cathode, a high charged capacity of 3.25 mAh cm(-2) can be maintained through 20 cycles, demonstrating its great potentials for practical application.
引用
收藏
页数:9
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