Diagnosing and Correcting the Failure of the Solid-State Polymer Electrolyte for Enhancing Solid-State Lithium-Sulfur Batteries

被引:27
|
作者
Meng, Xiangyu [1 ]
Liu, Yuzhao [1 ]
Ma, Yanfu [2 ]
Boyjoo, Yash [2 ]
Liu, Jian [2 ]
Qiu, Jieshan [3 ]
Wang, Zhiyu [1 ,4 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Liaoning Key Lab Energy Mat & Chem Engn, Dalian 116024, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China
[4] Valiant Co Ltd, Branch New Mat Dev, Yantai 265503, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysis; failure mechanisms; Li-S batteries; solid-state batteries; solid-state polymer electrolytes; LI-S BATTERIES; HIGH-ENERGY; PERFORMANCE; INTERFACE;
D O I
10.1002/adma.202212039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state polymer electrolytes (SPEs) attract great interest in developing high-performance yet reliable solid-state batteries. However, understanding of the failure mechanism of the SPE and SPE-based solid-state batteries remains in its infancy, posing a great barrier to practical solid-state batteries. Herein, the high accumulation and clogging of "dead" lithium polysulfides (LiPS) on the interface between the cathode and SPE with intrinsic diffusion limitation is identified as a critical failure cause of SPE-based solid-state Li-S batteries. It induces a poorly reversible chemical environment with retarded kinetics on the cathode-SPE interface and in bulk SPEs, starving the Li-S redox in solid-state cells. This observation is different from the case in liquid electrolytes with free solvent and charge carriers, where LiPS dissolve but remain alive for electrochemical/chemical redox without interfacial clogging. Electrocatalysis demonstrates the feasibility of tailoring the chemical environment in diffusion-restricted reaction media for reducing Li-S redox failure in the SPE. It enables Ah-level solid-state Li-S pouch cells with a high specific energy of 343 Wh kg(-1) on the cell level. This work may shed new light on the understanding of the failure mechanism of SPE for bottom-up improvement of solid-state Li-S batteries.
引用
收藏
页数:10
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