All-Solid-State Lithium-Sulfur Batteries Enhanced by Redox Mediators

被引:85
|
作者
Gao, Xin [1 ]
Zheng, Xueli [1 ]
Tsao, Yuchi [2 ]
Zhang, Pu [1 ]
Xiao, Xin [1 ]
Ye, Yusheng [1 ]
Li, Jun [1 ,2 ]
Yang, Yufei [1 ]
Xu, Rong [1 ]
Bao, Zhenan [3 ]
Cui, Yi [1 ,4 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[4] SLAC Natl Accelerator Lab, Stanford Inst Mat & Energy Sci, Menlo Pk, CA 94025 USA
关键词
LI-S BATTERIES; POLYMER ELECTROLYTES; IN-SITU; CATHODE;
D O I
10.1021/jacs.1c07754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Redox mediators (RMs) play a vital role in some liquid electrolyte-based electrochemical energy storage systems. However, the concept of redox mediator in solid-state batteries remains unexplored. Here, we selected a group of RM candidates and investigated their behaviors and roles in all-solid-state lithium-sulfur batteries (ASSLSBs). The soluble-type quinone-based RM (AQT) shows the most favorable redox potential and the best redox reversibility that functions well for lithium sulfide (Li2S) oxidation in solid polymer electrolytes. Accordingly, Li2S cathodes with AQT RMs present a significantly reduced energy barrier (average oxidation potential of 2.4 V) during initial charging at 0.1 C at 60 degrees C and the following discharge capacity of 1133 mAh gs(-1). Using operando sulfur K-edge X-ray absorption spectroscopy, we directly tracked the sulfur speciation in ASSLSBs and proved that the solid-polysulfide-solid reaction of Li2S cathodes with RMs facilitated Li2S oxidation. In contrast, for bare Li2S cathodes, the solid-solid Li2S-sulfur direct conversion in the first charge cycle results in a high energy barrier for activation (charge to similar to 4 V) and low sulfur utilization. The Li2S@AQT cell demonstrates superior cycling stability (average Coulombic efficiency 98.9% for 150 cycles) and rate capability owing to the effective AQT-enhanced Li-S reaction kinetics. This work reveals the evolution of sulfur species in ASSLSBs and realizes the fast Li-S reaction kinetics by designing an effective sulfur speciation pathway.
引用
收藏
页码:18188 / 18195
页数:8
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