Designer Anion Enabling Solid-State Lithium-Sulfur Batteries

被引:124
|
作者
Zhang, Heng [1 ]
Oteo, Uxue [1 ]
Judez, Xabier [1 ]
Eshetu, Gebrekidan Gebresilassie [2 ,3 ]
Martinez-Ibanez, Maria [1 ]
Carrasco, Javier [1 ]
Li, Chunmei [1 ]
Armand, Michel [1 ]
机构
[1] CIC Energigune, Parque Tecnol Alava, Elect Energy Storage Dept, Albert Einstein 48, Minano 01510, Alava, Spain
[2] Rhein Westfal TH Aachen, Inst Power Elect & Elect Drives ISEA, Jagerstr 17, D-52066 Aachen, Germany
[3] Mekelle Univ, Coll Nat & Computat Sci, Dept Chem, POB 231, Mekelle, Ethiopia
关键词
POLYMER ELECTROLYTES; METAL ANODE; SAFE;
D O I
10.1016/j.joule.2019.05.003
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
With an extremely high theoretical energy density, solid-state lithium-sulfur (Li-S) batteries (SSLSBs) are emerging as one of the most feasible chemistries; however, their energy efficiency and long-term cyclability are severely hampered by the lithium metal (Li degrees) dendrite formation during repeated discharge/charge cycles and the shuttling of aggressive polysulfide intermediates between two electrodes. Herein, we report (difluoromethanesulfonyl) (trifluoromethanesulfonyl)imide anion [N(SO2CF2H)(SO2CF3)](-), hereafter DFTFSI-, as a designer anion for high-performance polymer-based SSLSBs. In contrast to the widely used bis(trifluoromethanesulfonyl)imide anion [N(SO2CF3)(2)](-)(TFSI-), DFTFSI-based SSLSBs provide superior interfacial stability against Li degrees, extremely high discharge and areal capacities, very high Coulombic efficiency, and long-term cyclability, surpassing the reported literature values, in terms of gravimetric energy density. This work opens a new door for accelerating the practical deployment of SSLSBs in the future.
引用
收藏
页码:1689 / 1702
页数:14
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