arrow
Return

Realizing an Applicable Solid → Solid Cathode Process via a Transplantable Solid Electrolyte Interface for Lithium-Sulfur Batteries

delete2019-07-30
delete38
PRE
AI
C
Chen Xue
L
Lixia Yuan
Z
Zhen Li
陈思静 cover
陈思静 (Sijing Chen)
H
Haijin Ji
Y
Yufei Qin
L
Longsheng Wu
Y
Yue Shen
王立宾 cover
王立宾 (Libin Wang)
J
Jingping Hu *
Y
Yunhui Huang *
DOI:10.1021/acsami.9b07787delete
deleteOriginal
deleteOriginal request for help
deleteShare
deleteSave
Abstract

Abstract

En 中文
The conventional lithium-sulfur battery (LSB) undergoes a solid-liquid-solid cathode process during which the intermediate polysulfides dissolve into the electrolyte, leading to a serious shuttle reaction and significantly shortened lifespan. Here, we realize a novel solid -> solid cathode mode for LSBs via a transplantable solid electrolyte interface (SEI). The SEI is in situ formed in a carbonate-based electrolyte with high-concentration dualsalt during the initial discharge process. The solid -> solid cathode process does not involve any dissolution of the intermediates; hence, the shuttle effect can be totally eliminated. Furthermore, the SEI shows a high electrolyte compatibility and can be transplanted to the conventional carbonate-based/ether-based electrolytes. The sulfur/carbon composite with 65% sulfur a reversible specific capacity of 1009 mA h g(-1) and negligible self-discharge. The SEI strategy can successfully break the limitation from the traditional catholyte electrode mechanism. Meanwhile, it provides large flexibility for designing high-loading carbon hosts and selecting an electrolyte for high-performance LSBs.
Keywords:
lithium-sulfur batteries
high-concentration electrolyte
transplantable SEI
solid -> solid conversion
negligible self-discharge
AI Summary

AI Summary

Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.

Journal

ACS Applied Materials and Interfaces cover
ACS Applied Materials and Interfaces
IF:
8.2
Papers:
6.1W
Citations:
38.7W

Organization

No organization information available