原位
降级(电信)
X射线
吸收能力
吸收(声学)
机制(生物学)
材料科学
分析化学(期刊)
化学
化学工程
光学
物理
环境化学
计算机科学
复合材料
工程类
有机化学
电信
量子力学
作者
Yan Xu,Yifan Ye,Shuyang Zhao,Jun Feng,Jia Li,Hao Chen,Ankun Yang,Feifei Shi,Lujie Jia,Yang Wu,Xiaoyun Yu,Per‐Anders Glans,Yi Cui,Jinghua Guo,Yuegang Zhang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-04-01
卷期号:19 (5): 2928-2934
被引量:73
标识
DOI:10.1021/acs.nanolett.8b05208
摘要
The Mg/S battery is attractive because of its high theoretical energy density and the abundance of Mg and S on the earth. However, its development is hindered by the lack of understanding to the underlying electrochemical reaction mechanism of its charge-discharge processes. Here, using a unique in situ X-ray absorption spectroscopic tool, we systematically study the reaction pathways of the Mg/S cells in Mg(HMDS)2-AlCl3 electrolyte. We find that the capacity degradation is mainly due to the formation of irreversible discharge products, such as MgS and Mg3S8, through a direct electrochemical deposition or a chemical disproportionation of intermediate polysulfide. In light of the fundamental understanding, we propose to use TiS2 as a catalyst to activate the irreversible reaction of low-order MgS x and MgS, which results in an increased discharging capacity up to 900 mAh·g-1 and a longer cycling life.
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