氧化还原
调解人
化学
无机化学
醌
化学工程
氧化还原
组合化学
材料科学
纳米技术
有机化学
医学
生物化学
内科学
工程类
作者
Yuchi Tsao,Minah Lee,Elizabeth C. Miller,Guoping Gao,Jihye Park,Shucheng Chen,Toru Katsumata,Helen Tran,Lin‐Wang Wang,Michael F. Toney,Yi Cui,Zhenan Bao
出处
期刊:Joule
[Elsevier BV]
日期:2019-01-27
卷期号:3 (3): 872-884
被引量:264
标识
DOI:10.1016/j.joule.2018.12.018
摘要
In lithium-sulfur (Li-S) batteries, the insulating nature of sulfur and lithium sulfide (Li2S) results in large polarization and low sulfur utilization while the soluble polysulfides lead to internal shuttle upon cycling. Furthermore, the redox reaction via the dissolution-precipitation route destroys the electrode architecture by passivating the active interface responsible for the redox reaction, and thus the performance deteriorates with cycling. Here, we employ the redox chemistry of quinone to realize efficient, fast, and stable operation of Li-S batteries using Li2S microparticles. By adding a quinone derivative with tailored properties (e.g., oxidation potential, solubility, and electrochemical stability) to an electrolyte as a redox mediator (RM), initial charging of Li2S electrodes occurs below 2.5 V at 0.5C, and the subsequent discharge capacity is as high as 1,300 mAh gs−1. Moreover, deposition of dead Li2S, which was the primary cause of increasing polarization and decreasing capacity upon cycling, is effectively prevented with the RM.
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