多硫化物
电化学
阴极
锂(药物)
电池(电)
溶解
材料科学
化学
化学工程
有机化学
工程类
电解质
聚合物
内分泌学
物理化学
功率(物理)
物理
医学
量子力学
电极
作者
Jaebeom Jeon,Jung‐Keun Yoo,Soonmin Yim,Kiung Jeon,Gun Ho Lee,Jong Hyuk Yun,Do Kyung Kim,Yeon Sik Jung
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2019-09-27
卷期号:7 (21): 17580-17586
被引量:48
标识
DOI:10.1021/acssuschemeng.9b01924
摘要
It is highly desirable to develop advanced electrode structures of lithium–sulfur (Li–S), which enable high energy density, long life, low cost, and environmental benignity. In particular, suppression of polysulfide (PS)-shuttle behavior that occurs during electrochemical reaction in Li–S batteries is the most important challenge for practical, large-scale applications. In this work, a natural-wood-derived polymer, lignosulfonate sodium salt (LSS), is employed as a binder material for Li–S, showing superior capacity and cycle retention because of its unique chemical structure. LSS with amphiphilic functional groups can easily disperse hydrophobic electrode components in water and effectively block PS dissolution by its electrostatic repulsion force. Moreover, with enhanced Li ionic conductivity, the rate capability of the S cathode is maintained at ∼661 mA h g–1 at a current rate of 1675 mA g–1 and stable areal capacity of ∼1.55 mA h cm–2 is obtained with pristine S active material.
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