多硫化物
法拉第效率
材料科学
催化作用
阴极
电化学
聚合物
比能量
电极
硫黄
储能
氧化还原
化学工程
纳米技术
化学
有机化学
物理化学
复合材料
功率(物理)
冶金
工程类
物理
电解质
量子力学
作者
Hongwei Chen,Changhong Wang,Yafei Dai,Jun Ge,Wei Lü,Jinlong Yang,Liwei Chen
出处
期刊:Nano Energy
[Elsevier BV]
日期:2016-05-02
卷期号:26: 43-49
被引量:35
标识
DOI:10.1016/j.nanoen.2016.04.052
摘要
While Li–S batteries are poised to be the next generation high-density energy storage devices, the low sulfur utilization and intrinsic polysulfide shuttle have limited their practical applications. Here, we report that radical polymer Poly(2,2,6,6-tetramethyl-1-piperidinyloxy-4-yl methacrylate) (PTMA)—a stable free radical polymer reported to be potential organic electrode materials–can perform as a multifunctional sulfur-trapping and catalytic binder for high performance Li-S batteries once activated via in-situ electrochemical oxidation. The activated PTMA+ not only displays strong binding affinity to polysulfides but also provides PTMA+-assisted additional redox sites and improves the kinetics of the cathode reaction. Thus the novel multifunctional additive for Li-S batteries results in improved cycle life, faster rate performance and most importantly, a significantly increase in specific discharge capacity by ~80%, with specific capacity of 1254 mAh/g and Coulombic efficiency of 96% at a four-hour charge/discharge (C/4) current rate.
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