多硫化物
储能
材料科学
阴极
纳米技术
商业化
能量密度
桥接(联网)
锂(药物)
阳极
电极
计算机科学
工程物理
电解质
化学
电气工程
工程类
医学
计算机网络
功率(物理)
物理
物理化学
量子力学
内分泌学
政治学
法学
作者
Sreekala Kunhi Kannan,Jithu Joseph,Mary Gladis Joseph
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-04-13
卷期号:37 (9): 6302-6322
被引量:10
标识
DOI:10.1021/acs.energyfuels.3c00155
摘要
Lithium–sulfur (Li–S) batteries have received paramount attention as a next-generation energy storage device due to their remarkably high specific capacity (1675 mAh g–1), energy density (2600 Wh kg–1), and cost-effectiveness compared to the forefront lithium-ion batteries. However, certain issues still hamper the smooth working of Li–S batteries, which need to be addressed to fill the gap between fundamental research and commercialization. Polymer binders, as an inevitable part of the cathode structure, play a vital role in upholding the structural robustness and firmness of the electrode. However, conventional binders like PVDF are not capable of effectively accommodating the large volume changes within the electrode, facilitating electronic/ionic conductivity, entrapping the soluble polysulfide intermediates, and enhancing polysulfide redox kinetics. Therefore, novel multifunctional binder designs are adopted in Li–S batteries to tackle the above-mentioned issues. This review summarizes the recent progress in this research area employing advanced multifunctional polymer binders in Li–S batteries. The action of the binder through various mechanisms is discussed in detail. The role of binder is given immense attention in the emerging field of various energy storage devices, including Li–S batteries, and, thus, here discussed as well.
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