多硫化物
阴极
储能
电解质
材料科学
电池(电)
锂(药物)
电化学
化学工程
溶解
有机自由基电池
硫黄
纳米技术
电极
化学
工程类
冶金
物理
物理化学
功率(物理)
内分泌学
医学
量子力学
作者
Quanquan Pang,Xiao Liang,Chun Yuen Kwok,Linda F. Nazar
出处
期刊:Nature Energy
[Springer Nature]
日期:2016-09-08
卷期号:1 (9)
被引量:1849
标识
DOI:10.1038/nenergy.2016.132
摘要
Amid burgeoning environmental concerns, electrochemical energy storage has rapidly gained momentum. Among the contenders in the ‘beyond lithium’ energy storage arena, the lithium–sulfur (Li–S) battery has emerged as particularly promising, owing to its potential to reversibly store considerable electrical energy at low cost. Whether or not Li–S energy storage will be able to fulfil this potential depends on simultaneously solving many aspects of its underlying conversion chemistry. Here, we review recent developments in tackling the dissolution of polysulfides — a fundamental problem in Li–S batteries — focusing on both experimental and computational approaches to tailor the chemical interactions between the sulfur host materials and polysulfides. We also discuss smart cathode architectures enabled by recent materials engineering, especially for high areal sulfur loading, as well as innovative electrolyte design to control the solubility of polysulfides. Key factors that allow long-life and high-loading Li–S batteries are summarized. Li–S batteries are a low-cost and high-energy storage system but their full potential is yet to be realized. This Review surveys recent advances in understanding polysulfide chemistry at the positive electrode and the electrolyte and discusses approaches towards long-life and high-loading batteries.
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