阴极
过电位
阳极
锂(药物)
电解质
电化学
惰性
材料科学
硫黄
储能
纳米技术
化学
无机化学
化学工程
电极
冶金
工程类
有机化学
物理
功率(物理)
物理化学
内分泌学
医学
量子力学
作者
Hualin Ye,Matthew Li,Tongchao Liu,Yanguang Li,Jun Lü
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-06-04
卷期号:5 (7): 2234-2245
被引量:153
标识
DOI:10.1021/acsenergylett.0c00936
摘要
Lithium–sulfur batteries are considered a possible next-generation energy-storage solution, but their commercial viability is still in question because of several technical challenges, including the use of a highly reactive lithium anode. Using Li2S as the cathode to couple with Li-free anodes presents a feasible approach to circumvent the safety issue of lithium. Unfortunately, Li2S is largely electrochemically inert and needs a high activation potential during the initial oxidation. Here, we provide an overview of recent progress on electrochemically activating Li2S as a lithium-containing cathode for lithium–sulfur batteries. We first discuss the origin of its large charging overpotential and current understanding of its activation process. This is then followed by an up-to-date account of different strategies to activate Li2S and promote its electrochemical performance by engineering the electrode material, the cathode catalyst, or the electrolyte. Finally, a short perspective is offered about the possible future directions of this exciting field.
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