多硫化物
法拉第效率
阴极
电池(电)
材料科学
硫黄
过渡金属
纳米技术
锂硫电池
储能
锂(药物)
化学
电化学
电极
冶金
催化作用
有机化学
医学
内分泌学
功率(物理)
物理化学
物理
电解质
量子力学
作者
Luzhi Liu,Xiangshao Yin,Wenjiao Li,Ding Wang,Jianguo Duan,Xianshu Wang,Yiyong Zhang,Dong Peng,Yingjie Zhang
出处
期刊:Small
[Wiley]
日期:2023-12-04
卷期号:20 (17)
被引量:11
标识
DOI:10.1002/smll.202308564
摘要
Abstract Lithium–sulfur batteries (LSBs) with ultra‐high energy density (2600 W h kg −1 ) and readily available raw materials are emerging as a potential alternative device with low cost for lithium‐ion batteries. However, the insulation of sulfur and the unavoidable shuttle effect leads to slow reaction kinetics of LSBs, which in turn cause various roadblocks including poor rate capability, inferior cycling stability, and low coulombic efficiency. The most effective way to solve the issues mentioned above is to rationally design and control the synthesis of the cathode host for LSBs. Transition metal phosphides (TMPs) with good electrical conductivity and dual adsorption‐conversion capabilities for polysulfide (PS) are regarded as promising cathode hosts for new‐generation LSBs. In this review, the main obstacles to commercializing the LSBs and the development processes of their cathode host are first elaborated. Then, the sulfur fixation principles, and synthesis methods of the TMPs are briefly summarized and the recent progress of TMPs in LSBs is reviewed in detail. Finally, a perspective on the future research directions of LSBs is provided.
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