Advances in the Catalytic Mechanism of Metal Oxides for Lithium-Sulfur Batteries

被引:0
|
作者
Min, Yi [1 ]
Zou, Xiaohong [2 ]
Lu, Qian [1 ]
Cai, Wei [1 ]
Bu, Yunfei [1 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Sch Environm Sci & Technol, UNIST NUIST Energy & Environm Jointed Lab, Nanjing 210044, Peoples R China
[2] Hong Kong Polytech Univ, Dept Mech Engn, Hung Hom, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
catalytic mechanism; lithium-sulfur batteries; metal oxides; polysulfide conversion; GRAPHENE; CATHODE; ENERGY; LI4TI5O12; HOST; ENTRAPMENT; CONVERSION; STRATEGY; GREEN;
D O I
10.1002/smll.202411794
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur (Li-S) batteries are one of the promising next-generation energy storage/conversion devices, considering their high energy density and low cost. However, the shuttle of polysulfides hinders the practical application of Li-S batteries, which leads to reduced cycling stability. Although chemical adsorption strategies have made significant progress in improving the cycling stability of Li-S batteries, the poor catalytic conversion ability of the polysulfide host results in an imbalance between chemical adsorption and catalytic conversion. Recent studies have revealed that metal oxides with adjustable electronic structures exhibit good catalytic ability as polysulfide hosts. However, there is currently no systematic review of the catalytic mechanism of metal oxides in Li-S batteries. Herein, the working principle and primary challenge of Li-S batteries are first introduced, followed by a categorization of catalyst design strategies. Furthermore, a comprehensive review of recent advancements in understanding the reaction mechanism of metal oxide catalysts in Li-S batteries is also provided. Finally, personal perspectives on the future development of Li-S batteries enhanced by metal oxide catalysis are offered. It is hoped that this review can provide valuable insights into the catalytic role of metal oxides in accelerating polysulfide conversion for Li-S batteries.
引用
收藏
页数:19
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