硫黄
材料科学
共聚物
氧化还原
阴极
动力学
电化学
金属有机骨架
锂(药物)
化学工程
电极
化学
有机化学
物理化学
聚合物
冶金
内分泌学
吸附
复合材料
工程类
物理
医学
量子力学
作者
Qinghan Zeng,Xin Li,Wei Gong,Sijia Guo,Yuan Ouyang,Dixiong Li,Yingbo Xiao,Chao Tan,Lin Xie,Haibin Lu,Qi Zhang,Shaoming Huang
标识
DOI:10.1002/aenm.202104074
摘要
Abstract Lithium−sulfur batteries (LSBs) are regarded as one of the most promising candidates for energy storage devices. However, the severe shuttling effect of soluble polysulfides (PSs) limits its further application. Metal−organic frameworks (MOFs) have emerged as a new kind of sulfur host for their talents in confining and trapping PSs. However, the shuttle effect has not been fully stressed as a significant drawback for most MOFs that leads to sluggish redox kinetics, resulting in low specific capacity and short lifetime, especially at high sulfur loading. In this work, a MOF‐sulfur copolymer (CNT@UiO‐66‐V‐S) is elaborated by copolymerization of sulfur with vinyl functionalized MOFs. Systematic electrochemical experiments and in situ Raman spectroscopy analysis indicate that the cathode exhibits a radical reaction mechanism and can accelerates LiPSs conversion. The CNT@UiO‐66‐V‐S cathode delivers over 100% improved discharge capacity and lowers decay rate at both low and high (5.6 mg cm –2 ) sulfur loadings compared to the physically mixed MOF/S cathode. The strategy of MOF‐sulfur copolymerization provides a new solution for promoting reaction kinetics and tackling the shuttle effect, and is expected to inspire the design of advanced sulfur hosts applied for high‐performance LSBs.
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