Polyoxometalate-Cyclodextrin-Based Cluster-Organic Supramolecular Framework for Polysulfide Conversion and Guest-Host Recognition in Lithium-sulfur Batteries

被引:126
作者
Ni, Lubin [1 ]
Gu, Jie [1 ]
Jiang, Xinyuan [1 ]
Xu, Hongjie [1 ]
Wu, Zhen [1 ]
Wu, Yuchao [1 ]
Liu, Yi [1 ]
Xie, Ju [1 ]
Wei, Yongge [2 ]
Diao, Guowang [1 ]
机构
[1] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[2] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Minist Educ, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Cluster-Organic Supramolecular Framework; Cyclodextrin; Lithium-Sulfur Batteries; Polyoxometalates; Polysulfide; LI-S; BETA-CYCLODEXTRIN; PERFORMANCE; GRAPHENE; ELECTROCATALYST; COMPLEXATION; MECHANISM; CATHODES; REDOX; OXIDE;
D O I
10.1002/anie.202306528
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing polyoxometalate-cyclodextrin cluster-organic supramolecular framework (POM-CD-COSF) still remains challenging due to an extremely difficult task in rationally interconnecting two dissimilar building blocks. Here we report an unprecedented POM-CD-COSF crystalline structure produced through the self-assembly process of a Krebs-type POM, [Zn-2(WO2)(2)(SbW9O33)(2)](10-), and two & beta;-CD units. The as-prepared POM-CD-COSF-based battery separator can be applied as a lightweight barrier (approximately 0.3 mg cm(-2)) to mitigate the polysulfide shuttle effect in lithium-sulfur batteries. The designed Li-S batteries equipped with the POM-CD-COSF modified separator exhibit remarkable electrochemical performance, attributed to fast Li+ diffusion through the supramolecular channel of & beta;-CD, efficient polysulfide-capture ability by the dynamic host-guest interaction of & beta;-CD, and improved sulfur redox kinetics by the bidirectional catalysis of POM cluster. This research provides a broad perspective for the development of multifunctional supramolecular POM frameworks and their applications in Li-S batteries.
引用
收藏
页数:9
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