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Dual electrocatalytic heterostructures for efficient immobilization and conversion of polysulfides in Li-S batteries

Lithium sulfur (Li-S) batteries have been investigated as ideal candidates for future high-density energy storage systems with the advantages of abundant reserves, high energy density and competitive cost. The key issues are the severe shuttling of polysulfides and sluggish redox kinetics. Herein, w...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-09, Vol.9 (34), p.18477-18487
Main Authors: Yang, Menghua, Wang, Xuewei, Wu, Jinfeng, Tian, Yue, Huang, Xingyu, Liu, Ping, Li, Xianyang, Li, Xinru, Liu, Xiaoyan, Li, Hexing
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cited_by cdi_FETCH-LOGICAL-c281t-4535f9744320e313aa0dee0034a514d0dca9b284faebcb42705e6858360a15c93
cites cdi_FETCH-LOGICAL-c281t-4535f9744320e313aa0dee0034a514d0dca9b284faebcb42705e6858360a15c93
container_end_page 18487
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container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 9
creator Yang, Menghua
Wang, Xuewei
Wu, Jinfeng
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Liu, Xiaoyan
Li, Hexing
description Lithium sulfur (Li-S) batteries have been investigated as ideal candidates for future high-density energy storage systems with the advantages of abundant reserves, high energy density and competitive cost. The key issues are the severe shuttling of polysulfides and sluggish redox kinetics. Herein, we report a novel metal-organic framework-derived Co 2 P-ZnS/ZnS-C nanocomposite constructed from inner Co 2 P-ZnS and outer ZnS-C heterostructures. Both the experimental results and theoretical calculations demonstrated that these dual electrocatalytic heterostructures enabled strong affinity with polysulfides and facilitated the reaction kinetics. Meanwhile, the hollow carbon polyhedron provided fast electron/ion transfer channels and effectively buffered volume expansion during cycling. As anticipated, a high initial capacity of 1503 mA h g −1 was achieved at 0.2C with Co-Zn/Zn-C/S as a cathode, together with excellent stability after 500 cycles at 1C. Even a high reversible capacity of 540 mA h g −1 was achieved at 1C after 200 cycles under an elevated sulfur loading of 3.65 mg cm −2 . This work presents a new strategy for designing dual electrocatalytic hosts for immobilization and conversion of polysulfides, which may offer more opportunities as cathodes in stable Li-S batteries with high energy density. Dual Co 2 P-ZnS/ZnS-C electrocatalytic heterostructures were constructed for synergistic immobilization of polysulfides and promotion of the conversion kinetics.
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subjects Batteries
Cathodes
Conversion
Energy storage
Flux density
Heterostructures
Immobilization
Kinetics
Lithium
Lithium sulfur batteries
Metal-organic frameworks
Nanocomposites
Polysulfides
Reaction kinetics
Storage batteries
Storage systems
Sulfur
Zinc
Zinc sulfide
title Dual electrocatalytic heterostructures for efficient immobilization and conversion of polysulfides in Li-S batteries
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