4.8 Article

Design of Quasi-MOF Nanospheres as a Dynamic Electrocatalyst toward Accelerated Sulfur Reduction Reaction for High-Performance Lithium-Sulfur Batteries

期刊

ADVANCED MATERIALS
卷 34, 期 2, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202105541

关键词

electrocatalysts; lithium-sulfur batteries; polysulfides; quasi-metal-organic-frameworks; sulfur reduction reaction

资金

  1. Department of Science and Technology of Guangdong province [2019JC01L203, 2020B0909030004]
  2. Science and Technology Program of Guangzhou [2019050001]
  3. China Postdoctoral Science Foundation [2021M691087]
  4. Science and Technology Program of Zhaoqing [2019K038]
  5. Program for the Outstanding Young Talents of Hebei Province, China
  6. Chunhui Project of Ministry of Education of the People's Republic of China [Z2017010]
  7. Natural Sciences and Engineering Research Council of Canada
  8. University of Waterloo
  9. Waterloo Institute for Nanotechnology

向作者/读者索取更多资源

This study presents a strategy to design quasi-MOF nanospheres as sulfur electrocatalysts by incorporating a transition-state structure between MOF and metal oxides via controlled ligand exchange strategy. The quasi-MOF inherits the porous structure of MOF and exposes abundant metal nodes to act as active sites for strong LiPs absorbability, resulting in remarkable catalytic activity and long-term cycling stability in Li-S batteries.
Lithium-sulfur (Li-S) batteries are considered as one of the most promising next-generation rechargeable batteries owing to their high energy density and cost-effectiveness. However, the sluggish kinetics of the sulfur reduction reaction process, which is so far insufficiently explored, still impedes its practical application. Metal-organic frameworks (MOFs) are widely investigated as a sulfur immobilizer, but the interactions and catalytic activity of lithium polysulfides (LiPs) on metal nodes are weak due to the presence of organic ligands. Herein, a strategy to design quasi-MOF nanospheres, which contain a transition-state structure between the MOF and the metal oxide via controlled ligand exchange strategy, to serve as sulfur electrocatalyst, is presented. The quasi-MOF not only inherits the porous structure of the MOF, but also exposes abundant metal nodes to act as active sites, rendering strong LiPs absorbability. The reversible deligandation/ligandation of the quasi-MOF and its impact on the durability of the catalyst over the course of the electrochemical process is acknowledged, which confers a remarkable catalytic activity. Attributed to these structural advantages, the quasi-MOF delivers a decent discharge capacity and low capacity-fading rate over long-term cycling. This work not only offers insight into the rational design of quasi-MOF-based composites but also provides guidance for application in Li-S batteries.

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