| Literature DB >> 34613619 |
Dan Luo1,2, Chaojie Li1,3, Yongguang Zhang3, Qianyi Ma2, Chuyin Ma1,4, Yihang Nie1,4, Matthew Li2, Xuefei Weng5, Rong Huang5, Yan Zhao3, Lingling Shui1, Xin Wang1,4, Zhongwei Chen2.
Abstract
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.Entities:
Keywords: electrocatalysts; lithium-sulfur batteries; polysulfides; quasi-metal-organic-frameworks; sulfur reduction reaction
Year: 2021 PMID: 34613619 DOI: 10.1002/adma.202105541
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849