期刊
JOURNAL OF ENERGY CHEMISTRY
卷 81, 期 -, 页码 432-442出版社
ELSEVIER
DOI: 10.1016/j.jechem.2023.03.008
关键词
Nanoscale transition metal; Lithium polysulfide; Catalytic activity; Redox reaction; Lithium-sulfur battery
To achieve high-performance lithium-sulfur (Li-S) batteries, it is crucial to design electrocatalytic materials that can efficiently facilitate sulfur electrochemical reactions. In this study, a novel heterostructured material consisting of nanoscale transition metals anchored on perovskite oxide was developed. This material demonstrated excellent catalytic activity for the oxidation and reduction reactions of lithium polysulphide (LiPSs), leading to a high-performance Li-S battery with stable cycling under rapid charge-discharge conditions.
To obtain high-performance lithium-sulfur (Li-S) batteries, it is necessary to rationally design electrocat-alytic materials that can promote efficient sulfur electrochemical reactions. Herein, the robust heterostructured material of nanoscale transition metal anchored on perovskite oxide was designed for efficient catalytic kinetics of the oxidation and reduction reactions of lithium polysulphide (LiPSs), and verified by density functional theory (DFT) calculations and experimental characterizations. Due to the strong interaction of nanoscale transition metals with LiPSs through chemical coupling, heterostructured materials (STO@M) (M = Fe, Ni, Cu) exhibit excellent catalytic activity for redox reactions of LiPSs. The bifunctional heterostructure material STO@Fe exhibits good rate performance and cycling stability as the cathode host, realizing a high-performance Li-S battery that can maintain stable cycling under rapid charge-discharge cycling. This study presents a novel approach to designing electrocatalytic materials for redox reactions of LiPSs, which promotes the development of fast charge-discharge Li-S batteries. (c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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