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MOF衍生的MoC/WC异质结构作为锂多硫化物的双向催化剂助力高性能锂硫电池

MOF-Derived MoC/WC Heterostructure as Bidirectional Catalyst for Lithium Polysulfide Enables High-Performance Lithium-Sulfur Batteries.

作者信息

Zhang Xingxing, Zhang Fang, Su Qingmei, Hou Xuehan, Chen Rui, Chen Zhuo, Du Gaohui, Shi Weihao, Shi Yang, Lv Yujie, Huang Wenhuan, Xu Bingshe

机构信息

School of Materials Science & Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.

Materials Institute of Atomic and Molecular Science, School of Physics & Information Science, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.

出版信息

Small. 2024 Dec 4:e2407283. doi: 10.1002/smll.202407283.

Abstract

Since lithium-sulfur (Li-S) batteries have high energy density and environmental friendliness, they have garnered a lot of attention as a new type of energy storage technology. However, the shuttle effect of lithium polysulfides (LiPSs) and low utilization of sulfur (S) in Li-S batteries reduce the cycle stability and energy efficiency and limit their practical application. Therefore, it is urgent to achieve simultaneous immobilization and conversion of LiPSs utilizing catalysts. Herein, a metal-organic framework (MOF)-derived MoC/WC@NC heterojunction is synthesized as a bidirectional catalyst for LiPSs in high-performance Li-S batteries. Experimental and theoretical calculations indicate that the catalyst is expected to improve the catalytic activity for reduction and oxidation reactions of LiPSs, thereby accelerating the kinetics of Li-S batteries. In conclusion, with the incorporation of the novel catalyst between the cathodes and separators in Li-S batteries, the assembled batteries demonstrate excellent rate performance, with an initial discharge capacity of 1752.1 mAh g at 0.1 C, and a discharge-specific capacity of 783.2 mAh g even at 2 C. More significantly, the coulombic efficiency stayed above 99% and the capacity of 589.1 mAh g after 1000 cycles at 1 C with a decay rate of only 0.062% each cycle.

摘要

由于锂硫(Li-S)电池具有高能量密度和环境友好性,作为一种新型储能技术受到了广泛关注。然而,锂硫电池中多硫化锂(LiPSs)的穿梭效应以及硫(S)的低利用率降低了循环稳定性和能量效率,限制了它们的实际应用。因此,迫切需要利用催化剂实现LiPSs的同时固定和转化。在此,合成了一种金属有机框架(MOF)衍生的MoC/WC@NC异质结,作为高性能锂硫电池中LiPSs的双向催化剂。实验和理论计算表明,该催化剂有望提高LiPSs还原和氧化反应的催化活性,从而加速锂硫电池的动力学。总之,通过在锂硫电池的阴极和隔膜之间引入这种新型催化剂,组装的电池表现出优异的倍率性能,在0.1 C下初始放电容量为1752.1 mAh g,即使在2 C下放电比容量仍为783.2 mAh g。更显著的是,库仑效率保持在99%以上,在1 C下经过1000次循环后容量为589.1 mAh g,每次循环的衰减率仅为0.062%。

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