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在用于长寿命锂硫电池的中空结构MoS/CoS/C异质结主体中实现与工作协同的多硫化物吸附-转化

Achieving job-synergistic polysulfides adsorption-conversion within hollow structured MoS/CoS/C heterojunction host for long-life lithium-sulfur batteries.

作者信息

Li Fangyuan, Wu Yujie, Lin Yongxian, Li Junhao, Sun Yajie, Nan Haoxiong, Wu Ming, Dong Huafeng, Shi Kaixiang, Liu Quanbing

机构信息

Guangzhou Key Laboratory of Clean Transportation Energy Chemistry, Guangdong Provincial Key Laboratory of Plant Resources Biorefinery, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.

School of Science, Hainan University, Haikou 570228, China.

出版信息

J Colloid Interface Sci. 2022 Nov 15;626:535-543. doi: 10.1016/j.jcis.2022.06.091. Epub 2022 Jun 24.

Abstract

Lithium-sulfur batteries are considered one of the most promising next-generation energy storage devices owing to their ultrahigh theoretical energy density and environmental friendliness. However, the sluggish electrode reaction kinetics of the sulfur cathode and shuttle effects of lithium polysulfide (LiPSs) restrict their active material utilization and cycling stability. Herein, a hollow, free-standing MoS/CoS/C heterojunction was fabricated and employed as a cathode host for high-performance lithium-sulfur batteries (LSBs). The unique hollow nanostructured MoS/CoS/C can achieve job-synergistic polysulfide adsorption-conversion, in which the conductive nitrogen-doped carbon framework facilitates rapid electron/ion diffusion; polar CoS species provide strong chemisorption capability and endow intrinsic catalytic sites towards LiPSs, and MoS serves as a nanocrystal to accelerate the reaction dynamics. As a result, MoS/CoS/C/S exhibited high reversible specific capacities at 2C and was maintained at 394 mAh g after 1000 cycles, with a 0.04% capacity decay rate. Impressively, the high reversible specific capacities with high sulfur loading of 4.1 mg cm were maintained at 906.7 mAh g.

摘要

锂硫电池因其超高的理论能量密度和环境友好性而被认为是最有前途的下一代储能装置之一。然而,硫正极缓慢的电极反应动力学和多硫化锂(LiPSs)的穿梭效应限制了其活性材料的利用率和循环稳定性。在此,制备了一种中空的、自支撑的MoS/CoS/C异质结,并将其用作高性能锂硫电池(LSBs)的正极主体。独特的中空纳米结构MoS/CoS/C可以实现协同的多硫化物吸附-转化,其中导电的氮掺杂碳骨架促进快速的电子/离子扩散;极性CoS物种提供强大的化学吸附能力并赋予对LiPSs的固有催化位点,而MoS作为纳米晶体加速反应动力学。结果,MoS/CoS/C/S在2C时表现出高可逆比容量,在1000次循环后保持在394 mAh g,容量衰减率为0.04%。令人印象深刻的是,在硫负载量为4.1 mg cm的情况下,高可逆比容量保持在906.7 mAh g。

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