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导电且具催化性的VTe@MgO异质结构作为锂硫电池的有效多硫化物促进剂

Conductive and Catalytic VTe@MgO Heterostructure as Effective Polysulfide Promotor for Lithium-Sulfur Batteries.

作者信息

Wang Menglei, Song Yingze, Sun Zhongti, Shao Yuanlong, Wei Chaohui, Xia Zhou, Tian Zhengnan, Liu Zhongfan, Sun Jingyu

机构信息

College of Energy, Soochow Institute for Energy and Materials InnovationS (SIEMIS), Jiangsu Provincial Key Laboratory for Advanced Carbon Materials and Wearable Energy Technologies , Soochow University , Suzhou 215006 , P.R. China.

Physical Sciences and Engineering Division , King Abdullah University of Science and Technology , Thuwal 23955-6900 , Saudi Arabia.

出版信息

ACS Nano. 2019 Nov 26;13(11):13235-13243. doi: 10.1021/acsnano.9b06267. Epub 2019 Oct 29.

Abstract

Lithium-sulfur (Li-S) batteries are recognized as one of the most promising energy storage systems due to the high energy density and cost effectiveness. However, their practical implementation has still been handicapped due to notorious lithium polysulfide (LiPS) shuttle and depressed sulfur redox kinetics. It is therefore desirable to exploit key mediators synergizing electrical conductivity and electrocatalytic activity for the cathode. Herein, we report the employment of atmospheric pressure chemical vapor deposition to harness the efficient and controllable synthesis of metallic VTe over particulated MgO substrates, which has scarcely been demonstrated by conventional wet-chemical synthetic routes thus far. The thus-derived VTe@MgO heterostructure as an efficient promotor enables effective regulation of LiPSs with respect to polysulfide capture/conversion and LiS decomposition. As a result, a S/VTe@MgO cathode with a sulfur loading of 1.6 mg cm harvests long-term cyclability with a negligible capacity decay of 0.055% per cycle over 1000 cycles at 1.0 C. Even at a sulfur loading of 6.9 mg cm, the cathode still delivers electrochemical performances that can rival the state-of-the-art high-loading counterparts. Our work might offer a feasible solution for developing heterostructured promotors with multifunctionality and electrocatalytic activity for high-performance Li-S batteries.

摘要

锂硫(Li-S)电池因其高能量密度和成本效益而被认为是最具前景的储能系统之一。然而,由于臭名昭著的多硫化锂(LiPS)穿梭效应和缓慢的硫氧化还原动力学,其实际应用仍然受到阻碍。因此,需要开发关键的介导剂,以协同提高正极的电导率和电催化活性。在此,我们报道了利用常压化学气相沉积法在颗粒状MgO衬底上高效、可控地合成金属VTe,而传统的湿化学合成路线至今几乎无法实现这一点。由此得到的VTe@MgO异质结构作为一种高效的促进剂,能够有效地调控多硫化锂的多硫化物捕获/转化和LiS分解。结果,硫负载量为1.6 mg cm的S/VTe@MgO正极在1.0 C下经过1000次循环,实现了长期循环稳定性,每次循环的容量衰减可忽略不计,仅为0.055%。即使在硫负载量为6.9 mg cm时,该正极仍能提供可与最先进的高负载正极相媲美的电化学性能。我们的工作可能为开发具有多功能性和电催化活性的异质结构促进剂以用于高性能锂硫电池提供了一种可行的解决方案。

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