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高效捕获和催化转化多硫化锂在中空金属氧化物亚微米球上作为锂硫电池正极。

Efficient entrapment and catalytic conversion of lithium polysulfides on hollow metal oxide submicro-spheres as lithium-sulfur battery cathodes.

机构信息

State Key Laboratory of Material Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.

Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA.

出版信息

Nanoscale. 2018 Mar 28;10(12):5634-5641. doi: 10.1039/c7nr09216d. Epub 2018 Mar 12.

DOI:10.1039/c7nr09216d
PMID:29528070
Abstract

Li-S battery technology, with high theoretical capacity and energy density, has drawn much attention in recent years as a possible replacement for current Li-ion battery technologies. A major drawback of Li-S batteries is a severe capacity fading effect which, to a large extent, stems from the dissolution and diffusion of lithium polysulfides (LiPS) that are formed during both charge and discharge cycles. The self-discharge caused by the LiPS migration during the charge process (the so-called "shuttle effect") often leads to the capacity decay of Li-S batteries. Herein, hollow structured metal oxide (CoO, MnO, and NiO) submicro-spheres are prepared by a novel method and employed as efficient LiPS immobilizers. These Li-S batteries, based on the developed metal oxide spheres, possess outstanding rate capability and cycling stability. The best performing S/C/CoO electrode delivers excellent cycling stability with only a 0.066% capacity decay per cycle during 550 cycles. Moreover, its discharge capacity is as high as 428 mA h g at a 3C rate which is far superior to that of bare S/C (115 mA h g) at 3C. The fast kinetics of the electrocatalytic conversion of LiPS on the developed CoO electrode and its unique hollow structure are the key factors that lead to its outstanding performance as a Li-S battery cathode material.

摘要

锂硫电池技术具有高的理论容量和能量密度,近年来作为可能替代现有锂离子电池技术的一种选择而受到广泛关注。锂硫电池的一个主要缺点是严重的容量衰减效应,这在很大程度上源于在充放电循环过程中形成的多硫化锂(LiPS)的溶解和扩散。在充电过程中 LiPS 迁移引起的自放电(所谓的“穿梭效应”)常常导致锂硫电池的容量衰减。在此,通过一种新方法制备了空心结构的金属氧化物(CoO、MnO 和 NiO)亚微米球,并将其用作有效的 LiPS 固定剂。基于所开发的金属氧化物球的这些锂硫电池具有出色的倍率性能和循环稳定性。表现最佳的 S/C/CoO 电极在 550 次循环中具有仅 0.066%的每循环容量衰减率的出色循环稳定性。此外,其在 3C 倍率下的放电容量高达 428 mA h g,远高于裸 S/C(115 mA h g)在 3C 下的容量。在开发的 CoO 电极上 LiPS 的电催化转化的快速动力学及其独特的空心结构是导致其作为锂硫电池阴极材料具有出色性能的关键因素。

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