Issue 24, 2024

MoS2 quantum dot-decorated CNT networks as a sulfur host for enhanced electrochemical kinetics in advanced lithium–sulfur batteries

Abstract

The slow redox kinetics and shuttle effect of polysulfides severely obstruct the further development of lithium–sulfur (Li–S) batteries. Constructing sulfur host materials with high conductivity and catalytic capability is well acknowledged as an effective strategy for promoting polysulfide conversion. Herein, a well-designed MoS2 QDs-CNTs/S@Ni(OH)2 (labeled as MoS2 QDs-CNTs/S@NH) cathode was synthesized via a hydrothermal process, in which conductive polar MoS2 quantum dot-decorated carbon nanotube (CNT) networks coated with an ultrathin Ni(OH)2 layer acted as an efficient electrocatalyst. MoS2 QD nanoparticles with a high conductivity and catalytic nature can enhance the kinetics of polysulfide conversion, expedite Li2S nucleation, and decrease the reaction energy barrier. The thin outer Ni(OH)2 layer physically confines active sulfur and meanwhile provides abundant sites for adsorption and conversion of polysulfides. Benefiting from these merits, a battery using MoS2 QDs-CNTs/S@NH as the sulfur host cathode exhibits excellent electrochemical performances with rate capabilities of 953.7 mA h g−1 at 0.1C and 606.6 mA h g−1 at 2.0C. A prominent cycling stability of a 0.052% decay rate per cycle after 800 cycles is achieved even at 2C.

Graphical abstract: MoS2 quantum dot-decorated CNT networks as a sulfur host for enhanced electrochemical kinetics in advanced lithium–sulfur batteries

Supplementary files

Article information

Article type
Paper
Submitted
24 Jan 2024
Accepted
18 Oct 2024
First published
22 Oct 2024
This article is Open Access
Creative Commons BY license

Nanoscale Adv., 2024,6, 6386-6397

MoS2 quantum dot-decorated CNT networks as a sulfur host for enhanced electrochemical kinetics in advanced lithium–sulfur batteries

M. Wei, H. Lu, Z. Wang, B. Lu, P. Wang, X. Zhang, B. Feng, Y. Xie, T. Zhang, G. Liu and S. Xu, Nanoscale Adv., 2024, 6, 6386 DOI: 10.1039/D4NA00068D

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