Issue 9, 2023

Molecular engineering on a MoS2 interlayer for high-capacity and rapid-charging aqueous ion batteries

Abstract

Rechargeable aqueous ion batteries (AIBs) play essential roles in the increasing demand for high-performance energy storage systems, and yet they are hampered by the lack of suitable cathode materials because of the sluggish intercalation kinetics. In this work, we develop an effective and feasible strategy to enhance the performance of AIBs by broadening the interlayer spacing by using intercalated CO2 molecules to promote the intercalation kinetics by using first principles simulations. Compared with pristine MoS2, the intercalation of CO2 molecules with a 3/4 ML coverage significantly increases the interlayer spacing to 9.383 Å from 6.369 Å and the diffusivity is boosted by 12 orders of magnitude for Zn ions, 13 orders for Mg ions and one order for Li ions. Moreover, the concentrations of intercalating Zn, Mg and Li ions are enhanced by 7, 1 and 5 orders of magnitude, respectively. The significantly increased diffusivity and intercalation concentration of metal ions signify that intercalating CO2 bilayer MoS2 is a promising cathode material to realize metal ion batteries with a rapid charging capability and high storage capacity. The strategy developed in this work can be generally applied to increase the metal ion storage capacity in transition metal dichalcogenide (TMD)- and other layered material-based cathodes and make them promising for next-generation rapidly rechargeable batteries.

Graphical abstract: Molecular engineering on a MoS2 interlayer for high-capacity and rapid-charging aqueous ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
30 Jan 2023
Accepted
01 Apr 2023
First published
04 Apr 2023
This article is Open Access
Creative Commons BY license

Nanoscale Adv., 2023,5, 2639-2645

Molecular engineering on a MoS2 interlayer for high-capacity and rapid-charging aqueous ion batteries

X. Han, J. Yang, Y. Zhang and Z. G. Yu, Nanoscale Adv., 2023, 5, 2639 DOI: 10.1039/D3NA00068K

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