The influences of Mg intercalation on the structure and supercapacitive behaviors of MoS2

Hao Liu, Bochao Chen, Libing Liao, Peng Fan, Yun Hai, Yuanyuan Wu, Guocheng Lv, Lefu Mei, Huiying Hao, Jie Xing, Jingjing Dong

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Metallic 1T MoS2 greatly benefits the supercapacitance of MoS2 due to its considerably higher conductivity as compared to semiconducting 2H MoS2. Alkali metals, such as Li, Na and K, are always used to prepare 1T MoS2 through intercalation of alkali metal ions into the interlayer of 2H MoS2. Nevertheless, the influences of the alkali-earth metals as the guest in the interlayer of MoS2 on its structure and electrochemical capacitor performance are rarely investigated. Herein, we introduced hydrated Mg ions as the guest into MoS2 nanosheets. The interlayer spacing was increased to 1.144 nm after the introduction of hydrated Mg ions, larger than that of the pristine MoS2 (0.620 nm) and restacking MoS2 (0.626 nm). The enlarged interlayer spacing can accommodate more ions during intercalation process. Moreover, the 1T phase concentration after the introduction of hydrated Mg ions was as high as ~ 90%, which benefits the charge transfer during the charging/discharging processes. Consequently, the specific capacitance of the MoS2 with Mg guest ions as well as the energy densities and power densities was greatly improved as compared to those of the restacking MoS2 or pristine MoS2 counterparts. The present work not only demonstrated a new strategy for engineering the physical properties and improving the electrochemical performance of MoS2 supercapacitor electrode through pre-intercalation of alkali-earth metal ions in the interlayer of MoS2, but also has directive significance for the design of other layered electrode materials for energy storage systems.

Original languageEnglish
Pages (from-to)13247-13254
Number of pages8
JournalJournal of Materials Science
Volume54
Issue number20
DOIs
StatePublished - Oct 30 2019
Externally publishedYes

Funding

This work was supported by the National Natural Science Foundation of China (No. 21875223) and the Fundamental Research Funds for the Central Universities (No. 649911023).

FundersFunder number
National Natural Science Foundation of China21875223
Fundamental Research Funds for the Central Universities649911023

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