Construction of 1T@2H MoS2heterostructures: In situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries

13Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Natural molybdenite, an inexpensive and naturally abundant material, can be directly used as an anode material for lithium-ion batteries. However, how to release the intrinsic capacity of natural molybdenite to achieve high rate performance and high capacity is still a challenge. Herein, we introduce an innovative, effective, and one-step approach to preparing a type of heterostructure material containing 1T@2H MoS2 crafted from insertion and expansion of natural molybdenite. The metallic 1T phase formed in situ can significantly improve the electronic conductivity of MoS2. At the same time, 1T@2H MoS2 heterostructures can provide an internal electric field (E-field) to accelerate the migration rate of electrons and ions, promote the charge transfer behaviour, and ensure the reaction reversibility and lithium storage kinetics. Such worm-like 1T@2H MoS2 heterostructures also have a large specific surface area and a large number of defects, which will help shorten the lithium-ion transmission distance and provide more ion transmission channels. As a result, it exhibits a discharge capacity of 788 mA h g-1 remarkably at 100 mA g-1 after 485 cycles and stable cycling performance. It also shows excellent magnification performance of 727 mA h g-1 at 1 A g-1, compared to molybdenite concentrate. Briefly, this work's heterostructure architectures open up a new avenue for applying natural molybdenite in lithium-ion batteries, which has the potential to achieve large-scale commercial applications. This journal is

Cite

CITATION STYLE

APA

Peng, C., Shi, M., Li, F., Wang, Y., Liu, X., Liu, H., & Li, Z. (2021). Construction of 1T@2H MoS2heterostructures: In situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries. RSC Advances, 11(53), 33481–33489. https://doi.org/10.1039/d1ra05565h

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free