One-Step Hydrothermal Reaction Induced Nitrogen-Doped MoS2/MXene Composites with Superior Lithium-Ion Storage
Source abstract
Abstract
MoS2, a typical transition metal dichalcogenide (TMDs), inheriting high theoretical capacity, open framework and unique electrochemical properties, is regarded as a promising electrode material. However, the low electronic conductivity and slow chemical kinetics of two-dimensional (2D) MoS2 lamellars, along with the large volume expansion during cycling hinder their application in Li-ion batteries. MXene inherits the strengths of excellent metallic conductivity, a low lithium-ion diffusion potential barrier and superior mechanical stability; however, its low reversible capacity and self-stacking problems as anode still need to be solved. Herein, the MXene Ti3C2Tx compound with MoS2 through a simple one-step hydrothermal reaction is introduced. The introduction of nitrogen-doped Ti3C2Tx can effectively restrain the volume change of MoS2 and ameliorate the electronic conductivity of the whole electrode, while MoS2 can alleviate the self-stacking of Ti3C2Tx during cycling. The as-prepared MoS2/MXene electrode delivers an initial discharge capacity of 1087 mA h g−1 with an initial Coulombic efficiency (ICE) of 81.6% at 100 mA g−1, and a specific discharge capacity of 731 mA h g−1 can be retained after 100 cycles. The excellent electrochemical performance demonstrates that nitrogen-doped MoS2/MXene can be a potential electrode material for Li-ion batteries.
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Research context
OpenAlex topics: MXene and MAX Phase Materials · Advancements in Battery Materials · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Joint International Laboratory on Environmental and Energy Frontier Materials, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China
Centre for Clean Energy Technology, Faculty of Science, University of Technology Sydney, Broadway, Sydney, NSW 2007, Australia
Funding
Australian Research Council
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