Conversion of MoS2 to a Ternary MoS2–xSex Alloy for High-Performance Sodium-Ion Batteries
Source abstract
Abstract
MoS2 has attracted tremendous attention as an anode for Na-ion batteries (NIBs) owing to its high specific capacity and layered graphite-like structure. Herein, MoS2 is converted to a ternary MoS2- xSe x alloy through the selenizing process in order to boost the electrochemical performance for Na-ion batteries. Conversion of MoS2 to MoS2- xSe x expands interlayer spacing, improves electronic conductivity, and creates more defects. The expanded interlayer spacing decreases Na+ diffusion resistance and facilitates Na+ fast transfer. The integrated graphene as a conductive network offers effective pathway for electron migration and maintains structural stability of electrodes during cycles. The ternary MoS1.2Se0.8/graphene (MoS1.2Se0.8/G) electrode demonstrates an extremely high reversible capacity of 509 mA h g-1 after 200 cycles at 0.1 A g-1 (capacity retention of 109%) as an anode for sodium-ion batteries. Even at 2 A g-1 and after 700 cycles, the MoS1.2Se0.8/G electrode also displays a relatively high reversible capacity of 178 mA h g-1. Full cells assembled with Na3V2(PO4)2F3 cathodes and MoS1.2Se0.8/G anodes reveal high charge/discharge capacities. This work demonstrates that the ternary MoS2- xSe x alloy could be a potential anode material for Na-ion storage.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advancements in Battery Materials · MXene and MAX Phase Materials · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Materials and Chemical Engineering, China Three Gorges University, Yichang, Hubei 443002, China
Collaborative Innovation Center for Microgrid of New Energy, Yichang, Hubei 443002, China
Funding
National Natural Science Foundation of China · Ministry of Science and Technology of the People's Republic of China · Hubei Educational Committee
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