Manganese sulfide (MnS) has been
found to be a suitable electrode
material for lithium-ion batteries (LIBs) owing to its considerable
theoretical capacity, high electrochemical activity, and low discharge
voltage platform, while its poor electrical conductivity and severe
pulverization caused by volume expansion of the material limit its
practical application. To improve the rate performance and cycle stability
of MnS in LIBs, the structure-control strategy has been used to design
and fabricate new anode materials. Herein, the MnS@MXene@CNF (MMC,
CNFs means carbon nanofibers) electrode has been prepared by electrospinning
and a subsequent high-temperature annealing process. The MMC electrode
exhibits excellent cyclic stability with a capacity retention rate
close to 100% after 1000 cycles at 1000 mA/g and an improved rate
performance with a specific capacity up to 500 mAh/g at a high current
density of 5000 mA/g, much higher than the 308 mAh/g of the MnS@CNF
(MC) electrode. The elevated electrochemical performance of the MMC
electrode not only benefits from the unique structure of MnS nanoparticles
evenly dispersed in the well-designed flexible self-supporting three-dimensional
(3D) CNF network but, more importantly, also benefits from the formation
of sulfur-bridged Mn–S–C bonds at the MnS/MXene interface.
The newly formed bonds between MnS and MXene nanosheets can stabilize
the structure of MnS near the interfaces and provide a channel for
fast charge transfer, which notably increase both the reversibility
and the rate of the conversion reaction during the charge/discharge
process. This work may pave a new path for designing stable and self-supporting
anodes for high-performance LIBs.