摘要
Despiting the technological promise and environmental friendliness of sodium-ion batteries (SIBs), relatively large sizes of Na-ions and moderate oxidation-reduction response slows down their wider-spread industrial implementation. To overcome this obstacle, we developed carbon-coated MoSe 2 /MXene heterostructures , in which MXene was covered on the MoSe 2 particles and the loose carbon linked all the coated particles while providing porosity. The density-functional theory was used to understand the electronic structure of the carbon-coated MoSe 2 /MXene (MoSe 2 /Mo 2 CT x /C) and the mechanism of exchanging charge between MoSe 2 and MXene. MoSe 2 /Mo 2 CT x /C as active anode material showed exceptional stability even after 2200 cycles in SIBs. Specifically, the capacities and retention rates observed for the batteries containing MoSe 2 /Mo 2 CT x /C and cycled at 0.5, 1, and 2 A g −1 rates were equal to 652.2, 484.4, and 238.4 mAh g −1 and 102.5%, 103.9%, and 86.3%, respectively. Thus, carbon-coated MoSe 2 /MXene can be utilized as active SIB anode materials.
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