Transition metal oxides (TMOs) are considered as the prospective anode materials in lithium-ion batteries (LIBs). Nevertheless, the disadvantages, including large volume variation and poor electrical conductivity, obstruct these materials to meet the needs of practical application. Well-designed mesoporous nanostructures and electronic structure modulation can enhance the electron/Li-ions diffusion kinetics. Herein, a unique mesoporous molybdenum dioxide/molybdenum phosphide heterostructure nanobelts (meso-MoO2 /MoP-NBs) composed of uniform nanoparticles is obtained by one-step phosphorization process. The Mott-Schottky tests and density functional theory calculations demonstrated that meso-MoO2 /MoP-NBs possesses superior electronic conductivity. The detailed lithium storage mechanism (solid solution reaction for MoP and partial conversion for MoO2 ), small change ratio of crystal structure and fast electronic/ionic diffusion behavior of meso-MoO2 /MoP-NBs are systematically investigated by operando X-ray diffraction, ex situ transmission electron microscopy, and kinetic analysis. Benefiting from the synergistic effects, the meso-MoO2 /MoP-NBs displays a remarkable cycling performance (515 mAh g-1 after 1000 cycles at 1 A g-1 ) and excellent rate capability (291 mAh g-1 at 8 A g-1 ). These findings can shed light on the behavior of the electron/ion regulation in heterostructures and provide a potential route to develop high-performance lithium-ion storage materials.
Keywords: MoO2/MoP; heterosturctures; lithium-ion batteries; long-term cycling stability.
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