Abstract

Owing to energy density, powder density, and eco-friendliness, Li-ion batteries (LIBs) are increasingly used in transportable electronic devices and electric vehicles. Monoclinic VO2 (B) has been broadly used as a cathode owing to its abundance, affordability, high capacity, and multiple oxidation states, but it's low repeatability and slow kinetics have restricted its practical applications. To mitigate these shortcomings, novel 1D/2D VO2 (B) nanowire/g-C3N4 hybrid architecture cathode materials were synthesized via hydrothermal method, and its electrochemical activity (i.e., repeatability constancy and rate capability) for LIBs was investigated. X-ray diffraction experiments confirmed that VO2 (B) exhibited a monoclinic crystal phase. SEM images revealed that the g-C3N4 and VO2 (B) presented sheet-like morphologies and comprised nanowires of uniform thickness, respectively. Electrochemical experiments revealed that the hybrid architectures showed a capacity of 779 mAh/g, and VO2 (601.4 mAh/g) and g-C3N4 (340.6 mAh/g) at 0.1 C current density. The remarkable electrochemical activity of the materials was attributed to their distinctive structures, excellent electronic conductivity associated with g-C3N4 sheets, small transport distances for Li+ ions, and fast charge transmission owing to the presence of VO2 (B) nanowires attached to g-C3N4 sheets. Consequently, distinct VO2 (B) nanowire/g-C3N4 hybrid architectures delivered suitable electrode performance to facilitate the design of high-power LIBs and these hybrid composites can serve as suitable cathode materials for rechargeable LIBs.

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