Abstract
AbstractStructural engineering and creating atomic disorder in electrodes are promising strategies for highly efficient and rapid charge storage in advanced batteries. Herein, a nanohybrid architecture is presented with amorphous vanadium oxide conformally coated on layered V2C MXene (a‐VOx/V2C) via tunable anodic oxidation, which exhibits a high reversible capacity of 307 mAh g–1 at 50 mA g–1, decent rate capability with capacity up to 96 mAh g–1 at 2000 mA g–1, and good cycling stability as a cathode for sodium‐ion batteries. The a‐VOx layer enables reversible and fast Na+ insertion/extraction by providing sufficient vacancies and open pathways in the amorphous framework, unlike the irreversible phase transition in its crystalline counterpart, while layered V2C MXene offers abundant electron/ion transfer channels, which are joined together to boost the electrochemical performance. Notably the improved reversibility and structural superiority of the a‐VOx/V2C nanohybrid are clearly revealed by in situ Raman, in situ transmission electron microscopy, in situ synchrotron X‐ray absorption spectroscopy, and density functional theory calculations, demonstrating a reversible V–O vibration and valence oscillation between V4+ and V5+ in the disordered framework, with robust structural stability and unobstructed Na+ diffusion. This work provides a meaningful reference for the elaborate design of MXene‐based nanostructured electrodes toward advanced rechargeable batteries.
Published Version
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