In Situ Lattice Tunnel Distortion of Vanadium Trioxide for Enhancing Zinc Ion Storage

Abstract Research on aqueous zinc‐ion batteries is still in its initial stages owing to the limited choice of cathode materials, especially those having tunnel structures with high capacity and fast kinetics. Furthermore, their zinc ion storage mechanisms are not well established as yet. Here, a novel in situ electrochemical lattice distortion of vanadium trioxide (V 2 O 3 ) is demonstrated. The obtained defect‐rich V 2 O 3 is applied as a cathode for ultrafast Zn 2+ storage. Operando X‐ray diffraction and operando Raman spectroscopy corroborate the unique lattice conversion reaction of V 2 O 3 during the initial charging process. Transmission electron microscopy and X‐ray photoelectron spectroscopy further demonstrate the stability of the main crystal planes of V 2 O 3 during the initial lattice distortion and subsequent zinc ion storage processes. This unique in situ electrochemical lattice conversion reaction allows V 2 O 3 to achieve a high capacity of 382.5 mAh g −1 , remarkable rate performance (154.3 mAh g −1 at 51.2 A g −1 ), and high energy and power densities (139 Wh kg −1 at 46 KW kg −1 ), revealing the potential of tunnel‐type cathodes via an in situ electrochemical lattice distortion reaction to achieve ultrafast zinc ion storage with high capacity.