Ming Lu, C. K. John Wang, Fangyuan Chen, Kang Xiao, Zhao‐Qing Liu
ABSTRACT Aqueous zinc‐ion batteries (AZIBs) are promising candidates for grid‐scale energy storage owing to their intrinsic safety, low‐cost, and environmental benignity. Manganese dioxide (MnO 2 ) cathodes, in particular, offer high theoretical capacity and natural abundance but suffer from irreversible Jahn–Teller distortion induced by Mn 3+ species and subsequent manganese dissolution, leading to severe capacity degradation. Herein, we propose an innovative axial compressive strain engineering strategy to tackle this challenge via the substitution of O 2− with highly electronegative F − anions in the MnO 2 lattice. This deliberate anion doping effectively shortens the axial Mn‐O bond, thereby directly suppressing the Jahn–Teller distortion. More profoundly, the incorporation of F − ions disrupts the lone electron occupancy in the e g orbital. During the battery discharge process, the electron configuration transitions from the high‐spin t 2g 3 e g 1 state to the more stable t 2g 3 e g 2 configuration, which stabilizes the Mn 3+ state and drastically inhibits Mn dissolution. As a result, the F‐doped MnO 2 (F‐MnO 2 ) cathode delivers exceptional cycling stability, retaining 81% of its initial capacity after 1000 cycles at 2 A g −1 . This work not only demonstrates an effective cathode material but also provides fundamental insights into stabilizing crystal structures of manganese oxides for advanced energy storage technologies.