摘要: Spinel LiMn₂O₄ (LMO) is deemed to be a promising cathode material for commercial lithium-ion batteries (LIBs) in prospect of its cost-effectiveness, nontoxicity, fabulous rate capability, and high energy density. Nevertheless, the LMO is inevitably confronted with sluggish diffusion kinetics and drastic capacity degradation triggered by multiple issues, including Jahn–Teller distortion, Mn dissolution, and structural attenuation. Thereinto, a metal-organic framework (MOF) chemistry engineering for hierarchical micro-/nano-structural F, O-dual-doped carbon embedded oxygen vacancy enriched LiMn₂O₄ cathode (OV-LMO@FOC) is proposed for longevous LIBs. Bestowed by experimental and theoretical implementations, systematic investigations of OV-LMO@FOC endow that the meticulous integration of F, O-dual-doped carbon and oxygen vacancy in LMO-based cathode reconfigures the electronic structure, boosts electronic conductivity, expedites diffusion capability, facilitates energetically preferable Li⁺ adsorption, and suppresses Mn dissolution in the electrolyte, consequently achieving fabulous long-term cycling stability. As expected, the OV-LMO@FOC behaves with compelling electrochemical performance with prosperous reversible capacity (130.2 mAh g^-1 at 0.2 C upon 200 cycles), exceptional rate capacity (93.7 mAh g^-1 even at 20 C), and pronounced long-term cyclability (112.5 mAh g^-1 after 1200 cycles with 77.6% capacity retention at 1 C). Even at the ultrahigh current density of 5 C, the OV-LMO@FOC bears a brilliant capacity of 96.9 mAh g^-1 upon 1000 cycles with an extraordinary capacity retention of 90.7%, and maintains a discharge capacity of 70.9 mAh g^-1 upon 4000 cycles. This work envisions the MOF-chemistry in surface modification and electronic modulation engineering of high-performance cathode materials towards industrialization in automotive market.