and suitable redox potential (−0.76 V vs standard hydrogen electrode). [2] However, corrosion, passivation, and dendrites on the Zn anode, as well as parasitic side reactions severely hinder the application of AZIBs in energy-storage systems. [3] In addition, the limited specific area of commercial Zn foil results in inadequate contact between electrolyte and anode, thus preventing Zn ion transport at the electrolyte-anode interface. The inherent rough surface results in the continuous deposition of Zn 2+ on the tips with an enhanced electric field, which gradually evolves into the formation of Zn dendrites. [4] Interface modification, structural design, and Zn alloying are typical strategies for improving the performance of Zn anodes. [5] However, the 3D structure and eutectic alloy design of Zn anodes weaken the inherent strengths of AZIBs, that is, their low cost and environmental benignity. [6] Similar to the optimization strategy for lithium metal, the protective layer coated on the surface of zinc acts as a continuous solid-electrolyte interface (SEI) between the metal zinc anode and electrolyte. [7] Hence, interface modification is an effective method for improving the stability of zinc electrode interface and for alleviating the disordered deposition of Zn 2+ and dendrite growth. [8] However, many coating strategies Metal zinc is recognized as a promising anode candidate for aqueous zinc-ion batteries (AZIBs), however, dendrites and byproducts formation severe deteriorate its reversibility and practical lifespan. Herein, a polydopamine (PDA) layer, which offers the dual effects of fast desolvation and ion confinement, is constructed on the surface of a Zn anode for efficient AZIBs. The abundant polar functional groups in PDA significantly enhance interfacial contact in aqueous media, which reduces the number of water molecules reaching the zinc surface through fast desolvation, thus lowering the energy barrier for Zn 2+ migration. Furthermore, the porous PDA coating controls the ion flux via the ion-confinement effect, thereby accelerating Zn 2+ kinetics on the zinc surface. Consequently, Zn@PDA exhibits significantly improved Zn 2+ deposition kinetics (nucleation potential of only 32.6 mV vs 50.2 mV of bare Zn) compared with bare Zn at 2.0 mA cm −2 , with a dendrite-free surface and negligible byproduct formation. When paired with a MnO 2 cathode, the Zn@PDA// MnO 2 cell delivers high discharge capacity and long cycle stability without significant performance deterioration over 1000 cycles at 1.0 A g −1 . Additionally, the cell demonstrates excellent shelving-restoring performance.