Trace molecular chelation engineering of a self-healing hybrid interphase for highly stable aqueous zinc-ion batteries

Aqueous Zn-ion batteries (AZIBs) hold promise for grid-scale storage due to their intrinsic safety and low cost, yet face critical irreversible anode degradation from dendritic proliferation and parasitic reactions. Here, we introduce a molecular chelation-driven interfacial engineering strategy using trace polyglutamate sodium (PS) to construct a dynamically selfhealing hybrid interphase on Zn anodes. PS reorganizes interfacial water networks and chelates Zn 2+ , forming an adaptive hydrogel-like PS-Zn layer (PSZ), which further in situ generates an inorganic solid-electrolyte interphase (SEI). This synergistic PSZ-SEI layer provides robust electrode shielding, precise hydration regulation, and continuous self-repair. Consequently, Zn||Zn symmetric cells achieve >4500 h cycling, Zn||Na 2 V 6 O 16 •3H 2 O full cells exhibit stable cycling for 1000 cycles in coin cells and 180 cycles in pouch cells (N/P ratio = 1.62) under high cathode loading (~12 mg cm -2 ). The universality of this approach is further demonstrated in Zn||I 2 batteries over 5000 cycles. This ppm-level dynamic interface control resolves long-standing interfacial conflicts in practical AZIBs.