Critical triple roles of sodium iodide in tailoring the solventized structure, anode-electrolyte interface and crystal plane growth to achieve highly reversible zinc anodes for aqueous zinc-ion batteries

Aqueous rechargeable Zn-ion batteries (ARZIBs) are promising for energy storage. However, the Zn dendrite and corrosive reactions on the surface of Zn anode limit the practical uses of ARZIBs. Herein, we present a valid electrolyte additive of NaI, in which I^- can modulate the morphology of Zn crystal growth by adsorbing on specific crystal surfaces (0 0 2), and guide Zn deposition by inducing a negative charge on the Zn anode. Simultaneously, it enhances the reduction stability of water molecules by participating in the solvation structure of Zn(H₂O)₆²⁺ by forming ZnI(H₂O)₅⁺. At 10 mA cm⁻², the assembled Zn symmetrical batteries can run stably over 1,100 h, and the depth of discharge (DOD) can reach 51.3 %. At 1 A g⁻¹, the VO₂||Zn full-cell in 2 M ZnCl₂ electrolyte with 0.4 M NaI (2 M ZnCl₂-0.4 M NaI) maintains of the capacity retention of 75.7 % over 300 cycles. This work offers an insight into inorganic anions as electrolyte additives for achieving stable zinc anodes of ARZIBs.