The unavoidable dendrite growth and side reactions are two major issues that lead to unsatisfactory cycling stability of the Zn metal anode and premature battery failure, which constrains the wide practical application of aqueous Zn-ion batteries. Herein, a bilayered zinc fluoride-indium interface-modified zinc anode (ZnF2-In@Zn) is in situ-constructed to solve these two issues through a simple solution-dipping strategy. The outer ZnF2 layer assures sufficient desolvation of hydrated Zn2+ and even Zn2+ flux; meanwhile, the interior In layer further contributes to the uniform distribution of the electric field and lower energy barrier of Zn2+ nucleation, achieving dendrite-free and side reaction-free Zn deposition. With synergistic regulation from the bilayered composite interface, the ZnF2-In@Zn anode exhibits outstanding cycling stability (over 4200 h at 1 mA cm-2), achieving a cumulative capacity of over 5250 mAh cm-2 even under a high current density of 5 mA cm-2. This work proposes an advanced understanding of reasonable interface engineering for tackling multiple challenges faced by metal anodes.
Keywords: Zn anode; Zn dendrite; aqueous zinc-ion batteries; bilayered interface; side reactions.