摘要
Although aqueous zinc-ion batteries (ZIBs) have demonstrated great potential for large-scale energy storage, dendrite growth in the Zn metal anode leads to poor electrochemical stability and unsatisfactory cycling life, restricting widespread utilization of ZIBs. Herein, a zincophilic covalent organic framework (COF; TpPa-SO 3 H) film is fabricated via interfacial reaction to stabilize the Zn anode (TpPa-SO 3 H@Zn-foil). The sulfonic acid groups on the TpPa-SO 3 H film coordinate with Zn 2+ ions and regulate the uniform deposition of Zn 2+ ions to inhibit the dendrite formation. Additionally, the TpPa-SO 3 H can release abundant protons (H + ) and achieve a dynamic equilibrium with OH − , thereby adjusting the desolvation of [Zn(H 2 O) 6 ] 2+ to prevent secondary reactions. This work demonstrates that COF film-coated Zn anodes are a family of promising electrode candidates and provides inspiration to other fields of batteries, such as the material design for separator and electrolyte.
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