阴极保护
锌
水溶液
化学
无机化学
阳极
共价键
电化学
沉积(地质)
离子
电偶阳极
电极
有机化学
物理化学
古生物学
沉积物
生物
作者
Qianchuan Yu,Tianyu Shen,Si‐Wen Ke,Kaiqiang Zhang,Xinmei Song,Jingjie Sun,Zuoao Wu,Miao Wang,Xin Yang,Zedong Zhang,Anqi Zhang,Zuoxiu Tie,Yichao Yan,Jing Ma,Jing‐Lin Zuo,Zhong Jin
标识
DOI:10.1002/ange.202507352
摘要
Abstract In response to the increasing demand for sustainable energy storage solutions, aqueous zinc‐ion batteries (AZIBs) have garnered significant attention for their high safety, low cost, and environmental friendliness. However, two major challenges to battery stability persist: developing efficient cathode materials and addressing zinc dendrite formation. Here, we report a dual‐functional covalent organic framework (COF), named Ni–DAPTO, designed to improve both Zn 2+ storage on the cathode and zinc deposition kinetics on the anode. The incorporation of Ni coordination centers achieves an expected low energy gap, enhancing the intrinsic conductivity, while selectively guiding uniform Zn 2+ deposition. As a result, the Ni–DAPTO cathode demonstrated superior cycling stability and rate performance, retaining a specific capacity of 127.0 and 119.7 mAh g −1 at 0.5 and 10.0 A g −1 , respectively after 10 000 cycles. Besides, when employed as artificial solid electrolyte interphase (SEI), Ni–DAPTO can improve zinc utilization and inhibit dendrite formation. The full AZIBs assembled with Ni–DAPTO cathodes and Ni–DAPTO modified Zn anodes deliver a discharge capacity of 100.9 mAh g −1 after 1000 cycles at a current density of 5.0 A g −1 . These findings suggest that multifunctional COFs hold great potential for advancing high‐performance and long‐lasting aqueous secondary batteries.
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