Yu Qianchuan, Shen Tianyu, Ke Si-Wen, Zhang Kaiqiang, Song Xinmei, Sun Jingjie, Wu Zuoao, Wang Miao, Yang Yongxin, Zhang Zedong, Zhang Anqi, Tie Zuoxiu, Yan Yichao, Ma Jing, Zuo Jinglin, Jin Zhong
State Key Laboratory of Coordination Chemistry, MOE Key Laboratory of Mesoscopic Chemistry, MOE Key Laboratory of High Performance Polymer Materials and Technology, Jiangsu Key Laboratory of Advanced Organic Materials, Suzhou Key Laboratory of Green Intelligent Manufacturing of New Energy Materials and Devices, Tianchang New Materials and Energy Technology Research Center, Institute of Green Chemistry and Engineering, School of Chemistry and Chemical Engineering, School of Sustainable Energy and Resources, Nanjing University, Nanjing, Jiangsu, 210023, P.R. China.
College of Chemistry and Materials Science, Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, Anhui Key Laboratory of Functional Molecular Solids, Anhui Normal University, 189 Jiuhua Southern Road, Wuhu, 241002, P.R. China.
Angew Chem Int Ed Engl. 2025 Jul 29:e202507352. doi: 10.1002/anie.202507352.
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 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 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 at 0.5 and 10.0 A g, 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 after 1000 cycles at a current density of 5.0 A g. These findings suggest that multifunctional COFs hold great potential for advancing high-performance and long-lasting aqueous secondary batteries.
为响应可持续储能解决方案日益增长的需求,水系锌离子电池(AZIBs)因其高安全性、低成本和环境友好性而备受关注。然而,电池稳定性仍存在两个主要挑战:开发高效的阴极材料和解决锌枝晶的形成问题。在此,我们报道了一种双功能共价有机框架(COF),名为Ni-DAPTO,旨在改善阴极上的锌存储以及阳极上的锌沉积动力学。引入镍配位中心实现了预期的低能隙,提高了本征导电性,同时选择性地引导均匀的锌沉积。结果,Ni-DAPTO阴极表现出卓越的循环稳定性和倍率性能,在10000次循环后,在0.5和10.0 A g的电流密度下分别保持127.0和119.7 mAh g的比容量。此外,当用作人工固体电解质界面(SEI)时,Ni-DAPTO可以提高锌的利用率并抑制枝晶形成。采用Ni-DAPTO阴极和Ni-DAPTO改性锌阳极组装的全水系锌离子电池在5.0 A g的电流密度下循环1000次后,放电容量为100.9 mAh g。这些发现表明,多功能COF在推进高性能和长寿命水系二次电池方面具有巨大潜力。