水溶液
阴极
锌
碳纤维
离子
材料科学
化学工程
化学
冶金
复合材料
工程类
有机化学
物理化学
复合数
作者
Tianbing Song,Qianli Ma,Baojuan Wang,Xirong Zhang,Yonggang Wang,Huan‐Ming Xiong
标识
DOI:10.1002/anie.202503655
摘要
Carbon dots (CDs) have been explored widely in the electrochemistry field owing to their unique structures and rich properties. However, in the reported devices, such as batteries and supercapacitors, CDs are always used as additives to modify the electrodes or regulate the electrolytes, because they have been regarded as inert and low‐capacity materials all along. Here for the first time, o‐phenylenediamine derived CDs are selected as the only protagonist to construct cathode materials for aqueous zinc‐ion batteries (ZIBs). Such CDs (p‐CDs) have a special π‐conjugated phenazine‐based structure, with carbon cores for electrical conductivity and active sites for embedding Zn2+ and H+. The p‐CDs solely constructed cathode material delivers a decent capacity of 290 mAh g‐1 at 0.1 A g‐1, and a superior capacity of 103 mAh g‐1 at an ultra‐high current density of 10 A g‐1, as well as an ultrahigh ion diffusion coefficient of 10‐8 ~ 10‐7 cm2 s‐1. The p‐CDs assembled ZIBs exhibits a stable long‐term cycling, retaining 87.4% of the original capacity after 10000 cycles. Various characterizations and theoretical calculations prove that the electron‐deficient N as the active sites on p‐CDs can embed/release Zn2+ and H+ reversibly.
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