High‐Capacity and Long‐Life Cathode Constructed Solely by Carbon Dots for Aqueous Zinc‐Ion Batteries

T Tian‐Bing Song (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 China) Q Qian‐Li Ma (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 China) B Bao‐Juan Wang (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China) X Xi‐Rong Zhang (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China) Y Yong‐Gang Wang (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China) H Huan‐Ming Xiong (Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China)

Abstract

Abstract 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 Zn 2+ and H + . The p‐CDs solely constructed cathode material delivers a superior capacity of 290 mAh g −1 at 0.1 A g −1 and a decent 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  cm 2 s −1 . The p‐CDs assembled ZIBs exhibit a stable long‐term cycling, retaining 87.4% of the original capacity after 10 000 cycles. Various characterizations and theoretical calculations prove that the electron‐deficient N as the active sites on p‐CDs can embed/release Zn 2+ and H + reversibly.

Article Details

Volume / Issue Vol. 64, Issue 34
Published August 18, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

T

Tian‐Bing Song

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 China

Q

Qian‐Li Ma

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 China

B

Bao‐Juan Wang

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China

X

Xi‐Rong Zhang

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China

Y

Yong‐Gang Wang

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China

H

Huan‐Ming Xiong

Department of Chemistry Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling Fudan University Shanghai 200438 P.R. China