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Updated: May 26, 2026

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Dual-ion Co-storage in a donor-acceptor covalent organic framework for high-performance low-temperature
Xinya Zhang1, Shuangqin Yang1, Yihao Zhang1
1College of Energy Materials and Chemistry, State Key Laboratory of New Textile Materials and Advanced Processing, Inner Mongolia University Hohhot 010070 China yuanchen@imu.edu.cn zwzhao@imu.edu.cn.
Abstract:
The development of covalent organic framework (COF) cathodes for low-temperature sodium-ion batteries (SIBs) remains challenging due to sluggish reaction kinetics at low temperatures. Herein, we demonstrate a donor-acceptor (D-A) covalent organic framework constructed from p-type triphenylamine and n-type naphthalimide units as a robust cathode for low-temperature SIBs. The stable naphthalimide-based building blocks endow the constructed D-A framework with faster charge transport capability and enhanced redox kinetics, achieving a capacity of 135 mAh g-1 at 0.1 A g-1 and an impressive capacity retention of 80% after 2000 cycles at 1 A g-1. Remarkably, it maintains high capacities of 108 mAh g-1 at 0 °C and 85 mAh g-1 at -20 °C, with a capacity retention rate of 91% after 300 cycles at -20 °C. The dual-ion co-storage mechanism of Na+ and PF6 - has been elucidated through in situ spectroscopic characterization and theoretical calculations. This work provides a feasible molecular design strategy towards stable and high-performance porous organic cathodes for low-temperature SIBs.
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