Two-dimensional conjugated N-rich covalent organic frameworks for superior sodium storage

被引:28
作者
Yang, Xiya [1 ]
Jin, Yucheng [1 ]
Yu, Baoqiu [1 ]
Gong, Lei [1 ]
Liu, Wenbo [1 ]
Liu, Xiaolin [1 ]
Chen, Xin [1 ]
Wang, Kang [1 ]
Jiang, Jianzhuang [1 ]
机构
[1] Univ Sci & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing Key Lab Sci & Applicat Funct Mol & Crysta, Dept Chem & Chem Engn,Sch Chem & Biol Engn, Beijing 100083, Peoples R China
关键词
covalent organic frameworks; sodium-ion batteries; phthalocyanine; anode materials; pi-conjugated 2D COFs; ELECTROCHEMICAL ENERGY-STORAGE; ION BATTERIES; STRATEGIES;
D O I
10.1007/s11426-022-1269-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sodium-ion batteries (SIBs) are considered as a promising next-generation energy storage system. To achieve the large-scale application of SIBs, it is crucial to develop cost-effective anode materials with high Na-ion storage capacity. Herein two-dimensional (2D) conjugated covalent organic frameworks (cCOFs) with N-rich phthalocyanine (Pc) units fused via benzene moieties (named MPc-2D-cCOFs) were explored as the SIBs anode materials. Electrochemical tests reveal their high reversible capacities of 538 and 342 mA h g(-1) at 50 and 1000 mA g(-1), respectively, good rate performance, and excellent stability, comparable to the state-of-the-art anode materials of SIBs, indicating their outstanding Na-ion storage performance. Ex situ X-ray photoelectron and Fourier transform infrared spectroscopies together with theoretical calculations disclose the N atoms at the pore channels and conjugated pyrrole moieties of MPc-2D-cCOFs provide abundant Na-ion storage sites. This, in cooperation with the enhanced electrical conductivity owing to the 2D conjugated structure, contributes to the outstanding Na-ion storage capacity of MPc-2D-cCOFs. The present result is surely helpful for developing high-performance and cost-effective COFs as electroactive materials for SIBs.
引用
收藏
页码:1291 / 1298
页数:8
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