共价有机骨架
碳纳米管
阴极
氧化还原
共价键
芘
化学工程
电化学
复合数
材料科学
离子键合
多孔性
离子
纳米技术
纳米管
化学
电极
无机化学
复合材料
有机化学
物理化学
工程类
作者
Lei Chen,Yuke Li,Yuemiao Zhang,Shi‐Bin Ren,Jinhai Bi,Xinxian Xue,Deman Han,Di Wu,Yujing Wang,Xianlang Chen,Yingpeng Wu
标识
DOI:10.1016/j.cej.2024.154743
摘要
Covalent organic frameworks (COFs) have attracted significant interest in the field of rechargeable batteries on account of their unique properties, including robust frameworks, well-defined porosity, abundant redox-active sites, and flexible structure designability. However, the limited active site utilization and low electrical conductivity always bring about poor electrochemical performance, thereby hindering practical applications. Herein, we reported a pyrene-4,5,9,10-tetraone-based covalent organic framework composite (Tp-PTO-COF@CNTs) grown on multi-walled carbon nanotubes via in-situ polycondensation. The Tp-PTO-COF@CNTs with numerous active sites (C=O groups) and strong π-π interaction between CNTs and COFs could accommodate more Na-ions and boost structural stability. Moreover, the existence of 1D CNTs could improve electronic conductivity, which facilitates fast transport of electrons and enhances reaction kinetics. In view of the two synergistic effects, Tp- PTO-COF@CNTs cathode displays an outstanding sodium-ion storage property with high initial capacity of 223.2 mA h/g at 0.1 A/g, remarkable rate capability at as high as 20 A/g, and ultra-long cycling stability (163.0 mA h/g exceeding 5000 cycles at 5 A/g). Furthermore, the ex-situ measurements are proposed to better confirm the role of carbonyl groups as redox-active centers. Such ultra-stable structural advantage might inspire the development of COF cathode materials for sodium-ion batteries.
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