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作 者:Nan Jiang Mengpei Qi Yalong Jiang Yin Fan Shiwei Jin Yingkui Yang
机构地区:[1]School of Chemistry and Materials Science,South-Central Minzu University,Wuhan 430074,China [2]State Key Laboratory of New Textile Materials and Advanced Processing Technologies,Wuhan Textile University,Wuhan 430200,China
出 处:《Energy & Environmental Materials》2024年第6期150-157,共8页能源与环境材料(英文)
基 金:supported by the National Natural Science Foundation of China(Grant No.52173091 and 52102300);the Program for Leading Talents of National Ethnic Affairs Commission of China(MZR21001);the Hubei Provincial Natural Science Foundation of China(2021CFA022).
摘 要:Covalent organic frameworks(COFs)after undergoing the superlithiation process promise high-capacity anodes while suffering from sluggish reaction kinetics and low electrochemical utilization of redox-active sites.Herein,integrating carbon nanotubes(CNTs)with imine-linked covalent organic frameworks(COFs)was rationally executed by in-situ Schiff-base condensation between 1,1′-biphenyl]-3,3′,5,5′-tetracarbaldehyde and 1,4-diaminobenzene in the presence of CNTs to produce core–shell heterostructured composites(CNT@COF).Accordingly,the redox-active shell of COF nanoparticles around one-dimensional conductive CNTs synergistically creates robust three-dimensional hybrid architectures with high specific surface area,thus promoting electron transport and affording abundant active functional groups accessible for electrochemical utilization throughout the whole electrode.Remarkably,upon the full activation with a superlithiation process,the as-fabricated CNT@COF anode achieves a specific capacity of 2324 mAh g^(−1),which is the highest specific capacity among organic electrode materials reported so far.Meanwhile,the superior rate capability and excellent cycling stability are also obtained.The redox reaction mechanisms for the COF moiety were further revealed by Fourier-transform infrared spectroscopy in conjunction with X-ray photoelectron spectroscopy,involving the reversible redox reactions between lithium ions and C=N groups and gradual electrochemical activation of the unsaturated C=C bonds within COFs.
关 键 词:heterostructured anode core-shell nanostructures carbon nanotubes polymeric Schiff-bases covalent organic frameworks
分 类 号:TB383[一般工业技术—材料科学与工程] TM912[电气工程—电力电子与电力传动]
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