阳极
共价有机骨架
锂(药物)
离子
聚酰亚胺
共价键
电流密度
共轭体系
电池(电)
氧化还原
锂离子电池
材料科学
酰亚胺
化学工程
化学
纳米技术
聚合物
高分子化学
复合材料
有机化学
电极
物理
物理化学
冶金
内分泌学
量子力学
功率(物理)
医学
工程类
图层(电子)
作者
Yue Qian,Zhoujia Liu,Haixin Song,Ruize Yin,Hanni Yang,Siyang Li,Weiwei Xiong,Sàisài Yuán,Junhao Zhang,Huan Pang
标识
DOI:10.1016/j.cclet.2023.108785
摘要
Covalent organic frameworks (COFs) exhibiting reversible redox behaviors have been identified as promising candidates for constructing electrode materials in lithium-ion batteries (LIBs). However, their extensive application has been limited due to finite redox sites and poor structural stability. In this study, we design and synthesize a novel polyimide covalent organic framework (PI-COF) using the traditional solvothermal method and successfully apply it as an anode material for LIBs. The large conjugated structure of PI-COF accelerates charge transfer, while its large surface area provides more active sites, making PI-COF an attractive anode material for LIBs. Furthermore, the PI-COF anode material demonstrates high reversible specific capacity and excellent long-term cycling stability due to its COF characteristics. Specifically, the PI-COF electrodes deliver a specific capacity of 800 mAh/g at a current density of 200 mA/g after 200 cycles, while a specific capacity of 450 mAh/g at a current density of 1000 mA/g is sustained after 800 cycles. The outstanding lithium storage capacity, particularly the satisfactory long-term cycling stability, establishes PI-COF as a promising material for LIBs.
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