杂原子
超级电容器
法拉第效率
电容
材料科学
化学工程
储能
碳纤维
多孔性
兴奋剂
共价键
共价有机骨架
纳米技术
电极
电化学
有机化学
化学
光电子学
复合数
物理化学
复合材料
戒指(化学)
功率(物理)
工程类
物理
量子力学
作者
Yue Wang,Jifan Zhao,Yuzhu Xing,Yan Dong,Zhong Lin Wang,Yasushi Hasebe,Ray H. Baughman
标识
DOI:10.1002/asia.202400930
摘要
Heteroatom‐doped porous carbons (HPCs) have been considered promising electrode materials for supercapacitors due to their improvement of energy density by providing extra pseudocapacity. Covalent organic frameworks (COFs) are obtaining great importance in energy storage because of their designable structure and versatile functionality. Herein, we designed and fabricated oxygen and sulfur dual‐doped covalent organic framework (COF) derived HPCs with very high heteroatoms content (up to 25.76 atom%) via a facile coupling reaction. The optimized HPCs exhibit a porous structure with high specific surface area (up to 2835 m2 g‐1) along with a high specific capacitance (430 F g‐1 at 0.5 A g‐1), excellent capacitance retention (96.9%), and high coulombic efficiency (98.5%) after 10000 cycles at 5 A g‐1. As electrodes for aqueous symmetric supercapacitors, the HPCs exhibits a high energy density of 60 Wh kg‐1 at a 250 W kg‐1 power density, excellent cycling stability of capacity retention (82.2%) and a high coulombic efficiency (92.3%) after 10000 cycles at 10 A g‐1, indicating attractive application potential in chemical energy storage. This work establishes a promising strategy for preparation of high heteroatom content HPCs using COFs and demonstrates great potential for energy storage/conversion devices.
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