循环伏安法
超级电容器
介电谱
材料科学
共价有机骨架
电容
原电池
电化学
化学工程
储能
电极
离子液体
单体
水平扫描速率
三嗪
化学
聚合物
高分子化学
有机化学
复合材料
多孔性
物理化学
工程类
物理
催化作用
功率(物理)
冶金
量子力学
作者
Piyali Bhanja,Kousik Bhunia,Sabuj Kanti Das,Debabrata Pradhan,Ryuto Kimura,Yuh Hijikata,Stephan Irle,Asim Bhaumik
出处
期刊:Chemsuschem
[Wiley]
日期:2017-01-06
卷期号:10 (5): 921-929
被引量:145
标识
DOI:10.1002/cssc.201601571
摘要
Abstract The new covalent organic framework material TDFP‐1 was prepared through a solvothermal Schiff base condensation reaction of the monomers 1,3,5‐tris‐(4‐aminophenyl)triazine and 2,6‐diformyl‐4‐methylphenol. Owing to its high specific surface area of 651 m 2 g −1 , extended π conjugation, and inherent microporosity, TDFP‐1 exhibited an excellent energy‐storage capacity with a maximum specific capacitance of 354 F g −1 at a scan rate of 2 mV s −1 and good cyclic stability with 95 % retention of its initial specific capacitance after 1000 cycles at 10 A g −1 . The π‐conjugated polymeric framework as well as ionic conductivity owing to the possibility of ion conduction inside the micropores of approximately 1.5 nm make polymeric TDFP‐1 a favorable candidate as a supercapacitor electrode material. The electrochemical properties of this electrode material were measured through cyclic voltammetry, galvanic charge–discharge, and electrochemical impedance spectroscopy, and the results indicate its potential for application in energy‐storage devices.
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