材料科学
超级电容器
氟化物
氨
钴
咪唑酯
沸石咪唑盐骨架
无机化学
衍生工具(金融)
比表面积
法拉第效率
氟
配体(生物化学)
化学工程
电容
电极
金属有机骨架
有机化学
电解质
化学
物理化学
催化作用
吸附
冶金
经济
受体
金融经济学
生物化学
工程类
作者
Chung‐Hsien Wu,Yung‐Fu Wu,Pin‐Yan Lee,Sibidou Yougbaré,Lu‐Yin Lin
标识
DOI:10.1021/acsami.2c09787
摘要
The zeolitic imidazolate framework 67 (ZIF67) derivative is a potential active material of supercapacitors (SC), owing to high specific surface area and porosity and possible formation of cobalt compounds. A novel ZIF67 derivative is synthesized using a one-step solution process with cobalt precursor 2-methylimidazole (2-Melm) and ammonia fluoride in our previous work. Due to its facile synthesis and excellent electrocapacitive behavior, it is crucial to understand the competition between ammonia fluoride and 2-Melm on forming derivatives with cobalt ions and to create more efficient ZIF67 derivatives for charge storage. In this work, several ZIF67 derivatives are designed using a one-step solution process with 2-Melm and ammonia fluoride incorporated in different sequences. The reaction durations for a single ligand and two ligands are controlled. The largest capacity of 176.33 mAh/g corresponding to the specific capacitance of 1057.99 F/g is achieved for the ZIF67 derivative electrode prepared by reacting ammonia fluoride and a cobalt precursor for 0.5 h and then incorporating 2-Melm for another 23.5 h of reaction (NM0.5). This derivative composed of highly conductive CoF2, NiF2, Co(OH)F, and Ni(OH)F presents high specific surface area and porosity. The relevant SC presents a maximum energy density of 19.5 Wh/kg at 430 W/kg, a capacity retention of 92%, and Coulombic efficiency of 96% in 10000 cycles.
科研通智能强力驱动
Strongly Powered by AbleSci AI