微型多孔材料
假电容
儿茶酚
热解
对苯二酚
碳纤维
材料科学
化学工程
无机化学
化学
复合材料
有机化学
超级电容器
工程类
物理化学
复合数
电极
电化学
作者
Junyan Wang,Xinta Li,Kesong Tian,Wanchun Guo,Bosen Zhang,Jiamin Zhang,Mengran Li,Zhankun Xing,Xueai Li,Junjie Xu,Haiyan Wang
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-09-03
卷期号:6 (10): 4571-4580
标识
DOI:10.1021/acsmaterialslett.4c01175
摘要
Unavoidable complicated oxygen functionalities in porous carbons restrict identification of their electrochemically active sites. Herein, we report 3D interconnected macroporous/microporous catechol-enriched carbon through first-step low-temperature pyrolysis and second-step melted KOH etching of resorcinol-formaldehyde resin and its excellent pseudocapacitance. First, high-content hydroxyl groups in a carbonaceous framework stem from preservation after low-temperature pyrolysis and introduction after KOH treatment. Second, molten KOH removes some carbon atoms in carbonaceous resin to form micropores and unstable domains to form macropores. Third, molten KOH promotes removal of some sp3-carbon atoms and/or their conversion to sp2-carbon atoms, forming a large-size conjugated plane to ensure electrical conductivity. Obvious reversible redox conversion between catechol and quinone groups during charge/discharge according to ex-situ O 1s XPS and GCD/CV analyses reliably confirms accessible catechol configurations in macro/microporous carbon as pseudocapacitive sites. Catechol-enriched carbon could be expanded to explore more electrochemical mechanisms.
科研通智能强力驱动
Strongly Powered by AbleSci AI