电解质
化学工程
超级电容器
材料科学
碳纤维
电化学
多孔性
石墨烯
比表面积
纳米片
电导率
纳米技术
化学
复合数
电极
有机化学
复合材料
催化作用
工程类
物理化学
作者
Panpan Chang,Xuguang Li,Linze Li,Jirui Wang,Jinshi Dong,Ting Yang,Jingying Duan
标识
DOI:10.1016/j.cej.2023.146732
摘要
The operating voltage of over 3.0 V is a severe challenge for commercial supercapacitors in organic electrolyte, which raises rigorous requirements for the structure and composition characteristics of porous carbon. There are few reports regarding the construction of ultra-high voltage withstanding porous carbon derived from cheap biomass carbon sources. Herein, using cheap and renewable fulvic acid (FA) and graphene oxide (GO) as carbon precursors, the ultra-high withstanding voltage 2D porous carbon nanosheets are synthesized through KOH activation and annealing treatment, assisted by the π-π conjugation and hydrogen bonding. The incorporation of GO plays an important role in modulating the 2D nanosheet morphology of FA derived porous carbon, enhancing the e-conductivity and reducing the OFGs of porous carbons, which makes significant contribution to improving the structural stability and electrochemical performance of material. The obtained FG1% C/C composite simultaneously exhibits high specific surface area (2593 m2/g) and desirable e-conductivity (101 S m−1). More critically, it possesses highly stable surface chemical microenvironment with very-low surface oxygen content of 2.7 at.%, mainly existing as stable ether and quinone bonds. Thus, FG1% exerts ultra-high withstanding voltage up to 3.3 V in commercial TEABF4/PC electrolyte with the maximum energy density of 68.6 Wh kg−1, superior to most of the literatures, also it shows excellent stability throughout its lifespan, maintaining improved capacity retention rate (88.9%) at 2.5 A/g over 10,000 cycles. This work pares the way for the architecture design of high withstanding voltage porous carbon.
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