碳纤维
化学工程
超级电容器
材料科学
电解质
杂原子
吸附
多孔性
比表面积
纳米技术
惰性气体
烷基
催化作用
化学
电容
有机化学
电极
复合材料
复合数
工程类
物理化学
作者
Juan Du,Miao Li,Junzhen Song,Xueqing Gao,Senlin Hou,Aibing Chen
标识
DOI:10.1016/j.jcis.2022.09.113
摘要
Carbonaceous materials with diverse morphologies have shown unique and excellent performance in many fields, such as catalysis, adsorption, separation and energy storage. However, regulating the structural changes of these morphologies accurately using simple approaches is a difficult process. In this study, porous carbon materials with a morphology that changed from carbon spindles to fold-carbon spheres and then to regular carbon spheres were prepared assisted by in-situ activator of KNO3 in co-assembly of resorcinol/phenol resin and 1-alkyl-3-methylimidazolium bromide. The activation of KNO3 greatly improves the hydrophily, pore volume and surface area of the inert carbon skeleton, and increases heteroatom defects for the carbon framework. As electrode materials of supercapacitors, the influence of different structures on energy storage performance was studied. The obtained fold-carbon spheres showed a higher capacitance (405 F g-1) than flake, spindle and spherical porous carbon, which is due to convenient electrolyte transmission and completely available active sites.
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