超级电容器
氨基
材料科学
氢氧化钾
聚合物
碳纤维
化学工程
碳化
微型多孔材料
电容
无机化学
电极
化学
有机化学
复合材料
物理化学
扫描电子显微镜
复合数
工程类
作者
Fei Li,Xinhua Huang,Nuoya Wang,Xingxing Zhu,Vincent Chan,Ruikun Zhao,Yimin Chao
标识
DOI:10.1002/celc.202001165
摘要
Abstract In this study, a polymer‐containing aminal and imine (C=N) linkages was synthesized from the reaction between p‐phthalaldehyde and 2,6‐diaminepyridine through nucleophilic addition. Subsequently, nitrogen‐doped carbon nanospheres (N‐CNSs) were fabricated by a process of sequential potassium hydroxide (KOH) activation and direct carbonization of the polymer. Interestingly, the mass ratio ( x ) of the polymer to KOH was found to play a crucial role in dictating the porosity, surface chemistry, and capacitive performance of the resulting CNSs. The optimization of x led to the formation of N‐CNS‐2 with a significantly larger specific surface area (809 m 2 g −1 , 98 % microporous content) and a high specific capacitance (732 F g −1 ) at 8 A g −1 in 6 M KOH aqueous electrolyte. In addition, the electrode fabricated with N‐CNS‐2 showed excellent cycling stability along with 98 % of the initial specific capacitance after 5000 charge/discharge cycles. The carbon precursor with the aminal linkage network has shown very promising potential in energy storage materials.
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