微型多孔材料
碳化
超级电容器
聚吡咯
材料科学
化学工程
碳纤维
聚合
比表面积
多孔介质
多孔性
电容
纳米技术
聚合物
化学
有机化学
催化作用
电极
扫描电子显微镜
复合材料
复合数
工程类
物理化学
作者
Fei Xu,Yongjie Lai,Ruowen Fu,Dingcai Wu
摘要
Controlling carbon frameworks of nanocarbons from microporous to nonporous without imposing any additional treatment on a given type of precursor currently remains a great challenge. Here, a facile approach for tailoring different pore characteristics of carbon frameworks for nanocarbons from polypyrrole (PPy) precursors has been achieved based on the significant effect of reaction medium on the conjugation degree of PPy chains. Nanocarbon from PPy synthesized in NaOH solution (CPPy-NaOH) has numerous micropores with a BET surface area up to 482 m2 g−1, which is 10-fold higher than that of nanocarbon with an almost nonporous carbon framework from PPy polymerized in HCl solution (CPPy-HCl). This could be attributed to a distinct difference in the conjugation degree of the PPy chains. A much lower conjugation degree for the PPy precursor of CPPy-NaOH facilitates formation of micropores during carbonization. CPPy-NaOH exhibits much higher specific capacitance than CPPy-HCl. Furthermore, CPPy-NaOH gives much larger surface efficiency and higher capacitance retention ratios as compared to a commercial activated carbon for supercapacitors.
科研通智能强力驱动
Strongly Powered by AbleSci AI