Plasma Treatment of Carbon Nanotubes Applied to Improve the High Performance of Carbon Nanofiber Supercapacitors

被引:24
作者
Chang, Wei-Min [1 ]
Wang, Cheng-Chien [2 ]
Chen, Chuh-Yung [1 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 701, Taiwan
[2] Southern Taiwan Univ Sci & Technol, Dept Chem & Mat Engn, Tainan, Taiwan
关键词
Plasma treatment; Carbon nanotube; Carbon nanofiber; Supercapacitor; Conductivity; DOUBLE-LAYER CAPACITANCE; ACTIVATED CARBON; NITROGEN; CONDUCTIVITY; ELECTROSPUN; COMPOSITES; FIBERS; OXIDE;
D O I
10.1016/j.electacta.2015.11.038
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Plasma-treatment carbon nanotubes (CNTs) grafted with maleic anhydride (MA) were embedded in polyacryonitrile nanofibers via electrospinning and subsequently carbonizated at 800 degrees C to fabricate carbon nanofibers (CNFs). The grafted degree of MA on CNTs (CNTs-MA) was determined via Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The morphology, surface composition and conductivity of the CNTs-MA/CNF were characterized using electron microscopy, X-ray photoelectron and electrochemical impedance spectroscopy, respectively. CNTs-MA not only affected the conductivity of the CNFs but also the types of the nitrogen functional groups that could be represented as active sites on the CNFs to enhance the performance of the supercapacitors. When 2.5 wt.% CNTs-MA was embedded in the CNFs, the highest conductivity was obtained at 5.2 s/cm, and the amount of pyridinic and pyrrolic species increased to 70.3%. However, the highest capacitance was not obtained with 2.5 wt.% CNTs-MA added because of current leakage present in the system. The highest capacitance was 382 F/g with 1.0 wt.% CNTs-MA embedded in CNF with proper conductivity of 2.2 s/cm. Furthermore, galvanostatic charge/discharge, cyclic voltammetry and electrochemical impedance spectroscopy measurements also demonstrated that 1.0 wt.% CNTs-MA embedded in CNF resulted in better electrochemical reversibility and impendence properties. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:530 / 541
页数:12
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