详细信息
Fabrication and electrochemical characterization of polyaniline nanorods modified with sulfonated carbon nanotubes for supercapacitor applications ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Fabrication and electrochemical characterization of polyaniline nanorods modified with sulfonated carbon nanotubes for supercapacitor applications
作者:Zhu, Zhong-ze[1];Wang, Geng-chao[1];Sun, Min-qiang[1];Li, Xing-wei[1];Li, Chun-zhong[1]
机构:[1]E China Univ Sci & Technol, Key Lab Ultrafine Mat, Sch Mat Sci & Engn, Shanghai Key Lab Adv Polymer Mat,Minist Educ, Shanghai 200237, Peoples R China
年份:2011
卷号:56
期号:3
起止页码:1366
外文期刊名:ELECTROCHIMICA ACTA
收录:;EI(收录号:20105213523208);WOS:【SCI-EXPANDED(收录号:WOS:000289225400050)】;
基金:We greatly appreciate the financial supports of Shanghai Municipal Science and Technology Commission (0852nm02000), National Natural Science Foundation of China (50773020), Innovation Program of Shanghai Municipal Education Commission (11ZZ55), Shanghai Leading Academic Discipline Project (B502) and Shanghai Key Laboratory Project (08DZ2230500).
语种:英文
外文关键词:Polyaniline nanorods; Functionalized carbon nanotubes; Electrochemical properties; Supercapacitors
摘要:The novel composites of sulfonated multi-walled carbon nanotubes (sMWCNTs) modified polyaniline (PANI) nanorods (PANI/sMWCNTs) were synthesized successfully by in situ oxidative polymerization method in the HClO4 solution. FTIR and Raman spectra revealed the presence of pi-pi interaction between the PANI and the sulfonated carbon nanotubes and the formation of charge transfer composites. It was found that the specific capacitance of the PANI/sMWCNT composites was markedly influenced by their morphological structure and the content of PANI which was coated onto the sMWCNT. The specific capacitance of the PANI/sMWCNT composite exhibited a maximum value of 515.2 F g(-1) at the 76.4 wt% PANI. The charge-discharge tests showed the PANI/sMWCNT composites possessed a good cycling stability (below 10% capacity loss after 1000 cycles) compared to PANI nanorods. (C) 2010 Elsevier Ltd. All rights reserved.
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