Effect Nd2O3 content on electrochemical performance of polyaniline/Nd2O3 composites

被引:24
作者
Li, Hui [1 ,2 ]
Wang, Shao-Xu [1 ]
Huang, Zihang [1 ]
Zhang, Shihui [1 ]
Li, Yini [1 ]
Han, Liangjun [1 ]
Tan, Zhicheng [3 ]
机构
[1] Dalian Jiaotong Univ, Coll Environm & Chem Engn, Dalian 116028, Peoples R China
[2] Taiyuan Iron & Steel Grp Co Ltd, Taiyuan 030003, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
polyaniline; Nd2O3; composite electrode; electrochemical properties; WALLED CARBON NANOTUBE; ELECTRODE MATERIAL; THERMAL-ANALYSIS; SUPERCAPACITOR; CAPACITANCE; NANOCOMPOSITE;
D O I
10.1002/pat.3372
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyaniline/neodymium(III) oxide (PANI/Nd2O3) composites were synthesized by in situ chemical oxidative polymerization method, and the new electrode materials were used for supercapacitor. The composites were characterized physically by scanning electron microscope (SEM), Fourier transform infrared spectra (FTIR) and X-ray diffraction (XRD). SEM, IR and XRD results showed the existence of interactions between PANI and Nd2O3. The electrochemical capacitance performance of the composites was investigated by cyclic voltammetry, galvanostatic charge-discharge tests and ac impedance spectroscopy with a three-electrode system in 6M KOH solution. Cyclic voltammetry and galvanostatic charge/discharge tests proved that the addition of Nd2O3 enhanced the capacitance of the composites. However, the conductivity of the composites decreases with increasing the amount of Nd2O3. Electrochemical impedance tests manifest that the charge-transfer resistance of the composites is smaller than that of the pure PANI, which indicates the addition of Nd2O3 could lower resistance and facilitate the charge transfer of the active materials. All results support that Nd2O3 has a significant contribution to the performance of PANI and makes the composites have more active sites for faradiac reaction and larger specific capacitance than pure PANI. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:1163 / 1168
页数:6
相关论文
共 36 条
[21]   A scalable CVD synthesis of high-purity single-walled carbon nanotubes with porous MgO as support material [J].
Li, QW ;
Yan, H ;
Cheng, Y ;
Zhang, J ;
Liu, ZF .
JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (04) :1179-1183
[22]  
Liu F. J., 2009, J POWER SOURCES, V117, P6
[23]   Supercapacitor behavior of new substituted manganese dioxides [J].
Machefaux, E. ;
Brousse, T. ;
Belanger, D. ;
Guyomard, D. .
JOURNAL OF POWER SOURCES, 2007, 165 (02) :651-655
[24]   The Scherrer formula for x-ray particle size determination [J].
Patterson, AL .
PHYSICAL REVIEW, 1939, 56 (10) :978-982
[25]   Fabrication and evaluation of 450 F electrochemical redox supercapacitors using inexpensive and high-performance, polyaniline coated, stainless-steel electrodes [J].
Prasad, KR ;
Munichandraiah, N .
JOURNAL OF POWER SOURCES, 2002, 112 (02) :443-451
[26]   Thermal stability, decomposition and glass transition behavior of PANI/NiO composites [J].
Qi, Yanni ;
Zhang, Jian ;
Qiu, Shujun ;
Sun, Lixian ;
Xu, Fen ;
Zhu, Min ;
Ouyang, Liuzhang ;
Sun, Dalin .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2009, 98 (02) :533-537
[27]  
Sabatani E., 2005, J PHYS CHEM, V9, P3660
[28]   Electrochemical performance of polyaniline nanofibres and polyaniline/multi-walled carbon nanotube composite as an electrode material for aqueous redox supercapacitors [J].
Sivakkumar, S. R. ;
Kim, Wan Ju ;
Choi, Ji-Ae ;
MacFarlane, Douglas R. ;
Forsyth, Maria ;
Kim, Dong-Won .
JOURNAL OF POWER SOURCES, 2007, 171 (02) :1062-1068
[29]   High dissolution and strong light emission of carbon nanotubes in aromatic amine solvents [J].
Sun, Y ;
Wilson, SR ;
Schuster, DI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (22) :5348-5349
[30]   Synthesis, characterization and thermal analysis of polyaniline (PANI)/Co3O4 composites [J].
Wang, S. X. ;
Sun, L. X. ;
Tan, Z. C. ;
Xu, F. ;
Li, Y. S. .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2007, 89 (02) :609-612