Synthesis of mesoporous polythiophene/MnO2 nanocomposite and its enhanced pseudocapacitive properties

被引:150
作者
Lu, Qing [1 ]
Zhou, Yikai [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, MOE Key Lab Environm & Hlth, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
Manganese oxide; Polythiophene; Mesoporous nanocomposite; Supercapacitor; MANGANESE OXIDE NANOCOMPOSITE; ELECTROCHEMICAL PROPERTIES; NANOSTRUCTURED MATERIALS; COMPOSITE ELECTRODES; ENERGY-CONVERSION; MNO2; PERFORMANCE; CAPACITANCE; DEPOSITION; NANOTUBES;
D O I
10.1016/j.jpowsour.2010.12.059
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mesoporous nanocomposite of polythiophene and MnO2 has been synthesized by a modified interfacial method, aiming to develop electrode materials for supercapactitors with an enhanced cycle performance and high-rate capability. The N-2 adsorption/desorption isotherm test of the prepared hybrid indicates a high surface area and a typical mesoporous feature. A uniform hierarchical microstructure with submicron-spheres assembled from ultrathin nanosheet with diameters less than 10 nm has been confirmed by field-emission scanning electron microscopy and transmission electron microscopy. The employed interfacial synthesis is found to be advantageous to retard the overgrowth of nuclei. The retention of 97.3% of its initial capacitance after 1000 cycles at a charge/discharge rate of 2 A g(-1) indicates excellent cycle performance of the nanocomposite electrode. At a high-rate charge/discharge process of 10 A g(-1), the nanocomposite electrode retained 76.6% of its capacitance at 1 A g(-1), suggesting good high-power capability. The important roles of polythiophene in the as-prepared nanocomposite are highlighted in terms of their functions on enhancing the electrical conductivity and constraining the dissolution of manganese oxides during charge-discharge cycles. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:4088 / 4094
页数:7
相关论文
共 49 条
[1]   Nanostructured materials for advanced energy conversion and storage devices [J].
Aricò, AS ;
Bruce, P ;
Scrosati, B ;
Tarascon, JM ;
Van Schalkwijk, W .
NATURE MATERIALS, 2005, 4 (05) :366-377
[2]   Variation of the MnO2 birnessite structure upon charge/discharge in an electrochemical supercapacitor electrode in aqueous Na2SO4 electrolyte [J].
Athouel, Laurence ;
Moser, Francois ;
Dugas, Romain ;
Crosnier, Olivier ;
Belanger, Daniel ;
Brousse, Thierry .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (18) :7270-7277
[3]  
Belanger D., 2008, Interface, V17, P49
[4]   Electrochemical Properties of Poly(3,4-ethylenedioxythiophene)/Manganese Oxide Synthesized by Interfacial Polymerization [J].
Chen Li ;
Zhang Xiao-Gang ;
Yuan Chang-Zhou ;
Chen Sheng-Yao .
ACTA PHYSICO-CHIMICA SINICA, 2009, 25 (02) :304-308
[5]   Material and electrochemical characterization of tetrapropylammonium manganese oxide thin films as novel electrode materials for electrochemical capacitors [J].
Chin, SF ;
Pang, SC ;
Anderson, MA .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (04) :A379-A384
[6]   Effect of crystallographic structure of MnO2 on its electrochemical capacitance properties [J].
Devaraj, S. ;
Munichandraiah, N. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (11) :4406-4417
[7]   Electroless deposition of nanoscale MnO2 on ultraporous carbon nanoarchitectures:: Correlation of evolving pore-solid structure and electrochemical performance [J].
Fischer, Anne E. ;
Saunders, Matthew P. ;
Pettigrew, Katherine A. ;
Rolison, Debra R. ;
Long, Jeffrey W. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (03) :A246-A252
[8]   Microstructural Effects on Charge-Storage Properties in MnO2-Based Electrochemical Supercapacitors [J].
Ghodbane, Ouassim ;
Pascal, Jean-Louis ;
Favier, Frederic .
ACS APPLIED MATERIALS & INTERFACES, 2009, 1 (05) :1130-1139
[9]   Nanostructured materials for electrochemical energy conversion and storage devices [J].
Guo, Yu-Guo ;
Hu, Jin-Song ;
Wan, Li-Jun .
ADVANCED MATERIALS, 2008, 20 (15) :2878-2887
[10]   Ideal capacitive behavior of hydrous manganese oxide prepared by anodic deposition [J].
Hu, CC ;
Tsou, TW .
ELECTROCHEMISTRY COMMUNICATIONS, 2002, 4 (02) :105-109