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Controlled synthesis of hierarchical polyaniline nanowires/ordered bimodal mesoporous carbon nanocomposites with high surface area for supercapacitor electrodes

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dc.title Controlled synthesis of hierarchical polyaniline nanowires/ordered bimodal mesoporous carbon nanocomposites with high surface area for supercapacitor electrodes en
dc.contributor.author Yan, Yanfang
dc.contributor.author Cheng, Qilin
dc.contributor.author Zhu, Zhengju
dc.contributor.author Pavlínek, Vladimír
dc.contributor.author Sáha, Petr
dc.contributor.author Li, Chunzhong
dc.relation.ispartof Journal of Power Sources
dc.identifier.issn 0378-7753 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2013
utb.relation.volume 240
dc.citation.spage 544
dc.citation.epage 550
dc.type article
dc.language.iso en
dc.publisher Elsevier S.A. en
dc.identifier.doi 10.1016/j.jpowsour.2013.03.190
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0378775313006058
dc.subject Electrochemical properties en
dc.subject Nanocomposite en
dc.subject Ordered bimodal mesoporous carbon en
dc.subject Polyaniline nanowires en
dc.description.abstract A facile strategy is developed for the synthesis of hierarchical polyaniline nanowires/ordered bimodal mesoporous carbon (PANI/OBMC) composites via chemical oxidative polymerization. Structural and morphological characterizations indicate that the polyaniline nanowire arrays with 20-30 nm diameters are grown on the surface of the OBMC. The bimodal pore distribution and hierarchical nanostructure endow the PANI/OBMC composite with high surface area of 599 m2 g-1. Electrochemical performance of the hierarchical PANI/OBMC composite as supercapacitor electrode materials has been evaluated by cyclic voltammetry and galvanostatic charge-discharge techniques. The hierarchical composite with 60 wt% PANI possesses the highest specific capacitance of 517 F g-1 and outstanding cycling stability with a capacitance retention of 91.5% after 1000 cycles. The coexistence of primary mesopores and abundant small mesopores is in favor of the fast penetration of electrolyte and the unique hierarchical structure facilitates the ion diffusion and shortens the charge transfer distance, which lead to superior electrochemical performance of PANI/OBMC-60%. © 2013 Elsevier B.V. All rights reserved. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1003244
utb.identifier.obdid 43869818
utb.identifier.scopus 2-s2.0-84877864191
utb.identifier.wok 000321803700067
utb.identifier.coden JPSOD
utb.source j-scopus
dc.date.accessioned 2013-06-05T12:00:08Z
dc.date.available 2013-06-05T12:00:08Z
utb.contributor.internalauthor Cheng, Qilin
utb.contributor.internalauthor Pavlínek, Vladimír
utb.contributor.internalauthor Sáha, Petr
utb.fulltext.affiliation Yanfang Yan a , Qilin Cheng a,b,*, Zhengju Zhu a , Vladimir Pavlinek b , Petr Saha b , Chunzhong Li a,* a Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 200237 Shanghai, China b Centre of Polymer Systems, Polymer Centre, Tomas Bata University in Zlin, nam. T.G. Masaryka 5555, 760 01 Zlin, Czech Republic *Corresponding authors. Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 200237 Shanghai, China. Tel.: þ86 21 64250949; fax: þ8621 64250624. E-mail addresses: chengql@ecust.edu.cn (Q. Cheng), czli@ecust.edu.cn (C. Li).
utb.fulltext.dates Received 19 November 2012 Received in revised form 21 March 2013 Accepted 29 March 2013 Available online 10 April 2013
utb.fulltext.sponsorship This work was supported by the National Natural Science Foundation of China (20925621, 21236003, 21206043), the Shanghai Pujiang Program (12PJ1401900), the Fundamental Research Funds for the Central Universities and the Project sponsored by SRF for ROCS, SEM.
utb.fulltext.faculty University Institute
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Polymer Centre
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