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dc.contributor.authorLi, Heng
dc.contributor.author李恒
dc.contributor.authorNie, Jia Cai
dc.contributor.authorKunsagi-Mate, Sandor
dc.date.accessioned2013-04-11T08:24:43Z
dc.date.available2013-04-11T08:24:43Z
dc.date.issued2012-04-02
dc.identifier.citationCHEMICAL PHYSICS LETTERS,2012,531:183-187zh_CN
dc.identifier.issn0009-2614
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2012.02.033
dc.identifier.uriWOS:000301931800035
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/15576
dc.description.abstractMultiwalled carbon nanotubes (MWCNTs) were etched by EtOH treating. Such treated MWCNTs were deposited from solution phase onto the nanostructured CeO2 films. High resolution images by both transmission and scanning electron microscopy showed that the nanographite fractions are existed in the solution and they were also reorganized on the surface. On the nanostructured surface of specific morphology, the nanographite fractions are deposited into the valleys between the CeO2 islands and therefore a selective pattern of nanographite was formed. Molecular dynamics calculations highlighted that adsorption and reorganization properties of the nanographite layers have considerable dependence on the morphology of CeO2 nanostructures. (C) 2012 Elsevier B.V. All rights reserved.zh_CN
dc.description.sponsorshipChinese-Hungarian Intergovernmental S&T Cooperation Programme [CH-5-21/2010, TET_10-1-2011-0126]; National Natural Science Foundation of China [91121012, 51172029, 50772015, 10974019]; Fundamental Research Funds for the Central Universities of China; Developing Competitiveness of Universities in the South Transdanubian Region [SROP-4.2.1.B-10/2/KONV-2010-0002]; Laboratory of Organic Optoelectronic Functional Materials and Molecular Engineering, TIPC, CASzh_CN
dc.language.isoenzh_CN
dc.publisherELSEVIER SCIENCE BVzh_CN
dc.subjectCARBON NANOTUBESzh_CN
dc.subjectRAMAN-SPECTROSCOPYzh_CN
dc.titleEtOH induced formation of nanographite fractions and their reorganization on nanostructured CeO2 filmszh_CN
dc.typeArticlezh_CN


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