Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/32121
DC FieldValueLanguage
dc.contributorDepartment of Applied Physics-
dc.creatorFei, LF-
dc.creatorSun, TY-
dc.creatorLu, W-
dc.creatorAn, XQ-
dc.creatorHu, ZF-
dc.creatorYu, JC-
dc.creatorZheng, RK-
dc.creatorLi, XM-
dc.creatorChan, HLW-
dc.creatorWang, Y-
dc.date.accessioned2014-12-19T07:00:59Z-
dc.date.available2014-12-19T07:00:59Z-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10397/32121-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleDirect observation of carbon nanostructure growth at liquid-solid interfacesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage826-
dc.identifier.epage828-
dc.identifier.volume50-
dc.identifier.issue7-
dc.identifier.doi10.1039/c3cc46264a-
dcterms.abstractOur TEM observation revealed that in a carbon-Pt3Co system, amorphous carbon first crystallized into nanoclusters at step-edges on melting Pt3Co surfaces before merging into graphene layers through a kinetic restructuring via oriented-attachment, leading to the final formation of few-layered graphene nanostructures. The result obtained from density-functional theory calculations further suggested that Co atoms rather than Pt atoms acted as initial nucleation centers.-
dcterms.bibliographicCitationChemical communications, 2014, v. 50, no. 7, p. 826-828-
dcterms.isPartOfChemical communications-
dcterms.issued2014-
dc.identifier.scopus2-s2.0-84890836286-
dc.identifier.eissn1364-548X-
dc.identifier.rosgroupidr69015-
dc.description.ros2013-2014 > Academic research: refereed > Publication in refereed journal-
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