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dc.contributor.authorSun, Chia-Liangen_US
dc.contributor.authorPao, Chih-Wenen_US
dc.contributor.authorTsai, Huang-Mingen_US
dc.contributor.authorChiou, Jau-Wernen_US
dc.contributor.authorRay, Sekhar C.en_US
dc.contributor.authorWang, Houng-Weien_US
dc.contributor.authorHayashi, Michitoshien_US
dc.contributor.authorChen, Li-Chyongen_US
dc.contributor.authorLin, Hong-Jien_US
dc.contributor.authorLee, Jyh-Fuen_US
dc.contributor.authorChang, Lien_US
dc.contributor.authorTsai, Min-Hsiungen_US
dc.contributor.authorChen, Kuei-Hsienen_US
dc.contributor.authorPong, Way-Faungen_US
dc.date.accessioned2014-12-08T15:31:43Z-
dc.date.available2014-12-08T15:31:43Z-
dc.date.issued2013en_US
dc.identifier.issn2040-3364en_US
dc.identifier.urihttp://hdl.handle.net/11536/22438-
dc.identifier.urihttp://dx.doi.org/10.1039/c3nr01234den_US
dc.description.abstractThe atomistic nucleation sites of Pt nanoparticles (Pt NPs) on N-doped carbon nanotubes (N-CNTs) were investigated using C and N K-edge and Pt L-3-edge X-ray absorption near-edge structure (XANES)/extended X-ray absorption fine structure (EXAFS) spectroscopy. Transmission electron microscopy and XANES/EXAFS results revealed that the self-organized Pt NPs on N-CNTs are uniformly distributed because of the relatively high binding energies of the adsorbed Pt atoms at the imperfect sites. During the atomistic nucleation process of Pt NPs on N-CNTs, stable Pt-C and Pt-N bonds are presumably formed, and charge transfer occurs at the surface/interface of the N-CNTs. The findings in this study were consistent with density functional theory calculations performed using cluster models for the undoped, substitutional-N-doped and pyridine-like-N-doped CNTs.en_US
dc.language.isoen_USen_US
dc.titleAtomistic nucleation sites of Pt nanoparticles on N-doped carbon nanotubesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3nr01234den_US
dc.identifier.journalNANOSCALEen_US
dc.citation.volume5en_US
dc.citation.issue15en_US
dc.citation.spage6812en_US
dc.citation.epage6818en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000321675600023-
dc.citation.woscount8-
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