Please use this identifier to cite or link to this item: https://doi.org/10.1021/la802805w
DC FieldValue
dc.titleEngineering inorganic hybrid nanoparticles: Tuning combination fashions of gold, platinum, and iron oxide
dc.contributor.authorZhang, H.-T.
dc.contributor.authorDing, J.
dc.contributor.authorChow, G.-M.
dc.contributor.authorDong, Z.-L.
dc.date.accessioned2014-06-17T07:58:22Z
dc.date.available2014-06-17T07:58:22Z
dc.date.issued2008-11-18
dc.identifier.citationZhang, H.-T., Ding, J., Chow, G.-M., Dong, Z.-L. (2008-11-18). Engineering inorganic hybrid nanoparticles: Tuning combination fashions of gold, platinum, and iron oxide. Langmuir 24 (22) : 13197-13202. ScholarBank@NUS Repository. https://doi.org/10.1021/la802805w
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64863
dc.description.abstractMultistep colloidal chemical routes were employed to synthesize Pt/Au, Pt/iron oxide (IO), and Au/Pt/IO hybrid nanoparticles (NPs). The starting templates, Pt NPs, were synthesized by controlling the decomposition kinetics of platinum acetylacetonate in oleylamine. The morphologies of binary metal Pt/Au hybrid NPs were modulated by controllable attachment of Au nanoscale domains to Pt templates. Similarly, Pt/IO and Au/Pt/IO hybrid NPs were fabricated by the controllable attachment of Fe to the Pt or Pt/Au template NPs. The noble metal domains of as-prepared hybrid NPs had face center cubic crystal structures and did not alloy, as verified by high resolution transmission electron microscopy and X-ray diffraction spectrometry. X-ray diffraction spectrometry study indicates that the IO domains in the as-prepared NPs have a spinel structure. UV-vis study of binary metal Pt/Au hybrid NPs revealed that they have a characteristic plasmon resonance around 525 nm, while dumbbell-like Au/Pt/IO NPs had a plasmon resonance around 600 nm. Furthermore, magnetism study of the binary Pt-IO NPs clearly indicated that the interfacial interactions between Pt and IO domains could result in a shift of the blocking temperature. © 2008 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/la802805w
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1021/la802805w
dc.description.sourcetitleLangmuir
dc.description.volume24
dc.description.issue22
dc.description.page13197-13202
dc.description.codenLANGD
dc.identifier.isiut000260874800067
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