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dc.contributor.authorKelly, Anna T.
Filgueira, Carly S.
Schipper, Desmond E.
Halas, Naomi J.
Whitmire, Kenton H.
dc.date.accessioned 2017-05-23T19:32:18Z
dc.date.available 2017-05-23T19:32:18Z
dc.date.issued 2017
dc.identifier.citation Kelly, Anna T., Filgueira, Carly S., Schipper, Desmond E., et al.. "Gold coated iron phosphide core–shell structures." RSC Advances, 7, (2017) Royal Society of Chemistry: 25848-25854. https://doi.org/10.1039/C7RA01195D.
dc.identifier.urihttps://hdl.handle.net/1911/94359
dc.description.abstract Core–shell particles Fe2P@Au have been prepared beginning with Fe2P nanorods, nanocrosses and nanobundles prepared from the solvothermal decomposition of H2Fe3(CO)9(μ3-PtBu). Iron phosphide structures can be produced from a single-source organometallic precursor with morphological control by varying the surfactant conditions to yield fiber bundles and dumbbell-shaped bundles ranging from nanometers to microns. Derivatization of the surfaces with γ-aminobutyric acid was used to attach Au nanoparticle seeds to the surface of the Fe2P nanoparticles followed by completion of the Au shell by reduction with formaldehyde or aqueous HAuCl4/CO, with the latter giving somewhat better results. Shell thickness ranged from an incomplete, partially coated Au shell to a thickness of 65 ± 21 nm by varying the amount of gold decorated precursor particles. Increasing the thicknesses of the Au shells produced a redshift in the plasmonic resonance of the resulting structures as was observed previously for FeOx@Au.
dc.language.iso eng
dc.publisher Royal Society of Chemistry
dc.rights This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/
dc.title Gold coated iron phosphide core–shell structures
dc.type Journal article
dc.citation.journalTitle RSC Advances
dc.citation.volumeNumber 7
dc.type.dcmi Text
dc.identifier.doihttps://doi.org/10.1039/C7RA01195D
dc.type.publication publisher version
dc.citation.firstpage 25848
dc.citation.lastpage 25854


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