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dc.contributor.authorMcDonagh, Birgitte Hjelmeland
dc.contributor.authorSingh, Gurvinder
dc.contributor.authorBandyopadhyay, Sulalit
dc.contributor.authorLystvet, Sina Maria
dc.contributor.authorRyan, Joseph Anthony
dc.contributor.authorVolden, Sondre
dc.contributor.authorKim, Eugene
dc.contributor.authorSandvig, Ioanna
dc.contributor.authorSandvig, Axel
dc.contributor.authorGlomm, Wilhelm
dc.date.accessioned2018-05-08T08:42:39Z
dc.date.available2018-05-08T08:42:39Z
dc.date.created2015-11-24T14:25:51Z
dc.date.issued2015
dc.identifier.citationRSC Advances. 2015, 5 (122), 101101-101109.nb_NO
dc.identifier.issn2046-2069
dc.identifier.urihttp://hdl.handle.net/11250/2497495
dc.description.abstractWhile the size-dependent optical properties of BSA-stabilized gold nanoclusters are well known, the time-dependent growth mechanism remains to be described. Herein, we systematically compare two synthesis methods with and without ascorbic acid, and show that tuning of BSA-stabilized gold nanoclusters (AuNCs) of different sizes can be performed without the aid of an extrinsic reducing agent and with good reproducibility. We also show that adding ascorbic acid yields larger BSA-stabilized gold nanoparticles (AuNPs), and that AuNPs can only form above a threshold gold precursor concentration. Using computed tomography, we describe how these biomineralized AuNPs show size-dependent X-ray attenuation. Growth of BSA-stabilized AuNCs and AuNPs, over a range of gold precursor concentrations, was followed with steady-state fluorescence and UV-vis spectroscopy for one week, constituting the first study of its kind. Based on our results, we propose a mechanism for BSA-stabilization of AuNCs and AuNPs that can further aid in selective growth of discrete AuNCs and AuNPs.nb_NO
dc.language.isoengnb_NO
dc.publisherRoyal Society of Chemistrynb_NO
dc.titleControlling the self-assembly and optical properties of gold nanoclusters and gold nanoparticles biomineralized with bovine serum albuminnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber101101-101109nb_NO
dc.source.volume5nb_NO
dc.source.journalRSC Advancesnb_NO
dc.source.issue122nb_NO
dc.identifier.doi10.1039/c5ra23423a
dc.identifier.cristin1292773
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46056814nb_NO
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46056629nb_NO
dc.relation.projectEU/7F14057nb_NO
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46052400nb_NO
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2015 by Royal Society of Chemistrynb_NO
cristin.unitcode194,66,30,0
cristin.unitcode194,66,35,0
cristin.unitcode194,65,25,0
cristin.unitcode194,65,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.unitnameInstitutt for materialteknologi
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for nevromedisin og bevegelsesvitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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