Please use this identifier to cite or link to this item: https://doi.org/10.1039/b509223j
DC FieldValue
dc.titleRe-examining the origins of spectral blinking in single-molecule and single-nanoparticle SERS
dc.contributor.authorEmory, S.R.
dc.contributor.authorJensen, R.A.
dc.contributor.authorWenda, T.
dc.contributor.authorHan, M.
dc.contributor.authorNie, S.
dc.date.accessioned2014-06-19T08:59:08Z
dc.date.available2014-06-19T08:59:08Z
dc.date.issued2006
dc.identifier.citationEmory, S.R., Jensen, R.A., Wenda, T., Han, M., Nie, S. (2006). Re-examining the origins of spectral blinking in single-molecule and single-nanoparticle SERS. Faraday Discussions 132 : 249-259. ScholarBank@NUS Repository. https://doi.org/10.1039/b509223j
dc.identifier.issn13596640
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/74929
dc.description.abstractSingle metal nanoparticles and nanoaggregates are known to emit intense bursts of surface-enhanced Raman scattering (SERS) in an intermittent on and off fashion. The characteristic "blinking" timescales range from milliseconds to seconds. Here we report detailed temperature dependence (both heating and cooling) and light-intensity studies to further examine the origins of this intriguing phenomenon. The results indicate that blinking SERS contains both a thermo-activated component and a light-induced component. Several lines of evidence suggest that the observed fluctuations are caused by thermally activated diffusion of individual molecules on the particle surface, coupled with photo-induced electron transfer and structural relaxation of surface active sites or atomic-scale roughness features. © The Royal Society of Chemistry 2005.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b509223j
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1039/b509223j
dc.description.sourcetitleFaraday Discussions
dc.description.volume132
dc.description.page249-259
dc.identifier.isiut000236772600020
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