Differences in single and aggregated nanoparticle plasmon spectroscopy

dc.bibliographicCitation.date2015
dc.bibliographicCitation.firstPage2991
dc.bibliographicCitation.issue5
dc.bibliographicCitation.journalTitlePhysical chemistry, chemical physics : PCCPeng
dc.bibliographicCitation.lastPage2995
dc.bibliographicCitation.volume17
dc.contributor.authorSingh, Pushkar
dc.contributor.authorDeckert-Gaudig, Tanja
dc.contributor.authorSchneidewind, Henrik
dc.contributor.authorKirsch, Konstantin
dc.contributor.authorvan Schrojenstein Lantman, Evelien M.
dc.contributor.authorWeckhuysen, Bert M.
dc.contributor.authorDeckert, Volker
dc.date.accessioned2022-06-27T08:33:48Z
dc.date.available2022-06-27T08:33:48Z
dc.date.issued2014
dc.description.abstractVibrational spectroscopy usually provides structural information averaged over many molecules. We report a larger peak position variation and reproducibly smaller FWHM of TERS spectra compared to SERS spectra indicating that the number of molecules excited in a TERS experiment is extremely low. Thus, orientational averaging effects are suppressed and micro ensembles are investigated. This is shown for a thiophenol molecule adsorbed on Au nanoplates and nanoparticles.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/9286
dc.identifier.urihttps://doi.org/10.34657/8324
dc.language.isoengeng
dc.publisherCambridge : RSC Publ.
dc.relation.doihttps://doi.org/10.1039/c4cp04850d
dc.relation.essn1463-9084
dc.rights.licenseCC BY 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/
dc.subject.ddc540
dc.titleDifferences in single and aggregated nanoparticle plasmon spectroscopyeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTger
wgl.subjectChemieger
wgl.subjectPhysikger
wgl.typeZeitschriftenartikelger
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