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dc.contributor.authorSokołowska, Karolina
dc.contributor.authorLuan, Zhongyue
dc.contributor.authorHulkko, Eero
dc.contributor.authorRameshan, Christoph
dc.contributor.authorBarrabés, Noelia
dc.contributor.authorApkarian, Vartkess A.
dc.contributor.authorLahtinen, Tanja
dc.date.accessioned2020-01-30T11:48:04Z
dc.date.available2020-01-30T11:48:04Z
dc.date.issued2020
dc.identifier.citationSokołowska, K., Luan, Z., Hulkko, E., Rameshan, C., Barrabés, N., Apkarian, V. A., & Lahtinen, T. (2020). Chemically Selective Imaging of Individual Bonds through Scanning Electron Energy-Loss Spectroscopy : Disulfide Bridges Linking Gold Nanoclusters. <i>Journal of Physical Chemistry Letters</i>, <i>11</i>(3), 796-799. <a href="https://doi.org/10.1021/acs.jpclett.9b03496" target="_blank">https://doi.org/10.1021/acs.jpclett.9b03496</a>
dc.identifier.otherCONVID_34190042
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/67629
dc.description.abstractAs proof-of-principle of chemically selective, spatially resolved imaging of individual bonds, we carry out electron energy-loss spectroscopy in a scanning transmission electron microscopy instrument on atomically precise, thiolate-coated gold nanoclusters linked with 5,5′-bis(mercaptomethyl)-2,2′-bipyridine dithiol ligands. The images allow the identification of bridging disulfide bonds (R–S–S–R) between clusters, and X-ray photoelectron spectra support the finding.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofseriesJournal of Physical Chemistry Letters
dc.rightsIn Copyright
dc.subject.otherdisulfides
dc.subject.othersulfur
dc.subject.otherscanning transmission electron microscopy
dc.subject.othergold nanoclusters
dc.titleChemically Selective Imaging of Individual Bonds through Scanning Electron Energy-Loss Spectroscopy : Disulfide Bridges Linking Gold Nanoclusters
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202001301898
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineFysikaalinen kemiafi
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiainePhysical Chemistryen
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange796-799
dc.relation.issn1948-7185
dc.relation.numberinseries3
dc.relation.volume11
dc.type.versionacceptedVersion
dc.rights.copyright© 2020 American Chemical Society
dc.rights.accesslevelopenAccessfi
dc.subject.ysonanohiukkaset
dc.subject.ysoelektronimikroskopia
dc.subject.ysokemialliset sidokset
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p23451
jyx.subject.urihttp://www.yso.fi/onto/yso/p18917
jyx.subject.urihttp://www.yso.fi/onto/yso/p10130
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1021/acs.jpclett.9b03496
jyx.fundinginformationThis work was supported by the National Science Foundation Center for Chemical Innovation on Chemistry at the Space-Time Limit (CaSTL), Grant Number CHE-1414466. STEM-EELS characterization was performed at the user facilities of the UC Irvine Materials Research Institute (IMRI), including instrumentation funded in part by the National Science Foundation Major Research Instrumentation Program under Grant No. CHE-1338173. We thank Dr. Toshiro Aoki for support measuring STEM-EELS at IMRI and C.R. for providing XPS spectra. We acknowledge Zhipei Sun and Mika Pettersson for fruitful discussions and financial support.
dc.type.okmA1


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