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dc.contributor.authorWattanavichean, Nungniten_US
dc.contributor.authorGilby, Matthewen_US
dc.contributor.authorNichols, Richard J.en_US
dc.contributor.authorArnolds, Heikeen_US
dc.date.accessioned2019-04-02T05:58:16Z-
dc.date.available2019-04-02T05:58:16Z-
dc.date.issued2019-02-19en_US
dc.identifier.issn0003-2700en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.analchem.8b03576en_US
dc.identifier.urihttp://hdl.handle.net/11536/148918-
dc.description.abstractVibrational modes play a key role in characterizing metal-molecule-metal junctions, but their detection currently either requires single-molecule sensitivity or the generation of defect-free large-scale junctions. Here we demonstrate that surface-enhanced Raman scattering (SERS) on nonideal surfaces can provide a significant amount of information despite many defects in the layer. We determine the vibrational signature of the molecular electronic junction for palladium ions complexed and reduced on 4-mercaptopyridine adsorbed on rough gold and gold nanoparticles using SERS and density functional theory. We show that these nonideal surfaces can be used to probe kinetics of metal ion complexation and establish the success of electrochemical metallization. SERS on nonideal surfaces is thus revealed as a useful tool to rapidly establish the key process parameters in making molecular electronic junctions before embarking on more detailed studies on single molecules or single crystal surfaces.en_US
dc.language.isoen_USen_US
dc.titleDetection of Metal-Molecule-Metal Junction Formation by Surface Enhanced Raman Spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.analchem.8b03576en_US
dc.identifier.journalANALYTICAL CHEMISTRYen_US
dc.citation.volume91en_US
dc.citation.spage2644en_US
dc.citation.epage2651en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000459642400014en_US
dc.citation.woscount0en_US
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