Please use this identifier to cite or link to this item: https://doi.org/10.1021/jp053429r
DC FieldValue
dc.titleDodecanethiol-protected copper/silver bimetallic nanoclusters and their surface properties
dc.contributor.authorAng, T.P.
dc.contributor.authorChin, W.S.
dc.date.accessioned2014-10-16T08:26:30Z
dc.date.available2014-10-16T08:26:30Z
dc.date.issued2005-12-01
dc.identifier.citationAng, T.P., Chin, W.S. (2005-12-01). Dodecanethiol-protected copper/silver bimetallic nanoclusters and their surface properties. Journal of Physical Chemistry B 109 (47) : 22228-22236. ScholarBank@NUS Repository. https://doi.org/10.1021/jp053429r
dc.identifier.issn15206106
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93629
dc.description.abstractDodecanèthiol-protected copper/silver bimetallic nanoclusters were prepared by a liquid-phase method using different copper to silver feed ratios. The morphology and size of the prepared nanoclusters were analyzed with X-ray diffraction (XRD) and transmission electron microscopy (TEM), while their spectroscopic and surface properties were characterized by infrared (IR) and X-ray photoelectron spectroscopy (XPS), thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC), and 13C cross-polarization magic angle spinning NMR (13C CPMAS NMR). TEM analysis indicated that all the bimetallic clusters prepared are ∼4-6 nm in size. On the other hand, the results of XRD, XPS, and Fourier transform infrared (FTIR) spectroscopy suggested that the surfaces of the alloy nanoclusters are mostly enriched with the less noble metal copper atoms. This surface enrichment of copper may be attributed to a galvanic exchange process during preparation, and the extent of enrichment is directly related to the copper feed ratio used. Interestingly, DSC studies showed two melting transitions in some of these alloy samples, suggesting different packing behavior of the dodecanethiol chains onto the heterogeneously intercalated silver- and copper-rich surfaces. © 2005 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/jp053429r
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/jp053429r
dc.description.sourcetitleJournal of Physical Chemistry B
dc.description.volume109
dc.description.issue47
dc.description.page22228-22236
dc.description.codenJPCBF
dc.identifier.isiut000233684500023
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