Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja301805u
DC FieldValue
dc.titleAqueous-phase reactions on hollow silica-encapsulated semiconductor nanoheterostructures
dc.contributor.authorLian, J.
dc.contributor.authorXu, Y.
dc.contributor.authorLin, M.
dc.contributor.authorChan, Y.
dc.date.accessioned2014-10-16T08:20:48Z
dc.date.available2014-10-16T08:20:48Z
dc.date.issued2012-05-30
dc.identifier.citationLian, J., Xu, Y., Lin, M., Chan, Y. (2012-05-30). Aqueous-phase reactions on hollow silica-encapsulated semiconductor nanoheterostructures. Journal of the American Chemical Society 134 (21) : 8754-8757. ScholarBank@NUS Repository. https://doi.org/10.1021/ja301805u
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93135
dc.description.abstractWe introduce a facile and robust methodology for the aggregation-free aqueous-phase synthesis of hierarchically complex metal-semiconductor heterostructures. By encapsulating semiconductor nanostructures within a porous SiO 2 shell with a hollow interior, we can isolate each individual particle while allowing it access to metal precursors for subsequent metal growth. We illustrate this by Pt deposition on CdSe-seeded CdS tetrapods, which we found to be facilitated via the surprising formation of a thin interfacial layer of PtS coated onto the original CdS surface. We took advantage of this unique architecture to perform cation exchange reactions with Ag + and Pd 2+, thus demonstrating the feasibility of achieving such transformations in complex metal-semiconductor nanoparticle systems. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja301805u
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja301805u
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume134
dc.description.issue21
dc.description.page8754-8757
dc.description.codenJACSA
dc.identifier.isiut000304570700007
Appears in Collections:Staff Publications

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