Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja302518n
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dc.titleHollow and cage-bell structured nanomaterials of noble metals
dc.contributor.authorLiu, H.
dc.contributor.authorQu, J.
dc.contributor.authorChen, Y.
dc.contributor.authorLi, J.
dc.contributor.authorYe, F.
dc.contributor.authorLee, J.Y.
dc.contributor.authorYang, J.
dc.date.accessioned2014-10-09T06:50:13Z
dc.date.available2014-10-09T06:50:13Z
dc.date.issued2012-07-18
dc.identifier.citationLiu, H., Qu, J., Chen, Y., Li, J., Ye, F., Lee, J.Y., Yang, J. (2012-07-18). Hollow and cage-bell structured nanomaterials of noble metals. Journal of the American Chemical Society 134 (28) : 11602-11610. ScholarBank@NUS Repository. https://doi.org/10.1021/ja302518n
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/89123
dc.description.abstractMastery of the structure of nanomaterials enables control of their properties to enhance their performance for a given application. Herein we demonstrate the synthesis of metal nanomaterials with hollow interiors or cage-bell structures based on the inside-out diffusion of Ag in core-shell structured nanoparticles. It begins with the synthesis of core-shell Ag-M or core-shell-shell M A-Ag-M B nanoparticles in an organic solvent. Ag is then extracted from the core or the inner shell by bis(p-sulfonatophenyl)phenylphosphane, which binds strongly with Ag(I)/Ag(0) to allow the complete removal of Ag in 24-48 h, leaving behind an organosol of hollow or cage-bell structured metal nanomaterials. Because of their relatively lower densities, which usually translate to a higher surface area than their solid counterparts, the hollow and cage-bell structured metal nanomaterials are especially relevant to catalysis. For example, cage-bell structured Pt-Ru nanoparticles were found to display outstanding methanol tolerance for the cathode reaction of direct methanol fuel cells (DMFCs) as a result of the differential diffusion of methanol and oxygen in the cage-bell structure. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja302518n
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/ja302518n
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume134
dc.description.issue28
dc.description.page11602-11610
dc.description.codenJACSA
dc.identifier.isiut000306457900049
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