Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja073521w
DC FieldValue
dc.titleHollowing Sn-doped TiO2nanospheres via Ostwald ripening
dc.contributor.authorLi, J.
dc.contributor.authorHua, C.Z.
dc.date.accessioned2011-09-26T09:20:24Z
dc.date.available2011-09-26T09:20:24Z
dc.date.issued2007
dc.identifier.citationLi, J., Hua, C.Z. (2007). Hollowing Sn-doped TiO2nanospheres via Ostwald ripening. Journal of the American Chemical Society 129 (51) : 15839-15847. ScholarBank@NUS Repository. https://doi.org/10.1021/ja073521w
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/26594
dc.description.abstractThe well-known physical phenomenon Ostwald ripening in crystal growth has been widely employed in template-free fabrication of hollow inorganic nanostructures in recent years. Nevertheless, all reported works so far are limited only to stoichiometric phase-pure solids. In this work we describe the first investigation of doped (nonstoichiometric) materials using Ostwald ripening as a means of creating interior space. In particular, we chose the xSnO2-(1 - x)TiO2 binary system to establish preparative principles for this approach in synthesis of structurally and compositionally complex nanomaterials. In this study, uniform Sn-doped TiO2 nanospheres with hollow interiors in 100% morphological yield have been prepared with an aqueous inorganic route under hydrothermal conditions. Furthermore, our structural and surface analyses indicate that Sn4+ ions can be introduced linearly into TiO2, and preferred structural phase(s) can also be attained (e.g., either anatase or rutile, or their mixtures). Fluoride anions of starting reagents are adsorbed on the surface sites of oxygen. The resultant anion overlayer may contribute to stabilization of surface and creation of repulsive interaction among the freestanding nanospheres. On the basis of these findings, we demonstrate that Ostwald ripening can now be employed as a general hollowing approach to architect interior spaces for both simple and complex nanostructures. © 2007 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja073521w
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.contributor.departmentOPHTHALMOLOGY
dc.description.doi10.1021/ja073521w
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume129
dc.description.issue51
dc.description.page15839-15847
dc.identifier.isiut000251974000033
dc.published.statePublished
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