Please use this identifier to cite or link to this item: https://doi.org/10.1021/cg9007153
DC FieldValue
dc.titleMesoscale Self-Assembly of Highly Luminescent Zinc Tellurite Nanoclusters
dc.contributor.authorBatabyal, S.K.
dc.contributor.authorVenkatram, N.
dc.contributor.authorWei, J.
dc.contributor.authorVittal, J.J.
dc.date.accessioned2014-10-16T08:33:20Z
dc.date.available2014-10-16T08:33:20Z
dc.date.issued2009-11-04
dc.identifier.citationBatabyal, S.K., Venkatram, N., Wei, J., Vittal, J.J. (2009-11-04). Mesoscale Self-Assembly of Highly Luminescent Zinc Tellurite Nanoclusters. Crystal Growth and Design 9 (11) : 4951-4956. ScholarBank@NUS Repository. https://doi.org/10.1021/cg9007153
dc.identifier.issn15287483
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94204
dc.description.abstractZinc tellurite (ZnTeO3 or ZTO) nanoclusters synthesized in aqueous medium from zinc acetate and sodium tellurite are amorphous in nature and exhibit intense photoluminescence when excited at the UV region. These nanoclusters assembled in two different compositions with different morphologies by refluxing in water, depending on the pH of the refluxing medium. At pH 5.5, the ZTO transformed to a crystalline phase with rod-like morphology. At pH 4.5, crystalline Zn2Te3O8 resulted and the as-obtained nanoplates of this compound self-assembled in oval-shaped microstructures. On further decreasing the pH to 3.5, the nanoplates self-assembled to rose-like patterns (nanorose). Very big microspheres and a mixture of microcrystals were formed on further reduction of pH to 3. Interestingly, all the crystalline products with different morphologies display luminescence properties. Further, these new materials exhibit three-photon absorption with positive third-order and negative fifth-order nonlinear refraction. © 2009 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cg9007153
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/cg9007153
dc.description.sourcetitleCrystal Growth and Design
dc.description.volume9
dc.description.issue11
dc.description.page4951-4956
dc.identifier.isiut000271272900055
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