Confinement of zinc oxide nanoparticles in ordered mesoporous silica MCM-41

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dc.contributor.authorLihitkar, P.B.en_US
dc.contributor.authorViolet, Samuelen_US
dc.contributor.authorShirolkar, Mandar M.en_US
dc.contributor.authorSingh, Jaien_US
dc.contributor.authorSrivastava, O.N.en_US
dc.contributor.authorNaik, R.H.en_US
dc.contributor.authorKULKARNI, SULABHAen_US
dc.contributor.departmentDept. of Physicsen_US
dc.date.accessioned2019-07-23T11:09:56Z
dc.date.available2019-07-23T11:09:56Z
dc.date.issued2012-04en_US
dc.description.abstractMesoporous silica (MS) and zinc loaded MS composites have been synthesized and characterized using high resolution transmission electron microscopy, X-ray diffraction, UV–visible spectroscopy, photoluminescence spectroscopy, N2 adsorption–desorption isotherms, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. Thermal treatment of the zinc loaded MS composite lead to the formation of ZnO–MS composite. The well ordered uniform pore structure of MS (pore size ∼3.4 nm) is found to remain stable even after 30% Zn loading albeit decrease in the pore size 1.2 nm indicates the formation of ZnO inside the pores.en_US
dc.identifier.citationMaterials Chemistry and Physics, 133(2-3), 850-856.en_US
dc.identifier.issn0254-0584en_US
dc.identifier.sourcetitleMaterials Chemistry and Physicsen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3661
dc.identifier.urihttps://doi.org/10.1016/j.matchemphys.2012.01.106
dc.language.isoenen_US
dc.publication.originofpublisherForeignen_US
dc.publisherElsevier B.V.en_US
dc.subjectMesoporousen_US
dc.subjectPhotoluminescence spectroscopyen_US
dc.subjectSurface propertiesen_US
dc.subjectDefect Energy spectroscopyen_US
dc.subjectChemical analysis (ESCA)en_US
dc.subject2012en_US
dc.titleConfinement of zinc oxide nanoparticles in ordered mesoporous silica MCM-41en_US
dc.typeArticleen_US

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