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dc.contributor.authorSINGH, SUKHVINDERen_US
dc.contributor.authorSRINIVASA, RSen_US
dc.contributor.authorTALWAR, SSen_US
dc.contributor.authorMAJOR, SSen_US
dc.date.accessioned2009-04-24T09:12:37Zen_US
dc.date.accessioned2011-12-08T06:27:25Zen_US
dc.date.accessioned2011-12-26T13:01:37Zen_US
dc.date.accessioned2011-12-27T05:45:36Z
dc.date.available2009-04-24T09:12:37Zen_US
dc.date.available2011-12-08T06:27:25Zen_US
dc.date.available2011-12-26T13:01:37Zen_US
dc.date.available2011-12-27T05:45:36Z
dc.date.issued2007en_US
dc.identifier.citationThin Solid Films 515(24), 8714-8717en_US
dc.identifier.issn0040-6090en_US
dc.identifier.uri10.1016/j.tsf.2007.03.178en_US
dc.identifier.urihttp://hdl.handle.net/10054/1233en_US
dc.identifier.urihttp://dspace.library.iitb.ac.in/xmlui/handle/10054/1233en_US
dc.description.abstractZnO and Zn1−xCdxO nanocrystallites were prepared by oxidation of zinc arachidate–arachidic acid and zinc arachidate–cadmium arachidate–arachidic acid LB multilayers, respectively. The metal content of the multilayers was controlled by manipulation of subphase composition and pH. Precursor multilayers were oxidized in the temperature range of 400 °C–700 °C. The formation of ZnO and Zn1−xCdxO was confirmed by UV–Visible spectroscopy. Uniformly distributed, isolated and nearly mono-dispersed nanocrystallites of ZnO (11 ± 3 nm) and Zn1−xCdxO (18 ± 6 nm) were obtained.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPh Effectsen_US
dc.subjectOxidationen_US
dc.subjectNanocrystallitesen_US
dc.subjectLangmuir Blodgett Filmsen_US
dc.titleZnO and Zn1-xCdxO nanocrystallites obtained by oxidation of precursor Langmuir-Blodgett multilayersen_US
dc.typeArticleen_US
dc.description.copyright© Elsevieren_US


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