Please use this identifier to cite or link to this item: https://doi.org/10.1111/j.1551-2916.2010.03922.x
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dc.titleMorphology, optical, and magnetic properties of Zn1-xCo xO nanorods grown via a wet chemical route
dc.contributor.authorKartawidjaja, F.C.
dc.contributor.authorLim, Z.Y.
dc.contributor.authorNg, S.L.G.
dc.contributor.authorZhang, Y.
dc.contributor.authorWang, J.
dc.date.accessioned2014-10-07T09:52:13Z
dc.date.available2014-10-07T09:52:13Z
dc.date.issued2010-11
dc.identifier.citationKartawidjaja, F.C., Lim, Z.Y., Ng, S.L.G., Zhang, Y., Wang, J. (2010-11). Morphology, optical, and magnetic properties of Zn1-xCo xO nanorods grown via a wet chemical route. Journal of the American Ceramic Society 93 (11) : 3798-3802. ScholarBank@NUS Repository. https://doi.org/10.1111/j.1551-2916.2010.03922.x
dc.identifier.issn00027820
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86567
dc.description.abstractCo-doped ZnO nanorods (Zn1-xCoxO) with x=0.05, 0.1, and 0.2 were successfully grown on indium-doped tin oxide glass substrates via a wet chemical route at 70°C for 10 h. The effect of Co-doping level on the morphology, crystalline phases, optical, and magnetic properties of the ZnO nanorods was studied. Based on scanning electron microscopy, TEM, and XRD studies, it is confirmed that Co-doped ZnO nanorods were grown along the [0001] direction. Co doping affects the d-spacing and with an increasing Co concentration, the lattice parameter c is increased slightly. The incorporation of Co in ZnO is confirmed with XPS, whereby it is shown that the excitation state of Co is (+2), which rules out the formation of a secondary phase such as Co2O3 or Co3O4, which is consistent with XRD phase analysis results. The near-band edge emission peak of ZnO nanorods is red shifted in response to Co doping, and the band gap energy of (Zn1-xCoxO) nanorods decreases with the increasing Co doping. Zn0.95Co0.05O and Zn0.9Co 0.1O nanorods exhibit a degree of paragmagnetism, while the nanorods with higher Co concentration (Zn0.8Co0.2O) exhibit ferromagnetic behavior at room temperature. © 2010 The American Ceramic Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1111/j.1551-2916.2010.03922.x
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1111/j.1551-2916.2010.03922.x
dc.description.sourcetitleJournal of the American Ceramic Society
dc.description.volume93
dc.description.issue11
dc.description.page3798-3802
dc.identifier.isiut000283987400052
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