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New insights on physico-chemical transformations of ZnO: From clustered multipods to single crystalline nanoplates

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dc.contributor.author Anas, S
dc.contributor.author Mahesh, K V
dc.contributor.author Ambily, K J
dc.contributor.author Chandran, M R
dc.contributor.author Uma, K
dc.contributor.author Warrier, K G K
dc.contributor.author Ananthakumar, S
dc.date.accessioned 2013-06-13T09:32:09Z
dc.date.available 2013-06-13T09:32:09Z
dc.date.issued 2012-05-15
dc.identifier.citation Materials Chemistry and Physics 134(1):435-442;15 May 2012 en_US
dc.identifier.uri http://hdl.handle.net/123456789/451
dc.description.abstract Physico-chemical transformations of ZnO have been investigated in low temperature reflux reactions involving zinc nitrate, arious ZnO micro/nano structures were systematically examined from 4 to 60 h. The study showed the formation and transformation of multidimensional ZnO structures such as multipods,microtubes, microplates, nanoplates, nanoflowers, nanoblades and diffused nano networked structures including single crystalline nanoplates in a simple reflux synthesis. The crystalline nature, phase purity,associated structural features and surface characteristics were studied using powder X-ray, Raman, SEM,TEM, AFM, FT-IR, XPS and TG analytical techniques and the results were discussed. The kinetics involved in the evolution of ZnO structures and % yield of the ZnO products has also been studied and a possible growth mechanism is proposed on the basis of time-triggered transformations. The inherent anisotropic nature of ZnO as well as the change in chemical environment over the time of reflux is found to control the growth and evolution of diverse ZnO morphologies en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Nanostructures en_US
dc.subject Chemical synthesis en_US
dc.subject Electron microscopy en_US
dc.subject Microstructures en_US
dc.title New insights on physico-chemical transformations of ZnO: From clustered multipods to single crystalline nanoplates en_US
dc.type Article en_US
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