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dc.contributor.authorKemmitt, Tim
dc.contributor.authorIngham, Bridget
dc.contributor.authorLinklater, Rachael Annette
dc.date.accessioned2011-09-01T23:34:06Z
dc.date.available2011-09-01T23:34:06Z
dc.date.issued2011
dc.identifier.citationKemmitt, T., Ingham, B. & Linklater, R.A. (2011). Optimization of Sol–Gel-Formed ZnO:Al Processing Parameters by Observation of Dopant Ion Location Using Solid-State ²⁷Al NMR Spectrometry. The Journal of Physical Chemistry C, 115(30), 15031-15039.en_NZ
dc.identifier.urihttps://hdl.handle.net/10289/5674
dc.description.abstractWe report the discrimination of Al doping sites in sol–gel-formed ZnO powders by solid-state 27Al nuclear magnetic resonance (NMR) spectrometry. A degree of control of dopant placement is demonstrated by modifying sol precursors and processing parameters. ZnO powders containing 1–8 at. % aluminum ions were prepared from aqueous citrate-amino-alcohol-based gels calcined at 500 °C. The powders were characterized using ²⁷Al NMR spectrometry, X-ray diffraction (XRD), and scanning electron microscopy (SEM). Solid-state ²⁷Al NMR spectrometry clearly distinguished between different Al environments and was effective in determining the relative amounts of incorporation of Al dopant ions into the Zn lattice sites in the zincite structure. This allowed a synthesis protocol to be developed to optimize the doping effectiveness. Relatively minor variations in processing conditions could influence the degree and mode of Al incorporation. Optimal conditions were found to include a 90 °C drying step, followed by placement in a preheated (500 °C) furnace for 1 h. An ethanolamine-containing precursor was shown to perform much better than precursors containing alternative amino alcohols.en_NZ
dc.language.isoen
dc.publisherACS Publicationsen_NZ
dc.relation.urihttp://pubs.acs.org/doi/abs/10.1021/jp204283ken_NZ
dc.subjectchemistryen_NZ
dc.titleOptimization of Sol–Gel-Formed ZnO:Al Processing Parameters by Observation of Dopant Ion Location Using Solid-State ²⁷Al NMR Spectrometryen_NZ
dc.typeJournal Articleen_NZ
dc.identifier.doi10.1021/jp204283ken_NZ
dc.relation.isPartOfThe Journal of Physical Chemistryen_NZ
pubs.begin-page15031en_NZ
pubs.elements-id36316
pubs.end-page15039en_NZ
pubs.volume115en_NZ


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