On the agent role of Mn 2+ in redirecting the synthesis of Zn(OH) 2 towards nano-ZnO with variable morphology
One of the simplest routes to prepare polycrystalline Zn(OH) 2 is by coprecipitation, with zinc nitrate as a cation source. However, the addition of even minute amounts of manganese nitrate to the precursors used to prepare pure Zn(OH) 2 results in Mn 2+ doped nanostructured ZnO. The comparison with...
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Veröffentlicht in: | RSC advances 2016, Vol.6 (108), p.106732-106741 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | One of the simplest routes to prepare polycrystalline Zn(OH)
2
is by coprecipitation, with zinc nitrate as a cation source. However, the addition of even minute amounts of manganese nitrate to the precursors used to prepare pure Zn(OH)
2
results in Mn
2+
doped nanostructured ZnO. The comparison with other Mn
2+
doped metal hydroxides prepared by the same coprecipitation method, involving metal nitrates precursors, shows that this behavior is unique, pertaining only to Zn(OH)
2
. A systematic study of the samples prepared without and with variable amounts of Mn
2+
ions, in the 1 to 5000 ppm nominal concentrations range showed that the re-routing of the reaction takes place even for the lowest nominal dopant concentration of 1 ppm. According to X-ray diffraction, transmission electron microscopy and Fourier transform infrared spectroscopy investigations, both crystallite size and morphology of the resulting nanostructured ZnO samples varied with the Mn
2+
nominal concentration. Moreover, quantitative electron paramagnetic resonance investigations showed that the incorporation rate of the Mn
2+
ions at different sites in the nanostructured ZnO depended on the nominal Mn
2+
concentration. The results are discussed in terms of the coordination properties of the Mn
2+
and Zn
2+
ions and the nature of the reaction precursors. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C6RA23065B |