This work focuses on the microwave-assisted hydrothermal synthesis of praseodymium-doped zirconia and on the subsequent evaluation of the effect of synthesis conditions on powder properties. Pure and 10 mol% Pr-doped zirconia samples have been analyzed by X-ray diffraction (XRD) and the perturbed angular correlations hyperfine technique, which probes the nearest environments of zirconium ions. At atomic scale, as determined from perturbed angular correlation data, the XRD amorphous fraction of the as-obtained powders exhibits a tetragonal-like structure. The pure powder becomes partially stabilized and the doped powder is a substitutional solid solution of praseodymium in tetragonal zirconia.
Microwave-hydrothermal synthesis and hyperfine characterization of praseodymium-doped nanometric zirconia powders / F., Bondioli; Leonelli, Cristina; Manfredini, Tiziano; Ferrari, Anna Maria; M. C., Caracoche; P. C., Rivas; A. M., Rodriguez. - In: JOURNAL OF THE AMERICAN CERAMIC SOCIETY. - ISSN 0002-7820. - STAMPA. - 88:3(2005), pp. 633-638. [10.1111/j.1551-2916.2005.00093.x]
Microwave-hydrothermal synthesis and hyperfine characterization of praseodymium-doped nanometric zirconia powders
LEONELLI, Cristina;MANFREDINI, Tiziano;FERRARI, Anna Maria;
2005
Abstract
This work focuses on the microwave-assisted hydrothermal synthesis of praseodymium-doped zirconia and on the subsequent evaluation of the effect of synthesis conditions on powder properties. Pure and 10 mol% Pr-doped zirconia samples have been analyzed by X-ray diffraction (XRD) and the perturbed angular correlations hyperfine technique, which probes the nearest environments of zirconium ions. At atomic scale, as determined from perturbed angular correlation data, the XRD amorphous fraction of the as-obtained powders exhibits a tetragonal-like structure. The pure powder becomes partially stabilized and the doped powder is a substitutional solid solution of praseodymium in tetragonal zirconia.File | Dimensione | Formato | |
---|---|---|---|
2005_ZrPrPAC_J. Am. Ceram. Soc., 88 [3] 633–638.pdf
Accesso riservato
Tipologia:
Versione pubblicata dall'editore
Dimensione
467.77 kB
Formato
Adobe PDF
|
467.77 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
Pubblicazioni consigliate
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris