TY - JOUR
T1 - Transformation of Yttrium-Doped Hydrated Zirconium into Tetragonal and Cubic Nanocrystalline Zirconia
AU - Bokhimi, X.
AU - Morales, A.
AU - García-Ruiz, A.
AU - Xiao, T. D.
AU - Chen, H.
AU - Strutt, P. R.
PY - 1999/2/1
Y1 - 1999/2/1
N2 - Nanostructured yttrium-stabilized zirconia powders, with yttria concentrations between 0.0 and 10.0 mol%, were prepared via the hydrolysis of an aqueous solution of zirconyl and yttrium chloride, and ammonium hydroxide. Powder phases were characterized by using X-ray powder diffraction; their crystalline structures were refined with the Rietveld technique. When samples were annealed below 200°C, their diffraction patterns corresponded to an amorphous atom distribution and were independent of yttria concentration. The doped amorphous phases crystallized, at 400°C, into tetragonal or cubic nanocrystalline zirconia, which were stabilized by yttrium. These results suggest that yttrium atoms served as a substitute for zirconium atoms not only in the crystalline phases but also in the amorphous phases, which are determined by the fast condensation of zirconyl clusters. Nondoped samples contained a mixture of monoclinic and tetragonal nanocrystalline zirconia; those with 2.5 to 5.0 mol% yttria contained only the tetragonal zirconia nanophase, and those with 7.5 to 10.0 mol% had only the nanocrystalline cubic phase. The average crystallite size of the nanophases diminished when Y2O3concentration was increased.
AB - Nanostructured yttrium-stabilized zirconia powders, with yttria concentrations between 0.0 and 10.0 mol%, were prepared via the hydrolysis of an aqueous solution of zirconyl and yttrium chloride, and ammonium hydroxide. Powder phases were characterized by using X-ray powder diffraction; their crystalline structures were refined with the Rietveld technique. When samples were annealed below 200°C, their diffraction patterns corresponded to an amorphous atom distribution and were independent of yttria concentration. The doped amorphous phases crystallized, at 400°C, into tetragonal or cubic nanocrystalline zirconia, which were stabilized by yttrium. These results suggest that yttrium atoms served as a substitute for zirconium atoms not only in the crystalline phases but also in the amorphous phases, which are determined by the fast condensation of zirconyl clusters. Nondoped samples contained a mixture of monoclinic and tetragonal nanocrystalline zirconia; those with 2.5 to 5.0 mol% yttria contained only the tetragonal zirconia nanophase, and those with 7.5 to 10.0 mol% had only the nanocrystalline cubic phase. The average crystallite size of the nanophases diminished when Y2O3concentration was increased.
KW - Cubic zirconia
KW - Hydrated zirconium
KW - Nanocrystalline zirconia
KW - Rietveld technique
KW - Tetragonal zirconia
KW - X-ray diffraction
KW - Yttrium-doped zirconia
KW - Zirconyl cluster
UR - http://www.scopus.com/inward/record.url?scp=0001652691&partnerID=8YFLogxK
U2 - 10.1006/jssc.1998.8056
DO - 10.1006/jssc.1998.8056
M3 - Artículo
SN - 0022-4596
VL - 142
SP - 409
EP - 418
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
IS - 2
ER -