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Crystallization in hafnia‐ and zirconia‐based systems
Author(s) -
Ushakov S. V.,
Navrotsky A.,
Yang Y.,
Stemmer S.,
Kukli K.,
Ritala M.,
Leskelä M. A.,
Fejes P.,
Demkov A.,
Wang C.,
Nguyen B.Y.,
Triyoso D.,
Tobin P.
Publication year - 2004
Publication title -
physica status solidi (b)
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.51
H-Index - 109
eISSN - 1521-3951
pISSN - 0370-1972
DOI - 10.1002/pssb.200404935
Subject(s) - hafnia , crystallization , cubic zirconia , materials science , amorphous solid , tetragonal crystal system , monoclinic crystal system , chemical engineering , mineralogy , crystallography , metallurgy , crystal structure , chemistry , ceramic , engineering
Abstract Crystallization of hafnia and zirconia and their alloys with silica and lanthana was studied in bulk and thin film samples by thermal analysis, X‐ray diffraction and electron microscopy. Crystallization temperatures of hafnia and zirconia increase by more than 300 °C with increase of surface/interface area of the amorphous phase. Crystallization temperatures of zirconia and hafnia alloys with silica and lanthana increase with dopant content and exceed 900 °C for 50 mol% SiO 2 and LaO 1.5 . Energies for tetragonal HfO 2 and ZrO 2 interfaces with amorphous silica were derived from their crystallization enthalpies from silicates as 0.25 ± 0.08 and 0.13 ± 0.07 J/m 2 , respectively. The crystallization pathways in bulk powders and films of zirconia and hafnia can be interpreted as resulting from thermodynamic stabilization by the surface energy term of tetragonal and amorphous phases over monoclinic. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)