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Characterization of Sc2O3&CeO2-Stabilized ZrO2 Powders Via Co-Precipitation or Hydrothermal Synthesis

Published online by Cambridge University Press:  06 August 2013

Justyna Grzonka*
Affiliation:
Faculty of Materials Science and Engineering, Warsaw University of Technology, 02-507 Warsaw, Poland
Victor Vereshchak
Affiliation:
Laboratory for Chemistry & Technology of Powder Materials, Ukrainian State University of Chemical Engineering, Dnipropetrovs'k, 49005, Ukraine
Oleksiy Shevchenko
Affiliation:
Frantcevych Institute for Problems of Materials Science, National Academy of Sciences of Ukraine, Kyiv 03680, Ukraine
Oleksandr Vasylyev
Affiliation:
Frantcevych Institute for Problems of Materials Science, National Academy of Sciences of Ukraine, Kyiv 03680, Ukraine
Krzysztof J. Kurzydłowski
Affiliation:
Faculty of Materials Science and Engineering, Warsaw University of Technology, 02-507 Warsaw, Poland
*
*Corresponding author. E-mail: [email protected]
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Abstract

As the presence of Sc2O3 and CeO2 is known to largely enhance the ionic conductivity in the temperature range of 600–800°C, compared with the conventional yttria-stabilized ZrO2, Sc2O3&CeO2-stabilized ZrO2 provide its applicability as electrolytes in solid oxide fuel cells. The current study introduces the methodology to synthesize Sc2O3&CeO2-stabilized ZrO2 powders by using co-precipitation technique or high-temperature hydrothermal reaction, and further describes the structural characterization of the zirconia powders synthesized by the above-mentioned two methods. The co-precipitation technique was found to allow obtaining powders of cubic phase, whereas high-temperature hydrothermal synthesis results in the presence of a monoclinic phase as well. The scanning transmission electron microscope observations also confirm that the size of the synthesized ZrO2 powders in this study is found to be much smaller than that of commercially available powders.

Type
Research Article
Copyright
Copyright © Microscopy Society of America 2013 

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References

Baur, E. & Preis, H. (1937). Über Brennstoff-ketten mit Festleitern. Zeitschrift für Elektrochemie 43, 727732.Google Scholar
Haering, C., Roosen, A., Schichl, H. & Schnöller, M. (2005). Degradation of the electrical conductivity in stabilized zirconia system. Part II: Scandia-stabilized zirconia. Solid State Ionics 176, 261268.10.1016/j.ssi.2004.07.039Google Scholar
Kilner, J.A. & Brook, R.J. (1982). A study of oxygen ion conductivity in doped nonstoichiometric oxides. Solid State Ionics 6, 237252.Google Scholar
Lei, Z. & Zhu, Q. (2005). Low temperature processing of dense nanocrystalline scandia-doped zirconia (ScSZ) ceramics. Solid State Ionics 176, 27912797.Google Scholar
Lei, Z., Zhu, Q. & Zhang, S. (2006). Nanocrystalline scandia-doped zirconia (ScSZ) powders prepared by a glycine-nitrate solution combustion route. J Eur Ceram Soc 26, 397401.10.1016/j.jeurceramsoc.2005.06.007Google Scholar
Mizutani, Y., Tamura, M., Kawai, M. & Yamamoto, O. (1994). Development of high-performance electrolyte in SOFC. Solid State Ionics 72, 271275.10.1016/0167-2738(94)90158-9Google Scholar
Okamoto, M., Akimune, Y., Furuya, K., Hatano, M., Yamanaka, M. & Uchiyama, M. (2005). Phase transition and electrical conductivity of scandia-stabilized zirconia prepared by spark plasma sintering process. Solid State Ionics 176, 675680.10.1016/j.ssi.2004.10.022Google Scholar
Tietz, F., Fischer, W., Hauber, T. & Mariotto, G. (1997). Structural evolution of Sc-containing zirconia electrolytes. Solid State Ionics 100, 289295.10.1016/S0167-2738(97)00356-1Google Scholar
Tu, H., Liu, X. & Yu, Q. (2011). Synthesis and characterization of Scandia ceria stabilized zirconia powders prepared by polymeric precursor method for integration into anode-supported solid oxide fuel cells. Power Sources 196, 31093113.10.1016/j.jpowsour.2010.11.108Google Scholar