Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-27T02:22:37.259Z Has data issue: false hasContentIssue false

Hydrothermal Synthesis and Properties of Ceria Solid Electrolytes

Published online by Cambridge University Press:  10 February 2011

M. Greenblatt
Affiliation:
Department of Chemistry, Rutgers, the State University of New Jersey, 610 Taylor Rd, Piscataway, NJ 08854–8087, [email protected]
W. Huang
Affiliation:
Department of Chemistry, Rutgers, the State University of New Jersey, 610 Taylor Rd, Piscataway, NJ 08854–8087, [email protected]
P. Shuk
Affiliation:
Department of Chemistry, Rutgers, the State University of New Jersey, 610 Taylor Rd, Piscataway, NJ 08854–8087, [email protected]
Get access

Abstract

The structure, thermal expansion coefficients and ionic/electronic conductivity of (Ce1−xSmx)1-y(Tb/Pr)yO2-x/2)+δ (x=0–0.30; y=0–0.10) and Ce1−xCaxO2-x ( x= 0–0.17) solid electrolytes prepared hydrothermally were investigated. The uniformly small particle size (7–68 nm) of the hydrothermally prepared materials allows sintering of the samples into highly dense ceramic pellets at 1400°C, a significantly lower temperature, compared to that at 1600–1650°C required for samples prepared by solid state techniques. The maximum ionic conductivity in Ce1−x(Sm/Ca)xO2-δ was found at x= 0.17 for the Sm (σ600°c = 5.7×10−3 S/cm). In (Ceo0.83Sm0.17)1-y(Tb/Pr)yO1.915+δ the maximum conductivity was found at y= 0.17 for the Pr and Tb substituted ceria (σ600°c=7.6x10−3S/cm, Ea= 0.55 eV and σ600°c = 10−2 S/cm, Ea= 0.72 eV respectively) with electronic contribution to total conductivity around 20–30 %. When the Tb or Pr substitution in Ce0.83Sm0.17OO1.915 is reduced, the conductivity becomes more ionic, and is purely ionic at 2 %. However the conductivity at this lower level doping is not significantly lower.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Trovarelli, A.,. Catal. Rev. - Sci. Eng. 38, 439 (1996).10.1080/01614949608006464Google Scholar
2. Inaba, H. and Tagawa, H., Solid State Ionics 83, 1 (1996).10.1016/0167-2738(95)00229-4Google Scholar
3. Takahashi, T. and Kozawa, A., eds. Application of Solid Electrolytes (JEC Press, Ohio, 1980).Google Scholar
4. Takahashi, T., ed. High Conductivity Solid Ionic Conductors (World Scientific, Singapore, 1989).10.1142/0729Google Scholar
5. Göpel, W., Jones, T. A., Kleitz, M., Lundström, I. and Seiyama, T, eds. Chemical and Biochemical Sensors, Vol. 2, 3 ( VCH, Weinheim, 1991/1992).10.1002/9783527620142Google Scholar
6. Etsell, T. H. and Flengas, S. N., Chem. Rev. 70, 339 (1970).10.1021/cr60265a003Google Scholar
7. Badwal, S. P. S., ed. Science and Technology of Zirconia (Technomic, Lancaster, 1993).Google Scholar
8. Takahashi, T. and Iwahara, H., Mat. Res. Bull. 13, 1447 (1978).10.1016/0025-5408(78)90138-1Google Scholar
9. Shuk, P., Wiemhöfer, H.-D., Guth, U., Göpel, W. and Greenblatt, M., Solid State Ionics 89, 179 (1996).10.1016/0167-2738(96)00348-7Google Scholar
10. Egushi, K., Setoguchi, T., Inoue, T., Arai, H., Solid State Ionics 52, 165 (1992).10.1016/0167-2738(92)90102-UGoogle Scholar
11. Zhou, Y. C. and Rahaman, M. N., J. Mater. Res. 8, 1680 (1993).10.1557/JMR.1993.1680Google Scholar
12. Yamashita, K., Ramanujachary, K. V., Greenblatt, M., Solid State Ionics 81, 53 (1995).10.1016/0167-2738(95)99031-HGoogle Scholar
13. Huang, W., Shuk, P. and Greenblatt, M., Chem. Mater. 9, 2240(1997).10.1021/cm970425tGoogle Scholar
14. Maride, D. L., Swarrm, T. E. and Karavolis, S., Solid State Ionics 52, 173 (1992).Google Scholar
15. Shannon, R. D. and Prewitt, C. T., Acta Crystallogr. 32A, 751 (1976).10.1107/S0567739476001551Google Scholar