Hostname: page-component-76fb5796d-skm99 Total loading time: 0 Render date: 2024-04-26T01:37:46.108Z Has data issue: false hasContentIssue false

Thermoelectric Properties of Cd3−xAxTeO6 (A = In3+, La3+ and Bi3+) Ceramics1

Published online by Cambridge University Press:  21 March 2011

Weiling Luan
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Utsunomiya University 7-1-2 Yoto, Utsunomiya 321-8585, Japan
Yue Jin Shan
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Utsunomiya University 7-1-2 Yoto, Utsunomiya 321-8585, Japan
Mitsuru Itoh
Affiliation:
Materials and Structures Laboratory, Tokyo Institute of Technology 4259 Nagatsuta, Yokohama 226-8503, Japan
Hideo Imoto
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Utsunomiya University 7-1-2 Yoto, Utsunomiya 321-8585, Japan
Get access

Abstract

Perovskite oxide Cd3TeO6 was electron-doped by the introduction of oxygen vacancies and substitution of trivalent cations, In3+, La3+ and Bi3+. Their electric properties were investigated and compared with that of undoped Cd3TeO6. Negative temperature dependence of resistivity was observed in undoped, air-sintered Cd3TeO6. The resis tivity of Cd3−xAxTeO6 (A = In3+, La3+ and Bi3+) showed a metallic behavior with very slight temperature dependence. Indium-doped samples gave a low resistivity, which were decreased by more than three orders of magnitudes than that of air-sintered, undoped Cd3TeO6. The negative Seebeck coefficient and Hall coefficient obtained from all samples indicate that electrons are the charge carriers. The absolute Seebeck coefficients values of doped samples are decreased by 5 ∼ 10 times than that observed in undoped Cd3TeO6. Fortunately, the resistivity of indium-doped samples is low enough to provide a good thermoelectric power factor, and the optimum value of Cd2.97In0.03TeO6 was calculated as 1.35×10−4 Wm−1K−2. This result is close to that of the current best n-type perovskite thermoelectric material Ba0.4Sr0.6PbO3.

Type
Research Article
Copyright
Copyright © Materials Research Society 2002

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.)

Footnotes

1

This work is supported by the Satellite Venture Business Laboratory of Utsunomiya University

References

REFERENCES

1 Kasper, H., Z. Anorg. Allg. Chem., 356, 329 (1968).Google Scholar
2 Burckhardt, V. H-G, Platte, C. and Tromel, M., Acta Cryst., B38, 2450 (1982).Google Scholar
3 Politova, E. D. and Venevtsev, Y. N., Mat. Res. Bull., 10, 319 (1975).Google Scholar
4 Yang, H., Phys. Chem. Minerals, 19,528 (1993).Google Scholar
5 Yasukawa, M. and Murayama, N., Mater. Sci. & Eng. B54, 64 (1998)Google Scholar
6 Mahan, G. D., Solid State Phys., 51, 81 (1998)Google Scholar