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Synthesis and thermoelectric properties of p-type barium-filled skutterudite BayFexCo4−xSb12

Published online by Cambridge University Press:  31 January 2011

X. F. Tang
Affiliation:
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, People's Republic of China
L. D. Chen
Affiliation:
State Key Laboratory of High Performance Ceramics and Superfine Structure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China
T. Goto
Affiliation:
Institute for Materials Research, Tohoku University, Sendai 980–8577, Japan
T. Hirai
Affiliation:
Institute for Materials Research, Tohoku University, Sendai 980–8577, Japan
R. Z. Yuan
Affiliation:
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, People's Republic of China
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Abstract

Single-phase barium-filled skutterudite compounds, BayFexCo4−xSb12 (x = 0 to 3.0, y = 0 to 0.7), were synthesized by a two-step solid-state reaction method. The maximum filling fraction of Ba (ymax) in BayFexCo4–xSb12 increased with increasing Fe content and was found to be rather greater than that of CeyFexCo4–xSb12. The ymax varied from 0.35 to near 1.0 when Fe content changed from 0 to 4.0. BayFexCo4–xSb12 showed p-type conduction at a composition range of x = 0 to 3.0, y = 0 to 0.7. Carrier concentration and electrical conductivity increased with increasing Fe content and decreased with increasing Ba filling fraction. The Seebeck coefficient increased with increasing Ba filling fraction and with decreasing Fe content. Lattice thermal conductivity decreased with increasing Ba filling fraction and reached a minimum at a certain Ba filling fraction (y = 0.3 to 0.4). The greatest ZT value of 0.9 was obtained at 750 K for p-type Ba0.27Fe0.98Co3.02Sb12. It is expected that further investigation on the optimization of filling fraction would result in a higher ZT value at the moderately low Fe content region.

Type
Articles
Copyright
Copyright © Materials Research Society 2002

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References

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