Enhancing the Thermoelectric Properties of p-Type Bulk Bi-Sb-Te Nanocomposites via Solution-Based Metal Nanoparticle Decoration

Embedding nanosized particles in bulk thermoelectric materials is expected to lower the lattice thermal conductivity by enhancing the degree of interface phonon scattering, thus improving their thermoelectric figure of merit ZT . We have developed a wet chemical process to fabricate Bi 0.5 Sb 1.5 Te...

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Veröffentlicht in:Journal of electronic materials 2013-07, Vol.42 (7), p.1411-1416
Hauptverfasser: Hwang, Sungwoo, Kim, Sang-Il, Ahn, Kyunghan, Roh, Jong Wook, Yang, Dae-Jin, Lee, Sang-Mock, Lee, Kyu-Hyoung
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Sprache:eng
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Zusammenfassung:Embedding nanosized particles in bulk thermoelectric materials is expected to lower the lattice thermal conductivity by enhancing the degree of interface phonon scattering, thus improving their thermoelectric figure of merit ZT . We have developed a wet chemical process to fabricate Bi 0.5 Sb 1.5 Te 3 -based thermoelectric nanocomposites which include nanometer-sized metal particles. By simple solution mixing of metal acetate precursors and Bi 0.5 Sb 1.5 Te 3 powders in ethyl acetate as a medium for homogeneous incorporation, it is possible to apply various types of metal nanoparticles onto the surfaces of the thermoelectric powders. Next, bulk Bi 0.5 Sb 1.5 Te 3 nanocomposites with homogeneously dispersed metal nanoparticles were fabricated using a spark plasma sintering technique. The lattice thermal conductivities were reduced by increasing the long-wavelength phonon scattering in the presence of metal nanoparticles, while the Seebeck coefficients increased for a few selected metal-decorated nanocomposites, possibly due to the carrier-energy-filtering effect. Finally, the figure of merit ZT was enhanced to 1.4 near room temperature. This approach highlights the feasibility of incorporating various types of nanoparticles into an alloy matrix starting by wet chemical routes, which is an effective means of improving the thermoelectric performance of Bi-Te-based alloys.
ISSN:0361-5235
1543-186X
DOI:10.1007/s11664-012-2280-6