Electrochemical Deposition and Characterization of Thermoelectric Ternary (BixSb1-x)(2)Te-3 and Bi-2(Te1-ySey)(3) Thin Films
Journal article, 2012

Thermoelectric thin films of the ternary compounds (Bi Sb1- )(2)Te-3 and Bi-2(Te1- Se )(3) were synthesized using potentiostatic electrochemical deposition on gold-coated silicon substrates from aqueous acidic solutions at room temperature. The surface morphology, elemental composition, and crystal structure of the deposited films were studied and correlated with preparation conditions. The thermoelectric properties of (Bi Sb1- )(2)Te-3 and Bi-2(Te1- Se )(3) films, i.e., Seebeck coefficient and electrical resistivity, were measured after transferring the films to a nonconductive epoxy support. (Bi Sb1- )(2)Te-3 thin films showed -type semiconductivity, and the highest power factor was obtained for film deposited at a relatively large negative potential with composition close to Bi0.5Sb1.5Te3. In addition, Bi-2(Te1- Se )(3) thin films showed -type semiconductivity, and the highest power factor was obtained for film deposited at a relatively small negative potential, having composition close to Bi2Te2.7Se0.3. In contrast to Bi2Te2.7Se0.3 thin films, an annealing treatment was required for Bi0.5Sb1.5Te3 thin films to achieve the same magnitude of power factor as Bi2Te2.7Se0.3. Therefore, Bi2Te2.7Se0.3 thin films appear to be good candidates for multilayer preparation using electrochemical deposition, but the morphology of the films must be further improved.

electrodeposition

alloys

thin films

telluride

(BixSb1-x)(2)Te-3

characterization

devices

bi2te3

Bi-2(Te1-ySey)(3)

Thermoelectric

Author

Yi Ma

Chalmers, Chemical and Biological Engineering, Applied Surface Chemistry

Waruna Wijesekara

Chalmers, Chemical and Biological Engineering

Anders Palmqvist

Chalmers, Chemical and Biological Engineering, Applied Surface Chemistry

Journal of Electronic Materials

0361-5235 (ISSN) 1543-186X (eISSN)

Vol. 41 6 1138-1146

Subject Categories

Physical Sciences

DOI

10.1007/s11664-011-1790-y

More information

Created

10/7/2017