AI Article Synopsis

  • Bismuth telluride materials are popular for thermoelectric applications, but there's a need for better performance, especially at higher temperatures due to a bipolar effect caused by their narrow band gap.
  • This study explores alloying commercial BiSbTe with AgSbTe using advanced techniques, which effectively lowers thermal conductivity and increases electrical conductivity by raising hole carrier concentration.
  • The optimal alloy composition (0.15 wt % AgSbTe) achieved a thermoelectric performance improvement of 20.5% at 393 K and 27.6% between 303 K and 483 K compared to commercial samples.

Article Abstract

Bismuth telluride-based materials have been widely used in commercial thermoelectric applications due to their excellent thermoelectric performance in the near-room-temperature range, yet further improvement of their thermoelectric properties is still necessary. Moreover, the narrow band gap of these materials results in a bipolar effect at elevated temperatures, which causes severe degradation of the thermoelectric performance. In this work, the commercial BiSbTe was alloyed with AgSbTe by using high-energy ball milling method combined with spark plasma sintering. It was found that ball milling can effectively reduce the lattice thermal conductivity of the samples. The alloying of AgSbTe leads to a gradual increase in hole carrier concentration, resulting in an enhanced electrical conductivity and optimized power factor. Additionally, the bipolar effect is also weakened due to the increased hole carrier concentration. Furthermore, the substitution of Ag in the Bi/Sb sublattice causes further reduction in the lattice thermal conductivity. Ultimately, the sample alloyed with 0.15 wt % AgSbTe demonstrates its best thermoelectric performance with a maximum of 1.35 at 393 K, showing a 20.5% improvement compared to the commercial sample. Besides, its average reaches a high value of 1.25 between 303 and 483 K, with a 27.6% improvement compared to that of the commercial sample.

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http://dx.doi.org/10.1021/acsami.4c12307DOI Listing

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