Synthesis, crystal structure, and transport properties of Cu2.2Zn0.8SnSe4-xTex (0.1
KAUST Grant NumberKAUST Faculty Initiated Collaboration grant
Permanent link to this recordhttp://hdl.handle.net/10754/672852
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AbstractQuaternary chalcogenides, particular compounds with the stannite structure-type, are of interest for thermoelectrics applications however tellurium-containing compositions have not been extensively investigated. We report on the synthesis and high temperature thermoelectric properties of p-type stannites Cu2.2Zn0.8SnSe4−xTex (x = 0.1, 0.2, 0.3, and 0.4). The compositions for each specimen were confirmed with a combination of Rietveld refinement and elemental analysis. Hall measurements indicate that holes are the dominant charge carriers in these materials. The electrical resistivity shows little temperature dependence up to 500 K and then increases with increasing temperature. The thermal conductivity decreases with increasing temperature with no indication of increase at higher temperatures suggesting a minimal bipolar diffusion effect in the thermal conductivity although these materials possess relatively small band-gaps as compared to that of other stannite compositions. A maximum ZT value of 0.56 was obtained at 700 K for Cu2.2Zn0.8SnSe3.7Te0.3 due to a relatively high Seebeck coefficient and low thermal conductivity.
CitationDong, Y., Eckert, B., Wang, H., Zeng, X., Tritt, T. M., & Nolas, G. S. (2015). Synthesis, crystal structure, and transport properties of Cu2.2Zn0.8SnSe4−xTex (0.1 ≤ x ≤ 0.4). Dalton Transactions, 44(19), 9014–9019. doi:10.1039/c5dt00910c
SponsorsThe work was supported by the National Science Foundation grant no. DMR-1400957. H.W. would like to thank the support of the assistant secretary for Energy Efficiency and Renewable Energy of the Department of Energy and the Propulsion Materials program under the Vehicle Technologies program. Oak Ridge National Laboratory is managed by UT-Battelle LLC under contract DE-AC05000OR22725. The work in Dr Tritt's laboratory acknowledges, in a small part, the support of a KAUST Faculty Initiated Collaboration grant and also internal funding from Clemson University.
PublisherROYAL SOC CHEMISTRY