Investigation of PbSnTeSe High-Entropy Thermoelectric Alloy: A DFT Approach - Aix-Marseille Université Access content directly
Journal Articles Materials Year : 2022

Investigation of PbSnTeSe High-Entropy Thermoelectric Alloy: A DFT Approach


Thermoelectric materials have attracted extensive attention because they can directly convert waste heat into electric energy. As a brand-new method of alloying, high-entropy alloys (HEAs) have attracted much attention in the fields of materials science and engineering. Recent researches have found that HEAs could be potentially good thermoelectric (TE) materials. In this study, special quasi-random structures (SQS) of PbSnTeSe high-entropy alloys consisting of 64 atoms have been generated. The thermoelectric transport properties of the highest-entropy PbSnTeSe-optimized structure were investigated by combining calculations from first-principles density-functional theory and onthe-fly machine learning with the semiclassical Boltzmann transport theory and Green-Kubo theory. The results demonstrate that PbSnTeSe HEA has a very low lattice thermal conductivity. The electrical conductivity, thermal electronic conductivity and Seebeck coefficient have been evaluated for both n-type and p-type doping. N-type PbSnTeSe exhibits better power factor (PF = S 2 σ) than p-type PbSnTeSe because of larger electrical conductivity for n-type doping. Despite high electrical thermal conductivities, the calculated ZT are satisfactory. The maximum ZT (about 1.1) is found at 500 K for n-type doping. These results confirm that PbSnTeSe HEA is a promising thermoelectric material.
Fichier principal
Vignette du fichier
materials-16-00235.pdf (4.41 Mo) Télécharger le fichier
Origin : Publisher files allowed on an open archive
Licence : CC BY - Attribution

Dates and versions

hal-03983417 , version 1 (10-02-2023)





Ming Xia, Marie-Christine Record, Pascal Boulet. Investigation of PbSnTeSe High-Entropy Thermoelectric Alloy: A DFT Approach. Materials, 2022, 16 (1), pp.235. ⟨10.3390/ma16010235⟩. ⟨hal-03983417⟩
2 View
26 Download



Gmail Facebook Twitter LinkedIn More