High thermoelectric performance of Ge1−xPbxSe0.5Te0.5 due to (Pb, Se) co-doping
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Abstract
Abstract Ge-rich Ge1−xPbxTe0.5Se0.5 (x = 0, 0.1, 0.2, 0.25, 0.3, 0.4 and 0.5) alloys with high thermoelectric performance were prepared through a conventional melting, solutioning and quenching route, followed by a spark plasma sintering technique. Se doping extends the solid solubility of Pb in GeTe. The samples maintain the rhombohedral GeTe-based solid solution up to x = 0.3, while the samples with x = 0.4 and 0.5 are composites containing the major rhombohedral GeTe-based supersaturated solid solution and a mixture of the minor NaCl-type PbTe-based and rhombohedral GeTe-based phases separated from the supersaturated solid solution. All the samples show p-type conduction. The solute Pb and Se atoms in the GeTe lattice may modify the carrier concentration, leading to a significant increase in the Seebeck coefficient. The solute Pb and Se atoms, twinning microstructures and the grain boundaries or secondary phase may form broad-based phonon scattering centers, leading to alloys with extremely low thermal conductivity. In the results, the overall high thermoelectric properties were obtained in the alloys due to (Pb, Se) co-doping. A maximum ZT of 1.6 at 673 K was eventually achieved in Ge0.75Pb0.25Te0.5Se0.5; this value is higher than that of pure PbTe or GeTe compounds and any other reported PbTe–GeTe composites.
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Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Chalcogenide Semiconductor Thin Films · Perfectionism, Procrastination, Anxiety Studies
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References (25)
Show source-provided references
1. Vining · Nature Mater · 2009 · 8 · 8310.1038/nmat2361 ↗
2. Venkatasubramanian · Nature · 2001 · 413 · 59710.1038/35098012 ↗
3. Harman · Science · 2002 · 297 · 222910.1126/science.1072886 ↗
4. Poudel · Science · 2008 · 320 · 63410.1126/science.1156446 ↗
5. Gelbstein · J Electron Mater · 2009 · 38 · 147810.1007/s11664-008-0652-8 ↗
6. Biswas · Nature · 2012 · 489 · 41410.1038/nature11439 ↗
7. Biswas · Energy Environ Sci · 2011 · 4 · 467510.1039/c1ee02297k ↗
8. Biswas · Nature Chem · 2011 · 3 · 16010.1038/nchem.955 ↗
9. Ohta · Adv Energy Mater · 2012 · 2 · 111710.1002/aenm.201100756 ↗
10. Zhao · Energy Environ Sci · 2013 · 6 · 334610.1039/c3ee42187b ↗
11. Gelbstein · J Electron Mater · 2009 · 38 · 147810.1007/s11664-008-0652-8 ↗
12. Cook · J Appl Phys · 2007 · 101 · 05371510.1063/1.2645675 ↗
13. Salvador · J Solid State Chem · 2009 · 182 · 208810.1016/j.jssc.2009.05.024 ↗
14. Parker · J Mater Sci · 1974 · 9 · 182910.1007/BF00541753 ↗
15. Ramachandrarao · J Mater Sci · 1975 · 10 · 184910.1007/BF00754472 ↗
16. Gorsse · Chem Mater · 2010 · 22 · 98810.1021/cm901862m ↗
17. Gelbstein · Acta Mater · 2011 · 61 · 149910.1016/j.actamat.2012.11.027 ↗
18. Gelbstein · Adv Energy Mater · 2013 · 3 · 81510.1002/aenm.201200970 ↗
19. Gelbstein · Chem Mater · 2010 · 22 · 105410.1021/cm902009t ↗
20. Pei · J Alloy · 2012 · 514 · 4010.1016/j.jallcom.2011.10.036 ↗
21. Gelbstein · J Electron Mater · 2009 · 38 · 147810.1007/s11664-008-0652-8 ↗
22. Bulusu · Superlattices Microst · 2008 · 44 · 110.1016/j.spmi.2008.02.008 ↗
23. Li · J Electron Mater · 2011 · 40 · 206310.1007/s11664-011-1715-9 ↗
24. Cao · J Phys D: Appl Phys · 2009 · 42 · 01540610.1088/0022-3727/42/1/015406 ↗
25. Søndergaard · J Solid State Chem · 2011 · 184 · 117210.1016/j.jssc.2011.02.028 ↗