Synthesis and Thermoelectric Properties of Charge-Compensated SyPdxCo4–xSb12 Skutterudites
Source abstract
Abstract
Recently, the electronegative elements (e.g., S, Se, Cl, and Br) filled skutterudites have attracted great attention in thermoelectric community. Via doping of some electron donors at the Sb sites, these electronegative elements can be filled into the voids of CoSb 3 forming thermodynamically stable compounds, which greatly extends the scope of filled skutterudites. In this study, we show that doping appropriate elements at the Co sites can also stabilize the electronegative elements in the voids of CoSb 3 . A series of S y Pd x Co 4– x Sb 12 compounds were successfully fabricated by a traditional solid state reaction method combined with a spark plasma sintering technique. The phase composition and electrical and thermal transport properties were systematically characterized, and the related mechanisms were deeply discussed. It is found that the charge compensation between Pd doping and S filling is the main reason for the formation of thermodynamically stable S y Pd x Co 4– x Sb 12 compounds. Filling S element in the voids of CoSb 3 provides additional holes to reduce the carrier concentration while scarcely affecting the carrier mobility. However, doping Pd at the Co sites not only changes the carrier scattering mechanism but also deteriorates the carrier mobility. Low lattice thermal conductivities are observed in these S y Pd x Co 4– x Sb 12 compounds, which are attributed to the low resonant frequency of the S element. Finally, a maximal figure of merit of 0.85 is obtained for S 0.05 Pd 0.25 Co 3.75 Sb 12 at 700 K.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Optical properties and cooling technologies in crystalline materials · Phase-change materials and chalcogenides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
College of Materials Sciences and Opto-Electronic Technology, University of Chinese Academy of Sciences, Beijing 100049, China
Funding
Youth Innovation Promotion Association of the Chinese Academy of Sciences · Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China
References (40)
Show source-provided references
1. 10.1038/nmat464310.1038/nmat4643 ↗
2. 10.1038/nmat209010.1038/nmat2090 ↗
3. 10.1002/adma.20170281610.1002/adma.201702816 ↗
4. 10.1002/aenm.20120051410.1002/aenm.201200514 ↗
5. Slack, G. A.InCRC Handbook of Thermoelectrics;Rowe, D. M., Ed.CRC Press:Boca Raton, FL, 1995; p407.
6. 10.1126/science.272.5266.132510.1126/science.272.5266.1325 ↗
7. 10.1080/09506608.2016.118307510.1080/09506608.2016.1183075 ↗
8. 10.1109/ICT.1997.66696810.1109/ICT.1997.666968 ↗
9. 10.1146/annurev.matsci.29.1.8910.1146/annurev.matsci.29.1.89 ↗
10. 10.1063/1.273742210.1063/1.2737422 ↗
11. 10.1063/1.131159710.1063/1.1311597 ↗
12. 10.1063/1.292021010.1063/1.2920210 ↗
13. 10.1021/ja808933410.1021/ja8089334 ↗
14. 10.1021/ja111199y10.1021/ja111199y ↗
15. 10.1016/j.actamat.2013.09.03910.1016/j.actamat.2013.09.039 ↗
16. 10.1103/PhysRevLett.95.18550310.1103/PhysRevLett.95.185503 ↗
17. 10.1039/C4TA05285D10.1039/C4TA05285D ↗
18. 10.1063/1.239753810.1063/1.2397538 ↗
19. 10.1002/adfm.20120257110.1002/adfm.201202571 ↗
20. 10.1039/C3EE43240H10.1039/C3EE43240H ↗
21. 10.1039/c4ta00487f10.1039/c4ta00487f ↗
22. 10.1039/C6EE00322B10.1039/C6EE00322B ↗
23. 10.1021/acsami.7b0588710.1021/acsami.7b05887 ↗
24. 10.1063/1.37128710.1063/1.371287 ↗
25. 10.1016/j.jallcom.2004.03.10410.1016/j.jallcom.2004.03.104 ↗
26. 10.1103/PhysRevB.55.147610.1103/PhysRevB.55.1476 ↗
27. 10.1063/1.367797110.1063/1.3677971 ↗
28. 10.1002/adfm.20150278210.1002/adfm.201502782 ↗
29. Li, S. S.Semiconductor Physical Electronics;Springer, 2006; pp211–223.10.1007/0-387-37766-2 ↗
30. 10.1063/1.487225010.1063/1.4872250 ↗
31. 10.1016/0020-0891(84)90066-610.1016/0020-0891(84)90066-6 ↗
32. 10.1017/S030500410002056910.1017/S0305004100020569 ↗
33. 10.1016/j.jallcom.2014.09.17310.1016/j.jallcom.2014.09.173 ↗
34. 10.1063/1.488031510.1063/1.4880315 ↗
35. 10.1016/j.actamat.2009.03.01810.1016/j.actamat.2009.03.018 ↗
36. 10.1126/science.115972510.1126/science.1159725 ↗
37. 10.1002/adfm.20090181710.1002/adfm.200901817 ↗
38. 10.1063/1.493682910.1063/1.4936829 ↗
39. 10.1063/1.355384210.1063/1.3553842 ↗
40. 10.1063/1.224520410.1063/1.2245204 ↗