Thermal-Driven Cobalt Intercalation Enhances Thermoelectric ZT of n-Type Bi2Te2.7Se0.3
Source abstract
Abstract
Layered materials have emerged as stars in the realm of nanomaterials, showcasing exceptional versatility in various fields. This investigation employed a thermally driven method to intercalate cobalt (Co) into the van der Waals gaps of (CuI) 0.002 Bi 2 Te 2.7 Se 0.3 crystals and investigated the mechanism by which the intercalated Co enhances the thermoelectric performance of the material. Co intercalation decreases the carrier concentration, thereby improving the Seebeck coefficient and decreasing both the mobility and the electrical conductivity. These effects result in a significant enhancement of the power factor above 400 K. Theoretical electronic structure calculations provide insights into the role of Co in this material. Additionally, the presence of intercalated Co significantly enhances phonon scattering, thereby boosting the thermoelectric figure-of-merit, ZT to 1.33 at 350 K for 0.17% Co intercalation. These findings highlight the potential of Co incorporation for improving the thermoelectric energy efficiency of n-type Bi 2 Te 2.7 Se 0.3, offering avenues for further optimization in thermoelectric applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Topological Materials and Phenomena · Advanced Thermodynamics and Statistical Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Engineering and Center for Plasma and Thin Film Technologies, Ming Chi University of Technology, New Taipei City 243, Taiwan
Graduate School of Materials Science, National Yunlin University of Science and Technology, Yunlin 64002, Taiwan
Funding
National Science and Technology Council
References (38)
Show source-provided references
1. 10.1016/j.pmatsci.2015.02.00210.1016/j.pmatsci.2015.02.002 ↗
2. 10.1021/acsaem.3c0149310.1021/acsaem.3c01493 ↗
3. 10.1021/acsaem.1c0256010.1021/acsaem.1c02560 ↗
4. 10.1021/acs.jpcc.7b0300210.1021/acs.jpcc.7b03002 ↗
5. 10.1016/j.physe.2016.08.01510.1016/j.physe.2016.08.015 ↗
6. 10.1039/C5QI00242G10.1039/C5QI00242G ↗
7. 10.1021/acsaem.1c0323910.1021/acsaem.1c03239 ↗
8. 10.1038/nmat417010.1038/nmat4170 ↗
9. 10.1038/nnano.2015.34010.1038/nnano.2015.340 ↗
10. 10.1021/jacs.9b1166810.1021/jacs.9b11668 ↗
11. 10.1021/acsnano.9b0828810.1021/acsnano.9b08288 ↗
12. 10.1038/s41467-020-16717-410.1038/s41467-020-16717-4 ↗
13. 10.1038/nature2577410.1038/nature25774 ↗
14. 10.1038/s41699-021-00211-610.1038/s41699-021-00211-6 ↗
15. 10.1002/smll.20170164910.1002/smll.201701649 ↗
16. 10.1021/acsaem.3c0146510.1021/acsaem.3c01465 ↗
17. 10.1039/C5CS00758E10.1039/C5CS00758E ↗
18. 10.1126/sciadv.aay409210.1126/sciadv.aay4092 ↗
19. 10.1088/2053-1591/ab63fd10.1088/2053-1591/ab63fd ↗
20. 10.1021/acsaem.8b0110110.1021/acsaem.8b01101 ↗
21. 10.1063/5.007448910.1063/5.0074489 ↗
22. 10.1103/physrevb.97.24120310.1103/physrevb.97.241203 ↗
23. 10.1002/advs.20220135310.1002/advs.202201353 ↗
24. 10.1039/D1MH01601F10.1039/D1MH01601F ↗
25. 10.1103/PhysRevApplied.15.06402310.1103/PhysRevApplied.15.064023 ↗
26. 10.1039/D1EE00356A10.1039/D1EE00356A ↗
27. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
28. 10.1016/0022-3093(95)00355-X10.1016/0022-3093(95)00355-X ↗
29. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
30. 10.1002/jcc.2175910.1002/jcc.21759 ↗
31. 10.1063/1.338234410.1063/1.3382344 ↗
32. 10.1007/s11664-019-06973-610.1007/s11664-019-06973-6 ↗
33. 10.1039/c2ee21536e10.1039/c2ee21536e ↗
34. 10.1021/acsnano.6b0115610.1021/acsnano.6b01156 ↗
35. 10.1021/acsami.4c0203210.1021/acsami.4c02032 ↗
36. 10.1016/j.cej.2022.14092310.1016/j.cej.2022.140923 ↗
37. 10.1016/j.mtchem.2024.10200810.1016/j.mtchem.2024.102008 ↗
38. 10.1063/1.511898110.1063/1.5118981 ↗