Liquid-Phase Manipulation Securing Enhanced Thermoelectric Performance of Ag2Se
Source abstract
Abstract
Developing n-type materials with high peak and/or average ZT (ZT is the figure of merit) is an urgent need for the lower ZT of the existing n-type BiTeSe materials compared with the p-type BiSbTe materials. Here, we demonstrate that liquid-phase sintering can lead to lowered thermal conductivity and an improved power factor in n-type Ag2Se, which originates from the greatly lowered electronic thermal conductivity attributed to the decreased mobility and improved Seebeck coefficients because of increased effective mass. Benefiting from this, the maximum ZT (ZTmax) of ∼1.21 and the average ZT (ZTave) of 1.06 are successfully achieved in polycrystalline Ag2Se. In this work, ZTave is the highest reported value, being 26% larger than that of Ag2Se reported. Our work shows that liquid-phase sintering to achieve improved thermoelectric (TE) performance opens a great opportunity for designing prospective thermoelectrics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Perfectionism, Procrastination, Anxiety Studies · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Lab of Photovoltaic and Energy conservation Materials, Institute of Solid State Physics, HFIPS, Chinese Academy of Sciences, Hefei 230031, China
School of Foreign Languages, Chaohu University, Chaohu 238000 China
Funding
National Natural Science Foundation of China · Key projects of Humanities and Social Sciences in Anhui Universities
References (28)
Show source-provided references
1. 10.1016/j.mtphys.2021.10035510.1016/j.mtphys.2021.100355 ↗
2. 10.1016/j.mtphys.2020.10024710.1016/j.mtphys.2020.100247 ↗
3. 10.1016/j.nanoen.2019.10426110.1016/j.nanoen.2019.104261 ↗
4. 10.1021/jacs.7b1187510.1021/jacs.7b11875 ↗
5. 10.1016/j.scriptamat.2019.07.01610.1016/j.scriptamat.2019.07.016 ↗
6. 10.1039/C8TA00525G10.1039/C8TA00525G ↗
7. 10.1063/1.487050910.1063/1.4870509 ↗
8. 10.1021/acsami.0c1534110.1021/acsami.0c15341 ↗
9. 10.1039/D0TA02614J10.1039/D0TA02614J ↗
10. 10.1016/0365-1789(63)90064-X10.1016/0365-1789(63)90064-X ↗
11. 10.1063/1.37374110.1063/1.373741 ↗
12. 10.1063/1.242972710.1063/1.2429727 ↗
13. 10.1002/aenm.20170202410.1002/aenm.201702024 ↗
14. 10.1038/s41467-019-08835-510.1038/s41467-019-08835-5 ↗
15. 10.1039/C9EE01609K10.1039/C9EE01609K ↗
16. 10.1016/j.nanoen.2017.10.03410.1016/j.nanoen.2017.10.034 ↗
17. 10.1007/s10853-018-2209-410.1007/s10853-018-2209-4 ↗
18. 10.1016/j.scriptamat.2017.11.04510.1016/j.scriptamat.2017.11.045 ↗
19. 10.1126/science.aaa416610.1126/science.aaa4166 ↗
20. 10.1016/j.nanoen.2016.10.05610.1016/j.nanoen.2016.10.056 ↗
21. 10.1039/C9QM00487D10.1039/C9QM00487D ↗
22. 10.1063/1.221859210.1063/1.2218592 ↗
23. 10.1039/c2ee21536e10.1039/c2ee21536e ↗
24. 10.1039/C4TA04912H10.1039/C4TA04912H ↗
25. 10.1039/c3tc31810a10.1039/c3tc31810a ↗
26. 10.1039/D0NR08045D10.1039/D0NR08045D ↗
27. 10.1039/C7TA08726H10.1039/C7TA08726H ↗
28. 10.1021/acsaem.9b0223110.1021/acsaem.9b02231 ↗