journal article·2024-12-13

Directional Regulation of Photogenerated Carriers in Tin Halide Perovskites for Enhanced Thermoelectrics

Ruisi Chen, Lidong Chen, Ziqi Liang

ACS Energy Letters· Volume 9· Issue 12
Publisher page

Abstract

Metal halide perovskites hold good prospects for thermoelectric applications. Photoexcitation is manifested to effectively increase carrier density of perovskites, yet the severe carrier recombination due to the bipolar effect leads to the significant Seebeck voltage loss. Herein, we discover a remarkably photo-enhanced thermoelectric effect in FASnI 3 thin film by depositing an electron transport layer, delivering a 28-fold enhancement in thermoelectric power factor (PF). It is found that carrier recombination is greatly suppressed via directional regulation of photogenerated carrier transport, leading to a concurrent increase of electrical conductivity (σ) and Seebeck coefficient ( S ). Such a strategy is applicable to other compositional tin perovskite films with higher carrier and defect densities, which are however less pronounced owing to the inferior photocarriers and the restrained electron extraction. Nonetheless, we achieve a champion PF up to ∼342 μW m –1 K –2 in CsSnI 3 films by virtue of their outstanding σ that plays a decisive role in comparison to that of S .
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Research context

OpenAlex topics: Perovskite Materials and Applications · Advanced Thermoelectric Materials and Devices · Chalcogenide Semiconductor Thin Films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science, Fudan University, Shanghai 200433, China

State Key Laboratory of High-Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China

Funding

Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China

References (35)

Show source-provided references
1. 10.1016/j.nanoen.2022.10694910.1016/j.nanoen.2022.106949 ↗
2. 10.1021/acsenergylett.1c0201510.1021/acsenergylett.1c02015 ↗
3. 10.1002/advs.20190338910.1002/advs.201903389 ↗
4. 10.1002/adma.20210279710.1002/adma.202102797 ↗
5. 10.1021/acs.chemmater.1c0186710.1021/acs.chemmater.1c01867 ↗
6. 10.1002/adfm.20230377410.1002/adfm.202303774 ↗
7. 10.1038/s41578-021-00286-z10.1038/s41578-021-00286-z ↗
8. 10.1002/aenm.20190405410.1002/aenm.201904054 ↗
9. 10.1021/acs.jpcc.5b0393910.1021/acs.jpcc.5b03939 ↗
10. 10.1016/j.orgel.2018.01.01410.1016/j.orgel.2018.01.014 ↗
11. 10.1016/j.matlet.2023.13385810.1016/j.matlet.2023.133858 ↗
12. 10.1021/acs.accounts.5b0041110.1021/acs.accounts.5b00411 ↗
13. 10.1146/annurev-physchem-040215-11222210.1146/annurev-physchem-040215-112222 ↗
14. 10.1016/j.joule.2018.04.01010.1016/j.joule.2018.04.010 ↗
15. 10.1039/C4EE01463D10.1039/C4EE01463D ↗
16. 10.1016/j.mtphys.2019.10013010.1016/j.mtphys.2019.100130 ↗
17. 10.1002/adma.20200593110.1002/adma.202005931 ↗
18. Sze M. · 200610.1002/0470068329 ↗
19. 10.1016/j.joule.2023.08.00210.1016/j.joule.2023.08.002 ↗
20. 10.1039/C5TA09011C10.1039/C5TA09011C ↗
21. 10.1002/adma.20220560310.1002/adma.202205603 ↗
22. 10.1002/smsc.20220000410.1002/smsc.202200004 ↗
23. 10.1002/aesr.20200003310.1002/aesr.202000033 ↗
24. 10.1038/s41467-019-13773-310.1038/s41467-019-13773-3 ↗
25. 10.1039/D0TA09329G10.1039/D0TA09329G ↗
26. 10.1021/jacs.0c0342710.1021/jacs.0c03427 ↗
27. 10.1557/adv.2019.27910.1557/adv.2019.279 ↗
28. 10.1021/acs.jpclett.8b0255510.1021/acs.jpclett.8b02555 ↗
29. 10.1016/j.xcrp.2023.10170310.1016/j.xcrp.2023.101703 ↗
30. 10.1039/D1TA11093D10.1039/D1TA11093D ↗
31. 10.1021/acs.jpcc.0c0045910.1021/acs.jpcc.0c00459 ↗
32. 10.1021/acsaem.2c0177310.1021/acsaem.2c01773 ↗
33. 10.1073/pnas.171174411410.1073/pnas.1711744114 ↗
34. 10.1039/c0dt01601b10.1039/c0dt01601b ↗
35. 10.1007/s11664-020-07958-610.1007/s11664-020-07958-6 ↗