Surface Dedoping for Methylammonium-Free Tin–Lead Perovskite Solar Cells
Source abstract
Abstract
For Sn–Pb-based perovskite solar cells (PSCs), surface p-doping-related defects including Sn vacancies, FA vacancies, and I-related defects substantially impact the local work function and band structure, thus resulting in inefficient carrier transfer kinetics at the perovskite/C 60 interface. Herein, a surface dedoping strategy is rationally designed based on synergistic passivation of p-doping-related defects, in which shallow-level defects are compensated and localized electronic states caused by deep-level defects are removed. Accordingly, the back surface electrical-field by a concomitantly formed n/n + homojunction as well as reduced surface potential fluctuations minimize the electron extraction barrier. The electron mobility and built-in voltage are greatly enhanced, and carrier lifetimes are elongated to over 7 μs. Meanwhile, the cooperative stabilization of surface components suppresses I – ion migration and Sn 2+ oxidation. The resulting MA-free Sn–Pb PSCs deliver a champion efficiency of 22.05%, along with maintaining 94% of the initial efficiency after 1200 h of aging in N 2 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory for Liquid−Solid Structural Evolution and Processing of Materials, Ministry of Education, School of Materials Science and Engineering, Shandong University, Jinan 250061, P. R. China
Funding
Government of Shandong Province · National Natural Science Foundation of China
References (40)
Show source-provided references
1. 10.1002/adma.20211024110.1002/adma.202110241 ↗
2. 10.1038/s41563-022-01448-210.1038/s41563-022-01448-2 ↗
3. 10.1021/acsenergylett.1c0210510.1021/acsenergylett.1c02105 ↗
4. 10.1038/s41578-020-0221-110.1038/s41578-020-0221-1 ↗
5. 10.1038/nenergy.2016.20710.1038/nenergy.2016.207 ↗
6. 10.1038/s41578-021-00286-z10.1038/s41578-021-00286-z ↗
7. 10.1016/j.joule.2022.05.01210.1016/j.joule.2022.05.012 ↗
8. 10.1038/nenergy.2016.14910.1038/nenergy.2016.149 ↗
9. 10.1039/C8EE01447G10.1039/C8EE01447G ↗
10. 10.1021/acsenergylett.2c0203510.1021/acsenergylett.2c02035 ↗
11. 10.1038/s41467-021-22864-z10.1038/s41467-021-22864-z ↗
12. 10.1002/aenm.20220124310.1002/aenm.202201243 ↗
13. 10.1038/s41560-018-0219-810.1038/s41560-018-0219-8 ↗
14. 10.1002/aenm.20210356710.1002/aenm.202103567 ↗
15. 10.1063/1.486477810.1063/1.4864778 ↗
16. 10.1038/s41586-022-05268-x10.1038/s41586-022-05268-x ↗
17. 10.1002/adom.20170013910.1002/adom.201700139 ↗
18. 10.1002/adma.20210230010.1002/adma.202102300 ↗
19. 10.1021/acs.jpclett.0c0072510.1021/acs.jpclett.0c00725 ↗
20. 10.1039/D0CS00573H10.1039/D0CS00573H ↗
21. 10.1002/anie.20221200210.1002/anie.202212002 ↗
22. 10.1021/acsaem.2c0143710.1021/acsaem.2c01437 ↗
23. 10.1021/acsenergylett.1c0011110.1021/acsenergylett.1c00111 ↗
24. 10.1039/C8CP00280K10.1039/C8CP00280K ↗
25. 10.1002/aenm.20220411510.1002/aenm.202204115 ↗
26. 10.1016/j.chempr.2021.04.00210.1016/j.chempr.2021.04.002 ↗
27. 10.1126/science.abn891010.1126/science.abn8910 ↗
28. 10.1002/aenm.20220041710.1002/aenm.202200417 ↗
29. 10.1021/acsenergylett.1c0121710.1021/acsenergylett.1c01217 ↗
30. 10.1016/j.joule.2021.11.00310.1016/j.joule.2021.11.003 ↗
31. 10.1021/acsenergylett.1c0034210.1021/acsenergylett.1c00342 ↗
32. 10.1126/science.add878610.1126/science.add8786 ↗
33. 10.1021/jacs.0c1280210.1021/jacs.0c12802 ↗
34. 10.1016/j.joule.2021.06.00110.1016/j.joule.2021.06.001 ↗
35. 10.1002/aenm.20200195810.1002/aenm.202001958 ↗
36. 10.1002/adma.20210592010.1002/adma.202105920 ↗
37. 10.1021/acsenergylett.2c0243510.1021/acsenergylett.2c02435 ↗
38. 10.1038/ncomms849710.1038/ncomms8497 ↗
39. 10.1126/science.abp887310.1126/science.abp8873 ↗
40. 10.1002/adma.20230187110.1002/adma.202301871 ↗