Enhancing a Perovskite Solar Cell and Module by Suppressing Protonation through Chelating Agents
Source abstract
Abstract
Formamidinium-based perovskites (FA perovskites) often incorporate methylammonium chloride (MACl) to stabilize the α-FAPbI 3 phase and prevent formation of the δ phase. However, MACl undergoes deprotonation and reacts with FA, leading to the generation of unstable byproducts that can cause component degradation and negatively impact the device performance. In this study, we introduce ethylenediaminetetramethylenephosphonic acid as a corrosion inhibitor, which effectively prevents the formation of these byproducts and stabilizes α-FAPbI 3 . The resulting perovskite solar module achieved a power conversion efficiency of 22.44%. Furthermore, the device maintained approximately 83% of its initial efficiency after 2136 h of damp-heat testing (85 °C and 85% RH), while maximum power point tracking retained 88.7% of the initial efficiency after 1000 h.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The College of Electronic Information
Qingdao University
Institute of New Energy Technology, College of Physics and Optoelectronic Engineering
Jinan University
Guangdong Mellow Energy Company, Ltd., Yuanming Road, Zhuhai 519075, Guangdong, China
Funding
Basic and Applied Basic Research Foundation of Guangdong Province · Guangzhou Municipal Science and Technology Project · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
References (38)
Show source-provided references
1. 10.1002/pssr.20200061310.1002/pssr.202000613 ↗
2. 10.1021/ja809598r10.1021/ja809598r ↗
3. 10.1002/pip.383110.1002/pip.3831 ↗
4. 10.1007/s40820-023-01046-010.1007/s40820-023-01046-0 ↗
5. 10.1063/5.014519910.1063/5.0145199 ↗
6. 10.1002/eom2.1202510.1002/eom2.12025 ↗
7. 10.1021/acs.jpclett.5b0038010.1021/acs.jpclett.5b00380 ↗
8. 10.1021/jp411112k10.1021/jp411112k ↗
9. 10.1016/j.joule.2019.06.01410.1016/j.joule.2019.06.014 ↗
10. 10.1016/j.nanoen.2017.08.00910.1016/j.nanoen.2017.08.009 ↗
11. 10.1126/science.abb898510.1126/science.abb8985 ↗
12. 10.1002/advs.20230628010.1002/advs.202306280 ↗
13. 10.1016/j.xcrp.2021.10043210.1016/j.xcrp.2021.100432 ↗
14. 10.1002/ange.20221579910.1002/ange.202215799 ↗
15. 10.1039/D2EE01634F10.1039/D2EE01634F ↗
16. 10.1002/admi.20220143610.1002/admi.202201436 ↗
17. 10.1002/elt2.5210.1002/elt2.52 ↗
18. 10.1002/aenm.20240050010.1002/aenm.202400500 ↗
19. 10.1002/aenm.20180347610.1002/aenm.201803476 ↗
20. 10.1002/aenm.20170339910.1002/aenm.201703399 ↗
21. 10.1002/adma.20170714310.1002/adma.201707143 ↗
22. 10.1021/acsami.9b2308610.1021/acsami.9b23086 ↗
23. 10.1016/j.chempr.2020.02.01610.1016/j.chempr.2020.02.016 ↗
24. 10.1002/adfm.20241118310.1002/adfm.202411183 ↗
25. 10.1002/ange.20241170810.1002/ange.202411708 ↗
26. 10.1039/D4EE02793K10.1039/D4EE02793K ↗
27. 10.1038/s41560-024-01471-410.1038/s41560-024-01471-4 ↗
28. 10.1038/s41586-024-08546-y10.1038/s41586-024-08546-y ↗
29. 10.1002/adma.20241077910.1002/adma.202410779 ↗
30. 10.1021/acsenergylett.8b0030510.1021/acsenergylett.8b00305 ↗
31. 10.1021/acs.jpclett.1c0134910.1021/acs.jpclett.1c01349 ↗
32. 10.1557/jmr.2016.27210.1557/jmr.2016.272 ↗
33. 10.1002/solr.20200071510.1002/solr.202000715 ↗
34. 10.1007/s40843-024-3071-810.1007/s40843-024-3071-8 ↗
35. 10.1016/j.joule.2023.11.01410.1016/j.joule.2023.11.014 ↗
36. 10.1002/aenm.20220065010.1002/aenm.202200650 ↗
37. 10.1016/j.cej.2022.13510710.1016/j.cej.2022.135107 ↗
38. 10.1016/j.mssp.2024.10813810.1016/j.mssp.2024.108138 ↗