Self-Sacrificed Additive in Preparing PbI2 Film Enables the Oriented Growth of Perovskite Crystals for Improved Solar Cell Performance
Source abstract
Abstract
Due to the limitation of the diffusion kinetics of organic amine salts on the PbI 2 layer in the two-step method, prepared perovskite particles are small in size, have many defects, and are randomly oriented, and the cell efficiency and stability are difficult to guarantee due to PbI 2 residues. Here, we added a volatile additive, N, N, N ′, N ′-tetramethylethylenediamine (TMEDA), to the PbI 2 precursor solution and formed preaggregated atomic clusters with PbI 2 through TMEDA, which reduced the Gibbs free energy of nucleation to obtain a porous PbI 2 layer, and finally obtained a perovskite film with large particles, few defects, ideal crystal plane orientation, and no additive residues. The results show that the photoelectric conversion efficiency of the optimized device is increased by 1.68% (from 21.68% to 23.36%), and the unpackaged optimized device still maintains the maximum efficiency of 77% after being placed in the air for 1200 h. This study provides an effective way to fabricate efficient and stable perovskite solar cells by promoting the nucleation-induced crystallization orientation by volatile additives.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, P. R. China
Funding
National Natural Science Foundation of China · Priority Academic Program Development of Jiangsu Higher Education Institutions
References (34)
Show source-provided references
1. 10.1021/ja809598r10.1021/ja809598r ↗
2. 10.1038/s41586-023-06745-710.1038/s41586-023-06745-7 ↗
3. 10.1126/science.abp887310.1126/science.abp8873 ↗
4. 10.1016/j.joule.2020.12.00910.1016/j.joule.2020.12.009 ↗
5. 10.1002/aenm.20210153810.1002/aenm.202101538 ↗
6. 10.1002/adma.20220004110.1002/adma.202200041 ↗
7. 10.1039/D2EE03342A10.1039/D2EE03342A ↗
8. 10.1016/j.joule.2020.09.01110.1016/j.joule.2020.09.011 ↗
9. 10.1002/adma.20211048210.1002/adma.202110482 ↗
10. 10.1002/inf2.1236910.1002/inf2.12369 ↗
11. 10.1021/jacs.1c1084210.1021/jacs.1c10842 ↗
12. 10.1039/D2EE03418B10.1039/D2EE03418B ↗
13. 10.1002/smll.20230721910.1002/smll.202307219 ↗
14. 10.1002/inf2.1243110.1002/inf2.12431 ↗
15. 10.1021/acs.jpclett.1c0339910.1021/acs.jpclett.1c03399 ↗
16. 10.1039/C6EE03014A10.1039/C6EE03014A ↗
17. 10.1002/adfm.20200262210.1002/adfm.202002622 ↗
18. 10.1002/anie.20191080010.1002/anie.201910800 ↗
19. 10.1002/aenm.20230045110.1002/aenm.202300451 ↗
20. 10.1002/adfm.20200577610.1002/adfm.202005776 ↗
21. 10.1002/adfm.20221483410.1002/adfm.202214834 ↗
22. 10.1002/aenm.20220312710.1002/aenm.202203127 ↗
23. 10.1002/aenm.20230125910.1002/aenm.202301259 ↗
24. 10.1002/adma.20230111510.1002/adma.202301115 ↗
25. 10.1016/j.joule.2022.09.01210.1016/j.joule.2022.09.012 ↗
26. 10.1126/science.adn964610.1126/science.adn9646 ↗
27. 10.1038/s41566-019-0398-210.1038/s41566-019-0398-2 ↗
28. 10.1002/adfm.20170692310.1002/adfm.201706923 ↗
29. 10.1002/adma.20231023710.1002/adma.202310237 ↗
30. 10.1039/D2EE00663D10.1039/D2EE00663D ↗
31. 10.1021/acsenergylett.0c0184810.1021/acsenergylett.0c01848 ↗
32. 10.1002/adma.20240147610.1002/adma.202401476 ↗
33. 10.1021/acsaem.3c0241510.1021/acsaem.3c02415 ↗
34. 10.1021/acsami.4c0060610.1021/acsami.4c00606 ↗