journal article·2025-03-14

Nickel Oxide Thin Films Formed from the pH-Adjusted Solutions for Inverted Perovskite Solar Cells

Yun-Sung Jeon, Nam-Gyu Park

ACS Energy Letters· Volume 10· Issue 3
Publisher page

Abstract

We report here a facile approach for fabricating a p-type nickel oxide (NiO x ) thin film for inverted perovskite solar cells (PSCs) by a direct conversion of the pH-adjusted aqueous precursor solutions into solid NiO x . pH control influenced both the p-type characteristics of the NiO x film and the phase stability of the perovskite layer deposited on the NiO x film. Formic acid (HCOOH) increased the Ni 3+ /(Ni 2+ + Ni 3+ ) ratio from 4.65% to 5.77%, enhancing charge extraction capability, while ammonium hydroxide reduced it to 4.13%. The HCOOH-derived NiO x films also improved the perovskite stability by eliminating residual nitrates. As a result, under ISOS-L1 conditions, the T 90 lifespan (90% of the initial efficiency) was extended to 900 h, compared to less than 200 h for other films. A power conversion efficiency of 24.19% was achieved by using the HCOOH-derived NiO x film with carbazole-based phosphonic acid passivation.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films · Conducting polymers and applications

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

Affiliations

School of Chemical Engineering and Center for Antibonding Regulated Crystals

Sungkyunkwan University

SKKU Institute of Energy Science and Technology (SIEST)

Funding

National Research Foundation of Korea

References (38)

Show source-provided references
1. 10.1038/srep0059110.1038/srep00591 ↗
2. 10.1002/pip.383110.1002/pip.3831 ↗
3. 10.1002/adma.20200743110.1002/adma.202007431 ↗
4. 10.1038/s41586-023-06784-010.1038/s41586-023-06784-0 ↗
5. 10.1126/science.ade312610.1126/science.ade3126 ↗
6. 10.1038/s41586-024-07723-310.1038/s41586-024-07723-3 ↗
7. 10.1038/s41560-023-01377-710.1038/s41560-023-01377-7 ↗
8. 10.1039/C6NR01601D10.1039/C6NR01601D ↗
9. 10.1002/solr.20230093310.1002/solr.202300933 ↗
10. 10.1016/j.mtsust.2023.10043810.1016/j.mtsust.2023.100438 ↗
11. 10.1126/science.adj885810.1126/science.adj8858 ↗
12. 10.1021/acsomega.2c0404210.1021/acsomega.2c04042 ↗
13. 10.5935/0103-5053.2014027010.5935/0103-5053.20140270 ↗
14. 10.1002/admi.20230075110.1002/admi.202300751 ↗
15. 10.1016/j.solener.2019.06.04010.1016/j.solener.2019.06.040 ↗
16. 10.1007/s12678-021-00686-310.1007/s12678-021-00686-3 ↗
17. 10.2109/jcersj2.118.19310.2109/jcersj2.118.193 ↗
18. 10.1021/acs.jcim.3c0021710.1021/acs.jcim.3c00217 ↗
19. 10.1021/acs.jpcc.4c0210910.1021/acs.jpcc.4c02109 ↗
20. 10.1016/j.matlet.2013.03.07710.1016/j.matlet.2013.03.077 ↗
21. 10.1016/j.jtice.2020.02.02110.1016/j.jtice.2020.02.021 ↗
22. Smith D. W. · 2006
23. 10.1021/ja01177a00810.1021/ja01177a008 ↗
24. 10.1063/1.474299310.1063/1.4742993 ↗
25. 10.1021/cm300739y10.1021/cm300739y ↗
26. 10.1149/2.0191804jes10.1149/2.0191804jes ↗
27. 10.1021/acsami.2c0181310.1021/acsami.2c01813 ↗
28. 10.1021/acsenergylett.4c0203110.1021/acsenergylett.4c02031 ↗
29. 10.1016/j.joule.2020.06.00410.1016/j.joule.2020.06.004 ↗
30. 10.1021/acsenergylett.4c0014010.1021/acsenergylett.4c00140 ↗
31. 10.1002/anie.20211653410.1002/anie.202116534 ↗
32. 10.1116/6.000266710.1116/6.0002667 ↗
33. 10.1016/S1001-0742(12)60226-510.1016/S1001-0742(12)60226-5 ↗
34. 10.1039/D2TA08488K10.1039/D2TA08488K ↗
35. 10.1021/acsenergylett.4c0115010.1021/acsenergylett.4c01150 ↗
36. 10.1038/s41560-022-01045-210.1038/s41560-022-01045-2 ↗
37. 10.1002/eom2.1247010.1002/eom2.12470 ↗
38. 10.1039/D3TC03575A10.1039/D3TC03575A ↗