Increasing VOC of Inverted Inorganic Perovskite Solar Cells Through Nickel Oxide Modification
Source abstract
Abstract
Abstract Compared to conventional structure inorganic perovskite solar cells (PSC), the power conversion efficiency (PCE) of inverted structure devices still falls behind. In inverted structures, the commonly used hole transport layer (HTL), nickel oxide (NiOx), is hindered by low carrier transport efficiency. To address this issue, nickel oxide nanoparticles with potassium hexafluorosilicate (KSiF6) in inverted CsPbI3 perovskite solar cells are modified. The high electronegativity of KSiF6 leads to an increased content of Ni3⁺ in NiOx, greatly enhancing the electrical conductivity. Meanwhile, potassium (K) from the modified HTL diffuses into the perovskite layer after annealing, which further passivates defects at the grain boundaries. As a result, a PCE of 19.8% is achieved under ambient air conditions, with the open–circuit voltage (VOC) significantly increasing from 1.14 to 1.21 V.
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Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Solid-state spectroscopy and crystallography
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Photoelectronic Thin Film Devices and Technology State Key Laboratory of Photovoltaic Materials and Cells Tianjin Key Laboratory of Efficient Solar Energy Utilization Ministry of Education Engineering Research Center of Thin Film Photoelectronic Technology Nankai University Tianjin 300350 China
Funding
National Key Research and Development Program of China · National Natural Science Foundation of China
References (28)
Show source-provided references
1. 10.1038/s41560-023-01250-710.1038/s41560-023-01250-7 ↗
2. 10.1016/j.esci.2024.10024310.1016/j.esci.2024.100243 ↗
3. 10.1039/D1EE01562A10.1039/D1EE01562A ↗
4. 10.1002/ange.20210880010.1002/ange.202108800 ↗
5. 10.1039/D3NJ00231D10.1039/D3NJ00231D ↗
6. 10.1002/adfm.20241611810.1002/adfm.202416118 ↗
7. 10.1016/j.esci.2023.10018510.1016/j.esci.2023.100185 ↗
8. 10.1039/D4EE02486A10.1039/D4EE02486A ↗
9. 10.1002/adma.20231223710.1002/adma.202312237 ↗
10. 10.1002/anie.20230581510.1002/anie.202305815 ↗
11. 10.1016/j.esci.2024.10027310.1016/j.esci.2024.100273 ↗
12. 10.1021/acsenergylett.2c0121910.1021/acsenergylett.2c01219 ↗
13. 10.1002/solr.20230002210.1002/solr.202300022 ↗
14. 10.1039/C5TA06398A10.1039/C5TA06398A ↗
15. 10.1126/science.aag270010.1126/science.aag2700 ↗
16. 10.1002/solr.20170004810.1002/solr.201700048 ↗
17. 10.1002/eem2.1203910.1002/eem2.12039 ↗
18. 10.1016/j.joule.2020.06.00410.1016/j.joule.2020.06.004 ↗
19. 10.1002/aenm.20190164210.1002/aenm.201901642 ↗
20. 10.1039/C9TC05759E10.1039/C9TC05759E ↗
21. 10.1126/science.adj885810.1126/science.adj8858 ↗
22. 10.1002/aenm.20240501610.1002/aenm.202405016 ↗
23. 10.1002/adfm.20241939310.1002/adfm.202419393 ↗
24. 10.1016/j.joule.2022.06.02610.1016/j.joule.2022.06.026 ↗
25. 10.1002/adfm.20220304910.1002/adfm.202203049 ↗
26. 10.1039/C7TC04696K10.1039/C7TC04696K ↗
27. 10.1016/j.tsf.2005.04.06110.1016/j.tsf.2005.04.061 ↗
28. 10.1002/aenm.20190308310.1002/aenm.201903083 ↗