Tin–Lead Perovskite Solar Cells Fabricated on Hole Selective Monolayers
Source abstract
Abstract
According to the detailed balanced limit for a single-junction solar cell, tin–lead (Sn–Pb) perovskite solar cells (PSCs) can achieve power conversion efficiencies (PCEs) more than Pb-PSCs. However, the rise in PCE of Sn–Pb PSCs is limited by the choice of hole transport layer to PEDOT:PSS only. Inspired by the use of hole selective monolayers (HSM) in Pb only PSCs, here, we employed 2-(9H-carbazol-9-yl) ethyl] phosphonic acid (2PACz), leading to PCE (21.39%) comparable to PSCs fabricated on conventional PEDOT:PSS (21.37%). Moreover, we reported a small molecule, methyl phosphonic acid (MPA), employing which an equipotential performance (PCE= 21.08%) was obtained owing to its passivation effect on the transparent conducting oxide (TCO) layer. Furthermore, by taking motivation from the idea of cosensitization in dye sensitized solar cells, we explored the point that the coabsorption of 2-(9H-carbazol-9-yl) ethyl] phosphonic acid (2PACz) and a small molecule MPA on TCO glass led to the Sn–Pb PSC (1.25 eV) with a PCE of 23.3% and open-circuit voltage of 0.88 V.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
i-Powered Energy System Research Center (i-PERC), The University of Electro-Communications, 1-5-1 Chofugaoka, Chofu, Tokyo 182-8585, Japan
The University of Tokyo, Research center for Advanced Science and Technology, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan
FUJICO Company, Ltd., 4-31 Makiyamashinmachi, Tobata, Kitakyushu 804-0054, Japan
Funding
New Energy and Industrial Technology Development Organization
References (39)
Show source-provided references
1. 10.1021/ja809598r10.1021/ja809598r ↗
2. 10.1038/s41586-021-03406-510.1038/s41586-021-03406-5 ↗
3. 10.1126/science.abc441710.1126/science.abc4417 ↗
4. 10.1016/j.solener.2016.02.01510.1016/j.solener.2016.02.015 ↗
5. 10.1021/acs.chemrev.8b0031810.1021/acs.chemrev.8b00318 ↗
6. 10.1021/acs.chemrev.8b0055810.1021/acs.chemrev.8b00558 ↗
7. 10.1039/C5EE03874J10.1039/C5EE03874J ↗
8. 10.1126/science.aah555710.1126/science.aah5557 ↗
9. 10.1021/ja503325910.1021/ja5033259 ↗
10. 10.1021/jz500211710.1021/jz5002117 ↗
11. 10.1038/nature1413310.1038/nature14133 ↗
12. 10.1039/C7TA00929A10.1039/C7TA00929A ↗
13. 10.1038/s41560-018-0190-410.1038/s41560-018-0190-4 ↗
14. 10.1016/j.coelec.2018.10.01710.1016/j.coelec.2018.10.017 ↗
15. 10.1038/s41560-020-00705-510.1038/s41560-020-00705-5 ↗
16. 10.1002/aenm.20210106910.1002/aenm.202101069 ↗
17. 10.1038/s41560-020-00692-710.1038/s41560-020-00692-7 ↗
18. 10.1021/acsenergylett.0c0025510.1021/acsenergylett.0c00255 ↗
19. 10.1016/j.scib.2019.08.00210.1016/j.scib.2019.08.002 ↗
20. 10.1039/C9EE02268F10.1039/C9EE02268F ↗
21. 10.1021/acs.jpclett.5b0042010.1021/acs.jpclett.5b00420 ↗
22. 10.1002/adfm.20140149310.1002/adfm.201401493 ↗
23. 10.1016/j.orgel.2019.10558310.1016/j.orgel.2019.105583 ↗
24. 10.1021/acsaem.9b0014110.1021/acsaem.9b00141 ↗
25. 10.1126/science.abf560210.1126/science.abf5602 ↗
26. 10.1039/C8EE01831F10.1039/C8EE01831F ↗
27. 10.1039/D0EE03807E10.1039/D0EE03807E ↗
28. 10.1021/acsenergylett.1c0212410.1021/acsenergylett.1c02124 ↗
29. 10.1002/ange.20070310610.1002/ange.200703106 ↗
30. 10.1002/anie.20110861010.1002/anie.201108610 ↗
31. 10.1002/cssc.20120065510.1002/cssc.201200655 ↗
32. 10.1021/acs.chemrev.8b0063210.1021/acs.chemrev.8b00632 ↗
33. 10.1021/jz501050f10.1021/jz501050f ↗
34. 10.1021/acsenergylett.9b0123710.1021/acsenergylett.9b01237 ↗
35. 10.1039/C5TA01246E10.1039/C5TA01246E ↗
36. 10.1038/s41560-019-0466-310.1038/s41560-019-0466-3 ↗
37. 10.1126/science.aav791110.1126/science.aav7911 ↗
38. 10.1016/j.joule.2021.07.01610.1016/j.joule.2021.07.016 ↗
39. 10.1126/sciadv.aao561610.1126/sciadv.aao5616 ↗