journal article·2018-04-13Open access

Coating Evaporated MAPI Thin Films with Organic Molecules: Improved Stability at High Temperature and Implementation in High-Efficiency Solar Cells

Francisco Palazon, Daniel Pérez-del-Rey, Sergio Marras, Mirko Prato, Michele Sessolo, Henk J. Bolink, Liberato Manna

ACS Energy Letters· Volume 3· Issue 4

Abstract

Methylammonium lead iodide (MAPI) has proven to be an exceptional light-absorber for single-junction thin-film solar cells. Nonetheless, degradation induced by environmental agents (air, moisture, heat) limits the stability of this hybrid perovskite. Here, we demonstrate that coating evaporated MAPI thin films with different hydrophobic molecules leads to a significant improvement in their stability. We especially investigated the degradation of MAPI and the subsequent formation of PbI2 at 150 °C by in situ XRD analysis and showed that this transformation is remarkably slowed down in films coated with trioctyl phosphine oxide and tridodecyl methylammonium iodide. This enhances the processability of such films, which is an important aspect for the fabrication of thin-film devices. Eventually, we demonstrate that such protected films can be implemented in single-junction n–i–p solar cells without any loss in the device efficiency.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films · Thin-Film Transistor Technologies

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

Affiliations

Instituto de Ciencia Molecular, ICMol, Universidad de Valencia, C/ Catedrático J. Beltrán 2, 46980 Paterna, Spain

Funding

Generalitat Valenciana · Ministerio de Econom?a y Competitividad · H2020 Marie Sklodowska-Curie Actions · FP7 Ideas: European Research Council

References (28)

Show source-provided references
1. 10.1038/nnano.2015.9010.1038/nnano.2015.90 ↗
2. 10.1039/C4CS00458B10.1039/C4CS00458B ↗
3. 10.1038/nphoton.2016.6210.1038/nphoton.2016.62 ↗
4. 10.1073/pnas.160747111310.1073/pnas.1607471113 ↗
5. 10.1126/science.124398210.1126/science.1243982 ↗
6. 10.1021/jz500279b10.1021/jz500279b ↗
7. 10.1002/aenm.20170026410.1002/aenm.201700264 ↗
8. 10.1021/acs.accounts.5b0045510.1021/acs.accounts.5b00455 ↗
9. 10.1039/C7TA00434F10.1039/C7TA00434F ↗
10. 10.1039/C6EE03014A10.1039/C6EE03014A ↗
11. 10.1021/jacs.7b0722310.1021/jacs.7b07223 ↗
12. 10.1021/acsenergylett.6b0069710.1021/acsenergylett.6b00697 ↗
13. 10.1039/C6TA10727C10.1039/C6TA10727C ↗
14. 10.1038/ncomms1568410.1038/ncomms15684 ↗
15. 10.1038/nature1830610.1038/nature18306 ↗
16. 10.1002/anie.20140646610.1002/anie.201406466 ↗
17. 10.1021/jacs.5b0379610.1021/jacs.5b03796 ↗
18. 10.1038/nenergy.2017.11510.1038/nenergy.2017.115 ↗
19. 10.1126/science.aah555710.1126/science.aah5557 ↗
20. 10.1039/C6EE02941H10.1039/C6EE02941H ↗
21. 10.1038/nenergy.2015.1610.1038/nenergy.2015.16 ↗
22. 10.1002/adma.20160306210.1002/adma.201603062 ↗
23. 10.1021/acsenergylett.6b0023610.1021/acsenergylett.6b00236 ↗
24. 10.1039/C7TA09646A10.1039/C7TA09646A ↗
25. 10.1039/C6EE02100J10.1039/C6EE02100J ↗
26. 10.1039/C6RA05718G10.1039/C6RA05718G ↗
27. 10.1016/j.nanoen.2017.05.04910.1016/j.nanoen.2017.05.049 ↗
28. 10.1002/sia.74021030210.1002/sia.740210302 ↗