journal article·2024-04-03

Tuning Surface Defect States in Sputtered Titanium Oxide Electron Transport Layers for Enhanced Stability of Organic Photovoltaics

Mehrad Ahmadpour, Mariam Ahmad, Michela Prete, John Lundsgaard Hansen, Denys I. Miakota, William Greenbank, Yunlin Jacques Zheng, Michiel Top, Thomas Ebel, Horst-Günter Rubahn, Vida Turkovic, Stela Canulescu, Nadine Witkowski, Morten Madsen

ACS Applied Materials & Interfaces· Volume 16· Issue 13
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Abstract

Nonfullerene acceptors (NFAs) have dramatically improved the power conversion efficiency (PCE) of organic photovoltaics (OPV) in recent years; however, their device stability currently remains a bottleneck for further technological progress. Photocatalytic decomposition of nonfullerene acceptor molecules at metal oxide electron transport layer (ETL) interfaces has in several recent reports been demonstrated as one of the main degradation mechanisms for these high-performing OPV devices. While some routes for mitigating such degradation effects have been proposed, e.g., through a second layer integrated on the ETL surface, no clear strategy that complies with device scale-up and application requirements has been presented to date. In this work, it is demonstrated that the development of sputtered titanium oxide layers as ETLs in nonfullerene acceptor based OPV can lead to significantly enhanced device lifetimes. This is achieved by tuning the concentration of defect states at the oxide surface, via the reactive sputtering process, to mitigate the photocatalytic decomposition of NFA molecules at the metal oxide interlayers. Reduced defect state formation at the oxide surface is confirmed through X-ray photoelectron spectroscopy (XPS) studies, while the reduced photocatalytic decomposition of nonfullerene acceptor molecules is confirmed via optical spectroscopy investigations. The PBDB-T:ITIC organic solar cells show power conversion efficiencies of around 10% and significantly enhanced photostability. This is achieved through a reactive sputtering process that is fully scalable and industry compatible.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications

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

Affiliations

Mads Clausen Institute, Center for Advanced Photovoltaics and Thin Film Energy Devices (SDU CAPE), University of Southern Denmark, So̷nderborg 6400, Denmark

SDU Climate Cluster, University of Southern Denmark, Odense 5230, Denmark

Department of Physics and Astronomy/Interdisciplinary Nanoscience Center (iNano), Aarhus University, Ny Munkegade 120, Aarhus C DK-8000, Denmark

Department of Electrical and Photonics Engineering, Technical University of Denmark, Frederiksborgvej 399, Roskilde DK-4000, Denmark

Centre for Industrial Electronics, Department of Mechanical and Electrical Engineering, University of Southern Denmark, Alsion 2, So̷nderborg DK-6400, Denmark

UMR CNRS 7588, Institut des Nanosciences de Paris, Sorbonne Université, Paris F-75005, France

Fraunhofer Institute for Organic Electronics, Electron Beam and Plasma Technology FEP, Winterbergstrasse 28, Dresden 01277, Germany

University of Southern Denmark, SDU NanoSYD, Mads Clausen Institute, So̷nderborg 6400, Denmark

Funding

Danmarks Frie Forskningsfond · Uddannelses- og Forskningsministeriet

References (44)

Show source-provided references
1. 10.1039/C1EE02728J10.1039/C1EE02728J ↗
2. 10.1016/S1369-7021(12)70019-610.1016/S1369-7021(12)70019-6 ↗
3. 10.1088/2058-8585/ab556f10.1088/2058-8585/ab556f ↗
4. 10.1002/pip.333610.1002/pip.3336 ↗
5. 10.1021/acsaelm.9b0082610.1021/acsaelm.9b00826 ↗
6. 10.1002/adma.20190221010.1002/adma.201902210 ↗
7. 10.1002/ente.20200023410.1002/ente.202000234 ↗
8. 10.1002/adma.20220208910.1002/adma.202202089 ↗
9. 10.1021/acs.chemrev.1c0095510.1021/acs.chemrev.1c00955 ↗
10. 10.1039/C5EE02871J10.1039/C5EE02871J ↗
11. 10.1021/ja513189710.1021/ja5131897 ↗
12. 10.1039/C6EE02851A10.1039/C6EE02851A ↗
13. 10.1016/j.ultramic.2017.03.02510.1016/j.ultramic.2017.03.025 ↗
14. 10.1063/1.492136710.1063/1.4921367 ↗
15. 10.1038/nmat315910.1038/nmat3159 ↗
16. 10.1021/acsaem.8b0145210.1021/acsaem.8b01452 ↗
17. 10.1016/j.jallcom.2014.01.23810.1016/j.jallcom.2014.01.238 ↗
18. 10.1016/S0040-6090(00)01410-310.1016/S0040-6090(00)01410-3 ↗
19. 10.1016/j.jpowsour.2013.07.09610.1016/j.jpowsour.2013.07.096 ↗
20. 10.1016/S0167-2738(01)00901-810.1016/S0167-2738(01)00901-8 ↗
21. 10.1016/j.apmt.2018.11.01110.1016/j.apmt.2018.11.011 ↗
22. 10.1021/acsami.6b1422810.1021/acsami.6b14228 ↗
23. 10.1007/s13391-019-00163-610.1007/s13391-019-00163-6 ↗
24. 10.1016/j.nanoen.2019.05.00410.1016/j.nanoen.2019.05.004 ↗
25. 10.1021/acsaem.9b0145410.1021/acsaem.9b01454 ↗
26. 10.1016/j.orgel.2013.05.02810.1016/j.orgel.2013.05.028 ↗
27. 10.1038/s41467-019-10351-510.1038/s41467-019-10351-5 ↗
28. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
29. 10.1039/C9TA07417A10.1039/C9TA07417A ↗
30. 10.1016/j.scib.2019.10.01910.1016/j.scib.2019.10.019 ↗
31. 10.1002/solr.20200063810.1002/solr.202000638 ↗
32. 10.1002/aenm.20140160610.1002/aenm.201401606 ↗
33. 10.1002/eem2.1262010.1002/eem2.12620 ↗
34. 10.1021/acsami.1c0070010.1021/acsami.1c00700 ↗
35. 10.1002/adma.20230140410.1002/adma.202301404 ↗
36. 10.1002/ente.20200029510.1002/ente.202000295 ↗
37. 10.1063/1.35630610.1063/1.356306 ↗
38. 10.1016/S0039-6028(00)00420-910.1016/S0039-6028(00)00420-9 ↗
39. 10.1021/jp068606i10.1021/jp068606i ↗
40. 10.1021/jp111335w10.1021/jp111335w ↗
41. 10.1016/S0039-6028(97)00863-710.1016/S0039-6028(97)00863-7 ↗
42. 10.1039/C5CC05853H10.1039/C5CC05853H ↗
43. 10.1063/1.172157910.1063/1.1721579 ↗
44. 10.1021/jz401214610.1021/jz4012146 ↗