journal article·2019-01-28Open access

Crystalline Molybdenum Oxide Layers as Efficient and Stable Hole Contacts in Organic Photovoltaic Devices

Mehrad Ahmadpour, André L. Fernandes Cauduro, Christophe Méthivier, Birgit Kunert, Chiara Labanti, Roland Resel, Vida Turkovic, Horst-Günter Rubahn, Nadine Witkowski, Andreas K. Schmid, Morten Madsen

ACS Applied Energy Materials· Volume 2· Issue 1

Abstract

High work function metal oxides such as molybdenum oxide (MoOx) have demonstrated good hole contact properties in organic photovoltaic (OPV) devices in the past years and have replaced the otherwise conventionally used PEDOT:PSS. In this work, we introduce new crystalline MoOx layers that outperform the otherwise commonly used thermally grown MoOx layers in OPV devices. These hole contact layers are developed from superoxidized MoO3.2 films grown by reactive sputtering, followed by postannealing in high vacuum to induce crystallization of the otherwise amorphous MoOx films. Standard configuration organic solar cell devices based on DBP as electron donor and C70 as electron acceptor were developed on top of the sputtered MoOx, and a large increase in power conversion efficiency as a function of the MoOx annealing temperature was observed, which is in clear contrast to devices grown on thermally deposited MoOx. The crystallization of the sputtered MoOx at elevated temperatures is shown to lead to high work function films with improved conductivity, resulting in the appealing device properties. Importantly, long-term stability investigations revealed that devices based on these crystalline MoOx films exhibit superior stability as compared to devices based on thermally grown MoOx. These characteristics show that crystalline MoOx prepared by postannealing sputter deposited films forms a superior hole contact layer material for future air-stable organic optoelectronic devices.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Organic Light-Emitting Diodes Research

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

Affiliations

SDU NanoSYD, Mads Clausen Institute, University of Southern Denmark, Alsion 2, 6400 Sønderborg, Denmark

National Center for Electron Microscopy, Molecular Foundry, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, California 94720, United States

Laboratoire de Réactivité de Surface (LRS), Sorbonne Université, CNRS UMR 7197, 4 Place Jussieu, 75005 Paris, France

Institute of Solid State Physics, Graz University of Technology, Petersgasse 16, 8010 Graz, Austria

Institut des Nanosciences de Paris (INSP), Sorbonne Université, UMR CNRS 7588, 4 Place Jussieu, 75005 Paris, France

Funding

Teknologi og Produktion, Det Frie Forskningsr?d · Advanced Research Projects Agency - Energy · Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico · Villum Fonden · European Cooperation in Science and Technology

References (41)

Show source-provided references
1. 10.1038/nmat315910.1038/nmat3159 ↗
2. 10.1038/nenergy.2015.3110.1038/nenergy.2015.31 ↗
3. 10.1021/acsenergylett.6b0001310.1021/acsenergylett.6b00013 ↗
4. 10.1063/1.337433310.1063/1.3374333 ↗
5. 10.1063/1.217409310.1063/1.2174093 ↗
6. 10.1002/adma.20120163010.1002/adma.201201630 ↗
7. 10.1116/1.369275310.1116/1.3692753 ↗
8. 10.1002/adma.1995007012210.1002/adma.19950070122 ↗
9. 10.1557/JMR.2004.025210.1557/JMR.2004.0252 ↗
10. 10.1557/mrs2005.210.1557/mrs2005.2 ↗
11. 10.1039/b817952b10.1039/b817952b ↗
12. 10.1126/science.aat261210.1126/science.aat2612 ↗
13. 10.1038/s41560-018-0134-z10.1038/s41560-018-0134-z ↗
14. 10.1088/0022-3727/49/12/12560410.1088/0022-3727/49/12/125604 ↗
15. 10.1007/s00339-016-9758-710.1007/s00339-016-9758-7 ↗
16. Krebs F. C. · 201210.1002/9781119942436 ↗
17. 10.1063/1.131534410.1063/1.1315344 ↗
18. 10.1063/1.345653010.1063/1.3456530 ↗
19. 10.1016/j.orgel.2014.01.01110.1016/j.orgel.2014.01.011 ↗
20. 10.1002/adfm.20110042910.1002/adfm.201100429 ↗
21. 10.1002/adma.20110003810.1002/adma.201100038 ↗
22. 10.1021/acsami.7b0118310.1021/acsami.7b01183 ↗
23. 10.1016/j.solmat.2004.02.02810.1016/j.solmat.2004.02.028 ↗
24. 10.1016/S0040-6090(00)01410-310.1016/S0040-6090(00)01410-3 ↗
25. 10.1016/j.jpowsour.2013.07.09610.1016/j.jpowsour.2013.07.096 ↗
26. 10.1016/j.jallcom.2014.01.23810.1016/j.jallcom.2014.01.238 ↗
27. 10.1016/S0167-2738(01)00901-810.1016/S0167-2738(01)00901-8 ↗
28. 10.1063/1.492136710.1063/1.4921367 ↗
29. 10.1021/acsami.6b1422810.1021/acsami.6b14228 ↗
30. 10.1016/j.ultramic.2017.03.02510.1016/j.ultramic.2017.03.025 ↗
31. 10.1109/JPHOTOV.2017.271340510.1109/JPHOTOV.2017.2713405 ↗
32. 10.1088/1361-6463/aa7f1c10.1088/1361-6463/aa7f1c ↗
33. 10.1016/j.solmat.2008.11.03410.1016/j.solmat.2008.11.034 ↗
34. 10.1063/1.343244710.1063/1.3432447 ↗
35. 10.1002/adfm.20120099310.1002/adfm.201200993 ↗
36. 10.1016/j.vacuum.2006.08.00610.1016/j.vacuum.2006.08.006 ↗
37. 10.1007/s10854-015-4206-610.1007/s10854-015-4206-6 ↗
38. 10.1002/aenm.20140073410.1002/aenm.201400734 ↗
39. 10.1016/j.jcrysgro.2010.10.14910.1016/j.jcrysgro.2010.10.149 ↗
40. 10.1063/1.12684910.1063/1.126849 ↗
41. 10.1103/PhysRevB.32.831710.1103/PhysRevB.32.8317 ↗