Enhanced photo-stability of inverted organic solar cells via using polyethylenimine in the electron extraction layers

dc.contributor.authorSadeghianlemraski, Mozhgan
dc.contributor.authorLee, Brenda Yasie
dc.contributor.authorDavidson-Hall, Tyler
dc.contributor.authorLeonenko, Zoya
dc.contributor.authorAziz, Hany
dc.date.accessioned2020-02-04T16:46:00Z
dc.date.available2020-02-04T16:46:00Z
dc.date.issued2019-10
dc.descriptionThe final publication is available at Elsevier via https://doi.org/10.1016/j.orgel.2019.05.048. © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.description.abstractThe influence of using Polyethylenimine (PEI) in the electron extraction layers (EELs) on the photo-stability of inverted organic solar cells (OSCs) is investigated. Results show that introducing PEI in the commonly used ZnO EELs, either mixed in the same layer with the ZnO (ZnO:PEI mixture) or in a separate layer in the form of a bilayer EEL configuration (ZnO/PEI), reduces the susceptibility of OSCs to photo-degradation with the mixture giving more significant stability enhancements. In comparison to the widely used ZnO EEL, the use of ZnO:PEI mixture is found to lead to ∼ 5× higher PCE stability under continuous UV irradiation, the latter being the main factor behind the limited stability of the cells under sunlight, primarily due to a more stable and FF. Tests on electron only devices show that the higher photo-stability is mainly due to the role of the ZnO:PEI mixture in minimizing light-induced deterioration in electron collection efficiency at OSCs electron collection contacts under sunlight. Kelvin probe force microscopy (KPFM) measurements show that the use of ZnO:PEI helps maintain a more stable surface potential at the electron collection contact, hence the more stable and FF. X-ray photoelectron spectroscopy (XPS) measurements reveal that the stability enhancement is likely associated with chemical interactions between PEI and ITO at the ITO/ZnO:PEI interface that produce a more electronically and energetically stable contact that is less susceptible to changes in surface potential or work function by UV illumination. Using PEI in the form of a neat layer next to the ITO in a bilayer EEL (PEI/ZnO) is found to provide a similar significant enhancement in photo-stability, further ascertaining the above conclusions. The findings not only reveal the potential of utilizing PEI in the EEL, but also shed light on some of the root causes of the limited photo-stability of OSCs and approaches to mitigate their effect.en
dc.description.sponsorshipThe support by the Natural Sciences and Engineering Research Council of Canada and Canadian General-Tower (CGT) Corporation is gratefully acknowledged.en
dc.identifier.urihttps://doi.org/10.1016/j.orgel.2019.05.048
dc.identifier.urihttp://hdl.handle.net/10012/15610
dc.language.isoenen
dc.publisherElsevieren
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectelectron extraction layeren
dc.subjectpolyethylenimine (PEI)en
dc.subjectorganic solar cellsen
dc.subjectphoto-stabilityen
dc.subjectphoto-induced deteriorationen
dc.subjectsurface potentialen
dc.titleEnhanced photo-stability of inverted organic solar cells via using polyethylenimine in the electron extraction layersen
dc.typeArticleen
dcterms.bibliographicCitationM. Sadeghianlemraski, B.Y. Lee, T. Davidson-Hall, Z. Leonenko, H. Aziz, Enhanced photo-stability of inverted organic solar cells via using polyethylenimine in the electron extraction layers, Organic Electronics (2019), doi: https://doi.org/10.1016/j.orgel.2019.05.048.en
uws.contributor.affiliation1Faculty of Engineeringen
uws.contributor.affiliation1Faculty of Scienceen
uws.contributor.affiliation2Electrical and Computer Engineeringen
uws.contributor.affiliation2Physics and Astronomyen
uws.contributor.affiliation2Waterloo Institute for Nanotechnology (WIN)en
uws.peerReviewStatusRevieweden
uws.scholarLevelFacultyen
uws.scholarLevelGraduateen
uws.typeOfResourceTexten

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