Field Effect Passivation in Perovskite Solar Cells by a LiF Interlayer

dc.contributor.affiliationPontificia Universidad Católica del Perú. Departamento de Ciencias
dc.contributor.authorMenzel, D.
dc.contributor.authorAl-Ashouri, A.
dc.contributor.authorTejada, A.
dc.contributor.authorLevine, I.
dc.contributor.authorGuerra Torres, J.A.
dc.contributor.authorRech, B.
dc.contributor.authorAlbrecht, S.
dc.contributor.authorKorte, L.
dc.date.accessioned2026-03-13T16:59:19Z
dc.date.issued2022
dc.description.abstractThe fullerene C60 is commonly applied as the electron transport layer in high-efficiency metal halide perovskite solar cells and has been found to limit their open circuit voltage. Through ultra-sensitive near-UV photoelectron spectroscopy in constant final state mode (CFSYS), with an unusually high probing depth of 5–10 nm, the perovskite/C60 interface energetics and defect formation is investigated. It is demonstrated how to consistently determine the energy level alignment by CFSYS and avoid misinterpretations by accounting for the measurement-induced surface photovoltage in photoactive layer stacks. The energetic offset between the perovskite valence band maximum and the C60 HOMO-edge is directly determined to be 0.55 eV. Furthermore, the voltage enhancement upon the incorporation of a LiF interlayer at the interface can be attributed to originate from a mild dipole effect and probably the presence of fixed charges, both reducing the hole concentration in the vicinity of the perovskite/C60 interface. This yields a field effect passivation, which overcompensates the observed enhanced defect density in the first monolayers of C60.
dc.description.sponsorshipFunding: The authors acknowledge funding by the Federal Ministry of Education and Research (BMBF) under the Grant 03SF0631 (PEROWIN), the Helmholtz Association within the HySPRINT Innovation lab project, and the HyPerCells joint Graduate School. Furthermore, this work was supported in part by the German Federal Ministry for Economic Affairs and Climate Action under Grants 03EE1017B (Project P3T) and 03EE1086C (PrEsto), and the joint agreement between the DAAD (German Academic Exchange Service) and FONDECYT (National Fund for Scientific, Technological Development and Technological Innovation) under the agreements 57508544 DAAD and 423‐2019‐FONDECYT. Further support had been provided by the PUCP vice chancellorship for research (VRI, Project No. CAP‐2019‐3‐0041/702). The authors thank Thomas Lußky for technical support and Bor Li for part of the sample preparation. Danbi Yoo is acknowledged for assistance with optical spectroscopy. Additionally, the authors thank Tilmann Neubert for the fruitful discussion about the XPS core level modeling. I.L. thanks the AiF project (ZIM‐KK5085302DF0) for financial support.
dc.identifier.doihttps://doi.org/10.1002/aenm.202201109
dc.identifier.urihttp://hdl.handle.net/20.500.14657/206256
dc.language.isoeng
dc.publisherJohn Wiley and Sons
dc.relation.ispartofurn:issn:1614-6832
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.sourceAdvanced Energy Materials; Vol. 12, Núm. 30 (2022)
dc.subjectPassivation
dc.subjectMaterials science
dc.subjectPerovskite (structure)
dc.subjectX-ray photoelectron spectroscopy
dc.subjectMonolayer
dc.subjectOpen-circuit voltage
dc.subjectHalide
dc.subjectAnalytical Chemistry (journal)
dc.subjectPhotoemission spectroscopy
dc.subjectOptoelectronics
dc.subjectLayer (electronics)
dc.subjectChemical engineering
dc.subjectVoltage
dc.subjectInorganic chemistry
dc.subjectNanotechnology
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#2.04.00
dc.titleField Effect Passivation in Perovskite Solar Cells by a LiF Interlayer
dc.typehttp://purl.org/coar/resource_type/c_6501
dc.type.otherArtículo
dc.type.versionhttps://vocabularies.coar-repositories.org/version_types/c_970fb48d4fbd8a85/

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