Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/37255
Title: The Role of SnF2 Additive on Interface Formation in All Lead-Free FASnI(3) Perovskite Solar Cells
Authors: Zillner, Julia
BOYEN, Hans-Gerd 
Schulz, Philip
Hanisch, Jonas
Gauquelin, Nicolas
Kueffner, Johannes
Verbeeck, Johan
DESTA, Derese 
Eisele, Lisa
Ahlswede, Erik
Powalla, Michael
Issue Date: 2022
Publisher: WILEY-V C H VERLAG GMBH
Source: ADVANCED FUNCTIONAL MATERIALS, (Art N° 2109649)
Status: Early view
Abstract: Tin-based perovskites are promising alternative absorber materials for leadfree perovskite solar cells but need strategies to avoid fast tin (Sn) oxidation. Generally, this reaction can be slowed down by the addition of tin fluoride (SnF2) to the perovskite precursor solution, which also improves the perovskite layer morphology. Here, this work analyzes the spatial distribution of the additive within formamidinium tin triiodide (FASnI(3)) films deposited on top of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) hole transporting layers. Employing time-of-flight secondary ion mass spectrometry and a combination of hard and soft X-ray photoelectron spectroscopy, it is found that Sn F2 preferably accumulates at the PEDOT:PSS/perovskite interface, accompanied by the formation of an ultrathin SnS interlayer with an effective thickness of approximate to 1.2 nm.
Notes: Zillner, J; Ahlswede, E (corresponding author), Ctr Solar Energy & Hydrogen Res Baden Wurttemberg, Meitnerstr 1, D-70563 Stuttgart, Germany.; Boyen, HG (corresponding author), Hasselt Univ, Inst Mat Res IMO IMOMEC, Wetenschapspk 1, B-3590 Diepenbeek, Belgium.
julia.zillner@zsw-bw.de; hansgerd.boyen@uhasselt.be;
erik.ahlswede@zsw-bw.de
Keywords: hard X-ray photoelectron spectroscopy; poly(3,4-ethylenedioxythiophene):;poly(styrenesulfonate); Sn-based perovskite solar cells; SnF2 additives;;SnS interlayer; time-of-flight secondary ion mass spectrometry
Document URI: http://hdl.handle.net/1942/37255
ISSN: 1616-301X
e-ISSN: 1616-3028
DOI: 10.1002/adfm.202109649
ISI #: WOS:000779891000001
Rights: © 2022 Wiley-VCH GmbH
Category: A1
Type: Journal Contribution
Validations: ecoom 2023
Appears in Collections:Research publications

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