Effects of Alkaline Earth Metal Additives on Methylammonium-Free Lead Halide Perovskite Thin Films and Solar Cells

dc.contributor.author Yüce, Hürriyet
dc.contributor.author LaFollette, Diana K.
dc.contributor.author Demir, Mustafa Muammer
dc.contributor.author Perini, Carlo A.R.
dc.contributor.author Correa-Baena, Juan-Pablo
dc.date.accessioned 2022-07-28T10:50:49Z
dc.date.available 2022-07-28T10:50:49Z
dc.date.issued 2022
dc.description National Science Foundation (NSF) (ECCS-1542174) and (DGE-2039655) en_US
dc.description.abstract Organic–inorganic lead halide perovskite solar cells are regarded as one of the most promising technologies for the next generation of photovoltaics due to their high power conversion efficiency (PCE) and simple solution manufacturing. Among the different compositions, the formamidinium lead iodide (FAPbI3) photoactive phase has a bandgap of 1.4 eV, which enables the corresponding higher PCEs according to the Shockley–Queisser limit. However, the photoactive crystal phase of FAPbI3 is not stable at room temperature. The most high-performing compositions to date have reduced this problem by incorporating the methylammonium (MA) cation into the FAPbI3 composition, although MA has poor stability at high temperatures and in humid environments, which can limit the lifetime of FAxMA1−xPbI3 films. CsxFA1−xPbI3 perovskites are also explored, but despite better stability they still lag in performance. Herein, the additive engineering of MA-free organic−inorganic lead halide perovskites using divalent cations Sr2+ and Ca2+to enhance the performances of CsxFA1−xPbI3 perovskite compositions is explored. It is revealed that the addition of up to 0.5% of Sr2+ and Ca2+ leads to improvements in morphology and reduction in microstrain. The structural improvements observed correlate with improved solar cell performances at low additive concentrations. en_US
dc.identifier.doi 10.1002/solr.202100999
dc.identifier.issn 2367-198X en_US
dc.identifier.scopus 2-s2.0-85130508779
dc.identifier.uri https://doi.org/10.1002/solr.202100999
dc.identifier.uri https://hdl.handle.net/11147/12214
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.relation.ispartof Solar RRL en_US
dc.rights info:eu-repo/semantics/embargoedAccess en_US
dc.subject Solar cells en_US
dc.subject High performance en_US
dc.subject Photoelectric conversion efficiencies en_US
dc.subject UV solidification en_US
dc.title Effects of Alkaline Earth Metal Additives on Methylammonium-Free Lead Halide Perovskite Thin Films and Solar Cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0002-7459-2833
gdc.author.id 0000-0003-1309-3990
gdc.author.institutional Yüce, Hürriyet
gdc.author.institutional Demir, Mustafa Muammer
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
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gdc.coar.access embargoed access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.contributor.affiliation Izmir Institute of Technology en_US
gdc.contributor.affiliation Georgia Institute of Technology en_US
gdc.contributor.affiliation Izmir Institute of Technology en_US
gdc.contributor.affiliation Georgia Institute of Technology en_US
gdc.contributor.affiliation Georgia Institute of Technology en_US
gdc.description.department İzmir Institute of Technology. Materials Science and Engineering en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 6
gdc.description.wosquality Q2
gdc.identifier.openalex W4280607651
gdc.identifier.wos WOS:000798535300001
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.diamondjournal false
gdc.oaire.impulse 5.0
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gdc.oaire.isgreen false
gdc.oaire.popularity 5.926231E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration International
gdc.openalex.fwci 0.5382336
gdc.openalex.normalizedpercentile 0.6
gdc.opencitations.count 4
gdc.plumx.mendeley 19
gdc.plumx.scopuscites 4
gdc.scopus.citedcount 4
gdc.wos.citedcount 4
relation.isAuthorOfPublication.latestForDiscovery dd55ee8a-44b0-42ff-bbe9-2f2e7467a491
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