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dc.contributor.authorKaulachs, I.
dc.contributor.authorIvanova, A.
dc.contributor.authorHolsts, A.
dc.contributor.authorRoze, M.
dc.contributor.authorFlerov, A.
dc.contributor.authorTokmakov, Andrei
dc.contributor.authorMihailovs, Igors
dc.contributor.authorRutkis, Martins
dc.date.accessioned2021-08-26T14:44:59Z
dc.date.available2021-08-26T14:44:59Z
dc.date.issued2021
dc.identifier.issn0868-8257
dc.identifier.urihttps://www.sciendo.com/article/10.2478/lpts-2021-0006
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/56495
dc.description.abstractThe main drawback of the methylammonium lead halide perovskite solar cells is their degradation in ambient atmosphere. To investigate ambient-air-induced cell degradation, spec-tral dependencies of open-circuit voltage (VOC), fill factor (FF) and the power conversion effi-ciency (PCE) have been acquired (for the first time reported in literature). Our custom-made measurement system allowed us to perform measurements of the above-mentioned entities in situ directly in vacuum during and after thermal deposition of the elec-trode. We also studied how these parameters in vacuum changed after cell exposure to ambient air for 85 min (50 nm top electrode) and for 180 min (100 nm top Ag electrode). For fresh CH3NH3PbI3–xClx cell (never been in open air) with very high shunt resistance of 3·107 Ω·cm2 (with practically no shorts and therefore FF could be determined mainly by charge carrier recombination processes) we found that FF in vacuum increased along with an increase of the incident photon energy from 0.55 at 760 nm up to 0.82 at 400 nm. Hypothesis considering hot polaron participation in charge carrier photogeneration and recombination processes as well as another competing hypothesis were offered as possible explanations for the observed FF increase. The kinetics of short-circuit photocurrent EQE with a change in pressure was also inves-tigated. It was also shown that perovskite solar cell degradation could be noticeably reduced by increasing the top Ag electrode thickness to at least 100 nm, which could possibly facilitate the usual encapsulation process.---//---This work is licensed under a CC BY 4.0 license.en_US
dc.description.sponsorshipInstitute of Solid State Physics, University of Latvia as the Centre of Excellence has received funding from the European Union’s Horizon 2020 Framework Pro-gramme H2020-WIDESPREAD-01-2016-2017-Teaming Phase2 under grant agreement No. 739508, project CAMART²en_US
dc.language.isoengen_US
dc.publisherDe Gruyteren_US
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739508/EU/Centre of Advanced Material Research and Technology Transfer/CAMART²en_US
dc.relation.ispartofseriesLatvian Journal of Physics and Technical Sciences;58 (1)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES:Physicsen_US
dc.subjectDegradation kineticsen_US
dc.subjectfill factor spectral dependenceen_US
dc.subjectlead halide perovskiteen_US
dc.subjectpower conversion efficiencyen_US
dc.subjectsolar cellsen_US
dc.titlePerovskite CH3NH3PbI3–XClx Solar Cells. Experimental Study of Initial Degradation Kinetics and Fill Factor Spectral Dependenceen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.rights.licenseCC BY 4.0 license
dc.identifier.doi10.2478/lpts-2021-0006


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