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dc.contributor.authorGünzler, Antonio
dc.contributor.authorBermúdez Ureña, Esteban
dc.contributor.authorMuscarella, Loreta A.
dc.contributor.authorOchoa Gómez, Mario 
dc.contributor.authorOchoa Martínez, Efraín
dc.contributor.authorEhrler, Bruno
dc.contributor.authorSaliba, Michael
dc.contributor.authorSteiner, Ullrich
dc.date.accessioned2023-05-29T14:28:09Z
dc.date.available2023-05-29T14:28:09Z
dc.date.issued2021-02-10
dc.identifier.issn1944-8252
dc.identifier.issn1944-8244
dc.identifier.urihttps://hdl.handle.net/10902/29132
dc.description.abstractUnderstanding and controlling the crystallization of organic-inorganic perovskite materials is important for their function in optoelectronic applications. This control is particularly delicate in scalable single-step thermal annealing methods. In this work, the crystallization mechanisms of flash infrared-annealed perovskite films, grown on substrates with lithographically patterned Au nucleation seeds, are investigated. The patterning enables the in situ observation to study the crystallization kinetics and the precise control of the perovskite nucleation and domain growth, while retaining the characteristic polycrystalline micromorphology with larger crystallites at the boundaries of the crystal domains, as shown by electron backscattering diffraction. Time-resolved photoluminescence measurements reveal longer charge carrier lifetimes in regions with large crystallites on the domain boundaries, relative to the domain interior. By increasing the nucleation site density, the proportion of larger crystallites is increased. This study shows that the combination of rapid thermal annealing with nucleation control is a promising approach to improve perovskite crystallinity and thereby ultimately the performance of optoelectronic devices.es_ES
dc.description.sponsorshipThis work was partially supported by the Swiss National Science Foundation (SNSF) through grants numbers 153990 and 186453. A.G., E.B.-U., E.O.-M., and U.S. acknowledge the financial support by the Adolphe Merkle Foundation. The work of L.A.M. and B.E. is part of the Dutch Research Council (NWO) and was performed at the research institute, AMOLF. The work of L.A.M. was supported by NWO Vidi grant 016.Vidi.179.005. M.O. acknowledges financial support partially from the Swiss State Secretary for Education, Research, and Innovation (SERI) under contract number 17.00105 (EMPIR project HyMet). The EMPIR program is co-financed by the participating states and by the European Union’s Horizon 2020 research and innovation program. E.O.-M. acknowledges support from the Marie Skłodowska Curie fellowship, H2020 grant agreement no. 841005.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rights© ACS under an ACS AuthorChoice License via Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceACS Applied Materials and Interfaces, 2021, 13(5), 6854-6863es_ES
dc.subject.otherPerovskite patterninges_ES
dc.subject.otherIn situes_ES
dc.subject.otherFlash infrared annealinges_ES
dc.subject.otherCrystallizationes_ES
dc.subject.otherNucleationes_ES
dc.titleShaping perovskites: in situ crystallization mechanism of rapid thermally annealed, prepatterned perovskite filmses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1021/acsami.0c20958es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1021/acsami.0c20958
dc.type.versionpublishedVersiones_ES


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