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Zastosuj identyfikator do podlinkowania lub zacytowania tej pozycji: http://hdl.handle.net/20.500.12128/9516
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dc.contributor.authorMinns, J.L.-
dc.contributor.authorZajdel, Paweł-
dc.contributor.authorChernyshov, D.-
dc.contributor.authorVan Beek, W.-
dc.contributor.authorGreen, M.A.-
dc.date.accessioned2019-06-19T06:42:10Z-
dc.date.available2019-06-19T06:42:10Z-
dc.date.issued2017-
dc.identifier.citationNature Communications, Vol. 8 (2017), art. no. 15152pl_PL
dc.identifier.issn2041-1723-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/9516-
dc.description.abstractHybrid perovskites form an emerging family of exceptional light harvesting compounds. However, the mechanism underpinning their photovoltaic effect is still far from understood, which is impeded by a lack of clarity on their structures. Here we show that iodide ions in the methylammonium lead iodide migrate via interstitial sites at temperatures above 280 K. This coincides with temperature dependent static distortions resulting in pseudocubic local symmetry. Based on bond distance analysis, the migrating and distorted iodines are at lengths consistent with the formation of I2 molecules, suggesting a 2I -I2þ2e redox couple. The actual formula of this compound is thus (CH3NH3)PbI3 2x(I2)x where xB0.007 at room temperature. A crucial feature of the tetragonal structure is that the methylammonium ions do not sit centrally in the A-site cavity, but disordered around two off-centre orientations that facilitate the interstitial ion migration via a gate opening mechanism.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectiodide ionpl_PL
dc.subjectammoniumpl_PL
dc.titleStructure and interstitial iodide migration in hybrid perovskite methylammonium lead iodidepl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.relation.journalNature Communicationspl_PL
dc.identifier.doi10.1038/ncomms15152-
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