Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/25874
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dc.contributor.authorVAN GOMPEL, Wouter-
dc.contributor.authorHERCKENS, Roald-
dc.contributor.authorREEKMANS, Gunter-
dc.contributor.authorRUTTENS, Bart-
dc.contributor.authorD'HAEN, Jan-
dc.contributor.authorADRIAENSENS, Peter-
dc.contributor.authorLUTSEN, Laurence-
dc.contributor.authorVANDERZANDE, Dirk-
dc.date.accessioned2018-04-12T12:24:24Z-
dc.date.available2018-04-12T12:24:24Z-
dc.date.issued2018-
dc.identifier.citationThe Journal of Physical Chemistry C, 112 (8), p. 4117-4124-
dc.identifier.issn1932-7447-
dc.identifier.urihttp://hdl.handle.net/1942/25874-
dc.description.abstractThe highest efficiency in perovskite solar cells is currently achieved with mixed-cation hybrid perovskites. The ratio in which the cations are present in the perovskite structure has an important effect on the optical properties and the stability of these materials. At present, the formamidinium cation is an integral part of many of the highest efficiency perovskite systems. In this work, we introduce a nuclear magnetic resonance (NMR) spectroscopy protocol for the identification and differentiation of mixed perovskite phases and of a secondary phase due to formamidinium degradation. The influence of the cooling rate used in a precipitation method on the FA/MA ratio in formamidinium–methylammonium lead iodide perovskites (FAxMA1–xPbI3) was investigated and compared to the FA/MA ratio in thin films. In order to obtain the FA/MA ratio from fast and accessible liquid-state 1H NMR spectra, the influence of the acidity of the solution on the line width of the resonances was elucidated. The ratio of the organic cations incorporated into the perovskite structure could be reliably quantified in the presence of the secondary phase through a combination of liquid-state 1H NMR and solid-state 13C NMR spectroscopic analysis.-
dc.description.sponsorshipW.T.M.V.G. is an SB Ph.D. fellow at FWO (project number 1S17516N), and the FWO is acknowledged for the funding of the research. R.H. is a special research fund (BOF) Doctoral (Ph.D.) student at UHasselt/IMO. This work has been carried out in the context of the Solliance network (www.solliance.eu), from which the UHasselt is a full member. Research Foundation Flanders (FWO) and the EU funded network MERA.NET are acknowledged for the funding of the PROMISES project.-
dc.language.isoen-
dc.rightsCopyright 2018 American Chemical Society-
dc.subject.otherhybrid perovskites; nuclear magnetic resonance spectroscopy-
dc.titleDegradation of the Formamidinium Cation and the Quantification of the Formamidinium–Methylammonium Ratio in Lead Iodide Hybrid Perovskites by Nuclear Magnetic Resonance Spectroscopy-
dc.typeJournal Contribution-
dc.identifier.epage4124-
dc.identifier.issue8-
dc.identifier.spage4117-
dc.identifier.volume112-
local.bibliographicCitation.jcatA1-
dc.description.notesVanderzande, D (reprint author), Hasselt Univ, Organ & Biopolymer Chem, Inst Mat Res IMO, Hybrid Mat Design HyMaD, Agoralaan 1 Bldg D, B-3590 Diepenbeek, Belgium, IMEC, IMOMEC Div, Wetenschapspk 1, B-3590 Diepenbeek, Belgium, dirk.vanderzande@uhasselt.be-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1021/acs.jpcc.7b09805-
dc.identifier.isi000426802500001-
item.contributorVAN GOMPEL, Wouter-
item.contributorHERCKENS, Roald-
item.contributorREEKMANS, Gunter-
item.contributorRUTTENS, Bart-
item.contributorD'HAEN, Jan-
item.contributorADRIAENSENS, Peter-
item.contributorLUTSEN, Laurence-
item.contributorVANDERZANDE, Dirk-
item.validationecoom 2019-
item.fullcitationVAN GOMPEL, Wouter; HERCKENS, Roald; REEKMANS, Gunter; RUTTENS, Bart; D'HAEN, Jan; ADRIAENSENS, Peter; LUTSEN, Laurence & VANDERZANDE, Dirk (2018) Degradation of the Formamidinium Cation and the Quantification of the Formamidinium–Methylammonium Ratio in Lead Iodide Hybrid Perovskites by Nuclear Magnetic Resonance Spectroscopy. In: The Journal of Physical Chemistry C, 112 (8), p. 4117-4124.-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
crisitem.journal.issn1932-7447-
crisitem.journal.eissn1932-7455-
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