Polaron-Mediated Luminescence in Lithium Niobate and Lithium Tantalate and Its Domain Contrast

dc.bibliographicCitation.firstPage214
dc.bibliographicCitation.issue5
dc.bibliographicCitation.journalTitleCrystals : open access journaleng
dc.bibliographicCitation.volume8
dc.contributor.authorReichenbach, Philipp
dc.contributor.authorKämpfe, Thomas
dc.contributor.authorHaußmann, Alexander
dc.contributor.authorThiessen, Andreas
dc.contributor.authorWoike, Theo
dc.contributor.authorSteudtner, Robin
dc.contributor.authorKocsor, Laura
dc.contributor.authorSzaller, Zsuzsanna
dc.contributor.authorKovács, László
dc.contributor.authorEng, Lukas M.
dc.date.accessioned2022-12-21T13:10:35Z
dc.date.available2022-12-21T13:10:35Z
dc.date.issued2018-5-15
dc.description.abstractIn this review article, we discuss photoluminescence phenomena mediated by polarons in lithium niobate (LNO). At first we present the fundamentals on polaron states in LNO and their energy levels, i.e., on free and bound electron polarons, on hole polarons as well as on bipolarons. We discuss the absorption measurements on reduced as well as on doped LNO that made the characterization of the formed polaron states possible by their absorption bands. Next, we proceed by reporting on the two polaron-mediated photoluminescence bands that have been observed in LNO: (1) A near-infrared luminescence band in the range of 1.5 eV shows a mono-exponential decay and a strong dependence on iron doping. This luminescence is emitted by bound polarons returning from an excited state to the ground state. (2) A luminescence band at visible wavelengths with a maximum at 2.6 eV shows a stretched-exponential decay and is strongly enhanced by optical damage resistant doping around the doping threshold. This luminescence stems from the recombination of free electron and hole polarons. The next major topic of this review are domain contrasts of the visible photoluminescence that have been observed after electrical poling of the substrate, as singly inverted domains show a slightly reduced and faster decaying luminescence. Subsequent annealing results in an exponential decrease of that domain contrast. We show that this contrast decay is strongly related to the mobility of lithium ions, thus confirming the role of polar defect complexes, including lithium vacancies, for these domain contrasts. Finally we discuss the extension of our investigations to lithium tantalate (LTO) samples. While the results on the domain contrast and its decay are similar to LNO, there are remarkable differences in their luminescence spectra.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10715
dc.identifier.urihttp://dx.doi.org/10.34657/9751
dc.language.isoeng
dc.publisherBasel : MDPI
dc.relation.doihttps://doi.org/10.3390/cryst8050214
dc.relation.essn2073-4352
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540
dc.subject.otherDefecteng
dc.subject.otherDefect complexeng
dc.subject.otherDomain contrasteng
dc.subject.otherDoping thresholdeng
dc.subject.otherFerroelectriceng
dc.subject.otherLithium niobateeng
dc.subject.otherLithium tantalateeng
dc.subject.otherMultiphoton luminescenceeng
dc.subject.otherPolaroneng
dc.subject.otherThermal relaxationeng
dc.titlePolaron-Mediated Luminescence in Lithium Niobate and Lithium Tantalate and Its Domain Contrasteng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIFWD
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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