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dc.contributor.authorWinterstein, A.en
dc.contributor.authorAkamatsu, H.en
dc.contributor.authorMoencke, D.en
dc.contributor.authorTanaka, K.en
dc.contributor.authorSchmidt, M. A.en
dc.contributor.authorWondraczek, L.en
dc.date.accessioned2015-02-18T06:34:02Z-
dc.date.available2015-02-18T06:34:02Z-
dc.date.issued2013-02-01-
dc.identifier.issn2159-3930-
dc.identifier.urihttp://hdl.handle.net/2433/194095-
dc.description.abstractTransition metal ions such as Mn[2+], Fe[2+], or Co[2+] provide an interesting alternative to rare earth dopants in optically active glasses. In terms of their magneto-optical properties, they are not yet very well exploited. Here, we report on the effect of Mn[2+] on Faraday rotation in a metaphosphate glass matrix along the join Mn{x}Sr{1-x}(PO{3}){2} with x = 0...1. Mn[2+] shows small optical extinction in the visible spectral range and, compared to other transition metal ions, a high effective magnetic moment. At high Mn- levels, however, the magneto-optical activity of Mn[2+] is strongly quenched due to ionic clustering. The magnetic properties of the heavily Mn[2+]-loaded phosphate matrix are dominated by a superexchange interaction in the Mn[2+]-O-Mn[2+] bridge with antiparallel spin alignment between Mn[2+] and O[2-] species. The apparent paramagnetic potential of Mn[2+] species can therefore not be exploited at room temperature.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherOptical Society of Americaen
dc.rights© 2013 Optical Society of America. One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modifications of the content of this paper are prohibited.en
dc.titleMagnetic and magneto-optical quenching in (Mn[2+], Sr[2+]) metaphosphate glassesen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleOptical Materials Expressen
dc.identifier.volume3-
dc.identifier.issue2-
dc.identifier.spage184-
dc.identifier.epage193-
dc.relation.doi10.1364/OME.3.000184-
dc.textversionpublisher-
dcterms.accessRightsopen access-
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