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Frequency upconversion in rare-earth doped fluoroindate glasses

dc.contributor.authorAraújo, Cid B. de
dc.contributor.authorMaciel, Glauco S.
dc.contributor.authorMenezes, Leonardo de S.
dc.contributor.authorRakov, Nikifor
dc.contributor.authorFalcão-Filho, Edilson L.
dc.contributor.authorJerez, Vladimir A.
dc.contributor.authorMessaddeq, Younes [UNESP]
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:20:32Z
dc.date.available2014-05-27T11:20:32Z
dc.date.issued2002-12-01
dc.description.abstractWe present recent results on frequency upconversion (UPC) obtained in fluoroindate glasses (FIG) doped with Ho3+, Tm3+ and Nd3+ ions and codoped with Pr3+/Nd3+ and Yb3+/Tb3+ ions. The results for the Ho3+-doped samples show strong evidence of energy transfer (ET) between Ho3+ ions resonantly excited at 640 nm. The origin of the blue-green upconverted fluorescence observed was identified and the dynamics of the signals revealed the pathways involved in the UPC process. In the case of Tm3+-doped FIG, the samples were resonantly excited at 650 nm and the main mechanism that contributes for the red-to-blue upconversion is excited-state absorption (ESA). The FIG samples codoped with Pr3+/Nd3+ were excited at 588 nm in resonance with transitions starting from the ground state of the Nd 3+ and the Pr3+ ions. It was observed that the presence of Nd3+ ions enhanced the Pr3+ emission at 480 nm by two orders of magnitude. Multiphonon (MP)-assisted upconversion is also discussed for Nd3+-doped FIG pumped at 866 nm. Emission at 750 nm with a peculiar linear dependence with the laser intensity was observed and explained. A rate-equation model that includes MP absorption via thermally coupled electronic excited states of Nd3+ was developed and describes well the experimental results. The role played by effective phonon modes is clearly demonstrated. MP-assisted UPC process was also studied in Yb3+/ Tb3+-codoped FIG samples excited at 1064 nm, which is off-resonance with electronic transitions starting from the ground state. It was determined that the mechanism leading to Tb3+ emission in the blue is due to ET from a pair of excited Yb3+ ions followed by ESA in the Tb 3+ ions. © 2002 Académie des sciences/Éditions scientifiques et médicales Elsevier SAS.en
dc.description.affiliationDepartamento de Física Universidade Federal de Pernambuco, 50670-901 Recife, PE
dc.description.affiliationInstituto de Química Universidade do Estado de São Paulo, 14801-970, Araraquara, SP
dc.format.extent885-898
dc.identifierhttp://dx.doi.org/10.1016/S1631-0748(02)01460-1
dc.identifier.citationComptes Rendus Chimie, v. 5, n. 12, p. 885-898, 2002.
dc.identifier.doi10.1016/S1631-0748(02)01460-1
dc.identifier.issn1631-0748
dc.identifier.lattes2998503841917815
dc.identifier.scopus2-s2.0-17644416144
dc.identifier.urihttp://hdl.handle.net/11449/67035
dc.language.isoeng
dc.relation.ispartofComptes Rendus Chimie
dc.relation.ispartofjcr1.877
dc.relation.ispartofsjr0,438
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectFluoroindate glass
dc.subjectFrequency upconversion
dc.subjectRare-earth ions
dc.titleFrequency upconversion in rare-earth doped fluoroindate glassesen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes2998503841917815
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Inorgânica - IQARpt

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