364 resultados para Yb3


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In this report we investigate the optical properties and energy-transfer upconversion luminescence of Ho3+- and Tb3+/Yb 3+-codoped PbGeO3-PbF2-CdF2 glass-ceramic under infrared excitation. In Ho3+/Yb 3+-codoped sample, green(545 nm), red(652 nm), and near-infrared(754 nm) upconversion luminescence corresponding to the 4S 2(5F4) 5I8, 5F5 5I8, and 4S2(5F4) 5I 7, respectively, was readly observed. Blue(490 nm) signals assigned to the 5F2,3 5I8 transition was also detected. In the Tb3+/Yb3+ system, bright UV-visible emission around 384, 415, 438, 473-490, 545, 587, and 623 nm, identified as due to the 5D3(5G6) 7FJ(J=6,5,4) and 5D4 7FJ(J=6,5,4,3) transitions, was measured. The comparison of the upconversion process in glass ceramic and its glassy precursor revealed that the former samples present much higher upconversion efficiencies. The dependence of the upconversion emission upon pump power, and doping contents was also examined. The results indicate that successive energy-transfer between ytterbium and holmium ions and cooperative energy-transfer between ytterbium and terbium ions followed by excited-state absorption are the dominant upconversion excitation mechanisms herein involved. The viability of using the samples for three-dimensional solid-state color displays is also discussed.

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Erbium Er3+ and ytterbium Yb3+ codoped fluoro-phosphate glasses belonging to the system NaPO3-YF 3-BaF2-CaF2 have been prepared by the classical melt-quenching technique. Glasses containing up to 10 wt% of erbium and ytterbium fluorides have been obtained and characterized using differential scanning calorimetry (DSC) and UV-visible and near-infrared spectroscopy. Transparent and homogeneous glass-ceramics have been then reproducibly synthetized by appropriate heat treatment above glass transition temperature of a selected parent glass. Structural investigations of the crystallization performed through X-ray diffractometry (XRD) and scanning electron microscopy (SEM) have evidenced the formation of fluorite-type cubic crystals based during the devitrification process. Finally, infrared to visible up-conversion emission upon excitation at 975 nm has been studied on the Er3+ and Yb 3+ codoped glass-ceramics as a function of thermal treatment time. A large enhancement of intensity of the up-conversion emissions-about 150 times- has been observed in the glass-ceramics if compared to the parent glass one, suggesting an incorporation of the rare-earth ions (REI) into the crystalline phase. 2012 The American Ceramic Society.

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Coordenao de Aperfeioamento de Pessoal de Nvel Superior (CAPES)

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Fundao de Amparo Pesquisa do Estado de So Paulo (FAPESP)

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Ps-graduao em Qumica - IQ

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This manuscript reports the first example of up-conversion properties involving Yb3+ and Tb3+ ions in five isostructural Lanthanide-Organic Frameworks (LnOFs), herein designated as UCMarker-1 to UCMarker-5, respectively, and their application as optical probes for the identification of gunshot residues (GSRs) and the ammunition encryption procedure. The excitation of the Yb3+2 F-7/2 <-> F-2(5/2) transition (980 nm) at room temperature leads to visible up-conversion (UC) emission of Tb3+ D-5(4) -> F-7(J). The GSR and lead-free primer residues are easily identified upon UV radiation (lambda = 254 nm). These results prove that the exploration of LnOFs to identify GSR is attractive for the identification of ammunition origins or caliber recognition.

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The aim of this Ph.D. project has been the design and characterization of new and more efficient luminescent tools, in particular sensors and labels, for analytical chemistry, medical diagnostics and imaging. Actually both the increasing temporal and spatial resolutions that are demanded by those branches, coupled to a sensitivity that is required to reach the single molecule resolution, can be provided by the wide range of techniques based on luminescence spectroscopy. As far as the development of new chemical sensors is concerned, as chemists we were interested in the preparation of new, efficient, sensing materials. In this context, we kept developing new molecular chemosensors, by exploiting the supramolecular approach, for different classes of analytes. In particular we studied a family of luminescent tetrapodal-hosts based on aminopyridinium units with pyrenyl groups for the detection of anions. These systems exhibited noticeable changes in the photophysical properties, depending on the nature of the anion; in particular, addition of chloride resulted in a conformational change, giving an initial increase in excimeric emission. A good selectivity for dicarboxylic acid was also found. In the search for higher sensitivities, we moved our attention also to systems able to perform amplification effects. In this context we described the metal ion binding properties of three photoactive poly-(arylene ethynylene) co-polymers with different complexing units and we highlighted, for one of them, a ten-fold amplification of the response in case of addition of Zn2+, Cu2+ and Hg2+ ions. In addition, we were able to demonstrate the formation of complexes with Yb3+ an Er3+ and an efficient sensitization of their typical metal centered NIR emission upon excitation of the polymer structure, this feature being of particular interest for their possible applications in optical imaging and in optical amplification for telecommunication purposes. An amplification effect was also observed during this research in silica nanoparticles derivatized with a suitable zinc probe. In this case we were able to prove, for the first time, that nanoparticles can work as off-on chemosensors with signal amplification. Fluorescent silica nanoparticles can be thus seen as innovative multicomponent systems in which the organization of photophysically active units gives rise to fruitful collective effects. These precious effects can be exploited for biological imaging, medical diagnostic and therapeutics, as evidenced also by some results reported in this thesis. In particular, the observed amplification effect has been obtained thanks to a suitable organization of molecular probe units onto the surface of the nanoparticles. In the effort of reaching a deeper inside in the mechanisms which lead to the final amplification effects, we also attempted to find a correlation between the synthetic route and the final organization of the active molecules in the silica network, and thus with those mutual interactions between one another which result in the emerging, collective behavior, responsible for the desired signal amplification. In this context, we firstly investigated the process of formation of silica nanoparticles doped with pyrene derivative and we showed that the dyes are not uniformly dispersed inside the silica matrix; thus, core-shell structures can be formed spontaneously in a one step synthesis. Moreover, as far as the design of new labels is concerned, we reported a new synthetic approach to obtain a class of robust, biocompatible silica core-shell nanoparticles able to show a long-term stability. Taking advantage of this new approach we also showed the synthesis and photophysical properties of core-shell NIR absorbing and emitting materials that proved to be very valuable for in-vivo imaging. In general, the dye doped silica nanoparticles prepared in the framework of this project can conjugate unique properties, such as a very high brightness, due to the possibility to include many fluorophores per nanoparticle, high stability, because of the shielding effect of the silica matrix, and, to date, no toxicity, with a simple and low-cost preparation. All these features make these nanostructures suitable to reach the low detection limits that are nowadays required for effective clinical and environmental applications, fulfilling in this way the initial expectations of this research project.

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We demonstrate a multicore multidopant fiber which, when pumped with a single pump source around 800nm , emits a more than one octave-spanning fluorescence spectrum ranging from 925 to 2300nm . The fiber preform is manufactured from granulated oxides and the individual cores are doped with five different rare earths, i.e., Nd3+ , Yb3+ , Er3+ , Ho3+ , and Tm3+ .

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Unfavorable environmental and developmental conditions may cause disturbances in protein folding in the endoplasmic reticulum (ER) that are recognized and counteracted by components of the Unfolded Protein Response (UPR) signaling pathways. The early cellular responses include transcriptional changes to increase the folding and processing capacity of the ER. In this study, we systematically screened a collection of inducible transgenic Arabidopsis plants expressing a library of transcription factors for resistance toward UPR-inducing chemicals. We identified 23 candidate genes that may function as novel regulators of the UPR and of which only three genes (bZIP10, TBF1, and NF-YB3) were previously associated with the UPR. The putative role of identified candidate genes in the UPR signaling is supported by favorable expression patterns in both developmental and stress transcriptional analyses. We demonstrated that WRKY75 is a genuine regulator of the ER-stress cellular responses as its expression was found to be directly responding to ER stress-inducing chemicals. In addition, transgenic Arabidopsis plants expressing WRKY75 showed resistance toward salt stress, connecting abiotic and ER-stress responses.

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Este trabalho concentra-se na preparao e caracterizaes estrutural e espectroscpica de materiais nanoestruturados base de SiO2-Nb2O5 dopados e codopados com ons Er3+, Yb3+ e Eu3+ na forma de ps e guias de onda planares. Os nanocompsitos foram preparados atravs de uma nova rota sol-gel utilizando xido de nibio como precursor em substituio ao alcxido de nibio. A correlao estrutura propriedades luminescentes foi estudada por difrao de raios X, microscopia eletrnica de transmisso, espectroscopia vibracional de absoro no infravermelho, espectroscopia vibracional de espalhamento Raman, anlise trmica, reflectncia difusa e especular, espectroscopia de fotoluminescncia e acoplamento M-line. Inicialmente foi avaliado a influncia da concentrao de nibio nas propriedades estruturais e luminescentes de nanocompsitos (100-x)Si-xNb dopados e codopados com ons Er3+, Yb3+ e Eu3+ tratados termicamente a 900 C por 3h. A cristalizao do Nb2O5 foi dependente da concentrao de Nb na matriz, com a distribuio dos ons lantandeos preferencialmente no Nb2O5, afetando as propriedades luminescentes. Para os nanocompsitos codopados com ons Er3+ e Yb3+ foram obtidos valores de largura de banda a meia altura (FWHM) da ordem de 70 nm na regio de 1550 nm e tempos de vida de at 5,2 ms. A emisso na regio do visvel, decorrente de processos de converso ascendente, revelou-se dependente da concentrao de nibio. Foi verificada emisso preferencial na regio do verde para menores concentraes de Nb. Enquanto que, para as maiores concentraes, processos de relaxao cruzada levaram a um aumento relativo na intensidade de emisso na regio do vermelho. A eficincia quntica de emisso dos nanocompsitos (100-x)Si-xNb dopados com Eu3+ variou com o comprimento de onda de excitao, refletindo os diferentes stios de simetria ocupados por este ons nesta estrutura complexa. A influncia da temperatura de tratamento trmico no processo de cristalizao do Nb2O5 em nanocompsitos 70Si:30Nb codopados com ons Er3+ e Yb3+ foi avaliada. Material amorfo foi obtido a 700 C enquanto que a 900 e 1100 C foram identificas as fases ortorrmbica (fase T) e monoclnica (fase M) do Nb2O5. Intensa emisso na regio de 1550 nm com valores de FWHM de 52 e 67 nm e tempos de vida de 5,6 e 5,4 ms foram verificados a 700 e 900 C sob excitao em 977 nm, respectivamente. Por fim, foram obtidos guias de onda planares com excelentes propriedades pticas e com grande potencial de aplicao em dispositivos de amplificao ptica. Especificamente, materiais fotnicos com banda larga de emisso na regio do infravermelho foram preparados, indicando fortemente a potencialidade para a aplicao em telecomunicaes envolvendo no somente a banda C como tambm as bandas L e S em materiais contendo somente ons Er3+ como centros emissores.

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O presente trabalho tem como objetivo estudar a produo e caracterizao de filmes finos do tipo GeO2-Bi2O3 (BGO) produzidos por sputtering-RF com e sem nanopartculas (NPs) semicondutoras, dopados e codopados com ons de Er3+ ou Er3+/Yb3+ para a produo de amplificadores pticos. A produo de guias de onda do tipo pedestal baseados nos filmes BGO foi realizada a partir de litografia ptica seguida por processo de corroso por plasma e deposio fsica a vapor. A incorporao dos ons de terras-raras (TRs) foi verificada a partir dos espectros de emisso. Anlises de espectroscopia e microscopia foram indispensveis para otimizar os parmetros dos processos para a construo dos guias de onda. Foi observado aumento significativo da luminescncia do Er3+ (regio do visvel e do infravermelho), em filmes finos codopados com Er3+/Yb3+ na presena de nanopartculas de Si. As perdas por propagao mnimas observadas foram de ~1,75 dB/cm para os guias pedestal em 1068 nm. Para os guias dopados com Er3+ foi observado aumento significativo do ganho na presena de NPs de silcio (1,8 dB/cm). O ganho ptico nos guias de onda amplificadores codopados com Er3+/Yb3+ e dopados com Er3+ com e sem NPs de silcio tambm foi medido. Ganho de ~8dB/cm em 1542 nm, sob excitao em 980 nm, foi observado para os guias pedestal codopados com Er3+/Yb3+ (Er = 4,64.1019 tomos/cm3, Yb = 3,60.1020 tomos/cm3) com largura de 80 m; para os guias codopados com concentrao superior de Er3+/Yb3+ (Er = 1,34.1021 tomos/cm3, Yb = 3,90.1021 tomos/cm3) e com NPs de Si, foi observado aumento do ganho ptico de 50% para guia com largura de 100 m. Os resultados apresentados demonstram que guias de onda baseados em germanatos, com ou sem NPs semicondutoras, so promissores para aplicaes em dispositivos fotnicos.

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We review progress on laser cooling of solids. The general process that enables cooling to occur is based on anti-Stokes fluorescence. Candidate materials for laser cooling are discussed, including gases, dyes, crystals, semiconductors, and ionically doped glasses. Cooling processes and necessary conditions for cooling are outlined, and general thermodynamic limitations are discussed. This is followed by a more detailed discussion of one specific material, ytterbium-doped ZBLAN, with consideration given to optimization of the laser cooling process and applications. (C) 2003 Optical Society of America.