Emissão luminescente no titanato de cálcio dopado com íons de terras-raras

Through the polymeric precursor method were synthesized samples Ca0.98Sr0.01X0.01TiO3 (X= Eu3+, Sm3+ and Pr3+), which under different heat treatments were obtained with levels of distinct structural order-disorder. The synthesized materials were characterized by X-ray diffraction, confirming the obtaining of ahomogeneous material with perovskite-type orthorhombic structure. This characterization allowed evaluating the average crystallite size of the samples that varies depending on the rare-earth ion. The results of photoluminescence emission confirmed the presence of this optical phenomenon at room temperature and its relationship to the level of order-disorder structural system. The photoluminescence emission is more intense in samples annealed at 500 ° C (independent on the dopant ion), the variation of the dopant influence on the emission intensity due to charge transfer between the host and emitting rare-earth ion, where the doped with Pr3+ ion has charge transfer more efficient and hence more intense emission in the photoluminescence. Another factor that favors the optical property of the samples is the charge compensation, as it contributes to the increase in structural disorder due to formation of Ca2+ vacancies.Através do método dos precursores poliméricos foram sintetizadas amostras de Ca0,98Sr0,01X0,01TiO3 (X= Eu3+, Sm3+ ou Pr3+), que submetidas a diferentes tratamentos térmicos foram obtidas com níveis de ordem-desordem estrutural distintos. Os materiais sintetizados foram caracterizados por difração de raios X, confirmando a obtenção de um material homogêneo com estrutura perovsquita do tipo ortorrômbica. Essa caracterização permitiu ainda calcular o tamanho médio de cristalito das amostras, que varia em função do íon terra-rara presente. Os resultados da emissão fotoluminescente confirmaram a presença desse fenômeno óptico à temperatura ambiente e sua relação com o nível de ordem-desordem estrutural do sistema. A emissão fotoluminescente mais intensa ocorre nas amostras tratadas termicamente a 500 °C (independente do íon dopante), a variação do dopante influencia na intensidade da emissão devido à transferência de carga entre a matriz hospedeira e o íon terra-rara emissor, onde a amostra dopada com íon Pr3+ apresenta transferência de carga mais eficiente e consequentemente maior intensidade na emissão fotoluminescente. Outro fator que favorece a propriedade óptica das amostras é a compensação de carga, pois contribui para o aumento da desordem estrutural devido à formação de vacâncias do íon Ca2+.UFG CACUSP IFSCUNESP Instituto de QuímicaUFRN DEMat-CTUNESP Instituto de Químic

Structural and luminescence properties of Eu3+ doped BaxSr1 12xTiO3 (BST) nanocrystalline powders prepared by different methods

Eu3+ doped BaxSr1-xTiO3 (BST) nanocrystalline powders have been prepared using molten salts, sol-gel and hydrothermal techniques in order to compare their structural and luminescence properties. The sizes of the particles are around 50 nm for the BST powders obtained by the sol-gel and hydrothermal methods while they are around 400 nm for the samples prepared by the molten salts method. The Eu3+ doped BST samples show strong emission in the visible range. The luminescence spectra of the Eu3+ ions for the investigated samples depend strongly upon the preparation method. The luminescence bands are affected by a notable amount of inhomogeneous broadening. The broadening of the emission bands and the non-exponential behavior of the emission decay curves point to the presence of significant structural disorder

Up-conversion emission and in vitro cytotoxicity characterization of blue emitting, biocompatible SrTiO₃ nanoparticles activated with Tm³⁺ and Yb³⁺ ions

Blue emitting, up-converting NP's of SrTiO3:Tm3+/Yb3+ synthesized using the citric route are biocompatible towards J774.E whereas the cytotoxic effect to U2OS cells is not particle size dependent but most probably is related to Sr2+ ion release.</p

Structural and spectroscopic features of Ca9M(PO4)7 (M\ua0=\ua0Al3+, Lu3+) whitlockites doped with Pr3+ ions

In this work we present the structural and spectroscopic properties of Ca9M(PO4)7 (M = Al, Lu) whitlockite compounds doped with Pr3+ ions. The Al containing samples were prepared by the citrate route, while the Lu based samples were prepared by standard solid state reaction. The structural properties were investigated by XRD measurements and Rietveld analysis. Detailed spectroscopic properties like emission and excitation spectra, luminescence kinetics and luminescence temperature quenching were measured to determine the influence of different trivalent host metal on the Pr3+ ions. Pr3+ enter in the three Ca2+ sites in the Ca9Al(PO4)7 compounds, creating some defect to compensate the charge mismatch, whereas in the Ca9Lu(PO4)7 Pr3+ ions occupy four Ca2+/Lu3+ sites, where no charge compensation is needed. The emission spectra are similar for both materials. Efficient quenching of the 1D2 emission was observed, while the 3P0 emission remains stable for all dopant concentrations. Decay times were found to be non-single exponential due to the occupation of different sites by the Pr3+ ions. The luminescence temperature quenching measurements have revealed that two different mechanisms (multi-phonon relaxation and cross-relaxation processes) are responsible for the emission quenchin

A new approach in the synthesis of La_1−xGd_xFeO₃ perovskite nanoparticles – structural and magnetic characterization

A series of highly crystalline orthoferrite nanoparticles (type La1−xGdxFeO3, where x = 0 to 1) were prepared using the self-combustion method.</p