Luminescent behavior of Eu3+ doped BaHfO3 perovskite ceramic under UV radiation.

In this paper, luminescent properties of Europium trivalent ion in the matrix with unbalanced charge of barium hafnate under UV radiation, with special emphasis on the 5D0 → 7F0 transition are reported. The synthesis was conducted by the hydrothermal route at 200 °C with a reaction time of 90 min using chlorides as raw materials. In order to determinate the luminescent quenching concentration, the samples were doped with different amounts of Europium trivalent ions being the sample doped with 1 and 3% at of Eu3+ which shows the highest luminescent emission. X-ray diffraction analysis showed that the material crystallize in the cubic perovskite structure with space group Pm-3m. The Energy Dispersive Spectroscopy (EDS) shows there are not elements other those that Ba, Hf, O and Eu in the synthesized material. Photoluminescent emission spectra show peaks of emission associated with the 5D0 → 7FJ (J = 0,1,2,3,4) transitions, characteristics of europium ion. The 5D0 → 7F0 transition centered at 580 nm showed an unusual great intensity when it was excited with the wavelength associated with the charge transfer band (272 nm). Finally the decay time was measured in the 5D0 → 7FJ (J = 0,1,2,3,4) transitions using the sample doped with Eu3+ (3% at).

Photo-, cathodo- and thermoluminescent properties of dysprosium-doped HfO2 films deposited by ultrasonic spray pyrolysis.

In this work, the photoluminescent (PL), cathodoluminescent (CL) and thermoluminescent (TL) properties of hafnium oxide films doped with trivalent dysprosium ions are reported. The films were deposited on glass substrates at temperatures ranging from 300 to 600°C, using chlorides as precursor reagents. The surface morphology of films showed a veins shaped microstructure at low deposition temperatures, while at higher temperatures the formation of spherical particles was observed on the surface. X-ray diffraction showed the presence of HfO2 monoclinic phase in the films deposited at temperatures greater than 400°C. The PL and CL spectra of the doped films showed the highest emission band centered at 575nm corresponding to the transitions (4)F9/2→(6)H13/2, which is a characteristic transition of Dy(3+) ion. The greatest emission intensities were observed in samples doped with 1 atomic percent (at%) of DyCl3 in the precursor solution. Regarding the TL behavior, the glow curve of HfO2:Dy(+3) films exhibited spectrum with one broad band centered at about 150°C. The highest intensity TL response was observed on the films deposited at 500°C.

Thermoluminescent characterization of HfO2:Tb3+ synthesized by hydrothermal route.

Thermo and photoluminescent properties of nanoparticles (NPs) of hafnium oxide (HfO2), both intrinsic and doped with terbium (Tb(3+)) are reported. The NPs of HfO2 were synthesized by hydrothermal route, using hafnium tetrachloride (HfCl4) and terbium chloride hexahydrated (TbCl3∙6H2O) as precursors and sodium hydroxide (NaOH) to adjust the pH. Deionized water was used as solvent in all cases. The synthesis was carried out at different dopant concentrations from 0 to 20 at% of terbium with respect to the amount of hafnium in the precursor solution. The temperature of hydrothermal treatment was 200 °C and 80 min of reaction time. X-ray diffraction results show that at terbium concentrations higher than 15 at% the HfO2 nanoparticles have a crystalline structure corresponding to the tetragonal phase. Thermoluminescent (TL) characterization was performed after 5 min irradiation of the samples with ultraviolet light of 200 nm wavelength. The highest TL emission was observed on samples with 7 at% of Tb, with the TL peak centered at 128 °C. Thermoluminescence analysis shows behavior associated with second-order kinetics with activation energy of 0.49 eV. Photoluminescent spectrum present the characteristics (5)D4→(7)FJ (J=3-6) terbium ion electronic transitions lines centered on 489 nm, 543 nm, 584 nm and 622 nm.