Browsing by Author "Muresan, LE"

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    Preparation and characterization of Yttrium based luminescence phosphors
    Muresan, LE; Ayvacikli, M; Guinea, JG; Canimoglu, A; Karabulut, Y; Can, N
    Ce doped Yttrium aluminate modified by replacing different molar part of aluminium or gallium (Y(3)Al(5-x)GaxO(12)) and Yttrium silicate phosphors activated with Ce and Tb (Y2SiO5:Ce3+,Tb3+) were synthesized by solid state reaction and a gel combustion method, respectively. X-ray diffraction and Scanning electron microscope (SEM) techniques are used to identify their structures and morphologies. Luminescence characteristics are measured and spectroscopic data confirm that Y2SiO5:Ce3+, Tb3+ phosphors can be effectively excited upon UV excitation light and X-ray irradiation, resulting in intense blue and green emissions, respectively. This energy transfer takes place by means of a non-radiative process inside Ce3+-Tb3+ clusters formed in the host matrix. Tb3+ doped Y2SiO5 yields both blue emission D-5(3) -> F-7(j) (j = 3,4,5,6) and green emission D-5(4) -> F-7(J) (J = 3,4,5,6) of Tb3+. Y(3)Al(5-x)GaxO(12):Ce3+ phosphors exhibit a broad blue emission band originating from allowed 5d-4f transition of the Ce3+ ions under different excitation sources but the broad emission band shifts with increasing of Ga3+ content. This work presents a quantitative understanding of host material's on dopant's luminescence properties and thereby provides an optimization guideline, which is extremely demanding for the development of new luminescent materials. (C) 2017 Elsevier B.V. All rights reserved.
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    Synthesis and influence of ultrasonic treatment on luminescence of Mn incorporated ZnS nanoparticles
    Cadis, AI; Muresan, LE; Perhaita, I; Munteanu, V; Karabulut, Y; Guinea, JG; Canimoglu, A; Ayvacikli, M; Can, N
    Manganese (Mn) doping of ZnS phosphors was achieved by precipitation method using different ultrasound (US) maturation times. The structural and luminescence properties of the samples were carried out by means of X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), photoluminescence (PL), and cathodoluminescence (CL). The real amount of manganese incorporated in ZnS lattice was calculated based on ICP-OES results. According with XRD patterns, the phase structure of ZnS:Mn samples is cubic. EDS spectra reveal deviations of the Mn dopant concentration from the target composition. Both 300 K PL and CL emission spectra of the Mn doped ZnS phosphors display intense orange emission at 590 and 600 nm, respectively, which is characteristic emission of Mn ion corresponding to a T-4(1) -> (6)A(1) transition. Both PL and CL spectra confirmed manganese is substitutionally incorporated into the ZnS host as Mn2+. However, it is suggested that the origin of broad blue emission around 400 nm appeared in CL is due to the radiative recombination at deep level defect states in the ZnS. The ultrasound treatment at first enhances the luminescent intensity by similar to 3 times in comparison with samples prepared by classical way. This study gives rise to an optimization guideline, which is extremely demanded for the development of new luminescent materials. (C) 2017 Elsevier B.V. All rights reserved.
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    The role of calcination temperature on structural and luminescence behaviour of novel apatite-based Ca2Y 8(SiO4)6O2: Ce3+,Tb3+ phosphors
    Perhaita, I; Muresan, LE; Silipas, DT; Borodi, G; Karabulut, Y; Guinea, JG; Ayvacikli, M; Can, N
    A series of novel apatite-based Ca2Y8(SiO4)(6)O-2 phosphors doped with Ce3+ and Tb3+ were synthesized by a solid-state reaction method at different calcination temperatures and times. The comparative results of thermal analysis (TG-DTA), FTIR, X-ray diffraction (XRD) and environmental scanning electron microscope (ESEM) reveal that the firing temperature for Ca2Y (8)(SiO4)(6)O-2:Ce3+, Tb3+ was optimized to be 1200 degrees C. The systematic studies on the influences of thermal treatment conditions on photoluminescence (PL) and cathodoluminescence (CL) properties were also reported. The excitation spectra of Ca2Y8(SiO4)(6)O-2:Ce3+, Tb3+ exhibited one strong excitation band at 325 run. The PL and CL results indicated that the violet-blue emission intensities about 400 nm from the Ce3+ and efficient green emission at 544 nm from Tb3+ were highly dependent on the calcination conditions.
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    Structural and luminescence effects of Ga co-doping on Ce-doped yttrium aluminate based phosphors
    Ayvacikli, M; Canimoglu, A; Muresan, LE; Tudoran, LB; Guinea, JG; Karabulut, Y; Jorge, A; Karali, T; Can, N
    Herein, we primarily focus on luminescence spectrum measurements of various types of green emitting yttrium aluminate phosphors modified with gallium (Y3Al5-xGaxO12) synthesised by solid state reaction. The luminescent emission of samples depends on sample temperature and excitation radiation such as incident X-ray, electron and laser beam. Here, we measured radioluminescence (RL), cathodoluminescence (CL), photoluminescence (PL) along with XRD in order to clarify relationship between lattice defects and the spectral luminescence emissions. The RL and CL spectra of YAG:Ce exhibit an emission band ranging from 300 to 450 nm related to Y-Al antisite defects. The broad emission band of garnet phosphors is shifted from 526 nm to 498 nm with increasing of Ga3+ content, while full width at half maximum (FWHM) of the band tends to be greater than the width of unmodified YAG: Ce garnet. Deconvolution of the spectrum reveals that three emission bands centred at 139, 234 and 294 degrees C occur in aluminate host garnets. (C) 2016 Elsevier B.V. All rights reserved.
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    Optical spectroscopy of the Ce-doped multicomponent garnets
    Canimoglu, A; Karabulut, Y; Ayvacikli, M; Muresan, LE; Perhaita, I; Barbu-Tudoran, L; Guinea, JG; Karali, T; Can, N
    Here, we report our results referring to the preparation of Ce doped Y2.22MgGa2Al2SiO12, Y1.93MgAl4SiO12 and Y2.22Gd0.75Ga2Al3O12 using solid state reaction at high temperature. Several complementary methods (i.e. powder x-ray diffraction (XRPD), energy dispersive analysis of X-rays (EDX), scanning electron microscopy (SEM) and Fourier transforms infrared spectroscopy (FTIR)) were studied to examine the effects of the synthesis procedure on the morphology and structure. XRD analyses revealed that all compounds include yttrium aluminate phase with garnet structure. Cathodoluminescence (CL), radioluminescence (RL) and photoluminescence (PL) measurements were carried out for clarification of relationship between host lattice defects and the spectral luminescence emissions. Luminescence emission of phosphors is peaked at 530 nm assigned to 5d-4f transitions of the dopant Ce3+ ions with a broad emission band in 400-700 nm range. Under electron irradiation, the emission spectrum of Ce doped (YGd)(3)Ga2Al3O12 is well defined and has a characteristic fairly narrow and sharp emission band peaking at 312 nm and 624 nm corresponding to transition of P-6(7/2) -> S-8(7/2) and (6)G(J) -> P-6(J) (Gd3+), respectively. We suggest some of phosphors might be excellent phototherapy phosphor materials under electron excitation. (C) 2016 Elsevier Ltd. All rights reserved.
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    Tunable luminescence of broadband-excited and narrow line green emitting Y2SiO5:Ce3+, Tb3+ phosphor
    Muresan, LE; Karabulut, Y; Cadis, AI; Perhaita, I; Canimoglu, A; Guinea, JG; Tudoran, LB; Silipas, D; Ayvacikli, M; Can, N
    Cerium and terbium activated white emitting yttrium silicate phosphors (Y-2-x-yCe(x)Tb(y)SiO(5)) having average size between 96 and 123 nm were synthesised by a gel-combustion, and their phase and crystal structures, morphologies and ultraviolet (UV)-visible spectroscopic properties were studied. All rare earth doped yttrium silicate (YSO) phosphors are well crystallized powders containing only monoclinic X2-Y2SiO5 phase. No significant changes in the cell parameters were observed with increasing of Tb amount as ionic radii of Tb3+ (0.923 angstrom) and Y3+ (0.9 angstrom) have almost the same. Under different excitations, YSO:Ce3+ exhibits blue emission due to the 5d-4f transitions of Ce3+ ions. The series of emission states at different wavelengths of YSO:Tb3+ associated to f-f transition of Tb3+ ion were detected from luminescence measurements. The emission observed at 544 nm (green) corresponding to D-5(4) -> F-7(5) of Tb3+ is strongest one. Incorporation of variable amounts of Tb3+ in the YSO host lattice determines the modification of emission colour from blue through light blue and eventually to bluish green. A possible energy transfer mechanism taking place from Ce3+ to Tb3+ was also discussed in terms of excitation and emission spectra. (C) 2015 Elsevier B.V. All rights reserved.