Y. Karabulut

Catholuminescence properties of rare earth doped CaSnO3 phosphor

The present study describes cathodoluminescence (CL) properties of CaSnO3 phosphors doped with Eu(3+), Tb(3+) and Dy(3+) synthesized by a solid-state method. X-ray diffraction (XRD) patterns confirm that CaSnO3 sintered at 1200°C exhibits orthorhombic structure. The evidence and rationale for two strong broad emission bands appeared at 360 and 780nm for undoped CaSnO3 are presented. The CL measurements exhibit that the 4f-4f emissions from (5)D4→(7)F6 (490nm), (5)D4 →(7)F5 (544nm), (5)D4 →(7)F4 (586nm) and (5)D4 →(7)F3 (622nm), assigned to possible transitions of Tb(3+) ions are seen. The strongest one, observed at 544nm, due to its probability of both magnetic and electric transitions make the sample emission green. Emissions at 480, 574, 662 and 755nm were detected for the CaSnO3:Dy(3+) and attributed to the transitions from the (4)F9/2 to various energy levels (6)H15/2, (6)H13/2, (6)H11/2 and (6)H9/2+(6)F11/2 of Dy(3+), respectively. CL spectra of Eu doped CaSnO3 reveal that there is a strong emission peak appeared at 615nm due to the electric dipole transition (5)D0→(7)F2 (red). Finally, our results show that the rare earth doped CaSnO3 have remarkable potential for applications as optical materials since it exhibits efficient and sharp emission due to rare earth ions.

Synthesis and Luminescence Properties of Trivalent Rare-Earth Element-Doped Calcium Stannate Phosphors

ABSTRACT The phosphors of calcium stannate activated with individual trivalent rare-earth element (REE) ions (Neodymium III, Europium III, Terbium III, Dysprosium III, and Samarium III) were synthesized by high-temperature solid-state reaction (SSR), and their characterization and luminescent properties were investigated. The crystal structures and morphologies of the resultant materials were well characterized by experimental techniques such as X-ray powder diffraction (XRD) and environmental scanning electron microscopy (ESEM). The XRD results display that the rare-earths substitution of Calcium II does not change the structure of calcium stannate host. Obviously, the ESEM image exhibits that phosphors aggregate and their particles with irregular shape exist. The calcined powders of the Europium III, Neodymium III, Samarium III, Dysprosium III, and Terbium III ions doped in calcium stannate exhibits bright red, reddish orange, yellowish, orange white, and green light, respectively. Although there is some intrinsic emission ranging from UV to near-infrared (NIR) due to the host lattice, the dominant signals are from the rare-earth sites, with signals characteristic of the trivalent rare-earth states. The emission spectrum from undoped-calcium stannate phosphor is characterized by two broad bands centered at ∼800 and ∼950 nm. The shapes of the emission bands are different for each dopant. The sharp emission properties show that the calcium stannate is a suitable host for rare-earth ion-doped phosphor material. Furthermore the influence of different rare-earth dopants, that is, Europium III, Neodymium III, Samarium III, Dysprosium III, and Terbium III, on thermally stimulated luminescence (TSL) of calcium stannate phosphor under the beta irradiation was discussed. Among these trivalent rare-earth-doped phosphors samarium-doped material showed maximum TSL sensitivity with favorable glow curve shape.

Luminescence studies of zinc borates activated with different concentrations of Ce and La under x-ray and electron excitation

Several ZnB2O4 powder samples having dopants concentrations of 0.1, 0.01, 0.04wt% Ce and La were prepared using the nitric acid method via the starting oxides. Several complementary methods such as powder X-ray diffraction (XRD), thermal analyses environmental scanning electron microscopy (ESEM), Radioluminescence (RL) and Cathodoluminescence (CL) techniques were used. Unique luminescence properties of Ce doped ZnB2O4 powder samples are reported for the first time. A new luminescence bands appearing in red part of the spectrum and having all the characteristics of Ce3+ were obtained from RL results. Changing the Ce and La concentration of 0.01-0.1wt% leads to an increase in RL and CL intensities of Ce3+ and La3+ ions and also CL emission spectra of ZnB2O4 show gradual shift towards longer wavelength. When we compare the luminescence intensity of the samples it is seen that Ce doped ZnB2O4 has the highest intense whereas La doped ZnB2O4 has the lowest one. However, emission spectra of both Ce and La doped samples kept unchanged.

Thermoluminescence studies of Nd doped Bi4Ge3O12 crystals irradiated by UV and beta sources.

Thermoluminescence (TL) glow curves of pure and rare earth doped bismuth germanate (BGO) were investigated under UV and beta radiation. The glow curves of pure BGO crystal present different patterns for both kinds of radiation. The TL glow curves of BGO crystals doped with Nd ions are similar to that of pure BGO under UV radiation. The kinetic parameters, kinetic order (b), activation energy (E) and frequency factor (s) of the TL glow curves of pure BGO crystal have been determined by peak shape method. Activation energies of 3 peaks obtained by PS were found to be 1.81, 1.15 and 1.78, respectively.

Characterisation and luminescence studies of Tm and Na doped magnesium borate phosphors.

In this study, structural and luminescence properties of magnesium borate of the form MgB4O7 doped with Tm and Na were investigated by X-ray diffraction (XRD), Raman spectroscopy and cathodoluminescence (CL). The morphologies of the synthetised compounds exhibit clustered granules and road-like materials. As doping trivalent ions into a host with divalent cations requires charge compensation, this effect is discussed. The CL spectra of undoped MgB4O7 shows a broad band emission centred around 350 nm which is postulated to be produced by self-trapped excitons and some other defects. From the CL emission spectrum, main emission bands centred at 360, 455, 475 nm due to the respective transitions of (1)D2→(3)H6,(1)D2→(3)F4 and (1)G4→(3)H6 suggest the presence of Tm(3+) ion in MgB4O7 lattice site. CL mechanism was proposed to explain the observed phenomena which are valuable in possibility of the developing new luminescent materials for different applications. In addition, the experimental Raman spectrum of doped and undoped MgB4O7 were reported and discussed.

Visible to infrared low temperature photoluminescence of rare earth doped bismuth germanate crystals.

In this paper, the influence of a series of rare earth (Eu, Tm, Nd) and Cr ion doping on the optical properties of BGO was investigated by means of photoluminescence (PL) from visible to IR region in the 10-300K temperature range using different types of detectors, namely, photomultiplier tube (PMT), InGaAs (IGA), and Si. Several samples were investigated having dopants concentrations of 0.3wt%Nd, 0.4wt%Tm, 0.06wt% Cr and 3ppm Eu. The PL spectra of the samples showed different luminescence behaviour which is assigned to the 4f intra shell transition from rare earth ions. The temperature dependence of the PL from rare earth doped BGO crystals is also examined.

Optical spectroscopy of the Ce-doped multicomponent garnets.

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 530nm assigned to 5d-4f transitions of the dopant Ce(3+) ions with a broad emission band in 400-700nm range. Under electron irradiation, the emission spectrum of Ce doped (YGd)3Ga2Al3O12 is well defined and has a characteristic fairly narrow and sharp emission band peaking at 312nm and 624nm corresponding to transition of (6)P7/2 →(8)S7/2 and (6)GJ→(6)PJ (Gd(3+)), respectively. We suggest some of phosphors might be excellent phototherapy phosphor materials under electron excitation.

Preparation and cathodoluminescence characteristics of rare earth activated BaAl 2 O 4 phosphors

Undoped and Pr, Sm and Tb activated BaAl2O4 phosphors have been synthesized by solid state reaction method and combustion method. The structure and morphological observation of the phosphor samples were monitored by X-ray powder diffraction (XRD) and environmental scanning electron microscope (ESEM) coupled to an energy dispersive X-ray spectrometer (EDS). The all diffraction peaks are well assigned to standard data card (PDF♯17-306). Emission properties of the samples were explored using light emission induced by an electron beam (i.e cathodoluminescence, CL) at room temperature (RT). Undoped BaAl2O4 sample exhibits a broad defect emission from 300 to 500 nm from the aluminate defect centres. CL spectra recorded at room temperature display that the as-prepared BaAl2O4:Ln (Ln=Pr, Sm and Tb) phosphors exhibit different luminescence colors coming from different rare earth activator ions. The transition 4G5/2 → 6H7/2 located at 606 and 610 nm for Sm3+ can occur as hypersensitive transition having the selection rule ΔJ = ± 1. For the Tb3+ doped samples, they exhibit D45 green line emissions. The proposed luminescent mechanisms of all doped rare earth ions are also discussed.

Luminescent, Structural, and Thermal Properties of the Unusual “Anatolian” Diaspore (Zultanite) from Turkey

ABSTRACT Results are presented for the cathodoluminescence (CL) probe of an environmental scanning electron microscopy (ESEM) with an energy-dispersive spectrometry analyzer (EDS), thermoluminescence (TL), thermo X-ray diffraction in situ (TXRD), and simultaneous differential thermal analysis and thermogravimetric analysis (DTA/TGA) techniques of gem-quality zultanite samples collected from the Muğla region of southwest Turkey. Micro-Raman measurements were also performed on different zultanite orientations and preheated aliquots to study the spectral phase transition diaspore-corundum also detected by the other thermal techniques in the 450°C–500°C thermal range. The thermal phenomena of TL are synchronous with this dehydroxylation process, involving consecutive breaking-linking bonds of Al-O, Cr-O, Fe-O, Al-OH, Cr-OH, and Fe-OH, including the formation of hydrolyzed ions such , and and redox reactions. Assuming that zultanite oxygen atoms are distributed as a hexagonal close packed layer, the experimental spectrum CL of zultanite is characteristic of the 2E → 4A2 transitions of substitutional Cr3+ luminescent centers in positions of Al3+ in sixfold coordination.

Strong Visible and Near-Infrared Cathodoluminescence in Alkali Feldspar

ABSTRACT In this study, cathodoluminescence (CL) spectroscopy at direct current and alternating current under the sample temperature condition of 40–293 K using different modulation frequencies is presented for alkali feldspar from the Dartmoor granite (UK). These feldspars contain strain-controlled lamellar crypto- and microperthites that are cross-cut by strain-free deuteric microperthites. The CL spectra of the alkali feldspar at room and low temperature confirm that the observed emission peaked at ∼460 nm could be associated with Al-O−-Al or Ti impurity centers, yellow emission ∼560 nm could be associated with the presence of the centers such as radiation-induced defect centers, and ∼756 nm emission could be associated with the Fe3+ impurity center on T1 and T2 sites. The consequence of their association is to produce different luminescence properties such as intensity, peak wavelength, and band shape.