Luminescence centers in thin films of yttrium oxide and yttrium-aluminum garnet activated with bismuth

Luminescence spectra and photoluminescence excitation spectra of Y₂O₃:Bi and Y₃Al₅O₁₂:Bi thin films were investigated. Luminescence was stimulated by the emission from two types of centers that were associated with the substitution of Bi³⁺ for Y³⁺ in sites of the crystal lattice of Y₂O₃ (Y₃Al₅O₁₂) with point symmetries C₂ and C_3i (D₂ and C_3i). The emission of Bi³⁺ in the site with point symmetry C_3i causes blue luminescence in both Y₂O₃:Bi and Y₃Al₅O₁₂:Bi films with maxima at 3.03 eV and 3.15 eV, respectively, that is related to the ³P₁-¹S₀ transition. The emission of Bi³⁺ in the site with point symmetry C₂ gives green luminescence in Y₂O₃:Bi with the maximum at 2.40 eV that is also related to the ³P₁-¹S₀ transition. The emission of Bi³⁺ in the site with point symmetry D₂ leads to ultraviolet luminescence in Y₃Al₅O₁₂:Bi with the maximum at 3.75 eV that corresponds to the ³P₁-¹S₀ transition. The red luminescence band with the maximum at 1.85 eV in Y₂O₃:Bi is due to the presence of structural defects. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 75, No. 2, pp. 202–207, March–April, 2008.     

Thermally stimulated luminescence of urine salts

We investigated thermally stimulated luminescence (TSL) of urine salts in the normal state and with oxalate, urate, and phosphate salts. We found that the presence of pathological salts leads to a decrease of TSL intensity and to the appearance of additional TLS bands with maxima at 118 and 205 K in addition to the characteristic bands at 173 and 260 K. The TLS bands are related to the urine components. The TSL intensities of urine salts of different chemical composition are compared. The thermal activation energy of the strongest TSL bands is determined. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 4, pp. 548–551, July–August, 2007.     

Thermally stimulated luminescence of Mg-doped ZnO Nanophosphors

Nanosized ZnO:Mg phosphors were synthesized through a controlled chemical reaction. X-ray diffraction patterns confirmed that Mg entered in a substitutive way in Zn sites. To investigate their thermoluminescence (TL) properties, some samples were exposed to beta-particle irradiation. The results reported here show that Mg doping improves ZnO TL features that are important for TL dosimetry applications, such as the shape of the glow curve, the temperature at which the maximum TL intensity is observed, and the TL fading and reproducibility. No saturation clues of the TL response as a function of the dose is observed for doses below 1600 Gy.     

Thermally stimulated luminescence origin in LiF crystals irradiated in a reactor at different temperatures

Thermally stimulated luminescence as well as optical absorption and emission spectra have been studied in LiF crystals irradiated in a reactor at different temperatures. It was shown that aggregate colour centres give rise to thermally stimulated luminescence peaks registered below 450°C. Peak at 470°C is observed only in crystals that have been irradiated at standard temperature of the reactor experimental channels. The peak is caused by interaction of dislocations and F centres.     

Cooperative up-conversion luminescence of ytterbium doped yttrium lanthanum oxide transparent ceramic

The up-conversion luminescence of Yb³⁺-doped yttrium lanthanum oxide transparent ceramic was investigated. It was ascribed to cooperative luminescence originated from the coupled states of the Yb³⁺ ion pairs. The proper doping of La₂O₃ can remove the cooperative luminescence of Yb³⁺ ion. But excessive La₂O₃ (at least 10 at.%) the cooperative up-conversion of Yb³⁺:Y₂O₃ is obtained again, and the intensity of up-conversion luminescence strengthens with the increase of La₂O₃ content.     

Spectral properties of Ce3+ doped yttrium lanthanum oxide transparent ceramics

Ce3+-doped yttrium lanthanum oxide (Y0.9La0.1)2O3 transparent ceramics is fabricated with nanopowders and sintered in H2 atmosphere. The spectral properties of Ce:(Y0.9La0.1)2O3 transparent ceramics are investigated. There appear two characteristic absorption peaks of Ce3+ ions at 230 nm and 400 nm, separately. It is found that Ce3+ ions can efficiently produce emission at 384 nm from (Y0.9La0.1)2O3 transparent ceramic host, while the emission is completely quenched in Re2O3 (Re=Y, Lu, La) host materials.     

Thermoluminescence and low-temperature luminescence of beryllium oxide

Beryllium oxide in the forms of either single crystals (pristine, additively-colored) or hot-pressed ceramic samples was studied in the energy range of 1.2–6.2 eV using both the thermoluminescence (TL) and steady-state X-ray induced luminescence (XRL) techniques. The XRL emission spectra were recorded at 6 and 293 K, whereas TL glow curves were studied after X-ray exposure at T₀ = 6 K upon linear heating in the temperature range from 6 to 293 K. A search for TL manifestations of shallow trapping centers was carried out using a sensitive channel for TL registration in the range of more than six decades of change in intensity. The participation of shallow trapping centers in the process of recombination luminescence excitation at 6–293 K; branching electronic excitations between different recombination channels; the dominance of the self-trapped exciton and F-center emissions in spectra of the low-temperature recombination luminescence in BeO at 6–293 K were discussed.     

Thermally stimulated luminescence studies of undoped,Cu- and Mn-doped CaSO4 compounds

Thermally stimulated luminescence (TSL) of undoped and doped CaSO₄ with activators such as Cu and Mn has been investigated. The polycrystalline samples of undoped and doped CaSO₄ are prepared by the melting method. The formation of CaSO₄ compound is confirmed by X-ray diffraction and Fourier transform infrared studies. Scanning electron microscopic studies of CaSO₄ are also carried out.

The TSL glow curves of undoped CaSO₄, Cu- and Mn-doped CaSO₄ are studied. Comparison of the thermoluminescence (TL) intensity of the most intensive glow peak of Cu-doped CaSO₄ compound with that of undoped CaSO₄ shows that addition of Cu impurity in CaSO₄ compound enhances the TL intensity by about four times. However, the addition of Mn impurity to undoped CaSO₄ increases the TL intensity by about three times when compared with that of undoped CaSO₄. The TL-dose dependence of all three samples was studied and was observed to be almost linear in the studied range of irradiation time. Among the samples studied, namely undoped CaSO₄ and Cu- and Mn-doped CaSO₄, Cu-doped CaSO₄ is found to be the most sensitive. The trap parameters, namely order of kinetics (b), activation energy (E) and frequency factor (s) associated with the most intensive glow peaks of CaSO₄:Mn, CaSO₄:Cu and CaSO₄ phosphors were determined using the glow curve shape (Chen's) method.     

Thermally stimulated luminescence and electron paramagnetic resonance studies of actinide doped calcium chloro phosphate

Electron paramagnetic resonance [EPR] and thermally stimulated luminescence [TSL] studies were conducted on self [α]-irradiated²³⁹Pu doped calcium chloro phosphate andγ-irradiated²³⁹Pu/²³⁸UO ₂ ²⁺ doped calcium chloro phosphate to elucidate the role of the electron/hole traps in thermally stimulated reactions and to obtain trap parameters from both TSL and EPR data. TSL glow peaks around 135 K (# peak 1), 190 K (# peak 2), 435 K (# peak 5) and 490 K (# peak 7) were observed and their spectral characteristics have shown that Pu³⁺ and UO ₆ ⁶⁻ act as luminescent centres in calcium chloro phosphate with respective dopants. EPR studies have shown the formation of the radical ions H⁰, PO ₄ ²⁻ , O⁻, O ₂ ⁻ and [ClO]²⁻ under different conditions. Whereas the [ClO]²⁻ radical being stable up to 700 K, was not found to have any role in TSL processes, the thermal destruction of other centres was found to be primarily responsible for the TSL peaks observed. The trap depth values were determined both by using the TSL data and also the temperature variation of EPR spectra of these centres.     

Tunneling luminescence of Y2O3 and Sc2O3 ceramics

In the present work we investigate the tunneling luminescence (TL) of Y₂O₃, Y₂O₃:Eu, and Sc₂O₃ ceramics. From an analysis of the decay kinetics of the TL it is established that the recombinational processes are described by a model involving recombination with a complex interaction. In addition, using the method of partial light sums, we show that in the ceramics investigated the mechanisms of TL are the same and the majority of radiation-induced defects in pairs are removed to distances exceeding the radius of effective tunneling transitions with a time constant of 10–100 sec. In the Y₂O₃:Eu ceramics the distances between defects decrease. TL occurs in pairs whose electron component is F-centers that are thermally released at 176 K in the Y₂O₃ ceramics and 200 K in the Sc₂O₃ ceramics. The hole components of tunneling pairs are associated with centers that are thermally released at 110 and 122 K in the Y₂O₃ ceramics and at 121 and 146 K in the Sc₂O₃ ceramics. To whom correspondence should be addressed. I. Franko Lvov State University, 50, Dragomanov Str., Lvov, 290005, Ukraine. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 5, pp. 649–651, September–October, 1999.     

Thermally stimulated luminescence of polycrystalline CdWO4 at low temperatures

CdWO₄ scintillator powders were produced via solid state reaction and investigated by thermally stimulated luminescence technique after UV irradiation. Under a heating rate of 0.1 K/s, the glow curve presented a superposition of peaks at low temperatures. Four peaks were identified below 80 K by partial heating method and their kinetic parameters were evaluated from the initial rise analysis. Measurements were also performed for heating rates of 0.05 and 0.2 K/s and allowed the kinetic study by peak position method. Surface effects due to the polycrystalline feature of the sample were investigated by comparing the results with those reported for CdWO₄ single crystals.     

Thermally stimulated luminescence of bismuth germanate ceramics with the benitoite,eulitine, and sillenite structures

Thermally stimulated luminescence (TSL) of Bi₂Ge₃O₉, Bi₄Ge₃O₁₂, and Bi₁₂GeO₂₀ and the primary components Bi₂O₃ and GeO₂ was studied under x-ray excitation. Thermal activation energies and frequency factors of trapping centers in the studied ceramics were determined. The relationships of TSL bands of the studied ceramics with maxima at 141–145 and 166–170 K and damage to the Ge sublattice and of TSL bands with maxima at 104–110 and 180–190 K and recombination processes in the Bi sublattice were demonstrated. Recombination processes causing luminescence upon nonequilibrium charge carrier release from trapping centers occur in structural complexes of similar configuration that contain the Bi ion in a nearest environment of O atoms. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 75, No. 3, pp. 359–364, May–June, 2008.     

Luminescence centers in yttrium silicate and germanate

Luminescence spectra for isostructural Y₂SiO₅ and Y₂GeO₅ are investigated. The spectra are resolved into elementary components by the Alentsev—Fock method. Bands with maxima in regions of 2.6, 2.3, and 2.05 eV in the spectra of Y₂SiO₅ luminescence and in regions of 2.55, 2.25, and 2.0 eV in the spectra of Y₂GeO₅ luminescence are considered as radiative recombination of excited associative donor-acceptor Y³⁺−O²⁻ pairs. The indicated bands are related to certain distances between yttrium (the donor) and oxygen (the acceptor). A band with a maximum of 2.95 eV in Y₂SiO₅ and 3.0 eV in Y₂GeO₅ occurs in recombination of electrons with holes trapped by an anionic sublattice. I. Franko L’vov State University, 50, Dragomanov St., L’vov, 290005, Ukraine. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 65, No. 4, pp. 528–531, July–August, 1998.     

Investigation of a fibre-coupled beryllium oxide (BeO) ceramic luminescence dosimetry system

The purpose of this study is to investigate the potential use of a beryllium oxide (BeO) ceramic as a radioluminescence (RL) and optically stimulated luminescence (OSL) probe material for fibre-coupled luminescence dosimetry. A portable dosimetry system, named RL/OSL BeO FOD was developed, consisting of a 1 mm diameter, 1 mm long BeO ceramic cylinder coupled to a silica/silica optical fibre. The reader measures the RL signal and also uses a 450 nm laser diode to stimulate the BeO ceramic. A second background optical fibre is used to remove the stem effect. The RL/OSL BeO FOD was characterised in a solid water phantom, using a 6 MV x-ray beam. The RL was found to be reproducible and have a linear response to doses ranging from 30 cGy–15 Gy and dose rates from 100 cGy/min – 600 cGy/min. The OSL response was linear to doses of 10 Gy, becoming supralinear at higher doses. Measured percentage depth curves using the RL/OSL BeO FOD agreed with those measured using an IC15 ion chamber to within 5%, beyond the build up region. It was also found that the RL from BeO ceramic is unaffected by the delivered dose to the probe and hence, it remains constant for a given dose-rate. The insensitivity of the RL to accumulated dose makes BeO ceramic potentially capable of accurate dose-rate measurements without any corrections for the accumulated dose. This study demonstrates the feasibility of BeO ceramic as a versatile fibre-coupled luminescence dosimeter probe.     

Optically stimulated luminescence of dosimetric anion-defective corundum crystals

The relationship between the characteristics of optically stimulated luminescence (OSL) and thermally stimulated luminescence (TSL) of dosimetric crystals based on nominally pure single-crystal, ion-defective corundum is considered. It is established that the TSL and OSL characteristics of these crystals are closely interrelated and are caused by the same active traps. It is shown that the OSL of deep traps has a form difficult to interpret, which can be due to the effect of both more shallow and deeper traps.__________Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 1, pp. 140–142, January–February, 2005.     

Thermally stimulated luminescence and electron paramagnetic resonance studies on uranium doped K2Ca2(SO4)3

Thermally stimulated luminescence (TSL) studies of gamma-irradiated uraniumdoped K₂Ca₂(SO₄)₃ revealed two glow peaks around 400 K and 435 K. Electron paramagnetic resonance (EPR) studies carried out on these samples have shown the formation of the radical ions SO ₄ ⁻ , SO ₃ ⁻ , SO ₂ ⁻ and O ₃ ⁻ . From the study of the thermal stabilities of these radical ions, it was found that the thermal destruction of SO ₂ ⁻ and SO ₄ ⁻ radical ions are associated with the glow peaks observed around 400 K and 435 K respectively. Uranate ion was identified as the luminescent centre for the observed TSL glow. The trap depth values for the glow peaks have been determined from TSL data.     

Luminescence of Bismuth‐Activated Ceramics of Yttrium and Scandium Oxides

The luminescence spectra of Y₂O₃:Bi and Sc₂O₃:Bi ceramics have been investigated. The spectra have been resolved into elementary components by the Alentsev–Fock method. It has been established that the luminescence is attributed to emission centers of three types, two of which are due to the replacement of Y³⁺ (or Sc³⁺) by Bi³⁺ at the nodes of the crystal lattice of Y₂O₃ (or Sc₂O₃) with the point symmetry C ₂ and C _3i . The emission center Bi³⁺ in the position C_3i leads to the appearance of blue luminescence with maxima at 3.03 eV for Y₂O₃:Bi and at 3.05 eV for Sc₂O₃:Bi; this luminescence is attributed to the transition ³ P ₁–¹ S ₀. The emission center Bi³⁺ in the position C ₂ initiates green luminescence (which is also related to the ³ P ₁–¹ S ₀ transition in Bi³⁺) with a maximum in the region of 2.40 eV in Y₂O₃:Bi and in the region of 2.46 eV in Sc₂O₃:Bi. The red luminescence band with maxima at 1.85 eV in Y₂O₃:Bi and at 1.95 eV in Sc₂O₃:Bi is related to the presence of structural defects.     

Nd3+掺杂的氧化镧钇透明激光陶瓷的光谱性能研究

采用传统无压烧结工艺制备了Nd³⁺掺杂的Y_2-2xLa_2xO₃(x=0.08)透明陶瓷并对其光谱性能进行了研究. 结果表明：Nd³⁺:Y_1.84La_0.16O₃透明陶瓷在780—850 nm的波长范围内有较宽的吸收带. 当Nd³⁺掺杂量为1.5at%时，在820 nm和激光二极管抽运的808 nm处的吸收截面分别为σ_abs(820 nm)=1.81×10^-20 cm²，σ_abs(808 nm)=1.54×10^-20 cm². 最强的发射峰位于1078 nm处，并具有荧光寿命长、发射带宽宽、量子效率高等特点. 加入La₂O₃后，基质的光谱品质参数X_Nd由1.6减小到0.46，因此和⁴F_3/2—⁴I_11/2跃迁相对应的荧光分支比β_J,11/2增大为56.82%. Nd³⁺:Y_1.84La_0.16O₃透明陶瓷的这些性质有利于高效率的激光输出和超短锁模激光脉冲的实现. 关键词： 氧化镧钇透明陶瓷 光谱性能 3+')" href="#">Nd³⁺     

Thermally and optically stimulated radiative processes in LiBaF3 crystals

In LiBaF₃ crystals both valence–core transitions (5.4–6.5 eV) and so-called self-trapped exciton luminescence (about 4.3 eV) are important for practical application. Here, we present a study of 4.3 eV luminescence under photo- and thermostimulation after X-irradiation of undoped LiBaF₃ crystals at various temperatures. Optically stimulated luminescence as a result of electron recombination with both self-trapped holes and holes localized at some defects, were observed after X-irradiation below 130 K and that of electron recombination with defect-localized holes was observed after X-irradiation above 130 K. The spectra of thermo-stimulated luminescence (TSL) contain a broad band about 4 eV related to the electron (high-energy side) or hole (low-energy side) recombination depending on TSL peak temperature.