Thermoluminescence characteristics of rare-earth-doped LiCaBO3 phosphor

LiCaBO₃ was synthesized by high-temperature solid-state reaction. The influence of different rare earth dopants, i.e. Dy³⁺, Tb³⁺, Tm³⁺ and Ce³⁺, on thermoluminescence (TL) of LiCaBO₃ phosphor was discussed. We studied the TL properties and some dosimetric characteristics of Ce³⁺-activated LiCaBO₃ phosphor in detail. The effect of the concentration of Ce³⁺ on TL was investigated, the result of which showed that the optimum Ce³⁺ concentration was 1 mol%. The TL kinetic parameters of LiCaBO₃:0.01Ce³⁺ were studied by computer glow curve deconvolution (CGCD) method. The three-dimensional (3D) TL emission spectra were also studied, peaking at 431 and 474 nm due to the characteristic transition of Ce³⁺. We also studied the linearity, annealing condition, reproducibility, fading and different heating rate of the LiCaBO₃:0.01Ce³⁺ phosphor.     

Energy levels in YPO4:Ce3+,Sm3+ studied by thermally and optically stimulated luminescence

Energy-resolved optically stimulated luminescence (OSL) spectra and thermoluminescence (TL) glow curves of a powder sample of YPO₄:Ce³⁺,Sm³⁺ were measured to investigate the nature of the trapping centre and to locate its energy level relative to the valence and conduction bands of the YPO₄ host. The high-temperature glow peak could unequivocally be assigned to Sm²⁺ (thus Sm³⁺ acts as an electron trap). The trap depth of this centre, as derived from the OSL excitation spectra, is in good agreement with the Dorenbos model prediction. The OSL excitation spectra also reveal excited states of Sm²⁺ well below the conduction band. These excited states produce a broadening of the high-temperature TL glow peak and also cause the activation energy determined by the Hoogenstraten method to underestimate the trap depth.     

Comparative investigations of TL and OSL in KCI:Eu2+ crystals irradiated with UV and X-rays

Abstract

We present thermoluminescence (TL) glow curves and optical stimulated luminescence (OSL) response from both KCl:Eu²⁺ crystals irradiated with soft X-rays (20 KV, 80 μA) and ultraviolet light (230 nm). Two situations take place. First, we observed that for long time F-light bleaching (560 nm) the typical TL glow curve of X-rays irradiated KCl:Eu²⁺ resembles the TL glow curve of UV-irradiated samples. Second, along with OSL measurements, we have performed a thermal bleaching and we have addressed F and F_z participation in OSL. These results provide us a supportable correlation between F and F_z as responsible centers for OSL and TL processes.     

Modelling the optical bleaching of the thermoluminescence of K2YF5:Pr3+

Optical bleaching of the thermoluminescence (TL) curve of K₂YF₅:Pr³⁺ has been observed after optically stimulated luminescence (OSL) readout of pre-irradiated crystals. The traps being responsible for the TL signal are not emptied completely by the optical stimulation. Furthermore, if the illumination time is increased a constant intensity level of the residual TL glow curve is eventually achieved. On the other hand, if the low temperature peak of the glow curve is thermally cleaned, no subsequent OSL is measured. This behavior has been successfully explained by assuming that part of the electrons in the trap being responsible for the low temperature glow peak of K₂YF₅:Pr³⁺ recombine with holes via localized transitions during optical stimulation. During TL all trapped electrons recombine via delocalized transitions. Simulations have been carried out in order to demonstrate the feasibility of the model.     

Time-resolved OSL studies of YAlO3:Mn2+ crystals

Time-Resolved Optically Stimulated Luminescence (TR-OSL) from single crystalline YAlO₃:Mn²⁺ samples was investigated using a green light emitting diode (λ ∼ 525 nm) as stimulation light source. The TR-OSL decay curve of the material can be described with a single exponential decay function with a lifetime about 80 ms that does not depend on irradiation dose in the range from 50 mGy to 1 kGy. This OSL decay is superposed on a photoluminescence signal with a much shorter (3.5 ms) decay lifetime. The Mn²⁺ photoluminescence decay with a lifetime of 3.5 ms can be easily eliminated by corresponding time resolution using pulsed OSL readout. Dose response and thermal stability of the OSL signal are consistent with the previous thermoluminescent (TL) studies of the material.     

Luminescence studies on gamma irradiated KCl: Ce crystals

This paper reports thermoluminescence(TL), optical absorption and TL emission studies that are made on Ce³⁺ doped KCl single crystals irradiated at room temperature. The glow curve and optical absorption studies indicate the participation of Ce³⁺ ions in the TL process. The TL study suggests the presence of low concentration of Ce³⁺ ions which reduces the TL efficiency with respect to pure KCl samples. On F bleaching γ irradiated crystals Z₁ centers are observed. A broader and strongly intense violet blue emission at 290, 370, 423 and 488 nm has been observed with 240 nm excitation. This emission has been attributed due to the transition from 5d(2D) excited energy level to the 4f¹ ground stable energy level (2F_5/2 and 3F_7/2) of Ce³⁺ doped KCl crystals.     

Scintillation properties of Ce3+-doped YCl3 and YBr3

The dependence of the scintillation properties of Ce³⁺-doped YCl₃ and YBr₃ on activator concentration (0.5, 1 and 2 mol%) has been studied. The radioluminescence spectra of both materials contain asymmetric bands with maxima located at 3.13 eV (383 nm) for YCl₃:Ce³⁺ and 2.84 eV (422 nm) for YBr₃:Ce³⁺. The scintillation pulse decay curves for both materials are described by two components with decay constants of 37 and 640 ns for YCl₃:Ce³⁺ and 36 and 450 ns for YBr₃:Ce³⁺, the fractions of the faster component being 86 and 79 per cent, respectively. The dependences of the light yield of the studied materials on Ce³⁺ concentration pass through a maximum near 1 mol% of the activator, and the maximum light yields (relative to NaI:Tl) are 8700 photons per MeV for YCl₃:Ce³⁺ and 20,600 photons per MeV for YBr₃:Ce³⁺.     

Ce and Pr5d-energy levels in the (pseudo) perovskites KMgF3 and NaMgF3

The location of the 5d-energy levels of Ce³⁺ and Pr³⁺ in the cubic perovskite KMgF₃ and in the distorted perovskite NaMgF₃ was determined from spectroscopic studies in the vacuum ultraviolet. It is established that Ce³⁺ and Pr³⁺ ions both occupy the same site in each host: K⁺ sites for KMgF₃ and Na⁺ sites for NaMgF₃. The small crystal field splitting and the small value of the centroid shift of the 4fⁿ⁻¹5d-configuration yield a relatively high energy for the lowest 5d state of both Ce³⁺ and Pr³⁺. The lowest 5d state of Pr³⁺ in both hosts is found at energy higher than the 4f² state, enabling the photon cascade emission to occur.     

Synthesis and luminescence in some fluoro-silicates for the possible applications in OSL dosimetry

Various fluoro-silicates, viz. M₂SiF₆ (M=Li, Na, K) were synthesized by reacting the mixture of corresponding salt and silicic acid with Hydrofluoric acid. The thermal analysis of these materials was performed. These materials were doped with ions Ce³⁺, Cu⁺, Ag⁺ and photoluminescence, TL, OSL properties were studied. Intense TL and OSL was observed from these materials. Due to decomposition during heating, these materials may not be suitable as TL Phosphors, but will be good phosphors for radiation dosimetry using OSL.     

Analysis of TL and OSL kinetics of lithium aluminate

Lithium aluminate (LiAlO₂) polycrystalline material showing high OSL sensitivity and linear dose response was prepared at IFJ Krakow. The kinetic parameters of OSL and TL processes were evaluated using various experimental techniques: LM-OSL deconvolution, TL glow-curve deconvolution, variable heating rate and isothermal decay. The OSL signal was found to consist of four components, one of them exhibiting a very slow decay. The TL glow-curve possesses two apparent peaks at approximately 85 °C and at 165 °C, which both seem to follow first order kinetics. These peaks seem to have a composite structure and as many as six peaks were found in the glow-curve.     

Photoluminescence and EPR studies on gamma irradiated Ce doped potassium halide single crystals

Electron Paramagnetic Resonance(EPR), Photoluminescence(PL), Thermoluminescence (TL) and other optical studies of γ-irradiated KBr, KCl:Ce³⁺ single crystals. Cerium when doped into the KBr, KCl is found to enter the host lattice in its trivalent state and act as electron trap during γ-irradiation, thereby partially converting itself to Ce²⁺. The Photoluminescence(PL) spectra of both KCl and KBr crystals doped with Ce exhibit the strong blue emissions of Ce corresponding to ⁵d(²D)→²F_5/2 and ⁵d(²D)→²F_7/2 transitions. The defect centers formed in the Ce³⁺ doped KBr and KCl. Crystals are studied using the technique of EPR. A dominant TL glow peak at 374, 422 K and KCl:Ce³⁺ at 466, 475 K is observed in the crystal. EPR studies indicate the presence at two centers at room temperature. Spectral distribution under the thermoluminescence emission(TLE) and optically stimulated emission(OSL) support the idea that defect annihilation process to be due to thermal release of F electron in KBr, KCl:Ce³⁺ crystals. Both Ce³⁺ and Ce²⁺ emissions were observed in the thermoluminescence emission of the crystals.     

Optical and gain properties of series of crystals LiF-YF3-LuF3 doped with Ce and Yb ions

Here, we present first results of systematic studies of host cation variation impact on spectral-kinetic, photochemical and gain properties of Ce³⁺-doped LiYF₄ (YLF), LiLuF₄ (LLF) and LiY_1−xLu_xF₄ family crystals. 5d-4f luminescence decay of Ce³⁺ ions studies, together with pump-probe experiments, indicate that previously reported twice higher luminescence quantum yield in LLF compared with that of YLF crystals is provided by more efficient upper lasing level feeding due to recombination and higher color center destruction rate in LLF against YLF crystals. Namely, it is responsible for higher energetic characteristics of laser based on Ce³⁺:LLF crystals. Strong and wide pump-induced absorption band centered at 310 nm is observed in Ce³⁺:YLF. This band is shifted to blue and its intensity goes down with Lu content. We have evaluated free charges recombination rate, excited state absorption cross-section for Ce³⁺ ions and some other photodynamic processes related microparameters. Fitting results indicate that pump-induced color centers lifetime decreases with Lu-content in LiYF₄-LiLuF₄ mixture and it can be associated with more efficient color center bleaching by Ce³⁺ ions 5d-4f fluorescence.     

EPR and optical spectroscopy of neodymium ions in KMgF3 and KZnF3 crystals

KMgF₃ and KZnF₃ crystals doped with Nd³⁺ ions were studied using EPR and optical spectroscopy methods. Several types of paramagnetic centers of Nd³⁺: KMgF₃ — two of tetragonal and one of rhombic symmetry; KZnF₃ — one of tetragonal and one of trigonal symmetry were found. Parameters of the corresponding spin Hamiltonians were determined. Using optical spectroscopy paramagnetic centers Nd²⁺ and Nd⁴⁺ in KMgF₃ were found.     

Optically stimulated luminescence in doped K3Na(SO4)2 phosphors

Optically stimulated luminescence (OSL) in Cu and Eu doped K₃Na(SO₄)₂ is reported for the first time. The Cu-doped sample shows OSL sensitivity which gets enhanced by co-doping with Mg²⁺ ions. The Cu-doped and quenched sample shows better sensitivity which is almost double than that of the slowly cooled sample, whereas the sensitivity of Mg co-doped sample remains nearly same irrespective of the thermal treatment. The Cu-doped sample shows TL peak around 200 °C and moderate OSL sensitivity. Doping of Mg shifts the TL peak to around 160 °C and is correlated with good OSL sensitivity. Eu-doped sample does not show OSL sensitivity. However, relatively good OSL sensitivity is observed in Aluminium co-doped and slowly cooled sample, which is about 15% of the commercial Al₂O₃:C(Landuer Inc.). A near fully optically sensitive TL peak around 155 °C is observed. The dose response is linear and practically no OSL fading is observed in first five days of storage in slowly cooled sample. This study on conventional sulphate-based TL phosphors will be useful in developing OSL phosphors for radiation dosimetry.     

Luminescence properties and energy transfer in Ba2Y(BO3)2Cl:Ce3+,Tb3+ phosphors

Novel green-emitting Ba₂Y(BO₃)₂Cl:Ce³⁺,Tb³⁺ phosphors were synthesized by a solid-state method. X-ray diffraction and photoluminescence spectra were utilized to characterize the structures and luminescence properties of the as-synthesized phosphors, respectively. Ba₂Y(BO₃)₂Cl:Ce³⁺,Tb³⁺ phosphors exhibit blue and green emission bands under the excitation of near-ultraviolet light. An asymmetric blue emission originates from the Ce³⁺ ion, whereas the green emission originates from the Tb³⁺ ion. A spectral overlap is found between the emission band of the Ce³⁺ ion and the excitation band of the Tb³⁺ ion, which supports the occurrence of the energy transfer from the Ce³⁺ ion to the Tb³⁺ ion. Meanwhile, the energy transfer is thoroughly investigated by their photoluminescence decay behaviors. The energy-transfer efficiency from the Ce³⁺ ion to the Tb³⁺ ion is also calculated, and a possible mechanism is proposed.     

Influence of high hydrostatic pressure on Eu-luminescence in KMgF3:Eu crystal

Spectroscopic investigations are presented of KMgF₃:Eu²⁺ crystal under high hydrostatic pressure from ambient to 310 kbar. The sample was excited by 30 ps pulses generated by optical parametric generator (OPG) system with wavelength controlled between 210 and 325 nm. The Grüneisen parameters of individual phonons are obtained from the pressure shift of the Eu²⁺ emission related to the ⁶P_7/2→⁸S_7/2 transition accompanied by phonon sideband. The luminescence decays exponentially for the pressure below 135 kbar with lifetime of 3.30 ms and slightly nonexponential above 135 kbar, while the average decay time is nearly independent of the pressure. The results obtained for KMgF₃:Eu²⁺ are compared with those for LiBaF₃:Eu²⁺ in which the ⁶P_7/2→⁸S_7/2 emission is replaced by the broadband emission of the 4f⁶5d¹→4f⁷ transition at high hydrostatic pressure.     

α-Al2O3:C晶体的热释光和光释光特性

以高纯α-Al₂O₃和石墨为原料,采用温梯法生长了α-Al₂O₃：C晶体,使用Ris TL/OSL-DA-15型热释光和光释光仪研究了其热释光和光释光特性.α-Al₂O₃：C晶体在462K附近有单一热释光峰,发射波长位于410nm.随着辐照剂量的增加,热释光强度逐渐增强,462K的热释光特征峰位置保持不变.α-Al₂O₃：C晶体的 关键词： 2O₃：C')" href="#">α-Al₂O₃：C 热释光 光释光     

Decay of the Ce3+ luminescence of LaMgAl11O19 : Ce3+ and of CeMgAl11O19 activated with Tb3+ or Eu3+

Decay measurements have been performed on the Ce³⁺ luminescence of LaMgAl₁₁O₁₉ : Ce³⁺ and of CeMgAl₁₁O₁₉ activated with Tb³⁺. For all samples, the decay was found to be nearly exponential over at least two decades, and the decay time constant was practically the same, being ≈20 ns. From these results and from quantum efficiency data of the Ce³⁺ luminescence, conclusions are drawn about the various energy transfers and quenching interactions occurring in these compounds.     

Investigation of defect centres responsible for TL/OSL in MgAl2O4:Tb

Magnesium aluminate doped with Tb³⁺ (MgAl₂O₄:Tb³⁺) was prepared by combustion synthesis. Three thermoluminsence (TL) peaks at 120, 220 and 340 °C were observed. PL and TL emission spectrum shows that Tb³⁺ acts as the luminescent centre. Optically stimulated luminescence (OSL) was observed when stimulated by 470 nm blue light.Electron spin resonance (ESR) studies were carried out to identify the defect centres responsible for the TL and OSL processes in MgAl₂O₄:Tb³⁺. Two defect centres were identified in irradiated MgAl₂O₄:Tb³⁺ phosphor by ESR measurements which was carried out at room temperature and these were assigned to V and F⁺ centres. V centre (hole centre) is correlated to 120 and 220 °C TL peaks and F⁺ centre (electron centre), which acts as a recombination centre is correlated to 120, 220 and 340 °C.