Novel Tb³âº-Doped LaAl2B4O10 phosphors: Structural analysis, luminescent properties, and energy transfer mechanism.

This study explores the structural and luminescent properties of terbium (Tb³âº)-doped lanthanum aluminium borate (LaAl2B4O10, abbreviated as LAB) phosphors, a novel host lattice for Tb³âº doping. LAB:Tb³âº phosphors, with varying dopant concentrations, were synthesized using a microwave-assisted combustion synthesis approach and characterized using X-ray diffraction (XRD), Rietveld refinement, and photoluminescence spectroscopy at both room and low temperatures. The structural analysis confirmed the hexagonal crystal structure of LAB and revealed successful incorporation of Tb³âº ions without altering the fundamental lattice. Luminescence studies demonstrated that the LAB:Tb³âº phosphors show strong green emission primarily attributed to the 5D4→7F5 transition of Tb³âº. The optimal doping concentration was determined to be 5 wt% Tb³âº, which provided maximum luminescence efficiency. This concentration also allowed for a critical study of energy transfer mechanisms within the phosphor, revealing dipole-dipole interactions with a critical distance of 9.80 Å between Tb³âº ions. Additionally, the CIE chromaticity coordinates of LAB:0.05 Tb³âº were precisely determined to be (0.289, 0.4460), indicating the potential for high-quality green emission suitable for solid-state lighting and display technologies. This work not only demonstrates the potential of LAB:Tb3+ as a highly efficient green luminescent material, but also sheds light on the mechanisms responsible for energy transfer and concentration quenching.

Enhanced luminescence of Eu3+ in LaAl2B4O10 via energy transfer from Dy3+ doping.

In this study, an investigation was conducted on the structural and photoluminescence (PL) characteristics of LaAl2B4O10 (LAB) phosphors initially incorporated with Dy3+ and Eu3+ ions. Subsequently, the impact of varying Eu3+ concentration while maintaining a constant Dy3+ concentration was examined. Structural characterization was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (EDS). XRD analysis confirmed the effective embedding of both dopants into the hexagonal framework of the LAB. The PL emission spectra revealed characteristic emissions of Dy3+ (blue and yellow) and Eu3+ (red) ions. The optimized dopant concentrations of both Dy3+ and Eu3+ were observed to be 3 wt%. The dominant mechanism for concentration quenching in doped LAB phosphors was determined to be the electric dipole-dipole interaction. Co-doping with Eu3+ led to a substantial decrease in Dy3+ emission intensity (∼0.18-fold) while enhancing Eu3+ emission intensity (∼3.72-fold). The critical energy transfer distance (RC = 11.64 Å) and the analysis based on the Dexter theory confirmed that the energy transfer mechanism corresponds to dipole-dipole interaction. The color purities and correlated color temperatures (CCT) were estimated, suggesting the potential of these phosphors for warm white and red lighting applications, respectively. The observed energy transfer and luminescence properties, along with the structural and compositional characterization, highlight the promising potential of LAB:Dy3+/Eu3+ co-doped phosphors for advanced lighting and display technologies.

Beta irradiation-induced thermoluminescence: Glow curve analysis and kinetic parameters in combustion-synthesized undoped Ca4YO(BO3)3.

This study examines the thermoluminescent (TL) properties of undoped Ca4YO(BO3)3 phosphor, focusing on how it behaves under a variety of experimental conditions. The IRSL-TL 565 nm was chosen as the appropriate detection filter among various optical detection filter combinations. During the preheating trials conducted at a rate of 2 °C/s, the TL peak exhibited increased intensity, particularly around 200 °C. The experimental outcomes demonstrated a reliable linear relationship (R2 = 0.996 and b = 1.015) in the dose response of undoped preheated Ca4YO(BO3)3 within the range of 1-200 Gy. The investigation encompasses a range of techniques, including the TM-Tstop method, computerized glow curve deconvolution (CGCD) analysis, and theoretical modelling. The application of the TM-Tstop method to samples irradiated with a 5 Gy dose revealed distinct zones on the TM versus Tstop diagram, signifying the presence of at least two discernible components within the TL glow curve, specifically, a single general order kinetics peak and a continuous distribution. The analysis of activation energy versus preheated temperature exhibited a stepwise curve, indicating five trap levels with depths ranging between 1.13 eV and 1.40 eV. The CGCD method also revealed the superposition of at least five distinct TL glow peaks. It was observed that their activation energies were consistent with the Tm-Tstop experiment. Furthermore, the low Figure of Merit (FOM) value of 1.18% indicates high reliability in the goodness-of-fit measure. These findings affirm the reliability and effectiveness of the employed methods in characterizing the TL properties of the Ca4YO(BO3)3 phosphor under investigation. Theoretical models, including the semi-localized transition model, were introduced to explain anomalous observations in TL glow peak intensities and heating rate patterns. While providing a conceptual framework, these models may require adjustments to accurately capture the specific characteristics uncovered through CGCD analysis. As a potential application, the study suggests that the characterized TL properties of Ca4YO(BO3)3 phosphor could be utilized in dosimetric applications, such as radiation dose measurements, owing to its reliable linear response within a broad dose range.

Temperature-dependent photoluminescence of novel Eu3+, Tb3+, and Dy3+ doped LaCa4O(BO3)3: Insights at low and room temperatures.

This study explores the structural and optical qualities of LaCa4O(BO3)3 (LACOB) phosphors doped with Eu3+, Dy3+, and Tb3+ using a microwave-assisted sol-gel technique. It uncovers oxygen-related luminescence defects in LACOB, highlighting emission peaks at 489 and 585 nm for Dy3+, a distinct sharp peak at 611 nm for Eu3+ in the red spectrum, and a notable green emission for Tb3+ due to specific transitions. The photoluminescence (PL) analysis indicates that luminescence is optimized through precise doping, leveraging dipole interactions, and localized resonant energy transfer, which are influenced by dopant concentration and spatial configuration. Temperature studies show emission intensity variations, particularly noticeable below 100 K for Tb3+ doped samples, demonstrating the nuanced balance between thermal quenching and luminescence efficiency. This temperature dependency, alongside the identified optimal doping conditions, underscores the potential of these materials for advanced photonic applications, offering insights into their thermal behavior and emission mechanisms under different conditions.

Temperature-responsive insights: Investigating Eu3+ and Dy3+ activated yttrium calcium oxyborate phosphors for structure and luminescence.

An investigation into the luminescent behavior of YCOB (Yttrium Calcium Oxyborate) doped with Eu3+ and Dy3+ ions, synthesized via the combustion method, is presented. The study, employing X-ray diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), and Energy-Dispersive X-ray Spectroscopy (EDS) analyses, confirms the structural integrity and purity of the synthesized nanophosphors. An XRD pattern exhibiting distinct crystalline peaks indicates that the dopant ions were successfully integrated into the YCOB lattice. The photoluminescence (PL) response of YCOB with Eu3+ and Dy3+ ions is thoroughly examined, uncovering distinct excitation and emission spectra. In the case of Eu3+ doping, excitation spectra reveal a significant charge transfer (CT) band at 254 nm, indicative of electron transfer between oxygen and europium ions. This CT transition enhances our understanding of the excitation behavior, with the dominant and Laporte-forbidden 5D0 → 7F2 transition. Characteristic peaks at 345 nm in the excitation spectra efficiently stimulate YCOB:Dy3+ when Dy3+ is used as a dopant. The primary emission peak at 585 nm corresponds to the hypersensitive electric dipole transition 4F9/2-6H13/2. Concentration quenching phenomena are observed, with a maximum Eu3+ concentration of 7 wt % attributed to the dipole-quadrupole interaction. Dy3+ doping, with a maximum concentration of 2 wt % primarily shows multipolar interactions, especially dipole-dipole interactions. The study extends to CIE chromaticity analysis, emphasizing Eu3+ doping's suitability for white light-emitting diode (WLED) applications and ensuring color stability. Conversely, varying Dy3+ concentrations do not yield consistent chromaticity coordinates. These findings have significant implications for the development of advanced phosphor materials across diverse applications, offering a roadmap for optimizing their optical performance.

Luminescence of undoped and Eu3+ activated zinc gallate phosphor: Synthesis, unusual intense 5D0 → 7F4 red emission.

A series of Eu3+-doped ZnGa2O4 samples were synthesized via the urea-glycine combustion route. Powder X-ray diffraction (XRD) was used to investigate the crystallinity of the samples, energy dispersive spectroscopy (EDS) to explore the elemental composition, Fourier transform infrared (FTIR), to observe the vibrational modes of the samples, photoluminescence (PL) to determine the luminescence properties. The XRD data prove that the samples remain single cubic structure even at high concentrations of Eu³âº, enabling the formation of a unique emission spectrum. The active ion concentration was varied to examine the influence of concentration on luminescent properties. This study revealed a 5D0 →7F4 transition located at 700 nm with unusual intensity that has not been documented in the literature, which suggests that the active ion concentration can influence the luminescent characteristics of the phosphors. The increasing Eu3+ content increases the number of Eu3+ ions in ZnGa2O4 host lattice, which enhances the luminescence efficiency of the phosphor. However, beyond a certain level of Eu3+content (i.e., 3 wt% Eu3+), the number of Eu3+ ions becomes excessive, resulting in a reduction in luminescence efficiency due to concentration quenching. The dipole dipole interaction is elucidated to play a prominent role in the mechanism of Eu3+ quenching in the ZnGa2O4. An assessment of color coordinates based on emission spectra reveals that the coordinates shift from blue to the white light region, and then to red as Eu3+ content increases. This suggests that there is a substantial relationship between the Eu3+ concentration and the measured color coordinates.

Thermoluminescence in GdAl3(BO3)4 phosphors: Unusual heating rate dependencies, dose responses and kinetic parameters.

The current study focuses on the production of GdAl3(BO3)4 (GAB) phosphors using gel combustion. X-ray diffraction (XRD) and thermoluminescent (TL) methods were used to investigate the structural and thermoluminescence (TL) features of the samples. XRD results revealed that GAB phosphors were crystallized in a rhombohedral crystal system. TL experimental data exhibited an unusual heating rate behaviour, which was explained by the semi-localized transition model, and this provides valuable insight into the properties of the GAB sample. Beta-irradiated GAB hosts exhibit two primary peaks at 106 °C and 277 °C on their TL glow curves. We have employed a variety of heating rates (VHRs), TM-Tstop method, and computerized glow curve deconvolution (CGCD) techniques. By using a combination of these techniques, we can identify the kinetic parameters of the GAB samples more accurately, including peak numbers, activation energy, and frequency factors. Both Tm-Tstop and CGCD techniques produce similar results in terms of trap numbers and trap depths. In the trap centers, electrons were trapped at 1.05 eV, 0.84 eV, 1.12 eV, 1.20 eV, 1.42 eV, 1.63 eV and 1.42 eV. There was a linear behaviour of GAB samples over a dose range of 0.1 Gy-10 Gy. GAB phosphors did not show any significant changes in TL response with repeated irradiation cycles, suggesting that it is a reliable radiation dosimeter. GAB is therefore a potential candidate for radiotherapy dose measurement based on these findings.

Anomalous dose behaviour of thermoluminescence glow curves and kinetic analysis of beta irradiated YAl3(BO3)4:Tb phosphor.

With the aid of thermoluminescence (TL), we have extensively studied YAl3(BO3)4 host matrices incorporated with Tb3+ at different doping contents, which have been produced by combustion. The measured the TL glow curves exposed to beta rays at different doses consisted of four broad peaks located at around 76, 126, 230, and 378 °C. The peak maximum of the 230 °C TL peak shifts toward higher temperatures after 5 Gy beta irradiation while the other peak maxima almost remain constant. It is peculiar that 230 °C peak maximum shifts to higher temperatures with increased radiation dose and can be attributed to the multiple phases of the sample. A TL glow curve exhibits a proportional increase in intensity with increased the heating rate. A discussion of the possible causes of this pattern is provided. Observed peaks using the Tm─Tstop method are due to the presence of a quasi-continuous distribution of traps. The parameters of the traps have also been estimated using various heating rate methods in excellent agreement with one another.

Thermoluminescence glow curve analysis of Ca3Y2B4O12 phosphor prepared using combustion method.

Ca3Y2B4O12 (CBYO) phosphor was synthesized using a gel combustion method. X-ray diffraction (XRD) measurement confirmed a single-phase structure (space group Pnma (62)) of synthesized compound. TL measurements were conducted between room temperature (RT) and 450 °C at a heating rate of 2 °Cs-1. Significant glow peaks were observed at 64, 116, and 242 °C in CYBO phosphor sample exposed to different beta doses. In the range of 0.1-100 Gy, the TL intensity of the glow peak displayed good linearity. Different methods were employed to determine the number of peaks, the trap structure, and the kinetic parameters of the thermoluminescence glow curve of CBYO; the Hoogenstraaten method, various heating rates (VHR), and glow curve deconvolution method (CGCD) implemented through tgcd:An R package. Currently available findings confirm that CYBO host is a promising candidate for environmental studies because one exhibits adequate TL dose response coupled with a good sensitivity and linearity.

Novel Dy incorporated Ca3Y2B4O12 phosphor: Insights into the structure, broadband emission, photoluminescence and cathodoluminescence characteristics.

This study reports cathodoluminescence (CL) and photoluminescence (PL) properties of undoped borate Ca3Y2B4O12 and Ca3Y2B4O12:x Dy3+ (x = 0.5, 1, 2, 3, 5, and 7) synthesized by gel combustion method. Micro-X-Ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), CL and PL under electron beam and 359 nm pulse laser excitation, respectively were used to investigate characterization and luminescence studies of synthesized samples in the visible wavelength. As-prepared samples match the standard Ca3Y2BO4 phase that belongs to the orthorhombic system with space group Pnma (62) based on XRD results. Under electron beam excitation, this borate host shows a broad band emission from about 250 to 450 nm, peaked at 370 nm which is attributed to NBHOC. All as-prepared phosphors exhibited the characteristic PL and CL emissions of Dy3+ ions corresponding to 4F9/2→6HJ transitions when excited with laser at 359 nm. The CL emission spectra of phosphors were identical to those of the PL spectra. Concentration quenching occurred when the doping concentration was 1 mol% in both the CL and PL spectra. The underlying reason for the concentration quenching phenomena observed in the discrete orange-yellow emission peaked at 574 nm of Dy3+ ion-doped Ca3Y2B4O12 phosphor is also discussed. According to these data, we can infer that this new borate can be used as a yellow emitting phosphor in solid-state illumination.

Synthesis and beta particle excited thermoluminescence of BaSiF6 phosphor.

BaSiF6 phosphor was synthesized by a gel combustion method. The crystalline size was found to be 54.17 ± 4.36 nm using Williamson-Hall (W-H) approximation. The TL data collected by means of a combination of a commercial BG39 and HC575/25 filters was studied to evaluate basic kinetic parameters. Three TL glow peaks of BaSiF6 phosphors are centered at around 84, 190 and 322 °C. Tm-Tstop, various heating rate (VHR) and computerized glow-curve deconvolution (CGCD) method were utilized to analyse collected data. Our findings indicate that luminescence process in scrutinized material may obey second order kinetics. The TL dose response of the TL glow peaks exhibits a linear characteristic up to 100 Gy. Deconvolution of the glow curve reveals that the number of the component TL glow peaks in the complex glow curve is composed of well-isolated six overlapping glow peaks. The FOM value is 2.32.

Adsorption of thorium (IV) ions by metal ion doped ZnO nanomaterial prepared with combustion synthesis: Empirical modelling and process optimization by response surface methodology (RSM).

Environmental problems have reached enormous dimensions, driving efforts to remove and recycle waste from energy and industrial production. In particular, removing the radionuclide contamination that occurs as the nuclear industry grows is difficult and costly, but it is vital. Technologic and economical methods and advanced facilities are needed for the separation and purification of radioactive elements arising from the nuclear industry and uranium and thorium mining. With the adsorption method, which is the most basic separation and recovery method, the use of high-capacity nanomaterials has recently gained great importance in reducing the activity of the waste, reducing its volume by transforming it into solid form, and recovering and removing liquid radioactive wastes that might harm the ecological environment. This study aimed to determine the adsorption properties of metal ion-doped nano ZnO (nano-ZnO:Al) material synthesized by the microwave-assisted gel combustion method for the adsorption of thorium (IV) from aqueous media. First, characterization processes such as XRD, SEM, BET and zeta potential were performed to observe changes in the host ZnO adsorbent structure caused by the doping process. Later, this was optimized via the response surface method (RSM), which is widely used in the characterization of the adsorption properties of thorium (IV) from aqueous solutions. Such characterization is commonly used in industrial research. We tested how pH (3-8), temperature (20-60 °C), Th (IV) concentration (25-125 mg/L) and adsorbent amount (0.01-0.1 g) affect adsorption efficiency. The best possible combinations of these parameters were determined by RSM. It was calculated by RSM that the design fits the second order (quadratic) model using the central composite design (CCD) for the design of experimental conditions. R2 and R2 adjusted values from the parameters showing the model fit were 0.9923 and 0.9856, respectively. According to the model, the experimental adsorption capacity was 192.3 mg/g for the doped-ZnO nanomaterial under the theoretically specified optimum conditions. Also, the suitability of Th (IV) adsorption to isotherms was examined and thermodynamic parameters were calculated.

Synthesis and photoluminescence characteristics of a novel Eu and Tb doped Li2MoO4 phosphor.

Li2MoO4:x Eu3+ and Li2MoO4:xTb3+ phosphors, where x = 0.5, 1, 2, 3, 5 and 7 wt%, were synthesized through a gel-combustion method. The XRD data reveals that Eu3+ and Tb3+ doped Li2MoO4 phosphors exhibit a Rhombohedral structure belonging to the space group R3 which matched well with the standard JCPDS files (No.012-0763). We present photoluminescence (PL) spectra from Eu and Tb doped Li2MoO4 under 349 nm Nd:YLF pulses laser excitation over the temperature range of 10-300 K. Undoped Li2MoO4 shows a wide broad band around 600 nm because of the intrinsic PL emission of tetrahedral of MoO42- which was in good agreement with previous findings. Under the excitation of 394 nm, the as-synthesized phosphors exhibited sharp and strong intensity PL emission signals in the red (612 nm, 5D0→7F2 transition) and green (544 nm, 5D4→7F5 transition), respectively. The critical doping concentration of Eu3+ and Tb3+ ions in the Li2MoO4 were estimated to be 2 wt%. The concentration quenching phenomena were discussed, and the critical distances for energy transfer have also been evaluated by the concentration quenching.

Cathodoluminescence properties of La2MoO6:Ln3+ (Ln: Eu, Dy, and Sm) phosphors.

La2MoO6 orange-red phosphors with high efficiency incorporated with Eu, Dy and Sm have been synthesized through a gel combustion method. The influences of rare earth doping in synthesized samples were analysed by X-ray diffraction (XRD), scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), and cathodoluminescence. Rare earth doped La2MoO6 samples show strong emission bands in the range of 400-750 nm and optimal doping concentration for all samples was 2 mol%. La2MoO6 host doped Eu ion showed intense and predominant emission peaks in 450-750 nm range. The electrical multipolar interaction contributed to the non-radiative energy transfer between Eu3+ ions in La2MoO6 host matrix. Sm doped La2MoO6 host exhibited orange-red CL emission peaks at 564, 608, 652 and 708 nm La2MoO6:Dy3+ phosphor displayed emissions at 484, 574 and 670 nm, respectively. The observed intense and sharp emission peaks indicate that La2MoO6 is promising host for lanthanides doped phosphor materials in the applications of optoelectronic.

Synthesis and photoluminescence characteristics of Dy incorporated MoO3 phosphor: Suppression concentration quenching.

A series of MoO3:Dy3+ phosphors have been synthesized via the gel-combustion method. The X-ray and photoluminescence (PL) emission spectra were employed to characterize the obtained phosphors. The prepared samples were characterized through XRD measurements and exhibited that Dy3+ ions can be successfully incorporated into the host material. The PL emission bands of Dy3+ doped MoO3 were observed at 486 nm, 574 nm and 666 nm which are assigned to the transitions of 4F9/2 â†’ 6H15/2, 4F9/2 â†’ 6H13/2 and 4F9/2 â†’ 6H11/2, respectively. Concentration quenching were largely taken into consideration as one of the crucial aspects limiting the application range of phosphors in today's modern world. An abnormal thermal quenching dependence was reported when Dy3+ ions were incorporated into MoO3 host matrix. In order to understand the origin of this beneficial behaviour, energy transfer processes occurring via radiative and nonradiative mechanisms were investigated to elucidate this suppression of the concentration quenching.

Preparation and cathodoluminescence characteristics of rare earth activated BaAl2O4 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 = ±â€¯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.

The role of calcination temperature on structural and luminescence behaviour of novel apatite-based Ca2Y 8(SiO4)6O2: Ce3+,Tb3+ phosphors.

A series of novel apatite-based Ca2Y8(SiO4)6O2 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 Ca 2Y 8 (SiO4)6O2:Ce3+, Tb3+ was optimized to be 1200°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)6O2:Ce3+, Tb3+exhibited one strong excitation band at 325nm. The PL and CL results indicated that the violet-blue emission intensities about 400nm from the Ce3+ and efficient green emission at 544nm from Tb3+ were highly dependent on the calcination conditions.

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.

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.

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.