Abstract
Microcrystalline SrB4O7:Eu3+ (SBO) synthesized using strontium carbonate, boric acid and europium chloride as precursors by solid state diffusion method with different concentrations of europium. The microcrystalline powder samples were annealed and quenched at different temperatures in the range of 400–900 °C for 2 h in air and were characterized by XRD, SEM, EDS techniques. The phosphor material with 0.2 mol% europium doping and annealed at 700 °C shows maximum TL intensity and PL studies show presence of Eu in 2 + and 3 + ionic states. The dosimetry characteristics show that the phosphor could be used for high dose measurements.
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Introduction
Thermoluminescence (TL) is a familiar technique, used for various applications in radiation dosimetry. The materials activated with certain impurities (popularly known as phosphors) when irradiated with high-energy (ionizing radiations) produce electron traps and holes (luminescence centers). They are mostly stable at room temperature but emit visible light during their recombinations on stimulating optically or simply by heating. The intensity of luminescence thus produced by thermal stimulation (TL) has generally linear relationship (in a specific dose range) with the ionizing radiation dose(s) (absorbed doses) given to the phosphor material and unknown absorbed dose(s) could thus be estimated by calibration. In other words, some little amount of energy is stored in the material in the form of defects which gets released on stimulation in the form of visible light, converted into electrical signal and used for estimating/monitoring high-energy radiation doses. This is necessary as high-energy radiations are hazardous to living beings. TL has expanded its applications in personnel, clinical and environmental dosimetry, medical dosimetry, space dosimetry, archaeological and geological dating, etc. [1,2,3,4]. Luminescence of rare earth ions activated alkaline earth borates has been well studied by several workers as found in the literature [5,6,7,8,9,10,11,12,13,14], particularly strontium tetraborate (SrB4O7, here represented as SBO) because of its special structure [15]. The crystal structure of SBO is orthorhombic with space group Pnm21(31). The structure of SBO contain a rigid 3-dimentisonal B4O7 network of which each corner attached to BO4 tetrahedrons, with the strontium atoms positioned in the larger confinement of atomic structure by nine oxygen atoms [16, 17]. These confinements of oxygen are large enough to house the activator ions (rare earth ions such as, Eu2+, Eu3+, Dy2+, Sm2+, etc.) without breaking the borate networks, hence targeted for various applications. Strontium tetraborate is unique compound which devises excellent non-linear optical properties with high mechanical strength, non-hygroscopic in nature and high optical damage threshold [18].
Rare-earth and non-rare-earth-doped inorganic phosphors are widely used in a range of applications, such as, medical dosimetry, radiation dosimetry, dose mapping, lamp industry, X-ray imaging, colour display, radiological incidents and imaging, etc. [19]. Rare-earth ion doped phosphors have been widely studied for their superior luminescence properties. Doped alkaline-earth borates such as MgB4O7:Dy,Na [7], CaB4O7:Dy,Eu [8, 9], SrB4O7:Cu [10], SrB4O7:Dy [11], SrB4O7:Eu,Gd [12], SrB4O7:Eu,Tb [13] SrB4O7:Sm2+ [14] are some of the most promising materials for individual doses owing to their high sensitivity and, in certain cases, their TL tissue-like properties for radiation absorption. To be more specific, the luminescent properties of europium-ion doped phosphors have been studied expansively. SBO on doping with rare earth ions [20,21,22] is no exception and has been used as a host medium for several luminescence applications. The synthesis of rare earth doped SBO phosphors has been carried out by using various techniques, such as, combustion method, Kyropoulos method, micro-pulling-down method, Pechini-type sol–gel method, conventional melt-quenching method and so on [23,24,25,26]. Due to simplicity and larger product formation, solid state diffusion method was widely used for the synthesis of SBO. Also, this method provides the advantage for controlling the particle size of the sample from micro to nano scale.
In this work, SrB4O7:Eu3+ microphosphor has been synthesized by using solid state diffusion method and its thermoluminescence (TL) and photoluminescence (PL) properties were studied. The influence of impurity doping concentrations and that of annealing and quenching temperatures on structural, morphological, compositional and luminescent (TL) properties of the SrB4O7:Eu3+ microphosphor has also been studied. Moreover, the investigation of the formation of different local energy levels due to the presence of the impurity in different ionic forms was carried out using photoluminescence (PL) technique. The phosphor material in the microcrystalline form was irradiated with different gamma radiation doses using 60Co gamma source and its thermoluminescence (TL) dosimetry study was carried out. These were the absorbed doses of the radiation. The exact peak positions and the number of peaks of TL glow curve were confirmed by Tm-Tstop method. The TL glow curve was also deconvoluted by using Computerized Glow Curve Deconvolution (CGCD) method and the trapping parameters, such as, order of kinetics, activation energy, frequency factor, were determined.
Experimental
Synthesis of SrB 4 O 7 :Eu 3+
SrB4O7:Eu3+ microphosphor synthesized by using solid state diffusion method. In this method Europium chloride (EuCl3) (0.2 mol%) and Strontium carbonate (SrCO3) are mixed in distilled water and stirred on a magnetic stirrer at room temperature (RT) for 30 min. Few drops of concentrated hydrochloric acid (HCl) were added into the solution to dissolve/disperse the EuCl3 compound completely. This solution was further heated in an oven to form the powder by removing all water molecules. The powder thus formed was then transferred to an agate mortar with addition of boric acid (H3BO3) and grinded for 20 h. After grinding, the mixture was annealed at 500 °C for 2 h in muffle furnace. With the help of sieves, particles with size in the range of 90–120 µm were collected and further annealed and quenched at different temperatures (in the range of 400–900 °C) for 2 h. Finally, the microcrystalline samples were irradiated with different gamma radiation doses by using 60Co gamma source. Likewise, to study the effect of Eu concentration on SBO structure, synthesis of SrB4O7:Eu3+ microphosphor with different concentrations of europium (0.1–1.0 mol%) was carried out by using same the procedure. Figure 1 shows schematic diagram for synthesis of SrB4O7:Eu3+ microphosphor by solid state diffusion method.
Characterization techniques
The structural characterization of prepared sample was carried out by XRD using Cu-target (Cu-Kα = 1.54 Å) on Bruker AXS D-8 Advance X-ray Diffractometer. The morphological study was done by scanning electron microscope (SEM) attached with energy-dispersive X-ray spectrometer (EDS) (JEOL JSM-6360A). The Photoluminescence (PL) excitation and emission spectra were recorded using Horiba FluoroLog Spectrophotometer (Horiba Inc., Worldwide). For PL measurements, same weight of powder sample (~ 50 mg) was used for all the measurements. For TL measurement, SrB4O7:Eu3+ powder samples were exposed to gamma rays from the 60Co radioactive source for various doses. The TL glow curves were recorded using a computerized Nucleonix TLD Reader (Model TL1009I), by taking ~ 5.0 mg of the sample each time and heating it with a constant rate of 5 °Cs−1 with the help of a temperature programmer and controller.
Results and discussion
X-ray diffraction spectroscopy
The XRD patterns of the SrB4O7:Eu3+ (0.2 mol%) as prepared and annealed at different temperatures (400 ºC and 500 ºC) are shown in Fig. 2. The XRD peaks of the sample shows the orthorhombic phase (space group Pmn21(31)) with lattice parameters are, a = 3.9190 Å, b = 4.4632 Å and c = 10.8788 Å which matches well with the same found in JCPDS file # 71–2191. A sharp peak at ~ 36º may be due to unreacted strontium carbonate during the chemical reaction.
Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS)
The morphological study of the prepared sample was carried out using scanning electron microscope technique. Figures 3 a-c show SEM images of as prepared SrB4O7:Eu3+ (0.8 mol%) microphosphor and Figs. 3 d–f show SEM images of the same phosphor but annealed and quenched at 700 ° for 2 h. The SEM results show, the prepared samples have irregular shaped particles with average size around 20–30 μm.
The elemental compositional analysis of SrB4O7:Eu3+ microphosphor was obtained from the energy dispersive spectroscopy (EDS). Figures 4 a and b show EDS of as prepared and annealed SrB4O7:Eu3+ (0.8 mol%) microphosphor, respectively. It reveals that they are mainly composed of Sr, B, and O with a small amount of Eu. The EDS patterns confirm the presence of Eu in the SrB4O7:Eu3+ powder and percentage of the impurity is very nearly equal to the doped value of the impurity (Eu). The Figs. 4 c-f show the elemental mapping of Sr, B, O and Eu elements in SrB4O7:Eu3+ (0.8 mol%) microphosphor (annealed and quenched at 700 °C). It was found that the components (i.e., Sr, B, O, and Eu) were evenly distributed among the particles. Table 1 represents the atomic percentage of the compositional elements in the SrB4O7:Eu3+ sample.
Photoluminescence
The photoluminescence (PL) properties of the SrB4O7-Eu3+ (0.2 mol%) sample annealed and quenched at 700 °C was carried out by PL excitation and emission spectra, with maintaining equal amount of sample during each measurements. Figure 5 shows the excitation spectra (recorded at 420 nm and 615 nm emission wavelengths) of SrB4O7:Eu3+ (0.2 mol%) microphosphor annealed and quenched at 700 °C for 2 h obtain in the range 200–600 nm. It is very difficult to observe different distinct peaks in the excitation spectrum. It shows two visible shoulders at ~ 300 nm and 358 nm with corresponding to f-d transition (4f65d- 4f7) (8S7/2) of Eu2+ ions in the host lattice [27]. These transitions arise from divalent europium ion (Eu2+) in the host lattices. A less intense peaks at ~ 250 nm and hidden peak at 300 nm are observed which corresponds to 5d orbital splitting in t2g and eg compounds, respectively [28, 29]. These transition bands in the spectral range 250–360 nm are connected with energy transfer between Eu2+ and Eu3+ [30]. In the range 450–550 nm, excitation peaks are assigned to the 7F0-5H3, 7F0-5D4, 7F0-5L7, 7F0-5F6, and 7F0-5d3 intra-configurational 4f-4f transitions of Eu3+, respectively [30]. Other noticeable peaks were observed at higher wavelength region between 360 and 500 nm range. These peaks are appearing due to inter-configurational f-f transitions of Eu3+ ions resulting from excitation of the Eu3+ ground state to the higher levels of 4f 6 arrangements, some of them assigns as 7F0—5L6 (394 nm), 7F0—5D3 (419 nm), and 7F0—5D2 (467 nm). For 420 nm and 615 nm emission wavelengths, the excitation spectra look very much similar with very slight shifts in the peak positions and small changes in their relative intensities with respect to each other.
The emission spectra of SrB4O7:Eu3+ (0.2 mol%) microphosphor annealed and quenched at 700 °C for 2 h was recorded in the range of 200–800 nm with different excitation wavelength (250 nm, 260 nm, and 280 nm), shown in Fig. 6. It is observed that the PL spectra shows a blue emission bands appearing at around 310 nm and 420 nm which could be attributed for Eu2+ (4f—5d) transitions [31]. Some other small peaks in the range 500–710 nm were recognized as transitions of Eu3+ ions from 5D0 – 7FJ, (J = 0, 1, 2, 3 and 4). These appearances of peaks between 300 to 420 nm suggest the existence of Eu2+ ions in different surrounding environment. Figure 7 shows the emission spectrum of the SrB4O7:Eu3+ (0.2 mol% sample) microphosphor annealed and quenched at 700 ºC for 2 h with excitation at 395 nm. The emission spectrum consists of several prominent peaks at 579 nm, 591 nm, 615 nm, 652 nm, and 703 nm which were attributed to 5D0-7F0, 5D0-7F1, 5D0-7F2, 5D0-7F3, and 5D0-7F4, (i.e., 5D0-7FJ, J = 0, 1, 2, 3 and 4), respectively, for Eu3+ ions. A peak Centered at 615 nm represents the red emission from 5D0–7F2 transition corresponds to electric dipole transition, while peak at 591 nm from 5D0–7F1 is a typical magnetic dipole transition [27]. It was initially thought that as the source of impurity consists of Eu3+ ions they might have been incorporated inside the material in this form only but the PL studies show that they are in different ionic forms, plausibly, due to charge compensation in different surrounding atmosphere or there might be some redox reactions occurring inside the material on annealing.
Thermoluminescence glow curves
The SrB4O7:Eu3+ (0.2 mol%) microphosphor, annealed and quenched at different temperature (400–900 °C) for 2 h, exposed to 100 Gy, 1.0 kGy and 6.0 kGy of gamma radiation doses from 60Co source. Figures 89 and 10 show TL glow curves of SrB4O7:Eu3+ (0.2 mol%) microphosphor; annealed and quenched at different temperatures; exposed to 100 Gy, 1.0 kGy and 6.0 kGy; respectively. Figure 11 represents the graph of total TL intensity vs. annealing temperature for SrB4O7:Eu3+ (0.2 mol%) microphosphor exposed to 100 Gy, 1.0 kGy and 6.0 kGy of gamma radiation doses. In these figures, the ordinate value needs to be multiplied by the number shown near the corresponding curves to get the relative intensities. It is observed that TL intensity increases with annealing temperature maximum up to 700 °C and then starts decreasing on annealing at higher temperatures. This might be due to the impurity aggregation at low temperatures and acting as self-quenchers [32]. Also, during synthesis, europium chloride and strontium carbonate were mixed in distilled water, therefore; some water molecules are present in sample and act as quenchers for TL. At higher temperatures they disperse making maximum luminescence centres at around 700 °C. If sample annealed beyond 700 °C, there could be more complexes formation resulting in TL quenching [32]. It also shows that TL glow curve changes with annealing temperature, it may be due to phase change of SrB4O7:Eu3+ phosphor or conversion of Eu3+ to Eu2+, these results change in the energy level structure and hence there may be corresponding changes in the TL glow curve [33]. Bakshi et. al. [34] mentioned that the change in TL glow curve structure is attributed to the diffusion of atmospheric oxygen at high temperatures. This may form some clusters of strontium oxide SrO and change the glow curve structure.
The TL glow curve of SrB4O7:Eu3+ (0.2 mol%) microphosphor, annealed and quenched at 700 °C for 2 h was found to be the most sensitive to radiation amongst the samples annealed at different temperatures (optimized for impurity concentrations and annealing temperatures) and was used for further studies. It was further exposed to 100 Gy (Fig. 8), apparently shows major peak (high intensity) at ~ 102 °C, a hump at ~ 163 °C and a small peak (low intensity) at ~ 317 °C. If it is exposed to 1.0 kGy (Fig. 9), TL glow curve apparently shows major peak at ~ 98 °C, a hump at ~ 154 °C and a small peak (low intensity) at ~ 319 °C and for 6.0 kGy (Fig. 10); TL glow curve shows major peak (high intensity) at ~ 101 °C, a hump at ~ 147 °C and a small peak (low intensity) at ~ 308 °C. Thus, the shifting of TL peak position is observed with dose. This shifting of TL peak with dose is due to the disorganization of trapping centers (TCs)/luminescent centers (LCs) [35, 36]. The TL peaks are may be a first order, second order or general order of kinetics. In a second-order or general order reaction released electrons are re-trapped before they recombine. This results in the shift in the peak temperatures of a glow curve with dose as well as with the heating rate. Thus, a TL peak may be second or general order of kinetics [36, 37]. To find the order of kinetics and activation energy, deconvolution of glow curve is necessary. The peaks are deconvoluted (in the following section Deconvolution of TL glow curves) and it is verified that the peaks are of general order (Table 2).
The synthesis of SrB4O7 microphosphor doped with different mole concentrations of Eu in the range of 0.1–1.0 mol% with annealing and quenching at 700 °C for 2 h was carried out for studying the behavior of dopant on the luminescent properties of the sample. Figure 12 represents the TL glow curves of SrB4O7:Eu3+ microphosphor doped at different molar concentrations of Eu ions, annealed and quenched at 700 °C for 2 h, and exposed to 1.0 kGy of gamma dose from 60Co source. Figure 13 shows the total TL intensity vs. different Eu concentrations (0.1–1.0 mol%) of SrB4O7:Eu3+ microphosphor. The effect of impurity concentrations on the TL sensitivity attributed to the concentration quenching. The luminescence of a material is very sensitive to the impurity concentration. If the impurity concentration is too high, they may act as self-quenchers by causing nonradiative cross transitions resulting in quenching of the luminescence [32]. In SrB4O7:Eu3+ microphosphor, the optimum impurity concentration was found for 0.2 mol% of europium doping, and above this quantity the TL intensity starts decreasing (Fig. 13).
Comparison with standard phosphors
The intensity of the newly developed SrB4O7:Eu3+ phosphor was compared with that of some standard (commercially available) TLD phosphors, such as, CaSO4:Dy (TLD-900) and LiF: Mg,Cu,P (TLD-700H). The results are as shown in Fig. 14. It could be seen that the first peak (88 °C with a shoulder at 138 °C) of the SrB4O7:Eu3+ phosphor is highly sensitive (approx. twice that of TLD-900 and around 1.33 times that of TLD-700H) but it is at quite low temperature, mostly (around 70%) fades in 48 h and therefore, it is not very useful for dosimetry. However, the isolated high temperature peak (318 °C) is quite stable and could be used. The relative sensitivity of this peak for 10 Gy dose is of the same order (~ 0.5 times than that of TLD-900 and ~ 0.42 that of TLD-700H considering the peak heights of the dosimetry peaks). As it is appearing at quite high temperature as compared to the standard phosphors and thus shows better stability.
Dose response
The dose vs. TL intensity plots (dose response) for the SrB4O7:Eu (0.2 mol%) is shown in Fig. 15. From the figure it could be observed that the response of the complete glow curve as well as individual peaks (peak 1 appearing at around 88 °C and another peak appearing at around 138 °C) is very much linear (little sublinear) and unlike in commercially available phosphors (which saturate around 100 Gy) it saturates at around 2.0 kGy except for peak 3 which becomes supralinear after 1.0 kGy before saturating at around 10 kGy.
Reusability
The SrB4O7:Eu3+ phosphor under investigation was irradiated for 100 Gy dose and TL was taken. The same sample was annealed at 700 °C for 2 h and again TL was recorded after irradiating for the same dose. The procedure was repeated several times (at least 25 times). The results given in Fig. 14 show excellent reusability, the material is quite stable even for high doses and not much radiation hardening was observed (Fig. 16).
Fading
Several samples (~ 5.0 mg each) of the phosphor material was irradiated to 10 Gy dose and stored at room temperature (27 °C) in dark. The TL was recorded at different intervals of time by taking out one sample at a time. It could be seen from the TL intensity vs. storage time plots as shown in Fig. 17 that there is about 70% fading of the first peak (88 °C along with a shoulder at around 138 °C), however, that of the high temperature peak is only around 5% in approx. over a week’s time.
T m -T stop method
To find the trapping parameters such as, order of kinetics, activation energy, frequency factor, etc., deconvolution of the TL glow curve is necessary. Before doing the deconvolution the exact peak positions and the number of TL glow peaks were confirmed by Tm-Tstop method. The individual peaks were resolved by Tm-Tstop method suggested by McKeever [38]. The SrB4O7:Eu3+ (0.2 mol%) microphosphor (annealed at 700 °C for 2 h) was irradiated by 1.0 kGy dose of γ -rays from Co60 source. The 5.0 mg sample was heated with a linear rate (5 °Cs−1) to a temperature Tstop corresponding to a position on the low-temperature tail of the first glow peak.
The sample was then cooled rapidly to room temperature and then re-heated at the same linear rate in order to record all of the remaining TL glow-curve. The position of the first maximum (Tm) in the glow-curve was noted. Again, a freshly irradiated 5.0 mg sample was heated up to new Tstop temperature, it was cooled to room temperature, TL was taken and the position of TM was recorded. The whole process was repeated using a different value of Tstop each time. The Tstop was increased each time by 5 °C and the corresponding TM value was noted on each occasion. The Tm vs. Tstop values were plotted (Fig. 14) to obtain a staircase type of curve where the TM values corresponding to the stairs (horizontally flat portions of the curve) are the respective maximum peak temperatures. The three peaks were revealed in TL glow curve SrB4O7:Eu3+ (0.2 mol%) microphosphor at positions 88, 138 and 318 °C.
Deconvolution of TL glow curves
For the deconvolution of TL glow curves, SrB4O7:Eu3+ (0.2 mol%) microphosphor (annealed at 700 °C for 2 h) was irradiated by 1.0 kGy dose of γ -rays from 60Co source. Initially the peak positions were confirmed by Tm-Tstop method. The three peaks were revealed at positions 88, 138 and 318 °C. By keeping these peak positions TL glow curve was deconvoluted. The Computerized Glow Curve Deconvolution (CGCD) curve fitting was done using glow curve deconvolution (GCD) functions (Eqs (1) and (2), suggested by Kitis [39], for general and first order kinetics glow curves, respectively. For kinetic analysis the experimentally obtained TL glow curve was fitted with CGCD method which was given by Pagonis et. al. [40].
For General order
For First order:
Here, I (T) is the TL intensity at temperature T (K), Im, the maximum peak intensity, Tm, is the temperature corresponding to maximum peak intensity Im, E, trap depth or the thermal activation energy (eV) needed to free the trapped electrons, b, order of kinetics, k, the Boltzmann’s constant (8.6 × 10−5 eVK−1).
The frequency factor s is obtained from the following equations.
For general order:
For first order:
where β is the linear heating rate and b is the order of kinetics.
The de-convoluted TL curves and the theoretical curve fitting with the experimental after convolution are shown in Fig. 15. The goodness of the fitting, i.e., figure of merit (FOM), is found to be less than 1%. This shows that experimental and theoretical glow curves are in good agreement and very much overlapping on either side. The deconvolution of the experimental curve has revealed three peaks at 88, 138 and 318 °C.
Calculation of trapping parameters by Chen’s formulae
To verify further, the thermal activation energy (E) and order of kinetics (b) of the deconvoluted glow peaks were calculated using Chen’s set of empirical formulae [41] as follows.
with
\(\alpha = \tau ,{ }\delta ,{ }\omega\),
\(\tau = T_{m} - T_{1} ,{ }\delta = T_{2} - T_{m}\),\({ }\omega = T_{2} - T_{1}\),
\(c_{\tau } = 1.51 + 3.0{ }\left( {\mu_{g} - 0.42} \right),\)
\(c_{\delta } = 0.976 + 7.3{ }\left( {\mu_{g} - 0.42} \right),\)
\(c_{\omega } = 2.52 + 10.2{ }\left( {\mu_{g} - 0.42} \right)\),
\(b_{\tau } = 1.58 + 4.2{ }\left( {\mu_{g} - 0.42} \right)\),
\(b_{\delta } = 0,{ }\)
\(b_{\omega } = 1\).
To determine the order of kinetic, the form factor was calculated by using the equation,
Theoretically the form factor, μg, ranges between 0.42 and 0.52, the value is close to 0.42 for first order kinetics and 0.52 for second order kinetics. To determine the general order of kinetics (other than first or second order), use of the correlation between order of kinetics (b) and the form factor (μg) given by Chen was made [42]. The values calculated by Chen’s set of equations are very well matches with the values calculated by CGCD program using Kitis functions. As discussed earlier, (in the section ‘Thermoluminescence Glow Curves), the shift in the TL peak position with dose indicates that the peak is not of first order; it may be second or general order of kinetics. It is also confirmed by deconvolution of TL glow curve. The order of kinetics of first peak is 1.8, and that of second and third peak is 1.3 (Table 2), i.e., retrapping taking place in SrB4O7:Eu3+ (0.2 mol%) microphosphor. The thermal activation energy or trap depth (eV) needed to free the trapped electrons are given Table 2. The values of frequency factor or attempt to escape factor vary from 104–1012 s−1.
Conclusions
The SrB4O7:Eu3+ microphosphor was synthesized by solid state diffusion method. It exhibits orthorhombic structure (space group Pmn21(31)) and lattice parameters a = 3.9190 Å, b = 4.4637 Å, c = 10.8788 Å. The compositional studies determine the presence of strontium, boron, oxygen, and europium with the appropriate amount of concentration. The Photoluminescence study of SrB4O7:Eu3+ (0.2 mol%) microcrystalline phosphor annealed and quenched at 700 °C for 2 h shows the excitation peaks (recorded at 420 nm and 615 nm emissions) in the range 200–600 nm. It shows two visible shoulders at ~ 300 nm and 358 nm with corresponding to f-d transitions (4f65d—4f7) (8S7/2) of these transitions are arises from divalent europium ion in the host lattices. The PL emission spectra shows a blue emission band with ~ 310 nm and ~ 420 nm peaks which can be attributed for Eu2+ (4f 5d) transitions. The series of emission peaks between 500 and 770 nm which corresponds to 5D0—7FJ (J = 0, 1, 2, 3, and 4) transition of Eu3+ ions under excitation with wavelengths 250, 260, 280 and 395 nm. The SrB4O7:Eu3+ microphosphor was irradiated for different doses of gamma rays from 60Co source. The TL intensity found to be maximum for the 0.2 mol% doping of europium for the sample which was annealed and quenched at 700 °C for 2 h. The exact peak positions and the number of peaks in TL glow curve were confirmed by Tm-Tstop method. The three peaks were revealed at positions 88, 138 and 318 °C. The TL glow curve was deconvoluted by the Computerized Glow Curve Deconvolution (CGCD) method and trapping parameters were calculated. All the three peaks were found to follow general order of kinetics. The dosimetry characteristics, such as, high sensitivity (comparable to TLD-900 and LiF TLD-700H), low fading (around 5% fading that of 318 °C peak), wide dose response (commercially available phosphors saturate around 100 Gy while the newly developed SrB4O7:Eu3+ microphosphor does not saturate up to 10 kGy). All these properties make it a good candidate for TL dosimetry of high-energy radiations (Figs. 18, 19).
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Acknowledgements
One of the authors would like to thank the Inter-University Accelerator Centre (IUAC) for financial assistance under the UFUP project (File # UFR-64325).
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Ali, N., Sahare, P.D., Kachere, A.R. et al. Luminescence and dosimetric characteristics of microcrystalline SrB4O7:Eu3+ synthesized by solid state diffusion method. J Radioanal Nucl Chem 330, 1397–1408 (2021). https://doi.org/10.1007/s10967-021-07965-9
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DOI: https://doi.org/10.1007/s10967-021-07965-9