Comprehensive kinetic analysis of thermoluminescence peaks of α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116142 , vital:34323 , https://doi.org/10.1016/j.jlumin.2017.01.003
- Description: A comprehensive kinetic analysis of the glow peaks in α-Al2O3:C,Mg is reported. A thermoluminescence glow curve measured at 1 °C/s after beta irradiation to 1 Gy shows a high intensity peak hereafter referred to as the main peak at 161 °C and six lower intensity secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. For ease of reference, the secondary peaks are labelled as I, II, IV, V, VI and VII respectively and the main peak denoted peak III. Kinetic analysis of the glow peaks has been carried out using the initial rise, whole glow peak, peak shape, variable heating rate and glow curve deconvolution methods as well as by way of phosphorescence. Using Tm-Tstop, Tm-dose and phosphorescence analyses, the order of kinetics of the peaks has been evaluated as first order. Analysis by the peak shape, whole glow peak and deconvolution methods produce the same conclusion. The activation energy of peaks I through VII are calculated as ~0.83, 0.96, 1.37, 1.20, 1.15, 1.61 and 1.94 eV respectively. The frequency factors for all the peaks are of the order of 109 to 1014 s−1. The question of thermal quenching affecting the peaks was considered. The peaks III, IV and V, the only ones that could be conveniently studied in this regard, were found to be affected by thermal quenching. The activation energy for thermal quenching was calculated for peak III as 0.96±0.03 eV, for peak VI as 0.95±0.07 eV and for peak V as 1.26±0.08 eV. The thermal quenching phenomenon has been discussed with reference to F+ and F centres. An energy band model has been developed to discuss the luminescence mechanisms in α-Al2O3:C,Mg in light of finding in this work.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116142 , vital:34323 , https://doi.org/10.1016/j.jlumin.2017.01.003
- Description: A comprehensive kinetic analysis of the glow peaks in α-Al2O3:C,Mg is reported. A thermoluminescence glow curve measured at 1 °C/s after beta irradiation to 1 Gy shows a high intensity peak hereafter referred to as the main peak at 161 °C and six lower intensity secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. For ease of reference, the secondary peaks are labelled as I, II, IV, V, VI and VII respectively and the main peak denoted peak III. Kinetic analysis of the glow peaks has been carried out using the initial rise, whole glow peak, peak shape, variable heating rate and glow curve deconvolution methods as well as by way of phosphorescence. Using Tm-Tstop, Tm-dose and phosphorescence analyses, the order of kinetics of the peaks has been evaluated as first order. Analysis by the peak shape, whole glow peak and deconvolution methods produce the same conclusion. The activation energy of peaks I through VII are calculated as ~0.83, 0.96, 1.37, 1.20, 1.15, 1.61 and 1.94 eV respectively. The frequency factors for all the peaks are of the order of 109 to 1014 s−1. The question of thermal quenching affecting the peaks was considered. The peaks III, IV and V, the only ones that could be conveniently studied in this regard, were found to be affected by thermal quenching. The activation energy for thermal quenching was calculated for peak III as 0.96±0.03 eV, for peak VI as 0.95±0.07 eV and for peak V as 1.26±0.08 eV. The thermal quenching phenomenon has been discussed with reference to F+ and F centres. An energy band model has been developed to discuss the luminescence mechanisms in α-Al2O3:C,Mg in light of finding in this work.
- Full Text: false
- Date Issued: 2017
Thermoluminescence of α-Al2O3: C, Mg annealed at 1200° C
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111030 , vital:33365 , https://doi.org/10.1016/j.nimb.2018.03.003
- Description: Stimulated luminescence in α-Al2O3:C,Mg has thus far been studied for samples annealed at temperature no higher than 900 °C as can be seen by an examination of the literature. We report the thermoluminescence (TL) features of α-Al2O3:C,Mg annealed at 1200 °C. A glow curve measured at 1 °C/s from the samples annealed at 1200 °C shows eight peaks at 54, 80, 102, 173, 238, 290, 330 and 387 °C. Kinetic analyses show that the peak at 54 °C follows general order kinetics (b = 1.3) whereas the rest follow first order kinetics. The values of the activation energy of the peaks are between 0.77 eV and 1.90 eV and the frequency factors are of the order of 1010–1014 s−1. The intensity of the peaks at 54, 80, 102 and 173 °C increase with heating rate whereas those of the peaks at 238 and 290 °C decrease with heating rate. The decrease of intensity of the peaks at 238 and 290 °C with heating rate is due to thermal quenching whereas the increase of intensity of the peaks with heating rate indicates an inverse thermal-quenching-like behaviour. Interestingly this behaviour is observed only after annealing at 1200 °C. The activation energy for thermal quenching as calculated using the peaks at 238 and 290 °C are (1.02 ± 0.16) eV and (1.33 ± 0.15) eV respectively. Regarding the dosimetric features, the dose response of the peaks at 54, 80 and 102 °C are sublinear within 1–10 Gy and the peak at 54 °C saturates above 6 Gy. In contrast, the response of the peak at 173 °C is sublinear with 1–4 Gy and superlinear between 4 and 10 Gy. The peaks are found to fade at different rates and the rate of fading is also affected by annealing.
- Full Text: false
- Date Issued: 2018
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111030 , vital:33365 , https://doi.org/10.1016/j.nimb.2018.03.003
- Description: Stimulated luminescence in α-Al2O3:C,Mg has thus far been studied for samples annealed at temperature no higher than 900 °C as can be seen by an examination of the literature. We report the thermoluminescence (TL) features of α-Al2O3:C,Mg annealed at 1200 °C. A glow curve measured at 1 °C/s from the samples annealed at 1200 °C shows eight peaks at 54, 80, 102, 173, 238, 290, 330 and 387 °C. Kinetic analyses show that the peak at 54 °C follows general order kinetics (b = 1.3) whereas the rest follow first order kinetics. The values of the activation energy of the peaks are between 0.77 eV and 1.90 eV and the frequency factors are of the order of 1010–1014 s−1. The intensity of the peaks at 54, 80, 102 and 173 °C increase with heating rate whereas those of the peaks at 238 and 290 °C decrease with heating rate. The decrease of intensity of the peaks at 238 and 290 °C with heating rate is due to thermal quenching whereas the increase of intensity of the peaks with heating rate indicates an inverse thermal-quenching-like behaviour. Interestingly this behaviour is observed only after annealing at 1200 °C. The activation energy for thermal quenching as calculated using the peaks at 238 and 290 °C are (1.02 ± 0.16) eV and (1.33 ± 0.15) eV respectively. Regarding the dosimetric features, the dose response of the peaks at 54, 80 and 102 °C are sublinear within 1–10 Gy and the peak at 54 °C saturates above 6 Gy. In contrast, the response of the peak at 173 °C is sublinear with 1–4 Gy and superlinear between 4 and 10 Gy. The peaks are found to fade at different rates and the rate of fading is also affected by annealing.
- Full Text: false
- Date Issued: 2018
On the sensitivity of thermally and optically stimulated luminescence of α-Al2O3: C and α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119803 , vital:34784 , https://doi.org/10.1016/j.radmeas.2017.03.006
- Description: The luminescence sensitivity of α-Al2O3:C and α-Al2O3:C, Mg is of interest because of the contemporary use of these materials in dosimetry related applications. We report investigations concerning the change in sensitivity of thermoluminescence (TL) and optically stimulated luminescence (OSL) from α-Al2O3:C and α-Al2O3:C, Mg with re-use. The study was carried out on a set of un-annealed samples and others annealed at 700 and 900 °C. The TL and OSL sensitivity in α-Al2O3:C and α-Al2O3:C, Mg was found to increase with sample re-use whether the intensity was monitored as peak area or peak height for the main TL peak or, in the case of OSL, as the maximum intensity or the area under a decay curve. The fractional increase in area under either the main TL peak or the OSL decay curve exceeds that of the TL peak height or maximum OSL intensity when samples are re-used. However, when un-annealed samples are used, any increase in TL peak height or peak area per measurement is less than observed in annealed samples. It is also interesting to note that the change in maximum OSL intensity or OSL area is minimal for samples annealed at 900 °C. In general, the TL sensitivity in α-Al2O3:C increases more than that in α-Al2O3:C, Mg with re-use. On the other hand, the OSL sensitivity in α-Al2O3:C, Mg increases more than that in α-Al2O3:C with re-use. These findings suggest that it is advisable to take into account the fractional increase in sensitivity per measurement when one uses α-Al2O3:C as a TL dosimeter and α-Al2O3:C, Mg as an OSL dosimeter.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119803 , vital:34784 , https://doi.org/10.1016/j.radmeas.2017.03.006
- Description: The luminescence sensitivity of α-Al2O3:C and α-Al2O3:C, Mg is of interest because of the contemporary use of these materials in dosimetry related applications. We report investigations concerning the change in sensitivity of thermoluminescence (TL) and optically stimulated luminescence (OSL) from α-Al2O3:C and α-Al2O3:C, Mg with re-use. The study was carried out on a set of un-annealed samples and others annealed at 700 and 900 °C. The TL and OSL sensitivity in α-Al2O3:C and α-Al2O3:C, Mg was found to increase with sample re-use whether the intensity was monitored as peak area or peak height for the main TL peak or, in the case of OSL, as the maximum intensity or the area under a decay curve. The fractional increase in area under either the main TL peak or the OSL decay curve exceeds that of the TL peak height or maximum OSL intensity when samples are re-used. However, when un-annealed samples are used, any increase in TL peak height or peak area per measurement is less than observed in annealed samples. It is also interesting to note that the change in maximum OSL intensity or OSL area is minimal for samples annealed at 900 °C. In general, the TL sensitivity in α-Al2O3:C increases more than that in α-Al2O3:C, Mg with re-use. On the other hand, the OSL sensitivity in α-Al2O3:C, Mg increases more than that in α-Al2O3:C with re-use. These findings suggest that it is advisable to take into account the fractional increase in sensitivity per measurement when one uses α-Al2O3:C as a TL dosimeter and α-Al2O3:C, Mg as an OSL dosimeter.
- Full Text: false
- Date Issued: 2017
Features of an annealing-induced thermoluminescence peak in α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116013 , vital:34289 , DOI: 10.1016/j.optmat.2017.05.034
- Description: We report the thermoluminescence glow curves of beta irradiated single crystal α-Al2O3:C,Mg after annealing at 700 and 900 °C. A glow curve measured at 1 °C/s from samples irradiated to 1 Gy following annealing at 700 and 900 °C shows a high intensity peak at 163 °C and seven secondary peaks of weaker intensity at 43, 73, 100, 195, 280, 329 and 370 °C. Comparing the position of the peaks in the annealed samples with those in an un-annealed one, it is observed that the peak at 100 °C appears only after annealing at and above 700 °C. Kinetic analysis of this annealing-induced peak was carried out using the initial rise, whole glow peak, peak shape, curve fitting and variable heating rate methods. The order of kinetics of the peak was determined as first order using various methods including the Tm-Tstop technique and the dependence of Tm on irradiation dose. The activation energy of the peak is about 1.01 eV and the frequency factor of the order of 1012 s−1. The peak was found to be affected by thermal quenching in analysis based on change of peak intensity with heating rate. The activation energy of thermal quenching was evaluated as 1.06 ± 0.08 eV. We speculate that the annealing-induced peak is due to formation of a new electron trap after destruction of the F22+(2 Mg) centre when the sample is annealed at 700 °C. The annealing-induced peak fades with storage between irradiation and measurement. It was also concluded that electrons from traps corresponding to secondary peaks get re-trapped at the main electron trap.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116013 , vital:34289 , DOI: 10.1016/j.optmat.2017.05.034
- Description: We report the thermoluminescence glow curves of beta irradiated single crystal α-Al2O3:C,Mg after annealing at 700 and 900 °C. A glow curve measured at 1 °C/s from samples irradiated to 1 Gy following annealing at 700 and 900 °C shows a high intensity peak at 163 °C and seven secondary peaks of weaker intensity at 43, 73, 100, 195, 280, 329 and 370 °C. Comparing the position of the peaks in the annealed samples with those in an un-annealed one, it is observed that the peak at 100 °C appears only after annealing at and above 700 °C. Kinetic analysis of this annealing-induced peak was carried out using the initial rise, whole glow peak, peak shape, curve fitting and variable heating rate methods. The order of kinetics of the peak was determined as first order using various methods including the Tm-Tstop technique and the dependence of Tm on irradiation dose. The activation energy of the peak is about 1.01 eV and the frequency factor of the order of 1012 s−1. The peak was found to be affected by thermal quenching in analysis based on change of peak intensity with heating rate. The activation energy of thermal quenching was evaluated as 1.06 ± 0.08 eV. We speculate that the annealing-induced peak is due to formation of a new electron trap after destruction of the F22+(2 Mg) centre when the sample is annealed at 700 °C. The annealing-induced peak fades with storage between irradiation and measurement. It was also concluded that electrons from traps corresponding to secondary peaks get re-trapped at the main electron trap.
- Full Text: false
- Date Issued: 2017
Temperature dependence of optically stimulated luminescence of α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115708 , vital:34217 , https://doi.org/10.1016/j.radmeas.2017.08.009
- Description: Thermal assistance and thermal quenching are two independently acting thermodynamic phenomena that simultaneously affect the stimulation of luminescence. We have studied thermal assistance to luminescence optically stimulated from α-Al2O3:C,Mg. Since thermal assistance causes only a minor change in the luminescence intensity, measurements were made after the sample had been pre-exposed to stimulating light to reduce its intensity significantly, that is, in the slow component of its decay curve. The luminescence intensity was monitored as a function of measurement temperature between 30 and 130 °C. The intensity goes through a peak at 60 °C due to competing effects of thermal assistance and thermal quenching. The initial increase of intensity is attributed to dominant thermal assistance whereas the subsequent decrease of intensity is ascribed to dominant thermal quenching. The activation energy for thermal assistance was calculated for the main electron trap of an un-annealed sample as 0.324 ± 0.020 eV and in a sample annealed at 900 °C as 0.416 ± 0.028 eV. Implications of such differences in the value of the activation energy for thermal assistance are considered.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115708 , vital:34217 , https://doi.org/10.1016/j.radmeas.2017.08.009
- Description: Thermal assistance and thermal quenching are two independently acting thermodynamic phenomena that simultaneously affect the stimulation of luminescence. We have studied thermal assistance to luminescence optically stimulated from α-Al2O3:C,Mg. Since thermal assistance causes only a minor change in the luminescence intensity, measurements were made after the sample had been pre-exposed to stimulating light to reduce its intensity significantly, that is, in the slow component of its decay curve. The luminescence intensity was monitored as a function of measurement temperature between 30 and 130 °C. The intensity goes through a peak at 60 °C due to competing effects of thermal assistance and thermal quenching. The initial increase of intensity is attributed to dominant thermal assistance whereas the subsequent decrease of intensity is ascribed to dominant thermal quenching. The activation energy for thermal assistance was calculated for the main electron trap of an un-annealed sample as 0.324 ± 0.020 eV and in a sample annealed at 900 °C as 0.416 ± 0.028 eV. Implications of such differences in the value of the activation energy for thermal assistance are considered.
- Full Text: false
- Date Issued: 2017
A comparative study of the dosimetric features of α-Al2O3: C, Mg and α-Al2O3: C
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/113058 , vital:33694 , https://doi.org/10.1093/rpd/ncx039
- Description: A comparative study of the dosimetric features of α-Al2O3:C,Mg and α-Al2O3:C relevant to thermoluminescence dosimetry is reported. A glow curve of α-Al2O3:C,Mg measured at 1°C/s after beta irradiation to 1 Gy shows two subsidiary peaks at 42°C (labelled as I) and 72°C (II) and the main peak at 161°C (III) whereas a glow curve of α-Al2O3:C measured under the same conditions shows the main peak at 178°C (II′) and a lower intensity peak at 48°C (I′). Apart from these ones, there are several other peaks at temperatures beyond that of the main peak in both α-Al2O3:C,Mg and α-Al2O3:C. However, the latter are not included in this study. We report a comparative quantitative analysis of dose response and fading of peaks I, II and III of α-Al2O3:C,Mg and peaks I′ and II′ of α-Al2O3:C. Analysis shows that the dose response of peaks I and III is sublinear within 1–10 Gy whereas that of peak II is superlinear within 1–4 Gy followed by a sublinear region within 4–10 Gy. In comparison, the dose response of peak I′ is superlinear within 1–4 Gy followed by a sublinear region within 4–10 Gy whereas that of peak II′ is sublinear within 1–4 Gy followed by a superlinear region within 4–10 Gy. As regards to fading corresponding to 1 Gy, peak I is very unstable and fades within 300 s, peak II is more stable and takes up to 43200 s to fade. In comparison, peak III fades down to 30% of its initial intensity within 2400 s. Interestingly, between 2400 and 800 s, the intensity fades by 17% only. Regarding fading in α-Al2O3:C, peak I′ fades within 600 s whereas peak II′ shows an inverse fading behaviour up to 64800 s. The rate of fading for peaks I, II and III in α-Al2O3:C,Mg was found to decrease with increase in dose. However, no such behaviour was observed in α-Al2O3:C. The fading in both samples is discussed on the basis of a charge hopping mechanism.
- Full Text:
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/113058 , vital:33694 , https://doi.org/10.1093/rpd/ncx039
- Description: A comparative study of the dosimetric features of α-Al2O3:C,Mg and α-Al2O3:C relevant to thermoluminescence dosimetry is reported. A glow curve of α-Al2O3:C,Mg measured at 1°C/s after beta irradiation to 1 Gy shows two subsidiary peaks at 42°C (labelled as I) and 72°C (II) and the main peak at 161°C (III) whereas a glow curve of α-Al2O3:C measured under the same conditions shows the main peak at 178°C (II′) and a lower intensity peak at 48°C (I′). Apart from these ones, there are several other peaks at temperatures beyond that of the main peak in both α-Al2O3:C,Mg and α-Al2O3:C. However, the latter are not included in this study. We report a comparative quantitative analysis of dose response and fading of peaks I, II and III of α-Al2O3:C,Mg and peaks I′ and II′ of α-Al2O3:C. Analysis shows that the dose response of peaks I and III is sublinear within 1–10 Gy whereas that of peak II is superlinear within 1–4 Gy followed by a sublinear region within 4–10 Gy. In comparison, the dose response of peak I′ is superlinear within 1–4 Gy followed by a sublinear region within 4–10 Gy whereas that of peak II′ is sublinear within 1–4 Gy followed by a superlinear region within 4–10 Gy. As regards to fading corresponding to 1 Gy, peak I is very unstable and fades within 300 s, peak II is more stable and takes up to 43200 s to fade. In comparison, peak III fades down to 30% of its initial intensity within 2400 s. Interestingly, between 2400 and 800 s, the intensity fades by 17% only. Regarding fading in α-Al2O3:C, peak I′ fades within 600 s whereas peak II′ shows an inverse fading behaviour up to 64800 s. The rate of fading for peaks I, II and III in α-Al2O3:C,Mg was found to decrease with increase in dose. However, no such behaviour was observed in α-Al2O3:C. The fading in both samples is discussed on the basis of a charge hopping mechanism.
- Full Text:
- Date Issued: 2017
Temperature dependence of persistent luminescence in CaAl2O4: Eu2+, Nd3+ related to beta irradiation and optical excitation
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2019
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105158 , vital:32470 , https://doi.org/10.1016/j.jlumin.2018.10.062
- Description: Mechanisms responsible for the emission of persistent luminescence in CaAl2O4:Eu2+,Nd3+ are typically studied following excitation by ultraviolet or visible light. In contrast, we have studied the persistent luminescence from this material after beta irradiation and optical excitation. These studies have been carried out at 25 °C as well as at various temperatures up to 100 °C. A thermoluminescence (TL) glow curve measured at 1 °C/s following beta irradiation showed a glow peak at 63 °C. On the other hand, a glow curve measured after 15 s of optical excitation by polychromatic white light shows a peak at 102 °C. The partial heating procedure reveals that each of the TL peaks consist of several overlapping components. The TL in each case was analysed for kinetic parameters. The initial rise analysis carried out on the rising edge of the overlapping components shows that the activation energy of the component peaks corresponding to beta irradiation is consistent at (0.59 ± 0.01) eV. In comparison, activation energies corresponding to optical excitation increases with the partial heating temperature from (0.71 ± 0.01) eV to (0.76 ± 0.01) eV. The activation energy of (0.59 ± 0.01) eV is ascribed to an oxygen vacancy whereas the range of activation energies between (0.71 ± 0.01) eV and (0.76 ± 0.01) eV is ascribed to the 4 f levels of the Nd dopant.
- Full Text: false
- Date Issued: 2019
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2019
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105158 , vital:32470 , https://doi.org/10.1016/j.jlumin.2018.10.062
- Description: Mechanisms responsible for the emission of persistent luminescence in CaAl2O4:Eu2+,Nd3+ are typically studied following excitation by ultraviolet or visible light. In contrast, we have studied the persistent luminescence from this material after beta irradiation and optical excitation. These studies have been carried out at 25 °C as well as at various temperatures up to 100 °C. A thermoluminescence (TL) glow curve measured at 1 °C/s following beta irradiation showed a glow peak at 63 °C. On the other hand, a glow curve measured after 15 s of optical excitation by polychromatic white light shows a peak at 102 °C. The partial heating procedure reveals that each of the TL peaks consist of several overlapping components. The TL in each case was analysed for kinetic parameters. The initial rise analysis carried out on the rising edge of the overlapping components shows that the activation energy of the component peaks corresponding to beta irradiation is consistent at (0.59 ± 0.01) eV. In comparison, activation energies corresponding to optical excitation increases with the partial heating temperature from (0.71 ± 0.01) eV to (0.76 ± 0.01) eV. The activation energy of (0.59 ± 0.01) eV is ascribed to an oxygen vacancy whereas the range of activation energies between (0.71 ± 0.01) eV and (0.76 ± 0.01) eV is ascribed to the 4 f levels of the Nd dopant.
- Full Text: false
- Date Issued: 2019
Phototransferred thermoluminescence in α-Al2O3: C, Mg under 470 nm blue light stimulation
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116026 , vital:34290 , https://doi.org/10.1016/j.jlumin.2017.04.059
- Description: Phototransferred thermoluminescence (PTTL) in α-Al2O3:C,Mg under 470 nm blue light has been investigated. Conventional thermoluminescence (TL) measured at 1 °C/s following irradiation to 10 Gy shows the main peak (labelled as III) at 163 °C and six secondary peaks I, II, IV, V, VI and VII at 45, 74, 200, 279, 328, 370 °C respectively. When a sample irradiated to 10 Gy is preheated to 220 °C at 1 °C/s to remove peaks I, II, III and IV and then exposed to 470 nm blue light for 100 s, it is found that three peaks I, II and III are reproduced under phototransfer. Kinetic analysis of the PTTL peaks shows that their kinetic parameters are similar to those of peaks I, II and III from conventional TL. Pulse annealing experiments, intended to study the dependence of PTTL peak intensity on preheating temperature, show that the electron traps corresponding to peaks V, VI and VII act as donor traps whereas the traps corresponding to peaks I, II and III act as acceptor traps. Further, it was found that no PTTL can be generated when all the traps corresponding to peaks I, II…VII are erased by preheating after irradiation. The primary conclusion here is that α-Al2O3:C,Mg does not have any deep traps beyond 400 °C sensitive to 470 nm stimulation or if there are any, their concentration is negligible. The PTTL for any of the PTTL peaks mentioned earlier increases with illumination time to a maximum within 400 s for measurements corresponding to doses between 6 and 15 Gy. The dose response of PTTL peaks II and III is linear within 1–15 Gy. Regarding fading, PTTL peak II fades to background level within 18000 s whereas in the same time, PTTL peak III fades down to 40% of its initial intensity.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116026 , vital:34290 , https://doi.org/10.1016/j.jlumin.2017.04.059
- Description: Phototransferred thermoluminescence (PTTL) in α-Al2O3:C,Mg under 470 nm blue light has been investigated. Conventional thermoluminescence (TL) measured at 1 °C/s following irradiation to 10 Gy shows the main peak (labelled as III) at 163 °C and six secondary peaks I, II, IV, V, VI and VII at 45, 74, 200, 279, 328, 370 °C respectively. When a sample irradiated to 10 Gy is preheated to 220 °C at 1 °C/s to remove peaks I, II, III and IV and then exposed to 470 nm blue light for 100 s, it is found that three peaks I, II and III are reproduced under phototransfer. Kinetic analysis of the PTTL peaks shows that their kinetic parameters are similar to those of peaks I, II and III from conventional TL. Pulse annealing experiments, intended to study the dependence of PTTL peak intensity on preheating temperature, show that the electron traps corresponding to peaks V, VI and VII act as donor traps whereas the traps corresponding to peaks I, II and III act as acceptor traps. Further, it was found that no PTTL can be generated when all the traps corresponding to peaks I, II…VII are erased by preheating after irradiation. The primary conclusion here is that α-Al2O3:C,Mg does not have any deep traps beyond 400 °C sensitive to 470 nm stimulation or if there are any, their concentration is negligible. The PTTL for any of the PTTL peaks mentioned earlier increases with illumination time to a maximum within 400 s for measurements corresponding to doses between 6 and 15 Gy. The dose response of PTTL peaks II and III is linear within 1–15 Gy. Regarding fading, PTTL peak II fades to background level within 18000 s whereas in the same time, PTTL peak III fades down to 40% of its initial intensity.
- Full Text: false
- Date Issued: 2017
The influence of dose on the kinetic parameters and dosimetric features of the main thermoluminescence glow peak in α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119834 , vital:34787 , https://doi.org/10.1016/j.nimb.2016.12.027
- Description: The influence of dose (0.1–100 Gy) on the kinetic parameters and the dosimetric features of the main glow peak of α-Al2O3:C,Mg have been investigated. Thermoluminescence (TL) measured at 1 °C/s shows a very high intensity glow peak at 161 °C and six secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. Analysis shows that the main peak follows first order kinetics irrespective of the irradiation dose. The activation energy is found to be consistent at 1.37 eV and the frequency factor is of the order of 1014 s−1 for any dose between 0.1 and 100 Gy. Further, the analysis for thermal quenching of the main peak of 0.1 Gy irradiated sample shows that the activation energy for thermal quenching is (0.94 ± 0.04) eV.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119834 , vital:34787 , https://doi.org/10.1016/j.nimb.2016.12.027
- Description: The influence of dose (0.1–100 Gy) on the kinetic parameters and the dosimetric features of the main glow peak of α-Al2O3:C,Mg have been investigated. Thermoluminescence (TL) measured at 1 °C/s shows a very high intensity glow peak at 161 °C and six secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. Analysis shows that the main peak follows first order kinetics irrespective of the irradiation dose. The activation energy is found to be consistent at 1.37 eV and the frequency factor is of the order of 1014 s−1 for any dose between 0.1 and 100 Gy. Further, the analysis for thermal quenching of the main peak of 0.1 Gy irradiated sample shows that the activation energy for thermal quenching is (0.94 ± 0.04) eV.
- Full Text: false
- Date Issued: 2017
The effect of pre-dose on thermally and optically stimulated luminescence from α-Al2O3C, Mg and α-Al2O3: C
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111011 , vital:33363 , https://doi.org/10.1016/j.apradiso.2018.06.012
- Description: We report the effect of pre-dose on the thermoluminescence (TL) and optically stimulated luminescence (OSL) dose response of α-Al2O3:C,Mg and α-Al2O3:C. Before any luminescence measurement, the samples were irradiated with different doses, namely 100, 500 and 1000 Gy to populate the deep electron traps. This is the pre-dose. The results from TL and OSL studies are compared with results from samples used without any pre-measurement dose. The TL glow curves and OSL decay curves of α-Al2O3:C,Mg recorded after pre-doses of 100, 500 and 1000 Gy are identical to those from a sample used without any pre-dose. Further, the TL and OSL dose response of all α-Al2O3:C,Mg samples are similar regardless of pre-dose. In comparison, the TL glow curves and OSL decay curves of α-Al2O3:C are influenced by pre-dose. We conclude that the differences in the TL and OSL dose response of various pre-dosed samples of α-Al2O3:C are due to the concentration of charge in the deep traps. On the other hand, owing to the lower concentration of such deep traps in α-Al2O3:C,Mg, the TL or OSL dose responses are not affected by pre-dose in this material.
- Full Text: false
- Date Issued: 2018
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111011 , vital:33363 , https://doi.org/10.1016/j.apradiso.2018.06.012
- Description: We report the effect of pre-dose on the thermoluminescence (TL) and optically stimulated luminescence (OSL) dose response of α-Al2O3:C,Mg and α-Al2O3:C. Before any luminescence measurement, the samples were irradiated with different doses, namely 100, 500 and 1000 Gy to populate the deep electron traps. This is the pre-dose. The results from TL and OSL studies are compared with results from samples used without any pre-measurement dose. The TL glow curves and OSL decay curves of α-Al2O3:C,Mg recorded after pre-doses of 100, 500 and 1000 Gy are identical to those from a sample used without any pre-dose. Further, the TL and OSL dose response of all α-Al2O3:C,Mg samples are similar regardless of pre-dose. In comparison, the TL glow curves and OSL decay curves of α-Al2O3:C are influenced by pre-dose. We conclude that the differences in the TL and OSL dose response of various pre-dosed samples of α-Al2O3:C are due to the concentration of charge in the deep traps. On the other hand, owing to the lower concentration of such deep traps in α-Al2O3:C,Mg, the TL or OSL dose responses are not affected by pre-dose in this material.
- Full Text: false
- Date Issued: 2018
Thermally-assisted optically stimulated luminescence from deep electron traps in α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L, Polymeris, G S
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L , Polymeris, G S
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116133 , vital:34322 , https://doi.org/10.1016/j.nimb.2017.04.075
- Description: We report thermally-assisted optically stimulated luminescence (TA-OSL) in α-Al2O3:C,Mg. The OSL was measured at elevated temperatures between 50 and 240 °C from a sample preheated to 500 °C after irradiation to 100 Gy. That OSL could be measured even after the preheating is direct evidence of the existence of deep electron traps in α-Al2O3:C,Mg. The TA-OSL intensity goes through a peak with measurement temperature. The initial increase is ascribed to thermal assistance to optical stimulation whereas the subsequent decrease in intensity is deduced to reflect increasing incidences of non-radiative recombination, that is, thermal quenching. The activation energy for thermal assistance corresponding to a deep electron trap was estimated as 0.667 ± 0.006 eV whereas the activation energy for thermal quenching was calculated as 0.90 ± 0.04 eV. The intensity of the TA-OSL was also found to increase with irradiation dose. The dose response is sublinear from 25 to 150 Gy but saturates with further increase of dose. The TA-OSL dose response has been discussed by considering the competition for charges at the deep traps. This study incidentally shows that TA-OSL can be effectively used in dosimetry involving large doses.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L , Polymeris, G S
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116133 , vital:34322 , https://doi.org/10.1016/j.nimb.2017.04.075
- Description: We report thermally-assisted optically stimulated luminescence (TA-OSL) in α-Al2O3:C,Mg. The OSL was measured at elevated temperatures between 50 and 240 °C from a sample preheated to 500 °C after irradiation to 100 Gy. That OSL could be measured even after the preheating is direct evidence of the existence of deep electron traps in α-Al2O3:C,Mg. The TA-OSL intensity goes through a peak with measurement temperature. The initial increase is ascribed to thermal assistance to optical stimulation whereas the subsequent decrease in intensity is deduced to reflect increasing incidences of non-radiative recombination, that is, thermal quenching. The activation energy for thermal assistance corresponding to a deep electron trap was estimated as 0.667 ± 0.006 eV whereas the activation energy for thermal quenching was calculated as 0.90 ± 0.04 eV. The intensity of the TA-OSL was also found to increase with irradiation dose. The dose response is sublinear from 25 to 150 Gy but saturates with further increase of dose. The TA-OSL dose response has been discussed by considering the competition for charges at the deep traps. This study incidentally shows that TA-OSL can be effectively used in dosimetry involving large doses.
- Full Text: false
- Date Issued: 2017
Thermoluminescence of α-Al2O3: C, Mg: kinetic analysis of the main glow peak
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119844 , vital:34788 , https://doi.org/10.1016/j.jlumin.2016.10.031
- Description: The kinetic analysis of the thermoluminescence of aluminium oxide doped with carbon and co-doped with magnesium (α-Al2O3:C,Mg) is reported. Measurements were made at 1 °C/s following beta irradiation to 1 Gy. The glow curve consists of a dominant peak at a peak-maximum Tm of 161 °C and six secondary peaks of weaker intensity at 42, 72, 193, 279, 330 and 370 °C. Kinetic analysis of the main peak, the subject of this report, was carried out using initial rise, whole glow peak, peak shape, curve fitting and variable heating rate methods. The order of kinetics of the main peak was determined as first order using various methods including the Tm–Tstop technique and the dependence of Tm on irradiation dose. The activation energy of the peak is about ~1.36 eV and the frequency factor of the order of 1014 s−1. The peak area changes with heating rate in a manner that shows that the peak is affected by thermal quenching. The activation energy of thermal quenching was evaluated as 0.99±0.08 eV. A comparison of analytical results from the main peak before and after correction for thermal quenching show that the kinetic parameters of the main peak are not that affected by thermal quenching.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119844 , vital:34788 , https://doi.org/10.1016/j.jlumin.2016.10.031
- Description: The kinetic analysis of the thermoluminescence of aluminium oxide doped with carbon and co-doped with magnesium (α-Al2O3:C,Mg) is reported. Measurements were made at 1 °C/s following beta irradiation to 1 Gy. The glow curve consists of a dominant peak at a peak-maximum Tm of 161 °C and six secondary peaks of weaker intensity at 42, 72, 193, 279, 330 and 370 °C. Kinetic analysis of the main peak, the subject of this report, was carried out using initial rise, whole glow peak, peak shape, curve fitting and variable heating rate methods. The order of kinetics of the main peak was determined as first order using various methods including the Tm–Tstop technique and the dependence of Tm on irradiation dose. The activation energy of the peak is about ~1.36 eV and the frequency factor of the order of 1014 s−1. The peak area changes with heating rate in a manner that shows that the peak is affected by thermal quenching. The activation energy of thermal quenching was evaluated as 0.99±0.08 eV. A comparison of analytical results from the main peak before and after correction for thermal quenching show that the kinetic parameters of the main peak are not that affected by thermal quenching.
- Full Text: false
- Date Issued: 2017
Structural and optical properties of sol-gel derived α-Fe2O3 nanoparticles
- Mathevula, Langutani E, Noto, L L, Mothudi, Bakang M, Chithambo, Makaiko L, Dhlamini, M S
- Authors: Mathevula, Langutani E , Noto, L L , Mothudi, Bakang M , Chithambo, Makaiko L , Dhlamini, M S
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115467 , vital:34145 , DOI: 10.1016/j.jlumin.2017.07.055
- Description: α-Fe2O3 nanoparticles of crystallite size between 3.9 and 9.5 nm were synthesized by a simple sol-gel method using iron (III) nitrate nonahydrate (Fe(NO3)3·9H2O) as a precursor. Polyvinyl alcohol (PVA) was added as a capping agent to avoid agglomeration of the nanoparticles. A single pure phase was obtained when the sample was annealed at 300 °C and 600 °C. The purity was further confirmed with the Fourier Transform Infrared Spectroscopy. The energy band gap of the materials was extrapolated from the Kubelka-Munk relation and it ranges between 1.8 and 2.3 eV. The Photoluminescence of the 3 samples shows a broad emission spectrum centered at about 422 nm when excited by a 336 nm lamp. The emission peaks intensities increased with an increase in the annealing temperature, accept for the 576 nm peak, which was quenched as the temperature increased from 300 °C to 600 °C. The thermoluminescence glow curves were carried out at different heating rates and the samples were exposed to different beta particle doses (82–1315 Gy). The activation energy of the trapped electrons was determined.
- Full Text: false
- Date Issued: 2017
- Authors: Mathevula, Langutani E , Noto, L L , Mothudi, Bakang M , Chithambo, Makaiko L , Dhlamini, M S
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115467 , vital:34145 , DOI: 10.1016/j.jlumin.2017.07.055
- Description: α-Fe2O3 nanoparticles of crystallite size between 3.9 and 9.5 nm were synthesized by a simple sol-gel method using iron (III) nitrate nonahydrate (Fe(NO3)3·9H2O) as a precursor. Polyvinyl alcohol (PVA) was added as a capping agent to avoid agglomeration of the nanoparticles. A single pure phase was obtained when the sample was annealed at 300 °C and 600 °C. The purity was further confirmed with the Fourier Transform Infrared Spectroscopy. The energy band gap of the materials was extrapolated from the Kubelka-Munk relation and it ranges between 1.8 and 2.3 eV. The Photoluminescence of the 3 samples shows a broad emission spectrum centered at about 422 nm when excited by a 336 nm lamp. The emission peaks intensities increased with an increase in the annealing temperature, accept for the 576 nm peak, which was quenched as the temperature increased from 300 °C to 600 °C. The thermoluminescence glow curves were carried out at different heating rates and the samples were exposed to different beta particle doses (82–1315 Gy). The activation energy of the trapped electrons was determined.
- Full Text: false
- Date Issued: 2017
Photoluminescence and thermoluminescence properties of BaGa2O4
- Noto, L L, Poelman, D, Orante-Barrón, V R, Swart, H C, Mathevula, Langutani E, Nyenge, R, Chithambo, Makaiko L, Mothudi, B M, Dhlamini, M S
- Authors: Noto, L L , Poelman, D , Orante-Barrón, V R , Swart, H C , Mathevula, Langutani E , Nyenge, R , Chithambo, Makaiko L , Mothudi, B M , Dhlamini, M S
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116037 , vital:34292 , https://doi.org/10.1016/j.physb.2017.07.059
- Description: Rare–Earth free luminescent materials are fast becoming important as the cost of rare earth ions gradually increases. In this work, a Rare–Earth free BaGa2O4 luminescent compound was prepared by solid state chemical reaction, which was confirmed to have a single phase by X-ray Diffraction. The Backscattered Electron image and Energy Dispersive X-ray spectroscopy maps confirmed irregular particle and homogeneous compound formation, respectively. The Photoluminescence spectrum displayed broad emission between 350 to 650 nm, which was deconvoluted into two components. The photoluminescence excitation peak was positioned at 254 nm, which corresponds with the band-to-band position observed from the diffuse reflectance spectrum. The band gap was extrapolated to 4.65 ± 0.02 eV using the Kubelka-Munk model. The preliminary thermoluminescence results indicated that the kinetics involved were neither of first nor second order. Additionally, the activation energy of the electrons within the trap centres was approximated to 0.61 ± 0.01 eV using the Initial Rise model.
- Full Text: false
- Date Issued: 2018
- Authors: Noto, L L , Poelman, D , Orante-Barrón, V R , Swart, H C , Mathevula, Langutani E , Nyenge, R , Chithambo, Makaiko L , Mothudi, B M , Dhlamini, M S
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116037 , vital:34292 , https://doi.org/10.1016/j.physb.2017.07.059
- Description: Rare–Earth free luminescent materials are fast becoming important as the cost of rare earth ions gradually increases. In this work, a Rare–Earth free BaGa2O4 luminescent compound was prepared by solid state chemical reaction, which was confirmed to have a single phase by X-ray Diffraction. The Backscattered Electron image and Energy Dispersive X-ray spectroscopy maps confirmed irregular particle and homogeneous compound formation, respectively. The Photoluminescence spectrum displayed broad emission between 350 to 650 nm, which was deconvoluted into two components. The photoluminescence excitation peak was positioned at 254 nm, which corresponds with the band-to-band position observed from the diffuse reflectance spectrum. The band gap was extrapolated to 4.65 ± 0.02 eV using the Kubelka-Munk model. The preliminary thermoluminescence results indicated that the kinetics involved were neither of first nor second order. Additionally, the activation energy of the electrons within the trap centres was approximated to 0.61 ± 0.01 eV using the Initial Rise model.
- Full Text: false
- Date Issued: 2018
Influence of argon-implantation on conventional and phototransferred thermoluminescence of synthetic quartz
- Nsengiyumva, S, Chithambo, Makaiko L, Pichon, L
- Authors: Nsengiyumva, S , Chithambo, Makaiko L , Pichon, L
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124732 , vital:35656 , DOI: 10.1080/10420150.2016.1194412
- Description: Conventional and phototransferred thermoluminescence of crystalline synthetic quartz implanted with 70 keV Ar ions at fluences in the range 1 × 1014–5 × 1015 ions/cm2 is reported. The glow curves, recorded at 5°C/s from beta-irradiated samples of similar mass, show a prominent peak between 100°C and 120°C. The thermoluminescence intensity of all implanted samples was greater than that of the unimplanted one. The increase in sensitivity is attributed to a corresponding increase in the concentration of point defects, as a result of the implantation, which act as electron traps or recombination centres. Kinetic analysis carried out using the peak shape, whole glow-peak and curve-fitting methods produced values of the activation energy, frequency factor and order of kinetics that are generally independent of implantation fluence. This result suggests that implantation did not necessarily affect the nature of the electron traps. With respect to phototransferred thermoluminescence, it was observed that it only appeared in the sample implanted at the highest fluence of 5 × 1015 ions/cm2. This may be so because the concentration of deep traps produced as a result of implantation at low fluence is too low to give rise to phototransferred thermoluminescence. The intensity of the phototransferred thermoluminescence goes through a peak with illumination time. We attribute this behaviour to the relative concentration of holes at recombination centres and phototransferred electrons at shallow traps.
- Full Text: false
- Date Issued: 2016
- Authors: Nsengiyumva, S , Chithambo, Makaiko L , Pichon, L
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124732 , vital:35656 , DOI: 10.1080/10420150.2016.1194412
- Description: Conventional and phototransferred thermoluminescence of crystalline synthetic quartz implanted with 70 keV Ar ions at fluences in the range 1 × 1014–5 × 1015 ions/cm2 is reported. The glow curves, recorded at 5°C/s from beta-irradiated samples of similar mass, show a prominent peak between 100°C and 120°C. The thermoluminescence intensity of all implanted samples was greater than that of the unimplanted one. The increase in sensitivity is attributed to a corresponding increase in the concentration of point defects, as a result of the implantation, which act as electron traps or recombination centres. Kinetic analysis carried out using the peak shape, whole glow-peak and curve-fitting methods produced values of the activation energy, frequency factor and order of kinetics that are generally independent of implantation fluence. This result suggests that implantation did not necessarily affect the nature of the electron traps. With respect to phototransferred thermoluminescence, it was observed that it only appeared in the sample implanted at the highest fluence of 5 × 1015 ions/cm2. This may be so because the concentration of deep traps produced as a result of implantation at low fluence is too low to give rise to phototransferred thermoluminescence. The intensity of the phototransferred thermoluminescence goes through a peak with illumination time. We attribute this behaviour to the relative concentration of holes at recombination centres and phototransferred electrons at shallow traps.
- Full Text: false
- Date Issued: 2016
Factors influencing the shape of CW-OSL signal obtained by stimulation of very deep traps in carbon-doped aluminium oxide: an experimental study
- Nyirenda, Angel N, Chithambo, Makaiko L
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115493 , vital:34149 , https://doi.org/10.1016/j.jlumin.2017.07.016
- Description: The optically stimulated luminescence from carbon-doped aluminium oxide (α-Al2O3:C) displays a peak with time under certain measurement conditions. In this paper, we present factors that influence the peak-like shape of continuous-wave optically stimulated luminescence (CW-OSL) signal. The report is based on the experimental study of OSL signals obtained by stimulation of very deep traps in α-Al2O3:C. Methods exploiting post-irradiation annealing, variable dose and temperature dependent OSL measurements were used in the investigation. It is found that the rising part of the CW-OSL peak is obtained when the rate of retrapping at the most optically active trap (main trap) exceeds the rate of direct radiative recombination following optical release of charges from all optically active traps. This is possible if, during optical stimulation, the primary trap responsible for OSL i.e. the main trap, is substantially unoccupied and the very deep, donor traps are substantially filled up. The rate of charge retrapping itself is deduced to depend on the occupancy of the acceptor traps i.e. shallow, main and secondary traps; concentration of charge carriers in the very deep, donor traps; the post-irradiation annealing temperature and the temperature at which the OSL is measured.
- Full Text: false
- Date Issued: 2017
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115493 , vital:34149 , https://doi.org/10.1016/j.jlumin.2017.07.016
- Description: The optically stimulated luminescence from carbon-doped aluminium oxide (α-Al2O3:C) displays a peak with time under certain measurement conditions. In this paper, we present factors that influence the peak-like shape of continuous-wave optically stimulated luminescence (CW-OSL) signal. The report is based on the experimental study of OSL signals obtained by stimulation of very deep traps in α-Al2O3:C. Methods exploiting post-irradiation annealing, variable dose and temperature dependent OSL measurements were used in the investigation. It is found that the rising part of the CW-OSL peak is obtained when the rate of retrapping at the most optically active trap (main trap) exceeds the rate of direct radiative recombination following optical release of charges from all optically active traps. This is possible if, during optical stimulation, the primary trap responsible for OSL i.e. the main trap, is substantially unoccupied and the very deep, donor traps are substantially filled up. The rate of charge retrapping itself is deduced to depend on the occupancy of the acceptor traps i.e. shallow, main and secondary traps; concentration of charge carriers in the very deep, donor traps; the post-irradiation annealing temperature and the temperature at which the OSL is measured.
- Full Text: false
- Date Issued: 2017
The influence of radiation-induced defects on thermoluminescence and optically stimulated luminescence of α-Al2O3: C
- Nyirenda, Angel N, Chithambo, Makaiko L
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119818 , vital:34786 , https://doi.org/10.1016/j.nimb.2017.02.077
- Description: It is known that when α-Al2O3:C is exposed to excessive amounts of ionising radiation, defects are induced within its matrix. We report the influence of radiation-induced defects on the thermoluminescence (TL) and optically stimulated luminescence (OSL) measured from α-Al2O3:C after irradiation to 1000 Gy. These radiation-induced defects are thermally unstable in the region 450–650 °C and result in TL peaks in this range when the TL is measured at 1 °C/s. Heating a sample to 700 °C obliterates the radiation-induced defects, that is, the TL peaks corresponding to the radiation induced defects are no longer observed in the subsequent TL measurements when moderate irradiation doses below 10 Gy are used. The charge traps associated with these radiation-induced defects are more stable than the dosimetric trap when the sample is exposed to either sunlight or 470-nm blue light from LEDs. TL glow curves measured following the defect-inducing irradiation produce a dosimetric peak that is broader and positioned at a higher temperature than observed in glow curves obtained before the heavy irradiation. In addition, sample sensitization/desensitization occurs due to the presence of these radiation-induced defects. Furthermore, both the activation energy and the kinetic order of the dosimetric peak evaluated when the radiation-induced defects are present in the sample are significantly lower in value than those obtained when these defects are absent. The radiation-induced defects also affect the shape and total light sum of the OSL signal as well as the position and width of the resultant residual phototransferred thermoluminescence main peak.
- Full Text: false
- Date Issued: 2017
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/119818 , vital:34786 , https://doi.org/10.1016/j.nimb.2017.02.077
- Description: It is known that when α-Al2O3:C is exposed to excessive amounts of ionising radiation, defects are induced within its matrix. We report the influence of radiation-induced defects on the thermoluminescence (TL) and optically stimulated luminescence (OSL) measured from α-Al2O3:C after irradiation to 1000 Gy. These radiation-induced defects are thermally unstable in the region 450–650 °C and result in TL peaks in this range when the TL is measured at 1 °C/s. Heating a sample to 700 °C obliterates the radiation-induced defects, that is, the TL peaks corresponding to the radiation induced defects are no longer observed in the subsequent TL measurements when moderate irradiation doses below 10 Gy are used. The charge traps associated with these radiation-induced defects are more stable than the dosimetric trap when the sample is exposed to either sunlight or 470-nm blue light from LEDs. TL glow curves measured following the defect-inducing irradiation produce a dosimetric peak that is broader and positioned at a higher temperature than observed in glow curves obtained before the heavy irradiation. In addition, sample sensitization/desensitization occurs due to the presence of these radiation-induced defects. Furthermore, both the activation energy and the kinetic order of the dosimetric peak evaluated when the radiation-induced defects are present in the sample are significantly lower in value than those obtained when these defects are absent. The radiation-induced defects also affect the shape and total light sum of the OSL signal as well as the position and width of the resultant residual phototransferred thermoluminescence main peak.
- Full Text: false
- Date Issued: 2017
Spectral study of radioluminescence in carbon-doped aluminium oxide
- Nyirenda, Angel N, Chithambo, Makaiko L
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110067 , vital:33220 , https://doi.org/10.1016/j.radmeas.2018.06.026
- Description: The spectral emission study of the radioluminescence (RL) measured from carbon-doped aluminium oxide (α-Al2O3:C) at various temperatures between 30 and 300∘C is reported. The energy-resolved RL emission spectra measured at room temperature show seven gaussian emission bands centred at 1.75, 1.79, 1.85, 2.22, 2.96, 3.72 and 4.44 eV. The 2.96-eV emission, associated with F-centres, is the primary RL emission whereas the narrow (R-line) emission centred at 1.79 eV, associated with Cr3+ impurity ions, is the most intense secondary emission. However, the intensity of 1.79-eV emission decreases with repeated RL measurements. The central emission energy for F-centres is constant throughout the temperature range of investigation. The full width at half maximum (FWHM) for the F-centre emission band increases with temperature whereas the F-centre peak intensity exhibits thermal quenching behaviour at temperatures above 160∘C. On the other hand, the emission energy for the R-line emission of Cr3+ is constant for temperatures between 30 and 160∘C, whereas its peak intensity generally decreases with temperature. F-centres experience strong-coupling in their crystallographic sites with estimated electron-lattice coupling parameters of S = 5.0 ± 0.9, Ep = 0.079 ± 0.008 eV and ν = 1.91 × 1013 Hz where S, Ep and ν are the Huang-Rhys factor, the phonon energy and the phonon frequency, respectively. The RL spectra recorded while ramping the temperature of a sample at a constant rate have been compared against conventional TL spectra.
- Full Text: false
- Date Issued: 2018
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110067 , vital:33220 , https://doi.org/10.1016/j.radmeas.2018.06.026
- Description: The spectral emission study of the radioluminescence (RL) measured from carbon-doped aluminium oxide (α-Al2O3:C) at various temperatures between 30 and 300∘C is reported. The energy-resolved RL emission spectra measured at room temperature show seven gaussian emission bands centred at 1.75, 1.79, 1.85, 2.22, 2.96, 3.72 and 4.44 eV. The 2.96-eV emission, associated with F-centres, is the primary RL emission whereas the narrow (R-line) emission centred at 1.79 eV, associated with Cr3+ impurity ions, is the most intense secondary emission. However, the intensity of 1.79-eV emission decreases with repeated RL measurements. The central emission energy for F-centres is constant throughout the temperature range of investigation. The full width at half maximum (FWHM) for the F-centre emission band increases with temperature whereas the F-centre peak intensity exhibits thermal quenching behaviour at temperatures above 160∘C. On the other hand, the emission energy for the R-line emission of Cr3+ is constant for temperatures between 30 and 160∘C, whereas its peak intensity generally decreases with temperature. F-centres experience strong-coupling in their crystallographic sites with estimated electron-lattice coupling parameters of S = 5.0 ± 0.9, Ep = 0.079 ± 0.008 eV and ν = 1.91 × 1013 Hz where S, Ep and ν are the Huang-Rhys factor, the phonon energy and the phonon frequency, respectively. The RL spectra recorded while ramping the temperature of a sample at a constant rate have been compared against conventional TL spectra.
- Full Text: false
- Date Issued: 2018
On luminescence stimulated from deep traps using thermally-assisted time-resolved optical stimulation in α-Al2O3: C
- Nyirenda, Angel N, Chithambo, Makaiko L, Polymeris, G S
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L , Polymeris, G S
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124627 , vital:35639 , https://doi.org/10.1016/j.radmeas.2016.01.016
- Description: We report a study of charge transfer mechanisms of electrons stimulated optically from very deep traps, also known as donor traps, in α-Al2O3:C. The investigations were carried out using thermally-assisted time-resolved optical stimulation, thermoluminescence and by way of residual thermoluminescence from the main electron trap. When the charges are optically stimulated from the deep traps, they are redistributed via the conduction band to the main electron trap and the shallow trap from where they are optically or thermally released for recombination at luminescence centres. The luminescence is strongly quenched at high measurement temperature as evident by very short luminescence lifetimes at these temperatures. The main peak due to residual thermoluminescence is located at a higher temperature than the conventional main peak.
- Full Text: false
- Date Issued: 2016
- Authors: Nyirenda, Angel N , Chithambo, Makaiko L , Polymeris, G S
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124627 , vital:35639 , https://doi.org/10.1016/j.radmeas.2016.01.016
- Description: We report a study of charge transfer mechanisms of electrons stimulated optically from very deep traps, also known as donor traps, in α-Al2O3:C. The investigations were carried out using thermally-assisted time-resolved optical stimulation, thermoluminescence and by way of residual thermoluminescence from the main electron trap. When the charges are optically stimulated from the deep traps, they are redistributed via the conduction band to the main electron trap and the shallow trap from where they are optically or thermally released for recombination at luminescence centres. The luminescence is strongly quenched at high measurement temperature as evident by very short luminescence lifetimes at these temperatures. The main peak due to residual thermoluminescence is located at a higher temperature than the conventional main peak.
- Full Text: false
- Date Issued: 2016
Thermoluminescence of kunzite: a study of kinetic processes and dosimetry characteristics
- Ogundare, F O, Alatishe, M A, Chithambo, Makaiko L, Costin, G
- Authors: Ogundare, F O , Alatishe, M A , Chithambo, Makaiko L , Costin, G
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124701 , vital:35650 , https://doi.org/10.1016/j.nimb.2016.02.059
- Description: Since the use of natural minerals for dating and dose reconstruction using luminescence techniques is well-established and always of interest, we present thermoluminescence characteristics of kunzite, a gem variety of spodumene. The chemical composition of the sample was determined using an Electron Probe MicroAnalyzer.
- Full Text: false
- Date Issued: 2016
- Authors: Ogundare, F O , Alatishe, M A , Chithambo, Makaiko L , Costin, G
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124701 , vital:35650 , https://doi.org/10.1016/j.nimb.2016.02.059
- Description: Since the use of natural minerals for dating and dose reconstruction using luminescence techniques is well-established and always of interest, we present thermoluminescence characteristics of kunzite, a gem variety of spodumene. The chemical composition of the sample was determined using an Electron Probe MicroAnalyzer.
- Full Text: false
- Date Issued: 2016