Thermoluminescence due to simultaneous recombination of two electrons into two-hole centers

2021 ◽  
Vol 141 ◽  
pp. 106521
Author(s):  
R. Chen ◽  
J.L. Lawless ◽  
V. Pagonis
Keyword(s):  
MRS Advances ◽  
2016 ◽  
Vol 1 (63-64) ◽  
pp. 4227-4232 ◽  
Author(s):  
S.V. Stefanovsky ◽  
O.I. Stefanovsky ◽  
M.I Kadyko ◽  
V.A. Zhachkin ◽  
L.D. Bogomolova

ABSTRACTGlasses of the series (mol.%) 40 Na2O, (20-x) Al2O3, x Fe2O3, 40 P2O5 were irradiated with 8 MeV electrons to doses equivalent of 0.1, 0.5, and 1.0 MGy and characterized by FTIR spectroscopy and ESR at room temperature. FTIR spectra of all the glasses consist of strong bands due to O-P-O stretching modes in (PO4)3- and (P2O7)4- units at 1000-1200 cm-1, P-O-P stretching modes at 900-950 cm-1 (νas) and 700-750 cm-1 (νs), and bending modes in the PO4 units. The wavenumber range lower 800 cm-1 has some contribution due to stretching modes in MO4 and MO6 (M = Al, Fe) units. Moreover the bands at 3300-3700 cm-1 and 1550-1650 cm-1 due to stretching and bending modes in both absorbed and structurally bound H2O molecules were present. As irradiation dose increases the bands due to stretching and bending modes in water molecules and M-O-H bonds become stronger and are split. No essential changes with increasing dose were observed within the spectral range of stretching modes of the O-P-O and P-O-P bonds. Irradiation yields phosphorus-oxygen hole centers - PO42- (D5) and PO42- (D6), and PO32- ion-radicals (D2) observable in ESR spectra of low-Fe glasses. At x>5 their responses are overlapped with strong broad line due to Fe(III). On the whole, with the increase in iron content the glass structural evolution decrease.


1975 ◽  
Vol 46 (10) ◽  
pp. 4531-4536 ◽  
Author(s):  
C. Manfredotti ◽  
A. Rizzo ◽  
C. De Blasi ◽  
S. Galassini ◽  
L. Ruggiero
Keyword(s):  

1993 ◽  
Vol 63 (25) ◽  
pp. 3440-3442 ◽  
Author(s):  
S. Kannan ◽  
M. E. Fineman ◽  
J. Li ◽  
G. H. Sigel

2020 ◽  
Vol 105 (7) ◽  
pp. 1051-1059
Author(s):  
José R. Toledo ◽  
Raphaela de Oliveira ◽  
Lorena N. Dias ◽  
Mário L.C. Chaves ◽  
Joachim Karfunkel ◽  
...  

Abstract Montebrasite is a lithium aluminum phosphate mineral with the chemical formula LiAlPO4(Fx,OH1–x) and considered a rare gemstone material when exhibiting good crystallinity. In general, montebrasite is colorless, sometimes pale yellow or pale blue. Many minerals that do not have colors contain hydroxyl ions in their crystal structures and can develop color centers after ionization or particle irradiation, examples of which are topaz, quartz, and tourmaline. The color centers in these minerals are often related to O− hole centers, where the color is produced by bound small polarons inducing absorption bands in the near UV to the visible spectral range. In this work, colorless montebrasite specimens from Minas Gerais state, Brazil, were investigated by electron paramagnetic resonance (EPR) for radiation-induced defects and color centers. Although γ irradiation (up to a total dose of 1 MGy) did not visibly modify color, a 10 MeV electron irradiation (80 MGy) induced a pale greenish-blue color. Using EPR, O− hole centers were identified in both γ- or electron-irradiated montebrasite samples showing superhyperfine interactions with two nearly equivalent 27Al nuclei. In addition, two different Ti3+ electron centers were also observed. From the γ irradiation dose dependency and thermal stability experiments, it is concluded that production of O− hole centers is limited by simultaneous creation of Ti3+ electron centers located between two equivalent hydroxyl groups. In contrast, the concentration of O− hole centers can be strongly increased by high-dose electron irradiation independent of the type of Ti3+ electron centers. From detailed analysis of the EPR angular rotation patterns, microscopic models for the O− hole and Ti3+ electron centers are presented, as well as their role in the formation of color centers discussed and compared to other minerals.


Nukleonika ◽  
2015 ◽  
Vol 60 (2) ◽  
pp. 289-292 ◽  
Author(s):  
Vitaliy P. Zhurenko ◽  
Oganes V. Kalantaryan ◽  
Sergiy I. Kononenko

AbstractThis paper deals with the luminescence of silica (KV-type) induced by beam of hydrogen ions with the energy of 210 keV per nucleon. An average implantation dose of up to 3.5 × 1021cm−3(5 × 1010Gy) was accumulated during irradiation over an extended period. The luminescent spectra consisted of the blue band (maximum at 456 nm) and the red band (650 nm) in the visible range. It was shown that increase in the absorption dose had an effect on the silica luminescence. It was found that the most significant changes in the spectrum occurred during the dose accumulation in the region of 550–700 nm. The shape of the spectrum of the luminescent radiation in this wavelength range was affected both by the oxygen deficient centres (blue band) and non-bridging oxygen hole centers (red band). Mathematical processing of the experimental spectra permitted to identify contributions to the luminescent radiation coming from both types of defects.


2019 ◽  
Vol 122 ◽  
pp. 17-21 ◽  
Author(s):  
Roman Shendrik ◽  
Alexandra Myasnikova ◽  
Alexey Rupasov ◽  
Alexey Shalaev
Keyword(s):  

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