Abstract:SrAl 2 O 4 :Eu,Dy is presumably the best known persistent luminescent phosphor. At room temperature, its green emission remains visible for hours after switching off the excitation. It is known that upon lowering the temperature of the phosphor a second photoluminescence emission band arises in the blue part of the visible spectrum, although its origin is still the subject of discussion. In this paper we thoroughly study the origin of both emission bands in SrAl 2 O 4 :Eu,Dy and we attribute this to europium i… Show more
“…Hölsä et al [6] proposed the possibility of anomalous low-temperature luminescence, but the reported experimental data and theoretical calculations allow to conclude that the emission comes indeed from two different sites [4,7]. Nakazawa et al [8] observed the thermal quenching of SrAl 2 O 4 :Eu 2+ (doped with 1 mol%) but at much lower temperatures (100 K less) than all other publications.…”
Section: Introductionmentioning
confidence: 92%
“…The band gap of SrAl 2 O 4 is 6.6 eV [12]. The positions of the ground states can be estimated by the Dorenbos model [13], as it was done in [7] or it can be measured [14]. The europium ions in the two sites can be excited with UV-light.…”
SrAl 2 O 4 doped with europium and dysprosium is a powerful and widely used afterglow material. Within this material strontium is found in two crystallographic different sites. Due to the similar ion radii and same charge, Eu 2+ -ions can occupy both sites, resulting in two different Eu 2+ -ions, one emitting in the blue and one in the green spectral range. The blue emission is thermally quenched at room temperature. In this paper we investigate the energy transfer between different Eu ions depending on the concentration and temperature using two different approaches: lifetime measurements and integrated intensity. We find an activation energy for the thermal quenching of the blue emission of 0.195 ± 0.023 eV and a critical radius for the energy transfer of 3.0 ± 0.5 nm. These results can help in designing better afterglow materials due to the fact that with energy transfer parts of the lost emission in the blue region at room temperature can be converted to the green site.
“…Hölsä et al [6] proposed the possibility of anomalous low-temperature luminescence, but the reported experimental data and theoretical calculations allow to conclude that the emission comes indeed from two different sites [4,7]. Nakazawa et al [8] observed the thermal quenching of SrAl 2 O 4 :Eu 2+ (doped with 1 mol%) but at much lower temperatures (100 K less) than all other publications.…”
Section: Introductionmentioning
confidence: 92%
“…The band gap of SrAl 2 O 4 is 6.6 eV [12]. The positions of the ground states can be estimated by the Dorenbos model [13], as it was done in [7] or it can be measured [14]. The europium ions in the two sites can be excited with UV-light.…”
SrAl 2 O 4 doped with europium and dysprosium is a powerful and widely used afterglow material. Within this material strontium is found in two crystallographic different sites. Due to the similar ion radii and same charge, Eu 2+ -ions can occupy both sites, resulting in two different Eu 2+ -ions, one emitting in the blue and one in the green spectral range. The blue emission is thermally quenched at room temperature. In this paper we investigate the energy transfer between different Eu ions depending on the concentration and temperature using two different approaches: lifetime measurements and integrated intensity. We find an activation energy for the thermal quenching of the blue emission of 0.195 ± 0.023 eV and a critical radius for the energy transfer of 3.0 ± 0.5 nm. These results can help in designing better afterglow materials due to the fact that with energy transfer parts of the lost emission in the blue region at room temperature can be converted to the green site.
“…TL was recorded in a homebuilt setup, details of which can be found in Botterman et al 26 Before each TL measurement, the sample was thermally cleaned by heating to 220…”
The near-infrared emitting persistent phosphor LiGa 5 O 8 :Cr 3+ (LGO:Cr) has promising applications in bioimaging. In order to improve the persistent luminescence of LGO:Cr and other Cr-doped persistent phosphors, a better understanding of trapping and detrapping mechanisms is necessary. In this work, we study the afterglow and thermoluminescence via a thermal fading experiment. The results show that there is a broad trap distribution present in LGO:Cr. The emission spectrum of chromium changes during the afterglow, which indicates that different Cr ions experience a varying crystal field in the LGO host, due to different defect configurations, and that the detrapping process occurs locally. The results of thermoluminescence and spectral decay measurements show that chromium ions residing near deep traps are subject to a smaller crystal field. Vacancies formed during the synthesis are most probably causing this effect. Codoping LGO with Si 4+ or Ge 4+ significantly improves the persistent luminescence and increases the number of deep-lying traps in the phosphor.
“…Some authors assigned the 445 and 520 nm emission bands to emission of the Eu 2+ ion located at two nonequivalent strontium sites in the SrAl 2 O 4 host. 53,61 However, the two strontium sites in the SrAl 2 O 4 are very similar and differ only by a slight distortion of their square planes. 51 The similar coordination for both sites is expected to give rise similar luminescence properties due to comparable crystal field strengths and centroid shifts.…”
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