87 research outputs found

    Avoiding concentration quenching and self-absorption in Cs4EuX6 (X = Br, I) by Sm2+ doping.

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    The benefits of doping Cs4EuBr6 and Cs4EuI6 with Sm2+ are studied for near-infrared scintillator applications. It is shown that undoped Cs4EuI6 suffers from a high probability of self-absorption, which is almost completely absent in Cs4EuI6:2% Sm. Sm2+ doping is also used to gain insight in the migration rate of Eu2+ excitations in Cs4EuBr6 and Cs4EuI6, which shows that concentration quenching is weak, but still significant in the undoped compounds. Both self-absorption and concentration quenching are linked to the spectral overlap of the Eu2+ excitation and emission spectra which were studied between 10 K and 300 K. The scintillation characteristics of Cs4EuI6:2% Sm is compared to that of the undoped samples. An improvement of energy resolution from 11% to 7.5% is found upon doping Cs4EuI6 with 2% Sm and the scintillation decay time shortens from 4.8 s to 3.5 s in samples of around 3 mm in size

    The role of Yb2+ as a scintillation sensitiser in the near-infrared scintillator CsBa2I5:Sm2+

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    The feasiblity of using Yb2+ as a scintillation sensitiser for CsBa2I5:Sm2+ near-infrared scintillators has been assessed. CsBa2I5 samples with concentrations ranging from 0.3% to 2% Yb2+ and 0–1% Sm2+ have been studied. The scintillation properties have been determined and the dynamics of the scintillation mechanism have been studied through photoluminescence measurements. Radiationless energy transfer between Yb2+ ions plays a key role in increasing the ratio between the spinforbidden and spin-allowed emission with increasing Yb2+ concentration in samples where Yb2+ is the only dopant. In samples co-doped with Sm2+, the Yb2+ 4f13[2F7/2]5d1[LS] and 4f13[2F7/2]5d1[HS] states both serve as donor states for radiationless energy transfer to Sm2+ with a rate of energy transfer that is inversely proportional to the luminescence lifetime the respective donor states. At a Sm2+ concentration of 1%, 85% of the Yb2+ excitations are transferred to Sm2+ through radiationless energy transfer. Almost all of the remaining Yb2+ emission is reabsorbed by Sm2+, resulting in nearly complete energy transfer

    Charging mechanisms in persistent phosphors

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    The development of novel persistent phosphors is currently hampered by a limited understanding of the charging mechanism. Using x-ray absorption and thermoluminescence spectroscopy we evaluate the validity of recently proposed models for the charging mechanism

    Light yield and thermal quenching of Ce3+ and Pr3+ co-doped LaBr3:Sm2+ near-infrared scintillators

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    LaBr3:Ce3+ is a compound with excellent scintillation properties, but its ultraviolet emission does not match well with the detection efficiency curves of silicon based photodetectors. In this work, Sm2+ is studied as an activator for LaBr3 as its near-infrared emission can be detected with close to 100% efficiency by such photodetectors. LaBr3:Sm2+ single crystals were grown with and without co-doping of Ce3+ or Pr3+. The samples were studied by means of X-ray excited and photoluminescence spectroscopy at temperatures between 10 K and 300 K. Their spectroscopic properties are compared to LaBr3:Ce3+ and LaBr3:Eu2+. The effect of using Ce3+ or Pr3+ as scintillation sensitiser for Sm2+ is assessed. It is found that energy transfer from host to Sm2+ greatly improves upon Ce3+ co-doping, but the quenching temperature of the Sm2+ emission decreases. The quenching mechanism of both the Ce3+ and Sm2+ emission in LaBr3 is elaborated on. Furthermore, the effect of charge compensating defects on the light yield and spectroscopic properties is discussed
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