Low-temperature luminescence and thermally stimulated luminescence of BeO: Mg single crystals

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Luminescence and thermally stimulated luminescence (TL) of BeO: Mg crystals are studied at T = 6–380 K. The TL glow curves and the spectra of luminescence (1.2–6.5 eV), luminescence excitation, and reflection (3.7–20 eV) are obtained. It is found that the introduction of an isovalent magnesium impurity into BeO leads to the appearance of three new broad luminescence bands at 6.2–6.3, 4.3–4.4, and 1.9–2.6 eV. The first two are attributed to the radiative annihilation of a relaxed near-impurity (Mg) exciton, the excited state of which is formed as a result of energy transfer by free excitons. The impurity VUV and UV bands are compared with those for the intrinsic luminescence of BeO caused by the radiative annihilation of self-trapped excitons (STE) of two kinds: the band at 6.2–6.3 eV of BeO: Mg is compared with the band at 6.7 eV (STE1) of BeO, and the band at 4.3–4.4 eV is compared with the band at 4.9 eV (STE2) of BeO. In the visible region, the luminescence spectrum is due to a superposition of intracenter transitions in an impurity complex including a magnesium ion. The manifestation of X-ray-induced luminescence bands at T = 6 K in BeO: Mg indicates their excitation during band-to-band transitions and in recombination processes. The energy characteristics of the impurity states in BeO: Mg are determined; the effect of the isovalent impurity on the fluctuation rearrangement of the BeO: Mg structure in the thermal transformation region of STE1 → STE2 is revealed.

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The effect of magnesium impurity on luminescent properties of alumina ceramics sintered at high temperatures under vacuum is studied by pulsed cathodoluminescence, photoluminescence, and thermoluminescence. At dopant concentrations >1 wt %, high-temperature synthesis results in formation of defects associated with magnesium, which were identified in the pulsed cathodoluminescence (520 nm) and photoluminescence (767 nm) spectra, as well as in the thermoluminescence curves (380 K). It is found that increased magnesium concentration leads to luminescence quenching of the intrinsic centers (F centers) of alumina in the PCL emission band at 400 nm, impurity defects (Mn4+ and Cr3+) in the photoluminescence emission bands at 673 and 689 nm, and all the recorded thermoluminescence peaks at 380, 450, and 615 K.

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Luminescence and thermally stimulated luminescence (TL) of BeO: Mg crystals are studied at T = 6–380 K. The TL glow curves and the spectra of luminescence (1.2–6.5 eV), luminescence excitation, and reflection (3.7–20 eV) are obtained. It is found that the introduction of an isovalent magnesium impurity into BeO leads to the appearance of three new broad luminescence bands at 6.2–6.3, 4.3–4.4, and 1.9–2.6 eV. The first two are attributed to the radiative annihilation of a relaxed near-impurity (Mg) exciton, the excited state of which is formed as a result of energy transfer by free excitons. The impurity VUV and UV bands are compared with those for the intrinsic luminescence of BeO caused by the radiative annihilation of self-trapped excitons (STE) of two kinds: the band at 6.2–6.3 eV of BeO: Mg is compared with the band at 6.7 eV (STE_1) of BeO, and the band at 4.3–4.4 eV is compared with the band at 4.9 eV (STE^2) of BeO. In the visible region, the luminescence spectrum is due to a superposition of intracenter transitions in an impurity complex including a magnesium ion. The manifestation of X-ray-induced luminescence bands at T = 6 K in BeO: Mg indicates their excitation during band-to-band transitions and in recombination processes. The energy characteristics of the impurity states in BeO: Mg are determined; the effect of the isovalent impurity on the fluctuation rearrangement of the BeO: Mg structure in the thermal transformation region of STE_1 → STE_2 is revealed.

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