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Durable crystalline actinide host phases of ceramic waste forms are considered as advanced materials which are prospective for safe use of Pu and minor actinides before their final disposal. Development of self-glowing actinide-doped materials with matrices that are chemically inert and resistant to radiation damage may significantly change the approaches to actinide immobilization. Single crystals of zircon doped with different amount of Tb and 238Pu were synthesized by the flux method. Different non-radioactive crystals of Tb-doped zircon were studied first by cathodoluminescence method in order to identify the optimal content of Tb3+ that provides the highest luminescence emission. Then self-glowing crystals of zircon were grown with the optimal Tb content and small admixture of 238Pu (less than 0.1 wt. %). It was proposed that the valence state of Tb incorporated into zircon crystals can be (3+) and (4+), but only trivalent Tb is responsible for intensive luminescence. It is demonstrated that a small addition of Zr-phosphate to the flux supports Tb incorporation into zircon lattice and stabilizes preferably Tb3+. At the same time the addition of Zr-phosphate caused the crystallization of zirconia as a minor phase. Zircon crystals with very intensive self-glowing were successfully synthesized. The 238Pu content was 0.02 wt.% and the Tb concentration varied between 0.2 and 0.3 wt.%. Zirconia crystals obtained from the same experiment are characterized by weak self-glowing, although the Tb content was only 0.02 wt.%, while the content of 238Pu was comparable to that of zircon, i.e. 0.03 wt. %.
We studied the defect properties present in rapid thermal oxidized porous silicon (RTOPS) by Electron Spin Resonance (ESR). Two different types of defects are distinguished, one similar to the ones observed in damaged c-Si, and in a-Si. The second one is probably related to the Pbo center at the Si/SiO2 interface. The minimum density of 1016 cm-3 is observed for the as etched and for the 900°C oxidized samples, but reaches a maximum of 8×1018 cm-3for the 600°C samples. The PL intensity anticorrelates with the defect densities, which shows that nonradiative recombination via defects is a very powerful channel in quenching the PL efficiency.
The characteristics of organic light-emitting devices
based on aluminum tris-(8-hydroxy-quinoline) (Alq3), N,N'-bis(3-methylphenyl)-N,N'-diphenylbenzidine (TPD) with novel
p-isopropenyl-calixarenestyrene copolymer buffer layer and Al cathode were
investigated. The devices with TPD/Alq3/Al were also fabricated in the
same way for comparison. The p-isopropenylcalixarenestyrene copolymer used
as buffer layer greatly improved the performance of the device and increased
the device efficiency and stability.
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