2014
DOI: 10.1016/j.materresbull.2014.09.076
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On the photo and thermally stimulated luminescence properties of U doped SrBPO 5

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Cited by 23 publications
(13 citation statements)
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“…The uneven shape of the particles observed in this case was due to the synthesis procedure. The spectra is similar to the data reported by Kumar et al [20] that showed a five band structure for the samples with peaks at 481 nm (20,790 cm À 1 ), 498 nm (20,080 cm À 1 ), 519 nm (19,268 cm À 1 ), 539 nm (18,518 cm À 1 ) and 560 nm (17,875 cm À 1 ). Another weak but prominent hump in the spectra was observable at 595 nm (16,806 cm À 1 ).…”
Section: Crystal Structure and Morphologysupporting
confidence: 89%
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“…The uneven shape of the particles observed in this case was due to the synthesis procedure. The spectra is similar to the data reported by Kumar et al [20] that showed a five band structure for the samples with peaks at 481 nm (20,790 cm À 1 ), 498 nm (20,080 cm À 1 ), 519 nm (19,268 cm À 1 ), 539 nm (18,518 cm À 1 ) and 560 nm (17,875 cm À 1 ). Another weak but prominent hump in the spectra was observable at 595 nm (16,806 cm À 1 ).…”
Section: Crystal Structure and Morphologysupporting
confidence: 89%
“…Recently Kumar et al have reported the stabilization of uranium as uranyl in one of the borophosphate based host i.e. SrBPO 5 (SBP) prepared through solid state reaction route [20]. However, the dopant ion concentration in the work was arbitrarily fixed at 1 mol%.…”
Section: Introductionmentioning
confidence: 99%
“…The efficient green emission around 535 nm observed in this case, suggests the absence of tetrahedral UO 4 2 À (red emission). The broad green emission band spectral profile (its symmetry around the 535 nm peak) seems to match better with the UO 6 6 À unit [12]. The origin of this emission is assigned to the parity forbidden charge transfer transition 5f-t 1u that is vibronically coupled by the ungerade vibrational modes of the UO 6 6 À octahedron.…”
Section: Luminescence Studymentioning
confidence: 77%
“…in case of the silicate [3], pyrophosphate [11], borophosphate [12] and borate matrices [13], uranium gets stabilized as uranyl (UO 2 2 þ ), whereas, in case of the tetraborate [14] and zirconate [15] matrices, it was the octahedral uranate species, UO 6 6 À that gets stabilized preferentially. This difference is probably because of U-O bond length.…”
Section: Luminescence Studymentioning
confidence: 99%
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