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Luminescence of Sb3+ in rare earth orthoborates LnBO3 (Ln = Sc,Y, La,Gd, Lu)
Affiliation:1. Co-creative Research Center of Industrial Science and Technology, Kanazawa Institute of Technology, Hakusan, Ishikawa 924-0838, Japan;2. Oarai Research Center, Chiyoda Technol Corporation, Oarai-machi, Ibaraki 311-1313, Japan;3. Division of Materials Science, Nara Institute of Science and Technology, Ikoma, Nara 630-0192, Japan;4. Department of Electrical and Computer Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada
Abstract:The luminescence of several Sb3+-activated rare earth orthoborates (LnBO3Sb3+; Ln = Sc, Y, La, Gd, Lu) are reported. In all compositions the Stokes shift of the Sb3+ luminescence is rather large, resulting in rather low quenching temperatures (200 K or lower). The Stokes shift appears to be dependent on the coordination number and on the radius of the host lattice cation. This is explained from the assumed tendency of the Sb3+ ion to occupy an off-center position which becomes more apparent when the space available for the Sb3+ ion increases. The present results are compared with those on LnBO3Bi3+. It appears that the Stokes shift of the Bi3+ luminescence is more sensitive to the host lattice and is smaller than the Stokes shift of the Sb3+ luminescence. This is explained by the large radius of the Bi3+ ion compared to the Sb3+ ion. In GdBO3Sb3+ thermally activated energy transfer is observed from Gd3+ to Sb3+.
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