Luminescence of dysprosium doped strontium aluminate phosphors by codoping with manganese ion


Karabulut Y., Canimoglu A., Kotan Z., Akyuz O., Ekdal E.

JOURNAL OF ALLOYS AND COMPOUNDS, cilt.583, ss.91-95, 2014 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 583
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1016/j.jallcom.2013.08.172
  • Dergi Adı: JOURNAL OF ALLOYS AND COMPOUNDS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.91-95
  • Anahtar Kelimeler: SrAl2O4, Rare earths, Radioluminescence, Photoluminescence, Cathodoluminescence, Solid state reaction method
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

The authors report here the luminescence properties of strontium aluminate doped with dysprosium and manganese. The dysprosium, manganese co-doped powders were prepared by a solid state reaction at temperatures at 1600 degrees C under H-2 (15%)-Ar (85%) atmosphere. The dysprosium, manganese co-doped strontium aluminate phosphors have the monoclinic structure with lattice parameters a approximate to 8.440 angstrom, b approximate to 8.821 angstrom, c approximate to 5.157 angstrom and beta approximate to 93.4 degrees. The characteristic (4)F9/2 -> H-6(15/2) (blue), F-4(9/2) -> H-6(13/2) (yellow), F-4(9/2) -> H-6(11/2) (red) and F-4(9/2) -> H-6(9/2) (NIR) transitions of Dy3+ for different luminescence techniques (radioluminescence, photoluminescence and cathodoluminescence) were detected in the emission spectra at the room temperature. The luminescence of Mn2+ co-doped SrAl2O4:Dy3+ exhibits a broad greenorange emission band (T-4(1) -> (6)A(1) transition) from the synthesized phosphor particles under different excitation sources. This corresponds to the spin-forbidden transition of the d-orbital electron associated with the Mn2+ ion. Multiple emission lines observed at each of these techniques are due to the crystal field splitting of the ground state of the emitting ions. The nature of the emission lines is discussed. (C) 2013 Elsevier B.V. All rights reserved.