کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1489825 992313 2013 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis and photoluminescence characteristics of Dy3+ doped NaY(WO4)2 phosphors
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد سرامیک و کامپوزیت
پیش نمایش صفحه اول مقاله
Synthesis and photoluminescence characteristics of Dy3+ doped NaY(WO4)2 phosphors
چکیده انگلیسی

The novel phosphor powders of NaY(WO4)2 doped with Dy3+ were synthesized by solid state reaction. X-ray diffraction analysis showed that the phosphors sintered at 900 °C for 6 h were a pure NaY(WO4)2 phase for all the Dy3+ doping concentrations. The room temperature excitation spectra of the phosphors vary with the Dy3+ concentration and consist of an intense charge transfer band of WO42− groups and weak f–f transition absorption peaks of Dy3+. The photoluminescence spectra, excited at the peak wavelength of charge transfer band, exhibit three bands centered at 488, 575 and 662 nm, which originate from the transitions of 4F9/2 → 6H15/2 (blue), 4F9/2 → 6H13/2 (yellow) and 4F9/2 → 6H11/2 (red) of Dy3+, respectively. The effects of Dy3+ concentration on luminescence intensity and the yellow-to-blue intensity ratio of the phosphors were investigated. The different behaviors for the doping concentration dependence of luminescence intensity resulted from the different kinds of excitation was discussed.

The phosphor powders of NaY(WO4)2: Dy3+ were prepared by solid state reaction. For the different kinds of excitations, the dependence of luminescence intensity on the Tb3+ concentration was investigated.Figure optionsDownload as PowerPoint slideHighlights
► We synthesize NaY(WO4)2:Dy3+ phosphors by the solid-state reaction technique.
► We observe and explain the change of Y/B ratio with Dy3+ content.
► The I−x curve shows different behavior for different excitations.
► The concentration quenching mechanism is the d–d interaction.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Research Bulletin - Volume 48, Issue 2, February 2013, Pages 281–285
نویسندگان
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