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Photoluminescence properties of (Ba1−xEux)WO4 red synthesized by the coprecipitation/calcination method
► Ba1−xEuxWO4 red phosphors are synthesized by coprecipitation/calcination method. ► The obtained powders are identified by X-ray diffraction, scanning electron microscope (SEM) and fluorescence spectrometer. ► Spectroscopic study of Eu3+ ions was made at room temperature. The optimal doping concent...
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Published in: | Journal of alloys and compounds 2012-04, Vol.521, p.146-149 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Ba1−xEuxWO4 red phosphors are synthesized by coprecipitation/calcination method. ► The obtained powders are identified by X-ray diffraction, scanning electron microscope (SEM) and fluorescence spectrometer. ► Spectroscopic study of Eu3+ ions was made at room temperature. The optimal doping concentration and concentration quenching mechanism are discussed.
In this paper, we report on the series of novel red phosphors (Ba1−xEux)WO4 were synthesized by coprecipitation/calcination method. The morphology and structure were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). Photoluminescence (PL) excitation and emission spectra were also used to characterize the (Ba1−xEux)WO4. The results showed that all phosphors present a scheelite-type tetragonal structure with space group (I41/a). The SEM images showed that the grains were like shuttles with sizes ranging from 3.0 to 7.0μm. The obtained (Ba1−xEux)WO4 phosphor emitted red emission centered at 612nm corresponding to the 5D0→7F2 transition of Eu3+ when was excited by 394nm and 465nm which well matched with near-ultraviolet and blue chips. The optimized concentration of Eu3+ was 20mol.% for the highest PL emission intensity which was excited at 534nm. The concentration quenching occurred when the Eu3+ concentration was beyond 20mol.%. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2012.01.098 |