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作 者:廉世勋[1] 田科明[1] 尹笃林[1] 朱爱玲[1] 刘利民[1]
出 处:《高等学校化学学报》2007年第6期1024-1026,共3页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:20371017);湖南省科技厅基金(批准号:06FJ3095)资助
摘 要:Carbonate coprecipitate precursors were prepared by mixed nitrate solutions containing M2+(M2+=Sr2+,Ba2+),Y3+ and Er3+ as the cation sources and(NH4)2CO3 as the precipitator.MY2S4:Er3+ phosphors were synthesized by calcining the carbonate precursors with CS2 as the sulfurization reagent at 1050 ℃ for 4 h.XRD patterns show that the synthesized SrY2S4 and BaY2S4 crystalline powders possess the orthorhombic [CaFe2O4]-type structure.Photoluminescent measurements indicate that there were mainly red emitting(4F9/2→4I15/2) and green emitting(2H11/2→4I15/2 and 4S3/2→4I15/2) of Er3+ in the SrY2S4 while there was only red emitting(4F9/2→4I15/2) in BaY2S4:Er3+.BaY2S4:Er3+ is considered as a novel red phosphor candidate with a high monochromaticity.Carbonate coprecipitate precursors were prepared by mixed nitrate solutions containing M^2+( M^2+ = Sr^2+, Ba^2+) , y^3+ and Er^3+ as the cation sources and ( NH4 )2CO3 as the precipitator. MY2S4: Er^3+ phosphors were synthesized by calcining the carbonate precursors with CS2 as the sulfurization reagent at 1050 °C for 4 h. XRD patterns show that the synthesized SrY2S4 and BaY2S4 crystalline powders possess the ortho-rhombic [CaFe204]-type structure. Photoluminescent measurements indicate that there were mainly red emit-ting ( ^4F9/2→^4I15/2 ) and green emitting(^2H11/2→^4I15/2 and ^4S3/2→^4I15/2 ) of Er^3+ in the SrY2S4 while there was only red emitting(^4F9/2→^4I15/2 ) in BaY2S4: Er^3+.BaY2S4: Er^3+ is considered as a novel red phosphor candi-date with a high monochromaticity.
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