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Compositional tuning and site selective excitations in SrTiO3:Y3+, Eu3+ red phosphors
Dyes and Pigments ( IF 4.1 ) Pub Date : 2017-10-28 , DOI: 10.1016/j.dyepig.2017.10.040
G. Jyothi , K.G. Gopchandran

The paper reports the effective control of charge transfer transitions in perovskite based titanate red emitting phosphors by site selective substitution and the resulting enhanced emission with increased colour purity. The influence of altering the substitution sites of Y3+ and Eu3+ ions at different cationic sites on local structure variations and photoluminescence properties is investigated by adopting three different protocols of composition, viz., Sr1-x-yYxTiO3: yEu3+, Sr1-x/2-yYxTi1-x/2O3: yEu3+ and Sr1-x/2-y/2YxTi1-x/2-y/2O3: yEu3+. It is found that optimum substitution of Y3+ ions at Sr2+ and Ti4+ sites in Sr0.95Eu0.05TiO3 enhances the intensity of luminescence by 14 times, accompanied by an increase in asymmetric ratio between 5D07F2 and 5D07F1 transitions from 1 to 5.6. Further, the double site substitution of Eu3+ and Y3+ ions in this system yields emission having close resemblance with that of the commercial red phosphor, Y2O3:Eu3+ with 99.9% colour purity, asymmetric ratio 6.8 and chromaticity co-ordinates (0.66, 0.34), close to that of standard red. The biexponential luminescence decay curves propose the occurrence of two nonequivalent Eu3+ crystallographic sites in Sr1-x-yYxTiO3: yEu3+ phosphors and the triple exponential behavior observed in the case of Sr1-x/2-yYxTi1-x/2O3: yEu3+ and Sr1-x/2-y/2YxTi1-x/2-y/2O3: yEu3+ shows the occurrence of three nonequivalent Eu3+ crystallographic sites. The increase in local asymmetry for Sr1-x/2-y/2YxTi1-x/2-y/2O3: yEu3+, which prompted the colour pure emission, compared to that of Sr1-x/2-yYxTi1-x/2O3: yEu3+, is evident in the increase of J-O intensity parameter (Ω2) from 6.07 × 10−20 to 8.98 × 10−20 cm2.



中文翻译:

SrTiO 3:Y 3+,Eu 3+红色荧光粉的组成调谐和位点选择性激发

该论文报道了通过位点选择性取代有效控制钙钛矿基钛酸红色发光磷光体中电荷转移跃迁的方法,并通过提高色纯度提高了发射效率。通过采用三种不同的组成方案,即Sr 1- xy Y x TiO 3y,研究了改变Y 3+和Eu 3+离子在不同阳离子位点上的取代位点对局部结构变化和光致发光性能的影响。Eu 3+,Sr 1- x / 2- y Y x Ti 1- x / 2 O3y Eu 3+和Sr 1- x / 2- y / 2 Y x Ti 1- x / 2- y / 2 O 3y Eu 3+。发现在Sr 0.95 Eu 0.05 TiO 3中Sr 2+和Ti 4+处Y 3+离子的最佳取代将发光强度提高了14倍,并伴随着5 D 07 F之间不对称比的增加。25 D 07 F 1从1转换为5.6。另外,在该系统中Eu 3+和Y 3+离子的双位取代产生的发射与商业红色荧光粉Y 2 O 3:Eu 3+的发射近似,具有99.9%的色纯度,不对称比6.8和色度。坐标(0.66,0.34),接近标准红色。双指数发光衰减曲线表明在Sr 1- xy Y x TiO 3y Eu 3+中存在两个不等价的Eu 3+晶体学位点Sr 1- x / 2- y Y x Ti 1- x / 2 O 3y Eu 3+和Sr 1- x / 2- y / 2 Y x Ti 1- x情况下观察到的荧光粉和三重指数行为x / 2- y / 2 O 3y Eu 3+显示出三个非等价的Eu 3+晶体位点。Sr 1- x / 2- y / 2 Y的局部不对称性的增加x Ti 1- x / 2- y / 2 O 3 y Eu 3+,与Sr 1- x / 2- y Y x Ti 1- x / 2 O 3 y相比,它促进了颜色的发出。的Eu 3+,在JO强度参数的增加(Ω是显而易见2)从6.07×10 -20到8.98×10 -20 厘米2

更新日期:2017-10-28
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