Synthesis, Persistent Luminescence, and Thermoluminescence Properties of Yellow Sr3SiO5:Eu2+, RE3+ (RE=Ce, Nd, Dy, Ho, Er, Tm, Yb) and Orange-Red Sr3-xBaxSiO5:Eu2+, Dy3+ Phosphor

被引:47
|
作者
Li, Ye [1 ]
Li, Baohong [2 ]
Ni, Chenchen [1 ]
Yuan, Shuxia [1 ]
Wang, Jing [1 ]
Tang, Qiang [2 ]
Su, Qiang [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, State Key Lab Optoelect Mat & Technol, Minist Educ,Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sch Phys & Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
persistent luminescence; rare earths; silicates; thermoluminescence; LONG-LASTING PHOSPHORESCENCE; LLP; CAALSIN3-EU2+; SRAL2O4EU2+; MECHANISM; BLUE; SR; EU;
D O I
10.1002/asia.201301045
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sunlight-excitable orange or red persistent oxide phosphors with excellent performance are still in great need. Herein, an intense orange-red Sr3-xBaxSiO5:Eu2+,Dy3+ persistent luminescence phosphor was successfully developed by a two-step design strategy. The XRD patterns, photoluminescence excitation and emission spectra, and the thermoluminescence spectra were investigated in detail. By adding non-equivalent trivalent rare earth co-dopants to introduce foreign trapping centers, the persistent luminescence performance of Eu2+ in Sr3SiO5 was significantly modified. The yellow persistent emission intensity of Eu2+ was greatly enhanced by a factor of 4.5 in Sr3SiO5:Eu2+,Nd3+ compared with the previously reported Sr3SiO5:Eu2+, Dy3+. Furthermore, Sr ions were replaced with equivalent Ba to give Sr3-xBaxSiO5:Eu2+,Dy3+ phosphor, which shows yellow-to-orange-red tunable persistent emissions from =570 to 591nm as x is increased from 0 to 0.6. Additionally, the persistent emission intensity of Eu2+ is significantly improved by a factor of 2.7 in Sr3-xBaxSiO5:Eu2+,Dy3+ (x=0.2) compared with Sr3SiO5:Eu2+,Dy3+. A possible mechanism for enhanced and tunable persistent luminescence behavior of Eu2+ in Sr3-xBaxSiO5:Eu2+,RE3+ (RE=rare earth) is also proposed and discussed.
引用
收藏
页码:494 / 499
页数:6
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