Energy transfer, multi-colour emission and high thermal stability behaviour of K2Tb1-xEuxHf(PO4)3 with langbeinite-type structure

被引:7
|
作者
Zhao, Dan [1 ,2 ]
Zhang, Shi-Rui [1 ]
Zhang, Rui-Juan [1 ]
Fan, Yan-Ping [1 ]
Liu, Bao-Zhong [3 ]
Shi, Lin-Ying [3 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Henan, Peoples R China
[2] State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Henan Polytech Univ, Henan Key Lab Coal Green Convers, Jiaozuo 454000, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH QUANTUM EFFICIENCY; LUMINESCENCE PROPERTIES; TUNABLE LUMINESCENCE; CRYSTAL-STRUCTURE; PHOSPHOR; EU3+; TB3+; PHOTOLUMINESCENCE; MECHANISM; MIGRATION;
D O I
10.1039/d0ce00322k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Eu3+/Tb(3+)codoped phosphors usually present multi-color emitting performances ranging from green and yellow to red, which not only have theoretical but also practical significance. In this work, we prepared a new langbeinite-type compound, K2TbHf(PO4)(3), determined its structureviasingle-crystal X-ray diffraction, and prepared solid solutions of K2Tb1-xEuxHf(PO4)(3)(x= 0-1) with multi-color emitting properties. The structure of the solid solutions was refined by the Rietveld method, showing a constant lattice structure with a change in Eu(3+)concentration from 0 to 100%. For the typical sample, K2Tb0.99Eu0.01Hf(PO4)(3), both Tb(3+)and Eu(3+)emission peaks were observed upon excitation by near ultraviolet light of 378 nm, whereas only the characteristic peaks of Eu(3+)were observed when the excitation source was 393 nm. This suggests that the energy transfer from Tb(3+)to Eu(3+)occurred, but not the reverse transfer. The emitting color of K2Tb1-xEuxHf(PO4)(3)could change from green and yellow to red by simply modulating the concentration of Eu3+. Meanwhile, the temperature-dependent analysis proved the high thermal stability of the prepared phosphor. Finally, green, yellow, and red near-ultraviolet pumped LEDs were fabricated using three typical phosphors withx= 0, 0.005, and 0.10, respectively.
引用
收藏
页码:4914 / 4922
页数:9
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