Photoluminescence properties of solid-state Tb^3＋ doped NaY（MoO4）2
A series of Tb^3＋ doped Na Y（Mo O4）2 are synthesized by a solid-state reaction at 550 °C for 4 h, and their luminescent properties are investigated. The phase formation is carried out with X-ray powder diffraction analysis, and there is no other crystalline phase except Na Y（Mo O4）2. Na Y（Mo O4）2：Tb...
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| creator | 刘海燕 张坤 庞立斌 高少杰 高占军 段平光 张子才 王志军 |
| description | A series of Tb^3＋ doped Na Y（Mo O4）2 are synthesized by a solid-state reaction at 550 °C for 4 h, and their luminescent properties are investigated. The phase formation is carried out with X-ray powder diffraction analysis, and there is no other crystalline phase except Na Y（Mo O4）2. Na Y（Mo O4）2：Tb^3＋ can produce the green emission under 290 nm radiation excitation, and the luminescence emission peak at 545 nm corresponds to the 5D4→7F5 transition of Tb^3＋. The emission intensity of Tb^3＋ in Na Y（Mo O4）2 is enhanced with the increase of Tb^3＋ concentration, and there is no concentration quenching effect. The phenomena are proved by the decay curves of Tb^3＋. Moreover, the Commission International de I＇Eclairage（CIE） chromaticity coordinates of Na Y（Mo O4）2：Tb^3＋ locate in the green region. |
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The phase formation is carried out with X-ray powder diffraction analysis, and there is no other crystalline phase except Na Y（Mo O4）2. Na Y（Mo O4）2：Tb^3＋ can produce the green emission under 290 nm radiation excitation, and the luminescence emission peak at 545 nm corresponds to the 5D4→7F5 transition of Tb^3＋. The emission intensity of Tb^3＋ in Na Y（Mo O4）2 is enhanced with the increase of Tb^3＋ concentration, and there is no concentration quenching effect. The phenomena are proved by the decay curves of Tb^3＋. 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The phase formation is carried out with X-ray powder diffraction analysis, and there is no other crystalline phase except Na Y（Mo O4）2. Na Y（Mo O4）2：Tb^3＋ can produce the green emission under 290 nm radiation excitation, and the luminescence emission peak at 545 nm corresponds to the 5D4→7F5 transition of Tb^3＋. The emission intensity of Tb^3＋ in Na Y（Mo O4）2 is enhanced with the increase of Tb^3＋ concentration, and there is no concentration quenching effect. The phenomena are proved by the decay curves of Tb^3＋. 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The phase formation is carried out with X-ray powder diffraction analysis, and there is no other crystalline phase except Na Y（Mo O4）2. Na Y（Mo O4）2：Tb^3＋ can produce the green emission under 290 nm radiation excitation, and the luminescence emission peak at 545 nm corresponds to the 5D4→7F5 transition of Tb^3＋. The emission intensity of Tb^3＋ in Na Y（Mo O4）2 is enhanced with the increase of Tb^3＋ concentration, and there is no concentration quenching effect. The phenomena are proved by the decay curves of Tb^3＋. Moreover, the Commission International de I＇Eclairage（CIE） chromaticity coordinates of Na Y（Mo O4）2：Tb^3＋ locate in the green region.</abstract></addata></record> |
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| ispartof | 光电子快报：英文版, 2014 (6), p.451-454 |
| issn | 1673-1905 1993-5013 |
| language | eng |
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| source | SpringerNature Complete Journals; Alma/SFX Local Collection |
| subjects | NaY X射线粉末衍射分析 反应合成 发光性能 发光特性 固态 掺杂 铽 |
| title | Photoluminescence properties of solid-state Tb^3＋ doped NaY（MoO4）2 |
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