Photoluminescence properties of (Eu, Tb, Tm) co-doped PbMoO4 obtained by sonochemical synthesis

被引:31
作者
Gurgel, G. M. [1 ]
Lovisa, L. X. [1 ]
Pereira, L. M. [1 ]
Motta, F. V. [1 ]
Li, M. S. [2 ]
Longo, E. [3 ]
Paskocimas, C. A. [1 ]
Bomio, M. R. D. [1 ]
机构
[1] Univ Fed Rio Grande do Norte, CT, DEMAT, Ave Sen Salgado Filho 3000, BR-59072970 Natal, RN, Brazil
[2] Univ Sao Paulo, IFSC, Ave Trabalhador Sao Carlense 400, BR-13566590 Sao Carlos, SP, Brazil
[3] UNESP, IQ, LIEC, Rua Francisco Degni S-N, BR-14801907 Araraquara, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
PbMoO4; Earth rare; Sonochemistry; Photoluminescence; PHOTOCATALYTIC ACTIVITY; GROWTH-MECHANISM; LEAD MOLYBDATE; DEGRADATION; NANOSTRUCTURES; MICROCRYSTALS; NANOCRYSTALS; LUMINESCENCE; REFINEMENT; ULTRASOUND;
D O I
10.1016/j.jallcom.2016.12.409
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The PbMoO4 co-doped with Tm3+, Tb3+ Eu3+ with scheelita structure was synthesized by the sono-chemical method. The photoluminescent properties, structural and color coordinates emitted by phosphors were investigated. The structural analysis of the crystal and the changes in lattice parameters confirm that the rare earth ions (RE3+) were successfully introduced into the host of the PbMoO4. The relationship between energy gap (Egap) and the concentration of RE3+ ions was also discussed, the Egap is significantly influenced by the degree of structural order-disorder present in the crystal lattice. The PbMoO4:RE3+ shows light emission in green. Under UV excitation, Photoluminescence (PL) shows a broad band centered at 520 nm and smaller bands belonging to transitions of RE3+: (1)G(4) -> F-3(4) and D-1(2) -> H-3(4) at 480 and 533 nm (Tm3+), D-5(4) -> F-7(j) = 6, 5) at 493 and 550 rim (Tb3+) D-5(0) -> 7Fj =1, 2, 4) 593, 615 and 702 nm (Eu3+). (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:130 / 137
页数:8
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