In Situ Preparation and Luminescent Properties of CeF3 and CeF3:Tb3+ Nanoparticles and Transparent CeF3:Tb3+/PMMA Nanocomposites in the Visible Spectral Range

被引:43
作者
Chai, Ruitao
Lian, Hongzhou
Li, Chunxia
Cheng, Ziyong
Hou, Zhiyao
Huang, Shanshan
Lin, Jun [1 ]
机构
[1] Acad Sinica, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
LAYERED SILICATE NANOCOMPOSITES; LIQUID-PHASE SYNTHESIS; PHOTOLUMINESCENT PROPERTIES; HYBRID MATERIALS; CONTROLLABLE SYNTHESIS; QUANTUM DOTS; POLYMERIZATION; METHACRYLATE); CEF3-TB3+; FILMS;
D O I
10.1021/jp900269b
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
CeF3 and CeF3:Tb3+ nanoparticles were prepared by reverse microemulsion with a functional monomer, methyl methacrylate (MMA), as the oil phase, and CeF3:Tb3+/poly (methyl methacrylate) (PMMA) nanocomposites were obtained via polymerization of the MMA monomer. The nanoparticles and nanocomposites have been well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), low- and high-resolution transmission electron microscope (TEM), selected-area electron diffraction (SAED), thermogravimetric analysis (TGA), UV/vis transmission spectra, photoluminescence excitation, and emission spectra and luminescence decays. The well-crystallized CeF3 and CeF3:Tb3+ nanoparticles are spherical with a mean diameter of 15 nm. They show the characteristic emission of Ce3+ 5d-4f (313 nm, D-2-F-2(5/2); 323 nm, D-2-F-2(7/2)) and Tb3+ D-5(4)-F-7(J) (J = 6-3, with D-5(4)-F-7(5) green emission at 541 nm as the strongest one) transitions, respectively. The energy transfer from Ce3+ to Tb3+ was investigated in CeF3:Tb3+ nanoparticles in detail. The obtained solid CeF3:Tb3+/PMMA nanocomposites are highly transparent (in the visible spectral range) and exhibit strong green photoluminescence upon UV excitation, due to the integration of luminescent CeF3:Tb3+ nanoparticles. The luminescent lifetime of Tb3+ is determined to be 4.1 ms in the nanocomposite.
引用
收藏
页码:8070 / 8076
页数:7
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