Synthesis and luminescence properties of ternary complexes of SmxTb1-x(TTA)3Phen nanoparticles and their surface modification

被引:8
作者
Ni, Yaru [1 ]
Tao, Jing [1 ]
Lu, Chunhua [1 ]
Xu, Zhongzi [1 ]
Kang, Zhitao [2 ,3 ]
Xu, Feng [4 ]
机构
[1] Nanjing Univ Technol, Nanjing 210009, Peoples R China
[2] Georgia Inst Technol, Georgia Tech Res Inst, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[4] Southeast Univ, Minist Educ, Key Lab MEMS, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
INTRAMOLECULAR ENERGY-TRANSFER; RARE-EARTH COMPLEXES; LANTHANIDE; ENHANCEMENT; LIGANDS; ACID;
D O I
10.1007/s10853-013-7325-6
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of Sm (x) Tb1-x (TTA)(3)Phen (x = 1.0, 0.9, 0.7, 0.5, 0.3, 0.1, 0) complexes was synthesized by wet chemical method and characterized using Fourier transform infrared spectroscopy and fluorescence spectroscopy. The IR absorption spectra indicate that alpha-thenoyltrifluoroacetone was coordinated to the rare earth ions and that chemical bonds were formed between rare earth ions and the nitrogen atoms in 1,10-Phenanthroline (Phen). The fluorescence spectra of the complexes indicate that the emission intensity of Sm3+ was enhanced by the addition of substitutive Tb3+. These data show that not only the ligands (TTA and Phen) but also Tb3+ could absorb and transmit energy to Sm3+ in the complexes. Formation of dual-core complexes appears to be responsible for co-fluorescence, which can greatly promote the illuminant ability of Sm (TTA)(3)Phen complex. After further encapsulation by SiO2, the Sm (x) Tb1-x (TTA)(3)Phen@SiO2 core-shell structure was very stable to UV light.
引用
收藏
页码:5309 / 5315
页数:7
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