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首页> 外文期刊>Optics and Spectroscopy >Luminescent Properties of Hybrid Nanostructures Based on Quantum Dots of CdS, Europium 1,3-Diketonate, and Methylene Blue Molecules
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Luminescent Properties of Hybrid Nanostructures Based on Quantum Dots of CdS, Europium 1,3-Diketonate, and Methylene Blue Molecules

机译:基于量子点,1,3-二酮和亚甲基蓝分子的量子点的杂化纳米结构的发光性能

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The luminescent properties of hybrid nanostructures constructed from colloidal quantum dots (QDs) of CdS passivated with thioglycolic acid, europium(III) tris(tenoyltrifluoroacetonate), and methylene blue dye molecules are studied. Spectral features typical for the formation of core/shell QDs of the CdS/CdS:Eu3+ type are found. It is noted that the adsorption of the europium complex at the QD interfaces and the formation of QDs of the CdS/TGA/Eu3+ are probable. Spectral patterns that reveal nonradiative energy transfer from the recombination luminescence centers of CdS QDs to the Eu3+ ions in the CdS/CdS:Eu3+ and CdS/TGA/Eu3+ structures are obtained. This is manifested in quenching the recombination luminescence of QDs and in the ignition of the intracentric luminescence of Eu3+, which enhance with an increase in the concentration of the europium complex. When such structures are combined with methylene blue molecules, the half-width of the absorption spectra is found to increase by 10-15% with an unchanged position of the absorption band maximum. With an increase in the concentration of methylene blue molecules, decreases in the intensity of the recombination luminescence band of CdS QDs at a wavelength of 530 nm and in the luminescence intensity of Eu3+ ions and simultaneously the rise up of the fluorescence of methylene blue at a wavelength of about 675 nm are observed. At the same time, a decrease in the luminescence lifetime of the bands of QDs and europium ions are observed. It is concluded that the nonradiative excitation energy transfer from both the recombination luminescence centers and Eu3+ ions to methylene blue molecules takes place.
机译:研究了用硫酸乙酸,铕(III)Tris(Tenoyltrifluoroogetonate)和亚甲基蓝染料分子钝化Cds的杂交纳米结构的发光性能。发现CDS / CDS的核心/壳QDS的典型光谱特征:找到EU3 +类型。应注意,在QD界面处吸附铕络合物和CDS / TGA / EU3 +的QDS的形成。将来自CDS QD的重组发光中心的光谱图案揭示了Cds / Cds中的Cds / Cds:Eu3 +和Cds / Tga / Eu3 +结构的Eu3 +离子。这表现为猝灭QD的重组发光和Eu3 +的英属核感觉点的点火,这增加了铕络合物浓度的增加。当这种结构与亚甲基蓝色分子组合时,发现吸收光谱的半宽度增加10-15%,吸收带的不变位置最大。随着亚甲基蓝色分子的浓度的增加,CDS QDS的重组发光带的强度降低530nm的波长和Eu3 +离子的发光强度,并同时升高亚甲基蓝色的荧光观察到波长约675nm。同时,观察到QDS和铕离子的带的发光寿命的减少。结论是,从重组发光中心和Eu3 +离子到亚甲基蓝色分子的非抗激发能量转移。

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