OPTICAL MATERIALS
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2020
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IF 2.779
Yicheng Zeng,Biwei Qiu,FangFang Wang,Lei Zhou,Ying Li
Two kinds of hybrid luminescence films ([C 8 VIM][Eu (nta) 4 ]@PMMA and [C 8 VIM][Tb (acac) 4 ]@PMMA) have been synthesized by the copolymerization of MMA with lanthanide functionalized ionic liquid [C 8 VIM][Eu (nta) 4 ]. The structure and composition of the as-synthesized films have been characterized by 1 HNMR, XPS , FTIR, UV–vis, XRD , TGA and SEM. In addition, the photophysical properties of as-synthesized films have been investigated in detail by luminescence spectroscopy. It was found that the transparent and thermal stability of as-synthesized films are improved by the long chains of PMMA . More significantly, [C 8 VIM][Eu (nta) 4 ] @PMMA exhibits the improvement of photo physical properties (ƞ = 52.6%) and is selected as the representative sample to examine the potential fluorescence sensing of metal ions and anions. It has been showed highly selective and sensitive fluorescence sensing for Cu 2+ and CrO 4 2− . Meanwhile, [C 8 VIM][Eu (nta) 4 ]@PMMA exhibits a good stability in the aqueous solution, which is further used as fluorescence probe for detecting CO 3 2− . The good stability, sensitive fluorescence response and good mechanical processing properties of [C 8 VIM][Eu (nta) 4 ]@PMMA show a great potential to establish a fast response anion and cationic of aqueous solution fluorescence colorimetric sensor devices.
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高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2016
·Vol. 28
·期 7
·5615-5622
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IF 1.798
Chu Yang,Hao Haixia,Xie Hongde,Chen Cuili,Cai Peiqing,Seo Hyo Jin
In this work, we report the preparation of lanthanide (Eu 3+ , Tb 3+ )-complex-grafted copolymer of methyl methacrylate and maleic anhydride films. The lanthanide complex with three amino groups was used to react with poly(methyl methacrylate-co-maleic anhydride) (P(MMA-MAH)) via the amidation method. Fourier transform infrared (FT-IR), Transmission electron microscope (TEM), Scanning electron microscope (SEM), Thermogravimetric analysis (TGA) were employed to characterize those polymers. Luminescent properties were evaluated through conducting Photoluminescence (PL) excitation spectra, emission spectra and fluorescence decay curves measurements. The infrared analysis reveals the amidation between amino groups and anhydride rings. The comparatively uniform morphology can be observed in the images of TEM and SEM. These polymers can emit intense characteristic lights including red light from Eu 3+ ions and green light from Tb 3+ ions under 294 nm excitation. The lifetimes of polymers are short (about 1 ms). Meanwhile, these luminescent polymers exhibit high thermal stability (T 5 > 200 °C). We also stimulate a lamp to illustrate the possible application. All these approved interesting results suggest that they hold significant promising applications as luminous layers for optoelectronic devices.
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高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
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2014
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IF 3.209
Bing Yan,Qiu-Ping Li
Several kinds of novel lanthanide organic–inorganic mesoporous hybrid luminescent materials have been assembled by introducing the ternary lanthanide ions (Eu 3+ , Tb 3+ ) and beta-diketone (TTA, TAA) into the functionalized mesoporous hosts through the coordination bond and covalent bond by using 3-chloropropyltriethoxysilane modified 1,4,7,10-tetraazacyclododecane (Cyclen-Si) as an organic bridge molecule. These multicomponent hybrids are characterized by FTIR, TEM, XRD, thermogravimetric analysis, diffuse reflectance UV–Vis spectra and nitrogen adsorption–desorption isotherms, especially the photoluminescence properties of them. The luminescent spectra of the hybrids reveal that the MCM-41 based materials show strong emission intensities, high luminescent quantum efficiencies, long luminescent lifetimes and exhibit characteristic red and green luminescence originated from lanthanide ions (Eu 3+ or Tb 3+ ), which suggesting the Cyclen-Si bridge molecule is favorable for the assembly of lanthanide functionalized luminescent hybrids.
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Journal of Materials Chemistry C
·
2025
·
IF 5.1
Jin Liu,Boying Wang,Shuxin Li,Yao Wang,Jun Li,Yan Zhang,Christopher D. Snow,Matt J. Kipper,Soo Wohn Lee,Laurence A. Belfiore,Jianguo Tang
Advanced data storage and anti-counterfeiting technologies are critical in addressing modern information safety. In this work, novel nanocomposites of Eu3+, Tb3+, Zn2+ and -hyaluronan for down-conversion and NaGdF4:Yb,Er nanoparticles for up-conversion have been synthesized and applied for innovative anticounterfeiting luminescent inks. These inks exhibit excellent fluorescence under dual UV or NIR excitation, and sensitive quenching in response to some ions or compounds, enabling multi-level data encoding, reversible Cu2+ detection, and dynamic information concealment. Utilizing electrohydrodynamic (EHD) printing, we achieved precise patterns with line widths of approximately 20–50 μm, facilitating dynamic information concealment and secure data storage. The printed patterns, invisible under natural light, displayed distinct and bright fluorescence when stimulated by UV and NIR light, offering orthogonal readout capabilities for secure information retrieval. Additionally, the luminescent inks demonstrated remarkable sensitivity to Cu2+ ions, with fluorescence quenching efficiency reaching 85.3% at a Cu2+ concentration of 100 μg mL−1. The quenching process was reversible upon introducing ethylenediaminetetraacetic acid (EDTA), enabling up to three cycles of fluorescence recovery and suppression with minor degradation (<15%) in intensity after repeated use. The high-resolution EHD printing technology combined with excellent sensing performance, such as a detection limit of 1.2 μg mL−1 for Cu2+, enables a promising strategy for advancing intelligent information systems and hazardous ion detection. This work offers a versatile solution for secure information coding, anti-counterfeiting, and environmental sensing, providing a significant advancement in multifunctional luminescent materials, especially for smart quadruplicate information coding and hazard sensing, with dual UV/IR excitation.
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