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1.
Zhiyong Huang Chenhan Xiong Jianhua Huang Tianxiang Zhao Wei Cao Guoping Du Nan Chen 《Luminescence》2022,37(6):944-952
Inorganic–organic hybrid nanoparticles formed by lanthanide-doped nanostructures and organic ligands have been intensively studied, which could greatly increase their photoluminescence performance as a result of the energy transfer process from organic ligands to Ln3+ ions. However, the photoluminescence intensity and excitation spectral width are still quite limited on coordinating with a single type of organic ligand. In this work, Eu3+-doped LaF3 (LaF3:Eu3+) nanoparticles were prepared using a hydrothermal method, and were then hybridized with benzoic acid and thenoyltrifluoroacetone to form the hybrid nanostructures. After that, the hybrid nanostructures were mixed with 2,2′-azobisisobutyronitrile and methyl methacrylate to prepare the composites. The sample obtained by hybridization and composite doping with 5% Eu3+ exhibited the best photoluminescence performance. The excitation peak width and luminescence intensity of the hybrid nanostructures were significantly increased. The excitation spectral width of the inorganic–organic mixed hybrid nanostructures was particularly enhanced, and covered the whole ultraviolet band region of solar light on Earth. The prepared composites exhibited good optical properties. 相似文献
2.
Utility of gold nanoparticles in luminescence determination of trovafloxacin: comparison of chemiluminescence and fluorescence detection
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Two novel sensitive sequential injection chemiluminescence analysis and fluorescence methods for trovafloxacin mesylate detection have been developed. The methods were based on the enhancement effect of gold nanoparticles on luminol–ferricyanide–trovafloxacin and europium(III)–trovafloxacin complex systems. The optimum conditions for both detection methods were investigated. The chemiluminescence signal was emitted due to the enhanced effect of gold nanoparticles on the reaction of luminol–ferricyanide–trovafloxacin in an alkaline medium. The response was linear over a concentration range of 1.0 × 10–9 to 1.0 × 10–2 mol/L (%RSD = 1.3), (n = 9, r = 0.9991) with a detection limit of 1.7 × 10–10 mol/L (S/N = 3). The weak fluorescence intensity signal of the oxidation complex of europium(III)–trovafloxacin was strongly enhanced by gold nanoparticles and detected at λex = 330 and λem = 540 nm. Fluorescence detection enabled the determination of trovafloxacin mesylate over a linear range of 1.0 × 10–8 to 1.0 × 10–3 mol/L (%RSD = 1.2), (n = 6, r = 0.9993) with a detection limit of 3.3 × 10–9 mol/L. The proposed methods were successfully applied to the determination of the studied drug in its bulk form and in pharmaceutical preparations. The results were treated statistically and compared with those obtained from other reported methods. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
3.
Effects of Ce doping on the luminescent property of Ca3SiO4Cl2:Eu phosphor for green lighting
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Jingsheng Chen 《Luminescence》2015,30(2):159-162
White light‐emitting diodes (LEDs) for green lighting are new solutions for energy saving and environmental protection. Ca3SiO4Cl2:Ce,Eu is an efficient phosphor for white LEDs. Effective energy transfer from Ce3+ to Eu2+ occurs in Ca3SiO4Cl2:Ce,Eu due to good spectrum overlap between the emission band of Ca3SiO4Cl2:Ce and the excitation band of Ca3SiO4Cl2:Eu, and hues vary systematically from blue to green at different Ce concentrations. A great improvement in the luminescent property of Ca3SiO4Cl2:Eu has been observed on Ce3+ doping, which is attributed to energy transfer from Ce3+ to Eu2+ and an increase in the number of luminescent centers (Eu2+) on Ce doping. The optimal sample has a quantum efficiency of up to 75%, and can be an efficient green phosphor for white LEDs. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
4.
Hui Wang Lingling Wang Meihua Wu Minghao Fang Zhaohui Huang Xin Min 《Luminescence》2023,38(2):208-215
This paper reports a sequence of a Ca3YAl3B4O15:xEu3+ red phosphor prepared using a high-temperature solid-state reaction. At the excitation of 396 nm, the samples emitted intense red emission centred at ~623 nm, which could be attributed to the 5D0→7F2 transition of the Eu3+ ion. The results showed that the optimum Eu3+ doping concentration of Ca3YAl3B4O15:Eu3+ phosphor was x = 80 mol%, and the concentration quenching mechanism of Ca3YAl3B4O15:Eu3+ red phosphor belonged to the exchange coupling between Eu3+ ions. The Commission Internationale de l'éclairage (CIE) coordinates and colour purity of Ca3Y0.2Al3B4O15:0.8Eu3+ were calculated as (0.6375, 0.3476) and 95.5%, respectively. Moreover, the red emission of the obtained phosphor Ca3YAl3B4O15:0.8Eu3+ exhibited a low thermal quenching behaviour with an intensity retention rate of 92.85% at 150°C. The above results manifest that the Eu3+-activated Ca3YAl3B4O15 phosphor is predicted to be a promising red luminescent component for white light-emitting diodes. 相似文献
5.
Summary The NMR shift reagent, Europium(III)-tris-(1,1,1,2,2,3,3)-heptafluoro-7,7-dimethyl-4-6-octanedione [Eu(fod)3], complexes efficiently with-amino acid esters in chloroform. These complexes exhibit characteristic circular dichroism (CD) spectral patterns in the 350-250 nm region. A fast and simple procedure (also in microscale) has been worked out which utilizes the signs of these CD bands for the determination of the absolute configuration at the-carbon atomin situ. In the L-series, a positive CD band is observed at around 310 nm and a negative one in the 290-280 nm region. The CD spectra of the Eu complexes of the D-isomers are mirror images of those of the L-configurations. An empirical rule is proposed.Presented in part at the 2nd International Congress on Amino Acids and Analogues, Vienna, Austria, August 5–9, 1991. 相似文献
6.
Ca3(PO4)2:Eu3+ phosphor preparation with different morphologies and their fluorescence properties
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Ca3(PO4)2:Eu3+ phosphor was prepared using a facile chemistry method in the presence of surfactants. The effects of surfactants on the morphology and photoluminescence properties of Ca3(PO4)2:Eu3+ phosphor were investigated. The morphology of the phosphor was significantly influenced by the surfactants employed. When nonionic surfactant glyceryl monostearate and anionic surfactant sodium dodecylbenzene sulfonate were employed, the phospor powders are composed of a large number of homogeneous spherical particles with sizes of 0.3–0.6 µm and 2–3 µm, respectively. By contrast, when cationic surfactant cetyltrimethylammonium bromide was used, the morphology of the phosphor is completely different. The product is an excellent cuboid, and the phosphor prepared with 2.5 mmol cetyltrimethylammonium bromide showed higher luminescent intensity than phosphors prepared with the other two types of surfactants. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
7.
The protonation constants of 1,3,5-trideoxy-1,3,5-tris(2-hydroxyl-benzyl)amino-cis-inositol (thci) in I = 1 M (NaClO4) were determined to be: pKa1 5.96 ± 0.03, pKa2 7.21 ± 0.01, pKa3 8.32 ± 0.07, pKa4 8.95 ± 0.06. The solvent extraction studies were consistent with the formation of the Ln(thci)3+ and complexes. The log of the stability constants (log β1 and log β2) at 25 °C in 1 M (NaClO4) at pH 4 for formation of these complexes are reported. Laser luminescence measurements of the 7F0-5D0 transition of Eu(III) complexed by thci indicated two species. The shifts in the peaks relative to that of Eu(aq)3+ were comparable to the values reported for other complexes of Eu(III) with organic ligands, but the intensities were greater. Luminescence lifetime measurements of the fluorescence spectra indicated that the complex has 5 inner sphere water molecules bound to the Eu(III) cation at pH 6.71-8.52. This was consistent with bidentate chelation of Eu(III) with each thci molecule. gaussian view energy calculations indicated bonding for M(III) to the amino and hydroxyl groups of the cyclohexanetriol and (2-hydroxybenzyl)amino moieties in the Ln(thci)3+ complex. 相似文献
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9.
Thyroid-hormone effects on putative biochemical pathways involved in UCP3 activation in rat skeletal muscle mitochondria 总被引:2,自引:0,他引:2
Silvestri E Moreno M Lombardi A Ragni M de Lange P Alexson SE Lanni A Goglia F 《FEBS letters》2005,579(7):1639-1645
In vitro, uncoupling protein 3 (UCP3)-mediated uncoupling requires cofactors [e.g., superoxides, coenzyme Q (CoQ) and fatty acids (FA)] or their derivatives, but it is not yet clear whether or how such activators interact with each other under given physiological or pathophysiological conditions. Since triiodothyronine (T3) stimulates lipid metabolism, UCP3 expression and mitochondrial uncoupling, we examined its effects on some biochemical pathways that may underlie UCP3-mediated uncoupling. T3-treated rats (Hyper) showed increased mitochondrial lipid-oxidation rates, increased expression and activity of enzymes involved in lipid handling and increased mitochondrial superoxide production and CoQ levels. Despite the higher mitochondrial superoxide production in Hyper, euthyroid and hyperthyroid mitochondria showed no differences in proton-conductance when FA were chelated by bovine serum albumin. However, mitochondria from Hyper showed a palmitoyl-carnitine-induced and GDP-inhibited increased proton-conductance in the presence of carboxyatractylate. We suggest that T3 stimulates the UCP3 activity in vivo by affecting the complex network of biochemical pathways underlying the UCP3 activation. 相似文献
10.
We have studied the fluorescence of Mg-Al-Eu ternary layered hydroxides (TLH) quenched by tryptophan (Trp). IR spectroscopy was used to evaluate the change of Trp structure which was caused by TLH. XRD and TG-DTA results further suggested a structural change of Trp after being reacted with TLH. XPS characterization confirmed a strong chemical reaction between Trp and TLH. These studies may present more direct evidence to explain the interrelation between the structural change of Trp and the fluorescent quenching of TLH. 相似文献