SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2023
·
IF 4.4
Jie Fu,Yanling Chen,Jianhua Lin,Renguang Ye,Lei Lei,Yang Shen,Degang Deng,Shiqing Xu
Bi 3+ , Eu 3+ co-doped Ba 2 Y 2 Si 4 O 13 phosphors with multi-color luminescence properties were prepared by high temperature solid state method. The structure, luminescent properties and temperature characteristics were studied by X-ray diffraction, scanning electron microscope, fluorescence spectrum and temperature-dependence of emission spectrum. Ba 2 Y 2 Si 4 O 13 : Bi 3+ , Eu 3+ phosphors can emit color from cyan to red when the excitation wavelength was changed from 340 nm to 390 nm, which is attributed to that there are two Bi 3+ ion emission centers, and their emission intensity will change with the change of excitation wavelength. Moreover, the emission of the phosphor has good temperature sensing characteristics, based on the fluorescence intensity ratio of the two blue emission bands of Bi 3+ and the red emission peak of Eu 3+ , a multimode thermometer with high temperature sensitivity was constructed. At the same time, based on the dynamic luminescence characteristics of the phosphor, the dynamic anti-counterfeiting experiments are designed. Therefore, the results show that the material has a bright prospect in the field of temperature sensing and anti-counterfeiting.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2019
·Vol. 43
·期 21
·8315-8324
·
IF 3.069
Hui Yang,Rui Wang,Yaozu Wang,Jianzhong Jiang,Xingzhong Guo
Macroporous europium-doped Ca12Al14O33 (C12A7:Eu3+) was prepared via a sol–gel method followed by heat-treatment, and the crystal structure, luminescence performance and metal ion luminescence sensing of C12A7:Eu3+ were investigated and evaluated in detail. The process of the sol–gel method and heat-treatment promotes the formation of a single mayenite phase C12A7:Eu3+, and the Eu3+ ions are incorporated into the crystal lattice and replace the position of the Ca2+ ions without destroying the lattice structure of C12A7. The interconnected macropores not only increase the lighting area but also reduce the concentration quenching effect, leading to a significant enhance of luminescence intensity. The resultant macroporous C12A7:Eu3+ can be used as a luminescence performance sensor and displays the potential practical application for metal ion detection. The macroporous C12A7:Eu3+ sensor has a good response to Pb2+ ions, whose linear equation between concentration (CPb) and luminescence intensity (F) of (F0 − F)/F0 = 1.412 + 0.3428 log10(CPb) can be obtained.
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DALTON TRANSACTIONS
·
2018
·Vol. 47
·期 46
·16696-16703
·
IF 4.099
Lifei Xu,Yan Xu,Xianliang Li,Zhuopeng Wang,Ting Sun,Xia Zhang
The rational design strategy to construct lanthanide ion functionalized metal organic frameworks (MOFs) has attracted tremendous attention as they are promising candidates for developing novel luminescence materials and optical sensors owing to their intense, long-lived and tunable luminescence performances. In this work, a series of Eu3+/Tb3+ singly doped or codoped bismuth-based MOFs were prepared under in situ facile solvothermal conditions using BiOBr nanoplates as bismuth resources. A red-green-blue-based trichromatic white-light emission can be finely achieved by modulating the doping ratio of Eu3+/Tb3+ in the blue-emitting Bi-MOF host material and such photoluminescence tuning can also be realized by controlling the excitation wavelength. In addition, the Eu3+/Tb3+ singly incorporated Bi-MOF can serve as a multifunctional fluorescent probe for sensing Fe3+ and Cr2O72− ions in aqueous solution, as well as small organic pollutants of acetone molecules, and their sensing mechanisms have also been analyzed. These lanthanide ion functionalized Bi-MOF materials exhibit great potential in exploring white-light emitting devices and construction of supersensitive multifunctional sensors.
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Journal of the Taiwan Institute of Chemical Engineers
·
2017
·
IF 4.217
Long Huang,Weihua Luo,Meiying Liu,Jianwen Tian,Qiang Huang,Hongye Huang,Junfeng Hui,Yuanqing Wen,Xiaoyong Zhang,Yen Wei
The luminescent hydroxyapatite nanorods co-doped with Eu 3+ and F − (named as FAp:Eu 3+ ) were synthesized through liquid-solid-solution strategy to control their size and morphology as well as improve their fluorescence. However, these luminescent FAp:Eu 3+ nanorods are hydrophobic nature and cannot be directly used for biomedical applications. In this work, we developed a novel strategy for surface modification of FAp:Eu 3+ nanorods with the combination of the surface ligand exchange reaction and photo-initiated reversible addition-fragmentation chain transfer (photo-RAFT) polymerization using the biocompatible and hydrophilic poly(ethylene glycol) methacrylate (PEGMA) as the monomer. We demonstrated that the photo-RAFT polymerization is a facile and efficient route to fabricate hydrophilic FAp:Eu 3+ -polyPEGMA composites based on a series of characterization techniques. The FAp:Eu 3+ -polyPEGMA composites still well maintained the morphology and luminescent properties. Furthermore, the resultant FAp:Eu 3+ -polyPEGMA composites showed low cytotoxicity and desirable cell uptake behavior. These features suggested that the FAp:Eu 3+ -polyPEGMA composites are of great potential for biological imaging applications. More importantly, the photo-RAFT polymerization should be promising for preparation of many other luminescent nanocomposites owing to their advantages of photo-RAFT polymerization such as low polymerization temperature, high efficiency, absence of metal catalysts and good monomer applicability. It is therefore, the photo-RAFT could be extended for fabrication of many other multifunctional fluorescent composites for different biomedical applications.
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NEW JOURNAL OF CHEMISTRY
·
2017
·Vol. 41
·期 24
·15187-15194
·
IF 3.269
Jing Wu,Yue Xing,Huan Wang,Hongjing Liu,Mei Yang,Jingli Yuan
Although molecular luminescent probes capable of detecting target analytes in an organelle of interest are especially appreciated, lanthanide complex-based organelle-targetable luminescent probes have rarely been developed. Herein, by using an anthryl-substituted terpyridine derivative, 4′-(9-anthryl)-2,2′:6′,2′′-terpyridine (ATPY), as a singlet oxygen (1O2)-recognition ligand, and a diphenyl-containing β-diketone coligand, 6-(1′,1′′-diphenyl-4′-yl)-1,1,1,2,2,3,3-heptafluoro-4,6-hexanedione (DHH), a new β-diketonate–Eu3+ complex-based luminescent probe, Eu(DHH)3(ATPY), has been designed and synthesized for the time-gated luminescence imaging detection of 1O2 in the mitochondria of living cells. The probe showed only weak luminescence due to the quenching effect of the 9-anthryl group. After the specific reaction of the 9-anthryl group with 1O2, the corresponding endoperoxide derivative that exhibited great quantum yield (Φ = 53%), Eu(DHH)3(EP-ATPY), was formed, accompanied by a remarkable luminescence enhancement. The luminescence response behaviors of Eu(DHH)3(ATPY) to 1O2 were investigated using two different 1O2 reaction systems in aqueous media. In addition, the time-gated luminescence imaging study has demonstrated the applicability of the probe for monitoring the 1O2 generation in 5-aminolevulinic acid (a drug for photodynamic therapy) loaded HepG2 cells with high sensitivity and selectivity. Furthermore, by coloading the probe and a mitochondrial indicator, Mito-Tracker Green, into HepG2 cells, the mitochondria-targetable feature of the probe has also been confirmed by confocal luminescence imaging measurements.
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Materials Today Chemistry
·
2024
·
IF 6.7
Hanyu Xu,Yanling Wei,Rong Wang,Guiying Liang,Tianqi Sheng,Zuoling Fu
The cesium-based fluoride Cs 3 YF 6 has increasingly attracted curiosity due to its potential in up-conversion luminescence applications, signifying a possible revolutionary change in the next generation of lanthanide-doped luminescent functional materials. However, the nature of the photoluminescence process involving Cs 3 YF 6 has still not been studied in detail. Developing Cs 3 YF 6 luminescence applications is an intricate endeavor. Herein, we present the optimal doping concentration required for Eu 3+ and Tb 3+ doping in Cs 3 YF 6 . Meanwhile, by spectra analyses and theoretical model simulations, we have been able to decipher the intricacies of the energy transfer interaction that transpires between Tb 3+ and Eu 3+ ions. Furthermore, a water-sensitive fluorescence response system tailored for anti-counterfeiting applications was designed, which relied on the superior luminescence characteristics of Cs 3 YF 6 doped with Tb 3+ /Eu 3+ under excitation at 254 nm, whilst simultaneously exploiting the easily deliquescent nature of Cs 3 YF 6 . This work not only enhances the understanding of Cs 3 YF 6 materials in the field of rare-earth luminescence but also introduces a novel anti-counterfeiting strategy, that propels the development of applications for rare-earth-doped fluoride materials.
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OPTICAL MATERIALS
·
2015
·
IF 1.981
Wenjun Zhang,Haiyan Wang
A novel precursor PMA–Si was synthesized by modifying 1,2,4,5-benzene-tetracarboxylic acid (PMA) with 3-aminopropyltriethoxysilane (APTES). Then the hybrids were prepared by PMA–Si coordinating to lanthanide ions (Eu 3+ and Tb 3+ ) in sol–gel process. In order to improve luminescent efficiency, 1,10-Phenanthroline (Phen) was introduced to the system as the second ligand. As-prepared compounds in sol condition were coated on quartz plates to form a layer of thin film, which was different from other similar hybrids. The properties of the hybrids were characterized by FT-IR, fluorescence spectra, TG and SEM. The results showed that the obtained materials enhanced thermal stability, mechanical resistances, waterproofness as well as machining properties.
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ACS Sustainable Chemistry & Engineering
·
2017
·
IF 5.951
Wentao Gan,Shaoliang Xiao,Likun Gao,Runan Gao,Jian Li,Xianxu Zhan
Natural wood is functionalized using the index matching poly(methyl methacrylate) (PMMA) and luminescent γ-Fe2O3@YVO4:Eu3+ nanoparticles to form a novel type of luminescent and transparent wood composite. First, the delignified wood template was obtained from natural wood through a lignin removal process, which can be used as a support for transparent polymer and phosphor nanoparticles. Then, the functionalization occurs in the lumen of wood, which benefits from PMMA that fills the cell lumen and enhances cellulose nanofiber interaction, leading to wood composites with excellent thermal properties, dimensional stability, and mechanical properties. More importantly, this wood composite displays a high optical transmittance in a broad wavelength range between 350 and 800 nm, magnetic responsiveness, and brightly colored photoluminescence under UV excitation at 254 nm. The unique properties and green nature of the luminescent wood composite have great potential in applications including green LED lighting equipment, luminescent magnetic switches, and anti-counterfeiting facilities.
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RSC Advances
·
2017
·Vol. 7
·期 87
·55489-55495
·
IF 3.108
Yumei Bu,Bin Cui,Weiwei Zhao,Zhenfeng Yang
A carrier possessing simple structure and composition, but with microwave-targeted-fluorescence multifunctional properties to precisely control the delivery of the drug was prepared. Herein, we have constructed the multifunctional Fe3O4@ZnAl2O4:Eu3+@mSiO2–APTES core–shell drug-carrier via direct precipitation method and sol–gel process with surfactant-assistance approach. This carrier is a monodisperse microsphere with an average particle size of 325 nm. Fe3O4 in the core has a high saturation magnetization and provides the Fe3O4@ZnAl2O4:Eu3+@mSiO2–APTES with good drug targeting properties. The ZnAl2O4:Eu3+ interlayer has the characteristic of fluorescent luminescence and can be used to monitor the transport of drugs in the body in real time. In addition, the ZnAl2O4:Eu3+ as a dielectric loss microwave absorbing material combines with the high magnetic loss Fe3O4 to form a composite material, which improved the microwave thermal response. Over 78.2% of VP16 molecules were released under microwave trigger. In addition, mesoporous silica nanoparticles in the outer layer improve the drug loading efficiency through organic modification. The results indicated that this multifunctional drug-carrier with simple structure and composition is a potential controlled drug delivery system in cancer therapy.
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JOURNAL OF APPLIED PHYSICS
·
2014
·Vol. 115
·期 4
·
IF 2.185
Wang Pei,He Duanwei,Xu Chao,Ren Xiangting,Lei Li,Wang Shanmin,Peng Fang,Yan Xiaozhi,Liu Dongqiong,Wang Qiming,Xiong Lun,Liu Jing
Angle-dispersive synchrotron X-ray diffraction measurements were performed on vaterite-type YBO 3 /Eu 3+ , GdBO 3 , and EuBO 3 , respectively, up to 41 GPa at room temperature using a diamond-anvil cell. Pressure-induced amorphization was observed in hexagonal GdBO 3 with a significant compression along the c -axis. Compared to the ions of the distorted GdBO 3 phase, its anions may lose their long-range order prior to the cations at high pressures. Based on the experimental pressure-volume data, the obtained bulk moduli of YBO 3 /Eu 3+ and GdBO 3 are 329 and 321 GPa, respectively, which are more than 90% larger than that of EuBO 3 (167 GPa) and are presumably attributed to Gd 3+ and Y 3+ with a high density of d valence electrons.
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PHOTOCHEMISTRY AND PHOTOBIOLOGY
·
2014
·Vol. 90
·期 6
·1462-1466
·
IF 2.684
Ying Mei,Bing Yan
A special multifunctional ionic liquid compound (1-methyl-3-(2-(thiocarboxyoxy)-ethyl)-2H-imidazole-1,3-diium bromide (SHIL)) is used as the chemical bridge to link lanthanide beta-diketonates and polymer resin, which are designated as Ln(L) 4 -SHIL-WR/MR (Ln = Eu, Tb, Sm; L = thenoyltrifluoroacetonate (TTA), acetylacetonate (AA), dibenzoylmethane (DBM); WR = Wang resin, MR = Merrifield resin). Among SHIL and polymer resin are assembled to form covalently bonded system through condensation reaction. Then tetrakis lanthanide beta-diketonates are linked to SHIL through ion-exchange reaction. Physical characterization and especially the photoluminescent performance of the multicomponent hybrids are studied. The hybrid materials possess good stability and excellent luminescent property. The results provide useful path to obtain luminescent hybrids for further practical application.
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LANGMUIR
·
2014
·
IF 4.384
Jun Liu,Xiumei Tian,Ningqi Luo,Chuan Yang,Jun Xiao,Yuanzhi Shao,Xiaoming Chen,Guowei Yang,Dihu Chen,Li Li
Monoclinic Gd2O3:Eu3+ nanoparticles (NPs) possess favorable magnetic and optical properties for biomedical application. However, how to obtain small enough NPs still remains a challenge. Here we combined the standard solid-state reaction with the laser ablation in liquids (LAL) technique to fabricate sub-10 nm monoclinic Gd2O3:Eu3+ NPs and explained their formation mechanism. The obtained Gd2O3:Eu3+ NPs exhibit bright red fluorescence emission and can be successfully used as fluorescence probe for cells imaging. In vitro and in vivo magnetic resonance imaging (MRI) studies show that the product can also serve as MRI good contrast agent. Then, we systematically investigated the nanotoxicity including cell viability, apoptosis in vitro, as well as the immunotoxicity and pharmacokinetics assays in vivo. This investigation provides a platform for the fabrication of ultrafine monoclinic Gd2O3:Eu3+ NPs and evaluation of their efficiency and safety in preclinical application.
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