Journal of Food Measurement and Characterization
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2025
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IF 3.3
Jie Mingsha,Zhu Amei,Zhu Bing,Guo Ruipeng,Lan Shengkai,He Jiaxin,Lang Xingang,Bai Yanhong
The overuse of antibiotics leads to significant health risks and environmental challenges. Therefore, selective and sensitive detection of antibiotic residues is a critical issue. Here, a double-emission ratiometric fluorescence probe (Lu-Eu-DPA) was constructed for the selective detection of gentamicin sulfate (GEN), neomycin (NEO), and erythromycin (EM). The Lu-Eu-DPA coordination polymer nanoparticles composed of luminol, the coordinated nuclear metal Eu 3+ , and 2,6-pyridinedicarboxylic acid (DPA). The coordination reaction between luminol molecules and Eu 3+ ions produce the aggregation-induced emission (AIE) effect, while DPA acts as a ligand for the antenna, absorbing energy from the excitation light and then transferring the energy to Eu 3+ . Based on the AIE effect and antenna effect (AE), the fluorescence intensity of Lu-Eu-DPA at 426 nm and 617 nm was correlated with the concentration of GEN, NEO, and EM, and the detection limits of GEN, NEO, and EM were 20, 25, and 48 nmol/L, respectively. The detection capability of the proposed method in pork samples was also studied. In addition, semi-quantitative determination of GEN, NEO, and EM was conveniently and efficiently performed using a smartphone-based visualization method. These results suggested that this probe with good selectivity and specificity was a promising method for swiftly detecting multiple antibiotic residues.
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高影响因子
JOURNAL OF FLUORESCENCE
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2011
·Vol. 22
·期 2
·729-736
·
IF 1.966
Li Yan-Yan,Yan Bing,Guo Lei
In this paper, the organic ligands TTA and TAA are grafted onto the coupling agent to achieve the organic precursors (TTA-Si, TAA-Si) as first ligand and the organic 4-(4-nitrostyryl)pyridine (Nspy) is synthesized as the second ligand. Both of them are coordinated to the rare ions with the carbonyl group and nitrogen atom respectively. After the hydrolysis and copolycondensation between the teraethoxysilane (TEOS) and the ternary rare earth organic complex via the sol–gel process, the chemical bonded hybrid materials are constructed and characterized in detail. The obtained hybrid materials present superior thermal stabilities and regular and homogenous square blocks microstructure. Among the hybrids Eu(TTA-Si) 3 Nspy shows a more strong characteristic emission and longer lifetime than the hybrids Eu(TAA-Si) 3 Nspy, while hybrids Tb(TAA-Si) 3 Nspy exhibits the stronger characteristic emission and longer lifetime than the hybrids Tb(TTA-Si) 3 Nspy. For Sm 3+ hybrid materials, the photoluminescence of Sm(TAA-Si) 3 Nspy is too weak to find in the characteristic emission spectra, meanwhile, Sm(TTA-Si) 3 Nspy has the excellent luminescent intensity.
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Inorganic Chemistry Frontiers
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2025
·
IF 6.4
Jiayu Zheng,Longxiao Zhou,Qiufen Liu,Senwei Wu,Yuting Peng,Xiujian Zhao,Shouqin Tian
Ratiometric optical thermometry has emerged as a vital platform for non-contact temperature monitoring in industrial and scientific applications, demanding sensors with high sensitivity, non-invasiveness, and spatial resolution. Although zeolitic imidazolate framework-8 (ZIF-8) possesses attractive thermal stability and structural tunability, its limited luminescence intensity hinders practical thermometric applications. Meanwhile, ZIF-L, a two-dimensional (2D) polymorph of ZIF-8 with identical ligands, remains unexplored for temperature sensing. Herein, we propose a dual-modulation strategy synergizing lanthanide valence engineering with MOF phase control to develop a multi-emission center Eu3+/Eu2+ co-doped ZIF-L film (Eu/ZIF-L). By introducing Eu3+ into ZIF-8 precursors, the partial reduction of Eu3+ to Eu2+ under thermal treatment triggers a structural evolution from 3D ZIF-8 to 2D ZIF-L. The resultant Eu/ZIF-L exhibits dual emission peaks at 450 nm (Eu2+) and 495 nm (ligand-centered), with their intensity ratio (I495/I450) demonstrating remarkable linear temperature dependence over 296–373 K and achieving a relative sensitivity of 1.95% K−1. This work pioneers the integration of valence-state manipulation and MOF phase transition for thermometric optimization, providing a novel paradigm to design advanced ratiometric MOF thermometers for industrial thermal management.
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Analytical Methods
·
2025
·
IF 2.6
Nanhai Zhang,Deyan Liu,Rui Zhang,Qinghe Song,Guangjun He,Shixing Wang,Libo Zhang
The design and preparation of fluorescent sensors for detecting toxic ions in aqueous environments are of paramount importance. In this study, a europium metal–organic framework (Eu-MOF), constructed from Eu3+, the rigid 2,2′-biphenyldicarboxylic acid (2,2′-H2bpdc) ligand, and the auxiliary 1,10-phenanthroline (Phen) ligand, was synthesized through hydrothermal synthesis. The synthesized Eu-MOF demonstrated remarkable water stability, pH stability, thermal stability, and photostability. It showed a high quantum yield of 42.6%, along with an average fluorescence lifetime of 0.9002 ms, which could enhance its sensitivity when employed as a fluorescent probe. The Eu-MOF could function as a fluorescent probe to quantitatively detect trace amounts of Fe3+, CrO42− and Cr2O72− via fluorescence quenching. Their detection sensitivities are 1.527 × 104 M−1, 1.378 × 104 M−1 and 1.463 × 104 M−1 respectively, with detection limits as low as 0.28 μM, 0.19 μM and 0.09 μM. Additionally, the Eu-MOF sensor exhibited excellent selectivity, anti-interference ability, repeatability (after undergoing five cycles) and practical feasibility. Furthermore, a detailed investigation of its fluorescence properties and sensing mechanisms was carried out. Based on density functional theory calculations, two energy transfer pathways in the process of Eu3+ ion luminescence sensitized by the double ligands 2,2′-H2bpdc and Phen were identified. The fluorescence sensing mechanism of the Eu-MOF for detecting Fe3+, CrO42− and Cr2O72− involved photoinduced electron transfer from the antenna ligand to the organic molecules and competitive absorption of excitation energy. Owing to its high stability and sensitivity, the Eu-MOF holds great potential for practical applications as a sensor for Fe3+, CrO42− and Cr2O72− in aqueous environments.
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INORGANIC CHEMISTRY
·
2023
·
IF 4.6
Dongsheng Zhao,Wenqian Li,Rongmei Wen,Nana Lei,Wencui Li,Xin Liu,Xiutang Zhang,Liming Fan
With the introduction of Eu3+ ions as the secondary fluorescent signal reporter and sensing active sites, a dual-emission ratiometric sensor of Eu3+@NiMOF (Eu3+ functional NiMOF) for hippuric acid (HA) detection in urine and serum was fabricated via the postsynthetic encapsulating strategy. Based on the two emission signals at 441 nm (turn-on) and 628 nm (turn-off), the produced Eu3+@NiMOF ratiometric sensor provided enhanced sensitivity, higher selectivity, and 9.7 times lower limits of detection (LOD) for the detection of HA (2.38 μM, 0.42 μg·mL–1) than that of the pristine NiMOF. Considering the high sensitivity and visualization results, further exploration of intelligent applications in the HA sensing process was carried out by constructing a tandem combinational logic gate to improve the practicability and convenience with the help of a smartphone. This work provides a promising approach for developing MOF-based ratiometric sensors to detect biomarkers.
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JOURNAL OF LUMINESCENCE
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2022
·
IF 4.171
Gen Li,Yaqi Wang,Min Tao,Siqi Chen,Bozhi Zhou,Quan Li,Xin Li,Heming Deng,Hao Huang,Haoshuang Gu,Yuebin Li
Developing efficient strategies to fabricate planar photoluminescence scintillators is of great importance to explore X-ray detectors with new platform. Rare-earth (RE) doped Lu 2 O 3 thin films are successfully fabricated by mild aqueous phase electrochemical deposition on ITO/glass substrates with low-temperature post-annealing treatment. The as-prepared Lu 2 O 3 :RE 3+ (RE = Eu, Tb and Tm) thin films exhibit steerable thickness, high transparency in the visible-NIR range, and low transmittance at UV band mainly due to the oxygen-metal (O 2- -RE 3+ ) charge transfer processes and the 4f-4f transitions of the RE 3+ . The Lu 2 O 3 :RE 3+ thin films emit intense red, green and blue (RGB) photoluminescence, which mainly correspond to the 5 D 0 - 7 F 2 transition of Eu 3+ , 5 D 4 - 7 F 5 transition of Tb 3+ and 1 G 4 - 3 H 6 transition of Tm 3+ respectively. Moreover, the transparent Lu 2 O 3 :RE 3+ thin films also exhibit high sensitivity and linearity luminescence to the X-ray stimulation in a dose rate from 30 to 160 mGy s −1 . This rapid and energy-saving synthesis show high efficiency to fabricate rare-earth doped thin-film with a tunable optical performance for optoelectrical application in the fields of solar light concentrators, agricultural light conversion thin films, biosensors , photodetectors and especially the X-ray detectors.
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Polymers
·
2022
·Vol. 14
·期 17
·3578
·
IF 4.967
Jiawen Chen,Jun Ye,Mingming Zhang,Jian Xiong
The residual acrylamide in food paper packaging can be transferred into water and food, which will cause harmful effects on human beings. In this paper, a rapid and easily available fluorescent probe based on carboxymethyl cellulose (CMC)/Eu (Ⅲ) nanocomposites was designed to detect the residue acrylamide with high sensibility. The probe could respond in 1 min. The concentration of acrylamide was linearly correlated to the fluorescence intensity of the probe at the emission wavelength of 615 nm in the concentration range of 0.1–100 μmol/L. The limit of detection (LOD) of the probe was 0.085 μg/L, which is lower than the guideline value of the European Union, the U.S. EPA, and the WHO. An experiment was performed to simulate the acrylamide migrating from food-contacting paper materials to different foods, including waterborne food, alcohol beverage, acidic food, and greasy food. The recoveries and RSDs of acrylamide in all samples indicated that the CMC/Eu (Ⅲ) fluorescent probe was efficient for acrylamide detection. The possible mechanism of the probe for acrylamide detection involved both dynamically quenching and static quenching by forming of non-fluorescent substances.Keywords:CMC/Eu (Ⅲ);fluorescence probe;acrylamide;food contacting material
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JOURNAL OF LUMINESCENCE
·
2018
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IF 2.732
Wenzhi Wang,Jinkai Li,Zhengyang Zhang,Zongming Liu
The new systems of the (Gd 0.95- x Dy 0.05 Tb x ) 2 (WO 4 ) 3 ( x = 0–0.1) and (Gd 0.95- y Dy 0.05 Eu y ) 2 (WO 4 ) 3 ( y = 0–0.2) phosphors have been successfully obtained using the hydrothermal method at 900 °C in this work. The crystal structure, morphology, PL/PLE spectra, fluorescence and decay analysis have been studied in detail via the combined techniques of XRD , FE-SEM, PLE/PL spectra and decay kinetic. The phase-pure of the (Gd 0.95- x Dy 0.05 Tb x ) 2 (WO 4 ) 3 and (Gd 0.95- y Dy 0.05 Eu y ) 2 (WO 4 ) 3 with good dispersions have been formed at the lower sintering temperature of 900 °C. Under 273 nm and 270 nm excitation (the 6 P 7/2 → 8 S 7/2 transitions of Gd 3+ ), the Gd 2 (WO 4 ) 3 :Dy 3+ /Tb 3+ and Gd 2 (WO 4 ) 3 :Dy 3+ /Eu 3+ phosphors exhibit both Dy 3+ (yellow, at 574 nm) and Tb 3+ (green, at 547 nm) as well as Dy 3+ (yellow, at 574 nm) and Eu 3+ (red, at 616 nm) emissions, respectively. The presences of WO 4 2- , Gd 3+ and Dy 3+ excitation bands on the PLE spectra by monitoring the Tb 3+ and Eu 3+ emissions directly provide an evidence of energy transfer of WO 4 2- →Tb 3+ , Gd 3+ →Tb 3+ and Dy 3+ →Tb 3+ , as well as WO 4 2- →Eu 3+ , Gd 3+ →Eu 3+ and Dy 3+ →Eu 3+ , respectively. The quenching concentrations of both two systems are determined to be 7 at% ( x = 0.07 for Tb 3+ ) and 10 at% ( y = 0.10 for Eu 3+ ), and the quenching mechanisms of both two systems are mainly due to the Tb 3+ -Tb 3+ and Eu 3+ -Eu 3+ energy transfers, respectively. The color-tunable emission can be achieved though adjusting the relative content ratios of Dy 3+ /Tb 3+ or Dy 3+ /Eu 3+ , which has been verified by the CIE chromaticity coordinates analysis. The energy transfer efficiencies of Dy 3+ →Tb 3+ and Dy 3+ →Eu 3+ have been calculated, and the energy transfer mechanisms have been analyzed in detail. The (Gd 0.95- x Dy 0.05 Tb x ) 2 (WO 4 ) 3 and (Gd 0.95- y Dy 0.05 Eu y ) 2 (WO 4 ) 3 phosphors with color-tunable emission may have a potential application for w-LEDs.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Yunchuan Dai,Pengyu Hu,Tingting Chu,Meihong Niu,Haiqiang Shi,Haiming Li,Zhiwei Wang,Yanzhu Guo
As a novel fluorescent carbon nanomaterial, carbon dots are restricted by their poor fluorescence in the solid state, although they exhibit favorable photoluminescence in solution. N-doped carbon dots (N-CDs) and solid-state fluorescence films were prepared using green and renewable cellulose-derived materials, respectively. The hydrogen bonding network of carboxymethyl cellulose (CMC) inhibits the self-aggregation behavior of N-CDs, which leads to solid-state fluorescence. The N-CDs was initially obtained with CMC as the carbon source, which showed excellent blue fluorescence. Subsequently, the white-emitting films (N-CDs@Eu-MOF/CMC) were successfully constructed by combining the blue fluorescent N-CDs with the red fluorescence of the europium metal-organic framework. The prepared films showed stable luminescence within 30 days and in the heat environment at 120 °C for 3 h. After covering the N-CDs@Eu-MOF/CMC films on the UV-LED chip with ultraviolet emissive at 365 nm, the white light-emitting diodes were obtained, which exhibited excellent color characteristics with the color coordinates, a correlated color temperature, and a color rendering index of (0.31, 0.32), 6580 K, and 92, respectively. The strategy proposed in this work will provide ideas for generating optical luminescent films from biomass and provide guidance for solid-state fluorescence biomass materials.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Xiaoping Jiang,Yue Guo,Lixi Wang,Qitu Zhang
Multi-mode dynamic anti-counterfeiting materials can provide complex anti-counterfeiting performance and ensure the anti-counterfeiting strategy becomes more secure. Herein, a new type of multi-mode anti-counterfeiting encryption material of CaAl 12 O 19 :Eu, Er with different Er doping concentration was developed by sol–gel method. Interestingly, the CaAl 12 O 19 :Eu, Er phosphor and its composite have multi-mode anti-counterfeiting characteristics of multi-color down-conversion luminescence, up-conversion luminescence, dynamic luminescence, and photochromism. Effect of different Er doping concentration on the down-conversion luminescence, up-conversion luminescence, dynamic luminescence, and photochromism of CaAl 12 O 19 :Eu, Er was systematically investigated, and the relevant mechanisms were discussed. These anti-counterfeiting features can be simultaneously applied in both bright and dark fields, which can achieve high-level anti-counterfeiting in both spatial and temporal dimensions. The CaAl 12 O 19 :Eu, Er phosphors cannot be easily replaced by other materials with the same anti-counterfeiting properties. They display good application foreground in the field of anti-counterfeiting encryption.
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Materials Today Chemistry
·
2024
·
IF 6.7
Jian Gou,Yousong Hu,Luxin Xing,Jun Xu,Fengzhi Yue,Lina Zhang,Lei Jia
Traditional luminescent materials for anti-counterfeiting usually adopt encryption of low-level systems with limited security, which seriously hinders their application in preventing counterfeiting and information leakage. Therefore, it is urgent to develop materials for higher-level anti-counterfeiting. In this work, a stimulus-responsive intelligent luminescent material (AC@CDs-Eu-MOFs) was prepared by co-loading green-fluorescence CDs and red-fluorescence Eu-MOFs on Amino clay (AC). 5D security barcodes, which were easy to observe while difficult to clone, were ulteriorly designed based on the nanocomposite owing to the tunable fluorescence by optical stimulation and chemical stimulus. Owing to the large capacity, low cost, and easy authentication, the 5D security barcodes possess enormous potential in optical data storage and multi-dimensional information encryption. In addition, the chemical stimulus-response enables the nanocomposite achievable in detection of Cu 2+ and Bacillus anthracis. Particularly, quantitative determination of copper in environmental water samples could be realized with a detection limit as low as 10.67 nM. Therefore, the material shows potential for detection of environmental pollutants besides advanced anti-counterfeiting.
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Foods
·
2022
·Vol. 11
·期 19
·3138
·
IF 5.561
Xiaoyue Yue,Chaoyun Wu,Zijun Zhou,Long Fu,Yanhong Bai
Rapid, facile, and accurate detection of antibiotic residues is vital for practical applications. Herein, we designed a sensitive, visual, and rapid analytical method for sensitive detection of ciprofloxacin and chloramphenicol based on a nanosized rod-shaped Europium metal organic framework (Eu-MOF). The fluorescent Eu-MOF was firstly synthesized by a simple synthetic route at room temperature, which displays a red emission. The mechanisms of detecting ciprofloxacin and chloramphenicol were confirmed to be the inner filter effect (IFE) and photoinduced electron transfer (PET). Under the optimized experimental conditions, the detection limits of the developed method for ciprofloxacin and chloramphenicol detection were 0.0136 and 3.16 μM, respectively. Moreover, the sensor was effectively applied for quantitative determination of ciprofloxacin and chloramphenicol milk samples with satisfactory recoveries of 94.5–102% and 97–110%, respectively. This work developed a new method for rapid detection of ciprofloxacin and chloramphenicol residues. In addition, the established method has potential practical application value for on-site safety regulation on antibiotic residues in animal-derived food.Keywords:fluorescent sensing;antibiotic detection;inner filter effect;photoinduced electron transfer;metal organic framework
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