FOOD CHEMISTRY
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2024
·
IF 8.5
Yin-Xia Sun,Bo-Tao Ji,Jiang-Hai Chen,Lu-Lu Gao,Yu Sun,Zhe-Peng Deng,Biao Zhao,Jin-Guo Li
Diquat (DQ) is a typical bipyridine herbicide widely used to control weeds in fields and orchards. The severe toxicity of diquat poses a serious threat to the environment and human health. Metal-organic frameworks (MOFs) have received widespread attention due to their unique physical and chemical properties and applications in the detection of toxic and harmful substances. In this work, a two-dimensional (2D) Tb(III) functionalized MOF Tb(III)@ 1 ( 1 = [Cd(HTATB)(bimb)] n ·H 2 O (Cd-MOF), H 3 TATB = 4,4′,4″-triazine-2,4,6-tribenzoicacid, bimb = 1,4-bis((1H-imidazol-1-yl)methyl)benzene) has been prepared and characterized. Tb(III)@ 1 has excellent optical properties and high water and chemical stability. After the Tb(III) is fixed by the uncoordinated -COO- in the 1 framework, Tb(III)@ 1 emits the typical green fluorescence of the lanthanide ion Tb(III) through the “antenna effect”. It is worth noting that Tb(III)@ 1 can be used as a dual emission fluorescence chemical sensor for the ratio fluorescence detection of pesticide DQ, exhibiting a relatively low detection limit of 0.06 nM and a wide detection range of 0–50 nM. After the addition of DQ, a rapid color change of Tb(III)@ 1 fluorescence from green to blue was observed due to the combined effects of IFE, FRET and dynamic quenching. Therefore, a simple test paper box has been designed for direct on-site determination of pesticide DQ. In addition, the developed sensor has been successfully applied to the detection of DQ in real samples (fruits a Yin-Xia Sun and Bo-Tao Ji contributed equally to this work and should be considered co-first authors.nd vegetables) with satisfactory results. The results indicate that the probe developed in this study has broad application prospects in both real sample detection and actual on-site testing.
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INORGANIC CHEMISTRY
·
2019
·
IF 4.85
Xiao Zhou,Hongwei Wang,Sha Jiang,Guotao Xiang,Xiao Tang,Xiaobing Luo,Li Li,Xianju Zhou
A series of lanthanide organic complexes, namely, [Ln2PDC3(H2O)3]H2O (Ln = Eu, Tb, EuxTb2–x, H2PDC: pyridine-3,5-dicarboxylic acid), were synthesized via hydrothermal method. Eu-PDC was characterized by single-crystal X-ray diffraction. The powder X-ray diffraction, Fourier transform infrared spectra, and thermogravimetric analysis illustrate that Eu-PDC, Tb-PDC, and EuxTb2–x-PDC complexes are isostructural. All the complexes exhibit strong emission even though water molecules coordinated in the structure. Tunable emission color from green, yellow to red is realized by adjusting the Eu/Tb ratio in mixed EuxTb2–x-PDC complexes. Energy transfer from Tb3+ to Eu3+ is discussed in detail via fluorescence decay and time resolution spectra. The detailed energy transfer process sees that the emitting color of Eu0.15Tb1.85-PDC shifts from green to orange in a time interval of 153–790 μs. In addition, temperature-dependent emission of the Eu0.05Tb1.95-PDC complex indicates that it is a potential solid state material for a luminescence thermometer in the range of 293–333 K. The temperature resolution is less than 0.16 K. The optical properties of the EuTb-PDC complex indicate that it is a multifunctional luminescent material with promising applications in temperature sensing, time resolution imaging, lighting, and displaying.
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INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Chengyu Ni,Chunyu Li,Zihao Xu,Wubin Dai
(Co)doping luminescent center(s) in a host is a universal strategy to photoluminescence (PL) modulations for extensive applications, yet its mechanism and interactions between structure and behavior in many phosphors remain ambiguous. Herein, via a facile sol–gel reaction method, differently tendentious occupations of Ce3+ in distinct crystallographic sites of K3YSi2O7 (KYS) lead to tunable PL in between blue and bluish-green under diverse excitations with high quantum efficiency. The generation of wide trap energy levels originating from heterovalent substitution Tb3+ → K+ could entrust Tb3+ as both PL and long-persistent PL (LPL) centers in green. Due to temperature-dependent filling/releasing rates of captured carriers, strong thermal-induced LPL could be obtained in KYS: Tb. By codoping Ce/Tb in KYS, multimode anticounterfeiting and information storage/encryption of KYS: Ce/Tb are realized with high security level via a screen printing technique. Because Ce and Tb possess different temperature-dependent quenching behaviors, optical temperature sensing is achieved with high absolute/relative sensitivity. To further enhance the KYS: Ce/Tb performance, trap depth engineering via equivalent substitution Gd → Y is further executed. The colorimetric/photometric analyses here provide new insights into designing novel stable and single-phased phosphor for applications in advanced anticounterfeiting technology and optical thermometry.
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Materials Science & Engineering C-Materials for Biological Applications
·
2018
·
IF 5.08
Chunning Heng,Xin Zhou,Xiaoyan Zheng,Meiying Liu,Yuanqing Wen,Hongye Huang,Daidi Fan,Junfeng Hui,Xiaoyong Zhang,Yen Wei
Rare-earth ions doped hydroxyapatite nanoparticles (HAp:Ln NPs) have demonstrated to be very promising candidates for biological imaging applications owing to their small size and chemical compositions similar to bone. However, these HAp:Ln NPs with controllable size and morphology should be prepared under hydrothermal treatment with hydrophobic molecules as the protective layers. The hydrophobic nature of these luminescent HAp:Ln NPs largely impeded their applications in biomedical fields. In this study, a novel and effective strategy has been developed for the surface modification of HAp:Ln nanorods through the combination of surface ligand exchange reaction and reversible-addition fragmentation chain transfer (RAFT) polymerization using 2-methacryloyloxyethyl phosphorylcholine (MPC) and itaconic acid (IA) as the monomers. Herein, a small molecule adenosine 5′-monophosphate disodium salt (AMP) that contains a phosphate group and two hydroxyl groups was used to displace the hydrophobic oleic acid on pristine HAp NPs through surface ligand exchange reaction owing to its stronger interaction with HAp NPs. On the other hand, the MPC and IA were introduced on HAp NPs through RAFT polymerization after the chain transfer agent was immobilized on the HAp NPs through the esterification reaction. The poly(IA-MPC) could not only endow the high water dispersibility but also be used for loading anticancer agent cisplatin (CDDP) through coordination interaction. To evaluate their potential biomedical applications, the cell uptake behavior, drug loading capacity and release behavior as well as cell viability of HAp:Ln-AMP-poly(IA-MPC) polymeric composites were examined. We demonstrated that the method developed in this work is very effective for introduction of functional polymers onto HAp:Ln nanorods. The HAp:Ln-AMP-poly(IA-MPC) composites are promising for cell imaging and controlled delivery of CDDP.
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TALANTA
·
2018
·
IF 4.244
Sobia Niazi,Xiaole Wang,Imran Pasha,Imran Mahmood Khan,Sen Zhao,Muhammad Shoaib,Shijia Wu,Zhouping Wang
Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by fungi on stored grains. The earlier detection methods used for ZEN rely on expensive equipment, time-consuming sample preparation and temperature sensitive antibodies. The current work, proposed a novel strategy based on ZEN aptamer labeled with amine-functionalized magnetic nanoparticle (MNPs) as a capture probe and time-resolved fluorescence (TRFL) nanoparticles labeled with complementary DNA (cDNA) as a signal probe. Under the optimized conditions, TRFL intensity at 544 nm was used to measure ZEN (R 2 = 0.9920) in the range of 0.001–10 ng mL −1 and limits of detection (LOD) for proposed method was 0.21 pg mL −1 . The specificity of bioassay was also determined by using other mycotoxins (OTA, AFB 2 , DON and Patulin) and results showed that the aptamer are specific to recognize only ZEN. The analytical applications of the present bioassay in maize and wheat samples were also examined and results were compared with existing methods. Based on these findings, it is suggested to use current rapid and simple bioassay for the determination of ZEN in food and agricultural products.
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MICROCHIMICA ACTA
·
2015
·Vol. 182
·期 9
·1653-1660
·
IF 3.741
Ge Xiaoqian,Sun Lining,Dang Song,Liu Jinliang,Xu Yanxia,Wei Zuwu,Shi Liyi,Zhang Hongjie
A new multifunctional nanocomposite is described that displays both upconversion and downconversion luminescence. It is based on upconversion nanoparticles (UCNPs) with a mesoporous coating that is boned with a terbium(III) complex. The modified mesoporous nanocomposite was characterized by transmission electron microscopy, X-ray powder diffraction, nitrogen adsorption-desorption isotherms, and photoluminescence spectra. They display dual (green and red) fluorescence under 980-nm excitation, and green fluorescence under 365-nm excitation. Both emissions can be easily detected by bare eyes. The material has low cytotoxicity and good biocompatibility as proven by the methyl thiazolyltetrazolium (MTT) assay. The nanocomposite was successfully applied to upconversion luminescence based in-vitro confocal imaging of the cytosol of murine macrophage cells (RAW264.7), and this resulted in images of excellent contrast. In addition, the particles display strongly temperature-dependent luminescence in the range from 280 K to 330 K.
A new multifunctional nanocomposite was designed and prepared with dual green luminescence based on the upconversion and downconversion emission for in vitro bioimaging and temperature sensing
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MICROCHIMICA ACTA
·
2024
·Vol. 192
·期 1
·1-12
·
IF 5.3
Liu Xiang,Li Huijun,Sun Junjun,Shi Jianchao,Xu Zhouqing,Wang Yan
A HPU-23@Ru@Tb-NH 2 sensor array with light-driven oxidase-mimicking activity and triple-emission fluorescence was developed. It was composed of a Tb 3+ -functionalized metal organic framework and Ru(bpy) 3 2+ and applied to the simultaneous detection of Hg 2+ , ClO − , and PO 4 3− via differently responsive channels. HPU-23@Ru@Tb-NH 2 had a photoresponsive colorimetric response toward Hg 2+ with a LOD as low as 4.18 nM. In addition, the three emissions of the HPU-23@Ru@Tb-NH 2 sensor array were influenced by ClO − and PO 4 3− to varying degrees, causing remarkably distinguishable responses for the fluorescence channels to discriminate ClO − and PO 4 3− from each other. The detection limits of ClO − and PO 4 3− were 12.26 µM and 0.197 nM, respectively. Therefore, this work demonstrates the feasibility of multi-emission and multi-mode sensing platform, which is able to combine the advantages of different strategies for solving the problems of various toxic substances coexisting in the environment while meeting the needs of accurate and precise results and no side interferences. Graphical
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2019
·Vol. 411
·期 7
·1453-1465
·
IF 3.286
Niazi Sobia,Khan Imran Mahmood,Yan Lv,Khan Muhammad Issa,Mohsin Ali,Duan Nuo,Wu Shijia,Wang Zhouping
A rapid and highly sensitive time-resolved fluorescence (TRF)-based aptasensor for simultaneous recognition of mycotoxins ochratoxin A (OTA) and fumonisin B 1 (FB 1 ) was developed using multi-color, Ln 3+ -doped time-resolved fluorescence nanoparticles (TRF-NPs) (NaYF 4 : Ce, Tb and NH 2 -Eu/DPA@SiO 2 NPs) coupled with complementary strand DNA (cDNA) as luminescence probe and aptamers-conjugated amine-functionalized Fe 3 O 4 magnetic nanoparticles (MNPs) act as a capture probe. Under the optimized conditions, the time-resolved fluorescence intensities at 544 and 618 nm corresponded with Tb 3+ and Eu 3+ , respectively, were used to measure FB 1 ( Y = 19,177.1 + (− 12,054.4) x , R 2 = 0.9917) and OTA ( Y = 4138.8 + (− 11,182.6) x , R 2 = 0.9924), respectively. The limits of detection (LODs) for FB 1 and OTA were 0.019 pg mL −1 and 0.015 pg mL −1 , respectively, which were much lower than previously described methods for simultaneous recognition of mycotoxins OTA and FB 1 while detection range varied from 0.0001–0.5 ng mL −1 . This aptasensor was effectively applied to quantity FB 1 and OTA in maize samples and results were compared with ELISA method. This is the first reported time-resolved fluorescence (TRF)-based aptasensor to detect two agriculturally important toxins in the maize. The developed aptasensor has potential to be used for detection of toxins in food safety fields.
Graphical abstract
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Yong Xu,Yue Wang,Ping Wang,Yishun Wang,Weili Dai,Jianping Zou,Xubiao Luo
Employing electric energy to convert carbon dioxide (CO 2 ) into valuable small molecules is a potentially practical method in energy storage and greenhouse gas alleviation. A huge challenge for electrocatalytic CO 2 reduction is to reduce overpotential to improve energy efficiency. Herein, we demonstrate that doping alloy Pd 49 Ag 30 Te 4 (PAT) with rare-earth element Tb is beneficial for selective exposure of (1 1 1) crystal plane, which is a highly active crystal plane for producing carbon monoxide (CO). The as-prepared Tb 2.9 PAT exhibited high electrocatalytic performance with 95.7 % CO faradic efficiency at − 0.8 V (vs RHE), far exceeding that of PAT, and coupled with good durability. In situ spectral study and theoretical calculations disclose that the introduction of Tb regulates the d-band center of PAT alloy, weakens the Pd − C bonding ability, and promotes the desorption of *CO in the rate-determining step. This study provides a method for doping induced selective exposure of crystal face, which provides new idea for improving catalytic performance.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Tianshuai Lyu,Pieter Dorenbos,Zhanhua Wei
Developing X-ray charged dosimeters with excellent charge carrier storage capacity and stability is challenging. Such energy storage dosimeters have fascinating use in developing novel applications, for instance, in radiation detection, advanced multimode anti-counterfeiting, and flexible X-ray imaging of curved objects. Herein, novel LiTaO 3 :Ln 3+ ,Eu 3+ (Ln = Tb or Pr) perovskite dosimeters are reported by combining the vacuum referred binding energy (VRBE) diagram of LiTaO 3 and the optimization of dopant’s concentration and compound synthesis condition. Based on the VRBE diagram prediction, charge carrier capturing and de-trapping processes in Eu 3+ and/or Ln 3+ (Ln = Tb or Pr) doped LiTaO 3 will be studied to unravel the role of Eu 3+ as a good electron trapping centre and to discover a record storage phosphor. The ratios of the thermoluminescence intensity of the optimized LiTaO 3 :0.005Tb 3+ ,0.001Eu 3+ to that of the state-of-the-art BaFBr(I):Eu 2+ , Al 2 O 3 :C, or NaLuF 4 :Tb 3+ are 5.2, 8.8, or 2.8, respectively. The charge carriers can be stored more than 1000 h in LiTaO 3 :0.005Tb 3+ ,0.001Eu 3+ . Proof-of-concept anti-counterfeiting application will be demonstrated by combining the colour-tailorable photoluminescence, afterglow, thermally, or optically stimulated luminescence in LiTaO 3 :0.005Tb 3+ ,xEu 3+ and LiTaO 3 :0.005Pr 3+ ,0.001Eu 3+ . Multimode anti-counterfeiting application will be proposed by combining a high absolute X-ray scintillation light yield of 19000 ± 1800 ph/MeV of LiTaO 3 :0.005Tb 3+ ,0.001Eu 3+ . Proof-of-concept flexible X-ray imaging application will be demonstrated by using the optimized LiTaO 3 :0.005Tb 3+ , 0.001Eu 3+ dispersed in a silicone gel film.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2023
·
IF 4.4
Chengxiang Chu,Xianfeng Wang,Yuanyi Deng,Yi Ma,Chengyue Zou,Mei Yang,Huibo Luo,Danqun Huo,Changjun Hou
A facile and rapid fluorescence sensor array based on Tb (III) and Eu (III) doped Zr (IV) metal–organic frameworks was proposed for Chinese green tea discrimination. According to large porosity of Tb@UiO-66-(COOH) 2 and Eu@UiO-66-(COOH) 2 , phenolic hydroxyl groups of tea polyphenols could coordinate with free carboxylic acid groups and was captured into the pores, which led to the disturbance of electronic structure of ligand and inhibited the energy transfer efficiency from ligand to Tb (III) and Eu (III) center, causing the fluorescence quenching effect. Based on Hierarchy Cluster Analysis and Linear Discrimination Analysis, the fluorescence sensor array was employed for successful tea polyphenols classification through the analysis of different fluorescence quenching effect to tea polyphenols. Green tea samples within different categories and grades were also successfully discriminated using this assay according to tea polyphenols, providing a new method for Chinese green tea identification.
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Materials
·
2023
·Vol. 16
·期 20
·6667
·
IF 3.4
Yukun Li,Svenja Hanson,Cheng Heng Pang,Peng Lyu,Jun Jiang
In order to attain phosphor ceramics with a high Color-Rendering Index (CRI), samples with the composition of Y0.997−xRexCe0.003)3(Al0.9748Mn2+0.024Cr3+0.0012)5O12(Rex= 0, Gd0.333, Gd0.666, Gd0.997, Tb0.333, Tb0.666, Tb0.997and Lu0.997were prepared by solid-state reaction and vacuum sintering, and exhibited potential for high-quality, solid-state lighting. Doping with Cr3+and Mn2+effectively enhanced the red component of Ce3+spectra through the intense energy transfer from Ce3+ions to Mn2+/Cr3+ions. The crystal field splitting of [GdO8] and [TbO8] was more extensive than that of [YO8], causing a massive redshift in the Ce3+emission peaks from 542 to 561 and 595 nm, while [LuO8] had an opposite effect and caused a blueshift with a peak position at 512 nm. White LED devices incorporating Ce/Mn/Cr: (Gd0.333Y0.664)3Al5O12phosphor ceramic exhibited a high CRI of 83.97, highlighting the potential for enhancing the red-light component of white LED lighting.Keywords:garnet phosphor;laser lighting;full spectrum;spectral modulation;Ce/Mn/Cr: (Re,Y)3Al5O12
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