ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 29
·期 24
·36337-36350
·
IF 5.19
Wang Bing,Cao Qingtong,Li Guomin,Zhang Jian
Given that the biological treatment of antibiotic wastewater can easily induce resistant bacteria, the photocatalytic degradation of antibiotics is considered as a better method for treating antibiotic wastewater. Therefore, the ability to remove Tylosin (TYL) and Tetracycline (TC) in aqueous solution using rare earth element Tb-doped g-C 3 N 4 under simulated natural solar radiation was investigated. A series of rare earth Tb 3+ doped mesoporous g-C 3 N 4 were successfully prepared by nitric acid treatment and Tb(NO 3 ) 3 ·5H 2 O samples showed significantly higher degradation efficiency for TYL and TC than pure g-C 3 N 4 . Leaching toxicity experiments were carried out on the catalyst using chard seeds and demonstrated negligible toxicity of the leachate from the catalyst. The structure, elemental state, optical properties, morphology, and photogenerated carrier separation of the prepared xTCN catalysts were characterized by XRD, XPS, UV–Vis DRS, TEM, and PL. The results show that Tb doping enhanced the photocatalytic activity of the g-C 3 N 4 catalyst by narrowing the band gap while improving the light-trapping ability; The separation and transport rate of photogenerated carriers were significantly increased after Tb doping. Finally, a simple, efficient, and non-polluting Tb-doped carbon nitride photocatalyst is successfully developed in this paper.
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ANALYST
·
2020
·Vol. 145
·期 24
·7849-7857
·
IF 3.978
Chang Liu,Chunyu Huang,Ruixue Ma,Wanying Zhai,Jingjing Deng,Tianshu Zhou
This work demonstrates a new strategy for sensing cerebrospinal acetylcholinesterase (AChE) as a cholinergic biomarker for brain dysfunction based on graphene quantum dot (GQD)-functionalized lanthanide infinite coordination polymer (Ln-ICP) nanoparticles. The ICPs used in this work were comprised of two components, i.e. a supramolecular Ln-ICP host formed by the coordination between the GMP ligand and central metal ion Tb3+, and guest GQDs with abundant functional groups, which were utilized as antenna ligands to further sensitize the fluorescence of Tb/GMP. Upon excitation at 300 nm, the obtained GQD@Tb/GMP ICP nanoparticles exhibited enhanced green fluorescence from Tb/GMP. With the addition of Cu2+, the competitive coordination between Cu2+ and GQDs weakened the antenna effect, leading to a decrease in the fluorescence of GQD@Tb/GMP ICPs. However, in the presence of thiocholine (TCh), a thiol-containing compound hydrolyzed from acetylthiocholine (ATCh) by AChE, a stronger coordination interaction between Cu2+ and TCh occurred, resulting in the restoration of the fluorescence of GQD@Tb/GMP ICPs. Using the method established herein, the cerebrospinal AChE fluctuation of rats with acute organophosphorus pesticide (OP) poisoning or chronic Alzheimer's disease (AD) could be monitored. This study essentially provides a novel approach to realize the direct monitoring of a biomarker for brain dysfunction by regulating the competitive coordination interaction reversibly, which is critical in the early diagnosis and therapy of brain diseases.
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TALANTA
·
2023
·
IF 6.1
Jingyu Li,Miao Liu,Jiaxuan Li,Xianhua Liu
The establishment of simple and sensitive detection methods for fluoride ion (F − ) is of great importance for its effective prevention and control, and metal-organic framework (MOF) has attracted much attention for sensing applications due to its high surface areas and tunable structures. Herein, we successfully synthesized a fluorescent probe for ratiometric sensing of F − by encapsulating sensitized Tb 3+ in a MOF-on-MOF material (UIO66/MOF801, with the formula of C 48 H 28 O 32 Zr 6 and C 24 H 2 O 32 Zr 6 , respectively). We found that Tb 3+ @UIO66/MOF801 can be used as a built-in fluorescent probe for fluorescence-enhanced sensing of F − . Interestingly, the two fluorescence emission peaks of Tb 3+ @UIO66/MOF801 at 375 nm and 544 nm exhibit different fluorescence responses to F − under excitation at 300 nm. The 544 nm peak is sensitive to F − , while the 375 nm peak is insensitive to it. Photophysical analysis indicated that the photosensitive substance was formed, which promotes the absorption of 300 nm excitation light by the system. Self-calibrating fluorescent detection of F − was achieved due to the unequal energy transfer toward the two different emission centers. The detection limit of Tb 3+ @UIO66/MOF801 for F − was 4.029 μM, which is far lower than the WHO guideline for drinking water . Moreover, the ratiometric fluorescence strategy showed a high concentration tolerance of interference, because of its inner-reference effect. This work highlights the high potential of lanthanide ion encapsulated MOF-on-MOF as environmental sensors, and offers a scalable way for construction of the ratiometric fluorescence sensing systems.
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JOURNAL OF MATERIALS SCIENCE
·
2017
·Vol. 53
·期 7
·4861-4873
·
IF 2.599
Ding Yang,Liu Jie,Zhu Yan,Nie Siyang,Wang Weili,Shi Junli,Miu Yanru,Yu Xibin
One-dimensional CaMoO 4 :RE 3+ (RE = Eu, Sm, Dy, Tb) nanofibers were successfully synthesized through a facile supersaturated recrystallization process. These CaMoO 4 :Ln 3+ nanofibers have the length ranging from 40 to 70 nm and the width of nearly 2 nm. Under UV excitation, these single-doped CaMoO 4 nanofibers shown stronger emission, and the photoluminescence quantum efficiency is 25.7% (CaMoO 4 :Eu 3+ ), 22.4% (CaMoO 4 :Sm 3+ ), 23.2% (CaMoO 4 :Dy 3+ ) and 27.7% (CaMoO 4 :Tb 3+ ), respectively. Moreover, our work reveals that various emission colors can be obtained and tuned from pure red to delight green via co-doping Tb 3+ and Eu 3+ in the CaMoO 4 host, and the energy transfer properties from Tb 3+ to Eu 3+ are also demonstrated. Finally, we apply the green CaMoO 4 :Tb 3+ , red CaMoO 4 :Eu 3+ and white CaMoO 4 :0.05Tb 3+ , 0.02Eu 3+ for LED devices, and these nanofiber-based LEDs present high efficiency and stability, which indicates the promising application in future optoelectronic fields.
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MICROCHIMICA ACTA
·
2017
·Vol. 184
·期 10
·4021-4027
·
IF 4.58
Wang Xiaole,Niazi Sobia,Yukun Huang,Sun Weijia,Wu Shijia,Duan Nuo,Hun Xu,Wang Zhouping
The authors describe an aptasensor based on time-resolved fluorescence resonance energy transfer (TR-FRET) for the identification of Salmonella typhimurium ( S. typhimurium ). Aptamer-functionalized nanoparticles (NPs) is used as the energy donor, and a complementary oligonucleotide (cDNA) labeled with carboxyfluorescein (FAM) acts as the acceptor. The detection scheme is based on the hybridization between aptamer and cDNA, upon which photonic energy is transferred from NPs to FAM unless aptamer interacts with S. typhimurium . Due to the highly specific recognition ability of aptamer and the strong fluorescence intensity of NPs, the method is highly sensitive and selective for S. typhimurium . Under the optimal conditions, at excitation wavelength of 273 nm, a delay time of 100 μs and a gating time of 1 ms, the integrated time-resolved fluorescence intensity ratio (FAM 520 /Tb 489 ) is linear in the 100 to 10 6 cfu·mL −1 range, and the limit of detection is as low as 25 cfu·mL −1 . The assay was applied to the analysis of eggs and chicken meat for S. typhimurium , and the results were consistent with those of a plate-counting method.
Schematic of a homogeneous time-resolved FRET assay for the determination of Salmonella typhimurium by FRET between NaYF 4 :Ce/Tb nanoparticle-tagged aptamer and FAM-cDNA, with a good linearity and the limit of detection of 25 cfu mL −1 .
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ACS Applied Electronic Materials
·
2025
·
IF 4.7
Na Chu,Zhihua Wang,Fubo Gu
Tb-doped SnO2 (represented as Tb–SnO2) was prepared by calcining Tb-doped Sn MOF synthesized by a solvothermal method. 5% Tb–SnO2 exhibits excellent selectivity, high response (28.2), and fast response/recovery time (28 s/135 s) toward 50 ppb (volume concentration in parts per billion) formaldehyde (HCHO) at low operating temperature (200 °C). The low detection limit of the HCHO gas sensor is mainly due to the large number of oxygen vacancies in Tb–SnO2 caused by the charge imbalance between Tb ions and Sn ions during the high-temperature calcination process of Tb-doped Sn MOF. Oxygen vacancies promote the conversion of oxygen molecules into active adsorbed oxygen species, narrow the band gap of semiconductor oxides, and reduce the activation energy of formaldehyde gas-sensing reactions, thereby improving the performance of gas sensors. 5% Tb–SnO2 gas sensor has strong moisture resistance, with a response value of 209.3 to 10 ppm of HCHO at a high relative humidity of 80%. The moisture resistance mechanism of the material is explained as Tb3+/Tb4+ redox pairs acting as water molecule capture agents, which reduce the occupation of gas-sensing reaction active sites by water molecules on the material surface.
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Magnetochemistry
·
2025
·Vol. 11
·期 9
·70
·
IF 2.5
Ya-Wei Geng,Tong Guo,Xiao-Qin Wang,Tian Han
As an important branch of lanthanide-based complexes, clusters show unique properties in magnetocaloric effect (MCE) and single-molecule magnets (SMMs) using O/N ligands, while research on heavy p-block elements (e.g., S atom) with larger atomic radii and more diffuse p valence orbitals as coordinating atoms remains relatively scarce. Herein, using the sulfur-containing ligand of 2-pyridinethiol 1-oxide (HL), we successfully synthesized a series of hourglass-like Ln9clusters [Ln9(L)17(μ3-OH)9(μ4-OH)]·nH2O (1: Ln = Gd,n= 3;2: Ln = Tb,n= 3;3: Ln = Dy,n= 1). Magnetic data analysis reveals that cluster1shows a significant MCE, with the entropy change (−ΔSm) reaching a maximum of 34.41 J kg−1K−1at 2 K under ΔH= 7 T. Cluster3, meanwhile, exhibits distinct frequency- and temperature-dependent behavior, indicating its SMM characteristics. Interestingly, despite possessing the highest molar mass among reported Gd9clusters with MCE,1exhibits a competitive −ΔSmvalue, highlighting the critical role of sulfur-containing ligand on the structure and even exchange interactions. This work offers new insights into synthesizing high-performance MCE materials and understanding magneto-structural relationships.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2019
·
IF 2.931
Yan Su,Dan Zhang,Peng Jia,Weichen Gao,Youbing Li,Zhuyu Bai,Xin Liu,Qunying Deng,Jing Xu,Chaolong Yang
Developing novel rare-earth complexes to rapidly and reliably sensing anions in pure water is highly challenging. Here, a series of long fluorescence lifetime polyurethane foam bonded Tb(BAA) 3 chromophore porous material (Tb-PUFs) have been designed and synthesized via a simple one-step co -polycondensation reaction as an efficient fluorescent sensor for H 2 PO 4 − in pure water. All Tb-PUFs exhibited strong green emission and long fluorescence lifetime in water, which was ascribed to Tb-complex can be dispersed very well in polyurethane foam, effectively avoiding the emission quenching of Tb 3+ ions caused by water molecules vibration. The titration experimental results showed that precursor Tb(BAA) 3 can effective recognize F − , CH 3 COO − , and H 2 PO 4 − in DMSO solution. Interestingly, Tb-PUFs can only selectively recognize H 2 PO 4 − in pure water, this phenomenon can be explained that H 2 PO 4 − is acidic, and can occur deprotonation with -NH group of ligand BAA , thus making the fluorescence quenching effect was more sensitive for H 2 PO 4 − in pure water. In addition, the sensing ability of Tb-PUFs for H 2 PO 4 − is highly reversible by washing them with deionized water for three times. In a word, all results implied that Tb-PUFs was an excellent candidate for H 2 PO 4 − ions detection selectively in pure water.
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JOURNAL OF FLUORESCENCE
·
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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JOURNAL OF LUMINESCENCE
·
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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FOOD CHEMISTRY
·
2023
·
IF 8.8
Junya Song,Beibei Zhao,Yiren Wang,Xinfang Liu,Zheng Cheng,Xiaoyu Zhang,Xun Feng
In this study, a new Tb-MOF fluorescence probe was developed for the detection of malachite green (MG) in real aquatic products. Fluorescence sensing experiments revealed that MG can effectively quench the green fluorescence of Tb-MOF suspensions, and the detection process exhibits the advantages of high sensitivity, a wide linear range (0–80 μM), a low detection limit (10.8 nM) and a rapid response time. Selective detection of MG is achieved primarily through fluorescence resonance energy transfer (FRET) and photoinduced electron transfer (PET) mechanisms. Furthermore, a smartphone-assisted Tb-MOF-based agar slice detection platform was constructed for the visual and quantitative detection of MG. Additionally, the on-site detection of MG in crucian and shrimp samples was accomplished with high recoveries (99.8 %-107.99 %) and low relative standard deviations (RSD < 2.2 %). This developed detection platform introduced a low-cost, portable and user-friendly approach for MG detection.
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CRYSTAL GROWTH & DESIGN
·
2024
·
IF 3.2
Pengju Xia,Yifeng Lei,Wanyuan Li,Kaiting Wu,Chengyu Ni,Man Xu,Wubin Dai
With the growing public awareness of protecting vision and prevention of hazardous effects, there is much-needed research on a “healthy” full visible spectrum under near-ultraviolet (nUV) excitation in phosphor-converted white light-emitting diodes (pc-wLEDs) to fill the “cyan gap” and avoid employing a blue LED chip. Herein, a novel series of borosilicates Ba2CaB2Si4O14 (BCBS): Ce3+/Tb3+/Sm3+/Sr2+/Na+ phosphors, presenting color-tunable photoluminescence (PL), high quantum yield (QY), and thermal stability, were designed and synthesized via a facile solid-phase reaction. The Rietveld analyses, density functional theory (DFT) simulations, and theoretical calculations of bond energy together imply the site occupations of Ce/Tb/Sm on Ba2+/Ca2+ sites with a preferred location on Ca2+ over the Ba2+ site. The broad/bright cyan-PL from BCBS: Ce under nUV excitation is associated with the allowed f–d transitions of Ce3+ and dual-site occupancies. The forbidden f–f transitions of both the green-PL of Tb and the red-PL of Sm were insensitive to the site environment and helpful to PL color regulation. The cascading Ce → Tb → Sm energy transfer is confirmed, where Tb is regarded as an energy transfer (ET) bridge to avoid the metal–metal charge transfer (MMCT) effect. The introduction of Na+ as both flux and charge compensator is for the sake of decreasing defects from heterovalent substitutions and regulating morphology. Further incorporation of Sr2+ is to modulate the lattice environments of dopants for controlling the shift of PL. Finally, as a proof-of-concept implement, a pc-wLED assembled by BCBS: Ce/Tb/Sm/Sr/Na and an nUV LED chip via a remote “capping” packaging strategy show attractive performance.
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