OPTICAL MATERIALS
·
2025
·
IF 4.2
Aihua Zhou,Chengguo Ming,Yumiao Pei,Yuanxue Cai,Tingting Guo,Hanbo Li
Reasonable modulation of temperature-dependent luminescence color has attracted significant attention due to its promising applications in anti-counterfeiting and temperature sensing. Although research on thermochromic materials is growing, the detailed exploration of the causes remain insufficiently explored. In this study, we successfully synthesized SrMoO 4 :Tb/Eu samples exhibiting thermal-responsive color tuning. Under 280 nm excitation, the intensity ratio of Eu 3+ ( 5 D 0 → 7 F 2 ) to Tb 3+ ( 5 D 4 → 7 F 5 ) in SrMoO 4 :0.08Tb/0.12Eu gradually increases from 0.81 to 5.8 over the temperature range of 303K–573K, accompanied by a distinct color shift from red to yellow. Experimental investigations demonstrated that the thermochromic behavior of the sample is primarily governed by nonradiative relaxation rates and local site symmetry. These results indicated that the samples can have potential for anti-counterfeiting and temperature sensing, particularly suitable as temperature sensing in the high-temperature reactor observation window.
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高影响因子
OPTICAL MATERIALS
·
2024
·
IF 3.8
Renjie Jiang,Jie Chen,Mingqin Li,Yanna Tian,Shiji Shen,Xuan Yang,Yanru Tang,Yan Sun,Hui Lin,Shengming Zhou
Ce: YAG- Al 2 O 3 composite ceramics are regarded as highly promising materials for laser illumination application due to their high luminous efficacy and thermal stability. Nevertheless, the Ce: YAG ceramics exhibit limited color rendering index (CRI) for indoor lighting due to their low red emission component. In this study, we synthesized high-performance Ce, Mn-doped (Y, Tb) 3 Al 5 O 12 –Al 2 O 3 composite ceramic phosphors via a vacuum solid-state sintering method. It was observed that the introduction of Mn 2+ ions created a second luminescence center with an emission peak centered at 580 nm. As the Mn 2+ concentration increased, the emission peak redshifted from 580 nm to 591 nm, leading to a significant enhancement in the color rendering index of the ceramics. The cross-energy transfer between Tb 3+ and Mn 2+ , Ce 3+ ions augmented the absorption and conversion of blue light by the ceramics, thereby reducing the correlated color temperature greatly. Based on these findings, ceramics with a Ce 3+ concentration of 3 at% and a Mn 2+ concentration of 4 at% exhibited the highest CRI values (81.3 and 75.6) under both laser excitation and LED excitation, establishing them as strong candidates for achieving high color rendering in white LED/LD illumination applications.
研究领域:
材料科学
·
光学工程
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高影响因子
DALTON TRANSACTIONS
·
2022
·Vol. 52
·期 3
·644-651
·
IF 4.569
Xiao Lian,Lele Cheng,Jingrui Shan,Mingzai Wu,Fangcai Zheng,Helin Niu
The identification of drugs or biomolecules for public health monitoring requires facile analytical technologies with excellent sensitivity, portability and reliability. In the past decades, different sensing materials have inspired the development of various bioanalytical strategies. However, sensing platforms based on powder materials are not suitable for medical diagnosis, which limits further exploration and application of biosensors. Herein, a point-of-care testing (POCT) membrane was designed from an energy competition mechanism and achieved the detection of the nonsteroidal antiphlogistic diclofenac, and exhibited remarkable testing efficacy at the ppb level. The mixed matrix membrane (MMM) sensor consists of electrospun polyacrylonitrile nanofibers and luminescent Tb-MOFs and possess the advantages of high stability, outstanding anti-interference ability, efficient detection (LOD = 98.5 ppb) and easy visual recognition. Furthermore, this MMM sensor exhibits excellent recyclability in serum, which is beneficial for developing a portable and convenient device to distinguish diclofenac in practical sensing applications. Meanwhile, the feasibility and mechanism of this recyclable sensor were verified by theory and experiments, indicating that it is a promising device for diclofenac detection in biological environments to evaluate the toxic effect caused by the accumulation of nonsteroidal drugs.
研究领域:
分析化学
·
材料科学
·
生物医学工程
·
环境健康
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高影响因子
Journal of Materials Chemistry C
·
2020
·Vol. 8
·期 41
·14548-14558
·
IF 7.059
Zhihao Wang,Qinghong Meng,Chunyun Wang,Dianyuan Fan,Yu Wang
Phosphor-converted white light-emitting diodes (pc-WLEDs) integrated with deep UV chips and single-component white light-emitting phosphors have attracted widespread research interest recently. (Y,Tb,Eu)NbO4 nanophosphors with full-color emission properties were achieved in this work by a facile calcination-assisted hydrothermal method, and the elaborately designed white light-emitting (Y0.988Tb0.010Eu0.002)NbO4 phosphor was successfully applied to a 275 nm chip excited pc-WLED with a relatively low correlated color temperature (CCT) of 5517 K and a high color-rendering index (CRI) of 86.7. Through a comprehensive characterization by XRD, elemental analysis, FE-SEM, TEM, TG, FT-IR, UV-vis, and optical spectroscopy, the YNbO4 nanophosphor with optimal PL properties was evidenced to be obtainable through calcining the hydrothermally crystallized precursor at 1000 °C. The quenching concentrations of Tb3+ and Eu3+ in YNbO4 were determined to be ∼4 and 5 at%, respectively, and the efficiency of the NbO43− → Tb3+ energy transfer was calculated to be ∼47.93%. Upon excitation at 260 nm, the ternary (Y,Tb,Eu)NbO4 phosphor simultaneously displays blue NbO43−, green Tb3+, and red Eu3+ emissions. Benefiting from the NbO43− → Tb3+ → Eu3+ energy transfer, full color emission was achieved via adjusting the Tb3+ and Eu3+ concentrations in (Y,Tb,Eu)NbO4. The white light-emitting (Y0.988Tb0.010Eu0.002)NbO4 phosphor with color coordinates of (0.336, 0.334) can maintain its emission color and ∼67% of its overall emission intensity at 150 °C, indicating that the phosphor is highly promising for application in deep UV chip-based pc-WLEDs.
研究领域:
材料科学
·
光学工程
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高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2026
·
IF 4.6
Yulong Han,Huanhuan Lu,Haili Liu,Hengye Chen,Wei Lan,Xinming Lv,Wanjun Long,Haiyan Fu
In this work, a ratiometric fluorescent sensing platform based on the antenna effect of Tb-doped metal – organic framework (Tb-MOF) was constructed for sensitive and visual detection of enoxacin (Eno). The coordination of Tb 3+ with the β-diketone structure of the Eno molecule activates yellowish-green fluorescence emission through the “antenna effect”. The Tb-MOF fluorescent probe exhibits excellent response-sensitivity and selectivity for Eno with a low detection limit (LOD) of 0.09 μM, showing a good linear response in the concentration range of 0–20 μM. Under excitation with 365 nm ultraviolet light, the fluorescence color of the sensor system gradually changes from blue to yellow-green as the Eno concentration increases. Further, Tb-MOF ratiometric fluorescent sensor combined with cloud-based machine learning algorithm-assisted WeChat Mini Program realized the intelligent quantification of Eno in complex matrices such as honey, milk, and beef was achieved, which overcomes the reliance of traditional methods on large-scale instruments and provides a portable and efficient solution for on-site monitoring of food safety.
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BIOSENSORS & BIOELECTRONICS
·
2020
·
IF 10.257
Juncong Miao,Kang Du,Xuan Li,Xiaoting Xu,Xue Dong,Jinglong Fang,Wei Cao,Qin Wei
Procalcitonin (PCT) as a disease marker is of great significance in the early diagnosis of septicemia and pyemia. Biosensor have good prospects for analysis and detection of disease markers, but developing highly sensitive detection methods for detecting PCT remains a daunting task. In this paper, we develop a ratiometric electrochemical immunosensor with Au NPs modified SiO 2 -Fc-COOH complex as matrix and UiO-66 loaded with Toluidine blue (TB) as a marker for quantitative detection of procalcitonin (PCT). The SiO 2 modified by APTES not only has a large specific surface area but also contains abundant amino groups, which can be connected to the electrochemical probe of ferrocenecarboxylic acid (Fc-COOH). UiO-66 has the advantages of large specific surface area, high porosity and adjustable structure, which can adsorb toluidine blue electrochemical probe through electrostatic attraction . Measurement and analysis of the prepared immunosensor by Differential Pulse Voltammetry (DPV) show that the oxidation peak currents of Fc-COOH and TB appear at potentials of 0.30 V and −0.30 V respectively. As the PCT concentration increases, the oxidation peak current of TB increases and the oxidation peak current of Fc-COOH decreases. The ratios ( ΔI = ΔI TB /ΔI Fc-COOH ) between the double signals could show a certain linear relationship with the concentration of the PCT within a certain range. Under optimal conditions, the linear range of detection obtained by the immunosensor was 1 pg/mL-100 ng/mL and the detection limit was 0.3 pg/mL. In this work, the developed ratiometric electrochemical immunosensor not only provides a simple, reliable and sensitive strategy for quantitative detection of PCT but also provides a useful method for clinical detection of other disease markers.
研究领域:
生物传感器
·
医学检测
·
电化学分析
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高影响因子
BIORESOURCE TECHNOLOGY
·
2021
·
IF 9.642
Zeyu Wang,Luyao Dai,Jiachao Yao,Tianjiao Guo,Dzmitry Hrynsphan,Savitskaya Tatsiana,Jun Chen
Aiming at the accumulation of NO 2 − -N and N 2 O during denitrification process, this work focused to improve the denitrification performance by Pd-Fe embedded multi-walled carbon nanotubes (MWCNTs). The main conclusions were as follows: 30 mg/L Pd-Fe/MWCNTs have shown an excellent promotion on denitrification (completely TN removal at 36 h). Meanwhile, enzyme activity results indicated that the generation of NO 2 − -N, NH 4 + -N by Pd-Fe/MWCNTs led the occur of short-cut denitrification by increasing 203.9% the nitrite reductase activity. Furthermore, electrochemical results and index correlation analysis confirmed that the electron exchange capacity (1.401 mmol eg −1 ) of Pd-Fe/MWCNTs was positively related to nitrite reductase activity, indicating its crucial role in electron transport activity (0.46 μg O 2 /(protein·min) at 24 h) during denitrification process by Pd-Fe/MWCNTs played a role of chemical reductant and redox mediator.
研究领域:
环境工程
·
生物技术
·
微生物学
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高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
·
IF 4.3
Xinru Wu,Chen Ruan,Siqi Zhou,Lina Zou,Rong Wang,Gaiping Li
Tandem enzyme can catalyze some cascade reactions with high efficiency, and some few tandem enzyme-like mimics have been discovered recently. Further improving the catalytic efficiency of tandem nanoenzymes with facile method may undoubtedly promote and broaden their applications in various fields. In this work, cupric oxide nanoparticles (CuO NPs) with dual-functional enzyme mimics were synthesized using the rapid deposition method in advance, which simultaneously combined with lanthanide infinite coordination polymers (Ln ICPs) during the self-assemble of Tb 3+ , guanine-5′-triphosphate (GTP) and auxiliary ligand terephthalic acid (TA). Excitingly, the obtained Tb-GTP/TA@CuO ICPs, not only displayed obviously enhanced tandem catalytic activity compared with pure CuO NPs, but also provided a versatile ratiometric platform for ultrahigh selective and sensitive detection of glutathione (GSH) under single-wavelength excitation. A good linear relationship between the ratio signal and the GSH concentration was spanning from 0.001 to 20 μM with an impressive detection limit of 0.50 nM. This study opens a new and universal avenue for preparing integrated multifunctional probes by coupling of nanoenzyme catalytic activity with superior luminescent Ln ICPs through facile method.
研究领域:
材料科学
·
纳米技术
·
分析化学
·
生物化学
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 17
·8029-8036
·
IF 3.925
Qingju Liu,Saixue Tang,Hui Wang,Ping Han
The current luminescent metal–organic framework (MOF) based fluorescence detection mostly focuses on achiral molecules. The stereospecific recognition and determination of MOF-based detection remain challenging. A novel luminescent terbium-based MOF (Tb-MOF) based biosensing system with excellent performance for stereoselective detection of D-amino acids (D-AAs) was introduced in this paper. D-Amino acid oxidase catalyzes stereospecific oxidative deamination of D-AAs, producing H2O2. The generated H2O2 effectively quenches the fluorescence of Tb-MOF. Under optimum conditions, the D-AAs were detected with excellent efficiency. The linear working range was 0.5–100 μM for D-Alanine (D-Ala) and 0. 5–5 μM for D-Proline (D-Pro), respectively. The limit of detection (Ksv detection) for D-Ala and D-Pro was 0.09 μM and 0.14 μM, respectively. The detection can be performed within 30 min with high selectivity and long-term stability. The fluorescent sensing platform required simple fabrication and operation and was free from complicated reaction processes and expensive reagents. The present sensing system was successfully applied in D-AA detection in human serum with good recovery, indicating its potential application in detection in biological samples.
研究领域:
分析化学
·
生物技术
·
材料科学
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高影响因子
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.
研究领域:
分析化学
·
材料科学
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高影响因子
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.
研究领域:
材料科学
·
光物理学
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高影响因子
Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 2
·121155
·
IF 7.2
Yaqi Liu,Hui Lu,Changfei Gao,Yameng Wang,Haoran Liu,Huiqiang Ma,Bo Wang,Lifen Liu,Yihua Li,Xianbo Chang
The persistent threat posed by radioactive metal contamination necessitates the development of innovative and sustainable remediation strategies. In this study, we proposed a self-sustaining bioelectrocatalytic reduction system (BECRs) incorporating an in situ co-synthesized ternary Fe/Cu/Co@Z-CF cathode derived from zeolite imidazole salt skeleton (ZIF) -functionalized carbon felt. The engineered electrode demonstrated outstanding electrocatalytic performance, characterized by an ultrahigh exchange current density of 7.68 × 10 −3 A cm −2 and minimal charge transfer resistance of 0.11 Ω. These properties were attributed to the synergistic redox cycling of Fe-Cu-Co species and the enhanced exposure of active sites facilitated by the ZIF structure. Under optimized conditions at pH 11, the BECRs achieved removal efficiencies exceeding 98.28 % for targeted radionuclides (Cs + : 99.00 %, Sr 2+ : 98.28 %, Tb 3+ : 99.95 %, Eu 3+ : 99.97 %) while generating a stable bio-voltage of 730 mV. The removal mechanisms operated synergistically through three primary pathways: direct electroreduction of metals to elemental or metallic oxide forms at the catalytic cathode; electroflocculation mediated by in situ formation of Fe(OH) x species and microbial adsorption by enriched pollutant-resistant microbial consortia, notably with a 16.3 % increase in Bacteroidota abundance. Density Functional Theory (DFT) calculations revealed charge complementarity among Fe/Cu/Co sites, accelerating oxygen reduction kinetics. Crucially, the electrode demonstrated negligible metal leaching across pH 3–11, confirming ecological safety. Kinetic analysed distinguish radionuclide-specific pathways: pseudo-first-order for Cs⁺/Sr²⁺ versus pseudo-second-order for Tb 3+ /Eu 3+ , informing selective recovery strategies. This work established a green, energy-positive paradigm for radioactive wastewater treatment, achieving simultaneous decontamination, resource recovery (metallic Cs/Sr/Tb/Eu) with significant potential for closed-loop nuclear effluent management.
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