JOURNAL OF SOLID STATE CHEMISTRY
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2023
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IF 3.3
Yun Xie,Da-Li Chen,Yu-Long Wei,Nan Zhang,Wen-Dong Yao,Sheng-Ping Guo
Exploration of new compounds belonging to unusual families is always attractive for the everlasting development of material science. Here, three isomorphic rare-earth sulfide borates RE 3 S 3 BO 3 (RE = Nd, Tb, Dy) have been obtained via a facile metal oxide-boron-sulfur solid-state routine. Their centrosymmetric triclinic structures feature 3 D framework built by three types of REO x S y units, viz. REOS 6 , REO 4 S 3 , and REO 3 S 6 . Their structural relationship with similar phases and lanthanide contraction rule are discussed. Their optical band gaps are measured to be 2.59–2.70 eV, and the corresponding theoretical calculations are also performed. This work enriches the rarely studied chalcogenide borate system and is conducive to discovering more inorganic materials .
研究领域:
材料科学
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无机化学
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光学材料
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产品关联
DOI
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2021
·Vol. 413
·期 16
·4227-4236
·
IF 4.157
Chen Li,Liu Donghao,Zheng Limin,Yi Simin,He Hua
In the present work, a structure-dependent ratiometric fluorescence (RF) sensor constructed with boric acid–modified carbon quantum dots (B-CQDs) and Tb-MOF(MOF-76) was developed for sensing 2,6-pyridinedicarboxylic acid (DPA). Based on the distinct fluorescent responses of B-CQDs and MOF-76 to DPA, MOF-76/B-CQDs can be developed as a RF sensor for DPA detection. In this RF sensor, the reticulated cross-linked structure of MOF-76/B-CQDs can be destroyed by DPA due to a strong coordination effect between DPA and the Tb of MOF-76, resulting in the quenching of the fluorescence of B-CQD and the restoration of the fluorescence of MOF-76 after the addition of DPA. Benefiting from the confinement effect of the special structure change, the presented sensor showed high sensitivity toward DPA with a detection limit of 3.05 μM and excellent selectivity over the monochromatic fluorescence sensor. Graphical abstract
研究领域:
分析化学
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材料科学
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传感器
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DOI
PubMed
高影响因子
Crystals
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2022
·Vol. 12
·期 7
·963
·
IF 2.67
Weili Wang,Shihai Miao,Dongxun Chen,Yanjie Liang
Trivalent lanthanides (Ln3+) doped bismuth-based inorganic compounds have attracted considerable interest as promising candidates for next-generation inorganic luminescent materials. Here, a series of K0.3Bi0.7F2.4(KBF) nanocrystalline particles with controlled morphology have been synthesized through a low-temperature aqueous-phase precipitation method. Using KBF as the host matrix, Eu3+, Tb3+, Pr3+, Nd3+, Sm3+,and Dy3+ions are introduced to obtain K0.3Bi0.7F2.4:Ln3+(KBF:Ln) nanophosphors. The as-prepared KBF:Ln nanophosphors exhibit commendable photoluminescence properties, in which multicolor emissions in a single host lattice can be obtained by doping different Ln3+ions when excited by ultraviolet light. Moreover, the morphology and photoluminescence performance of these nanophosphors remain unchanged under different soaking times in water, showing good stability in a humid environment. The proposed simple and rapid synthesis route, low-cost and nontoxic bismuth-based host matrix, and tunable luminescent colors will lead the way to access these KBF:Ln nanophosphors for appealing applications such as white LEDs and optical thermometry.
研究领域:
材料科学
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纳米技术
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光学
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化学
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DOI
高影响因子
OPTICAL MATERIALS
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2016
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IF 2.183
Chen Yuan,Hongde Xie,Haijun Cai,Cuili Chen,Peiqing Cai,Hyo Jin Seo
A green-emitting Tb(III) complex based on siloxane-modified pressure sensitive adhesives (SPSA-Tb(III)) was successfully synthesized by emulsion polymerization . Siloxane-modified pressure sensitive adhesives (SPSA) were used as host materials. The structural coordination, photoluminescence excitation (PLE) and luminescence (PL) spectra, and thermal characterization of this luminescent polymer were investigated. The result from the FT-IR spectra reveals that SPSA have successfully coordinated with the Tb(III) ions. The luminescent analysis indicates that SPSA-Tb(III) displays Tb(III) typical emission peaks at 489, 545, 583, and 622 nm under the excitation of 369 nm. When monitored at 545 nm, strong and sharp excitation bands appear from 300 to 500 nm. And SPSA-Tb(III) has short lifetime (0.25 ms). Meanwhile, SPSA-Tb(III) exhibits high thermal stability (T d = 402 °C) owing to the high bond dissociation energy of Si O bonds. All the results suggest that it is expected to be used as a superior green-emitting material under high temperature.
研究领域:
材料科学
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发光材料
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高分子化学
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无机-有机杂化材料
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DOI
高影响因子
MICROCHEMICAL JOURNAL
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2026
·
IF 5.2
Hui Cao,Run Gao,Lin Chen,Zixia Huang,Xiuxiu Wu,Jinsong Yu,Fei Xu
Hg(II) is a widespread environmental contaminant with high toxicity and severe adverse effects on human health. Although aptamers are commonly used as recognition elements for Hg(II), their binding performance is highly susceptible to pH. In this study, we designed a dual-functional Hg(II)-specific aptamer and developed a biosensor based on Tb(III)-DNA self-assembled coordination polymers (Tb-DNA CPs) for the rapid detection of Hg(II). In the designed aptamer, the G-rich region functions as a luminescent antenna ligand to sensitize Tb(III) emission, while the T-rich region serves as the Hg(II) recognition unit. The resulting Tb-DNA CPs retained 90.2% of their original fluorescence intensity after 30 days in aqueous solution and demonstrated high stability over a broad pH range (pH 4–11). This improved stability is attributed to the role of Tb(III) as a structural crosslinker that promotes the assembly of coordination polymers. The sensor exhibited a limit of detection (LOD) of 3.89 nM for Hg(II), with a linear response range of 5 to 250 μg·L −1 . In vegetable samples, Hg(II) was rapidly quantified with recoveries of 96.49% to 113.40% and RSDs of 1.98%–4.83%. Mechanistic analysis indicated that the sensing response of the Tb-DNA CPs was mainly driven by photoinduced electron transfer (PET) and Hg(II)-induced conformational changes. This work overcomes the pH-dependent limitation of conventional aptamer-based sensors and provides a practical platform for on-site Hg(II) monitoring. The Tb-DNA CP strategy also offers a versatile foundation for the development of stable lanthanide-based biosensors.
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DOI
高影响因子
CERAMICS INTERNATIONAL
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2025
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IF 5.6
Chaochao Tao,Songsong Ding,Shengqian Wang,Lin Liu,Houfa Mao,Genyuan Chen,Hualan Xu,Chongfeng Guo,Shengliang Zhong
Multicolor emission has long been a critical scientific challenge in the field of persistent luminescence (PersL) materials, with the achievement of multicolor PersL emission within a single host matrix representing a primary research objective. Herein, a new and effective method of using coordination polymers (CPs) as precursors is designed to synthesize multicolored CdSiO 3 :RE 3+ (RE = Pr, Sm, Eu, Tb, Tm) PersL materials. Through variation of rare earth dopants, we successfully achieved color-tunable PersL emission spanning brown, pink, purple, red, green, and blue spectra. The influence of RE 3+ dopants on the crystal structure, morphology and optical properties are studied in detail. Notably, this straightforward synthesis strategy enabled the effective production of nanospherical particles exhibiting regular morphology and uniform size distribution. The electronic band structure of the material was theoretically analyzed using density functional theory (DFT) calculations. Combined with thermoluminescence (TL) measurements were performed to elucidate the underlying PersL mechanism. To demonstrate practical applications, we designed a dynamic anti-counterfeiting pattern and evaluated the potential utility of CdSiO 3 :RE 3+ materials. This study not only enhances our fundamental understanding of CdSiO 3 -based PersL materials, but also provides novel insights into morphology and size control strategies that could be extended to other PersL material systems.
研究领域:
材料科学
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光学
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产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
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2025
·
IF 5.1
Raj Kumar Parajuli,Jin Liu,Shree Krishna Tamang,Govinda Gurung,Kumar Neupane,Yao Wang,Christopher D. Snow,Matt J. Kipper,Laurence A. Belfiore,Jianguo Tang
Patient urine may provide relatively convenient access to biomarkers, but it is challenging to directly and visibly sense drugs via fluorescence quenching or enhancement. This study reports the synthesis of water-soluble and fluorescence-stable terbium-induced nanoaggregates (TIPAs) of polystyrene-poly(acrylic acid) (PS- b -PAA), containing a novel [Tb( acac )Cl 2 ( phen )Cyclen] complex, to sense doxorubicin ( dox ) in urine. The TIPAs demonstrated remarkable water stability, maintaining high fluorescence intensity in aqueous environments, with a fluorescence lifetime of 55.5 ms and a quantum yield (QY) of 4.60 %, making them ideal for smart sensing applications. The novel aggregate exhibits an orthorhombic structure, with its photophysical properties elucidated through simulated modeling. Fluorescence quenching studies indicate dynamic interactions between TIPAs and dox in urine, achieving a limit of detection (LOD) of 13.77 μM, highlighting the method's sensitivity for real-time dox monitoring. The emission of TIPAs in the visible range (450–600 nm) overlaps with the absorption spectrum of dox , enabling efficient energy transfer and fluorescence quenching. These findings highlight the potential of TIPAs as stable, fluorescence-based sensors for drug monitoring, with promising applications in bioimaging and diagnostics within cancer therapy.
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DOI
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
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2025
·
IF 4.7
Qiang Zhao,Han Peng,He-zhen Wang,Shu-ran Gao,Jun-zhao Wang,Lin-Xi Qin,Meng-ting Fan
In order to better study the properties of rare earth complexes in terms of fluorescence, magnetism, and fluorescent probes, in this work, 5-(2-carboxyphenoxy)isophthalic acid (H 3 ocpia) and rare metal ions Eu 3+ , Tb 3+ , Dy 3+ were used to synthetic metal complexes by solvothermal reaction. Then three complexes Eu(ocpia) (1) , Tb(ocpia) (2) and Dy(ocpia) (3) were synthesized, their structural formulas are as follows: EuC 15 H 7 O 7, TbC 15 H 7 O 7 and DyC 15 H 7 O 7 . Data on the structure acquired via an X - ray single - crystal diffractometer indicates that complexes 1, 2 , and 3 possess the same spatial structures. They are two-dimensional planar structures with undulating ripples. Moreover, solid - state fluorescence tests were carried out on complexes H 3 ocpia, 1 , and 2 , and magnetic property tests were done on complexes 2 and 3 . Fluorescence recognition studies were conducted on complexes 1 and 2 in dispersed systems. The solid-state fluorescence results show that complexes 1 and 2 have excellent fluorescence properties, with higher fluorescence intensity than the ligand. The CIE chromaticity coordinates of complexes 1 and 2 are (0.59, 0.34) and (0.33, 0.62), respectively, and exhibit bright characteristic lights of europium and terbium under fluorescent lamps. Magnetic susceptibility measurements reveal that compounds 2 and 3 exhibit antiferromagnetic coupling behavior between adjacent metal centers. Fluorescence recognition studies have shown that complexes 1 and 2 exhibit good recognition of acetone in dispersed systems, the detection thresholds were determined to be 0.063 vol.% for complex 1 and 0.136 vol.% for complex 2 .
研究领域:
无机化学
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配位化学
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材料科学
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荧光光谱学
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磁性材料
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传感器技术
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晶体学
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分析化学
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产品关联
DOI
高影响因子
Journal of Materials Chemistry C
·
2024
·
IF 5.7
Yao Li,Qingxing Yang,Huwei Li,Xinyu Fu,Hongxia Yue,Zheyu Li,Jing Feng,Hongjie Zhang
Metal halide double perovskites are a promising alternative to lead-based perovskites. Especially, rare earth (RE)-based halide double perovskites have attracted much attention due to their unique optical properties. As RE3+ ions could be served not only as the component of the matrix but also as the luminescence centers, the chemical composition of RE-based halide double perovskites can be simplified and tunable luminescence could be achieved. In this work, Cs2NaRECl6 (RE = Tb, Eu) halide double perovskite nanocrystals were synthesized by the hot injection method. Cs2NaRECl6 nanocrystals exhibit not only the intrinsic host emission but also the characteristic emissions of RE3+ ions. Furthermore, the excitation-wavelength-dependent multicolor emissions of Cs2NaRECl6 nanocrystals make them highly potential for anticounterfeiting applications. Multicolor LED devices based on various components of Cs2NaRECl6 could be obtained, providing promising candidates for optoelectronic applications.
研究领域:
材料科学
·
光学工程
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产品关联
DOI
高影响因子
APPLIED CATALYSIS A-GENERAL
·
2020
·
IF 5.006
Hui Huang,Jun Wang,Yafei Xu,Rui Xu,Wuke Li
In this paper, a luminescent and thermo-responsive catalyst based on SiO 2 @Pt@PABI-Tb@PNIPAM was prepared by incorporating Pt nanoparticles , luminescent material and mesoporous silica with thermo-responsive polymer. The obtained catalyst was characterized by IR, TGA, UV–vis, SEM, TEM, X-ray photoelectron spectroscopy and luminescence. The hybrid catalyst exhibits “on-off” green luminescence in solution under UV irradiation, which could be observed by eyes. The catalytic results indicate that the dehydrogenation of ammonia borane (AB) catalyzed by SiO 2 @Pt@PABI-Tb@PNIPAM is thermo-controllable and switchable. The SiO 2 @Pt@PABI-Tb@PNIPAM shows high catalytic activity for the generation of hydrogen at room temperature. However, it exhibits much lower catalytic activity at high temperature. The catalysts exhibit excellent durability because the support and polymer could prevent the aggregation and leaching of Pt nanoparticles during catalysis. The catalytic research offers a new approach to the thermo-controllable application in the generation of hydrogen from AB.
研究领域:
材料科学
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催化化学
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能源化学
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产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Jie Chen,Yanhua Song,Ye Sheng,Meiqi Chang,Xiaoming Xie,Murad M.A. Abualrejal,Hongxia Guan,Zhan Shi,Haifeng Zou
Novel luminescent one-dimensional Ln 3+ (Eu, Tb) doped SiO 2 hollow nanofibers were successfully fabricated using a facile and economical co-axial electrospinning technique with subsequent calcination . The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that the as-obtained samples present obvious hollow morphology with an average diameter of 303 ± 11 nm and thin walls approximate 76 nm. For SiO 2 :xEu 3+ hollow nanofibers, the highest luminescence intensity, the longest lifetime and the largest quantum efficiency were both in the composition of 6 mol% Eu 3+ . The large value of R 21 indicated a highly disordered environment around Eu 3+ ions in the host, which was better for intense visible red emission. Meanwhile, the spectral characteristics and radiative properties were also analyzed according to the Judd-Ofelt theory from the emission spectra. What's more, under ultraviolet excitation, the emission colors of samples could be tuned from red to green, including bisque by doping Eu 3+ , Tb 3+ and co-doping Eu 3+ /Tb 3+ ions, which indicated the obtained SiO 2 :Ln 3+ hollow nanofibers are potential phosphors in nanostructured optical devices applications.
研究领域:
材料科学
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光学
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产品关联
DOI
高影响因子
APPLIED SPECTROSCOPY
·
2025
·
IF 2.2
XingYi Guo,Chun Zhu,Guoqing Chen,Lei Li,Chaoqun Ma,Taiqun Yang,Anqi Hu,WenHui Yang,YaLi Qian
In this paper, a lanthanide complex-based fluorescent sensor Tb(4-MBA) was developed for the selective recognition of diabetic ketoacidosis (DKA) and the diabetes biomarker β-hydroxybutyric (β-Hb). β-Hb significantly enhanced the fluorescence emission of the Tb(4-MBA) complex at 539 nm. Based on the analysis of the surface electrostatic potential distribution and time-resolved spectra, we speculate that in the reaction system of β-Hb with Tb(4-MBA), β-Hb and Tb(4-MBA) may form a complex through hydrogen bonding interactions, which brings β-Hb closer to Tb3+ and thus reduces the non-radiative energy loss of the solvent molecules to Tb3+ and significantly enhances the Tb(4-MBA) fluorescence intensity. The linear range of Tb(4-MBA) for β-Hb was 2–55 μM, and the limit of detection (LOD) was 50.6 nM. This sensor has high sensitivity and selectivity and shows great potential in the field of screening and diagnosis of diabetes mellitus and DKA.
研究领域:
分析化学
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生物无机化学
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荧光传感
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糖尿病研究
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材料科学
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）