OPTICAL MATERIALS
·
2020
·
IF 2.779
Yicheng Zeng,Biwei Qiu,FangFang Wang,Lei Zhou,Ying Li
Two kinds of hybrid luminescence films ([C 8 VIM][Eu (nta) 4 ]@PMMA and [C 8 VIM][Tb (acac) 4 ]@PMMA) have been synthesized by the copolymerization of MMA with lanthanide functionalized ionic liquid [C 8 VIM][Eu (nta) 4 ]. The structure and composition of the as-synthesized films have been characterized by 1 HNMR, XPS , FTIR, UV–vis, XRD , TGA and SEM. In addition, the photophysical properties of as-synthesized films have been investigated in detail by luminescence spectroscopy. It was found that the transparent and thermal stability of as-synthesized films are improved by the long chains of PMMA . More significantly, [C 8 VIM][Eu (nta) 4 ] @PMMA exhibits the improvement of photo physical properties (ƞ = 52.6%) and is selected as the representative sample to examine the potential fluorescence sensing of metal ions and anions. It has been showed highly selective and sensitive fluorescence sensing for Cu 2+ and CrO 4 2− . Meanwhile, [C 8 VIM][Eu (nta) 4 ]@PMMA exhibits a good stability in the aqueous solution, which is further used as fluorescence probe for detecting CO 3 2− . The good stability, sensitive fluorescence response and good mechanical processing properties of [C 8 VIM][Eu (nta) 4 ]@PMMA show a great potential to establish a fast response anion and cationic of aqueous solution fluorescence colorimetric sensor devices.
研究领域:
材料科学
·
光学
·
分析化学
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高影响因子
JOURNAL OF SOLUTION CHEMISTRY
·
2020
·Vol. 49
·期 2
·166-178
·
IF 1.273
Zhu Liqing,Liu Bijun,Yang Xia,Zhuo Liangang,Mu Wanjun,Chen Yue,Yang Yuchuan,Wei Hongyuan,Li Xingliang
Thermodynamic equilibria of complexes of 1,3-diamino-2-hydroxypropane- N , N , N ', N '-tetraacetic acid (DHPTA) with heavy lanthanides (Tb 3+ , Ho 3+ and Lu 3+ ) in aqueous solution have been investigated with potentiometry, spectrophotometry, luminescence spectroscopy and nuclear magnetic resonance spectroscopy (NMR). The results identified three 1:1 Ln/DHPTA (Ln: Tb 3+ , Ho 3+ and Lu 3+ ) complexes with different degrees of deprotonation, LnL − , Ln(H −1 L) 2− , and Ln(OH)(H −1 L) 3− , where H −1 represents the deprotonation of the hydroxyl group between two methyliminodiacetate groups in the DHPTA structure. The alkoxide form of the DHPTA hydroxyl group directly binds to the lanthanide atom, forming highly strong chelation. The complex of Ln(H −1 L) 2− could be present as a dimeric or polymeric complex in solution.
研究领域:
配位化学
·
无机化学
·
物理化学
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高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Hangqing Xie,Zi Chen,Xiaoqin Wei,Qing Han,Haotuo Wang,Xiaolei Yang,Shiqing Xu,Xiang Wang
The fluoride ion (F – ) concentration in serum is an important indicator of fluorosis. However, the biofluorescence of serum itself makes the concentration of F – difficult to detect. Herein, a Tb‐1@F127 nanoprobe is synthesized by Flash NanoPrecipitation of Tb 3+ , Ga 3+ , organic ligands and block copolymer Pluronic (F127). The absorbance and photoluminescence (PL) of the Tb‐1@F127 nanoprobe are enhanced by the "antenna" effect of the organic ligands and the energy transfer of triplet excitons . The molar extinction coefficient of Tb‐1@F127 nanoprobe is 28,000 times higher than the f-f transfer in free Tb 3+ . Moreover, the addition of F – blocks the above energy transfer process , resulting in a decrease in the PL intensity of Tb‐1@F127 nanoprobe. In the serum solution, the PL intensity of Tb‐1@F127 nanoprobe has a linear response to the concentration of F – in the range of 0–18.81 ppm, and the detection limit is 0.056 ppm. The Tb‐1@F127 nanoprobe demonstrates high sensitivity and selectivity for the detection of F concentration, and is not affected by biological autofluorescence.
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Journal of Materials Chemistry C
·
2020
·Vol. 8
·期 13
·4408-4420
·
IF 7.059
Shaoying Wang,Balaji Devakumar,Qi Sun,Jia Liang,Liangling Sun,Xiaoyong Huang
Inorganic phosphors with broadband near-ultraviolet (near-UV) excitation and efficient visible emission are highly important for fabricating high-performance near-UV-pumped white light-emitting diodes (LEDs). Herein, we report on novel efficient near-UV-excitable Ce3+/Tb3+ ion co-activated Ca2YHf2Al3O12 (CYHA) green-emitting garnet phosphors, which were successfully prepared through a high-temperature solid-state reaction process. X-ray diffraction, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, photoluminescence, CIE color coordinates, the internal and external quantum efficiency, and temperature-dependent emission spectra were used to characterize the samples. Interestingly, due to the efficient energy transfer from Ce3+ to Tb3+ ions in CYHA, the CYHA:Ce3+,Tb3+ samples presented a wide excitation band in the 370–470 nm region peaking around 408 nm owing to the 4f–5d transition of Ce3+ ions, and under 408 nm excitation they showed intense characteristic sharp green emission around 543 nm corresponding to the 5D4 → 7F0–6 transitions of Tb3+ ions. The energy transfer mechanism from Ce3+ to Tb3+ ions was ascribed to the quadruple–quadruple interaction, and the energy transfer efficiency reached as high as 93.2%. Notably, the composition-optimized CYHA:0.03Ce3+,0.6Tb3+ sample exhibited a high internal quantum efficiency (IQE) of 78.5% and external quantum efficiency (EQE) of 56%, which were much higher than those of the Tb3+ singly-activated CYHA:0.6Tb3+ sample (IQE = 8%, EQE = 2.2%). Finally, a prototype white LED device was made by combining a 400 nm near-UV-emitting LED chip with a phosphor blend of the as-prepared CYHA:0.03Ce3+,0.6Tb3+ green phosphors, commercial BaMgAl10O17:Eu2+ blue phosphors and commercial CaAlSiN3:Eu2+ red phosphors, which emitted bright warm-white light with good CIE chromaticity coordinates of (0.391, 0.356), a low correlated color temperature of 3528 K and a high color rendering index of 92.3 under 120 mA driving current. This work opens up new opportunities for the development of efficient color converters toward near-UV-pumped warm-white LEDs with high color rendering index.
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MATERIALS RESEARCH BULLETIN
·
2015
·
IF 2.288
Qiang Zhang,Ye Sheng,Keyan Zheng,Xuming Qin,Pingchuan Ma,Haifeng Zou
Novel organic–inorganic hybrid amorphous thin films were synthesized by linking lanthanide (Tb 3+ , Eu 3+ ) complexes through 3,4-bis(3-(triethoxysilyl)propylcarbamoyloxy)benzoic acid using sol–gel method. These inorganic–organic hybrids were characterized in detail by Fourier transform infrared spectroscopy, wide angle X-ray diffraction, themogravimetric analysis, scanning electron microscope, and fluorescence spectra. The above research results indicate that the hybrids possess high thermal-stability, amorphous structure features and especially favorable luminescent performances, such as long luminescent decay lifetime, high quantum yield etc.
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JOURNAL OF CRYSTAL GROWTH
·
2024
·
IF 1.7
Sibo Zhao,Dan Xiu,Min Zhang,Yao Wang,Miao Qiu,Christopher D. Snow,Yanxin Wang,Laurence A. Belfiore,Jianguo Tang
In this study, a highly sensitive anticancer drug sensor was synthesized using DNA crystals loaded with luminescent Ln 3+ (Eu 3+ /Tb 3+ ) complexes. The sensors exhibited a pronounced color transformation property due to the differential quenching of Eu 3+ and Tb 3+ emissions upon drug interactions. These luminescent hybrid DNA crystals present a significant advancement in sensing anticancer drugs like curcumin, transitioning from monitoring fluorescence intensity changes to a visually discernable color change. This new approach eliminates the need for specialized instrumentation. Owing to the intrinsic biocompatibility of materials composed of DNA, this hybrid sensor has the potential to sense drugs within the human body. Hybrid crystals loaded with a single complex will lose their fluorescence properties due to drug quenching; however, crystals loaded with mixed complexes emit distinct fluorescent colors, such as yellow-green and orange-red, at different drug concentrations. This color transformation allows for the direct determination of drug concentration based on crystal color, making the sensing process more simple and easily observable.
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INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Huangyao Chen,Chonghui Qi,Xiang Guo,Jun Zhang,Chaoyong Deng,Ruirui Cui
In lead-free halide double perovskites, doping and alloying are key strategies for optical performance enhancement. However, achieving stable full-spectrum white emission in single-component phosphors remains challenging. Herein, high-quality single-phase white emission is realized in Cs2NaGdCl6 via Sb3+/Tb3+/Mn2+ codoping. Pristine Cs2NaGdCl6 shows a weak sky-blue emission, while Sb3+ doping significantly enhances the self-trapped exciton (STE) intensity. Density functional theory calculations show that Sb3+ doping creates new sensitizing states, boosting the STE emission. Under Sb3+ sensitization, STE energy transfers to Tb3+ and Mn2+. The incorporation of Tb3+ elevates the photoluminescence quantum yield from 0.66% (pristine) to 68.38% (CNGC: Sb3+, Tb3+), while the broadband red emission from Mn2+ plays a critical role in achieving full-spectrum coverage. Tunable white-light emission is achieved via a dopant ratio optimization. Combining the phosphor with a 340 nm commercial light-emitting diode chip produces a white light-emitting diode with a correlated color temperature of 4658 K and a color rendering index of 91.9. Temperature-dependent photoluminescence spectra confirm ratiometric sensing capability, yielding maximum relative sensitivities (Sr) of 1.06%/K (I463 nm/I608 nm) and 1.12%/K (I548 nm/I608 nm) at 298 K. These results demonstrate that this material exhibits multifunctional application potential in the fields of white-light illumination, optical thermometry, and fluorescent anticounterfeiting.
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DOI
PubMed
高影响因子
Journal of Materials Chemistry C
·
2019
·Vol. 8
·期 7
·2336-2342
·
IF 6.641
Rui Shi,Baohua Zhu,Mixia Hu,Haofei Zhou,Jianming Fan,Zhen Tao,Fei Chang,Shiyong Yu
The graphene oxide (GO)/rare earth Tb3+ complex hybrid, GO-1,1′:2′,1′′-terphenyl-4,4′′-dicarboxylic acid-Tb3+ (GO-L-Tb), luminescent micron crystals with special multi-layered six-petal flower shape were facilely obtained by treatment of the L-Tb with graphene oxide (GO) in N,N-dimethylformamide (DMF) solution using a solvothermal method. The as-prepared L-Tb and GO-L-Tb complex hybrids are characterized via Fourier-transform infrared spectroscopy, powder X-ray diffraction, thermogravimetric analysis, scanning electron microscopy, fluorescence microscopy, fluorescence spectroscopy, and X-ray photoelectron spectroscopy. The composite shows excellent fluorescence properties and can emit bright characteristic green fluorescence of rare earth Tb3+ with a long fluorescence lifetime. The unique six-petal flower fractal structure, good thermostability and brilliant fluorescence properties of the GO-L-Tb complex make it a promising candidate for application in micro-scale fluorescence anti-counterfeiting.
研究领域:
材料科学
·
光学
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DOI
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Polymers
·
2022
·Vol. 14
·期 9
·1655
·
IF 4.967
Jun Ye,Zichang Fu,Jiawei Rao,Jian Xiong
The influences of interactions between carboxymethyl cellulose (CMC) and CMC/europium (III)–terbium (III) (CET) on the structure and properties of the resultant CMC/CET films were investigated by rheology at three stages of the film-drying process. According to the water content at different drying times, the kinetics curves during the film-drying process were drawn. Then, the rheology properties of film-forming solutions during the drying process were characterized by dynamic modulus, Han plots, zero shear complex viscosity and relaxation time. When the water content was 90%, the film contained either 0.1 or 0.2 g of CET, which had good fluidity, while the film with 0.3 g of CET was elastic-dominated. Han plots and XRD analyses showed that the interactions between the CMC and CET were not hydrogen bonds but random entanglements. The zero-shear complex viscosity and relaxation time spectrum confirmed that the entanglements enhanced as the CET content increased. Meanwhile, aggregation formed in the solution of CMC with 0.3 g of CET. When CMC-CET films with different CET additions were compared, the film with 0.2 g of CET had an even and tight sheet structure, the greatest fluorescence intensity, and superior tensile strength of 78.76 MPa.Keywords:fluorescent carboxymethyl cellulose;rheological properties;mechanical property;polymer chain
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PubMed
高影响因子
ACS Applied Nano Materials
·
2021
·
IF 5.097
Jianzhong Yu,Song Ye,Yanling Shi,Huazhen Liao,Xinling Xv,Deping Wang
In this research, highly luminescent silver nanoclusters (Ag NCs) were prepared by using Na-FAUY zeolite as a scaffold to hinder their aggregation, and efficient energy transfer from Ag NCs to Tb3+ was realized in Ag+-Tb3+ dual-exchanged Na-FAUY zeolites and then proved by steady spectral and luminescence lifetime measurements. Furthermore, the effects of Ag+ loading amount, thermal treatment, and Tb3+ loading on the luminescence properties of Ag NCs were studied, and the optimized doping and preparing conditions were obtained. X-ray photoelectron spectroscopy together with spectral measurements indicated that the available sites for Tb3+ and Ag+ are competitive and Tb3+ doping may hinder the effective formation of Ag NCs. It is also indicated that the loading of Tb3+ may lead to reduced Si/Al ratios, which greatly influence the luminescence property and chemical state of Ag NCs, e.g., a high Si/Al ratio leads to blueshift emission and stronger ionic of Ag NCs. This research may benefit the design of Ag NCs-involved luminescent zeolites that have potential applications for photonic devices like LEDs and 3D displays.
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高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2016
·Vol. 28
·期 7
·5615-5622
·
IF 1.798
Chu Yang,Hao Haixia,Xie Hongde,Chen Cuili,Cai Peiqing,Seo Hyo Jin
In this work, we report the preparation of lanthanide (Eu 3+ , Tb 3+ )-complex-grafted copolymer of methyl methacrylate and maleic anhydride films. The lanthanide complex with three amino groups was used to react with poly(methyl methacrylate-co-maleic anhydride) (P(MMA-MAH)) via the amidation method. Fourier transform infrared (FT-IR), Transmission electron microscope (TEM), Scanning electron microscope (SEM), Thermogravimetric analysis (TGA) were employed to characterize those polymers. Luminescent properties were evaluated through conducting Photoluminescence (PL) excitation spectra, emission spectra and fluorescence decay curves measurements. The infrared analysis reveals the amidation between amino groups and anhydride rings. The comparatively uniform morphology can be observed in the images of TEM and SEM. These polymers can emit intense characteristic lights including red light from Eu 3+ ions and green light from Tb 3+ ions under 294 nm excitation. The lifetimes of polymers are short (about 1 ms). Meanwhile, these luminescent polymers exhibit high thermal stability (T 5 > 200 °C). We also stimulate a lamp to illustrate the possible application. All these approved interesting results suggest that they hold significant promising applications as luminous layers for optoelectronic devices.
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JOURNAL OF LUMINESCENCE
·
2024
·
IF 3.3
Chenglong Xia,Jiahui Yang,Bingyang Zeng,Chunmiao Cui,Haoyuan Weng,Yue Guo,Xiaoguang Liu,Ling Li
This study successfully synthesized Na 5 Y(WO 4 ) 4 doped with Sm³⁺, Pr³⁺, and Tb³⁺ using a high-temperature solid-state method. Photoluminescence spectra revealed that Na 5 Y(WO 4 ) 4 :Sm³⁺ phosphors emits a strong red glow at 646 nm under the excitation of 405 nm, and has an extremely high quantum yield, suggesting their suitability for plant growth LED lighting applications. In contrast, Na 5 Y(WO 4 ) 4 :Pr³⁺ phosphors displayed a lower efficiency but still aligned well with the red-wavelength absorption spectra of plants. Additionally, Na 5 Y(WO 4 ) 4 :Tb³⁺ phosphors demonstrated strong green emission under UV light, indicating potential applications in fingerprint detection. The Site Occupancy Theory (SOT) was utilized to explain the preferential occupation of dopant ions, showing that Sm³⁺ and Tb³⁺ preferred Y1 sites, whereas Pr³⁺ favored Na2 sites.
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