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JOURNAL OF LUMINESCENCE · 2022 · IF 4.171

Eu3+/Tb3+ bimetallic complex-doped siloxane-polyether hybrid film for luminescent thermometry

Guangmin Xie,Yuan Wang,Xinzhe Zhou,Liang He,Huanrong Li

Developing a contactless ratiometric luminescent thermometry with high sensitivity, widely available temperature range, and reliable performance is still a challenge in materials science. Herein, we adopted an in-situ formation strategy to synthesize luminescent lanthanide complexes in siloxane-polyether matrix by the reaction between 4′-(4-carboxyphenyl)- 2,2′:6′,2″- terpyridine (Hcptpy) ligand and lanthanide ions (Eu 3+ /Tb 3+ ) to realize a ratiometric luminescent thermometer. The unique energy cascade from Hcptpy → Tb 3+ → Eu 3+ in siloxane-polyether enables the luminescent films to be not only the multi-color emission, but also provide highly temperature-sensitive over the wide temperature range. The EuTb 15 @SP film for luminescent thermometry performance is fine-tuned to reach a maximum relative sensitivity of 7.26% K −1 at 397 K and shows repeated utilization without sensitivity loss. Furthermore, the multi-color emission ranging from red through yellow to green can be achieved by tuning the Eu 3+ /Tb 3+ molar ratio. Consequently, utilizing siloxane-polyether as matrix has been proven to be an effective strategy for constructing lanthanide-based hybrid films with temperature sensor properties. We believe that the reported strategies for preparing a bimetallic complex-doped siloxane-polyether hybrid film will broaden potential applications.

CAS / MDL: 24801-88-5
研究领域: 材料科学 · 光学
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JOURNAL OF LUMINESCENCE · 2015 · IF 2.719

Au@NaYF4:Tb3+ core@shell nanostructures: Synthesis and construction of luminescence resonance energy transfer

Yan Song,Guixia Liu,Xiangting Dong,Jinxian Wang,Wensheng Yu

Luminescence resonance energy transfer (LRET) system can be constructed using NaYF 4 :Tb 3+ luminescence nanocrystals and gold nanoparticles (AuNPs) served as energy donor and acceptor, respectively. The AuNPs modified by cetyltrimethylammonium bromide (CTAB) were synthesized first and NaYF 4 :Tb 3+ shells encapsulated Au cores via a hydrothermal method . The synthesized materials were well characterized by X-ray diffraction (XRD), Fourier-transform infrared spectra (FT-IR), Transmission electron microscopy (TEM), X-ray photoelectron spectrum (XPS), UV–vis absorption spectra (UV–vis) and photoluminescence (PL) measurement. The results indicate that the synthesized Au@NaYF 4 :Tb 3+ core–shell nanoparticles have spherical morphology with a size of 80–90   nm and the shell layers of NaYF 4 :Tb 3+ nanocrystals have pure cubic structure. The luminescence properties of Au@NaYF 4 :Tb 3+ core–shell nanoparticles are same as those of NaYF 4 :Tb 3+ particles. The LRET process was realized using the core–shell nanoarchitectures due to the absorption spectrum of AuNPs matches well with the major emission peaks of Tb 3+ ions. The LRET experiments have successfully verified the energy transfer between NaYF 4 :Tb 3+ nanocrystals and AuNPs. Additionally, the emission intensities of Tb 3+ ions and the content of AuNPs exhibited a fair linear correlation.

研究领域: 材料科学 · 光物理学 · 纳米技术
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CRYSTENGCOMM · 2018 ·Vol. 20 ·期 26 ·3657-3665 · IF 3.304

Tb3+- and Yb3+-doped novel KBaLu(MoO4)3 crystals with disordered chained structure showing down- and up-conversion luminescence

G. Q. Wang,L. Y. Li,Y. N. Feng,H. Yu,X. H. Zheng

In this study, a novel dual-mode luminescence phosphor KBaLu(MoO4)3:Tb3+,Yb3+ has been synthesized by high-temperature solid-state reactions, and the crystal structures have been determined for the first time. Single-crystal X-ray diffraction data reveal that its space groups are C2/c. The crystalline structure is constituted by K/BaO8 distorted square antiprisms, distorted LuO8 polyhedra and two kinds of distorted MoO4 tetrahedra, which form chains lying along the c-axis. Spectroscopic properties and energy transfer mechanisms are investigated by detailed analyses of emission and excitation spectra and excited-state lifetimes. The KBaLu(MoO4)3:Tb3+,Yb3+ phosphor shows dominant green emissions in the visible region, which are due to 5D4 → 7F5 transition of Tb3+ under excitation light in ultraviolet region as well as a 980 nm laser, and the CIE coordinates are close to the Society of Motion Picture and Television Engineers (SMPTE) standard values for primary green (0.310, 0.595). With the increasing temperature, the luminescence of KBaLu(MoO4)3:Tb3+,Yb3+ phosphor decreases almost linearly with the CIE coordinate variation from (0.326, 0.616) to (0.327, 0.530), which results in photoluminescence color variation from primary green to yellowish-green. The present results demonstrate the successful synthesis of a dual-mode luminescence material KBaLu(MoO4)3:Tb3+,Yb3+ phosphor with both up- and down-conversion luminescence properties; moreover, it can be used as a potential spectrum converter in display lighting and anti-counterfeiting.

研究领域: 光学材料 · 固体化学 · 发光材料 · 晶体学 · 光谱学
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Journal of Materials Chemistry C · 2020 ·Vol. 8 ·期 13 ·4408-4420 · IF 7.059

Highly efficient near-UV-excitable Ca2YHf2Al3O12:Ce3+,Tb3+ green-emitting garnet phosphors with potential application in high color rendering warm-white LEDs

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.

CAS / MDL: 12055-23-1
研究领域: 材料科学 · 光学工程
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2019 · IF 2.931

Multi-component luminescence responsive Eu3+/Tb3+ hybrids based with metal-organic frameworks and zeolites A

Jing Ma,Bing Yan

Both Zeolite A (ZA) and two kinds of 2,2′-bipyridine-5,5′-dicarboxylic acid (H 2 bpydc) linking meta-organic frameworks (MOFs) (MOF-253 (Al(OH)(bpydc)) and UiO-67 ([Zr 6 O 4 (OH) 4 (bpydc) 6 ])) have been used to construct novel photofunctional multi-component lanthanide hybrid materials through covalent-coordination cooperative assembly. Microporous ZA is firstly functionalized by covalently grafting of the surface hydroxyl groups using special silane crosslinking reagent 3-methacryloxypropyltrimethoxysilane (MPTMS). Then the multi-component assembly are realized by coordination interaction between lanthanide ions (Eu 3+ /Tb 3+ ), ZA through the carbonyl group of MPTMS unit and MOF-253 (or UiO-67) through the double nitrogen of bpydc linker. Subsequently, the obtained multicomponent hybrid materials (ZA-MPTMS-Eu/Tb-MOF-253(UiO-67)) are characterized by means of XRD, FT-IR, SEM and especially the photoluminescence properties are studied in details. These hybrids with both ZA and MOFs host show the main characteristic crystal framework morphology of ZA together with the composition of MOFs. They display the feature luminescence of Eu 3+ /Tb 3+ ions for the energy transfer from bpydc linker of MOFs. Furthermore, ZA-MPTMS-Eu-UiO-67 hybrid material is selected to check the luminescence response to volatile substances, whose luminescence quenching is found for ammonia vapor.

研究领域: 材料科学 · 化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Nanoarchitectonics of Ln3+ (Eu3+/Tb3+)-induced polyelectrolyte aggregates (LIPAs) for multicolor luminescence in 3D-printed poly(Lactic acid)

Jin Liu,Yaowei Guo,Yupeng Bi,Yao Wang,Yanxin Wang,Matt J. Kipper,Laurence A. Belfiore,Jianguo Tang

Reversible bright-dark luminescence nanomaterials have been developed for information storage and anti-counterfeiting in recent years, however, their monochrome characteristic and 2D patterning impose limits on the effective information storage density. In this work, a new strategy for producing ultraviolet switchable and stable luminescent patterns is proposed, based on Ln 3+ (Eu 3+ /Tb 3+ ) induced-polyelectrolyte aggregates (LIPAs) with sharp multi-color optical properties . Under 365 nm excitation, a multicolor pattern can be observed using both red and green, which is not visible when this excitation light source is off. The LIPAs enable the luminescent lanthanide complexes to be compatibilized with poly(lactic acid) (PLA). Functional anti-counterfeiting patterns were prepared by 3D printing using luminescent PLA containing by Ln 3+ (Eu 3+ /Tb 3+ ) LIPAs. Invisible, adjustable and ultra-stable multicolor luminescent patterns well enable information storage and enhance information security for anti-counterfeiting applications.

研究领域: 材料科学 · 纳米技术 · 光学
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2014 ·Vol. 16 ·期 29 ·15139-15145 · IF 4.198

Synthesis and luminescence resonance energy transfer based on noble metal nanoparticles and the NaYF4:Tb3+ shell

Yan Song,Guixia Liu,Jinxian Wang,Xiangting Dong,Wensheng Yu

A core–shell hybrid nanostructure was prepared by combining NaYF4 doped with the lanthanide dopant Tb3+ as shell layer materials and noble metal nanoparticles (Au and Ag) as cores. For the core–shell system, the luminescence resonance energy transfer (LRET) was demonstrated, in which noble metal nanoparticles as fluorescence quenchers can absorb the emission energy of the α-NaYF4:Tb3+ donor. The morphology, structure, composition and properties of the as-prepared samples were characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), UV-Vis absorption and photoluminescence (PL) spectroscopy, respectively. In the Au/Ag@NaYF4:Tb3+ system, it is observed that the plasmonic absorption bands of gold or silver nanoparticles overlap with the emission bands of 5D4 → 7Fj (j = 6, 5) transition of the Tb3+ ions, and the emission intensity of the 5D4 → 7F5 transition is clearly attenuated. The photoluminescence decay curve measurements show that the lifetimes of the 5D4 → 7F6 and 5D4 → 7F5 transitions of Tb3+ are slightly decreased in the presence of gold or silver cores. The quenching efficiency of the gold and silver nanoparticles implies that the efficiency of energy transfer is highly dependent on the extent of spectral overlap in the LRET system.

CAS / MDL: 16903-35-8 7761-88-8
研究领域: 材料科学 · 光学
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CRYSTENGCOMM · 2013 ·Vol. 15 ·期 41 ·8262-8272 · IF 3.879

Synthesis of NaYF4:Eu3+/Tb3+ nanostructures with diverse morphologies and their size- and morphology-dependent photoluminescence

Qin Wang,Yunxia Liu,Baocang Liu,ZhanLi Chai,Guangran Xu,ShengLi Yu,Jun Zhang

Cubic α- and hexagonal β-phase lanthanide luminescent NaYF4:Eu3+/Tb3+ nanostructures with diverse morphologies were successfully synthesized via a mild solvothermal method. The effects of the synthetic parameters on the crystal phase structure, size and morphology of NaYF4:Eu3+/Tb3+ nanostructures were systematically investigated. By modifying the synthetic parameters, the crystal phase structure, size and morphology were well controlled, and the phase transition from cubic α- to hexagonal β- can be easily realized. Furthermore, the morphology evolution is revealed, and the surfactant modulating formation mechanisms with diverse morphologies was proposed. The photoluminescence properties were found to be in close correlation with their composition, phase structure and morphology. NaYF4:Eu3+/Tb3+ nanostructures possessing unique morphologies and highly efficient luminescence may find potential applications in optoelectronics, sensors and biolabels.

CAS / MDL: 1308-96-9 12036-41-8
研究领域: 材料科学 · 光学 · 纳米技术
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DALTON TRANSACTIONS · 2020 ·Vol. 49 ·期 43 ·15433-15442 · IF 4.174

The morphology evolution, tunable down-conversion luminescence, and energy transfer of [CaY]F2 crystals doped with Li+/Ce3+/Tb3+

Yini Mao,Zhiyi Wang,Rui Ye,Li Jiang,Shanshan Hu,Jun Yang

Octahedral [CaY]F2 crystals with an average particle size of 1 μm were synthesized via a mild one-step hydrothermal route without employing any surfactants. Various morphologies, including cubes, truncated cubes, truncated octahedrons, and spheres, were achieved via manipulating the amount of EDTA used, and a possible growth mechanism was proposed based on the surface energies of different crystal planes and the influence of the surfactant. XRD, SEM, EDS, TEM, HRTEM, and PL analysis were used to characterize the products. The effects of the morphologies and Li+ doping concentrations on the luminescence intensities of the [CaY]F2:Ce3+/Tb3+ phosphors were explored, and the strongest luminescence intensity is obtained when the sample is cubic with (100) crystal faces and the doping concentration of Li+ is 0.25 mol%. Additionally, multicolor emission (blue → aquamarine blue → green) was obtained from [CaY]F2:Ce3+/Tb3+ phosphors via adjusting the doping concentration of Tb3+, which resulted from the Ce3+ → Tb3+ energy transfer behavior; the energy transfer here happened through a dipole–dipole mechanism. This work may result in the as-synthesized phosphors having great application potential in many optoelectronic device fields, such as in displays and multicolor lighting.

CAS / MDL: 60-00-4
研究领域: 材料科学 · 光学
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ACS Applied Nano Materials · 2021 · IF 5.097

Confinement of Highly Luminescent Silver Nanoclusters in FAUY Zeolite: A Study on the Formation Effects of Silver Nanoclusters and the Sensitization of Tb3+

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.

CAS / MDL: 7761-88-8 57584-27-7
研究领域: 材料科学 · 光电子学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

Ce3+/Tb3+ co-doped β-NaYF4 dual-emitting phosphors for self-referencing optical thermometry

Mingye Ding,Chunhua Lu,Le Chen,Zhenguo Ji

Traditional FIR (fluorescence intensity ratio)-based optical thermometers, requiring narrow energy gap between two thermally coupled states (TCS) of single rare-earth ion, have inherent drawbacks including low signal discriminability and large measuring error. To overcome the intrinsic limitation, a new thermometry strategy involving the usage of dual-emitting activators with diverse temperature-dependent emission behaviours has been proposed. Impressively, β-NaYF 4 :Ce 3+ /Tb 3+ phosphor exhibits good temperature sensing performance, excellent signal discriminability and superior thermal stability by using the linearly temperature-dependent FIR between Ce 3+ and Tb 3+ as detecting parameter. Hopefully, the developed dual-emitting sample could have a promising application in self-calibrated luminescent thermometry and this strategy provides a reference for developing high-performance optical thermometers.

研究领域: 材料科学 · 光学工程 · 无机化学 · 生物医学工程 · 纳米技术 · 传感器
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 24 ·19477-19489 · IF 2.779

A novel blue-emitting Tm3+ and Tb3+ co-doped Ca9Nd(PO4)7 phosphor for white light-emitting diodes

Zhao Jianwen,Dong Jun,Zhou Jian,Wang Linsheng

White light-emitting diodes (WLEDs) are of paramount importance in the development of lighting and display in replace of inefficient fluorescence as well as incandescent lamps. In this work, Tb 3+ , and Tm 3+ were both introduced into a novel phosphate host Ca 9 Nd(PO 4 ) 7 . The X-ray diffraction (XRD) analyses make sure that the materials have been synthesized successfully. Further XRD Rietveld refinements were used to shed light on the site preference and the variations of crystal lattice parameters. Strong blue light emission was observed after careful optimization of the doping concentration. Theoretical computation on the basis of density functional theory checks the reliability of the phosphate host for doping luminescent centers. At last, a near-ultraviolet commercial LED chip was used with these materials to make a prototype WLED device. They possess a highly stable warm white light emission upon various driving currents (color temperature is constant 4000 K). The work has shown intriguing prospects of Ca 9 Nd(PO 4 ) 7 : Tm 3+ , Tb 3+ in lighting and display applications.

研究领域: 材料科学 · 光学工程
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