Synthesis and luminescent properties of BaGd2O4:Eu3+ phosphors with highly efficient red-emitting

The BaGd_(2-2 x)Eu_(2 x)O_4(BG, x = 0.01-0.09) phosphors were successfully synthesized via the sol-gel method,and BaY_(2-2 y)Eu_(2 y)O_4(BY, y = 0.005-0.07) phosphors were included for comparison. The pure phase BG phosphors with the ordered CaFe_2 O_4-type structure are obtained by annealing at 1300℃ for5 h. The phosphors with uniform particle size of 120 nm and good dispersion display typical Eu~(3+)emission with the strongest peak at 613 nm(~5 D_0→~7 F_2 transition of Eu3+) under optimal excitation band at 262 nm(CTB band). The presence of Gd~(3+) excitation bands on the PLE spectra monitoring the Eu3+emission directly proves an evidence of Gd~(3+)-Eu~(3+) energy transfer. Owing to the concentration quenching, the optimum content of Eu3+ addition is 5 at%(x = 0.05), and the quenching mechanism is determined to be the exchange reaction between Eu3+. All the BG samples have similar color coordinates and temperature of(0.64 ± 0.02, 0.36 ± 0.01) and 2000 ± 100 K,respectively. The lifetime value of BaGd_(1.9)Eu_(0.1)O_4 for 613 nm is fitted to be 2.19 ± 0.01 ms, and the Eu~(3+) concentration does not change the lifetime significantly. Owing to the Gd~(3+)-Eu~(3+) energy transfer, the luminescent intensity of the BaGd_(1.9)Eu_(0.1)O_4 phosphor is better than BY system. The BG system served as a new type of phosphor is expected to be widely used in lighting and display areas.     

Synthesis and luminescence properties of Tb3+/Eu3+ co-doped GdAlO3 phosphors with enhanced red emission

The(Gd_(0.97-x)Eu_xTb_(0.03))AIO_3(x= 0.005-0.07) phosphors were synthesized by the co-precipitation method,using ammonium bicarbonate as a precipitant.The combined technologies of FT-IR,XRD,FESEM,PLE/PL and photo luminescence decay analysis were used to study the phase evolution,morphologies and luminescent properties.The phosphors with good dispersion exhibit strong vivid red emission located at 617 nm(~5 D_0-~7 F_2 transition of Eu~(3+)) under the optimal excitation wavelength of 275 nm(~4 f~8-4 f~75 d~1 transition of Tb~(3+),~8 S_(7/2)→6~I_J transition of Gd~(3+)).The presence of Gd~(3+) and Tb~(3+) excitation bands on the PLE spectra monitoring the Eu~(3+) emission directly gives an evidence of Tb~(3+) → Eu~(3+) and Gd~(3+) → Eu~(~(3+)) energy transfer,The emission intensity varies with the Eu~(3+) amount,and the quenching concentration is ～5 at% which is close to the calculated value.The quenching mechanism is determined to be the exchange reaction between Eu~(3+).The temperature-dependent PL analysis indicates that the best(Gd_(0.92)Eu_(0.05)Tb_(0.03))AlO_3 sample possesses good thermally stable properties.All the(Gd_(0.97-x)Eu_xTb_(0.03))AIO_3 phosphors in this work have similar CIE chromaticity coordinates and color temperatures,which are(0.65 ± 0.02,0.35 ± 0.02) and ～2558 K,respectively.Fluorescence decay analysis shows that the lifetime for～617 nm emission decreases with the content of Eu~(3+) and temperature increasing.Owing to the Tb~(3+)→ Eu~(3+) energy transfer,the luminescent properties of the(Gd_(0.92)Eu_(0.05)Tb_(0.03))AlO_3 phosphors are superior to the single Eu~(~(3+)) doped sample(Gd_(0.95)Eu_(0.05))AlO_3.As a result,the prepared phosphors may be widely used in solid-state display and light emitting devices.     

Preparation,structure, luminescence properties of europium doped zinc spinel structure green-emitting phosphor ZnAl2O4:Eu2+

The Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders were synthesized by the solid-state reaction method.The synthesis temperature for ZnAl_2 O_4 was optimized,whereas the phase structure,TEM images,photoluminescence(PL) properties,the concentration quenching mechanism,the fluorescence decay curves,as well as the CIE chromaticity coordinates of the samples were investigated in details.Under the excitation at 379 nm,the phosphor exhibits an asymmetric broad-band green emission with a peak at 532 nm,which is ascribed to the 5 d-4 f transition of Eu2+.When the doping concentration of Eu2+ ions is 0.01,the luminescence intensity of the sample reaches the maximum value.It is further proved that the exchange interaction results in the concentration quenching of Eu2+ in the Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders.The thermal quenching property of ZnAl_2 O_4:Eu~(2+)phosphor was investigated and the quantum efficiency(QE) values of the selected Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) phosphor was measured and determined as 54.85%.The lifetime of the optimized sample Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) is 3.0852 μs and the CIE coordinate of the sample was calculated as(0.3323,0.5538) with high-color-purity green emission.All properties indicate that the green-emitting ZnAl_2 O_4:Eu~(2+) phosphor powder has potential application in white LEDs.     

Synthesis and optical characterization of Eu2+,Tb3+-codoped Sr3Y(PO4)3 green phosphors

A series of Eu~(2+),Tb~(3+)-codoped Sr_3 Y(PO_4)_3(SYP) green phosphors were synthesized by hightemperature solid-state reaction. Several techniques, such as X-ray diffraction, UV-vis spectrum,and photoluminescence spectrum, were used to investigate the obtained phosphors. The present study investigates in detail photoluminescence excitation and emission properties, energy transfer between the two dopants, and effects of doping ions on optical band gap. SYP:0.05 Eu2+ phosphor shows an intense and broad excitation band ranging from 220 to 400 nm and exhibits a bright green emission band with CIE chromaticity coordinates(0.189, 0.359) under 350 nm excitation. Green emission of SYP:0.03 Tb3+ is intensified by codoping with Eu~(2+), and energy transfer mechanism between them is demonstrated to be a dipole-dipole interaction. Upon 350 nm excitation, SYP:Eu~(2+),Tb~(3+) phosphors exhibits two dominating bands peaking at 466 and 545 nm, which are assigned to 4 f~65 d~1→4 f~7 transition of Eu~(2+) ions and ~5 D_4→~7 F_5 transition of Tb~(3+) ions, respectively. Optimal doping concentrations of Eu~(2+) and Tb~(3+) in the SYP host are 5 mol% and 15 mol%, respectively. Results indicate that SYP:Eu~(2+),Tb~(3+) phosphors are potentially used as green-emitting phosphors for white light-emitting diodes.     

Upconversion multicolor tuning of NaY(WO4)2:Tb3+ with Eu3+ doping

A series of Tb~(3+) and Eu~(3+) co-doped NaY(WO_4)_2 phosphors were synthesized by hydrothermal reactions.The crystal structure,morphology,upconversion luminescent properties,the energy transfer from Tb~(3+) to Eu~(3+)ions and the ~5 D_4→ ~7 F_5 transition of the Tb~(3+) ion in NaY(WO_4)_2:Tb~(3+),Eu~(3+) phosphors were investigated in details.The results indicate that all the synthesized samples are of pure tetragonal phase NaY(WO_4)2.Furthermore,the micrometer-sized needle spheres and excellent dispersion of the particles are obtained by adding polyethylene glycol(PEG-2000) as the surfactant.Phosphors of NaY(WO_4)_2:Tb~(3+),Eu~(3+) exhibit the492 nm blue emission peak,546 nm green emission peak,595 nm orange emission peak and 616 nm red emission peak under 790 nm excitation.The energy transfer from Tb~(3+) to Eu~(3+) is a resonant transfer,in which electric dipole-dipole interaction plays a leading role.By adjusting the doping concentration of Eu~(3+) in NaY(WO_4)_2: 1.0 mol%Tb~(3+),xmol%Eu~(3+) phosphors,the emitting color of UC phosphors can be tuned from green to red.     

Luminescence properties of Eu2＋ -doped Ba3Si6O12N2 green phosphor： concentration quenching and thermal stability

The efficient Eu2+ -doped Ba3 Si6O12N2 green phosphors were prepared by a traditional solid state reaction method under N2 /H2 atmosphere at a temperature up to 1350 oC for 12h. Photoluminescence (PL) properties showed a broad emission band with a peak of 525 nm and the full width of half-emission maximums (FWHM) of 70 nm under 460 nm light irradiation. The X-ray diffraction patterns (XRD) and scanning electron microscope (SEM) images of the synthesized powder demonstrated its pure phase and excellent crystallization. Quenching concentration in this phosphor was found to be 0.3. The mechanisms of concentration quenching and redshift of emission peak with increasing concentration of Eu2+ were studied. The temperature dependence measurement of this green phosphor revealed excellent thermal quenching property compared to silicate green phosphor. It is believed that Ba3 Si6O12N2 :Eu2+ is an excellent green phosphor for UV or blue chip based white LEDs.     

Optical characteristics of Ce,Eu:YAG single crystal grown by Czochralski method

Eu-doped Ce:YAG single crystal (SC) was fabricated by the Czochralski method. The crystal structure, optical and photoelectric property of the constructed w-LED was investigated. The XRD and HRTEM results show that YAG crystal structure has little change when Eu³⁺, Ce³⁺ are doped. Absorption spectra and photoluminescence spectra show that the Ce,Eu:YAG single crystal can effectively absorb the 460 nm blue light to form a broadband emission center at 530 nm, decay curves of the crystal show that the energy transfer between Ce³⁺ and Eu³⁺ is highly suppressed. Compared with commercial Ce:YAG phosphor, Ce,Eu:YAG exhibits better thermal stability.     

Luminescent properties of Eu~（3＋） doped Gd_2WO_6 and Gd_2（WO_4）_3 nanophosphors prepared via co-precipitation method

Eu3+ doped Gd2WO6 and Gd2(WO4)3 nanophosphors with different concentrations were prepared via a co-precipitation method. The structure and morphology of the nanocrystal samples were characterized by using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM), respectively. The emission spectra and excitation spectra of samples were measured. J-O parameters and quantum efficiencies of Eu3+ 5D0 energy level were calculated, and the concentration quenching of Eu3+ luminescence in different matrixes were studied. The results indicated that effective Eu3+:5D0-7F2 red luminescence could be achieved while excited by 395 nm near-UV light and 465 nm blue light in Gd2WO6 host, which was similar to the familiar Gd2(WO4)3:Eu. Therefore, the Gd2WO6:Eu red phosphors might have a potential application for white LED.     

Microstructure and Properties of Fe–Cr–B–Al Alloy After Heat Treatment

By means of optical microscope, scanning electron microscope, X-ray diffraction, energy dispersive spectrometer, Rockwell and Vickers hardness tester, and wear tester, the microstructure and properties of Fe–10Cr–1B–4Al alloy quenched in different temperature has been studied. The results show that the microstructure of as-cast Fe–10Cr–1B–4Al are composed of pearlite, ferrite and the eutectic borocarbide which shows a network distribution along grain boundaries. The eutectic borocarbides are composed of M₇(C, B)₃, M₂(B, C) and M₂₃(C, B)₆. As the quenching temperature increases, the network structure of eutectic borocarbide breaks, but the type of eutectic borocarbide has no obvious change, and the matrix structure changes gradually from ferrite to pearlite. As the quenching temperature increases, the macro-hardness and the matrix micro-hardness of Fe–10Cr–1B–4Al alloy increases gradually. The macro-hardness and matrix micro-hardness of alloy reach the highest value of 45.7 HRC and 388.1 HV, respectively when the quenching temperature is 1150 °C. The hardness of alloy decreases slightly when the quenching temperature is too high. While quenching at 1150 °C, the alloy has the highest wear resistance and good comprehensive properties.     

Influence of reaction parameters on the luminescence properties of monodisperse NaGd(1−x−y)(WO4)2:xEu3+,yTb3+ phosphor by molten salt synthesis

Eu~(3+) activated and Eu~(3+), Tb~(3+) co-activated monodisperse sodium double tungstates NaGd(WO4)2 phosphors were prepared by molten salt method at 750 ℃ for 10 h using NaCl as a flux. The crystal structure and morphology of the as-synthesized phosphors were measured by XRD and SEM, respectively. The photoluminescence properties were characterized by PL spectra, decay lifetime and CIE. The presence of NaCl plays an important role in the morphology and luminescence properties. In this work,NaCl and one of the raw material Na_2 CO_3 in a certain proportion will form a low eutectic salt to decrease the reaction temperature and benefit the formation of monodisperse NaGd(WO_4)_2 crystals. The color of Eu~(3+) and Tb~(3+) co-doped NaGd(WO_4)_2 phosphors can be tuned from creamy white to orange, red and green by adjusting the doping concentration of rare earth ions, since the emission contain the broad blue-green emission origin from NaGd(WO_4)_2 host and characteristic red and green emission origin from Eu~(3+) and Tb~(3+) ions. The electroluminescent spectra and CIE measurement shows that the LED device with NaGd_((1-x))(WO_4)_2:xEu~(3+)(x = 0.24) phosphor can be excited by 365 nm and 380 nm LED chip, and their CIE coordinate is(x = 0.45, y = 0.45) and(x = 0.36, y = 0.37), Ra is 80.3 and 86.3, T_c is 3196 and4556 K, respectively. As a single-component phosphor, NaGd(WO_4)_2:Eu~(3+),Tb~(3+) have potential application in UV-pumped WLEDs.     

Optical and luminescence characteristics of Eu3+-doped B2O3:SiO2:Y2O3:CaO glasses for visible red laser and scintillation material applications

Europium(Eu~(3+)) doped glasses of chemical compositions(55-x)B_2O_3:10 SiO_2:25 Y_2O_3:10CaO:xEu_2O_3,where x denotes mol% and ranges 0≤ x ≤ 2.5, were synthesized by adopting conventional melt quenching technique, Physical properties like density, molar volume, polaron radius, inter-ionic distance and field strength of the glass samples were investigated to assess the impact of Eu_2O_3. Optical and luminescence properties of the glasses were characterized with optical absorption, photoluminescence,X-ray induced emission spectra, temperature dependence emission spectra and decay times. Judd-Ofelt(JO) intensity parameters(Ω_λ) of the glasses were evaluated based on the absorption spectrum of 0.5 mol%. JO parameters, calculated from absorption spectra with thermal corrections on oscillator strength, were used to evaluate radiative properties such as radiative transition probability(A_R),branching ratio(β_R), stimulated cross section emission(σ) and radiative lifetime(τ_R) for ~5D_0→~7 F_J(J = 0,1,2,3 and 4) transitions. The decay rate of ~5D_0 fluorescent level for all the glass samples was single exponential. Lifetimes of the ~5D_0 level were decreased with increasing concentrations of Eu~(3+)ions from 0.05 mol% to 2.5 mol% which might be due to energy transfer through cross-relaxation in the glasses. The chromaticity coordinates(x, y) were similar for all BSYCaEu glasses and were located at the red region of CIE 1931 color chromaticity diagram. Hence, these results confirm that the Eu~(3+) doped BSYCaEu glasses could be useful for visible red lasers and glass scintillation applications.     

Synthesis and luminescence properties of CdSe:Eu NPs and their surface polymerization of poly(MMA-co-MQ)

CdSe:Eu nanoparticles(NPs) were synthesized using an oil phase method and the substitution of Cd~(2+)with Eu3+ was confirmed by XRD,TEM,UV-Vis absorption and fluorescence emission analyses.The CdSe:Eu NPs are monodispersed and uniform spherical particles with a diameter of 3.2 nm,bigger than the pure CdSe NPs(2.3 nm),but with a similar cubic structure as CdSe NPs.Compared with those of pure CdSe NPs,both emission spectrum and absorption spectrum of CdSe:Eu NPs are red-shifted.The CdSe:Eu NPs are incorporated into poly(MMA-co-MQ) to afford poly(MMA-co-MQ)-CdSe:Eu NPs with the cubic structure and particle size(～3-4 nm) similar to those of CdSe:Eu NPs.The TEM imaging suggests that the CdSe:Eu NPs are uniformly dispersed in poly(MMA-co-MQ,) without any obvious aggregation.The fluorescent emission peak and absorption peak of poly(MMA-co-MQ)-CdSe:Eu NPs are between those of CdSe:Eu NPs and poly(MMA-co-MQ),possibly due to the energy transfer caused by the interactions of Cd or Eu atoms on the surfaces of CdSe:Eu NPs with the N and O atoms of poly(MMA-co-MQ).These CdSe:Eu and poly(MMA-co-MQ)-CdSe:Eu NPs with tunable photoluminescence properties can be potentially used for the fabrication of optical and optoelectronic devices.     

Preparation,luminescence and photofunctional performances of a hybrid layered gadolinium-europium hydroxide

The design and fabrication of rare earth ions incorporated into the inorganic/organic hybrid materials have attracted growing attention for seeking improved optical properties and photofunctional performances.In this paper,a novel hybrid composite based on the layered rare earth hydroxides was successfully prepared by the ion-exchange and intercalation chemical process.The rare earth elements in the composite contain gadolinium(Gd) and europium(Eu) and the molar ratio of Gd to Eu is kept constan...     

Effect of Li+ ion concentration on upconversion emission and temperature sensing behavior of La2O3:Er3+ phosphors

The effects of Li~+ co-doping concentration on the structure, upconversion luminescence and temperature sensing behavior of Er~(3+):La_2O_3 phosphors were investigated. X-ray diffraction and scanning electron microscopy observations reveal that Li~+ ion co-doping can change the lattice parameter of La_2O_3 host and increase the particle size of the samples. The optical investigation shows that co-doping of Li~+ ions can enhance the upconversion emission of Er~(3+) ions in La_2O_3 matrix effectively. Most importantly, the temperature sensing sensitivity of the samples is found to be dependent on Li~+ co-doping concentration,when the emission intensity ratio of the(~2H_(11/2)→~4 I_(15/2)) and(~4 S_(3/2)→~4 I_(15/2)) transitions of Er~(3+) is chosen as the thermometric index. Both of the optimum upconversion luminescence and temperature sensing sensitivity are obtained for 7 mol% Li~+ co-doped sample. When the Li~+ concentration is beyond 7 mol%,both the quenching in upconversion intensity and the degradation of temperature sensitivity are observed, which may be due to the serious distortion in local crystal field around Er~(3+) ions caused by the excess Li~+ ions.     

One pot synthesis of TiO2:Eu3+ hierarchical structures as a highly specific luminescent sensing probe for the visualization of latent fingerprints

In the present work, TiO₂:Eu³⁺ (1 mol%–11 mol%) nano powders (NPs) were prepared via a facile one-pot hydrothermal method by using Epigallocatechin Gallate (EGCG) as bio-surfactant. The optimized TiO₂:Eu³⁺ (5 mol%) NPs can be used as fluorescent labeling agent for visualizing of latent fingerprints (LFPs) on various porous and non-porous surfaces. The obtained results exhibit well defined ridge details with high sensitivity, selectivity, and low background hindrance which show greater advantages as compared to conventional powders. We demonstrated the viability of high-performance security labels thorough excellent luminescence for practical anti-mimetic applications. Morphology of the prepared samples is highly dependent on pH, concentration of the bio-surfactant, temperature and time durations. Photoluminescence (PL) emission spectra exhibit intense red emission at ～ 615 nm due to electric dipole transition (⁵D₀→⁷F₂). Photometric (CIE and CCT) results clearly show the intense warm red emission of the optimized samples. Therefore, this work offers a superior and universal luminescent label, which can be applied to visualize miniature LFPs particulars for individualization and consequently display great prospective in forensic investigation.     

Physical,structural and optical studies on magnesium borate glasses doped with dysprosium ion

Intense visible emissions from dysprosium(Dy3+) ions doped glasses became prospective for diverse technological applications. In this paper, physical, optical and structural properties of magnesium borate glasses doped with varied concentrations of Dy_2 O_3 were examined. Such glasses were synthesised by melt quenching method and characterized at room temperature using several analytical techniques.Luminescence and absorption spectra(in the visible region) of as-quenched samples were used to evaluate the physical and optical properties. XRD pattern confims the amorphous state of as-quenched samples. The Fourier transform infrared(FTIR) spectra of glasses reveal various bonding vibrations assigned to different functional groups. UV-vis-NIR spectra disclose eight absorption bands accompanied by a band for hypersensitive transition positioned at 1260 nm(~6 H_(15/2)→~6 F_(11/2)). The values of direct and indirect optical energy band gap of the studied glasses are decreased with the increase of Dy~(3+) ion contents. The photoluminescence spectra of all glasses under the excitation of 380 nm display two prominent emission bands centred at 497 nm(~4 F_(9/2)→~6 H_(15/2), blue) and 587 nm(~4 F_(9/2) →~6 H_(13/2), green).The achieved intense luminescence from the proposed glass composition may be beneficial for solidstate laser applications.     

Structural,morphological and optical properties of new Eu-doped and vacancied lead molybdato-tungstates

A new tetragonal,scheelite-type Pb_(1-3 x)■_xEU_(2 x)(MoO_4)_(1-3 x)(WO_4)_(3 x)(0 x ≤0.1970 and ■ denotes A-site vacancies) solid solution was synthesized via solid state reaction method. The X-ray diffraction(XRD) and scanning electron microscopy(SEM) results confirm the formation of single, tetragonal scheelite-type phases(space group I4_1/a) with the average crystallite size in the range of ～20-100 μm. Substitution of Pb~(2+) with Eu~(3+) is relatively easy despite the large difference in ionic radii, and the formation of vacancies is necessary to compensate the excess positive charge in PbMoO_4 framework. A change in lattice parameters(both a and c as well as lattice parameter ratio c/a) and progressive deformation of MoO_4 and WO_4 tetrahedra with increasing Eu concentration are observed. Thermal stability of Eu-doped materials strongly depends on the concentration of Eu3+ ions. The Pb_(1-3 x)■_xEu_(2 x)(MoO_4)_(1-3 x)(WO_4)_(3 x) solid solution for x=0.0098 shows the highest melting point(1057 ℃) which is slightly higher than that of pure PbMoO_4(1040 ℃). The UV-vis diffuse reflectance spectroscopy(DRS) and the Tauc plots were used to extrapolate the optical indirect band gap(E_g) of doped materials. Eu-doped ceramics are insulators(E_g 3 eV) and their band gap nonlinearly decreases with increasing dopant concentration.     

Solid-state synthesis of LnOCl/Ln2O3 (Ln = Eu,Nd) by using chitosan and PS-co-P4VP as polymeric supports

A series of lanthanide materials of type LnOCl or Ln_2 O_3(Ln = Eu, Nd) were successfully prepared via a convenient and straightforward two-step procedure. Firstly, and by using chitosan and PS-co-P4 VP as polymeric supports, macromolecular complexes of type chitosan ·LnCl_3 and PS-co-P4 VP·LnCl3 were prepared. These macro molecular complexes were treated in solid state at 800 ℃ under air, leading to the corresponding LnOCl or Ln_2 O_3 materials(Ln = Eu, Nd) with moderate to good yields. The nature of the asprepared lanthanide materials(LnOCl and/or Ln_2 O_3) is strongly influenced by the polymeric template(i.e.,chitosan or PS-co-P4 VP), the lanthanide salt precursor, and the polymer/lanthanide molar ratio. Thus, when chitosan · EuCl_3 and PS-co-P4 VP·EuCl_3 are used as macromolecular precursors, a mixture of crystalline phases of both EuOCl and Eu_2 O_3 are obtained. However, when chitosan· NdCl_3 and PS-co-P4 VP· NdCl_3 are used, a sole pure crystalline phase of NdOCl is obtained. The nano structured lanthanide materials were characterized by means of XRD(X-ray diffraction of powder), SEM, EDS, TEM, and HRTEM. The luminescent spectra of the asprepared EuOCI/Eu_2 O_3 mixture materials show an emission pattern whose intensity is strongly influenced by the nature of the polymeric precursor, as well as on the metal/polymer molar ratios.     

Eu2+-doped Sr5(PO4)3Br blue-emitting phosphor with high color purity for near-UV-pumped white light-emitting diodes

Eu²⁺-doped bromophosphateapatite Sr₅(PO₄)₃Br phosphors were synthesized by the conventional high-temperature solid-state reaction. The crystal structure and luminescence properties of the phosphors, as well as their thermal stability and CIE chromaticity coordinates were systematically investigated. Photoluminescence spectra of Sr₅(PO₄)₃Br:Eu²⁺ exhibit a single blue emission at 450 nm under the excitation of 345 nm, which is ascribed to the 4f–5d transition of Eu²⁺. The phosphor shows very good thermal stability. The CIE color coordinates are very close to those of BaMgAl₁₀O₁₇:Eu²⁺ (BAM). All the properties indicate that the blue-emitting Sr₅(PO₄)₃Br:Eu²⁺ phosphor has potential application in white LEDs.     

A highly sensitive luminescent metal–organic framework thermometer for physiological temperature sensing

Thermal sensing and imaging in the physiological temperature range are of great importance for studying physiological processes and treating diseases. Metal-organic frameworks(MOFs) exhibit great promise for developing luminescent thermometers due to their remarkable structural diversities and tunable luminescence properties. Here, we synthesized a series of luminescent mixed-lanthanide MOFs,Eu_xTb_(1-x)BPT(x = 0.019, 0.058, 0.106; H3 BPT = biphenyl-3,4',5-tricarboxylate acid) and adopted powder X-ray diffraction(PXRD), thermogravimetric analysis(TGA) and Fourier transform infrared(FT-IR) to characterize the resulting products. The temperature-dependent photoluminescence emission spectra were recorded to investigate their potential applications in physiological temperature readout. It is found that the intensity ratio of Tb~(3+) to Eu~(3+) is linearly correlated with temperature and the relative sensitivity is higher than 1.5%/℃ over the entire physiological temperature range. Furthermore,the temperaturedependent luminescence color emission allows for visual colorimetric temperature measurements.Luminescence lifetime testing and triplet energy level measurement were further conducted to study the mechanism.