Effects of Eu content on the luminescent properties of Y2O3:Eu3+ aerogels and Y(OH)3/Y2O3:Eu3+@SiO2 glassy aerogels

This article describes the morphological, structural, and luminescent properties of Y₂O₃:Eu³⁺ aerogels and Y(OH)₃/Y₂O₃:Eu³⁺@SiO₂ glassy aerogels synthesized by the sol-gel method with Eu concentrations from 2.5 mol% to 30 mol%. XRD measurements indicated that both the aerogels and glassy aerogels had a monoclinic phase, but the crystallinity in the glassy aerogels was lower due to the presence of SiO₂. SEM images reveal that a three-dimensional porous network was formed in the aerogels due to the interconnection of coalesced Y₂O₃:Eu³⁺ nanoparticles. The 3D porous network was also observed in the glassy aerogels, coated with a silica shell. In both the aerogels and glassy aerogels, the size of the agglomerates decreased as the europium concentration increased. This, in turn, increased the average size of the macropores that formed their 3D network. Furthermore, the luminescent properties of the aerogels and glassy aerogels were studied under UV excitation, and it was observed that their red emission intensity increased continuously as the Eu³⁺ concentration increased. The luminescence of the aerogels was on average 50% higher than that of the glassy aerogels. Hence, our results indicate that porous and luminescent aerogels with and without silica are adequate for applications in sensing and catalysis.     

Influence of deposition temperature on luminescent efficiency of Y2O3:Eu3+ thin films deposited on quartz fabric by EBE

Y₂O₃:Eu³⁺ thin films were grown on quartz fabric substrate by electron beam evaporation (EBE) at different deposition temperatures. It was found that an increase of deposition temperature from room temperature (R.T.) to 250 °C results in improved morphologies of the films, such as reduced defects, spherical particle shape and dense surface topography. A change in the predominant orientation of Y₂O₃:Eu³⁺ thin films was detected from (222) at low temperatures of R.T.–150 °C to (400) at higher temperatures of 200–250 °C. The luminescent intensity of the films was gradually improved with an increase in deposition temperature and the optimal brightness was observed when the films were grown at 250 °C and improved by 32.67% in comparison with that of the films grown at R.T. The results reveal that the improved morphologies and effective crystallization can contribute to the enhanced luminescent properties of the Y₂O₃:Eu³⁺ thin films.     

Ultraviolet radiation excited strong red-emitting LaAlO3:Eu3+ nanophosphors: Synthesis and luminescent properties

We synthesized the trivalent europium ions (Eu³⁺) doped lanthanum aluminate (LaAlO₃, LAO) nanophosphors by a solvothermal method. Their structural, morphological, and luminescent properties were systematically investigated. The obtained nanoparticles possessed single nanocrystallinity with a rhombohedral structure. For the excitation originating from the charge transfer band (O^2- to Eu³⁺ ions) under 320 nm illumination, the featured emissions of Eu³⁺ ions were detected in all the compounds. The optimum doping concentration of Eu³⁺ ions in LAO was about 9 mol% and the concentration quenching was dominated by dipole-dipole interaction. Furthermore, the Judd-Ofelt (J-O) theory was used to estimate the J-O intensity parameters. Based on the temperature-dependent PL emission spectra, the thermal stability was analyzed and the activation energy was obtained to be 0.234 eV. Meanwhile, the decay time, color coordinate/purity, and cathodoluminescence behaviors of the synthesized nanophosphors were also studied. These characteristics make the Eu³⁺-doped LAO nanoparticles a promising red-emitting phosphor for both ultraviolet-based white light-emitting diodes and field-emission displays.     

Monodisperse nanospheres of yttrium oxysulfide: Synthesis,characterization, and luminescent properties

A red long-lasting phosphorescent material, monodisperse Y₂O₂S: Eu³⁺, Mg²⁺, Ti⁴⁺ nanospheres have been prepared successfully. Y(OH)(CO₃): Eu³⁺ nanospheres were firstly synthesized via an urea-based homogeneous precipitation technique to serve as the precursor. Nanospheres long-lasting phosphors Y₂O₂S: Eu³⁺, Mg²⁺, Ti⁴⁺ were obtained by calcinating the precursor in CS₂ atmosphere. XRD investigation shows a pure phase of Y₂O₂S, indicating no other impurity phase appeared. SEM observation reveals that the structures are nanosphere. The Y₂O₂S: Eu³⁺, Mg²⁺, Ti⁴⁺ nanospheres with particle size about 100–150 nm show uniform size and well-dispersed distribution. After irradiation by ultraviolet radiation with 325 nm for 5 min, the phosphor emitted red color long-lasting phosphorescence corresponding to typical emission of Eu³⁺ ion. The main emission peaks are ascribed to Eu³⁺ ions transition from ⁵D_J (J = 0, 1, 2) to ⁷F_J (J = 0, 1, 2, 3, 4). Both the PL spectra and luminance decay revealed that this phosphor had efficient luminescent and long-lasting properties. It was considered that the red-emitting long-lasting phosphorescence was due to the persistent energy transfer from the traps to the Ti⁴⁺ and Mg²⁺ ions.     

White luminescence of bismuth and samarium codoped Y2O3 phosphors

In this work Sm³⁺ (0–2.0 at%) and Bi³⁺ (0–2.0 at%) doped Y₂O₃ luminescent powders were prepared by a sol–gel method from yttrium acetylacetonate, samarium and bismuth nitrates as metal sources. The as prepared powders (chemical composition is close to stoichiometric Y₂O₃) present the cubic structure from 700 °C, and at 900 °C are characterized by the presence of rounded particles with heterogeneous size of 42.9 nm. Luminescent effect of ions of Sm³⁺ and Bi³⁺ into Y₂O₃ host as was studied on heat treated powders from 800 to 1100 °C. The combination of the red luminescence from the Sm³⁺ ions and the bluish from Bi³⁺, makes the synthesized phosphors candidates to be used in fabrication of phosphor-converted light-emitting diodes (LEDs).     

Structural and spectral properties of red light emitting Eu3+ activated TiO2 nanophosphor for white LED application

The structural and luminescent properties of Eu³⁺ doped TiO₂ nanophosphors synthesized by low cost combustion method were investigated. The X-ray diffraction analysis revealed that crystallite size decreases with doping concentration. Lattice volume expansion occurred due to the substitution of Ti⁴⁺ ions by larger ionic radii ions Eu³⁺. FESEM images showed prepared phosphors to be nano size spherical shaped particles. Energy band gap of 3 mol% Eu³⁺ doped samples decreased to 3.15 eV due to doping effect. The Eu³⁺ doped TiO₂ nanophosphors exhibited main red emission peak centered at 616 nm under 395 nm UV light excitation. Concentration quenching was observed at 3 mol% doping, that has been ascribed to dipole-dipole interaction. The covalent nature of Eu-O bond and environment around Eu³⁺ ions were discussed using Judd-Ofelt (J-O) intensity parameters. Internal quantum efficiency was calculated using excited state lifetime ⁵D₀ state of Eu³⁺ ion and J-O theory. The CIE colour coordinates and colour purity were calculated using the spectral energy distribution function. Low excited state life time indicated that Eu³⁺ doped TiO₂ can be used as red emitting phosphor for white light emitting diode applications.     

Luminescence and structural study of Bi4−xEuxTi3O12 solid solution

The Bi₄Ti₃O₁₂ (BIT) is a well known ferroelectric ceramic within the family of so called Aurivillius phases. The present work shows that when bismuth (Bi³⁺, r = 0.96 Å) is substituted by trivalent europium (r = 0.95 Å), a solid solution, Bi_4−xEu_xTi₃O₁₂ (BIET), is formed. This solid solution was obtained by coprecipitation and characterized by X-ray diffraction, electron microscopy and density measurements. The solubility limit x was determined, and the variation of the lattice parameters was measured through profile fitting of the whole pattern. In order to establish the europium substitution site, we studied the luminescent properties of the material. The excitation spectra, at room temperature, show a broad band associated with a charge transfer state and with the intrinsic absorption of Bi³⁺. We found at least two Eu³⁺ sites, selectively excited. The Eu³⁺ emission spectra reveal a significant rising of the point symmetry at the rare earth site with respect to the Bi C₁, deduced from the crystallographic analysis.     

Synthesis and characterization of Eu3+-doped C12H18Ca3O18 phosphor

A series of Eu³⁺-doped C₁₂H₁₈Ca₃O₁₈ phosphors were synthesized through a facile hydrothermal method and the properties of as-prepared phosphors were explored by X-ray diffractometer (XRD), scanning electron microscope (SEM), and photoluminescence (PL) spectrometer. The exploration results indicated that the C₁₂H₁₈Ca₃O_18:Eu³⁺ had been successfully synthesized. The morphology of C₁₂H₁₈Ca₃O_18:Eu³⁺ was a strip with the size of 100–4000 nm × 50–400 nm × 50–200 nm and the ratio of length to width of 2–80. The strongest emission peak of C₁₂H₁₈Ca₃O_18:Eu³⁺ around 620 nm was ascribed to ⁵D_o→⁷F₂ transition of Eu³⁺, and the peaks centered at 590, 653 and 694 nm respectively corresponded to ⁵D_o →⁷F₁, ⁷F₃, and ⁷F₄ transitions. C₁₂H₁₈Ca₃O_18: Eu³⁺ gave the red light emission, as indicated by color coordinate analysis. The photoluminescence intensity of the phosphors prepared under the Eu³⁺ concentration of 6% was the highest. The crystal structure of C₁₂H₁₈Ca₃O_18:Eu³⁺ was changed after europium ions occupied the lattice position of calcium ions. Europium ion could displace calcium arbitrarily. As a new kind of matrix, calcium citrate possesses the properties of both organic and inorganic compounds and the luminescent C₁₂H₁₈Ca₃O₁₈: x Eu³⁺ particles may be applied in biological fluorescent tags and luminescent materials.     

Novel amorphous precursor densification to transparent Nd:Y2O3 Ceramics

A novel approach of neodymium ion doped yttrium oxide (Nd:Y₂O₃) amorphous precursor compaction and sintering is being reported for the first time. Precursor of 2 at.% Nd³⁺ doped Y₂O₃ was synthesized by gelation of sol of yttrium and neodymium nitrates with l-alanine at 80 °C for 16 h followed by gel combustion in microwave. A part of microwave precursor was heat treated at 700 °C for 5 h to give the partially crystalline Nd:Y₂O₃ amorphous precursor. Thermogravimetric analysis (TGA) of partially crystalline amorphous precursor of Nd:Y₂O₃ gave 8.5% total weight loss indicating removal of maximum organics. X-Ray diffraction (XRD) showed broad peaks indicating incomplete crystallization of cubic Nd:Y₂O₃. Morphology was found to be close to spherical with particles in size range 17–19 nm by TEM. Another part of microwave precursor on calcination at 1000 °C for 3 h led to formation of fully crystalline Nd:Y₂O₃ with particles in size range of 35–85 nm. Both partially crystalline amorphous precursor and fully crystalline Nd:Y₂O₃ were compacted at 400 MPa by cold isostatic press and sintered at 1750 °C for 10 h under vacuum (10^?5 mbar). The partially crystalline Nd:Y₂O₃ amorphous precursor densified to 99% with 65% transmission at 2500 nm (0.5 mm thickness) compared to 96% densification with 34% transmission for fully crystalline Nd:Y₂O₃ without any sintering aids. Retention of cubic phase purity of Y₂O₃ was observed in both the ceramic pellets post sintering by XRD. Good grain fusion with grain growth to ≤2 μm was observed by scanning electron microscope (SEM) for partially crystalline Nd:Y₂O₃ amorphous precursor. Thus partially crystalline Nd:Y₂O₃ amorphous precursor nanopowders, with homogeneous close to spherical fine particles and high reactivity due to ionic mobility of amorphous phase, led to better densification.     

Microwave-assisted hydrothermal synthesis of Eu2O3-coated spherical Y2O3 ceramic particles

This paper reports on the synthesis of uncoated and Eu₂O₃-coated spherical Y₂O₃ ceramic particles using optimized hydrothermal (HM) and microwave-assisted hydrothermal (MWHM) routes. The integration of microwave and hydrothermal processes was shown to enhance the reaction kinetics during the synthesis of uncoated Y₂O₃. Spherical particles of pure Y₂O₃ phase with an average particle size of 600 nm and uniform size distribution were obtained via the MWHM process at 180 °C following reaction duration of only 1 h. Y₂O₃ spherical particles were coated with Eu₂O₃ via a hydrolysis method at room temperature. The band gap of the resulting phosphors was estimated at 5.7 eV. Eu₂O₃-coated Y₂O₃ particles synthesized via the HM and MWHM present bright red PL emission under UV excitations; however, Y₂O₃ particles obtained via the MWHM method are more efficient than those yielded via the HM technique. Eu₂O₃-coated Y₂O₃ particles derived using the optimized MWHM technique present efficient emissions of red light with color purity and down conversion efficiency of approximately 85% and 80%, respectively. The present study demonstrates the suitability of employing coated phosphors in optical display technologies.     

White light emitting from YVO4/Y2O3:Eu3+,Bi3+ composite phosphors for UV light-emitting diodes

A series of (1−x)YVO₄/xY₂O₃:Eu³⁺_0.006,Bi³⁺_0.006 (0≤x≤0.54) composite phosphors was synthesized in one step by high temperature solid state reaction and the photoluminescence properties were investigated. By means of co-doping Eu³⁺ and Bi³⁺ ions into the composite matrices composed of YVO₄ and Y₂O₃ crystals, the YVO₄/Y₂O₃:Eu³⁺,Bi³⁺ phosphor exhibits simultaneously the blue (418 nm), green (540 nm) and orange-red (595, 620 nm) emissions. The broad blue and green emissions are attributed to the ³P₁–¹S₀ transitions of Bi³⁺ ion both in Y₂O₃ and in YVO₄ matrices. Moreover, the sharp orange-red emissions are attributed to the ⁵D₀–⁷F_1,2 transitions of Eu³⁺ ion in YVO₄ matrix. By tuning the mole ratio of YVO₄/Y₂O₃ matrices the white light-emitting could be obtained. The results indicated that when the mole ratio of Y₂O₃ (x) is at 0.11–0.54 mol, the (1−x)YVO₄/xY₂O₃:Eu³⁺_0.006,Bi³⁺_0.006 phosphors emit white light by combining the blue, green and orange-red emissions under the excitation of 360–370 nm wavelength which matches the emission of the commercial UV-LED diode. This implies that the phosphors may be the promising white light materials with broad absorption band for white light-emitting diodes.     

Luminescence and structural properties of Gd2SiO5:Eu3+ phosphors synthesized from the modified solid state method

This paper reports the preparation of Eu³⁺ doped Gadolinium oxyorthosilicate (Gd₂SiO₅:Eu³⁺) phosphor with different concentration of Eu³⁺(0.1–2.5 mol%) using the modified solid state reaction method. The synthesis procedure of the Gd₂SiO₅:Eu³⁺phosphor using inorganic materials such as Gd₂O₃, silicon dioxide (SiO₂), europium oxide (Eu₂O₃) and boric acid (H₃BO₃) as flux is discussed in detail. The prepared phosphor samples were characterized by using X-Ray Diffraction (XRD), Field Emission Gun Scanning Electron Microscopy (FEGSEM), Transmission Electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FTIR), Photoluminescence (PL) and Thermoluminescence (TL). The Commission Internationale de l′Eclairage(CIE) coordinates were also calculated. The PL emission was observed in the 350–630 nm range for the Gd₂SiO₅:Eu³⁺ phosphor. PL excitation peaks were observed at 266, 275, 312 and 395 nm while the emission peaks were observed at 380, 416, 437, 545, 579, 589, 607, 615 and 628 nm. The emission peak at 615 nm was the most intense peak for all the different Eu³⁺ concentration samples. From the XRD data, using the Scherrer's formula, the average crystallite size of the Gd₂SiO₅:Eu³⁺ phosphor was calculated to be 33 nm. TL was carried out for the phosphor after both UV and gamma irradiation. The TL response of the Gd₂SiO₅:Eu³⁺ phosphor for the two different radiations was compared and studied in detail. It was found that the present phosphor can acts as a single host for red emission (1.5 mol%) for display devices and light emitting diode (LED) and white light emission for Eu³⁺(0.1 mol%) and it might be used as a TL dosimetric material for gamma dose detection.     

Translucent and persistent luminescent SrAl2O4:Eu2+Dy3+ ceramics

Ceramics that exhibit persistent luminescence are usually opaque, which limits their utility. In this work, a laser-sintering technique is employed to produce persistent luminescent SrAl₂O₄:Eu²⁺Dy³⁺ ceramics that has enhanced translucency in the visible spectral range. In this technique, a CO₂ laser was used as the main heating source for sintering with no atmosphere control employed. The ceramics sintered at a power density of 3.1 W/mm² yielded homogeneous grain size distributions and transmittance up to 40% in the range of 600–800 nm. Upon sintering in air, the ceramics exhibited the characteristic green emission from the Eu²⁺ ion, corresponding to the 5d→4f transition (514 nm) and a weak emission from the Eu³⁺ ion at 614 nm, corresponding to the ⁵D₀→⁷F₂ transition. The valence of europium ions was further studied by the X-ray absorption spectroscopy in the XANES region and those details are reported herein.     

Synthesis and photoluminescence properties of the high-brightness Eu3+-doped Sr3Y(PO4)3 red phosphors

A series of red-emitting phosphors Eu³⁺-doped Sr₃Y(PO₄)₃ have been successfully synthesized by conventional solid-state reaction, and its photoluminescence properties have been investigated. The excitation spectra reveal strong excitation bands at 392 nm, which match well with the popular emissions from near-UV light-emitting diode chips. The emission spectra of Sr₃Y(PO₄)₃:Eu³⁺ phosphors exhibit peaks associated with the ⁵D₀ → ⁷F_J (J = 0, 1, 2, 3, 4) transitions of Eu³⁺ and have dominating emission peak at 612 nm under 392 nm excitation. The integral intensity of the emission spectra of Sr₃Y_0.94(PO₄)₃:0.06Eu³⁺ phosphors excited at 392 nm is about 3.4 times higher than that of Y₂O₃:Eu³⁺ commercial red phosphor. The Commission Internationale de l’Eclairage chromaticity coordinates, the quantum efficiencies and decay times of the phosphors excited under 392 nm are also investigated. The experimental results indicate that the Eu³⁺-doped Sr₃Y(PO₄)₃ phosphors are promising red-emitting phosphors pumped by near-UV light.     

Study on luminescence properties of co-doped nanoparticles Gd2O3:Tb3+, Eu3+ synthesized by polyol route

Spherical-like Tb³⁺ and Eu³⁺ co-doped Gd₂O₃ nanoparticles with a particle size around 5.5 nm were synthesized by a polyol route. The optimized luminescence property was obtained when 5 mol% Tb³⁺ and 2 mol% Eu³⁺ were co-doped. The influence of different polyalcohol solvents (DEG/PEG) on particle size and luminescence properties was investigated. The results show that the nanoparticles Gd₂O₃:5%Tb³⁺ prepared in PEG presented greater particle size (around 79 nm) and higher luminescence intensity.     

Synthesis and characterization of the crystalline powders on the basis of Lu2O3:Eu3+spherical submicron-sized particles

This study is devoted to the preparation of the crystalline powders on the basis of non-agglomerated monodisperse Lu₂O₃:Eu³⁺ spherical particles with the diameters in the range of 50–250 nm by the soft chemistry co-precipitation route. The influence of the synthesis parameters on control morphology, particles size and agglomeration in the final Lu₂O₃:Eu³⁺ powder was considered. Lu₂O₃:Eu³⁺ crystalline powders were characterized by means of electron microscopy methods (TEM, SEM), FT-IR spectroscopy, thermal analysis (TG-DTA) and X-ray diffractometry. The mechanisms of the precursor decomposition and crystallization at the temperatures ranging from 60 to 900 °C were discussed. It was shown that the powders obtained were characterized by the effective luminescence under X-ray excitation in λ = 575–725 nm spectral region corresponding to ⁵D₀ → ⁷F_J transitions (J = 0–4) of Eu³⁺ ions with a maximum at 612 nm and the luminescence intensity strongly depends on annealing temperature. The relative densities of the green-bodies on the basis of Lu₂O₃:Eu³⁺ powders were estimated and the sintering of compacts at the temperatures up to 1500 °C was studied.     

Dielectric properties and bright red emission of Y3+/Eu3+-codoped ZrO2 thin films prepared by chemical solution deposition

We report on an effective combination of good dielectric properties with bright red emission in Y³⁺/Eu³⁺-codoped ZrO₂ thin films. The thin films were deposited on fused silica and Pt/TiO₂/SiO₂/Si substrates using a chemical solution deposition method. The crystal structure, surface morphology, electrical and optical properties of the thin films were investigated in terms of annealing temperature, and Y³⁺/Eu³⁺ doping content. The 5%Eu₂O₃–3%Y₂O₃–92%ZrO₂ thin film with 400 nm thickness annealed at 700 °C exhibits optimal photoluminescent properties and excellent electrical properties. Under excitation by 396 nm light, the thin film on fused silica substrate shows bright red emission bands centered at 593 nm and 609 nm, which can be attributed to the transitions of Eu³⁺ ions. Dielectric constant and dissipation factor of the thin films at 1 kHz are 30 and 0.01, respectively, and the capacitance density is about 65.5 nf/cm² when the bias electric field is less than 500 kV/cm. The thin films also exhibit a low leakage current density and a high optical transmittance with a large band gap.     

Variation in structures and photoluminescence spectra of BaxEu1−xAl2O4 powders

Barium europium(II) aluminate (Ba_xEu_1?xAl₂O₄) powders were prepared by a solid-state reaction among barium carbonate (BaCO₃), europium oxide (Eu₂O₃), and alumina (Al₂O₃) powders at 1400 °C for 3 h under a mixed gas flow of H₂ and N₂. The powders were characterized by powder X-ray diffraction (XRD), infrared and Raman spectroscopy, and photoluminescence (PL). With increasing Ba²⁺ content in Ba_xEu_1?xAl₂O₄, the structure of Ba_xEu_1?xAl₂O₄ changed from a monoclinic (P2₁) to hexagonal (P6₃) phase. The hexagonal (P6₃22) phase was also observed between the two phases. The XRD pattern of a single Ba_0.6Eu_0.4Al₂O₄ phase, which has not been reported in the literature, was refined by the Rietveld method and its structure was confirmed by selected-area electron diffraction. With increasing x value, the emission peak in the PL spectra of Ba_xEu_1?xAl₂O₄ became weaker (x = 0–0.4) and then more intense (x = 0.6–0.98), and its position showed a blue shift from 520 to 498 nm.     

Tunable white light and energy transfer of Dy3+ and Eu3+ doped Y2Mo4O15 phosphors

A series of Dy³⁺ or/and Eu³⁺ doped Y₂Mo₄O₁₅ phosphors were successfully synthesized at a low temperature of 600 °C via solid state reaction. The as-prepared phosphors were characterized by X-ray powder diffraction (XRD), scanning electronic microscope (SEM), photoluminescence (PL) excitation, emission spectra and PL decay curves. XRD results demonstrate that Y₂Mo₄O₁₅: Dy³⁺, Eu³⁺ has the monoclinic structure with the space group of p21/C(14). Under the excitation of ultraviolet (UV) or near-UV light, the Dy³⁺ and Eu³⁺ ions activated Y₂Mo₄O₁₅ phosphors exhibit their characteristic emissions in the blue, yellow and red regions. The emitting light color of the Y₂Mo₄O₁₅: 0.08Dy³⁺, yEu³⁺ phosphors can be adjusted by varying the concentration ratio of Dy³⁺ to Eu³⁺ ions and a white light is achieved when the doping concentration of Eu³⁺ is 5%. In addition, the energy transfer from Dy³⁺ to Eu³⁺ is also confirmed based on the luminescence spectra and decay curves.     

Citrate-based sol–gel synthesis and luminescent properties of Y6WO12:Eu3+, Dy3+ phosphors for solid-state lighting applications

The rare-earth ions (Eu³⁺, Dy³⁺) doped Y₆WO₁₂ phosphors were prepared by a citrate-based sol–gel method. The morphologies and structural properties of the as-prepared and doped samples were analyzed by scanning electron microscope images and X-ray diffraction patterns. The luminescent properties were studied by examining the excitation and emission spectra of the samples. The Eu³⁺ and Dy³⁺ ions doped samples exhibited their characteristic emission bands in the visible region under ultraviolet light excitation. The temperature-dependent photoluminescence (PL) properties of the samples were also investigated. The PL spectra of the synthesized samples by the sol–gel method were compared with those of the bulk sample prepared by a solid-state reaction. Similarly, the Commission International de I’Eclairage chromaticity coordinates and the decay times of Y₆WO₁₂:Eu³⁺ (3 mol%) and Y₆WO₁₂:Dy³⁺ (2 mol%) phosphors were studied.