Luminescence properties of composite material Sr2MgSi2O7:Eu2+,Dy3+/light conversion agent with multilayer structure

In order to improve the red luminescent properties,Sr₂ MgSi₂ O₇:Eu²⁺,Dy³⁺was selected as a blue persistent luminescent donor phosphor,while light conversion agent was utilized to tune the persistent luminescent spectra from blue to red.Composite red luminescent material Sr₂ MgSi₂ O₇:Eu²⁺,Dy³⁺/light conversion agent(SMED/LCA) was fabricated with light conversion agent and Sr₂ M...     

Characterization of Y2O2S： Eu^3＋, Mg^2＋, Ti^4＋ Long-Lasting Phosphor Synthesized by Flux Method

Long-lasting phosphor Y₂O₂S: Eu³⁺, Mg²⁺, Ti⁴⁺ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased with the increase of Eu₂O₃ content in Y₂O₂S: Eu_x³⁺ (0.01 ≤ x ≤ 0.10). On the other hand, the change of unit cell parameter a is not linear dependence. In the Y₂O₂S: Eu³⁺ crystal structure, Eu³⁺ ions only replaced Y³⁺ ions' places in which it posited center position of c axis. With the increase of Eu₂O₃ content, the position of the strongest emission peak changed from 540 nm (⁵D₁→⁷F₂ transition) to 626 nm (⁵D₀→⁷F₂ transition), and the maximum intensity was obtained when x = 0.09 in Y₂O₂S: Eu_x³⁺ (0.01 ≤ x ≤ 0.10). This is due to the environment of trivalent europium in the crystal structure of Y₂O₂S. Doping with Mg²⁺ or Ti⁴⁺ ions alone cannot get the good long-lasting afterglow effect, whereas co-doping with Mg²⁺ and Ti⁴⁺ ions and excited with 365 nm ultraviolet light, a strong thermoluminesence peak appeared, red and orange long-lasting phosphorescence (LLP) was also observed and the phosphorescence lasted nearly 3 h in the light perception of the dark-adapted human eye (0.32 mcd · m⁻²). Thus the LLP mechanism was analyzed.     

Study on Red Long-Time Luminescent Material Y2O2S:Eu,M (M = Mg,Ca, Sr,Ba)

The red long-time luminescent material Y₂O₂S:Eu³⁺, M (M = Mg, Ca, Sr, Ba) was prepared by high temperature solid-state method. The XRD result of the sample showed that the crystal phase was Y₂O₂S, which belong to hexagonal system, and no new crystal phase were by doping different amount of Mg, Ca, Sr, Ba. The excitation spectrum was a broad band within 200 × 400 nm region, the characteristic peaks of emission spectrum were located at 583, 595, 597, 617, 627, 707 nm. There was no marked change in excitation spectra, emission spectra and maximum of their wavelengths of the luminescent materials by doping with different ions. The luminescent intensity of the phosphors were stronger when the concentration of doping ions was Mg/Y = 6%, Ca/Y = 4%, Sr/Y = 8%, Ba/Y = 2.5%, respectively. Its sequence of luminescent intensity from high to low is Sr > Ba > Mg > Ca.     

Synthesis of Long Afterglow Phosphors Doped B SrAl2O4:Eu2+, Dy3+ and Its Luminescent Properties

The long afterglow luminescent material SrAl₂O₄: Eu²⁺, Dy³⁺ was prepared by high temperature solid-state method. Effects of doped B on the luminescent properties of phosphors SrAl₂O₄: Eu²⁺, Dy³⁺ were investigated by means of excitation spectra, emission spectra and X-ray diffraction analysis. As the result, the addition of H₃BO₃ as flux promotes the growth of crystalline and reduces the synthesizing temperature, but the wavelength of emission peak of photoluminescent material did not change with the variation of H₃BO₃ content. The effect of Dy³⁺ concentration on the luminescent properties of material was investigated. It was found that the luminescence of phosphors prepared under the condition of the amount of H₃BO₃ 5% and the mole ratio of Eu/Dy = 1/7(Eu = 0.02 mole) had better luminescent property and longer afterglow time.     

Structure and luminescent properties of luminous polypropylene fiber based on Sr2MgSi2OT：EU^2＋,Dy^3＋

The luminous polypropylene fiber based on long afterglow luminescent material Sr2MgSi2O7：Eu^2＋,Dy^3＋was prepared by melt-spinning process. Micro-morphology, phase composition, crystal structure, spectral features and afterglow properties of the lu-minescent fiber were tested and analyzed. The results indicated that the fiber had independent superposition phase features of both Sr2MgSi2O7：Eu2＋,Dy3＋and polypropylene. The range of its excitation wavelength was located between 250-450 nm;therefore, the luminescent fiber could be excited by ultraviolet or visible light. It could emit blue light of 460 nm wavelength after excitation, which was caused by the 5d-4f transition of Eu^2＋ions within the host lattice. The initial luminescent intensity was more than 0.8 cd/m^2, and afterglow life lasted 7 h. The afterglow decay was composed of rapid-decaying and slow-decaying processes, and the decay charac-teristics depended on the depth and concentration of trap level in the Sr2MgSi2O7：Eu^2＋,Dy^3＋.     

Synthesis and characterization of Ca0.9Mg0.1TiO3:Pr3+,Ag+ phosphor

Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+),Ag~+ phosphors were synthesized by solid-state reaction technique. The crystalline phase and luminescence performances of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+),Ag~+ were observed by X-ray powder diffractometer(XRD), transmission electron microscope(TEM), photoluminescence spectrometer and brightness meter, respectively. The addition of Ag~+ can diminish in the crystal particle sizes of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+). Because Ag+ can reduce the concentration of the undesirable defects in the phosphor, luminescence intensity of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+),Ag~+ is 2.3 times as high as that of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+)at the same preparation condition. The effect of Ag+ on the persistent afterglow properties is to deepen the energy storage traps and enhance the energy transfer efficiency from Ca_(0.9)Mg_(0.1)TiO_3 to Pr~(3+). The persistent afterglow properties of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+),Ag~+ are better than those of Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+) at the same preparation condition. In conclusion,Ca_(0.9)Mg_(0.1)TiO_3:Pr~(3+),Ag~+ phosphor with molar ratio of Ag~+to Pr~(3+) 3:1 obtained at 900 ℃ for 4 h exhibits the optimal photoluminescence performances.     

Photoluminescence properties of Tm~(3+)/Tb~(3+)/Sm~(3+)tri-doped Na_5Y_9F_(32)single crystal with high thermal stability for white light-emitting diodes

A novel Tm~(3+)/Tb~(3+)/Sm~(3+)tri-doped Na_5 Y_9 F_(32) single crystal was synthesized by a modified Bridgman method for the propose of white light emitting diodes.The fluorescence spectra of various Sm~(3+)ion concentrations and fixed 0.4 mol% Tm~(3+) and 0.5 mol% Tb~(3+) were measured and studied systematically excited by near-ultraviolet light of 355 nm.The Sm3+ion concentration takes apparent effect on the relative intensity of peaks in the visible region and the color coordinate combining from these emission bands.A near pure white light emission with color coordinates(0.3295,0.3057) and color temperature(5657 K) can be obtained when the concentrations of Tm~(3+),Tb~(3+) and Sm~(3+) ions are 0.4 mol%,0.5 mol%and 0.8 mol%,respectively.Furthermore,the practical down-conversion internal quantum yield was measured by integrating spheres at about 14.39%.The tri-doped Na_5 Y_9 F_(32) single crystal shows a high thermal stability inferring from the temperature dependent emission in which the integrated emission intensities are reduced only by～3% with the increase of temperature from 280 to 450 K.The present results demonstrate that the Tm~(3+)/Tb~(3+)/Sm~(3+)tri-doped Na_5 Y_9 F_(32) single crystal may provide a promising candidate for white light-emitting diodes,luminescent materials and fluorescent display devices.     

Researches on preparation and properties of polypropylene nonwovens containing rare earth luminous materials

Polypropylene composite nonwovens containing rare-earth strontium aluminates Sr Al2O4：Eu2＋,Dy3＋ and functional additives were fabricated by the spun-bonded technique.The optical properties, morphology and mechanical properties of the samples were characterized.Results from scanning electron microscopy photographs（SEM） indicated that the surface of the fiber was destroyed by the addition of rare earth luminescent materials lightly but the thickness of the fiber was uniform.Differential scanning calorimetry results showed that pure polypropylene has the double crystallization peak at 162.3 and 165.1 °C.Studies from X-ray diffraction showed that the nonwoven prepared with the luminescent materials contained the α-monoclinic crystal and β crystalline phase.Furthermore, the afterglow properties were tested, which showed that the afterglow curve of the luminous nonwoven was similar to that of strontium aluminate, and the intensity was more intensive than luminous nonwoven at the beginning.The nonwoven fabricated with the luminescent material did not affect the crystal lattice of the polymer making the materials have potential applications in fluorescent lamps and field emission displays（FEDs）.     

Preparation and luminescence properties of orange-red Ba3Y4O9:Sm3+ phosphors

A novel orange-red emitting Ba₃Y₄O₉:Sm³⁺ phosphors were prepared by a high temperature solid-state reaction in air. X-ray diffraction (XRD), photoluminescence spectra, fluorescence decay and temperature-dependent emission spectra were utilized to characterize the structure and luminescence properties. The results show that the excitation spectrum includes a series of linear peaks at 350, 367, 382, 410, 424, 445, 470 and 495 nm, respectively. Under 410 nm excitation, the emission peaks were located at 574 nm (⁴G_5/2—⁶H_5/2), 608 nm (⁴G_5/2—⁶H_7/2), 659 nm (⁴G_5/2—⁶H_9/2) and 722 nm (⁴G_5/2—⁶H_11/2), respectively. The concentration quenching occurs when x equals 0.08 for Ba₃Y_4–xO₉:xSm³⁺ phosphor and its mechanism is ascribed to the dipole–dipole interaction. The chromaticity coordinates of Ba₃Y_3.92O₉:0.08Sm³⁺ phosphor are in the orange-red region. The temperature-dependent study shows that this phosphor has excellent luminescence thermal-stability. And the luminescence intensity of Ba₃Y_3.92O₉:0.08Sm³⁺ phosphor at 473 K only declines by about 25.75% of its initial intensity. The experimental data indicate that Ba₃Y₄O₉:Sm³⁺ phosphor may be promising as an orange-red emitting phosphor for white light emitting diodes.     

Enhanced afterglow performance of CaAl_2O_4:Eu~(2+),Nd~(3+) phosphors by co-doping Gd~(3+)

In order to effectively improve the afterglow properties of CaAl_2 O_4:Eu~(2+),Nd~(3+) phosphors,a series of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)(x=0,0.012,0.024,0.036,0.048,0.060 mol) phosphors were prepared by a high-temperature solid-phase approach.Crystalline composition and microstructure were characterized by XRD,TEM,HRTEM,and XPS,luminescence properties were systematically analyzed by fluorescence spectra,afterglow decay curves and TL glow curve.Results show that all of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)phosphors belong to monoclinic CaAl_2 O_4,without other cystalline phase.The blue emission at 442 nm is observed,which is assigned to the 4 f~65 d→4 f~7 transition of Eu~(2+) ions.Doping with appropriate amount of Gd~(3+) ions(x=0.036 mol) significantly improves the afterglow properties of phosphors,but the excessive doping of Gd~(3+) induces the fluorescent quenching.The doping of moderate Gd3+changes the traps states,the trap depth varies from 0.598 to 0.644 eV and the trap concentration is also greatly improved,thus significantly improving afterglow performance.     

Factors affecting afterglow properties of red-emitting phosphor MgSiO3：Mn^2＋,Nd^3＋ for luminescent fiber

With stable physical properties,the rare-earth silicate phosphor of MgSiO3:Mn2+,Nd3+ is one of the suitable luminescent materials used in preparing functional fibers.In order to promote the afterglow properties of red-emitting phosphors,we prepared it by means of solid-state reaction,and the effect of manufacturing elements including H3BO3 and environmental factor of calcining temperature,type of flux on its luminescence property were investigated through evaluating their afterglow properties.The results showed that with the concentration of Nd 3+ increasing,the amounts of H3BO3 doping and calcining temperature,the afterglow time and initial brightness of the rare-earth silicate phosphor increased and then decreased gradually.The afterglow properties of different flux concentration were different from one to another as:H3BO3 >Na+>K+>No flux.     

Investigation on luminescence properties of Ln^3＋ doped Sr3EuMgSi2O8 （Ln=Dy, Er, Ho）

The luminescent properties of Sr2.97MgSi2O8:Eu2+0.01 phosphors were investigated with different Ln3+0.02(Ln3+:Dy3+,Er3+,Ho3+) co-dopants. The co-dopants had no influence on both the structure of the lattice and the position of the emission peak. However, the afterglow properties of samples were enhanced with different co-dopants. The afterglow duration of the Dy3+ co-doped sample was longer than that of the others. Furthermore, the co-doping samples had stronger thermoluminescence (TL) intensity and therefore longer afterglow duration. At last, the self-reduction of Eu3+→Eu2+ was observed in an silicate compound of Sr3-xMgSi2O8:xEu phosphor in air condition. This is the first time to show a blue long afterglow phosphor synthesized avoiding reducing atmosphere.     

Structure and luminescence properties of color-tunable phosphor Sr2La3(SiO4)3F:Tb3+,Sm3+

A series of single-phase and color-tunable phosphors Sr₂La₃(SiO₄)₃F:0.15Tb³⁺,xSm³⁺(SLSOF:0.15Tb³⁺,xSm³⁺) was prepared using solid-state route.The X-ray diffraction(XRD) was used to characterize the phase of the as-prepared samples.The synthesized phosphors have apatite-type structure without other impurities.Sm³⁺ and Tb³⁺ ions substitute La³⁺ into the lattice and form a single...     

Effect of y/x ratio on luminescence properties of xSrO·yAl2O3：Eu2＋,Dy3＋ luminous fiber

Rare earth strontium aluminate luminous fiber is a novel functional fiber. In order to investigate the influence of Al/Sr ratio on luminescence properties of xSrO·yAl2O3：Eu2＋,Dy3＋ luminous fibers, several kinds of rare earth strontium aluminate luminous fibers were prepared by using rare-earth strontium aluminate as the rare-earth luminescent material and fiber-forming polymers such as polymer polyethylene terephthalate（PET） as a matrix and combining them with functional additives. X-ray diffraction（XRD）, fluorescence spectrophotometer, and afterglow brightness tester as well as microcomputer thermo-luminescence dosimeters were used to characterize the resulting samples. Results from XRD demonstrated that the phase of xSrO·yAl2O3：Eu2＋,Dy3＋ luminous fibers were different from one another as the Al/Sr ratio changed. Emission spectra of the samples with different Al/Sr ratios showed that emission intensity increased with the decrease of A1/Sr ratio at first then increased when it was over 2/1. From afterglow decay results, it could be found that Sr-rich sample showed lower luminance and shorter persistent time.     

High thermal stability and blue-violet emitting phosphor CaYAlO4:Ti4+ with enhanced emission by Ca2+ vacancies

Blue-violet light can not only enhance the total content of biomass and glucoside but also enrich the taste of the fruit. Thus, it is meaningful to study the blue-violet luminescent materials for plant cultivation. In this study, titanium (IV) -activated CaYAlO₄ (CYAO) phosphors were synthesized by conventional high-temperature solid–state reaction. X-ray powder diffraction was employed to analyze the crystal-structure of CYAO. It is found that the doped Ti⁴⁺ ions do not change obviously the crystal structure of phosphors. Upon 246 nm excitation, CaYAl_1-xO₄:xTi⁴⁺ phosphors exhibit broad blue-violet emission band peaking at 395 nm, which can be attributed to the charge transfer of Ti⁴⁺–O^2–. Moreover, this phosphor exhibits strong thermal stability. The luminescence emission intensity at 150 °C maintained about 91 mol% of its initial value at room temperature. Additionally, the electron transition process and concentration quenching mechanism of CaYAl_1–xO₄:xTi⁴⁺ are discussed in detail. The excellent luminescent properties indicate that CaYAl_1-xO₄:xTi⁴⁺ phosphor may have promising application in indoor plant cultivation.     

Luminescent ionic lattice occupation and wide tunable emission spectra of La2MgZrO6:Bi3+,Eu3+ double perovskite phosphors for white light LED

La₂Mg_1-x/2Zr_1-x/2O₆:xBi³⁺(x=0.01-0.035,abbreviated as LMZ:Bi³⁺) and La_2-yMg_0.99Zr_0.99O₆:0.02Bi³⁺,yEu³⁺(y=0.1-0.11,abbreviated as LMZ:Bi³⁺,Eu³⁺) double-perovskite phosphors were prepared through high-temperature solid-phase method.The emission spectrum of LMZ:xBi³⁺(x=0.01-0.035)phosphors excited at 353 nm is asymmetric in the range be...     

Investigation on the amounts of Na2CO3 and sulphur to obtain pure Y2O2S and up-conversion luminescence of Y2O2S:Er

The process to prepare pure phase of hexagonal Y2O2S was investigated. Effect of mixed flux of Na2CO3 and S amounts was studied. The phase composition and morphology were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed that the single phase of Y2O2S with smooth morphology could not be obtained as the molar ratio of Y2O3, Na2CO3 and S was in the range of 1:(0.5-1):(2-3) until the molar ratio was increased to 1:1.5:4. Different Er3+ concentration doped Y2O2S...     

Optical and scintillation properties of Bi4Si3O12:RE (RE=Eu3+, Sm3+, Ho3+, Tb3+) single crystals

Bi_4 Si_3 O_(12):RE(BSO:RE, RE = Eu~(3+), Sm~(3+), Ho~(3+), Tb~(3+)) crystals were grown by the modified vertical Bridgeman method, and doping effects on scintillation properties were investigated. Under γ-ray irradiation, the light yield of BSO doped with small doses of Eu~(3+) increases slightly, and the energy resolution improves significantly compared to pure BSO, therefore the ability of distinguishing between particles will be improved for BSO crystals with a small amount of Eu~(3+) dopant. The results show that a small amount of Eu~(3+) doping can sensitize the Bi~(3+) ions. The sensitization effect enables the reduction of intrinsic defects, and thus improves the scintillation properties. However, the relative light yield of BSO:Tb(1.0 mol%) crystal is 4.3%, which is smaller than 5.0% of pure BSO. The improved light yield and energy resolution in the BSO:Eu and BSO:Sm crystals are considered an impressive achievement in the optimization of this scintillator which is already suitable for applications such as dual-readout calorimeters and homogeneous hadron calorimeters.     

Ferroelectric and Dielectric Behavior of Samarium-Substituted Bi<Subscript>4</Subscript>Ti<Subscript>3</Subscript>O<Subscript>12</Subscript> Nanomaterials Synthesized by Gel Combustion Method

Samarium (Sm) substituted bismuth titanate (Bi₄Ti₃O₁₂, BT) nanoparticles with compositions of Bi_4?xSm_xTi₃O₁₂ (BSmT) (where x = 0.0, 0.25, 0.50, 0.75, 1.0) were prepared by using the gel combustion method. X-ray diffraction pattern of prepared nanoparticles confirmed that all the BSmT compositions were of the single phase orthorhombic structure with the space group of B2ab. The dielectric loss at 100 Hz varied from 0.0925 to 0.056 with an increase in Samarium content. Dielectric loss confirmed the lower leakage current of BSmT nanoparticles. The ferroelectric behavior of BSmT nanoparticles showed that the Bi_3.50Sm_0.50Ti₃O₁₂ had good ferroelectric property and also had minimum leakage current. The increase of coercive field (Ec) and the increase of remnant polarizations (Pr) were pronounced with the increase in Sm content confirming to the fact that the substitution of Sm³⁺ had improved the ferroelectric properties of BT.     

Synthesis and enhanced photoluminescence properties of red emitting divalent ion (Ca2+) doped Eu:Y2O3 nanophosphors for optoelectronic applications

This work presents the synthesis of Y₂O₃:Eu³⁺,xCa²⁺ (x = 0 mol%, 1 mol%, 3 mol%, 5 mol%, 7 mol%, 9 mol%, 11 mol%) nanophosphors with enhanced photoluminescence properties through a facile solution combustion method for optoelectronic, display, and lighting applications. The X-ray diffraction (XRD) patterns of the proposed nanophosphor reveal its structural properties and crystalline nature. The transmission electron microscope (TEM) results confirm the change in the shape of the particle and aggregation of particles after co-doping with Ca²⁺. Fourier transform infrared spectroscopy (FTIR) and Raman vibrations also confirm the presence of Y–O vibration and subsequently explain the crystalline nature, structural properties, and purity of the samples. All the synthesized nanophosphors samples emit intense red emission at 613 nm (⁵D₀→⁷F₂) under excitation with 235, 394 and 466 nm wavelengths of Eu³⁺ ions. The photoluminescence (PL) emission spectra excited with 235 nm illustrate the highest emission peak with two other emission peaks excited with 466 and 394 nm that is 1.4 times higher than 466 nm and 1.9 times enhanced by 394 nm wavelength, respectively. The emission intensity of Y₂O₃:Eu³⁺,xCa²⁺ (5 mol%) is increased 8-fold as compared to Eu:Y₂O₃. Doping with Ca²⁺ ions enhances the emission intensity of Eu:Y₂O₃ nanophosphors due to an increase in energy transfer in Ca²⁺→Eu³⁺ through asymmetry in the crystal field and by introduction of radiative defect centers through oxygen vacancies in the yttria matrix. It is also observed that the optical band gap and the lifetime of the ⁵D₀ level of Eu³⁺ ions in Y₂O₃:Eu³⁺,xCa²⁺ nanophosphor sample gets changed with a doping concentration of Ca²⁺ ions. Nanophosphor also reveals high thermal stability and quantum yield as estimating activation energy of 0.25 eV and 81%, respectively. CIE, CCT, and color purity values (>98%) show an improved red-emitting nanophosphor in the warm region of light, which makes this material superior with a specific potential application for UV-based white LEDs with security ink, display devices, and various other optoelectronics devices.