Controllable hydrothermal synthesis and photoluminescence properties of CaGd2(WO4)4:Eu3+ red-emitting phosphor

CaGd₂(WO₄)₄:Eu³⁺ phosphors with controllable morphology were synthesized via the hydrothermal method. The influences of pH value, reaction time and Eu³⁺ concentration on the crystal structure, morphology, and photoluminescence properties of CaGd₂(WO₄)₄:Eu³⁺ were studied. The pure tetragonal structure CaGd₂(WO₄)₄ is obtained when the pH value is 8 and 9. Furthermore, by altering the pH value of the reaction solution, the morphologies of the CaGd₂(WO₄)₄:Eu³⁺ phosphors evolve from spindle-shaped grains to tetragonal plate-like grains and finally to aggregated bulk particles. Under the 394 nm excitation, the phosphors display a bright red emission corresponding to the characteristic 4f-4f transitions of Eu³⁺, and the intensity of emission peaks depends mainly on the pH value, the reaction time, and the Eu³⁺ concentration. The optimum photoluminescence performance is achieved for CaGd_2-x(WO₄)₄:xEu³⁺ (x = 1) phosphor synthesized at pH = 8 under the reaction time of 16 h. Finally, the thermal stability of the phosphors is analyzed at different ambient temperatures.     

A novel scheelite-type LiCaGd(WO4)3:Eu3+ red phosphors with prominent thermal stability and high quantum efficiency

A series of LiCaGd(WO4)3 : xEu³⁺ (0 ≤ x ≤ 1.0) red phosphors with tetragonal scheelite structure were synthesized via the conventional solid-state reaction. Their crystal structure, photoluminescence excitation (PLE), and photoluminescence (PL) spectra, thermal stability and quantum efficiency were investigated. The phosphors exhibit a typical red light upon 395 nm near ultraviolet excitation, and the strongest emission peak at 617 nm is dominated by the ⁵D₀→⁷F₂ transition of Eu³⁺ ions. The PL intensity of the phosphors gradually increases with the increase of Eu³⁺ doping concentration, and the concentration quenching phenomenon is hardly observed. The quantum efficiency and the color purity of the phosphor reach maximum values of about 94.2 and 96.6% at x = 1.0, respectively. More importantly, LiCaGd(WO₄)₃:xEu³⁺ phosphors have prominent thermal stability. The temperature-dependent PL intensity of the phosphors at 423 K is only reduced to 89.1% of the PL intensity at 303 K, which is superior to that of commercial red phosphors Y₂O₃:Eu³⁺. Finally, LiCaGd(WO₄)₃:Eu³⁺ phosphor is packaged with near ultraviolet InGaN chips to fabricate white light emitting diodes, which has a low color temperature (CCT = 4622 K) and a high color rendering index (CRI= 89.6).     

Anti-thermal quenching of Eu3+ luminescence in negative thermal expansion Zr(WO4)2

Thermal quenching of luminescence is the most critical problem for rare earth doped phosphors used in light-emitting diodes (LEDs). Herein, we demonstrate that thermal quenching can be considerably suppressed via the negative thermal expansion effect in Zr(WO₄)₂ that serves as host for Eu³⁺ red emission. The photoluminescence (PL) intensity is surprisingly enhanced by 130% when the temperature is raised from room temperature to 100 °C. As temperature further increases to 160 °C, the PL intensity turns to reduce, which is still 1.4 times of that at room-temperature. Moreover, Zr(WO₄)₂:15%Eu phosphor has good durability, which still exhibits strong red luminescence (only 13% loss) after being kept in 85 °C/85% relative humidity chamber for 240 h. The anti-thermal quenching of Eu³⁺ luminescence can be ascribed mainly to the following two factors: first one is the thermal-enhanced energy transfer between Eu³⁺ ions induced by the contraction of Zr(WO₄)₂ unit-cell volume that leads to the strong structural rigidity of host lattice; second one would be electron traps in the host that favors the increase of electrons on the excited energy levels. This important anti-thermal quenching effect induced from the negative thermal expansion of the host matrix may stimulates a novel and efficient approach to design highly thermal stable phosphors for next-generation LEDs.     

High luminescent brightness and thermal stability of red emitting Li3Ba2Y3(WO4)8:Eu3+ phosphor

A series of Li₃Ba₂Y_3−x(WO₄)₈:xEu³⁺ (x=0.1, 1, 1.5, 2 and 2.8) phosphors were synthesized by a high temperature solid-state reaction method. Under the excitation of near ultraviolet (NUV) light, the as-prepared phosphor exhibits intense red luminescence originating from the characteristic transitions of Eu³⁺ ions, which is 1.8 times as strong as the commercial Y₂O₂S:Eu³⁺ phosphor. The optimal doping concentration of Eu³⁺ ions here is confirmed as x=1.5. The electric dipole-quadrupole (D-Q) interaction is deduced to be responsible for concentration quenching of Eu³⁺ ions in the Li₃Ba₂Y₃(WO₄)₈ phosphor. The analysis of optical transition and Huang-Rhys factor reveals a weak electron-phonon coupling interaction. The temperature-dependent emission spectra also indicate that the as-prepared Li₃Ba₂Y₃(WO₄)₈:Eu³⁺ phosphor has better thermal stability than that of the commercial Y₂O₂S:Eu³⁺ phosphor. Therefore, our results show that the as-prepared Li₃Ba₂Y₃(WO₄)₈:Eu³⁺ phosphor is a promising candidate as red emitting component for white light emitting diodes (LEDs).     

Tunable emission of single-phased NaY(WO4)2:Sm3+ phosphor based on energy transfer

A series of NaY(WO₄)₂:Sm³⁺ phosphors were prepared by high temperature solid state reaction. When excited by ultraviolet and blue light, their emission spectra cover entirely visible light region, due to intrinsic luminescence of WO₄^2- group as well as Sm³⁺ 4f-4f transitions. White light emission was obtained from NaY_0.99Sm_0.01(WO₄)₂ phosphor under radiation of 265 nm UV light, and intense yellow and red emission from ⁶H_{J(J=5/2, 7/2, 9/2)} transitions were observed when pumped Sm^{3+ 4}G_5/2 by 405 nm blue light. With incorporation of Sm³⁺ into NaY(WO₄)₂ host, higher-level emission from Sm³⁺ at 650 nm was generated by energy transfer from WO₄^2- to Sm³⁺ under excitation of 265 nm. The corresponding energy transfer mechanism was demonstrated to be a dipole-dipole interaction. In addition, tunable emission from blue to white and, finally, to red was realized by increasing Sm³⁺ doping concentration. The band gap of NaY(WO₄)₂ calculated from diffuse reflection spectra indicates a semiconducting character. All these results show that NaY_1−xSm_x(WO₄)₂ phosphor provides promising application for conversion of frequencies emitted by UV or blue LEDs.     

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.     

Synthesis and luminescence properties of single‐component Ca5(PO4)3F:Dy3+, Eu3+ white‐emitting phosphors

A series of Ca₅(PO₄)₃F:Dy³⁺, Eu³⁺ phosphors was synthesized by a solid‐state reaction method. The XRD results show that all as‐prepared Ca₅(PO₄)₃F:Dy³⁺, Eu³⁺ samples match well with the standard Ca₅(PO₄)₃F structure and the doped Dy³⁺ and Eu³⁺ ions have no effect on the crystal structure. Under near‐ultraviolet excitation, Dy³⁺ doped Ca₅(PO₄)₃F phosphor shows blue (486 nm) and yellow (579 nm) emissions, which correspond to ⁴F_9/2→⁶H_15/2 and ⁴F_9/2→⁶H_13/2 transitions respectively. Eu³⁺ co‐doped Ca₅(PO₄)₃F:Dy³⁺ phosphor shows the additional red emission of Eu³⁺ at 631 nm, and an improved color rendering index. The chromaticity coordinates of Ca₅(PO₄)₃F:Dy³⁺, Eu³⁺ phosphors also indicate the excellent warm white emission characteristics and low correlated color temperature. Overall, these results suggest that the Ca₅(PO₄)₃F:Dy³⁺, Eu³⁺ phosphors have potential applications in warm white light‐emitting diodes as single‐component phosphor.     

Synthesis and photoluminescence properties of CaGd2(MoO4)4:Eu3+ red phosphors

The novel red-emitting Eu³⁺ ions activated CaGd₂(MoO₄)₄ phosphors were prepared by a citrate sol–gel method. The X-ray diffraction patterns confirmed their tetragonal structure when the samples were annealed above 600 °C. The photoluminescence excitation spectra of CaGd₂(MoO₄)₄:Eu³⁺ phosphors exhibited the charge transfer band (CTB) and intense f–f transitions of Eu³⁺ ion. The optimized annealing temperature and Eu³⁺ ion concentration were analyzed for CaGd₂(MoO₄)₄:Eu³⁺ phosphors based on the dominant red (⁵D₀→⁷F₂) emission intensity under NUV (394 nm) excitation. All decay curves were well fitted by the single exponential function. These luminescent powders are expected to find potential applications such as WLEDs and optical display systems.     

Structure and Luminescence of New Red‐Emitting Materials‐Eu3+‐Doped Triple Orthovanadates NaALa(VO4)2 (A = Ca,Sr, Ba)

The new red‐emitting phosphors of Eu³⁺‐doped triple orthovanadates NaALa(VO₄)₂ (A = Ca, Sr, Ba) were prepared by the high‐temperature solid‐state reaction. The formation of single phase compound with isostructural structure of Ba₃(VO₄)₂ was verified through X‐ray diffraction (XRD) studies. The photoluminescence excitation and emission spectra, the fluorescence decay curves and the dependence of luminescence intensity on doping level were investigated. The phosphor can be efficiently excited by near UV and blue light to realize an intense red luminescence (613 nm) corresponding to the electric dipole transition ⁵D₀→⁷F₂ of Eu³⁺ ions. Their potential applications as red‐emitting phosphors for solid‐state lighting were evaluated in comparison with the Eu³⁺‐doped lanthanum orthovanadate LaVO₄ and other reported references. The luminescence was discussed in detail on the base of the crystal structures. The luminescence thermal stability on temperature was investigated and the thermal activated energy was calculated. The phosphors can be suggested to be a potential red‐emitting phosphor for the application on white LEDs under irradiation of near‐UV or blue chips.     

Synthesis and photoluminescence enhancement of Ca3Sr3(VO4)4:Eu3+ red phosphors by co-doping with La3+

In this study, a series of red-emitting Ca₃Sr₃(VO₄)₄:Eu³⁺ phosphors co-doped with La³⁺ was prepared using the combustion method. The microstructures, morphologies, and photoluminescence properties of the phosphors were investigated. All Ca₃Sr₃(VO₄)₄:Eu³⁺, La³⁺ samples synthesized at temperatures greater than 700 ℃ exhibited the same standard rhombohedral structure of Ca₃Sr₃(VO₄)₄. Furthermore, the Ca₃Sr₃(VO₄)₄:Eu³⁺, La³⁺ phosphor was effectively excited by near-ultraviolet light of 393 nm and blue light of 464 nm. The strong excitation peak at 464 nm corresponded to the ⁷F₀→⁵D₂ electron transition of Eu³⁺. The strong emission peak observed at 619 nm corresponded to the ⁵D₀→⁷F₂ electron transition of Eu³⁺. Co-doping with La³⁺ significantly improved the emission intensity of Ca₃Sr₃(VO₄)₄:Eu³⁺ red phosphors. The optimum luminescence of the phosphor was observed at Eu³⁺ and La³⁺ concentrations of 5% and 6%, respectively. Moreover, co-doping with La³⁺ also improved the fluorescence lifetime and thermal stability of the Ca₃Sr₃(VO₄)₄:Eu³⁺ phosphor. The CIE chromaticity coordinate of Ca₃Sr₃(VO₄)₄:0.05Eu³⁺, 0.06La³⁺ was closer to the NTSC standard for red phosphors than those of other commercial phosphors; moreover, it had greater color purity than that of all the samples tested. The red emission intensity of Ca₃Sr₃(VO₄)₄:0.05Eu³⁺, 0.06La³⁺ at 619 nm was ~1.53 times that of Ca₃Sr₃(VO₄)₄:0.05Eu³⁺ and 2.63 times that of SrS:Eu²⁺. The introduction of charge compensators could further increase the emission intensity of Ca₃Sr₃(VO₄)₄:Eu³⁺, La³⁺ red phosphors. The phosphors synthesized herein are promising red-emitting phosphors for applications in white light-emitting diodes under irradiation by blue chips.     

Eu2+ activated novel eulytite Na3Bi5(PO4)6: Eu3+ phosphors: Enhanced luminescence and thermal stability for photonics application

For the first time, novel eulytite-like Eu²⁺/Eu³⁺: Na₃Bi₅(PO₄)₆ phosphor was synthesized via high temperature solid-state reaction method in reduction environment, and the structure, luminescence performances and thermal stability were investigated and discussed using various techniques. X-ray refinement diffraction and Raman spectra revealed the around 200 nm well-crystallized eulytite-type (I43d space group) phosphors were synthesized, and a diagram of crystal structure of Na₃Bi₅(PO₄)₆ was proposed. X-ray photoelectron spectroscopy analysis confirmed the co-existence of Eu²⁺ and Eu³⁺ ions which exhibited characteristic 4f⁶5d→⁸S_7/2 transition of Eu²⁺ and ⁷F₀→⁵D_0,1,2,3,4 transitions of Eu³⁺ ions. On the other hand, due to the activation of Eu²⁺, samples displayed good tunability on excited and emission behaviors under different excited laser. The JO parameters, emission cross-section, branching ratio and asymmetric ratio indicated that the Eu doping increased the covalency and asymmetry of host. Thermal quenching was studied and the reasons were discussed. Through the comparison of phosphors prepared in different conditions, the thermal stability& repeatability, radiative lifetime, color purity and activation energy were remarkably superior due to the Eu doping and in particularly Eu²⁺ activation. Finally, the energy level and CIE chromaticity diagrams were plotted to explain the mechanism of Eu²⁺ activation and energy transfer between Eu²⁺ and Eu³⁺ ions. The 0.5%Eu doped Na₃Bi₅(PO₄)₆ exhibited promising tunable red-emission performance with quantum efficiency of 92%, activation energy of 0.24 eV, red color purity of 93.74% and very low non-radiative transfer ratio 44.20 s^?1 with smaller CCT (<2200 K).     

White light emission from novel host-sensitized single-phase Y2WO6: Ln3+ (Ln3+=Eu3+, Dy3+) phosphors

A series of Eu³⁺- or Dy³⁺-doped and Eu³⁺/Dy³⁺ co-doped Y₂WO₆ in pure phase was synthesized via high-temperature solid-state reaction. X-ray diffraction, diffuse reflection spectra, photoluminescence excitation and emission spectra, the CIE chromaticity coordinates and temperature-dependent emission spectra were exploited to investigate the phosphors. Upon UV excitation at 310 nm, efficient energy transfer from the host Y₂WO₆ to dopant ions in Eu³⁺ or Dy³⁺ single-doped samples was demonstrated and those phosphors were suitable for the UV LED excitation. The intense red emission was observed in Y₂WO₆: Eu³⁺, and blue and yellow ones were observed in Y₂WO₆: Dy³⁺. Concentration quenching in Y₂WO₆: Dy³⁺ phosphors could be attributed to the electric dipole-dipole interaction. In Eu³⁺/Dy³⁺ co-doped Y₂WO₆ phosphors energy transfer process only took place from the host to Eu³⁺/Dy³⁺ ions and warm white-light emission can be obtained by adjusting the dopant concentrations. The temperature-dependent luminescence indicated Eu³⁺/Dy³⁺ co-doped Y₂WO₆ was thermally stable. Our overall results suggested that Y₂WO₆: Ln³⁺ (Ln³⁺=Eu³⁺, Dy³⁺) as warm white-light emitting host-sensitized phosphor might be potentially applied in WLEDs.     

Ca2Na2La6(SiO4)4(PO4)2O: Eu2+/Eu3+: A visual dual-emitting fluorescent ratiometric temperature sensor

A novel apatite-based UV-excited dual-emitting Ca₂Na₂La₆(SiO₄)₄(PO₄)₂O: Eu²⁺/Eu³⁺ phosphor (CNL: Eu²⁺/Eu³⁺) was designed and successfully synthesized by a solid-state reaction. Compared with previous reports on this family of materials, a structural study based on DFT calculation exhibited a new consequence that the monovalent ions in this system are more inclined to occupy the seven-coordinate cationic sites rather than the nine-coordinate sites. This result was confirmed by the structural refinement and high-resolution transmission electron microscopy (HRTEM) data. Due to the coexistence of Eu²⁺ and Eu³⁺ dopants in the material, under 345 or 392 nm excitation, CNL: 0.02Eu²⁺/Eu³⁺ exhibited a green Eu²⁺ emission band (528 nm) and red Eu³⁺ emission peaks (around 618 nm). The application potential of CNL:0.02Eu²⁺/Eu³⁺ in luminescent thermometry was studied by exploiting the temperature sensitivity of the fluorescent intensity ratio (green/red) at different temperatures. It was found that, under 345 nm excitation, the fluorescent intensity ratio of CNL: 0.02Eu²⁺/Eu³⁺ displayed linear correlation over the temperature range of 298 to 473 K with a high sensitivity of 2.82%K⁻¹. Additionally, the emission color of the CNL: 0.02Eu²⁺/Eu³⁺ sample under UV lamp (254 and 365 nm) excitation showed an obvious change (from green to red) as the temperature increased from 298 to 473 K (from green to red). These results indicated that CNL: Eu²⁺/Eu³⁺ can serve as an excellent visual luminescent ratiometric thermometer. Furthermore, this work provides a novel reference for developing high-performance luminescence temperature-sensing materials.     

Crystal structure,luminescent properties and white light emitting diode application of Ba3GdNa(PO4)3F:Eu2+ single-phase white light-emitting phosphor

A series of single-phase white-light-emitting phosphors, Eu²⁺-activated Ba₃GdNa(PO₄)₃F phosphors were synthesized by solid-state reactions. The crystal structure of Ba₃GdNa(PO₄)₃F was been identified by Rietveld refinement of X-ray diffraction pattern. The Eu²⁺-activated Ba₃GdNa(PO₄)₃F phosphors exhibit broad excitation spectra from 250 to 420 nm, which matched well with the n-UV LED chips. Under the excitation of 365 nm, the emission spectrum almost covered the entire visible region including two emission bands peaked at 472 nm and 640 nm. Three different Eu²⁺ emission centers in Ba₃GdNa(PO₄)₃F:Eu²⁺ phosphor were confirmed by their fluorescence decay lifetimes. The optimal concentration of Eu²⁺ in Ba₃GdNa(PO₄)₃F:xEu²⁺ was 3 mol% and the corresponding concentration quenching mechanism was verified to be exchange coupling interaction. Furthermore, the white light-emitting diode fabricated with Ba₃GdNa(PO₄)₃F:0.05Eu²⁺ phosphor and a 370 nm UV chip has a CIE of (0.3267, 0.2976) with a color-rendering index of 78.4 at the CCT of 5287 K.     

Efficient and tunable Mn2+ sensitized luminescence via energy transfer of a novel red phosphor Ca19Mn2(PO4)14: Eu2+ for white LED

The exploration of efficient and high-purity red phosphors is an urgent need in LED development. Due to the compact and compositional-tunable structure of whitlockite compound, manganese-based Ca₁₉Mn₂(PO₄)₁₄ is chosen as phosphor host for Eu²⁺ sensitization. Rietveld refinement, steady-state spectra, decay lifetime analysis and temperature-dependent emission spectra were investigated and clearly discussed. Under 360 nm excitation, Ca₁₉Mn₂(PO₄)₁₄: Eu²⁺ shows a strong Mn²⁺ sensitized emission at 655 nm with FWHM of 82 nm, benefiting from the short-distance-induced high-efficient Eu² -Mn²⁺ energy transfer. Emission engineering of Ca₁₉Mn₂(PO₄)₁₄: Eu²⁺ is achieved by Sr²⁺ co-doping, leading to both tunable peak wavelength (ranging from 650 to 610 nm) and improved intensity (130% of original value). Moreover, Ca₁₉Mn₂(PO₄)₁₄: Eu²⁺ exhibits a promising thermal stability where only 40% of emission intensity is lost at 200 °C. Finally, we explored the working performance of the fabricated RGB phosphor-converted white LED. The present work indicates that Ca₁₉Mn₂(PO₄)₁₄: Eu²⁺ phosphor is of great potential as a promising and efficient red phosphor in phosphor-converted white LED.     

Effects of Eu3+ doping on the luminescence properties of novel Sr2CaLa(VO4)3 from partial substitution of Sr2+ by Ca2+ in Sr3La(VO4)3

Eu³⁺-activated Sr_3−xCa_xLa(VO₄)₃ phosphors were fabricated via citric-acid-assisted sol combustion. Characterization of the Sr_3−xCa_xLa(VO₄)₃:Eu³⁺ samples with different concentrations of Ca²⁺ revealed a hexagonal crystal structure belonging to the R-3m space group. The amount of Ca²⁺ added (x) was controlled within 0 ≤ x ≤ 2 to yield high-purity phosphors. Scanning electron microscopy results showed that an increase in Ca²⁺ concentration resulted in a decrease in the particle size of Sr_3−xCa_xLa(VO₄)₃:Eu³⁺, with the shape gradually changing from nearly equiaxed to lath-shaped. The Sr₂CaLa(VO₄)₃:Eu³⁺ phosphor (denoted as SCLVO:Eu³⁺) exhibited the strongest photoluminescence (PL) intensity at 618 nm among the samples under excitation of 394-nm near-UV (NUV) light. The study of Eu³⁺ doping concentration confirmed that Eu³⁺ could enter the lattice of the SCLVO matrix without altering its crystal structure. SCLVO:Eu³⁺ was found to strongly absorb 394 nm NUV light and 464 nm blue light. The optimal concentration of the Eu³⁺ dopant in the SCLVO host was 0.11, which resulted in the phosphor achieving an excellent PL intensity and a color purity of 98.68%. Tunable luminescence from the orange area (0.5280, 0.4522) of Commission Internationale de l'éclairage (CIE) to the red area (0.6313, 0.3650) was achieved by adjusting the concentration of Eu³⁺. Under 394 nm excitation, SCLVO:0.11Eu³⁺ phosphor has a quantum yield (QY) of 28.2% and excellent thermal stability with 0.383 eV activation energy. Consequently, White-light-emitting diode (WLED) based on SCLVO:0.11Eu³⁺ phosphor yielded a high color rendering index (CRI), low correlated color temperature (CCT), and CIE coordinates of 91.8, 5196 K, and (0.3407, 0.3612), respectively, under the 20 mA driven current. These results indicated the tremendous potential of SCLVO:0.11Eu³⁺ phosphors for application in WLEDs excited by NUV or blue light.     

A single-phase white-emitting La10(SiO4)6O3：Eu2+/Eu3+ phosphor for near-UV LED-based application

A novel single-phase white-emitting phosphor La₁₀(SiO₄)₆O₃ (LSO): xEu has been synthesized by high-temperature solid-state reaction. Its crystal structure, luminescence properties, fluorescence decay time and oxygen vacancies have been characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectra. XRD result shows a typical oxyapatite structure with the space group of P6₃/m. Characteristic excitation and emission peaks of Eu²⁺ and Eu³⁺ were observed from PL studies. The optimum doping concentration of Eu was found to be 7.5 mol% (x = 0.075). In this work, the lifetimes of Eu³⁺ and Eu²⁺ were considerably longer than those from some references. Under the excitation of different near ultraviolet (n-UV) longer wavelengths (λex = 360, 370, and 380 nm), the white light emission can be realized with the CIE chromaticity coordinates (0.3907, 0.3595), (0.3472, 0.3282), and (0.3504, 0.3062) for the phosphor LSO: 0.075Eu. The chromaticity coordinates of the phosphor were all located in the white region. Therefore, it is suggested that the explored LSO: 0.075Eu phosphor can be a good candidate for white light-emitting diodes (W-LEDs) application.     

Luminescent properties of Na2GdMg2(VO4)3:Eu3+ red phosphors for NUV excited pc-WLEDs

Herein, a series of novel Na₂GdMg₂(VO₄)₃:Eu³⁺ (NGMVO:Eu³⁺) red phosphors were elaborated by conventional solid-state reaction process. Their structural features, luminescent properties, energy transfer were researched at length. XRD patterns indicate that NGMVO:Eu³⁺ crystallized in single cubic garnet structure. Under the excitation of near ultraviolet light at 356 nm, the emission spectra of NGMVO host could be divided in two parts that resulted from ³T₂ → ¹A₁ and ³T₁ → ¹A₁ transitions of VO₄^3?. While NGMVO:Eu³⁺ phosphors show intense sharp red emission peaks including 590, 610, 652 and 706 nm that originated from ⁵D₀ → ⁷F_J (J = 1–4) transitions of Eu³⁺, respectively. The optimal concentration of Eu³⁺ is 0.7. Importantly, NGMVO:0.7Eu³⁺ sample presents high energy transfer efficiency (89 %) and high external quantum efficiency (48.3 %). Besides, its emission intensity remains 79 % at 420 K compared with that at 300 K, proving the good thermal stability of phosphors. All above results suggest that NGMVO:Eu³⁺ red phosphors have latent applications in white light emitting diodes.     

Morphology control and temperature sensing properties of micro-rods NaLa(WO4)2:Yb3+,Er3+ phosphors

Uniform spindle-like micro-rods NaLa(WO₄)₂:Yb³⁺,Er³⁺ phosphors are prepared by the solvothermal method in the text. Controllable morphology of NaLa(WO₄)₂ crystal can be obtained by adjusting the prepared temperature, PH value, complexing agent content, and solvent ratio. Uniform NaLa(WO₄)₂:Yb³⁺,Er³⁺ micro-rods of 1.8 μm in length and 0.5 μm in width are synthesized at a low temperature of 120°C. The prepared NaLa(WO₄)₂:Yb³⁺,Er³⁺ phosphors present green upconversion luminescence under 980 nm excitation, luminescence intensity reaches to maximum at the Yb³⁺ and Er³⁺ concentration of 6 and 2 mol%. The temperature performance of the NaLa(WO₄)₂:Yb³⁺,Er³⁺ phosphors are evaluated based on thermal coupling technology. Temperature dependence of the two green emissions ratio of Er³⁺ ion is obtained, and the sensitivity of the sample can be calculated, the maximum sensitivity of NaLa(WO₄)₂:Yb³⁺,Er³⁺ is up to 0.019 K⁻¹ at the sample temperature of 564 K.     

Synthesis,structural characterization,and photoluminescence properties of Eu3+‐doped Mg3‐xEux(BO3)2 phosphor

Eu³⁺‐doped Mg_3‐xEu_x(BO₃)₂ (x = 0.000, 0.005, 0.010, 0.020, 0.050, and 0.100) phosphors were synthesized for the first time by solution combustion synthesis method, which is a fast synthesis method for obtaining nano‐sized borate powders. The optimization of the synthesis conditions of phosphor materials was performed by TG/DTA method. These phosphors were characterized by XRD, FTIR, SEM‐EDX, and photoluminescence, PL analysis. The XRD analysis exhibited that all of the prepared ceramic compounds have been crystallized in orthorhombic structure with space group Pnnm. Also, the influence of europium dopant ions on unit cell parameters of host material was analyzed using Jana2006 program and the crystalline size was determined by Debye‐Scherrer's formula. The luminescence properties of all Eu³⁺‐doped samples were investigated by excitation and emission spectra. The excitation spectra of Mg_3‐xEu_x(BO₃)₂ phosphors show characteristic peak at 420 nm in addition to other characteristic peaks of Eu³⁺ under emission at 613 nm. The emission spectra of Eu³⁺‐doped samples indicated most intensive red emission band dominated at 630 nm belonging to ⁵D₀→⁷F₂ magnetic dipole transition. Furthermore, the optimum or quenching concentration of Eu³⁺ ion has been determined as x = 0.010 showed the maximum emission intensity when it was excited at 394 nm.