Sr<Subscript>3</Subscript>GdLi(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>F: Sm<Superscript>3+</Superscript> phosphor: preparation and luminescence properties evaluation

A series of Sr₃Gd_1?xLi(PO₄)₃F: xSm³⁺ (x?=?0.02, 0.04, 0.06, 0.08) phosphors were synthesized by a high-temperature solid state method. The Sm³⁺ activated Sr₃GdLi(PO₄)₃F phosphors can be efficiently excited by the wavelengths in the range from 350 to 450 nm, which matches perfectly with that of the commercial near-UV LED chips. The optimal doping concentration of Sr₃Gd_1?xLi(PO₄)₃F: xSm³⁺ phosphors was determined to be x?=?0.04, corresponding to the quantum efficiency of 2.23%, and the CIE chromaticity coordinates (x?=?0.5172, y?=?0.4641). The concentration quenching mechanism of Sm³⁺ in Sr₃GdLi(PO₄)₃F host is mainly attributed to the dipole–dipole interaction, which was confirmed by the fluorescent lifetimes. The effect of temperature on the photoluminescence property of Sr₃GdLi(PO₄)₃F: Sm³⁺ was investigated. 90% of the intensity is preserved at 150 °C. In addition, a white light emitting diode (WLED) lamp was fabricated by a 405 nm n-UV LED chip coated with Sr₃Gd_0.96Li(PO₄)₃F:0.04Sm³⁺ phosphor and commercial yellow phosphor (YAG: Ce³⁺) of a certain mass ratio. The present work indicates that the Sr₃GdLi(PO₄)₃F: Sm³⁺ orange–red-emitting phosphors tend to be potential application in n-UV WLED.     

Tunable luminescence properties and energy transfer of single-phase Ca<Subscript>4</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>O: Dy<Superscript>3+</Superscript>, Eu<Superscript>2+</Superscript> multi-color phosphors for warm white light

The novel Ca_4?x(PO₄)₂O: xDy³⁺ and Ca_4?x?y(PO₄)₂O: xDy³⁺, yEu²⁺ multi-color phosphors were synthesized by traditional solid-state reaction. The crystal structure, particle morphology, photoluminescence properties and energy transfer process were investigated in detail. The X-ray diffraction (XRD) results demonstrate that the products showed pure monoclinic phase of Ca₄(PO₄)₂O when x < 0.1. The scanning electron microscopy (SEM) indicated that the phosphors were grain-like morphologies with diameters of ~ 3.7–7.0 μm. Under excitation of 345 nm, Dy³⁺-doped Ca₄(PO₄)₂O phosphors showed multi-color emission bands at 410, 481 and 580 nm originated from oxygen vacancies and Dy³⁺. Interestingly, Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors exhibited blue emission band at 481 nm and broad emission band from 530 to 670 nm covering green to red regions. The energy transfer process from Dy³⁺ to Eu²⁺ was observed for the co-doped samples, and the energy transfer efficiency reached to 60% when Eu²⁺ molar concentration was 8%. In particular, warm/cool/day white light with adjustable CCT (2800–6700 K) and high CRI (R_a > 85) can be obtained by changing the Eu²⁺ co-doping contents in Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors. The optimized Ca_3.952(PO₄)₂O: 0.04Dy³⁺, 0.008Eu²⁺ phosphor can achieve the typical white light with CCT of 4735 K and CRI of 87.     

Single phased Sr<Subscript>3</Subscript>La(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>:Eu<Superscript>2+</Superscript>/Mn<Superscript>2+</Superscript> phosphors: solid state synthesis,tunable luminescence and potential applications in white light LEDs

A series of Sr₃La(PO₄)₃:Eu²⁺/Mn²⁺ phosphors were synthesized by a solid state reaction. The phase and the optical properties of the synthesized phosphors were investigated. The XRD results indicate that the doped Eu²⁺ and Mn²⁺ ions do not change the phase of Sr₃La(PO₄)₃. The peak wavelengths of Eu²⁺ single doped and Eu²⁺/Mn²⁺ codoped Sr₃La(PO₄)₃ phosphors shift to longer wavelength due to the larger crystal field splitting for Eu²⁺ and Mn²⁺. The increases of crystal field splitting for Eu²⁺ and Mn²⁺ are induced by the substitution of Sr²⁺ by Eu²⁺ and Mn²⁺ in Sr₃La(PO₄)₃ host. Due to energy transfer from Eu²⁺ to Mn²⁺ in Sr₃La(PO₄)₃:Eu²⁺/Mn²⁺ phosphors, tunable luminescence was obtained by changing the concentration of Mn²⁺. And the white light was emitted by Sr₃La(PO₄)₃:3.0 mol%Eu²⁺/4.0 mol%Mn²⁺ and Sr₃La(PO₄)₃:3.0 mol%Eu²⁺/5.0 mol%Mn²⁺ phosphors.     

Color-tunable luminescence properties of Sm<Superscript>3+</Superscript>/Dy<Superscript>3+</Superscript> co-doped NaLa(MoO<Subscript>4</Subscript>)<Subscript>2</Subscript> phosphors and their energy transfer mechanism

The Sm³⁺, Dy³⁺ doped and Sm³⁺/Dy³⁺ co-doped NaLa(MoO₄)₂ spherical phosphors were hydrothermally synthesized by the EDTA-2Na mediated method. Under the excitation of 297 nm, the quenching concentration of Sm³⁺ in NaLa(MoO₄)₂ host was determined to be 13%, and the concentration quenching mechanism was discussed to be the electric quadrupole–quadrupole interaction. After Sm³⁺ and Dy³⁺ ions were co-doped into the NaLa(MoO₄)₂ host, the energy transfer behaviors resulted from Dy³⁺ to Sm³⁺ ions were investigated by the help of the luminescent spectra of the obtained phosphors. By varying co-doping concentrations of Sm³⁺/Dy³⁺ ions, the emission color of NaLa(MoO₄)₂:Sm³⁺/Dy³⁺ can be tuned from reddish-orange, pink and white to bluish-green. The CIE chromaticity coordinate, the correlated color temperature and the quantum efficiency of NaLa_0.87(MoO₄)₂:1%Sm³⁺, 12%Dy³⁺ were calculated to be (0.356, 0.320), 4353 K and 20%, respectively. Furthermore, in the temperature-dependent analysis, it presented good thermal stability, which can become a promising single-phased white-emitting phosphor for white LEDs devices. Based on these results, the possible energy transfer mechanism between Dy³⁺ and Sm³⁺ in NaLa(MoO₄)₂:Sm³⁺/Dy³⁺ was also proposed.     

The comparison: photoluminescence and afterglow behavior in CaSnO<Subscript>3</Subscript>:Dy<Superscript>3+</Superscript> and Ca<Subscript>2</Subscript>SnO<Subscript>4</Subscript>:Dy<Superscript>3+</Superscript> phosphors

This paper reports the comparison of photoluminescence and afterglow behavior of Dy³⁺ in CaSnO₃ and Ca₂SnO₄ phosphors. The samples containing CaSnO₃ and Ca₂SnO₄ were prepared via solid-state reaction. The properties have been characterized and analyzed by utilizing X-ray diffraction (XRD), photoluminescence spectroscope (PLS), X-ray photoelectron spectroscopy (XPS), afterglow spectroscopy (AS) and thermal luminescence spectroscope (TLS). The emission spectra revealed that CaSnO₃:Dy³⁺ and Ca₂SnO₄:Dy³⁺ phosphors showed different photoluminescence. The Ca₂SnO₄:Dy³⁺ phosphor showed a typical ⁴F_9/2 to ⁶H_j energy transition of Dy³⁺ ions, with three significant emissions centering around 482, 572 and 670 nm. However, the CaSnO₃:Dy³⁺ phosphor revealed a broad T₁ → S₀ transitions of Sn²⁺ ions. The XPS demonstrate the existence of Sn²⁺ ions in CaSnO₃ phosphor caused by the doping of Dy³⁺ ions. Both the CaSnO₃:Dy³⁺ and Ca₂SnO₄:Dy³⁺ phosphors showed a typical triple-exponential afterglow when the UV source switched off. Thermal simulated luminescence study indicated that the persistent afterglow of CaSnO₃:Dy³⁺ and Ca₂SnO₄:Dy³⁺ phosphors was generated by the suitable electron or hole traps which were resulted from the doping the calcium stannate host with rare-earth ions (Dy³⁺).     

Synthesis and annealing effects on the optical spectroscopy properties of red-emitting Gd(P<Subscript>0.5</Subscript>V<Subscript>0.5</Subscript>)O<Subscript>4</Subscript>: x at.% Eu<Superscript>3+</Superscript>

In this work, Gd(P_0.5V_0.5)O₄: x at.% Eu³⁺ phosphors with different dopant concentrations (x?=?1, 3, 5, 6, 7, 9) were synthesized through chemical coprecipitation method. The phosphors were characterized by XRD, SEM, infrared spectroscopy, photoluminescence excitation, emission spectra and CIE. The results of XRD indicate that the obtained phosphors have the tetragonal phase structure. Eu³⁺ emission transitions arise mainly from the ⁵D₀ level to the ⁷F_J (J?=?0, 1, 2, 3, 4) manifolds. The emission intensity and crystalline of Gd(P_0.5V_0.5)O₄:x at% Eu³⁺ powders are increasing with annealing temperature at 600, 800, 1000, 1100, and 1200 °C, respectively. The introduction of VO₄^3? can broaden the range of UV excitation spectrum wavelength and enhance the transition between ⁵D₀ → ⁷F₁ to ⁵D₀ → ⁷F₂ for long wavelength emission. And the most dominant emission peak of Eu³⁺ for ⁵D₀ → ⁷F₂ transition is closer to pure red light at 622 nm. The maximum emission intensity of the phosphors is the concentration of 6 at.% Eu³⁺ because of the distance of the neighbor Eu³⁺ ions reaching a certain critical value and the influence of multipolar interaction. Compared to commercial phosphors Y₂O₃:Eu³⁺ and (Y,Gd)BO₃:Eu³⁺, our work yielded a longer wavelength red light emission intensity and a higher proportion of red light to orange light. All our results indicate that color purity of this phosphor turns it into a promising red phosphor in ultraviolet-pumped light-emitting diodes.     

Luminescence properties and energy transfer of co-doped Ba<Subscript>3</Subscript>GdNa(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>F:Ce<Superscript>3+</Superscript>,Tb<Superscript>3+</Superscript> green-emitting phosphors

Phase pure Ce³⁺ and Tb³⁺ singly doped and Ce³⁺/Tb³⁺ co-doped Ba₃GdNa(PO₄)₃F samples have been synthesized via the high temperature solid-state reaction. The crystal structures, photoluminescence properties, fluorescence lifetimes, thermal properties and energy transfer of Ba₃GdNa(PO₄)₃F:Ce³⁺,Tb³⁺ were systematically investigated. Rietveld structure refinement indicates that Ba₃GdNa(PO₄)₃F crystallizes in a hexagonal crystal system with the space group P-6. For the co-doped Ba₃GdNa(PO₄)₃F:Ce³⁺,Tb³⁺ samples, the emission color can be tuned from blue to green by varying the doping concentration of the Tb³⁺ ions. The intense green emission was realized in the Ba₃GdNa(PO₄)₃F:Ce³⁺,Tb³⁺ phosphors on the basis of the highly efficient energy transfer from Ce³⁺ to Tb³⁺. Also the energy transfer mechanism has been confirmed to be quadrupole–quadrupole interaction, which can be validated via the agreement of critical distances obtained from the concentration quenching (13.84 Å). These results show that the developed phosphors may possess potential applications in near-ultraviolet pumped white light-emitting diodes.     

Ce and Eu activated Na<Subscript>2</Subscript>Zn<Subscript>5</Subscript>(PO<Subscript>4</Subscript>)<Subscript>4</Subscript>, a new promising novel phosphor

A new efficient phosphor, Eu²⁺/Eu³⁺ and Ce³⁺ activated Na₂Zn₅(PO₄)₄ has been synthesized by solid-state reaction technique at high temperature. X-ray powder diffraction analysis confirmed the formation of Na₂Zn₅(PO₄)₄ host lattice. Scanning electron microscopy indicated that the microstructure of the phosphor consisted of irregular fine grains with a size of about 0·5–2 μm. Photoluminescence excitation spectrum measurements of Ce³⁺ activated Na₂Zn₅(PO₄)₄ show that the phosphor can be efficiently excited by UV-Vis light from 280 to 310 nm to realize emission in the visible (blue) range due to the 5d-4f transition of Ce³⁺ ions which is applicable for scintillation purpose, whereas Eu²⁺/Eu³⁺ activated Na₂Zn₅(PO₄)₄ phosphor emits blue, green and red emission spectrum shows at 487 nm, 546 nm with a dominant peak at 611 nm respectively, due to Eu²⁺/Eu³⁺ ions which is promising candidate for solid state lighting. Therefore, newly synthesised, by low cost and easy technique prepared, novel phosphors may be useful as RGB phosphor for solid state lighting application.     

Hydrothermal synthesis of NaLa(WO<Subscript>4</Subscript>)<Subscript>2</Subscript>:Eu<Superscript>3+</Superscript> octahedrons and tunable luminescence by changing Eu<Superscript>3+</Superscript> concentration and excitation wavelength

NaLa(WO₄)₂:Eu³⁺ phosphors with different Eu³⁺ concentrations have been synthesized by a hydrothermal method. The phase is confirmed by XRD analysis, which shows a pure-phase NaLa(WO₄)₂ XRD pattern for all of NaLa(WO₄)₂:Eu³⁺ phosphors. The SEM and TEM images indicate that all of NaLa(WO₄)₂:Eu³⁺ phosphors have a octahedral morphology. These suggest that the Eu³⁺ doping has no influence on the structure and growth of NaLa(WO₄)₄ particles. By monitoring the emission of Eu³⁺ at 615 nm, NaLa(WO₄)₂:Eu³⁺ phosphors show excitation bands originating from both host and Eu³⁺ ions. Under the excitation at 271 nm corresponding to WO₄ ^2? groups, emission bands coming from the ¹A₁ → ³T₁ transition with the WO₄ ^2? groups and the ⁵D₀ → ⁷F_j (j = 0, 1, 2, 3 and 4) transitions of Eu³⁺ are observed. The emission intensity relating to WO₄ ^2? groups decreases with increasing Eu³⁺ concentration. But emission intensities of Eu³⁺ increase firstly and then decreases because of concentration quenching effect. Under the excitation at 395 nm corresponding to ⁷F₀ → ⁵L₆ transition of Eu³⁺, only characteristic Eu³⁺ emission bands can be observed. The results of this work suggest that tunable luminescence can be obtained for Eu³⁺ doped NaLa(WO₄)₂ phosphors by changing Eu³⁺ concentration and excitation wavelength.     

Synthesis and luminescence properties of LiBaPO<Subscript>4</Subscript>:Bi<Superscript>3+</Superscript> yellow-emitting phosphor for solid-state lighting

Novel LiBaPO₄:Bi³⁺ yellow-emitting phosphor is synthesized by high temperature solid-state reaction method in air. With excitation 260 nm, LiBaPO₄:Bi³⁺ phosphor emits yellow light with the chromaticity coordinate (0.4272, 0.4657) and color rendering index 77.7. Emission band peaking at ~?588 nm of LiBaPO₄:Bi³⁺ phosphor in the range of 400–790 nm is attributed to the ³P₁ → ¹S₀ electron transition of Bi³⁺ ion. Excitation band monitored at 588 nm in the range of 220–300 nm is assigned to the ¹S₀ → ³P₁ electron transition of Bi³⁺ ion. The optimal Bi³⁺ ion concentration in LiBaPO₄:Bi³⁺ phosphor is ~?1.0 mol%. Time resolved spectra and fluorescence lifetime data confirm that there is only Bi³⁺ ion luminous center in LiBaPO₄:Bi³⁺ phosphor. The luminous mechanism is analyzed by configurational coordinate diagram of Bi³⁺ ion. The experiment results are helpful to develop other new Bi³⁺-doped optical materials for solid-state lighting.     

Combusion synthesis,structural and photo-physical characteristics of Eu<Superscript>2+</Superscript> and Dy<Superscript>3+</Superscript> co-doped SrAl<Subscript>2</Subscript>O<Subscript>4</Subscript> phosphor nanopowders

In this research, we reported the synthesis of Eu²⁺ and Dy³⁺ co-doped SrAl₂O₄ phosphor nanopowders with high brightness and long afterglow by urea-nitrate solution combustion synthesis (SCS) at 600 °C, followed by heating the resultant combustion ash at 1,200 °C in a weak reductive atmosphere (5% H₂ + 95% N₂). The broad-band UV-excited luminescence of the SrAl₂O₄: Eu²⁺, Dy³⁺ nanopowders was observed at λ _max = 517 nm due to transitions from the 4f⁶5d¹ to the 4f⁷ configuration of the emission center (Eu²⁺ ions). The excitation spectra consist of 240- and 254 nm broad peaks. Finally, it was found that the optimum ratio of urea is 2.5 times higher than theoretical quantities for the best emission condition of SrAl₂O₄: Eu²⁺, Dy³⁺ phosphor nanopowders.     

Synthesis,structure and photoluminescence properties of (Sr,Ca)AlSiN<Subscript>3</Subscript>:Eu<Superscript>2+</Superscript> phosphor for white light emitting diodes with controllable optical performance

A series of Sr_yCa_1?x?yAlSiN₃:xEu²⁺ (x = 0–0.01, y = 0–0.8) phosphors have been successfully prepared by solid state reaction under atmospheric pressure. All the phosphors exhibit orthorhombic crystal structure similar with CaAlSiN₃ structure. It is found that the emission bands for all Ca_1?xAlSiN₃:xEu²⁺ phosphors are centered at ~650 nm and fluorescence quenching has been observed along with the increase of Eu²⁺ concentration in host materials. Through substitution of Ca²⁺ by Sr²⁺, an expected red emission peak (625 nm) and enhanced luminescent intensity can be achieved. The obtained Sr_0.8Ca_0.192AlSiN₃:0.008Eu²⁺ phosphor was further used as efficient red component to fabricate white light emitting diodes (LEDs). Under the optimized condition of LED packaging, the white LEDs own the excellent optical properties with luminous efficiency of 90.6 lm/W and an ideal color rendering index (Ra = 82). Furthermore, the color correlated temperature of white LEDs can be simply adjusted through changing the red phosphor concentration and dispensing package saves time.     

Synthesis and luminescent characterization of YAl<Subscript>3</Subscript>(BO<Subscript>3</Subscript>)<Subscript>4</Subscript>:Tb<Superscript>3+</Superscript> phosphors

YAl₃(BO₃)₄:Tb³⁺ phosphors were fabricated by the sol–gel method. The phosphor showed prominent luminescence in green due to the magnetic dipole transition of ⁵D₄–⁷F₅. Structural characterization of the luminescent material was carried out with X-ray powder diffraction (XRD) analysis. Luminescence properties were analyzed by measuring the excitation and photoluminescence spectra. Photoluminescence measurements indicated that the phosphor exhibited bright green emission at about 541 nm under UV excitation. It is shown that the 11% of doping concentration of Tb³⁺ ions in YAl₃(BO₃)₄:Tb³⁺ phosphors is optimum.     

Synthesis,photoluminescence properties of Sr<Subscript>1.95</Subscript>Ba<Subscript>0.05</Subscript>CeO<Subscript>4</Subscript>:Eu<Superscript>3+</Superscript> for LED applications

The Sr_1.95Ba_0.05 CeO₄:Eu³⁺ phosphors are synthesized by the solid-state reaction method. The samples are characterized using X-ray diffraction (XRD), diffuse reflectance spectroscopy and photoluminescence (PL) spectra. The XRD results reveal that the synthesized phosphors are genuine crystalline and belong to the orthorhombic structure. The intense PL emission is optimized from the PL spectra at various doping concentrations of europium ions. The results indicates that the phosphor can be effectively excited under 264 nm wavelength producing on intense emission spectrum of the synthesis material at 484 nm (blue region). The color purity of the phosphor is confirmed by CIE coordinates (x = 0.217, y = 0.265). The experimental data indicate that the prepared phosphors can be used as blue-emitting material in the field of illuminations and display devices.     

Luminescence properties and preparation of Lu<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript> powder doped with Ce and Pr ions

Lu₃Al₅O₁₂:Ce³⁺ phosphor powder, which exhibits green emission band, was synthesized by the high-temperature solid-state reaction method with a flux BaF₂. X-ray diffraction (XRD), photoluminescence (PL) spectra, and fluorescent lifetime spectra were used to characterize the structure and luminescent properties of the sample. The XRD patterns indicated that when prepared at 1550 °C for 3 h with 4 wt% flux, Lu₃Al₅O₁₂:Ce³⁺ phosphors powder is the garnet cubic crystal system structure. Photoluminescence (PL) spectra showed that the Lu₃Al₅O₁₂:Ce³⁺ phosphor powder can be effectively excited by near ultraviolet and blue light, emitting broad band peaking at 505 nm, which is attributed to ²F_5/2?→?²D_5/2 transition. The self-concentration quenching mechanism of Ce³⁺ is the dipole–dipole interaction. Small amount of Pr³⁺ increased red light emission at 610 nm. Photoluminescence (PL) spectra and fluorescent lifetime spectra indicated that there was an efficient energy transfer process between Ce³⁺ and Pr³⁺.     

Photoluminescence properties and charge compensation investigations of novel orange-emitting Eu<Superscript>3+</Superscript> doped Na<Subscript>4</Subscript>Ca<Subscript>4</Subscript>(Si<Subscript>6</Subscript>O<Subscript>18</Subscript>) phosphors

A series of polycrystalline Na₄Ca₄(Si₆O₁₈):Eu³⁺ orange emitting phosphors were synthesized by a conventional high-temperature solid-state reaction. The phase formation was confirmed by X-ray power diffraction analysis. The excitation spectra show a strong host absorption indicating an efficient energy transfer process from O^2? to Eu³⁺ ions. Upon NUV radiation, the phosphors showed strong red emission around 610 nm (⁵D₀ → ⁷F₂) and orange emission around 591 nm (⁵D₀ → ⁷F₁), but the ⁵D_1,2,3 emission nearly can not be seen. Compared with the luminescence properties of Li⁺, Na⁺, and K⁺ co-doped samples, we deduced that Na⁺ ions probably prefer to dope into the intrinsic Na vacancies rather than Ca²⁺ ions vacancies in Na₄Ca₄(Si₆O₁₈) crystal. Thermal stability properties, quantum efficiency and chromaticity coordinates of the phosphors have been investigated for the potential application in white LEDs.     

Synthesis and luminescence properties of a novel UV-emitting phosphor Sr<Subscript>3</Subscript>P<Subscript>4</Subscript>O<Subscript>13</Subscript>:Ce<Superscript>3+</Superscript>

The ultraviolet (UV)-emitting Sr₃P₄O₁₃:Ce³⁺ phosphors were synthesized via the solid-state reaction method, and their structural, morphological and luminescence properties were characterized by X-ray diffraction analysis, scanning electron microscopy, photoluminescence spectroscopy. The obtained results indicate that these phosphors can be effectively excited by short-wavelength ultraviolet (<300 nm), and exhibit long-wavelength ultraviolet (300–380 nm) emission with nanosecond-level fluorescence lifetime corresponding to the parity-allowed 5d–4f transitions of Ce³⁺. The concentration-quenching phenomenon of Ce³⁺ in Sr₃P₄O₁₃ host was also studied, in which the critical energy transfer distance between Ce³⁺ ions and concentration quenching mechanism were determined.     

Phase conversion and spectral properties of long lasting phosphor Zn<Subscript>3</Subscript> (PO<Subscript>4</Subscript>)<Subscript>2</Subscript>:Mn<Superscript>2+</Superscript>, Ga<Superscript>3+</Superscript>

A red long lasting phosphor Zn₃(PO₄)₂:Mn²⁺,Ga³⁺ (ZPMG) was prepared by ceramic method, and phase conversion and spectral properties were investigated. Results indicated that the phase conversion from α-Zn₃(PO₄)₂, β-Zn₃(PO₄)₂ toγ-Zn₃(PO₄)₂ occurs with different manganese concentration incorporated and sinter process. The structural change induced by the phase transformation results in a remarkable difference in the spectral properties. The possible luminescence mechanism for this red LLP with different forms has been illustrated.     

New NaSrPO<Subscript>4</Subscript>:Sm<Superscript>3+</Superscript> phosphor as orange-red emitting material

Sm³⁺-activated NaSrPO₄ phosphors could be efficiently excited at 403 nm, and exhibited a bright red emission mainly including four wavelength peaks of 565, 600, 646 and 710 nm. The highest emission intensity was found for NaSr _1?x PO₄: xSm³⁺ with a composition of x = 0.007. Concentration quenching was observed as the composition of x exceeds 0.007. The decay time values of NaSr_1?x PO ₄ : xSm³⁺ phosphors range from around 2.55 to 3.49 ms. NaSr_1?x PO₄: xSm³⁺ phosphor shows a higher thermally stable luminescence and its thermal quenching temperature T ₅₀ was found to be 350°C, which is higher than that of commercial YAG:Ce³⁺ phosphor and ZnS:(Al, Ag) phosphor. Because NaSr_1?x PO₄: xSm³⁺ phosphor features a high colour-rendering index and chemical stability, it is potentially useful as a new scintillation material for white light-emitting diodes.     

Enhanced red-emitting phosphor Na<Subscript>2</Subscript>Ca<Subscript>3</Subscript>Si<Subscript>2</Subscript>O<Subscript>8</Subscript>:Eu<Superscript>3+</Superscript> by charge compensation

A series of novel red-emitting Na₂Ca_3???x Si₂O₈:xEu³⁺ phosphors were synthesized by solid state reactions. The phosphors can strongly absorb 395 nm light, and show red emission with a good color purity. The excitation and emission spectra properties of Na₂Ca₃Si₂O₈:Eu³⁺ were characterized. Na₂Ca₃Si₂O₈:Eu³⁺ with self-compensated and alkali metal ions charge compensated approaches (2Ca²⁺→Eu³⁺ + M⁺, M?=?Li⁺, Na⁺, K⁺) have investigated, which found that the red emission of luminescent intensity can be greatly enhanced, and shows superior luminescent property to the commercial Y₂0₃S:Eu³⁺. The present work implies that the efficient charge compensated phosphors are promising candidates as red-emitting phosphor for w-LEDs.