Microstructure tailoring of red-emitting AlN-CaAlSiN3:Eu2+ composite phosphor ceramics with higher optical properties for laser lighting

Laser lighting is superior to light-emitting diodes (LEDs) in brightness, beam aperture and efficiency, which largely depends on the light extraction efficiency and thermal properties of color converters. In this paper, we proposed to improve the light extraction efficiency of red-emitting AlN-CaAlSiN₃:Eu composite phosphor ceramics by controlling the light scattering, and to improve the thermal conductivity of the phosphor ceramics by increasing grain size. The composite phosphor ceramics with moderate light scattering and high thermal conductivity can be obtained by gas pressure sintering (GPS) and the followed hot isostatic pressing (HIP). The saturation threshold of the sample is increased from 7.0 to 10.8 W, and the luminous flux is enhanced from 32.3 to 51.0 lm after the HIP post-treatment, which is 55.5% higher than the previously reported dense AlN-CaAlSiN₃:Eu composite phosphor ceramics (32.8 lm). This work emphasizes the role of pore size distribution in light extraction efficiency of phosphor ceramics.     

Highly thermal conductive red-emitting AlN-CaAlSiN3:Eu2+ composite phosphor ceramics for high-power laser-driven lighting

Thermally robust red-emitting phosphor ceramics are urgently required for laser lighting and displays with high luminance and better color saturation. The most promising CaAlSiN₃:Eu ceramics have a low thermal conductivity of 4.2 W m^?1 K^?1 and a small luminance saturation of 0.5 W, making it hard to be used under high power laser irradiation. In this work, we incorporated AlN into the CaAlSiN₃:Eu ceramic to produce red-emitting AlN-CaAlSiN₃:Eu composite phosphor ceramics by spark plasma sintering. The fully densified phosphor ceramics have the highest thermal conductivity reported so far (53.5 W m^?1 K^?1), which is about 13 times higher than the reported one. The luminance saturation of the composite ceramics occurs at a high threshold of 4.2 W under blue laser excitation, enabling them to be used for high power laser lighting. This work provides an idea of tackling the microstructure of nitride phosphor ceramics and of preparing thermally robust red-emitting color converters.     

Additive-free Y2O3:Eu3+ red-emitting transparent ceramic with superior thermal conductivity for high-power UV LEDs and UV LDs

To obtain red-emitting luminescent material for high-power UV LED and UV LD applications, an additive-free Y₂O₃:Eu³⁺ phosphor ceramic was successfully prepared in this work. The nitrate pyrogenation method is applied to obtain raw nanopowders with high reactivity, and a hybrid sintering method combining low-temperature presintering and subsequent hot isostatic pressing (HIP) is then applied to realize full densification of the final ceramic products. The effects of the presintering temperature on the density, microstructural, and optical properties are investigated in detail. The HIP-treated Y₂O₃:Eu³⁺ ceramic presintered at 1450 °C exhibits a high transmittance near 80 % at 600 nm. Due to the nonuse of sintering additives, the thermal conductivity of Y₂O₃:Eu³⁺ ceramic product reaches 10.9 Wm⁻¹ K⁻¹ at room temperature. The achieved Y₂O₃:Eu³⁺ ceramic also exhibits good applicability under the excitation of a UV LED chip and UV laser light, showing promise as a color converter for high-power UV LED and UV LD applications.     

Silica nanoparticles assisted preparation of reddish-yellow emitting Eu2+ activated remote-type CaSrSiO4 phosphor for warm white LED applications

A reddish-yellow emitting silicate-based remote phosphor has been developed via the wet-solid phase reaction technique. By employing silica nanoparticles (200 nm), Eu²⁺ doped CaSrSiO₄ phosphor was developed and its efficacy has been examined thoroughly. The developed remote phosphor can get excited over a broad region of the spectrum ranging from ultraviolet to blue (250–500 nm) and as generates a reddish-yellow emission peaked at 580 nm covering a broad range of spectral components (450–800 nm) with a quantum efficiency of 52%. The thermoluminescence studies of developed remote phosphor exhibit 50% of the stable emission up to 200 °C without any shift in the emission wavelength. The developed remote phosphor was then utilized for the making of a proto-type LED using 450 nm blue-emitting commercial LED. The output emission from the proto-type LED confirms the production of efficient warm white light with CCT <5000 K and CRI >85.     

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.     

Mn2+ activated MgAlON transparent ceramic: A new green-emitting transparent ceramic phosphor for high-power white LED

A novel Mn²⁺ activated green-emitting MgAlON transparent ceramic phosphor was synthesized from Mg_0.21Al_2.57O_3.80N_0.20:0.03Mn²⁺ (MgAlON:Mn) phosphor powder by pressureless sintering combining with hot isostatic pressing. By crystalline structure refinement and cathodoluminescence (CL) characterization, it is demonstrated that Mn²⁺ was dissolved in the spinel lattice and occupied the tetrahedral site. The ceramic, retaining high transmittance in UV–vis region (up to 82% at 800 nm) and excellent thermal-mechanical properties of MgAlON transparent ceramic-matrix, shows a strong green emission at 513 nm under 445 nm light excitation. Compared with its powder counterpart, the ceramic phosphor exhibits higher green color purity, higher internal quantum efficiency (47%) and lower thermal quenching. It is suggested that this novel green solid phosphor could be applied in high color rendering and high-power white light-emitting diodes when combined with a red solid phosphor and a blue LED chip.     

Sr3GdLi(PO4)3F:Eu2+, Mn2+: A tunable blue-white color emitting phosphor via energy transfer for near-UV white LEDs

A series of Eu²⁺ and Mn²⁺ co-doping Sr₃GdLi(PO₄)₃F phosphors have been synthesized through high temperature solid state reaction. Eu²⁺ single doped Sr₃GdLi(PO₄)₃F phosphors have an efficient excitation in the range of 230–430 nm, which is in good agreement with the commercial near-ultraviolet (n-UV) LED chips, and gives intense blue emission centering at 445 nm. The critical distance of the Eu²⁺ ions in Sr₃GdLi(PO₄)₃F is computed and demonstrated that the concentration quenching mechanism of Eu²⁺ is mostly caused by the dipole-dipole interaction. By co-doping Eu²⁺ and Mn²⁺ ions in the Sr₃GdLi(PO₄)₃F host, the energy transfer from Eu²⁺ to Mn²⁺ that can be discovered. With the increase of Mn²⁺ content, emission color can be adjusted from blue to white under excitation of 380 nm, corresponding to chromatic coordinates change from (0.189, 0.108) to (0.319, 0.277). The energy transfer from Eu²⁺ to Mn²⁺ ions is proven to be a dipole-dipole mechanism on the basis of the experimental results and analysis of photoluminescence spectra and decay curves. This study infers that the obtained Sr₃GdLi(PO₄)₃F:Eu²⁺, Mn²⁺ phosphors may be a potential candidate for n-UV LEDs.     

A new mechanoluminescence phosphor Na3Sc2(PO4)3:Eu2+: Phase transition-assisted defect formation in a polymorphic composition

A new mechanoluminescent phosphor was developed from a sodium (Na) superionic conductor (NASICON)-structured Na₃Sc₂(PO₄)₃:Eu²⁺ phosphor that is known for its self-healing properties. The compound that crystalized assuming monoclinic C2/c symmetry was found to be blue-emitting, with no noticeable persistent luminescence. Thermoluminescence analysis showed that the phosphor had two prominent distinct thermal emission bands corresponding to the high-temperature β- and γ-phases of the composition. The mechanoluminescence properties of the material that does not have any persistent luminescence at room temperature were investigated by imparting impulsive strain. The compound on charging with 365 nm radiation was found to have significant mechanoluminescent emission originating from shallow defects present in the β-phase of composition that formed by the stress-induced phase transition process. Its emission characteristics and temporal behavior were investigated by varying the impact velocity.     

Thermoluminescence study of Eu3+ doped Na2Sr2Al2PO4Cl9 phosphor via doping of singly,doubly and triply ionized ions

We report here thermoluminescence properties of Eu³⁺ doped Na₂Sr₂Al₂PO₄Cl₉ phosphor via doping of singly, doubly and triply ionized ions on the basis of PL studies done for this sample. The proposed sample was synthesized using solid state reaction method. Vibrational feature of this phosphor was confirmed by FT-IR spectra. This sample shows high degrees of crystallinity. All subseries are irradiated with ⁶⁰Co- γ (gamma) source and thermoluminescence studies were done for all subseries formed by doping of singly, doubly and triply ionized ions. The result shows that all the series give highest TL intensity at low dose rate. On doping of triply doped ionized ion (Y³⁺), TL intensity is enhanced to some extent. Deconvolution of broad TL glow data formed for some sample were done by using TLAnal computerized software. Thermoluminescence studies of these Eu³⁺ doped SrYAl₃O₇ phosphor were done by Nucleonix TL 1009I thermoluminescence (TL) reader. Trapping parameters of each phosphor such as activation energy (E), order of kinetics (b) and frequency factor (s) were calculated by Chen's peak shape method, Initial rise method and Ilich method. Thus, the singly, doubly and triply ionized ions co-doped with Na₂Sr₂Al₂PO₄Cl₉: Eu³⁺phosphor may be used in high dose thermoluminescence dosimetric application in various fields.     

Effect of singly,doubly and triply ionized ions on downconversion photoluminescence in Eu3+ doped Na2Sr2Al2PO4Cl9 phosphor: A comparative study

We report a change in the red photoluminescence of the Eu³⁺ doped Na₂Sr₂Al₂PO₄Cl₉ phosphor via doping of singly, doubly and triply ionized ions. The synthesized phosphors show good crystalline nature. The EDS analysis confirms the presence of desired elements in the phosphor samples. The vibrational feature of the phosphor was confirmed by FTIR analysis. The photoluminescence excitation spectra of the phosphor show three peaks at 317, 395 and 467 nm. The Eu³⁺ doped Na₂Sr₂Al₂PO₄Cl₉ phosphor emits intense red color on excitations with 395 and 467 nm wavelengths. However, the photoluminescence intensity of the phosphor is larger for 395 nm excitation. When the singly, doubly and triply ionized ions are co-doped in the Eu³⁺ doped Na₂Sr₂Al₂PO₄Cl₉ phosphor (i.e. F⁻, WO₄²⁻, MoO₄²⁻, VO₄³⁻, La³⁺, and Y³⁺) the photoluminescence intensity of the phosphor is decreased significantly. The decrease in photoluminescence intensity is due to change in local crystal structure created by these ions. Interestingly, the photoluminescence intensity of phosphor increases many times when the (Y³⁺) ion incorporated phosphor is excited with 317 nm wavelength. The CIE diagram shows color emitted in the red region of visible spectrum and the color purity is larger for triply ionized (Y³⁺) ion. Thus, the singly, doubly and triply ionized ions activated Na₂Sr₂Al₂PO₄Cl₉: Eu³⁺ phosphor may be used in displays devices, photonic devices, solid state lighting and white LEDs.     

Laser sintering and influence of the Dy concentration on BaAl2O4:Eu2+, Dy3+ persistent luminescence ceramics

This work reports the effect of the Dy concentration on the persistence luminescence properties of Eu doped barium aluminate (BaAl₂O₄) laser-sintered ceramics. For this study, the ceramics were first sintered using the laser sintering technique, based on a CO₂ laser as the heating source, in an ambient atmosphere. The structural and morphology characteristics of the samples were investigated by x-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques, respectively. The laser-sintered ceramics presented are shown to be phase pure (single phased), and, for highest Dy concentration sample, a spurious Dy-rich phase at the grain boundary was observed. All samples exhibit the characteristic blue-green emission from the Eu²⁺ ion, due to the 4f⁶5d¹–4f⁷ transition (495 nm), even when they have been sintered in air. Finally, a clear dependence of the persistent luminescence intensity and decay time with the Dy concentration was verified.     

A novel Li2CaSi2N4:Eu2+ orange-red phosphor for field-emission displays

The exploration of suitable phosphors with high efficiency, low saturation, and good stability has always been a key issue for field-emission displays (FEDs) development. In this work, a novel Li₂CaSi₂N₄:Eu²⁺ orange-red phosphors were prepared by solid reaction process and the cathodoluminescence (CL) properties were investigated in detail to explore the potential application for FEDs. Under a low voltage electron-beam excitation, the phosphors show an intense orange-yellow emission in the range of 500-700 nm, which belongs to the 4f⁶5d→4f⁷ electron transition of Eu²⁺ ion. The influences of the Eu²⁺ doping concentration, filament current, accelerating voltage, and bombardment time on the CL emission of Li₂CaSi₂N₄:Eu²⁺ were investigated in detail. The results indicate that Li₂CaSi₂N₄:Eu²⁺ phosphors exhibit an intense orange-red emission, no saturation effect, and excellent degradation property, which give the Li₂CaSi₂N₄:Eu²⁺ phosphors potential application in full color FEDs.     

Gd3Al3Ga2O12:Ce,Mg2+ transparent ceramic phosphors for high-power white LEDs/LDs

Gd₃Al₃Ga₂O₁₂:1.5%Ce, xMg²⁺ (GAGG:1.5%Ce, xMg²⁺) transparent ceramic phosphors (TCPs) were prepared via a two-step sintering method. The effects of MgO on microstructures and luminescent properties of GAGG:Ce TCPs are investigated for the first time. For the optimized Mg²⁺ of x = 0.5%, the in-line transmittance of the obtained TCP reaches 78.6%. Performances of the titled TCPs in high-power light-emitting diodes (LEDs) and laser diodes (LDs) lighting are illustrated. The optimized TCP shows the luminous efficacy of 84.0 lm W^?1 in LD lighting. This work provides a strategy to modify TCPs for the next-generation LD lighting.     

Analysis of fluorescence properties of novel Eu3+-doped ZnAl2O4-based ceramic aerogels for high-power optical device applications

A novel series of ZnAl₂O₄:Eu³⁺ aerogels (ZAE) and mullite ceramic phase reinforced ZnAl₂O₄:Eu³⁺ aerogels (MZAE) with high fluorescence thermal stability have been firstly synthesized for the encapsulation of high-power optical devices. However, due to the intrinsic structural brittleness of the aerogel, the structure of ZAE tends to collapse during the heat treatment and the fluorescence performance falls short of expectations. To this end, we propose a simple and effective strategy to enhance the structural rigidity of fluorescent aerogels by introducing the mullite ceramic phase into the network structure of ZAE. This can effectively suppress the agglomeration of Eu³⁺ caused by the collapse of the structure during the heat treatment, thus enhancing the optical properties of the aerogel. Compared with ZAE, MZAE has higher fluorescence thermal stability. The fluorescence intensity of MZAE at 498 K is still 75 % of that at 298 K, and the chromaticity shift is only 22 × 10⁻³.     

Optimization of Ce3+ concentration and Y4MgSi3O13 phase in Mg2+-Si4+ Co-doped Ce: YAG ceramic phosphors

As a promising replacement for nitride red phosphors, Ce: Y₃(Mg_1.8Al_1.4Si_1.8)O₁₂ (Ce: YMASG) ceramic phosphors have attracted significant attention recently for their advantages in inorganic encapsulation and massive red-shifting of Ce³⁺ emission. In this work, Ce: YMASG with different doping concentrations of Ce³⁺ and Al₂O₃, was fabricated by vacuum sintering to investigate its effects on the elimination of the impurity phase and the enhancement of the luminescent properties of white light-emitting diodes (w-LEDs). It was discovered that the emission wavelength redshifts from 592 to 606 nm as the Ce³⁺ concentration increases, while at 450 K, the emission intensity deteriorates from 0.47 to 0.36 of its initial value. The Rietveld analysis revealed the presence of an impurity phase of Y₄MgSi₃O₁₃ with a concentration of 17.021 wt% in Ce: YMASG. With the introduction of Al₂O₃, the impurity phase was eliminated from the matrix completely, the emission peak shifted to a shorter wavelength, and the thermal stability was greatly improved. When the correlated color temperature was controlled at around 3000 K in the packaged w-LEDs, the commission international de l'éclairage (CIE) chromaticity coordinates shifted toward the bottom left corner of the diagram with increasing concentration of Ce³⁺. Conversely, the luminous efficiency (LE) increased from 36 lm/W to 58.6 lm/W as the concentration of Al₂O₃ increased from 0 to 10 wt%, which demonstrated the application prospect of the fabricated phosphor in warm w-LEDs.     

High CRI white light-emitting phosphor-in-glass film for laser lighting applications by adding cyan phosphor BaSi2O2N2:Eu2+

PiGF (Phosphor-in-glass film) with high color rendering was successfully prepared at a low sintering temperature. The influence of sintering temperature, the mass ratio of glass and phosphor, and different fluorescent layers on the luminescence properties of PiGF was systematically studied. It is of note that the “cyan cavity” is significantly reduced due to the addition of “cyan phosphor” (BaSi₂O₂N₂:Eu²⁺). Under 455 nm blue light laser excitation, PiGF has the highest luminous efficiency of 94.55 lm/W and a white light composite PiGF with a correlated color temperature of 5500 K and a color rendering index of 95 can be obtained. In short, this work shows that the PiGF has great potential application in white light laser lighting.     

Enhanced luminescence and energy transfer performance of double perovskite structure Gd2MgTiO6:Bi3+, Mn4+ phosphor for indoor plant growth LED lighting

Deep-red light emitting phosphors are widely used in LEDs for indoor plant growth because of the critical role played by red light in plant growth. The luminescence properties of deep-red phosphors are still not well understood at present. An energy transfer strategy is a common and effective method to improve luminescence properties. In principle, the energy transfer process may occur when the sensitizer's emission spectra overlap with the activator's excitation spectra. In this work, Bi³⁺ and Mn⁴⁺ were incorporated into the matrix of Gd₂MgTiO₆ as sensitisers and activators, respectively. Mn⁴⁺ ions tend to occupy the [TiO₆] octahedral site and the Bi³⁺ ions are expected to substituted in the site of Gd³⁺. The energy transfer process from Bi³⁺ to Mn⁴⁺ was realised and the photoluminescence (PL) intensity of Mn⁴⁺ increased with the doping content of Bi³⁺. Upon excitation at 375 nm, the PL intensity of Mn⁴⁺ increased to 116.4% when the doping concentration of Bi³⁺ reached 0.3%. Finally, the pc-LED devices were prepared by a Gd₂MgTiO₆:Bi³⁺, Mn⁴⁺ phosphor. The high red luminescence indicated that this phosphor has potential applications in indoor LED lighting.     

A far-red-emitting (Gd,Y)3(Ga,Al)5O12:Mn2+ ceramic phosphor with enhanced thermal stability for plant cultivation

As for plants, far-red (FR) light with wavelength from 700 nm to 740 nm is critical for processes of photosynthesis and photomorphogenesis. Light-controlled development depends on light to control cell differentiation, structural and functional changes, and finally converge into the formation of tissues and organs. Phosphor converted FR emission under LED excitation is a cost-effective and high-efficient way to provide artificial FR light source. With the aim to develop an efficient FR phosphor that can promote the plant growth, a series of gadolinium yttrium gallium garnet (GYGAG) transparent ceramic phosphors co-doped with Mn²⁺ and Si⁴⁺ have been fabricated via chemical co-precipitation method, followed sintered in O₂ and hot isostatic pressing in this work. Under UV excitation, the phosphor exhibited two bright and broadband red emission spectra due to Mn²⁺: ⁴T₁ → ⁶A₁ spin-forbidden transition, and one of which located in the right FR region. And then, Ce³⁺ ions were co-doped as the activator to enhance the absorption at blue light region and the emission of Mn²⁺. It turns out that the emission band of GYGAG transparent ceramic phosphors matches well with the absorption band of phytochrome P_FR, which means they are promising to be applied in plant cultivation light-emitting diodes (LEDs) for modulating plant growth. Besides, the thermal stability of this material was investigated systematically, and an energy transferring model involves defects was also proposed to explain the phenomenon of abnormal temperature quenching.     

Host sensitized photoluminescence in Sr2.9-3x/2LnxAlO4F: 0.1Eu3+ (Ln = Gd,Y) for innovative flexible lighting applications

Tetragonal structured Sr₃AlO₄F is highly strained as reported from its global instability index estimation. Moreover, our results of X-ray photoelectron spectroscopy (XPS) also ascertained that the structure of Sr₃AlO₄F is highly strained with oxygen vacancies. Herein, aliovalent substitutions of divalent Sr ions with trivalent Ln (Ln = Gd/Y) ions were carried out to improve the stability of Sr₃AlO₄F lattice, which subsequently enhanced the photoluminescence in a series of Sr_2.9-3x/2Ln_xAlO₄F: 0.1Eu³⁺ phosphors. All the phosphors showed intense red-orange emission (⁵D₀ → ⁷F_1,2) at excitation with UV and near-UV light. The critical concentrations of Gd³⁺ and Y³⁺ up to which the Eu³⁺ emission intensities increased linearly were observed to be x = 0.09 and x = 0.07, respectively. Nevertheless, further enhancement in the Eu³⁺ luminescence of the optimized phosphors was realized by subsequently annealing in low oxygen atmospheres. The enhancement in oxygen deficiency during the post-annealing in Ar or vacuum led the energy transfer (O^2--Eu³⁺) to a greater extent which afterward increased the Eu³⁺ luminescence. The optimized Sr_2.765Gd_0.09AlO₄F: 0.1Eu³⁺ and Sr_2.795Y_0.07AlO₄F: 0.1Eu³⁺ phosphors showed high red color purity (~99%), as well as CIE coordinates of (0.62, 0.38), indicated that these phosphors could be appropriate red-emitting components for making flexible optical films for many lighting devices. Therefore, flexible polydimethylsiloxane based films were also fabricated using optimized Sr_2.765Gd_0.09AlO₄F: 0.1Eu³⁺ phosphor. The electroluminescence of a flexible PDMS-phosphor composite film showed an intense and pure red color with good thermal stability suggesting its suitability in flexible lighting and display devices.     

Site-selective occupation and luminescence property investigation of Ca18Na3Y(PO4)14:Eu2+ phosphor for full-spectrum LED

Cyan-emitting phosphors have attracted widespread attention as an integral part to realize full-spectrum lighting. Understanding the site occupation of luminescence centers is of great importance to design and clarify the luminescent mechanism for new cyan-emitting phosphors. Here, we report a cyan-emitting phosphor Ca₁₈Na₃Y(PO₄)₁₄:Eu²⁺ synthesized by the high-temperature solid-state method. The crystal structure is characterized by X-ray diffraction and refined by the Rietveld method. The diffuse reflectance spectra, excitation/emission spectra, fluorescence decay curves, thermal stability, and related mechanism are systematically studied. The results show that Ca₁₈Na₃Y(PO₄)₁₄:Eu²⁺ crystallizes in a trigonal crystal system with space group R3c. Under excitation at 350 nm, a broadband cyan emission can be obtained at 500 nm with a half-width of about 120 nm, which is caused by Eu²⁺ occupying five different sites in host, namely, Na2O₁₂ (450 nm), (Ca3/Na1)O₈ (485 nm), Ca2O₈ (515 nm), Ca1O₇ (565 nm), and (Ca4/Y)O₆ (640 nm), respectively. Moreover, crystal structure, room and low temperature spectroscopy, and luminescence decay time are used to skillfully verify the site-selective occupation of Eu²⁺. Finally, a full-spectrum light-emitting diode (LED) lamp is fabricated with an improved color rendering index (∼90.3), CCT (∼5492 K), and CIE coordinates (0.332, 0.318). The results show that Ca₁₈Na₃Y(PO₄)₁₄:Eu²⁺ has the potential to act as a cyan emission phosphor for full-spectrum white LEDs.