Garnet Research Articles

Exploring of the suitability of garnets for immobilizing nuclear waste and radiation shielding

In this study, the structural, chemical composition and gamma and nuclear shielding properties of some garnets were investigated. The experimental studies were made on the mass attenuation coefficients (MAC), linear attenuation coefficients (LAC), mean free path (MFP), half-value layer (HVL), effective atomic numbers (Zeff) and the radiation protection efficiency (RPE) in the high energy region. The fast neutron removal cross sections (ΣR), exposure buildup factors (EBF) were theoretically determined. The neutron absorption equivalent dose was measured of the garnet by 241Am–Be fast neutron source. It may be concluded that P1.21 has better photon shielding than the other samples investigated. The equivalent dose rate absorbed by the P1.21 garnet sample was found to be 36.80 % μSv/h and the P1.21 sample shows promise as a neutron shielding option. Also, the detection of inclusion minerals were made by EPMA and SEM analysis. It is observed that P1.21 sample is pyrope, P1.3 sample is andradite and P1.6 sample is grossular series. Also, according to ICP-MS results, it is possible to say that the P1.21 sample, which contains high amount of uranium, thorium, Y and Zr and has a high radiation absorption capacity, is a potential garnet structure for nuclear waste immobilization. Garnet's crystal structure and chemical durability enable safe containment and long-term storage of radioactive elements, facilitating their secure disposal.

Structure, Optical Properties and Magnetocaloric Effects in Gd3Fe5O12 Garnet Synthesized by Solid State Method

In this work, gadolinium iron garnet (Gd3Fe5O12) was synthesized using the solid-state ceramic method. The structural analysis, confirmed through Rietveld refinement, indicated the formation of a single-phase garnet structure. Scanning electron microscopy studies revealed uniform grain size and homogeneity in the sintered material, while UV-vis absorption studies showed a peak at 300 nm, indicating strong ultraviolet interaction and an optical band gap of 3.64 eV, suggesting optoelectronic potential. The fluorescence emission spectrum shows a band at 435 nm, while the excitation spectrum exhibits bands at 275 and 360 nm. The magnetic measurements demonstrated Gd ion ordering at low temperatures, with a compensation temperature around 290 K. Arrott plots confirmed the second-order magnetic phase transition. Importantly, Gd3Fe5O12 exhibited both normal and inverse magnetocaloric effects, with a maximum magnetic entropy change of 1.05 J kg–1 K–1 at 230 K under 9 T magnetic field. These properties indicate Gd3Fe5O12 material as a promising candidate for magnetic refrigeration and optoelectronic applications.

Gd3Ga5O12: a wide bandgap semiconductor electrolyte for ceramic fuel cells, effective at temperatures below 500 °C

Searching for compatible electrolytes with Ni0.8Co0.15Al0.05LiO2 (NCAL) electrodes with high ionic conductivity at low operational temperatures (<550 °C) is essential for the research on ceramics fuel cells (CFCs). In this work, the experimental and theoretical analyses demonstrate that the highly stable single-phase Gd3Ga5O12 (GGO) garnet structure, composed of Gd-O octahedrons and Ga-O tetrahedrons, provides more active sites for ion transport, resulting in enhanced peak power density (PPD) and stable open circuit voltage (OCV) at low operational temperature. The unique internal garnet structure effectively reduces the interfacial impedance of the prepared fuel cell device, provides many active sites at triple-phase boundaries and increases the electrochemical stability. As a result, the constructed cell can deliver a superior peak power density of 770 mW/cm2 at 490 °C. In addition, X-ray photoelectron spectroscopy, electrochemical impedance spectroscopy and theoretical calculations further demonstrate electrolyte effectiveness of GGO, enabling stable OCV even at a low temperature of 370 °C under a H2/air environment. This work can help in improving the understanding of the underlying mechanisms of a single-layer fuel cell device, which is essential to further develop this potential energy technology even at a very low temperature of 370 °C.

Synthesis of nanosized phases with a garnet structure using supercritical СО2 fluid

A method was developed for the production of nanosized complex oxides and oxysulfides. The first stage uses supercritical СО2 fluid (SAS – supercritical antisolvent method). This approach makes it possible to obtain precursor-free complex oxides in a narrow nanoscale range. Nanosized rare-earth iron garnets with the general formula R3Fe5O12, where R is a rare earth element, were obtained and studied by physicochemical methods. The resulting samples have a size of less than 100 nm, exhibit ferromagnetic ordering, and can be used as soft magnetic materials. The multi-stage method for the preparation of complex oxysulfides was not previously demonstrated anywhere in the literature. The method involves three stages. At the first stage, a nanosized X-ray amorphous solid solution of the original salts is obtained using the SAS method. Then a nanosized X-ray amorphous component – the oxide phase – is obtained by annealing in a furnace. After this, the resulting oxide phase is mixed with the disulfide of a transition element (Nb, Mo), and high-temperature annealing is performed in an evacuated quartz ampoule. As a result, compact and nanosized phases of the composition Eu3Fe5-3/2xMox□1/2xO12-2xS2x and Eu3Fe5-3/2xNbx□1/2xO12-2xS2x, where x = 0.15, were obtained for the first time. The introduction of the sulfide component, namely NbS2, into the garnet structure increases its magnetic parameters by the factor of 1.5.

Realization of narrow-band blue emission based on structurally engineering-designed Bi3+-doped phosphors

The exploration of efficient narrowband emission phosphors is crucial for white light-emitting diodes (WLEDs) in high-performance backlighting applications. Up to now, the discovery of narrow-band Bi3+-doped phosphors for emerging applications remains challenging because Bi3+ typically exhibits broadband emission properties. A novel narrow-band blue phosphor (Ca4SnGe3O12:Bi3+) was successfully synthesized, benefiting from the highly symmetric crystal environment and tightly connected rigid structure of the garnet structure. The phosphor demonstrates broad excitation in the near-ultraviolet (n-UV) region and emits narrowband blue light at 442 nm (FWHM = 36 nm) with a color purity of 94.7 %. In this paper, the assignment of different luminescence centers and the use of Zr/Hf to partially replace Sn to enhance luminescence performance are studied. The reasons for the consequent changes in luminescence behavior are explained in detail. The use of narrowband commercial red K2SiF6:Mn4+, green β-Sialon:Eu2+, and synthetic blue luminescent materials as RGB emitters covered 81 % of the National Television System Committee (NTSC) color space, demonstrating great potential for liquid-crystal-display (LCD) backlight use.

High-Performance Tunable Near-Infrared Emitters of Cr3+-Activated Garnet Phosphor Enabled by Chemical Unit Co-Substitution.

The escalating demand for portable near-infrared (NIR) light sources has posed a formidable challenge to the development of NIR phosphors characterized by high efficiency and exceptional thermal stability. Taking inspiration from the chemical unit co-substitution strategy, high-performance tunable (Lu3- xCax)(Ga5- xGex)O12:6%Cr3+ (x = 0-3) phosphors are designed with an emission center from 704 to 780nm and a broadest full width at half maximum (FWHM) of up to 172nm by introducing Ca2+ and Ge4+ ions into the garnet structure. In particular, Lu3Ga5O12:6%Cr3+ demonstrates an anti-thermal quenching phenomenon (I423K = 113.1%). Compared to Lu3Ga5O12:6%Cr3+, Lu2CaGa4GeO12:6%Cr3+ exhibits significantly improved FWHM and IQE by 108nm and 25.5%, respectively, while maintaining good thermal stability (I423K = 80.4%). Finally, Lu2CaGa4GeO12:6%Cr3+ phosphor is combined with a 465nm blue LED chip to fabricate NIR LED devices, exhibiting a NIR electroluminescence efficiency of 13.31%@100mA and demonstrating successful applications in nocturnal illumination and biomedical imaging technology. This work offers a fresh perspective on the design of highly efficient NIR garnet phosphors.

Reactive sintering of coaxial Yb3+:YAG/YAG transparent ceramics

15 at.% Yb3+:YAG/YAG transparent composite ceramics with a coaxial geometry were synthesized by a ceramic forming method combined with the reactive sintering at 1800 °C. Densification peculiarities, microstructure, optical properties, and laser characteristics of composite ceramic samples were studied. Powder mixtures of Yb3+:YAG and YAG stoichiometric compositions demonstrate almost the same densification enabling uniform shrinkage of composite without differential sintering. It was shown that in-line optical transmittance of 15 at.% Yb3+:YAG/YAG composite ceramics reaches 80 % at 1030 nm wavelength. The effective diffusion coefficient of Yb3+ ions in garnet structure has been determined. Efficient laser emission was generated from Yb3+:YAG/YAG composite ceramics with a slope efficiency of ηsa = 0.30.

Wet-chemical synthesis and luminescence studies of nano-crystalline gadolinium gallium garnet

Abstract This paper reports the photoluminescence studies of pure polycrystalline nano-sized gadolinium gallium garnet (Gd3Ga5O12, GGG) powders synthesized by the method of co-precipitation using ammonium hydrogen carbonate (NH4HCO3, AHC) as the precipitant. The prepared samples were characterized by X-ray diffraction, scanning electron microscopy, Fourier transform infrared, ultraviolet, visible, near-infrared (UV–Vis–NIR) spectroscopy and photoluminescence studies. The X-ray diffraction analysis confirms the formation of cubic structure of gadolinium gallium garnet (Gd3Ga5O12). The average particle sizes are found to be in the range of approximately 19 nm–88 nm, for different calcining temperatures. The formation of gadolinium gallium garnet is also confirmed by Fourier transform infrared studies. Scanning electron microscopy image measurement confirms the formation of nanosized particles. The photoluminescence studies of the pure gadolinium gallium garnet sample shows emission peaks around at 441 nm for an excitation wavelength of 350 nm for the sample calcined at 1,100 °C.

The structural, mechanical and chemical stability properties of HEG and YIG in response to α-irradiation

Ceramic materials with excellent radiation resistance stability play an indispensable role in the treatment of nuclear waste. This article uses spark plasma sintering (SPS) to synthesize high-entropy (HE) Y0.6Gd0.6Sm0.6Eu0.6Dy0.6Fe5O12 (HEG) and traditional garnet Y1.2Nd1.8Fe5O12 (YIG). Studied the effects of 2 MeV He2+ irradiation (1 × 1014 ions/cm2 - 1 × 1017 ions/cm2) on the crystal structure, mechanical properties, and chemical stability of ceramics. Research shows that the surface of YIG becomes completely amorphous under ∼30dpa irradiation. Under irradiation at∼30dpa, HEG underwent a small amount of amorphization (with an amorphization rate of 38 %), maintaining the structure of garnet, and the lattice expansion rate of HEG caused by irradiation was lower than that of YIG. After irradiation, the mechanical properties of HEG were improved, while YIG's hardness decreased due to its amorphous state. Radiation has almost no effect on the chemical stability of HEG, and its long-term release mechanism is dominated by diffusion. This study identified HEG as an ideal candidate substrate for immobilizing high-radioactive waste (HLW) the perspective of radiation resistance.

Relationship between structure and microwave dielectric properties of new low-K garnet-type Ca3Cr2Ge3O12 ceramics

In order to solve the problem of signal delay, a novel low-K Ca3Cr2Ge3O12 ceramic for 5G and millimeter-wave communication was prepared by a solid-state reaction method. XRD and Rietveld refinement results confirm that it belongs to the garnet structure with the Ia-3d space group. The shrinkage rate of the sample sintered at 1350 °C reached 11.9 %, and the relative density exceeded 94.3 %. Excellent microwave dielectric properties were obtained. The permittivity was 8.38, the quality factor was 23,107 GHz, and the temperature coefficient of resonant frequency was −43.57 ppm/°C. The relationship between the crystal structure and microwave dielectric properties of ceramics was further studied. The results show that lattice vibration, stacking fraction and bond strength have a great influence on the Q × f value of ceramics, and the bond valence parameter is the key factor affecting the temperature stability. In addition, the theoretical quality factor of the ceramic can reach ∼13,0000 GHz by far-infrared reflection spectroscopy, and the ceramic has great research potential. The development of Ca3Cr2Ge3O12 ceramics and the study of microwave dielectric properties have filled the research gap of related systems. The excellent microwave dielectric properties indicate that it can be used as an alternative material for the preparation of components in the field of communication.

Crystal chemistry and ionic conductivity of garnet-type solid-state electrolyte, Li5-xLa3(NbTa)O12-y

Crystal structures, microtopography, morphologies, elemental compositions, and ionic conductivity have been investigated for Li5-xLa3(Nb,Ta)O12-y using X-ray diffraction (XRD), field-emission analytical scanning and transmission electron microscopies (S/TEM), and electrochemical impedance spectroscopy. Using Rietveld refinements with powder XRD patterns, we determined that the number of Li atoms in the formula is less than 5 and that Li5-xLa3(NbTa)O12-y crystallizes in the cubic garnet structure with a space group Ia-3d. Sintering at varying temperatures (750–1000 °C) for 5 h in an ambient atmosphere produced distinct outcomes. Rietveld refinements disclosed that the sample sintered at 1000 °C (Li3.43(2)La3Nb1.07(2)Ta0.93(2)O12-y, a = 12.8361(7) Å, V = 2114.96(3) Å3) exhibited the highest ionic conductivity, while the 850 °C sample had the lowest conductivity, characterized by lower Li concentration and impurity phases (Li(Nb,Ta)3O88, Li2CO3). Analyses, including XRD and electron microscopy, confirmed the 1000 °C sample as a relatively phase pure with enhanced Li content (Li/La = 1.2), larger grains (15 μm), and uniform crystallinity. The 1000 °C sample introduced additional partially filled Li3 (96h) sites, promoting Li migration, and enhancing ionic conductivity. The resulting XRD pattern at 1000 °C has been submitted to the Powder Diffraction File as a reference.

Efficiency of Cr3+ → Cr4+ conversion in YSAG:Cr ceramics

In this study, we investigated the influence of the position and quantitative content of scandium in YSAG:Cr on the efficiency of chromium cation valence conversion. YSAG:Cr ceramic powders were synthesized using the chemical precipitation method. It was determined that the microstructure of ceramics and the luminescent properties of YSAG:Cr4+ depend on the predominant position of scandium, whether it replaces octahedral or dodecahedral positions in the garnet crystal lattice. An increase in Scdod content contributed to a decrease in grain size and a shift of the emission peak of Cr4+ ions towards the short-wavelength region. Conversely, an increase in Scoct content led to an increase in grain size and a shift of the maximum of the luminescent band towards the long-wavelength region. It was found that increasing the quantitative content of scandium in the octahedral position in the garnet structure by up to 50 % enhances the efficiency of the conversion of Cr3+ to Cr4+, while an increase in the proportion of Scdod resulted in a decrease in conversion efficiency.

Polymer-salt synthesis and study on structure of vanadium-doped yttrium-aluminum garnet

Polymer-salt synthesis and study on structure of vanadium-doped yttrium-aluminum garnet

Ion-irradiation effect on swelling and microstructure of BN particle dispersed liquid phase sintering SiC

The boron nitride (BN) particle dispersed silicon carbide (SiC) materials were fabricated by liquid phase sintering (LPS) with Al2O3 and Y2O3 sintering additives as the reference matrix material for SiC composites. They were irradiated to 0.1/1/3/10 dpa by 5.1 MeV Si2+ ions at 800 °C. Raman spectra indicated that the pure h-BN structure was partially destroyed following irradiation, while yttrium aluminum garnet (YAG) structure at grain boundaries formed from the sintering additives wasn’t destroyed. TEM images and diffraction patterns indicated that the mechanism of microstructure evolution of SiC after irradiation up to high fluence at 800 °C was defect clusters induced by irradiation.

Microwave heterostructures in the form of submicron Y&lt;sub&gt;3&lt;/sub&gt;Fe&lt;sub&gt;5&lt;/sub&gt;O&lt;sub&gt;12&lt;/sub&gt; films on non-oriented ferroelectric ceramic substrates: synthesis, properties, and prospects for applications

In the work monolithic structures of yttrium iron garnet (YIG, Y3Fe5O12) with a thickness of about 2 μm were obtained on ferroelectric ceramic substrates based on PbZr0.45Ti0.55O3 (PZT) and Ba0.4Sr0.6TiO3 (BST). The Y3Fe5O12 layer was deposited by ion beam sputtering deposition on substrates 400 μm thick by sputtering a polycrystalline Y3Fe5O12 target with with argon ions. The heterostructures were crystallized by annealing in air at a temperature of 820 °C for 5 min. The results of the characteristic X-ray radiation method showed that the elemental composition of the monolithic heterostructure corresponds to the specified one. During X-ray studies, it was found that the YIG crystallization process is completed and the resulting structure is single-phase. The results of magnetic and ferromagnetic resonance studies indicate the possibility of using the obtained heterostructures in logic circuits based on spin waves with low scattering, in memory elements, as well as in electrically controlled microwave devices.

MODELING OF THE ELECTRONIC AND ELASTIC PROPERTIES OF THE Y&lt;sub&gt;3&lt;/sub&gt;Al&lt;sub&gt;5&lt;/sub&gt;O&lt;sub&gt;12&lt;/sub&gt; CRYSTAL

In this scientific work, we conducted a comprehensive study of yttrium aluminum garnet using computer modeling methods. Our efforts are focused on the precise analysis of elastic properties, the development of equations of state, as well as a detailed study of crystal and band structures. We conducted a detailed study of the mechanical parameters of the material, such as the modulus of elasticity and the Poisson's ratio, using modern computational methods. Virtual modeling methods allow us to study in detail the mechanical characteristics of the material. The main focus is on the creation and verification of computer models that accurately reflect the elastic properties of the crystal. The values obtained using various hybrid functionals were compared with experimental data. Virtual models allowed not only to study in detail the mechanical characteristics of the material, but also provided results that are significantly close to real experimental data. Comparisons were carried out according to the following parameters: cell parameters, band gap energy, effective charges of crystal atoms, equations of state and elastic properties. Also, the error levels relative to the experimental data are determined. We present the results of the analysis of the crystal structure of yttrium aluminum garnet achieved using various exchange-correlation hybrid functionals such as B3PW, B3LYP, HSE06, PBE. This aspect of the study includes the analysis of the crystal lattice parameters, the distribution of atoms in the crystal and the band structure, which is important for a complete understanding of the properties of the material.

Исследование качества молодых игристых вин из крымских автохтонных сортов винограда

Most domestic sparkling wines are made of traditional champagne grape varieties. However, indigenous Crimean cultivars could increase the output of high-quality original beverages if a proper technology was introduced. &#x0D; This research featured young sparkling wines from Crimean grape varieties, i.e., Soldaya, Shabash, Kokur Beliy, Sary Pandas, Kefesiya, Dzhevat Kara, and Ekim Kara. Organic acids, sugars, glycerin, phenolic substances, and ethanol were determined by high performance liquid chromatography; the content of amine nitrogen was measured by formalin titration. The optical profile of the wine samples was subjected to the colorimetric method while their foamy properties were studied by bubbling the samples in a measuring cylinder. The sparkling properties depended on the rate of CO2 desorption; the volumetric method made it possible to define the CO2 content; the viscosity was measured using a viscometer. The sensory assessment followed State Standard 32051-2013, ISO 5492:2008, and ISO 11035:1994. &#x0D; The samples of Kokur Beliy, Sary Pandas, and Soldaya received high tasting ratings (≥ 9.0 points), as did the red variety of Kefesiya (8.95 points). They demonstrated a clear typical aroma and a harmonious taste, as well as good foamy and sparkling properties. The maximal foam volume correlated with amine nitrogen (r = 0.762) while the sparkling properties correlated with the mass fraction of bound CO2 (r = 0.977). The red sparkling wine from the Kefesiya variety had a dark garnet color due to its high anthocyanins. It also contained quercetin and glycoside, which are known for their biological (P-vitamin) activity and powerful antioxidant properties. The early low-sugar (&lt; 18 g/100 cm3) varieties of Dzhevat Kara and Ekim Kara had the same acidity but demonstrated a less diverse phenolic profile and were paler in color. &#x0D; In this research, the indigenous Crimean grape cultivars of Kokur Beliy, Sary Pandas, Soldaya, and Kefesia showed good prospects for young sparkling wines. Other varieties needed special technologies to preserve their typical properties and the aroma/taste balance. The new technology makes it possible to obtain unique high-quality products right in the harvest year, thus increasing the range and volume of sparkling wine production.

Effects of cerium oxide and cerium sulfate on the optical behavior of synthesized garnet glass ceramics

In this study, the YAG silicate glasses containing the cerium sulfate and cerium oxide salts (17YO3-33Al2O3-40SiO2-2AlF3-3NaF-2CeO2-3B2O3), separately were produced by melting method and glass ceramics were produced by heat treatment of base glasses. According to Photo Luminescence spectrums of both glasses there were emissions in the range of 466 and 435 nm wavelengths related to cerium ions. It was shown that by heating treatment, garnet crystal (in sulfated sample) formed less than the sample with cerium oxide. The emission spectra of both glass-ceramics, when excited at 240 nm, fall within the wavelength range of 460 nm. Also, the 534 and 660 nm emissions wavelengths were obtained by 340 nm wavelength excitation. Heat treatments were done by oxide atmosphere in tubular furnace (single step), SPS sintered powder and in hydrogen atmosphere (by two steps heating). According to XRD results the 24 hrs. heat treating time and the 1060 °C temperature affect the entry of cerium into the garnet structure. Finally, by comparing the spectroscopic results the optical response of the garnet glass-ceramic synthesized in the hydrogen atmosphere was obtained at 400 nm wavelength that indicated this garnet can be applied in the LED industry.

Synthesis of cerium-doped gadolinium gallium aluminum garnet (GGAG:Ce) scintillating powder via solvothermal method

The powder material Gd3Ga3Al2O12:Ce (GGAG doped with Cerium) has garnered significant attention in radiation detection due to its high light yield and rapid decay time. Despite its potential, the synthesis of high-quality and reproducible GGAG:Ce scintillating powder remains a considerable challenge. In this study, we present a solvothermal approach with an annealing temperature of 1300 °C for producing cerium-doped GGAG powder with varying concentrations (4, 2, and 0.5 mol%). The structural and luminescent characteristics were meticulously examined using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), photoluminescence (PL), radioluminescence (RL) spectroscopy, and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed the single-cubic phase garnet structure of the synthesized powder. By comparing the intermediate solvothermal products synthesized at different sintering temperatures (900 °C for 3 h and 1300 °C for 1 and 3 h), a direct correlation between solvothermal conditions and the structure/property relationships of the product was established. FESEM images revealed an ellipsoidal to irregular morphology of the as-synthesized GGAG:Ce microparticles, ranging from 0.1 to 0.3 μm, regardless of the Ce concentration. PL spectra demonstrated a strong emission peak at approximately 550 nm, characteristic of Ce3+ ions. RL data confirmed the peak luminescence at around 550 nm, with an almost twofold increase in intensity as the concentration of Ce3+ increased from 0.5 mol% to 4 mol%. XPS data disclosed the Ce3+/Ce4+ ratio in solvothermally synthesized GGAG:Ce, wherein Ce loading of 4 mol% demonstrated the increase in Ce3+ concentration to 95%, whereas the concentration of Ce4+ decreased to 5%. Notably, the highest luminescence efficiency was achieved with GGAG:Ce at a 4 mol% concentration. Thus, the solvothermal method employed in GGAG:Ce synthesis presents a straightforward approach, yielding rapid results with precise control over particle morphology and size.

Ce3+-Activated SrLu2Al3ScSiO12 Cyan-Green-Emitting Garnet-Structured Inorganic Phosphor Materials toward Application in Blue-Chip-Based Phosphor-Converted Solid-State White Lighting.

Phosphor-converted white-light-emitting diodes (WLEDs) with superhigh color rendering index (CRI) are the ongoing pursuit of next-generation solid-state lighting. One of the most important challenges is the limited improvement in CRI on account of the absence of a cyan component in the typical commercial combination. Here, a bright broad-band cyan-green-emitting phosphor with cubic garnet structure, SrLu2Al3ScSiO12:Ce3+ (SLASSO:Ce3+), was successfully reported, which can compensate for the absence of cyan cavity in the 480-520 nm blue-green emission region. With 439 nm blue-light irradiation, the as-fabricated SLASSO:Ce3+ phosphor yields a broad-band cyan-green emission with the maximum emission peak positioned at 525 nm and an appropriate full width at half-maximum (fwhm) of 111 nm, capable of providing more cyan emission component without sacrificing green emission. Meanwhile, the optimal SLASSO:2%Ce3+ phosphor features CIE color coordinates of (0.3254, 0.5470) with cyan-green hue, along with a high internal quantum efficiency of up to 93%. Additionally, thermal stability measurements at different temperatures reveal that the luminescence emission intensity of the proposed phosphor retains 44% of its original integral emission intensity at 423 K with respect to room temperature, while also demonstrating an excellent color stability (ΔE = 5.4 × 10-3). This work shows that the highly efficient SLASSO:Ce3+ garnet phosphor can be utilized as a potential cyan-green-emitting phosphor for filling the cyan gap, resulting in the construction of a high-quality warm WLED with high CRI for "human-centric" sunlight-like full-spectrum solid-state illumination.