Influence of UV irradiation on the luminescence properties of CsPbBr3 perovskite quantum dots and CsPbBr3 perovskite quantum dots/PVDF composite film - for white LED application.

Perovskite quantum dots (QDs) have been widely investigated for their excellent properties such as high color purity in displays, tunable emission wavelength, and high photoluminescence quantum yield. For device applications, improving the stability is an area of interest. In this study, the effects of UV irradiation on the structural and luminescence properties of CsPbBr3 perovskite quantum dots (CPB QDs) excited at 365 nm were investigated. To overcome the effects of UV irradiation, a CPB QDs/PVDF composite flexible film was prepared. It exhibits high structural and optical stability under UV irradiation and emits a highly intense green color. The emission wavelength and intensity were observed for three years, and the stability of the temperature-dependent emission intensity up to 400 K has been reported. In addition, it is stable in water. A white LED, fabricated by integrating a blue LED with CPB QDs/PVDF composite film and red phosphor, produces bright natural white light [(CIE x, CIE y) = (0.3704, 0.3611), and CCT = 4177 K] with a color gamut area coverage of 86.4% of the standard NTSC (1953) color space. .

Fluorescence Carbon Dots from Blood-Berries for Sensing Cr6+ Ions in Water and Application in White Light Emitting Diode.

Conventional techniques for identifying heavy metal ions in water are laborious and time-consuming. Therefore, it is necessary to create innovative sensing technologies that can detect with greater sensitivity and speed. Although there have been reports of optical-based assays utilising fluorescent nanomaterials, these assays usually rely on variations in signal strength. However, this approach has significant drawbacks when it comes to environmental monitoring. Fluorescence carbon dots (CDs) have been prepared by facile synthesis from Blood berries. A homemade heavy metal optical detector is constructed to accurately identify heavy metal ions, exclusively Cr6+ ions in a water medium. Their optical emission signature varies based on the specific chromium ions in solution, and the emission intensity also changes depending on its concentration. The quenching behaviour is attributed to the interaction between the metallic cations and the fluorescent surface states of the carbon dots. Another application is the encapsulation of CDs in PVDF polymer to form a flexible film and use it as a phosphor for LED conversion.

Modulation and Enhancement of Red Luminescence in Ca2GdSbO6: Eu3+ Phosphor by Co-Doping with Bi3.

The double perovskite structure of Ca2GdSbO6 as a fluorescent phosphor matrix material possesses a stable structure, making it an excellent candidate for a matrix material. In this study, single-doped Ca2GdSbO6: Eu3+ fluorescent phosphors and Bi3+ sensitized Ca2GdSbO6: Eu3+, Bi3+ fluorescent phosphor materials were synthesized using the high-temperature solid-state method. The luminescence of this phosphor is based on the 5D0→4F2 transition emission of Eu3+ ions, which occurs at 612 nm. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL) spectra, high-temperature fluorescence spectra, and fluorescence decay lifetimes to study the phase structure, optical properties, crystal structure, and chemical purity of the samples. The performance of the single-doped phosphor was significantly improved by the addition of Bi3+ sensitizer. The luminescence intensity increased by nearly 100% compared to Ca2GdSbO6: Eu3+ phosphor, with a quantum efficiency increase of 124%. The thermal quenching activation energy was found to be 0.299 eV, and the luminescence intensity remained at 70.3% of room temperature at 453 K. These results indicate that the co-doping of Bi3+ has a modulation and enhancement effect on the luminescence of Ca2GdSbO6: Eu3+ red phosphor, showing great potential for application in near-ultraviolet-excited white LED devices.

Recent Advances in Preparing Transparent Phosphor Ceramics for High-Index Color Rendering and High-Power Lighting.

In recent years, high-power white light-emitting diode (wLED)/laser diode (wLD) lighting sources based on transparent phosphor ceramic (TPC) materials have attracted increasing application interest in automotive headlights, projection displays, and space navigation lighting due to their superior brightness, lighting distance, compactness, lifespan, and environmental resistance compared with the widely used phosphor-converted wLEDs. However, preparing TPC-converted wLEDs/wLDs with high color rendering index (CRI) remains a huge challenge, which limits their widespread application. In this review, we summarize the recently adopted strategies for constructing TPCs to develop high-power wLEDs/wLDs with high CRI values (>75). The construction protocols were categorized into four groups: host regulation, red-emitter doping, host regulation/red-emitter doping combination, and composite structure design. A comprehensive discussion was conducted on the design principles, photoluminescent properties, and device performances for each strategy. The challenges and future trends of high-power and high-CRI wLEDs/wLDs based on TPCs are also discussed toward the end of this review.

Model and Methodology to Characterize Phosphor-Based White LED Visible Light Communication Links.

LED lighting has become the standard solution for illumination purposes thanks to its energy efficiency. Nowadays, there is growing interest in the use of LEDs for data transmission to develop future-generation communication systems. The low cost and widespread deployment of phosphor-based white LEDs make them the best candidate for visible light communications (VLC), although they have a limited modulation bandwidth. This paper presents a simulation model of a VLC link based on phosphor-based white LEDs and a method to characterize the VLC setup used to perform the data transmission experiments. Specifically, the simulation model incorporates the frequency response of the LED, the noise levels coming from the lighting source and the acquisition electronics, and the attenuation due to both the propagation channel and the angular misalignment between the lighting source and the photoreceiver. In order to validate the suitability of the model for VLC, carrierless amplitude phase (CAP) and orthogonal frequency division multiplexing (OFDM) modulation signals were employed for data transmission, and simulations with the proposed model and measurements over the equivalent scenario show high agreement.

White LED active α-Fe2O3/rGO photocatalytic nanocomposite for an effective degradation of tetracycline and ibuprofen molecules.

The formation of phase pure magnetically separable α-Fe2O3 and α-Fe2O3/rGO nanostructures were achieved through a simple hydrothermal technique. The properties of synthesized materials were investigated through different analytical techniques. The formation of phase pure FO and FO/rGO nanostructures were confirmed by XRD analysis with crystallite size of about ∼42 nm and ∼65 nm, respectively. The morphological analysis reveals the formation of sphere-like nanoparticles with high agglomeration. The UV-DRS analysis clearly shows the enhanced visible-light activity of FO/rGO nanoparticles. The BET analysis revealed the mesoporous property of FO/rGO nanocomposite. The enhancement in the photoinduced charge transfer process is observed after including rGO nanoparticles with FO. The photocatalytic efficiency of nanomaterials was analyzed using tetracycline and ibuprofen as model organic pollutants under white LED irradiation. The enhanced photocatalytic degradation ability of FO/rGO nanocomposite is studied against both tetracycline and ibuprofen molecules.

Luminescence properties of MgCaAl10 O17 :RE3+ (RE3+ = Sm3+ ,Dy3+ ) phosphor for eco-friendly solid-state lighting applications.

Different concentrations of rare earth Sm3+ - and Dy3+ -activated MgCaAl10 O17 phosphors were synthesized using the combustion route and their detailed luminescence investigations are reported in this paper. The photoluminescence excitation spectra of Sm3+ - and Dy3+ -activated MgCaAl10 O17 phosphor show multiple peaks in the ultraviolet light region of the electromagnetic spectrum. The characteristic emission spectra of the MgCaAl10 O17 :Sm3+ phosphor are located at 563 nm, 594 nm, and 644 nm, with the maximum emission intensity occurring at 594 nm. The emission spectra of the MgCaAl10 O17 :Dy3+ phosphor show two emission peaks, one at 476 nm wavelength in the blue light region and the other at 573 nm wavelength in the yellow region. The above results suggest that the prepared phosphor can be suitable for applications in eco-friendly solid-state lighting.

Enhanced photoluminescence in RE (Eu3+ , Ce3+ and Sm3+ )-activated Ca10 (PO4 )F2 phosphors by double or triple ionized mineral doping: a comparative study.

In this work, RE3+ (Eu, Ce and Sm)-activated Ca10 (PO4 )6 F2 (fluorapatite) phosphors were synthesized by doping with different apatite minerals (SO4 , VO4, WO4 ) using a solid-state diffusion method. Optical and structural characterizations were performed using X-ray diffraction (XRD), Fourier transform infrared spectroscopy, and photoluminescence (PL) spectroscopy. XRD characterization showed the crystalline nature of the phosphor. PL properties were investigated under ultraviolet light excitation for all three rare earths. CIE chromaticity revealed the colour emitted in the visible region. Luminescence intensity was enhanced considerably by tuning the host matrices after core-shell formation by substitution with other ions producing promising candidates for white light-emitting diode materials.

Automated diabetic retinopathy detection with two different retinal imaging devices using artificial intelligence: a comparison study.

PURPOSE: In this study, we evaluated the diagnostic performance of an automated artificial intelligence-based diabetic retinopathy (DR) algorithm with two retinal imaging systems using two different technologies: a conventional flash fundus camera and a white LED confocal scanner. METHODS: On the same day, patients underwent dilated colour fundus photography using both a conventional flash fundus camera (TRC-NW8, Topcon Corporation, Tokyo, Japan) and a fully automated white LED confocal scanner (Eidon, Centervue, Padova, Italy). All images were analysed for DR severity both by retina specialists and the AI software EyeArt (Eyenuk Inc., Los Angeles, CA) and graded as referable DR (RDR) or not RDR. Sensitivity, specificity and the area under the curve (AUC) were computed. RESULTS: A series of 165 diabetic subjects (330 eyes) were enrolled. The automated algorithm achieved 90.8% sensitivity with 75.3% specificity on images acquired with the conventional fundus camera and 94.1% sensitivity with 86.8% specificity on images obtained from the white LED confocal scanner. The difference between AUC was 0.0737 (p = 0.0023). CONCLUSION: The automated image analysis software is well suited to work with different imaging technologies. It achieved a better diagnostic performance when the white LED confocal scanner is used. Further evaluation in the context of screening campaigns is needed.

A Novel Surface Recovery Algorithm for Dual Wavelength White LED in Vertical Scanning Interferometry (VSI).

The two peaks characteristic of yellow and blue light in the spectrum of dual-wavelength white light emitting diodes (LEDs) introduce distinctive features to the interference signal of white light scanning interferometry (WLSI). The distinctive features are defined as discontinuities, so that the fringe contrast function cannot be modeled as a single Gaussian function, and causes the interferogram to have uneven distribution of fringes of different orders in the scanning interferometer. This phenomenon leads to the low accuracy of the zero-order fringe position in the envelope calculation, which affects the repeatability and accuracy of the interferometry. This paper proposes a new surface recovery algorithm based on the Hilbert phase envelope and adjacent reference points calculation, which can effectively overcome the influence of the discontinuous signal of dual-wavelength LED white light interference on the three-dimensional reconstruction of WLSI measurements. The reliability of the algorithm is verified by experiments, and the measurement accuracy of LED WLSI system is evaluated.

An untargeted metabolomic approach reveals significant postharvest alterations in vitamin metabolism in response to LED irradiation in pak-choi (Brassica campestris L. ssp. chinensis (L.) Makino var. communis Tsen et Lee).

The main objective of this study was to investigate the effect of low-level light emitting diode (LED) irradiation on the metabolite profile of pak-choi. A total of 633 different molecular features (MFs) were identified among sample groups (initial, dark-treated, light-treated) using an untargeted metabolomic approach. The identified metabolites were associated with 24 different metabolic pathways. Four of the pathways including carbon pool by folate, folate biosynthesis, thiamine metabolism, and glutathione metabolism, all of which are associated with vitamin biosynthesis, changed significantly. Metabolites in four of the pathways exhibited significant differences from the control in response to LED irradiation. Additionally, porphyrin and chlorophyll metabolism, as well as glucosinolate biosynthesis, riboflavin metabolism, and carotenoid biosynthesis were positively induced by LED irradiation. These results indicate that postharvest LED illumination represents a potential tool for modifying the metabolic profile of pak-choi to maintain quality and nutritional levels.

Synthesis and Applications of Red-Emissive Carbon Dots.

Carbon dots (CDs), a new class of fluorescent carbon nanoparticles (less than 10 nm in size), have been widely applied in various fields, including sensors, bioimaging, catalysis, light-emitting devices (LEDs), and photoelectronic devices, owing to their unique properties such as low toxicity, bio-compatibility, high photostability, easy surface modification, and up-conversion fluorescence, over the past decades. Recently, multiple-color-emissive CDs, especially red-emissive CDs (RCDs), have drawn much attention owing to their unique advantages, like the ability to penetrate the animal bodies without the disturbance of strong tissue autofluorescence, multiple-color fluorescence displaying or sensing, and the capacity to be one essential component to obtain white LED (WLED). In this review, we focused on the progress of recently-emerging RCDs in the past five years, including their synthetic methods (hydrothermal, solvothermal, reflux condensation and microwave techniques), influencing factors (precursors, solvents, elements doping, surface chemistry) and various applications (bioimaging, sensor, photocatalysis and WLEDs), with a perspective on the future advancements.

Near White Light Emission and Concentration Quenching of Calcium Titanate Doped with Dysprosium (III) Phosphors.

This paper reports the preparation of CaTiO3 doped with various concentrations of Dysprosium (II) using solid state reaction technique. X-ray diffraction patterns of the sample were taken. Observed XRD pattern was matched using software match2!. The pattern was matched significantly with the crystallographic open database card (COD - 96-101-1212) which is a standard card for CaTiO3. This matching exhibited that, the prepared sample is cubic in structure with space group P m - 3 m (221). Photoluminescence (PL) studies of the samples were also done. PL intensity was found increasing with increasing dopant concentration and maximum intensity was noted at 2.0 mol% concentration of Dy3+, thereafter concentration quenching occurred. Emission Peaks were centered at 483 nm (4F9/2➔6H15/2) and 576 nm (4F9/2➔6H13/2) respectively. For studying the concentration quenching, the critical distance for energy transfer and electric multipolar character were estimated. The value of multipolar character expressed that, the transition in emission spectra is a dipole - dipole (d-d) transition. Commission Internationale de l'Éclairage (CIE) coordinates was found as (0.36, 0.39), which is near to white light. Colour Correlated Temperature (CCT) was 4489 K which was indicative of cool appearance of the light emitted.

A comparison between a white LED confocal imaging system and a conventional flash fundus camera using chromaticity analysis.

BACKGROUND: Conventional flash fundus cameras capture color images that are oversaturated in the red channel and washed out in the green and blue channels, resulting in a retinal picture that often looks flat and reddish. A white LED confocal device was recently introduced to provide a high-quality retinal image with enhanced color fidelity. In this study, we aimed to evaluate the color rendering properties of the white LED confocal system and compare them to those of a conventional flash fundus camera through chromaticity analysis. METHODS: A white LED confocal device (Eidon, Centervue, Padova, Italy) and a traditional flash fundus camera (TRC-NW8, Topcon Corporation, Tokyo, Japan) were used to capture fundus images. Color images were evaluated with respect to chromaticity. Analysis was performed according to the image color signature. The color signature of an image was defined as the distribution of its pixels in the rgb chromaticity space. The descriptors used for the analysis are the average and variability of the barycenter positions, the average of the variability and the number of unique colors (NUC) of all signatures. RESULTS: Two hundred thirty-three color photographs were acquired with each retinal camera. The images acquired by the confocal white LED device demonstrated an average barycenter position (rgb = [0.448, 0.328, 0.224]) closer to the center of the chromaticity space, while the conventional fundus camera provides images with a clear shift toward red at the expense of the blue and green channels (rgb = [0.574, 0.278, 0.148] (p < 0.001). The variability of the barycenter positions was higher in the white LED confocal system than in the conventional fundus camera. The average variability of the distributions was higher (0.003 ± 0.007, p < 0.001) in the Eidon images compared to the Topcon camera, indicating a greater richness of color. The NUC percentage was higher for the white LED confocal device than for the conventional flash fundus camera (0.071% versus 0.025%, p < 0.001). CONCLUSIONS: Eidon provides more-balanced color images, with a wider richness of color content, compared to a conventional flash fundus camera. The overall higher chromaticity of Eidon may provide benefits in terms of discriminative power and diagnostic accuracy.

Luminescent properties of single-phase Ba2-x-1.5y-1.5z P2 O7 :xEu2+ ,yCe3+ , zTb3+ phosphors for white light-emitting diode.

A series of Ba2 P2 O7 :xEu2+ ,yCe3+ ,zTb3+ phosphors was synthesized via a co-precipitation method, then their crystal structure, quantum efficiency and luminescent properties were analyzed by XRD and FL, respectively. The results showed that these phosphors not only presented the excitation characteristics of Ba2 P2 O7 :xEu2+ ,zTb3+ , but also exhibited that of the Ba2 P2 O7 :yCe3+ ,zTb3+ phosphor. Meanwhile, the tri-doped phosphor showed a stronger absorption around 320 nm in contrast with the Eu2+ /Ce3+ :Tb3+ co-doped phosphor. Not only can energy transfer from Ce3+ →Eu2+ be observed; the energy transfer mechanism from Eu2+ to Tb3+ is discussed in the tri-doped system. Ce3+ affects the luminescence properties of Ba2 P2 O7 :xEu2+ ,yCe3+ ,zTb3+ phosphors just as the sensitizer whereas Eu2+ is considered both as the sensitizer and the activator. The chromaticity coordinates of tri-doped phosphors excited at 320 nm stayed steadily in the bluish-white light region,and the emitted color and color temperature (CCT) of these phosphors could be tuned by adjusting the relative contents of Eu2+ , Ce3+ and Tb3+ . Hence, the single phase Ba2 P2 O7 :xEu2+ ,yCe3+ ,zTb3+ phosphors may be considered as potential candidates for white light-emitting diodes.

Colour differences in Caucasian and Oriental women's faces illuminated by white light-emitting diode sources.

OBJECTIVE: To provide an approach to facial contrast, analysing CIELAB colour differences (ΔEab,10∗) and its components in women's faces from two different ethnic groups, illuminated by modern white light-emitting diodes (LEDs) or traditional illuminants recommended by the International Commission on Illumination (CIE). METHODS: We performed spectrophotometric measurements of spectral reflectance factors on forehead and cheek of 87 young healthy women (50 Caucasians and 37 Orientals), plus five commercial red lipsticks. We considered a set of 10 white LED illuminants, representative of technologies currently available on the market, plus eight main illuminants currently recommended by the CIE, representative of conventional incandescent, daylight and fluorescent light sources. Under each of these 18 illuminants, we analysed the magnitude and components of ΔEab,10∗ between Caucasian and Oriental women (considering cheek and forehead), as well as for cheek-forehead and cheek-lipsticks in Caucasian and Oriental women. Colour-inconstancy indices for cheek, forehead and lipsticks were computed, assuming D65 and A as reference illuminants. RESULTS: ΔEab,10∗ between forehead and cheek were quantitatively and qualitatively different in Orientals and Caucasians, but discrepancies with respect to average values for 18 illuminants were small (1.5% and 5.0% for Orientals and Caucasians, respectively). ΔEab,10∗ between Caucasians and Orientals were also quantitatively and qualitatively different both for forehead and cheek, and discrepancies with respect to average values were again small (1.0% and 3.9% for forehead and cheek, respectively). ΔEab,10∗ between lipsticks and cheek were at least two times higher than those between forehead and cheek. Regarding ΔEab,10∗ between lipsticks and cheeks, discrepancies with respect to average values were in the range 1.5-12.3%, although higher values of up to 54.2% were found for a white RGB LED. This white RGB LED provided the highest average colour-inconstancy indices: 17.1 and 11.5 CIELAB units, under reference illuminants D65 and A, respectively. CONCLUSION: Colour contrasts in women's faces under CIE standard illuminants for outdoor and indoor conditions may be strongly altered using specific white LEDs. More research needs to be performed on the impact of spectral power distribution of light sources with high colour rendering indices on visual colour appearance of cosmetic products.

Energy transfer rate and electron-phonon coupling properties in Eu3+ -doped nanophosphors.

A series of controllable emissions SrWO4 :Eu3+ and charge-compensated SrWO4 : Eum3+ (m = 0.01 or 0.20) phosphors was successfully prepared via a simple co-precipitation method. The energy transfer mechanism was studied based on the Huang's theory. A low magnitude of Huang-Rhys factor (10-2 ) was calculated using phonon sideband spectra. The Judd-Ofelt parameters Ωλ (λ = 2, 4 and 6) of Eu3+ -activated SrWO4 doped with charge compensation were obtained. The calculated Commission Internationale de l'Eclairage chromaticity coordinates were found to be about (0.67, 0.33) for SrWO4 : Eu0.203+ and charge-compensated SrWO4 : Eu0.203+ phosphors, which coincided with the National Television Standard Committee system standard values for red. A white light emission was obtained under 362 nm excitation. The correlated color temperature was computed by a simple equation to characterize light sources. Thus, warm white light-emitting diodes with higher Ra can be constructed by combining as-prepared high efficiency, low correlated color temperature and high color purity phosphor.

Sol-gel synthesis and luminescence property of Sr4 Al2 O7 :Re3+ ,R+ (Re = Eu and Dy; R = Li, Na and K) phosphors for white LEDs.

Sr4 Al2 O7 :Eu3+ and Sr4 Al2 O7 :Dy3+ phosphors with alkali metal substitution were prepared using a sol-gel method. The effects of a charge compensator R on the structure and luminescence of Sr4 Al2 O7 :Re3+ ,R+ (Re = Eu and Dy; R = Li, Na and K) phosphors were investigated in detail. Upon heating to 1400°C, the structure of the prepared samples was that of the standard phase of Sr4 Al2 O7 . Under ultraviolet excitation, all Sr4 Al2 O7 :Eu3+ ,R+ samples exhibited several narrow emission peaks ranging from 550 to 700 nm due to the 4f â†’ 4f transition of Eu3+ ions. All Sr4 Al2 O7 :Dy3+ ,R+ phosphors showed two emission peaks at 492 and 582 nm, due to the 4 F9/2  â†’ 6 H15/2 and 4 F9/2  â†’ 6 H13/2 transitions of Dy3+ ions, respectively. The luminescence intensity of Sr4 Al2 O7 :Re3+ ,R+ (Re = Eu and Dy; R = Li, Na and K) phosphors improved markedly upon the addition of charge compensators, promoting their application in white light-emitting diodes with a near-ultraviolet chip.

Direct Evidence of the Effect of Water Molecules Position in the Spectroscopy, Dynamics, and Lighting Performance of an Eco-Friendly Mn-Based Organic-Inorganic Metal Halide Material for High-Performance LEDs and Solvent Vapor Sensing.

Luminescent Mn(II)-based organic-inorganic hybrid halides have drawn attention as potential materials for sensing and photonics applications. Here, the synthesis and characterization of methylammonium (MA) manganese bromide ((MA)nBrxMn(H2O)2, (n = 1, 4 and x = 3, 6)) with different stoichiometries of the organic cation and inorganic counterpart, are reported. While the Mn2+ centers have an octahedral conformation, the two coordinating water molecules are found either in cis (1) or in trans (2) positions. The photophysical behavior of 1 reflects the luminescence of Mn2+ in an octahedral environment. Although Mn2+ in 2 also has octahedral coordination, at room temperature dual emission bands at ≈530 and ≈660 nm are observed, explained in terms of emission from Mn2+ in tetragonally compressed octahedra and self-trapped excitons (STEs), respectively. Above the room temperature, 2 shows quasi-tetrahedral behavior with intense green emission, while at temperatures below 140 K, another STE band emerges at 570 nm. Time-resolved experiments (77-360 K) provide a clear picture of the excited dynamics. 2 shows rising components due to STEs formation equilibrated at room temperature with their precursors. Finally, the potential of these materials for the fabrication of color-tunable down-converted light-emitting diode (LED) and for detecting polar solvent vapors is shown.

Reconstructing the Surface of K2SiF6:Mn4+ Phosphors toward Enhanced Moisture Resistance for White LED Applications.

The K2SiF6:Mn4+ (KSFM) phosphor featuring efficient ultranarrow red emissions is an outstanding candidate for white light-emitting diode (WLED) applications. However, poor moisture resistance seriously affects its application performance. In this study, a two-step surface reconstruction strategy is proposed to dramatically enhance the moisture resistance of commercially available KSFM phosphors, involving treatment with H2NbF7 and subsequent hydrothermal treatment. The modified KSFM phosphor exhibits a high internal quantum efficiency (IQE) of 98.9% after the two-step surface treatment. Meanwhile, nearly 100% of the initial emission intensity is retained for the modified KSFM phosphor even after aging in high temperature (85 °C) and high relative humidity (85% RH) environments for 6 days, in sharp contrast to only 18.6% retention for the original KSFM phosphor. The relative emission intensity of the modified KSFM remains at 98.9% even after being immersed in water for 6 h. Additionally, the phosphor-converted LED fabricated with the modified KSFM phosphor demonstrated excellent long-term stability, retaining up to 97.9% of initial luminous efficacy after aging under 85 °C and 85% RH conditions for 500 h. The moisture-resistance mechanism is elucidated on the basis of spectroscopic analysis as well as structural and compositional characterization of the phosphor surface layer, which can be attributed to the formation of a robust Mn4+-rare shell with high crystalline quality following this two-step surface treatment. The findings contribute to the performance improvements of KSFM phosphors for industrial applications.