Color Coordinates Research Articles

A Preliminary Study on the Modifying Effect of Strawberry Seed Oil and Sex on Rabbit Meat Quality

The aim of this research was to determine the effect of strawberry seed oil addition to rabbit feed on slaughter performance traits, meat quality traits and plasma cholesterol and triglycerides of purebred Termond White rabbits (n = 24). The experiment used young rabbits born to 6 does. From each litter, two rabbits were randomly assigned into one of the two groups. In each group (2 × n = 12; 6♂, 6♀), the animals were fed a complete pelleted feed. Rabbits from the experimental group received feed enriched with a 1% addition of strawberry seed oil. Animals were slaughtered on day 84. Rabbits fed with pellets with the addition of strawberry oil were characterized by a higher hind part and head and liver weight compared to the rabbits from the control group (p ≤ 0.05). The addition of strawberry seed oil significantly increased the pH of matured meat and affected the colour coordinates of the meat by increasing their values (p ≤ 0.05). The tested oil reduced the values of meat texture parameters such as springiness, cohesiveness and chewiness (p ≤ 0.05). The tested oil impacted the level of HDL, which was higher in the experimental group, as well as lowered the triglyceride level. The addition of strawberry seed oil was proven to significantly increase the linoleic acid content in rabbit meat (p ≤ 0.05).

Standardization of color measurement in the medical photography in clinical practice

BACKGROUND: For many medical specialties, photography is a routine element of work. Environmental factors equally and significantly influence the interpretation of colour light perception and the quality of photographic recording. Standardization of conditions in medical photography is necessary for subsequent quantitative assessment of the postoperative skin scar by analysing colour coordinates in the RGB system. AIM: To determine the impact of illumination and shooting distance at colour coordinates when studying unaltered skin. METHODS: Five volunteers without any skin diseases and no make-up on their facial skin were taken in the study. Skin type by the Fitzpatrick scale was II–III. Digital photography was made with a mobile device camera at distance 30 cm from the subject. For each participant, a series of digital photographs was taken at a distance of 20, 30, 40, 50, 60, 70 cm from the light source. Colour coordinates in the RGB system were measured in the digital graphics editor Adobe Photoshop CS6. Statistical analysis of the obtained data was carried out using Microsoft Office Excel 2019, Phyton 3.11. RESULTS: The analysis of variance by the ANOVA method was used as a statistical analysis. In order to determine a statistically significant difference between the sets, Tukey HSD test was performed. A total of 1764 coordinates of three colours were subjected to statistical analysis (R=588, G=588, B=588). When constructing a heat map of the cross-correlation of the absolute values of each colour at each distance, taking into account the type of light source among themselves, the data had a strong direct correlation, regardless of the study area. When constructing a linear graph, coordinates of any of the zones were located on the same straight line. CONCLUSION: Photography conditions were experimentally determined under which the color interpretation of light is constant. Results of the study should be taken into account during medical photography and subsequent color assessment of postoperative skin scars.

AUGITE-BASED CERAMICS OBTAINED BY SOLID-STATE SINTERING OF LOESS

Loess from the Danubian Plain (Bulgaria) was used as the raw material for the solid-state synthesis of ceramics.The mineral phase composition of the loess fraction used was determined by powder X-ray phase analysis, and the chemical composition by X-ray fluorescence analysis. The semi-quantitatively determined mineral phases are quartz, plagioclase, K-feldspar, mica, carbonates (calcite and dolomite), chlorite and amphibole. The major oxides of the chemical composition of loess fraction are (in wt. %): SiO2 - 53,61; Al2O3 - 12.57; Fe2O3 - 7.05; P2O5 - 0,23; TiO2 - 1.37; CaO - 19.36; and MgO - 1.48. Experiments were performed with sintering of pure loess without additives, and with addition of MgO and Na2O in order to obtain a composition corresponding to that of the pyroxene augite - (Ca,Na)(Mg,Fe,Al,Ti)(Si,Al)2O6. Ceramics were obtained at three temperatures: 1000, 1100 and 1200°C. The phase composition, spectral characteristics and colour coordinates of the obtained ceramics were determined. The results show that when magnesium and sodium are added to the loess raw material, the ceramics obtained after sintering at 1100 and 1200°C have a predominant content of augite and have a yellow-beige colour.

Lead‐free Halide Perovskites With ≈100% PLQY and Dual‐Color Emission for White Light‐Emitting Diodes

AbstractLead‐free halide perovskites (LHP) have attracted extensive attention in the field of next‐generation solid‐state lighting. However, single perovskite phosphor with tunable white‐light emission and ultra‐high photoluminescence quantum yield (PLQY) are rare. Here, the tunable dual‐color emission LHP phosphor is developed with a near‐unity PLQY of 99.5%. The LHP phosphor comprises Cs2NaInCl6: Sb3+/Bi3+ and Cs2InCl5·H2O: Sb3+/Bi3+ crystals, with the transition between these two perovskite structures being adjustable by the concentration of Na+. The addition of NaCl inhibits the hydrolysis of the [Sb(H2O)Cl5]2− octahedron, resulting in 3D connected [SbCl6]3− octahedron with less Jahn‐Teller distortion, and the PLQY of LHP is greater than 90%. Finally, the white‐light diode device is fabricated by assembling the LHP with a ultraviolet light‐emitting diode chip and the white light‐emitting diode device achieved Commission Internationale de l'Eclairage color coordinates of (0.34, 0.33), correlated color temperature of 4936 K, and a high color rendering index of 92.9. The LHP perovskite exhibited multimodal luminescence when excited by 365, 335, and 310 nm UV light, showing the multi‐mode anti‐counterfeiting capabilities of the LHP crystals.

Dy3+ ions in fluorophosphate glasses for luminescent white light applications

Abstract In this study, a series of fluorophosphate (FP) glasses, activated with Dy3+ ions and displaying concentration dependence, have been prepared and analysed for their suitability in luminescent white light applications. The melt quenching method was utilized to fabricate a set of FP glasses, doped with Dy3+ ions and possessing the composition of (60 − x) P2O5 + 10MgO + 10ZnO + 10BiF3 + 10KF + xDy2O3, where x ranges from 0.1 to 2.0 mol%. The structural properties of the samples were analysed using x-ray diffraction (XRD), scanning electron microscope (SEM), Fourier transform infrared (FTIR), and Raman spectroscopy while the optical properties of the samples were studied using absorption and emission spectra. The amorphous nature of the FP glasses was confirmed through SEM analysis and XRD profiles. Moreover, the presence of elements in their composition was verified using EDX. The FTIR spectra of the FP glasses exhibited vibration bands consistent with the characteristic phosphate groups, which was further supported by Raman analysis. The absorption spectra were used to calculate oscillator strengths (f exp & f cal) and Judd–Ofelt (JO) parameters Ω λ (λ = 2, 4, 6). The values of Ω λ (λ = 2, 4, 6) followed this order: Ω6 > Ω2 > Ω4. The emission spectra displayed three prominent transitions in the UV–visible region: (4F9/2 → 6H15/2) blue, (4F9/2 → 6H13/2) yellow, and (4F9/2 → 6H11/2) red. The peak at 553 nm (4F9/2 → 6H13/2) was the most intense and dominant. Radiative characteristics were evaluated from the emission spectra through the employment of JO intensity parameters and refractive indices. The Y/B intensity ratio values were greater than 1, indicating the high covalency of Dy3+ ions. The colour coordinates (x, y) and correlated colour temperature values of CIE 1931 were situated in the cool white region. The comprehensive analysis suggests that these glasses have the potential to become highly favourable candidates as luminescent components for solid-state white light emitting instruments.

Violet Light Excitable BaLiZn3(PO4)3: Eu3+ Orange-red-emitting Phosphor towards White LED Application

White light-emitting diode (WLED) has been widely used as solid-state lighting in recent years, with the advantages of energy saving, high luminous efficiency, and safety. Red phosphors are crucial to the color rendering index of WLED, and Eu3+-activated red phosphors can significantly improve the chromaticity performance of WLED. In this work, a series of new orange-red emitting BaLiZn3(PO4)3: Eu3+ phosphors were synthesized through high-temperature solid-state reaction method. The phase composition, crystal structure, morphology and photoluminescence properties of BaLiZn3(PO4)3: Eu3+ samples were investigated. The phosphors can be effectively excited by the violet light at 394 nm and emit orange-red lights corresponding to the electric dipole transition (5D0→7F1) at 594 nm. The optimal doping concentration of Eu3+ ions was about 5 mol%. The concentration quenching was caused by the electric dipole-dipole interaction between Eu3+ ions. Temperature-dependent PL spectra indicate that BaLiZn3(PO4)3: Eu3+ has excellent emission and color stability at high temperatures. The color coordinates were calculated and fall in the orange-red luminescent area. The color purity is about 98.3%, and the correlated color temperature is 1710K. These results indicate that the new orange-red phosphor BaLiZn3(PO4)3: Eu3+ has potential application prospects in WLED.

A well-performed green-emitting Lu1.5Ca1.5Al3.5Si1.5O12:Ce3+ garnet phosphor for high-quality pc-WLEDs

High-brightness and thermally-stable broadband green-emitting phosphors are highly demanded for the fabrication of high-quality phosphor-converted white light-emitting diodes (pc-WLEDs) with high color rendering index (CRI) and low correlated color temperature (CCT). Herein, we report on the synthesis, luminescent properties, thermal stability and application of a novel highly efficient green-emitting Lu1.5Ca1.5Al3.5Si1.5O12:Ce3+ garnet-type phosphor for blue-chip-pumped high-CRI pc-WLEDs. A series of Lu1.5Ca1.5Al3.5Si1.5O12:Ce3+ green phosphors doped with various Ce3+ concentrations (0.5-4 mol%) have been prepared by a conventional high-temperature solid-state reaction approach. Impressively, the composition-optimized Lu1.5Ca1.5Al3.5Si1.5O12:2%Ce3+ sample exhibits a broad excitation band in the 400-500 nm spectral range with an excitation peak around 451 nm, and it gives rise to a bright broad green emission band in the 470-700 nm wavelength region (emission peak: 533 nm; bandwidth: 108 nm) with CIE color coordinates of (0.3361, 0.5640). Notably, high luminescence efficiency is obtained for Lu1.5Ca1.5Al3.5Si1.5O12:2%Ce3+ phosphor (internal quantum efficiency: 92.2%; external quantum efficiency: 50.7%). Moreover, it is also found that Lu1.5Ca1.5Al3.5Si1.5O12:2%Ce3+ shows excellent resistance to thermal quenching, while its emission intensity at 423 K remains 76% of the initial value at room temperature. Amazingly, the color stability of Lu1.5Ca1.5Al3.5Si1.5O12:2%Ce3+ is also outstanding, and only a very small chromaticity shift (3.99 × 10−3) is observed at 423 K. A high-performance pc-WLED device has been fabricated by using a 450 nm blue-emitting LED chip and as-prepared Lu1.5Ca1.5Al3.5Si1.5O12:2%Ce3+ green phosphor as well as commercial CaAlSiN3:Eu2+ red phosphor. Such device produces a bright warm-white emission under 280 mA driving current, demonstrating super CIE chromaticity coordinates (0.3870, 0.3818), high CRI of 93.8, low CCT of 3865 K, and high luminous efficacy (51.86 lmW-1).

Evaluation of Luminescent and Thermal Properties of Dy³⁺ Doped Tungstate Phosphors for Optoelectronic and Thermometry Applications

Novel Ca2MgWO6: xDy3+ (x = 1, 2, 3, 4, and 6 mol%) phosphors were synthesized via solid-state reaction method. The phosphor structure remained unchanged upon doping with Dy3+ ions. Phosphors were optical optimizated using 4F9/2 → 6H13/2 transition, and 3 mol% of Dy3+ was found to be optimal concentration. We investigated optical quenching mechanisms including energy transfer, cross-relaxation, charge compensation, and multipole-multipole interactions. Colorimetric analyses assessed colour coordinates, purity, and correlated colour temperature (CCT). The optimized phosphor showed a direct band gap of 3.68 eV, a refractive index of 2.24, and covalent bonding between Dy3+ and the host. It exhibited exceptional thermal stability with only 0.31 wt% loss up to 440°C. Temperature-dependent emission spectra indicated high optical quenching temperature (498.82 K) and activation energy (0.21 eV). A multi-transition ratiometric approach confirmed suitability for non-contact thermometry and LED applications.

Synthesis and characterization of erbium silica glass and glass-ceramics for potential low-emissivity coating applications

Silica glasses co-doped with varying concentrations of Er3+ (0.8, 1.5, 4, and 8 mol %) were fabricated employing the sol-gel technique. The effects of erbium concentration were evaluated through several characterization techniques, including X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), UV-visible transmission spectroscopy, and photoluminescence analysis. The incorporation of erbium ions significantly altered the structural, optical, and photoluminescence properties of the doped glasses. XRD analysis revealed the presence of SiO2 in both tetragonal and hexagonal forms, along with Er2SiO5 crystalline phases. SEM images showed irregular rod-shaped structures with agglomeration and micro-flake cubic shapes. FTIR spectroscopy provided insights into the structural characteristics of the materials. Notably, the optical band gap energy of the glassy films increased, accompanied by fluctuating Urbach energy and a slight reduction in the refractive index, attributed to structural changes within the glass network. Photoluminescence spectra indicated strong emissions at 523 and 543 nm, corresponding to the transitions 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2, respectively. Additionally, a notable near-infrared emission at 1532 nm was observed, linked to the transition 4I13/2 → 4I15/2. The color coordinates of the produced glasses were found to be near the green or yellow regions, suggesting potential applications in optical amplifiers, lasers, and low-emissivity coatings.

Luminescent color modulation of Zn/BaAl2O4:0.2%Eu phosphors for LED application

Spinel-type aluminate (ZnAl2O4) doped with europium (Eu) ions has garnered considerable attention in the field of luminescence. This study explores a series of Zn/BaAl2O4:0.2%Eu phosphors (x=0∼0.25, x is for the mole fraction of BaAl2O4), fabricated through a high temperature solid-phase reaction method in air or reduction environment. In the case of phosphors synthesized in air, the photoluminescence emission (PL) spectra show a series of sharp emission peaks at 570nm, 589nm, 620nm, 660nm, and 710nm, which are generated by the 5D0-7FJ (J = 0, 1, 2, 3, 4) level transitions in Eu3+. Time-resolved photoluminescence and X-ray photoelectron spectroscopy (XPS) characteristics also validate the presence of Eu3+ in samples synthesized in air. An intriguing observation is the abnormally strong emission peak at 570nm under 346nm excitation, originating from the Eu3+5D0-7F0 level transition. For x=0.15, the corresponding CIE color coordinate is (0.3246, 0.3449), suggesting its potential application as a mono-doped and uni-matrix white phosphor. On the other hand, phosphors synthesized in reduction environment exhibit PL spectra with a wide emission band spanning from 400nm to 550nm, resulting from the electric-dipole-allowed transition of f-d state of Eu2+. The partial substitution of Zn2+ with Ba2+ significantly enhances the Eu2+ luminescence intensity. Moreover, an elevation of the mole fraction of Zn/BaAl2O4:0.2%Eu leads to a notable redshift (450nm→500nm) in the emission peaks of Eu2+ caused by lattice expansion, providing the adjustability of emitting color.

Color Stability of Bulk-Fill Flowable Resin Composites After Artificial Aging

Background: This study aimed to evaluate the color stability of bulk-fill flowable resin composites with 2 difference shades at baseline and after artificial aging. Methods: Disk-shaped specimens (Ø10 × 4 mm) were fabricated from three bulk-fill flowable resin resin composites (Filtek Bulk-Fill Flow, Venus Bulk-Fill Flow, and Estelite Bulk-Fill Flow). The specimens in each bulk-fill resin composite group were divided into two subgroups (n = 10 per subgroup) with two different shades, A1 (N = 30) and A3 (N = 30), and were polymerized with light curing (800 mW/cm2/Valo LED Unit, Ultradent) and polished. The color difference between bulk-fill resin composites was evaluated at baseline and after artificial aging using a spectrophotometer (CM-700d, Konica Minolta, Tokyo, Japan) under D65 illumination. Color coordinates were measured with CIEDE2000, and color differences (∆E00) and relative translucency parameter (RTP) values were calculated. Subsequently, the comparison of color changes (∆E00) before and after thermocycling was performed using the t-test for paired samples. Results: The bulk-fill flow resin composites evaluated in the present study were capable of mimicking important optical properties such as light transmission. All the resin composites provided acceptable color stability at baseline and after thermocycling when the color A1 was used. On the other hand, whenever the shade A3 was used, the Venus Bulk-Fill Flow demonstrated the best optical properties. There was no statistically significant difference when comparing baseline and after thermocycling in bulk-fill flowable resin composites (p > 0.05). After thermocycling, A1 bulk-fill flowable resin composites provided acceptable color stability, and all A3 bulk-fill flowable resin composites provided visible color change, except for the Venus Bulk-Fill Flow (∆E00 = 2.35). Conclusions: Estelite Bulk-Fill Flow displayed the best color stability (∆E00 = 2.22) between all the combinations evaluated.

Novel reddish-orange emitting BaBPO5:Eu3+ phosphor for n-UV warm white-LEDs: Synthesis and study of structural and spectroscopic investigations

A novel reddish-orange emitting 2Ba2-xO-B2O3-P2O5:xEu3+ (x= 0.04, 0.06, 0.08, 0.10, 0.12 and 0.14 mol%) phosphor with different concentrations of Eu3+ ions were synthesized through high temperature solid-state reaction technique. The crystal structure has been studied by X-ray diffraction technique for all the concentrations of Eu3+ ions. The morphology and elemental analysis of the optimal ∼0.1 mol% concentration was examined by the SEM-EDS images. The functional groups were analysed by the FTIR characterization technique. The thermal properties were studied by the TGA-DSC analysis. The energy band gap of all the samples were analysed by using UV–VIS DRS technique. The photoluminescence properties of BaBPO5:Eu3+ phosphor with different concentrations of Eu3+ ions were investigated at λem = 611 nm and λex = 394 nm. Variation in emission intensity with Eu3+ ion concentrations, phonon side bands, multi-phonon relaxation rate and energy transfer mechanisms were studied. The BaBPO5:Eu3+ phosphors exhibit characteristic emission peaks corresponding to 5D0 → 7FJ (J = 0, 1, 2, 3, 4) transitions of Eu3+ ions under n-UV excitation. Among all the transitions, 5D0 → 7F1 (593 nm) transition shows higher intensity and asymmetric ratio (R21) for all concentrations of Eu3+ ions were calculated. The lifetimes of 5D0 level of Eu3+ ions in BaBPO5: Eu3+ phosphor were calculated by using fluorescent decay curve analysis. The CIE color coordinates reveal, reddish-orange emission in the low CCT range. These findings imply that BaBPO5: 0.1Eu3+ phosphor is a promising candidate for solid-state lighting applications as well as phosphor-converted warm w-LEDs.

Synthesis and Properties of a Red Na5Zn2Gd1−x(MoO4)6: xEu3+ Phosphor

Novel Eu3+-doped Na5Zn2Gd(MoO4)6 triple molybdate phosphors were fabricated by the sol-gel method. The structure, morphology, and luminescent properties have been characterized by X-ray diffraction (XRD), thermogravimetric differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), FTIR spectroscopy, and luminescence spectroscopy. The results indicated that the synthesized Na5Zn2Gd1−x(MoO4)6: xEu3+ phosphor consisted of a pure phase with monoclinic structure. Under excitation at 465 nm, the Na5Zn2Gd1−x(MoO4)6: xEu3+ phosphor exhibits an intensive red emission band around 610 nm corresponding to the transition of 5D0→7F2 which is much higher than that 5D0→7F1 at 594 nm, which was appropriate for a blue LED. According to the influence of the synthesis conditions, the phosphors showed the highest emission intensity when the doping concentration of Eu3+ was 25 mol.% and the molar ratio of citric acid to metal ions was 2:1. Na5Zn2Gd0.75(MoO4)6: 0.25 Eu3+ with the color coordinates (x = 0.658, y = 0.341) is a more stable red phosphor for blue-based white LEDs than the commercial Y2O2S: Eu3+ red phosphor (0.48, 0.50) due to its being closer to the NTSC standard values (0.670, 0.330).

Application of nano-TiO2 and micro-ZnO on cementitious surfaces for self-cleaning façades by spray coating and dip coating: A comparative study

Building façades are constantly exposed to atmospheric pollution and various external agents that can degrade their aesthetic qualities and introduce degradation patterns that affect the durability and performance of the materials. Façades with self-cleaning properties are important in the modern construction industry and the conservation of historic buildings, as they reduce costs and allow the preservation of original surfaces without the need for invasive interventions that could compromise cultural heritage. This study does a comparative analysis of the application of photocatalytic coatings composed of aqueous dispersions of titanium dioxide nanoparticles (TiO₂) and zinc oxide microparticles (ZnO) on cementitious substrates for use on façades by two functionalisation methods: spray coating and dip coating. A comprehensive characterisation was carried out using techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), and diffuse reflectance spectroscopy (DRS) to assess the morphology, crystal structure and light absorption properties of the photocatalyst particles while Energy Dispersive Spectroscopy (EDS) and scanning electron microscopy (SEM) were employed to evaluate the substrate. The self-cleaning performance was evaluated by monitoring the degradation of Rhodamine B (RhB) dye under simulated sunlight. Spectrophotometric analysis was used to assess the colour coordinates using a standard colour system (CIELAB colour space). The results showed that the photocatalytic coatings improved the surfaces' self-cleaning properties while maintaining the substrate's original aesthetics. Spray-applied micro-ZnO-based coatings showed the most significant effectiveness in terms of self-cleaning.

Color Ranges and Distribution of Human Teeth: A Prospective Clinical Study.

This study investigated the in vivo color range of human teeth using a research-grade noncontact spectroradiometer, analyzing the effects of gender, age, ethnicity, and lifestyle factors, including diet, smoking, and oral hygiene. A total of 1004 participants were recruited at two research sites and stratified by gender, age, and ethnicity, and data on their dietary and oral habits were collected. Noninvasive color measurements of an upper central incisor were performed using a spectroradiometer and a fiber-coupled Xe-Arc light source. Color differences were computed using the CIELAB and CIEDE2000 color difference formulas, statistically analyzed, and interpreted through comparisons with 50:50% perceptibility (PT) and acceptability (AT) thresholds for dentistry. CIELAB and CIEDE2000 color coordinate values varied significantly. Female teeth appeared lighter and less yellow than men's. Age correlated with darker, more chromatic teeth, stabilizing only after Age 46. Significant ethnic differences were observed, particularly between African-American and Asian participants. Coffee consumption impacted teeth yellowness and chromaticity, while tea had no significant effect. Frequent tooth brushing led to lighter teeth, and tooth whitening considerably influenced color, emphasizing the effect of cosmetic dental treatments. Smoking showed minimal impact, with slight discoloration noted among light smokers compared to nonsmokers. Color coordinate values by gender, age, and ethnicity exhibited statistically significant differences and, in most cases, noticeable color differences. With exceptions, the dietary/oral habits of the patient had a significant impact on the color of human teeth. The findings from this study provide detailed information and understanding of the color range and distribution of human teeth, which can help enhance the esthetic outcome of dental care and, consequently, the patient's satisfaction.

Photoluminescence color-tuning with polymer-dispersed fluorescent films containing two fluorinated diphenylacetylene-type fluorophores.

The development of organic light-emitting devices has driven demand for new luminescent materials, particularly after the 2001 discovery of aggregation-induced emission. This study focuses on fluorinated diphenylacetylene-based luminescent molecules, revealing that specific molecular modifications can enhance fluorescence and achieve a wide range of photoluminescence colors. A simple and effective luminescence color-tuning method is proposed to investigate the photoluminescence behavior of two-component polymer dispersion films blended with two types of fluorinated diphenylacetylenes, namely blue- and yellow- or red-fluorescent fluorinated diphenylacetylenes. It is confirmed that if blue and green-yellow or yellow fluorophores are blended in appropriate ratios, a binary blend with color coordinates (0.20, 0.32) can be achieved, which approaches the white point of pure white emission. These findings contribute to the development of effective lighting and display devices as new white-light-emitting materials.

Designing LiDAR‐Detectable Dark‐Tone Materials with High Near‐Infrared Reflectivity for Autonomous Driving: A Comprehensive Review

AbstractAutonomous driving relies on the precise recognition of objects using light detection and ranging (LiDAR) technology, that operates at a specific wavelength of 905 nm. Black objects, such as carbon black used in vehicle coating, tend to absorb this specific wavelength significantly, which limits the performance of LiDAR sensors. To address this issue, researchers have explored creating dark‐toned materials that can be detected by LiDAR with high NIR reflectivity while maintaining a true blackness (L* < 20 based on the CIE color coordinates). These materials fall into two categories: organic and inorganic pigments. Organic pigments can be synthetically adjusted to achieve true blackness by manipulating their functional groups, but achieving high NIR reflectivity remains challenging, often requiring a bilayer structure with NIR‐reflective white base and an upper layer of organic black pigments. Additionally, the need for hydrophobic additives and resistance to degradation from sunlight further restricts their use. In the case of inorganic pigments, the desired LiDAR‐detectable properties can be obtained through careful control of their composition, structure, and morphology, allowing for single‐layer coatings with appropriate design. This review highlights recent advancements in developing organic and inorganic LiDAR‐detectable black pigments and outlines future material design strategies for autonomous vehicle systems.

High Efficiency Ultra-Narrow Emission Quantum Dot Light-Emitting Diodes Enabled by Microcavity.

A wide-color-gamut display enableby a narrow emission linewidth facilitates a visually immersive experience akin to the real world. Quantum dot light-emitting diodes (QLEDs) with excellent color purity and high efficiency hold great promise as future candidates for high-definition displays. However, most devices typically exhibit emission linewidths exceeding 20nm, and lack a universal strategy for further enhancing the color purity. In this study, a planar microcavity structure for realizing ultra-narrow emissions is developed by incorporating a distributed Bragg reflector into normal electroluminescent devices. By leveraging the strong optical resonance effect derived from this microcavity structure, red QLEDs are successfully fabricated with an extraordinary full width at half maximum of 11nm in the normal direction, beyond the BT.2020 color coordinates. The fabricated red-microcavity QLEDs exhibit a considerable enhancement in the external quantum efficiency, which increases from 28.2% to 35.6%, together with an extended operating lifetime. The strategy adopted herein will serve as an effective reference for achieving ultra-narrow emission and high-efficiency QLEDs.

Urban Color Perception and Sentiment Analysis Based on Deep Learning and Street View Big Data

The acceleration of urbanization has resulted in a heightened awareness of the impacts of urban environments on residents’ emotional states. This present study focuses on the Lixia District of Jinan City. By using urban street view big data and deep learning methods, we undertook a detailed analysis of the impacts of urban color features on residents’ emotional perceptions. In particular, a substantial corpus of street scene image data was extracted and processed. This was performed using a deep convolutional neural network (DCNN) and semantic segmentation technology (PSPNet), which enabled the simulation and prediction of the subjective perception of the urban environment by humans. Furthermore, the color complexity and coordination in the street scene were quantified and combined with residents’ emotional feedback to carry out a multi-dimensional analysis. The findings revealed that color complexity and coordination were significant elements influencing residents’ emotional perceptions. A high color complexity is visually appealing, but can lead to fatigue, discomfort, and boredom; a moderate complexity stimulates vitality and pleasure; high levels of regional harmony and aesthetics can increase perceptions of beauty and security; and low levels of coordination can increase feelings of depression. The environmental characteristics of different areas and differences in the daily activities of residents resulted in regional differences regarding the impacts of color features on emotional perception. This study corroborates the assertion that environmental color coordination has the capacity to enhance residents’ emotions, thereby providing an important reference point for urban planning. Planning should be based on the functional characteristics of the region, and color complexity and coordination should be reasonably regulated to optimize the emotional experiences of residents. Differentiated color management enhances urban aesthetics, livability, and residents’ happiness and promotes sustainable development. In the future, the influences of color and environmental factors on emotions can be explored in depth, with a view to assist in the formulation of fine urban design.

Structural, morphological and photoluminescence studies of Ca7Mg2P6O24:RE3+(RE3+= Tb3+, Dy3+) nanophosphor for solid state illumination

The Ca7Mg2P6O24:RE3+ (RE3+= Tb3+, Dy3+) nanophosphor material was synthesized by traditional wet chemical method. The XRD are used to determine phase and crystallinity of the synthesized sample; further FTIR, SEM, TEM, and PL properties were studied. The XRD pattern of prepared sample match well with standard JCPDS card no 00–020–0348, and it exhibits the rhombohedral structure along with space group R3c (161). The phosphate (PO4)3-group absorption band was observed at 990–1100 cm-1 in FTIR. Surface morphology (TEM analysis) reveals particle sizes in the range of 55–110 nm. The luminescence emission spectra of Ca7Mg2P6O24 phosphor activated by Tb3+ were studied at three different excitations: 352 nm, 370 nm, and 379 nm. The spectra show two emission peaks at 470 nm (blue) and 545 nm (green). These are due to the 5D4 → 7F6 and 5D4 → 7F5 transitions of Tb3+ ions. The highest intensity peak is located at 545 nm. The Ca7Mg2P6O24:Tb3+ phosphor's CIE chromaticity coordinates are (0.040, 0.316) at 491 nm and (0.265, 0.724) at 543 nm. These are in the blue and green areas on the edges of the CIE diagram, respectively. The photoluminescence emission spectra of Dy3+-doped Ca7Mg2P6O24 phosphor show two significant emission peaks located at 482 nm and 574 nm. These are caused by the 4F9/2 → 5H15/2 and 4F9/2 → 6H13/2 transitions of Dy3+ ions, which produce blue and yellow light, respectively, with an excitation wavelength of 350 nm. The sharp peak position at 482 nm produces the strongest emission. The effect of concentration quenching in between the Dy3+-Dy3+ions and Tb3+-Tb3+ ions is due to dipole-dipole interaction. The CIE color coordinate is found to be (0.082, 0.156) at 482 nm and (0.471, 0.527) at 574 nm which lies in blue and yellow border of CIE diagram. The lifespan of Tb3+, Dy3+activated Ca7Mg2P6O24 nanophosphor of highest concentration is found to be 1.917 ms and 0.9985 ms respectively. On investigation, the synthesized Tb3+, Dy3+activated Ca7Mg2P6O24 nanophosphor can be potential for solid lightning devices & other display application.