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Sustainable production of multifunctional nanomaterials is a key challenge for their widespread use. Phytochemical-assisted synthesis provides an environmentally benign route of nanoparticle modifications towards desired applications. Herein, Catharanthus roseus (CR) leaves extract has been used as a phytochemical modifier for copper oxide-doped yttrium oxide nanoparticles (CuO/Y2O3 NPs). The composition, structure, morphology and functional groups of CuO/Y2O3 NPs have been extensively modulated via green synthesis. The excellent antibacterial activities against gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) pathogens suggest an increasing rate of antibacterial behaviour. Besides, the sheet-like morphology of CuO/Y2O3 NPs promotes photocatalytic activities by methylene blue, phenol and methyl orange degradation under sunlight with rates of 0.0203, 0.0152 and 0.0167 min−1. Most importantly, CuO/Y2O3 NPs facilitate low oxidation peak potential (−0.58 V), extended frequency linear range (1–300 nM), and ultralow detection limit (up to 0.58 nM) for an important biomarker threonine, which is the best among any nanomaterials reported till date. Such achievement paved the way for sustainable nanomaterial modifications towards multifunctionality. [ABSTRACT FROM AUTHOR]

This research paper focuses on the development of additive-based erosion-resistant high-velocity oxy-fuel (HVOF) WC-10Co4Cr coating for pump steel. In this study, the WC-10Co4Cr cermet powder consists of yttria and zirconia, each with a concentration of 3 wt.%. The HVOF spraying method was utilised to develop the ceramics-added WC-10Co4Cr coatings. The study conducted erosion tests using a pot tester under mining conditions. The microstructure, crystalline phases and microhardness of the as-HVOF coatings were analysed and compared between the pure and ceramics-based WC-10Co4Cr coatings. The results revealed the effect of ceramics addition on surface erosion of WC-10Co4Cr coating. The results indicate that yttrium oxide enhances the performance of WC-10Co4Cr coating in terms of erosion resistance, while zirconium oxide is not suitable for use in WC-10Co4Cr coating in erosion wear environments. [ABSTRACT FROM AUTHOR]

Hydrogen production from the decomposition of ammonia is considered an effective approach for addressing challenges associated with hydrogen storage and transportation. However, their relatively high energy consumption and low efficiency hinder practical multi‐scenario applications. In this study, Y2O3‐stabilized catalysts with Co‐loaded onto porous nitrogen‐doped carbon (Y2O3–Co/NC) are synthesized by pyrolysis of Y(NO3)3‐modified ZIF‐67 under an inert atmosphere, followed by annealing in a reducing environment. The introduction of Y2O3 enhanced the recombination and desorption of N atoms and facilitated the gradual dehydrogenation of NHx on the catalyst surface, resulting in improved catalytic activity for the thermal decomposition of ammonia. Benefitting from the electron‐donating properties of Y2O3 and N‐doped carbon, the optimized catalyst achieved a remarkable NH3 conversion efficiency of 92.3% at a high gas hourly space velocity of 20 000 cm3·gcat−1${\mathrm{g}}_{{\mathrm{cat}}}^{ - {\mathrm{1}}}$·h−1 with an encouraging H2 production rate of 20.6 mmol·gcat−1${\mathrm{g}}_{{\mathrm{cat}}}^{ - {\mathrm{1}}}$·min−1 at 550 °C. Moreover, the synthesized catalyst undergoes a fast‐dynamic reconstruction process, resulting in exceptionally stable catalytic activity during the thermal decomposition of ammonia, rendering it a promising candidate for carbon‐free energy thermocatalytic conversion technology. [ABSTRACT FROM AUTHOR]

Laser Powder Bed Fusion (LPBF) enables the efficient production of near-net-shape oxide dispersion-strengthened (ODS) alloys, which possess superior mechanical properties due to oxide nanoparticles (e.g., yttrium oxide, Y-O, and yttrium-titanium oxide, Y-Ti-O) embedded in the alloy matrix. To better understand the precipitation mechanisms of the oxide nanoparticles and predict their size distribution under LPBF conditions, we developed an innovative physics-based multiscale modeling strategy that incorporates multiple computational approaches. These include a finite volume method model (Flow3D) to analyze the temperature field and cooling rate of the melt pool during the LPBF process, a density functional theory model to calculate the binding energy of Y-O particles and the temperature-dependent diffusivities of Y and O in molten 316L stainless steel (SS), and a cluster dynamics model to evaluate the kinetic evolution and size distribution of Y-O nanoparticles in as-fabricated 316L SS ODS alloys. The model-predicted particle sizes exhibit good agreement with experimental measurements across various LPBF process parameters, i.e., laser power (110–220 W) and scanning speed (150–900 mm/s), demonstrating the reliability and predictive power of the modeling approach. The multiscale approach can be used to guide the future design of experimental process parameters to control oxide nanoparticle characteristics in LPBF-manufactured ODS alloys. Additionally, our approach introduces a novel strategy for understanding and modeling the thermodynamics and kinetics of precipitation in high-temperature systems, particularly molten alloys. [ABSTRACT FROM AUTHOR]

ABSTRACT Objective Materials and Methods Results Conclusion Clinical Significance To evaluate the effect of staining, glazing, and polishing of stabilized zirconia with 5 mol% of yttrium oxide (5Y‐TZP) on the wear behavior of opposing tooth enamel.The plane specimens of 5Y‐TZP were divided into 6 groups (n = 10), according to surface treatment: as sintered, staining, glazing, polishing, staining followed by glazing, and staining followed by polishing, and positioned against tooth enamel during the two‐body wear test (20 N, 2 Hz, until completing 300,000 cycles). The wear rates of tooth enamel were evaluated using a profile projector and a digital pachymeter as a measure of vertical height loss. The data were analyzed by one‐way ANOVA and a Tukey post hoc test (α = 0.05).Polishing reduced the vertical height loss (p < 0.001) while there was no difference among other groups.Polishing is recommended as a finishing procedure to reduce the wear rates of tooth enamel, and finishing procedures (glazing or polishing) performed after staining did not affect the vertical height loss of tooth enamel.Polishing is the recommended finishing procedure for preshaded 5Y‐TZP to reduce the wear rates of opposing tooth enamel. Staining is applied to the occlusal surface to reproduce the pigmented groove appearance, and glazing or polishing performed after staining did not affect the wear rates of opposing tooth enamel. [ABSTRACT FROM AUTHOR]

A novel lactate biosensor based on a yttrium oxide/boron nitride (Y 2 O 3 /BN) nanocomposite modified electrode was developed. The BN nanosheets provided a supporting matrix for the Y 2 O 3 nanoparticles, combining their synergistic properties for electrochemical biosensing. The Y 2 O 3 /BN nanocomposite provided high surface area and excellent electrocatalytic effects, promoting the oxidation of hydrogen peroxide generated from lactate oxidase catalyzed lactate oxidation. The Y 2 O 3 /BN modified biosensor showed wide linear range from 0.005 to 500 μM, low detection limit of 2 nM, high sensitivity of 1.23 μA/μM, good reproducibility with 3.2 % RSD, and long-term stability over 56 days. The biosensor could detect lactate levels in athlete sweat samples with high accuracy and correlation to standard methods, distinguishing changes in sweat lactate corresponding to different exercise intensities. The nanocomposite modified biosensor showed potential for non-invasive, real-time monitoring of exercise levels and fatigue status based on sweat lactate detection in athletic training applications. [ABSTRACT FROM AUTHOR]

Multi-Arc Ion Plating (MAIP) technology was used to deposit yttrium oxide (Y 2 O 3) ceramic thin films on Al 2 O 3 ceramics and silicon wafers. The effects of varying the O-to-Ar gas flow ratio (Rc: 0.5, 1.0, 1.5, 2.0) and the annealing conditions on the phase composition, microstructure, mechanical properties, and tribological performance of the Y 2 O 3 films were assessed. The films deposited at Rc values of 1.0 and 1.5 consisted of a single cubic phase structure. In contrast, films deposited at Rc values of 0.5 and 2.0 contained a small monoclinic phase and the cubic phase structure. The film deposited at an Rc value of 1.0 (oxygen flow rate of 200 sccm) exhibited a dense microstructure, the best mechanical properties (hardness of 14.2 ± 0.191 GPa), and the lowest friction coefficient (0.142 ± 0.003). Furthermore, the colour of the film changed from grey-black to white after annealing at 800 °C for 6 h. The oxygen vacancy of the thin film increased, with improving crystallinity, decreasing hardness and elastic modulus, and increasing grain size, friction coefficient and wear rate. The film exhibited the best tribological properties at 25 °C. [ABSTRACT FROM AUTHOR]

The achievement of optimal performance is a crucial aspect of renewable energy resources. The study attempts to boost the power conversion efficiency of polycrystalline silicon (Si) photovoltaic cells by the application of anti-reflective coating (ARC). The solgel method is employed to synthesize yttrium oxide (Y 2 O 3). The electro spraying method was utilized to apply the ARC on photovoltaic cells. The effect of coating on PV cells were determined through the structural, electrical, optical and thermal analysis. The antireflective material was uniformly applied over the coated substrate for 45 min (Y-I), 90 min (Y-II), 135 min (Y-III), and 180 min (Y-IV). The sample coated for 135 min showed an optimal power conversion efficiency (PCE) of 21.65 % and 20.09 % in the presence of neodymium light and direct sunlight, respectively, and a minimum electrical resistivity of 3.96 × 10−3 Ω-cm. In addition, Y-III coated cells exhibit a maximum absorbance of 94 %. The Y-III coated photovoltaic cells demonstrated the lowest temperature of 34.6 °C when exposed to an open environment and 40.6 °C when exposed to a controlled environment. The results from numerous studies demonstrated that Y 2 O 3 can be a suitable ARC, which effectively improved the efficiency of photovoltaic cells. [ABSTRACT FROM AUTHOR]

This study presents both numerical modeling and experimental fabrication of three different partial-reflection (PR) coatings each optimized for quantum cascade lasers (QCLs) that emit radiation in the mid-infrared range. A novel double-layer PR coating comprising silicon dioxide (SiO2) and silicon nitride (Si3N4) was proposed as a potential solution for compatibility with QCLs fabrication processes. Subsequently, the PR coating was compared with two well-known PR coatings: a single layer of aluminum oxide (Al2O3) and a single layer of yttrium oxide (Y2O3). The coatings were designed to reduce the reflectivity of the front laser mirror from 30% to approximately 13%. The thickness of the dielectric layers was optimized for lasers emitting at 4.4 μm, with applicability in the 2.5–6 μm range. The proposed double-layer coating achieved the desired reflectivity while reducing the total coating thickness by 120 nm. By using the presented coatings it will be possible to increase the optical power of Mid-Infrared QCLs. [ABSTRACT FROM AUTHOR]

Objective: We assessed the changes in optical properties and biocompatibility of transition zones in multilayered translucent monolithic zirconia exposed to prolonged hydrothermal aging and compared the results to those with different yttrium oxide contents. Materials and Methods: Four types of zirconia blocks from IPS e.max ZirCAD were used: 3Y-TZP e.max ZirCAD LT (ZL), 4Y-TZP e.max ZirCAD MT (ZM), 5Y-TZP e.max ZirCAD MT Multi (ZT), and 3Y/5Y-TZP e.max ZirCAD Prime (ZP). A total of 120 specimens (15.0 mm diameter and 1.5 mm height) were fabricated and divided into three groups (n = 10). The aging process for the specimens was conducted in an autoclave set to 134 °C and 0.2 MPa, with durations of 0 h (control), 5 h (first aged), and 10 h (second aged). The optical properties and biocompatibility were analyzed, followed by a statistical analysis of the data (α = 0.05). Results: Before and after aging, ZL and ZP exhibited the lowest color changes. ZT exhibited the highest average transmittance and translucency parameter values, while ZL had the lowest. The water contact angle test showed the highest value in ZM and lowest in ZL across all the aging stages. ZL, ZM, and ZP showed a considerable decrease in the water contact angle; however, ZT did not. A cell counting kit-8 assay showed ZL had the highest value, while ZM had the lowest. A filamentous actin test exhibited the highest value in ZL and lowest in ZM. In the vinculin analysis, ZL and ZT exhibited the lowest values, whereas ZM and ZP had the highest. Conclusion: 3Y/5Y-TZP exhibited a balanced performance across critical parameters, such as color stability, translucency, and biocompatibility, aligning with 3Y-TZP. While 5Y-TZP demonstrated superior translucency, it confirmed the lowest color stability, whereas 3Y-TZP achieved the highest biocompatibility. These properties provide clinicians with a reliable material option that ensures superior esthetic outcomes and long-term prognosis, ultimately contributing to improved patient satisfaction and clinical longevity. [ABSTRACT FROM AUTHOR]

Oxygen vacancy is the key contributing to the rapid bonding in flash joining. Prior to this study, the specific formation process of oxygen vacancy and its influencing factors have not been systematically investigated. In this work, the based materials yttrium oxide and Ti are phased observed during the incubation stage and the flash stage of flash joining. Three periods are summarized to reveal the whole process and variation in oxygen vacancy generation, electron binding, and metal filling. Following the stable stage, the factors impacting the oxygen vacancy are systematically studied and characterized to quantify their contribution. These factors include bonding temperature, current density, joining time, furnace atmosphere, and electric field direction. These findings have significant implications for precisely controlling the strength of the transparent/metal flash joint, meanwhile, may have reference value for universal flash joining. [ABSTRACT FROM AUTHOR]

Different contributions of dopants based on Yttrium oxide (Y 2 O 3)/titanium(IV) oxide (TiO 2)/carbon nanotube (CNT)/have been incorporated into the polymeric matrix of Polystyrene (PS). These films were fabricated in films due to their feasibility and low cost. The contact angle revealed that the dopants supported the hydrophilicity of the films that Y 2 O 3 /TiO 2 /CNT/PS represents the second highest wettability with (56.15 ± 6.35°) films, while Y 2 O 3 /PS film displays rough surface with the highest wettability with (32.5 ± 0.9°). we examined the impact of Y 2 O 3 /TiO 2 /CNT/PS composite on the viability of a human lung cell-line to better understand its biological behavior. Specifically, we measured cell viability as a means to assess the effect of the composite. The results revealed that at a concentration of 5000 μg/ml, the cell viability was measured to be 31.8 %. However, at a lower concentration of 2.4 μg/ml, the cell viability increased significantly to 117.9 %. These findings highlight a concentration-dependent relationship between the composite and the viability of the human lung cell-line. The observed cell viability exceeding 100 % indicates that the Y 2 O 3 /TiO 2 /CNT/PS composite scaffold had a positive effect on cell proliferation and generation. This suggests that the modified PS scaffold is conducive to cellular growth and can be considered safe for human use. The results imply that the composite scaffold promotes a favorable cellular environment, potentially supporting tissue regeneration and indicating its potential suitability for biomedical applications. The surface morphology shows that the topography of the films was changed clearly with the dopants of Yttrium oxide, titanium(IV) oxide and CNT components. The TiO 2 granules implanted in the PS composition cause an increase in pore size to an average of 2.2 μm. Pore diameters ranging from 100 to 500 μm may enhance cell proliferation, while lower sizes lead to more stable implantable discs. [ABSTRACT FROM AUTHOR]

In recent years, yttrium oxide coatings prepared by atmospheric plasma spraying (APS) have been employed extensively in semiconductor processing equipment. Meanwhile, defects in yttrium oxide coating, such as unmelted particles and pores, reduce the etching resistance of the coating. In this work, two yttrium oxide coatings were prepared by in situ laser-assisted plasma spraying (LAPS) coupled with a 500 W and 600 W laser for comparison with a coating prepared by APS, and the effects of the laser on the coating properties were investigated. The results show that the surface roughness was reduced by 25.7% (500 W) and 25.3% (600 W) and the porosity was reduced by 52.3% (500 W) and 36.9% (600 W) after laser coupling. After being etched by CF4/CHF3 for a long time, it was observed from SEM, EDS and XPS analyses that the intensity ratios of the Y-F bonds in the coating were 1 (APS):1.3 (LAPS+500W):1.1 (LAPS+600W), which indicated that the LAPS+500W coating had a thicker fluorination layer. It was also observed that the fluorination layer at the defect was first eroded; then, the erosion area gradually spread to the surrounding area, and finally, the fluorination layer was etched. This indicated that the defects had a significant impact on the etching resistance. Consequently, the LAPS+500W coating with fewer defects and a thicker fluorination layer showed the lowest etching rate. Therefore, in situ laser-assisted plasma spraying coupled with an appropriate laser power is an effective method to improve the performance of yttrium oxide coatings. [ABSTRACT FROM AUTHOR]

Passive daytime radiative cooling (PDRC) presents a promising avenue for efficient thermal management without relying on electrical power. In this study, the potential of integrating Hollow Yttrium‐Oxide Spheres (HYSs) within a Polydimethylsiloxane (PDMS) matrix to enhance PDRC is investigated. Through a combination of experimental characterization and computational analysis, the optical properties and radiative cooling performance of PDMS films embedded with HYSs are evaluated. These results demonstrate that HYSs significantly improve both solar reflectivity and long‐wave infrared (LWIR) emissivity of the PDMS matrix. Finite‐Difference Time‐Domain (FDTD) simulations confirm the scattering efficiency of HYSs across various wavelength ranges, highlighting their effectiveness as additives for enhancing the radiative properties of passive cooling materials. Experimental validation reveals enhanced reflectivity and emissivity of PDMS films with embedded HYSs, resulting in superior cooling performance compared to non‐HYS counterparts. Overall, this study underscores the potential of HYS‐infused PDMS films as a promising solution for passive radiative cooling, with broad applicability in diverse domains requiring efficient thermal management solutions. Additionally, these research insights pave the way for establishing an AI database for passive radiative cooling research, offering new avenues for further exploration and application in this field. [ABSTRACT FROM AUTHOR]

Thermal shock resistance and mechanical reliability of aluminum nitride (AlN) ceramic substrates are essential in electronic device modules. In this study, the thermal shock behavior of AlN doped with aluminum - yttrium oxide (Al - Y 2 O 3) was explored. The results indicate that adding Al to AlN ceramics increases its flexural strength, thermal conductivity, and thermal expansion coefficient. The microcracks caused by thermal mismatch between the AlN matrix and the secondary phases relieved internal stress, thereby improving thermal shock resistance of AlN ceramics. Furthermore, the addition of Al isolates and homogenizes the secondary phases, resulting in a more uniform microstructure and strengthened grain boundaries, which enhance the flexural strength, Weibull modulus, and thermal shock resistance. After introducing 0.5 wt% Al, the Weibull modulus of AlN ceramics increased by 73.37 %, and their critical thermal shock temperature difference exceeded 800 °C, with a maximum residual strength of 488.01 ± 48.26 MPa at 600 °C. Overall, an appropriate amount of Al improves the reliability and thermal shock resistance of AlN ceramics. [ABSTRACT FROM AUTHOR]

Cerium oxide (CeO2) and yttrium oxide (Y2O3) nanoparticles possess interesting surface properties and interfacial interactions that make them attractive candidates for various applications. This study presents a comprehensive investigation into the synthesis and toxicity assessment of yttrium-doped cerium oxide (Ce-Y) nanocomposite using a combination of analytical techniques and biological assays. The nanocomposite was characterized using UV–Vis spectroscopy, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), electron microscopy imaging, dynamic light scattering (DLS), and zeta potential measurements to elucidate their structural, optical and physicochemical properties. The synthesized nanocomposite exhibited distinctive absorption spectra and precise alignment of diffraction peaks, confirming the successful incorporation of yttrium ions into the cerium oxide lattice. Electron microscopy images revealed well-dispersed yttrium particles within the ceria matrix, indicating uniform distribution and morphology. DLS and zeta potential analysis provided insights into the size distribution and stability of the nanocomposite. Furthermore, in vivo toxicity assessment using Drosophila melanogaster model revealed no significant toxicity of Ce:Y nanocomposite, as evidenced by survival assay and behavioral assays. Superoxide dismutase (SOD) activity and reactive oxygen species (ROS) levels were also evaluated, demonstrating no discernible nanoparticle-induced toxicity. Overall, this study highlights the potential applications of Ce:Y nanocomposite and underscores the importance of comprehensive toxicity evaluation in nanomaterial development. [ABSTRACT FROM AUTHOR]

Eu3+-doped Y2O3-based luminescent materials can be used as a scintillator for electron or high energy β-ray irradiation, which are essential for applications such as electron microscopy and nuclear batteries. Therefore, it is essential to understand their defect mechanisms and to develop materials with excellent properties. In this paper, Y2O3-based transparent ceramics with different Eu3+ doping concentrations were prepared by solid-state reactive vacuum sintering. This series of transparent ceramic samples exhibits strong red emission under electron beam excitation at the keV level. However, color change appears after the high-energy electron irradiation due to the capture of electrons by the traps in the Y2O3 lattice. Optical transmittance, laser-excited luminescence, X-ray photoelectron spectroscopy (XPS), and other analyses indicated that the traps, or the color change, mainly originate from the residual oxygen vacancies, which can be suppressed by high Eu doping. Seen from the cathodoluminescence (CL) spectra, higher doping concentrations of Eu3+ showed stronger resistance to electron irradiation damage, but also resulted in lower emissions due to concentration quenching. Therefore, 10% doping of Eu was selected in this work to keep the high emission intensity and strong radiation resistance both. This work helps to enhance the understanding of defect formation mechanisms in the Y2O3 matrix and will be of benefit for the modification of scintillation properties for functional materials systems. [ABSTRACT FROM AUTHOR]

Rare earth zirconate ceramic has been considered as one of the potential thermal barrier coating materials to replace 6–8% YSZ material (6–8% yttrium oxide stabilized zirconia), because of its low thermal conductivity and good high temperature phase stability. However, there is a problem that the coefficient of thermal expansion does not match the matrix. In this paper, rare earth high entropy zirconate ceramic powder with defective fluorite structure was prepared by molten salt synthesis(MSS). The results show that the reaction temperature and the ratio of reactants to molten salt will affect the synthesis effects. With the action of the high entropy effect, the synthesized ceramic powder has low thermal conductivity, improved thermal expansion coefficient and high infrared reflectivity. [ABSTRACT FROM AUTHOR]

An original procedure is proposed to refine unit cell parameters (UCPs) of single crystals in Bond's scheme. The procedure involves the use of a modern laboratory diffractometer equipped with a 2D detector and a three-circle goniometer. At the first stage, preliminary UCPs, diffraction class, and crystal orientation relative to goniometer axes are determined. Then φ and ω angles are calculated to bring an appropriate (occurrence of a well-resolved doublet, intensity) reflection hkl on the equatorial plane. The measurement in Bond's scheme is carried out at two symmetric positions of the detector ±2θD ≈ 2θhkl. The principal difference from the measurement on a single crystal spectrometer consists in refusing to plot the reflection profile I(ω) and passing to ω-scans with a width of 3-4°, which allows the measurement of the Kα1/Kα2 doublet profile. After its processing by two independent 2D functions, coordinates of the maxima are determined, and then the 4θhkl. Angle is found based on angular sizes of the detector pixel and the difference in the coordinates of X Kα1-component reflections obtained in symmetric positions. In this approach, measurement errors are related to the accuracy of placing the detector in two symmetric positions and the correctness of processing 2D reflection profiles. In the study of reference Si and Ge single crystals in the range of 2θD angles close to 100°, UCP deviations from the theoretical values are found to not exceed 0.0004 Å, and the relative measurement accuracy is 6·10–5. The refinement of UCPs of single crystals grown in the Y2O3–Eu2O3 system by the melt-solution technique indicates the formation of the (Y1–xEux)2O3 solid solution with the x value range of 0.27-0.40. A scheme is proposed to improve the measurement accuracy when the procedure is transferred to the diffractometer with synchrotron radiation. [ABSTRACT FROM AUTHOR]

Nanotechnology has a significant impact on different fields such as medicine, information technology, energy, advanced materials, textiles, and many other new areas. In this study, the characterization of the green synthesized and chemically synthesized nanoparticle from Tribulis terrestris was studied. Yttrium nitrate hexahydrate was employed as a precursor material for the synthesis of nanoparticles. Characterization study was performed by using UV–Vis spectroscopy, FTIR, FE-SEM. For green synthesis, the peak was observed at 311 nm while for chemically synthesized nanoparticles the maximum peak absorption was seen at 239 nm. The FTIR analysis for green synthesized nanoparticles reveals the presence of three prominent peaks due to C–O stretching vibration, C–O bending vibration and Y–O vibration. Chemically synthesized nanoparticles show the presence of C–O stretching vibration, C–O bending vibration and OH-stretching. The results of SEM studies indicated the particle shape and size of chemically synthesized nanoparticles and green synthesized nanoparticles. Green synthesized Y2O3 NPs are an appropriate option for use in medicinal applications. Furthermore, detailed in vivo studies are needed to determine the safety and effectiveness of these green synthesized Y2O3 nanoparticles. [ABSTRACT FROM AUTHOR]

Topological constraint theory (TCT) and molecular dynamics simulations (MD) are utilized to study the effect of Y2O3/SiO2 substitution on the short‐ and medium‐range structures and properties in aluminosilicate glasses containing Y2O3. Experimental methods have been applied to characterize the structures of the as‐prepared glasses to verify the accuracy of MD simulations. It was found that the Y–O bond distance is around 2.38 Å and the Y average coordination number is around 5.78. The introduction of Y2O3 disrupts the Si–O and Al–O bonds in the network structure and elevates the proportion of non‐bridging oxygen. Meanwhile, the calculation results of Si–O and Al–O bond distances show Y shortens the distance between Si, Al cations and oxygen ions, improving the network structure tightness. Furthermore, the glass transition temperature (Tg), Vickers hardness (HV), and elastic modulus (E) of glass increase with the increase of Y2O3 content, while the viscosity decreases. TCT was used to analyze the relationship among glass compositions, structures, and properties, and the properties prediction models for Tg, HV, and E were established. The effectiveness of TCT prediction models was proved by the comparison between the results predicted by the models and the data reported in the literature. [ABSTRACT FROM AUTHOR]

We present magnetic characterization, charge resistivity, and optical photoluminescence measurements on amorphous yttrium iron oxide thin films (a -Y–Fe–O), with supporting comparisons to amorphous germanium (a -Ge) films. We measured magnetic properties with both SQUID magnetometry and polarized neutron reflectometry. These results not only confirm that a -Y–Fe–O is a disordered magnetic material with strong predominantly antiferromagnetic exchange interactions and a high degree of frustration, but also that it is best understood electrically as a disordered semiconductor. As with amorphous germanium, a -Y–Fe–O obeys expectations for variable-range hopping through localized electron states over a wide range of temperature. We also clarify the consequences of charge transport through such a semiconducting medium for non-local voltage measurements intended to probe spin transport in nominally insulating magnetic materials. We further compare non-local resistance measurements made with "quasi-dc" automated current reversal to ac measurements made with a lock-in amplifier. These show that the "quasi-dc" measurement has an effective ac current excitation with frequency up to approximately 22 Hz, and that this effective ac excitation can cause artifacts in these measurements including incorrect sign of the non-local resistance. This comprehensive investigation of non-local resistance measurements in a -Y–Fe–O shows no evidence of spin transport on micrometer length scales, which is contrary to our original work, and in line with more recent investigations by other groups. [ABSTRACT FROM AUTHOR]

This report presents a new application for yttrium oxide (YOX) in the modification of carbon paste electrodes with excellent electroactivity for the independent detection of dopamine (DA) and ascorbic acid (AA). The surface of the YOX‐modified electrode was characterized with SEM and EDS. The electroactive properties of DP and AA were studied with cyclic voltammetry (CV), square wave voltammetry (SWV) and amperometry (Am). The activity of DA and AA increased by more than 100 % when YOX/CPE was used, which allowed us to obtain detection limits of 0.04 and 0.06 μmol/L for DA and AA, respectively. The usefulness of YOX/CPE was tested with real human urine, fresh orange juice and vitamin C tablets, and the results were acceptable. [ABSTRACT FROM AUTHOR]

Yttrium oxide (Y2O3)$( {{{\mathrm{Y}}}_2{{\mathrm{O}}}_3} )$ has the potential to be used as a host material for creating polycrystalline transparent ceramics (PTCs). This paper presents an experimental study on opto‐electrical properties of Y2O3${{\mathrm{Y}}}_2{{\mathrm{O}}}_3$ using zirconium oxide (ZrO2)$( {{\mathrm{ZrO}}_2} )$ and lanthanum oxide (La2O3)$({\mathrm{La}}_2{{\mathrm{O}}}_3)$ as sintering aids via the co‐precipitation technique. The sintering aids improve the properties, sintering process, and lower the sintering temperature. Five different compositions of Y2O3(((Y1−xZr0.02Lax)2O3),wherex=0,3,6,and9at.%)${{\mathrm{Y}}}_2{{\mathrm{O}}}_3\ ( {({{( {{{\mathrm{Y}}}_{1 - x}{\mathrm{Zr}}_{0.02}{\mathrm{La}}_x} )}}_2{{\mathrm{O}}}_3} ),{\mathrm{\ where\ }}x = 0,\ 3,\ 6,{\mathrm{\ and\ }}9{\mathrm{\ at}}.{\mathrm{\% }})$ were synthesized and they were then used to analyze for their structural, morphological, physio‐chemical, and electrical characteristics. For the system studied, the addition of ZrO2${\mathrm{ZrO}}_2$ and La2O3${\mathrm{La}}_2{{\mathrm{O}}}_3$ does not change the phase of pure Y2O3${{\mathrm{Y}}}_2{{\mathrm{O}}}_3$, but an increase in the crystal and grain size from 31.2$31.2$ to 42.5nm$42.5{\mathrm{\ nm}}$ and 10.2 µm to 16.4 µm was noticed. The thermal characterization over thermogravimetric analysis/differential thermal calorimetry (TGA/DSC) determines the temperature at which pure Y2O3${{\mathrm{Y}}}_2{{\mathrm{O}}}_3$ undergoes a phase transition, specifically over 700°C. A reduction in the band gap due to strain induced by the dopant resulted in a decrease in energy from 5.54$5.54$ to 4.8eV$4.8{\mathrm{\ eV}}$. The dielectric constant of Y2O3${{\mathrm{Y}}}_2{{\mathrm{O}}}_3$ doped with 9at.%La$9{\mathrm{\ at}}.{\mathrm{\% \ La}}$ exhibits a significant increase of ∼50%${\sim}50\%$. [ABSTRACT FROM AUTHOR]

This study systematically investigated the influence of varying yttrium(Y) additions on the interfacial reaction mechanism between the DD5 superalloy melt and Al 2 O 3 -based ceramic molds during directional solidification. The analysis revealed the formation of a complex multilayer reaction layer at the alloy-ceramic interface. The interfacial products changed from CaO·6Al 2 O 3 to a mixture of various yttrium oxides after Y was added. As the reaction time increased, the sequence of interfacial reaction products observed on the surface of Y-containing alloys progressed as follows: Y 2 O 3 , Y 4 Al 2 O 9 , YAlO 3 , and ultimately Y 3 Al 5 O 12. Increasing the Y additions promoted the formation of a reaction layer with a higher atomic percentage of Y. The interfacial reaction process between the DD5 superalloy and Al 2 O 3 -based ceramic molds involved ceramic decomposition and diffusion, Y element diffusion and displacement reactions, Al 2 O 3 dissolution and further diffusion of the Al element. This process resulted in the formation of different yttrium-aluminum oxides and related to the bidirectional erosion of the Y 2 O 3. These interfacial reactions significantly contributed to the consumption of Y element within the alloy. • Components of multilayer interfacial reaction layer varied with the Y additions. • The phases and microstructures of Y 2 O 3 , Y 4 Al 2 O 9 , YAlO 3 , and Y 3 Al 5 O 12 , were determined. • Four oxidation reaction products formed sequentially with extended reaction time. • The reaction involved dissolution, diffusion, displacement and dual erosion. [ABSTRACT FROM AUTHOR]

Engineering plastics, such as polyoxymethylene (POM), are high-performance thermoplastics designed to withstand high temperature or mechanical stress and are used in electronic equipment, the automotive industry, construction, or specific household utensils. POM is immiscible with other plastics but due to a low volume of production, no methods were developed to separate it from the residual plastic waste stream. Therefore, POM recycling is minimal despite its high market value. This paper provides a proof of concept for tracer-based sorting (TBS) as a potential solution for increasing the separation efficiency of low-volume, high-quality polymers. For this purpose, yttrium oxide (Y2O3) and cerium (IV) oxide (CeO2) have been embedded into the POM matrix. Mechanical tests of samples at varying concentrations (0.1 to 1000 ppm) of both tracers were conducted, followed by an analysis of detectability and dispersibility using a portable X-ray fluorescence spectrometer (p-XRF), subsequently optimizing detection time and tracer concentration. Finally, an experimental scenario was developed to test the fate and potential recovery of the tracer material after the thermal treatment of plastics. A low detectable concentration, short measurement time, low influence on mechanical parameters of the compound, and low loss ratio after simulated recycling prove Y2O3 to be a suitable tracer for the industrial implementation of TBS. [ABSTRACT FROM AUTHOR]

Photoacoustic (PA) is an infrequent form of spectroscopy where electromagnetic light waves directly interact with the molecules and an acoustic wave is produced. The absorbed energy is measured by detecting the pressure fluctuations in enclosed air volume. For this experiment, we have fabricated a PA cell and executed parametric studies for maximum sensitivity of its performance. The optimum inert cavity volume is found to be 84.3 × 10−7 m3 for maximum signal. Also, we have designed a pre-amplifier circuit and optimized it for desired frequency response by changing its basic components. Whole setup of the spectrosmeter was optimized using lamp carbon black as a reference sample. Finally, we have measured the thermal diffusivity of Yttrium oxide using PA spectroscopy and it is found to be 6.52 × 10−6 m2/s. [ABSTRACT FROM AUTHOR]

Hydrogen production from the decomposition of ammonia is one of the promising methods to solve the problem of hydrogen storage and transportation. Currently, ruthenium‐based catalysts are widely recognized as highly active catalysts for ammonia decomposition reactions. Here, Ru nanoparticles (NPs) on yttrium oxide derived from yttrium carbonate precursor (c‐Y2O3) was successfully prepared by the impregnation method. A hydrogen production rate up to 31.5 mmol gcat−1 min−1 can be obtained over the 5% Ru/c‐Y2O3 catalyst at 450 °C with a weight hour space velocity (WHSV) of 30000 mL gcat−1 h−1, and the activity is stable during a test period of 120 h. The catalysts were characterized by a series of techniques such as TEM, CO‐chemisorption, XPS, and CO2‐TPD. Characterization results reveal that high metal dispersion of Ru NPs, strong metal support interaction, high concentration of oxygen vacancies, and suitable basicity of Ru/c‐Y2O3 catalyst all strongly influence on the catalytic performance in ammonia decomposition. NH3 temperature‐programmed surface reaction (NH3‐TPSR) results indicate that a strong NH3 adsorption activation and binding desorption of nitrogen ability on the surface of Ru/c‐Y2O3 catalysts are also beneficial for the high activity. These results provide a reference for the design of efficient Ru‐based ammonia decomposition catalysts for hydrogen production by tuning the precursor of Y2O3 support. [ABSTRACT FROM AUTHOR]

The aqueous room temperature mono-dehydration of sugar alcohols (D-sorbitol and D-mannitol) was conducted using functionalized yttrium oxide nanocatalysts prepared via sol-gel methods. Materials exhibited high selectivity to mono-dehydration products. Solvent and catalyst effects were also investigated and discussed. The introduction of titanium into the yttrium oxide framework would decrease both substrate conversion and mono-dehydration efficiency. In addition, studies of the catalytic mechanism indicate high mono-dehydration efficiency may come from the stability of the formed intermediate during catalysis. This work provides a highly efficient and benign system for catalytic mono-dehydration of sugar alcohols. [ABSTRACT FROM AUTHOR]

ABSTRACT Objective Materials and Methods Results Conclusion Clinical Significance The purpose of this in vitro study was to evaluate the effect of staining, glazing, and polishing on the survival probability of monolithic crowns manufactured with preshaded stabilized zirconia with 5 mol% of yttrium oxide (5Y‐TZP).Monolithic crowns in the shape of an upper canine (1.5 mm of thickness) were manufactured by CAD/CAM, adhesively cemented on metallic foundation, and divided into 6 groups (n = 21): C (control), S (staining), G (glazing), P (polishing), SG (staining and glazing), and SP (staining and polishing). The survival probability was determined by step‐stress accelerated life testing with a load applied to the palatine concavity of the crown. First, the specimens were subjected to a single‐load to fracture test (SLF) and next to the fatigue test (5 Hz, thermocycling immersed in water varying 5–55°C), including the light (n = 9), moderate (n = 6), and aggressive (n = 3) loading profiles (load ranged between 20% and 60% of SLF). The survival probability was calculated considering the cycles for failure (CFF) and fatigue failure load (FFL) and illustrated using a Kaplan–Meier graph. The comparison among groups was performed using a Log‐Rank test (α = 0.05).The mean value of SLF was 586.7 N. There was no difference among groups in survival probability, considering CFF and FFL.Staining, glazing, and polishing can be performed safely without damaging the mechanical behavior of 5Y‐TZP monolithic crowns.Staining is used to characterize and improve the esthetic of zirconia monolithic crowns. It can be used to reproduce the color gradient in the cervical region of the crown and pigmented grooves. This study showed that staining, glazing, and polishing did not affect the survival probability and the use of finishing procedures (glazing or polishing) after staining did not improve the survival probability of zirconia monolithic crowns. [ABSTRACT FROM AUTHOR]

In this paper, high transmittance glass-ceramics containing Zirconium Yttrium Oxide (Zr 0.82 Y 0.18 O 1.91) nanocrystals were successfully prepared by melt cooling and crystallization heat-treatment method. The effects of Y 2 O 3 concentration on the structure, crystallization performance, transmittance, and indentation fracture toughness of Na 2 O–Al 2 O 3 –B 2 O 3 –SiO 2 –ZrO 2 glass and glass-ceramics were explored. The addition of Y 2 O 3 improved the Vickers hardness (4.81 GPa–5.25 GPa) and indentation fracture toughness (0.78 MPam1/2 to 0.95 MPam1/2) of the glasses. Y 2 O 3 successfully facilitated the precipitation of the non-alkaline crystalline phase Zr 0.82 Y 0.18 O 1.91 at low heat-treatment temperatures. The precipitation of Zr 0.82 Y 0.18 O 1.91 nanocrystals improves the Vickers hardness (5.17 GPa–5.56 GPa) and indentation fracture toughness (0.90 MPam1/2 to 1.01 MPam1/2) in glass-ceramics, while concurrently preserving a high level of visible light transmittance (∼90 %). This demonstrates its potential applications in the field of protective covers for electronic displays. [ABSTRACT FROM AUTHOR]

WC-Co composites are widely used in cutting tools but are expensive and harmful due to Co in the composites. Alternatives, such as WC-Ni composites have inferior mechanical properties, as a result, WC-Co composites are used in most cutting tools. This study investigated whether adding yttrium oxide (Y2O3) to WC-Ni composites, fabricated from recycled tungsten carbide (WC) and Ni, improved their mechanical properties. Changes in the composites' microstructure and mechanical properties depended on the amount of Y2O3 added. Y2O3 reacted with WC during sintering, promoting the formation of W and reducing the proportion of C in the composite. The added Y2O3 accelerated the dissolution of W in the Ni matrix, and increased the fractions of the eta phase and solid solution phase. Ni is strengthened by the dissolution of W in Ni, thereby supplementing the low toughness of the eta phase and ultimately yielding WC – Ni with improved hardness and fracture toughness (HV: max. 15.4 GPa, KIC: max. 13.4 MPa∙m1/2) compared to WC – Ni without Y2O3 (HV: 13.5 GPa, KIC: 12.7 MPa∙m1/2). The method for improving the properties of WC – Ni composites by the addition of Y2O3 has a high possibility of commercialization because it does not necessitate process changes. [ABSTRACT FROM AUTHOR]

Purpose: The sintering technique and cooling strategy influence the strength of zirconia. This study examined the impact of altering the cooling rate of glass‐infiltrated monolayer and multilayer 5 mol% yttria‐partially stabilized zirconia (5Y‐PSZ) on their strength. Materials and Methods: One‐hundred eighty (180) specimens (width × length × thickness = 10 × 20 × 2 mm) were prepared using monolayer (Mo: Cercon‐xt) and multilayer (Mu: Cercon‐xt ML) 5Y‐PSZ. Randomly distributed specimens (n = 15/group) were sintered with traditional (T) versus glass infiltrated (G) technique and cooled down with different cooling rates: slow (S: 5°C/min), normal (N: 35°C/min), and fast (F: 70°C/min). Four‐point bending test was used to measure flexural strength (σ). Microstructures were investigated by scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), and X‐ray diffraction (XRD). Three‐way ANOVA and Tamhane comparisons were determined for a significant difference of σ (p < 0.05). Weibull analysis was determined for Weibull modulus (m). Results: The highest σ (MPa) was seen for GMuS (696.8 ± 69.8). Mo‐PSZ and Mu‐PSZ showed no significant difference in σ. G‐sintering presented significantly higher σ (659.9 ± 79.3) than T‐sintering (426.0 ± 63.7). S‐cooling (560.9 ± 126.1) had the highest σ. The highest m‐value was observed in GMuN (12.1 ± 3.8). A significant difference in σ was indicated due to cooling rates and sintering techniques (p < 0.05). Conclusions: Glass infiltration significantly enhanced strength through elastic gradience. F‐cooling reduced grain size, impaired grain boundary integration, and increased the tetragonal to monoclinic phase transition, significantly decreasing flexural strength in traditional sintering. Nevertheless, F‐cooling was recommended for glass‐infiltrated 5Y‐PSZ to enhance strength while reducing processing time. [ABSTRACT FROM AUTHOR]

There is a high demand for plasma-resistant coatings that prevent the corrosion of the internal ceramic components of plasma etching equipment, thereby reducing particle contamination and process drift. Yttrium oxyfluoride (YOF) coatings were prepared using atmospheric plasma spraying (APS) with commercially available YOF/YF3 powder mixtures; namely YOF 3%, YOF 6%, and YOF 9%. The etching behaviour of YOF and yttrium oxide (Y2O3) coatings was investigated using an inductively coupled plasma consisting of NF3/He. X-ray photoelectron spectroscopy (XPS) showed that the YOF 6% coating had the thickest fluorinated layer. The scanning electron microscope (SEM) examination revealed that the YOF 6% coating showed exceptional resistance to erosion and generated a reduced quantity of contaminated particles in comparison to Y2O3. Consequently, it is more suitable as a protective material for the inner wall of reactors. The YOF coatings exhibit excellent stability and high resistance to erosion, indicating their appropriateness for use in the semiconductor industry. [ABSTRACT FROM AUTHOR]

Yttrium oxide (Y2O3) is a promising rare-earth compound that is rarely studied. This study reports on the synthesis, structural, morphological, optical and antimicrobial properties of Y2O3 nanoparticles (NPs) synthesized using Agathosma betulina leaf extract. XRD pattern indicated that the crystalline phase was achieved for the sample calcined at 5 0 0 ∘ C with body-centered cubic symmetry. SEM and TEM images of Y2O3 nanopowder showed the nearly spherical morphology of agglomerated NPs with an average diameter of 13 nm. Optical properties revealed that the bandgap of Y2O3 NPs (∼ 5. 6 7 eV) has been increased compared with the bulk Y2O3 (∼ 5. 5 eV). Moreover, the antimicrobial activity was also evaluated against gram-positive and gram-negative bacteria of clinical interest. Results demonstrated that the synthesized Y2O3 NPs exhibited higher bacteriostatic effects against gram-negative bacterial strains due to their thin cell wall structure. These results show that the synthesized Y2O3 NPs are suitable for antibacterial control systems and medicines. [ABSTRACT FROM AUTHOR]

Yttrium oxide (Y 2 O 3) nanoparticles have critical applications in many industries, including ceramics, optics, and biomedicine. However, conventional synthesis methods are typically cumbersome and time-consuming. Herein, a novel emulsion detonation method successfully achieved the one-step synthesis of Y 2 O 3 nanoparticles. In this method, yttrium nitrate hexahydrate was uniformly dispersed in the emulsion explosive as a precursor and an auxiliary oxidizer. After the emulsion explosive was detonated in a detonation chamber, the detonation products were collected, purified and characterized by X-ray diffraction, Fourier transform infrared spectrometer, Raman spectrometer, X-ray photoelectron spectroscopy, field emission scanning electron microscopy, field emission transmission electron microscopy, and ultraviolet spectrophotometer. The results show that the as-synthesized powders are high-purity cubic phase yttrium oxide nanoparticles with a spherical-like morphology and an average particle size of approximately 30 nm. These Y 2 O 3 nanoparticles have a wide (5.53 eV) energy band gap, close to the conventional methods. Based on detonation theory, thermochemical theory, and characterization results, this text discussed the mechanism of the Y 2 O 3 nanoparticles synthesized by the emulsion detonation method. During detonation, the formation of the Y 2 O 3 nanoparticles underwent three stages: the formation of the Y 2 O 3 molecules by the collision of Y and O ions, the formation of the crystal nucleus at supersaturation concentration, and crystal growth. This study provides a novel, cost-effective method for efficiently synthesizing Y 2 O 3 nanoparticles. [ABSTRACT FROM AUTHOR]

This study focused on synthesizing a cellulose-based hydrogel nanocomposite as a green hydrogel by adding a microcrystalline cellulose (MC) solution to carboxymethyl cellulose sodium (CMC-Na) with citric acid as a cross-linker. Y2O3 nanoparticles were incorporated during hydrogel preparation in different ratios (0.00% (0 mmol), 0.03% (0.017 mmol), 0.07% (0.04 mmol) and 0.10% (0.44 mmol)). FTIR analysis confirmed the cross-linking reaction, while XRD analysis revealed the hydrogels' amorphous nature and identified sodium citrate crystals formed from the reaction between citric acid and CMC-Na. The swelling test in deionized water (pH 6.5) at 25 °C showed a maximum swelling percentage of 150% after 24 h in the highest nanoparticle ratio. The resulting cellulose hydrogels were flexible and exhibited significant antibacterial activity against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). The synthesized cellulose-based hydrogel nanocomposites are eco-friendly and suitable for medical applications. [ABSTRACT FROM AUTHOR]

Green nanoparticles are synthesized using environmentally friendly methods, and natural materials hold significant importance. This makes the process environmentally sustainable and reduces the production of harmful waste by-products. Green nanoparticles exhibit reduced toxicity which is crucial for biomedical applications. The current study suggested that yttrium nanoparticles (YNPs) should be synthesized, characterized, and evaluated for their diverse biological applications due to the rise in antibacterial resistance. The YNPs were prepared using a pine needle leaf extract (PNLE). The structural and morphological features have been investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), and vibrating sample magnetometry (VSM). The XRD pattern demonstrated the presence of yttrium oxide and yttrium nitrate phases. The crystallite size and particle size of the synthesized YNPs measured 1.696 nm and 24.55 nm, respectively. The XPS peaks showed two components with binding energies at 530.940 eV and 532.18 eV due to the bond between O–Y and OH–Y, respectively. Additionally, the ferromagnetic nature of the YNPs was confirmed by VSM analysis. The YNPs were tested for antibacterial activity on six uropathogenic bacteria (S. aureus, S. haemolyticus, E. faecalis, E. coli, K. pneumonia, and P. aeruginosa) using the microdilution assays, to find the minimum inhibitory concentration (MIC) as well as the minimum bactericidal concentration (MBC), the agar well diffusion assay, and antibiofilm screening assays, where they showed bacteriostatic action against all isolates (0.5–1 mg/mL MIC) and significant inhibition of biofilm formation (80% inhibition rate). The antioxidant capacity assessed by 1,1, diphenyl-2-picrylhydrazyl (DPPH) radical scavenging revealed 50% DPPH scavenging. Moreover, docking studies exhibited that YNPs inhibit crucial bacterial enzymes, including DNA gyrase, penicillin-binding proteins, carbapenemase, LasR-binding protein, and dihydropteroate synthase. These findings may explain the mechanisms responsible for the observed antibacterial effects of YNPs. Overall, these findings underscore YNPs as promising candidates for antioxidant and antibacterial applications. [ABSTRACT FROM AUTHOR]

Low-dimensional yttrium oxide (Y2O3) nanostructures have garnered significant research interest due to their intriguing properties arising from the dimensional effect and the modulation of the band structure. However, the simple preparation of Y2O3 nanosheets is rarely investigated due to the inherent limitations posed by the counterpart bulk cubic or monoclinic crystal structure. Herein, the low-dimensional layered Y2O3 nanosheets are prepared by a facile route of rapid heating followed by centrifugation, in which its corresponding hydrous-chloride compound is used as the sole reagent. The formation stages of layered Y2O3 nanosheets and corresponding mechanisms are elucidated in detail. The x-ray diffraction results confirm that the intermediate product after rapid heating is yttrium oxychloride (YOCl), which converts to the single-phase Y2O3 with a 2D layered phase after centrifugation. In addition, the obtained Y2O3 nanosheets possess a direct optical bandgap of 5.49 eV, and thus may hold promise for use in electronic applications. This research provides a facile and low-cost method for the preparation of other low-dimensional nanosheets with similar structures. [ABSTRACT FROM AUTHOR]

CO2 methanation is an effective strategy for making full use of waste gases and converting them into valuable chemicals. Nowadays, the key challenge is the design of efficient catalysts to enhance low-temperature catalytic performance. The present work studies the effect of metal type on the catalytic performance of yttrium oxide-supported catalysts for CO2 methanation reaction. Ru/Y2O3, Ni/Y2O3, and Co/Y2O3 catalysts were prepared by wetness incipient impregnation method, characterized using N2-adsorption/desorption isotherm, XRD, FTIR, and H2-TPR and TGA techniques to evaluate the surface, crystal phase, and thermal stability. The catalytic test was conducted with the use of a fixed-bed reactor under atmospheric pressure. The temperature of catalytic performance was 350 °C with a supply of H2: CO2 molar ratio of 4 and a total flow rate of 200 mL/min. The main products of the reaction were CH4, and traces of carbon monoxide were present among the products. The methane yield reached 64.67%, 60.03%, and 50.82% over Ru/Y2O3, Ni/Y2O3, and Co/Y2O3 catalysts, respectively. [ABSTRACT FROM AUTHOR]

In this study, Y2O3 coating is used as an interlayer between Al2O3 substrate and a ceramic coating; this is in order to minimize the morphological distortion produced by a single deposition of the ceramic coating on the Al2O3 substrate, which is performed using the aerosol method. The interlayer coating, which comprises the Y2O3 phase, is deposited on the Al2O3 substrate using an e-beam evaporator. The crystal structure of the powder that was used to process the coating is identified as cubic Y2O3. In contrast, the crystal structure of the top-coating layer and interlayer indicates the presence of two kinds of Y2O3 phases, which possess cubic and monoclinic structures. The single Y2O3 coating without an interlayer exhibits microcracks around the interface between the coating and the substrate, which can be attributed to the stress that occurs during aerosol deposition. In contrast, no cracks are found in the aerosol-deposited Y2O3 coating and interlayer, which show a desirable microstructure. The single Y2O3 coating and the Y2O3 coating with an interlayer exhibit similar hardness and elastic modulus values. Nevertheless, the Y2O3 coating with an interlayer exhibits a higher level of adhesion than the single Y2O3 coating, with a value of 14.8 N compared to 10.2 N. [ABSTRACT FROM AUTHOR]

Synthesis and characterization of a Dy3+-activated calcium yttrium oxide (CaY2O4) phosphor are reported. The CaY2O4:Dy3+ (1.5 mol%) phosphor is synthesized using a modified solid-state reaction technique for calcination and sintering. The cubic structure is revealed by the X-ray diffraction technique. The morphology and particle size distribution of the prepared phosphor are investigated by the FEGSEM technique. The chemical bonds and functional group analysis are confirmed by the FTIR. A photoluminescence analysis of the CaY2O4:Dy3+ phosphor shows dual excitation wavelengths at 285 and 348 nm, especially in the ultraviolet region. At 383 nm, three distinct emission peaks are found at the wavelengths 238, 485, and 571 nm. The spectroscopic parameters are calculated using the CIE chromaticity coordinates. The CIE coordinates of the Dysprosium ion-activated CaY2O4 phosphor (1.5 mol%) show an emission near the white light region of the chromaticity diagram, suggesting that it is suitable for W-LED applications. [ABSTRACT FROM AUTHOR]

The utilization of 3D printing technology for the fabrication of intricate transparent ceramics overcomes the limitations associated with conventional molding processes, thereby presenting a highly promising solution. In this study, we employed direct ink writing (DIW) to prepare yttrium oxide transparent ceramics using a ceramic slurry with excellent moldability, solid content of 45 vol%, and shear-thinning behavior. A successfully printed transparent yttrium oxide ring measuring 30 mm in diameter, 10 mm in inner diameter, and 0.9 mm in thickness was obtained from the aforementioned slurry. After de-binding and sintering procedures, the printed ceramic exhibited in-line transmittance of 71% at 850 nm. This work not only produced complex yttria transparent ceramics with intricate shapes, but also achieved in-line transmittance that was comparable to that of the CIP method (79%), which can meet certain optical applications. [ABSTRACT FROM AUTHOR]

In recent years, multifunctional applications of the same material have gained wide recognition in various fields. The present study reports the synthesis, characterization, and multifunctional applications of europium (Eu)‐doped yttrium oxide (Y2O3) nanophosphor. Synergistic optimization of Eu‐doped Y2O3 results in enhanced photoluminescence (PL) and triboelectric nanogenerator (TENG) performance. Eu‐doped Y2O3 nanophosphors are synthesized using an autocombustion method, and comprehensive characterizations are conducted. The investigations indicate that the Eu doping significantly influences the PL intensity, with the highest emission observed at 3 mol% for powders. The synthesized nanophosphors are blended with silicone to fabricate hybrid films, which are utilized for energy harvesting applications using TENG technology. The TENG devices fabricated with these hybrid films demonstrate a notable relationship between the Eu concentration and the electrical output, achieving peak performance at 1 mol% Eu doping. The maximum output voltage of ≈535 V, short‐circuit current of ≈38 μA, and power density of 800 mW m−2 are observed. Further, TENG is demonstrated in a self‐powered UV photodetector application. The present results contribute to the improvement of sustainable energy technologies and open up a new window for multifunctional materials. [ABSTRACT FROM AUTHOR]

This study presents significant advancements in passive radiative cooling (PRC), achieved using assembled hollow yttrium oxide spherical particles (AHYOSPs). We developed PRC films with enhanced optical properties by synthesizing micro-sized hollow Y2O3 particles and integrating them into a polydimethylsiloxane (PDMS) matrix. The findings revealed that AHYOSPs achieved a remarkable solar reflectance of 73.72% and an emissivity of 91.75%, significantly outperforming nano-sized yttrium oxide (NYO) and baseline PDMS. Field tests demonstrated that the AHYOSPs maintained their lowest temperature during daylight, confirming their superior cooling efficiency. Additionally, theoretical calculations using MATLAB indicated that the cooling capacity of AHYOSPs reached 103.77 W/m2, representing a substantial improvement over NYO and robustly validating the proposed nanoparticle assembly strategy. These results highlight the potential of structurally controlled particles to revolutionize PRC technologies, thereby offering a path toward more energy-efficient and environmentally friendly cooling solutions. [ABSTRACT FROM AUTHOR]

As a promising material for the advanced thermal barrier coatings (TBCs), scandium oxide (Sc 2 O 3) and yttrium oxide (Y 2 O 3) co-stabilized zirconia (ScYSZ) has been given increasing attention during the past decade. In this study, three types of TBCs including YSZ, ScYSZ and ScYSZ-YSZ double ceramic layer (DCL) coatings were deposited by a wide-velocity range high-energy plasma spraying technology. The thermal physical property, phase stability and thermal cycling performance of TBCs were comparatively studied. The results suggested that the thermal conductivity from 200 °C to 1000 °C of ScYSZ coating was reduced by approximately 30 % compared to the YSZ coating. After exposure at 1400 °C for 1000 h, the ScYSZ coating still kept the initial tetragonal phase structure, while the tetragonal phase was completely disappeared in the YSZ coating after 300 h at 1400 °C. Notably, the ScYSZ-YSZ DCL coating demonstrated the highest thermal cycling life within the temperature range of 1320∼1370 °C, exhibiting a remarkable 43 % increase over the single ScYSZ coating and doubling that of the single YSZ coating. The outcomes of this study hold significant promise for practical applications in the realm of high-performance TBCs. [ABSTRACT FROM AUTHOR]

The precise synthetic control of yttrium oxide (Y 2 O 3) nanotube morphology is essential for their practical application. A comprehensive investigation into the growth mechanisms of these nanotubes is crucial for directing the regulation of their morphology. In this study, Y 2 O 3 nanotubes were successfully synthesized. The morphological evolution was characterized through scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and selected area electron diffraction (SAED), which elucidated the growth mechanism underlying the transformation from Y 4 O(OH) 9 (NO 3) nanosheets to nanotubes. The initiation of this process involves lattice distortions within the nanosheets, resulting in a spontaneous curling phenomenon driven by the minimization of surface energy. The presence of NaOH in the reaction milieu initiates a topotactic transformation, resulting in the conversion of the Y 4 O(OH) 9 (NO 3) nanosheets into Y(OH) 3 nanotubes. Subsequent calcination induces a phase transition from hexagonal Y(OH) 3 to cubic Y 2 O 3 phases, while preserving the tubular structure. These findings offer strategic insights into the controlled synthesis of nanomaterials. [ABSTRACT FROM AUTHOR]