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Osteochondral tissue is a highly specialized and complex tissue composed of articular cartilage and subchondral bone that are separated by a calcified cartilage interface. Multilayered or gradient scaffolds, often in conjunction with stem cells and growth factors, have been developed to mimic the respective layers for osteochondral defect repair. In this study, we designed a hyaline cartilage-hypertrophic cartilage bilayer graft (RGD/RGDW) with chondrocytes. Previously, we demonstrated that RGD peptide-modified chondroitin sulfate cryogel (RGD group) is chondro-conductive and capable of hyaline cartilage formation. Here, we incorporated whitlockite (WH), a Mg2+-containing calcium phosphate, into RGD cryogel (RGDW group) to induce chondrocyte hypertrophy and form collagen X-rich hypertrophic cartilage. This is the first study to use WH to produce hypertrophic cartilage. Chondrocytes-laden RGDW cryogel exhibited significantly upregulated expression of hypertrophy markers in vitro and formed ectopic hypertrophic cartilage in vivo, which mineralized into calcified cartilage in bone microenvironment. Subsequently, RGD cryogel and RGDW cryogel were combined into bilayer (RGD/RGDW group) and implanted into rabbit osteochondral defect, where RGD layer supports hyaline cartilage regeneration and bioceramic-containing RGDW layer promotes calcified cartilage formation. While the RGD group (monolayer) formed hyaline-like neotissue that extends into the subchondral bone, the RGD/RGDW group (bilayer) regenerated hyaline cartilage tissue confined to its respective layer and promoted osseointegration for integrative defect repair.

We investigated the effects of Co doping on Pr0.7Ca0.3MnO3−d in the perspective of an oxygen-bonding state change. In all compositions, Pr0.7Ca0.3Mn1−xCoxO3−d (PCMCx, x = 0, 0.1, 0.2, 0.3) showed an orthorhombic structure, and the lattice gradually contracted with increasing Co content. The doped Co was mostly present as 2+ and 3+, which decreased the average oxidation value of the B site and created oxygen vacancies for charge compensation. However, as the Co content increased, the proportion of Co3+ increased, and the content of oxygen vacancies gradually decreased. In addition, the ratio of adsorbed oxygen in PCMC0.1 was the highest, and the B-O covalency was enhanced. Accordingly, the electrochemical reaction of oxygen with the cathode material in PCMC0.1 could occur most easily, showing the smallest polarization resistance among the Co-doped Pr0.7Ca0.3MnO3−d. We can confirm the formation of oxygen vacancies via Co doping and the effect of B-O covalency on the oxygen-reduction reaction of Pr0.7Ca0.3MnO3−d.

This study investigates the electrical and mechanical properties of a Lu2O3–Y2O3–ZrO2 system (ZrO2 co-doped with Lu2O3 and Y2O3) and evaluates its possibility for use as a high-performance oxygen-ion conducting ceramic suitable for intermediate/high-temperature solid electrolytes. The use of electrochemical impedance spectroscopy (EIS) in the analysis and fitting of AC impedance spectra arcs on 8 mol% (Lu2O3–Y2O3)– ZrO2 has allowed to compare with the Y2O3-doped ZrO2 (YSZ) and Sc2O3-doped ZrO2 (ScSZ). (ZrO2)0.92(Y2O3)0.07(Lu2O3)0.01, with 1 mol% Lu2O3 co-doped with Y2O3, shows a bulk conductivity of 9.60 × 10−1 S/cm at 1000 °C and 3.47 × 10−2 S/cm at 800 °C, which are least several times higher than the corresponding values of any other sample in the experimental group, including Sc2O3-doped ZrO2, over the entire measured temperature range. (ZrO2)0.92(Y2O3)0.075(Lu2O3)0.005 also shows an outstanding conductivity; over two times higher than that of ScSZ. Thus, Lu2O3 co-doping can enhance mechanical properties such as flexural strength (19.5 % (1 mol% Lu2O3) and 21.5 % (2 mol% Lu2O3) higher than that of YSZ), as confirmed by the flexural strength and Vickers hardness tests. After 8 mol% sesquioxide doping of YSZ, the maximum improvement in the electrical and mechanical properties occurs at approximately 1 mol% (for electrical properties) and 2 mol% (for mechanical properties) Lu2O3 co-doping, respectively. The results of this work suggest that a small amount of Lu doping, performed during the development of materials for use in electrochemical devices (including high-efficiency energy conversion apparatus), could be a considerable approach to overcome the limitations of conventional solid oxide electrolytes.

Uncrewed aerial vehicles (UAVs) have become a vital element in nonterrestrial networks, especially with respect to 5G communication systems and beyond. The use of UAVs in support of 4G/5G base station (uncrewed aerial vehicle base station [UAV-BS]) has proven to be a practical solution for extending cellular network services to areas where conventional infrastructures are unavailable. In this study, we introduce a UAV-BS system that utilizes a high-capacity wireless backhaul operating in millimeter-wave frequency bands. This system can achieve a maximum throughput of 1.3 Gbps while delivering data at a rate of 300 Mbps, even at distances of 10 km. We also present the details of our testbed implementation alongside the performance results obtained from field tests.

For several years, a growing interest among numerous researchers and investors in predicting stock price movements has spurred extensive exploration into employing advanced deep learning models. These models aim to develop systems capable of comprehending the stock market’s complex nature. Despite the immense challenge posed by the diverse factors influencing stock price forecasting, there remains a notable lack of research focused on identifying the essential feature set for accurate predictions. In this study, we propose a Dynamic Feature Selection System (DFSS) to predict stock prices across the 10 major industries, as classified by the FnGuide Industry Classification Standard (FICS) in South Korea. We apply 16 feature selection algorithms from filter, wrapper, embedded, and ensemble categories. Subsequently, we adjust the settings of industry-specific index data to evaluate the model’s performance and robustness over time. Our comprehensive results identify the optimal feature sets that significantly impact stock prices within each sector at specific points in time. By analyzing the inclusion ratios and significance of the optimal feature set by category, we gain insights into the proportion of feature classes and their importance. This analysis ensures the interpretability and reliability of our model. The proposed methodology complements existing methods that do not consider changes in the types of variables significantly affecting stock prices over time by dynamically adjusting the input variables used for learning. The primary goal of this study is to enhance active investment strategies by facilitating the creation of diversified portfolios for individual stocks across various sectors, offering robust models and feature sets that consistently demonstrate high performance across industries over time.

We investigated the impact of CaCO3 addition on the density and compressive strength of calcium aluminate cement (CAC)-based cementitious materials in binder jetting additive manufacturing (BJAM). To confirm the formation of a uniform powder bed, we examined the powder flowability and powder bed density for CaCO3 contents ranging from 0 to 20 wt.%. Specifically, powders with avalanche angles between 40.1–45.6° formed a uniform powder bed density with a standard deviation within 1%. Thus, a 3D printing specimen (green body) fabricated via BJAM exhibited dimensional accuracy of less than 1% across the entire plane. Additionally, we measured the hydration characteristics of CAC and the changes in compressive strength over 30 days with the addition of CaCO3. The results indicate that the addition of CaCO3 to CAC-based cementitious materials forms multimodal powders that enhance the density of both the powder bed and the green body. Furthermore, CaCO3 promotes the formation of highly crystalline monocarbonate (C4AcH11) and stable hydrate (C3AH6), effectively inhibiting the conversion of CAC and showing compressive strengths of up to 5.2 MPa. These findings suggest a strong potential for expanding the use of BJAM across various applications, including complex casting molds, cores, catalyst supports, and functional architectural interiors.

Many birds develop brood patches on their ventral apterium under hormonal regulation to effectively transmit body heat to eggs during incubation. The developed patch has several characteristics, including de-feathering, vascularization, and edema. However, little is known about whether avian brood parasites that do not incubate their eggs exhibit brood patch development during the breeding season. In this study, we measured the size of the ventral apterium in 114 Common Cuckoos (Cuculus canorus) captured in the field throughout the breeding season and examined the appearance of the ventral apterium to confirm the development of brood patches. We also examined whether morphological traits and various factors correlated with the size of the ventral apterium (sternal apterium and abdominal apterium) and how it changed during the breeding season. We found no clear signs of brood patch development in Common Cuckoos captured throughout the breeding season, indicating that they likely did not develop brood patches on the ventral apterium during this period. We also found that ventral apterium size was positively correlated with wing length and body weight. In addition, Common Cuckoos with newly growing feathers on the boundary of the ventral apterium with pteryla were frequently observed as seasons progressed to the end. In conclusion, Common Cuckoos exhibit neither brood patch development nor the vestigial characteristics of ancestral brood patches, except for the growth of feathers on boundary the ventral apterium. Further studies examining brood patches across different groups of avian brood parasites are valuable for enhancing our understanding of the developmental and physiological adaptations of avian brood parasites.

Geopolymers exhibit broad application prospects, including construction and radiation shielding, which require excellent mechanical performances. However, investigations on the nature of geopolymerization reactions and their consequential impact on mechanical performance are still vague. In this study, the effect of the major factors of Si/Al ratio and curing time on the geopolymerization reaction and flexural strength were studied based on the microstructure evolution and chemical bonding formation analyzed using the SEM, FTIR, peak deconvolution, and XRD methods. The microstructure of geopolymers was transferred from initially layered smooth particles of kaolinite to a 3D network porous structure, corresponding to sodalite. A spectrum exclusive to the geopolymer structure occurred at 973 cm−1, corresponding to the sodium aluminum silicate hydrate (N-A-S-H) links, the integral area of which represents the degree of geopolymerization reaction. Furthermore, a controllable reaction degree was achieved by adjusting the Si/Al ratio and curing time, where the maximum reaction degree of 55% was achieved at a Si/Al ratio of 1.94 when cured for 7 d. The correlation between the flexural strength and reaction degree was found to follow a proportional relationship, achieving a flexural strength of 21.11 MPa with a degree of 45%. This study provides insight into the development of mechanical strength through controlling the reaction process.

Highly selective etching of silicon nitride (Si3N4) and silicon dioxide (SiO2) has received considerable attention from the semiconductor community owing to its precise patterning and cost efficiency. We investigated the etching selectivity of Si3N4 and SiO2 in an NF3/O2 radio-frequency glow discharge. The etch rate linearly depended on the source and bias powers, whereas the etch selectivity was affected by the power and ratio of the gas mixture. We found that the selectivity can be controlled by lowering the power with a suitable gas ratio, which affects the surface reaction during the etching process. X-ray photoelectron spectroscopy of the Si3N4 and QMS measurements support the effect of surface reaction on the selectivity change by surface oxidation and nitrogen reduction with the increasing flow of O2. We suggest that the creation of SiOxNy bonds on the surface by NO oxidation is the key mechanism to change the etch selectivity of Si3N4 over SiO2.

In this paper, we present a two-stage scalable channel estimator (TSCE), a deep learning (DL)-based scalable, and robust channel estimator for wireless cellular networks, which is made up of two DL networks to efficiently support different resource allocation sizes and reference signal configurations. Both networks use the transformer, one of cutting-edge neural network architecture, as a backbone for accurate estimation. For computation-efficient global feature extractions, we propose using window and window averaging-based self-attentions. Our results show that TSCE learns wireless propagation channels correctly and outperforms both traditional estimators and baseline DL-based estimators. Additionally, scalability and robustness evaluations are performed, revealing that TSCE is more robust in various environments than the baseline DL-based estimators.

Double buffer layers composed of (AlxGa1−x)2O3/Ga2O3 structures were employed to grow a Sn-doped α-Ga2O3 epitaxial thin film on a sapphire substrate using mist chemical vapor deposition. The insertion of double buffer layers improved the crystal quality of the upper-grown Sn-doped α-Ga2O3 thin films by blocking dislocation generated by the substrates. Rapid thermal annealing was conducted for the double buffer layers at phase transition temperatures of 700–800 °C. The slight mixing of κ and β phases further improved the crystallinity of the grown Sn-Ga2O3 thin film through local lateral overgrowth. The electron mobility of the Sn-Ga2O3 thin films was also significantly improved due to the smoothened interface and the diffusion of Al. Therefore, rapid thermal annealing with the double buffer layer proved advantageous in achieving strong electrical properties for Ga2O3 semiconductor devices within a shorter processing time.

The thermomechanical properties of carbon fiber reinforced silicon carbide ceramic matrix composites (Cf/SiC CMCs) were studied up to 2000 °C using high-temperature in situ flexural testing in argon. The CMC specimens were fabricated using an ultrahigh concentration (66 vol%) aqueous slurry containing nano-sized silicon carbide powder. The SiC powder compacts were obtained by drying the slurry and were densified using the precursor impregnation and pyrolysis (PIP) method with field assisted sintering technology/spark plasma sintering (FAST/SPS). The high relative density of the SiC green body (77.6%) enabled densification within 2.5 days using four PIP cycles. In contrast, conventional PIP processes take over 7 days. The in situ flexural strength of the Cf/SiC CMC was 434 MPa at 1750 °C, which was 84% higher than the room temperature value. The value further increased to 542 MPa at 2000 °C. Possible mechanisms to explain the excellent strength of the CMC at elevated temperatures are discussed.

The oxygen vacancy formation behavior and electrochemical and thermal properties of Ba0.5Sr0.5Fe1−xMnxO3−δ (BSFMnx, x = 0–0.15) cathode materials were investigated. For thermogravimetric analysis, the weight decreased from 1.98% (x = 0) to 1.81% (x = 0.15) in the 400–950 °C range, which was due to oxygen loss from the lattice. The average oxidation state of the B-site increased, the Oads/Olat ratio decreased, and the binding energy of the Olat peak increased with Mn doping. These results indicate that Mn doping increases the strength of the metal–oxygen bond and decreases the amount of oxygen vacancies in the lattice. The electrical conductivity of BSFMnx increased with the temperature due to the thermally activated small-polaron hopping mechanism showing a maximum value of 10.4 S cm−1 (x = 0.15) at 450 °C. The area-specific resistance of BSFMn0.15 was 0.14 Ω cm2 at 700 °C and the thermal expansion coefficient (TEC) gradually decreased to 12.7 × 10−6 K−1, which is similar to that of Ce0.8Sm0.2O2 (SDC) (12.2 × 10−6 K−1). Mn doping increased the metal–oxygen bonding energy, which reduced the oxygen reduction reaction activity but improved the electrical conductivity and thermal stability with SDC.

We doped carbon into a TiZrN coating to reduce hydrogen permeability, and investigated the phase formation, bonding state, microstructure, and surface roughness of the carbon-doped TiZrN. The laser output for laser carburization was limited to a range of 20–50%. The grain size of the TiZrN coatings decreased from 26.49 nm before carburization to 18.31 nm after carburization. For XPS analysis, the sp2/sp3 ratio was 1.23 at 20% laser output, but it showed 2.64 at 40% laser output, which means that amorphous carbon was formed. As the grain size decreased with the formation of amorphous carbon, the surface microstructure of the carbon-doped TiZrN coatings transitioned to an intergranular structure, indicating the creation of amorphous carbon-embedded (Ti, Zr)(C, N) in the coating. The surface roughness (Ra) of the carbon-doped TiZrN coating was decreased to a maximum of 7.12 nm, and the hydrogen permeability correspondingly decreased by 78% at 573 K.

We studied the influence of the ethylenediaminetetraacetic acid (EDTA) content used as combustion fuel when fabricating nickel oxide (NiO) nanocatalysts via solution combustion synthesis, as well as the growth behavior of carbon nanotubes (CNTs) using this catalyst. Nickel nitrate hexahydrate (Ni(NO3)2∙6H2O) was used as the metal precursor (an oxidizer), and the catalysts were synthesized by adjusting the molar ratio of fuel (EDTA) to oxidizer in the range of 1:0.25 to 2.0. The results of the crystal structure analysis showed that as the EDTA content increased beyond the chemical stoichiometric balance with Ni(NO3)2∙6H2O (F/O = 0.25), the proportion of Ni metal within the catalyst particles decreased, and only single-phase NiO was observed. Among the synthesized catalysts, the smallest crystallite size was observed with a 1:1 ratio of Ni ions to EDTA. However, an increase in the amount of EDTA resulted in excessive fuel supply, leading to an increase in crystallite size. Microstructure analysis revealed porous NiO agglomerates due to the use of EDTA, and differences in particle growth based on the fuel ratio were observed. We analyzed the growth behavior of CNTs grown using NiO nanocatalysts through catalytic chemical vapor deposition (CCVD). As the F/O ratio increased, it was observed that the catalyst particles grew excessively beyond hundreds of nanometers, preventing further CNT growth and leading to a rapid termination of CNT growth. Raman spectroscopy was used to analyze the structural characteristics of CNTs, and it was found that the ID/IG ratio indicated the highest CNT crystallinity near an F/O ratio of 1:1.

MnO2 and CeO2 were doped to improve the corrosion resistance of CSZ (calcia-stabilized zirconia), and we studied the phase formation, mechanical properties, and corrosion resistance by molten mold flux. The volume fraction of the monoclinic phase gradually decreased as the amount of MnO2 doping increased. The splitting phenomenon of the t(101) peak was observed in 2Mn_CSZ, and in 4Mn_CSZ, it was completely split, forming a cubic phase. The relative density increased and the monoclinic phase decreased as the doping amount increased, leading to an increase in Vickers hardness and flexural strength. However, in 3Mn_CSZ and 4Mn_CSZ, where cubic phase formation occurred, the tetragonal phase decreased, leading to a reduction in these properties. MnO2-doped CSZ exhibited a larger fraction of the monoclinic phase compared to the original CSZ after the corrosion test, indicating worsened corrosion resistance. These results are attributed to the predominant presence of Mn3+ and Mn2+ forms, rather than the Mn4+ form, which has a smaller basicity difference with SiO2, and due to the low melting point. The monoclinic phase fraction decreased as the doping amount of CeO2 increased in CeO2-doped CSZ, but the rate of decrease was lower compared to MnO2-doped CSZ. The monoclinic phase decreased as the doping amount increased, but the Vickers hardness and flexural strength showed a decreasing trend due to the low relative density. The destabilization behavior of Ca in SEM-EDS images before and after corrosion was difficult to identify due to the presence of Ca in the slag, and the destabilization behavior of Ce due to slag after corrosion was not observed. In the XRD data of the specimen surface after the corrosion test, the fraction of the monoclinic phase increased compared to before the test but showed a lower monoclinic phase fraction compared to CSZ. It is believed that CeO2 has superior corrosion resistance compared to CaO because Ce predominantly exists in the form of Ce4+, which has a smaller difference in basicity within the zirconia lattice.

Although 4Ce4YSZ has high corrosion resistance, it faces challenges concerning its sinterability and ionic conductivity. Therefore, we studied destabilization behavior caused by corrosion and oxygen vacancy ordering according to ZnO doping. Powders of (4Ce4YSZ)1−x(ZnO)x (x = 0.5, 1, 2, 4 mol%) were synthesized using the sol-gel method. With the addition of ZnO, the cubic phase increased, and secondary phases were not observed. The (111) peak showed a higher angle shift in ZnO-doped 4Ce4YSZ compared to 4Ce4YSZ, and TEM-SAED revealed a reduction in the spacing of the (011)t plane, suggesting lattice contraction due to the substitution of the smaller Zn2+ (60 Å) for Zr4+ (84 Å) in the lattice. The local atomic structure analysis was conducted using EXAFS to investigate the oxygen vacancy ordering behavior. Zr K-edge Fourier transform data revealed a decrease in the Zr-O1 peak intensity with an increasing amount of ZnO doping, indicating an increase in oxygen vacancies. The Zr-O1 peak position shifted to the right, leading to an increase in the Zr-O1 interatomic distance. In the Y K-edge Fourier transform data, the Y-O1 peak intensity did not decrease, and there was little variation in the Y-O1 interatomic distance. These results suggest that the oxygen vacancies formed due to ZnO doping are located in the neighboring oxygen shell of Zn, rather than in the neighboring oxygen shells of Y and Zr. Impedance measurements were conducted to measure the conductivity, and as the amount of ZnO doping increased, the total conductivity increased, while the activation energy decreased. The increase in oxygen vacancies by ZnO doping contributed to the enhancement of conductivity, and it is considered that these created oxygen vacancies did not interact with Zn2+ and did not form defect associations. Fluoride-based molten salts were introduced to the specimens to assess the corrosion behavior in a molten salt environment. Yttrium depletion layers (YDLs) were formed on the surfaces of all specimens due to the leaching of yttrium. However, Ce remained relatively stable at the interface according to EDS line scans, suggesting a reduction in the phase transformation (cubic, tetragonal to monoclinic) typically associated with yttrium leaching in YSZ.

The effects of CaO content and post-heat treatment were investigated on the phase stability and mechanical and thermal properties of Ca-PSZ. ZrO2 specimens with 5–10 mol% CaO were sintered, and post-heat treatment was performed at 1200 °C for 100 h. Subsequently, to test and analyze the crystal structure and the microstructure, the mechanical and thermal properties of the specimens were evaluated. All specimens were partially stabilized by 5–10 mol% CaO (5CSZ–10CSZ) in a mixed monoclinic and tetragonal phase; however, peaks of the secondary phase of CaZrO3 were observed in 10CSZ. The ratio of the monoclinic phase decreased from 62.50% (5CSZ) to 21.02% (10CSZ) as the CaO content increased. Additionally, the monoclinic phase ratio decreased from 59.38% (5CSZ) to 19.57% (9CSZ) after the post-heat treatment; an increase to 24.84% was observed for 10CSZ. An increase in Vickers hardness from 676.02 to 1256.25 HV and flexural strength from 437.7 to 842.7 MPa was observed with increasing CaO content. The post-heat treatment resulted in further increases in these values as the CaO content increased from 5CSZ to 9CSZ; however, the Vickers hardness and flexural strength of 10CSZ decreased by approximately 8% and 9%, respectively. The thermal expansion coefficient exhibited the same tendency as the mechanical properties. This coefficient increased from 8.229 × 10−6 to 9.448 × 10−6 K−1 with increasing CaO content and was enhanced after the post-heat treatment in 5CSZ to 9CSZ; however, the thermal expansion coefficient of 10CSZ decreased by approximately 4% after the post-heat treatment. The mechanically and thermally stable tetragonal phase increased, and the monoclinic phase decreased as the doped Ca replaced the Zr sites, as was confirmed by the X-ray diffraction (XRD) analysis. The post-heat treatment and the increased Ca addition further facilitated the replacement of Zr sites by Ca. However, at high Ca concentrations of 10CSZ, an equilibrium phase of CaZrO3 was formed as a secondary phase at the post-heat treatment temperature, resulting in low performance.

We proposed a new channel edge doping (CED) technique for hump reduction in n-type low-temperature polycrystalline silicon (LTPS) thin-film transistors (TFTs) and validated it through experiments and technology computer-aided design (TCAD) simulations. The TCAD simulations indicate that the hump effect in LTPS TFTs is due to the high electron (e−) concentration (∼1016 cm−3) induced by an enhanced electric field (e-field) at the channel edge region along the width direction. In order to reduce the hump effect, we focused on decreasing the e− concentration at the channel edge. The CED process led to the selective control of the e− concentration at the channel edge. The decrease in the maximum e− concentration from 3.4 × 1016 to 2.9 × 1014 cm−3 at the channel edge using CED led to an effective reduction in the hump characteristic of LTPS TFTs. Furthermore, the CED process does not require any additional masks and is highly effective in hump reduction, rendering it beneficial for manufacturing active-matrix organic light-emitting diode displays.

Sperm competition has been studied in numerous species as a representative example of postcopulatory sexual selection, where sampling sperm from male is the most basic and important step. Sperm collection can be tricky in birds, however, because unlike mammals, the genitals of birds are generally latent in the cloacal region and their characteristics vary among species. Various methods to collect sperm from different birds have been tested, such as cloacal massage, feces collection, and electro-stimulation, but their applicability varies depending on species. In this study, we introduced the urodeum stimulation method (UroS method) to collect sperm from Cuculus cuckoos, such as the Common Cuckoo (C. canorus). These species are expected to have interesting patterns of pair bonding and sperm competition because of their unique breeding strategy called brood parasitism; however, it remains unexplored. In this study, we described the application of our new method to expel semen from male common cuckoos, measured the volume of semen collected, checked the presence of sperm in the semen sample, and finally estimated its success rate among 82 males. Samples were successfully collected from 76 cuckoos (approximately 93%) and the colors and volumes of the samples were very diverse. Sperm was present in 43 of these samples (57%), showing a sperm observation rate approximately twice as high as that of the conventional cloacal massage method. We believe that this novel method will contribute to a better understanding of postcopulatory sexual selection in avian brood parasites and facilitate the process of sperm collection and artificial insemination in other medium-sized birds.

The improved mechanical properties of carbon-doped TiZrN coatings were investigated in terms of the microstructure and bonding state. The carbon incorporation and structural change were confirmed as a shift to lower degree of the diffraction pattern and the decreased grain size from 24.64 to 22.19 nm. The clear grain boundaries (GBs) were observed in the carbon-doped coating, and its fast Fourier transform (FFT) exhibited a diffused ring pattern. Edge dislocations were also observed in the inverse FFT image, indicating the formation of an amorphous phase due to laser carburization. From the X-ray photoelectron spectroscopy depth profile analysis, the carbon concentration decreased to 37.26 at.% after carburization, which is non-stoichiometric behavior that suggests the formation of the amorphous carbon (a-C) rather than carbides. Both sp2- and sp3-hybridized bonds were detected in the C 1s spectrum of the carbon-doped coating, indicating that the diffused carbon atoms were trapped in the GBs as a-C. The change in the GB structure increased the compressive residual stress from 3.97 to 4.63 GPa. In addition, the hardness, elastic strain to failure (H/E), and plastic deformation resistance (H3/E2) of the carbon-doped TiZrN increased by 19.22%, 12.64%, and 49.59%, respectively, demonstrating the effect of GB strengthening.

Introduction : Since the population increases and the industry develops, the demand for fossil fuels continues to increase, creating problems of energy resource depletions and accelerating global warming. Thus, many countries are making active efforts to replace fossil fuels with bioenergy as a renewable energy. In particular, trees managed and produced by forest industry have a high potential as energy sources for biofuel industry, because they have a conceptual characteristic of carbon neutrality. Recently, energy plan and policy are being developed to cultivate trees on fallow lands, environmentally restored sites, and ground-level work places of abandoned mines; however, economic feasibility for such plans and policies cannot be readily evaluated due to insufficient information on the amount of the energy to be produced from tree cultivation. Thus, the objective of this study is to develop a methodology which can be used to estimate the potential energy amount of the bioenergy from tree cultivation based on tree species, cultivation time, and cultivation area conditions. Methodology : The methodology consists of three stages. In the first stage, the total volume of the trees per area is estimated by using the number of trees per unit area and the average stem volume of the tree, which are affected by the site index representing the environmental conditions of cultivation area. In the second stage, the total mass of biomass is calculated by using the density of wood, the biomass expansion factors for the above-ground biomass, and root-shoot ratio. In the last stage, the amount of the energy produced from the tree cultivation is estimated by taking into account the caloric value evaluated based on the carbon, hydrogen, and oxygen compositions of the tree. Case Study : A case study for conifers and broad-leaved trees is performed to demonstrate the methodology. The conifers are Jungbu local pine, Korean white pine, and Japanese larch, and the broad-leaved trees are oak, red oak, and birch. The results of the case study validate the developed methodology and clearly showed the procedure and necessity for the methodology by estimating the bioenergy productions from the trees. Conclusions : The developed methodology can be used to provide practical information needed to determine the economic feasibility of the plan, policy, and project for tree cultivations.

For fast access to the cell, we propose an enhanced random access scheme exploiting multiple transmissions of random access preambles and random access responses. The proposed random access scheme decreases the latency of the random access procedure, by avoiding random access retrials from the beginning of the random access procedure due to the expiry of a random access response window. We also provide a model and analysis of random access latency with the average delay and the failure probability of random access procedure. The model of random access latency considers the collisions of random access preambles transmitted by multiple mobile stations to a base station as well as the error of random access response corresponding to the received random access preamble transmitted by the base station to the mobile station. Our numerical results in accordance with the model show that the proposed scheme provides lower latency.

The oxygen reduction reaction (ORR) activity of a Cu-doped Ba0.5Sr0.5FeO3−δ (Ba0.5Sr0.5Fe1−xCuxO3−δ, BSFCux, x = 0, 0.05, 0.10, 0.15) perovskite cathode was investigated in terms of oxygen vacancy formation and valence band structure. The BSFCux (x = 0, 0.05, 0.10, 0.15) crystallized in a cubic perovskite structure (Pm3¯m). By thermogravimetric analysis and surface chemical analysis, it was confirmed that the concentration of oxygen vacancies in the lattice increased with Cu doping. The average oxidation state of B-site ions decreased from 3.583 (x = 0) to 3.210 (x = 0.15), and the valence band maximum shifted from −0.133 eV (x = 0) to −0.222 eV (x = 0.15). The electrical conductivity of BSFCux increased with temperature because of the thermally activated small polaron hopping mechanism showing a maximum value of 64.12 S cm−1 (x = 0.15) at 500 °C. The ASR value as an indicator of ORR activity decreased by 72.6% from 0.135 Ω cm2 (x = 0) to 0.037 Ω cm2 (x = 0.15) at 700 °C. The Cu doping increased oxygen vacancy concentration and electron concentration in the valence band to promote electron exchange with adsorbed oxygen, thereby improving ORR activity.

The degradation behavior of yttria-stabilized zirconia by thermal aging was investigated in terms of phase transformation, local atomic structure, and electrical conductivity. The average grain size of 8YSZ was increased from 20.83 μm to 25.81 μm with increasing aging temperature. All 8YSZ samples degraded at different temperatures had a predominantly cubic structure. The (400) peak of 8YSZ deteriorated at 1300 and 1400 °C shifted to a high angle, and the peak of tetragonal was not indexed. For 8YSZ degraded at 1500 °C, the (400) peak shifted to a lower angle, and the peak of tetragonal was identified. Analysis of the local microstructure of aged 8YSZ using extended X-ray absorption fine structure showed that the intensity of the Zr-O peak gradually increased and that the intensity of the peak of cationic Zr decreased as the aging temperature increased. The changes in the peaks indicate that the oxygen vacancies were reduced and Y3+ ions escaped from the lattice, leading to the destabilization of 8YSZ. The activation energies of 8YSZ at 1300 °C and 1400 °C were derived to be 0.86 and 0.87 eV, respectively, and the activation energy of 8YSZ at 1500 °C increased significantly to 0.92 eV. With the thermal deterioration of 8YSZ, the cation (Y3+) escaped from the lattice and the number of oxygen vacancies decreased, resulting in the formation of a tetragonal structure and high activation energy at 1500 °C.

The phase formation and stabilization behaviors of calcia partially stabilized zirconia (Ca-PSZ) were investigated with regard to the CaO content and post-heat treatment. Sintered specimens were prepared by adding 2, 3, 4, and 5 mol% to CaO to ZrO2, and post-heat treatment were conducted. In the X-ray diffraction pattern, the monoclinic peak decreased, the tetragonal peak increased upon CaO doping, and no CaZrO3 peak was observed. Transmission electron microscopy images of the Ca-PSZ showed that the d-spacing of 4CSZ (200)m extended from 0.260 nm to 0.266 nm subsequent to post-heat treatment. The coefficient of thermal expansion gradually increased in accordance with the dopant concentration, in addition, it increased even after the post-heat treatment. These results are related to the increase in tetragonal phase, which has a relatively higher coefficient of thermal expansion than that of the monoclinc phase. According to the Vickers hardness measurement, the hardness of all specimens increased gradually as the concentration of CaO increased, and the hardness of the 5CSZ was improved from 676 to 774 Hv by the post-heat treatment.

Lattice distortion and amorphization of carbon-doped SUS304 by variation of the laser output were investigated in terms of phase formation and the bonding state. The laser output was changed by 10% in the range of 60% to 100% after covering the SUS304 with carbon paste. A graphite peak and expanded austenite (S-phase) peak were observed in the carbon-doped SUS304, and Rietveld refinement was performed to identify the lattice distortion. The lattice constant of SUS304 was initially 3.612 Å, but expansion lattice distortion occurred in the carbon-doped SUS304 as a result of the S phase formation and carbon doping, and the lattice constant increased to 3.964 Å (100% laser output). X-ray photoelectron spectroscopy analysis for the bonding state of the carbon-doped SUS304 showed that the sp2/sp3 ratio decreased from 3.21 (70% laser output) to 2.52 (100% laser output). The residual stress in the lattice was accumulated due to carbon doping by high thermal energy, which resulted in the formation of amorphous carbon. The bonding environment was represented by the ID/IG ratio using Raman analysis, and it increased from 0.55 (70% laser output) to 1.68 (100% laser output). During microstructure analysis of the carbon-doped SUS304, disordered structures by amorphization were observed in the carbon-doped SUS304 by the greater than 90% laser output. The amorphous carbon filled the lattice grains or voids to lubricate the surface, which improved the friction coefficient and wear rate from 0.23 and 7.63 mm3(Nm)−110−6 to 0.09 and 1.43 mm3(Nm)−110−6, respectively.

Typically, to meet emission regulations, the selective catalytic reduction of NOX with NH3 (NH3-SCR) technology cause NH3 emissions owing to high NH3/NOX ratios to meet emission regulations. In this study, V-Cu/BN-Ti was used to remove residual NOX and NH3. Catalysts were evaluated for selective catalytic oxidation of NH3 (NH3-SCO) in the NH3-SCR reaction at 200–300 °C. The addition of vanadium and copper increased the number of Brønsted and Lewis acid sites available for the reaction by increasing the ratio of V5+ and forming Cu+ species, respectively. Furthermore, h-BN was dispersed in the catalyst to improve the content of vanadium and copper species on the surface. NH3 and NOX conversion were 98% and 91% at 260 °C, respectively. Consequently, slipped NH3 (NH3-Slip) emitted only 2% of the injected ammonia. Under SO2 conditions, based on the NH3 oxidation reaction, catalytic deactivation was improved by addition of h-BN. This study suggests that h-BN is a potential catalyst that can help remove residual NOX and meet NH3 emission regulations when placed at the bottom of the SCR catalyst layer in coal-fired power plants.

This study examined the microstructural gradation in Sn-doped, n-type Ga2O3 epitaxial layers grown on a two-inch sapphire substrate using horizontal hot-wall mist chemical vapor deposition (mist CVD). The results revealed that, compared to a single Ga2O3 layer grown using a conventional single-step growth, the double Ga2O3 layers grown using a two-step growth process exhibited excellent thickness uniformity, surface roughness, and crystal quality. In addition, the spatial gradient of carrier concentration in the upper layer of the double layers was significantly affected by the mist flow velocity at the surface, regardless of the dopant concentration distribution of the underlying layer. Furthermore, the electrical properties of the single Ga2O3 layer could be attributed to various scattering mechanisms, whereas the carrier mobility of the double Ga2O3 layers could be attributed to Coulomb scattering owing to the heavily doped condition. It strongly suggests the two-step-grown, lightly-Sn-doped Ga2O3 layer is feasible for high power electronic devices.

Powder bed 3D printing can be applied to sandcasting mold manufacturing to ensure high quality and economy through process innovation. In this study, refractory alumina cement was used as an aqueous binder to ensure high-temperature thermal stability to minimize the addition of organic matter to reduce gas generation. In addition, spherical silica sand, the study material, was selected to a size of 30 µm to improve the casting mold resolution. To improve the surface quality through the post-treatment process, we confirmed the change in the surface roughness of the mold depending on the surface treatment of colloidal silica and the presence or absence of heat treatment, and finally made the mold through actual casting. Changes in the surface roughness and flowability of the cast body after mold post-treatment were confirmed. For aluminum castings, the shrinkage rate and surface roughness were confirmed in a box-shaped mold via gravity casting, and the flowability of the molten metal in the mold was confirmed in a hand-shaped mold. There was a change in the roughness and porosity of the mold, owing to the post-treatment, and the influence of the surface roughness and flowability of the cast body during actual casting was confirmed.

The degradation behavior of PrBaCo2−xCuxO5+δ (x = 0, 0.2, 0.5) under thermal stress was investigated in terms of phase formation and polarization resistance. The tetragonal phase was indexed in all compositions of PBCCux, and the secondary phase, BaO, was identified after thermal degradation in the crystal structure analysis. BaO formation is induced by the nature of perovskite to terminate the surface with AO layer. For pristine specimens, the oxygen vacancy peak ratio was increased from 57% to 60% according to the decrease in the average oxidation number of the B-site ion with Cu doping. After thermal deterioration, the oxidation number of B-site ions was increased, and the M = O bonding peak increased due to the decrease in oxygen vacancies and BaO formation according to the thermal stress. In all compositions, the electrical conductivity decreased from 1000 S/cm to 17 S/cm, and the polarization resistance increased approximately 200 times. These results are considered to be related to the increase in the oxidation number of B-site ions along with the formation of secondary phases.

With the development of the powder bed 3D printing process, sand casting can be performed with methods that are more advanced than the traditional ones, thus enabling new research on applied materials. When sand is 3D-printed with cement as a binder, its casting performance is improved and sufficient thermal stability of conventional organic and inorganic binders is ensured. In this study, to ensure high resolution and strength in a physical and simple mixture of cement and sand, the compatibility for casting was confirmed using submicron-level cement with ingredients and sizes similar to commercial sand, which is uniformly controlled at 4 µm, instead of conventional sand. To enable quick 3D printing, calcium aluminate cement, which has quick binding properties, was used for high-temperature casting. The strength up to 6 h after hydration was compared to determine the curing rate of silica, mullite, and alumina sand containing cement components. By investigating the change in strength due to heat treatment and comparing the adhesion drop test results after powder bed formation, the material containing silica sand was determined as the most suitable for powder layer 3D printing for application to the mold.

Amorphous CeO2-TiO2 nanoparticles synthesized by the H2O2-modified sol-gel method were investigated in terms of the Ce-O-Ce and Ti-O-Ti linkage, local structure, and redox properties. The decrease in the crystallinity of CeO2-TiO2 by H2O2 addition was confirmed. The metal–oxygen linkage analysis showed the difference in size of the metal–oxygen network between crystalline CeO2-TiO2 and amorphous CeO2-TiO2 due to the O22− formed by H2O2. The local structure of CeO2-TiO2 was analyzed with an extended X-ray absorption fine structure (EXAFS), and the oscillation changes in the k space revealed the disordering of CeO2-TiO2. The decrease in Ce-O bond length and the Ce-O peak broadening was attributed to O22− interfering with the formation of the extended metal–oxygen network. The temperature-programmed reduction of the H2 profile of amorphous CeO2-TiO2 exhibited the disappearance of the bulk oxygen reduction peak and a low-temperature shift of the surface oxygen reduction peak. The H2 consumption increased compared to crystalline CeO2-TiO2, which indicated the improvement of redox properties by amorphization.

Conductive oxides are widely studied as cathode materials for electrochemical cells, such as solid oxide fuel cells (SOFCs), because of their chemical stability and high electrical conductivity at high temperatures (800–950 °C). The cathode is a key component of SOFCs, accounting for the greatest resistance loss among the SOFC components. It is important to precisely determine the conductivity of the cathode material, but it is difficult to achieve consistency among measurements because of errors caused by differences in the measurement methods and conditions employed by various research teams. In this study, the total electrical conductivity of an SOFC cathode material was measured by the DC 4-point method by investigating the geometrical parameters of the sample and the measurement terminal and the measurement device using La0.8Sr0.2MnO3+d (LSM). The measurement variables included the spacing between the measurement terminals (1 and 2 cm), lead wire diameter (0.25 and 0.5 mm), specimen thickness (3, 4, and 5 mm), and the applied current (10, 50, and 100 mA). The larger the spacing between the measurement terminal and the thinner the specimen, the smaller the standard deviation.

Carbon-doped TiZrN nanocomposite coatings were investigated for phase formation and wear behavior. They were prepared by laser carburization using carbon paste, and the thermal energy of the pulsed laser was limited to the range of 20 to 50%. X-ray photoelectron spectroscopy analysis revealed that the ratio of carbide (TiC, ZrC) increased as the thermal energy of the laser increased. The sp2/sp3 ratio increased by approximately 16% when the laser thermal energy was raised from 30 to 40%, and the formation of amorphous carbon was confirmed in the carbon-doped TiZrN coatings. As a result of microstructural analysis, the carbon-doped TiZrN nanocomposite was formed by an increase of hybrid bonds in expanded localized carbon clusters. Wear resistance was evaluated using a ball-on-disc tester, which showed that the friction coefficient decreased from 0.74 to 0.11 and the wear rate decreased from 7.63 × 10−6 mm3 (Nm)−1 to 1.26 × 10−6 mm3 (Nm)−1. In particular, the friction coefficient and wear rate improved by 71 and 66%, respectively, owing to the formation of carbon-doped TiZrN nanocomposite with amorphous carbon while the thermal energy was increased from 30 to 40%.

Chemical and biological investigation of green tea has been generally performed while using different infusions that are prepared without consideration of the effects of sample preparation conditions. In this study, for the first time, the effects of green tea brewing conditions on the antioxidant activity and chemical profiles of metabolome and catechin compounds were examined at 60 °C and 95 °C for a period of 5−300 min. The antioxidant capacities of the tea infusions, which were assessed as per 2,2-diphenyl-1-picryl-hydrazyl hydrate (DPPH) radical scavenging activity, depended more on temperature than time. Metabolomics study that was based on ultra-high performance liquid chromatography-quadrupole-time-of-flight mass spectrometry (UHPLC-QTOF/MS) revealed that the metabolic profiles, including 33 differential metabolites, were significantly changed by temperature and time, with the effects of time being more evident at 95 °C starting after 30 min. Infusions that were brewed at 95 °C for greater than 30 min yielded distinct profiles in the hierarchical clustering analysis. The quantification of eight catechins by UHPLC-QqQ/MS showed that the total catechin level peaked at 95 °C brewing at 10 min, after which the levels of four epi-forms of catechins decreased and those of four non-epi-forms increased, implying the epimerization of catechins over time. These results suggest that the brewing conditions for sample preparation of green tea should be put into careful consideration in studies where green tea extracts are applied as aqueous infusions.