In this study, quantum dots with Au/CdSe complex cores composed of Au as a metal base were synthesized, syrup was prepared, and coated on natural simulated LED unit modules, and the optical properties of traffic signs using them were investigated, and the following conclusions were obtained. The nanoparticles synthesized at 260°C and 280°C grew into irregular shapes with PL wavelengths of 624-627㎛, half-widths of 35㎛, PL-QY ratios of 55-61%, and grain diameters of 5-7㎛. The quantum dot syrup was applied to the LED unit module to produce a traffic sign composed of 4CL unit modules, and the luminance of 179 ㏅/㎡, insulation resistance of 10,000㏁, and insulation withstand of 500V were achieved, meeting the performance and specifications of the standard guidelines for luminescent traffic safety signs. The surface temperature of the unit module laminated with 4CL resin is 24~25℃, which shows a stable heat distribution, confirming that it can be applied as a sign using unit modules.

Encapsulating living cells within porous crystalline materials has emerged as a powerful strategy for improving cellular stability in chemically or physically harsh conditions. In this study, individual yeast cells were encapsulated with a zeolitic imidazolate framework-8 (ZIF-8) crystals via a biomimetic self-assembly process. Morphological analysis using electron microscopy confirmed the successful formation of a uniform and continuous protective shell around each cell. To evaluate the cytoprotective effect of the ZIF-8 coating, the encapsulated yeast cells were exposed to a range of pH conditions (pH 2~12). Fluorescence microscopy using fluorescein diacetate (FDA) staining revealed that over 50 % of the ZIF-8 encapsulated cells remained viable in alkaline environments (pH 8, 10, and 12), whereas non-encapsulated yeast cells showed 0 % viability across all tested conditions. The enhanced survival in alkaline media was attributed to the stability of the crystalline ZIF-8 shell, which remained partially intact and provided structural protection. In contrast, acidic conditions degraded the ZIF-8 shell, leading to cell membrane rupture and loss of viability. These findings demonstrate that ZIF-8 encapsulation can significantly improve the chemical resilience and survival of living yeast cells. This strategy holds great promise for applications in long-term cell preservation, transport, and pH-responsive biotechnological systems.

In this paper, the structural optimization and experimental validation of lightweight, high stiffness rollers for roll-to-roll(R2R) processing of lithium metal electrodes are presented. Precise dimensional control of electrode thickness below 50㎛ is essential for next-generation high energy density batteries, yet elastic recovery during rolling hinders the achievement of target specifications. To address this challenge, finite element(FE) analysis was employed to determine the optimal rolling gap and roller geometry, and the results were verified through R2R experiments. Simulations indicated that a rolling gap of 153㎛ yielded a final sheet thickness of about 49.6㎛, meeting the design requirement. Experimental results confirmed the validity of the numerical model, with thickness measurements deviating less than ±10% from FE analysis predictions. These findings demonstrate that the proposed roller design not only ensures thickness precision but also improves system efficiency, offering practical guidelines for scalable lithium metal electrode manufacturing.

The plausibility factors influencing heterogeneous nucleation at the metal/glass interface were systematically investigated as a function of temperature. Secondary phase formation at the metal/glass interface is governed by the contact angle, which is affected by volumetric changes, microstructural evolution driven by metal ion diffusion, and redox reactions influenced by the arrangement of oxygen layers on the metal surface. A comprehensive model was developed to describe these plausibility factors based on observed interfacial phenomena. Despite the inherent non-uniformity in ion distribution within the glass, the interfacial diffusion coefficient, derived from an Arrhenius plot, exhibited a clear temperature dependence, reflecting thermally activated diffusion processes. Above the glass transition temperature (Tg), chemical interactions between diffusing metal ions and migrating glass constituents were identified as the main driving force for secondary phase formation at the metal/glass interface. These chemical reactions not only alter the local stoichiometry but also contribute to structural rearrangements at the interface. The results highlight the complex interplay between the thermal, chemical, and structural factors that control nucleation at the metal/glass boundary. The proposed model provides valuable insight into the mechanisms of interfacial phase formation and offers a useful framework for the design and processing of metal/glass composite systems with tailored properties.

The Public Procurement Service was established to ensure efficient supply of necessary goods for public institutions and their quality stability. The Public Procurement Service operates the Excellent Product Designation System for quality improvement. Due to the convenience of sole-source contracts and pricing advantages, suppliers prefer to obtain excellent product certification. However, despite these advantages, the designation does not guarantee customer satisfaction, as consumers pay higher prices without assured quality improvements. The goal of this study is to propose a new evaluation system better reflecting customer satisfaction and repurchase intention. Metal window products were selected as the study subject. Candidate factors were derived through literature review, and surveys were conducted to identify significant items for the new evaluation system. Item weights were then calculated using AHP analysis. The proposed system was validated through case analysis comparing two excellent products with two general products.

It is addressed that the challenges of poor cyclic stability and low conductivity in metal–organic frameworks (MOFs) hinder their application in energy storage. Here, we synthesized binary metal MOFs through a one-step hydrothermal process, subsequently calcined to produce Co–Mn/reduced graphene oxide (rGO). This approach not only carbonized the organic framework but also enhanced its electrical conductivity and stability. Our findings demonstrated that the synergistic effects of Co and Mn within the assembled electrode resulted in remarkable performance, achieving a specific capacitance of 3558.65 F g− 1 at 1 A g− 1 and a rate capability of 1000 F g− 1 at 30 A g− 1. The Co–Mn/rGO anode in the asymmetric supercapattery exhibited a broadened operating potential window of 1.5 V, delivering an energy density of 54.65 W h kg− 1 at a power density of 125 W kg− 1, and maintaining 11.375 W h kg− 1 at a high power density of 12,500 W kg− 1. Notably, the capacitance retention rate reached 99.99% after 10,000 cycles at a current density of 10 A g− 1. These results suggest that the developed Co–Mn/rGO composite represents a promising candidate for advanced energy storage systems, offering both high performance and stability.

The development of high-performance metal filters is essential for maintaining ultra-clean environments in semiconductor manufacturing. In this study, cross-sealed honeycomb filters were fabricated using STS316L powder via material extrusion additive manufacturing (MEAM) for semiconductor gas filtration. The effects of filter geometry (4 or 9 channels) and sintering temperature (850°C, 950°C, or 1,050°C) on performance were examined. First, 4-channel and 9-channel filters sintered at the same temperature (950°C) exhibited similar porosities of 50.08% and 50.57%, but the 9-channel filter showed a higher pressure-drop (0.26 bar) and better filtration-efficiency (3.55 LRV) than the 4-channel filter (0.19 bar and 3.25 LRV, respectively). Second, for filters with the same geometry (4-channel) increasing the sintering temperature reduced porosity from 64.52% to 40.33%, while the pressure-drop increased from 0.13 bar to 0.22 bar and filtration-efficiency improved from 2.53 LRV to 3.51 LRV. These findings demonstrate that filter geometry and sintering temperature are key factors governing the trade-off between air permeability, pressure-drop, and filtration efficiency. This work provides insights and data for optimizing MEAM-based high-performance metal powder filter design.

본 연구에서는 온대산재 및 남양재 원목을 표층재로하고, 금속, 유리섬유, 탄소섬유로 보강한 코르크 보드를 중층에 배열한 코르크 복합 원목마루판 의 치수안정성을 평가하였다. 표층재에 따른 코르크 복합 원목마루판의 평균 흡수율은 백합나무(Tu)가 6.1%로 가장 높은 값을 나타내었고, 티크와 멀바우가 4.7%로 가장 낮은 값을 나타내었으며, 밀도가 낮은 온대산재를 배열한 원목마루판보다 남양재에서 낮은 값을 나타내는 것이 확인되었다. 중층보강재는 CM (cork board-metal) 타입이 CG (cork board-glass fiber) 및 CC (cork board-carbon fiber)타입에 비하여 높은 흡수율을 나타내어 밀도에 따른 흡수량의 차이가 확인되었다. 표층 수종에 따른 흡수두께팽창률은 백합나무가 7.2%로 가장 높은 값을, 티크(T)가 3.9%로 가장 낮은 값을 나타내었다. 전반적으로 금속 보강 원목마루판(CM)의 흡수두께팽창률은 유리섬유(CG)와 탄소섬유(CC)에 비하여 금속이 2–3배 높은 값을 나타내었다. 금속 보강 원목마루판을 제외한 모든 원목마루판은 목질 마루판에 관한 KS 규격 기준을 충족하는 우수한 치수안정성을 나타내는 것이 확인되었다.

The use of aluminum-based hybrid metal matrix composite (HMMC) materials, especially in engine components like pistons, is intended to improve wear resistance and overall performance. Crucial tribological indicators, such as wear and friction coefficients, underscore the significance of these materials. However, present aluminum alloys have limited wear because of clustered reinforced particles and relatively high coefficients of thermal expansion (CTE), resulting in inadequate anti-seizure properties during dry sliding conditions. This research introduces a novel “Hybrid Metal Matrix Composite of Al7068 Reinforced with Fly Ash-SiC-Al2O3”. Al7068 is employed for its superior strength-to-weight ratio and specific modulus, which is ideal for components exposed to cyclic loads and varying temperatures. The integration of fly Ash (FA), silicon carbide (SiC), and alumina (Al2O3) as reinforcements enhances wear resistance, diminishes particle clustering, improves stiffness, mitigates CTE discrepancies, and fortifies the composite against strain and corrosion, thereby enhancing its overall performance. The Stir-casting method was used with optimized reinforcement percentages (10 % total), and comprehensive evaluations through wear tests and mechanical property analyses determined the composite's optimal composition. The proposed HMMC variant with the most suitable reinforcement percentage exhibited enhanced engine piston functionality, reduced wear, low deformation of 0.20 mm, and a comparatively higher ultimate tensile strength of 190 megapascals (Mpa).

This study incorporates the formation of carbon quantum dots (CQDs) via a hydrothermal approach, recording the first-time use of castor leaves as a natural precursor. The used precursor offers various benefits including novelty, abundance, elemental composition, and biocompatibility. CQDs were further characterized with multiple techniques including high-resolution transmission electron microscope (HR-TEM), X-ray photoelectron microscopy (XPS), X-ray diffraction (XRD), Fouriertransform infrared spectroscopy (FTIR), Raman spectroscopy, UV–visible spectroscopy, Zeta analysis, and optical spectroscopy. They are fundamentally composed of carbon (71.37%), nitrogen (3.91%), and oxygen (24.73%) and are nearly spherical, and uniformly distributed with an average diameter of 2.7 nm. They possess numerous interesting characteristics like broad excitation/emission bands, excitation-sensitive emission, marvelous photostability, reactivity, thermo-sensitivity, etc. A temperature sensor (thermal sensitivity of 0.58% C− 1) with repeatability and reversibility of results is also demonstrated. Additionally, they were found selective and sensitive to ions in aqueous solutions. So, they are also utilized as a fluorescent probe for metal ion ( Fe3+) sensing. The lowest limit of detection (LOD) value for the current metal ion sensor is 19.1 μM/L.

As the demand for sustainable hydrogen (H₂) production grows, catalytic decomposition of methane (CDM) has emerged as a CO2- free pathway for H2 generation, producing valuable multi-walled carbon nanotubes (MWCNTs) as byproducts. This study examines the role of fuel type in shaping the properties and performance of NiOx/AlOx catalysts synthesized via solution combustion synthesis (SCS). Catalysts prepared with citric acid, urea, hexamethylenetetramine (HMTA), and glycine exhibited varying NiO nanoparticle (NP) sizes and dispersions. Among them, the HMTA catalyst achieved the highest Ni dispersion (~ 3.2%) and specific surface area (21.6 m2/ gcat), attributed to vigorous combustion facilitated by its high pH and amino-group-based fuel. Catalytic tests showed comparable activation energy (55.7–59.7 kJ/mol) across all catalysts, indicating similar active site formation mechanisms. However, the HMTA catalyst demonstrated superior CH4 conversion (~ 68%) and stability, maintaining performance for over 160 min under undiluted CH₄, while others deactivated rapidly. MWCNT characterization revealed consistent structural properties, such as graphitization degree and electrical conductivity, across all catalysts, emphasizing that fuel type influenced stability rather than MWCNT quality. H2 temperature-programmed reduction ( H2-TPR) analysis identified moderate metal-support interaction (MSI) in the HMTA catalyst as a key factor for optimizing stability and active site utilization. These findings underscore the importance of fuel selection in SCS to control MSIs and dispersion, offering a strategy to enhance catalytic performance in CDM and other thermocatalytic applications.

Biochar is considered as key anode material for alkali metal (lithium, sodium, and potassium) ion batteries (AIBs) owing to its rich microstructural features, high specific surface area, active sites, excellent conductivity, and mechanical strength. The multidimensional structures and diverse functional groups of biochar make it enable easy modification to improve ion transport, interface deposition behavior, and electrolyte stability. In addition, biochar-based derivatives, such as silicon/biochar composite anode materials, combine the advantages of high-energy density and low lithiation potential of silicon materials, as well as the superior conductive ability and outstanding mechanical qualities of biochar. In this review, the microstructure, properties, and synthesis methods of biochar materials are systematically clarified, and then, their applications in AIBs are presented followed by summarizing the energy storage mechanism and advanced physicochemical characterizations. Common structural configurations and preparative technique for biochar/silicon-based composites are summarized, such as core–shell, yolk–shell, and embedded coating structures with improved electrochemical and mechanical stability. Finally, toward practical application of biochar and biochar-based derivatives in future AIBs, the issues and challenges are outlined.

In recent years, there has been growing interest in the potential applications of carbon-based non-metallic catalysts in various fields, such as electrochemical energy storage, electrocatalysis, thermal catalysis, and photocatalysis, owing to their unique physical and chemical properties. Modifying carbon catalyst surfaces or incorporating non-metallic heteroatoms, such as nitrogen (N), phosphorus (P), boron (B), and sulfur (S), into the carbon structure has emerged as a promising approach to improve the catalytic performance. This method enables the adjustment of the electronic structure of the carbon catalyst's surface, leading to the formation of new active sites or the reduction of side reactions, ultimately enhancing the catalyst's performance. Here, the preparation methods for doped non-metallic heteroatom carbon catalysts have been systematically explored, encompassing techniques, such as impregnation, pyrolysis, chemical vapor deposition (CVD), and templating. Finally, the existing challenges in the application of non-metallic atomic catalysts have been discussed, insights into potential future development opportunities and new preparation methods of carbon catalysts in the future have been offered.

본 연구는 프로판탈수소(PDH) 공정의 배가스내에 포함되어 있는 탄화수소(HC)를 이용하여 질 소산화물(NOx)을 저감하는 Metal Corrugated HC-SCR 촉매 개발을 목적으로 하였다. 산성도(Si/Al 비) 가 다른 제올라이트계 Chabazite 3종을 Metal Corrugated에 워시코팅하였고, 가장 우수한 NOx 저감 성 능을 나타낸 Chabazite에 구리 함량을 1.5%, 3.0%, 4.5%, 6.0%로 함침하여 촉매를 제조하였다. 제조된 촉 매의 NOx 저감 성능은 실험실 규모의 마이크로 상압반응기상에서 측정하였으며, 촉매 특성분석은 BET, XRF, ICP를 이용하여 분석하였다. 측정 결과, 산성도가 가장 낮은 A-Chabazite가 가장 높은 NOx 저감 성능을 보였고, 구리 함량이 높을수록 Total NOx 저감 성능은 증가되었지만 NO2 저감 성능은 감소되는 것으로 확인되었다. 3.0-A-CHA 촉매는 NO2가 완전 저감되었고, Total NOx 저감에도 큰 효과를 나타내 상용 PDH 공정에서 NO2를 중점적으로 저감하고자 한다면 충분히 적용 가능할 것으로 보인다.

Lithium (Li) metal is a promising anode for next-generation batteries due to its high capacity, low redox potential, and low density. However, dendrite growth and interfacial instability limit its use. In this study, an artificial solid electrolyte interphase layer of LiF and Li-Sn (LiF@Li-Sn) was fabricated by spray-coating SnF2 onto Li. The LiF@Li-Sn anode exhibited improved air stability and electrochemical performance. Electrochemical impedance spectroscopy indicated a charge transfer resistance of 25.2 Ω after the first cycle. In symmetric cells, it maintained a low overpotential of 27 mV after 250 cycles at 2 mA/cm2, outperforming bare Li. In situ microscopy confirmed dendrite suppression during plating. Full cells with NMC622 cathodes and LiF@Li-Sn anodes delivered 130.8 mAh/g with 79.4% retention after 300 cycles at 1 C and 98.8% coulombic efficiency. This coating effectively stabilized the interface and suppressed dendrites, with promising implications for practical lithium metal batteries.