Search Results (677)

The quantitative analysis of cardio selective beta-blockers, such as the antihypertensive and antiarrhythmic medication acebutolol (ABT), is critical for biomedical and environmental monitoring. This study describes the development of a high-performance electrochemical sensing platform for ABT based on a screen-printed carbon electrode (SPCE) modified with a silver nanoparticle/hexagonal boron nitride (Ag NPs/h-BN) nanocomposite. The morphological and structural properties of the synthesized materials were examined by using a microscopic and spectroscopic techniques. The Ag NPs/h-BN/SPCE demonstrated exceptional electrocatalytic activity toward ABT oxidation, characterized by a significant reduction in overpotential and a substantial enhancement in peak current relative to unmodified and mono-component electrodes. This superior performance is attributed to the synergistic integration of Ag NPs and h-BN, which provides a high density of active sites, an expanded electroactive surface area, and accelerated charge transfer kinetics. Under optimized experimental conditions, the sensor exhibited a broad linear dynamic range of 0.01–284 μM, a remarkably low limit of detection (LOD) of 0.0049 μM, and a high sensitivity of 0.873 µA µM⁻¹ cm⁻² for ABT detection. Furthermore, the platform displayed excellent selectivity in the presence of common interfering species and robust reproducibility (RSD of 4.8%). The practical utility of the Ag NPs/h-BN/SPCE was successfully validated through the precise quantification of ABT in complex biological and environmental matrices. This work provides a versatile strategy for the rational design of metal nanocatalysts confined within h-BN frameworks for the development of advanced electrochemical diagnostic tools. Full article

Two-dimensional (2D) materials exhibit electronic and collective excitation properties that are highly sensitive to surface chemistry and thickness, requiring surface-sensitive characterization at low electron energies. Here, we investigate graphene, hexagonal boron nitride (h-BN), molybdenum disulfide (MoS₂), and titanium carbide (Ti₃C₂) MXene using an advanced home-built scanning low-energy electron microscopy system combined with time-of-flight electron spectroscopy (SLEEM/ToF). The system uniquely records electron energy-loss spectra (EELS) from transmitted electrons rather than from the reflected electrons used in conventional SLEEM. Compared with high-energy EELS, our low-energy ToF-EELS approach offers enhanced surface sensitivity and reduced beam-induced damage, enabling direct probing of π and π + σ plasmon excitations. Additionally, complementary techniques, including scanning transmission electron microscopy (STEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS), were employed to characterize structural and chemical properties. EELS were acquired for all investigated 2D materials at electron landing energies of 500–1500 eV, and in the 5–50 eV range for selected materials, including graphene and MoS₂. Analysis of these spectra enabled determination of the average plasmon positions across the measured energy range for all studied materials. Furthermore, a quantitative determination of the inelastic mean free path (IMFP) was achieved for graphene in the 10–50 eV range, yielding a value of 1.9 ± 0.2 nm. These results demonstrate the potential of SLEEM–ToF for surface-sensitive analysis of 2D materials. Full article

Three Ni-based composite coatings with varying TiCN/h-BN contents were fabricated on the surface of Ti-6Al-4V (TC4) alloy by laser cladding. The coatings were formulated with a fixed 15% TiCN and 0%, 2% and 5% h-BN, corresponding to L1–L3 coatings. The microstructure and phase composition were fully characterized and investigated. In addition, the microhardness and wear resistance of the coating were evaluated too. The analysis revealed that the L1–L3 coatings primarily consisted of Ti, TiNi, Ti(C, N) and TiAl₃ phases. Microstructural analysis indicated that the top region of the coating was predominantly composed of granular crystals, while the middle and bonding regions featured a combination of dendrites and white granular crystals. The average microhardness values for the L1–L3 coatings were measured at 1203.8, 1216.8 and 1235.5 HV_0.2, respectively, while the corresponding wear volumes were 0.098, 0.094 and 0.086 mm³. As the h-BN content increased, the microstructure of the Ni-based composite coating became finer and finer. Some TiB particles were also generated in the coating, which made the average microhardness and wear resistance increase gradually. Notably, the coating with 5% h-BN demonstrated the highest average microhardness and optimal wear resistance. Compared with the substrate, 5% h-BN increased the wear resistance of the substrate by 47.6%. The primary wear mechanism observed was abrasive wear. Full article

Developing effective metal-free electrocatalysts for acidic hydrogen evolution is challenging because both catalytic activity and electronic conductivity must be optimized simultaneously. Here, h-BN/carbon nano-onion (CNO) hybrid electrocatalysts were synthesized by integrating layered hexagonal boron nitride with conductive carbon nano-onions to generate accessible heterointerfaces for the hydrogen evolution reaction (HER). Structural characterization by XRD, SEM/TEM, and STEM-EDS confirmed intimate contact between h-BN sheets and quasi-spherical CNO domains. Similarly, XPS revealed B–N-rich frameworks with interfacial B–C/C–N surface environments and oxygen-associated defect sites. Among the prepared compositions, the h-BN/CNO20 eletrocatalyst exhibited the best apparent HER performance in 0.5 M H₂SO₄, delivering an overpotential of ~270 mV at 5 mA cm⁻² and a Tafel slope of 76 mV dec⁻¹, along with stable chronoamperometric behavior for 15 h. The improved electrocatalytic activity is due to the enhanced charge transport through the CNO network, suppression of h-BN restacking, increased exposure of interfacial sites, and charge redistribution across B–N/C heterojunctions. These findings identify h-BN/CNO20 as the optimum composition within this series and demonstrate that heterointerface engineering between boron nitride and curved graphitic nanocarbons is a promising strategy for developing metal-free HER electrocatalysts. However, further validation using a non-Pt counter electrode is necessary to confirm intrinsic catalytic activity. Full article

In this study, polysiloxane-containing polyimide (si-PI) composite coatings containing hexagonal boron nitride (hBN) particles of four different sizes and at different contents were prepared, and their mechanical and tribological properties were investigated. The coatings were deposited on steel substrates via dip coating and cured at 160 °C. Their tribological properties were measured using reciprocating sliding tests under unlubricated conditions against a steel ball. The composite coatings containing nano-hBN with the smallest mean primary particle size of 0.05 μm exhibited the lowest wear. Subsequently, coatings containing 1–15 wt% nano-hBN were prepared to examine the effect of filler content. The results showed that the coatings with low nano-hBN contents (1–2 wt%) had relatively high friction coefficients and significantly reduced wear on both the coating and the counterpart. Cross-sectional scanning electron microscopy (SEM) observations revealed that dispersed small hBN aggregates suppress crack propagation through dispersion strengthening. Coatings with low nano-hBN contents (1–2 wt%) also exhibited sufficient electrical insulation. However, as the hBN content increased further, hBN agglomeration was promoted, weakening the crack-propagation suppression effect and increasing wear. These findings indicate that low-content nano-hBN/si-PI composite coatings are promising electrical erosion-resistant coatings for the outer rings of the bearings used in electric vehicle motors. Full article

To cope with the increasing pressure from diseases and pests under climate change, the effect of 6 maize sowing dates on the plant health of an ultra-early maize variety (Pyroxenia, FAO 130) was analyzed in studies conducted from 2016 to 2018. The assessment of the response of the ultra-early variety to climate change will contribute to the identification of its predisposition to cultivation in terms of health recognition. The extent of plant damage caused by the frit fly (Oscinella frit L.), the European corn borer (Ostrinia nubilalis Hbn.), and the cereal leaf beetle (Oulema melanopus L.), as well as the severity of plant infection by Fusarium ear rot (Fusarium spp.) and maize smut (Ustilago maydis (D.C.) Corda), was assessed. Air temperature, precipitation, and the length of the growing period at individual sowing dates were also analyzed. The lowest level of insect damage and the highest level of disease infection were recorded in the final year of the study (2018), which was dry and had higher mean air temperature. Precipitation and temperature during the sowing dates ranged between 110.5 and 146.1 mm and 17.5 and 19.9 °C, respectively. The optimal sowing date for reducing maize losses caused by insect pests and diseases was found to be the earliest time points, i.e., between April 12 and 26. Full article

Hexagonal boron nitride (h-BN) has been widely applied in catalysis. Nevertheless, most research has focused on using h-BN as a substrate to anchor active transition metals, without probing the intrinsic activity of h-BN vacancies. In this work, we investigated the stability and catalytic activity of different h-BN vacancies. We found that B-terminated vacancies are more likely to be exposed under static conditions. The N_v, BN₂, and BN₃ vacancies show intermediate reaction energies for CH₄ activation. Although the B–N pair over the BN₂ vacancy model has the lowest barrier for CH₄ activation, the negative reaction energy could lead to a high potential for surface poisoning. Interestingly, the unsaturated B–B pair over N_v is a promising site for C–H bond activation. Further COHP analysis implies that the high C–H bond homolytic cleavage activity of the B–B pair arises from its relatively weak interaction, which can promote H insertion. Full article

The escalating power density in Active Phased Array Radar has made the thermal management of Transmitter and Receiver (T/R) modules a critical bottleneck for radar performance. To address the thermal resistance of traditional cold plates, this study investigates an innovative embedded cooling strategy utilizing micro-pyramid arrays and advanced nanofluids. Thermal performance was evaluated using maximum temperature, maximum temperature difference and surface temperature standard deviation (ST). Higher pyramid density markedly enhances temperature uniformity, an effect that scales positively with the power load. Under a 100 W condition, the 8-circle micro-pyramids configuration (the densest structure with roughness Ra = 1.3) achieved a 22.58 K reduction in maximum temperature and a 22.5% improvement in temperature uniformity compared to the 2-circle structure, and outperformed the 4-circle structure by 16.98 K and 17.9%, respectively. Furthermore, a comparative analysis of nanofluids (Al₂O₃, CuO, graphene, and h-BN) is conducted and it is found that graphene nanofluid exhibits the best overall heat transfer enhancement because of its high thermal conductivity and moderate reduction in specific heat capacity. The thermal performance of the nanofluid is evaluated by comparing the maximum temperatures of the heat source at the 8-circle structure. The synergistic coupling of graphene nanofluid with the 8-circle array yields a remarkable 35.38% enhancement in temperature uniformity at 100 W. The enhancement mechanisms are mainly attributed to intrinsic thermophysical properties of the nanoparticles and convection caused by denser pyramid array. The aforementioned findings provide important guidance for the thermal management design of antenna and other high-density integrated electronic systems with embedded cold plate design demand. Full article

In this work, we present a theoretical investigation of electron–surface optical phonon (SOP) interactions and Auger recombination processes in monolayer PtSe₂ and PtS₂ supported on polar dielectric substrates such as SiO₂ and hBN. The analysis is based on a low-energy effective Hamiltonian describing the electronic structure near the K and K′ valleys of the Brillouin zone, combined with the Fröhlich interaction model to account for the coupling between charge carriers and substrate-induced optical phonons. The comparison between Auger recombination and SOP scattering is performed at a representative carrier density of ${n=10}^{12} {\mathrm{c}\mathrm{m}}^{-2}$ within the investigated temperature range. We analyze the formation of polaronic states arising from the hybridization between electronic excitations and SOPs and evaluate the associated Rabi splitting energies and oscillator strengths. The temperature dependence of the SOP-induced scattering rates and the influence of the monolayer–substrate separation on carrier–phonon interactions are also examined. Our results show that electron–phonon coupling strongly depends on the dielectric properties of the supporting substrate, with larger anticrossing gaps predicted for hBN-supported structures compared with SiO₂-supported systems. Auger recombination constitutes the dominant carrier relaxation channel within the investigated temperature range, whereas SOP scattering becomes increasingly significant at elevated temperatures, where both mechanisms approach a comparable inelastic phonon-limited regime. These findings highlight the role of dielectric engineering in controlling carrier relaxation dynamics in Pt-based TMDC heterostructures. Full article

In this study, the effect of boron carbide (B₄C), hexagonal boron nitride (hBN), holy super graphene (HSG), and hybrid (B₄C + hBN + HSG) nano-additives on the tribological performance of SAE 5W-30 gasoline engine oil was investigated on Al-Si-based samples (Al 4032) prepared by cutting from a single-cylinder gasoline engine block. The addition of nano-additives regularly increased the kinematic viscosity; the 63.80 mm²/s (BO) value rose to 68.90 mm²/s at the highest level of B₄C and to 70.50 mm²/s in the hybrid oil (≈10.5% increase). The lowest and most stable friction performance was found in the hybrid 0.025 g/25 mL nano-additive oil, which remained between 0.03 and 0.05 during the entire COF test. The EDS mapping and line scan results confirmed the formation of tribofilm by identifying the additive elements (B for B₄C, B and N for hBN, C for HSG) in the wear scar, and the presence of increased O elements showed the restricted formation of tribo-oxidation. The results show that hybrid nano-additive oils provide the most effective friction and wear improvement, especially at low concentrations, while at high additive levels, performance does not show a consistent increase due to particle accumulation and third-body effects. Full article

The commercialization of V-based catalysts for the selective catalytic reduction of NOx by NH₃ (NH₃-SCR) is hindered by their narrow operating temperature window, insufficient low-temperature (LT) activity, and severe SO₂-to-SO₃ oxidation. To bridge this gap, we herein introduced Nb and hexagonal BN into a VW/TiO₂ system to simultaneously enhance its LT SCR activity, suppress undesired side reactions, and improve durability. Nb incorporation promoted V⁵⁺/V⁴⁺ redox cycling and enhanced lattice oxygen mobility, thus reducing the apparent activation energy and suppressing SO₂ oxidation at elevated temperatures. However, excessive Nb loading induced NH₃ oxidation and N₂O formation. This drawback was mitigated by introducing BN as a dispersion promoter, which helped secure high catalytic performance at a reduced Nb content. The VWNb/Ti-BN catalyst achieved superior NOx conversion and N₂ selectivity over a wide temperature range and benefited from notably suppressed NH₃ oxidation and SO₂-to-SO₃ oxidation. Kinetic analysis revealed that Nb primarily lowered the reaction energy barrier via redox property enhancement, whereas BN accelerated surface reaction turnover by stabilizing and dispersing active acidic sites, markedly increasing the turnover frequency without reducing the activation energy. In situ spectroscopic analysis confirmed the accelerated consumption of adsorbed NH₃ species and enhanced formation of reactive NOx intermediates, indicating SCR pathway enhancement. After aging in the presence of SO₂ and H₂O, the best-performing honeycomb-type monolithic catalyst retained and NOx conversion of >80%, demonstrating excellent long-term durability under practical conditions. A composition-aware machine learning model based on log-ratio-transformed variables quantitatively identified the synergistic balance among V, Nb, W, BN, and TiO₂ as the dominant factor governing LT SCR performance. Thus, this work provides valuable mechanistic insights and a strategy for designing wide-temperature-window SCR catalysts with improved activity, selectivity, and resistance to sulfur poisoning. Full article

Fiber-reinforced polymer (FRP) composites used in marine environments suffer progressive degradation due to hydrothermal aging, which undermines their structural, physical and morphological integrity. In this study, a novel polyester-based nano-gelcoat reinforced with hexagonal boron nitride (h-BN) nanoparticles was developed as an advanced FRP composite coating for marine applications. Glass fiber/epoxy laminates coated with h-BN/polyester nano-gelcoat were subjected to accelerated hydrothermal aging (immersion in 80 °C artificial seawater for 90 days). Mechanical (tensile/flexural tests), viscoelastic (creep and stress relaxation), thermal (DSC/TGA), and morphological (optical microscopy/SEM) analyses were performed on aged and unaged samples. The h-BN-enhanced nano-gelcoat increased the composite’s resistance to hydrothermal aging. In particular, the optimally doped nano-gelcoat (~1 wt% h-BN) retained the highest tensile and flexural strength and modulus, reducing the property losses seen in the unreinforced system by about half (flexural strength 531.29 MPa vs. 1070.52 MPa for the uncoated laminate). Thermal analysis indicated elevated decomposition onset temperatures and higher char yields with h-BN, confirming improved thermal stability. Morphological observations revealed well-dispersed h-BN at 1 wt% with minimal microcracking, whereas higher filler loadings led to agglomeration. Additionally, a TOPSIS-based multi-criteria decision-making (MCDM) analysis was performed across mechanical, viscoelastic, and thermal metrics, which identified the 1 wt% h-BN coating as the most balanced formulation after hydrothermal aging. Full article

The reaction of the pyridylalcohol Ph₂C(OH)CH₂-2-py-6-Me (IH) with Me₃Al in refluxing toluene led to the isolation of the dimer [AlMe₂(μ-OC(Me)Ph₂)]₂ (1), whilst at ambient temperature the complex [(I)AlMe₂]·MeCN (2·MeCN) was isolated. Complex 1 is also readily available via the interaction of diphenylethanol and Me₃Al. Similar treatment of iPr₂C(OH)CH₂-2-py-6-Me (IIH) at ambient temperature afforded [(II)AlMe₂] (3). Treatment of IH and IIH with [VO(OiPr)₃] led to oxo-bridged complexes of the type [(VO)(μ₂-O)(I/II)]₂ (I (4·0.67MeCN), II (5)). The molecular structures of 1–5 are reported. These complexes have been employed as catalysts for the ring-opening polymerization (ROP) of the cyclic esters ε-caprolactone (ε-CL) and δ-valerolactone (δ-VL). For aluminium, complex 1/BnOH produced medium- to high-molecular-weight (M_n) PCL at 20 to 110 °C in solution, though some bi-/multi-modal behaviour was observed; for melts the M_n values were toward the lower end. For complexes 2 and 3, far lower M_n values for PCL were observed at 20 °C in solution and as melts, whilst in solution at 110 °C higher M_n values were achieved, though with less control. In general, M_n values for the PCL obtained using the vanadium complexes were low (≤8560 Da for 4, ≤2920 Da for 5). In the case of PVL, 1/BnOH in solution exhibited higher M_n values at lower temperatures with good control, and when employed as a melt, the M_n was toward the higher end (30,830 Da) observed. For 2/BnOH, much lower M_n values (≤2740 Da) were recorded both in solution and as a melt, whilst for 3, high M_n values were only observed in the absence of BnOH. Low M_n values (≤2920 Da) were also observed for the vanadium complexes 4 and 5. Kinetic results (both ε-CL and δ-VL) revealed that the vanadium complexes, particularly 4, outperformed the aluminium complexes. MALDI-ToF spectra revealed the formation of linear PCL polymers with BnO/H end groups for the aluminium/BnOH complexes in solution, and cyclic polymers when employed as melts. For vanadium, cyclic PCL polymers were the major family present. In the case of PVL, linear (BnO/H end groups) and cyclic polymers were observed when employing the Al/BnOH systems, whilst cyclic polymers were observed for vanadium. Copolymerization of ε-CL and δ-VL using 4/BnOH at 110 °C over 24 h led to incomplete conversion and formation of a random-type copolymer. Full article

Reconfigurable logic is crucial for future adaptive computing, but is challenging to realize with conventional complementary metal-oxide-semiconductor technology due to the limited field-effect characteristics of the fundamental silicon devices. Two-dimensional materials offer a promising platform, yet enhancing their functional versatility requires novel operational mechanisms. Here, we demonstrate a single WSe₂/h-BN/graphene heterojunction capable of dynamically switching between distinct logic functions—XNOR and IMP (implication gate or “IF-THEN” gate)—simply by modulating the drain-source voltage. At a low bias of 0.3 V, the carrier distribution is governed by capacitive coupling, realizing an XNOR gate. Increasing the bias to 3 V activates Fowler–Nordheim tunneling between the graphene floating gate and the drain, enabling IMP logic operation. The interplay and voltage-induced transition between these two physical mechanisms underpin the device’s multifunctional capability. This work introduces a novel operational strategy for two-dimensional material-based reconfigurable logic, providing a pathway toward compact, adaptive hardware for post-CMOS computing. Full article

A composite meeting the UL94 V-0 rating was produced by adding 30 wt% epoxy silane-modified aluminum trihydrate (EPATH) to a 60/40 epoxy/benzoxazine matrix. Various bimodal and trimodal composites containing 20–40 wt% of three types of ceramic fillers, i.e., aluminum oxide (Al₂O₃), boron nitride (BN), and magnesium oxide (MgO), were prepared to simultaneously achieve flame-retardant and thermal conductive properties. The bimodal composites with 40 wt% of Al₂O₃ and MgO exhibited thermal conductivities of 1.22 W/m∙K and 1.29 W/m∙K, respectively, which were superior to that of the composite containing the same amount of ATH (1.0 W/m∙K). In contrast, both the coefficient of thermal expansion (CTE) and shear strength decreased with increasing ceramic filler content. For agglomerated BN, the filler loading was constrained above 30 wt% because its high specific volume caused a significant rise in the viscosity. In the trimodal composites with a total filler content of 40 wt% of Al₂O₃ and BN, a BN fraction of 7.5 wt% yielded the highest thermal conductivity of 1.64 W/m∙K and the lowest water absorption of 0.69%. When the trimodal composites were exposed to −55 °C and 150 °C for 1000 h, they exhibited a reduction in shear strength of less than 30% compared to their initial values. Full article