Search Results (105)

Boronic acids are an important class of molecules diversely used in organic synthesis, catalysis, medicinal chemistry, and for the design of functional materials. Particularly, aryl boronic acids in the solid state are known to exhibit pharmaceutical and photoluminescent properties for antimicrobial, sensing, and drug delivery applications. Furthermore, the phenazine molecule is known for its diverse pharmacological properties, including antibiotic activity. In the case of molecular crystalline solids, it is well established that understanding noncovalent interactions remains key to designing or engineering their functional properties. While both aryl boronic acids and phenazine molecules individually represent an important class of compounds, their co-assembly in the crystalline state is of interest within the context of supramolecular chemistry and crystal engineering. Herein, we report the supramolecular features of two newly synthesized cocrystals, which are composed of para-F/CF₃-substituted phenylboronic acids, respectively, and phenazine, as demonstrated by structure analysis by single-crystal X-ray diffraction. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article

Direct chemical vapor deposition (CVD) growth of hexagonal boron nitride (h-BN) on insulating substrates offers a promising pathway to circumvent transfer-induced defects and enhance device integration. This comprehensive review systematically evaluates recent advances in CVD techniques for h-BN synthesis on insulating substrates, including metal–organic CVD (MOCVD), low-pressure CVD (LPCVD), atmospheric-pressure CVD (APCVD), and plasma-enhanced CVD (PECVD). Key challenges, including precursor selection, high-temperature processing, achieving single-crystalline films, and maintaining phase purity, are critically analyzed. Special emphasis is placed on comparative performance metrics across different growth methodologies. Furthermore, crucial research directions for future development in this field are outlined. This review aims to serve as a reference for advancing h-BN synthesis toward practical applications in next-generation electronic and optoelectronic devices. Full article

This study synthesized boron-doped diamond (BDD) thin films using hot-filament chemical vapor deposition at different carbon-to-hydrogen (C/H) ratios in the range of 0.3–0.9%. The C/H ratio influence, a key parameter controlling the balance between diamond growth and hydrogen-assisted etching, was systematically investigated while maintaining other deposition parameters constant. Microstructural and electrochemical analysis revealed that increasing the C/H ratio from 0.3% to 0.7% led to a reduction in sp2-bonded carbon and enhanced the crystallinity of the diamond films. The improved conductivity under these conditions can be attributed to effective substitutional boron doping. Notably, the film deposited at a C/H ratio of 0.7% exhibited the highest electrical conductivity and the widest electrochemical potential window (2.88 V), thereby indicating excellent electrochemical stability. By contrast, at a C/H ratio of 0.9%, the excessively supplied carbon degraded the film quality and electrical and electrochemical performance, which was owing to the increased formation of sp² carbon. In addition, this led to an elevated background current and a narrowed potential window. These results reveal that precise control of the C/H ratio is critical for optimizing the BDD electrode performance. Therefore, a C/H ratio of 0.7% provides the most favorable conditions for applications in advanced oxidation processes. Full article

4H-silicon carbide (4H-SiC) is a cornerstone for next-generation optoelectronic and power devices owing to its unparalleled thermal, electrical, and optical properties. However, its chemical inertness and low dopant diffusivity for most dopants have historically impeded effective doping. This study unveils a transformative laser-assisted boron doping technique for n-type 4H-SiC, employing a pulsed Nd:YAG laser (λ = 1064 nm) with a liquid-phase boron precursor. By leveraging a heat-transfer model to optimize laser process parameters, we achieved dopant incorporation while preserving the crystalline integrity of the substrate. A novel optical characterization framework was developed to probe laser-induced alterations in the optical constants—refraction index ($\mathrm{n}$) and attenuation index ($\mathrm{k}$)—across the MIDIR spectrum (λ = 3–5 µm). The optical properties pre- and post-laser doping were measured using Fourier-transform infrared spectrometry, and the corresponding complex refraction indices were extracted by solving a coupled system of nonlinear equations derived from single- and multi-layer absorption models. These models accounted for the angular dependence in the incident beam, enabling a more accurate determination of $\mathrm{n}$ and $\mathrm{k}$ values than conventional normal-incidence methods. Our findings indicate the formation of a boron-acceptor energy level at 0.29 eV above the 4H-SiC valence band, which corresponds to λ = 4.3 µm. This impurity level modulated the optical response of 4H-SiC, revealing a reduction in the refraction index from 2.857 (as-received) to 2.485 (doped) at λ = 4.3 µm. Structural characterization using Raman spectroscopy confirmed the retention of crystalline integrity post-doping, while secondary ion mass spectrometry exhibited a peak boron concentration of 1.29 × 10¹⁹ cm⁻³ and a junction depth of 450 nm. The laser-fabricated p–n junction diode demonstrated a reverse-breakdown voltage of 1668 V. These results validate the efficacy of laser doping in enabling MIDIR tunability through optical modulation and functional device fabrication in 4H-SiC. The absorption models and doping methodology together offer a comprehensive platform for paving the way for transformative advances in optoelectronics and infrared materials engineering. Full article

In sealing, sliding, and power transmission operations, surface quality and contact tolerances have high impacts on material system efficiency. Although the boriding process improves the wear resistance of metallic surfaces, it increases surface roughness, affecting the tribological efficiency of material systems. This study presents the tribological results of AISI 4140 boriding surfaces tested using a dehydrated paste pack boriding method with and without a finishing polish process to reduce the roughness. The duration of the boriding process was 1 h at 1123, 1173, 1223, and 1273 K using boron paste obtained from a commercial source and using a pot-polishing process with Al₂O₃ with a particle size of 0.5 μm for 25 min. The samples with and without the finishing polish process were structurally characterized using X-ray diffraction, and the boride coating adhesion was determined using Rockwell C indentation. The tribological properties of the boride surface with and without the finishing polish process were determined using a reciprocating sliding test, with a ZrO₂ ball as a counter body. The boride surfaces’ crystalline structure changed with polishing, which revealed the FeB phase and reduced the roughness value. These modifications in the surface characteristics altered the adhesion and tribological performance of the coating, resulting in a more stable tribological performance on the polished boride surfaces, with a reduction in the coefficient of friction (Cof) value from 0.75 ± 0.02 for the tribological test on the 1123 K-P sample to 0.59 ± 0.002 for the 1273 K-P sample surface at 20 N of applied load. Full article

This study explored the use of boron nitride nanotubes (BNNTs) as reinforcing fillers to enhance the mechanical properties of polymer-derived carbon matrix composites. BNNT-reinforced carbon matrix composites containing 0.5–5 wt% BNNTs were fabricated with pyrolysis conducted at different temperatures. X-ray diffraction and Raman spectroscopy revealed enhanced crystallinity and reduced defects in carbon matrix composites with BNNT addition. At 1200 °C pyrolysis temperature, sample shrinkage decreased from 28% in the control sample without BNNT addition to 12% with 5 wt% BNNTs, demonstrating BNNTs’ significant influence on the matrix. The density increased by 20.1% with 5 wt% BNNTs. Mechanical testing demonstrated an enhancement in the failure strain from 0.7% to 0.8% and an 87.8% increase in the work of fracture with 5 wt% BNNTs. Furthermore, the flexural strength and modulus improved by 68.7% and 55.6%, respectively, at this BNNT concentration. Increasing the pyrolysis temperature to 1500 °C further boosted the mechanical properties, with the flexural strength increasing by 283.7% and the flexural modulus by 528.6% when comparing samples containing 5 wt% BNNTs to those without BNNT reinforcement. Samples processed at 1500 °C with 5 wt% BNNT composition exhibited optimal performance. Full article

The full potential of glauconite-based nanocomposites as micronutrient fertilizers remains underexplored, particularly their interaction with Zn, Cu, and B. Despite the promising applications, the mechanisms of nutrient sorption and their effects on plant growth require further investigation, especially concerning structural changes and nutrient delivery efficiency. This study investigates the modification of glauconite with Zn, Cu, and B solutions to create multifunctional nanocomposites with enhanced properties. It was established that the activation process preserves the primary globular–lamellar morphology of glauconite while introducing structural changes. Nanocomposites were synthesized using chemical activation and characterized using XRD, SEM-EDS, TEM, FTIR, and BET analyses. Agrochemical tests evaluated their effects on oat growth under controlled conditions. Nanocomposites with zinc sulfate exhibited an increase in specific surface area and mesoporosity, enhancing sorption capacity and facilitating the formation of inner-sphere complexes on the mineral’s basal surface. Modification with copper led to the formation of secondary phases, such as sulfates, on the surfaces of microflakes and globules while preserving the crystalline structure with inner-sphere coordination of Cu²⁺. Boron-modified nanocomposites were characterized by localized restructuring, pore channeling, and an increase in mesopore diameter, along with the formation of outer-sphere complexes relative to the basal surface of glauconite. Thermogravimetric and calorimetric analyses with mass spectrometry revealed specific endothermic and exothermic effects, particularly in Zn-modified samples, confirming changes in dehydration energetics. Agricultural tests on oats (Avena sativa) demonstrated the effectiveness of Cu- and B-modified nanocomposites in improving plant growth parameters, including a 7% increase in plant height and a 6.4% increase in dry weight. Zn-modified nanocomposites showed high germination rates (up to 100%) at low dosages but require optimization to avoid phytotoxicity at higher concentrations. The findings highlight the potential of adapting nanocomposites for targeted nutrient release. Additionally, glauconite nanocomposites have potential applications in restoring degraded soils, treating polluted runoff, and developing slow-release agrochemical systems. Full article

Boron nitride nanostructures (BNNs), including nanotubes, nanosheets, and nanoribbons, are renowned for their exceptional thermal stability, chemical inertness, mechanical strength, and high surface area, making them suitable for advanced material applications. Metal–organic frameworks (MOFs), characterized by their porous crystalline structures, high surface area, and tunable porosity, have emerged as excellent candidates for gas adsorption and storage applications, particularly in the context of hydrogen. This paper explores the synthesis and properties of BNNs and MOFs, alongside the innovative approach of integrating BNNs within MOFs to create composite materials with synergistic properties. The integration of BNNs into MOFs enhances the overall thermal and chemical stability of the composite while improving hydrogen sensing and storage performance. Various synthesis methods for both BNNs and MOFs are discussed, including chemical vapor deposition, solvothermal synthesis, and in situ growth, with a focus on their scalability and reproducibility. Furthermore, the mechanisms underlying hydrogen sensing and storage are examined, including physisorption, chemisorption, charge transfer, and work function modulation. Electrochemical characterization techniques, such as cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge–discharge, are used to analyze the performance of BNN-MOF systems in hydrogen storage and sensing applications. These methods offer insights into the material’s electrochemical behavior and its potential to store hydrogen efficiently. Potential industrial applications of BNN-MOF composites are highlighted, particularly in fuel cells, hydrogen-powered vehicles, safety monitoring in hydrogen production and distribution networks, and energy storage devices. The integration of these materials can contribute significantly to the development of more efficient hydrogen energy systems. Finally, this study outlines key recommendations for future research, which include optimizing synthesis techniques, improving the hydrogen interaction mechanisms, enhancing the stability and durability of BNN-MOF composites, and performing comprehensive economic and environmental assessments. BNN-MOF composites represent a promising direction in the advancement of hydrogen sensing and storage technologies, offering significant potential to support the transition toward sustainable energy systems and hydrogen-based economies. Full article

Recent research has focused on immunotherapy with no side effects as an innovative medical treatment for cancer. However, typical drugs for immunotherapy are very expensive. Here, we propose the use of immunoceramics that activate immune cells by contact with their surface. Previous studies demonstrated that polymers, including the phenylboronic acid group, could activate lymphocytes. This activation may be due to the interaction between the sugar chains in cells and the OH group in B(OH)₃ formed via the dissociation of the BO₂ group. We have clarified that boron-containing apatite (BAp) activated lymphocytes in vitro. In this study, we fabricated the ceramic surfaces using the CaO-P₂O₅-SiO₂-B₂O₃ system (CPSB ceramics) containing BAp as a main crystalline phase. The results of the in vitro evaluation indicated that killer T cells in splenocytes cocultured with the CPSB ceramics were more numerous than in splenocytes cocultured on a control surface. The results of the in vivo evaluation indicated that the CPSB ceramics significantly inhibited tumor growth when CD8-positive T cells were cultured on individual ceramics and subsequently injected into tumor-bearing mice. The present CPSB ceramics are expected to be a valuable biomaterial for immunotherapy. Full article

Fused deposition modeling (FDM) 3D printing has the advantages of a simple molding principle, convenient operation, and low cost, making it suitable for the production and fabrication of complex structural parts. Moving forward to mass production using 3D printing, the major hurdle to overcome is the achievement of high dimensional stability and adequate mechanical properties. In particular, engineering plastics require precise dimensional accuracy. In this study, we overcame the issues of FDM 3D printing in terms of ternary material compounds for polyamides with gradient structures. Using multi-walled carbon nanotubes (MWCNTs) and boron nitride (BN) as fillers, polyamide 6 (PA6)-based 3D-printed parts with high dimensional stability were prepared using a single-nozzle, two-component composite fused deposition modeling (FDM) 3D printing technology to construct a gradient structure. The ternary composites were characterized via DSC and XRD to determine the optimal crystallinity. The warpage and shrinkage of the printed samples were measured to ensure the dimensional properties. The mechanical properties were analyzed to determine the influence of the gradient structures on the composites. The experimental results show that the warpage of pure polymer 3D-printed parts is as high as 72.64%, and the introduction of a gradient structure can reduce the warpage to 3.40% by offsetting the shrinkage internal stress between layers. In addition, the tensile strength of the gradient material reaches up to 42.91 MPa, and the increasing filler content improves the interlayer bonding of the composites, with the bending strength reaching up to 60.91 MPa and the interlayer shear strength reaching up to 10.23 MPa. Therefore, gradient structure design can be used to produce PA6 3D-printed composites with high dimensional stability without sacrificing the mechanical properties of PA6 composites. Full article

The paper presents the results of the study of the processes of self-propagating high-temperature synthesis of Zr-1%B alloy and its refining by electron beam melting. Experiments on the influence of boron’s amorphous and crystalline modifications on the safety parameters of the synthesis process of Zr-1%B alloy necessitated the conversion of amorphous boron into crystalline form by electron beam melting, with an increase in its purity from 94% to 99.9%. High efficiency of vacuum induction and electron beam equipment was demonstrated, which provided a high purity of the Zr-1%B alloy of at least 99.9%. The alloy ingots had a uniform distribution of the alloying element (boron) all over the volume. The obtained alloy is suitable for the production of materials with thermal neutron capture cross-sections of up to 40 barns for neutron protection. Full article

Crystalline calcium fluoride (CaF₂) is drawing significant attention due to its great potential of being the gate dielectric of two-dimensional (2D) material MOSFETs. It is deemed to be superior to boron nitride and traditional silicon dioxide (SiO₂) because of its larger dielectric constant, wider band gap, and lower defect density. Nevertheless, the CaF₂-based MOSFETs fabricated in the experiment still present notable reliability issues, and the underlying reason remains unclear. Here, we studied the various intrinsic defects and adsorbates in CaF₂/molybdenum disulfide (MoS₂) and CaF₂/molybdenum disilicon tetranitride (MoSi₂N₄) interface systems to reveal the most active charge-trapping centers in CaF₂-based 2D material MOSFETs. An elaborate Table comparing the importance of different defects in both n-type and p-type devices is provided. Most impressively, the oxygen molecules (O₂) adsorbed at the interface or surface, which are inevitable in experiments, are as active as the intrinsic defects in channel materials, and they can even change the MoSi₂N₄ to p-type spontaneously. These results mean that it is necessary to develop a high-vacuum packaging process, as well as prepare high-quality 2D materials for better device performance. Full article

The distinct spin, optical, and coherence characteristics of solid-state spin defects in semiconductors have positioned them as potential qubits for quantum technologies. Both bulk and two-dimensional materials, with varying structural properties, can serve as crystalline hosts for color centers. In this study, we conduct a comparative analysis of the spin–optical, electron–nuclear, and relaxation properties of nitrogen-bound vacancy defects using electron paramagnetic resonance (EPR) and electron–nuclear double resonance (ENDOR) techniques. We examine key parameters of the spin Hamiltonian for the nitrogen vacancy (${NV}^{-}$) center in 4H-SiC: D = 1.3 GHz, A_zz = 1.1 MHz, and C_Q = 2.53 MHz, as well as for the boron vacancy ($V_B^{-}$) in hBN: D = 3.6 GHz, A_zz = 85 MHz, and C_Q = 2.11 MHz, and their dependence on the material matrix. The spin–spin relaxation times T₂ (${NV}^{-}$ center: 50 µs and $V_B^{-}$: 15 µs) are influenced by the local nuclear environment and spin diffusion while Rabi oscillation damping times depend on crystal size and the spatial distribution of microwave excitation. The ENDOR absorption width varies significantly among color centers due to differences in crystal structures. These findings underscore the importance of selecting an appropriate material platform for developing quantum registers based on high-spin color centers in quantum information systems. Full article

Due to the increasing demands for improved radiation safety and the growing concerns regarding the excessive use of plastics, this work aimed to develop effective and eco-friendly thermal-neutron-shielding materials based on recycled high-density polyethylene (r-HDPE) composites containing varying surface-treated gadolinium oxide (Gd₂O₃) contents (0, 5, 10, 15, and 20 wt%). The results indicate that the overall thermal-neutron-shielding properties of the r-HDPE composites were enhanced with the addition of Gd₂O₃, as evidenced by large reductions in I/I₀, HVL, and TVL, as well as the substantial increases in ∑_t and ∑_t/ρ of the composites. Furthermore, the results reveal that the values for tensile properties initially increased up to 5–15 wt% of Gd₂O₃ and then gradually decreased at higher contents. In addition, the results show that the addition of Gd₂O₃ particles generally increased the density (ρ), the remaining ash at 600 °C, and the degree of crystallinity (%XC) of the composites. This work also determined the effects of gamma irradiation on relevant properties of the composites. The findings indicate that following gamma aging, the tensile modulus slightly increased, while the tensile strength, elongation at break, and hardness (Shore D) showed no significant (p < 0.05) differences, except for the sample containing 5 wt% of Gd₂O₃, which exhibited a noticeable reduction in elongation at break. Furthermore, by comparing the neutron-shielding and mechanical properties of the developed r-HDPE composites with common borated polyethylene (PE) containing 5 wt% and 15 wt% of boron, the results clearly indicate the superior shielding and tensile properties in the r-HDPE composites, implying the great potential of r-HDPE composites to replace virgin plastics as effective and more eco-friendly shielding materials. Full article