Search Results (7,707)

Boron is a chemically distinctive bioelement whose electron-deficient structure enables reversible coordination with oxygen-rich functional groups such as diols and hydroxyls. This property allows boron to modulate molecular stability, conformation, and biological reactivity, giving rise to both beneficial pharmacological effects and toxicological outcomes. This review examines the dual biological role of boron through the framework of bioactive boron-containing natural products and natural compounds capable of forming reversible boron complexes. Particular attention is given to naturally occurring boron-containing antibiotics, including the polyketide macrodiolides boromycin, aplasmomycin, tartrolons, and hyaboron, where boron plays a direct structural and functional role in antimicrobial activity. These compounds demonstrate how boron coordination can influence ion transport, membrane interactions, and molecular assembly, contributing to potent antibacterial properties. Beyond intrinsically boron-containing metabolites, many natural antibiotics and toxins possess oxygen-rich architectures capable of forming transient borate complexes through vicinal 1,2-diol motifs. Examples include polyene macrolide antibiotics such as amphotericin B, fungichromin, and nystatin, as well as tetracyclines, rifamycins, and macrolides such as sorangicin A, where boron coordination may affect solubility, aggregation, ionophoric behavior, and biological selectivity. Similar chemistry is observed in marine neurotoxins and polyether toxins—including tetrodotoxin, saxitoxin derivatives, azaspiracids, pectenotoxins, ciguatoxins, and gambierones—whose hydroxyl-rich frameworks enable reversible interactions with boron species present in seawater. Such complexation may enhance aqueous stability and contribute to trophic transfer and bioaccumulation within marine ecosystems. By framing boron as a molecular “double edge,” this review integrates chemical, biological, and environmental perspectives to highlight how boron coordination can simultaneously enhance antimicrobial activity while influencing toxicity and ecological persistence. Recognizing the role of boron in shaping the activity of natural products provides new insight into antibiotic function, toxin behavior, and the broader impact of boron chemistry in biological systems. Full article

The rapid growth of polyethylene terephthalate (PET) waste and the limitations of conventional recycling methods for mixed waste streams emphasize the need for chemical recycling routes that deliver high-value monomers in a sustainable, resource-efficient manner. This work explores N-heterocyclic carbenes (NHCs) as organocatalysts for the glycolysis of PET with ethylene glycol to bis(hydroxyethyl)terephthalate (BHET), aiming for milder conditions and higher activity. A systematic catalyst screening links steric and electronic properties (percent buried volume, Tolman electronic parameter) of the NHCs to performance in the glycolysis process, resulting in a catalyst system with high PET conversion (up to 97%) and BHET yield (up to 65%). Mechanistic investigations (experimental and computational) support an anionic activation pathway for glycolysis. To lower the reaction temperature, selective cosolvent systems were explored, albeit with some loss of catalytic activity. Cooperative catalysis combining NHCs with Lewis acids enhances activity, leading to a high conversion (up to 90%) while maintaining lower temperatures than state-of-the-art glycolysis methods. The process was successfully transferred to post-consumer waste streams to validate the practicality. Full article

The bioconversion of propionate, a well-known intermediate of anaerobic digestion (AD), to methane is energetically unfavorable under standard conditions, which typically occurs in the syntrophy of bacteria and methanogens via methylmalonyl-CoA (MMC) and the dismutation pathway. Since the latter, which is reported only in Smithella, possessed a thermodynamic advantage over the former, enriching Smithella and promoting the syntrophic interaction and metabolism of the microbiota are important for improving AD efficiency. In this study, lysine-modified Fe₃O₄ (Lys@Fe₃O₄) significantly enhanced the bioconversion of propionate to methane. The methane yield and the maximum methane production rate (R_max) in a Lys@Fe₃O₄ reactor were 278.7% and 271.7% of Blank, and the corresponding values were 201.9% and 201.6% of bare Fe₃O₄, respectively. The metaproteomic results indicated that Lys@Fe₃O₄ increased not only the abundance of Smithella but also the expression of cell surface and adhesion proteins, thereby promoting syntrophic interaction between Smithella and methanogens and facilitating electron and acetate transfer from Smithella to methanogens. Moreover, the expression of quorum-sensing proteins was enhanced, benefiting the cooperation of Smithella and its associated bacterium (Syntrophomonas). Furthermore, the expressions of key enzymes related to metabolism and electron transfer in propionate oxidation, butyrate oxidation, CO₂-reductive methanogenesis and acetoclastic methanogenesis were all significantly upregulated. The results are of great significance for maintaining low propionate concentration and stability of AD. Full article

As one of the three fundamental modes of heat transfer, thermal radiation has long attracted interest due to its independence from a medium and its strong temperature dependence. In extreme environments such as deep space exploration and cryogenic engineering, thermal radiation often becomes the dominant heat transfer mechanism. Consequently, the radiative properties of materials are crucial for achieving precise thermal control, directly influencing the thermal stability and overall performance of advanced systems, including space probes, cryogenic devices, and superconducting components operating under high-vacuum and low-temperature conditions. This paper provides a systematic review of the physical mechanisms, key factors affecting emissivity, major measurement methods, and technological developments related to material radiative properties at cryogenic temperatures. Particular attention is given to experimental methods and techniques describing material radiative behavior, along with a comparative analysis of the suitability of different measurement techniques for cryogenic applications. Finally, the study highlights the significant practical value of this research for fields such as aerospace, precision electronics, and cryogenic instrumentation, aiming to offer insights for optimizing cryogenic thermal management and guiding the design of novel functional materials. Full article

In₂O₃ has high electron mobility, strong affinity for oxidizing gases, and abundant tunable surface oxygen species. These features enable efficient charge transfer during ozone adsorption, making In₂O₃ a promising ozone-sensing material. However, conventional In₂O₃-based gas sensors still suffer from insufficient sensitivity at low ozone concentrations and slow response/recovery rates, limiting their performance for high-precision gas detection. In this study, morphology-controlled In₂O₃ nanorods were synthesized via a glucose-assisted hydrothermal method, enabling coordinated regulation of the material structure and surface properties. Compared with conventional In₂O₃ nanocubes, the glucose-modulated In₂O₃ nanorods exhibited an approximately sevenfold increase in response toward 1 ppm O₃, indicating markedly improved capability for detecting low-concentration ozone. In addition, the sensor demonstrated a relatively low detection limit of about 80 ppb and fast response/recovery behavior (108 s/238 s). This strategy improves gas sensing performance through morphology optimization, increased surface active sites, and enhanced electron transport, offering a feasible materials design route for high-performance ozone gas sensors and showing potential for real-time environmental ozone monitoring and related applications. Full article

Hybrid nanomaterials that integrate surface functionality, colloidal stability, and efficient electron-transfer pathways are highly attractive for improving electrochemical sensing performance. Herein, we report the fabrication and evaluation of polyethyleneimine-functionalized gallium nitride nanoparticles (GaN) decorated with gold nanoparticles (GaN-PEI-Au) as a tunable electrode modifier for enhanced differential pulse voltammetry (DPV) detection of erythromycin. Branched polyethyleneimine was employed as a multifunctional interfacial layer to stabilize GaN dispersions, introduce amine-rich surface chemistry, and enable in situ gold nanoparticle formation at the GaN-PEI. The optimized GaN-PEI-Au material exhibited high colloidal stability, a characteristic Au localized surface plasmon resonance in the ~520–525 nm range, and well-defined Au nanoparticles attached to the GaN surface. When applied as an electrode coating, GaN-PEI-Au significantly enhanced the erythromycin oxidation response compared to bare Au and GaN-PEI interfaces, consistent with synergistic increases in electroactive surface area and interfacial charge-transfer efficiency. Under optimized DPV conditions, GaN-PEI-Au-modified electrodes enabled quantitative erythromycin determination with a linear range of 5 nM–2 µM (R² = 0.990), sensitivity of 1.32 × 10⁻³ µA nM⁻¹, and a limit of detection of 52.5 nM, while maintaining stable baseline behavior during repeated scans. The reported GaN-PEI-Au nanocomposites represent a robust platform for sensitive electrochemical detection of pharmaceutical compounds. Full article

Nanoscale electrical contacts, especially those between materials of dissimilar electronic properties, often represent one of the main causes of drops in energy transfer efficiency. They are also among the sources of above-threshold noise, and their performance often decreases over the lifetime of the nanodevices. Scale-down limitations from mesoscopic to nanoscale devices, and likewise, of nanoscale to quantum-scale devices are also impeded by contacts’ quality. Making more reliable, energy-efficient electrical contacts is among the goals of the nanoelectronics research within the framework of energy-efficient electronic systems. This report focuses on the design, nanofabrication, and testing of novel shapes of electrical contacts. Lithography and nanofabrication were utilized to mimic the approximate shape of insect setae for mesoscale contacts design. The contacts are tested for elementary charge transport via I–V curves and for the broadband, 1/f noise. Tests show that contacts design leads to a measurable decrease in the energy necessary to operate a contact as a switch by at least 12–20%, depending on temperature, while broadband noise shows measurably lower power spectra, for bio-inspired contacts. The proposed method is open to modifications and improvements as required by various on-chip applications. Full article

Background/Objectives: Medicinal plants are widely investigated due to their rich content of biologically active secondary metabolites with potential therapeutic applications. This study aimed to investigate the phytochemical profile and antioxidant activity of extracts with different polarities obtained from Justicia thunbergioides (Lindau) Leonard (Acanthaceae). Methods: Phytochemical screening was initially performed through qualitative analysis, followed by fractionation and characterization of dichloromethane and methanolic extracts using thin-layer chromatography (TLC) and gas chromatography–mass spectrometry (GC–MS). Antioxidant activity was evaluated using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay and electrochemical techniques. Results: GC–MS analysis of the dichloromethane extract revealed a chemically diverse composition, including compounds such as spathulenol, vitamin E, sesamin, squalene, and β-sitosterol, which are widely reported in the literature for their antioxidant and bioactive properties. The methanolic extract exhibited a distinct chemical profile, with a predominance of phenolic and redox-active compounds. DPPH assays demonstrated that the methanolic extract showed the highest radical scavenging capacity in a concentration-dependent manner, whereas the dichloromethane and hexane extracts required higher concentrations to achieve moderate antioxidant effects. Electrochemical analyses indicated that the methanolic extract is rich in electroactive metabolites capable of partially reversible electron transfer, consistent with its enhanced antioxidant performance. Conclusions: Collectively, these findings highlight the antioxidant efficacy of the polar extracts from J. thunbergioides and contribute to a better understanding of the bioactivity of their phytochemical constituents. Full article

Biochar provides a porous scaffold, conductive carbon framework and redox-active surface functional that can promote microbial attachment and extracellular electron flow. However, how feedstock-dependent biochar properties regulate the biochar–cell interface and microbial metabolism during contaminant removal remains insufficiently understood. Here, biochar derived from rice husk, corn straw and corn cob was used to immobilize Pseudomonas chlororaphis for triclocarban removal in batch microcosms. Multiscale analyses, including scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), (electrochemical impedance spectroscopy (EIS) and liquid chromatography–mass spectrometryLC-MS, were combined to link the biochar structure, interface and extracellular metabolism signatures with triclocarban (TCC) removal. Compared with free cells, all composites enhanced TCC removal and exhibited altered interfacial functional-group features together with substantially reduced fitted charge-transfer resistance, indicating facilitated interfacial electron exchange. Untargeted metabolomics further revealed consistent remodeling of extracellular redox-associated metabolite signatures upon immobilization, with increased quinone/polyphenol-associated features and pathway-level shifts related to redox homeostasis. Among feedstocks, the corn cob composite showed the highest triclocarban removal. Overall, this work proposes an evidence-supported “structure–interface–metabolism” framework for interpreting how agricultural-residue biochars modulate biofilm interfaces and redox-related metabolic signatures to improve triclocarban removal, providing guidance for designing biochar-supported bioprocesses for halogenated micropollutants. Full article

Rare Earth Elements (REEs) represent strategic and critical raw materials for the energy transition and must therefore be integrated into efficient and functional recycling processes. Their adoption in electric motors is rapidly expanding, raising significant challenges for end-of-life (EoL) management, starting from the collection phase. In this context, this work proposes the integration of an image-based classification framework within the Waste Electrical and Electronic Equipment (WEEE) recycling pipeline to selectively identify electric motors containing permanent magnets (PMs) and direct them toward dedicated recycling processes for rare earth recovery. The proposed methodology relies on a Discriminative Transfer Learning (DTL) approach based on a ResNeXt convolutional neural network (CNN), adapted to a proprietary and heterogeneous dataset of electric motors acquired in an industrial recycling facility. The objective is twofold: first, to identify motors containing PMs; second, to classify motors into construction categories according to their likelihood of incorporating PMs. Experimental results show promising performance in terms of PM-containing motor detection capability, establishing a robust foundation for the automated recovery of REEs at an industrial scale. Furthermore, the model’s generalization capabilities can be further enhanced through the expansion of collaborative datasets and the integration of advanced scanning technologies. Full article

We report a versatile, CMOS-compatible fabrication module for sub-100 nm TiN and TaN pillar electrodes, a key building block for sandwich-type test structures. As a demonstration, the electrodes were integrated into carbon nanotube-based nonvolatile random-access memory (CRAM) test structures. High-resolution hydrogen silsesquioxane (HSQ) masks defined by electron beam lithography were transferred into TiN films using optimized Ar/Cl₂ inductively coupled plasma reactive ion etching. Optical emission spectroscopy was used for real-time endpoint detection, ensuring precise etch control. The process achieved a TiN-to-HSQ selectivity of ~1.6 and reproducible nanoscale features with smooth sidewalls and an average taper angle of ~77°. Buffered hydrogen fluoride treatment effectively removed residual HSQ, revealing sharp TiN features and preserving pillar geometry. Atomic force microscopy (AFM) confirmed pillar height and profile fidelity, while conductive AFM verified electrical conductivity after planarization. The module was further demonstrated through the fabrication of TiN pillar arrays, TaN pillars, and sub-100 nm TiN line arrays. A CRAM test structure incorporating TiN pillars exhibited preliminary switching, indicating that both the test structure and fabrication process are feasible. This fabrication module provides a reproducible platform for nanoscale TiN and TaN electrodes, supporting laboratory-scale research and providing a pathway toward future integration of emerging memory and nanoelectronic technologies. Full article

This paper proposed an ultra-miniaturized four-port dual-band multi-input multi-output (MIMO) antenna designed for wireless biomedical implantable devices, including wireless capsule endoscopy (WCE) and cardiac leadless pacemakers. The antenna supports operation in the wireless medical telemetry service (WMTS) band of 1.395–1.4 GHz and the industrial, scientific, and medical (ISM) band of 2.4–2.4835 GHz for wireless power transfer and data telemetry applications. Miniaturization is achieved through a partial meandered structural configuration, yielding an overall size of 8 × 6.4 × 0.5 mm³. The antenna is encapsulated within implantable biomedical devices containing batteries, sensors, and electronic components, and evaluated in both homogeneous and realistic heterogeneous body phantoms, including the large intestine and heart. The full-wave electromagnetic simulation results demonstrate good performance, including reflection coefficients of −31.19 dB and −30.07 dB, gains of −27.5 dBi and −17.5 dBi, −10 dB impedance bandwidths of 170 MHz and 370 MHz, mutual coupling below 20 dB, and fractional bandwidths of 12.2% and 15.1% at 1.4 GHz and 2.45 GHz, respectively. Specific absorption rate (SAR) analysis satisfies implantation safety limits. Link budget analysis confirms reliable communication over distances more than 20 m in both frequency bands with high-data rates up to 100 Mbps. MIMO channel parameters such as envelope correlation coefficient (ECC), diversity gain (DG), channel capacity loss (CCL), and total active reflection coefficient (TARC) confirm the usefulness of the proposed MIMO antenna. Consequently, the proposed MIMO antenna emerges as a highly promising candidate with, ultra-miniaturization, isolation, multiband operation ability with omnidirectional-like radiation pattern characteristics for several biomedical implants in wireless health monitoring systems. Full article

To enable the efficient and environmentally benign treatment of phenol-containing wastewater, a nitrogen-doped porous carbon material (denoted as 900-CN) was synthesized via high-temperature annealing of a composite composed of humic acid (HA) and g-C₃N₄. The as-prepared materials were characterized, and their catalytic performance in activating peroxymonosulfate (PMS) for phenol degradation was investigated. The results demonstrate that g-C₃N₄ acts as a layered template; upon high-temperature annealing, it gradually evolves into a highly wrinkled and porous architecture. This morphology substantially increases the specific surface area, thereby facilitating pollutant removal. PMS formed metastable surface complexes on 900-CN, enabling concomitant electron transfer. Concurrently, functional groups on the HA-derived carbon reacted with PMS to generate singlet oxygen (¹O₂), a highly oxidative species that markedly enhanced phenol degradation. The 900-CN composite achieved complete phenol removal (100%) within 60 min. Variations in reaction temperature (20–50 °C) and initial pH (2–10) exhibited negligible influence on the performance of the 900-CN/PMS system. Reactive species in the 900-CN/PMS/phenol system included •OH, SO₄^•−, O₂^•−, and ¹O₂, indicating that phenol degradation occurred through combined radical and non-radical pathways. These findings highlight the strong potential of 900-CN as a promising catalyst for the treatment of phenolic wastewater. Full article

Background: Tumor-derived small extracellular vesicles (sEV), which we call TEX, carry a cargo of molecules that resembles the producer tumor cells. Circulating freely in body fluids, TEX potentially serve as a liquid tumor biopsy. TEX horizontally transfer their cargo to various recipient cells, imparting to them pro-tumor activity. Mechanisms of TEX-driven reprogramming might involve nucleic acids, especially double-stranded (ds)DNA. Methods: TEX isolated from supernatants of human tumor cells were identified as sEV, based on their size, endocytic origin and morphology. TEX treated with DNase/RNase cocktail were examined by transmission and cryo-electron microscopy and tested for biologic activity. DNA was extracted from enzyme-treated TEX, quantified by Qubit and analyzed for fragment sizes. The presence of genomic DNA in TEX was confirmed by PCR, and sequencing of the TP53 gene fragment for a mutational signature was performed. Results: Enzymatic and microscopic studies of TEX showed that nucleic acids are present in the biocorona on the outer surface. Their removal interfered with the biocorona integrity. A short TEX exposure to DNase/RNase altered their morphology without impairing vesicle functions; longer treatments induced TEX re-organization into smaller membrane-bound vesicles. The TEX lumen contained long fragments of protected genomic DNA with a mutational signature reflecting that of the tumor. Conclusions: Nucleic acids present on the TEX surface support the vesicular integrity. The TEX lumen contains membrane-protected large (ds)DNA fragments with the mutational signature of the parent tumor. The presence of surface and luminal nucleic acids in TEX, and especially their mutational signature, suggests that TEX may serve as highly promising cancer-specific biomarkers. Full article

To mitigate the intrinsic high corrosion susceptibility of AZ31B magnesium alloy, a three-step synergistic surface modification strategy was developed in this work: initially, a MgO ceramic coating was in situ fabricated on the AZ31B substrate via micro-arc oxidation (MAO); subsequently, a TiO₂ sealing barrier layer was deposited on the MAO coating through a deep ultraviolet (DUV)-assisted sol–gel method; finally, a superhydrophobic top layer was constructed via fluoroalkylsilane (FAS) self-assembly. The microstructural characteristics, chemical compositions and corrosion resistance of the coatings at different modification stages were comprehensively characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), water contact angle (WCA) measurements and electrochemical tests. The results showed that the as-deposited TiO₂ was predominantly anatase phase, and FAS molecules were firmly anchored on the coating surface via Si-O-Ti covalent bonds, endowing the composite coating with a WCA of up to 160°. Electrochemical tests demonstrated that the FAS-TiO₂-MAO composite coating exhibited an ultra-low corrosion current density of 1.31 × 10⁻⁹ A/cm² and a remarkably high charge transfer resistance (R_ct) of 3.46 × 10⁸ Ω·cm². Compared with the bare AZ31B substrate, the corrosion current density was decreased by nearly four orders of magnitude, while the charge transfer resistance was enhanced by approximately six orders of magnitude, indicating a significant improvement in corrosion resistance. Moreover, the composite coating exhibited excellent interfacial adhesion, favorable mechanical durability, and outstanding chemical stability, confirming its reliable long-term corrosion protection and high practical application potential. This work provides a feasible strategy for fabricating high-performance superhydrophobic anticorrosive coatings on magnesium alloys. Full article