Search Results (1,110)

The rapid development of electronic devices has led to increasing requirements for higher-performance thermal interface materials (TIMs). Based on the finite element method, this study investigates the heat transfer enhancement mechanism of polymer-based TIMs reinforced by carbon fiber and boron nitride fillers. An ordered aggregation algorithm and a collision detection algorithm were developed to construct representative volume element models, enabling filler volume fractions exceeding 50 vol% in the simulation. A predictive thermal resistance model was developed and validated, demonstrating good agreement with experimental results. Then, the effects of filler ratio, orientation angle, and size on thermal conductivity were systematically analyzed. Results demonstrate that a high CF/BN ratio can construct more efficient thermal conduction pathways and the optimal ratio is 4 (13.72 W/m∙K). The thermal conductivity exhibits extreme sensitivity to filler orientation, showing an increase of 17.68 times when the angle decreases from 45° to 0°. Meanwhile, the BN particle diameters have less impact on heat transfer; thermal conductivity only increased by 19.9% when D_BN rose from 10 μm to 45 μm. The predictive model based on thermal resistance theory was developed, and the average prediction error was only 5.18%. These findings provide quantitative design principles for developing high-efficiency thermal interface materials through rational filler selection and structural optimization. Full article

The drive to utilize ammonia as a carbon-free hydrogen source necessitates the development of effective, non-precious metal catalysts for ammonia decomposition. We successfully synthesized a series of Ce-based perovskite oxides (CeXO₃; X = Co, Ni, Fe) via combustion method using citric acid. These catalyst precursors were tested for NH₃ decomposition to study the effect of the perovskite structure on catalytic activity. The results were directly compared to corresponding impregnated catalysts, X/CeO₂, which had similar metal concentrations. A remarkable enhancement in catalytic performance was observed with the perovskite catalysts, particularly at lower temperatures, relative to their impregnated counterparts. The exception was the CeFeO₃ catalyst, which exhibited lower activity, likely due to the formation of metal nitrides. Both CeNiO₃ and CeCoO₃ showed good NH₃ decomposition activity, but CeNiO₃ emerged as the most active catalyst at lower temperatures. This superior performance attributed to the presence of oxygen vacancies—confirmed by Raman and XPS analyses—and enhanced metal reducibility at lower temperatures, both of which accelerate NH₃ decomposition. Furthermore, CeNiO₃ also displayed a high surface metal concentration. These Ce-based perovskite materials are cost-effective, easily synthesized, and highly stable; hence, they are attractive candidates for large-scale hydrogen production. Full article

Developing efficient photocatalysts is essential for sustainable wastewater treatment and tackling global water pollution. Graphitic carbon nitride (g-C₃N₄) is a promising material because it is active under visible light and chemically stable. However, its practical application is limited by fast recombination of charge carriers and a low surface area. In this study, we report a simple hydrothermal method to synthesize exfoliated porous g-C₃N₄ (E-PGCN) combined with Ti₃C₂ MXene to form a heterojunction composite that addresses these issues. Various characterization techniques (FTIR, XRD, XPS, SEM, BET) confirmed that adding MXene improves light absorption, increases surface area (53.7 m²/g for the composite versus 21.4 m²/g for bulk g-C₃N₄ (BGCN)), and enhances charge separation at the interface. Under UV-visible light irradiation with Rhodamine B (RhB) as the model pollutant, the E-PGCN/Ti₃C₂ MXene composite containing 3 wt% MXene demonstrated an impressive degradation efficiency of 93.2%. This performance is superior to BGCN (66.6%), E-PGCN (82.5%), and E-PGCN/Ti₃C₂ MXene-5 wt% composites (81%). This is due to the excess Mxene which caused agglomeration and reduced activity. Scavenger studies identified electron radicals as the dominant reactive species, with optimal activity at pH ~4.5. This enhanced performance, 1.4 times greater than BGCN and 1.13 times higher than E-PGCN, is ascribed to the synergistic interplay between the excellent electrical conductivity of MXene and the porous structural features of E-PGCN. This work highlights the importance of morphological engineering and heterojunction design for advancing metal-free photocatalysts, offering a scalable strategy for sustainable water purification. Full article

Aqueous zinc-ion batteries (AZIBs) have attracted considerable attention due to their intrinsic safety, low cost, and environmental friendliness. However, drastic volume expansion, sluggish reaction kinetics, and the insufficient structural stability of electrode materials still remain key challenges. In this work, a cascade structure-guided electron transport strategy was used to construct a vanadium nitride@carbon nanosheet/carbon nanofiber (VN@CNS/CNF) composite as a high-performance cathode for AZIBs. In this rationally engineered architecture, carbon-coated VN nanoparticles are uniformly anchored on a conductive carbon nanofiber network, forming a multidimensional interconnected structure that enables fast electron/ion transport and robust mechanical stability. The carbon shell effectively alleviates volume expansion and prevents VN nanoparticle agglomeration, while the continuous carbon fiber backbone reduces charge transfer resistance and enhances reaction kinetics. Benefiting from this synergistic structural design, the VN@CNS/CNF electrode delivers a high specific capacity of 564 mAh g⁻¹ at 0.1 A g⁻¹, maintains 99% capacity retention after 50 cycles, and retains 280 mAh g⁻¹ even at 8 A g⁻¹ after prolonged cycling. This study provides a new structural engineering strategy for vanadium nitride-based electrodes and provides strategic guidance for the development of fast-charging, durable aqueous zinc-ion batteries. Full article

The green synthesis of hydrogen peroxide (H₂O₂) is crucial for sustainable chemical production, but pristine graphitic carbon nitride (g-C₃N₄) suffers from low H₂O₂ yield owing to limited visible light absorption and swift charge recombination. Herein, a novel metal-free carbon nitride oxide/biochar photocatalytic system (CNO-B) was developed via a simple low-temperature calcination without post-treatment. The synergistic effect of carbonyl functionalization and biochar integration significantly enhanced light harvesting capabilities and charge carrier separation efficiency, achieving an exceptional H₂O₂ production rate of 2483 μmol g⁻¹ h⁻¹ upon irradiation (five times higher compared with pure g-C₃N₄). This work provides valuable insights into minimalist synthesis strategies for designing functional materials and demonstrates a practical approach for valorizing biomass waste in sustainable photocatalytic applications. Full article

Nitrogen oxides (NO_x) are major atmospheric pollutants, and their escalating emissions, driven by rapid economic development and urbanization, pose a severe threat to both the ecological environment and human health. Conventional denitrification technologies are often hampered by high costs, significant energy consumption, and stringent operational conditions, making them increasingly inadequate in the face of tightening environmental regulations. In this context, photocatalytic technology, particularly systems based on graphitic carbon nitride (g-C₃N₄), has garnered significant research interest for NO_x removal due to its visible-light responsiveness, high stability, and environmental benignity. To advance the performance of g-C₃N₄, numerous modification strategies have been explored, including morphology control, elemental doping, defect engineering, and heterostructure construction. These approaches effectively broaden the light absorption range, enhance the separation efficiency of photogenerated electron-hole pairs, and improve the adsorption and conversion capacities for NO_x. Notably, constructing heterojunctions between g-C₃N₄ and other materials (e.g., metal oxides, noble metals, metal–organic frameworks (MOFs)) has proven highly effective in boosting catalytic activity and stability. Furthermore, the underlying photocatalytic mechanisms, encompassing the generation and migration pathways of charge carriers, the redox reaction pathways of NO_x, and the influence of external factors like light intensity and reaction temperature, have been extensively investigated. From an application perspective, g-C₃N₄-based photocatalysis demonstrates considerable potential in flue gas denitrification, vehicle exhaust purification, and air purification. Despite these advancements, several challenges remain, such as limited solar energy utilization, rapid charge carrier recombination, and insufficient long-term stability, which hinder large-scale implementation. Future research should focus on further optimizing the material structure, developing greener synthesis routes, enhancing catalyst stability and poison resistance, and advancing cost-effective engineering applications to facilitate the practical deployment of g-C₃N₄-based photocatalytic technology in air pollution control. Full article

Photocatalytic CO₂ reduction holds great potential for sustainable solar fuel production, yet its practical application is often limited by inefficient charge separation and poor product selectivity. The photothermal effect presents a viable strategy to address these challenges by reducing activation energies and accelerating reaction kinetics. In this work, we report a rationally designed CN-B/Ti₃C₂ heterojunction that effectively leverages photothermal promotion for enhanced CO₂ reduction. The black carbon nitride (CN-B) framework, synthesized via a one-step calcination of urea and Phloxine B, exhibits outstanding photothermal conversion, reaching 131.4 °C under 300 mW cm⁻² illumination, which facilitates CO₂ adsorption and charge separation. Coupled with Ti₃C₂ MXene, the optimized composite (3:1) achieves remarkable CO and CH₄ production rates of 80.21 and 35.13 μmol g⁻¹ h⁻¹, respectively, without any cocatalyst—representing a 2.9-fold and 8.8-fold enhancement over CN-B and g-C₃N₄ in CO yield. Mechanistic studies reveal that the improved performance stems from synergistic effects: a built-in electric field prolongs charge carrier lifetime (3.15 ns) and reduces interfacial resistance, while localized heating under full-spectrum light further promotes CO₂ activation. In situ Fourier transform infrared (FTIR) spectroscopy confirms the accelerated formation of key intermediates (*COOH and *CO). The catalyst also maintains excellent stability over 24 h. This study demonstrates the promise of combining photothermal effects with heterojunction engineering for efficient and durable CO₂ photoreduction. Full article

This study investigated the variation in precipitation in Fe-25Cr-5Al-Ti-RE ferritic stainless steel under different quenching heat treatment temperatures. Quenching heat treatments were performed at five temperatures, namely 600 °C, 700 °C, 800 °C, 900 °C, and 1000 °C. To analyze the alloy’s microstructure and precipitation behavior, comprehensive characterization techniques were employed, including X-ray Diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results demonstrated that after quenching at these temperatures, the main precipitation in the alloy was a chromium-rich phase (α′), aluminum oxide (Al₂O₃), titanium carbide (TiC), and titanium nitride (TiN). Specifically, Al₂O₃ was detected exclusively after heat treatments at 800 °C, 900 °C, and 1000 °C, with its particle size ranging from 10 nm to 100 nm. During high-temperature heat treatment, aluminum atoms and oxygen atoms in the matrix interacted with each other, and fine Al₂O₃ particles precipitated through a solid-state phase transition. Regarding titanium-containing precipitates, TiC precipitated after heat treatments at 700 °C, 800 °C, and 900 °C, whereas TiN was only observed after the quenching treatment at 1000 °C. The size of TiC particles fell within the range of 100 nm to 400 nm, while TiN particles exhibited a significantly larger size, spanning from 5 μm to 10 μm. Thermodynamic and kinetic analyses revealed that at elevated temperatures, nitrogen (N) exhibited a relatively high diffusion coefficient in the matrix; meanwhile, titanium (Ti) demonstrated an extremely strong chemical affinity for N. Consequently, even when the N content in the alloy was at a low level, N tended to preferentially react with Ti rather than with carbon (C) to form TiN. Full article

Insufficient harvesting of visible photons, limited adsorption, and fast recombination of photogenerated electron-hole pairs restrict the application of graphitic carbon nitride (g-C₃N₄). Here, we propose a straightforward solid-phase synthesis method for fabricating 2D/2D graphitic carbon nitride/reduced graphene oxide (SCN/GR) hybrid photocatalysts. The synthesis process involves the thermal condensation of three precursors: dicyandiamide (as the g-C₃N₄ source), NH₄Cl (as a pore-forming agent), and graphene oxide (GO, which is in situ reduced to rGO during thermal treatment). The incorporation of reduced graphene oxide (rGO) into the g-C₃N₄ matrix not only narrows the bandgap of the material but also expedites the separation of photogenerated carriers. The photocatalytic activity of the SCN/GR hybrid was systematically evaluated by degrading ciprofloxacin in aqueous solution under different light conditions. The results demonstrated remarkable degradation efficiency: 72% removal within 1 h under full-spectrum light, 81% under UV light, and 52% under visible light. Notably, the introduction of rGO significantly improved the visible light absorption capacity of g-C₃N₄. Additionally, SCN/GR exhibits exceptional cyclic stability, maintaining its structural integrity and photocatalytic properties unchanged across five successive degradation cycles. This study offers a simple yet effective pathway to synthesize 2D/2D composite photocatalysts, which hold significant promise for practical applications in water treatment processes. Full article

One-pot hydrothermal synthesis of boron nitride quantum dots (BNQDs) offers a simple and widely accessible approach to produce nanoparticles with tailored properties for biomedical purposes, including bioimaging and drug delivery. However, growing evidence suggests that most reported BNQD syntheses yield products with insufficient purity and poorly defined structures, limiting their bioapplications where precise composition and controlled synthesis are paramount. In this study, we present a formation mechanism and demonstrate multiple BNQD synthesis pathways that can be precisely controlled by modulating the reaction equilibrium during hydrothermal synthesis under varying experimental conditions. We demonstrate that carbon-related defects shift BNQD photoluminescence (PL) from the UV to the 400–450 nm region, making them suitable for bioimaging, while BO₂⁻ enrichment introduces additional phosphorescence. Furthermore, we show that as-synthesized BNQD suspensions contain significant contamination by non-luminescent ammonium polyborate salts, which is overlooked in prior studies, and disclose the mechanism of their formation as well as effective purification method. Finally, we assess the biocompatibility of purified BNQDs with tuned PL properties and demonstrate their application in bioimaging using Vero cells. The elucidated nanoparticle formation mechanisms, combined with methods for precise control of optical properties, structural defects and sample purity, enable the reproducible production of reliable and effective BNQDs for bioimaging. Full article

This review addresses the environmental and health risks caused by antibiotic abuse, focusing on the inefficiency of traditional treatment methods and their tendency to cause secondary pollution, as well as the limitations of g-C₃N₄ in photocatalytic antibiotic degradation, such as insufficient visible light utilization and high carrier recombination rates. It systematically summarizes modification strategies and application advances of g-C₃N₄. Compared with previous reviews on carbon nitride, this work distinguishes itself by precisely targeting the cutting-edge application scenario of antibiotic-specific degradation, providing an in-depth analysis of how precursor selection and preparation methods regulate material properties, and emphasizing the role of modification approaches—including crystal optimization, element doping, surface modification, and heterojunction construction—in enhancing catalytic efficiency. It offers targeted and forward-looking insights for the practical application of this material in controlling antibiotic pollution in complex water environments. Full article

Photocatalytic oxidation technology harnesses solar energy for pollutant mineralization, presenting significant potential for environmental applications. A critical bottleneck remains the development of high-performance photocatalysts. This study centers on the non-metallic semiconductor material graphitic carbon nitride (g-C₃N₄). To overcome the inherent limitations of pristine g-C₃N₄, including limited surface area, rapid charge carrier recombination, and inadequate active sites, it implements surface engineering strategies employing acidic (H₂SO₄) or basic (K₂CO₃) agents to modulate microstructure, introduce defect sites (cyano/amino groups), and optimize bandgap engineering. These modifications synergistically enhanced photogenerated charge carrier separation efficiency and surface reactivity, leading to efficient dye degradation. Notably, the K₂CO₃-modified catalyst (g-C₃N₄-OH), synthesized with a mass ratio of m(g-C₃N₄):m(K₂CO₃) = 1:1, achieved 92.2% Rhodamine B degradation within 50 min under visible light, surpassing pristine g-C₃N₄ (20.6%), the optimized H₂SO₄-modified sample (g-C₃N₄-HS, 60.9%), and even template-synthesized g-C₃N₄-SBA (79.6%). The g-C₃N₄-OH catalyst demonstrated exceptional performance under both visible light and natural solar illumination. Combining facile synthesis, cost-effectiveness, superior activity, and robust stability, this work provides a novel approach for developing high-efficiency non-metallic photocatalysts applicable to dye wastewater. Full article

This study aimed to develop an industrially scalable coating route for enhancing the oxidation resistance of carbon fiber fabrics, a critical requirement for next-generation aerospace and high-temperature composite structures. To achieve this goal, synthesis of hexagonal boron nitride (h-BN) layers was achieved via a single wet step in which the fabric was impregnated with an ammonia–borane/THF solution and subsequently nitrided for 2 h at 1000–1500 °C in flowing nitrogen. Thermogravimetric analysis coupled with X-ray diffraction revealed that amorphous BN formed below ≈1200 °C and crystallized completely into (002)-textured h-BN (with lattice parameters a ≈ 2.50 Å and c ≈ 6.7 Å) once the dwell temperature reached ≥1300 °C. Complementary XPS, FTIR and Raman spectroscopy confirmed a near-stoichiometric B:N ≈ 1:1 composition and the elimination of O–H/N–H residues as crystallinity improved. Low-magnification SEM (100×) confirmed the uniform and large-area coverage of the BN layer on the carbon fiber tows, while high-magnification SEM revealed a progressive densification of the coating from discrete nanospheres to a continuous nanosheet barrier on the fibers. Oxidation tests in flowing air shifted the onset of mass loss from 685 °C for uncoated fibers to 828 °C for the coating produced at 1400 °C; concurrently, the peak oxidation rate moved ≈200 °C higher and declined by ~40%. Treatment at 1500 °C conferred no additional benefit, indicating that 1400 °C provides the optimal balance between full crystallinity and limited grain coarsening. The resulting dense h-BN film, aided by an in situ self-healing B₂O₃ glaze above ~800 °C, delayed carbon fiber oxidation by ≈140 °C. Overall, the process offers a cost-effective, large-area alternative to vapor-phase deposition techniques, positioning BN-coated carbon fiber fabrics for robust service in extreme oxidative environments. Full article

Alzheimer’s disease (AD) requires early and accurate identification of affected brain regions, which can be achieved through the detection of specific biomarkers to enable timely intervention. Carbon nanomaterials (CNMs), including graphene derivatives, carbon nanotubes, graphitic carbon nitride, carbon black, fullerenes, and carbon dots, offer high conductivity, large electroactive surface area, and versatile surface chemistry that enhance biosensor performance. While such properties benefit a wide range of transduction principles (e.g., electrochemical, optical, and plasmonic), this review focuses on their role in electrochemical biosensors. This review summarizes CNM-based electrochemical platforms reported from 2020 to mid-2025, employing aptamers, antibodies, and molecularly imprinted polymers for AD biomarker detection. Covered topics include fabrication strategies, transduction formats, analytical performance in complex matrices, and validation. Reported devices achieve limits of detection from the femtomolar to picogram per milliliter range, with linear ranges typically spanning 2–3 orders of magnitude (e.g., from femtomolar to picomolar, or from picogram to nanogram per milliliter levels). They exhibit high selectivity against common interferents such as BSA, glucose, uric acid, ascorbic acid, dopamine, and non-target peptides, along with growing capabilities for multiplexing and portable operation. Remaining challenges include complex fabrication, limited long-term stability and reproducibility data, scarce clinical cohort testing, and sustainability issues. Opportunities for scalable production and integration into point-of-care workflows are outlined. Full article

Highly permeable and selective membranes are crucial for energy-efficient gas separation. Two-dimensional (2D) graphitic carbon nitride (g-C₃N₄) has attracted significant attention due to its unique structural characteristics, including ultra-thin thickness, inherent surface porosity, and abundant amine groups. However, the interfacial defects caused by poor compatibility between g-C₃N₄ and polymers deteriorate the separation performance of membrane materials. In this study, amino-functionalized g-C₃N₄ nanosheets (CN@PEI) was prepared by a post-synthesis method, then blended with the polymer Pebax to fabricate Pebax/CN@PEI mixed matrix membranes (MMMs). Compared to g-C₃N₄, MMMs with CN@PEI loading of 20 wt% as nanofiller exhibited a CO₂ permeance of 241 Barrer as well as the CO₂/CH₄ and CO₂/N₂ selectivity of 39.7 and 61.2, respectively, at the feed gas pressure of 2 bar, which approaches the 2008 Robeson upper bound and exceeded the 1991 Robeson upper bound. The Pebax/CN@PEI (20) membrane showed robust stability performance over 70 h continuous gas permeability testing, and no significant decline was observed. SEM characterization revealed a uniform dispersion of CN@PEI throughout the Pebax matrix, demonstrating excellent interfacial compatibility between the components. The increased free volume fraction, enhanced solubility, and higher diffusion coefficient demonstrated that the incorporation of CN@PEI nanosheets introduced more CO₂-philic amino groups and disrupted the chain packing of the Pebax matrix, thereby creating additional diffusion channels and facilitating CO₂ transport. Full article