Search Results (926)

Pt-based intermetallics are high-efficiency electrocatalysts for the hydrogen evolution reaction (HER) in proton exchange membrane water electrolysis (PEMWE). However, the synthesis of intermetallics usually relies on high-temperature annealing, which easily induces particle agglomeration and limits the improvement of catalytic performance. In this study, a synergistic strategy of spatial confinement and ordered structure regulation is adopted, and indene-derived mesoporous carbon (IMC) is used as the support to controllably synthesize the intermetallic Pt₃Fe catalyst. The IMC support can anchor and spatially confine nanoparticles, thereby preventing particle sintering and agglomeration during high-temperature annealing. In 0.5 mol·L⁻¹ H₂SO₄ electrolytes, the catalyst exhibits excellent catalytic performance: it achieves an overpotential of only 19.1 mV at a current density of 10 mA·cm⁻², which is 9.4 mV lower than that of commercial Pt/C; its mass activity reaches 2.76 A·mg_Pt⁻¹, 8 times that of commercial Pt/C. Chronopotentiometry measurements show negligible potential variation after 190 h of operation at 10 mA·cm⁻². This strategy suppresses particle agglomeration through the spatial confinement effect of IMC and modulates electronic states via the ordered structure, providing a practical route for the scalable preparation of low-cost, highly active and high-stability Pt-based intermetallics for PEMWE applications. Full article

Nickel nanoparticles were synthesized via liquid-phase reduction of NiCl₂·6H₂O with N₂H₄·H₂O. The efficacy of different dispersing agents in preventing agglomeration was systematically compared, establishing a clear processing-dispersion correlation. Four different types of dispersants were selected to compare their effects on the microstructure and dispersibility of nano nickel powder. Among them, Ni nanoparticles prepared using sodium dodecyl sulfate (SDS) as dispersants exhibit superior microscopic morphology and dispersion. And then, the mass ratio between the precursor and dispersant was systematically optimized, resulting in spherical nickel nanoparticles with controllable particle size and favorable physical properties. When the mass ratio of SDS to Ni salt reached 150%, the prepared spherical Ni nanoparticles had the optimal dispersion and a minimum average particle size of 79 ± 12 nm. By estimating N_v, the concentration of nickel nanoparticles is about 2.15 × 10¹⁷ particles cm⁻³ at this ratio. After thermal treatment, the quality of the samples became stable beyond 415 °C with a maximum weight reduction of 6.75% at 150% SDS/Ni-salt ratio, and no residual surface sulfur was detected. The saturation magnetization of Ni nanopowders gently decreased with decreasing dispersant content from 35.3 emu·g⁻¹ to 31.6 emu·g⁻¹ at 300 K, while soft ferromagnetic behavior was maintained, which is more beneficial for the stability of multilayer ceramic capacitor performance. Full article

With the progressive decline of tailpipe emissions, non-exhaust sources such as brake wear are becoming an increasingly important contributor to traffic-related particulate matter in urban environments. In this context, improving real-world characterization of brake wear particles is essential for air-pollution assessment, source apportionment, and the development of cleaner and more sustainable road transport systems. Here, we investigated the emissions levels, particle size distribution and elemental composition of particles released during harsh real-world braking events by a single light-duty vehicle braking system equipped with an original manufacturer (OEM) non-asbestos organic (NAO) pad formulation. Using a direct on-vehicle sampling system combined with real-time particle sizing and high-resolution microscopy, we observed that particle emissions remained close to background levels at speeds up to 100 km/h, but rose sharply at 120 km/h, reaching 3.7 × 10⁷ #/cm³ in the 8–10 nm size range. This increase suggests that higher speeds are associated with elevated particle emissions, likely due to the higher braking temperatures reached at increased vehicle speeds. The emitted particles were mainly spherical agglomerates rich in iron, titanium, barium, zirconium, and sulphur, consistent with NAO pad formulations. Our results show that the investigated NAO pad system can deteriorate under thermal stress, potentially leading to higher levels of nanoparticle emissions compared to low-metallic or semi-metallic pads investigated under similar conditions. These findings provide real-world evidence relevant to urban air quality research, support the refinement of non-exhaust emissions inventories, and highlight the importance of thermally resilient friction-material formulations for mitigating residual particulate emissions in increasingly cleaner transport systems. Full article

ZnO–ZnCr₂O₄ heterojunction nanocomposites were synthesized via co-precipitation with nominal spinel loadings of 10, 20, and 30 wt.% (denoted ZnCr-10, ZnCr-20, ZnCr-30) to evaluate structure–property–performance relationships in photocatalytic dye degradation. Rietveld refinement of XRD data revealed actual crystalline phase fractions of 12.1%, 32.4%, and 39.9% ZnCr₂O₄, respectively, with systematic morphological evolution from dispersed nanoparticles (ZnCr-10) to densely agglomerated structures (ZnCr-30) observed by SEM. Optical analysis demonstrated that ZnCr-10 (apparent band gap 3.09 eV) retains ZnO-dominated absorption with moderate interfacial electronic coupling, while ZnCr-20 shows enhanced visible response (2.89 eV) through interface-mediated transitions. ZnCr-30 exhibits strong sub-bandgap absorption (1.63 eV) originating from defect states rather than intrinsic band narrowing. Photoluminescence studies under UV excitation revealed optimal radiative recombination suppression in ZnCr-10, consistent with efficient interfacial charge separation, whereas excessive loading (ZnCr-30) introduced defect-mediated recombination centers. Photocatalytic degradation of Rhodamine B (5 mg/L, 0.5 g/L catalyst, solar irradiation) followed the order: ZnCr-10 (k = 0.0307 min⁻¹) > ZnO (0.0203 min⁻¹) > ZnCr-20 (0.0230 min⁻¹) > ZnCr₂O₄ (0.0166 min⁻¹) > ZnCr-30 (0.0113 min⁻¹). The optimal ZnCr-10 performance is attributed to balanced interfacial contact between phases enabling charge separation without excessive agglomeration or defect accumulation. Operational parameters (pH 7, 50 mg/100 mL, 100 µL H₂O₂) were optimized, achieving 98% degradation in 60 min. This study demonstrates that photocatalytic enhancement in ZnO–spinel heterojunctions is governed by interfacial architecture and defect management rather than optical absorption alone, providing design principles for efficient solar-driven environmental remediation. Full article

This study investigated the effect of post-silanization processing on the surface chemistry and dispersion stability of 3 mol% yttria-stabilized tetragonal zirconia polycrystal (3Y-TZP) nanoparticles intended for the reinforcement of dental photopolymer resins. The nanoparticles were silanized using 3-Methacryloxypropyltrimethoxysilane and subjected to different post-treatment protocols, including control, drying, and centrifugation. Particle morphology was examined using field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). Dispersion behavior was analyzed by dynamic light scattering (DLS) and zeta potential measurements, performed in triplicate (n = 3), while surface chemical modifications were evaluated using Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). Post-silanization processing significantly influenced nanoparticle surface chemistry and dispersion stability. Centrifugation promoted the formation of Si–O–Zr and Si–O–Si linkages, reduced loosely adsorbed silane species, decreased particle agglomeration, and increased zeta potential magnitude, resulting in a more uniform hydrodynamic size distribution compared to the dried group (Z-average ≈ 814 nm, PDI ≈ 0.44). These findings suggest that post-silanization centrifugation acts as an interfacial selection mechanism that distinguishes covalently grafted silane from weakly adsorbed species. Within the limitations of this in vitro study, further investigations under varied conditions are required to confirm broader applicability. Full article

Efficient, low-cost catalysts are required for on-demand H₂ generation from chemical hydrides. This study utilized piezoelectric poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofibers (NFs) as a support to encapsulate bimetallic Co–Mo nanoparticles (NPs) for H₂ production via sodium borohydride (SBH) methanolysis. The PVDF-HFP membranes were synthesized through electrospinning, followed by in situ SBH reduction, which resulted in the uniform dispersion of amorphous Co–Mo NPs within the nanofibrous matrix. The optimized CoMo-0.2@PVDF-HFP membrane exhibited a hydrogen generation rate (HGR) of 1.9 × 10³ mL·min⁻¹·g⁻¹ (Co) at 298 K, indicating a 3.6-fold improvement relative to monometallic Co. Kinetic studies showed a nearly first-order relationship with catalyst dose and a nearly zero-order relationship with respect to SBH concentration, suggesting kinetics controlled by surface saturation. The activation energy (E_a) was determined to be 14.03 kJ·mol⁻¹. Moreover, the catalyst maintained over 80% of its original activity after five cycles. This enhanced performance is attributed to the combined effects of Co and Mo, the amorphous nature of the active sites, and the piezoelectric polarization of PVDF-HFP during mechanical stirring, which together improve charge transfer and reduce NP agglomeration. Full article

This study investigates the valorization of dredged sludge as a sustainable subgrade fill material through stabilization with a nano-calcium carbonate–cement composite. Unconfined compressive strength (UCS) tests were systematically conducted to determine the optimal dosage of nano-CaCO₃ as a supplementary additive at a fixed cement content of 8% by dry soil mass. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and quantitative pore structure analysis were employed to elucidate the underlying solidification mechanisms. The results demonstrate that the addition of 2% nano-CaCO₃ yields the highest 28-day UCS of 721 kPa, representing a statistically significant 21% improvement over the cement-only reference (596 kPa) and a more than threefold increase relative to untreated sludge (213 kPa). Conversely, increasing the nano-CaCO₃ dosage to 2.5% leads to a significant strength reduction, attributed to nanoparticle agglomeration and hindered cement hydration. Microstructural characterization reveals that the optimal nano-CaCO₃ dosage accelerates early-age hydration through a nucleation effect, promotes the consumption of portlandite, and enhances the formation of calcium silicate hydrate (C–S–H) gel. Semi-quantitative XRD analysis further confirms the conversion of less stable monosulfate (AFm-SO₄) into stable monocarboaluminate (AFm-CO₃) phases. These synergistic mechanisms—nucleation, physical pore filling, and chemical reaction—result in a densified matrix with a refined pore structure, reduced total porosity, and a more homogeneous pore-size distribution. The findings provide a robust theoretical basis for the resource-oriented utilization of dredged sludge and the design of low-carbon composite stabilizers for soft soil treatment. Full article

This review comprehensively examines the incorporation of nanoparticles (NPs) into biopolymers for 3D printing in biomedical applications, integrating material design, processing strategies, and translational considerations within a unified framework. Different types of NPs are analyzed regarding their effects on mechanical reinforcement, rheological modulation, and structural organization of biopolymeric matrices. The discussion covers principal additive manufacturing technologies, including extrusion-based systems such as fused deposition modeling (FDM) and direct ink writing (DIW), vat photopolymerization, powder-bed fusion (SLS), and emerging in situ nanoparticle formation approaches, emphasizing how nanoparticle loading and surface functionalization govern yield stress, shear-thinning behavior, viscoelastic recovery, and dimensional fidelity while mitigating agglomeration and optimizing interfacial interactions. Comparative evaluation of compressive modulus, strength, toughness, crystallinity, and porosity establishes structure–property–processing relationships directly linked to printability and functional performance. Biomedical applications are addressed in tissue engineering, biosensing, controlled and targeted drug delivery, and bioimaging, highlighting the balance between bioactivity and manufacturability. Finally, critical challenges—including compatibility, reproducibility, biological safety, long-term stability, regulatory adaptation, and environmental impact—are discussed, alongside future perspectives focused on green nanomaterials, AI-driven predictive formulation design, and digital twins for real-time monitoring and quality control in nano-enabled additive manufacturing. Full article

This study reports that titanium nanoparticles can be used as a surface coating to enhance the corrosion resistance of 316 stainless steel. It specifically examines the influence of the deposition temperature (T_dep) on the coating’s structural and morphological properties, including corrosion behavior. TiO₂ nanoparticles were thoughtfully deposited on steel substrates at temperatures of 300, 400, and 500 °C using a horizontal hot-wall tubular reactor. This equipment was expertly engineered at the CIDETEQ laboratory through the metal–organic chemical vapor deposition (MOCVD) concept. Titanium isopropoxide [Ti(OC₃H₇)₄] was used as the precursor for the coating synthesis. Structural analysis was conducted using X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM). Corrosion performance was evaluated under accelerated conditions in 0.5 M H₂SO₄ using potentiodynamic anodic polarization (AP), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The corrosion test indicates that increasing T_dep significantly differentiates the coating morphology and improves corrosion resistance. AP revealed that the pitting potential (E_pit) shifted to more positive values, ranging from +1.4 to +1.5 V. CV voltammograms indicated that coated samples had lower passive current densities (I_p ≈ 10⁴ to 10⁵ A/cm²) than the bare substrate. EIS analysis demonstrated that the coating deposited at 500 °C processed the most favorable electrochemical performance, resisting corrosion for over 28 days. This coating achieved the highest electrical resistance (297 kΩ·cm²) and the lowest capacitance (2.7 μF/cm²), attributed to the formation of a crystalline anatase phase composed of pyramidal-like nanoparticle agglomerates (~40 nm). The dense packing structure effectively blocks charge-transfer pathways, restricting electron and ion transfer. Finally, MOCVD-based chemical surface modification with TiO₂ nanoparticles is considered an innovative method to improve the corrosion resistance of stainless steel, thereby prolonging its durability under accelerated sulfuric acid exposure. Full article

Controlling the microstructure of electroless nickel coatings is crucial for optimizing the interfacial properties of carbon fibers. However, a systematic understanding of how dispersants can effectively leverage the refining effect of nanoparticles in composite plating systems remains lacking. This paper proposes the use of a composite dispersant, comprising polyethylene glycol (PEG) and sodium methylene bis-naphthalene sulfonate (NNO) at a 1:1 mass ratio, for nano-Al₂O₃ to achieve microstructure refinement of nickel coatings on carbon fiber surfaces. The results demonstrate that the composite dispersant modifies the surface state and dispersion stability of Al₂O₃ particles through synergistic adsorption, thereby regulating the nucleation and growth behavior of the Ni-P alloy. At an optimal composite dispersant concentration of 3 g/L, the coating exhibits the most compact structure, with Ni-P particle size refined to approximately 181 nm. The coating consists of two phases: crystalline Ni₃P and amorphous Ni-P. The dual adsorption effect of the dispersant—inhibiting Al₂O₃ agglomeration while improving the surface wettability of carbon fibers—is key to enhancing the refinement efficiency. Conversely, excessive dispersant addition leads to deteriorated coating quality. This study provides experimental evidence for understanding the multiphase interfacial interaction mechanism involving organic additives, nanoparticles, and metal deposition, and offers a novel strategy for controlling the surface functionalization of carbon fibers. Full article

This study investigates magnetic harvesting of Chlorella vulgaris cultivated under saline and wastewater conditions using Fe₃O₄ and polyethylene-glycol-coated Fe₃O₄ (Fe₃O₄@PEG) nanoparticles synthesized by ultrasound-assisted coprecipitation. TEM showed agglomerated, quasi-spherical particles with mean diameters of 13 ± 1 nm (Fe₃O₄) and 15 ± 1 nm (Fe₃O₄@PEG). FTIR confirmed the Fe–O vibrational bands of magnetite and the characteristic PEG vibrations in the coated sample. VSM measurements indicated superparamagnetic behavior, with saturation magnetizations of 72.74 emu/g for Fe₃O₄ and 32.25 emu/g for Fe₃O₄@PEG. SEM–EDX of native and functionalized cells verified nanoparticle attachment on the algal surface. Magnetic separation experiments (OD684) showed a decrease in supernatant absorbance with increasing nanoparticle dose, consistent with biomass removal; the PEG-coated system showed a lower apparent biomass concentration after functionalization. Full article

Surface discharge-induced degradation poses a significant threat to the operational reliability of high-voltage insulation systems. This research investigates the dielectric endurance of polyester-based nanocomposites reinforced with seven distinct nano-additives: iron oxide (Fe₃O₄), copper oxide (CuO), titanium oxide (TiO₂), aluminum oxide (Al₂O₃), silicon dioxide (SiO₂), zinc borate (ZnB) and graphene oxide (GO). Specimens were fabricated at 0.5% and 0.75% weight concentrations and subjected to constant AC electrical stress of 4.5 kV at 50 Hz until failure using the first-plane tracking method. To accurately monitor the aging process, a sophisticated signal processing framework involving Hankel-matrix-enhanced Robust Principal Component Analysis (RPCA) was developed to extract high-frequency discharge features from captured leakage current signals. The degradation characteristics were quantified using various statistical metrics, including Kurtosis, RMS and Burst Discharge Index (BDI). Experimental findings demonstrate that the incorporation of nanoparticles significantly extends the time-to-failure compared to neat polyester, although the effectiveness is highly dependent on both additive type and concentration. At 0.5 wt.%, ZnB exhibited the superior performance in delaying carbonized track formation. However, at 0.75 wt.%, Al₂O₃ emerged as the most effective additive, achieving a maximum endurance time of 31.61 min. In contrast, certain additives like TiO₂ showed a performance decline at higher loadings, likely due to nanoparticle agglomeration. The Hankel-RPCA methodology successfully isolated discharge-specific signatures from background noise, establishing a strong correlation between signal features and material failure stages. This study confirms that the synergy between advanced nanomaterial modification and robust signal processing provides an effective diagnostic tool for monitoring insulation health, offering a vital pathway for the designing of high-performance dielectrics for real-world power system applications. Full article

In the present work, the elastic modulus of several types of polymer nanocomposites has been analyzed with a semiempirical model which takes into consideration agglomerate formation and their impact on the nanocomposites’ mechanical performance. The nanocomposites under investigation were either hybrids with a combination of graphene oxide (GO) with multi-walled carbon nanotubes (MWCNTs) or carbon nanofibers (CNFs) at various loadings, or monofillers with varying nanoparticle sizes, at a constant nanofiller loading. In addition, the effect of the type of polymeric matrix on the same nanofiller combinations has been examined. The basic assumption of two phases, namely a matrix with finely dispersed nanoparticles coexisting with agglomerates, was analyzed. The elastic stiffness of the first phase was calculated by the Mori–Tanaka model, and hereafter a semiempirical model was utilized for the estimation of the agglomerates’ stiffness. Within the context of this model, it was shown that the agglomerates’ volume fraction, combined with the nanoparticles’ density, namely the nanoparticles’ volume fraction in the agglomerates and consequently the inclusions’/agglomerates’ enhanced modulus, may cause a substantial improvement in the Young’s modulus, which cannot be explained by conventional mechanical models. These results apply to both nanocomposite types, hybrids at various nanofiller loadings and monofillers with varying particle sizes. Full article

Environmental contamination by persistent industrial dyes such as Amido Black demands highly efficient photocatalysts for advanced water treatment. Structural, chemical, and optical strategies based on TiO₂ nanotube engineering are widely explored for this purpose. In this work, highly ordered TiO₂ nanotube arrays were fabricated by electrochemical anodization and subsequently decorated with Pd nanoparticles via potentiostatic electrodeposition (10–300 s), enabling precise control of Pd nanoparticle size and loading. The resulting materials were systematically characterized by SEM, TEM, XRD, XPS, UV–vis DRS, and PL spectroscopy, and their properties were correlated with the photocatalytic degradation of Amido Black under both UV and visible light irradiation. The study reveals a clear size-dependent duality in the role of Pd. For intermediate Pd nanoparticles (≈9 nm, 20 s), Pd behaves predominantly as an electron sink, forming an efficient Schottky junction with anatase TiO₂ that markedly suppresses charge carrier recombination. This configuration yields ≈ 97% Amido Black removal after 120 min of UV irradiation, with an apparent rate constant about three times higher than that of bare TiO₂ nanotubes. In contrast, for ultra-small Pd nanoparticles (≈6 nm, 10 s), interfacial defect states sensitize TiO₂ to visible light, enabling ≈ 65% degradation after 270 min and a rate constant roughly four times higher than that of undecorated nanotubes under visible illumination. At long deposition times (≥150 s), Pd agglomeration leads to enhanced photoluminescence and markedly reduced photocatalytic activity, indicating increased recombination and less effective utilization of photogenerated charges. This provides a practical design rule to rationally tailor Pd–TiO₂ nanotube photocatalysts for targeted UV or visible light applications in dye removal and broader environmental remediation scenarios Full article

Hybrid nanofluids possess exceptional thermal conductivity, but one of the major concerns with nanoparticles is agglomeration. While the usage of surfactants or dispersants can be used to mitigate this issue, numerical investigation and sensitivity analyses can be more affordable when attempting to optimize and design a thermal device. The consideration of thermal radiation with conductive and convective heat transfer and appropriate nanoparticles may provide a greater solution without compromising the efficacy of hybrid nanofluids. In the present work, the concept of magnetohydrodynamics (MHD) is used to examine the impact of thermal radiation on a stable, two-dimensional, incompressible hybrid fluid consisting of nanoparticles (MWNCT)${\mathrm{-Fe}}_3{\mathrm{O}}_4$ and water flowing over a vertical surface. The flow is governed by established equations of fluid dynamics, which use the Rosseland diffusion model to incorporate radiation effects. The implicit finite difference (IFD) was used to solve the mathematical equations. Sensitivity analyses were conducted as functions of volume fraction, radiation and magnetic variables. This study also examines the streamlines and isotherm lines with respect to the volume fraction, radiation parameter and magnetic parameter of the heat source. The results indicate that for a fixed radiation parameter, increasing the nanoparticle volume fraction by up to $20\%$ leads to a reduction of approximately $37\%$ in the skin friction coefficient, while the corresponding Nusselt number increases by nearly $50\%$. Furthermore, the introduction of a magnetic field parameter significantly suppresses wall shear stress and modifies the thermal boundary layer thickness, demonstrating the competing interaction between Lorentz-force-induced momentum damping and radiation-enhanced thermal diffusion. These quantified trends highlight the sensitivity of coupled momentum and heat transport to combined magnetic and radiative effects in hybrid nanofluid systems. Full article