Agglomeration Of Nanoparticles Research Articles

Fabrication of an antibacterial polybenzimidazole/Ag@UiO-66-NH2 mixed matrix membrane for dye-salt separation: Solvent evaporation effects

In textile water treatment, nanofiltration membranes are susceptible to biofilm layer formation on their surface due to microbial colonization, which can significantly reduce the separation efficiency of the membrane. Therefore, maintaining long-term antimicrobial efficacy of the membrane is of paramount importance. In this study, UiO-66-NH2 nanoparticles were fabricated via the solvothermal method, then Ag-loaded UiO-66-NH2 (Ag@UiO-66-NH2) nanoparticles were produced by stirring and reduction with silver nitrate solution, and the nanoparticles were integrated into the polybenzimidazole (PBI) matrix through a blending process to fabricate mixed matrix membranes (MMMs) with antimicrobial properties. During the preparation of mixed matrix membranes, the phenomenon of nanoparticle agglomeration on the membrane surface is frequently encountered. In order to solve this problem, we used solvent evaporation and cross-linking post-treatment methods to further improve the compatibility between the membrane and the particles, the membranes showed a good water flux (53.7 L·m−2·h−1), excellent separation capabilities for dyes and salts, NaCl rejection (9.50 %), Na2SO4 rejection (12.70 %), MgCl2 rejection (7.44 %), MgSO4 rejection (9.34 %), Crystal violet, Acid fuchsin, Congo red, Coomassie brilliant blue and Acid red 94 dyes rejection (all over 99 %). And the antibacterial rate is 98.7 % against E. coli and 99.1 % against S. aureus and it has the function of long-term stable Ag+ release.

Nitrogen-doped carbon coated Na3V2O2(PO4)2F as a cathode for high-performance sodium-ion batteries

Na3V2O2(PO4)2F (NVOPF), a cathode known for the advantages of high voltage, exceptional energy density, and thermal stability, is seen as a promising candidate for sodium-ion battery cathodes. However, the NVOPF exhibits poor performance in sodium storage. Here, we report a NVOPF composite cathode with a nitrogen-doped carbon produced from dopamine hydrochloride at an elevated temperature. Firstly, neutron power diffraction (NPD) is employed to determine the structure of pure NVOPF at different temperatures, including oxygen coordination and the mobility of Na+. The nitrogen-doped carbon layer facilitates electron conduction, prevents NVOPF nanoparticle agglomeration, and thus promotes efficient electron and ion transfer during sodium ion insertion/extraction processes, thereby improving the stability of the material structure. These results indicate that the N doped carbon@NVOPF cathode material exhibits outstanding electrochemical performance (111mAh/g at 0.1C and 85mAh/g at 1C), while maintaining 91.06 % capacity retention after 500 cycles. The enhanced electrochemical performance attributes to efficient charge transfer kinetics offer novel perspectives, and the methodology can be effectively adapted to other cathode materials.

Mesoporous Electrodes Enhance the Electrocatalytic Performance of [FeFe]‐Hydrogenase

The metalloenzyme [FeFe]‐hydrogenase is of interest to future biotechnologies targeting the production of “green” hydrogen (H2). We recently developed a simple two‐step functionalized procedure to immobilize the [FeFe]‐hydrogenase from Clostridium pasteurianum (“CpI”) on mesoporous indium tin oxide (ITO) electrodes to achieve elevated H2 production with high operational stability, with current densities of 8 mA cm–2. Here, we use a combination of atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrochemical quartz crystal microbalance (EQCM) to understand how mesoporous ITO stabilizes and activates CpI for electroenzymatic H2 production. Examination of the topography and morphology of the mesoporous ITO surface revealed a hierarchical morphology containing cavities and well‐defined nanoparticle agglomerates. Any potential effect of mesoporosity was investigated by comparing the stability and electroenzymatic activity of CpI on mesoporous ‘nanoITO’ and planar ITO, where we determined that CpI has a higher turnover frequency and absorbs with greater stability (with respect to electroenzymatic activity over time) to nanoITO surfaces.

Mesoporous Electrodes Enhance the Electrocatalytic Performance of [FeFe]-Hydrogenase.

The metalloenzyme [FeFe]-hydrogenase is of interest to future biotechnologies targeting the production of "green" hydrogen (H2). We recently developed a simple two-step functionalized procedure to immobilize the [FeFe]-hydrogenase from Clostridium pasteurianum ("CpI") on mesoporous indium tin oxide (ITO) electrodes to achieve elevated H2 production with high operational stability, with current densities of 8 mA cm-2. Here, we use a combination of atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrochemical quartz crystal microbalance (EQCM) to understand how mesoporous ITO stabilizes and activates CpI for electroenzymatic H2 production. Examination of the topography and morphology of the mesoporous ITO surface revealed a hierarchical morphology containing cavities and well-defined nanoparticle agglomerates. Any potential effect of mesoporosity was investigated by comparing the stability and electroenzymatic activity of CpI on mesoporous 'nanoITO' and planar ITO, where we determined that CpI has a higher turnover frequency and absorbs with greater stability (with respect to electroenzymatic activity over time) to nanoITO surfaces.

Recent Advances in Hybrid Nanocomposites for Aerospace Applications

Hybrid nanocomposites have emerged as a groundbreaking class of materials in the aerospace industry, offering exceptional mechanical, thermal, and functional properties. These materials, composed of a combination of metallic matrices (based on aluminum, magnesium, or titanium) reinforced with a mixture of nanoscale particles, such as carbon nanotubes (CNTs), graphene, and ceramic nanoparticles (SiC, Al2O3), provide a unique balance of high strength, low weight, and enhanced durability. Recent advances in developing these nanocomposites have focused on optimizing the dispersion and integration of nanoparticles within the matrix to achieve superior material performance. Innovative fabrication techniques have ensured uniform distribution and strong bonding between the matrix and the reinforcements, including advanced powder metallurgy, stir casting, in situ chemical vapor deposition (CVD), and additive manufacturing. These methods have enabled the production of hybrid nanocomposites with improved mechanical properties, such as increased tensile strength, fracture toughness, wear resistance, and enhanced thermal stability and electrical conductivity. Despite these advancements, challenges remain in preventing nanoparticle agglomeration due to the high surface energy and van der Walls forces and ensuring consistent quality and repeatability in large-scale production. Addressing these issues is critical for fully leveraging the potential of hybrid nanocomposites in aerospace applications, where materials are subjected to extreme conditions and rigorous performance standards. Ongoing research is focused on developing novel processing techniques and understanding the underlying mechanisms that govern the behavior of these materials under various operational conditions. This review highlights the recent progress in the design, fabrication, and application of hybrid nanocomposites for aerospace applications. It underscores their potential to revolutionize the industry by providing materials that meet the demanding requirements for lightweight, high-strength, and multifunctional components.

Self-assembly fabrication of SASN@GO composites with high electrostatic safety and thermal stability performances

ABSTRACT The high electrostatic discharge (ESD) sensitivity and mechanical sensitivity of silver acetylide-silver nitrate (SASN) seriously affects its application. For solving this problem, novel SASN@GO nanocomposites were successfully prepared by a self-assembly method. Thin sheet graphene oxide (GO) was coated on the surface of SASN, and prevented the agglomeration of SASN nanoparticles effectively. GO content in SASN@GO nanocomposites was controlled (0.5 ~ 1.5 wt%) to balance explosive performance and safety. Results reveal that SASN@(1%)GO exhibits the best thermal safety and desensitization, with thermal decomposition temperature, impact sensitivity (I s), friction sensitivity (F s) and electrostatic energy at 50% ignition probability (E 50) of 208.2°C, 1.96 J, 128 N and 0.64 mJ respectively, which are much better than that of SASN, indicating safety performances of SASN are improved through the introducetion of a small amount of GO. This work provides a strategy for reducing the explosion risk of SASN.

Photocatalytic Degradation of Four Organic Dyes Present in Water Using ZnO Nanoparticles Synthesized with Green Synthesis Using Ambrosia ambrosioides Leaf and Root Extract

Currently, several organic dyes found in wastewater cause severe contamination problems for flora, fauna, and people in direct contact with them. This research proposes an alternative for the degradation of polluting dyes using ZnO nanoparticles (NPs) synthesized by an ecological route using leaf and root extracts of Ambrosia ambrosioides as a reducing agent (with a weight/volume ratio = 4%). Scanning Electron Microscopy (SEM) was used to determine the morphology, showing an agglomeration of cluster-shaped NPs. Using Transmission Electron Microscopy (TEM), different sizes of NPs ranging from 5 to 56 nm were observed for both synthesized NPs. The composition and structure of the nanomaterial were analyzed by infrared spectroscopy (FT-IR) and X-ray diffraction (XRD), showing as a result that the NPs have a wurtzite-like crystalline structure with crystallite sizes around 32–37 nm for both samples. Additionally, the bandgap of the NPs was calculated using Ultraviolet Visible Spectroscopy (UV–Vis), determining values of 2.82 and 2.70 eV for the NPs synthesized with leaf and root, respectively. Finally, thermogravimetric analysis demonstrated that the nanoparticles contained an organic part after the green synthesis process, with high thermal stability for both samples. Photocatalytic analysis showed that these nanomaterials can degrade four dyes under UV irradiation, reaching 90% degradation for methylene blue (MB), methyl orange (MO) and Congo red (CR) at 60, 100 and 60 min, respectively, while for methyl red (MR) almost 90% degradation was achieved at 140 min of UV irradiation. These results demonstrate that it is effective to use Ambrosia ambrosioides root and leaf extracts as a reducing agent for the formation of ZnO NPs, also evidencing their favorable application in the photocatalytic degradation of these four organic dyes.

Study on the inhibitory behavior of high-voltage electric field on the agglomeration and sedimentation of nanoparticles in suspension

Nanoparticles can improve the heat transfer effect of fluids, however, they are difficult to dissolve in the base fluid and are prone to fouling, agglomeration and sedimentation during flow, which affects their efficient heat transfer characteristics. In this paper, the inhibitory effect of high-voltage electric field on the agglomeration and deposition of TiO2 nanoparticles in suspension was comparatively studied by comprehensive gravity sedimentation, spectrophotometer, particle size analysis, and zeta potential method. Studies have shown that the absorbance of suspensions is basically the same in neutral and acidic environments. However, in a highly alkaline environment, the agglomeration rate of nanoparticles increases significantly, resulting in a decrease in the absorbance of the suspension. The high-voltage non-uniform electric field generated by the active Cu rod electrode can effectively inhibit the agglomeration of TiO2 nanoparticles. However, the suppression effect of an external electric field is not necessarily the higher the voltage, the better. Different nanomaterials have different critical voltages. The high-voltage electric field of 1 kV has the best inhibitory effect on the agglomeration and deposition of TiO2 nanoparticles. An in-depth analysis of the mechanisms of the movement and agglomeration of TiO2 particles in suspension under high-voltage electric field excitation was conducted. The result shows that the agglomeration and sedimentation of particles in suspension depend on the Zeta potential of the nano particles. The higher the absolute value, the more stable the dispersion system is.

Thermophysical and Corrosion Inhibitor Evaluation of Graphene, Aluminum Nitride and Barium Titanate Nanolubricants

A newly developed kind of fluid known as nanolubricant is produced by dispersing nanometer-sized materials in base oil. The main issue with nanolubricant is particle stability, which occurs when nanoparticles aggregate due to van der Waals forces. The aim of the study is to evaluate the performance of graphene (GR), aluminium nitride (AlN), and barium titanate (BTO) nanolubricants at 0.05 and 0.1 vol. % concentrations. The stability was identified by using sedimentation photograph capturing method and zeta potential analysis, while KD2 Pro Analyzer was used to measure the thermal conductivity, and the effect of corrosion inhibitor evaluation was measured according to ASTM D130-19. The nanolubricants are prepared by two-step method and undergo ultrasonication process to ensure the nanoparticles are well dispersed in base oil. The results showed that nanolubricants containing 0.05 vol. % nanoparticles are more stable than 0.1 vol. % nanolubricants. Nanolubricants with 0.1 vol. % showed signs of instability based on low zeta potential values. This is due to the fact that the higher the concentration of nanoparticles, the closer the nanoparticles are to one another. This increased van der Waals attraction and potentially causing nanoparticle agglomeration. Improvement in thermal conductivity was obtained with high volume concentration of GR, AlN and BTO nanoparticles. All nanolubricants achieved an ASTM Standard D130 classification of 1a based on the Copper Strip Corrosion Test Standard (slight tarnish, slight colour change). As a result, it was discovered that all prepared samples are effective anticorrosion lubricating oil additives.

Cu2SnS3/rGO nanocomposites with optimized pore structure for high-performance lithium-ion batteries

Developing advanced anode materials is essential for enhancing the rate performance and stability of lithium-ion batteries (LIBs), which is critical for meeting the demands for next-generation energy storage solutions. In this research, Cu2SnS3/rGO nanocomposites were synthesized via a rapid microwave-assisted one-step method, followed by post-synthetic annealing. The incorporation of reduced graphene oxide (rGO) not only significantly improves its electrical conductivity, but also effectively inhibits the agglomeration of CTS nanoparticles. The nanocrystal size in the CTS/rGO nanocomposites has been dramatically downsized, transitioning from the pristine CTS dimensions of 0.9–1.5 μm to a mere 100 nm. This downsizing is a critical advancement in the electrode, as it enhances the surface area and reactivity of the composite. The subsequent high-temperature annealing process shrinks the pore size in the CTS/rGO nanocomposite, decreasing from an average of 42.13 nm to a more confined range of 7.81 to 8.77 nm, depending on the annealing temperatures. Electrochemical testing reveals that the CTS/rGO-A nanocomposite annealed at 300 °C exhibits superior electrochemical performance to the unmodified CTS and non-annealed CTS/rGO composite. The performance is evidenced by an initial capacity of 1856.97 mAh g−1 at a current density of 1 A g−1 and retains a capacity of 1250.32 mAh g−1 after 500 cycles. To elucidate the underlying mechanisms governing the lithium ion diffusion kinetics, capacitance and diffusion behavior of the CTS/rGO-A electrode, advanced techniques such as galvanostatic intermittent titration technique (GITT) and rate cyclic voltammetry (CV) were utilized. These analyses revealed that the synergistic effect of an increased Li+ diffusion coefficient (DLi+), coupled with a notable capacitive contribution, is demonstrated to the enhanced electrochemical performance observed. Furthermore, the COMSOL Multiphysics simulation also indicates improved structural stability of CTS/rGO-A, attributed to minimized stress from volume expansion during discharge. The CTS/rGO-A nanocomposites, featuring enhanced electrochemical performance, coupled with a straightforward and efficient fabrication method, emerge as a promising material for scalable and practical energy storage solutions.

Layered double hydroxides-derived CoNi alloy nanoparticles encapsulated by porous N-doped carbon nanofibers as efficient methanol electrocatalysts for alkaline direct methanol fuel cells

The exploration of inexpensive electrocatalysts possessing high activity and increased stability to replace precious metal catalysts in the methanol oxidation reaction (MOR) is highly desirable for alkaline direct methanol fuel cells (ADMFCs). This study presents a novel approach to synthesize layered double hydroxides (LDHs)-derived CoNi alloy nanoparticles confined within porous N-doped carbon nanofibers (CoNi@NCNFs) via facile electrospinning and pyrolysis for methanol electrooxidation.The one-dimensional N-doped carbon nanofibers could effectively prevent nanoparticle agglomeration during the pyrolysis of LDH precursors. The optimized CoNi@NCNF3-900 composite exhibits exceptional catalytic activity (80.3mAcm−2) for MOR in alkaline solution, attributed to its hierarchical porous structure, high surface area, and abundant accessible active sites. Furthermore, the catalyst demonstrates competitive electrocatalytic stability, retaining over 90% of its initial current density after 1000 consecutive cyclic voltammetry (CV) cycles. Notably, a single-cell ADMFC assembled with CoNi@NCNF3-900 as the anode catalyst achieves a promising maximum power density of 29.5mWcm−2, highlighting the potential of CoNi@NCNF3-900 for application in DMFC technology and clean energy sources.

The synergistic effect of micro/nanostructure length scale and fluid thermophysical properties on pool boiling heat transfer

Facile surface micro/nanostructuring techniques for additively-manufactured (AM) aluminum alloy (AlSi10Mg) have recently been developed. The structuring techniques are not only highly scalable, but they also enable the tailoring of structure length scale and morphology to enhance the pool boiling heat transfer coefficient. Our past study revealed that the structure cavity size of 5 µm is favorable for bubble nucleation during pool boiling of dielectric fluid, HFE-7100, resulting in significant enhancements in the heat transfer coefficients (h). However, owing to the differences in thermophysical properties between different coolant fluids, including saturation temperature, latent heat of vaporization and surface tension, the required structure size range for bubble nucleation and capillary wicking force for liquid re-supply are expected to differ significantly. To explore the effect of structure length scale on the pool boiling performance of coolants with different thermophysical properties, this work develops a new surface structuring technique consisting of a dual-stage metallurgic heat treatment process and single-stage crystallographic etching process to tune the structure length scale across nearly two orders of magnitude, viz., from 0.3 μm to 15 μm. Using coolant media of vastly different thermophysical properties, i.e., dielectric fluid HFE-7100 and deionized water, we show that while microcavities with sizes ranging from 3 to 8 μm are favorable bubble nucleation sites for boiling of HFE7100, which results in the enhancement of the maximum heat transfer coefficient (hmax) by 83.4 to 103.8 % as compared to a conventional plain Al6061 surface, larger microcavity sizes of 10 to 15 μm are required to effectively promote bubble nucleation of water. This large microcavity size range of 10 to 15 μm, produced through rational nanoparticle agglomeration of the rich Si-phase in AM AlSi10Mg in elevated temperature, followed by an indirect removal process using a chemical process, is found to significantly increase hmax of water by up to 259.9 % as compared to conventional nanostructures formed on Al6061. In addition, the new AM structured surfaces also exhibit up to 26.6 % enhancement in critical heat flux (CHF) as compared to highly-wicking conventional nanostructured Al6061. In summary, by utilizing scalable fabrication techniques to tailor the structure length scale on AM AlSi10Mg, this work not only reveals the favorable microcavity sizes for bubble nucleation of different coolant fluids to enhance boiling, but also provides useful micro/nanostructure design guidelines that can be adopted to enhance boiling of other coolants and phase change applications.

Heterostructured GCN Nanosheets/ZnO nanoflowers for enhanced TMO loading: From high-performance three electrode systems to printed flexible asymmetric supercapacitors

Transition metal oxides (TMOs) are widely used in the development of high-energy-density devices due to their multiple oxidation states and their frequent heterostructuring with carbon-based materials. However, the synthesis process often leads to severe nanoparticle agglomeration and weak synergistic effects with carbon-based templates, thereby limiting their application potential. In this study, we constructed graphitic carbon nitride (GCN) nanosheets/ZnO nanoflowers (NFs) structures with high TMOs loading by utilizing GCN nanosheets, which are rich in surface nitrogen content, as enriched templates for metal ions in conjunction with ultrasonic cavitation. Compared with GCN nanosheets/ZnO nanoparticles (NPs), the ZnO NFs exhibited vertical growth and a fluffy structure on a 2D material template, which resulted in high electronic conductivity, a large effective surface area, hierarchical pores, and strong synergistic interactions with GCNs, thus improving electrochemical performance. This structural enhancement enabled the GCN/ZnO NFs electrodes to achieve a high specific capacitance of 1524F g−1 at a current density of 1 A g−1 in a three-electrode supercapacitor system. Additionally, we formulated GCN/ZnO NFs into electronic inks and used them for the mass production of flexible supercapacitors with the aid of dispensing printing technology. These flexible supercapacitors retained 94% of their specific capacitance even under extreme conditions of 90° torsion. Our proposed strategy of modulating TMOs and 2D structures can create active electrode materials with higher loading capacities, thereby enabling comprehensive customization in material design and device preparation processes.

Formation and agglomeration of nanoparticles and carbon debris in MnO2@C/GO

Carbon-loaded manganese dioxide (MnO2) nanoparticle materials have potential applications in energy storage and conversion, environmental and sensing applications. Carbon-coated MnO2 nanoparticles can avoid particle agglomeration. However, the process of forming MnO2 nanoparticles and carbon shells is unclear when carbon material is used as a carrier. In this work, the generation and convergence processes of nanoparticles and carbon debris were probed at bulk and monolayer levels using graphene oxide as carrier. And it is deduced that MnO2 nanoparticles first nucleate and aggregate at GO plane. As the size of the nanoparticles increases, the surrounding nanoparticles further aggregate. GO is etched during the formation of nanoparticles, resulting in the formation of carbon debris. Amorphous carbon shells are mainly formed by the aggregation of carbon debris. The MnO2@C/GO obtained was tested for H2O2 detection and showed superior H2O2 reduction properties.

Self-healing efficiency of ceria-doped Zn-Co coatings: Insights into particle-free versus biphasic plating baths

Achieving the superior properties of nanocomposite materials involves addressing several challenges, particularly the agglomeration of nanoparticles in the plating bath. This study focuses on the electrodeposition and characterization of Zn-Co-CeO2 composite coatings using a particle-free plating bath, which is an effective strategy to mitigate agglo¬meration. For comparison, the composite coatings were also deposited from a traditional biphasic plating solution. The coatings were deposited galvanostatically, at various current densities. Scanning electron microscopy revealed that using a particles free plating solution in conjunction with lower current densities enhanced the compactness and the overall quality of the coatings. Lower current densities favoured the codeposition of particles, as indicated by energy-dispersive X-ray spectroscopy results. Notably, the coatings produced from the particle-free bath exhibited significantly improved corrosion resistance and durability in chloride-rich environments, attributed to their self-healing properties, as shown by electrochemical impedance spectroscopy.

Green synthesis of boehmite-reinforced cashew gum/polypyrrole biopolymer blend for advanced biomaterials

Electrically conducting biopolymer blend nanocomposites based on different contents of boehmite (BHM) reinforced cashew gum (CG) /polypyrrole (PPy) blend is synthesized by an in situ polymerization technique using water as a green solvent. The resulting bio-blend nanocomposites underwent comprehensive analysis concerning their structural, morphology, thermal, and electrical properties, such as dielectric constant, dielectric loss, electric modulus, and AC conductivity. The Fourier transform infrared spectroscopy (FTIR) spectra revealed the presence of metal oxide stretching in the blended nanocomposite at 512 cm−1. Field emission scanning electron microscopy (FE-SEM) confirmed the attachment and uniform dispersion of BHM within the CG/PPy blend at 7 wt% loading, and beyond this loading, the nanoparticles get agglomerated in the biopolymer blend. The glass transition temperature and thermal stability of all the blended nanocomposites are higher than that of the pure CG/PPy blend and these thermal properties increase with the loading of nanoparticles. Conductivity experiments demonstrated that as the nanofiller content increases up to 7 wt%, there is a concurrent rise observed in AC conductivity, dielectric loss, and dielectric constant. There is a substantial difference of 1.21 Scm−1 between the maximum and minimum AC electrical conductivity, at 102 Hz. However, a decrease in electrical properties is observed at the highest loadings of BHM due to the agglomeration of nanoparticles in the polymer blend matrix. The lowest activation energy value (0.049 × 10−4 eV) is also exhibited by 7 wt% BHM nanocomposites. Furthermore, the electrical properties of both CG/PPy and CG/PPy/BHM nanocomposites exhibited a temperature-dependent behavior, progressively increasing until reaching maximum values. This study suggests that such bio-based polymer dielectrics could be promising materials for various applications, offering enhanced thermal and electrical properties through careful control of nanofiller content and dispersion.

Production and Characterization of Hybrid Al6061 Nanocomposites

Aluminum-based hybrid nanocomposites, namely the Al6061 alloy, have gained prominence in the scientific community due to their unique properties, such as high strength, low density, and good corrosion resistance. The production of these nanocomposites involves incorporating reinforcing nanoparticles into the matrix to improve its mechanical and thermal properties. The Al6061 hybrid nanocomposites were manufactured by conventional powder metallurgy (cold pressing and sintering). Ceramic silicon carbide (SiC) nanoparticles and carbon nanotubes (CNTs) were used as reinforcements. The nanocomposites were produced using different reinforcement amounts (0.50, 0.75, 1.00, and 1.50 wt.%) and sintered from 540 to 620 °C for 120 min. The characterization of the Al6061 hybrid nanocomposites involved the analysis of their mechanical properties, such as hardness and tensile strength, as well as their micro- and nanometric structures. Techniques such as optical microscopy (OM) and scanning electron microscopy (SEM) with electron backscatter diffraction (EBSD) were used to study the distribution of nanoparticles, the grain size of the microstructure, and the presence of defects in the matrix. The microstructural evaluation revealed significant grain refinement and greater homogeneity in the hybrid nanocomposites reinforced with 0.75 wt.% of SiC and CNTs, resulting in better mechanical performance. Tensile tests showed that the Al6061/CNT/SiC hybrid composite had the highest tensile strength of 104 MPa, compared to 63 MPa for the unreinforced Al6061 matrix. The results showed that adding 0.75% SiC nanoparticles and CNTs can significantly improve the properties of Al6061 (65% in the tensile strength). However, some nanoparticle agglomeration remains one of the challenges in manufacturing these nanocomposites; therefore, the expected increase in mechanical properties is not observed.

Unveiling the heterojunction of Fe3O4@MXene nanocatalyst for ultrafast degradation of antibiotics via non-radical pathway

The transfer of advanced oxidation processes (AOPs) to real-world applications faces several technology challenges involving oxidation performance, catalyst cost, poor reactive oxygen species (ROS) yield, and long-term stability. This work aims to develop a reactive, efficient, and stable MXene-based nanocatalyst, namely Fe3O4@Ti3C2Tx, for ultrafast removal of the selected sulfonamide antibiotics. As revealed by extensive nanocatalyst characterization, the MXene surface not only anchors Fe/Fe3O4 nanoparticles (NPs) but also prevents NP agglomeration. Notably, the conductive interface between MXene and Fe3O4 promotes the Fe(II)/Fe(III) redox cycle and accelerates peroxymonosulfate (PMS) activation. The Fe3O4@Ti3C2Tx demonstrates excellent catalytic activity by achieving complete sulfamethoxazole (SMX) degradation within 6 min and maintained its catalytic activity after 5 continuous cycles. In the Fe3O4@Ti3C2Tx/PMS system, multiple ROS (e.g., •OH, SO4•-, O2•-) are involved but 1O2 was found to be the primary ROS for SMX degradation. The presence of co-exiting inorganic impurities and pH changes may hinder SMX degradation. Finally, elucidating possible degradation pathways of SMX would greatly aid in treating antibiotic-containing wastewater.

Nitrogen-doped carbon nanosheet confined PtNi alloy for efficient acidic electrocatalytic hydrogen evolution reaction

Low intrinsic electrocatalytic activity and inferior conductivity limit the application of Ni/NC in acidic electrocatalytic hydrogen evolution reaction (HER). Herein, we prepared nitrogen-doped carbon nanosheet confined PtNi alloy electrocatalysts (PtNi/NC-10) using PtCl62− electrostatic adsorption coupling melamine pyrolysis nitriding strategy. PtNi alloying was confirmed by the crystallinity decrease and lattice expansion of Ni/NC. The alloying and confinement effect of Metal-Organic Frameworks (MOFs) suppresses the oxidation and agglomeration of metal nanoparticles during pyrolysis, thus significantly reducing particle size, increasing specific surface area, and promoting the exposure of active sites. The strong electronic interaction between Pt and Ni optimizeds the surface charge distribution, enhancing the adsorption of H species on electron-rich Pt sites, thereby improving reaction kinetics. In addition, PtNi alloying improves the conductivity of the material, accelerating charge transfer and proton transport. Consequently, the prepared PtNi/NC-10 exhibits superior HER performance than Ni/NC in 0.5 M H2SO4 solution, even comparable to commercial 20 wt% Pt/C, with the overpotentials of 35 mV at 0.01 A cm−2. Furthermore, the electrocatalysts assembled PtNi/NC-10-CP‖RuO2-TFF proton exchange membrane (PEM) electrolyzer only requires 2.32 V cell voltage to achieve 1 A cm−2, presenting practical application prospects. Our work provides a novel idea for designing efficient and stable MOFs confined to alloy-based HER electrocatalysts.

Ultrasound-assisted freeze-drying graphitization process for the fabrication of two-dimensional carbon/Fe3O4 composite aerogels for microwave absorption

Magnetic Fe3O4 materials have received attention from researchers due to their significant wave absorption potential, but there are limitations to their efficient electromagnetic wave absorption and lightweight applications. Combining materials with dielectric properties to optimize the performance of Fe3O4 has become one of the research directions. In particular, carbon nanomaterials, such as graphene, show great application prospects in the field of microwave absorption due to their physical properties. To improve the impedance mismatch issue of graphene, researchers consider combining it with magnetic nanoparticles. Commercial applications require materials that are cost-effective, easy to produce, and environmentally sustainable, driving research on novel 2D carbon materials. In this study, 2D carbon materials were prepared by ultrasound-assisted freeze-drying/graphitization process using polymers as precursors, which simplifies the preparation process and avoids the use of expensive sacrificial templates and catalysts. The 2D carbon materials prepared by this method were used as the dielectric component in the wave-absorbing composites, and the nano effect was utilized to significantly improve the microwave absorption properties of the materials. The maximum reflection loss of the prepared graphite nano-aerogel reaches −84.16 dB and the EAB reaches 3.74 GHz. In addition, by adding Fe3O4 nanoparticles and applying an ultrasonic field for dispersion in the freeze-drying process, the nanoparticle agglomeration is effectively prevented, which provides a simple and efficient pathway for the preparation of nanocomposites.