Search Results (95)

The burgeoning electromagnetic pollution from 5G/6G technologies demands lightweight, broadband, and mechanically robust electromagnetic microwave absorbers (EMWAs). Conventional carbon aerogels suffer from structural fragility and inadequate electromagnetic dissipation. Herein, we propose a defect-engineering strategy through precise optimization of the chitosan (CS)/cellulose nanocrystal (CNC) ratio to fabricate elastic boron nitride nanosheet (BNNS)-embedded carbon aerogels. By fixing BNNS content for optimal impedance matching and modulating the CS/CNC ratio of the aerogel, we achieve synergistic control over hierarchical microstructure, defect topology, and electromagnetic response. The aerogel exhibits a wide effective absorption bandwidth (EAB) of 8.3 GHz at a thickness of 3.6 mm and an excellent reflection loss of −52.79 dB (>99.999% attenuation), surpassing most biomass-derived EMWAs. The performance stems from CNC-derived topological defects enabling novel polarization pathways and BNNS-triggered interfacial polarization, while optimal graphitization (I_D/I_G = 1.08) balances conductive loss. Simultaneously, the optimal CS/CNC ratio facilitates the formation of a stable and flexible framework. The long-range ordered micro-arch lamellar structure endows the aerogel with promising elasticity, which retains 82% height after 1000 cyclic compression at 50% strain. This work paves the way for biomass-derived carbon aerogels as next-generation wearable and conformal EMWAs with broadband absorption. Full article

We systematically investigated the morphology-controlled synthesis of Cu₂O micro-nano crystals, especially under surfactant-free conditions, targeting a simple, rapid, and morphologically controllable preparation strategy for polyhedral Cu₂O micro-nano crystals. By systematically investigating the effects of NaOH concentration, types of reducing agents, and copper salt precursors on crystal growth, precise control over the morphology of Cu₂O crystals under surfactant-free conditions was achieved. This method can rapidly prepare variously faceted Cu₂O crystals under mild conditions (70 °C, 7 min), including regular polyhedra with low-index facets exposure including cubes, octahedra and rhombic dodecahedra, as well as more complex polyhedra with high-index facets exposure such as 18-faceted, 26-faceted, 50-faceted and 74-faceted crystals. NaOH concentration is found to be the key factor in controlling Cu₂O crystal morphology: as the concentration of NaOH increases, the morphology of Cu₂O crystals gradually transforms from cubes that fully expose the {100} faces to regular polyhedra that expose the {110}, {111} faces, and even other high-index faces, ultimately presenting octahedra that fully expose the {111} faces. Additionally, Cu₂O crystals with unique morphologies such as hollow cubes and 18-faceted with {110} face etched can be obtained by introducing surfactants or prolonging reaction durations. This work provides new insights into the morphology control of Cu₂O crystals and establishes foundation in acquiring distinct Cu₂O polyhedra in a facile manner for their application in catalysis, optoelectronics, sensing, and energy conversion fields. Full article

Costs are increasing due to the addition of alloying elements such as V, W, and Mo to prevent damage to Cr-Mo steel for fastening bolts, but field tests have shown that it is not an appropriate solution for improving physical properties through heat treatment. In this study, the characteristics of fatigue cracks using Cr-Mo steel for fastening bolts before and after UNSM (ultrasonic nanocrystal surface modification) treatment were studied using fracture mechanics and fracture analysis methods. Specifically, using untreated and UNSM-treated materials: (1) the characteristics of small surface fatigue cracks existing on the surface, and (2) the surface fatigue cracks in the depth direction were observed and analyzed. The microstructure of Cr-Mo steel was refined by severe plastic deformation (SPD) from the surface to a depth of about 100 μm according to the static load of UNSM, and the fatigue limit increased by 30% as a large compressive residual stress was formed. Additionally, like the untreated materials, fisheye cracks did not occur in UNSM-treated materials, even when inclusions were present, and all specimens fractured while forming surface cracks. Accordingly, one or more of the multiple small surface fatigue cracks (MSFC) grew and developed into a major crack that determines the fatigue life, and a major ridge was formed among the many micro-ridges in the internal direction. In other words, this major crack grew and developed a major ridge in the internal direction, determining the lifespan of the test specimen. Full article

This study investigates the impact of micro- and nanocellulose coatings on the properties of wool fabrics using the solution blow spinning technique. The objective is to assess how varying cellulose sizes influence key fabric attributes, including physical properties, UV-shielding ability, air permeability and water vapour permeability, with a focus on their practical applications. Coating with microcrystalline cellulose (MCC) was found to increase the air permeability of fabric significantly, whereas coating with cellulose nanocrystals (CNCs) enhanced water vapour permeability and reduced pore size. The air permeability could relate to the breathability, and water vapour permeability could relate to the comfortability. Coated fabric with both sizes of cellulose could have different applications, like pollen filtration and printable cloth, and further functionality could be achieved by modifying the cellulose structure. This research establishes a platform for the effective application of cellulose coatings on wool fabric, offering promising advancements for textile performance and sustainability. Full article

Mesoporous HZSM-5 zeolites with nanocrystal stacking morphology were directly synthesized via hydrothermal methods without mesoporous templates. The synthesized mesoporous HZSM-5 was subjected to hydrothermal–citric acid washing treatment. The structural and acidic properties of the samples before and after modification were characterized using various techniques. The catalytic performance for butene conversion to propylene was investigated under atmospheric pressure, 500 °C, and a butene weight hourly space velocity (WHSV) of 10 h⁻¹ in a continuous-flow micro-fixed bed reactor. The results show that propylene selectivity increased significantly from 24.7% before modification to 44%, and propylene yield increased from 22% to 38%. After 2 h of hydrothermal–citric acid washing modification, the catalyst maintained a butene conversion rate of 76% and a selectivity of 47% at 525 °C and a WHSV of 10 h⁻¹ after 130 h of continuous reaction, with a propylene yield of 37%. The results indicate that moderate hydrothermal–citric acid washing modification leads to the removal of aluminum from the zeolite framework, reducing the amount and strength of acid but increasing the mesopore quantity. This helps control the reaction pathways and diffusion of intermediate products, suppresses some side reactions, and improves the selectivity and yield of the desired product, propylene, while significantly enhancing catalytic stability. Full article

Ce³⁺-doped lithium alumino-silicate (Li-Al-Si) scintillating glass was prepared using a melting method and crystallized via heat treatment. X-ray diffraction and transmission electron microscopy confirmed the presence of nanocrystals in the materials. Radioluminescence spectra, obtained by X-ray excitation, and luminescence spectra, obtained by 338 nm excitation, showed that the luminescence intensity increased after crystallization. The glass was combined with pure silica as the inner cladding to fabricate a hybrid fiber core using a melt-in-tube technique. The composition of the fiber core was examined using an electron probe microanalyzer. The glass fiber produced strong blue luminescence under UV excitation. After a micro-crystallizing heat treatment of the hybrid fiber at 850 °C in a reducing atmosphere, a Ce³⁺-doped lithium alumino-silicate glass–ceramic scintillating hybrid fiber was obtained. The nanocrystal structure of the fiber core was examined using micro-Raman spectroscopy. Excitation and luminescence spectra of the hybrid fiber before and after micro-crystallization were measured using microspectrofluorimetry. The results demonstrated that the fiber remained luminous after micro-crystallization. Hence, this work provides a new way to prepare scintillating glass–ceramic hybrid fibers for neutron detection. Full article

Photocurable hybrid organic–inorganic composites were prepared via surface modification and 3D-patterned structures were fabricated by utilizing a continuous roll-to-roll manufacturing strategy. The surfaces of nanocrystals were engineered with a bifunctional ligand that is a 2-carboxyethyl acrylate, which possesses a carboxylic acid moiety at one end and an acrylate functionality moiety at the other end, yielding acrylate-functionalized nanocrystals. Micro-scale 3D patterns (protruding pyramidal shapes with each side measuring 147 μm) were continuously manufactured at a speed of 2.5 m/min via UV curing with a soft engraved mold. The surface properties of the functionalized nanocrystals and their UV curing condition were explored with Fourier transform infrared spectroscopy. The morphology of the 3D film was measured using scanning electron microscopy. A pin-on-disk tribometer measurement revealed an improved interaction between the functionalized particles and resins. Full article

Membranes are a selective barrier that allows certain species (molecules and ions) to pass through while blocking others. Some rely on size exclusion, where larger molecules get stuck while smaller ones permeate through. Others use differences in charge or polarity to attract and repel specific species. Membranes can purify air and water by allowing only air and water molecules to pass through, while preventing contaminants such as microorganisms and particles, or to separate a target gas or vapor, such as H₂ and CO₂, from other gases. The higher the flux and selectivity, the better a material is for membranes. The desirable performance can be tuned through material type (polymers, ceramics, and biobased materials), microstructure (porosity and tortuosity), and surface chemistry. Most membranes are made from plastic from petroleum-based resources, contributing to global climate change and plastic pollution. Cellulose can be an alternative sustainable resource for making renewable membranes. Cellulose exists in plant cell walls as natural fibers, which can be broken down into smaller components such as cellulose fibrils, nanofibrils, nanocrystals, and cellulose macromolecules through mechanical and chemical processing. Membranes made from reassembling these particles and molecules have variable pore architecture, porosity, and separation properties and, therefore, have a wide range of applications in nano-, micro-, and ultrafiltration and forward osmosis. Despite their advantages, cellulose membranes face some challenges. Improving the selectivity of membranes for specific molecules often comes at the expense of permeability. The stability of cellulose membranes in harsh environments or under continuous operation needs further improvement. Research is ongoing to address these challenges and develop advanced cellulose membranes with enhanced performance. This article reviews the microstructures, fabrication methods, and potential applications of cellulose membranes, providing some critical insights into processing–structure–property relationships for current state-of-the-art cellulosic membranes that could be used to improve their performance. Full article

Scholars are looking for solutions to substitute hazardous substances in manufacturing nanocellulose from bio-sources to preserve the world’s growing environmental consciousness. During the past decade, there has been a notable increase in the use of cellulose nanocrystals (CNCs) in modern science and nanotechnology advancements because of their abundance, biocompatibility, biodegradability, renewability, and superior mechanical properties. Spherical cellulose nanocrystals (J–CNCs) were successfully synthesized from Jenfokie micro-cellulose (J–MC) via sulfuric acid hydrolysis in this study. The yield (up to 58.6%) and specific surface area (up to 99.64 m²/g) of J–CNCs were measured. A field emission gun–scanning electron microscope (FEG-SEM) was used to assess the morphology of the J–MC and J–CNC samples. The spherical shape nanoparticles with a mean nano-size of 34 nm for J–CNCs were characterized using a transmission electron microscope (TEM). X-ray diffraction (XRD) was used to determine the crystallinity index and crystallinity size of J–CNCs, up to 98.4% and 6.13 nm, respectively. The chemical composition was determined using a Fourier transform infrared (FT–IR) spectroscope. Thermal characterization of thermogravimetry analysis (TGA), derivative thermogravimetry (DTG), and differential thermal analysis (DTA) was conducted to identify the thermal stability and cellulose pyrolysis behavior of both J–MC and J–CNC samples. The thermal analysis of J–CNC indicated lower thermal stability than J–MC. It was noted that J–CNC showed higher levels of crystallinity and larger crystallite sizes than J–MC, indicating a successful digestion and an improvement of the main crystalline structure of cellulose. The X-ray diffraction spectra and TEM images were utilized to establish that the nanocrystals’ size was suitable. The novelty of this work is the synthesis of spherical nanocellulose with better properties, chosen with a rich source of cellulose from an affordable new plant (studied for the first time) by stepwise water-retted extraction, continuing from our previous study. Full article

In this paper, we report on the solvothermal preparation and detailed characterization of pristine and intentionally doped zirconium dioxide (ZrO₂) nanocrystals (NCs, ~5 nm) with Eu³⁺ or Ti⁴⁺/Eu³⁺ ions using alkoxide precursors. The results indicated that the ZrO₂ NCs were dominantly of a tetragonal phase (t-ZrO₂) with a small proportion of monoclinic ZrO₂ (m-ZrO₂). The high purity of t-ZrO₂ NCs could be synthesized with more Eu³⁺ doping. It was found that the as-obtained ZrO₂ NCs contain some naturally present Ti⁴⁺ ions originating from precursors, but were being overlooked commonly, and some carbon impurities produced during synthesis. These species showed distinct photoluminescence (PL) properties. At least two types of Eu³⁺, located at low- and high-symmetry sites (probably sevenfold and eightfold oxygen coordination), respectively, were demonstrated to build into the lattice structure of t-ZrO₂ NCs together. The cationic dopants were illustrated to be distributed non-randomly over the sites normally occupied by Zr, while Ti impurities preferentially occupied the sites near the low-symmetry site of Eu³⁺, yielding efficient energy transfer from the titanate groups to the neighboring Eu³⁺. Luminescence nanothermometry could measure temperature in a non-contact and remote way and could find great potentials in micro/nano-electronics, integrated photonics, and biomedicine. On the basis of the dual-emitting combination strategy involving the white broadband CT (Ti³⁺→O⁻) emissions of the titanate groups and red sharp Eu³⁺ emissions, t-ZrO₂:Eu³⁺ nanophosphors were demonstrated to be ratiometric self-referencing optical thermometric materials, with a working range of 130–230 K and a maxima of relative sensitivity of ~1.9% K⁻¹ at 230 K. Full article

While adding different micro- and nanocellulose types into epoxy coating formulations with waterborne phenalkamine crosslinker, effects on processing conditions and coating performance were systematically investigated. The variations in viscosity, thermal and thermomechanical properties, mechanical behavior, abrasive wear, water contact angles, and coating morphologies were evaluated. The selected additives include microcrystalline cellulose (MCC) at 1 to 10 wt.% and cellulose nanocrystals (CNC), cellulose nanofibers (CNF), cellulose microfibers (CMF), and hydrophobically modified cellulose microfibers (mCMF) at 0.1 to 1.5 wt.%. The viscosity profiles are determined by the inherent additive characteristics with strong shear thinning effects for epoxy/CNF, while the epoxy/mCMF provides lower viscosity and better matrix compatibility owing to the lubrication of encapsulated wax. The crosslinking of epoxy/CNF is favored and postponed for epoxy/(CNC, CMF, mCMF), as the stronger interactions between epoxy and CNF are confirmed by an increase in the glass transition temperature and reduction in the dampening factor. The mechanical properties indicate the highest hardness and impact strength for epoxy/CNF resulting in the lowest abrasion wear rates, but ductility enhances and wear rates mostly reduce for epoxy/mCMF together with hydrophobic protection. In addition, the mechanical reinforcement owing to the specific organization of a nanocellulose network at percolation threshold concentrations of 0.75 wt.% is confirmed by microscopic analysis: the latter results in a 2.6 °C (CNF) or 1.6 °C (CNC) increase in the glass transition temperature, 50% (CNF) or 20% (CNC) increase in the E modulus, 37% (CNF) or 32% (CNC) increase in hardness, and 58% (CNF) or 33% (CNC) lower abrasive wear compared to neat epoxy, while higher concentrations up to 1.5 wt.% mCMF can be added. This research significantly demonstrates that nanocellulose is directly compatible with a waterborne phenalkamine crosslinker and actively contributes to the crosslinking of waterborne epoxy coatings, changing the intrinsic glass transition temperatures and hardness properties, to which mechanical coating performance directly relates. Full article

Amorphous alloys or metallic glasses (MGs) thin films have attracted extensive attention in various fields due to their unique functional properties. Here, we use in situ heating transmission electron microscopy (TEM) to investigate the thermal stability and crystallization behavior of Pd-Au-Si thin films prepared by a pulsed laser deposition (PLD) method. Upon heating treatment inside a TEM, we trace the structural changes in the Pd-Au-Si thin films through directly recording high-resolution images and diffraction patterns at different temperatures. TEM observations reveal that the Pd-Au-Si thin films started to nucleate with small crystalline embryos uniformly distributed in the glassy matrix upon approaching the glass transition temperature ${\mathrm{T}}_{\mathrm{g}}=625\mathrm{K}$, and subsequently, the growth of crystalline nuclei into sub-10 nm Pd-Si nanocrystals commenced. Upon further increasing the temperature to $673\mathrm{K}$, the thin films transformed to micro-sized patches of stacking-faulty lamellae that further crystallized into ${\mathrm{Pd}}_9{\mathrm{Si}}_2$ and ${\mathrm{Pd}}_3\mathrm{Si}$ intermetallic compounds. Interestingly, with prolonged thermal heating at elevated temperatures, the ${\mathrm{Pd}}_9{\mathrm{Si}}_2$ transformed to ${\mathrm{Pd}}_3\mathrm{Si}$. Simultaneously, the solute Au atoms initially dissolved in glassy alloys and eventually precipitated out of the ${\mathrm{Pd}}_9{\mathrm{Si}}_2$ and ${\mathrm{Pd}}_3\mathrm{Si}$ intermetallics, forming nearly spherical Au nanocrystals. Our TEM results reveal the unique thermal stability and crystallization processes of the PLD-prepared Pd-Au-Si thin films as well as demonstrate a possibility of producing a large quantity of pure nanocrystals out of amorphous solids for various applications. Full article

The current work introduces the synthesis of inorganic salt nano/micro-crystals during the reduction of hydrogen tetrachloroaurate(III) by Pluronic triblock copolymers (P123, PEO₂₀–PPO₇₀–PEO₂₀). The morphologies and component were confirmed using an electron microscope with an electronic differential system (EDS), and the crystal structures were determined with X-ray diffraction (XRD). The morphologies highly depend on the concentrations of Pluronic and pH values. The mean size of the nanocrystal and hollow micro-crystal were controlled typically in the range of 32–150 nm (side length) and 1.4 μm, respectively. Different from the electrospray–ionization (EI) method, a model in which KCl forms a supersaturated solution in the micellar core of Pluronic is used to explain the formation process. This work provides the new insight that inorganic salt nanocrystals could be synthesized with the template of micelles in pure aqueous solutions. Full article

The aim of this study is to prove that resistive heating enables the synthesis of metal/metal oxide composites in the form of core–shell structures. The thickness and morphology of the oxide layer depends strongly on the nature of the metal, but the influences of parameters such as the time and current profiles and the presence of an external field have also been investigated. The systems chosen for the present study are Zn/ZnO, Ti/TiO₂, and Ni/NiO. The characterization of the samples was performed using techniques based on scanning electron microscopy (SEM). The thicknesses of the oxide layers varied from 10 μm (Zn/ZnO) to 50 μm (Ni/NiO). In the case of Zn- and Ti-based composites, the growth of nanostructures on the oxide layer was observed. Micro- and nanoneedles formed on the ZnO layer while prism-like structures appeared on the TiO₂. In the case of the NiO layer, micro- and nanocrystals were observed. Applying an external electric field seemed to align the ZnO needles, whereas its effect on TiO₂ and NiO was less appreciable, principally affecting the shape of their grain boundaries. The chemical compositions were analysed using X-ray spectroscopy (EDX), which confirmed the existence of an oxide layer. Structural information was obtained by means of X-ray diffraction (XRD) and was later checked using Raman spectroscopy. The oxide layers seemed to be crystalline and, although some non-stoichiometric phases appeared, the stoichiometric phases were predominant; these were wurtzite, rutile, and cubic for Zn, Ti, and Ni oxides, respectively. The photoluminescence technique was used to study the distribution of defects on the shell, and mainly visible bands (2–2.5 eV), attributed to oxygen vacancies, were present. The near-band edges of ZnO and TiO₂ were also observed around 3.2–3.3 eV. Full article

Owning to merits such as bandgap tunability, solution processability, large absorption coefficients, and high photoluminescence quantum yields, colloidal quantum dots (CQDs) emerged as a promising gain material to make on-chip micro/nanoscale lasers with high silicon compatibility. In this paper, we review the recent progress in CQD on-chip micro/nanoscale lasers, with a special focus on the physical properties achieved through field manipulation schemes in different types of cavities. Key aspects include manipulating and engineering wavelength, polarization, and direction as well as coupling and light extraction. Finally, we give our prospects for future research directions toward the integration of robust CQD nano/microscale lasers with photonic integrated circuits. Full article