Search Results (154)

Carbon nanotube yarns (CNTYs) have received more consideration recently due to their excellent specific mechanical, electrical and thermal properties, making them promising materials for different applications. Until now, the axial properties of the yarn have been thoroughly investigated; however, the transverse or radial properties, orthogonal to the fiber axis, remain relatively unknown due to the challenges associated with their measurement. In this study, the transverse or radial response of the CNTY including its elastic modulus was determined using Atomic Force Microscopy (AFM) and Raman Spectroscopy. Determining transverse properties in fibrous materials presents challenges owing to their geometry, inherent anisotropy, whereby mechanical characteristics exhibit directional disparities; i.e., the properties in the transverse direction may be several orders of magnitude smaller than those in the axial direction. To overcome these difficulties, AFM was utilized to perform nanoindentation experiments, where a tipless flexible cantilever probe was used to apply a controlled force to the CNTY surface. The resulting indentation depth was then analyzed to determine the transversal elastic modulus. Preliminary findings indicate that the transverse elastic modulus of the CNTYs ranges from 10–54 kPa for strain levels below 3%. Complementary Raman spectroscopy provided insight into the bulk-scale mechanical behavior of CNTYs. Incremental compressive loading between microscope slides induced nonlinear upshifts in the 2D Raman band (from ~2686.6 to 2691.4 cm⁻¹), indicating nanoscale tube realignment, inter-tube densification, and compaction. From lateral diameter measurements under load, a stress–strain curve was constructed, revealing three distinct regimes: one with an initial elastic modulus of 3.12 MPa (0.3–11.2% strain), another one with an elastic modulus increasing to 8.46 MPa (11.2–14.4%), and finally one with an elastic modulus peaking at 16.86 MPa beyond 14.4% strain. Together, these methods delineate the hierarchical and anisotropic nature of CNTYs, validating the importance of multiscale mechanical characterization for their deployment in piezoresistive sensors and multifunctional composites. This study establishes a robust framework for quantifying the transverse mechanical response of CNTYs. Full article

Biodegradable nanocomposite materials possessing self-healing behavior are emerging as an attractive option of being used in advanced mechatronic systems. The current study is focused on a thorough examination of the micromechanical properties of graphene–reinforced polylactic acid (PLA)/polycaprolactone (PCL) composite samples, followed by estimation of their self-healing behavior upon heating. Polymer blend–based nanocomposite materials were prepared using the green and reliable in terms of good nanofiller dispersion melt extrusion method. 3D printed nanocomposite specimens with impeccable flatness were subjected to fine microscratch testing by applying a constant force experimental mode. The surface resistance of the three-component polymer materials against the lateral movement of the stylus fulfilling the scratch and the impact of the dual-phase PLA/PCL ratio on the nanocomposite mechanical performance were estimated by calculation of the coefficient of friction (COF = F_x/F_z). COF values in the range of 0.8–1.4 indicated excellent nanocomposite resilience against scratch. Creating a heterogeneous polymer system that combines phase-separated soft and hard domains with close melt and glass transition temperatures, respectively, may facilitate the physical flow of macromolecular chains into voids or free volume areas. This aspect can be critical in the achievement of thermally–induced self-healing properties of the composite material. Scanning electron microscopy (SEM) imaging of the microscratches, made before and after Joule heating of the polymer samples, revealed a significant degree of surface recovery and a sensible reduction in the width of the adjusted scratch grooves. Full article

Cardiolipin (CL), a unique dimeric phospholipid predominantly enriched in the inner mitochondrial membrane, is a crucial determinant of mitochondrial structure and function. Its content, fatty acyl composition, and oxidation state are associated with mitochondrial bioenergetics, dynamics, and cellular signaling. Disruptions in CL metabolism are increasingly implicated in the pathogenesis of various central nervous system (CNS) disorders, including Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, epilepsy, and traumatic brain injury. This narrative review summarizes recent advances in the analytical techniques employed for CL analysis. The principles and applications of mass spectrometry-based platforms, nuclear magnetic resonance, Fourier-transform infrared spectroscopy, atomic force microscopy-infrared spectroscopy, and fluorescent probes were discussed, with an emphasis on their strengths in revealing the structure, composition, dynamics, and spatial distribution of CL. Furthermore, the evidence of CL abnormalities in various CNS disorders was assessed, often showing decreased CL levels, loss of polyunsaturated species, and increased oxidation associated with mitochondrial dysfunction and neuronal apoptosis. Furthermore, the nutritional interventions for CL modulation were discussed, such as polyunsaturated fatty acids, polyphenols, carotenoids, retinoids, alkaloids, and triterpenoids, which summarize their potential health-beneficial effects in remodeling the CL acyl chain, preventing oxidation, and regulating mitochondrial homeostasis. Overall, this review provided insight into integrating CL analysis and dietary modulation in understanding CL-related pathologies in CNS disorders. Full article

Glycation-induced modifications of extracellular matrix (ECM) proteins, including collagen, are increasingly recognized as critical modulators of cellular behavior, particularly in pathophysiological contexts such as aging and diabetes. While their impact on general cell adhesion has been explored, the specific consequences for mesenchymal stem cell (MSC) mechanotransduction remain poorly defined. In this study, we investigated the temporal and mechanistic aspects of adhesion and mechanosensitive signaling in adipose-derived MSCs (ADMSCs) cultured on native versus glycated collagen substrates. Our findings identify two temporally distinct adhesion mechanisms: an initial pathway mediated by the receptor for advanced glycation end-products (RAGE), which is activated within the first 30 min following substrate engagement, and a later-stage adhesion process predominantly governed by integrins. Immunofluorescence analysis demonstrated maximal nuclear localization of YAP/TAZ transcriptional regulators during the initial adhesion phase, coinciding with RAGE engagement. This nuclear enrichment was progressively attenuated as integrin-mediated focal adhesions matured, suggesting a dynamic shift in receptor usage and mechanotransductive signaling. Interestingly, glycated collagen substrates accelerated early cell attachment but impaired focal adhesion maturation, suggesting a disruption in integrin engagement. Endogenous collagen synthesis was consistently detected at all examined time points (30 min, 2 h, and 5 h), suggesting a constitutive biosynthetic activity that remains sensitive to the glycation state of the substrate. Atomic force microscopy (AFM) demonstrated that glycation disrupts collagen fibrillogenesis: while native collagen forms a well-organized network of long, interconnected fibrils, GL-1 substrates (glycated for 1 day) displayed sparse and disordered fibrillary structures, whereas GL-5 substrates (5-day glycation) exhibited partial restoration of fibrillar organization. These matrix alterations were closely associated with changes in adhesion kinetics and mechanotransduction profiles. Taken together, our findings demonstrate that collagen glycation modulates both adhesion dynamics and mechanosensitive signaling of MSCs through a dual-receptor mechanism. These insights have significant implications for the design of regenerative therapies targeting aged or metabolically compromised tissues, where ECM glycation is prevalent. Full article

This paper innovatively proposes a high-precision fabrication strategy for silicon-based micro–nano-composite layered structures composed of micron-scale platforms and nanopillars, effectively addressing the challenges of alignment errors and material mismatch during manufacturing. By integrating electron beam lithography (EBL), inductively coupled plasma (ICP) etching, and ultraviolet nanoimprint lithography (NIL) into a unified multi-step workflow, the method achieves exceptional precision and efficiency in producing complex micro–nano-composite architectures. Comprehensive structural characterization is performed using scanning electron microscopy (SEM) and atomic force microscopy (AFM), with probe convolution effects carefully corrected to ensure accurate dimensional analysis. Experimental results confirm the outstanding stability and uniformity of the fabricated structures, exhibiting minimal deviations in both feature size and spatial layout. Nanopillars with diameters ranging from 50 to 200 nm are successfully integrated onto 1-µm square platforms, with the lateral deviation of 50 nm features maintained within 5% or less. Furthermore, the method effectively mitigates thermal stress-induced misalignment during the fabrication of multi-material layers, demonstrating strong potential for scalable production of advanced photonic devices and integrated nanophotonic systems. Overall, this work establishes a robust and versatile technical pathway for the precise manufacturing and quantitative characterization of micro–nano-composite structures, providing a key foundation for the next generation of photonic integration technologies. Full article

Diamond, as an exceptional material with many superior properties, requires a single crystal in a reasonably large size for practical industrial applications. However, achieving large-area single-crystal diamond (SCD) growth without the formation of polycrystalline rims remains challenging. Microwave plasma chemical vapor deposition (MPCVD) using a gas mixture of 10% CH₄-H₂ was used for the homoepitaxial growth of (001) SCD. The effect of nitrogen gas addition in the range of 0–2000 ppm on lateral growth was investigated. Deposition with 180 ppm N₂ over a growth duration of 20 h to reach a thickness of 0.95 mm resulted in significantly enhanced lateral growth without the appearance of a polycrystalline diamond (PCD) rim for the grown diamond, and the total top surface area of SCD increased by an area gain of 1.6 relative to the substrate. The corresponding vertical and lateral growth rates were 47.3 µm/h and 52.5 µm/h, respectively. Characterization by Raman spectroscopy and atomic force microscopy (AFM) revealed uniform structural integrity across the whole surface from the laterally grown regions to the center, including the entire expanded area, in terms of surface morphology and crystalline quality. Moreover, measurements of the etch pit densities (EPDs) showed a substantial reduction in the laterally grown regions, approximately an order of magnitude lower than those in the central region. The high quality of the homoepitaxial diamond layer was further verified with (004) X-ray rocking curve analysis, showing a narrow full width at half maximum (FWHM) of 11 arcsec. Full article

The detection of volatile organic compound (VOC) biomarkers from the volatolome for the anticipated diagnosis of severe diseases such as cancers is made difficult due to the presence of high quantities of H₂O in the collected samples. It has been shown that water molecules tend to compete or combine themselves with analytes, which requires either their removal or the development of more sensitive and discriminant sensors. In this later prospect, a positive effect of poly(hedral oligomeric silsesquioxanes) (POSS) is sought out to enhance the sensitivity of carbon nanotube-based quantum resistive vapour sensors (vQRS). POSS, once copolymerized with methyl methacrylate or styrene, can be used as nano-spacers amplifying the disconnection of the nano-junctions due to swelling of the polymer upon the diffusion of VOC. The amplitude of this phenomenon, which is at the origin of the chemo-resistive behaviour of vQRS, was compared with that of homologue transducers made of poly(styrene) (PS) and poly(methyl methacrylate) (PMMA)-coated carbon nanotube (CNT) random networks. The presence of POSS in PS-based sensors has enhanced their sensitivity by 213 times for toluene, by 268 times for acetone, by 4 times for ethanol, and by 187 times for cyclohexane. Similarly, the presence of POSS in PMMA chains increases the sensitivity of sensors to cyclohexane by 10 times, to ethanol by 45 times, to toluene by 244 times, and to acetone and butanone by 4 times. All transducers were made by spray layer by layer (sLbL) to obtain a hierarchically structured conducting architecture. The transducers’ surface was characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM) to observe the CNT coating and dispersion level in the matrix. All sensors were tested with twenty-one VOC part of lung and skin cancer biomarkers by using a dynamic vapour analysis (DVA). The vQRS based on POSS copolymers demonstrated much larger chemo-resistive responses (A_R) than the sensors based only on pure polymers and were found to be very selective towards cyclohexane and hexene-1. The PMMA-co-POSS/CNT sensor was able to detect down to 12 ppm of VOC with a very high signal-to-noise ratio (SNR) and to discriminate six VOC among them all with a PCA (principal component analysis) projection. Full article

Nanostructures obtained as a by-product of the electrochemical synthesis of ZrO₂ nanotube membranes have scarcely received any attention despite their enormous potential. This is mainly due to their size properties, morphology, and composition. In the present work, these nanostructures are characterized, and their potential application as an additive in PVA-based coatings is analyzed. The characterization was performed by X-ray fluorescence, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, and X-ray diffraction. The results showed that the nanostructures consist of tubular fragments generated during the formation of the ZrO₂ membrane, with a dimension of 626.74 nm in width, a length of 1906.39 nm, and a clear cubic structure. The ZrO₂-PVA coating, which is prepared by using the spin coating technique, presented a uniform and homogenous particle distribution, which was later confirmed by Fourier transform infrared spectroscopy, scanning electron microscopy, and atomic force microscopy. The optical transparency and thermal resistance were evaluated through UV-Vis spectroscopy and thermogravimetric analysis, showing that the incorporation of ZrO₂ as an additive improved its UV absorption properties and thermal stability during the pyrolysis stage. The results suggest that the ZrO₂ nanostructures enhance the thermal and protective properties of the PVA-based coatings by acting as physical barriers and stabilizers within the polymer matrix. Full article

This review paper provides a comprehensive overview of selected 3D surface texture parameters defined by ISO 25178-2, with a focus on their metrological aspects in high-resolution measurements using atomic force microscopy (AFM). The parameters Sa, Sz, Sq, Sdq, and Sdr are analyzed in terms of their practical application, sensitivity to measurement conditions, and role in assessing surface functionality. Through a review of the literature and simulations of surface profiles with controlled geometric variations, the study demonstrates how the selected parameters respond to changes in step pitch, step width, slope, and lateral calibration errors. Experimental AFM measurements performed on a certified step height standard further illustrate the impact of calibration on the quality of measurement results. Special emphasis is placed on the importance of evaluating measurement uncertainty. The results confirm the need for rigorous instrument calibration and uncertainty assessment to ensure reliable and comparable surface characterization across different instruments and laboratories. Full article

Tomato waste (TW) was employed as a sustainable source for the synthesis of fluorescent carbon dots (CDs) via a microwave-assisted hydrothermal carbonization (Mw-HTC) method, aiming at its valorization. Several amines were used as nitrogen additives to enhance the fluorescence quantum yield (QY) of CDs, and a set of reaction conditions, including additive/TW mass ratio (0.04–0.32), dwell time (15–60 min), and temperature (200–230 °C) of the HTC process, were scrutinized. The structural analysis of the tomato waste carbon dots (TWCDs) was undertaken by FTIR and ¹H NMR techniques, revealing their most relevant features. In solid state, transmission electron microscopy (TEM) analysis showed the presence of nearly spherical nanoparticles with an average lateral size of 8.1 nm. Likewise, the topographical assessment by atomic force microscopy (AFM) also indicated particles’ heights between 3 and 10 nm. Their photophysical properties, revealed by UV–Vis, steady-state, and time-resolved fluorescence spectroscopies, are fully discussed. Higher photoluminescent quantum yields (up to 0.08) were attained when the biomass residues were mixed with organic aliphatic amines during the Mw-HTC process. Emission tunability is a characteristic feature of these CDs, which display an intensity average fluorescence lifetime of 8 ns. The new TWCDs demonstrated good antioxidant properties by the ABTS radical cation method (75% inhibition at TWCDs’ concentration of 5 mg/mL), which proved to be related to the dwell time used in the CDs synthesis. Moreover, the synthesized TWCDs suppressed the growth of Escherichia coli and Staphylococcus aureus at concentrations higher than 2000 μg/mL, encouraging future antibacterial applications. Full article

In ultra-precision polishing tests, due to the corrosive and adhesive properties of the polishing abrasive, the spray system faces wear, blockage and oxidation problems. To solve these problems, this paper studied nozzles and verified the wear mechanism of the coated and uncoated nozzles by simulating the operating conditions after assembling the spray system. In the early stages of the experiment, the polishing speed of the spray system (v = 10 L/min), the feed rate (v_f = 7.8 mm/min) and the polishing pressure (2~3.5 MPa) were maintained. The wear mechanism and surface morphology features of the nozzles in each case were analyzed by Hitachi S-3400N electron microscopy. When comparing the surface morphology of the nozzle coated with titanium alloy and the uncoated one, the results show that there is a significant difference in the corrosion resistance of the coatings to the abrasive particles. A significant effect was seen on the wear morphology, proving that the nozzle wear mechanism includes wear, adhesion and diffusion. Under the experimental conditions of a lateral velocity of 7.8 mm/min and a polishing force of 2 MPa, BK7 was polished using nozzles 1 and 2, resulting in a surface roughness of 75 nm and 35 nm while PV values were 125 nm and 67 nm, respectively. The excellent quality of nozzle 2 (coating nozzle) was proven, further demonstrating the superiority of the coating nozzle. Finally, the lifespan of the nozzle was extended and the surface accuracy of BK7 was improved by coating titanium alloy composite material on the 304 stainless steel nozzle. Full article

Due to the bio-inert nature of titanium (Ti) and subsequent accompanying chronic inflammatory response, an implant’s stability and function can be significantly affected, which is why various surface modifications have been employed, including the deposition of titanium oxide (TiO₂) nanotubes (TNTs) onto the native surface through the anodic oxidation method. While the influence of nanotube diameter on cell behaviour and osteogenesis is very well documented, information regarding the effects of nanotube lateral spacing on the in vivo new bone formation process is insufficient and hard to find. Considering this, the present study’s aim was to evaluate the mechanical properties and the osteogenic ability of two types of TNTs-based pins with different lateral spacing, e.g., 25 nm (TNTs) and 92 nm (spTNTs). The mechanical properties of the TNT-coated implants were characterised from a morphological point of view (tube diameter, spacing, and tube length) using scanning electron microscopy (SEM). In addition, the chemical composition of the implants was evaluated using X-ray photoelectron spectroscopy, while surface roughness and topography were characterised using atomic force microscopy (AFM). Finally, the implants’ hardness and elastic modulus were investigated using nanoindentation measurements. The in vivo new bone formation was histologically evaluated (haematoxylin and eosin—HE staining) at 6 and 30 days post-implantation in a rat model. Mechanical characterisation revealed that the two morphologies presented a similar chemical composition and mechanical strength, but, in terms of surface roughness, the spTNTs exhibited a higher average roughness. The microscopic examination at 1 month post-implantation revealed that spTNTs pins (57.21 ± 34.93) were capable of promoting early new bone tissue formation to a greater extent than the TNTs-coated implants (24.37 ± 6.5), with a difference in the average thickness of the newly formed bone tissue of ~32.84 µm, thus highlighting the importance of this parameter when designing future dental/orthopaedic implants. Full article

In the fabrication of optical polymer-based components, such as diffractive gratings and waveguides, high throughput and high precision are required. The non-destructive evaluation of these complex polymer-based structures is a significant challenge. Different measurement techniques can measure the structure geometry directly or via its functionality indirectly. This study investigates various measurement techniques aimed at assessing these structures from 200 nm up to 20 µm. Environmental scanning electron microscopy (ESEM), white light interferometry (WLI), atomic force microscopy (AFM), micro computed tomography (µCT), optical coherence tomography (OCT), phase contrast microscopy (PCM), and Mueller matrix ellipsometry (MME) are investigated for their practical limits of lateral resolution and aspect ratio. The impact of the specimens’ complexity factors, including structure width and aspect ratio, on measurement quality is discussed. A particular focus of this study is on the suitability of different measurement systems for evaluating undercuts and enclosed structures while considering structure size, slant angle, and cover thickness. The aim is to discuss the specific advantages of the individual measurement systems and their application areas in order to be able to quickly select suitable measurement systems for a non-destructive evaluation of polymer-based micro and nanostructures. Full article

The structural properties of lattice-matched InAlAs/InP layers grown by molecular beam epitaxy have been studied using atomic force microscopy, scanning electron microscopy and micro-photoluminescence spectroscopy. The formation of the surface pits with lateral sizes in the micron range and a depth of about 2 ÷ 10 nm has been detected. The InP substrate annealing temperature and value of InAlAs alloy composition deviation from the lattice-matched In_xAl_1−xAs/InP case (x = 0.52) control the density of pits ranging from 5 × 10⁵ cm⁻² ÷ 10⁸ cm⁻². The pit sizes are controlled by the InAlAs layer thickness and growth temperature. The correlation between the surface pits and threading dislocations has been detected. Moreover, the InAlAs surface is characterized by composition inhomogeneity with a magnitude of 0.7% with the cluster lateral sizes and density close to these parameters for surface pits. The experimental data allow us to suggest a model where the formation of surface pits and composition clusters is caused by the influence of a local strain field in the threading dislocation core vicinity on In adatoms incorporating kinetic. Full article

Controlling the balance between piezoelectric and flexoelectric effects is crucial for tailoring the electromechanical responses of a material. In twisted graphene, it is found that the electromechanical response near the domain walls (DWs) is dominated by either the flexoelectric effect as in twisted bilayer graphene (tBLG) or the piezoelectric effect as in twisted monolayer–bilayer graphene (tMBG). The codominance of both effects in a single system is rare. Here, utilizing lateral piezoresponse force microscopy (LPFM), we show that piezoelectric and flexoelectric effects can coexist and are equally important in twisted double bilayer graphene (tDBG), termed as the piezo-flexoelectric effect. Unlike tBLG and tMBG, distinctive two-step LPFM spatial profiles are captured across the moiré DWs of tDBG. By decomposing the LPFM signal into axisymmetric and antisymmetric components, we find that the angular dependence of both components satisfies sinusoidal relations. Quantitatively, the in-plane piezoelectric coefficient of DWs in tDBG is determined to be 0.15 pm/V by dual AC resonance tracking (DART) LPFM measurement. The conclusion is further supported by continuum mechanics simulations. Our results demonstrate that the stacking configuration serves as a powerful tuning knob for modulating the electromechanical responses of twisted van der Waals materials. Full article