Search Results (11,786)

Raman spectroscopy allows for analyzing local molecular matrix components while preserving spatial resolution in tissue samples. The aim of this study was to use Raman line scans to discriminate between healthy and diseased cartilage tissue based on the depth-dependent sulfated glycosaminoglycans (sGAG) and total GAGs distribution. Full-thickness articular cartilage tissue was harvested from human individuals at different maturation stages (skeletally immature, skeletally mature) and from patients with diagnosed osteoarthritis. Raman spectroscopic line scans (30 µm step size) were utilized to analyze the sub-zonal sGAG (1062 cm⁻¹) and total GAG (1370–1380 cm⁻¹) distribution relative to the organic matrix (CH₂ band 1430–1480 cm⁻¹). We found a linear trend of the sGAG/CH₂ ratio over the tissue depth in all samples (p < 0.0001). The total GAG/CH₂ ratio of the skeletally immature and mature cartilage showed a characteristic non-linear behavior over the tissue distance. The elderly osteoarthritic cartilage exhibited lower total GAG/CH₂ ratios compared to the ratios of the skeletally immature and mature samples, without a pronounced increase in the superficial area. Raman spectroscopic line scans are a fast and representative method allowing us to identify the local and tissue depth-dependent distribution of GAGs at higher specificity and resolution compared to histological staining. Full article

Indium phosphide (InP) is a promising photoactive material for solar-driven hydrogen production owing to its optimal bandgap, high carrier mobility, and broad solar absorption. However, conventional InP fabrication relies on costly wafers and toxic precursors, limiting its scalability and sustainability. Here, we demonstrate a simple and environmentally friendly route to synthesize n-type InP thin-film photoanodes by phosphidating indium films prepared via doctor blade coating on ITO substrates, using NaH₂PO₂ as a phosphorus source. Structural and spectroscopic analyses (XRD, Raman, XPS, PL) confirmed the successful formation of crystalline InP with optimum quality at 425 °C. Photoelectrochemical measurements revealed a significant photocurrent density of 1.8 mA·cm⁻² under AM 1.5 illumination, with extended photoresponse into the near-infrared region. Mott–Schottky and EIS analyses indicated efficient charge separation, low transfer resistance, and unintentional n-type doping due to Sn diffusion from the ITO substrate. This facile and green synthesis route not only provides a scalable approach to III–V semiconductors but also highlights InP thin films as cost-effective and efficient photoanodes for sustainable solar hydrogen generation. Full article

This research presents the study of utilizing the cocoa husk biomass waste to obtain active carbon through carbonization method, followed by chemical–thermal activation. The activated carbon (CH) was characterized using BET, SEM–EDX, XPS, and Raman techniques. The obtained material showed a high specific surface area of 1661 m²·g⁻¹, and XPS confirmed the presence of oxygen-containing surface functionalities. The adsorption of reactive dye Drimaren Red K-7B by CH was studied to assess the impact of the initial concentration in water solution, temperature, and contact time. The adsorbent achieved over 90% removal within three minutes at 40 °C. The experimental data for the adsorption of Drimaren Red K-7B using CH showed a good fit with the Dubinin–Radushkevich isotherm and a pseudo-second-order kinetic model. This research offers a promising approach for advancing the circular economy through the obtaining of eco-friendly adsorbents derived from biomass waste, exhibiting high initial adsorption efficiency and rapid uptake kinetics towards reactive dye. Full article

In this study, a new way of protecting textile wearable electronics is proposed. A natural product, silk fibroin, known for its high biocompatibility, biodegradability, and low cytotoxicity, was selected to cover the functionalized fabric to improve its stability and enable washability. Silk fabric was selected as a non-toxic material, suitable for further application on skin and for wearable devices. Silk fabric was functionalized with various amounts of high-pressure carbon monoxide single-walled carbon nanotubes (HiPCO SWNTs). HiPCO SWNTs made the fabric electroconductive, but they are easily washed out of the fabric. The fabric functionalized with HiPCO SWNTs was covered with silk fibroin (SF) protein, which was subsequently crystallized by ethanol vapor to make it insoluble in water. The functionalization and silk fibroin coverage processes were studied using electrical resistance measurements, infrared and Raman spectroscopies, thermogravimetric technique, and surface wettability analysis. The coverage of the fabric with crystallized silk fibroin enables the washing process. The resistance of the functionalized fabric with silk fibroin did not increase significantly. The presented silk fibroin coating can facilitate the construction of future wearable electronics, protect the electroconductive nanomaterials on the fabric surface, and make textile structures reusable. Full article

Hydrogels of acrylamide (AM)–acrylic acid (AA) and nanocomposite hydrogels of AM–AA and carbon nanotubes (CNTs) functionalized with acyl chloride groups (CNTs_OxCl) were synthesized and characterized, and their ability to release folic acid was analyzed. Both hydrogel types were synthesized via redox polymerization. CNTs were prepared via chemical vapor deposition. The prepared samples were analyzed via transmission electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, differential scanning calorimetry, and field-emission scanning electron microscopy. Their swelling ability and their mechanical properties (compression tests) were determined at room temperature ~298.15 K, whereas their ability to release folic acid was studied using UV–VIS spectroscopy. The equilibrium swelling of the AM–AA hydrogels was greater than that of the AM–AA/CNTs_OxCl nanocomposite hydrogels prepared at the same monomeric relation (wt%), whereas the Young moduli of these nanocomposite hydrogels were higher than that of AM–AA hydrogels. For the AM–AA/CNTs_OxCl nanocomposite hydrogels, polymer chains containing AM and AA units were grafted to CNTs_OxCl. The glass–transition temperatures of AM–AA nanocomposite hydrogels were higher than that of AM–AA hydrogels. Folic acid release from the AM–AA hydrogels and AM–AA/CNTs_OxCl nanocomposite hydrogels was successfully adjusted using the Weibull model. Full article

Biosensing plays a vital role in medical diagnostics, environmental monitoring, and food safety, enabling highly sensitive and specific detection of diverse biological and chemical targets. However, conventional biosensing platforms still suffer from limited sensitivity, poor nanoscale resolution, and restricted multiplexed or dynamic detection capabilities. DNA origami, as an emerging bottom-up nanofabrication strategy, enables the construction of programmable nanostructures with high spatial precision. This capability allows the rational arrangement of functional molecules at the nanoscale, thereby offering significant advantages for biosensing applications. Specifically, DNA origami can enhance signal amplification, improve spatial resolution, and enable multiplexed detection under complex conditions. In this review, we provide a systematic overview of recent advances in the application of DNA origami across various classes of biosensors, including microscopy-based biosensors, nanopore biosensors, electrochemical biosensors, fluorescent biosensors, SERS biosensors, and other related biosensors. We aim for this review to advance the development of DNA origami-based biosensing and to provide new insights for researchers working in related fields. Full article

Most biomarkers exhibit abnormal expression in more than one disease, making conventional single-biomarker detection strategies prone to false-negative results. Detecting multiple biomarkers associated with a single disease can therefore substantially improve diagnostic accuracy. Accordingly, recent research has focused on precise multiplex detection, leading to the development of sensors employing various readout methods, including electrochemical, fluorescence, Raman, and colorimetric approaches. This review focuses on optical sensing applications, such as fluorescence, Raman spectroscopy, and colorimetry, which offer rapid and straightforward detection and are well suited for point-of-care testing (POCT). These optical sensors exploit nanoscale phenomena derived from the intrinsic properties of nanomaterials, including metal-enhanced fluorescence (MEF), Förster resonance energy transfer (FRET), and surface-enhanced Raman scattering (SERS), which can be tailored through modifications in material type and structure. We summarize the types and properties of commonly used nanomaterials, including plasmonic and carbon-based nanoparticles, and provide a comprehensive overview of recent advances in multiplex biomarker detection. Furthermore, we address the potential of these nanosensors for clinical translation and POCT applications, highlighting their relevance for next-generation disease diagnostic platforms. Full article

The optical microscope is an indispensable observation instrument that has fundamentally contributed to progress in science and technology. Dark-field microscopy and scattered light imaging techniques enable high-contrast observation of nanoparticles in water. However, the scattered light is focused by the optical lenses, resulting in a blurred image of the nanoparticle structure. Here, we developed a projection optical microscope (PROM), which directly observes the scattered light from the nanoparticles without optical lenses. In this method, the sample is placed below the focus position of the microscope’s objective lens and the projected light is detected by an image sensor. This enables direct observation of the sample with a spatial resolution of approximately 20 nm. Using this method, changes in the aggregation state of nanoparticles in solution can be observed at a speed faster than the video frame rate. Moreover, the mechanism of such high-resolution observation may be related to the quantum properties of light, making it an interesting phenomenon from the perspective of optical engineering. We expect this method to be applicable to the observation and analysis of samples in materials science, biology and applied physics, and thus to contribute to a wide range of scientific, technological and industrial fields. Full article

Carbyne, a linear chain of carbon atoms, possesses extraordinary properties but has remained elusive due to its extreme instability. While encapsulation within carbon nanotubes stabilizes carbyne, a lack of synthetic control over its location has prevented practical use. Here, we introduce a spatially localized plasma jet technique that enables the guided spatially selective self-assembly of carbyne encapsulated within multiwalled carbon nanotube (carbyne@MWCNT) hybrids on graphite surfaces. This method uses intense, localized plasma energy to simultaneously grow nanotubes and synthesize carbyne within them, where the nanotube structure and carbyne encapsulation are governed by the localized heat flux distribution. Beyond confirming carbyne formation via its characteristic Raman mode, we discover its second-order vibrational spectrum, confirming anharmonic interactions between the chain and its nanotube container. This spatial control can be used to architect functional carbyne@MWCNT arrays, whose potential applications are discussed in detail. Full article

Poly(5-indolylboronic acid) was synthesized electrochemically via cyclic voltammetry using various electrodes, including screen-printed carbon electrodes, glassy carbon electrodes, highly oriented pyrolytic graphite, and 304 stainless steel. This study provides a thorough analysis of the resulting conducting polymer’s electrochemical behavior, morphological and structural characteristics, and potential applications. The following techniques were employed: cyclic voltammetry, electrochemical impedance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, and field-emission scanning electron microscopy. The polymer exhibits pH-dependent redox activity within the pH range of 4–10, displaying Nernstian behavior and achieving a specific areal capacitance of 0.234 mF∙cm⁻² on an SPCE electrode. This result highlights the electrode’s efficiency in terms of charge storage. Impedance data indicate that the modified electrodes demonstrate a substantial decrease in charge transfer resistance and improved interfacial conductivity compared to bare electrodes. Contact angle measurements show that the presence of boronic acid groups makes the polymer hydrophilic. However, when 5PIBA was incubated in the presence of molecules containing hydroxyl groups or certain proteins, such as casein, no adsorption was observed. This suggests limited interaction with functional groups such as amino, hydroxide, and carboxyl groups present in these molecules, indicating the potential application of the polymer in biocorrosion. 5PIBA forms homogeneous, stable, and electroactive coatings on various substrates, making it a promising and versatile material for electrochemical technologies, and paving the way for future functionalization strategies. Full article

Searching anode materials is an important task for the development of sodium-ion batteries. In this regard, bronze-phase titanium dioxide, TiO₂(B), has been considered as one of the promising materials, owing to its crystal structure with open channels and voids facilitating Na⁺ diffusion and storage. However, the electrochemical de-/sodiation mechanism of TiO₂(B) has not been clearly comprehended, and further experiments are required. Herein, in situ and ex situ observations by a combination of X-ray photoelectron spectroscopy, X-ray diffraction, Raman spectroscopy, gas chromatography–mass spectrometry was used to provide additional insights into the electrochemical reaction scenario of bronze-phase TiO₂ in Na-ion batteries. The findings reveal that de-/sodiation of TiO₂(B) occurs through a reversible intercalation reaction and without the involvement of the conversion reaction (no metallic titanium is formed and no oxygen is released). At the same time, upon the first Na⁺ uptake process, crystalline TiO₂(B) becomes partially amorphous, but is still driven by the Ti⁴⁺/Ti³⁺ redox couple. Importantly, TiO₂(B) has pseudocapacitive electrochemical behavior during de-/sodiation based on a quantitative analysis of the cyclic voltammetry data. The results obtained in this study complement existing insights into the sodium storage mechanisms of TiO₂(B) and provide useful knowledge for further improving its anode performance for SIBs application. Full article

Foodborne pathogenic bacteria in meat pose a serious threat to human health. Traditional detection methods for these bacteria are often time-consuming and labor-intensive. In this study, we applied surface-enhanced Raman scattering (SERS) combined with portable Raman spectroscopy as a rapid and convenient detection technique. SERS is a sensitive and fast method that enhances light scattering on rough metal surfaces. Silver nanoparticles (AgNPs) were used as SERS substrates to identify and analyze four pathogenic bacteria, including Escherichia coli (E. coli) O157:H7, Salmonella typhimurium (S. typhimurium), Staphylococcus aureus (S. aureus), and Listeria monocytogenes (L. monocytogenes), in beef. We optimized the detection conditions of AgNPs and established the limit of detection (LOD) for these four pathogenic bacteria in both pure culture and beef samples. The LODs were as low as 4–23 CFU/mL in beef samples, indicating high detection sensitivity. Linear discriminant analysis (LDA) was used to analyze the SERS spectra, yielding an accuracy of 91.7–97.3%. This study not only provides a rapid and portable detection method for pathogenic bacteria in beef but also overcomes the limitations of traditional methods that are often time-consuming and not suitable for on-site detection. However, the current study is limited to the detection of the four specific pathogenic bacteria, and further research is needed to expand the range of detectable pathogens and to improve the robustness of the detection models for more complex meat samples. Overall, this research demonstrates the potential of SERS combined with portable Raman spectroscopy as a powerful tool for the rapid detection of pathogenic bacteria in meat products, which could significantly enhance food safety monitoring and control. Full article

In this work, diamond/Si heterojunctions were fabricated by synthesizing a diamond layer directly on a monocrystalline n-type Si substrate. The diamond layers were characterized using micro-Raman spectroscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD). The current–voltage (I–V) characteristics of the heterojunctions were measured at room temperature. The heterojunctions exhibited rectifying behavior, confirming their diode-like nature. Based on thermionic emission theory, key electrical parameters of the heterojunction diodes—including the ideality factor (n) and carrier mobility (μ)—were estimated from the I–V characteristics. The I–V curves revealed large ideality factors ranging from 1.5 to 6.5, indicating the presence of deep trap states with densities between 2 × 10¹⁵ and 8 × 10¹⁶ eV⁻¹·cm⁻³. These variations were attributed to differences in the structural quality of the diamond layers and the effects of surface hydrogen termination. Full article

Background: currently, there is a growing trend toward multifunctional cosmetics, which combine several active ingredients in a single product to enhance efficacy and user convenience. As ingredients may influence one another, it is important to study the behavior of mixing multiple compounds in complex formulations, especially regarding their interaction with the skin. Piceatannol, for instance, is a naturally occurring stilbene recognized for its in vitro potent antioxidant, anti-inflammatory, and anti-aging activities, making it a promising candidate for dermocosmetic use in suncare. But despite its beneficial biological activities, its cutaneous permeation remains poorly understood, particularly when delivered from complex formulations containing multiple ingredients. Objectives: in this sense, this study aimed to evaluate the in vitro skin diffusion profile of piceatannol from a passion fruit seed extract (P_ext) incorporated into a topical base (B_em) or an organic sunscreen emulsion (O_em), with or without a spilanthol-rich Acmella oleracea extract (J_ext) used as a natural permeation enhancer. Methods: due to ethical and variability issues with human and animal skins, the Strat-M™ synthetic membrane was chosen as a standardized model for the in vitro skin permeation assays. Piceatannol localization within membrane layers was examined by confocal Raman microscopy (CRM), while compound identification in donor and receptor compartments was performed via UHPLC-DAD. Results: piceatannol from B_em was detected up to 140 µm from the Strat-M™ surface and exceeded 180 µm in depth when J_ext and organic sunscreens were included in the formulation. Notably, formulations containing J_ext and those based on O_em promoted enhanced accumulation in both the stratum corneum and deeper skin layers, suggesting an improved delivery potential in lipid-rich vehicles. Conclusions: even though some instability issues were observed, piceatannol penetration into Strat-M™ from the proposed formulations was confirmed, and the results provide a foundation for further research on its topical delivery, supporting the rational development of formulations capable of harnessing its demonstrated biological properties. Full article

This work examines the effect of gadolinium (Gd) promotion on nickel-based SBA-16 catalysts for the dry reforming of methane (DRM), with the goal of improving syngas production by optimizing catalyst composition and operating conditions. Catalysts with varying Gd loadings (0.5–3 wt.%) were synthesised using co-impregnation. XRD, N₂ physisorption, FTIR, XPS, and H₂-TPR–CO₂-TPD–H₂-TPR were used to examine the structural features, textural properties, surface composition, and redox behaviour of the catalysts. XPS indicated formation of enhanced metal–support interactions, while initial and post-treatment H₂–TPR analyses showed that moderate Gd loadings (1–2 wt.%) maintained a balanced distribution of reducible Ni species. The catalysts were tested for DRM performance at 800 °C and a gas hourly space velocity (GHSV) of 42,000 mL g⁻¹ h⁻¹. 1–2 wt.% Gd-promoted catalysts achieved the highest H₂ (~67%) and CO yield (~76%). Response surface methodology (RSM) was used to identify optimal reaction conditions for maximum H₂ yield. RSM predicted 848.9 °C temperature, 31,283 mL g⁻¹ h⁻¹ GHSV, and a CH₄/CO₂ ratio of 0.61 as optimal, predicting a H₂ yield of 96.64%, which closely matched the experimental value of H₂ yield (96.66%). The 5Ni–2Gd/SBA-16 catalyst exhibited minimal coke deposition, primarily of a graphitic character, as evidenced by TGA–DSC and Raman analyses. These results demonstrate the synergy between catalyst design and process optimization in maximizing DRM efficiency. Full article