Search Results (203)

The response of titanium (Ti) thin films is closely related to their microstructure, which is extremely sensitive to the selected deposition parameters and geometrical configurations. The present study investigates the impact of geometrical factors on the growth of Ti thin films, focusing on how variations in growth geometry influence film microstructure, surface morphology, and corrosion resistance. Three Ti thin films were prepared using Glancing Angle Deposition (GLAD) in a custom-built DC reactive magnetron sputtering system. For the first sample, the target was positioned perpendicular to the substrate surface (α = 0°); for the second and third samples, the substrate holder was positioned at an angle of 85° regarding the target direction (α = 85°), incorporating a 180° azimuthal rotation for the last (to obtain a zigzag-like deposition). The thickness and morphological features of the thin films were investigated by SEM, while the surface morphology, specifically roughness, and crystallinity of the thin films were assessed by AFM and XRD, respectively. Continuous and alternating current techniques were used for electrochemical characterization of behavior in simulated body fluid. The obtained results show a clear tendency to an improvement in anticorrosion performances varying the nanoarchitecture of the films in comparison to the conventional-grown sample, with the inclined sample presenting a slight enhancement in corrosion resistance and the zigzag-grown sample having the best corrosion resistance properties of the three. Full article

Metal sulfides are promising anode candidates for sodium–ion batteries (SIBs) due to their high theoretical capacities. However, their practical application is limited by significant volume extension and sluggish Na⁺ diffusion during cycling, which lead to rapid capacity degradation and poor long-term stability. In this work, we report the rational design of a hollow triple-shelled high-entropy sulfide (NaFeZnCoNiMn)₉S₈, synthesized through sequential templating method under hydrothermal conditions. Transmission electron microscopy confirms its well-defined three-shelled architecture. The inter-shell voids effectively buffer Na⁺ insertion/desertion-induced volume extension, while the tailored high-entropy matrix enhances electronic conductivity and accelerates Na⁺ transport. This synergistic design yields outstanding performance, including a high initial Coulombic efficiency (ICE) of 94.1% at 0.1 A g⁻¹, low charge-transfer resistance (0.32~2.54 Ω), fast Na⁺ diffusion efficiency (10^−8.5–10^−10.5 cm² s⁻¹), and reversible capacity of 582.6 mAh g⁻¹ after 1600 cycles at 1 A g⁻¹ with 91.2% capacity retention. These results demonstrate the potential of high-entropy, multi-shelled architectures as a robust platform for next-generation durable SIB anodes. Full article

The paraventricular nucleus of the hypothalamus (PVN) regulates, among others, the stress response, sexual behavior, and energy metabolism through its magnocellular and parvocellular neurosecretory cells. Within the PVN, ensemble coordination occurs through the many long-range synaptic afferents, whose activity in time relies on retrograde neuromodulation by, e.g., endocannabinoids. However, the nanoarchitecture of endocannabinoid signaling in the PVN, especially during neuronal development, remains undescribed. By using single-cell RNA sequencing, in situ hybridization, and immunohistochemistry during fetal and postnatal development in mice, we present a spatiotemporal map of both the 2-arachidonoylglycerol (2-AG) and anandamide (AEA) signaling cassettes, with a focus on receptors and metabolic enzymes, in both molecularly defined neurons and astrocytes. We find type 1 cannabinoid receptors (Cnr1), but neither Cnr2 nor Gpr55, expressed in neurons of the PVN. Dagla and Daglb, which encode the enzymes synthesizing 2-AG, were found in all neuronal subtypes of the PVN, with a developmental switch from Daglb to Dagla. Mgll, which encodes an enzyme degrading 2-AG, was only found sporadically. Napepld and Faah, encoding enzymes that synthesize and degrade AEA, respectively, were sparsely expressed in neurons throughout development. Notably, astrocytes expressed Mgll and both Dagl isoforms. In contrast, mRNA for any of the three major cannabinoid-receptor subtypes could not be detected. Immunohistochemistry validated mRNA expression and suggested that endocannabinoid signaling is configured to modulate the activity of afferent inputs, rather than local neurocircuits, in the PVN. Full article

By combining density functional theory with the non-equilibrium Green’s function method, we conducted a first-principles investigation of spin-dependent transport properties in a molecular device featuring a dynamic covalent chemical bridge connected to zigzag graphene nanoribbon electrodes. The effects of spin-filtering and spin-rectifying on the I–V characteristics are revealed and explained for the proposed molecular device. Interestingly, our results demonstrate that all three devices exhibit significant single-spin-filtering behavior in parallel (P) magnetization and dual-spin-filtering effects in antiparallel (AP) configurations, achieving nearly 100% spin-filtering efficiency. At the same time, from the I–V curves, we find that there is a weak negative differential resistance effect. Moreover, a high rectifying ratio is found for spin-up electron transport in AP magnetization, which is explained by the transmission spectrum and local density of state. The fundamental mechanisms governing these phenomena have been elucidated through a systematic analysis of spin-resolved transmission spectra and spin-polarized electron transport pathways. These results extend the design principles of spin-controlled molecular electronics beyond graphene-based systems, offering a universal strategy for manipulating spin-polarized currents through dynamic covalent interfaces. The nearly ideal spin-filtering efficiency and tunable rectification suggest potential applications in energy-efficient spintronic logic gates and non-volatile memory devices, while the methodology provides a framework for optimizing spin-dependent transport in hybrid organic–inorganic nanoarchitectures. Our findings suggest that such systems are promising candidates for future spintronic applications. Full article

This study seeks to develop and implement a non-enzymatic fluorescent labeling for immunoassay and immunochromatographic assay (ICAs) targeting SARS-CoV-2, to meet the extensive interest and need for effective COVID-19 diagnosis. In this manuscript, we delineate the development, synthesis, and evaluation of a novel quinone polymer zinc hybrid nanoarchitecture, referred to as polymerized alizarin red–inorganic hybrid nanoarchitecture (PARIHN), which integrates an antibody for direct use in fluorescent immunoassays, offering enhanced sensitivity, reduced costs, and improved environmental sustainability. The designed nanoarchitecture can enhance the sensitivity of the immunoassay and enable rapid results without the complexities associated with enzymes, such as their low stability and high cost. At first, a chitosan–alizarin polymer was synthesized utilizing quinone–chitosan conjugation chemistry (QCCC). Then, the chitosan–alizarin polymer was embedded with the detection antibody using zinc ion, forming PARIHN, which was proven to be a stable label with the ability to enhance the assay stability and sensitivity of the immunoassay. PARIHN can react with phenylboronic acid (PBA) or boric acid through its alizarin content to produce fluorescence signals with an LOD of 15.9 and 2.6 pm for PBA and boric acid, respectively, which is the first use of a boric acid derivative in signal generation in the immunoassay. Furthermore, PARIHN demonstrated high practicality in detecting SARS-CoV-2 nucleoprotein in fluorescence (PBA and boric acid) systems with an LOD of 0.76 and 10.85 pm, respectively. Furthermore, owing to the high brightness of our PARIHN fluorogenic reaction, our labeling approach was extended to immunochromatographic assays for SARS-CoV-2 with high sensitivity down to 9.45 pg/mL. Full article

The rapid evolution of micro- and nano-architectures is revolutionizing biomedical engineering, particularly in the fields of therapeutic and diagnostic micromechanics. This review explores the recent innovations in micro- and nanostructured materials and their transformative impact on healthcare applications, ranging from drug delivery and tissue engineering to biosensing and diagnostics. Key advances in fabrication techniques, such as lithography, 3D printing, and self-assembly, have enabled unprecedented control over material properties and functionalities at microscopic scales. These engineered architectures offer enhanced precision in targeting and controlled release in drug delivery, foster cellular interactions in tissue engineering, and improve sensitivity and specificity in diagnostic devices. We examine critical design parameters, including biocompatibility, mechanical resilience, and scalability, which influence their clinical efficacy and long-term stability. This review also highlights the translational potential and current limitations in bringing these materials from the laboratory research to practical applications. By providing a comprehensive overview of the current trends, challenges, and future perspectives, this article aims to inform and inspire further development in micro- and nano-architectures that hold promise for advancing personalized and precision medicine. Full article

The fast development of portable electronics demands electrodes for supercapacitors that are compatible with miniaturized device applications. In this study, an orderly aligned coaxial bilayer nanotube array made of transition metal/transition metal oxides was adopted as a nanostructure-integrated electrode for applications as miniaturized micro-supercapacitors. Using Ni and NiO as our model materials, the corresponding Ni/NiO-CBNTA electrodes were fabricated using templated growth and post-thermal oxidation. The Ni shells served as parts of the 3D nano-architectured collector, providing a large specific surface area, and the pseudocapacitive NiO layers were directly attached and electrically connected to the collector without any additives. The vertical growth of orderly aligned Ni/NiO-CBNTAs successfully avoided the underutilization of capacitive nanomaterials and allowed the electrolyte to be fully accessed, which manifested full charge storage capabilities under the miniaturizing. It was demonstrated that Ni/NiO-CBNTAs can serve as miniaturized electrodes with an improved specific capacitance of 1125 F/g ≅ 3 A/g, which is comparable to that obtained in a massive load electrode prepared by the conventional slurry-coating technique. Full article

The conversion of carbon dioxide into fuels and fine chemicals is a highly desirable route for mitigating flue gas emissions. However, achieving selectivity toward olefins remains challenging and typically requires high temperatures and pressures. Herein, we address this challenge using 12 nm copper nanoparticles supported on FeOx micro-rods, which promote the selective hydrogenation of CO₂ to light olefins (C₂–C₄) under atmospheric pressure. This catalyst achieves up to 27% conversion and 52% selectivity toward C₂–C₄ olefins, along with the production of C₂–C₄ paraffins, C₅+ hydrocarbons (with all C₁₊ products totalling to up to about 75%), and methane, while suppressing CO formation to just 1% at 340 °C. The enhanced performance of the Cu/FeOx pre-catalyst is attributed to the efficient in situ generation of iron carbides (Fe₅C₂) in the presence of copper nanoparticles, as confirmed by ex situ XRD analysis. Copper facilitates the reduction of FeOx to form Fe₅C₂, a crucial intermediate for shifting the reaction equilibrium toward higher hydrocarbons. The hydrogenation of CO₂ to higher hydrocarbons proceeds through the reverse water–gas shift reaction coupled with Fischer–Tropsch synthesis. Full article

(1) Background: This review study will delve into the potential of chitosan nanoparticles (NPs) as adaptable carriers for targeted drug delivery in different therapeutic areas. Chitosan is a biopolymer derived from chitin that has attracted interest in drug delivery applications because of its high biocompatibility and biodegradability. (2) Methods: A comprehensive literature review was conducted by following a careful systematized protocol for searching databases like PubMed, Google Scholar and ScienceDirect. (3) Results: Chitosan NPs are good drug delivery vehicles, notably for cancer. Studies reveal that doxorubicin-loaded chitosan NPs dramatically enhance toxicity to tumor cells compared to free medicines, yielding tumor suppression rates of up to 60%. Researchers found that chemotherapeutics had an 85% encapsulation efficiency (EE), lowering systemic toxicity. Magnetic and pH-responsive chitosan NPs boost drug accumulation by 63% and apoptosis by 54%. Chitosan also boosts medication retention in the lungs by 2.3×, per pulmonary delivery trials. Chitosan NPs also boost ocular medication bioavailability by 3× and improve nasal absorption by 30%, crossing the blood–brain barrier. For bone regeneration, chitosan scaffolds enhance bone mineral density by 46%, facilitating osteogenesis and healing. (4) Conclusions: NPs made of chitosan provide a solid foundation for improving drug delivery systems; yet there are still issues with material variability, scalability, and meeting regulatory requirements that need fixing. Research into combination treatments, ways to increase their specificity, and ways to optimize these NPs offers promising prospects for the creation of novel therapeutic approaches with the potential to improve patient outcomes. Full article

The nano-architecture of titanium oxide is a key element of a wide range of applications, mainly optical and catalytic activities. Therefore, the current study focuses on engineering and designing three interesting nanostructures of titanium oxides: nanoplates, nanotubes, and nanoparticle-supported nanolayers. The nanoplates of titanium oxides were prepared and confirmed by TEM images, X-ray diffraction, and EDX analysis. These nanoplates have an anatase phase, with the distance across the corners in the range of 15 nm. These nanoplates were modified and developed through a rolling process with sodium doping to generate the Na-doped TiO₂ nanotubes. These nanotubes were observed by TEM images and X-ray diffraction. In addition, the doping process of titanium oxides with sodium was confirmed by EDX analysis. A novel nano-architecture of titanium oxide was designed by supporting titanium oxide nanoparticles over Zn/Al nanolayers. The optical properties and activity of titanium oxides with the different morphologies indicated that titanium oxides became a highly photo-active photocatalyst after conversion to nanotubes. This finding was observed through the reduction in the band gap energy to 2.7 eV. Additionally, after 37 min of exposure to UV light, the titanium oxide nanotubes totally broke down and transformed the green dye of NGB into carbon dioxide and water. Furthermore, the kinetic analysis verified that the green dyes’ degradation was expedited by the high activity of nanotubes. Ultimately, based on these findings, it was possible to design an efficient photocatalyst for water purification by converting nanoplates into nanotubes, doping titanium sites with sodium ions, and creating new active sites for titanium oxides through defect-induced super radical formation. Full article

The development of efficient electrocatalysts for the complete oxidation of ethylene glycol (EG) is crucial for enhancing the practicality of direct EG fuel cells (DEGFCs). However, significant challenges persist in developing highly active Pd-based catalytic electrodes. In this work, PdIrNi ternary telluride nanospheres (PdIrNiTe-MNSPs) with mesoporous morphology and an amorphous structure were successfully synthesized and applied in electrocatalytic EG oxidation reaction. Brunauer–Emmett–Teller analysis revealed typical mesoporous characteristics, with a surface area of 8.33 m²·g⁻¹ and a total pore volume of 0.055 cm³·g⁻¹, respectively. Transmission electron microscopy characterization showed that the outer layer of PdIrNiTe-MNSPs is entirely amorphous in structure. Electrochemical tests demonstrated that PdIrNiTe-MNSPs exhibit enhanced electrocatalytic specific activity (16.75 mA·cm⁻²) and mass activity (1372.22 mA·mg⁻¹) for EG oxidation reaction (EGOR), achieving 3.17 and 2.09 times higher than commercial Pd/C, which can be attributed to its unique nanoarchitecture and optimized electron configuration. In situ spectroscopy revealed that with the incorporation of IrNi, PdIrNiTe-MNSPs facilitate C-C bond cleavage of EG, achieving a higher selectivity (≈93%) in oxidizing EG to C1 products, while PdTe-MNSPs demonstrated higher selectivity for glycolic acid in EGOR. Taken together, this work provides new insights into the application of Pd-based telluride nanomaterials in electrocatalysis for EGOR. Full article

Photocatalysis has attracted more and more attention as a possible solution to environmental, water, and energy crises. Although some photocatalytic materials have already proven to perform well, there are still some problems that should be solved for the broad commercialization of photocatalysis-based technologies. Among them, cheap and easy recycling, as well as stability issues, should be addressed. Accordingly, the application of gels, either as a photocatalytic material or as its support, might be a good solution. In this review, various propositions of gel-based photocatalysts have been presented and discussed. Moreover, an easy nanoarchitecture design of gel-based structures enables fundamental studies, e.g., on mechanism clarifications. It might be concluded that gels with their unique properties, i.e., low density, high specific surface area, great porosity, and low-cost preparation, are highly prospective for solar-energy-based reactions, water treatment, photodynamic cancer therapies, and fundamental research. Full article

Advances in nanotechnology have made it possible to observe and evaluate structures down to the atomic and molecular level. The next step in the development of functional materials is to apply the knowledge of nanotechnology to materials sciences. This is the role of nanoarchitectonics, which is a concept of post-nanotechnology. Nanoarchitectonics is defined as a methodology to create functional materials using nanounits such as atoms, molecules, and nanomaterials as building blocks. Nanoarchitectonics is very general and is not limited to materials or applications, and thus nanoarchitecture is applied in many fields. In particular, in the evolution from nanotechnology to nanoarchitecture, it is useful to consider the contribution of nanoarchitecture in device applications. There may be a solution to the widely recognized problem of integrating top-down and bottom-up approaches in the design of functional systems. With this in mind, this review discusses examples of nanoarchitectonics in developments of advanced devices. Some recent examples are introduced through broadly dividing them into organic molecular nanoarchitectonics and inorganic materials nanoarchitectonics. Examples of organic molecular nanoarchitecture include a variety of control structural elements, such as π-conjugated structures, chemical structures of complex ligands, steric hindrance effects, molecular stacking, isomerization and color changes due to external stimuli, selective control of redox reactions, and doping control of organic semiconductors by electron transfer reactions. Supramolecular chemical processes such as association and intercalation of organic molecules are also important in controlling device properties. The nanoarchitectonics of inorganic materials often allows for control of size, dimension, and shape, and their associated physical properties can also be controlled. In addition, there are specific groups of materials that are suitable for practical use, such as nanoparticles and graphene. Therefore, nanoarchitecture of inorganic materials also has a more practical aspect. Based on these aspects, this review finally considers the future of materials nanoarchitectonics for further advanced devices. Full article

Researchers are developing innovative electrode materials with high energy and power densities worldwide for effectual energy storage systems. Transition metal dichalcogenides (TMDs) are arranged in two dimensions (2D) and have shown great promise as materials for photoelectrochemical activity and supercapacitor batteries. This study reports on the fabrication of WS₂@NiCoS and WS₂@NiCoS@ZnS hybrid nano-architectures through a simple hydrothermal approach. Because of the strong interfacial contact between the two materials, the resultant hierarchical hybrids have tunable porosity nanopetal decorated morphologies, rich exposed active edge sites, and high intrinsic activity. The specific capacities of the hybrid supercapacitors built using WS₂@NiCoS and WS₂@NiCoS@ZnS electrodes are 784.38 C g⁻¹ and 1211.58 C g⁻¹ or 2019.3 F g⁻¹, respectively, when performed at 2 A g⁻¹ using a three-electrode setup. Furthermore, an asymmetric device (WS₂@NiCoS@ZnS//AC) shows a high specific capacity of 190.5 C g⁻¹, an energy density of 49.47 Wh kg^−1, and a power density of 1212.30 W kg⁻¹. Regarding the photoelectrochemical activity, the WS₂@NiCoS@ZnS catalyst exhibits noteworthy characteristics. Our findings pave the way for further in-depth research into the use of composite materials doped with WS₂ as systematic energy-generating devices of the future. Full article

It is difficult for carbonaceous materials to combine a large specific surface area with flexibility. Here, a flexible all-carbon nanoarchitecture based on the in situ growth of nanoporous graphene within “skeletal-capillary” carbon nanotube (CNT) networks has been achieved by a chemical vapor deposition (CVD) process. Multi-path long-range conductivity is established, and the porous graphene provides a large specific surface area for charge storage. The flexibility of the films allows them to be directly used as binder-free electrodes for supercapacitors. Since the polymeric binders are saved, the supercapacitors exhibit a higher overall storage density. Full article