Search Results (2,216)

Perylene bisimide derivatives are typical n-type semiconductors as well as redox-active materials. However, it has been difficult to produce thin films by solution processes because of their low solubilities in organic solvents. Perylene bisimide derivatives bearing oligosiloxane moieties exhibit columnar phases over wide temperature ranges, including room temperature and high solubilities in organic solvents. The columnar phases are stabilized by nanosegregation between crystal-like one-dimensional π-stacks and liquid-like mantle consisting of oligosiloxane moieties. The electron mobility at room temperature exceeded 0.1 cm²V⁻¹s⁻¹ in the ordered columnar phases of perylene bisimide derivatives bearing four disiloxane chains. Uniaxially aligned thin films of the perylene bisimide derivatives bearing oligosiloxane moieties could be produced by a spin-coating method. The spin-coated films of the perylene bisimide derivatives bearing cyclotetrasiloxane rings could be insolubilized via in situ ring-opening polymerization by the exposure of the thin films to trifluoromethanesulfonic acid vapors. Uniaxially aligned thin films of perylene bisimide derivatives bearing an ethylene oxide chain as well as cyclotetrasiloxane rings could be doped in an aqueous solution of sodium dithionate, resulting in an anisotropic electrical conductivity. Polymerized thin films of perylene bisimide derivatives bearing a crown ether ring exhibited electrochromism in electrolyte solutions. These compounds formed 1:1 complexes with lithium triflate, exhibiting columnar phases at room temperature. The nanostructures of the complexes were stabilized by the electrostatic interaction between cationic crown-metal units and triflate anions. Full article

Background/Objectives: Oral diseases remain among the most prevalent noncommunicable conditions worldwide, with biofilm-driven dysbiosis playing a central role in dental caries, gingivitis, periodontitis, and oral candidiasis. Curcumin has attracted considerable interest because of its anti-inflammatory, antioxidant, antimicrobial, and regenerative properties. However, its clinical use remains limited by poor water solubility, chemical instability, rapid metabolism, and low bioavailability. This review aimed to provide a comprehensive analysis of curcumin-based nanoformulations for oral health applications, with emphasis on their mechanistic actions, antibiofilm activity, and translational relevance. Methods: This review examined representative nanocarrier systems developed for curcumin delivery in oral health. These included polymeric nanoparticles, nanomicelles and nanoemulsions, solid lipid nanoparticles and nanostructured lipid carriers, nanogels, hydrogels, mucoadhesive films, and metallic or hybrid nanosystems. The analysis focused on molecular mechanisms of action, antimicrobial and antibiofilm effects against major oral pathogens, and key translational challenges. Results/Findings: Across the reviewed studies, nanoformulations consistently improved curcumin solubility, stability, tissue penetration, mucosal retention, and controlled release. Mechanistically, they enhanced anti-inflammatory activity through inhibition of nuclear factor kappa B (NF-κB), strengthened antioxidant defenses via the nuclear factor erythroid 2-related factor 2/heme oxygenase-1 (Nrf2/HO-1) axis, supported tissue repair and osteogenic responses, disrupted oral biofilms, and modulated local immune responses. Antimicrobial activity was reported against Streptococcus mutans, Porphyromonas gingivalis, Aggregatibacter actinomycetemcomitans, and Candida albicans, with reduced exopolysaccharide production, impaired adhesion, and improved biofilm penetration. Conclusions: Curcumin-based nanoformulations represent promising adjunctive platforms for oral healthcare. However, their clinical translation still requires improved stability in the oral-environment standardized manufacturing and characterization, rigorous safety evaluation, and well-designed controlled clinical studies. Full article

Nanostructured calcium phosphate-based (CaP) biocomposites have proven to be ideal candidates for the creation of multifunctional systems with applications in biomedicine. This review presents a critical and integrative overview of recent advances in the synthesis of CaP nanocomposites with applications in bone tissue regeneration. An analysis of calcium phosphate-based nanocomposites is thus provided by correlating their composition, synthesis routes and biological properties, guiding the rational development of next-generation biomaterials for bone tissue engineering. The first section presents calcium phosphates, such as hydroxyapatite (HAp) or β-tricalcium phosphate (β-TCP), used in the preparation of nanocomposite materials. Next, the main biocomposite materials are analyzed as a result of the functionalization of calcium phosphates by metal ion substitutions or by the addition of polymers, bioglass or metal additives. Thus, biomaterials with excellent properties in applications such as tissue engineering have been obtained. The synergistic effect of materials in the composition of biocomposites favored the improvement of properties such as bioactivity, mechanical strength, antimicrobial activity, structure and porosity. Beyond classical osteoconductivity, CaP-based nanocomposites demonstrate a broad spectrum of biological activities like immunomodulatory effects, pro-healing signaling, anti-inflammatory pathways, antibacterial and antifungal mechanisms, and capabilities for precise drug delivery or theranostic applications. Full article

Antimicrobial resistance represents one of the most formidable global health crises of the 21st century, driven by the diminishing efficacy of conventional antibiotics due to bacterial adaptation and biofilm formation. In response, antimicrobial nanoformulations have emerged as a transformative therapeutic paradigm, offering multifaceted and innovative mechanisms to combat resistant pathogens. This comprehensive review delineates the broad scope and distinct novelty of nano-enabled antimicrobial strategies, moving beyond the single-target limitations of traditional drugs. We systematically explore the diverse architectural classes of nanoformulations—including metallic, polymeric, and self-assembling nanostructures—and elucidate their unique mechanistic actions. These encompass (1) physical disruption of microbial membranes via electrostatic interactions; (2) catalytic generation of reactive oxygen and nitrogen species to induce an ‘oxidative storm’; (3) intracellular sabotage of essential metabolic pathways; (4) the ‘Trojan horse’ strategy for enhanced drug delivery and bioavailability; (5) efflux pump bypass to counteract a major resistance mechanism; (6) penetration and eradication of resilient biofilms; and (7) disarming pathogens through quorum sensing and virulence inhibition. Furthermore, this review highlights the immunomodulatory potential of nanoformulations; their activity beyond bacteria against fungi, viruses, and parasites; and the critical role of the nano-bio interface defined by surface physicochemistry. We also address the translational pathway, considering challenges in nanotoxicology, scalability, and regulatory approval, alongside the ecological impact and economic horizon of these technologies. This sector is projected to reach USD 5.4 to 8.96 billion by 2033 to 2034, with compound annual growth rates of 11 to 21% across antimicrobial nanomaterials, nanocoatings, and nanomedicine applications. By integrating insights from computational modeling and in silico design, this review underscores how nanoformulations leverage synergistic, multi-target approaches to overcome resistance, enhance therapeutic efficacy, and represent a significant leap forward in the future of infectious disease management. The novelty lies in the holistic and mechanistic synthesis of how nanotechnology is redefining antimicrobial warfare, offering a promising arsenal to avert a post-antibiotic era. Full article

The oxygen evolution reaction (OER), a key half-reaction in electrochemical water splitting, is limited by sluggish multi-electron transfer kinetics, starting extensive research into efficient, low-cost nanoscale electrocatalysts, particularly those based on nickel, cobalt, and iron, as well as mixed-metal, hybrid, and heteroatom-doped carbon-based metal-free systems, as presented here. Ni- and Co-based electrocatalysts show high efficiency for alkaline OER due to optimized nanostructures, surface modifications, heterostructure design, and multi-metal doping, which enhance activity, stability, and electronic properties. Their performance relies on precise atomic-level control of structure and synergistic interactions, enabling them to approach or rival noble-metal catalysts. Iron-based electrocatalysts are also promising due to their abundance, low cost, and flexible redox chemistry, forming active iron oxyhydroxide species during operation; however, their low conductivity requires structural and electronic optimization. Beyond Fe, Ni, and Co, copper-based compounds, zeolitic imidazolate framework-derived structures, and manganese phosphide–cerium oxide composites offer enhanced oxygen vacancies, tunable structures, and strong interfacial synergy. Furthermore, heteroatom-doped carbon materials incorporating nitrogen, phosphorus, or sulfur improve catalytic activity by modifying electronic structure, creating active sites, and enhancing charge transfer. Overall, careful control of composition, structure, and electronic properties enables the development of efficient, durable, and scalable noble-metal-free catalysts for OER. Full article

Organic dye-, pharmaceutical-, and heavy metal-contaminated water are emerging environmental issues, and thus there is a requirement for the development of efficient and sustainable purification methods. Semiconductor (SmC) material-based photocatalysis using TiO₂ and Fe₂O₃ nanostructures is considered a promising field for pollutant degradation due to its chemical stability, nontoxicity, and ability to perform photocatalytic degradation using light irradiation. Understanding the thermal, optical, and charge transport properties governing their photocatalytic activity requires advanced characterisation methods. In this context, photothermal (PT) techniques provide powerful tools for probing non-radiative processes and energy transport in photocatalytic materials. The photocatalytic activity of these materials strongly depends on their structural, optical, thermal, and electronic properties. These properties can be enhanced through several modification strategies, including metal and non-metal doping (e.g., C, N, Cu, Ag, Au), surface modification, forming a complex with SiO₂, and the formation of Fe₂O₃–TiO₂ heterostructure nanocomposites. In this review, a comprehensive overview is provided of TiO₂ and Fe₂O₃-based nanocomposites with a specific focus on characterisation techniques for photothermal characterisation techniques, including thermal lens spectroscopy (TLS), beam deflection spectrometry (BDS), and photoacoustic spectroscopy (PAS), for determining thermal diffusivity, thermal conductivity, bandgap energy, carrier lifetime, surface roughness, porosity, etc., which are related to photocatalytic activity. The properties of these nanocomposites are correlated with photocatalytic activity for pollutant degradation using these nanocomposites. The challenges faced while using these nanocomposites for pollutant degradation are also discussed, along with future prospects for designing efficient photocatalysts for water purification applications. Full article

In this work, we demonstrate a functional and previously insufficiently explored route for converting cyclic olefin copolymer (COC) TOPAS^® thin films into antibacterial hybrid materials through a combination of solvent casting, plasma activation, noble-metal sputtering, and subsequent thermal or laser treatment. While COC is already well-known as a transparent, chemically resistant material for pharmaceutical and optical applications, its coupling with post-treated noble-metal nanostructures for antibacterial functionality has not been systematically described. The main contribution of this study lies in showing that COC can serve not only as a passive packaging substrate, but also as an active platform for the formation of biologically relevant surface nanostructures. Compared with previously reported metal/polymer systems, the present work provides clear evidence that noble-metal layers on COC undergo substantial structural evolution after thermal and excimer-laser treatment, resulting in regular nanoclustered morphologies. A particularly important finding is the detection of Au particle implantation below the COC surface during sputtering, as revealed by Rutherford backscattering spectrometry, which distinguishes this system from conventional surface-only metal coatings. Furthermore, we show that laser and thermal processing do not merely reshape the deposited layer, but significantly influence the final biological response of the material. Ag-based structures showed strong bactericidal behavior against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. The prepared samples were comprehensively characterized by AFM, DSC, RBS, SEM, and TGA, and their roughness and wettability were also evaluated, enabling direct correlation between physicochemical changes and antibacterial performance. These results introduce a new strategy for upgrading conventionally used pharmaceutical COC materials into multifunctional surfaces with added antibacterial value. Full article

Metal-enhanced fluorescence (MEF) has found widespread application in biomedical sensing and in vivo tissue imaging systems. To enhance MEF efficiency, it is necessary to optimize the interaction between the metal nanoparticle plasmon and the fluorophore molecule. The size and shape of the nanoparticle, the nanoscale gap between the fluorescent molecule and the nanoparticle, and the excitation wavelength are critical parameters. In this study, we propose a model for a more complete and accurate description of the processes of molecular excitation and generation of the fluorescence spectral response, introducing a new concept of effective properties for the field enhancement factor, quantum yield, and fluorescence enhancement factor. The influence of the spectral properties of both the nanostructure plasmon and the fluorophore molecule on the optimal tuning of fluorescent complexes is studied. Particular attention is paid to the analysis of the spectral properties of plasmon resonance and calculations of the near-field intensity enhancement of the plasmonic nanostructure’s excitation field. Numerical results for optimizing the MEF of fluorescent complexes based on TagRFP and gold (silver) nanorod composites are presented. The advantages of the proposed model for the optimal design of new nanomaterials with unique fluorescent properties are discussed. Full article

The objective of this work was to investigate the effect of a special activating component, under the ZB-3 brand, on the welding and technological properties of a welding electrode when incorporated into the coating of a rutile welding electrode. Pulsed radiation activation was used to produce the nanostructured activating component ZB-3. The results showed the beneficial effect of the electrode doped with ZB-3 on the formation of welding beads. At the same time, an improvement in the quality of weld formation is observed with a ZB-3 activator content of up to 8%. The qualities of the weld formation were significantly improved. Also, an increase in the breaking length of the electrode arc by more than 10% was established with a ZB-3 activator content of up to 2%, and the depth of penetration of the welded metal increased to 40%. Full article

Catalytic materials are central to the advancement of hydrogen generation technologies, playing a pivotal role in enabling sustainable, carbon-neutral energy systems. Hydrogen can be produced via electrochemical water splitting, thermochemical reforming, or photocatalysis—each imposing unique performance requirements on catalysts in terms of activity, selectivity, stability, and efficiency. While traditional noble metals (e.g., platinum, ruthenium, iridium) provide benchmark catalytic activity, their widespread use is hindered by scarcity, high cost, and limited long-term durability. Consequently, researchers have increasingly focused on earth-abundant alternatives such as transition metals (Ni, Co, Fe, Mo), alloys, metal oxides, carbides, sulfides, nitrides, and carbon-based systems. Among these, two-dimensional materials, particularly the MXene family, have attracted significant attention due to their metallic conductivity, layered structure, and tunable surface chemistry. These features enable rapid charge transfer and abundant active sites, making MXenes and related nanostructured catalysts promising for both the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) across a wide range of electrochemical conditions. Parallel efforts have integrated novel semiconductors, plasmonic nanomaterials, and hybrid heterostructures to improve the efficiency of solar-to-hydrogen energy conversion. This paper reviews the main types of catalytic materials used in hydrogen production, explains their design strategies and structure–performance relationships, and discusses key engineering challenges such as integrating renewable energy sources, scaling up manufacturing, and ensuring long-term durability in real-world systems. Future research goals are also highlighted, including the development of affordable non-noble catalysts, enhancing catalyst stability through surface and defect engineering, and coupling hydrogen production with circular economy principles, all of which are essential to making hydrogen generation more efficient, scalable, and cost-effective as the world transitions to clean and sustainable energy. Full article

Metal packaging materials remain fundamental across food, beverage, pharmaceutical, cosmetic, and technical sectors owing to their combination of mechanical robustness, total light and gas barrier performance, thermal resistance, and established recyclability. Aluminum alloys, tinplate, tin-free steel (TFS/ECCS), stainless steels, metal–matrix composites (MMCs), and metal–polymer or metal–paper laminates define distinct metal-based packaging architectures whose metallurgical and interfacial design governs forming behaviour, corrosion and migration pathways, coating integrity, and mechanical reliability. In this review, these architectures are examined from a materials- and systems-oriented perspective, linking composition, microstructure, processing routes, and surface engineering to functional performance across rigid, semi-rigid, and flexible formats. The analysis also considers the ongoing transition from bisphenol A (BPA)-based epoxy linings to BPA-free and hybrid coating chemistries, the use of nano-structured metallic and metal-oxide surfaces, and the role of composite laminates in which thin metallic foils are combined with polymeric or paper-based structural layers. These material and architectural aspects are discussed together with safety, regulatory, and circularity considerations that increasingly influence the design and selection of metal-based packaging. Ion migration, coating degradation, and corrosion under realistic storage environments are considered in relation to EU, FDA, ISO, and sector-specific requirements, while attention is also paid to the contrast between well-established closed-loop recycling infrastructures for aluminum and steel and the more complex end-of-life management of coated metals and multilayer laminates. The review provides a unified framework connecting materials selection, metallurgical design, processing, performance, regulatory compliance, and sustainability in metal-based packaging systems. Applications spanning consumer goods, pharmaceuticals, cosmetics, and advanced electronics are integrated to support an overall understanding of how metallic and hybrid metal-based architectures underpin functional reliability and life-cycle sustainability. Full article

Nanostructured metallic materials are widely applied in various fields due to their excellent comprehensive properties. Enhancing mechanical properties through microstructure design has emerged as a novel strengthening strategy. In this contribution, the microscopic mechanical behavior of coarse-grained and gradient-structured nanocrystalline NiCoAl alloys during tensile deformation was investigated via molecular dynamics simulations. Based on the investigation of compositional effects, the Ni₆₀Co₃₀Al₁₀ alloy composition was selected, exhibiting a yield strength of 4.92 GPa. The results indicate that increasing Al content reduces the material’s strength, Young’s modulus, and work hardening effect. Furthermore, by introducing a gradient structure with grain sizes gradually varying from 1.8 nm to 6.5 nm into the alloy, the yield strength reaches 1.8 GPa and the flow stress reaches 3.35 GPa, demonstrating a significant improvement compared to the uniform coarse-grained structure. Upon introducing the gradient structure into the alloy, it was observed that geometrically necessary dislocations (GNDs) nucleate in the coarse-grained region during deformation and gradually extend towards the fine-grained region. The increased grain boundary density effectively impedes dislocation motion and enhances dislocation pinning capability, thereby inducing continuous strain hardening and improving plasticity. By promoting the accumulation and interaction of grain boundary dislocations, the gradient structure achieves further strengthening and strain hardening in the alloy, providing a theoretical basis and simulation foundation for designing high-performance advanced alloys. Full article

Hollow nanostructures have emerged as a pivotal class of nanomaterials in electrocatalysis, offering intrinsic advantages such as high surface-to-volume ratios, reduced density, and economical utilization of precious metals. However, the prevailing research paradigm has predominantly focused on the external shell characteristics while overlooking the decisive role of the interior cavity microenvironment. This review introduces a novel conceptual framework that positions the rational engineering of the cavity microenvironment—encompassing mass transport dynamics, localized electronic structure modulation, active site exposure, and structural stability—as a unified design principle for next-generation electrocatalysts. We systematically elucidate how precise control over cavity geometry, composition, and interfacial properties can optimize electrocatalytic performance for oxygen reduction (ORR), oxygen evolution (OER), and hydrogen evolution (HER) reactions. By correlating microenvironmental parameters with catalytic metrics, we establish structure–property–performance relationships and highlight recent breakthroughs. Finally, we outline future challenges in achieving atomic-level precision in cavity design, understanding dynamic evolution under operating conditions, and scaling up synthesis for industrial applications. Full article

Phase-change materials (PCMs) are capable of storing or releasing a substantial amount of thermal energy within a small volume through the latent heat of fusion during phase transitions of melting and solidification, i.e., from solid to liquid or vice versa, in a near isothermal process. However, commonly used organic PCMs, such as paraffin wax, exhibit very low thermal conductivity, contributing to an adverse increase in overall thermal resistance and, thus, a slow thermal response. This limitation often becomes a bottleneck for the system from a thermal performance standpoint. To mitigate this issue, the present work explores the fabrication of heat sinks incorporating nano-structured graphitic foams, including carbon foam (CF) and expanded graphite (EG), as well as micro-structured metal foams such as open-cell copper foam (OCCF), all impregnated with a paraffin-based PCM with a melting temperature near 37 °C. This study focuses on applying passive thermal management strategies to design efficient heat sinks capable of maintaining the temperatures of battery modules and electronic circuits within an acceptable thermal safety threshold for small satellites and spacecrafts, exemplified by the OPTIMUS and Pumpkin battery modules designed for CubeSats with a nominal cross-sectional area of almost 4″ × 4″. Temperature responses and average overall thermal resistances for fabricated heat sinks are accordingly assessed and compared in a vacuum chamber to simulate space conditions. Furthermore, the impact of operating pressure on the thermal performances of various heat sinks will be investigated by executing the same tests in both atmospheric and vacuum conditions. The findings demonstrate a superior thermal performance of composite heat sinks integrating carbon foam and copper foam into the paraffin PCM compared to the baseline PCM heat sink under both vacuum and atmospheric operating pressure conditions. Full article