Search Results (22,047)

Background: Menthol is a naturally occurring volatile terpene alcohol, widely used in food, pharmaceutical, and tobacco products; however, its high volatility leads to significant flavor loss during storage and handling. Methods: Herein, bimodal mesoporous silica materials (BMMs) were employed as carriers to encapsulate menthol, the loading and release behaviors were systematically compared using normal-temperature and alcohol-thermal loading methods. Results: Comprehensive characterizations (XRD and SAXS patterns, FT-IR spectra, SEM images, and N₂-sorption isotherms) confirmed that menthol incorporation did not disrupt the hierarchical mesoporous channels of BMMs. The alcohol-thermal loading method achieved a superior menthol loading capacity of 87%, significantly outperforming the normal-temperature loading (58%). Release performances revealed a transition in the dominant release mechanism, from diffusion-controlled behavior at low loading levels to concentration gradient-driven desorption at high loadings. Molecular dynamics simulations further demonstrated that alcohol-thermal loading enabled faster molecular diffusion and a more uniform distribution of menthol within the mesopores due to weaker interfacial interactions, whereas normal-temperature loading induced localized multilayer adsorption, resulting in mesopore blockage and hindered diffusion. In addition, long-term atmospheric release tests assessed sustained menthol retention over 30 days. Conclusions: Overall, this work establishes alcohol-thermal loading as an effective approach for regulating adsorption and release in mesoporous carriers, providing a foundation for developing volatile compound encapsulation strategies. Full article

The development of efficient and biocompatible sorbent nanomaterials for cesium removal is critical for environmental and biomedical decontamination. Here, hybrid composites based on ultra-small Prussian blue or Zn Prussian blue-type nanoparticles confined within porous chitosan beads are proposed for Cs⁺ extraction. Nanoparticle confinement ensures homogeneous dispersion and improved accessibility of ion-exchange sites, while preserving the porous polymeric network, as confirmed by physicochemical characterization. Cs⁺ adsorption was investigated under neutral and acidic conditions (pH 7.2 and 1.2), at concentrations of 0–9 mmol/L and contact times of 0–50 h, showing efficient uptake and favorable kinetics, with confirmed stability in simulated gastric fluid. In vivo performance was assessed in a mouse model of cesium contamination (70 mg Cs⁺/kg). Treatment with nanocomposites (225 mg/kg) was compared to bulk Prussian blue (75 mg/kg), revealing enhanced detoxification efficiency. Histological analysis of liver, spleen, and kidney tissues showed no detectable structural damage, consistent with unchanged systemic biomarkers. Overall, the proposed chitosan-confined Prussian blue-type nanocomposites combine high Cs⁺ removal efficiency, kinetic accessibility, and in vivo safety, highlighting their potential for decorporation applications. Full article

This communication discusses the problem of depositing equiatomic metal alloy films. It is shown that this problem can be solved using a magnetron equipped with a target constructed using a new “multilayer target” paradigm. This target, sputtered in an argon environment, consists of several parallel metal plates mounted on the magnetron axis. A method based on the equality of the sputtered fluxes generated by the plates is proposed for calculating the geometric dimensions of the plates. This equality leads to a system of algebraic equations, which are proposed to be solved under the assumption of a uniform discharge current density distribution in the sputtering region of the target. The communication describes two types of targets in which the plates have slots of different shapes. In one case, the slots are shaped as sectors of a ring with a given angle. In the other, the plates are shaped as rings. As examples, the geometric dimensions of targets for a balanced magnetron system intended for the deposition of films of equiatomic Ti_0.33Ta_0.33Nb_0.33 and Ti_0.25Ta_0.25Nb_0.25Mo_0.25 alloys are calculated. The presentation is accompanied by the results of individual experiments. This report is preliminary in nature; experimental verification is ongoing. The application of the new paradigm in magnetron target design facilitates the fabrication of films of nanostructured medium- and high-entropy alloys with specified chemical compositions, which is the central theme of the Special Issue devoted to functional nanomaterials. Full article

The search for harmless alternative solutions to protect crops has become urgent and has recently attracted widespread attention from researchers around the world focusing on natural polyphenols, which represent a treasure chest of molecules with potent activities. Due to the low water solubility of polyphenols, microemulsions were selected as nanovectors. Curcumin and mangiferin solubility in different excipients was evaluated by HPLC. Microemulsion was developed using pseudo-ternary phase diagrams. Sizes and polydispersity of microemulsion globules were evaluated by dynamic light scattering. Activity against Fusarium verticillioides was evaluated by a microdilution method. Vitamin E acetate was selected as the oily phase, Transcutol P as cosurfactant and Tween 80 as surfactant. S_mix was composed of Transcutol P and Tween 80 in a 1:2 gravimetric ratio and combined with oil-phase vitamin E acetate at a weight ratio of 3:1. Microemulsions were loaded with 5 mg/mL of each polyphenol and recovery results were 99.5% and 99.3% for curcumin and mangiferin, respectively. Sizes of the lipid phase were 121.7 ± 29.2 nm and 172.6 ± 19.3 nm, respectively, for mangiferin and curcumin microemulsions. F. verticillioides was very susceptible to both microemulsions with a very high activity at a dose of 0.9 mg/mL (log-4 reduction), evidencing a possible use of these nanoformulations to protect crops from F. verticillioides. Full article

Herein, we describe a versatile synthetic strategy for constructing Prussian Blue (PB)-coated polymeric nanocapsules (PB@nanocapsules) with tunable sizes and controlled PB loading. A soft template was first formed from a miniemulsion composed of water/chloroform/hexadecane (94.55:5:0.2, w/w/w), using P4VP₈₂-b-PDMAA₁₈₀ as a stabilizer and varying amounts of P4VP homopolymer as a hydrophobe and additional reactive site provider. Crosslinked nanocapsules were obtained by adding 1,2-bis-(2-iodoethoxy)ethane (BIEE) as a crosslinker. The resulting nanocapsules exhibited average hydrodynamic diameters ranging from approximately 282 nm (without P4VP homopolymer) down to 58 nm (with 0.01 g P4VP homopolymer), as determined by DLS and TEM. Subsequently, sequential coordination with sodium pentacyanoammine -ferroate(II) hydrate (Na₃ [Fe(CN)₅NH₃]), followed by the addition of FeCl₃, yielded a uniform PB coating, as confirmed by the appearance of a characteristic absorption peak at 780 nm in the UV–Vis spectra and a CN stretching shift from 2060 to 2070 cm⁻¹ in FT-IR. TEM and HAADF-STEM with EDX mapping revealed the homogeneous distribution of Fe across the nanocapsule shells. The PB loading could be further controlled by varying the Fe³⁺ addition (5.0 × 10⁻³–4.5 × 10⁻² mmol), with higher loading improving thermal stability. This rational design provides a robust and generalizable platform for engineering polymer–inorganic hybrid nanostructures with tailored functionalities. Full article

Crystalline silicon solar cells have long dominated the global photovoltaic market due to their mature manufacturing processes, excellent stability, and abundant raw material reserves, accounting for over 90% of the total PV market share. However, single−junction c−Si solar cells are approaching the Shockley–Queisser (SQ) efficiency limit of ~29.4%, creating an urgent need for next−generation PV technologies to achieve higher power conversion efficiency (PCE). Monolithic perovskite/silicon tandem solar cells (PSTSCs) stand as the most commercially promising technology to surpass the single−junction efficiency limit. Since their first demonstration in 2015, PSTSCs have experienced rapid technological advancement, with the certified PCE reaching 35.0% in 2026. This review posits that their rapid efficiency ascent is not serendipitous but driven by synergistic innovations across critical subsystems. We systematically deconstruct these efficiency drivers, encompassing top−cell materials, bottom−cell architecture, and optical management. We conclude by outlining future research frontiers essential for transforming this lab−champion technology into a mainstream energy solution. Full article

Carbon nanotube (CNT) materials exhibit ultrahigh electrical and thermal conductivity. Upon electrical excitation, CNT-based transparent conductive films (TCFs) can emit far-infrared radiation (FIR) and provide certain physiotherapeutic efficacy, making them ideal candidates for thermotherapy applications. This work systematically tests and analyzes the fundamental physical properties and physiotherapeutic performance of CNT flexible thin-film heaters (TFHs) for potential use in health physiotherapy. Two types of TFHs with different electrode connection modes were fabricated via the prepared TCFs. Experimental characterizations were conducted on their response time, electrothermal performance, and heat transfer characteristics. The results showed that the temperature rise per unit input power for TFH1 was 16.71 °C/W, while that of TFH2 was 4.29 °C/W at the same voltage of 10 V. In addition, the variation trends of maximum temperature with power density were highly consistent for the two films. This demonstrates that TFHs fabricated using the same TCFs exhibit excellent and high electrothermal conversion efficiency as well as outstanding comprehensive electrothermal performance. In addition, smaller L/W ratio leads to lower resistance of TFHs, resulting in a stronger thermal effect under identical applied voltage. After the temperature stabilized, the surface temperature of the TFHs decreased by approximately 5 °C when attached to the human arm, confirming that the heat generated by the TFHs under electrical excitation could be effectively absorbed by the human body. The TFHs emitted rapid FIR upon electrification, and the peak wavelength ranged from 8 to 12 µm, which fell within the range of 6–14 µm that was easily absorbable by the human body. The heat can be rapidly absorbed by the skin and distributed throughout the body via blood circulation, yielding favorable physiotherapeutic efficacy. This study provides key physical parameters for the application of TFHs in wearable medical devices and physiotherapy equipment. Full article

This work reports on the synthesis and electrochemical investigation of sustainable carbon–TiO₂ nanocomposites derived from marine biowaste, designed to elucidate light-assisted charge storage mechanisms in non-aqueous electrolytes. Porous carbons obtained from prawn chitin and blue shark gelatin were decorated in situ with TiO₂ nanoparticles using a deep eutectic solvent (DES) as a green synthesis medium. Structural and morphological characterisation revealed that TiO₂ incorporation induces significant nanoscale reorganisation of the carbon framework, resulting in hierarchical porosity, increased surface area, and intimate semiconductor–carbon interfaces. Electrochemical evaluation in a three-electrode configuration using an ethaline-based DES electrolyte demonstrated that TiO₂ decoration substantially enhances capacitive performance and cycling stability, with the prawn chitin-derived composite achieving a specific capacitance of 54 ± 3 F g⁻¹ and 91% retention after 10,000 cycles. Under illumination, all TiO₂-containing composites exhibited a pronounced increase in anodic current response and discharge time, indicating photo-assisted surface charge accumulation. Although the absolute capacitance values are modest compared to those of aqueous supercapacitor systems, the results provide mechanistic insight into the interplay among nanostructure, semiconductor photoactivity, and ion transport in viscous, hydrogen-bonded DES electrolytes. By combining waste-derived carbons, green synthesis routes, and photo-responsive nanostructures, this study highlights a sustainable strategy for developing multifunctional carbon-based nanomaterials with light-modulated electrochemical behaviour. Full article

This report presents a novel protocol for the recovery and utilization of recycled manganese oxide from used batteries through hydrothermal (HT) treatment. The recovered and treated material showed high activity towards rutin electro-oxidation (RT) on a screen-printed carbon electrode (SPCE) modified with recovered and treated MnO₂ within a hydrothermal reactor. Material characterization using scanning electron microscopy (SEM) and density distribution and particle size analysis revealed a more homogeneous and less dispersed particle size compared to the untreated material. This treatment increased the electroactive activity of the anodic current for RT by more than 70% compared to the SPCE without MnO₂ treated with HT. The electroanalytical application of this new electrode enabled the detection of RT, with a detection limit of 0.03 µmol/L, and its application in natural samples such as coffee and flavored beverages. Full article

Bacterial infections can delay wound healing and represent serious medical problems both in the hospital and community settings, especially skin wound infections caused by Staphylococcus aureus. In this work, a gelatin hydrogel modified with photo-cross-linkable methacrylamide groups at 10% concentration (GelMA10%), enriched with titanium dioxide nanoparticles (TiO₂NPs), and loaded with Neomycin sulphate was developed with the aim to realize a tissue for wound care with improved mechanical and antimicrobial properties. TiO₂ nanocomposite GelMA films with two concentrations of TiO₂NPs were characterized to assess physicochemical, structural and mechanical properties by scanning electron microscopy equipped with an energy-dispersive X-ray spectrometer (SEM/EDX), micro-computed tomography (micro-CT) and X-ray photoelectron spectroscopy (XPS). TiO₂ nanocomposite GelMA films showed a more compact structure, reduced pore sizes and a higher compressive modulus at the increasing concentration of TiO₂NPs. They were able to absorb and retain water for a prolonged time; however, no significant differences in the swelling degree at the increasing concentration of TiO₂NPs were observed. In vitro drug release and antibacterial activity against Staphylococcus aureus of TiO₂ nanocomposite GelMA film enriched with higher concentrations of TiO₂NPs, identified as a suitable candidate for wound healing, were investigated. Both GelMA10% and TiO₂ nanocomposite GelMA films loaded with drug exhibited a strong antibacterial action, whereas GelMA10% containing only TiO₂NPs did not show any antimicrobial properties. Full article

In biological systems, DNA serves as the primary carrier of genetic information, and the stability of its structure is fundamental to cellular function. Metal ions and temperature are critical environmental factors that modulate DNA conformation and activity. However, the differential morphological effects of alkali, alkaline earth, and transition metal ions, especially when combined with thermal treatment, have not been systematically visualized and quantified. In this work, atomic force microscopy (AFM) was employed to investigate the effects of different metal ions (Na⁺, K⁺, Mg²⁺, Ca²⁺, Cu²⁺) and temperature on DNA structure. The results demonstrated that monovalent ions (Na⁺ and K⁺) neutralized the negative charges on the DNA backbone, thereby reducing intermolecular electrostatic repulsion and promoting DNA aggregation into dendritic structures. Divalent ions (Mg²⁺ and Ca²⁺) not only provided more effective charge screening but also formed ion bridges between DNA strands, leading to more compact and cross-linked networks. In contrast, Cu²⁺ ions directly coordinated with DNA bases, causing local structural distortion and strand scission. Elevated temperatures induced DNA melting, with distinct morphological transitions from extended double strands to condensed single-stranded globules observed at temperatures exceeding the melting point (T_m). These findings elucidate the mechanisms by which environmental factors govern DNA morphology, providing in-sights relevant to nanotechnology and molecular biology applications. Full article

Molecular on-surface photochemistry has emerged as a promising alternative to thermal activation for fabricating low-dimensional carbon-based nanomaterials, offering unique advantages such as non-thermal initiation and high chemoselectivity. Controlling the selectivity and efficiency of on-surface photoreactions remains challenging due to the complex interplay among molecular excitation pathways, substrate properties, and reaction conditions. This review briefly summarizes recent advances in light-driven on-surface synthesis under ultra-high-vacuum conditions. We focus on molecular photoexcitation pathways that can be probed by scanning tunneling microscopy and spectroscopy (STM and STS). Studies of light-driven reactions in three categories are overviewed, i.e., dehalogenative C-C coupling, [2+2] and [4+4] cycloadditions, and photoisomerization. Typical strategies for tuning reactivity are exemplified, including molecular pre-organization via self-assembly, surface passivation, and wavelength/polarization control. The summary of successful case studies may not only facilitate the fundamental understanding of on-surface photochemistry but also inspire the design of functional low-dimensional architectures and light-responsive molecular devices. Full article

Currently, single-modal tumor therapy has significant limitations, while multi-modal combination therapy can overcome this bottleneck and open up new pathways for enhancing the efficacy of tumor therapy. However, it is still difficult to design a functionalized nanocarrier that can simultaneously mediate multiple therapeutic approaches. To tackle this challenge, we developed a multifunctional nano-codelivery system with glucose oxidase (GOx) loaded inside iron-doped zeolitic imidazolate framework-8 (Fe/ZIF-8), abbreviated as GFZ. This system effectively integrates the synergy and complementarity between ferroptosis therapy and starvation therapy (STT). Herein, GFZ innovatively combines the pH sensitivity of the ZIF-8 skeleton with the EPR effect of nanoparticles to achieve on-demand triggered release, significantly improving the accuracy of tumor targeting. Furthermore, GOx-mediated STT effectively alleviates the insufficiency of endogenous H₂O₂ during the ferroptosis process, thereby enhancing and synergizing with ferroptosis therapy. Experiments demonstrated both in vitro and in vivo that GFZ activates antitumor cascade reactions, inhibits tumor recurrence and metastasis, and exhibits excellent biocompatibility. Consequently, given its remarkable potential, GFZ is poised to emerge as a new mode of nano-delivery platform. Full article

Here, we report a highly efficient and stable catalytic system based on monometallic oxides supported on HY zeolites for the catalytic oxidation of chlorobenzene (CB). Among the transition and rare-earth metal oxides screened, the 30Cu/HY catalyst demonstrates exceptional performance, achieving near 100% CB conversion at 300 °C (500 ppm CB, 10,000 h⁻¹) alongside outstanding 24 h continuous stability without deactivation. Quantitative Py-IR analysis reveals that this superior activity is fundamentally driven by extensive solid-state ion exchange, forming robust Lewis acid centers (Cu-Y structures) that synergize with zeolitic Brønsted acid sites to efficiently polarize and cleave C-Cl bonds. Through an integrated approach combining in situ DRIFTS, real-time mass spectrometry, TGA, and NLDFT pore size analysis, we elucidate that the exceptional deep-oxidation capability of Cu/HY continuously mineralizes carbonaceous intermediates. This property minimizes coke deposition (2.91 wt%) and preserves the hierarchical pore architecture, preventing the coverage of active sites and severe pore blockage by partially oxidized intermediates (such as phenolic, aldehydic, and quinonic species) and stable carbonate species responsible for the deactivation of other metal oxides. These insights provide a mechanistic framework for the rational design of robust, chlorine-resistant catalysts for the sustainable abatement of persistent organic pollutants. Full article

In this study, N-doped carbon dots (CDs) functionalized with L-carnitine-loaded β-cyclodextrin were synthesized with a hydrothermal method using two different Rhododendron spp. (R. luteum and R. ponticum) as carbon sources. The synthesized carbon dots (LC/β-CD@Rh.l/N-CD (CD₁) and LC/β-CD@Rh.p/N-CD (CD₂)) showed monodisperse distributions, with a size of 3–5 nm and a spherical structure. The stability of these biogenic CDs in water and their effects on marine ecosystems were investigated using A. salina larvae (nauplii). Biogenic CDs were exposed to varying concentrations of 5–100 μL for 24, 48, 72, and 96 h, and the LC₅₀ values were calculated as 12.858 µg/L for CD₁ and 21.058 µg/L for CD₂. Bactericidal and fungicidal activities of CDs at sublethal concentrations were observed to have similar effects. Likewise, antioxidant activities (SOD, CAT), oxidative stress markers (ROS, MDA), and DPPH radical scavenging activities were investigated; SOD, CAT, and MDA activities varied depending on the exposure time of the larvae. Additionally, CDs induced high ROS generation and DPPH radical scavenging activity in nauplii. In fluorescence microscopy and TEM micrographs, different structural abnormalities were detected in larvae depending on the concentration of CDs, such as various degrees of abdominal fractures and fragmentation, and limb loss. Full article