Search Results (124)

Due to its persistence and potential negative effects on ecosystems and human health, microplastic pollution in aquatic environments has become a major worldwide concern. Photocatalytic degradation is a sustainable manner to degrade microplastics to non-toxic by-products. In this review, comprehensive discussion focuses on the synergistic effects of various photocatalytic materials including TiO₂, ZnO, WO₃, graphene oxide, and metal–organic frameworks for producing heterojunctions and involving multidimensional nanostructures. Such mechanisms can include the generation of reactive oxygen species and polymer chain scission, which can lead to microplastic breakdown and mineralization. The advancements of material modifications in the (nano)structure of photocatalysts, doping, and heterojunction formation methods to promote UV and visible light-driven photocatalytic activity is discussed in this paper. Reactor designs, operational parameters, and scalability for practical applications are also reviewed. Photocatalytic systems have shown a lot of development but are hampered by shortcomings which include a lack of complete mineralization and production of intermediary secondary products; variability in performance due to the fluctuation in the intensity of solar light, limited UV light, and environmental conditions such as weather and the diurnal cycle. Future research involving multifunctional, environmentally benign photocatalytic techniques—e.g., doped composites or composite-based catalysts that involve adsorption, photocatalysis, and magnetic retrieval—are proposed to focus on the mechanism of utilizing light effectively and the environmental safety, which are necessary for successful operational and industrial-scale remediation. Full article

In this study, we investigate the optical and structural properties of Cu-doped β-Ga₂O₃ nanostructures synthesized via a hydrothermal method, followed by annealing in ambient O₂. Different Cu doping concentrations (0, 1.6, and 4.8 at.%) are introduced to examine their effects on the crystal structure, chemical state, and optical bandgap of β-Ga₂O₃. X-ray diffraction (XRD) analysis reveals that the host β-Ga₂O₃ crystal structure is preserved at lower doping levels, whereas secondary phases (Ga₂CuO₄) appear at higher doping concentrations (4.8 at.%). X-ray photoelectron spectroscopy (XPS) confirms the presence of Cu²⁺ ions in both lattice substitution sites and surface-adsorbed hydroxylated species (Cu(OH)₂). The optical bandgap of β-Ga₂O₃ is found to decrease with increasing Cu concentration, likely due to the formation of localized states or secondary phases. These findings demonstrate the tunability of the optical properties of β-Ga₂O₃ via Cu doping, providing insights into the incorporation mechanisms and their impact on structural and electronic properties. Full article

Volatile organic compound (VOC) emissions have become a critical environmental concern due to their contributions to photochemical smog formation, secondary organic aerosol generation, and adverse human health impacts in the context of accelerated industrialization and urbanization. Catalytic oxidation over perovskite-type catalysts is an attractive technological approach for efficient VOC abatement. This review systematically evaluates the advancements in perovskite-based catalysts for VOC oxidation, focusing on their crystal structure–activity relationships, electronic properties, synthetic methodologies, and nanostructure engineering. Emphasis is placed on metal ion doping strategies and supported catalyst configurations, which have been demonstrated to optimize catalytic performance through synergistic effects. The applications of perovskite catalysts in diverse oxidation systems, including photocatalysis, thermal catalysis, electrocatalysis, and plasma-assisted catalysis, are comprehensively discussed with critical analysis of their respective advantages and limitations. It summarizes the existing challenges, such as catalyst deactivation caused by carbon deposition, sulfur/chlorine poisoning, and thermal sintering, as well as issues like low energy utilization efficiency and the generation of secondary pollutants. By consolidating current knowledge and highlighting future research directions, this review provides a solid foundation for the rational design of next-generation perovskite catalysts for sustainable VOC management. Full article

Molecular network conformations in the over-stoichiometric arsenoselenides of canonical As_xSe_100−x system (40 ≤ x ≤ 100) covering a full row of thioarsenide-type As₄Se_n entities (0 ≤ n ≤ 6) are analyzed with ab initio quantum-chemical modeling employing cluster-simulation code CINCA. Native (melt-quenching-derived) and nanostructurization-driven (activated by nanomilling) polymorphic and polyamorphic transitions initiated by decomposition of the thioarsenide-type As₄Se_n cage molecules and incorporation of their remnants into a newly polymerized arsenoselenide network are identified on the developed map of molecular network clustering in a binary As-Se system. Within this map, compositional counter lines corresponding to preferential molecular or network-forming tendencies in the examined arsenoselenides are determined, explaining that network-crystalline conformations prevail in the boundary compositions corresponding to n = 6 and n = 0, while molecular-crystalline ones dominate inside the rows corresponding to n = 4 and n = 3. A set of primary and secondary equilibrium lines is introduced in the developed clustering map to account for inter-phase equilibria between the most favorable (regular) and competitive (irregular) thioarsenide phases. Straightforward interpretation of decomposition reactions accompanying induced crystallization and amorphization (reamorphization) in the arsenoselenides is achieved, employing disproportionality analysis of thioarsenide-type molecular network conformations within the reconstructed clustering map. The preference of network clustering at the boundaries of the As₄Se_n row (at n = 6 and n = 0) disturbs inter-phase equilibria inside this row, leading to unexpected anomalies, such as absence of stable tetra-arsenic triselenide As₄Se₅ molecular-crystalline species; polyamorphism in mechanoactivated As₄Se_n alloys (2 ≤ n ≤ 6); breakdown in the glass-forming ability of melt-quenching-derived arsenoselenides in the vicinity of tetra-arsenic biselenide As₄Se₂ composition; plastically and normally crystalline polymorphism in tetra-arsenic triselenide As₄Se₃-based thioarsenides, and so on. Full article

Janus nanorods are a special class of nanorods composed of two distinct surface regions, one hydrophilic and one hydrophobic. This amphiphilic characteristic makes them promising candidates for stabilizing water–oil interfaces. Oily wastewater (OWW) contamination, resulting from industrial activities such as petroleum extraction and refining and vegetable oil processing, poses significant risks to ecosystems, water resources, and public health. Traditional surfactants used in enhanced oil recovery (EOR) and wastewater treatment often introduce secondary pollution due to their persistence and toxicity. In this work, we investigate the interfacial behavior of Janus NRs under two different conditions: a thin oil film surrounded by water and a nanoconfined system with purely repulsive walls. Using dissipative particle dynamics (DPD) simulations, we analyze how nanorod length and confinement influence interfacial tension and self-assembly. In bulk systems, shorter NRs (dimers and quadrimers) effectively reduce interfacial tension by adsorbing at the oil–water interface, while longer NRs (hexamers) exhibit bulk aggregation, limiting their surfactant efficiency. In contrast, under nanoconfinement, all NR sizes increase interfacial tension due to steric constraints, with longer NRs preferentially adsorbing onto the solid–liquid interface. These results pave the way for the rational design of nanostructured materials for applications in enhanced oil recovery, wastewater treatment, and membrane filtration. Full article

This study investigates the structural and catalytic properties of pure and Sr-doped LaCoO₃ and LaFeO₃ thin films for potential use as resistive gas sensors. Thin films were deposited via pulsed laser deposition (PLD) and characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), atomic force microscopy (AFM), nanoindentation, and scratch tests. XRD analysis confirmed the formation of the desired perovskite phases without secondary phases. XPS revealed the presence of La³⁺, Co³⁺/Co⁴⁺, Fe³⁺/Fe⁴⁺, and Sr²⁺ oxidation states. SEM and AFM imaging showed compact, nanostructured surfaces with varying morphologies (shape and size of surface irregularities) depending on the composition. Sr doping led to surface refinement and increased nanohardness and adhesion. Transmission electron microscopy (TEM) analysis confirmed the columnar growth of nanocrystalline films. Sr-doped LaCoO₃ demonstrated enhanced sensitivity and stability in the presence of NO₂ gas compared to pure LaCoO₃, as evidenced by electrical resistivity measurements within 230 ÷ 440 °C. At the same time, it was found that Sr doping stabilizes the catalytic activity of LaFeO₃ (in the range of 300 ÷ 350 °C), although its behavior in the presence of NO₂ differs from that of LaCo(Sr)O₃—especially in terms of response and recovery times. These findings highlight the potential of Sr-doped LaCoO₃ and LaFeO₃ thin films for NO₂ sensing applications. Full article

Nanocrystalline (NC) materials have widespread industrial usage. X-ray and neutron diffraction techniques are primary tools for studying the structural and microstructural features of NC materials. Selected area electron diffraction (SAED) patterns collected using a transmission electron microscope (TEM) on polycrystalline nanostructured materials, featuring nested rings, that are analogous to Debye–Scherrer patterns, possess similar potentials to aid materials characterisation. The utility of SAED patterns is further enhanced by the possibility of applying crystallographic approaches, like full pattern fitting procedures, based on Rietveld refinement algorithms, enabling the evaluation of material features, such as crystallite size, lattice distortions, defect structures, and the presence of secondary phases even from very small volume scale. In this paper, we have discussed the possibilities afforded by a Rietveld code applied to SAED patterns of NC materials, including the mathematical implementation of the two-beam dynamical correction model in MAUD software (version 2.9995), and a critical discussion of the results obtained on different NC materials. Full article

Transverse magnetic susceptibility is an excellent tool to study singularity points as anisotropy and switching fields in different bulk and nanostructured systems, as well as phase transitions. This technique has been carried out on polycrystalline Y-type hexaferrites, with compositions Ba_2−xSr_xCo₂Fe₁₂O₂₂, (0.0 ≤ x ≤ 2.0), and Ba_2−xSr_xZn₂Fe₁₂O₂₂, (1.3 ≤ x ≤ 1.7), promising candidates to exhibit multiferroic properties due to their noncollinear spin structure. In the Co₂Y system, different behavior is observed depending on the Sr substitution rate, with a secondary maximum observed for samples with x ≥ 1.0 and different shapes in the measurement temperature range analyzed. In the Zn₂Y system, several peaks related to the phase transitions that take place are observed, with certain variations depending on the degree of Ba substitution and the applied field in a more or less extended region around the ambient temperature. This type of measurement is a valuable tool to determine the bias field and temperature range of spin transitions. Full article

Plastic pollution, particularly from microplastics (MPs) and nanoplastics (NPs), has become a critical environmental and health concern due to their widespread distribution, persistence, and potential toxicity. MPs and NPs originate from primary sources, such as cosmetic microspheres or synthetic fibers, and secondary fragmentation of larger plastics through environmental degradation. These particles, typically less than 5 mm, are found globally, from deep seabeds to human tissues, and are known to adsorb and release harmful pollutants, exacerbating ecological and health risks. Effective detection and quantification of MPs and NPs are essential for understanding and mitigating their impacts. Current analytical methods include physical and chemical techniques. Physical methods, such as optical and electron microscopy, provide morphological details but often lack specificity and are time-intensive. Chemical analyses, such as Fourier transform infrared (FTIR) and Raman spectroscopy, offer molecular specificity but face challenges with smaller particle sizes and complex matrices. Thermal analytical methods, including pyrolysis gas chromatography–mass spectrometry (Py-GC-MS), provide compositional insights but are destructive and limited in morphological analysis. Emerging (bio)sensing technologies show promise in addressing these challenges. Electrochemical biosensors offer cost-effective, portable, and sensitive platforms, leveraging principles such as voltammetry and impedance to detect MPs and their adsorbed pollutants. Plasmonic techniques, including surface plasmon resonance (SPR) and surface-enhanced Raman spectroscopy (SERS), provide high sensitivity and specificity through nanostructure-enhanced detection. Fluorescent biosensors utilizing microbial or enzymatic elements enable the real-time monitoring of plastic degradation products, such as terephthalic acid from polyethylene terephthalate (PET). Advancements in these innovative approaches pave the way for more accurate, scalable, and environmentally compatible detection solutions, contributing to improved monitoring and remediation strategies. This review highlights the potential of biosensors as advanced analytical methods, including a section on prospects that address the challenges that could lead to significant advancements in environmental monitoring, highlighting the necessity of testing the new sensing developments under real conditions (composition/matrix of the samples), which are often overlooked, as well as the study of peptides as a novel recognition element in microplastic sensing. Full article

Skin represents an effective barrier against the penetration of external agents into the human body. Nevertheless, recent research has shown that small particles, especially in the nanosized range, can not only penetrate through the skin but also work as vectors to transport active molecules such as contrast agents or drugs. This knowledge has opened new perspectives on nanomedicine and controlled drug delivery. On the other hand, micro- and nanoplastics represent a form of emerging pollutants, and their concentration in the environment has been reported to drastically increase in the last years. The possible penetration of these particles through the skin has become a major concern for human health. If the actual primary toxicity of these materials is still debated, their possible role in the transport of toxic molecules through the skin, originating as secondary toxicity, is surely alarming. In this review paper, we analyze and critically discuss the most recent scientific publications to underline how these two processes, (i) the controlled delivery of bioactive molecules by micro- and nano-structures and (ii) the unwanted and uncontrolled penetration of toxic species through the skin mediated by micro- and nanoparticles, are deeply related and their efficiency is strongly affected by the nature, size, and shape of the particles. Full article

The impact of the interface phenomena on the properties of nanostructured materials is the focus of modern physics. We studied the magnetic properties of the nanostructured In–Ag alloy confined within a porous glass. The alloy composition was close to the eutectic point in the indium-rich range of the phase diagram. Temperature dependences of DC magnetization evidenced two superconducting transitions at 4.05 and 3.38 K. The magnetization isotherms demonstrated the superposition of two hysteresis loops with low and high critical fields below the second transition, a single hysteresis between the transitions and ferromagnetism with weak remanence in the normal state of the alloy. The shape of the loop seen below the second transition, which closes at a low magnetic field, corresponded to the intermediate state of the type-I superconductor. It was ascribed to strongly linked indium segregates. The loop observed below the first transition is referred to as type-II superconductivity. The secondary and tertiary magnetization branches measured at decreasing and increasing fields were shifted relative to each other, revealing the proximity of superconducting and ferromagnetic phases at the nanometer scale. This phenomenon was observed for the first time in the alloy, whose components were not magnetic in bulk. The sign of the shift shows the dominant role of the stray fields of ferromagnetic regions. Ferromagnetism was suggested to emerge at the interface between the In and AgIn₂ segregates. Full article

Water pollution is caused by heavy metals, minerals, and dyes. It has become a global environmental problem. There are numerous methods for removing different types of pollutants from wastewater. Adsorption is viewed as the most promising and financially viable option. Nanostructured materials are used as effective materials for adsorption techniques to extract metal ions from wastewater. Many types of nanomaterials, such as zero-valent metals, metal oxides, carbon nanomaterials, and magnetic nanocomposites, are used as adsorbents. Magnetic nanocomposites as adsorbents have magnetic properties and abundant active functional groups, and unique nanomaterials endow them with better properties than nonmagnetic materials (classic adsorbents). Nonmagnetic materials (classic adsorbents) typically have limitations such as limited adsorption capacity, adsorbent recovery, poor selective adsorption, and secondary treatment. Magnetic nanocomposites are easy to recover, have strong selectivity and high adsorption capacity, are safe and economical, and have always been a hotspot for research. A large amount of data has been collected in this review, which is based on an extensive study of the synthesis, characterization, and adsorption capacity for the elimination of ions from wastewater and their separation from water. The effects of several experimental parameters on metal ion removal, including contact duration, temperature, adsorbent dose, pH, starting ion concentration, and ionic strength, have also been investigated. In addition, a variety of illustrations are used to describe the various adsorption kinetics and adsorption isotherm models, providing insight into the adsorption process. Full article

This paper discusses the fabrication of three-dimensional dendritic Ag nanostructures, showcasing pronounced Localized Surface Plasmon Resonance (LSPR) effects. These nanostructures, employed in surface-enhanced Raman scattering (SERS), function as sensors for lactic acid in artificial sweat. The dendritic structures of the silver nanoparticles (AgNPs) create an effective SERS substrate, with additional hotspots at branch junctures enhancing LSPR. We achieve differential LSPR effects by varying the distribution and spacing of branches and the overall morphology. Adjustments to electrodeposition parameters, such as current and plating solution protective agents on an anodized aluminum oxide (AAO) base, allow for precise control over LSPR intensities. By pre-depositing AgNPs, the electron transmission paths during electrodeposition are modified, which leads to optimized dendritic morphology and enhanced LSPR effects. Parameter optimization produces elongated rods with main and secondary branches, covered with uniformly sized, densely packed, non-overlapping spherical AgNPs. This configuration enhances the LSPR effect by generating additional hotspots beyond the branch tips. Fine-tuning the electrodeposition parameters improved the AgNPs’ morphology, achieving uniform particle distribution and optimal spacing. Compared to non-SERS substrates, our structure amplified the Raman signal for lactic acid detection by five orders of magnitude. This method can effectively tailor SERS substrates for specific analytes and laser-based detection. Full article

The green synthesis of silver nanoparticles (AgNPs) can be developed using safe and environmentally friendly routes, can replace potentially toxic chemical methods, and can increase the scale of production. This study aimed to synthesize AgNPs from aqueous extracts of guarana (Paullinia cupana) leaves and flowers, collected in different seasons of the year, as a source of active biomolecules capable of reducing silver ions (Ag⁺) and promoting the stabilization of colloidal silver (Ag⁰). The plant aqueous extracts were characterized regarding their metabolic composition by liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS/MS), phenolic compound content, and antioxidant potential against free radicals. The synthesized AgNPs were characterized by UV/Vis spectrophotometry, dynamic light scattering (DLS), nanoparticle tracking analysis (NTA), transmission electron microscopy (TEM), and scanning electron microscopy coupled to energy-dispersive X-ray spectrometry (EDX). The results demonstrated that the chemical characterization indicated the presence of secondary metabolites of many classes of compounds in the studied aqueous extracts studied, but alkaloids and flavonoids were predominant, which are widely recognized for their antioxidant capabilities. It was possible to notice subtle changes in the properties of the nanostructures depending on parameters such as seasonality and the part of the plant used, with the AgNPs showing surface plasmon resonance bands between 410 and 420 nm using the leaf extract and between 440 and 460 nm when prepared using the flower extract. Overall, the average hydrodynamic diameters of the AgNPs were similar among the samples (61.98 to 101.6 nm). Polydispersity index remained in the range of 0.2 to 0.4, indicating that colloidal stability did not change with storage time. Zeta potential was above −30 mV after one month of analysis, which is adequate for biological applications. TEM images showed AgNPs with diameters between 40.72 to 48.85 nm and particles of different morphologies. EDX indicated silver content by weight between 24.06 and 28.81%. The synthesized AgNPs exhibited antimicrobial efficacy against various pathogenic microorganisms of clinical and environmental interest, with MIC values between 2.12 and 21.25 µg/mL, which is close to those described for MBC values. Therefore, our results revealed the potential use of a native species of plant from Brazilian biodiversity combined with nanotechnology to produce antimicrobial agents. Full article

Electrochemical pH sensors have a wide range of industrial applications such as in medicine due to their fast response and high sensitivity to pH changes. This work focuses on the preparation of samples based on the nanostructure of TiO₂ with potentiostatically deposited particles of iridium and its oxides (IrO₂), using a Ti-6Al-4V alloy as the base material, and subsequent surface characterization. Transmission electron microscopy and secondary ion mass spectroscopy showed Ir particles distributed in the nanotubes. Using a potentiostatic method, a stable pH sensor was prepared. By monitoring the open circuit potential, it was shown that this sensor is usable even without being kept in a storage medium and does not react to changes in the redox potential of the solution. Full article