The inclusion of carbon nanomaterials in cement-based materials influences a variety of properties, ranging from basic properties to electrical conductivity, which allows for the creation of functional materials. These materials can be utilized as sensors of strain and cracks, as well as to generate heat and harvest electricity. Through the combination of standard applications of construction materials and added functionality, it is possible to create modern construction materials combining higher durability and strength with additional functionality. The enhanced durability of functional cementitious nanocomposites can reduce the need for retrofitting and decrease resource consumption. Together with the increased safety offered by their functional applications, these characteristics make them well aligned with the growing demand for environmentally sustainable construction materials. The presented paper describes the application of various carbon nanomaterials in cement-based composites. Current research directions concerning the influence of the carbon nanomaterial addition on the most important properties of cement pastes, mortars and concretes have been described, along with a critical analysis of the acquired results and further recommendations. Furthermore, recent progress in the development of functional cement-based nanocomposites has also been reviewed.
Municipal solid waste incineration fly ash (MSWI FA) represents a significant environmental challenge due to its high content of toxic heavy metal (HM) and large-scale generation. This study demonstrates the feasibility pathway for converting hazardous MSWI FA into well-crystallized layered double hydroxide nanosheets (LDH-FA). Sodium dimethyl dithiocarbamate (SDD) was incorporated as a chelating stabilizer to enable synergistic HM immobilization during acid leaching and crystallization. High-resolution transmission electron microscopy (HRTEM) confirmed the characteristic two-dimensional nanosheet morphology with interlayer spacings consistent with LDH structures, while elemental mapping revealed homogeneous distribution of Pb and Zn within the nanosheet matrix. SDD dosages higher than 1.0 wt% effectively suppressed HM leaching, and Pb concentrations were controlled below 0.1 mg/L and Zn maintained at minimal levels. BCR sequential extraction analysis further demonstrated that SDD treatment effectively transformed HMs from bioavailable acid-soluble fractions to stable forms. This investigation establishes an innovative approach to MSWI FA resource utilization and provides mechanistic insights into HM stabilization within LDH nanostructures, offering a scientific basis for safer applications of waste-derived nanomaterials.
Dynamic interactions among cells, including immune cells, stromal cells, endothelial cells, epithelial cells, and extracellular matrix (ECM) components, are involved in the wound healing process. In chronic wounds, particularly diabetic wounds, these interactions are hampered by prolonged inflammation and excessive reactive oxygen species generation by dysregulated immune cells, bacterial infection, and impaired angiogenesis. These pathological features have shifted the therapeutic strategies from wound coverage and antimicrobial protection toward regulation of the immune microenvironment. Polymeric and hybrid materials have emerged as promising platforms for this purpose because their versatile composition, structure, degradation behavior, mechanical properties, and drug loading capacities can be widely engineered to match the dynamic requirements of wound healing, particularly in immunomodulation strategies. In this review, we focus on the major immunological barriers and potential targets in the wound healing process using polymer-based materials. Overall, this review covers recent advances, design strategies, and challenges in immunomodulatory materials including polymer-based nanoparticles, nanofibers, hydrogels, and hybrid materials for wound repair.
Nanotechnology continues to redefine the boundaries of science, medicine, energy, and environmental stewardship [...].
The journal retracts the article titled "Preparation of pH Responsive Polystyrene and Polyvinyl Pyridine Nanospheres Stabilized by Mickering Microgel Emulsions" [...].
In the original publication [...].
Demographic growth and the global environmental crisis have intensified the need to reconcile energy generation with the protection of terrestrial ecosystems. Traditional organic waste management systems are inefficient in handling high pollutant loads, leading to uncontrolled methane emissions and degradation of soil and water. In response to this challenge, the present study aimed to conduct a critical review of how Microbial Fuel Cells (MFCs) valorize biomass to align climate action (SDG 13) with the protection of terrestrial life (SDG 15). Through a bibliometric analysis of the Scopus database (2010-2026), supported by tools such as Bibliometrix, 460 documents were examined, complemented by a systematic literature review addressing biomass types, microbial interactions, and electrode modifications. The main findings indicate that MFC research is currently in an exponential growth phase (R2 = 0.99954), with Environmental Sciences (23%) and Chemical Engineering (15%) as the predominant fields. Industrial and plant residues exhibit the highest bioelectric potential, while mixed microbial consortia-particularly fungal-bacterial synergies-outperform pure cultures in degradative efficiency and energy generation, reaching up to 1760 mW/m2 with Geobacter sulfurreducens bioaugmentation. Electrode modification with nanomaterials such as NiO or MWCNTs substantially enhances charge transfer. Standardization of measurement protocols, ecological impact assessment of nanomaterials, and evaluation of the economic-environmental feasibility of MFC-integrated biorefineries are recommended to ensure scalability and effective contributions to SDGs 13 and 15.
Nanomaterials such as cellulose nanocrystals and fumed silica are emerging as excellent thickeners for liquids in a variety of practical applications. Surfactants are often incorporated into the thickening fluids to provide stabilizing components and to control the surface activity of fluids. To develop new thickening materials with desired surface-active properties, it is important to understand the interactions between surfactants and nanoparticles in suspensions. In this work, the interactions between surfactants and nanocrystals/nanoparticles were investigated. Two surfactants, anionic sodium lauryl sulfate-based surfactant (referred to as Stepanol) and cationic hexadecyltrimethylammonium bromide (referred to as HTAB), were studied. Cellulose nanocrystals (referred to as NCC) and fumed-silica nanoparticles (referred to as N20) were used as nanomaterials. The unique feature of this study is that it simultaneously measures rheology, surface activity, and electrical conductivity to determine the influence of ionic surfactants on the behavior and properties of cellulose nanocrystal and fumed silica nanoparticle suspensions. Furthermore, the interactions are observed in the low surfactant concentration range of 0 to 500 ppm. The NCC concentration of NCC-surfactant mixtures was fixed at 1 wt%. Two concentrations of N20 (2 and 5 wt%) were used for N20-surfactant mixtures. The influence of Stepanol was found to be weak whereas HTAB had a strong influence on the rheology of NCC and N20 suspensions. The NCC suspension and surfactant-NCC suspensions were highly non-Newtonian shear-thinning. The N20 suspensions and N20-Stepanol mixtures were nearly Newtonian. The N20-HTAB mixtures were shear-thinning at high HTAB concentrations. The power law model described the rheological behavior of non-Newtonian systems adequately. The consistency and flow behavior indices varied only marginally with the addition of the anionic surfactant Stepanol to NCC and N20 suspensions. With the addition of cationic surfactant HTAB to NCC and N20 suspensions, however, a large increase (20- to 70-fold) in consistency index was observed at high surfactant concentrations. The critical surfactant concentrations where sharp transitions in the rheological properties took place were identified using break points in surface tension and electrical conductivity plots. This study offers valuable insights into tailoring surfactant-nanoparticle systems for practical applications, where precise control of rheological and interfacial properties may be required.
We study the planar dynamics of a charged particle subjected to a radially repulsive inverted harmonic potential and a perpendicular uniform magnetic field, a configuration that is relevant to nanoscale-charged transport and confinement in low-dimensional systems. The competition between the destabilizing central repulsion and magnetic field-induced rotational motion gives rise to rich trajectory behavior, including spiraling, unbounded escape, and parameter-dependent quasi-confined motion. The governing coupled differential equations of motion are solved analytically. The resulting trajectories are classified as functions of system parameters. The proposed framework provides insight into charge carrier dynamics in nanostructured environments such as quantum wells, 2D materials, and plasma-like nanosystems, where effective repulsive potentials may arise from external gating or collective interactions. In addition, the model offers a classical analogue for interpreting features associated with magnetic confinement in non-equilibrium or unstable regimes. These results contribute to the theoretical foundation for designing and controlling charged particle motion in emerging nanomaterials and devices.
Precision nano-fertilization offers transformative potential for sustainable improvement of grape quality, yet the underlying molecular mechanisms remain poorly understood. Here, we investigated the effects of foliar-applied nano zero-valent iron (nZVI) and potassium dihydrogen phosphate (KH2PO4), in combination, on berry quality and secondary metabolic reprogramming in Vitis vinifera cv. Marselan. The combined nZVI/KH2PO4 treatment improved photosynthetic capacity, Fe/P co-accumulation, and berry quality traits including soluble solid content, sugar-acid ratio, and phenolic and aroma metabolite profiles. Crucially, integrated transcriptomic and metabolomic profiling identified 631 differentially expressed genes and 838 differentially accumulated metabolites, converging on flavonoid biosynthesis and glutathione metabolism as the dominant regulatory axes. Correlation network analysis pinpointed five hub regulatory genes-VvHCT, VvFLS1, VvLAR1/2, VvUGT88F5, and VvODC-as central orchestrators of nanomaterial-driven metabolic reprogramming: VvHCT and VvFLS1 coordinately redirected carbon flux toward hydroxycinnamic acid conjugates and flavonol accumulation, while VvLAR1/2 governed proanthocyanidin polymerization, and VvUGT88F5 modulated glycosylation-dependent metabolite stabilization. Notably, VvODC linked polyamine metabolism to glutathione-mediated stress buffering, revealing a previously uncharacterized crosstalk between nano-iron signaling and antioxidant reprogramming. These findings establish a mechanistic framework in which nZVI and KH2PO4 synergistically remodel the secondary metabolome through discrete yet interconnected transcriptional nodes, providing molecular targets for nano-enabled precision viticulture and broader applications of engineered nanomaterials in high-value crop improvement.
Nanoporous films assembled by low-kinetic-energy deposition of individual nanoparticles are complex nanomaterials for a variety of applications, from gas sensing to neuromorphic computing. We develop a numerical strategy for assembling metallic nanoparticles into 25-40 nm thick films from an arbitrary distribution of Au nanoparticles in terms of their initial size and shape. We characterize the structural properties of the assembled films as a function of the initial nanoparticle distribution. The morphology of the deposited nanoparticles affects nanofilm thickness, porosity, and its internal structure, including the length, type, and density of dislocations. Film porosity and the average dislocation length mainly correlate with the size of deposited nanoparticles. At the same time, thickness and dislocation density can also be affected by the shape of the larger nanoparticles deposited.
Cancer and multidrug-resistant microbial infections remain major global health challenges, underscoring the need for multifunctional, biocompatible, and environmentally sustainable therapeutic platforms. Herein, selenium-hyaluronic acid nanoconjugates (Se/HA NPs) were synthesized through an eco-friendly ascorbic acid-mediated reduction approach to improve the bio-functional stability and therapeutic performance of selenium-based nanomaterials. The formation of Se/HA NPs was confirmed by transmission electron microscopy (TEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), and Fourier-transform infrared spectroscopy (FTIR). FTIR analysis supported the involvement of ascorbic acid- and hyaluronic acid-associated functional groups in nanoparticle formation and stabilization. TEM revealed well-dispersed, predominantly spherical nanoparticles with diameters ranging from 29.72 to 80.38 nm, while XRD confirmed their crystalline nature with an average crystallite size of 31.2 nm. Biologically, Se/HA NPs exhibited strong antibacterial activity against Enterococcus faecalis (21 mm), Staphylococcus aureus (24 mm), Escherichia coli (25 mm), and Klebsiella pneumoniae (27 mm), outperforming hyaluronic acid alone and showing activity comparable to standard antibiotics, with a minimum inhibitory concentration (MIC) of 15.62 µg/mL. Notably, Se/HA NPs showed pronounced antifungal activity against Candida albicans, with an inhibition zone of 34 mm and an MIC of 7.8 µg/mL. In MG-63 osteosarcoma cells, Se/HA NPs demonstrated potent cytotoxicity, with a half-maximal inhibitory concentration (IC50) of 8.36 µg/mL compared with 746.37 µg/mL for hyaluronic acid. Moreover, Se/HA NPs enhanced wound closure to 73.41% and showed strong anti-inflammatory activity, with an IC50 of 5.37 µg/mL, demonstrating multifunctional bioactivity.
Self-assembling β-sheet-forming peptides are attractive building blocks for drug delivery nanomaterials. However, their strong intermolecular interactions often lead to high structural stability, which can hinder intracellular dissociation and limit cargo availability. Here, we propose a charge-compensated ampholytic design strategy for β-sheet peptide nanofibers that undergo destabilization and disassembly under reducing conditions. Six ampholytic peptides comprising an anionic main-chain peptide (β-sheet-forming motif, model antigenic cargo, and oligoglutamic acid segment) and a disulfide-linked cationic segment were designed and synthesized to vary the lengths and charges of the anionic and cationic segments, as well as the cationic insertion position. Four peptides formed nanofibers in 4×phosphate buffered saline (4×PBS) and the resulting nanofibers remained stable after dilution to 1×PBS, retaining β-sheet-rich secondary structures and fibrillar morphologies for at least 24 h. Under reducing conditions, the four preformed nanofibers exhibited distinct behaviors, including reduction-insensitive persistence, disassembly, and transient destabilization followed by re-stabilization, depending on peptide charge design. Redox-triggered disassembly was favored when the main-chain peptide had sufficient anionic character and the cationic segment was of moderate length and charge. This study therefore provides a molecular design strategy for controlling the destabilization of β-sheet peptide nanofibers under reducing conditions through disulfide-cleavage-induced disruption of charge compensation.
Carbon dots (CDs) are zero-dimensional carbon nanomaterials with sizes below 10 nm, with high fluorescence quantum yields, variable emission colours, and excellent photostability. Due to their different structural origins and complex surface chemicals, CDs display complex photoluminescence behaviors (PL) and different fluorescence suppression responses. This review systematically summarizes recent advances in understanding the PL mechanisms of CDs, including carbon-core emission, surface emission, molecular emission and crosslink emission. In addition, fluorescence quenching processes triggered by various analytical techniques are discussed, including dynamic quenching, static quenching, Förster resonance energy transfer (FRET), photoinduced electron transfer (PET), and the inner filter effect (IFE). Emphasis is placed on mechanistic understanding and experimental differentiation strategies. A clear understanding of these fundamental mechanisms is essential for optimizing the fluorescence properties of CDs and the design of highly sensitive and selective fluorescence sensors. Finally, potential research directions and applications of CDs based on these mechanical insights are also highlighted.
Antimicrobial resistance (AMR) is a growing global health concern driven by bacterial biofilm formation, which increases tolerance to treatments. Developing surface-based strategies to limit biofilm formation is therefore critical. Layered Double Hydroxides (LDHs) are 2D brucite-like nanomaterials with tuneable physicochemical properties that may reduce bacterial colonisation. Their ease of synthesis, with scalability potential for industrial production, alongside their characteristic and tunable physicochemical properties, makes them a promising nanostructured coating for antimicrobial applications. This study evaluates LDH thin-film coatings as intrinsic antimicrobial surfaces, focusing on the combined effects of chemical composition, nanotopography, and wettability on biofilm formation in Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Four aluminium-based LDHs (ZnAl-NO3, ZnAl-Cl2, MgAl-NO3, MgAl-Cl2) were synthesised via coprecipitation or in situ growth on aluminium substrates. Materials were characterised by XRD, SEM, EDS, and contact angle measurements. Antimicrobial performance was assessed by quantifying colony-forming units (CFU mL-1) after bacterial exposure. ZnAl-LDH surfaces showed significant antimicrobial activity against E. coli and S. aureus, while MgAl-LDHs showed no effect and occasionally increased bacterial growth. None of the LDH surfaces tested exhibited significant antimicrobial activity against P. aeruginosa strain. The antimicrobial performance of ZnAl-LDH can be attributed to the concurrent effect of the surface chemistry, wettability, and sharp platelet-like nanotopography. The results obtained demonstrate that ZnAl-LDH-based coatings are promising antimicrobial materials with potential relevance for translational research in clinical antimicrobial surface development.
Two-dimensional organic-inorganic hybrid perovskite (2D-OIHP) heterostructures provide a versatile platform for crystal engineering because their composition, dimensionality, excitonic structure and interfacial energy alignment can be tuned at the molecular level. However, the same ionic softness that enables facile chemical transformation also leads to ion migration under thermal, electrical and optical stimuli. In 2D-OIHP heterostructures, ion migration is not only a degradation pathway; it determines whether a heterointerface remains sharp, becomes compositionally graded, evolves into a mixed-halide alloy, or forms a bias-programmed functional junction. This review summarizes recent progress in understanding ion migration in 2D-OIHP-based heterostructures, with emphasis on migration species, driving forces, pathways and interface evolution. We first classify representative fabrication strategies according to the initial interface profiles they generate. We then discuss thermally driven in-plane and out-of-plane halide migration, spacer-cation engineering for suppressing interdiffusion, and electric-field-induced directional migration in functional devices. Finally, we extract design rules and unresolved challenges for achieving stable, sharp or dynamically programmable perovskite heterostructures. The aim is to provide a mechanistic framework for using ion migration as both a stability criterion and a crystal-engineering tool in layered hybrid perovskites.
The use of smartphones as analytical instruments is becoming increasingly widespread due to their ease of use and low cost. However, it has limitations, such as dependence on the smartphone's sensor, the light source and the environment, which hinders the reproducibility and comparability of results. This paper presents the development of a portable device, called DUNI, which can be attached to any smartphone and is designed to overcome these limitations. The device, manufactured using 3D printing and with an average cost of €35, consists of an integrating sphere, which incorporates a lighting-electronic system, as well as accessories for measuring on different surfaces. It has been optimised by evaluating the influence of the optical geometry, the size and reflective coating of the sphere, the lighting conditions, and the electronic stability on measurement performance. It has been applied to the determination of hydrogen peroxide and biogenic amines in synthetic samples, achieving relative errors of less than 5% and detection limits between 3 and 6 µM. Overall, the device we have developed constitutes a portable, versatile and low-cost platform that enables quantitative colorimetric measurements using smartphones under controlled lighting conditions, with potential applications in on-site analysis and resource-limited settings.
Biocorona (BC) formation is a critical determinant of nanoparticle (NP) biological identity and downstream interactions, yet lipid association within BCs remains comparatively understudied relative to proteins, despite its potential relevance to NP stability, biodistribution, cellular interactions, and clearance. A more complete understanding of NP-lipid interactions is essential for optimizing NP-based therapies and supporting their safe clinical translation. In this study, we evaluated how serum concentration, biological sex, and NP size influence lipid association with iron oxide (Fe3O4) NP BCs. Lipids associated with 50 or 100 nm Fe3O4 NPs were characterized following incubation in male or female human serum across increasing serum concentrations of 5%, 10%, 25%, 50%, or 75% (v/v). Increasing serum concentration promoted greater lipid association and increased BC complexity, with higher serum conditions yielding more compositionally diverse lipid coronas. BCs formed on 50 nm Fe3O4 NPs consistently contained more lipid species than those formed on 100 nm Fe3O4 NPs, indicating pronounced size-dependent differences in lipid recruitment. BCs formed in male serum also contained more lipid species and a greater number of unique lipids than corresponding female BCs, demonstrating that biological sex significantly influenced both lipid composition and abundance within the BC. Rank-based comparisons further indicated that lipid association was governed not only by serum abundance but also by selective binding behaviors. Together, these findings demonstrate that lipid corona formation is strongly shaped by both the biofluid environment and NP design variables, emphasizing the importance of considering lipid coronas in NP design and evaluation, particularly for applications in drug delivery, nanomedicine, and precision diagnostics.
Large-area MoS2 nanotube arrays were successfully prepared using a combination of simple and reliable electrochemical deposition and chemical etching techniques, with highly ordered ZnO nanorod arrays used as the template. The thickness of MoS2 nanotube walls can be effectively controlled by adjusting the deposition time. The characterization results of SEM and TEM showed the successful preparation of MoS2 nanotube arrays with different wall thicknesses. The composition of the obtained nanotube arrays was verified to be MoS2 by EDS, XRD, and XPS characterizations. It is worth noting that compared to MoS2 nanofilms, the as-prepared MoS2 nanotube arrays exhibit stronger photoelectric response properties; the on/off ratio and photoresponsivity increased by 2.8 times and 3.8 times, respectively, mainly attributed to its significantly increased specific surface area. These research results provide new ideas for the large-area controllable preparation of MoS2 low-dimensional nanostructures, as well as new material candidates for the development of low-cost and high-performance photodetectors.
Flexible transparent conductive films (TCFs) and their applications have attracted extensive interest. Silver nanowires (AgNWs) have been explored to replace conventional indium tin oxide (ITO) due to their high optical transmittance and superior electrical conductivity. Nevertheless, AgNWs tend to oxidize under ambient conditions, which weakens the conductive network and limits long-term performance. Spraying reduced graphene oxide (rGO) can stabilize the conductive network and inhibit oxidation, thereby enhancing the overall properties of the films. In this work, rGO/AgNW/PET TCFs were prepared using a spray-coating approach. The transmittance of the rGO/AgNW/PET TCFs was measured at 77% at 550 nm, accompanied by a sheet resistance of 6.8 Ω/sq. The films achieved the surface temperature of 95 °C at 6 V with stable operation while also achieving an electromagnetic interference shielding effectiveness of 27 dB. This structural design improves both performance and stability, offering great potential for flexible TCFs in advanced optoelectronic applications.