Explore the vast range of titles available.

BiFeO 3 (BFO) nanoparticles (NPs) were synthesized using the sol-gel method at different calcination temperatures from 400 °C to 600 °C. XRD studies have confirmed that all BFO NPs show distorted rhombohedral crystals that match the R3c space group. We found evidence of local structural strain that develops with increasing particle size as suggested by TEM and Raman spectroscopy measurements. Magnetic measurements suggest that NPs have two distinct regimes: a ferromagnetic-like one at low temperatures and a superparamagnetic-like one at room temperature. The crossover temperature increases with NPs size, suggesting a size-dependent blocking magnetic regime. Similarly, local piezoelectric measurements at room temperature in single NP have confirmed a ferroelectric order with a NP size-dependent d 33 coefficient. An analysis of both the ferroelectric and the magnetic results suggest that ferromagnetism and ferroelectricity coexist at room temperature in NPs. Our results lead to the possibility of tailoring the ferroic order in multifunctional materials by means of NP size.

While there are conventional chemical synthesis methods to generate metal nanoclusters (NCs), many of them are adversely affected by the unavoidable contamination of the nanoproduct solution, resulting in aggregation, background noise in analytical chemistry, toxicity, and deactivation of the catalyst. In this work, physical method of ultrafast laser ablation as a “green” synthesis approach together with mechanical centrifugation to obtain silver NCs, simplifying widely the chemical synthesis requirements, is proposed. Remarkably, compared with conventional methods for synthesizing Ag NCs, this new approach starts with a colloid that contains nanosized particles as well as smaller species, managing to obtain colloids with few atoms NCs by centrifugation. Those colloids were analyzed by fluorescence spectroscopy observing UV bands corresponding with HOMO-LUMO cluster transitions. Besides, independent HRTEM measurements were made confirming the presence of few atoms Ag NCs, as well as small NPs in different formation stages. Equally important, photocatalytic efficiency of the obtained NCs was studied through degradation of Methylene Blue (MB) when it was mixed with as-prepared or highly centrifuged colloid, showing an enhanced photocatalytic efficiency of 79% as compared to 57% for pure MB after 180 min of illumination. Consequently, this work contributes to establishing a simple approach to synthesize highly fluorescent and photocatalytic NCs.

Gold–iron oxide nano-heterostructures with a clear and well-defined morphology were prepared via a seed-assisted method. The synthesis process and the events of heterogeneous nucleation during the decomposition of the iron precursor were carefully studied in order to understand the mechanism of the reaction and to tailor the architecture of the fabricated heterostructures. When employing Au seeds of 3 and 5 nm, nanoparticles with a dimer-like morphology were produced due to the occurrence of a single iron oxide nucleation event. Otherwise, multi-nucleation events could be favored by two mechanisms: (i) by the incorporation of a reducing agent and the slowing down of the heating protocol, leading to a core–shell system; (ii) by the increase of the Au seed size to 8 nm, leading to a flower-like system. Further increase of the Au seed size to 12 nm using similar synthesis conditions promotes the homogeneous nucleation and growth of the iron oxide phase, without formation of heterostructures. An in-depth study was performed on the gold–iron oxide heterostructures to confirm the epitaxial growth of the oxide domain over the Au seed and to analyze the elemental distribution of the components within the heterostructures. Finally, it was found that the modification of the plasmonic properties of the Au nanoparticles are strongly influenced by the architecture of the heterostructure, with a more pronounced damping effect for the systems produced after multi-nucleation events.

Magnetic nanoparticles (MNps) have become powerful tools for multiple biomedical applications such as hyperthermia drivers, magnetic resonance imaging (MRI) vectors, as well as drug-delivery systems. However, their toxic effects on human health have not yet been fully elucidated, especially in view of their great diversity of surface modifications and functionalizations. Citrate-coating of MNps often results in increased hydrophilicity, which may positively impact their performance as drug-delivery systems. Nonetheless, the consequences on the intrinsic toxicity of such MNps are unpredictable. Herein, novel magnetite (Fe 3 O 4 ) nanoparticles covered with citrate were synthesized and their potential intrinsic acute toxic effects were investigated using in vitro and in vivo models. The proposed synthetic pathway turned out to be simple, quick, inexpensive, and reproducible. Concerning toxicity risk assessment, these citrate-coated iron oxide nanoparticles (IONps) did not affect the in vitro viability of different cell lines (HaCaT and HepG2). Moreover, the in vivo acute dose assay (OECD test guideline #425) showed no alterations in clinical parameters, relevant biochemical variables, or morphological aspects of vital organs (such as brain, liver, lung and kidney). Iron concentrations were slightly increased in the liver, as shown by Graphite Furnace Atomic Absorption Spectrometry and Perls Prussian Blue Staining assays, but this finding was considered non-adverse, given the absence of accompanying functional/clinical repercussions. In conclusion, this study reports on the development of a simple, fast and reproducible method to obtain citrate-coated IONps with promising safety features, which may be used as a drug nanodelivery system in the short run. (263 words)

BiFeO (BFO) nanoparticles (NPs) were synthesized using the sol-gel method at different calcination temperatures from 400 °C to 600 °C. XRD studies have confirmed that all BFO NPs show distorted rhombohedral crystals that match the R3c space group. We found evidence of local structural strain that develops with increasing particle size as suggested by TEM and Raman spectroscopy measurements. Magnetic measurements suggest that NPs have two distinct regimes: a ferromagnetic-like one at low temperatures and a superparamagnetic-like one at room temperature. The crossover temperature increases with NPs size, suggesting a size-dependent blocking magnetic regime. Similarly, local piezoelectric measurements at room temperature in single NP have confirmed a ferroelectric order with a NP size-dependent d coefficient. An analysis of both the ferroelectric and the magnetic results suggest that ferromagnetism and ferroelectricity coexist at room temperature in NPs. Our results lead to the possibility of tailoring the ferroic order in multifunctional materials by means of NP size.

Polyvinyl alcohol (PVA) ferrogels were easily obtained through a one-pot technique that involves co-precipitation of iron salts in the presence of a PVA solution, followed by freezing–thawing cycles of the resulting nanoparticles (NPs) dispersions. The protecting effect of PVA enabled the synthesis of small magnetic NPs that did not agglomerate in the initial solution allowing the synthesis of well-dispersed ferrogels by physical cross-linking. Physical properties of the physically cross-linked ferrogels, as swelling ability, melting temperature, and crystallinity, were barely affected by the presence of NPs, presenting similar or improved values when compared with chemically cross-linked systems. Ferrogels showed superparamagnetic properties at room temperature that combined with the absence of toxic residues arising from cross-linking agents make them ideal candidates for their use in biomedical applications (artificial muscles, drug delivery, and sensors among others).

A temperature pause introduced in a simple single-step thermal decomposition of iron, with the presence of silver seeds formed in the same reaction mixture, gives rise to novel compact heterostructures: brick-like Ag@Fe 3 O 4 core-shell nanoparticles. This novel method is relatively easy to implement and could contribute to overcome the challenge of obtaining a multifunctional heteroparticle in which a noble metal is surrounded by magnetite. Structural analyses of the samples show 4 nm silver nanoparticles wrapped within compact cubic external structures of Fe oxide, with curious rectangular shape. The magnetic properties indicate a near superparamagnetic like behavior with a weak hysteresis at room temperature. The value of the anisotropy involved makes these particles candidates to potential applications in nanomedicine.

We report for the first time on the formation of self-assembled fractals of spherical Ag nanoparticles (Nps) fabricated by femtosecond pulse laser ablation of a solid silver target in water. Fractal structures grew both in two and three Euclidean dimensions ( d ). Ramified-fractal assemblies of 2 nm height and 5–14 μm large, decorated with Ag Nps of 3 nm size, were obtained in a 2 d geometry when highly diluted drops of colloidal suspension were dried at a fast heating rate over a mica substrate. When less-diluted drops were dried at slow heating rate, isolated single Nps or rosette-like structures were formed. Fractal aggregates about 31 nm size in 3 d geometry were observed in the as-prepared colloidal suspension. Electron diffraction and optical extinction spectroscopy (OES) analyses performed on the samples confirmed the presence of Ag and Ag 2 O. The analysis of the optical extinction spectrum, using the electrostatic approximation of Mie theory for small spheres, showed the existence of Ag bare core, Ag–Ag 2 O and air–Ag core–shell Nps, Ag–Ag 2 O being the most frequent type [69 % relative abundance (r.a.)]. Core-size and shell-thickness distribution was derived from OES. In situ scattering measurements of the Ag colloidal suspension, carried out by small-angle X-ray scattering, indicate a mass fractal composed of packaged 〈 D SAXS 〉 = (5 ± 1) nm particles and fractal dimension d f  = 2.5. Ex situ atomic force microscopy imaging displayed well-ramified structures, which, analyzed with box-counting method, yield a fractal dimension d f  = 1.67. The growing behavior of these 2 d and 3 d self-assembled fractals is consistent with the diffusion-limited aggregation model.

In this study, the correlation between magnetic, structure, and electronic properties of Ag@Fe 3 O 4 hetero nanostructures are presented. These nanostructures were prepared using a two-step new chemical approach. Three different nanoparticle systems with different Ag concentrations have been prepared and characterized using high resolution transmission electron microscopy, dc magnetization (magnetization and coercive field as a function of temperature), X-ray absorption near edge spectroscopy, and magnetic circular dichroism studies (XMCD). From the correlation between XMCD and dc magnetic measurements (Verwey transition) the presence of non-stoichiometric magnetite in Ag@Fe 3 O 4 nanoparticle systems was confirmed. From the spin and orbital contribution to the total magnetic moment, we conclude that the sample with less Ag seeds particle concentration presents a non-quenched orbital contribution. These phenomena were analyzed based on the actual models and correlated with dc magnetic properties. From these, we conclude that the enhancement on the orbital contribution increases the spin orbital interaction, also increasing the magnetocrystalline anisotropy reflected on the dc magnetic properties.

A novel theoretical expression for the relaxation time of magnetic nanoparticles with dipolar interactions is derived from Kramers' theory, extending the Boltzmann-Gibbs framework to incorporate Tsallis statistics. The model provides a unified description of magnetic relaxation from weakly to strongly interacting regimes. It accounts for both the decrease and the increase of the relaxation time with increasing dipolar coupling, addressing a long-standing problem in nanoparticle magnetism that cannot be consistently described by classical phenomenological models. This result also offers an innovative interpretation of the cut-off condition inherent to the Tsallis distribution in terms of a cut-off temperature, T_cut-off, which naturally characterizes the onset of glassy freezing dynamics and provides an alternative interpretation of experimental relaxation data within a non-extensive statistical framework.