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Dodecanethiol capped Ag nanoparticles (NPs) have been independently synthesized by the well-known Brust method under the same physical-chemical conditions. The obtained NP present similar sizes (∼2 nm) but different magnetic behaviors. The extended x-ray absorption fine structure analyses at the K-edge of Ag did not reveal any noticeable structural nor topological differences among the samples. In clear contrast with the structure provided for thiol capped ferromagnetic Au NPs, the analysis also brings out the existence of Ag-S bonds in a diffuse region surrounding a reduced Ag core where the magnetism of the Ag NPs would be located. [ABSTRACT FROM AUTHOR]

The interaction of nanoparticles with cells has been a focus of interest during the past decade. We report the fabrication and characterization of hydrosoluble Fe3O4@Au nanoparticles functionalized with biocompatible and fluorescent molecules and their interaction with cell cultures by visualizing them with confocal microscopy. Gold covered iron oxide nanoparticles were synthesized by reducing metal salts in the presence of oleylamine and oleic acid. The functionalization of these particles with an amphiphilic polymer provides a water soluble corona as well as the possibility to incorporate different molecules relevant for bio-applications such as poly(ethylene glycol), glucose or a cadaverine derived dye. The particle size, and the presence of polymer layers and conjugated molecules were characterized and confirmed by transmission electron microscopy, thermogravimetric measurements and infrared spectroscopy. A complete magnetic study was performed, showing that gold provides an optimum coating, which enhances the superparamagnetic behaviour observed above 10–15 K in this kind of nanoparticle. The interaction with cells and the cytotoxicity of the Fe3O4@Au preparations were determined upon incubation with the HeLa cell line. These nanoparticles showed no cytotoxicity when evaluated by the MTT assay and it was demonstrated that nanoparticles clearly interacted with the cells, showing a higher level of accumulation in the cells for glucose conjugated nanoparticles. [ABSTRACT FROM AUTHOR]

Abstract: Polycrystalline samples of La0.8Ca0.2Fe0.8Ni0.2O3−δ (LCFN) with perovskite type structure have been prepared by combustion, freeze drying, citrate-gel process and liquid mix method. The analysis of X-ray powder diffraction indicated that the samples were single phase and crystallized in an orthorhombic (space group, Pnma no. 62) structure. Transmission electron microscopy (TEM) analysis on the synthesized powder at 600°C by liquid mix method showed clusters of 150nm formed by nanoparticles of 20nm. Electrochemical performance of LCFN cathodes, which are used for intermediate temperature solid oxide fuel cells, were investigated. The polarization resistance was studied using two different electrolytes: Y-doped zirconia (YSZ) and Sm-doped ceria (SDC). The dc four-probe measurement exhibits a total electrical conductivity, over 100Scm−1 at T ≥600°C, pointing out that strontium can be substituted for the cheaper calcium cation without destroying the electrochemical properties. Experimental results indicate that nanoparticles have more advantages in terms of smaller particle size and better electrochemical performance. [ABSTRACT FROM AUTHOR]

Abstract: The effect of Fe doping on the ferromagnetic Nd0.7Pb0.3Mn1− x Fe x O3 (, 0.025, 0.05, 0.075, 0.1) phases has been studied in order to analyze the double-exchange interaction. The structural and magnetic study has been carried out by neutron powder diffraction and susceptibility measurements between 1.7 and 300K. The substitution of Fe at the Mn site results in reductions in both the Curie temperature T c and the magnetic moment per Mn ion without appreciable differences in the crystal structures. All the compounds crystallize in space group. The thermal evolution of the lattice parameters of the Nd0.7Pb0.3Mn1− x Fe x O3 (, 0.05, 0.075) compounds shows discontinuities in volume and lattice parameters close to the magnetic transition temperature. Increasing amounts of Fe3+ reduces the double exchange interactions and no magnetic contribution for is observed. The magnetic structures of Nd0.7Pb0.3Mn1− x Fe x O3 (, 0.025, 0.05, 0.075) compounds show that the Nd and Mn ions are ferromagnetically ordered. [Copyright &y& Elsevier]

Abstract: Monodisperse magnetite nanoparticles coated with organic ligands have been chemically synthesised by using the poliol method. Modifying the synthetic conditions, particle diameter can be tuned from 3.5 to 7.1nm. In order to investigate the critical size effects on the magnetic behavior of the samples, Fe3O4 nanoparticles have been fully characterized by X-ray diffraction, thermogravimetric analysis, transmission electron microscopy, SQUID magnetometry and electron paramagnetic resonance spectroscopy. [Copyright &y& Elsevier]

Abstract: Three cathode compounds for lithium ion batteries, LiMn2O4, LiMn1.95Si0.05O4 and LiMn1.9Ga0.1O4 have been synthesized by the freeze-drying method. All samples present partially sintered particles of 80 nm average size, corresponding to single crystalline phases with cubic spinel structure. The substitution of a little portion of Mn(IV) by Si(IV) in the crystal framework leads to more expanded and regular MnO6 octahedra, whereas the replacement of some Mn(III) by Ga(III) induces the opposing effect. The ESR measurements support the effectiveness of doping as an evolution of the width of the resonance signal with the composition is observed. A complete magnetic study has been carried out, including ac and dc magnetic susceptibility measurements at different fields, FC and ZFC, and magnetization versus field. Due to the in-built magnetic frustration in spinel structure and the competition between different exchange pathways, the insertion of small quantities of dopants causes significant differences in the magnetic behaviour. The electrochemical study has revealed very good values of specific capacity for LiMn1.95Si0.05O4 reaching 146 mA h g− 1 and 139 mA h g− 1 at C/10 and 1C rates, respectively. A capacity retention up to 75% has been observed for the three samples after 300th cycles. [Copyright &y& Elsevier]

The double perovskites, Sr2FeReO6 and Sr2FeRe0.9M0.1O6 (M=Nb, Ta) have been obtained by soft synthesis methods which yield homogeneous particles of micrometric grain size. The materials have been studied by X-ray and neutron powder diffraction, scanning electron microscopy and magnetic measurements. Rietveld refinements show that the compounds adopt a tetragonal I4/mmm structure at high temperatures and monoclinic P21/n below the transition temperature. The magnetic structures were determined by neutron powder diffraction at 100 and 300 K for the Sr2FeReO6, Sr2FeRe0.9Nb0.1O6 and Sr2FeRe0.9Ta0.1O6 phases, respectively. Evidence for a ferrimagnetic coupling between the Fe3+ and Re5+ sublattices has been observed. Magnetic measurements yield magnetic moments lower than the theoretical ones being in accord with the antisite disorder of 25% in the B–B′ positions. [Copyright &y& Elsevier]

In recent years, much effort has been invested into developing multifunctional drug delivery systems to overcome the drawbacks of conventional carriers. Magnetic nanoparticles are not generally used as carriers but can be functionalised with several different biomolecules and their size can be tailored to present a hyperthermia response, allowing for the design of multifunctional systems which can be active in therapies. In this work, we have designed a drug carrier nanosystem based on Fe 3 O 4 nanoparticles with large heating power and 4-amino-2-pentylselenoquinazoline as an attached drug that exhibits oxidative properties and high selectivity against a variety of cancer malignant cells. For this propose, two samples composed of homogeneous Fe 3 O 4 nanoparticles (NPs) with different sizes, shapes, and magnetic properties have been synthesised and characterised. The surface modification of the prepared Fe 3 O 4 nanoparticles has been developed using copolymers composed of poly(ethylene-alt-maleic anhydride), dodecylamine, polyethylene glycol and the drug 4-amino-2-pentylselenoquinazoline. The obtained nanosystems were properly characterised. Their in vitro efficacy in colon cancer cells and as magnetic hyperthermia inductors was analysed, thereby leaving the door open for their potential application as multimodal agents.

The main objective of the preparation of the Fe 3- x Ga x O 4 (0.14 ≤ x ≤ 1.35) system was to further the knowledge of the magnetic response of Ga 3+ -doped magnetite for application as MRI contrast agents. With this purpose, monodisperse nanoparticles between 7 and 10 nm with different amounts of gallium were prepared from an optimized protocol based on thermal decomposition of metallo-organic precursors. Thorough characterization of the sample was conducted in order to understand the influence of gallium doping on the structural, morphological and magnetic properties of the Fe 3- x Ga x O 4 system. X-ray diffraction and X-ray absorption near-edge structure measurements have proved the progressive incorporation of Ga in the spinel structure, with different occupations in both tetrahedral and octahedral sites. Magnetization measurements as a function of field temperature have shown a clear dependence of magnetic saturation on the gallium content, reaching an M s value of 110 Am 2 kg -1 at 5 K for x = 0.14 (significantly higher than bulk magnetite) and considerably decreasing for amounts above x = 0.57 of gallium. For this reason, nanoparticles with moderate Ga quantities were water-transferred by coating them with the amphiphilic polymer PMAO to further analyse their biomedical potential. Cytotoxicity assays have demonstrated that Fe 3- x Ga x O 4 @PMAO formulations with x ≤ 0.57, which are the ones with better magnetic response, are not toxic for cells. Finally, the effect of gallium doping on relaxivities has been analysed by measuring longitudinal (T 1 -1 ) and transverse (T 1 -1 ) proton relaxation rates at 1.4 T revealing that nanoparticles with x = 0.14 Ga 3+ content present remarkable T 2 contrast and the nanoparticles with x = 0.26 have great potential to act as dual T 1 -T 2 contrast agents.

We present results concerning the fabrication of a new magnetorheological fluid with FeCo magnetic nanoparticles (NPs) as magnetic fillers. These NPs have been fabricated by using the chemical reduction technique and show a pure crystalline phase with size ranging among 30-50 nm and high magnetization, 212 ± 2 A m 2 kg -1 . They agglomerate due to the strong magnetic dipolar interaction among them. These FeCo nanoparticles were used to synthesize a magnetorheological fluid by using oleic acid as surfactant, mineral oil as carrier liquid and Aerosil 300 as additive to control the viscosity of the fluid. The synthesized fluid showed a strong magnetorheological response with increasing shear stress values as the magnetic field intensity increases. Thus, we have measured a superior performance up to 616.7 kA m -1 , with a yield stress value of 2729 Pa, and good reversibility after demagnetization process. This value competes with the best ones reported in the most recent literature. We have compared the obtained results with our previous reported ones by using high magnetization Fe NPs fabricated by the electrical explosion of wire method (Fe-EEW).

Local heat generation from magnetic nanoparticles (MNPs) exposed to alternating magnetic fields can revolutionize cancer treatment. However, the application of MNPs as anticancer agents is limited by serious drawbacks. Foremost among these are the fast uptake and biodegradation of MNPs by cells and the unpredictable magnetic behavior of the MNPs when they accumulate within or around cells and tissues. In fact, several studies have reported that the heating power of MNPs is severely reduced in the cellular environment, probably due to a combination of increased viscosity and strong NP agglomeration. Herein, we present an optimized protocol to coat magnetite (Fe 3 O 4 ) NPs larger than 20 nm (FM-NPs) with high molecular weight PEG molecules that avoid collective coatings, prevent the formation of large clusters of NPs and keep constant their high heating performance in environments with very different ionic strengths and viscosities (distilled water, physiological solutions, agar and cell culture media). The great reproducibility and reliability of the heating capacity of this FM-NP@PEG system in such different environments has been confirmed by AC magnetometry and by more conventional calorimetric measurements. The explanation of this behavior has been shown to lie in preserving as much as possible the magnetic single domain-type behavior of nearly isolated NPs. In vitro endocytosis experiments in a colon cancer-derived cell line indicate that FM-NP@PEG formulations with PEGs of higher molecular weight (20 kDa) are more resistant to endocytosis than formulations with smaller PEGs (5 kDa), showing quite large uptake mean-life (τ > 5 h) in comparison with other NP systems. The in vitro magnetic hyperthermia was performed at 21 mT and 650 kHz during 1 h in a pre-endocytosis stage and complete cell death was achieved 48 h posthyperthermia. These optimal FM-NP@PEG formulations with high resistance to endocytosis and predictable magnetic response will aid the progress and accuracy of the emerging era of theranostics.

Manganese/iron ferrite nanoparticles with different Mn 2+/3+ doping grades have been prepared by a thermal decomposition optimized approach so as to ascertain the doping effect on magnetic properties and, especially, on the magnetic hyperthermia response. The oxidation state and interstitial position of Mn in the spinel structure is found to be critical. The particle size effect has also been studied by growing one of the prepared samples (from 10 to 15 nm in diameter) by a seed mediated growth mechanism. After analyzing the main structural and chemical parameters such as the Mn/Fe rate, crystalline structure, particle diameter, shape and organic coating, some Mn doping induced changes have been observed, such as the insertion of Mn 2+ cations yielded more anisotropic shapes. Magnetic characterization, carried out by DC magnetometry (M(H), M(T)) and electron magnetic resonance (EMR) techniques, has shown interesting differences between samples with varying compositions. Lower Mn doping levels lead to larger saturation magnetization values, while an increase of the Mn content causes the decrease of the effective magnetic anisotropy constant at low T. The homogeneous magnetic response under applied magnetic fields, together with the great effect of nanoparticle size and shape in such a response, has been confirmed by the EMR analysis. Finally, a detailed magnetic hyperthermia analysis has demonstrated the large influence of NP size and shape on the magnetic hyperthermia response. The optimized Mn 0.13 Fe 2.87 O 4 _G sample with a diameter of 15 nm and slightly truncated octahedral shape is presented as an interesting candidate for future magnetic hyperthermia mediated biomedical treatments.

To improve the selectivity of magnetic nanoparticles for tumor treatment by hyperthermia, Fe 3 O 4 nanoparticles have been functionalized with a peptide of the type arginine-glycine-aspartate (RGD) following a "click" chemistry approach. The RGD peptide was linked onto the previously coated nanoparticles in order to target α v β 3 integrin receptors over-expressed in angiogenic cancer cells. Different coatings have been analyzed to enhance the biocompatibility of magnetic nanoparticles. Monodispersed and homogeneous magnetite nanoparticles have been synthesized by the seed growth method and have been characterized using X-ray diffraction, thermogravimetric analysis, infrared spectroscopy, transmission electron microscopy and magnetic measurements. The magnetic hyperthermia efficiency of the nanoparticles has also been investigated and cytotoxicity assays have been perfomed for functionalized nanoparticles., (Copyright © 2018 Elsevier B.V. All rights reserved.)

With the aim of studying the influence of synthesis parameters in structural and magnetic properties of cobalt-doped magnetite nanoparticles, Fe 3- x Co x O₄ (0 < x < 0.15) samples were synthetized by thermal decomposition method at different reaction times (30-120 min). The Co ferrite nanoparticles are monodisperse with diameters between 6 and 11 nm and morphologies depending on reaction times, varying from spheric, cuboctahedral, to cubic. Chemical analysis and X-ray diffraction were used to confirm the composition, high crystallinity, and pure-phase structure. The investigation of the magnetic properties, both magnetization and electronic magnetic resonance, has led the conditions to improve the magnetic response of doped nanoparticles. Magnetization values of 86 emu·g -1 at room temperature (R.T.) have been obtained for the sample with the highest Co content and the highest reflux time. Magnetic characterization also displays a dependence of the magnetic anisotropy constant with the varying cobalt content., Competing Interests: The authors declare no conflict of interest.

Nanoparticulate NiO and NiO/C composites with different carbon proportions have been prepared for anode application in lithium and sodium ion batteries. Structural characterization demonstrated the presence of metallic Ni in the composites. Morphological study revealed that the NiO and Ni nanoparticles were well dispersed in the matrix of amorphous carbon. The electrochemical study showed that the lithium ion batteries (LIBs), containing composites with carbon, have promising electrochemical performances, delivering specific discharge capacities of 550 mAh/g after operating for 100 cycles at 1C. These excellent results could be explained by the homogeneity of particle size and structure, as well as the uniform distribution of NiO/Ni nanoparticles in the in situ generated amorphous carbon matrix. On the other hand, the sodium ion battery (NIB) with the NiO/C composite revealed a poor cycling stability. Post-mortem analyses revealed that this fact could be ascribed to the absence of a stable Solid Electrolyte Interface (SEI) or passivation layer upon cycling., Competing Interests: The authors declare no conflict of interest.

Highly monodispersed palladium nanoparticles have been synthesized by a two-phase reduction method using two different capping agents, alkylamines and alkanethiols. The influence of ligand type in the properties of palladium nanoparticles have been analyzed in detail by means of several techniques as Infrared and Ultraviolet-Visible Spectroscopy, X-ray Diffraction and Transmission Electron Microscopy. It is shown how the size can be tuned easily between 2 and 4 nm by using alkylamines ligands with carbon chains of different lengths, while keeping up high purity and crystallinity. The transfer of these nanoparticles to water phase has been achieved by the ligand exchange process. In contrast, when alkanethiols are used as stabilizers no correlation between carbon chain length and size has been observed. This distinct chemical reactivity between palladium and mentioned ligands produces some particular electronic and magnetic properties that are analyzed by Electron Magnetic Resonance. The presence of free radicals associated with palladium and capping agent bond has been confirmed. No evidences of ferromagnetic behavior coming from Palladium nanoparticles have been found out in any of the studied samples.

Four LiMn0.8Fe0.1M0.1PO4/C (M = Fe, Co, Ni, Cu) cathode materials have been synthesized via a freeze-drying method. The samples have been characterized by powder X-ray diffraction, transmission electron microscopy, magnetic susceptibility, and electrochemical measurements. The composition and effective insertion of the transition-metal substituents in LiMnPO4 have been corroborated by elemental analysis, the evolution of the crystallographic parameters, and the magnetic properties. The morphological characterization of the composites has demonstrated that the phosphate nanoparticles are enclosed in a matrix of amorphous carbon. Among them, LiMn0.8Fe0.1Ni0.1PO4/C is the most promising cathode material, providing a good electrochemical performance in all aspects: high voltage and specific capacity values, excellent cyclability, and good rate capability. This result has been attributed to several factors, such as the suitable morphology of the sample, the good connection afforded by the in situ generated carbon, and the amelioration of the structural stress provided by the presence of Ni(2+) and Fe(2+) in the olivine structure.

Monodispersed Fe3O4 nanoparticles have been synthesized by a thermal decomposition method based on the seeded-growth technique, achieving size tunable nanoparticles with high crystallinity and high saturation magnetization. EMR spectroscopy becomes a very efficient complementary tool to determine the fine details of size distributions of MNPs and even to estimate directly the size in a system composed of a given type of magnetic nanoparticles. The size and size dispersity affect directly the efficiency of MNPs for hyperthermia and EMR provides a direct evaluation of these characteristics almost exactly in the same preparation and with the same concentration as used in hyperthermia experiments. The correlation observed between the Specific Absorption Rate (SAR) and the effective gyromagnetic factor (geff) is extremely remarkable and renders a way to assess directly the heating capacity of a MNP system.

Magnetite nanoparticles have been synthesized at different temperatures in order to get nanoparticles of different average sizes. Powders of the synthesized nanoparticles were introduced in a radio frequency electromagnetic apparatus built to perform hyperthermia measurements in laboratory animals. The nanoparticles synthesized at 80 degrees C, the ones giving the largest specific absorption rate values, have been functionalized with different organic ligands to study the influence of functionalization on specific absorption rate values. In all the synthesized nanoparticles, with and without organic surroundings, specific absorption rate measurements have been performed to study the influence of applied magnetic field intensity an frequency.