FeNi-based magnetoimpedance multilayers: Tailoring of the softness by magnetic spacers

The microstructure and magnetic properties of sputtered permalloy films and FeNi(170 nm)/X/FeNi(170 nm) (X=Co, Fe, Gd, Gd-Co) sandwiches were studied. Laminating of the thick FeNi film with various spacers was done in order to control the magnetic softness of FeNi-based multilayers. In contrast to the Co and Fe spacers, Gd and Gd-Co magnetic spacers improved the softness of the FeNi/X/FeNi sandwiches. The magnetoimpedance responses were measured for [FeNi/Ti(6 nm)] 2/FeNi and [FeNi/Gd(2 nm)] 2/FeNi multilayers in a frequency range of 1-500 MHz: for all frequencies under consideration the highest magnetoimpedance variation was observed for [FeNi/Gd(2 nm)] 2/FeNi multilayers. © 2012 American Institute of Physics

Crossover from superspin glass to superferromagnet in FexAg100-x nanostructured thin films ( 20 ≤ x ≤ 50 )

FexAg100?x granular thin films, with 20 x 50, have been prepared by the dc-magnetron sputtering deposition technique. With this technique we have been able to obtain samples comprising small Fe nanoparticles 2.5?3 nm embedded in a Ag matrix, remaining their size practically constant with increasing Fe content. Their magnetic behavior has been fully characterized by dc magnetic measurements between 5?350 K. They have revealed a crossover in the collective magnetic behavior of the Fe nanoparticles around a 35 at. %. Below such a concentration, a collective freezing of the magnetic moments is observed at low temperatures, while at high temperatures a transition, mainly mediated by dipolar interactions, to a magnetically disordered state is obtained. Above this concentration, direct exchange interactions overcome the dipolar magnetic interactions and a long-range order tends to prevail in the range of temperatures analyzed. ac magnetic measurements have indicated a crossover from a superspin glass x35 to a superferromagnetic x35 behavior for the magnetic moments of the Fe nanoparticles.This work was supported by the CICYT of Spain under Contracts No. MAT2008-06542-C04-02 and No. MAT2008- 06542-C04-04. SGIker technical support MEC, GV/EJ, European Social Fund is gratefully acknowledged. The financial support from the Basque Government Department of Education Project No. IT-347-07 is acknowledged

Magnetotactic bacteria for cancer therapy

Magnetotactic bacteria (MTB) are aquatic microorganisms that are able to biomineralize membrane-enclosed magnetic nanoparticles called magnetosomes. Inside the MTB, magnetosomes are arranged in a chain that allows MTB to align and navigate along the Earth's magnetic field. When isolated from the MTB, magnetosomes display a number of potential applications for targeted cancer therapies, such as magnetic hyperthermia, localized drug delivery, or tumor monitoring. The characteristics and properties of magnetosomes for these applications exceed in several aspects those of synthetic magnetic nanoparticles. Likewise, the whole MTB can also be considered as promising agents for cancer treatment, taking advantage of their self-propulsion capability provided by their flagella and the guidance capabilities ensured by their magnetosome chain. Indeed, MTB are envisaged as nanobiots that can be guided and manipulated by external magnetic fields and are naturally attracted toward hypoxic areas, such as the tumor regions, while retaining the therapeutic and imaging capacities of the isolated magnetosomes. Moreover, unlike most of the bacteria currently tested in clinical trials for cancer therapy, MTB are not pathogenic but could be engineered to deliver and/or express specific cytotoxic molecules. In this article, we will review the progress and perspectives of this emerging research field and will discuss the main challenges to overcome before the use of MTB can be successfully applied in the clinic.The Spanish and Basque Governments are acknowledged for funding under Project Nos. MAT2017-83631-C3-R and IT-1245-19, respectively

High-magnetic field characterization of magnetocaloric effect in FeZrB(Cu) amorphous ribbons

"The magnetic and magnetocaloric properties of a series of Fe-rich FeZrB(Cu) amorphous ribbons were investigated under magnetic field values up to mu H-0 of 8 T. A correlation between the saturation magnetization and the maximum magnetic entropy change vertical bar Delta S-M(peak)vertical bar is clearly evidenced. Although these metallic glasses show relatively low vertical bar Delta S-M(peak)vertical bar values (from 3.6 to 4.4 J kg(-1) K-1 for mu(0)Delta H - 8 T), the Delta S-M(T) curve broadens upon the increase in mu(0)Delta H, giving rise to a large refrigerant capacity RC (above 900 J kg(-1) for mu(0)Delta H-8 T). Using the universal curve method for rescaling the Delta S-M(T, mu(0)Delta H) curves, we found a collapse of the curves around the Curie temperature. However, in the low-temperature range the curves do not match into a single one due to the existence of magnetic frustration.

A Milestone in the Chemical Synthesis of Fe3O4 Nanoparticles Unreported Bulklike Properties Lead to a Remarkable Magnetic Hyperthermia

Among iron oxide phases, magnetite Fe3O4 is often the preferred one for nanotechnological and biomedical applications because of its high saturation magnetization and low toxicity. Although there are several synthetic routes that attempt to reach magnetite nanoparticles NPs , they are usually referred as IONPs iron oxide NPs due to the great difficulty in obtaining the monophasic and stoichiometric Fe3O4 phase. Added to this problem is the common increase of size shape polydispersity when larger NPs D gt; 20 nm are synthesized. An unequivocal correlation between a nanomaterial and its properties can only be achieved by the production of highly homogeneous systems, which, in turn, is only possible by the continuous improvement of synthesis methods. There is no doubt that solving the compositional heterogeneity of IONPs while keeping them monodisperse remains a challenge for synthetic chemistry. Herein, we present a methodical optimization of the iron oleate decomposition method to obtain Fe3O4 single nanocrystals without any trace of secondary phases and with no need of postsynthetic treatment. The average dimension of the NPs, ranging from 20 to 40 nm, has been tailored by adjusting the total volume and the boiling point of the reaction mixture. Mössbauer spectroscopy and DC magnetometry have revealed that the NPs present a perfectly stoichiometric Fe3O4 phase. The high saturation magnetization 93 2 A m2 kg at RT and the extremely sharp Verwey transition at around 120 K shown by these NPs have no precedent. Moreover, the synthesis method has been refined to obtain NPs with octahedral morphology and suitable magnetic anisotropy, which significantly improves the magnetic hyperthemia performance. The heating power of properly PEGylated nano octahedrons has been investigated by AC magnetometry, confirming that the NPs present negligible dipolar interactions, which leads to an outstanding magnetothermal efficiency that does not change when the NPs are dispersed in environments with high viscosity and ionic strength. Additionally, the heat production of the NPs within physiological media has been directly measured by calorimetry under clinically safe conditions, reasserting the excellent adequacy of the system for hyperthermia therapies. To the best of our knowledge, this is the first time that such bulklike magnetite NPs with minimal size shape polydispersity, minor agglomeration, and exceptional heating power are chemically synthesize

Size-induced superantiferromagnetism with reentrant spin-glass behavior in metallic nanoparticles of TbCu2

An unusual 4f -superantiferromagnetic state characterized by simultaneous antiferromagnetic and spin-glass behaviors induced by particle-size reduction is revealed in metallic nanoparticles (≈ 9 nm) of TbCu 2 . The Néel temperature is 46 K and the glassy freezing is below ≈ 9 K and governed by a critical slowing down process. Neutron diffraction at 1.8 K establishes the superantiferromagnetism. The latter is settled by the nanoparticle moments and the freezing mechanism is provided by the surface spins

Controlled Magnetic Anisotropy in Single Domain Mn-doped Biosynthesized Nanoparticles

Magnetotactic bacteria Magnetospirillum gryphiswaldense synthesize cubo-octahedral shaped magnetite nanoparticles, called magnetosomes, with a mean diameter of 40 nm. The high quality of the biosynthesized nanoparticles makes them suitable for numerous applications in fields like cancer therapy, among others. The magnetic properties of magnetite magnetosomes can be tailored by doping them with transition metal elements, increasing their potential applications. In this work, we address the effect of Mn doping on the main properties of magnetosomes by the combination of structural and magnetic characterization techniques. Energy-dispersive X-ray spectroscopy, X-ray absorption nearedge structure, and X-ray magnetic circular dichroism results reveal a Mn dopant percentage of utmost 2.3%, where Mn cations are incorporated as a combination of Mn2+ and Mn3+, preferably occupying tetrahedral and octahedral sites, respectively. Fe substitution by Mn notably alters the magnetic behavior of the doped magnetosomes. Theoretical modeling of the experimental hysteresis loops taken between 5 and 300 K with a modified Stoner-Wohlfarth approach highlights the different anisotropy contributions of the doped magnetosomes as a function of temperature. In comparison with the undoped magnetosomes, Mn incorporation alters the magnetocrystalline anisotropy introducing a negative and larger cubic anisotropy down to the Verwey transition, which appears shifted to lower temperature values as a consequence of Mn doping. On the other hand, Mn-doped magnetosomes show a decrease in the uniaxial anisotropy in the whole temperature range, most likely associated with a morphological modification of the Mn-doped magnetosomes.The Spanish and Basque Governments are acknowledged for funding under project numbers MAT2017- 83631-C3-R and IT-1245-19, respectively

Shaping Up Zn Doped Magnetite Nanoparticles from Mono and Bimetallic Oleates The Impact of Zn Content, Fe Vacancies, and Morphology on Magnetic Hyperthermia Performance

The currently existing magnetic hyperthermia treatments usually need to employ very large doses of magnetic nanoparticles MNPs and or excessively high excitation conditions H f gt; 1010 A m s to reach the therapeutic temperature range that triggers cancer cell death. To make this anticancer therapy truly minimally invasive, it is crucial the development of improved chemical routes that give rise to monodisperse MNPs with high saturation magnetization and negligible dipolar interactions. Herein, we present an innovative chemical route to synthesize Zn doped magnetite NPs based on the thermolysis of two kinds of organometallic precursors i a mixture of two monometallic oleates FeOl ZnOl , and ii a bimetallic ironzinc oleate Fe3 amp; 8722;yZnyOl . These approaches have allowed tailoring the size 10 amp; 8722;50 nm , morphology spherical, cubic, and cuboctahedral , and zinc content ZnxFe3 amp; 8722;xO4, 0.05 lt; x lt; 0.25 of MNPs with high saturation magnetization amp; 8805;90 Am2 kg at RT . The oxidation state and the local symmetry of Zn2 and Fe2 3 cations have been investigated by means of X ray absorption near edge structure XANES spectroscopy, while the Fe center distribution and vacancies within the ferrite lattice have been examined in detail through Mo amp; 776;ssbauer spectroscopy, which has led to an accurate determination of the stoichiometry in each sample. To achieve good biocompatibility and colloidal stability in physiological conditions, the ZnxFe3 amp; 8722;xO4 NPs have been coated with high molecular weight poly ethylene glycol PEG . The magnetothermal efficiency of ZnxFe3 amp; 8722;xO4 PEG samples has been systematically analyzed in terms of composition, size, and morphology, making use of the latest generation AC magnetometer that is able to reach 90 mT. The heating capacity of Zn0.06Fe2.94O4 cuboctahedrons of 25 nm reaches a maximum value of 3652 W g at 40 kA m and 605 kHz , but most importantly, they reach a highly satisfactory value 600 W g under strict safety excitation conditions at 36 kA m and 125 kHz . Additionally, the excellent heating power of the system is kept identical both immobilized in agar and in the cellular environment, proving the great potential and reliability of this platform for magnetic hyperthermia therapie

Morphological Transformations in the Magnetite Biomineralizing Protein Mms6 in Iron Solutions: A Small-Angle X-ray Scattering Study

Magnetotactic bacteria that produce magnetic nanocrystals of uniform size and well-defined morphologies have inspired the use of biomineralization protein Mms6 to promote formation of uniform magnetic nanocrystals in vitro. Small angle X-ray scattering (SAXS) studies in physiological solutions reveal that Mms6 forms compact globular three-dimensional (3D) micelles (approximately 10 nm in diameter) that are, to a large extent, independent of concentration. In the presence of iron ions in the solutions, the general micellar morphology is preserved, however, with associations among micelles that are induced by iron ions. Compared with Mms6, the m2Mms6 mutant (with the sequence of hydroxyl/carboxyl containing residues in the C-terminal domain shuffled) exhibits subtle morphological changes in the presence of iron ions in solutions. The analysis of the SAXS data is consistent with a hierarchical core–corona micellar structure similar to that found in amphiphilic polymers. The addition of ferric and ferrous iron ions to the protein solution induces morphological changes in the micellar structure by transforming the 3D micelles into objects of reduced dimensionality of 2, with fractal-like characteristics (including Gaussian-chain-like) or, alternatively, platelet-like structures