Modulation Of Magnetic Properties Research Articles

Modulation of magnetic properties in self-assembled one-dimensional CoxFe3-xO4 nano-chains with Co substitution

Modulation of magnetic properties on the low dimensional material under multiple fields is a captivating area of study in material science and nano-technology. In this paper, we focus on the self-assembly of chain-like nanostructures composed of CoxFe3−xO4 nanoparticles with an average size of 150 nm. These structures, consisting of more than 20 nanoparticles, are formed at 90 °C under a 0.25 T external magnetic field. The length of chains is surprising to decrease with increasing Co content due to an obvious additional cubic magneto-crystalline anisotropy superposed on the uniaxial induced anisotropy which is induced by the synthesized magnetic field with easy axis along the length of the chain. The additional magneto-crystalline anisotropy field of Co blocks the chain growing in length with Co doping. Additionally, our X-ray magnetic circular dichroism (XMCD) measurements confirm the doping of Co2+ ions in the CoxFe3−xO4 nano-chains, where they predominantly occupy the B sites and substitute the Fe2+ ions. This finding underlines the importance of spin-orbit coupling enhancement in the magnetic behavior resulting from the Fe2+ substitution with Co2+.

Wireless magneto-ionics: voltage control of magnetism by bipolar electrochemistry

Modulation of magnetic properties through voltage-driven ion motion and redox processes, i.e., magneto-ionics, is a unique approach to control magnetism with electric field for low-power memory and spintronic applications. So far, magneto-ionics has been achieved through direct electrical connections to the actuated material. Here we evidence that an alternative way to reach such control exists in a wireless manner. Induced polarization in the conducting material immersed in the electrolyte, without direct wire contact, promotes wireless bipolar electrochemistry, an alternative pathway to achieve voltage-driven control of magnetism based on the same electrochemical processes involved in direct-contact magneto-ionics. A significant tunability of magnetization is accomplished for cobalt nitride thin films, including transitions between paramagnetic and ferromagnetic states. Such effects can be either volatile or non-volatile depending on the electrochemical cell configuration. These results represent a fundamental breakthrough that may inspire future device designs for applications in bioelectronics, catalysis, neuromorphic computing, or wireless communications.

Ionic liquid modulation of exchange bias in epitaxial LaMnO3 thin films

The magnetic ground state of LaMnO3 (LMO) thin film is still a controversial issue, even though various mechanisms, such as cation/anion non-stoichiometry, epitaxial strain, interfacial charge reconstruction, and orbital ordering, have been proposed. Here, exchange bias (EB) was introduced into a high-quality epitaxial LMO thin film via relatively low oxygen growth pressure. The EB in LMO was modulated by +2 V gating via ionic liquid method with increased EB field (HEB), coercivity (HC), blocking temperature (TB), and reduced ferromagnetic (FM) magnetization. However, the −2 V gating has a much weaker tunability. By investigating the change of structure, surface morphology, and Mn oxidation state in LMO thin films, the modulation of magnetic properties is attributed to the creation/annihilation of oxygen vacancy in an LMO thin film. The suppressed FM phase in LMO can be ascribed to reduced Mn valence, structure disorders, and structure transition. However, the enriched antiferromagnetic phase results from the transition of the pseudocubic structure to the distorted orthorhombic structure. This work not only highlights the importance of functional defects in perovskite oxides but also sheds light on the potential of electric-field modulation of magnetism in spintronic devices.

Violation of the rule of parsimony: Mixed local moment and itinerant Fe magnetism in Fe3GeN

Ternary iron nitrides are of considerable interest due to their diverse magnetic properties. We find, based on first principles calculations, that the relatively minor structural distortion from the cubic antiperovskite structure in Fe$_3$GeN leads to unusual magnetic behavior. In particular, there is a separation into Fe sites with very different magnetic behaviors, specifically a site with Fe atoms having a stable local moment and a site where the Fe shows characteristics of much more itinerant behavior. This shows a remarkable flexibility of the Fe magnetic behavior in these nitrides and points towards the possibility of systems where minor structural and chemical changes can lead to dramatic changes in magnetic properties. The results suggest that, analogously to oxide perovskite materials, modulation of magnetic properties via chemical or strain control of octahedral rotation may be feasible. This may then lead to approaches for tuning magnetism to realize properties of interest, for example tuning magnetic transitions to quantum critical regimes or to proximity to metamagnetic transitions of interest for devices.

Modulation of Magnetic Properties in Ni0.4Zn0.6Fe₂O₄ Spinel Ferrite by Additives

Sintered NiSUB0.4/SUBZnSUB0.6/SUBFe₂O₄ ferrite with various additives, namely, CoO, Cu₂O, SiO₂, CaCO₃, and MgO was prepared by conventional ceramic processes. The formation of a single-phase cubic spinel structure was confirmed by powder X-ray diffraction. The microstructure and magnetic properties of the samples were significantly changed by the type of additive. In the frequency-dependent complex permeability (μ

Modulation of Magnetic Properties at the Nanometer Scale in Continuously Graded Ferromagnets.

Ferromagnetic alloy materials with designed composition depth profiles provide an efficient route for the control of magnetism at the nanometer length scale. In this regard, cobalt-chromium and cobalt-ruthenium alloys constitute powerful model systems. They exhibit easy-to-tune magnetic properties such as saturation magnetization MS and Curie temperature TC while preserving their crystalline structure over a wide composition range. In order to demonstrate this materials design potential, we have grown a series of graded Co1−xCrx and Co1−wRuw (100) epitaxial thin films, with x and w following predefined concentration profiles. Structural analysis measurements verify the epitaxial nature and crystallographic quality of our entire sample sets, which were designed to exhibit in-plane c-axis orientation and thus a magnetic in-plane easy axis to achieve suppression of magnetostatic domain generation. Temperature and field-dependent magnetic depth profiles have been measured by means of polarized neutron reflectometry. In both investigated structures, TC and MS are found to vary as a function of depth in accordance with the predefined compositional depth profiles. Our Co1−wRuw sample structures, which exhibit very steep material gradients, allow us to determine the localization limit for compositionally graded materials, which we find to be of the order of 1 nm. The Co1−xCrx systems show the expected U-shaped TC and MS depth profiles, for which these specific samples were designed. The corresponding temperature dependent magnetization profile is then utilized to control the coupling along the film depth, which even allows for a sharp onset of decoupling of top and bottom sample parts at elevated temperatures.

Influence of Tuned Linker Functionality on Modulation of Magnetic Properties and Relaxation Dynamics in a Family of Six Isotypic Ln2 (Ln = Dy and Gd) Complexes.

A coordination complex family comprising of six new dinuclear symmetric lanthanide complexes, namely, [Ln2(Lx)2(L')2(CH3OH)2]·yG (H2Lx: three related yet distinct Schiff-base linkers; x = 1-3, according to the nomenclature of the Schiff-base linker employed herein. HL': 2,6-dimethoxyphenol. yG refers to crystallographically assigned guest solvent species in the respective complexes; y = number of solvent molecules; LnIII = Dy/Gd) were isolated employing a mixed-ligand strategy stemming out of a strategic variation of the functionalities introduced among the constituent Schiff-base linkers. The purposeful introduction of three diverse auxiliary groups with delicate differences in their electrostatic natures affects the local anisotropy and magnetic coupling of LnIII ion-environment in the ensuing Ln2 dinuclear complexes, consequentially resulting into distinctly dynamical magnetic behaviors among the investigated new-fangled family of isotypic Ln2 complexes. Among the entire family, subtle alterations in the chemical moieties render two of the Dy2 analogues to behave as single molecule magnets, while the other Dy2 congener merely exhibits slow relaxation of the magnetization. The current observation marks one of the rare paradigms, wherein magnetic behavior modulation was achieved by virtue of the omnipresent influence of subtly tuned linker functionalities among the constituent motifs of the lanthanide nanomagnets. To rationalize the observed difference in the magnetic coupling, density functional theory and ab initio calculations (CASSCF/RASSI-SO/POLY_ANISO) were performed on all six complexes. Subtle difference in the bond angles leads to difference in the J values observed for Gd2 complexes, while difference in the tunnel splitting associated with the structural alterations lead to variation in the magnetization blockade in the Dy2 complexes.

Host-Guest [2+2] Cycloaddition Reaction: Postsynthetic Modulation of CO2 Selectivity and Magnetic Properties in a Bimodal Metal-Organic Framework.

Simultaneous tuning of permanent porosity and modulation of magnetic properties by postsynthetic modification (PSM) with light in a metal-organic framework is unprecedented. With the aim of achieving such a photoresponsive porous magnetic material, a 3D photoresponsive biporous framework, MOF1, which has 2D channels occupied by the guest 1,2-bis(4-pyridyl)ethylene (bpee), H2 O, and EtOH molecules, has been synthesized. The guest bpee in 1 is aligned parallel to pillared bpee with a distance of 3.9 Å between the ethylenic groups; this allows photoinduced PSM of the pore surface through a [2+2] cycloaddition reaction to yield MOF2. Such photoinduced PSM of the framework structure introduces enhanced CO2 selectivity over that of N2 . The higher selectivity in MOF2 than that of MOF1 is studied through theoretical calculations. Moreover, MOF2 unveils reversible changes in Tc with response to dehydration-rehydration. This result demonstrates that photoinduced PSM is a powerful tool for fabricating novel functional materials.

Synthesis and magnetic properties of Ni–BaTiO3 nanocable arrays within ordered anodic alumina templates

Modulation of magnetic properties and magnetoelectric coupling enhancement provided by ferromagnetic (Ni)/dielectric (BaTiO3) coaxial nanocable arrays.

Modulation of magnetic properties at room temperature: coordination-induced valence tautomerism in a cobalt dioxolene complex.

The valence-tautomeric six-coordinate complex [Co(tbdiox)2(4-papy)2] (1; tbdiox = redox-active 3,5-di-tert-butyl-o-dioxolene, 4-papy = 4-phenylazopyridine) was synthesized and its electronic structure examined. Whereas 1 shows regular thermally driven valence tautomerism in the solid state, it partially dissociates in solution to form the five-coordinate species [Co(tbdiox)2(4-papy)] (2) and free 4-papy. Species 1 and 2 exhibit different electronic structures-low-spin (ls) Co(III) and high-spin (hs) Co(II), respectively-in solution at room temperature and therefore different magnetic properties. Since 1 and 2 are in an equilibrium that is 4-papy-dependent, the magnetic moment of the solution species can be tuned by means of the ligand content. Thus, the concept of coordination-induced valence tautomerism (CIVT) has been introduced. The electronic structures of 1 and 2 as well as their CIVT were elucidated by X-ray crystallography, electrochemistry, titration experiments, and all variable-temperature SQUID susceptometry, NMR, EPR, and electronic absorption spectroscopy. The experimental findings are strongly supported by broken-symmetry DFT calculations. The magnetic exchange interactions in different types of valence-tautomeric cobalt complexes were explored computationally.

Modulation of magnetic properties and enhanced magnetoelectric effects in MnW1–xMoxO4 compounds

In this letter, we investigate the magnetic and ferroelectric properties of polycrystalline MnW1–xMoxO4 (x = 0, 0.05, 0.10, 0.20) compounds. The substitution of nonmagnetic Mo6+ ions for W6+ ions modifies the magnetic transition temperatures of MnW1–xMoxO4 by changing the Mn—O—Mn bond. As a result, distinct ferroelectric properties and enhanced magnetoelectric effects are observed in Mo6+ -doped MnWO4 compounds. The effects of substitution of Mo6+ ions on magnetic properties and magnetoelectric coupling are discussed.

Novel approaches to field modulation of electronic and magnetic properties of oxides

The interplay of electronic charge and spin in many of the novel multicomponent oxides presents opportunities for new device concepts. In this paper we summarize three different approaches to making field-modulated devices. The first is the observation of a giant electroresistance (ER) effect in the colossal magnetoresistive manganites, where it is shown that in the same system two phenomena operate, colossal magnetoresistance (CMR) and colossal electroresistance (CER) and both processes are complementary. In the second example we show the modulation of the magnetic property of a diluted magnetic semiconductor by an electric field but the role of unidentified ferromagnetic entities cannot be ruled out at this stage. In the third and last case we show the example of the multiferroic materials where the magnetic properties are field dependent as well, but for totally different reasons.

Ferromagnetism in II‐VI‐Based Semiconductor Structures

AbstractFor Abstract see ChemInform Abstract in Full Text.

Ferromagnetism in II–VI-based semiconductor structures

Experimental results obtained on Zn 1− x Mn x Te layers and Cd 1− x Mn x Te quantum wells are surprisingly well understood in the framework of a mean field model of the carrier-induced ferromagnetic transition, provided the real structure of the valence band is properly taken into account. Here we put the emphasis on effects leading to deviations from the standard model: RKKY oscillations in Zn 1− x Mn x Te when the Mn concentration is not high enough with respect to the carrier density, electronic disorder and localization at low carrier density in Zn 1− x Mn x Te epilayers and Cd 1− x Mn x Te quantum wells. Importantly, the modulation of magnetic properties through modulation of the carrier density, either optically or using the electric potential in a pin diode, is demonstrated.

Synthesis and magnetic properties of CoFe2O4 spinel ferrite nanoparticles doped with lanthanide ions

Lanthanide ions have been doped into cobalt spinel ferrites using an oil-in-water micellar method to form CoLn0.12Fe1.88O4 nanoparticles with Ln=Ce, Sm, Eu, Gd, Dy, or Er. Doping with lanthanide ions (LnIII) modulates the magnetic properties of cobalt spinel ferrite nanoparticles. In particular cases of Gd3+ or Dy3+ ions, a dramatic increase in the blocking temperature and coercivity is observed. Indeed, the introduction of only 4% of Gd3+ ions increases the blocking temperature ∼100 K and the coercivity 60%. Initial studies on the magnetic properties of these doped nanoparticles clearly demonstrate that the relationship between the modulation of magnetic properties and the nature of doped LnIII ions is interesting but very complex.

Simultaneous substitution of Co2+and Zn2+ions in submicronic acicular γ - Fe2O3particles

In iron sesquioxide of acicular shaded γ-Fe <inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</inf> O <inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</inf> simultaneous substitution of Co <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2+</sup> and Zn <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2+</sup> ions leads to the formation of mixed-defect ferrites and modulation of magnetic properties is of interest for their application to high density magnetic recording. It is shown that the coercive force, remanent magnetization and saturation-magnetization are controlled by a judicious choice of the contents of Co <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2+</sup> and Zn <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2+</sup> , while it is indispensable to optimize the morphological features like the average size of the crystallites, the shape, the size and texture of the particles. A high value of coercive force (650-700 Oe) and of the remanent magnetization (35-45 emu/g) had been obtained with a minimal content of cobalt ions (Co <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2+</sup> = 2.5 to 3% by wt.) permitting limits to the magnetocrystalline anisotropy of these compounds and their thermal variation near the ambient temperature. The influence of the zinc content had been systematically studied notably in relation to its effect on the structural, morphological and magnetic properties of the ferrites.