Increase In Coercivity Research Articles

Pr-modified microstructure enhances coercivity in Sm2Co17-type magnets

Optimizing components of the cellular structure is a strategy to enhance the magnetic performance of Sm2Co17-type magnets. In this study, Pr is used to modify the cellular structure in Sm2Co17-type magnets, achieving synergistic optimization of coercivity from 32.12 kOe to 34.71 kOe and remanence from 11.23 kGs to 11.36 kGs. Analyses reveal that the increased remanence is attributed to the enhanced saturation magnetization and better grain alignment in the Pr-5 magnet. The incomplete cellular structures and Cu-lean region near grain boundaries are ameliorated in the Pr-5 magnets. Meanwhile, the Pr-modified and Cu-enriched cellular boundary phase, which has a lower magnetocrystalline anisotropy field, enhances the pinning strength of the domain-wall and contributes to the increase in coercivity. The substitution of Pr for Sm has a lower substitution energy in SmCo5 than in Sm2Co17, leading to the slight enrichment of Pr in the 1:5H phase. However, excessive Pr leads to increased amounts of oxides and deteriorates magnetic properties. This work provides valuable insights into developing high-performance Sm2Co17-type magnets by optimizing the microstructure and microchemical components.

Strong Enhancement of Magnetic Coercivity Induced by Uniaxial Stress.

The performance of permanent magnets is intricately tied to their magnetic hysteresis loop. In this study, we investigate the heavy-fermion ferromagnet CeAgSb_{2} through magnetization measurements under uniaxial stress. We observe a 2400% increase in magnetic coercivity with just a modest stress of approximately 1kbar. This effect persists even after pressure release, attributable to stress-induced defects that efficiently pin domain walls. Other magnetic properties such as ordering temperature and saturation moment exhibit only weak pressure dependencies and display full reversibility. Our findings offer a promising route for increasing coercive field strength and enhancing the energy product in ferromagnetic materials and are potentially applicable to a broad spectrum of commercial or emerging magnetic applications.

Tailoring of magnetic phase: Co-doped SiC thin films grown by RF sputtering

In the present work, we investigate the influence of cobalt (Co) doping on the structural and magnetic properties of cobalt-doped silicon carbide (Co-SiC) thin films. The films were fabricated using DC/RF magnetron sputtering technique on Si (100) substrates at a temperature of 1200°C, with varying Co concentrations ranging from 5 to 16 at. (at%. X-ray diffraction (XRD) analysis unveiled the co-existence of CoSi2 and SiC phases in all the thin films. Surface morphological study through atomic force microscopy (AFM) revealed the densely packed nature of the films. Field emission scanning electron microscopy (FE-SEM) study showed that particles are uniformly distributed at the surface of the substrate. According to UV measurements, the films have high transmittance in the visible range, and as Co concentration rises, transmittance decreases. A magnetic phase transition from superparamagnetic to ferromagnetic behavior occurred with Co content surpassing 8 at% in the SiC thin films. Moreover, an increase in coercivity was observed from 38 Oe to 316 Oe as the doping concentration increased from 10 to 16 at%. This study represents an exploration into the induction of ferromagnetism through moderate Co doping in SiC thin films.

Swift heavy ions induced transformations in the structural and magnetic properties of Co/Pt multilayer thin films for magnetic storage applications

The integration of CoPt nanoparticles into an insulating matrix has garnered significant attention in material science, nanotechnology, and electronic engineering, particularly for their potential use in magnetic storage media. Precise control over the size, shape, and ordering of these nanoparticles is crucial. This study investigates the impact of swift heavy ion irradiation (120 MeV Ag+9) with varying ion fluences (1 × 1013 and 3 × 1013 ions/cm2) on the structural and magnetic properties of sputter-deposited Co/Pt multilayer thin films on quartz substrates. X-ray diffraction (XRD) analysis of the pristine samples reveals the presence of an FCC-structured CoPt alloy. In contrast, films irradiated with a fluence of 1 × 1013 ions/cm2 exhibit superlattice peaks (001) and (110), indicative of L10-structured CoPt alloy, whereas films subjected to 3 × 1013 ions/cm2 retain the FCC structure. This suggests that a fluence of 1 × 1013 ions/cm2 promotes ordering, while 3 × 1013 ions/cm2 induces disordering. Selected area electron diffraction (SAED) patterns from TEM confirm these structural transitions, while SQUID magnetometry reveals an increase in coercivity at 1 × 1013 ions/cm2, followed by a reduction at 3 × 1013 ions/cm2, consistent with the observed structural changes. These results demonstrate that carefully controlled ion fluences can effectively tailor the structural and magnetic properties of Co/Pt multilayers, enhancing their suitability for advanced magnetic storage applications.

Effect of 10 MeV electron irradiation on structural and magnetic properties of Ti- and Al- substituted strontium hexaferrite SrFe11.3Ti0.4Al0.3O19

The irradiation stability of Ti- and Al-substituted SrFe11.3Ti0.4Al0.3O19 strontium hexaferrite to 10 MeV electron irradiation with the fluences of 1014 and 2·1017 cm−2 was investigated using various characterization techniques such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectrum microanalysis, atomic force microscopy, Raman spectroscopy, vibrating sample magnetometry and magnetic force microscopy. Notable changes in lattice vibrations, magnetic domain microstructure and magnetization behavior were obtained after the electron irradiation with the fluence of 2·1017 cm−2. Phonon hardening observed by Raman spectroscopy confirms the increasing disorder in crystalline structure and the presence of spin-phonon coupling in the samples after electron irradiation with the fluence 2·1017 cm−2. It was found that the strongest spin-phonon interactions correspond to A1g vibration modes at trigonal bipyramidal 2b, 2a octahedral, 4f1 tetrahedral sites and E1g mode at 4f2 octahedral site in electron-irradiated SrFe11.3Ti0.4Al0.3O19 hexaferrite, while the most radiation-resistant phonon mode is A1g vibration of the Fe–O bonds at the 4f2 octahedral site. No significant change was observed in magnetic saturation magnitude after electron irradiation. The increase in coercivity and significant decrease of magnitude of the dM/dH derivative of magnetization curves with increasing radiation fluence is attributed to the increase in uniaxial magnetic-crystalline anisotropy. It is found that the fractal dimension of hierarchical magnetic domain structure in SrFe11.3Ti0.4Al0.3O19 continuously decreases with increasing fluence of 10 MeV electron irradiation, which can be caused by the distortion in uniaxial magnetocrystalline anisotropy and irradiation-induced defects.

Influence of Dy3+ doping on Mössbauer, magnetic and microwave absorption properties of M-type Ba0.5Ca0.5DyxFe12-xO19 hexaferrites

The present research paper reports a systematic study of the magnetic, and structural properties of Ba0.5Ca0.5DyxFe12-xO19 M-type hexaferrite. The dysprosium was doped @ x = 0 − 0.2, keeping Δx = 0.05, in BCDF by the sol–gel self-ignition technique. The sintering of the synthesized samples was performed for 4 h at 1050°C. The crystallographic analysis of the samples was made from the X-ray diffractograms (XRD), while the morphological and elemental analysis was made from field emission scanning electron microscopy (FESEM), and energy-dispersive X-ray spectroscopy (EDAX) profiles. The structural results revealed the formation of the M-type hexaferrite having P63/mmc as a space group along with the co-existence of a secondary Fe2O3 phase. FESEM micrographs exhibit the hexagonal platelets randomly arranged with agglomerations at some places giving rise to the random variations in particle size with varying ’x’. Magnetic measurements (VSM) show that the saturation magnetization (MS) and coercivity (HC) increase with the increasing Dy3+ doping pointing towards the fact that the Dy doping in Ba-Ca ferrite can be used to fabricate the hard ferrites with good saturation magnetization. The Mössbauer spectrum recorded at room temperature reveals five superimposed sextets representing the five Fe3+ ion sites. Investigating the Microwave absorption (MWA) characteristics in the frequency range 8 − 12 GHz (X-band), reveals that the sample with x = 0.1 having 3 mm thickness possesses good MWA power. Its minimum RL value for matching frequency 10.06 GHz is approximately −26.96 dB, indicating that more than 90 % of microwaves are absorbed. The current work offers the Dysprosium-doped BCDF hexaferrites, as promising candidatesfor microwave absorption applications.

Opening the Hysteresis Loop in Ferromagnetic Fe3GeTe2 Nanosheets Through Functionalization with TCNQ Molecules.

Ferromagnetic metal Fe3GeTe2 (FGT), whose structure exhibits weak van-der-Waals interactions between 5-atom thick layers, was subjected to liquid-phase exfoliation (LPE) in N-methyl pyrrolidone (NMP) to yield a suspension of nanosheets that were separated into several fractions by successive centrifugation at different speeds. Electron microscopy confirmed successful exfoliation of bulk FGT to nanosheets as thin as 6 nm. The ferromagnetic ordering temperature for the nanosheets gradually decreased with the increase in the centrifugation speed used to isolate the 2D material. These nanosheets were resuspended in NMP and treated with an organic acceptor, 7,7,8,8-tetracyano-quinodimethane (TCNQ), which led to precipitation of FGT-TCNQ composite. The formation of the composite material is accompanied by charge transfer from the FGT nanosheets to TCNQ molecules, generating TCNQ•- radical anions, as revealed by experimental vibrational spectra and supported by first principles calculations. Remarkably, a substantial increase in magnetic anisotropy was observed, as manifested by the increase in the coercive field from nearly zero in bulk FGT to 1.0 kOe in the exfoliated nanosheets and then to 5.4kOe in the FGT-TCNQ composite. The dramatic increase in coercivity of the composite suggests that functionalization with redox-active molecules provides an appealing pathway to enhancing magnetic properties of 2D materials.

Opening the Hysteresis Loop in Ferromagnetic Fe3GeTe2 Nanosheets Through Functionalization with TCNQ Molecules

Ferromagnetic metal Fe3GeTe2 (FGT), whose structure exhibits weak van‐der‐Waals interactions between 5‐atom thick layers, was subjected to liquid‐phase exfoliation (LPE) in N‐methyl pyrrolidone (NMP) to yield a suspension of nanosheets that were separated into several fractions by successive centrifugation at different speeds. Electron microscopy confirmed successful exfoliation of bulk FGT to nanosheets as thin as 6 nm. The ferromagnetic ordering temperature for the nanosheets gradually decreased with the increase in the centrifugation speed used to isolate the 2D material. These nanosheets were resuspended in NMP and treated with an organic acceptor, 7,7,8,8‐tetracyano‐quinodimethane (TCNQ), which led to precipitation of FGT‐TCNQ composite. The formation of the composite material is accompanied by charge transfer from the FGT nanosheets to TCNQ molecules, generating TCNQ•– radical anions, as revealed by experimental vibrational spectra and supported by first principles calculations. Remarkably, a substantial increase in magnetic anisotropy was observed, as manifested by the increase in the coercive field from nearly zero in bulk FGT to 1.0 kOe in the exfoliated nanosheets and then to 5.4 kOe in the FGT‐TCNQ composite. The dramatic increase in coercivity of the composite suggests that functionalization with redox‐active molecules provides an appealing pathway to enhancing magnetic properties of 2D materials.

Single-Phase L10-Ordered High Entropy Thin Films with High Magnetic Anisotropy.

The vast high entropy alloy (HEA) composition space is promising for discovery of new material phases with unique properties. This study explores the potential to achieve rare-earth-free high magnetic anisotropy materials in single-phase HEA thin films. Thin films of FeCoNiMnCu sputtered on thermally oxidized Si/SiO2 substrates at room temperature are magnetically soft, with a coercivity on the order of 10Oe. After post-deposition rapid thermal annealing (RTA), the films exhibit a single face-centered-cubic phase, with an almost 40-fold increase in coercivity. Inclusion of 50 at.% Pt in the film leads to ordering of a single L10 high entropy intermetallic phase after RTA, along with high magnetic anisotropy and 3 orders of magnitude coercivity increase. These results demonstrate a promising HEA approach to achieve high magnetic anisotropy materials using RTA.

Laser directed energy deposition of Alnico-8H from blended elemental powders: Effect of nickel increase on magnetic properties

Alnico-8H (14 wt% Ni) and Alnico-8H (19 wt% Ni) were additively fabricated from a blend of elemental powders with compositions (in wt.%) of 38Co-29Fe-14Ni-8Al-8Ti-3Cu and 33Co-29Fe-19Ni-8Al-8Ti-3Cu, respectively, using laser-directed energy deposition technique. Post additive fabrication both compositions were subjected to homogenization heat treatment at 1250 °C for 30 min and magnetic annealed at 650 °C under 2.5 T magnetic field for 60 mins (1 hr). X-ray diffraction was employed for studying the phase evolution. Scanning and transmission electron microscopes were utilized for characterization of Alnico alloys. The targeted compositions for Alnico-8H (14 wt% Ni) and Alnico-8H (19 wt% Ni) were nearly achieved in the L-DED processed samples. homogenization at 1250 °C, followed by magnetic annealing at 650 °C, resulted in an increase in grain size. The transmission electron microscopy revealed the presence of ferromagnetic α1 and paramagnetic α2 phases in the magnetic annealed microstructure. The increase in Nickel content from 14 to 19 wt% resulted in increase in coercivity (242 to 255 Oe), remanence (4437 to 8659 G), and maximum energy product (BHmax) (0.27 to 0.53 MGOe).

The effect of Ar+ and N+ ion irradiation on the thermally induced evolution of the structural and magnetic properties of Co/Pt and Pt/Co bilayered stacks

The application of Co–Pt thin films as functional elements of novel nanoelectronics and spintronics devices requires the formation of a homogeneous ferromagnetic CoPt phase with tunable magnetic properties. A diffusion-controlled synthesis of this ferromagnetic phase can be implemented through the annealing of deposited Co/Pt bilayers. Apart from thermal treatment, both structural and magnetic properties of such layered stacks can be affected by ion preirradiation. In this work, we, therefore, studied the effect of a two-stage process consisting of preirradiation with 110 keV Ar+/N+ ions followed by post-annealing in vacuum at 550°С for 30 min on the evolution of the structural, chemical, and magnetic properties of Co/Pt/substrate and Pt/Co/substrate heterostructures. The results obtained for such two-stage processing were compared to those received after single-stage vacuum annealing. It was found that when ion preirradiation is followed by annealing, the diffusion-driven intermixing of Pt and Co leading to the formation of the ferromagnetic Co–Pt phase is slowed down compared to the non-irradiated samples, which is associated with the barrier effect of implanted projectiles. Furthermore, we demonstrate that preirradiation does not compromise the magnetic properties of the samples. For instance, preirradiation leads to a coercivity increase of up to 38 % compared to the non-irradiated annealed samples which is attributed to the presence of remaining paramagnetic Pt between the grains of the ferromagnetic A1-CoPt phase. We demonstrate that the applied two-stage processing (consisting of ion preirradiation followed by thermal annealing) of magnetic thin films is a promising approach for tailoring their magnetic properties such as the in-plane coercivity, saturation, and effective magnetization.

Exploring Microstructure and Magnetic Domain Evolution in the As-cast Soft Magnetic Fe74B20Nb2Hf2Si2 Alloy: A Comprehensive Study Using STEM, Lorentz TEM, and LM-STEM DPC Microscopy

This study delves into subtle changes in the microstructure and domain arrangement of a Fe74B20Nb2Hf2Si2 soft magnetic amorphous alloy. Utilizing transmission electron microscopy in Lorentz mode, low-magnification STEM, and differential phase contrast analysis (DPC), the research explores both the as-cast state and annealed samples. The results confirmed the formation of α-Fe, Fe23B6, Fe2(Hf, Nb), and Fe2B crystalline phases with increasing annealing temperature. Consequently, these crystallization stages induce significant alterations in magnetic domain size and spatial distribution due to microstructural changes. As the crystallization temperature rises, the volume fraction of crystalline phases increases, leading to modifications in the arrangement and size of magnetic domains. The decrease in magnetic domain size, associated with the formation of pinning sites during heat treatment, leads to alterations in soft magnetic properties. This includes an increase in coercivity (Hc) up to 40 A/m in the sample annealed at the temperature range of the third crystallization stage compared to the as-cast sample (1.5 A/m). Furthermore, as the annealing temperature rises, there is a corresponding increase in saturation magnetization (Ms), which reached to 1.71 T in the sample annealed within the temperature range of the third crystallization stage. These findings hold substantial implications for the practical applications of the Fe-based soft bulk metallic glasses (BMGs) alloy across various industries.

Synthesis, characterization, and gas-sensing application of Cd0.5Zn0.5NdxFe2–xO4 nanoparticles

Fabrication of Cd0.5Zn0.5NdxFe2–xO4 nanoparticles, with x = 0.00, 0.01, 0.02, 0.04, 0.06, and 0.08, has been carried out using a wet chemical co-precipitation method. The effect of the rare earth Nd3+ doping on the prepared ferrites was structurally investigated using x-ray diffraction (XRD) along with Rietveld refinement. The results indicate great crystallinity in the FCC Fd3m spinel structure of Cd0.5Zn0.5NdxFe2–xO4 nanoparticles. The lattice parameter increases with the increase of doping concentration from 8.5378 until 8.5432 Å and the crystallite size obtained using Debye-Sherrer, Williamson–Hall, Size-strain plot (SSP), and Halder-Wagner (H-W) methods, decreases until the solubility limit of the materials is at x = 0.04. By using transmission electron microscopy (TEM), the morphological analysis reveals the spherical shape of the samples with minor agglomeration with the aid of using a Polyvinylpyrrolidone (PVP) capping agent. The grain size ranges from 14.37 to 15.24 nm. Raman spectroscopy verifies the incorporation of Nd3+ in the octahedral sites and the decrease in particle size. The elemental composition was verified using x-ray photoelectron spectroscopy (XPS). The magnetic properties were studied using a vibrating sample magnetometer (VSM) and it shows superparamagnetic behavior with a decrease in the saturation magnetization from 2.207 to 1.918 emu g−1 and an increase in coercivity from 7.194 to 14.397 G. The prepared materials were tested as liquefied petroleum gas (LPG) sensors by studying their sensitivity, selectivity, optimum working temperature, response, and recovery times. Nd3+ doping shows a great increase in LPG sensing sensitivity 4 to 20 times than the pure samples. The doping concentration also decreases the response and recovery times.

Insight into the effect of Ce content on the magnetic properties of Ce-magnets with grain boundary diffusion Pr-Al alloys

The development of cost-effective Ce-magnets with high Ce content is urgent to realize the vision of cost reduction and performance enhancement. Dual-main-phase Ce-magnets with different Ce content (Ce accounted for the total amount of rare earths is 40%, 50% and 60%) are prepared. The Pr80Al20 (at%) alloy is selected as diffusion source for the three magnets using the grain boundary diffusion technique under the same conditions. The correlation of magnetic properties and microstructures before and after diffusion with different Ce contents are systematically analyzed. According to the EPMA results, the presence of Ce in the magnets facilitates the diffusion of Pr elements along the grain boundaries, which significantly increases the diffusion depth of Pr inside the magnets. As a consequence, the percentage increment of coercivity increase with the Ce content due to the increased diffusion depth. This study provides new insight into the preparation of dual-main-phase Ce-magnets with high Ce content of 40–60%.

Effect of grain structure on the magnetic properties of AlNiCo 8 alloys

AlNiCo alloy has gained popularity again in recent years due to its good corrosion resistance, affordability, and superior performance at high temperature. However, the lower magnetic properties of AlNiCo limit its wide variety of applications. Directional solidification process is a key process that affects the properties of AlNiCo alloy. During the solidification process, grains with various structures are formed due to the difference of cooling rate at different positions of the ingot. As the cooling rate slows down, the average grain size gradually increases, and orientation degree of the grains becomes better, resulting in the increase of coercivity (Hc) and remanence (Br). Therefore, the top sample has the best Hc and Br, the bottom is the worst, and the middle is between the two. It is found that when the average grain size increases, the percentage of transverse grain boundaries and high angle grain boundaries (HAGBs) decrease, the truncated α1 phase decreases, and the Hc rises, whereas the magnetic moment along the easy-axis direction is not affected by the external magnetic field when the grain orientation coincides, and the Br value increases, and the Br value increases. Large and highly oriented grains are associated with excellent performance, providing a new method to enhancing magnetic properties by regulating the grain structure.

Magnetic Hardening: Unveiling Magnetization Dynamics in Soft Magnetic Fe-Ni-B-Nb Thin Films at Cryogenic Temperatures.

Recent advancements in amorphous materials have opened new avenues for exploring unusual magnetic phenomena at the sub-nanometer scale. We investigate the phenomenon of low-temperature "magnetic hardening" in heterogeneous amorphous Fe-Ni-B-Nb thin films, revealing a complex interplay between microstructure and magnetism. Magnetization hysteresis measurements at cryogenic temperatures show a significant increase in coercivity (HC) below 25 K, challenging the conventional Random Anisotropy Model (RAM) in predicting magnetic responses at cryogenic temperatures. Heterogeneous films demonstrate a distinct behavior in field-cooled and zero-field-cooled temperature-dependent magnetizations at low temperatures, characterized by strong irreversibility. This suggests spin-glass-like features at low temperatures, which are attributed to exchange frustration in disordered interfacial regions. These regions hinder direct exchange coupling between magnetic entities, leading to magnetic hardening. This study enhances the understanding of how microstructural intricacies impact magnetic dynamics in heterogeneous amorphous thin films at cryogenic temperatures.

Controllable synthesis and magnetization of Fe3O4 microspheres wrapped with amorphous carbon

A straightforward solvothermal methodology was employed to synthesize [Formula: see text] microspheres and [Formula: see text]@C hybrids, where amorphous carbon encapsulated [Formula: see text] microspheres. This encapsulation was achieved by meticulously controlling the reaction duration and glucose concentrations within the hydrothermal process. Analysis via X-ray diffraction and Raman spectroscopy confirmed that all specimens retained a homogeneous [Formula: see text] phase. Following encapsulation, the [Formula: see text] particles were uniformly distributed across the amorphous carbon spheres, with fine particle sizes in the hybrids measuring less than 20 nm. Magnetic characterization revealed that parameters such as saturation magnetization, remanent magnetization, and coercivity of the [Formula: see text] microspheres could be significantly adjusted by varying the hydrothermal reaction time. Notably, the hybrids exhibited a 5- to 10-fold increase in both coercivity and remanent magnetization when compared to the pristine [Formula: see text] microspheres. Nonetheless, the saturation magnetization of the hybrids reached up to 90% of that observed in bulk [Formula: see text]. These magnetic properties are predominantly influenced by the size effect associated with the nanostructured [Formula: see text].

Magnetic response of Ho3+ doped Ni0.4Cu0.6HoyFe2-yO4 spinel ferrites and their correlation with crystallite size

This study investigates the magnetic response of Ho3+ doped Ni0.4Cu0.6HoyFe2-yO4 (y = 0.0, 0.02, 0.04, 0.06, and 0.08) spinel ferrites (SFs) and their correlation with crystallite size. The synthesis was achieved using a sol-gel auto-combustion (SGAC) route and performed different characterizations, including X-ray diffraction (XRD), Scanning electron microscope (SEM), Energy dispersive x-ray (EDX), Inductively coupled plasma atomic emission spectroscopy (ICP-AES), and vibrating sample magnetometer (VSM) analysis. The cubic spinel phase was verified via XRD in pure NCF and Ho3+ doped NCF samples. The lattice constant (a) was improved from 8.344 Å to 8.378 Å. The substitution of Ho3+ ions led to a decrease in porosity from 42.22 % to 39.54 %. The introduction of Ho3+ ions also reduced the crystallite size (D) from 37.05 nm to 27.72 nm. The specific surface area (S) was increased from 27.44 g/cm2 to 36.14 g/cm2 with the doping of Ho3+. The average particle size (DS) was decreased from 54 nm to 35 nm. The EDX and ICP-AES analyses confirmed the good agreement with the theoretical composition. The VSM measurements provided insights into their magnetic properties. Furthermore, the doping of Ho3+ ions enhanced coercivity (HC), while reducing saturation magnetization (MS) from 64.35 emu/g to 16.22 emu/g. The decrease in crystalline anisotropy (K) observed at higher concentrations of Ho3+ may result from the increase in coercivity, potentially attributable to the smaller crystallite size of the single-domain SFs particles. The single-phase matrix and their magnetic behaviour showed that the Ho3+ doped Ni–Cu SFs samples are suitable for high-frequency applications.

Structural, magnetic, and thermal properties of nanocrystalline (Fe55Cu20Al25)90B10 alloy processed by mechanical alloying

In this study, we investigate the structural and magnetic properties of nanocrystalline (Fe55Cu20Al25)90B10 powders produced by mechanical alloying. We employ various characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron dispersive X-ray spectroscopy (EDS), and vibrating sample magnetometry (VSM) to analyze these properties. The XRD analysis reveals that after 80 h of milling, the powders undergo a transformation, resulting in the formation of a bcc-iron-based solid solution structure. After 16 h of milling, the average grain size is about 8.1 nm. Additionally, the maximum saturation magnetization reaches around 100.85 emu/g. The annealed sample exhibits structural ordering, as evidenced by the presence of Fe and Cu crystal phases, along with an increase in coercivity. The prepared alloy exhibits soft magnetic properties compared to previously investigated mechanically alloyed FeAl-based powders.

Magneto‐Ionic Control of Coercivity and Domain‐Wall Velocity in Co/Pd Multilayers by Electrochemical Hydrogen Loading

AbstractMagneto‐ionics, as the electrochemical reconfiguration of magnetic materials at low gating voltages, is a highly energy‐efficient alternative to control magnetism. For the fastest magneto‐ionic concept based on hydrogen, fundamental mechanisms are currently under debate, mainly because quantitative compositional information inside the magnetic materials upon gating is lacking. Using the electrochemical hydrogen loading of Co/Pd multilayers with perpendicular anisotropy, this study demonstrates that the hydrogen concentration inside the magnetic material determines its magnetic properties. Hydrogen concentrations up to a maximum of (0.24 ± 0.01) hydrogen atoms per metal atom can be set deterministically by voltage and are quantified via flow‐cell coulometry. With increasing hydrogen concentration, a continuous increase in coercivity of up to 15% and a decrease in magnetic domain‐wall velocity by an order of magnitude are observed using in situ MOKE microscopy. This enables the voltage‐controlled stop‐and‐go of domain walls. These magneto‐ionic effects can be explained by an increasing perpendicular anisotropy with increasing hydrogen content in Co/Pd multilayers, which is supported by theory. Importantly, the approach should be transferable to other ionic systems, such as lithium‐ or oxygen‐based ones, where it can uncover the yet hidden effects of ionic concentration on the magnetic properties and guide the design of functional magneto‐ionic devices.