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Comprehending the relationship between spin and phonons is essential to regulate the lattice thermal conductivity in 2D magnetic materials. Lattice thermal conductivity is a relevant part to consider in magnetic data storage and the working of spin-based devices. In this article, we examined the origin and effect of spin–phonon coupling (SPC) on the lattice thermal conductivity of pristine CrI 3 monolayer-based Janus monolayers Cr 2 X 3 S 3 (X = Br , I). We find a high SPC in these Janus monolayers due to in-plane Cr–S atomic vibrations. We observe a reduction in the lattice thermal conductivity at Janus monolayer magnetic states (∼ 52.3 % in Cr 2 Br 3 S 3 and ∼ 63.9% in Cr 2 I 3 S 3) compared to its paramagnetic states. The analysis is also conducted to determine which magnetic state has more anharmonicity using potential energy wells. A wide range of 2D magnetic materials can benefit from our results in the future development of spin-based thermal devices. [ABSTRACT FROM AUTHOR]

High-entropy perovskite ceramics (HEPCs) with equal atomic ratios have recently emerged as a highly promising class of materials due to their unique magnetic properties. However, the crystal structure, microstructure and magnetic properties of unequal atomic ratios HEPCs have yet to be fully investigated. In this paper, single-phase HEPCs (La 0.25 Nd 0.25 Sm 0.25 Gd 0.25) 1- x Ho x MnO 3 ((LNSG) 1- x H x MO) have been synthesized using solid-state reactions. The effect of Ho element content (x = 0.25, 0.3, 0.35 and 0.4) on the structure and magnetic properties was systematically investigated. All samples exhibit an orthorhombic perovskite structure with a Pbnm space group and show obvious crystallization characteristics after sintering at 1250 °C for 16 h (LNSG) 1- x H x MO HEPCs display a smooth surface texture and distinct grain boundaries, as well as significant hysteresis effects at T = 5 K. The spin-orbit interaction and magnetic anisotropy between Ho and Mn ions increase with the increase of Ho content, which increases the saturation magnetization (M s) of HEPCs. (LNSG) 0.6 H 0.4 MO exhibits the lowest magnetic hysteresis losses among the considered samples, attributed to its highest M s (50.95 emu/g) and the lowest coercivity H c (0.6 kOe). These characteristics endow it with a potential application in magnetic storage devices. [ABSTRACT FROM AUTHOR]

In this study, spinel NiFe2O4 nanoparticles were synthesized employing a one‐step flame spray pyrolysis technique and subjected to annealing at 500°C for 4 h. Thermal, structural, elemental, morphological, magnetic, and photoluminescence properties of the nanoparticles before and after annealing were evaluated using thermogravimetry–differential thermal analyzer, X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy, scanning electron microscopy, dynamic light scattering, vibrating sample magnetometry, and fluorescence spectrometer, respectively. Results revealed a pronounced increase in particle size from an average of 80 nm to approximately 140 nm postannealing. XRD verified the retention of the cubic spinel structure with enhanced crystallinity and grain enlargement post‐thermal treatment, without the emergence of additional phases. The photoluminescence analysis showed distinct blue and green emission bands, with excitation at about 364 nm leading to blue emission at 500 nm and green emission at 550 nm both as‐prepared and postannealing. Additionally, magnetic characterization revealed an improvement in saturation magnetization from 16.31 emu/g for the as‐prepared samples to 29.68 emu/g postannealing, underscoring the annealing process's positive impact on magnetic properties. These findings emphasize the potential of tailored NiFe2O4 nanoparticles for applications in magnetic data storage, targeted drug delivery, and bioimaging, driven by modifications in their magnetic and photoluminescence characteristics through thermal treatment. [ABSTRACT FROM AUTHOR]

Magnetic skyrmions and skyrmioniums have garnered significant attention due to their distinctive topologically nontrivial spin structures. Gaining a deep understanding of the magnetization dynamics of these structures and their interconversion processes is essential for fully leveraging their potential in magnetic storage technology. Here, the dynamics of strain-controlled generation and annihilation of skyrmions and skyrmioniums are investigated using phase field simulation methods. It is discovered that tensile strain can induce the transformation of a single domain into skyrmions and skyrmioniums, which can still exist stably after the strain is released. Notably, skyrmioniums demonstrate robust stability within a specific strain window of −0.2% to 0.5%. Beyond this, escalating the compressive strain magnitude induces a phase transition from skyrmioniums to skyrmions, culminating in a direct collapse to a single-domain state at a critical compressive strain of −0.8%. This study reveals that strain can effectively control a variety of topological magnetic domain structures and achieve their interconversion, providing guidance for the design of low-power, nonvolatile, multi-state spin storage devices. [ABSTRACT FROM AUTHOR]

Copper oxide (CuO) is an important transition metal oxide used in a wide variety of applications, such as gas sensors, magnetic storage media, lithium-ion electrodes, electronic device fabrication etc. CuO nanostructures (NS) exhibit exclusive properties considerably different from their bulk counterparts, such as highly reactive surfaces, different optical, electrical and catalytic properties which strongly depend on the shape, size and crystal structure of the NS. By altering the aspect ratio (length to diameter ratio) and shape of CuO NS, physical and chemical properties of these NS can be tailored. In this work, an array of CuO NS was synthesized on thin copper foil substrate through wet chemical route at different temperatures and times, followed by a thermal reduction in an Ar/H2 atmosphere. Cu foil itself was polished to different roughness levels and deformed to different thickness levels, prior to the reaction, to induce different growth conditions leading to the formation of CuO NS of different morphologies. The present study shows simple, scalable technique to synthesize various CuO NS that can be helpful in future to ameliorate various physical and chemical properties of CuO. [ABSTRACT FROM AUTHOR]

Holmium (Ho)‐doped bismuth ferrite (BiFeO3) nanoparticles are synthesized using the citrate‐gel autocombustion method to investigate their structural, dielectric, ferroelectric, and magnetic properties. X‐Ray diffraction analysis confirms the formation of a rhombohedral perovskite structure, with crystalline size decreasing from ≈14 to 7 nm as doping levels increase. Fourier‐transform infrared spectroscopy further validates the perovskite phase, while field emission scanning electron microscopy and energy‐dispersive X‐Ray spectroscopy confirm the nanocrystalline nature and composition of the samples. X‐Ray photoelectron spectroscopy verifies the successful incorporation of Ho3+ ions into the BiFeO3 matrix. The dielectric properties show high permittivity and low dielectric losses, while magnetic hysteresis loops reveal enhanced magnetic properties, including increased saturation magnetization, remanence, coercivity, squareness ratio, Bohr magneton, and magnetocrystalline anisotropy. These findings indicate that Ho‐doped BiFeO3 nanoparticles exhibit significantly improved electric and magnetic performance, positioning them as promising candidates for applications in magnetic storage devices and sensors. [ABSTRACT FROM AUTHOR]

Herein, the full potential linearized augmented plane wave (FP‐LAPW) method based on density functional theory has been used to compute the electro‐optical and magnetic characteristics of Mg1−xNixS (x = 0%, 6.25%, 12.5%, and 25%) alloys. The stability of the Mg1−xNixS alloys is verified by the enthalpy of formation energy. In electronic features, the band structure and density of states (DOS) demonstrate the semiconducting behavior in pristine MgS compound, while Mg1−xNixS alloys show half‐metallic ferromagnetic to metallic behavior based on the doping concentration. DOS exhibit a strong pd‐hybridization between Ni‐d and S‐p orbitals in the conduction band). For 6.25%, 12.5%, and 25% concentrations, the calculated total magnetic moment is 1.45364, 1.93086, and 0.71829 μB, respectively which is primarily owing to transition metal d states. Optical characteristics including refraction, absorption, complex dielectric function, and reflectivity are studied in the range of 0–10 eV at various concentrations. The absorption of light is noted from visible to UV spans which increase their significance for optoelectronic usages. Results of Mg1−xNixS alloys reveal their potential applications in optical and magnetic storage devices. [ABSTRACT FROM AUTHOR]

In this study, we investigate the thermal pinning and depinning behaviors of vortex domain walls (VDWs) in constricted magnetic nanowires, with a focus on potential applications in storage memory nanodevices. Using micromagnetic simulations and spin transfer torque, we examine the impacts of device temperature on VDW transformation into a transverse domain wall (TDW), mobility, and thermal strength pinning at the constricted area. We explore how thermal fluctuations influence the stability and mobility of domain walls within stepped nanowires. The thermal structural stability of VDWs and their pinning were investigated considering the effects of the stepped area depth (d) and its length (λ). Our findings indicate that the thermal stability of VDWs in magnetic stepped nanowires increases with decreasing the depth of the stepped area (d) and increasing nanowire thickness (th). For th ≥ 50 nm, the stability is maintained at temperatures ≥ 1200 K. In the stepped area, VDW thermal pinning strength increases with increasing d and decreasing λ. For values of d ≥ 100 nm, VDWs depin from the stepped area at temperatures ≥ 1000 K. Our results reveal that thermal effects significantly influence the pinning strength at constricted sites, impacting the overall performance and reliability of magnetic memory devices. These insights are crucial for optimizing the design and functionality of next-generation nanodevices. The stepped design offers numerous advantages, including simple fabrication using a single electron beam lithography exposure step on the resist. Additionally, adjusting λ and d allows for precise control over the pinning strength by modifying the dimensions of the stepped areas. [ABSTRACT FROM AUTHOR]

In the forefront of spintronic advancements, structures with strong perpendicular magnetic anisotropy (PMA) such as Pt/Co/Pt are essential for the miniaturization and performance enhancement of high-density magnetic storage technologies. The robust PMA characteristic of these systems facilitates the development of scalable spintronic devices, crucial for next-generation magnetic memory applications. This study investigates the interplay between PMA and the Dzyaloshinskii-Moriya interaction (DMI)—an antisymmetric exchange interaction prevalent in non-centrosymmetric magnetic systems—and its dissipative counterpart, chiral damping. While chiral damping arises from the same broken inversion symmetry as DMI, it typically introduces an additional energy dissipation channel, reducing device efficiency. Our research examines the effects of controlled helium ion (He+) irradiation on a Pt/Co/Pt system. We find that ion beam irradiation enhances interfacial intermixing, which correlates with a decrease in PMA. However, domain wall velocity measurements indicate a concurrent reduction in both DMI and chiral damping, along with enhanced velocities as irradiation fluence increases. These observations suggest that ion beam irradiation can be judiciously applied to achieve a balance between lower DMI, chiral damping, and reasonable PMA, thereby optimizing the system for improved device performance. [ABSTRACT FROM AUTHOR]

DFT studies are performed to investigate the crystal structure and geometry, electronic and magnetic properties of brownmillerite-type strontium-based oxygen-deficient perovskites SrTMO2.5 (TM = Mn, Fe, Co and Cu) in orthorhombic phase. The comparison of the calculated lattice parameters shows consistency with the experiments, and all these perovskites are thermodynamically stable as revealed by cohesive energy. The spin-dependent calculations of the electronic band profiles demonstrate the metallic behavior of all these deficient perovskites. The increase in electrical resistivity and electronic thermal conductivities with temperature also confirms the metallic behavior of these compounds. The optimized ground state energies in different magnetic phases and post-DFT treatment confirm that SrMnO2.5 and SrCoO2.5 are stable in C-type AFM, SrFeO2.5 is in G-type AFM and SrCuO2.5 in A-type AFM phase, respectively. The high specific heat of these deficient perovskites makes them good candidates for high-temperature technology. Based on the above physical properties, it is expected that these deficient perovskites are potential candidates for spintronics and magnetic storage devices. [ABSTRACT FROM AUTHOR]

Blade coating is a process that applies a fluid to a surface using a fixed blade. Among various coating technologies, blade coating offers significant economic advantages. It is commonly employed in the production of paper, information preservation, the application of coloring agents, and the manufacture of photographic films and magnetic storage devices. The novelty of this work lies in the investigation of the blade coating process for an electrically conducting Oldroyd 4‐constant liquid, incorporating velocity slippage at the blade surface in an area previously underexplored. The mathematical equations are modeled with the use of Lubrication Approximation Theory (LAT) and the normalized equations of the Oldroyd 4‐constant fluid are numerically solved by the Matlab built‐in function bvp4c using Regula‐Falsi Method. The impact of sundry parameters on physical quantities is examined through graphical representation. It is noted from the theoretical results that for the fixed value of the MHD parameter (M = 2.5), the coating thickness and blade load increased by 31% and 1648% respectively, for plane coater. For the exponential coater, these values increased by 29% and 1618% from their Newtonian value. These findings offer new insights into optimizing the blade coating process for complex fluid systems. [ABSTRACT FROM AUTHOR]

In this paper, we investigate the effects of spin-transfer torques within the ferromagnetic infinite medium through the short-wave approximation method. As a result, we have derived the new (1 + 1) dimensional nonlinear evolution system, which describes the propagation of electromagnetic short waves within the ferromagnet in the presence of electric current density. Using the Painlevé analysis and Hirota's bilinearization, we unearth the integrability properties of this new evolution system. In the wake of such an analysis, the typical class of excitations and its physical implications are presented. We remark that the current density acts on magnetization like an effective magnetic damping, which is important for the stabilization of magnetic information storage and data process elements. [ABSTRACT FROM AUTHOR]

La 0.7 Ca 0.3 MnO 3 (LCMO), with its high temperature coefficient of resistance (TCR) and large magnetoresistance (MR) effect, has emerged as a leading material in the field of new multi-functional ceramics. Enhancing the magnetoresistive effect of LCMO in low magnetic field and expanding its application range is one of the main research goals of this kind of materials. In this work, La 0.7- x Sm x Ca 0.3 MnO 3 (LSCMO) (0 ≤ x ≤ 0.09) ceramic targets with different doping amounts were successfully prepared by sol-gel method, and the influence mechanism of Sm3+ doping on the magnetoresistive effect and electrical transport performance of LSCMO was systematically analyzed. X-ray diffraction (XRD) results showed that the lattice parameters (a,b,c,V) of LSCMO decreased slightly, indicating that the doping amount of Sm3+ at the A-site increased. Scanning electron microscopy (SEM) showed that the grains were closely connected without obvious pores, the grain size decreased slightly. The ρ -T curve shows an obvious metal-insulator (M − I) transition, with the increase of Sm3+, the increase of resistivity, metal-insulator transition temperature (T MI) and ferromagnetic-paramagnetic (FM-PM) transition temperature (T C) move towards low temperature. When x = 0.015, the peak value of TCR reaches 41.94 %·K−1, and when x = 0.06, the peak value of MR reaches 80.25 %, both TCR and MR are improved. The results show that: Sm3+ doping can effectively enhance the electromagnetic transport performance of LSCMO. This material has a very wide application prospect in the fields of magnetic storage, and infrared detection. [ABSTRACT FROM AUTHOR]

The sol-gel self-combustion technique was applied to form Cd–Co-based La-doped (Cd 0.5 Co 0.5 La x Fe 2-x O 4) spinel ferrite nanoparticles. A series of six samples was synthesized by varying lanthanum content from x = 0.00 to 0.20. The structural characteristics of the prepared nanoparticles were carried out using X-ray diffraction (XRD) analysis. The (311) plane verified that the prepared nanomaterials are in the spinel phase in all observed XRD patterns. The crystallite size for each sample was determined using the Scherrer formula found in the 8.7–17.8 nm range, which is well correlated with the SSP model. The crystallite size decreased while the lattice constant increased from 8.38 to 8.45 Å with increasing La-content. The increasing trend in the bulk density and X-ray density has been analyzed with the effects of La3+ contents. In Fourier-transform infrared spectroscopy (FTIR), the high-frequency absorption band (υ 1) was found from 522.15 to 541.06 cm−1, whereas the low-frequency band (υ 2) varied from 419.80 to 414.31 cm−1. The surface morphology was carried out by scanning electron microscope (SEM), which positively correlated with XRD analysis. Impedance analyzer (IA) assisted in observing the variations in complex dielectric properties of the compound in the frequency range from 1 MHz to 3 GHz. The dielectric constant and impedance plots depicted that the nano ferrites have good dielectric properties in low-frequency regions due contribution of polarization. While conduction can be made possible in the high-frequency areas as observed through AC conductivity. The electric modulus revealed the relaxation phenomenon at high frequency due to the hopping of electrons at the octa and tetrahedral sites. The magnetic properties were investigated to study the impact of La3+ ion under the applied magnetic field from −15 to 15 kOe. The saturation magnetization, and magnetic remanence were found from 40.6 to 27.7 emu/g and 19.6 to 2.7 emu/g, respectively. The synthesized nanoparticles can be utilized for microwave applications and magnetic storage devices. [ABSTRACT FROM AUTHOR]

The present study explored the impacts of dysprosium (Dy³⁺) doping on the structure, optical, and magnetic characteristics of CuDy x Fe 2-x O 4 nanospinel ferrites synthesized via a hydrothermal method. X-ray diffraction revealed a tetragonal spinel matrix with increasing Dy³⁺ content, accompanied by a secondary Dy 2 O 3 phase at higher dopant levels for x ≥ 0.1. Crystallite size and microstrain increased with doping, while infrared spectroscopy confirmed the spinel structure and distinct vibrational modes. Interestingly, saturation magnetization displayed a non-monotonic trend, first rising due to spin polarization and cation redistribution, then decreasing with higher Dy³⁺ content attributable to the Dy 2 O 3 phase and larger grains. Coercivity exhibited a maximum at x = 0.2, reflecting the interplay between magnetocrystalline anisotropy, canting angles, and domain wall pinning. These findings highlight the complex interplay between Dy³⁺ doping and the resulting properties, paving the way for tailored CuDy x Fe 2-x O 4 nanospinel ferrites functionalities.. Further research involving advanced techniques and targeted dopant levels holds promise for optimizing properties for diverse technological applications such as magnetic storage, microwave devices, sensors, and hyperthermia treatment. [ABSTRACT FROM AUTHOR]

Element-modified La 0.67 Ca 0.33 MnO 3 (LCMO) ceramics have been a major research subject in the past decades due to their various electromagnetic properties and potential applications in infrared detection and magnetic storage devices. However, its electromagnetic transport mechanism has not been fully elucidated and its properties need to be further optimized for practical applications. Here, we report the effect of Ni2+ doping on the structural, magnetic, the temperature coefficient of resistivity (TCR) and magnetoresistance (MR) properties of La 0.67 Ca 0.33 Mn 1- x Ni x O 3 (LCMNO) ceramics. All samples were synthesized by the sol-gel method and were in pure phase. XRD refinement results show a decrease in lattice constants and cell volume of LCMNO ceramics with increasing Ni2+ content. The XPS study confirms the reduction of the Mn3+/Mn4+ ratio and indicates that oxygen vacancies occur in LCMNO ceramics due to the Ni2+ doping. Curie-Weiss fitting results suggest ferromagnetic superexchange coupling between Ni2+ and Mn3+(4+) ions. The electrical transport properties of LCMNO ceramics were further investigated using the spin polaron hopping model in the high temperature range and the various competing scattering mechanisms in the low temperature range. In addition, double resistivity peak behavior is observed at x = 0.04 and 0.05. Furthermore, the TCR of the LCMNO ceramics increased to 45.4 %·K−1 (x = 0.01), while the MR increased to 67.9 % (x = 0.03), respectively. Our studies contribute to a better understanding of the electromagnetic properties of LCMNO ceramics. [ABSTRACT FROM AUTHOR]

The density functional theory (DFT) framework in the generalized gradient approximation (GGA) was employed to study the mechanical, dynamical, and thermodynamic properties of the ordered bimetallic Fe-Pt alloys with stoichiometric structures Fe3Pt, FePt, and FePt3. These alloys exhibit remarkable magnetic properties, high coercivity, excellent chemical stability, high magnetization, and corrosion resistance, making them potential candidates for application in high-density magnetic storage devices, magnetic recording media, and spintronic devices. The calculations of elastic constants showed that all the considered Fe-Pt alloys satisfy the Born necessary conditions for mechanical stability. Calculations on macroscopic elastic moduli showed that Fe-Pt alloys are ductile and characterized by greater resistance to deformation and volume change under external shearing forces. Furthermore, Fe-Pt alloys exhibit significant anisotropy due to variations in elastic constants and deviation of the universal anisotropy index value from zero. The equiatomic FePt showed dynamical stability, while the others showed softening of soft modes along high symmetry lines in the Brillouin zone. Moreover, from the phonon densities of states, we observed that Fe atomic vibrations are dominant at higher frequencies in Fe-rich compositions, while Pt vibrations are prevalent in Pt-rich. [ABSTRACT FROM AUTHOR]

The Janus MoSSe and alloy MoSxSe(1-x), belonging to the family of two-dimensional (2D) transition metal dichalcogenides (TMDs), have gained significant attention for their potential applications in nanotechnology. The unique asymmetric structure of Janus MoSSe provides intriguing possibilities for tailored applications. The alloy MoSxSe(1-x) offers a tunable composition, allowing for the fine-tuning of the properties to meet specific requirements. These materials exhibit remarkable mechanical, electrical, and optical properties, including a tunable band gap, high absorption coefficient, and photoconductivity. The vibrational and magnetic properties also make it a promising candidate for nanoscale sensing and magnetic storage applications. Properties of these materials can be precisely controlled through different approaches such as size-dependent properties, phase engineering, doping, alloying, defect and vacancy engineering, intercalation, morphology, and heterojunction or hybridisation. Various synthesis methods for 2D Janus MoSSe and alloy MoSxSe(1-x) are discussed, including hydro/solvothermal, chemical vapour transport, chemical vapour deposition, physical vapour depositio, and other approaches. The review also presents the latest advancements in Janus and alloy MoSSe-based applications, such as chemical and gas sensors, surface-enhanced Raman spectroscopy, field emission, and energy storage. Moreover, the review highlights the challenges and future directions in the research of these materials, including the need for improved synthesis methods, understanding of their stability, and exploration of new applications. Despite the early stages of research, both the MoSSe-based materials have shown significant potential in various fields, and this review provides valuable insights for researchers and engineers interested in exploring its potential. [ABSTRACT FROM AUTHOR]

Owing to their high mobility and immunity to topological deflection, skyrmions in antiferromagnetic (AFM) systems are gaining attention as a potential solution for next‐generation magnetic data storage. Synthetic antiferromagnets (SAFs) offer a promising avenue to tune the properties of the individual magnetic layers, facilitating the conditions necessary for skyrmions to be used in practical devices. Despite recent advancements achieving fast skyrmion mobility, the nucleation of small and rigid circular skyrmions without an external field remains challenging in SAFs. Theoretical predictions suggest that optical vortex (OAM) beams can stabilize skyrmionic spin textures by transferring their spin and orbital angular momentum to the magnetic material. Here, this intriguing proposal is delved into and the creation of sub‐50 nm compact skyrmions in SAFs using OAM beams is successfully demonstrated, eliminating the need for external magnetic fields. Additionally, the results underscore the importance of beam energy and the number of pulses, as both factors play critical roles in the stabilization of these AFM skyrmionic textures. This breakthrough is significant as it paves the way for stabilizing true zero‐field skyrmions in AFM systems, where magnetization is minimally affected by external magnetic fields. This work will open a potential avenue for stabilizing small, compact skyrmions in antiferroic systems, facilitating their implementation in logic and memory devices. [ABSTRACT FROM AUTHOR]

Topological magnetic states are promising information carriers for ultrahigh‐density and high‐efficiency magnetic storage. Recent advances in two‐dimensional (2D) magnets provide powerful platforms for stabilizing various nanometer‐size topological spin textures within a wide range of magnetic field and temperature. However, non‐centrosymmetric 2D magnets with broken inversion symmetry are scarce in nature, making direct observations of the chiral spin structure difficult, especially for antiferromagnetic (AFM) skyrmions. In this work, it is theoretically predicted that intrinsic AFM skyrmions can be easily triggered in XY‐type honeycomb magnet NiPS3 monolayer by alloying of Cr atoms, due to the presence of a sizable Dzyaloshinskii–Moriya interaction. More interestingly, the diameter of the AFM skyrmions in Ni3/4Cr1/4PS3 decreases from 12 to 4.4 nm as the external magnetic field increases and the skyrmion phases remain stable up to an external magnetic field of 4 T. These results highlight an effective strategy to generate and modulate the topological spin texture in 2D magnets by alloying with magnetic element. [ABSTRACT FROM AUTHOR]

The Sm0.47La0.20K0.33MnO3 perovskite manganite was synthesized using the solid-state reaction method and its structural, magnetic, and critical properties were investigated. This work analyzed the structural characteristics of our sample through Rietveld refinement of the X-ray diffraction pattern and Hirshfeld surface mapping (HS) techniques. It was shown that the sample crystallized in the space group Pnma, with the lattice parameters: a = 5.461 (4) Å, b = 5.478(1) Å, and c = 7.706(8) Å. The Mn–O bond length ~ 1.9 Å obtained from the Rietveld refinement, agrees with the minimum distances between Mn and O atoms obtained from the characteristic 2D fingerprint plots of this manganite. From M vs. T measurements in the range of 5 K < T < 300 K and isothermal measurements M (H) in the range of 0 T < H < 6.5 T , two phase transitions were observed: (i) a paramagnetic (PM)—ferromagnetic (FM) second-order phase transition, and (ii) a FM—spin-glass-like transition. The latter is associated with the presence of samarium in the crystalline structure of the manganite studied. Furthermore, a collective freezing state occurs at T B = 72.83 K . The behavior of the inverse of susceptibility χ - 1 (T) vs. T shows the coexistence of FM clusters within the PM state ( T > 184 K ). Modified Arrott plots (applied to 3D-Heisenberg, 3D-Ising, and Tricritical mean-field models), as well as the Kouvel-Fisher method, were employed to obtain the critical coefficients that were found to be β = 0.367 , γ = 1.330 , and δ = 4.776 for the Sm0.47La0.20K0.33MnO3 manganite. It was confirmed that both critical exponents (β and γ) satisfy the Widom scaling relation (δ = 1 + γ β) . However, a slight deviation from the theoretical values exists of the critical exponent δ obtained with the 3D Heisenberg model. This may be due to the nanoscale dimensions of the secondary phase KMn 2 O 6 particles. In conclusion, critical coefficients and observed phase transitions are significant because they provide guidance for theoretical modeling, enabling real-world applications in diverse technical domains, and shed light on material behavior, all of which contribute to our understanding of manganites. Based on the results of the search, it appears that a better understanding of the critical magnetic behavior in polycrystalline manganites may greatly improve future research and applications in the following areas: Hard disk drives HDDs and magnetic tapes are magnetic data storage devices which can benefit from manganite research to be advanced. Spintronics is a technology, which is based on electron spin polarization mechanism to process information. It utilizes manganites as an important material. [ABSTRACT FROM AUTHOR]

Spintronic devices that utilize spin transfer torque are promising for integrated memory applications. However, these devices face substantial energy consumption challenges due to the high current densities required for switching. Conversely, voltage‐driven spintronic devices, using capacitive displacement charge, can realize switching operations that are energy‐efficient (≈1–10 fJ bit−1). This work investigates switching based on voltage control of the interlayer exchange coupling in perpendicular magnetic anisotropy (PMA) multilayered heterostructures. Unlike previous works that utilized gating techniques that employ ionic transport mechanisms to control interlayer exchange coupling, this study employs electrostatic gating by using MgO, which is more compatible with modern spintronic‐based memories. These results suggest that the magnetization anisotropy, and the magnitude, and phase of the Ruderman‐Kittel‐Kasuya‐Yosida (RKKY) coupling function with spacer layer thickness can be controlled through electric gating, providing a promising avenue for the development of energy‐efficient magnetic data storage devices. [ABSTRACT FROM AUTHOR]

In this study, computational techniques based on artificial neural networks for three models were used for training sets, Néel's relaxation time, particle Length and the decay of magnetization were used to perform superparamagnetic calculations for Co3Pt and FePt typical magnetic storage medium. The magnetic medium's magnetisation stability was studied using the thermal stability coefficient by determining the Néel relaxation time. The superparamagnetic limit was discovered to determine the size of the magnetic particle that can maintain its magnetization for over 10 years, larger particles (8 nm3 for FePt and 64 nm3 for Co3Pt) are required. The decay of magnetization occurs when the thermal stability factor exceeds 40. the effect of changing the neural network's parameters on its performance was examined. The results demonstrated the high sensitivity of the designed neural network's response, which relies on the backpropagation technique to change these parameters. [ABSTRACT FROM AUTHOR]

Co2Sn1−xTxO4 (T = Al, Sc, and Y; 0 ≤ x ≤ 0.2) magnetic spinel oxides have been synthesized through solid-state reaction. The XRD pattern displays a single-phase cubic structure with space group Fd3m. Moreover, magnetic susceptibility results show that substituting trivalent non-magnetic ions improves the para-ferrimagnetic transition temperature, TC. Magnetic susceptibility results of direct current (dc) and alternating current (ac) showed that the T3+ substitution increased the freezing temperature of the spin-glass state, and was also beneficial to the growth of the spin-glass phase. The apparent magnetic exchange bias effect at low temperatures (T < 20 K) was realized in the Co2Sn1−xTxO4 samples using the pinning effect in the spin-glass phase. Due to the magnetic exchange bias effect, the magnetism of the system dramatically increased at low temperatures. Thermal exchange bias results show that the coercivity field (HC) at 10 K increased from 0 for x = 0 samples to ~ 2.1, 1.3, and 2.9 kOe for Al-, Sc-, and Y-doped samples, respectively. It can optimize magnetic materials and architectures, improving performance and practicality in magnetic data storage, magnetic sensors, spintronics, and magnetic nanoparticles. [ABSTRACT FROM AUTHOR]

The exceptional properties of two‐dimensional (2D) magnet materials present a novel approach to fabricate functional magnetic tunnel junctions (MTJ) by constructing full van der Waals (vdW) heterostructures with atomically sharp and clean interfaces. The exploration of vdW MTJ devices with high working temperature and adjustable functionalities holds great potential for advancing the application of 2D materials in magnetic sensing and data storage. Here, we report the observation of highly tunable room‐temperature tunneling magnetoresistance through electronic means in a full vdW Fe3GaTe2/WSe2/Fe3GaTe2 MTJ. The spin valve effect of the MTJ can be detected even with the current below 1 nA, both at low and room temperatures, yielding a tunneling magnetoresistance (TMR) of 340% at 2 K and 50% at 300 K, respectively. Importantly, the magnitude and sign of TMR can be modulated by a DC bias current, even at room temperature, a capability that was previously unrealized in full vdW MTJs. This tunable TMR arises from the contribution of energy‐dependent localized spin states in the metallic ferromagnet Fe3GaTe2 during tunnel transport when a finite electrical bias is applied. Our work offers a new perspective for designing and exploring room‐temperature tunable spintronic devices based on vdW magnet heterostructures. [ABSTRACT FROM AUTHOR]

Due to the ever-increasing recording densities, disk-drive read channels are required to operate efficiently at high speeds. With the use of conventional design techniques, a compromise should be made between speed, power, latency and chip area. Improvements of head and media technology and the move from conventional single-track magnetic recording to two-dimensional magnetic recording help increase the areal density of magnetic data storage. Especially for the read channel, a performance gain is achieved by using more powerful coding and signal processing algorithms to mitigate inter-symbol and inter-track interferences. Timing recovery is essential to extract timing information in order to sample read data without a significant bit error, while calibration is performed to cancel the effects of gain and dc offset errors. Speed improvement and power consumption diminution are achieved in the resulting read channel system by using high-speed and power-efficient building blocks based on improved algorithms and pipeline stages to shorten critical paths. [ABSTRACT FROM AUTHOR]

We demonstrate direct printing from donor ink containing ferrite nanoparticles by employing laser induced forward transfer with an optical vortex possessing orbital angular momentum (OAM). We show, for the first time, that the as-printed dots are twisted and exhibit spinel Fe3O4 monocrystalline properties without the need for a sintering process. The helicity of the as-printed dots is shown to be selectively controlled merely by reversing the handedness of optical vortices. The diameter of the printed dots was typically measured to be less than 1/10th of the irradiated laser spot (diffraction limit). These results imply that the optical vortex twists and confines the sintered nanoparticles within its dark core to form chiral spinel monocrystalline dots. The observation of mono-crystallization with optical vortex induced forward transfer will offer new fundamental physics such as OAM light–matter interactions and could pave the way toward advanced printable magnetic devices, such as high-density magnetic data storage. [ABSTRACT FROM AUTHOR]

Antiferromagnetic spintronics has been receiving attention recently, while spin-texture dependent magnetoresistance (MR) represents one of the main mechanisms for magnetic data storage. In particular, sufficiently large MR with high operating temperatures would be highly required for advanced spintronic applications. In this work, we experimentally investigate the MR effect of well-known antiferromagnet α-Fe2O3 (hematite) in a single crystal form, which has the Morin transition temperature as high as Tm ∼ 260 K. It is revealed that the MR effect associated with the spin-texture re-alignment, i.e., the spin-flop from the out-of-plane direction (c axis) to the in-plane direction, driven by sufficiently low magnetic fields inclined along the [012] direction, reaches up to ∼2.5% at temperature T ∼ 250 K. The first-principles calculations suggest that this MR effect originates from the reduced bandgap due to the spin-flop and the finite spin–orbital coupling. The present work sheds light on the possibility of α-Fe2O3 as a favored MR-based candidate for near-room temperature spintronics. [ABSTRACT FROM AUTHOR]

Exploration and manipulation of topological protected magnetic swirls, such as skyrmion, antiskyrmion, meron, and vortex, holds significance for fundamental research and practical applications in high‐density magnetic information storage and spintronics because of their high storage density and low driven current. This study unveils the existence of field‐free spontaneous (anti)meron chains with a topological charge of ±1/2 in the centrosymmetric rare‐earth magnet Tb6Co2.17Si2.5 via in situ real‐space observation. The spin reorientation transition from in‐plane to uniaxial anisotropy contributes to the spontaneous transformation from straight domain walls to topological (anti)meron chains and to stripe domains along the [110] zone axis during in situ cooling. The study further confirms the critical role of the noncollinear magnetic structure of Tb atoms in the formation of topological (anti)meron chains via real‐space observations, first‐principles calculations, and micromagnetic simulations. The spontaneous topological magnetic texture is strongly correlated with the 4f electrons of rare‐earth atoms, enriching and stimulating alternative generation mechanisms of topological spin textures from emerging rare‐earth magnets, and further applications in spintronics. [ABSTRACT FROM AUTHOR]

We present an investigation into the magnetism exhibited by AMY2 compounds characterized by a chalcopyrite structure, where A can be Cu or Ag, M can be Sc, Ti, V, Cr, Mn, or Fe, and Y can be either S or Se. By substituting M atoms at the Ga position of AGaY2 compounds, the magnetic properties were calculated using the full potential linearized augmented plane wave method under the generalized gradient approximation and local spin density approximation with the WIEN2K code. The obtained spin-polarized results confirmed the presence of ferromagnetic and half-metallic (HM) properties in AMY2 compounds (A = Cu, Ag; M = Ti, V, Cr, Mn; Y = S, Se), wherein the HM property is preserved through p-d hybridization of p states of Y (S, Se) atoms with d (t2g) states of M (M = Ti, V, Cr, Mn) atoms, and minimal contribution of −s states of A (A = Cu, Ag) atoms. The total magnetic moments for AMY2 compounds were calculated as 1.00, 2.00, 3.00, and 4.00 µB/f.u. for M = Ti, V, Cr, Mn, respectively. For AFeY2 compounds (A = Cu, Ag; Y = S, Se), electronic band structures for both up spin and down spin states were identical, suggesting antiferromagnetic behavior at equilibrium, while AScY2 compounds (A = Cu, Ag; Y = S, Se) exhibited nonmagnetic properties at equilibrium. Overall, the accurate HM properties of AMY2 materials suggest promising prospects for their utilization in spintronics and magnetic storage device applications. [ABSTRACT FROM AUTHOR]

The Present work represents the Structural, morphological, magnetic, and optical properties of Pristine and Ni-doped La 2 SrFe 2 TiO 9 Triple Perovskite. The samples were synthesized by using the solid-state reaction approach. We have carried out the structural characterization of the La 2 SrFe 2-x Ni x TiO 9 (x = 0.0, 0.1, 0.2, 0.3 and 0.5) Triple Perovskite by using X-ray diffraction and found that all the synthesized samples were grown in a single phase with space group (Pnma) which has been confirmed further by Rietveld Refinement. The microstructural analysis and the elemental composition analysis were carried out using a Field Emission Scanning Electron Microscope (FE-SEM) and Energy dispersive spectroscopy (EDS) respectively. The morphological studies of the sample reveal that the grain size of the sample decreases (1.11–0.75 μm) with Ni Doping. The optical band gap of the samples was characterized by UV–vis spectroscopy measurements, and we have obtained the value of the energy band gap from 2.02 to 1.67 eV, confirming the application of the material in the Infrared region of the electromagnetic spectrum. The M − H measurements reveal the stabilized ferromagnetic character of the pure La 2 SrFe 2 TiO 9 Triple Perovskite upon Ni doping. The XPS Studies confirm that Ni exists in the form of Ni2+ while Fe exists in the form of Fe3+. The magnetic measurements were understood theoretically by using the mathematical equation. The current study indicates the stability of the samples, and their possible utilisation in spintronics, magnetic storage devices, magneto-optoelectronics, and solar cell applications. [ABSTRACT FROM AUTHOR]

Strontium-zirconium ferrite (Sr–ZrFe) nanocomposites are prepared by the co-precipitation method. Zirconium is taken in two ratios (20% & 50%) with strontium of (80% & 50%) in the synthesis process to make Sr 0.8 Zr 0.2 Fe 12 O 19 and Sr 0.5 Zr 0.5 Fe 12 O 19 which are mentioned as Sr–ZrFe1 and Sr–ZrFe2. The nanocomposites' crystallite size is ascertained by applying the Scherrer equation is 20.97 nm and 21.09 nm. The SEM micrographs show the hexagonal shape of the synthesized nanocomposites. The EDS spectrum depicts the nanocomposites' atomic percentage. The coercivity of the nanocomposites calculated is (H c) = 0.4353 Oe and 0.4450 Oe. From the magnetic hysteresis loop, both composites are found to be single-domain soft ferromagnetic materials. Therefore, the synthesized composites can be used as magnetic data storage devices. The Kubelka-Munk plot is used for obtaining the band gap energy from the UV-DRS reflectance data. The highest intensity peaks of Sr–ZrFe1 and Sr–ZrFe2 nanocomposites are studied from the PL analysis. [ABSTRACT FROM AUTHOR]

Searching for multiferroic materials with ferromagnetic (FM) and ferroelectric (FE) properties holds promise for ultra‐high‐density and low‐energy‐consumption memory device applications, but 2D materials with both properties are rare. Herein, a general strategy to achieve nonvolatile electric field control of magnetism in the bilayer (BL) α‐In2Se3 by hole doping is proposed. By first‐principles calculations, it is demonstrated that hole doping can induce robust ferromagnetism in the bilayer α‐In2Se3 due to its unique flat Mexican‐hat‐shape valence band structure. Such band edges cause van Hove singularities (VHS), and proper hole doping can lead to time‐reversal symmetry breaking. The bilayer α‐In2Se3 exhibits ferromagnetism and ferroelectricity within a wide range of doping concentrations, resulting in an unexpected multiferroic phase. Furthermore, when the electrical polarization of α‐In2Se3 flips from downward to upward, it becomes non‐magnetic (NM) from ferromagnetic states in the As‐substituted bilayer α‐In2Se3, which can work as a nonvolatile magnetic storage unit. Remarkably, the As‐substituted bilayer α‐In2Se3 exhibits an enhanced magnetic moment of 1.2 μB per AsSe due to substantial charge transfer across the interface. Notably, the mechanism of electrically controlled magnetism is elucidated as the coupling among the Mexican‐hat‐like dispersion, ferromagnetism, and ferroelectricity. The findings offer a promising strategy for electrical writing and the magnetic reading memory device. [ABSTRACT FROM AUTHOR]

The structure and the chemical composition of individual layers as well as of interfaces belonging to the two heterostructures M1 (BaFe12O19/YbFeO3/YSZ) and M2 (YbFeO3/BaFe12O19/YSZ) grown by pulsed laser deposition on yttria-stabilized zirconia (YSZ) substrates are deeply characterized by using a combination of methods such as high-resolution X-ray diffraction, transmission electron microscopy (TEM), and atomic-resolution scanning TEM with energy-dispersive X-ray spectroscopy. The temperature-dependent magnetic properties demonstrate two distinct heterostructures with different coercivity, anisotropy fields, and first anisotropy constants, which are related to the defect concentrations within the individual layers and to the degree of intermixing at the interface. The heterostructure with the stacking order BaFe12O19/YbFeO3, i.e., M1, exhibits a distinctive interface without any chemical intermixture, while an Fe-rich crystalline phase is observed in M2 both in atomic-resolution EDX maps and in mass density profiles. Additionally, M1 shows high c-axis orientation, which induces a higher anisotropy constant K1 as well as a larger coercivity due to a high number of phase boundaries. Despite the existence of a canted antiferromagnetic/ferromagnetic combination (T < 140 K), both heterostructures M1 and M2 do not reveal any detectable exchange bias at T = 50 K. Additionally, compressive residual strain on the BaM layer is found to be suppressing the ferromagnetism, thus reducing the Curie temperature (Tc) in the case of M1. These findings suggest that M1 (BaFe12O19/YbFeO3/YSZ) is suitable for magnetic storage applications. [ABSTRACT FROM AUTHOR]

Iron-metal clusters are crucial in a variety of critical biological and material systems, including metalloenzymes, catalysts, and magnetic storage devices. However, a synthetic high-nuclear iron cluster has been absent due to the extreme difficulty in stabilizing species with direct iron−iron bonding. In this work, we have synthesized, crystallized, and characterized a (Tp*)4W4S12(Fe@Fe12) cluster (Tp* = tris(3,5-dimethyl-1-pyrazolyl)borate(1−)), which features a rare trideca-nuclear, icosahedral [Fe@Fe12] cluster core with direct multicenter iron−iron bonding between the interstitial iron (Fei) and peripheral irons (Fep), as well as Fep···Fep ferromagnetic coupling. Quantum chemistry studies reveal that the stability of the cluster arises from the 18-electron shell-closing of the [Fe@Fe12]16+ core, assisted by its bonding interactions with the peripheral tridentate [(Tp*)WS3]4− ligands which possess both S→Fe donation and spin-polarized Fe−W σ bonds. The ground-state electron spin is theoretically predicted to be S = 32/2 for the cluster. The existence of low oxidation-state (OS ∼ +1.23) iron in this compound may find interesting applications in magnetic storage, spintronics, redox chemistry, and cluster catalysis. [ABSTRACT FROM AUTHOR]

Antiferromagnetic/ferromagnetic (AF/F) systems have been extensively investigated due to the importance that interfacial exchange coupling effects have in the development of magnetic storage technologies. Recently, these systems have garnered interest for the potential they have to imprint the magnetic moments of the AF into an F layer, offering the possibility of using it as a read-out mechanism in antiferromagnetic spintronics. In this study, we explored the importance of crystalline orientation and strains induced by the substrate in the exchange coupling properties of NiO/FeCo AF/F bilayers. For that, we have grown NiO/FeCo bilayers on MgO (001) and Al2O3 (0001) substrates varying the FeCo layer thickness. In addition, we have analyzed both deposited samples and those with induced interfacial unidirectional anisotropy. For inducing such interfacial anisotropy, we used a field cooling procedure, heating the bilayers to 650 K and subsequently cooling down to room temperature under the presence of an external magnetic field of 300 mT. We have investigated the effect of the substrate in terms of crystalline orientation and lattice mismatching on the AF/F exchange coupling as well as the dependence of the coercivity and exchange bias on the inverse F layer thickness that is consistent with the interfacial origin of the AF/F exchange coupling. Moreover, the angular dependence of the magnetic properties was explored by using vectorial Kerr magnetometry, confirming the presence of both magnetocrystalline anisotropy, arising from the epitaxial character of the growing process mainly when the bilayer is grown on MgO (001) substrates, and the field cooling (FC)-induced unidirectional anisotropy. [ABSTRACT FROM AUTHOR]

The exchange bias effect, pivotal in magnetic data storage and sensing devices, has been observed not only in interfacial regions but also in intrinsic ferromagnetic materials. Here, we have uncovered a robust and stable exchange bias effect within the layered van der Waals (vdW) ferromagnet VI3 employing magnetic circular dichroism microscopy. At 10 K, we observed a significant exchange field of approximately 0.1 T, accompanied by random shifts (positive or negative relative to zero magnetic field) after zero-field cooling. Notably, this effect is effectively controllable after field cooling, with shift direction opposing the applied magnetic field. The presence of strong magnetic anisotropic energy within VI3 results in larger coercivity-bound magnetic domains. These domains dictate the neighboring ferromagnetic alignment and induce shifts in the hysteresis loop. Our study not only contributes to comprehending fundamental nanoscale magnetic interactions but also sheds light on emergent phenomena within layered van der Waals magnets. [ABSTRACT FROM AUTHOR]

The New Journal of Chemistry, published by The Royal Society of Chemistry, has released its latest issue which includes a variety of articles covering different topics in the field of chemistry. The papers discuss recent progress in areas such as nitrogen-heterocycles, chemisorption of gases, photoactive derivatives, and potential applications of nanoribbons. The journal aims to connect the global community with the chemical sciences and provides scientific insights and advancements in various fields of study. [Extracted from the article]

We first constructed a new type of two-dimensional nanoribbon material by splicing a C2N-h2D nanoribbon with a BN nanoribbon, which is called the C2N-h2D/BN nanoribbon. The electronic properties of the C2N-h2D/BN nanoribbon were investigated using first-principles calculations, and its thermodynamic stability was verified through molecular dynamics simulations, demonstrating its dynamic stability at room temperature. Through analysis of the band structure, density of states, and charge density plots, we found that it is a nonmagnetic direct narrow bandgap semiconductor. To manipulate its electronic structure, we adsorbed transition metal atoms Mn, Fe, Co, and Ni into the nanoribbon. By analyzing the band structure and density of states after adsorption, we observed that the properties of the nanoribbon transitioned from a semiconductor to a metal upon adsorption of Mn, Co, and Ni atoms. Interestingly, after the adsorption of Fe atoms, the C2N-h2D/BN nanoribbon transformed from a semiconductor to a half-metal, indicating the generation of 100% spin-polarized current at the Fermi level and improved the electronic performance of the nanoribbon. This finding is exciting as it demonstrates that adsorption of different transition metal atoms can control the physicochemical properties of the nanoribbon, particularly the generation of 100% spin-polarized current at the Fermi level. This provides promising prospects for the application of this two-dimensional nanomaterial in spintronic devices and magnetic storage devices. [ABSTRACT FROM AUTHOR]

Two-dimensional (2D) magnetic materials have triggered tremendous interest in recent years due to their remarkable potential applications in magnetic storage and spintronics devices. Heat dissipation is of great significance in stability and durability of increasingly integrated magnetic devices. However, little investigation of thermal transport has been carried out in 2D magnetic materials and a comprehensive understanding of the underlying mechanism is still lacking. We experimentally demonstrate the thermal conductivity measurement of MnPSe3 nanoribbons and find a nonmonotonic thickness dependence, which is attributed to the phonon confinement effect in thin nanoribbons. The peaks of measured thermal conductivity are found to be modified with increasing thickness due to the magnon–phonon coupling. We propose that the magnon–phonon scattering rate increases with increasing thickness and causes a huge suppression in thermal conductivity. This study will deepen the understanding of the thermal properties of 2D magnetic materials and will benefit thermal management in designing magnetic devices. [ABSTRACT FROM AUTHOR]

Microalgae are highly regarded as ideal materials for the creation of liquid biofuels and have substantial potential for growth and utilization. However, traditional storage and culture methods for microalgae are plagued by challenges such as uncontrolled growth, bacterial contamination, and self-shading among algae. These issues severely impede the photosynthetic process and the efficient extraction of biomass energy. This study tackles these problems by utilizing magnetic hydrophobic protein particles to stabilize water-in-oil Pickering emulsions. This allows for the micro-compartment storage and magnetic transfer of algae. Additionally, the successful encapsulation of Chlorella cells in high-internal-phase water-in-oil Pickering emulsions effectively mitigates the settling problem of Chlorella cells in the liquid phase, thereby enabling the potential use of Pickering emulsions for the confined cultivation of microalgae. [ABSTRACT FROM AUTHOR]

Understanding of the laser-induced ultrafast demagnetization dynamics is one of the most challenging and hot topics in magnetism research due to its potential applications in magnetic storage devices and the field of spintronics. Recently, a laser-induced switching of ferromagnetism, driven by a disorder–order transition on FeAl thin films, has been experimentally demonstrated. The switching of ferromagnetic ordering by ultrafast laser pulses in FeAl thin films may open new possible applications of this material such as magnetic data storage and manipulation. Since the speed of the magnetic switching of magnetic states in thin films is one of the critical parameters for these applications, here we used time resolved magneto-optical Kerr measurements to investigate the demagnetization dynamics of Fe 60 Al 40 thin films at room temperature. We have for the first time observed a clear transition from one-step dynamics (type I) to two-step (type II) dynamics in the same material by increasing pump laser fluence. This experimental observation may give a strong confirmation that the ultrafast demagnetization process can be treated as a thermal process and is driven by the difference between temperatures of the electron and spin systems. [ABSTRACT FROM AUTHOR]

This article presents the technology for the preparation of a nitrogen-containing nanoporous bio-carbon and investigates its properties. It has been shown that the synthesised bio-carbon is characterised by a high degree of homogeneity, which has been confirmed by energy dispersive spectroscopy. The obtained bio-carbon has a micromesoporous structure, which has been confirmed by the results of studies using the method of low-temperature nitrogen adsorption and desorption. It was found that the specific surface area of biochar is 1247 m2/g. The data on nitrogen adsorption and desorption were compared with the data on small-angle X-ray scattering, and it was found that the micropores in the synthesised bio-carbon are open pores, while mesopores remain closed. The energy dispersion analysis showed that the structure of the bio-carbon does not contain ferromagnetic atoms, but due to the addition of nitrogen, the synthesised bio-carbon in a magnetic field has the properties of a ferromagnet with a characteristic hysteresis of the specific magnetisation. It was found that this material has a saturation magnetisation σs of 1.4 A∙m2∙kg−1 and a coercive force Hc of 10 kA/m. Symmetric supercapacitors were fabricated from the synthesised bio-carbon material with 30% aqueous KOH and 1 M Na2SO4 as electrolytes. It was found that for bio-carbon synthesised at 800 °C, the specific capacitance in a 30% aqueous solution of KOH is 180 F/g, and in a 1 M aqueous solution of Na2SO4, it is 124 F/g. The cyclic voltammetry of the fabricated supercapacitors at different rates of potential expansion was investigated and analysed. Impedance studies on these supercapacitors were carried out. The equivalent electrical circuits describing the electrochemical processes in the studied supercapacitors were constructed and characterised. [ABSTRACT FROM AUTHOR]

Using modern methodologies in the sectors and subareas of industrial design, where they currently find only marginal application, brings a potential for interrelating technology, the arts, and fine arts. To illustrate this, we present model procedures and options for designing a versatile storage cube that integrates magnetic structural components facilitating easy and quick assembly. In addition to being an item of real furniture, portable and readily convertible into a table or soft stool, the cube supports children's creative games and helps to develop their overall skills in the present-day household and in pre-primary and primary education. The basic material rests in birch plywood, and the joint edges between the individual walls are covered with smooth plastic guards manufactured via additive 3D printing from corn fodder-based filament. Thus, an interesting structural detail, namely, plastic edges, is generated, reinforcing the entire product. The walls comprise decorative, multicolor, polyurethane foam-based elements that can be removed and reinserted. Regarding the manufacturing technology, CNC machining and laser shaping are widely employed on the main parts, and the plastic edges are 3D-printed. In terms of the original idea, the product responds to customer requirements within a specific design project. The robustness and stability tests have proved that the cubes fully satisfy the relevant standards. [ABSTRACT FROM AUTHOR]

La 0.67 Ca 0.33 MnO 3 (LCMO) ceramics exhibit high temperature coefficient of resistance (TCR) and colossal magnetoresistance effect (CMR). Increasing their TCR and MR values can enhance potential applications in uncooled infrared detectors and magnetic storage devices. However, presence of inherent grain boundaries and defects within these ceramics significantly limits their performance. Therefore, this work proposed modifying grain boundaries of LCMO ceramic using low-resistivity and stable Au to enhance its electrical transport and improve magnetoresistance performance through competition between antiferromagnetic Au and ferromagnetic La 0.67 Ca 0.33 MnO 3. A series of La 0.67 Ca 0.33 MnO 3 : Au x (x = 0, 0.05, 0.10, 0.15) composite ceramics was prepared by sol-gel and solid-state methods. Introduction of Au increased TCR from 40.1 %·K−1 to 55.2 %·K−1 and MR from 60.4 % to 74.2 %, when x = 0.10. This study demonstrates that proposed strategy involving multiphase interactions can significantly improve electrical transport and magnetic properties of functional materials, with promising applications in areas such as thermoelectric and magnetoelectric conversion. [ABSTRACT FROM AUTHOR]

Bare Cu 0.26 Ni 0.74 alloy nanoparticles and those blended with multi-walled carbon nanotubes are synthesized by hydrothermal method. Nearly monodispersed and crystalline nanoparticles, which get attached onto the nanotube surfaces on blending, can be seen from the morphological characterizations. Single X-ray diffraction peaks occurring for each pair of (hkl) reflections from Cu and Ni are suggestive of the formation of Cu–Ni alloy. Small, concurrent binding energy shifts in the X-ray photoelectron peaks reveal a charge (electron) transfer from the nanotubes to the nanoparticles. Blue shifts in characteristic Raman peaks corroborate the charge transfer process. Magnetic studies show a significant enhancement in the low temperature coercivity of nanoparticles on their attachment with CNTs. This enhancement is attributable to the inferred charge transfer, which is further substantiated by an anomalous increase in the coercivity on temperature rise. This work demonstrates that a considerably large enhancement in the coercivity of Cu 0.26 Ni 0.74 alloy nanoparticles can be achieved by blending them with carbon nanotubes. Such composites could be very good candidates for applications such as magnetic storage devices. [ABSTRACT FROM AUTHOR]

Nanoimprint lithography presents unique opportunities for advanced magnetic storage media with ordered bit arrangements such as bit patterned media or heated dot magnetic recording. Providing sub-10 nm resolution and full disk imprinting capability, UV-nanoimprint lithography based on rigid quartz templates bears the entitlement for patterned recording media manufacturing with high throughput at low cost. However, a key challenge is the fabrication of the high-resolution template that can transfer the desired pattern onto the disk with high fidelity and low line edge roughness. In this article, we present fabrication routes and overcome challenges to the fabrication of quartz templates suitable for self-alignment and guiding purposes to be used for template replication toward full disk imprints. Guiding patterns down to 40 nm pitch are prepared using a rotary electron beam lithography tool. We compare three different process approaches to fabricate an etching mask for patterning the quartz. Two methods target chromium patterning, one with traditional lift-off and another by dry etching, both using an e-beam resist mask. The third approach is based on the development of a carbon-based Tri-layer hard mask. The template pattern profile is optimized for imprint-suitable sidewall angles using dry etching in a CF4/O2 chemistry. The templates were characterized using scanning electron microscopy and atomic force microscopy to evaluate the quality of the transferred pattern as well as line edge roughness. Our results show that the Tri-layer process using carbon resulted in the lowest line edge roughness of ≈0.65 nm at the imprinted disk level. In addition, we show that Tri-layer masking allowed for the use of conventional ZEP e-beam resist and fast writing speeds, while gaining high selectivity during quartz patterning. [ABSTRACT FROM AUTHOR]

Geometry-induced domain wall pinning has been studied in heterostructure with soft magnet Fe3Pt and hard magnet FePt. It is demonstrated that the domain wall is pinned at the interface region of the Fe3Pt/FePt heterostructure under a small current field owing to the spin-transfer torque. The pinning of the domain wall is strongly dependent on the geometry of both soft and hard magnets. The thickness of the heterostructure Fe3Pt/FePt has an important influence on the pinning of the domain wall, which is caused by the combined effects of demagnetization, exchange coupling, and anisotropy. Moreover, with an increase in the width of the hard magnet FePt, the current of the pinning domain wall increases. With an increase in the width of the soft magnet, Fe3Pt, the pinning current decreased to a minimum value and then increased. These results are helpful for the fabrication and design of magnetic storage devices. [ABSTRACT FROM AUTHOR]