Magnetic refrigeration relies on a substantial entropy change in a magnetocaloric material when a magnetic field is applied. Such entropy changes are present at first‐order magnetostructural transitions around a specific temperature at which the applied magnetic field induces a magnetostructural phase transition and causes a conventional or inverse magnetocaloric effect (MCE). First‐order magnetostructural transitions show large effects, but involve transitional hysteresis, which is a loss source that hinders the reversibility of the adiabatic temperature change ΔTad. However, reversibility is required for the efficient operation of the heat pump. Thus, it is the mastering of that hysteresis that is the key challenge to advance magnetocaloric materials. We review the origin of the large MCE and of the hysteresis in the most promising first‐order magnetocaloric materials such as Ni–Mn‐based Heusler alloys, FeRh, La(FeSi)13‐based compounds, Mn3GaC antiperovskites, and Fe2P compounds. We discuss the microscopic contributions of the entropy change, the magnetic interactions, the effect of hysteresis on the reversible MCE, and the size‐ and time‐dependence of the MCE at magnetostructural transitions.
Spin wave logic circuits using quantum oscillations of spins (magnons) as carriers of information have been proposed for next generation computing with reduced energy demands and the benefit of easy parallelization. Current realizations of magnonic devices have micrometer sized patterns. Here we demonstrate the feasibility of biogenic nanoparticle chains as the first step to truly nanoscale magnonics at room temperature. Our measurements on magnetosome chains (ca 12 magnetite crystals with 35 nm particle size each), combined with micromagnetic simulations, show that the topology of the magnon bands, namely anisotropy, band deformation, and band gaps are determined by local arrangement and orientation of particles, which in turn depends on the genotype of the bacteria. Our biomagnonic approach offers the exciting prospect of genetically engineering magnonic quantum states in nanoconfined geometries. By connecting mutants of magnetotactic bacteria with different arrangements of magnetite crystals, novel architectures for magnonic computing may be (self-) assembled.
This paper represents a detailed theoretical study of the role of the longrange magnetic dipole-dipole interaction evidenced by the ferromagnetic resonance (FMR) spectra for the ordered arrays of cubic nanoparticles. We show that the size of the array essentially controls the stability of the system, allowing to suppress the intermittent low-field excitations starting from the arrays formed by 6×6 nanoparticles. Our numerical simulations allow to determine the threshold inter-particle distance (around 80 ÷ 100 nm), after which the dipole-dipole interaction becomes negligible so that the FMR spectrum of the nanoparticle arrays becomes the same as the spectrum featured by a single nanoparticle. We also compare our simulations with experimental FMR-spectra of 24 Fe/Fe x O y -nanocubes irregularly placed on a substrate.
We report on the impact of magnetoelastic coupling on the magnetocaloric properties of LaFe11.4Si1.6H1.6 in terms of the vibrational (phonon) density of states (VDOS), which we determined with 57 Fe nuclear resonant inelastic X-ray scattering (NRIXS) measurements and with density-functional-theory (DFT)-based first-principles calculations in the ferromagnetic (FM) lowtemperature and paramagnetic (PM) high-temperature phase. In experiments and calculations, we observe pronounced differences in the shape of the Fe-partial VDOS between non-hydrogenated and hydrogenated samples. This shows that hydrogen does not only shift the temperature of the first-order phase transition, but also affects the elastic response of the Fe-subsystem significantly. In turn, the anomalous redshift of the Fe VDOS, observed by going to the low-volume PM phase, survives hydrogenation. As a consequence, the change in the Fe specific vibrational entropy ∆S lat across the phase transition has the same sign as the magnetic and electronic contribution. DFT calculations show that the same mechanism, which is a consequence of the itinerant electron metamagnetism associated with the Fe subsystem, is effective in both the hydrogenated and the hydrogen-free compounds. Although reduced by 50 % as compared to the hydrogen-free system, the measured change ∆S lat of (3.2 ± 1.9) J kgK across the FM to PM transition contributes with ∼ 35 % significantly and cooperatively to the total isothermal entropy change ∆Siso. Hydrogenation is observed to induce an overall blueshift of the Fe-VDOS with respect to the H-free compound; this effect, together with the enhanced Debye temperature observed, is a fingerprint of the hardening of the Fe sublattice by hydrogen incorporation. In addition, the mean Debye velocity of sound of LaFe11.4Si1.6H1.6 was determined from the NRIXS and the DFT data. arXiv:1911.11087v1 [cond-mat.mtrl-sci]
In this work a full angle dependent Ferromagnetic Resonance (FMR) investigation on a system of 20 separated Fe/FexOy nanocubes without dipolar coupling is reported. The angular magnetic field dependence of FMR spectra of 20 single particles and 2 dimers were recorded using a microresonator setup with a sensitivity of 106 μB at X-band frequencies. We determine an effective magnetocrystalline anisotropy field of 2K4,eff/M = 50 mT ± 5 mT for selected particles, which is smaller than the one of bulk Fe due to the core shell morphology of the particles. The FMR resonances have a linewidth of 4 mT ± 1 mT, corresponding to a magnetic effective damping parameter α = 0.0045 ± 0.0005 matching the values of high quality iron thin films. Numerical calculations taking into account the different angular orientations of the 24 particles with respect to the external magnetic field yield a good agreement to the experiment.
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