No Arabic abstract
We employ magnetic small-angle neutron scattering to investigate the magnetic interactions in $(Fe_{0.7}Ni_{0.3})_{86}B_{14}$ alloy, a HiB-NANOPERM-type soft magnetic nanocrystalline material, which exhibits an ultrafine microstructure with an average grain size below 10 nm. The neutron data reveal a significant spin-misalignment scattering, which is mainly related to the jump of the longitudinal magnetization at internal particle-matrix interfaces. The field dependence of the neutron data can be well described by the micromagnetic small-angle neutron scattering theory. In particular, the theory explains the clover-leaf-type angular anisotropy observed in the purely magnetic neutron scattering cross section. The presented neutron-data analysis also provides access to the magnetic interaction parameters, such as the exchange-stiffness constant, which plays a crucial role towards the optimization of the magnetic softness of Fe-based nanocrystalline materials.
Small angle neutron scattering (SANS) magnetic and electrical transport measurements were performed to study a single crystal of Pr0.7Ca0.3MnO3, a colossal magnetoresistive (CMR) material. While the magnetic field induced transformation of this phase separated compound consisting of an antiferromagnetic insulating phase (AFI) and a ferromagnetic insulating phase (FI), is continuous at high temperature (above 5K), at lower temperature a step like transformation is observed (around 5T at 2K). Macroscopic magnetization measurements and SANS indicate that this transformation occurs by the formation of mesoscopic ferromagnetic metallic (FM) domains in the AFI phase, and, eventually, in the FI phase. Although above 5K this transformation is continuous, below 5K a magnetization step marks the abrupt transition from a large scale FI/AFI phase separation to a large scale phase separation between AFI, FI and FM phases. Our results suggest that relaxation of elastic strains inherent to the coexistence of these different phases plays a crucial role in the mechanism of these transformations. The occurrence of magnetization steps could result from an intrinsic behavior of the AFI phase at low temperature.
Inelastic neutron scattering (INS) experiments under applied magnetic field at low temperatures show detailed low lying magnetic excitations in the so called tridiminshed iron icosahedron magnetic molecule. The magnetic molecule consists of nine iron Fe$^{3+}$ ($s = 5/2$) and three phosphorous atoms that are situated on the twelve vertices of a nearly perfect icosahedron. The three phosphorous atoms form a plane that separates the iron cluster into two weakly coupled three- and six-ion fragments, {Fe$_3$} and {Fe$_6$}, respectively. The magnetic field INS results exhibit an $S=1/2$ ground state expected from a perfect equilateral triangle of the {Fe$_3$} triad with a powder averaged $g$-value $=2.00$. Two sets of triplet excitations whose temperature and magnetic field dependence indicate an $S=0$ ground state with two non-degenerate $S=1$ states are attributed to the {Fe$_6$} fragment. The splitting may result from a finite coupling between the two fragments, single-ion anisotropy, antisymmetric exchange couplings, or from magnetic frustration of its triangular building blocks.
Magnetic tunnel junctions with perpendicular anisotropy form the basis of the spin-transfer torque magnetic random-access memory (STT-MRAM), which is non-volatile, fast, dense, and has quasi-infinite write endurance and low power consumption. Based on density functional theory (DFT) calculations, we propose an alternative design of magnetic tunnel junctions comprising Fe(n)Co(m)Fe(n)/MgO storage layers with greatly enhanced perpendicular magnetic anisotropy (PMA) up to several mJ/m2, leveraging the interfacial perpendicular anisotropy of Fe/MgO along with a stress-induced bulk PMA discovered within bcc Co. This giant enhancement dominates the demagnetizing energy when increasing the film thickness. The tunneling magnetoresistance (TMR) estimated from the Julliere model is comparable with that of the pure Fe/MgO case. We discuss the advantages and pitfalls of a real-life fabrication of the structure and propose the Fe(3ML)Co(4ML)Fe(3ML) as a storage layer for MgO-based STT-MRAM cells. The large PMA in strained bcc Co is explained in the framework of Brunos model by the MgO-imposed strain and consequent changes in the energies of dyz and dz2 minority-spin bands.
The charge ordered La$_{1/3}$Sr$_{2/3}$FeO$_{3-delta}$ (LSFO) in bulk and nanocrystalline forms are investigated using ac and dc magnetization, M{o}ssbauer, and polarised neutron studies. A complex scenario of short range charge and magnetic ordering is realized from the polarised neutron studies in nanocrystalline specimen. This short range ordering does not involve any change in spin state and modification in the charge disproportion between Fe$^{3+}$ and Fe$^{5+}$ compared to bulk counterpart as evident in the M{o}ssbauer results. The refinement of magnetic diffraction peaks provides magnetic moments of Fe$^{3+}$ and Fe$^{5+}$ are about 3.15$mu_B$ and 1.57$mu_B$ for bulk, and 2.7$mu_B$ and 0.53$mu_B$ for nanocrystalline specimen, respectively. The destabilization of charge ordering leads to magnetic phase separation, giving rise to the robust exchange bias (EB) effect. Strikingly, EB field at 5 K attains a value as high as 4.4 kOe for average size $sim$ 70 nm, which is zero for the bulk counterpart. A strong frequency dependence of ac susceptibility reveals cluster-glass like transition around $sim$ 65 K, below which EB appears. Overall results propose that finite size effect directs the complex glassy magnetic behavior driven by unconventional short range charge and magnetic ordering, and magnetic phase separation appears in nanocrystalline LSFO.
The magnetic system of the Mn$_{1-x}$Fe$_{x}$Ge solid solution is ordered in a spiral spin structure in the whole concentration range of $x in [0 div 1]$. The close inspection of the small-angle neutron scattering data reveals the quantum phase transition from the long-range ordered (LRO) to short range ordered (SRO) helical structure upon increase of Fe-concentration at $x in [0.25 div 0.4]$. The SRO of the helical structure is identified as a Lorentzian contribution, while LRO is associated with the Gaussian contribution into the scattering profile function. The scenario of the quantum phase transition with $x$ as a driving parameter is similar to the thermal phase transition in pure MnGe. The quantum nature of the SRO is proved by the temperature independent correlation length of the helical structure at low and intermediate temperature ranges with remarkable decrease above certain temperature $T_Q$. We suggest the $x$-dependent modification of the effective Ruderman-Kittel-Kasuya-Yosida exchange interaction within the Heisenberg model of magnetism to explain the quantum critical regime in Mn$_{1-x}$Fe$_{x}$Ge.