اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدProbing fractal magnetic domains on multiple length scales in Nd2Fe14B
399
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Using small-angle neutron scattering, we demonstrate that the complex magnetic domain patterns at the surface of Nd2Fe14B, revealed by quantitative Kerr and Faraday microscopy, propagate into the bulk and exhibit structural features with dimensions down to 6 nm, the domain wall thickness. The observed fractal nature of the domain structures provides an explanation for the anomalous increase in the bulk magnetization of Nd2Fe14B below the spin-reorientation transition. These measurements open up a rich playground for studies of fractal structures in highly anisotropic magnetic systems.
قيم البحث
اقرأ أيضاً
Long-range non-collinear all-in/all-out magnetic order has been directly observed for the first time in real space in the pyrochlore Cd$_2$Os$_2$O$_7$ using resonant magnetic microdiffraction at the Os L$_3$ edge. Two different antiferromagnetic doma
ins related by time-reversal symmetry could be distinguished and have been mapped within the same single crystal. The two types of domains are akin to magnetic twins and were expected - yet unobserved so far - in the all-in/all-out model. Even though the magnetic domains are antiferromagnetic, we show that their distribution can be controlled using a magnetic field-cooling procedure.
Neutron spherical polarimetry, which is directly sensitive to the absolute magnetic configuration and domain population, has been used in this work to unambiguously prove the multiferroicity of (ND4)2[FeCl5(D2O)]. We demonstrate that the application
of an electric field upon cooling results in the stabilization of a single-cycloidal magnetic domain below 6.9 K, while poling in the opposite electric field direction produces the full population of the domain with opposite magnetic chirality. We prove the complete switchability of the magnetic domains at low temperature by the applied electric field, which constitutes a direct proof of the strong magnetoelectric coupling. Additionally, we refine the magnetic structure of the ordered ground state, determining the underlying magnetic space group consistent with the direction of the ferroelectric polarization, and we provide evidence of a collinear amplitude-modulated state with magnetic moments along the a-axis in the temperature region between 6.9 and 7.2 K.
When a quantum dot is subjected to a thermal gradient, the temperature of electrons entering the dot can be determined from the dots thermocurrent if the conductance spectrum and background temperature are known. We demonstrate this technique by meas
uring the temperature difference across a 15 nm quantum dot embedded in a nanowire. This technique can be used when the dots energy states are separated by many kT and will enable future quantitative investigations of electron-phonon interaction, nonlinear thermoelectric effects, and the effciency of thermoelectric energy conversion in quantum dots.
Spontaneous self-assembly in molecular systems is a fundamental route to both biological and engineered soft matter. Simple micellisation, emulsion formation, and polymer mixing principles are well understood. However, the principles behind emergence
of structures with competing length scales in soft matter systems remain an open question. Examples include the droplet-inside-droplet assembly in many biomacromolecular systems undergoing liquid-liquid phase separation, analogous multiple emulsion formation in oil-surfactant-water formulations, and polymer core-shell particles with internal structure. We develop here a microscopic theoretical model based on effective interactions between the constituents of a soft matter system to explain self-organization both at single and multiple length scales. The model identifies how spatial ordering at multiple length scales emerges due to competing interactions between the system components, e.g. molecules of different sizes and different chemical properties. As an example of single and multiple-length-scale assembly, we map out a generic phase diagram for a solution with two solute species differing in their mutual and solvent interactions. By performing molecular simulations on a block-copolymer system, we further demonstrate how the phase diagram can be connected to a molecular system that has a transition from regular single-core polymer particles to multi-core aggregates that exhibit multiple structural length scales. The findings provide guidelines to understanding the length scales rising spontaneously in biological self-assembly, but also open new venues to the development and engineering of biomolecular and polymeric functional materials.
We present a study of the electronic and magnetic properties of the multiple-decker sandwich nanowires ($CP-M$) composed of cyclopentadienyl (CP) rings and 3d transition metal atoms (M=Ti to Ni) using first-principles techniques. We demonstrate using
Density Functional Theory that structural relaxation play an important role in determining the magnetic ground-state of the system. Notably, the computed magnetic moment is zero in $CP-Mn$, while in $CP-V$ a significant turn-up in magnetic moment is evidenced. Two compounds show a half-metallic ferromagnetic ground state $CP-Fe/Cr$ with a gap within minority/majority spin channel. In order to study the effect of electronic correlations upon the half-metallic ground states in $CP-Cr$, we introduce a simplified three-bands Hubbard model which is solved within the Variational Cluster Approach. We discuss the results as a function of size of the reference cluster and the strength of average Coulomb $U$ and exchange $J$ parameters. Our results demonstrate that for the range of studied parameters $U=2-4eV$ and $J=0.6-1.2eV$ the half-metallic character is not maintained in the presence of local Coulomb interactions.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
