Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userChiral asymmetry detected in a 2D array of permalloy square nanomagnets using circularly polarized X ray Resonant Magnetic Scattering
112
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The sensitivity of Circularly polarized X ray Resonant Magnetic Scattering (CXRMS) to chiral asymmetry has been demonstrated. The study was performed on a 2D array of Permalloy (Py) square nanomagnets of 700 nm lateral size arranged in a chess lattice of 1000 nm lattice parameter. Previous X ray Magnetic Circular Dichroism Photoemission Electron microscopy (XMCD-PEEM) images on this sample showed the formation of vortices at remanence and a preference in their chiral state. The magnetic hysteresis loops of the array along the diagonal axis of the squares indicate a non-negligible and anisotropic interaction between vortices. The intensity of the magnetic scattering using circularly polarized light along one of the diagonal axes of the square magnets becomes asymmetric in intensity in the direction transversal to the incident plane at fields where the vortex states are formed. The asymmetry sign is inverted when the direction of the applied magnetic field is inverted. The result is the expected in the presence of an unbalanced chiral distribution. The effect is observed by CXRMS due to the interference between the charge scattering and the magnetic scattering.
rate research
Read More
Chiral properties of the two phases - collinear motif (below Morin transition temperature, TM=250 K) and canted motif (above TM) - of magnetically ordered hematite ({alpha}-Fe2O3) have been identified in single crystal resonant x-ray Bragg diffraction, using circular polarized incident x-rays tuned near the iron K-edge. Magneto-electric multipoles, including an anapole, fully characterize the high-temperature canted phase, whereas the low-temperature collinear phase supports both parity-odd and parity-even multipoles that are time-odd. Orbital angular momentum accompanies the collinear motif, while it is conspicuously absent with the canted motif. Intensities have been successfully confronted with analytic expressions derived from an atomic model fully compliant with chemical and magnetic structures. Values of Fe atomic multipoles previously derived from independent experimental data, are shown to be completely trustworthy.
Magnetic spiral structures can exhibit ferroelectric moments as recently demonstrated in various multiferroic materials. In such cases the helicity of the magnetic spiral is directly correlated with the direction of the ferroelectric moment and measurement of the helicity of magnetic structures is of current interest. Soft x-ray resonant diffraction is particularly advantageous because it combines element selectivity with a large magnetic cross-section. We calculate the polarization dependence of the resonant magnetic x-ray cross-section (electric dipole transition) for the basal plane magnetic spiral in hexaferrite Ba0.8Sr1.2Zn2Fe12O22 and deduce its domain population using circular polarized incident radiation. We demonstrate there is a direct correlation between the diffracted radiation and the helicity of the magnetic spiral.
Chiral four-wave-mixing signals are calculated using the irreducible tensor formalism. Different polarization and crossing angle configurations allow to single out the magnetic dipole and the electric quadrupole interactions. Other configurations can reveal that the chiral interaction occurs at a given step within the nonlinear interaction pathways contributing to the signal. Applications are made to the study of valence excitations of S-ibuprofen by chiral Stimulated X-ray Raman signals at the Carbon K-edge and by chiral visible 2D Electronic Spectroscopy.teraction pathways contributing to the signal.
Heterostructures of PbTiO$_3$/SrTiO$_3$ superlattices have shown the formation of polar vortices, in which a continuous rotation of ferroelectric polarization spontaneously forms. Recently, Shafer {it{et al.}} [Proc. Natl. Acad. Sci. (PNAS) {bf{115}}, 915 (2018)] reported strong {it{non-magnetic}} circular dichroism (CD) in resonant soft x-ray diffraction at the Ti $L_3$ edge from such superlattices. The authors ascribe the CD to the chiral rotation of a polar vector. However, a polar vector is invisible to the parity-even electric-dipole transition which governs absorption in the soft x-ray region. A realistic, non-magnetic explanation of the observed effect is found in Templeton-Templeton scattering. Following this route, the origin of the CD in Bragg diffraction is shown by us to be the chiral array of charge quadrupole moments that forms in these heterostructures. While there is no charge quadrupole moment in the spherically symmetric $3d^0$ valence state of Ti$^{4+}$, the excited state $2p_{3/2}3d(t_{2g})$ at the Ti $L_3$ resonance is known to have a quadrupole moment. Our expressions for intensities of satellite Bragg spots in resonance-enhanced diffraction of circularly polarized x-rays, including their harmonic content, account for all observations reported by Shafer {it{et al.}} We predict both intensities of Bragg spots for the second harmonic of a chiral superlattice and circular polarization created from unpolarized x-rays, in order that our successful explanation of existing diffraction data can be further scrutinized through renewed experimental investigations. The increased understanding of chiral dipole arrangements could open the door to switchable optical polarization.
We demonstrate theoretically that a strong high-frequency circularly polarized electromagnetic field can turn a two-dimensional periodic array of interconnected quantum rings into a topological insulator. The elaborated approach is applicable to calculate and analyze the electron energy spectrum of the array, the energy spectrum of the edge states and the corresponding electronic densities. As a result, the present theory paves the way to optical control of the topological phases in ring-based mesoscopic structures.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
