Tuning magnetic chirality by dipolar interactions

Chiral magnetism has gained enormous interest in recent years because of the anticipated wealth of applications in nanoelectronics. The demonstrated stabilization of chiral magnetic domain walls and skyrmions has been attributed to the actively investigated Dzyaloshinskii-Moriya interaction. Recently, however, predictions were made that suggest dipolar interactions can also stabilize chiral domain walls and skyrmions, but direct experimental evidence has been lacking. Here we show that dipolar interactions can indeed stabilize chiral domain walls by directly imaging the magnetic domain walls using scanning electron microscopy with polarization analysis. We further show that the competition between the Dzyaloshinskii-Moriya and dipolar interactions can reverse the domain-wall chirality. Finally, we suggest that this competition can be tailored by a Ruderman-Kittel-Kasuya-Yosida interaction. Our work therefore reveals that dipolar interactions play a key role in the stabilization of chiral spin textures. This insight will open up new routes towards balancing interactions for the stabilization of chiral magnetism

Origin of the time dependence of wet oxidation of AlGaAs

The time-dependence of the wet oxidation of high-Al-content AlGaAs can be either linear, indicating reaction-rate limitation, or parabolic, indicating diffusion-limited rates. The transition from linear to parabolic time dependence can be explained by the increased rate of the formation of intermediate As{sub 2}O{sub 3} vs. its reduction to elemental As. A steadily increasing thickness of the As{sub 2}O{sub 3}-containing region at the oxidation front will shift the process from the linear to the parabolic regime. This shift from reaction-rate-limited (linear) to diffusion-limited (parabolic) time dependence is favored by increasing temperature or increasing Al mole fraction

Differences between students and physicians in their entitlement towards procedural skills education – a needs assessment of skills training in internal medicine

Objective: Procedural skills education has a high priority for medical students. However, it is not clear what kind of skills they consider important and whether their perception differs from the physicians’ view

Contributions of inelastically scattered electrons to defect images.

We have made measurements of the contribution of inelastically scattered electrons to images of dislocations in Ni{sub 3}Ga and nanometer-sized defects in ion-irradiated Au under weak-beam dark-field diffraction conditions [1]. The purpose is to determine the conditions for data acquisition required to eventually make detailed and quantitative comparisons to simulations of images for various defect models, thus determining defect structure, composition, and local strain field. Such image simulations usually consider only elastically scattered electrons, and thus it is important to understand and possibly eliminate the contribution of inelastically scattered electrons to the experimental images for quantitative comparisons with image simulations. Experimental data have been acquired with either JEOL 2010F or 3000F microscopes, both equipped with Gatan Imaging Filter electron spectrometers. Samples examined in the 2010F were Au, ion-irradiated to low dose (10{sup 11}Kr ions at 1 MeV energy) to form individual defects (1-10nm sized Frank dislocation loops and partial stacking fault tetrahedra). Samples examined in the 3000F were Ni{sub 3}Ga with long dislocation defects. Imaging conditions included weak-beam dark-field with deviation parameter generally > 0.2 nm{sup -1}. Energy filter slit width was set to 10 eV and centered on the zero loss peak in both instruments to obtain images produced by elastically scattered electrons. In the Au experiment an energy window was also set to image the 10-40 eV loss range to investigate the contribution to the defect images of plasmon-loss electrons. Electron intensity in defect images and backgrounds was measured by summing pixel values in appropriately sized rectangles using Digital Micrograph (Gatan) software

Magnetic chirality controlled by the interlayer exchange interaction

Chiral magnetism, wherein there is a preferred sense of rotation of the magnetization, has become a key aspect for future spintronic applications. It determines the chiral nature of magnetic textures, such as skyrmions, domain walls or spin spirals, and a specific magnetic chirality is often required for spintronic applications. Current research focuses on identifying and controlling the interactions that define the magnetic chirality. The influence of the interfacial Dzyaloshinskii-Moriya interaction (iDMI) and, recently, the dipolar interactions have previously been reported. Here, we experimentally demonstrate that an indirect interlayer exchange interaction can be used as an additional tool to effectively manipulate the magnetic chirality. We image the chirality of magnetic domain walls in a coupled bilayer system using scanning electron microscopy with polarization analysis (SEMPA). Upon increasing the interlayer exchange coupling, we induce a transition of the magnetic chirality from clockwise rotating N\'eel walls to degenerate Bloch-N\'eel domain walls and we confirm our findings with micromagnetic simulations. In multi-layered systems relevant for skyrmion research a uniform magnetic chirality across the magnetic layers is often desired. Additional simulations show that this can be achieved for reduced iDMI values when exploiting the interlayer exchange interaction. This work opens up new ways to control and tailor the magnetic chirality by the interlayer exchange interaction.Comment: Ms was off by a factor

Metal Core Bonding Motifs of Monodisperse Icosahedral Au13 and Larger Au Monolayer-Protected Clusters As Revealed by X-ray Absorption Spectroscopy and Transmission Electron Microscopy

The atomic metal core structures of the subnanometer clusters Au13[PPh3]4[S(CH2)11CH3]2Cl2 (1) and Au13[PPh3]4[S(CH2)11CH3]4 (2) were characterized using advanced methods of electron microscopy and X-ray absorption spectroscopy. The number of gold atoms in the cores of these two clusters was determined quantitatively using high-angle annular dark field scanning transmission electron microscopy. Multiple-scattering-path analyses of extended X-ray absorption fine structure (EXAFS) spectra suggest that the Au metal cores of each of these complexes adopt an icosahedral structure with a relaxation of the icosahedral strain. Data from microscopy and spectroscopy studies extended to larger thiolate-protected gold clusters showing a broader distribution in nanoparticle core sizes (183 ± 116 Au atoms) reveal a bulklike fcc structure. These results further support a model for the monolayer-protected clusters (MPCs) in which the thiolate ligands bond preferentially at 3-fold atomic sites on the nanoparticle surface, establishing an average composition for the MPC of Au180[S(CH2)11CH3]40. Results from EXAFS measurements of a gold(I) dodecanethiolate polymer are presented that offer an alternative explanation for observations in previous reports that were interpreted as indicating Au MPC structures consisting of a Au core, Au2S shell, and thiolate monolayer

Stress-driven instability in growing multilayer films

We investigate the stress-driven morphological instability of epitaxially growing multilayer films, which are coherent and dislocation-free. We construct a direct elastic analysis, from which we determine the elastic state of the system recursively in terms of that of the old states of the buried layers. In turn, we use the result for the elastic state to derive the morphological evolution equation of surface profile to first order of perturbations, with the solution explicitly expressed by the growth conditions and material parameters of all the deposited layers. We apply these results to two kinds of multilayer structures. One is the alternating tensile/compressive multilayer structure, for which we determine the effective stability properties, including the effect of varying surface mobility in different layers, its interplay with the global misfit of the multilayer film, and the influence of asymmetric structure of compressive and tensile layers on the system stability. The nature of the asymmetry properties found in stability diagrams is in agreement with experimental observations. The other multilayer structure that we study is one composed of stacked strained/spacer layers. We also calculate the kinetic critical thickness for the onset of morphological instability and obtain its reduction and saturation as number of deposited layers increases, which is consistent with recent experimental results. Compared to the single-layer film growth, the behavior of kinetic critical thickness shows deviations for upper strained layers.Comment: 27 pages, 11 figures; Phys. Rev. B, in pres