ABSTRACT
Non-collinear antiferromagnets are revealing many unexpected phenomena and they became crucial for the field of antiferromagnetic spintronics. To visualize and prepare a well-defined domain structure is of key importance. The spatial magnetic contrast, however, remains extraordinarily difficult to be observed experimentally. Here, we demonstrate a magnetic imaging technique based on a laser induced local thermal gradient combined with detection of the anomalous Nernst effect. We employ this method in one the most actively studied representatives of this class of materials-Mn3Sn. We demonstrate that the observed contrast is of magnetic origin. We further show an algorithm to prepare a well-defined domain pattern at room temperature based on heat assisted recording principle. Our study opens up a prospect to study spintronics phenomena in non-collinear antiferromagnets with spatial resolution.
ABSTRACT
An accurate material representation of polymeric interlayers in laminated glass panes has proved fundamental for a reliable prediction of their response in both static and dynamic loading regimes. This issue is addressed in the present contribution by examining the time-temperature sensitivity of the shear stiffness of two widely used interlayers made of polyvinyl butyral (TROSIFOL BG R20) and ethylene-vinyl acetate (EVALAM 80-120). To that end, an experimental program has been executed to compare the applicability of two experimental techniques, (i) dynamic torsional tests and (ii) dynamic single-lap shear tests, in providing data needed in a subsequent calibration of a suitable material model. Herein, attention is limited to the identification of material parameters of the generalized Maxwell chain model through the combination of linear regression and the Nelder-Mead method. The choice of the viscoelastic material model has also been supported experimentally. The resulting model parameters confirmed a strong material variability of both interlayers with temperature and time. While higher initial shear stiffness was observed for the polyvinyl butyral interlayer in general, the ethylene-vinyl acetate interlayer exhibited a less pronounced decay of stiffness over time and a stiffer response in long-term loading.
ABSTRACT
Magnetic properties are commonly used to identify new aromatic molecules because it is generally believed that magnetization and energetic stability are correlated. To verify the potential correlation between the energy and magnetic response properties, we examined a set of 198 isomers of C6 H6 . The energy and magnetic properties of these molecules can be directly compared with no need to invoke any arbitrary reference state because the studied systems are all isomers. Benzene is the global minimum on the potential energy surface of C6 H6 , 35â kcal mol-1 lower in energy than the second most stable isomer, fulvene. Unlike its electronic energy, isotropic magnetizability of benzene is slightly lower than the average magnetizability of its isomers. Altogether, 44 isomers of C6 H6 were identified to have more negative magnetic susceptibility than benzene but were between 67.0 to 168.6â kcal mol-1 higher in energy than benzene. However, benzene is unique in two ways. Analyzing the paramagnetic contribution to the magnetic susceptibility as originally suggested by Bilde and Hansen (Mol. Phys., 1997, 92, 237) revealed that 53â molecules have lower paramagnetic susceptibility than benzene but among monocyclic systems benzene has the least paramagnetic susceptibility. Furthermore, benzene has the largest out-of-plane magnetic susceptibility that originates from the strongest ring current among all studied species.
