RESUMEN
We report on the commissioning results of the cold neutron multiplexing secondary spectrometer CAMEA (Continuous Angle Multi-Energy Analysis) at the Swiss Spallation Neutron Source at the Paul Scherrer Institut, Switzerland. CAMEA is optimized for efficient data acquisition of scattered neutrons in the horizontal scattering plane, allowing for detailed and rapid mapping of low-energy excitations under extreme sample environment conditions.
RESUMEN
Although ultrafast manipulation of magnetism holds great promise for new physical phenomena and applications, targeting specific states is held back by our limited understanding of how magnetic correlations evolve on ultrafast timescales. Using ultrafast resonant inelastic X-ray scattering we demonstrate that femtosecond laser pulses can excite transient magnons at large wavevectors in gapped antiferromagnets and that they persist for several picoseconds, which is opposite to what is observed in nearly gapless magnets. Our work suggests that materials with isotropic magnetic interactions are preferred to achieve rapid manipulation of magnetism.
RESUMEN
We present a study of resonant inelastic x-ray scattering (RIXS) spectra collected at the rare-earth L edges of divalent hexaborides YbB6 and EuB6. In both systems, RIXS-active features are observed at two distinct resonances separated by [Formula: see text] eV in incident energy, with angle-dependence suggestive of distinct photon scattering processes. RIXS spectra collected at the divalent absorption peak resemble the unoccupied 5d density of states calculated using density functional theory. We discuss possible origins of this correspondence including a scenario which changes the 4fâ valence. In addition, anomalous resonant scattering is observed at higher incident energy, where no corresponding absorption feature is present. Our results demonstrate the potential for L-edge RIXS to assess the itinerant-state properties of fâ-electron materials.
RESUMEN
Coordination networks (CNs), such as, for instance, metal-organic frameworks (MOFs), can turn into remarkable magnets, with various topologies of spin carriers and unique opportunities of cross-coupling to other functionalities. Alternatively, distinct inorganic subnetworks that are spatially segregated by organic ligands can lead to coexisting magnetic systems in a single bulk material. Here, we present a system of two CNs of general formula Mn(H2O) x(OOC-(C6H4) y-COO). The compound with two water molecules and one aromatic ring ( x = 2; y = 1) has a single two-dimensional magnetic subnet, while the material with x = 1.5 and y = 2 shows, additionally, another type of magnetic layer. In analogy to magnetic multilayers that are deposited by physical methods, these materials can be regarded as metal-organic magnetic multilayers (MOMMs), where the stacking of different types of magnetic layers is controlled by the choice of an organic ligand during the chemical synthesis. This work further paves the way toward organic-inorganic nanostructures with functional magnetic properties.
