Synthesis and crystal growth

Abstract:

Resonant elastic X-ray scattering (REXS) at the Eu M5 edge reveals an antiferromagnetic structure in layered EuCd2Sb2 at temperatures below TN = 7.4 K with a magnetic propagation vector of (0, 0, 1/2) and spins in the basal plane. Magneto-transport and REXS measurements with an in-plane magnetic field show that features in the magnetoresistance are correlated with changes in the magnetic structure induced by the field. Ab initio electronic structure calculations predict that the observed spin structure gives rise to a gapped Dirac point close to the Fermi level with a gap of ∆E ∼ 0.01 eV. The results of this study indicate that the Eu spins are coupled to conduction electron states near the Dirac point.

Abstract:

Determining the fate of the Pauling entropy in the classical spin ice material Dy₂Ti₂O₇ with respect to the third law of thermodynamics has become an important test case for understanding the existence and stability of ice-rule states in general. The standard model of spin ice—the dipolar spin ice model—predicts an ordering transition at T≈0.15  K, but recent experiments by Pomaranski et al. suggest an entropy recovery over long timescales at temperatures as high as 0.5 K, much too high to be compatible with the theory. Using neutron scattering and specific heat measurements at low temperatures and with long timescales (0.35  K/10⁶  s and 0.5  K/10⁵  s, respectively) on several isotopically enriched samples, we find no evidence of a reduction of ice-rule correlations or spin entropy. High-resolution simulations of the neutron structure factor show that the spin correlations remain well described by the dipolar spin ice model at all temperatures. Furthermore, by careful consideration of hyperfine contributions, we conclude that the original entropy measurements of Ramirez et al. are, after all, essentially correct: The short-time relaxation method used in that study gives a reasonably accurate estimate of the equilibrium spin ice entropy due to a cancellation of contributions.

Abstract:

Neutron spectroscopy was applied to study the magnetic interactions of orbitally degenerate Co2+ on a host MgO rocksalt lattice where no long-range spin or orbital order exists. The paramagnetic nature of the substituted monoxide Co0.03Mg0.97O allows for the disentanglement of spin exchange and spin-orbit interactions. By considering the prevalent excitations from Co2+ spin pairs, we extract seven exchange constants out to the fourth coordination shell. An antiferromagnetic next-nearest-neighbor 180◦ exchange interaction is dominant; however, dual ferromagnetic and antiferromagnetic interactions are observed for pairings with other pathways. These interactions can be understood in terms of a combination of orbital degeneracy in the t2g channel and the Goodenough-Kanamori-Anderson rules. Our work suggest that such a hierarchy of exchange interactions exists in transition-metal-based oxides with a t2g orbital degeneracy.

Abstract:

Inelastic neutron scattering has been used to study the magnetoelastic excitations in the multiferroic manganite hexagonal YMnO3. An avoided crossing is found between magnon and phonon modes close to the Brillouin zone boundary in the (a,b) plane. Neutron polarization analysis reveals that this mode has mixed magnon-phonon character. An external magnetic field along the c axis is observed to cause a linear field-induced splitting of one of the spin-wave branches. A theoretical description is performed, using a Heisenberg model of localized spins, acoustic phonon modes, and a magnetoelastic coupling via the single-ion magnetostriction. The model quantitatively reproduces the dispersion and intensities of all modes in the full Brillouin zone, describes the observed magnon-phonon hybridized modes, and quantifies the magnetoelastic coupling. The combined information, including the field-induced magnon splitting, allows us to exclude several of the earlier proposed models and point to the correct magnetic ground state symmetry, and provides an effective dynamic model relevant for the multiferroic hexagonal manganites.