RESUMO
We report the evolution of the electronic structure at the surface of the layered perovskite Sr_{2}RuO_{4} under large in-plane uniaxial compression, leading to anisotropic B_{1g} strains of ϵ_{xx}-ϵ_{yy}=-0.9±0.1%. From angle-resolved photoemission, we show how this drives a sequence of Lifshitz transitions, reshaping the low-energy electronic structure and the rich spectrum of van Hove singularities that the surface layer of Sr_{2}RuO_{4} hosts. From comparison to tight-binding modeling, we find that the strain is accommodated predominantly by bond-length changes rather than modifications of octahedral tilt and rotation angles. Our study sheds new light on the nature of structural distortions at oxide surfaces, and how targeted control of these can be used to tune density of state singularities to the Fermi level, in turn paving the way to the possible realization of rich collective states at the Sr_{2}RuO_{4} surface.
RESUMO
The interplay between spin-orbit coupling and structural inversion symmetry breaking in solids has generated much interest due to the nontrivial spin and magnetic textures which can result. Such studies are typically focused on systems where large atomic number elements lead to strong spin-orbit coupling, in turn rendering electronic correlations weak. In contrast, here we investigate the temperature-dependent electronic structure of [Formula: see text], a [Formula: see text] oxide metal for which both correlations and spin-orbit coupling are pronounced and in which octahedral tilts and rotations combine to mediate both global and local inversion symmetry-breaking polar distortions. Our angle-resolved photoemission measurements reveal the destruction of a large hole-like Fermi surface upon cooling through a coupled structural and spin-reorientation transition at 48 K, accompanied by a sudden onset of quasiparticle coherence. We demonstrate how these result from band hybridization mediated by a hidden Rashba-type spin-orbit coupling. This is enabled by the bulk structural distortions and unlocked when the spin reorients perpendicular to the local symmetry-breaking potential at the Ru sites. We argue that the electronic energy gain associated with the band hybridization is actually the key driver for the phase transition, reflecting a delicate interplay between spin-orbit coupling and strong electronic correlations and revealing a route to control magnetic ordering in solids.
RESUMO
We show that atoms in tilted optical superlattices provide a platform for exploring coupled spin chains of forms that are not present in other systems. In particular, using a period-2 superlattice in one dimension, we show that coupled Ising spin chains with XZ and ZZ spin coupling terms can be engineered. We use optimized tensor network techniques to explore the criticality and nonequilibrium dynamics in these models, finding a tricritical Ising point in regimes that are accessible in current experiments. These setups are ideal for studying low-entropy physics, as initial entropy is "frozen-out" in realizing the spin models, and provide an example of the complex critical behavior that can arise from interaction-projected models.
RESUMO
We analyze the low-energy physics of nearly ferromagnetic metals in two spatial dimensions using the functional renormalization group technique. We find a new low-energy fixed point, at which the fermionic (electronlike) excitations are non-Fermi-liquid (z_{f}=13/10) and the magnetic fluctuations exhibit an anomalous Landau damping whose rate vanishes as Γ_{q}â¼|q|^{3/5} in the low-|q| limit. We discuss this renormalization of the Landau-damping exponent, which is the major novel prediction of our work, and highlight the possible link between that renormalization and neutron-scattering data on UGe_{2} and related compounds. Implications of our analysis for YFe_{2}Al_{10} are also discussed.
