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Register a new userTopological states in pyrochlore iridates: long-range anisotropy strongly competing with spin-orbit interaction
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Added by
Jeroen van den Brink
Publication date
2012
fields
Physics
and research's language is
English
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In the search for topological phases in correlated electron systems, iridium-based pyrochlores A2Ir2O7 -- materials with 5d transition-metal ions -- provide fertile grounds. Several novel topological states have been predicted but the actual realization of such states is believed to critically depend on the strength of local potentials arising from distortions of IrO6-cages. We test this hypothesis by measuring with resonant x-ray scattering the electronic level splittings in the A= Y, Eu systems, which we show to agree very well with ab initio electronic structure calculations. We find, however, that not distortions of IrO6-octahedra are the primary source for quenching the spin-orbit interaction, but strong long-range lattice anisotropies, which inevitably break the local cubic symmetry and will thereby be decisive in determining the systems topological ground state.
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Strong electronic interactions and spin orbit coupling can be conducive for realizing novel broken symmetry phases supporting quasiparticles with nontrivial band topology. 227 pyrochlore iridates provide a suitable material platform for studying such emergent phenomena where both topology and competing orders play important roles. In contrast to the most members of this material class, which are thought to display all-in all-out (AIAO) type magnetically ordered low-temperature insulating ground states, Pr$_2$Ir$_2$O$_7$ remains metallic while exhibiting spin ice (SI) correlations at low temperatures. Additionally, this is the only 227 iridate compound, which exhibits a large anomalous Hall effect (AHE) along [1,1,1] direction below 1.5 K, without possessing any measurable magnetic moment. By focusing on the normal state of 227 iridates, described by a parabolic semimetal with quadratic band touching, we use renormalization group analysis, mean-field theory, and phenomenological Landau theory as three complementary methods to construct a global phase diagram in the presence of generic local interactions among itinerant electrons of Ir ions. While the global phase diagram supports several competing multipolar orders, motivated by the phenomenology of 227 iridates we particularly emphasize the competition between AIAO and SI orders and how it can cause a mixed phase with three-in one-out (3I1O) spin configurations. In terms of topological properties of Weyl quasiparticles of the 3I1O state, we provide an explanation for the magnitude and the direction of the observed AHE in Pr$_2$Ir$_2$O$_7$. We propose a strain induced enhancement of the onset temperature for AHE in thin films of Pr$_2$Ir$_2$O$_7$ and additional experiments for studying competing orders in the vicinity of the metal-insulator transition.
Nonequilibrium many-body dynamics is becoming one of the central topics of modern condensed matter physics. Floquet topological states were suggested to emerge in photodressed band structures in the presence of periodic laser driving. Here we propose a viable nonequilibrium route without requiring coherent Floquet states to reach the elusive magnetic Weyl semimetallic phase in pyrochlore iridates by ultrafast modification of the effective electron-electron interaction with short laser pulses. Combining textit{ab initio} calculations for a time-dependent self-consistent reduced Hubbard $U$ controlled by laser intensity and nonequilibrium magnetism simulations for quantum quenches, we find dynamically modified magnetic order giving rise to transiently emerging Weyl cones that are probed by time- and angle-resolved photoemission spectroscopy. Our work offers a unique and realistic pathway for nonequilibrium materials engineering beyond Floquet physics to create and sustain Weyl semimetals. This may lead to ultrafast, tens-of-femtoseconds switching protocols for light-engineered Berry curvature in combination with ultrafast magnetism.
The recent discovery of magnetic topological insulators has opened new avenues to explore exotic states of matter that can emerge from the interplay between topological electronic states and magnetic degrees of freedom, be it ordered or strongly fluctuating. Motivated by the effects that the dynamics of the magnetic moments can have on the topological surface states, we investigate the magnetic fluctuations across the (MnBi$_{text{2}}$Te$_{text{4}}$)(Bi$_{text{2}}$Te$_{text{3}}$)$_{text{n}}$ family. Our paramagnetic electron spin resonance experiments reveal contrasting Mn spin dynamics in different compounds, which manifests in a strongly anisotropic Mn spin relaxation in MnBi$_{text{2}}$Te$_{text{4}}$ while being almost isotropic in MnBi$_{text{4}}$Te$_{text{7}}$. Our density-functional calculations explain these striking observations in terms of the sensitivity of the local electronic structure to the Mn spin-orientation, and indicate that the anisotropy of the magnetic fluctuations can be controlled by the carrier density, which may directly affect the electronic topological surface states.
The longitudinal spin-Seebeck effect (SSE) in magnetic insulator$|$non-magnetic metal heterostructures has been theoretically studied primarily with the assumption of an isotropic interfacial exchange coupling. Here, we present a general theory of the SSE in the case of an antisymmetric Dzyaloshinskii-Moriya interaction (DMI) at the interface, in addition to the usual Heisenberg form. We numerically evaluate the dependence of the spin current on the temperature and bulk DMI using a pyrochlore iridate as a model insulator with all-in all-out (AIAO) ground state configuration. We also compare the results of different crystalline surfaces arising from different crystalline orientations and conclude that the relative angles between the interfacial moments and Dzyaloshinskii-Moriya vectors play a significant role in the spin transfer. Our work extends the theory of the SSE by including the anisotropic nature of the interfacial Dzyaloshinskii-Moriya exchange interaction in magnetic insulator$|$non-magnetic metal heterostructures and can suggest possible materials to optimize the interfacial spin transfer in spintronic devices.
Very few topological systems with long-range couplings have been considered so far due to our lack of analytic approaches. Here we extend the Kitaev chain, a 1D quantum liquid, to infinite-range couplings and study its topological properties. We demonstrate that, even though topological phases are intimately linked to the notion of locality, the infinite-range couplings give rise to topological zero and non-zero energy Majorana end modes depending on the boundary conditions of the system. We show that the analytically derived properties are to a large degree stable against modifications to decaying long-range couplings. Our work opens new frontiers for topological states of matter that are relevant to current experiments where suitable interactions can be designed.
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