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Register a new userUsing thermal boundary conditions to engineer the quantum state of a bulk magnet
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The degree of contact between a system and the external environment can alter dramatically its proclivity to quantum mechanical modes of relaxation. We show that controlling the thermal coupling of cubic centimeter-sized crystals of the Ising magnet $LiHo_xY_{1-x}F_4$ to a heat bath can be used to tune the system between a glassy state dominated by thermal excitations over energy barriers and a state with the hallmarks of a quantum spin liquid. Application of a magnetic field transverse to the Ising axis introduces both random magnetic fields and quantum fluctuations, which can retard and speed the annealing process, respectively, thereby providing a mechanism for continuous tuning between the destination states. The non-linear response of the system explicitly demonstrates quantum interference between internal and external relaxation pathways.
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We have computed the low energy quantum states and low frequency dynamical susceptibility of complex quantum spin systems in the limit of strong interactions, obtaining exact results for system sizes enormously larger than accessible previously. The ground state is a complex superposition of a substantial fraction of all the classical ground states, and yet the dynamical susceptibility exhibits sharp resonances reminiscent of the behavior of single spins. These results show that strongly interacting quantum systems can organize to generate coherent excitations and shed light on recent experiments demonstrating that coherent excitations are present in a disordered spin liquid. The dependence of the energy spectra on system size differs qualitatively from that of the energy spectra of random undirected bipartite graphs with similar statistics, implying that strong interactions are giving rise to these unusual spectral properties.
Weyl fermions in an external magnetic field exhibit the chiral anomaly, a non-conservation of chiral fermions. In a Weyl semimetal, a spatially inhomogeneous Weyl node separation causes similar effect by creating an intrinsic pseudo-magnetic field with an opposite sign for nodes of opposite chirality. In the present work we study the interplay of external and intrinsic fields. In particular, we focus on quantum oscillations due to bulk-boundary trajectories. When caused by an external field, such oscillations are a proven experimental technique to detect Weyl semimetals. We show that the intrinsic field leaves hallmarks on such oscillations by decreasing the period of the oscillations in an analytically traceable manner. The oscillations can thus be used to test the effect of an intrinsic field and to extract its strength.
The relaxation time of a classical spin interacting with a large conduction-electron system is computed for a weak magnetic field, which initially drives the spin out of equilibrium. We trace the spin and the conduction-electron dynamics on a time scale, which exceeds the characteristic electronic scale that is set by the inverse nearest-neighbor hopping by more than five orders of magnitude. This is achieved with a novel construction of absorbing boundary conditions, which employs a generalized Lindblad master-equation approach to couple the edge sites of the conduction-electron tight-binding model to an external bath. The failure of the standard Lindblad approach to absorbing boundaries is traced back to artificial excitations initially generated due to the coupling to the bath. This can be cured by introducing Lindblad parameter matrices and by fixing those matrices to perfectly suppress initial-state artifacts as well as reflections of physical excitations propagating to the system boundaries. Numerical results are presented and discussed for generic one-dimensional models of the electronic structure.
Bulk-boundary correspondence, a central principle in topological matter relating bulk topological invariants to edge states, breaks down in a generic class of non-Hermitian systems that have so far eluded experimental effort. Here we theoretically predict and experimentally observe non-Hermitian bulk-boundary correspondence, a fundamental generalization of the conventional bulk-boundary correspondence, in discrete-time non-unitary quantum-walk dynamics of single photons. We experimentally demonstrate photon localizations near boundaries even in the absence of topological edge states, thus confirming the non-Hermitian skin effect. Facilitated by our experimental scheme of edge-state reconstruction, we directly measure topological edge states, which match excellently with non-Bloch topological invariants calculated from localized bulk-state wave functions. Our work unequivocally establishes the non-Hermitian bulk-boundary correspondence as a general principle underlying non-Hermitian topological systems, and paves the way for a complete understanding of topological matter in open systems.
We report high-resolution spin-resolved photoemission spectroscopy (Spin-ARPES) measurements on the parent compound Sb of the first discovered 3D topological insulator Bi{1-x}Sb{x} [D. Hsieh et al., Nature 452, 970 (2008) Submitted 2007]. By modulating the incident photon energy, we are able to map both the bulk and (111) surface band structure, from which we directly demonstrate that the surface bands are spin polarized by the spin-orbit interaction and connect the bulk valence and conduction bands in a topologically non-trivial way. A unique asymmetric Dirac surface state gives rise to a $k$-splitting of its spin polarized electronic channels. These results complement our previously published works on this materials class and re-confirm our discovery of first bulk (3D) topological insulator - topological order in bulk solids. [Invited article for NJP-IOP Focus issue on Topological Insulators]
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