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Periodic driving can be used to control the properties of a many-body state coherently and to realize phases that are not accessible in static systems. For example, exposing materials to intense laser pulses makes it possible to induce metal-insulator transitions, to control magnetic order and to generate transient superconducting behaviour well above the static transition temperature. However, pinning down the mechanisms underlying these phenomena is often difficult because the response of a material to irradiation is governed by complex, many-body dynamics. For static systems, extensive calculations have been performed to explain phenomena such as high-temperature superconductivity. Theoretical analyses of driven many-body Hamiltonians are more challenging, but approaches have now been developed, motivated by recent observations. Here we report an experimental quantum simulation in a periodically modulated hexagonal lattice and show that antiferromagnetic correlations in a fermionic many-body system can be reduced, enhanced or even switched to ferromagnetic correlations (sign reversal). We demonstrate that the description of the many-body system using an effective Floquet-Hamiltonian with a renormalized tunnelling energy remains valid in the high-frequency regime by comparing the results to measurements in an equivalent static lattice. For near-resonant driving, the enhancement and sign reversal of correlations is explained by a microscopic model of the system in which the particle tunnelling and magnetic exchange energies can be controlled independently. In combination with the observed sufficiently long lifetimes of the correlations in this system, periodic driving thus provides an alternative way of investigating unconventional pairing in strongly correlated systems experimentally.
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We study low-frequency linearly polarized laser-dressing in materials with valley (graphene and hexagonal-Boron-Nitride) and topological (Dirac- and Weyl-semimetals) properties. In Dirac-like linearly dispersing bands, the laser substantially moves the Dirac nodes away from their original position, and the movement direction can be fully controlled by rotating the laser polarization. We prove that this effect originates from band nonlinearities away from the Dirac nodes. We further demonstrate that this physical mechanism is widely applicable and can move the positions of the valley minima in hexagonal materials to tune valley selectivity, split and move Weyl cones in higher-order Weyl semimetals, and merge Dirac nodes in three-dimensional Dirac semimetals. The model results are validated with ab initio calculations. Our results directly affect efforts for exploring light-dressed electronic structure, suggesting that one can benefit from band nonlinearity for tailoring material properties, and highlight the importance of the full band structure in nonlinear optical phenomena in solids.
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The Haldane model on a honeycomb lattice is a paradigmatic example of a Hamiltonian featuring topologically distinct phases of matter. It describes a mechanism through which a quantum Hall effect can appear as an intrinsic property of a band structure, rather than being caused by an external magnetic field. Although physical implementation has been considered unlikely, the Haldane model has provided the conceptual basis for theoretical and experimental research exploring topological insulators and superconductors. Here we report the experimental realization of the Haldane model and the characterization of its topological band structure, using ultracold fermionic atoms in a periodically modulated optical honeycomb lattice. The Haldane model is based on breaking both time-reversal symmetry and inversion symmetry. To break time-reversal symmetry, we introduce complex next-nearest-neighbour tunnelling terms, which we induce through circular modulation of the lattice position. To break inversion symmetry, we create an energy offset between neighbouring sites. Breaking either of these symmetries opens a gap in the band structure, which we probe using momentum-resolved interband transitions. We explore the resulting Berry curvatures, which characterize the topology of the lowest band, by applying a constant force to the atoms and find orthogonal drifts analogous to a Hall current. The competition between the two broken symmetries gives rise to a transition between topologically distinct regimes. By identifying the vanishing gap at a single Dirac point, we map out this transition line experimentally and quantitatively compare it to calculations using Floquet theory without free parameters. We verify that our approach, which allows us to tune the topological properties dynamically, is suitable even for interacting fermionic systems. Furthermore, we propose a direct extension to realize spin-dependent topological Hamiltonians.
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Dirac points are central to many phenomena in condensed-matter physics, from massless electrons in graphene to the emergence of conducting edge states in topological insulators. At a Dirac point, two energy bands intersect linearly and the electrons behave as relativistic Dirac fermions. In solids, the rigid structure of the material determines the mass and velocity of the electrons, as well as their interactions. A different, highly flexible means of studying condensed-matter phenomena is to create model systems using ultracold atoms trapped in the periodic potential of interfering laser beams. Here we report the creation of Dirac points with adjustable properties in a tunable honeycomb optical lattice. Using momentum-resolved interband transitions, we observe a minimum bandgap inside the Brillouin zone at the positions of the two Dirac points. We exploit the unique tunability of our lattice potential to adjust the effective mass of the Dirac fermions by breaking inversion symmetry. Moreover, changing the lattice anisotropy allows us to change the positions of the Dirac points inside the Brillouin zone. When the anisotropy exceeds a critical limit, the two Dirac points merge and annihilate each other-a situation that has recently attracted considerable theoretical interest but that is extremely challenging to observe in solids. We map out this topological transition in lattice parameter space and find excellent agreement with ab initio calculations. Our results not only pave the way to model materials in which the topology of the band structure is crucial, but also provide an avenue to exploring many-body phases resulting from the interplay of complex lattice geometries with interactions.
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We report on the observation of antiferromagnetic correlations of ultracold fermions in a variety of optical lattice geometries that are well described by the Hubbard model, including dimers, 1D chains, ladders, isolated and coupled honeycomb planes, as well as square and cubic lattices. The dependence of the strength of spin correlations on the specific geometry is experimentally studied by measuring the correlations along different lattice tunneling links, where a redistribution of correlations between the different lattice links is observed. By measuring the correlations in a crossover between distinct geometries, we demonstrate an effective reduction of the dimensionality for our atom numbers and temperatures. We also investigate the formation and redistribution time of spin correlations by dynamically changing the lattice geometry and studying the time evolution of the system. Time scales ranging from a sudden quench of the lattice geometry to an adiabatic evolution are probed.
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We demonstrate a versatile method for creating state-dependent optical lattices by applying a magnetic field gradient modulated in time. This allows for tuning the relative amplitude and sign of the tunneling for different internal states. We observe substantially different momentum distributions depending on the spin state of fermionic ^{40}K atoms. Using dipole oscillations, we probe the spin-dependent band structure and find good agreement with theory. In situ expansion dynamics demonstrate that one state can be completely localized while others remain itinerant. A systematic study shows negligible heating and lifetimes of several seconds in the Hubbard regime.
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We realize and study the ionic Hubbard model using an interacting two-component gas of fermionic atoms loaded into an optical lattice. The bipartite lattice has a honeycomb geometry with a staggered energy offset that explicitly breaks the inversion symmetry. Distinct density-ordered phases are identified using noise correlation measurements of the atomic momentum distribution. For weak interactions the geometry induces a charge density wave. For strong repulsive interactions we detect a strong suppression of doubly occupied sites, as expected for a Mott insulating state, and the externally broken inversion symmetry is not visible anymore in the density distribution. The local density distributions in different configurations are characterized by measuring the number of doubly occupied lattice sites as a function of interaction and energy offset. We further probe the excitations of the system using direction dependent modulation spectroscopy and discover a complex spectrum, which we compare with a theoretical model.
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We study the anisotropic 3D Hubbard model with increased nearest-neighbor tunneling amplitudes along one direction using the dynamical cluster approximation and compare the results to a quantum simulation experiment of ultracold fermions in an optical lattice. We find that the short-range spin correlations are significantly enhanced in the direction with stronger tunneling amplitudes. Our results agree with the experimental observations and show that the experimental temperature is lower than the strong tunneling amplitude. We characterize the system by examining the spin correlations beyond neighboring sites and determine the distribution of density, entropy, and spin correlation in the trapped system. We furthermore investigate the dependence of the critical entropy at the Néel transition on anisotropy.
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We create an artificial graphene system with tunable interactions and study the crossover from metallic to Mott insulating regimes, both in isolated and coupled two-dimensional honeycomb layers. The artificial graphene consists of a two-component spin mixture of an ultracold atomic Fermi gas loaded into a hexagonal optical lattice. For strong repulsive interactions, we observe a suppression of double occupancy and measure a gapped excitation spectrum. We present a quantitative comparison between our measurements and theory, making use of a novel numerical method to obtain Wannier functions for complex lattice structures. Extending our studies to time-resolved measurements, we investigate the equilibration of the double occupancy as a function of lattice loading time.
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Quantum magnetism originates from the exchange coupling between quantum mechanical spins. Here, we report on the observation of nearest-neighbor magnetic correlations emerging in the many-body state of a thermalized Fermi gas in an optical lattice. The key to obtaining short-range magnetic order is a local redistribution of entropy, which allows temperatures below the exchange energy for a subset of lattice bonds. When loading a repulsively interacting gas into either dimerized or anisotropic simple cubic configurations of a tunable-geometry lattice, we observe an excess of singlets as compared with triplets consisting of two opposite spins. For the anisotropic lattice, the transverse spin correlator reveals antiferromagnetic correlations along one spatial axis. Our work facilitates addressing open problems in quantum magnetism through the use of quantum simulation.