We present a new model to realize artificial 2D lattices with cold atoms investigating the atomic artificial graphene: a 2D confined matter wave is scattered by atoms of a second species trapped around the nodes of a honeycomb optical lattice. The system allows an exact determination of the Green function, hence of the transport properties. The inter-species interaction can be tuned via the interplay between scattering length and confinements. Band structure and density of states of a periodic lattice are derived for different values of the interaction strength. Emergence and features of Dirac cones are pointed out, together with the appearance of multiple gaps and a non-dispersive and isolated flat band. Robustness against finite-size and vacancies effects is numerically investigated.
We present a new model to realize artificial 2D lattices with cold atoms investigating the atomic artificial graphene: a 2D confined matter wave is scattered by atoms of a second species trapped around the nodes of a honeycomb optical lattice. The system allows an exact determination of the Green function, hence of the transport properties. The inter-species interaction can be tuned via the interplay between scattering length and confinements. Band structure and density of states of a periodic lattice are derived for different values of the interaction strength. Emergence and features of Dirac cones are pointed out, together with the appearance of multiple gaps and a non-dispersive and isolated flat band. Robustness against finite-size and vacancies effects is numerically investigated.
We present a general scheme to realize a cold-atom quantum simulator of bidimensional atomic crystals. Our model is based on the use of two independently trapped atomic species: the first one, subject to a strong in-plane confinement, constitutes a two-dimensional matter wave which interacts only with atoms of the second species, deeply trapped around the nodes of a two-dimensional optical lattice. By introducing a general analytic approach we show that the system Green function can be exactly determined, allowing for the investigation of the matter-wave transport properties. We propose some illustrative applications to both Bravais (square, triangular) and non-Bravais (graphene, kagom\'e) lattices, studying both ideal periodic systems and experimental-size and disordered ones. Some remarkable spectral properties of these atomic artificial lattices are pointed out, such as the emergence of single and multiple gaps, flat bands, and Dirac cones. All these features can be manipulated via the interspecies interaction, which proves to be widely tunable due to the interplay between scattering length and confinements.
We study the ground-state properties of the interacting spinless fermions in the px,y-orbital bands in the two-dimensional honeycomb optical lattice, which exhibit different features from those in the pz-orbital system of graphene. In addition to two dispersive bands with Dirac cones, the tight-binding band structure exhibits another two completely flat bands over the entire Brillouin zone. With the realistic sinusoidal optical potential, the flat bands acquire a finite but much smaller bandwidth compared to the dispersive bands. The band flatness dramatically enhanced interaction effects giving rise to various charge and bond ordered states at commensurate fillings of n=6i(i=1−−6). At n=61, the many-body ground states can be exactly solved as the close-packed hexagon states which can be stabilized even in the weakly interacting regime. The dimerization of bonding strength occurs at both n=21 and 65, and the latter case is accompanied with the charge-density wave of holes. The trimerization of bonding strength and charge inhomogeneity appear at n=31,32. These crystalline orders exhibit themselves in the noise correlations of the time-of-flight spectra.
Abstract Cold atoms in an optical lattice with brick-wall geometry have been used to mimic graphene, a two-dimensional material with characteristic Dirac excitations. Here we propose to bring such artificial graphene into the proximity of a second atomic layer with a square lattice geometry. For non-interacting fermions, we find that such bilayer system undergoes a phase transition from a graphene-like semi-metal phase, characterized by a band structure with Dirac points, to a gapped band insulator phase. In the presence of attractive interactions between fermions with pseudospin-1/2 degree of freedom, a competition between semi-metal and superfluid behavior is found at the mean-field level. Using the quantum Monte Carlo method, we also investigate the case of strong repulsive interactions. In the Mott phase, each layer exhibits a different amount of long-range magnetic order. Upon coupling both layers, a valence-bond crystal is formed at a critical coupling strength. Finally, we discuss how these bilayer systems could be realized in existing cold atom experiments.
The band spectrum of bosonic atoms in two-dimensional honeycomb optical lattices with the graphene-type structure has been studied. The dispersion laws in the bands and the one-particle spectral densities are calculated for the normal phase in the random phase approximation. The temperature-dependent gapless spectrum with Dirac points located at the Brillouin zone boundary is obtained for the lattice with energetically equivalent sites, with the corresponding chemical potential lying outside the allowed energy band. Different on-site energies in the sublattices are shown to induce the appearance of a gap in the spectrum, so that the chemical potential can be located between the subbands, which gives rise to a substantial reconstruction of the band spectrum. The frequency dependences of the one-particle spectral density for both sublattices are determined as functions of the chemical potential level, the spectral gap magnitude, and the temperature.
Abstract Here, we present the application of a novel method for controlling the geometry of a state-dependent honeycomb lattice: the energy offset between the two sublattices of the honeycomb structure can be adjusted by rotating the atomic quantization axis. This enables us to continuously tune between a homogeneous graphene-like honeycomb lattice and a triangular lattice and to open an energy gap at the characteristic Dirac points. We probe the symmetry of the lattice with microwave spectroscopy techniques and investigate the behavior of atoms excited to the second energy band. We find a striking influence of the energy gap at the Dirac cones onto the lifetimes of bosonic atoms in the excited band.
Dirac points lie at the heart of many fascinating 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 particles behave as relativistic Dirac fermions. In solids, the rigid structure of the material sets the mass and velocity of the particles, as well as their interactions. A different, highly flexible approach is to create model systems using fermionic atoms trapped in an optical lattice, a method which so far has only been applied to explore simple lattice structures. In my talk I will report on the creation of Dirac points with adjustable properties in a tunable honeycomb optical lattice [1]. Using momentum-resolved interband transitions, we observe a minimum band gap inside the Brillouin zone at the position of the Dirac points. We exploit the unique tunability of our lattice potential to adjust the effective mass of the Dirac fermions by breaking the inversion symmetry of the lattice. Moreover, changing the lattice anisotropy allows us to move the position of the Dirac points inside the Brillouin zone. When increasing the anisotropy beyond a critical limit, the two Dirac points merge and annihilate each other. 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 where the topology of the band structure plays a crucial role, but also provide the possibility to explore many-body phases resulting from the interplay of complex lattice geometries with interactions.