No Arabic abstract
Itinerant electrons in a two-dimensional Kagome lattice form a Dirac semi-metal, similar to graphene. When lattice and spin symmetries are broken by various periodic perturbations this semi-metal is shown to spawn interesting non-magnetic insulating phases. These include a two-dimensional topological insulator with a non-trivial Z_2 invariant and robust gapless edge states, as well as dimerized and trimerized `Kekule insulators. The latter two are topologically trivial but the Kekule phase possesses a complex order parameter with fractionally charged vortex excitations. A charge density wave is shown to couple to the Dirac fermions as an effective axial gauge field.
High-order topological insulators (TIs) are a family of recently-predicted topological phases of matter obeying an extended topological bulk-boundary correspondence principle. For example, a two-dimensional (2D) second-order TI does not exhibit gapless one-dimensional (1D) topological edge states, like a standard 2D TI, but instead has topologically-protected zero-dimensional (0D) corner states. So far, higher-order TIs have been demonstrated only in classical mechanical and electromagnetic metamaterials exhibiting quantized quadrupole polarization. Here, we experimentally realize a second-order TI in an acoustic metamaterial. This is the first experimental realization of a new type of higher-order TI, based on a breathing Kagome lattice, that has zero quadrupole polarization but nontrivial bulk topology characterized by quantized Wannier centers (WCs). Unlike previous higher-order TI realizations, the corner states depend not only on the bulk topology but also on the corner shape; we show experimentally that they exist at acute-angled corners of the Kagome lattice, but not at obtuse-angled corners. This shape dependence allows corner states to act as topologically-protected but reconfigurable local resonances.
Twisting van der Waals heterostructures to induce correlated many-body states provides a novel tuning mechanism in solid-state physics. In this work, we theoretically investigate the fate of the surface Dirac cone of a three-dimensional topological insulator subject to a superlattice potential. Using a combination of diagrammatic perturbation theory, lattice model simulations, and ab initio calculations we elucidate the unique aspects of twisting a single Dirac cone with an induced moire potential and the role of the bulk topology on the reconstructed surface band structure. We report a dramatic renormalization of the surface Dirac cone velocity as well as demonstrate a topological obstruction to the formation of isolated minibands. Due to the topological nature of the bulk, surface band gaps cannot open; instead, additional satellite Dirac cones emerge, which can be highly anisotropic and made quite flat. We discuss the implications of our findings for future experiments.
We derive exact results for close-packed dimers on the triangular kagome lattice (TKL), formed by inserting triangles into the triangles of the kagome lattice. Because the TKL is a non-bipartite lattice, dimer-dimer correlations are short-ranged, so that the ground state at the Rokhsar-Kivelson (RK) point of the corresponding quantum dimer model on the same lattice is a short-ranged spin liquid. Using the Pfaffian method, we derive an exact form for the free energy, and we find that the entropy is 1/3 ln2 per site, regardless of the weights of the bonds. The occupation probability of every bond is 1/4 in the case of equal weights on every bond. Similar to the case of lattices formed by corner-sharing triangles (such as the kagome and squagome lattices), we find that the dimer-dimer correlation function is identically zero beyond a certain (short) distance. We find in addition that monomers are deconfined on the TKL, indicating that there is a short-ranged spin liquid phase at the RK point. We also find exact results for the ground state energy of the classical Heisenberg model. The ground state can be ferromagnetic, ferrimagnetic, locally coplanar, or locally canted, depending on the couplings. From the dimer model and the classical spin model, we derive upper bounds on the ground state energy of the quantum Heisenberg model on the TKL.
Electrons on the surface of a strong topological insulator, such as Bi2Te3 or Bi1-xSnx, form a topologically protected helical liquid whose excitation spectrum contains an odd number of massless Dirac fermions. A theoretical survey and classification is given of the universal features, observable by the ordinary and spin-polarized scanning tunneling spectroscopy, in the interference patterns resulting from the quasiparticle scattering by magnetic and non-magnetic impurities in such a helical liquid. Our results confirm the absence of backscattering from non-magnetic impurities observed in recent experiments and predict new interference features, uniquely characteristic of the helical liquid, when the scatterers are magnetic.
Quantum simulators are an essential tool for understanding complex quantum materials. Platforms based on ultracold atoms in optical lattices and photonic devices led the field so far, but electronic quantum simulators are proving to be equally relevant. Simulating topological states of matter is one of the holy grails in the field. Here, we experimentally realize a higher-order electronic topological insulator (HOTI). Specifically, we create a dimerized Kagome lattice by manipulating carbon-monoxide (CO) molecules on a Cu(111) surface using a scanning tunneling microscope (STM). We engineer alternating weak and strong bonds to show that a topological state emerges at the corner of the non-trivial configuration, while it is absent in the trivial one. Contrarily to conventional topological insulators (TIs), the topological state has two dimensions less than the bulk, denoting a HOTI. The corner mode is protected by a generalized chiral symmetry, which leads to a particular robustness against perturbations. Our versatile approach to quantum simulation with artificial lattices holds promises of revealing unexpected quantum phases of matter.