ﻻ يوجد ملخص باللغة العربية
We develop a theory of edge states based on the Hermiticity of Hamiltonian operators for tight-binding models defined on lattices with boundaries. We describe Hamiltonians using shift operators which serve as differential operators in continuum theories. It turns out that such Hamiltonian operators are not necessarily Hermitian on lattices with boundaries, which is due to the boundary terms associated with the summation by parts. The Hermiticity of Hamiltonian operators leads to natural boundary conditions, and for models with nearest-neighbor (NN) hoppings only, there are reference states that satisfy the Hermiticity and boundary conditions simultaneously. Based on such reference states, we develop a Bloch-type theory for edge states of NN models on a half-plane. This enables us to extract Hamiltonians describing edge-states at one end, which are separated from the bulk contributions. It follows that we can describe edge states at the left and right ends separately by distinct Hamiltonians for systems of cylindrical geometry. We show various examples of such edge state Hamiltonians (ESHs), including Hofstadter model, graphene model, and higher-order topological insulators (HOTIs).
We present a microwave realization of finite tight-binding graphene-like structures. The structures are realized using discs with a high index of refraction. The discs are placed on a metallic surface while a second surface is adjusted atop the discs
We present an accurate textit{ab-initio} tight-binding hamiltonian for the transition-metal dichalcogenides, MoS$_2$, MoSe$_2$, WS$_2$, WSe$_2$, with a minimal basis (the textit{d} orbitals for the metal atoms and textit{p} orbitals for the chalcogen
The topological order of single-crystal Bi and its surface states on the (111) surface are studied in detail based on empirical tight-binding (TB) calculations. New TB parameters are presented that are used to calculate the surface states of semi-inf
Motivated by recent nuclear magnetic resonance (NMR) experiments, we present a microscopic sp3 tight-binding model calculation of the NMR shifts in bulk Bi2Se3, and Bi2Te3. We compute the contact, dipolar, orbital and core polarization contributions
An earlier analysis of manganese oxides in various charge states indicated that free-atom term values and universal coupling gave a reasonable account of the cohesion. This approach is here extended to LaxSr(1-x)MnO3 in a perovskite structure, and a