No Arabic abstract
A study of the thermal properties of two-dimensional topological lattice models is presented. This work is relevant to assess the usefulness of these systems as a quantum memory. For our purposes, we use the topological mutual information $I_{mathrm{topo}}$ as a topological order parameter. For Abelian models, we show how $I_{mathrm{topo}}$ depends on the thermal topological charge probability distribution. More generally, we present a conjecture that $I_{mathrm{topo}}$ can (asymptotically) be written as a Kullback-Leitner distance between this probability distribution and that induced by the quantum dimensions of the model at hand. We also explain why $I_{mathrm{topo}}$ is more suitable for our purposes than the more familiar entanglement entropy $S_{mathrm{topo}}$. A scaling law, encoding the interplay of volume and temperature effects, as well as different limit procedures, are derived in detail. A non-Abelian model is next analysed and similar results are found. Finally, we also consider, in the case of a one-plaquette toric code, an environment model giving rise to a simulation of thermal effects in time.
When two identical fermions exchange their positions, their wave function gains phase factor $-1$. We show that this distance-independent effect can induce nonlocal entanglement in one-dimensional (1D) electron systems having Majorana fermions at the ends. It occurs in the system bulk and has nontrivial temperature dependence. In a system having a single Majorana at each end, the nonlocal entanglement has a Bell-state form at zero temperature and decays as temperature increases, vanishing suddenly at certain finite temperature. In a system having two Majoranas at each end, it is in a cluster-state form and its nonlocality is more noticeable at finite temperature. By contrast, thermal states of corresponding 1D spins do not have nonlocal entanglement.
Analytic solutions of the quantum relativistic two-body problem are obtained for an interaction potential modeled as a one-dimensional smooth square well. Both stationary and moving pairs are considered and the limit of the {delta}-function interaction is studied in depth. Our result can be utilized for understanding excitonic states in narrow-gap carbon nanotubes. We also show the existence of bound states within the gap for a pair of particles of the same charge.
The topological band theory predicts that bulk materials with nontrivial topological phases support topological edge states. This phenomenon is universal for various wave systems and has been widely observed for electromagnetic and acoustic waves. Here, we extend the notion of band topology from wave to diffusion dynamics. Unlike the wave systems that are usually Hermitian, the diffusion systems are anti-Hermitian with purely imaginary eigenvalues corresponding to decay rates. Via direct probe of the temperature diffusion, we experimentally retrieve the Hamiltonian of a thermal lattice, and observe the emergence of topological edge decays within the gap of bulk decays. Our results show that such edge states exhibit robust decay rates, which are topologically protected against disorders. This work constitutes a thermal analogue of topological insulators and paves the way to exploring defect-immune heat dissipation.
We point out that the momentum distribution is not a proper observable for a system of anyons in two-dimensions. In view of anyons as Wilczeks composite charged flux-tubes, this is a consequence of the fact that the orthogonal components of the kinetic momentum operator do not commute at the position of a flux tube, and thus cannot be diagonalized in the same basis. As a substitute for the momentum distribution of an anyonic (spatially localized) state, we propose to use the asymptotic single-particle density after expansion of anyons in free space from the state. This definition is identical with the standard one when the statistical parameter approaches that for bosons or fermions. Exact examples of expansion dynamics, which underpin our proposal, and observables that can be used to measure anyonic statistics, are shown.
We have extended our recent molecular-dynamic simulations of memristors to include the effect of thermal inhomogeneities on mobile ionic species appearing during operation of the device. Simulations show a competition between an attractive short-ranged interaction between oxygen vacancies and an enhanced local temperature in creating/destroying the conducting oxygen channels. Such a competition would strongly affect the performance of the memristive devices.