One-dimensional quasiperiodic systems with power-law hopping, 1/r^{a}, differ from both the standard Aubry-André (AA) model and from power-law systems with uncorrelated disorder. Whereas in the AA model all single-particle states undergo a transition from ergodic to localized at a critical quasidisorder strength, short-range power-law hops with a>1 can result in mobility edges. We find that there is no localization for long-range hops with a≤1, in contrast to the case of uncorrelated disorder. Systems with long-range hops rather present ergodic-to-multifractal edges and a phase transition from ergodic to multifractal (extended but nonergodic) states. Both mobility and ergodic-to-multifractal edges may be clearly revealed in experiments on expansion dynamics.
One-dimensional quasiperiodic systems with power-law hopping, 1/r^{a}, differ from both the standard Aubry-André (AA) model and from power-law systems with uncorrelated disorder. Whereas in the AA model all single-particle states undergo a transition from ergodic to localized at a critical quasidisorder strength, short-range power-law hops with a>1 can result in mobility edges. We find that there is no localization for long-range hops with a≤1, in contrast to the case of uncorrelated disorder. Systems with long-range hops rather present ergodic-to-multifractal edges and a phase transition from ergodic to multifractal (extended but nonergodic) states. Both mobility and ergodic-to-multifractal edges may be clearly revealed in experiments on expansion dynamics.
Pair localization in one-dimensional quasicrystals with nearest-neighbor hopping is independent of whether short-range interactions are repulsive or attractive. We numerically demonstrate that this symmetry is broken when the hopping follows a power law $1/{r}^{\ensuremath{\alpha}}$. In particular, for repulsively bound states, we find that the critical quasiperiodicity that signals the transition to localization is always bounded by the standard Aubry-Andr\'e critical point, whereas attractively bound dimers get localized at larger quasiperiodic modulations as the range of the hopping increases. Extensive numerical calculations establish the contrasting nature of the pair energy gap for repulsive and attractive interactions, as well as the behavior of the algebraic localization of the pairs as a function of quasiperiodicity, interaction strength, and power-law hops. The results here discussed are of direct relevance to the study of the quantum dynamics of systems with power-law couplings.
Models with correlated disorder are rather common in physics. In some of them, like the Aubry-André (AA) model, the localization phase diagram can be found from the (self)duality with respect to the Fourier transform. In others, like the all-to-all translation-invariant Rosenzweig-Porter (TI RP) ensemble or the many-body localization (MBL), one needs to develop more sophisticated and usually phenomenological methods to obtain the localization transition. In addition, such models contain not only localization, but also the ergodicity-breaking transition in the Hilbert-space eigenstate structure, giving way to the nonergodic (i.e., MBL) phase of states with nontrivial fractal dimensions D q > 0 . In this work, we suggest a method to calculate both the above transitions and a lower bound to the fractal dimensions D 2 and D ∞ , relevant for the physical observables. To verify this method, we apply it to the class of long-range (self-)dual models, interpolating between a tight-binding ballistic model and TI RP via both power-law dependencies of the hopping terms and the on-site disorder correlations, and, thus, being out of the validity range of the previously developed methods. We show that the interplay of the correlated disorder and the power-law decaying hopping terms leads to the emergence of the two types of nonergodic phases in the entire range of parameters, even without having any quasiperiodicity of the AA potential. The analytical results of the above method are in full agreement with the extensive numerical calculations.
We propose a general framework for constructing self-dual one-dimensional quasiperiodic lattice models with arbitrary-range hoppings and multifractal behaviors. Our framework generates a broad spectrum of one-dimensional quasicrystals, ranging from the off-diagonal Aubry-Andr\'e-Harper models on one end, to those featuring long-range hoppings with varied quasiperiodic modulations on another. Focusing on models with off-diagonal quasiperiodic hoppings with power-law decay, we exploit the fact that, when the self-dual condition is satisfied, the system must be in the critical state with multifractal properties. This enables the engineering of models with competing extended, critical, and localized phases, with richly structured mobility edges separating them. As an outstanding example, we show that a limiting case of our family of self-dual quasicrystals can be implemented using Rydberg-atom arrays. Our work offers a systematic route toward critical phases from self-duality considerations, and would facilitate the experimental simulation of these exotic states.
We study the single-particle properties of two-dimensional quasicrystals where the underlying geometry of the tight-binding lattice is crystalline but the on-site potential is quasicrystalline. We will focus on the two-dimensional (2D) generalized Aubry-André model which has a varying form to its quasiperiodic potential, through a deformation parameter and varied irrational periods of cosine terms, which allows a continuous family of on-site quasicrystalline models to be studied. We show that the 2D generalized Aubry-André model exhibits many single-particle mobility edges which we confirm for finite systems and supports critical states across large parameter regions. Critical states are neither fully localized nor extended. We observe that diagonal quasicrystalline models can support many energy intervals of critical states in the spectrum while stabilizing both localized and extended states in other energy intervals; we refer to these as anomalous mobility edges. We show that critical states are present independent of system size through a scaling analysis of the inverse participation ratio and that they are present in spectra that also contain extended and localized states, confirming that at least one anomalous mobility edge is present. Due to this, these models exhibit anomalous diffusion of initially localized states across the majority of parameter regions, including deep in the normally localized regime. The presence of critical states in large parameter regimes and throughout the spectrum will have consequences for the many-body properties of quasicrystals, including the formation of the Bose glass and the potential to host a many-body localized phase. Published by the American Physical Society 2024
Localization in non-Hermitian quasicrystals can differ fundamentally from its Hermitian counterpart when non-reciprocity is spatially disordered. Here we study a one-dimensional non-Hermitian Aubry-André-Harper chain with a Bernoulli imaginary gauge field and quasiperiodic onsite modulation. In the nearest-neighbor limit, we identify an anomalous transition from a fully erratic non-Hermitian skin effect (ENHSE) phase to a fully localized phase. Although the fractal dimension vanishes in both regimes, the Lyapunov exponent and the fluctuation of the eigenstate center of mass sharply distinguish them. For generic finite-size realizations, this transition is further accompanied by a complex-to-real spectral change under periodic boundary conditions and a change of spectral winding from nontrivial to trivial. With weak next-nearest-neighbor hopping, we uncover an anomalous mobility edge at the same location as in the Hermitian generalized Aubry-André-Harper model, but separating Anderson-localized states from ENHSE-type macroscopic-accumulation states rather than extended states. We further show that this anomalous localization structure is reflected in spectral winding and wave-packet dynamics: single realizations exhibit winding-dependent drift, winding-resolved averaging preserves opposite directional responses, and full disorder averaging largely restores Hermitian-like transport. Our results establish practical diagnostics of anomalous localization and mobility edges in non-Hermitian quasicrystals.
We investigate a one-dimensional tight-binding model in which onsite potentials [Formula: see text] exhibit power-law spatial correlations (with exponent α) and the hopping amplitudes decay as [Formula: see text]. This two-parameter family interpolates continuously between short-range Anderson-like disorder, correlated disorder with conventional hopping, and long-range hopping models with nontrivial delocalization tendencies. Using large-scale exact diagonalization, we construct a comprehensive phase map in the [Formula: see text] plane by combining spectral statistics, density-of-states analysis, and energy-resolved localization indicators such as the participation ratio, single-particle entanglement entropy, level-spacing ratio r, and the ratio of the geometric to arithmetic density of states. From these observables we define phase-indicator functions that compactly quantify localization behavior across the spectrum. Our analysis reveals robust mobility edges and multiple regimes of spectral coexistence between localized, extended, resonant, and critical states. Finite-size scaling, implemented via an explicit smoothness-based cost function, enables extraction of critical exponents and delineation of transition lines across the [Formula: see text] parameter space. To validate and complement these physics-based diagnostics, we employ a supervised autoencoder that learns high-level representations of eigenstate structure directly from raw features and reliably reproduces the phase classification defined by the indicator functions. Together, these approaches provide a coherent and internally consistent picture of the spectral transitions driven by correlated disorder and long-range hopping, establishing a unified framework for characterizing mobility edges in long-range one-dimensional systems.