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.
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 the interplay between the non-Hermitian skin effect and Aubry-André-Harper (AAH) quasiperiodic disorder in a one-dimensional Su-Schrieffer-Heeger (SSH) chain with nonreciprocal hopping. By exact diagonalization, transfer-matrix analysis, and an analytical similarity-transformation argument, we map the full ( , δ) phase diagram, where A is the AAH modulation strength and the nonreciprocity parameter. We identify five distinct regimes: ( ) topological with extended bulk, (II) AAH-localized, (III) skin-localized, (IV) fully localized, and a previously unreported (V) competition regime exhibiting reentrant partial delocalization, in which intermediate quasiperiodic disorder disrupts the directional skin accumulation before ultimately Anderson-localizing all states. Using phase-averaged diagnostics and finite-size scaling, we confirm that the reentrant regime is robust, characterized by a non-monotonic inverse participation ratio that sharpens with increasing system size. We derive an analytical expression for the modified localization boundary λc(δ)=2veffw with vvff=v2−δ2, which agrees with numerical Lyapunov exponent calculations. We further show that quasiperiodic disorder progressively unwinds the complex spectral loops, destroying the point-gap topology at a critical strength distinct from the band-topological transition ; that the skin effect suppresses entanglement entropy to near-zero values while sufficiently strong AAH disorder partially restores it ; and that the SSH sublattice structure absent in the widely studied non-Hermitian AAH chain is essential for producing the five-phase landscape, as demonstrated by direct comparison with the non-dimerized limit.
We investigate localization transitions and spectral topology in a one-dimensional non-Hermitian generalization of the Aubry-André model in which both the nearest-neighbor and the next-nearest-neighbor hopping amplitudes are nonreciprocal. By extending the Fermi-surface point-matching method to nonreciprocal hopping, we derive a closed-form expression for the energy-dependent mobility edge in which the two nonreciprocity parameters are absorbed into exponentially renormalized effective hopping amplitudes. The mobility edge forms a single parabola in the energy--potential plane: nearest-neighbor nonreciprocity rigidly shifts the localization boundary toward stronger potentials, whereas next-nearest-neighbor nonreciprocity reduces the curvature of the boundary and thereby broadens the energy window in which extended and localized states coexist. Exact diagonalization confirms the analytical boundary for purely nearest-neighbor, purely next-nearest-neighbor, and combined nonreciprocity, and recovers the known Hermitian mobility edge in the reciprocal limit. We further analyze the spectral topology under periodic boundary conditions and show that the spectral winding numbers evaluated at base energies near the two band edges directly bracket the mixed phase: the winding number at the lower band edge drops when the mobility edge enters the spectrum and the first localized states appear, while the winding number at the upper band edge drops when the last extended states localize, delineating the full potential-strength window over which extended and localized states coexist. These results provide a compact analytical framework that connects energy-dependent localization, spectral topology, and nonreciprocity in quasiperiodic lattices, and they are directly testable in photonic, atomic, and electrical-circuit platforms.
The erratic non-Hermitian skin effect (ENHSE), emerging from the interplay between disorders and locally nonreciprocal yet globally reciprocal couplings, has reshaped the conventional bulk-boundary correspondence through its disorder-dependent localization properties. Here, we experimentally observe the dynamical phenomena of ENHSE in phononic crystals with disordered imaginary gauge fields. The erratic localization occurs in the bulk independent of the excitation position, with the main and satellite peaks precisely located at the local maxima of the cumulative gauge field in accordance with random-walk extreme-value statistics. Remarkably, the selective manipulation of satellite peaks can be realized by tuning the staggered disorder strengths in a dimerized chain. These findings can deepen the understanding of non-Hermitian physics and establish a new route for disorder-engineered non-Hermitian wave control.
Non-Hermitian many-body physics reveals a rich interplay between topology, localization, and boundary effects, yet their collective behavior in interacting disordered systems remains largely unexplored. In this work, we study an interacting non-Hermitian spin chain subject to a quasi-periodic longitudinal field, providing a unified and controlled setting, where non-Hermitian dynamics, interactions, and localization mechanisms intertwine. Remarkably, we discover a "D-shaped" many-body mobility edge that separates extended and localized eigenstates, while simultaneously delineating regimes of many-body localization and the many-body skin effect (where many-body eigenstates acquire an anomalous drift towards a boundary under open boundaries) emerging from the combined action of interactions, non-Hermiticity, and driving amplitude. We demonstrate that the skin effect induces multifractal scaling in the non-Hermitian eigenstates, providing a clear signature of the many-body skin effect. Employing diagnostics such as the fractal dimension, complex eigenvalue fractions, and many-body inverse participation ratios, we map out a unified phase diagram in which all measures consistently identify the "D-shaped" mobility edge. Finally, we probe this interplay using both complex level-spacing statistics and dynamical observables such as density imbalance, entanglement growth, and wave-packet evolution, culminating in a rich many-body mobility phase diagram that captures both the many-body skin effect and localization transitions. Our results identify a clear, defining signature of the "D-shaped" many-body mobility edge, and underscore its pivotal role in shaping the physics of open quantum many-body systems.
The critical phase of a non-Hermitian quasicrystal can support stronger transport than its surrounding delocalized phase. We demonstrate this anomalous behavior in the one-dimensional nonreciprocal Aubry-André-Harper model through a combined study of dynamical quantum phase transitions (DQPTs) and wavepacket diffusion. Using a parity-sorted energy-spectrum classification that directly encodes the generalized PT symmetry, we find that DQPTs in this system are energy-resolved, in contrast to the energy-independent DQPTs of Hermitian quasicrystals. The energy-resolved features are most pronounced when the initial and final Hamiltonians belong to different phases (localized or extended), and they are tied to the even-odd index structure of the spectrum, which we exploit to organize the quench-dynamical landscape. For wavepacket dynamics after a single-site quench, the diffusion exponent β, extracted from the long-time power-law scaling of the root-mean-square displacement σ(τ), partitions the phase diagram into four distinct regimes. In the Hermitian limit the extended phase is ballistic (β=1), the critical phase is normally diffusive (β=0.5), and the localized phase yields β→0. Nonreciprocity reverses this hierarchy: the extended phase becomes normally diffusive, while the critical phase turns ballistic. We trace the anomalous β=1 at criticality to the self-similar multifractal structure of the critical eigenstates, whose nodal positions are organized by the golden ratio. A finite-size scaling ansatz built on the wave-front propagation yields σ(τ)∝τ. The parity-resolved DQPTs and the β-phase diagram establish two complementary dynamical diagnostics of nonreciprocal quasicrystals, in which nonreciprocity promotes transport at the critical point and suppresses it in the delocalized phase.
Quasiperiodic systems host exotic transport regimes that are distinct from those found in periodic or disordered lattices. In this work, we study quantum transport in the Aubry-André-Harper lattice in a two-terminal setup coupled to zero-temperature reservoirs, where the conductance is evaluated via the nonequilibrium Green's function method. In the extended phase, we uncover a universal subdiffusive transport when the bath chemical potential aligns with the band edges. Specifically, the typical conductance displays a scaling of Gtyp∼L−2 with system size L. We attribute this behavior to the emergence of an exceptional point (Jordan normal form) in the transfer matrix in the thermodynamic limit. In the localized phase, the conductance shows exponential decay governed by the Lyapunov exponent. Intriguingly, in the critical phase, we identify pronounced log-periodic oscillations of the conductance as a function of system size, arising from the discrete scale invariance inherent to the singular-continuous spectrum. We further extend our analysis to the generalized Aubry-André-Harper model and provide numerical evidence suggesting that the exact mobility edge resides within a finite spectral gap. This results in a counter-intuitive exponential suppression of conductance precisely at the mobility edge. Our work highlights the distinct transport behaviors in quasiperiodic systems and elucidates how they are rigorously dictated by the underlying local spectral structure.