Non-Hermitian lattices can host the non-Hermitian skin effect, a boundary-induced collapse of all bulk eigenstates into exponentially localized edge modes. This effect underlies anomalous bulk-boundary correspondence and remarkable enhancements in non-Hermitian sensing, yet direct energy-resolved access to the eigenmodes of non-Hermitian lattices has remained limited. Here we report band- and energy-resolved eigenmode spectroscopy of skin modes in a frequency synthetic dimension. By introducing strong frequency-domain boundaries in an electro-optically modulated ring resonator, we realize finite non-Hermitian lattices and use laser detuning as a spectroscopic axis for the eigenenergies of the effective Hamiltonian. Site-resolved heterodyne measurements then reconstruct the spatial profile of each mode, revealing boundary-localized skin states throughout the spectrum and their eigenenergy-dependent displacement from the edge. Beyond 1D, the same frequency-boundary architecture, upon incorporating long-range couplings between finite lattices, produces genuine 2D frequency lattices rather than the hitherto-realized folded 1D systems on twisted tubes. In these lattices we observe tunable directional transport and edge localization in two synthetic dimensions. Our results introduce eigenmode spectroscopy as a direct probe of non-Hermitian physics and establish strongly bounded frequency lattices as a flexible platform for Hamiltonian engineering.
Non-Hermitian lattices can host the non-Hermitian skin effect, a boundary-induced collapse of all bulk eigenstates into exponentially localized edge modes. This effect underlies anomalous bulk-boundary correspondence and remarkable enhancements in non-Hermitian sensing, yet direct energy-resolved access to the eigenmodes of non-Hermitian lattices has remained limited. Here we report band- and energy-resolved eigenmode spectroscopy of skin modes in a frequency synthetic dimension. By introducing strong frequency-domain boundaries in an electro-optically modulated ring resonator, we realize finite non-Hermitian lattices and use laser detuning as a spectroscopic axis for the eigenenergies of the effective Hamiltonian. Site-resolved heterodyne measurements then reconstruct the spatial profile of each mode, revealing boundary-localized skin states throughout the spectrum and their eigenenergy-dependent displacement from the edge. Beyond 1D, the same frequency-boundary architecture, upon incorporating long-range couplings between finite lattices, produces genuine 2D frequency lattices rather than the hitherto-realized folded 1D systems on twisted tubes. In these lattices we observe tunable directional transport and edge localization in two synthetic dimensions. Our results introduce eigenmode spectroscopy as a direct probe of non-Hermitian physics and establish strongly bounded frequency lattices as a flexible platform for Hamiltonian engineering.
Non-Hermitian skin effect (NHSE) is a distinctive phenomenon in non-Hermitian systems, marked by the accumulation of eigenstates at system boundaries. While well understood in one dimension, unraveling the NHSE in higher dimensions is challenging due to the diversity of lattice geometries. Here, we present a geometry-adaptive non-Bloch band theory in arbitrary dimensions, through the lens of spectral potential. Our formulation precisely determines the energy spectra and generalized Brillouin zone in the thermodynamic limit, unveiling their geometric dependency. We establish exact spectral relations that elucidate the geometric dependence of non-Bloch spectra and their connection to amoeba spectra. Moreover, we show that critical skin modes in higher dimensions exhibit scale-free localization along the boundary, thereby making the spectrum highly sensitive to the system size and boundary ratios. We demonstrate that these critical skin modes lead to spectral non-convergence and instability. Our findings pave the way toward a unified understanding of NHSE and non-Bloch bands in arbitrary dimensions. In non-Hermitian quantum systems, the skin effect causes states to cluster at the edges, which is straightforward in one dimension but gets complicated in higher dimensions because of different lattice shapes. Here, the authors report a flexible theory that adapts to any dimension and shape, revealing how these factors influence energy patterns and lead to unstable edge states sensitive to system size.
In non-Hermitian systems, spectra can be maximally boundary-sensitive, yet bulk physics need not be. Here we experimentally show that spectral moments provide boundary-robust bulk observables in finite non-Hermitian lattices, even when the spectra undergo dramatic geometry-dependent reshaping due to the skin effect. Using a unified acoustic platform with full spectral reconstruction and time-domain access, we probe one-, two- and three-dimensional lattices and demonstrate that spectral moments remain nearly invariant across distinct boundary geometries while the corresponding complex spectra differ strongly. To connect the thermodynamic theorem to realistic finite systems, we develop a loop-counting theory that identifies the physical origin of finite-size deviations in terms of missing boundary loops, quantitatively captures the corrections, and predicts a scaling law, which we verify experimentally. Beyond acoustic spectroscopy, we reveal a counterintuitive dynamical consequence of moment invariance: a dispersive-to-proliferative bulk transition governed by bulk moment structure rather than spectral boundary sensitivity. As a result, local bulk dynamics can remain stable (dispersive) even in a PT-broken spectral regime, challenging the conventional expectation that PT breaking necessarily implies feedback-induced dynamical instability (proliferation) through exponentially amplifying spectral components. These results establish spectral moments as practical bulk descriptors for finite non-Hermitian matter and open a route to extracting and controlling intrinsic bulk behavior in realistic wave-based non-Hermitian devices.
The well-established non-Bloch band theory predicts exponential localization of skin-mode eigenstates in one-dimensional (1D) non-Hermitian systems. Recent studies, however, have uncovered anomalous algebraic localization in higher dimensions. Here, we extend these ideas to Hermitian bosonic quadratic Hamiltonians incorporating quantum squeezing, offering a genuine quantum framework to explore non-Hermitian phenomena without external reservoirs. We construct a two-dimensional (2D) bosonic lattice model with two-mode squeezing and study its spectral properties of bosonic excitation within the Bogoliubov-de Gennes (BdG) formalism. We demonstrate an algebraic non-Hermitian skin effect (NHSE), characterized by quasi-long-range power-law localization of complex eigenstates. The system shows ultra spectral sensitivity to double infinitesimal on-site and long-range hopping impurities, while remaining insensitive to single impurities. Analytical treatment via the Green's function reveals that this sensitivity originates from the divergence of the nonlocal Green's function associated with the formation of nonlocal bound states between impurities. Our study establishes a framework for realizing novel higher-dimensional non-Hermitian physics in Hermitian bosonic platforms such as superconducting circuits, photonic lattices, and optomechanical arrays, with the demonstrated ultraspectral sensitivity enabling quantum sensing and amplification via bosonic squeezing.
In this paper, we investigate the non-Hermitian skin effect in a semi-infinite Fock-state lattice, where the inherent coupling scales as \sqrt{n}. By analytically solving a non-uniform, non-reciprocal SSH model, we demonstrate that the intrinsic inhomogeneous coupling, in combination with nonreciprocity, fundamentally modifies the conventional skin effect. Instead of accumulating at the physical boundary, all eigenmodes become compressed and skewed within a finite spatial range determined by the inhomogeneous profile-a phenomenon we term the confined non-Hermitian skin effect. Consequently, the evolution of the probability distribution on the lattice starting from a single site is doubly confined: it is spatially bounded to a finite range by the inhomogeneous coupling, and further restricted to a one-sided trajectory at the edge of this range by the non-reciprocity. Moreover, a feasible experimental scheme based on a single trapped ion is also proposed. This work reveals how engineered coupling profiles in synthetic dimensions can reshape non-Hermitian properties and enable new protocols for quantum state manipulation.
Non-Hermitian systems exhibit unique spectral properties, including the non-Hermitian skin effect and exceptional points, often influenced by boundary conditions. The modulation of these phenomena by generalized boundary conditions remains unexplored and not understood. Here, we analyze the Hatano-Nelson model with generalized boundary conditions induced by complex hopping amplitudes at the boundary. Using similarity transformations, we determine the conditions yielding real energy spectra and skin effect, and identify the emergence of exceptional points where spectra transition from real to complex. We demonstrate that tuning the boundary hopping amplitudes precisely controls the non-Hermitian skin effect, i.e., the localization of eigenmodes at the lattice edges. These findings reveal the sensitivity of spectral and localization properties to boundary conditions, providing a framework for engineering quantum lattice models with tailored spectral and localization features, with potential applications in quantum devices.
Non-Hermitian skin effect, which is a unique feature of non-Hermitian systems, exhibits the formation of an extensive number of boundary modes under open boundary conditions. However, its manifestation in higher dimensions remains elusive. In our work, we demonstrate a hybrid skin-topological effect arising from the interplay between first-order band topology and non-reciprocal hopping in an engineered two-dimensional brick-wall geometry. The non-Hermitian brick-wall lattice under open boundary conditions in both directions exhibits several unconventional spectral features. Notably, the eigenvalues associated with the corner skin modes do not exhibit non-trivial windings in the complex energy plane; instead, they exhibit dynamically stable exceptional point-like features that do not originate from eigenvector coalescence. In contrast, the remaining modes accumulate at the opposite pair. Of all the corner skin modes, only the two that originate from the topological corner states of the Hermitian brick-wall lattice remain localized at individual corners, while the rest accumulate at the pair of opposite corners. This spatial distribution contrasts sharply with the second-order skin effect, where corner skin modes are more uniformly distributed. Finally, for the non-Hermitian Brick-wall lattice, we design and implement the corresponding topolectrical circuit (circuit for a square lattice is included for comparison) to directly visualize the hybrid skin-topological modes.