In Hermitian impurity scattering, each isolated late-time exponential is the fingerprint of a bound state. We show that this correspondence breaks down in non-Hermitian bands. For a single impurity in a non-Hermitian lattice, the late-time signal is controlled by isolated complex frequencies selected by the analytic continuation of the Green's function relevant to real-time dynamics, which we term dynamical poles (DPs). DPs need not coincide with static bound states: one may appear without any bound-state counterpart, while a static bound state may be dynamically invisible. The remainder of the signal is an incoherent background set by complex continuum edges. Our results establish that the real-time analytic structure of the Green's function, not the static eigenvalue problem alone, organizes non-Hermitian impurity scattering.
In Hermitian impurity scattering, each isolated late-time exponential is the fingerprint of a bound state. We show that this correspondence breaks down in non-Hermitian bands. For a single impurity in a non-Hermitian lattice, the late-time signal is controlled by isolated complex frequencies selected by the analytic continuation of the Green's function relevant to real-time dynamics, which we term dynamical poles (DPs). DPs need not coincide with static bound states: one may appear without any bound-state counterpart, while a static bound state may be dynamically invisible. The remainder of the signal is an incoherent background set by complex continuum edges. Our results establish that the real-time analytic structure of the Green's function, not the static eigenvalue problem alone, organizes non-Hermitian impurity scattering.
The Hermitian properties of the Hamiltonian are related not only to the operator itself but also to the functions on which it acts. Hermitian Hamiltonians operate on functions in the L 2 Hilbert space which correspond to boundary conditions which vanish at infinity. In this chapter, in order to move into the non-Hermitian domain, we will impose on the solutions to the time-independent Schrödinger equation (TISE) different boundary conditions which lead to solutions which can be associated with different types of the complex poles of the scattering matrix. These solutions will contain information which was not available within the scope of functions in L 2 . By imposing outgoing boundary conditions on the eigenfunctions of the timeindependent Hamiltonian complex eigenvalues, E res = ε − (i/2)Г, are obtained. These complex energies are associated with decaying resonance states which were discussed in the previous two chapters. The bound states (if they exist) appear as real eigenvalues since they result from exactly such outgoing boundary conditions which appear under the threshold energy. When incoming boundary conditions are imposed two kind of solution are obtained. One type of solution is the complex conjugates of the decay resonance solutions mentioned above. In scattering theory text books (see Taylor for example) the physical resonance solutions are associated with the poles of the scattering matrix which are embedded in the lower half of the complex energy plane. However, in nuclear physics the complex poles embedded in the upper half of the complex energy plane, so-called virtual states , are denoted as capture resonances .
Time-independent scattering methods are widely employed to analyze transport in non-Hermitian systems. Their application, however, rests on a critical yet often overlooked assumption: that an incident wave is a pure superposition of scattering states. In practice, any physically realistic, spatially localized wave packet will generally have a nonzero overlap with the system's bound states, thereby violating this premise. While this violation is inconsequential in Hermitian systems, it can invalidate the conventional scattering picture in their non-Hermitian counterparts. The underlying cause is the emergence of time-growing bound states, which manifest as poles of the scattering matrix (S matrix) in the first quadrant of the complex wave-number plane. Any initial overlap with these states becomes exponentially amplified, eventually dominating the long-time dynamics. Consequently, the actual evolution of a wave packet diverges dramatically from the conventional scattering picture, rendering the transmission and reflection coefficients derived from time-independent scattering methods unphysical. Using tight-binding models with non-Hermiticity introduced via imaginary on-site potentials or asymmetric hopping, we demonstrate that parameter regimes supporting such growing states are common. We therefore conclude that an analysis of S-matrix poles is an indispensable step to confirm the physical relevance of time-independent scattering calculations in non-Hermitian systems.
The complex eigenvalues of some non-Hermitian Hamiltonians, e.g., parity-time-symmetric Hamiltonians, come in complex-conjugate pairs. We show that for non-Hermitian scattering Hamiltonians (of a structureless particle in one dimension) possessing one of four certain symmetries, the poles of the S-matrix eigenvalues in the complex momentum plane are symmetric about the imaginary axis, i.e., they are complex-conjugate pairs on the complex-energy plane. This applies even to states which are not bounded eigenstates of the system, i.e., antibound or virtual states, resonances, and antiresonances. The four Hamiltonian symmetries are formulated as the commutation of the Hamiltonian with specific antilinear operators. Example potentials with such symmetries are constructed and their pole structures and scattering properties are calculated.
Non-Hermitian lattice Hamiltonians generally exhibit strong boundary sensitivity, with periodic and open boundary conditions producing distinct density of states (DOS) in the complex-energy plane. This has led to the view that extended non-Hermitian systems lack a unique bulk DOS, with different prescriptions representing inequivalent bulk physics. Here, we show that this apparent ambiguity is largely illusory. For any finite-range tight-binding Hamiltonian, we establish a universal bulk structure: all DOS definitions arising as thermodynamic limits of finite systems share identical multipole moments and generate identical bulk dynamics at finite times and for observables measured far from boundaries. This universality is intimately tied to the thermodynamic Green's functions, which we show to be independent of the boundary condition for large enough complex frequencies. Among all equivalent descriptions, we identify the Brown measure - obtained via Hermitization and resolvent analysis - as a canonical and convenient representative of the bulk DOS, defined directly from the infinite-volume Hamiltonian. We further show that point-gap topology imposes additional universal constraints: boundary-dependent Green's functions are forced to coincide throughout topologically trivial point gaps. This, in particular, provides a systematic criterion, valid in arbitrary dimension, for determining where and how eigenvalues of different boundary truncations can accumulate in the complex plane, and precisely delineates the regime in which the DOS ambiguity retains physical significance.
A single quantum emitter coupled to a structured non-Hermitian environment shows anomalous bound states and real-time dynamics without Hermitian counterparts, as shown in Gong []. In this work, we establish a general approach for studying the scattering states of a single quantum emitter coupled to one-dimensional non-Hermitian single-band baths. We formally solve the exact eigenvalue equation for all the scattering states defined on finite periodic lattices. In the thermodynamic limit, the formal solution reduces to the celebrated Lippmann-Schwinger equation for generic baths. In this case, we find that the scattering states are no longer linear superpositions of plane waves in general, unlike those in Hermitian systems; instead, the wave functions exhibit a large, yet finite localization length proportional to the lattice size. Furthermore, we show and discuss the cases where the Lippmann-Schwinger equation breaks down. We find the analytical solutions for the Hatano-Nelson and unidirectional next-to-nearest-neighbor baths in the thermodynamic limit.
This dissertation develops the complex pole representation as a unified framework for compactly representing Green's functions in quantum many-body simulations, with applications to numerical analytic continuation, hybridization fitting, compact representation and quantum impurity solvers, accompanied with software implementation. The central idea is to replace continuous spectral and correlation functions by a small number of complex poles and complex weights, while preserving the analytic structure needed for physical interpretation and numerical simulation. By connecting analytic continuation, hybridization fitting, compact representation, impurity solvers, and software implementation within a single pole-based perspective, this dissertation provides a systematically improvable approach to extracting, representing, and directly manipulating real-frequency information in quantum many-body simulations.