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Critical non-Hermitian Skin Effect

Linhu Li [email protected] Department of Physics, National University of Singapore, Singapore 117542    Ching Hua Lee [email protected] Department of Physics, National University of Singapore, Singapore 117542 Institute of High Performance Computing, A*STAR, Singapore 138632    Sen Mu [email protected] Department of Physics, National University of Singapore, Singapore 117542    Jiangbin Gong [email protected] Department of Physics, National University of Singapore, Singapore 117542
Abstract

This work uncovers a new class of criticality where eigenenergies and eigenstates of non-Hermitian lattice systems jump discontinuously across a critical point in the thermodynamic limit, unlike established Hermitian and non-Hermitian critical scenarios where spectrum remains continuous across a transition. Such critical behavior, dubbed the “critical skin effect”, is rather generic, occuring whenever subsystems with dissimilar non-Hermitian skin localization lengths are coupled, however weakly. Due to the existence of this criticality, the thermodynamical limit and the zero-coupling limit cannot be exchanged, thus challenging the celebrated generalized Brillouin zone (GBZ) approach when applied to finite-size systems. As manifestations of the critical skin effect in finite-size systems, we present stimulating examples with anomalous scaling behavior regarding spectrum, correlation functions, entanglement entropy, and scale-free wavefunctions that decay exponentially rather than power-law. More spectacularly, topological in-gap modes can even be induced by changing the system size.

Introduction.– Lying at the boundary between distinct phases, critical systems exhibit a wide range of interesting universal properties from divergent susceptibilities to anomalous scaling behavior. They have broad ramifications in conformal and statistical field theory Coniglio and Klein (1980); Hu (1984); Aizenman et al. (1987); Boulatov and Kazakov (1987); Zamolodchikov (1987, 1989); Cardy (1992); Oshikawa and Affleck (1996); Dziarmaga (2005), Schramm-Loewner evolution Gruzberg (2006); Kozdron (2009); Stevenson and Weigel (2011); Werner (2007), entanglement entropy (EE) Vidal et al. (2003); Korepin (2004); Larsson and Johannesson (2005); Ryu and Takayanagi (2006); Barthel et al. (2006); Laflorencie et al. (2006); Swingle (2010); Swingle and Senthil (2013); Lee et al. (2015); Swingle and McGreevy (2016); Chang et al. (2019) and many other contexts. Recently, concepts crucial to criticality - like band gaps and localization - have been challenged by studies of non-Hermitian systems Bender and Boettcher (1998); Bender (2007); Moiseyev (2011); Gong et al. (2018); Kawabata et al. (2019a) exhibiting exceptional points Berry (2004); Dembowski et al. (2004); Rotter (2009); Jin and Song (2009); Longhi (2010); Heiss and Harney (2001); Heiss (2012); Xu et al. (2016); Hassan et al. (2017); Hu et al. (2017); Shen et al. (2018); Wang et al. (2019); Ghatak and Das (2019); Miri and Alù (2019); Zhang and Gong (2020); Yuce (2020); Jin et al. (2019); Kawabata et al. (2019b) or the non-Hermitian skin effect (NHSE), which are characterized by enigmatic bulk-boundary correspondence (BBC) violations, robust directed amplifications, discontinuous Berry curvature and anomalous transport behavior Lee (2016); Xiong (2018); Kunst et al. (2018); Yao and Wang (2018); Yokomizo and Murakami (2019); Lee et al. (2018); Lee and Thomale (2019); Song et al. (2019a, b); Li et al. (2019); Borgnia et al. (2020); Zhang et al. (2019); Yoshida et al. ; Yang et al. ; Lee et al. ; Longhi (2019); Luo (2020).

We uncover here a new class of criticality, dubbed the “critical skin effect” (CSE), where the eigenenergies and eigenstates in the thermodynamic limit “jump” discontinuously across the critical point. This is distinct from previously known phase transitions (Hermitian and non-Hermitian) [Fig. 1], where the eigenenergy spectrum can be continuously interpolated across the two bordering phases. A CSE transition, by contrast, is characterized by a discontinuous jump between two different complex spectra along with two different sets of eigenstates. As elaborated below, this behavior appears generically whenever systems of dissimilar NHSE localization lengths are coupled, no matter how weakly 111Not all subsystems need to be non-Hermitian; indeed, the CSE even occurs if a Hermitian chain is coupled a chain with NHSE. Importantly, at experimentally accessible finite system sizes 222Non-Hermitian system, particularly those exhibiting the NHSE, exhibit divergences in local density of states in the thermodynamic limit., the jump smooths out into an interpolation between the two phases in a strongly size-dependent manner, such that the system may exhibit qualitatively different properties i.e. real vs. complex spectrum or presence/absence of topological modes at different system sizes. Being strongly affected by minute perturbations around the critical point, such behavior may prove useful in sensing applications Brandenbourger et al. (2019); Schomerus (2020).

CSE as a limitation of the GBZ.– In non-Hermitian systems with unbalanced gain and loss, spectra under periodic boundary conditions (PBCs) and open boundary conditions (OBCs) can be very different Lee (2016); Xiong (2018); Yao and Wang (2018); Longhi (2020); Lee and Thomale (2019). Indeed, under OBC, eigenstates due to NHSE can exponentially localize at a boundary, in contrast to Bloch states under PBCs. This also explains the possible violation of the BBC, taken for granted in Hermitian settings.

The celebrated GBZ formalism aims to restore the BBC through a complex momentum deformation Yao and Wang (2018); Yokomizo and Murakami (2019); Lee and Thomale (2019); Yang et al. ; Okuma et al. (2020); Lee et al. . Rigorously applicable for bounded but infinitely large systems, it has however been an open question whether the GBZ can still accurately describe finite-size systems. The GBZ of a momentum-space Hamiltonian H(z)H(z), z=eikz=e^{ik} can be derived from its characteristic Laurent polynomial (energy eigenequation)

f(z,E):=det[H(z)E]=0,\displaystyle f(z,E):=\det[H(z)-E]=0, (1)

where EE is the eigenenergy. While the ordinary BZ is given by the span of allowed real quasimomenta kk, the GBZ is defined by the complex analytically-continued momentum kk+iκ(k)k\rightarrow k+i\kappa(k), with the NHSE inverse decay length κ(k)=log|z|\kappa(k)=-\log|z| determined by the smallest complex deformation zeikeκ(k)z\rightarrow e^{ik}e^{-\kappa(k)} such that f(z,E)f(z,E) possesses a pair of zeros zμz_{\mu}, zνz_{\nu} satisfying |zμ|=|zν||z_{\mu}|=|z_{\nu}| for the same EE Yao and Wang (2018); Lee and Thomale (2019); Lee et al. . Due to the double degeneracy of states with equal asymptotic decay rate at these EE, there exist a pair of eigenstates ψμ,ψν\psi_{\mu},\psi_{\nu} that can superpose to satisfy OBCs i.e. zero net amplitude at both boundaries. As such, provided that the characteristic polynomial cannot be made reducible by adding a small perturbation, the OBC spectrum in the thermodynamic limit (denoted as EE_{\infty}) can be obtained from the PBC spectrum via E(eik)E(eikeκ(k))E(e^{ik})\rightarrow E(e^{ik}e^{-\kappa(k)}), apart from isolated topological modes. Thus it is often claimed that the BBC is “restored” in the GBZ defined by kk+iκ(k)k\rightarrow k+i\kappa(k) or, at the operator level, with the surrogate Hamiltonian H(eik)H(eikeκ(k))H(e^{ik})\rightarrow H(e^{ik}e^{-\kappa(k)}) Lee et al. . In general, different EE (energy band) solutions can admit different functional forms of κ(k)\kappa(k), leading to band-dependent GBZs that have recently also been described with the auxiliary GBZ formalism Yang et al. . Since eikeκ(k)e^{ik}e^{-\kappa(k)} is generically non-analytic, it represents effectively non-local hopping terms Lee et al. . As such, the GBZ description challenges the very notion of locality, which is central to critical systems, by effectively “unraveling” the real-space eigenstate accumulation through replacing local hoppings with effectively non-local ones.

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Figure 1: Four different types of critical transitions. Hermitian phase transitions (Top) are marked by gap closures along the real line. In non-Hermitian cases (2nd to 4th rows, axis labels omitted), spectral phase transitions can take more sophisticated possibilities in the 2D complex energy plane. For instance, the spectral topology can change under line gap closures (2nd Row) or shrink to a point and re-emerge in a different topological configuration (3rd row), without the gap ever closing Lee et al. . The spectrum continuously passes through a gapless or point-like regime in the first three cases. The CSE (bottom row), however, is special in that OBC spectrum the thermodynamic limit, denoted EE_{\infty}, jumps discontinuously from one configuration (left), to a different one (middle), and to another (right) as certain parameter changes from ϵ-\epsilon to 0 (critical border), and to ϵ\epsilon, for an arbitrarily small ϵ\epsilon.

Due to the robustness of the NHSE, eigenspectra predicted from the GBZ typically converge rapidly to the exact numerically obtained OBC spectra even for small system sizes(𝒪(101)\mathcal{O}(10^{1}) sites) 333In principle, the convergence should be exact in the thermodynamic limit. But in practical computations, floating point errors ϵ\epsilon are continuously amplified as they propagate across the system, and we expect accurate numerical spectra only when L<log(ϵ)/max(κ)L<-\log(\epsilon)/\text{max}(\kappa). . However, this numerical agreement fails spectacularly near a critical point where f(z,E)f(z,E) changes from being reducible to irreducible. To understand the significance of this algebraic property of reducibility, consider a set of coupled irreducible subsystems described by the characteristic polynomial

f(z,E)=f0+ifi(z,E),f(z,E)=f_{0}+\prod_{i}f_{i}(z,E), (2)

where fi(z,E)f_{i}(z,E) is the characteristic polynomial of the ii-th subsystem, and f0f_{0} is a constant that represents the simplest possible form for the subsystem coupling. When f0=0f_{0}=0, f(z,E)f(z,E) completely factorizes into irreducible polynomials, as expected from a Hamiltonian H(z)H(z) that block-diagonalizes into irreducible sectors associated with the individual fi(z,E)f_{i}(z,E)’s. In particular, the OBC spectrum of this completely decoupled scenario is derived from the independent κi(k)\kappa_{i}(k)’s of each subsystem, each determined by zμ,zνz_{\mu},z_{\nu} from the same subsystem.

Yet, a nonzero coupling f0f_{0}, no matter how small, can have dramatic physical consequences. For arbitrarily small f00f_{0}\neq 0, the different sectors can hybridize significantly if the fif_{i}’s are different 444If two fif_{i}’s are equivalent, f0+fi2=(fi+if0)(fiif0)f_{0}+f_{i}^{2}=(f_{i}+i\sqrt{f_{0}})(f_{i}-i\sqrt{f_{0}}) is still reducible.. Indeed, such hybridization is inevitable in the thermodynamic limit, with OBC eigenstates formed from superpositions of eigenstates ψμ,ψν\psi_{\mu},\psi_{\nu} from dissimilar subsystems, each corresponding non-Bloch momenta ilogzμ/ν-i\log z_{\mu/\nu}. Hence the GBZs i.e. κ(k)\kappa(k)’s of the coupled system, which are defined in the thermodynamic limit, are thus determined by all pairs of |zμ|=|zν||z_{\mu}|=|z_{\nu}| not necessarily from the same subsystem. Therefore, the GBZs in the coupled case, no matter how small is f0f_{0}, can differ from the decoupled GBZs at f0=0f_{0}=0. That is, the thermodynamic limit and the f00f_{0}\rightarrow 0 limit are not exchangeable. However, since an actual finite physical system cannot possibly possess very different spectrum and band structure upon an arbitrarily small variation in its system parameter, the GBZ picture must be inapplicable in describing such finite-size systems in the presence of CSE.

Anomalous finite-size scaling from CSE.– For illustration, we turn to a minimal example of two coupled non-Hermitian 1D Hatano-Nelson chains Hatano and Nelson (1996, 1997, 1998) each containing only non-reciprocal (unbalanced) nearest neighbor (NN) hoppings [Fig. 2(a)]. Its Hamiltonian reads

H2-chain(z)=(ga(z)t0t0gb(z))\displaystyle H_{\text{2-chain}}(z)=\left(\begin{matrix}g_{a}(z)&t_{0}\\ t_{0}&g_{b}(z)\\ \end{matrix}\right) (3)

with ga(z)=ta+z+ta/z+Vg_{a}(z)=t_{a}^{+}z+t_{a}^{-}/z+V and gb(z)=tb+z+tb/zVg_{b}(z)=t_{b}^{+}z+t_{b}^{-}/z-V, ta/b±=t1±δa/bt_{a/b}^{\pm}=t_{1}\pm\delta_{a/b} being the forward/backward hopping of chains aa and bb. This model can be also realized with a reciprocal system with skin effect in a certain parameter regime Sup . When t0=0t_{0}=0, the two chains are decoupled, and the characteristic polynomial is reducible as f(z,E)=[ga(z)E][gb(z)E]f(z,E)=[g_{a}(z)-E][g_{b}(z)-E]. Each factor fa/b(z,E)=ga/b(z)Ef_{a/b}(z,E)=g_{a/b}(z)-E determines the skin eigensolutions of its respective chain. However, even an infinitesimal coupling t00t_{0}\neq 0 generically makes f(z,E)f(z,E) irreducible. Specifically, consider the simple case of ta+=tb=1t^{+}_{a}=t^{-}_{b}=1 and ta=tb+=0t_{a}^{-}=t_{b}^{+}=0. Without couplings (t0=0t_{0}=0), the two chains under OBC respectively yields a Jordan-block Hamiltonian matrix in real space, with the spectrum given by E=±VE=\pm V. Because the eigenstates of the decoupled chains are exclusively localized at the first or the last site, their GBZs collapse Longhi (2020). By contrast, for any t00t_{0}\neq 0, f(z,E)=E2E(z+z1)+(z+V)(z1V)t02f(z,E)=E^{2}-E(z+z^{-1})+(z+V)(z^{-1}-V)-t_{0}^{2} is irreducible (here t02=f0-t_{0}^{2}=f_{0} from Eq. 2), insofar as the eigenenergy roots E=cosk±t02+(V+isink)2E=\cos k\pm\sqrt{t_{0}^{2}+(V+i\sin k)^{2}} are no longer Laurent polynomials in z=eikz=e^{ik} that can be separately interpreted as de facto subsystems with local hoppings 555In higher degree polynomials, an algebriac expression for zz may not even exist as implied by the Abel-Ruffini theorem.. Importantly, the corresponding OBC EE_{\infty} spectrum and the GBZ for t00t_{0}\neq 0 are now qualitatively different. As derived in the Supplementary Material Sup , setting |za|=|zb||z_{a}|=|z_{b}| gives OBC spectrum (in the thermodynamic limit): E2=1η21+η2+V2+t02±2t02η2+η2t02/(1+η2)E_{\infty}^{2}=\frac{1-\eta^{2}}{1+\eta^{2}}+V^{2}+t_{0}^{2}\pm 2\sqrt{t_{0}^{2}-\eta^{2}+\eta^{2}t_{0}^{2}}/(1+\eta^{2}), with η\eta\in\mathbb{R}. Clearly, even one now takes the t00t_{0}\rightarrow 0 limit, E2E_{\infty}^{2} only simplifies to E2V2+1±iη1iηE_{\infty}^{2}\rightarrow V^{2}+\frac{1\pm i\eta}{1\mp i\eta}, which is not the above-mentioned OBC spectrum of the two decoupled chains. Likewise, the t00t_{0}\rightarrow 0 limit of the coupled GBZ, which can be shown to be the locus of z=±V2+eiθVz=\pm\sqrt{V^{2}+e^{i\theta}}-V, θ[0,2π]\theta\in[0,2\pi], has nothing in common with the collapsed GBZs of the decoupled case.

Refer to caption
Figure 2: (a) The two chain model [Eq. 3] with hopping asymmetry in chains a,ba,b denoted by δa/b\delta_{a/b}, and on-site energy offset ±V\pm V. A small inter-chain t0t_{0} can cause significant coupling when δaδb\delta_{a}\neq\delta_{b}. (b) OBC spectra (black dots) and eigenstate profiles (insets) at N=10,20N=10,20 and 8080 unit cells and coupling t0=0.01t_{0}=0.01, showing very different spectral behavior at different system sizes NN. At small N10N\approx 10, coupling effects are negligible, with the spectrum coinciding with the real OBC EE_{\infty} spectrum (green) in the decoupled thermodynamic limit. As NN increases, the spectrum gradually approaches the OBC EE_{\infty} spectrum (red) for the coupled thermodynamic limit, with hybridization becoming sharper. Parameters are t1=0.75t_{1}=0.75, δa=δb=0.25\delta_{a}=-\delta_{b}=0.25 and V=0.5V=0.5.

This paradoxical singular behavior is manifested as anomalous scaling behavior in finite-size systems that are more relevant to experimental setups. The discontinuous critical transition illustrated above becomes a smooth crossover between the different OBC EE_{\infty} solutions. As the size NN of a coupled system is varied, its physical OBC spectrum interpolates between the decoupled and coupled OBC EE_{\infty} solutions. As illustrated in Fig. 2(b) for the 2-chain model Eq. 3 at small coupling t0=0.01t_{0}=0.01 (with t1=0.75t_{1}=0.75 and δa=δb=0.25\delta_{a}=-\delta_{b}=0.25 for well-defined skin modes), the OBC spectrum (black dots) changes dramatically from N=10N=10 to 8080 unit cells. For small N=10N=10, it approximates the OBC EE_{\infty} (green) for t0=0t_{0}=0 lying on the real line, while at large N=80N=80, it converges towards the true OBC EE_{\infty} (red curve) with nonzero coupling. Indeed, the eigenstates for N=10N=10 are almost entirely decoupled across the two chains, while those for N=80N=80 are maximally coupled/decoupled depending on whether they approach the red/green EE_{\infty} curves. In the intermediate N=20N=20 case, the OBC spectrum lies far between the two EE_{\infty}’s, and cannot be characterized by their associated GBZs.

Refer to caption
(a)
Refer to caption
(b)
Figure 3: (a) Scale-free OBC skin eigenstate of the largest Im[E]\text{Im}[E] eigenenergy of H2-chainH_{\text{2-chain}} at system sizes N=20,40,60N=20,40,60 and 8080 (red,purple,blue,green). Its rescaled profile, despite decaying exponentially rather than power-law, remains invariant across different NN. This scale invariance persists in the N>20N>20 regime, and is due to the N1N^{-1} decay (dashed line) of the inverse skin depth (red dots), as plotted in the inset. Parameters follow Fig. 2’s, except with t0=103t_{0}=10^{-3}. (b) EE SS (blue) of a half-filled OBC H2-chainH_{\text{2-chain}} at odd system sizes NN, with real-space cut at N2\lfloor\frac{N}{2}\rfloor and parameters t1=0.58t_{1}=0.58, V=1V=1, t0=0.4t_{0}=0.4 and δa=δb=0.25\delta_{a}=-\delta_{b}=0.25. It saturates near zero in the gapless decoupled small NN regime, but scales like 13logN\sim\frac{1}{3}\log N (yellow) in the gapless coupled large NN regime.

Let us now explain the above-observed dramatic size-dependent spectrum via the competition between dissimilarly accumulated skin modes and the couplings across them. The general conditions for such are unveiled in Sec. I.a of Sup . In our model [Eq. 3], the inverse decay lengths in chains a,ba,b are given by κa/b=12log(ta/b+/ta/b)\kappa_{a/b}=\frac{1}{2}\log(t^{+}_{a/b}/t^{-}_{a/b}), which will be dissimilar as long as δaδb\delta_{a}\neq\delta_{b}. After performing a similarity transform that rescales each site jj by a factor of ejκbe^{j\kappa_{b}}, chain bb becomes reciprocal with κb=0\kappa^{\prime}_{b}=0 while chain aa has a rescaled inverse decay length κa=κaκb\kappa^{\prime}_{a}=\kappa_{a}-\kappa_{b}. If κa0\kappa^{\prime}_{a}\neq 0, chain aa always possesses exponentially growing skin modes scaling like eκaN~{}e^{\kappa^{\prime}_{a}N} at one end. As such, the coupling t0t_{0}, even if extremely small, still affects the spectrum and eigenstates dramatically as the system size NN increases.

Scale-free exponential wavefunctions.– A hallmark of conventional critical systems is scale-free power-law behavior, particularly in the wavefunctions. Interestingly, such scale-free behavior can also be found in the exponentially decaying wavefunctions i.e. skin modes. Shown in Fig. 3(a) are the profiles of the slowest decaying eigenstates ψ(x)\psi(x) of H2-chainH_{\text{2-chain}} at different system sizes N=20,40,60N=20,40,60 and 8080, with the horizontal axis normalized by NN. These featured eigenstates belong to the top of the central black ring in Fig. 2(b), with their distance from the coupled OBC EE_{\infty} ring (red) decreasing as N1\sim N^{-1}. Unlike usual exponentially decaying wavefunctions with fixed spatial decay length, here |ψ(x)|eκx|\psi(x)|\sim e^{-\kappa x} with κN1\kappa\sim N^{-1} [Fig. 3(b)], such that the overall profile ψ(x)\psi(x) has no fixed length scale. Such unique scale-free eigenmodes result from the slow critical migration of the eigenstates between EE_{\infty} solutions [Fig. 2(a) inset].

Anomalous correlations and entanglement entropy.– The CSE can also violate the usual logarithmic scaling of the EE Calabrese and Cardy (2004, 2009); Gioev and Klich (2006); Eisert et al. (2010), since the OBC spectrum can be gapped at some system sizes, and gapless at others. Consider for instance the OBC H2-chainH_{\text{2-chain}} [Eq. 3] with parameters chosen to gap out the OBC spectrum at small system sizes NN Sup . With all Re[E]<0\text{Re}[E]<0 states occupied by spinless free Fermions, the real-space entanglement entropy SS (blue curve in [Fig. 3(c)]) exhibits a crossover from the decoupled gapped regime at N5N\leq 5 to the gapless regime N>20N>20, where it approaches the usual 13logN\frac{1}{3}\log N behavior (yellow line). In generic CSE scenarios with multiple competing OBC EE_{\infty} loci, SS can scale differently at different system size regimes, choices of fillings and entanglement cuts, challenging the notion of a single well-defined scaling behavior. As shown in the Supplementary Material Sup , The two-Fermion correlator ψ(1)ψ(x)\langle\psi(1)\psi(x)\rangle characterizing the EE also crossovers from rapid exponential decay at small NN to 1/x1/x power-law decay at large NN. Remarkably, the probability of finding another Fermion nearby generally increases drastically when the system is enlarged (with filling fraction maintained).

Size-dependent topological modes.– Topological modes are usually associated with bulk invariants in the thermodynamic limit, with finite-size effects playing a diminishing role in the face of topological robustness. The CSE here can cause topological edge modes to appear only at certain system size regimes. Consider replacing the non-reciprocal intra-chain couplings of our H2-chainH_{\text{2-chain}} model with inter-chain couplings with non-reciprocity ±δab\pm\delta_{ab} between adjacent unit cells [Fig. 4(a)], as described by the following CSE Su-Schrieffer-Heeger (SSH) model:

HCSE-SSH(z)\displaystyle H_{\text{CSE-SSH}}(z) =\displaystyle= hy(z)σy+hz(z)σz+h0(z)𝕀\displaystyle h_{y}(z)\sigma_{y}+h_{z}(z)\sigma_{z}+h_{0}(z)\mathbb{I} (4)

where hy(z)=iδab(z+1/z)h_{y}(z)=i\delta_{ab}(z+1/z), hz(z)=V+δ(z1/z)h_{z}(z)=V+\delta_{-}(z-1/z), and h0(z)=t1(z+1/z)+δ+(z1/z)h_{0}(z)=t_{1}(z+1/z)+\delta_{+}(z-1/z), with δ±=(δa±δb)/2\delta_{\pm}=(\delta_{a}\pm\delta_{b})/2. HCSE-SSHH_{\text{CSE-SSH}} is so named because interestingly, at δ=δab\delta_{-}=\delta_{ab}, it can be transformed via a basis rotation σzσx\sigma_{z}\rightarrow\sigma_{x} into an extended (SSH) model Su et al. (1979) with non-reciprocal inter-cell couplings given by ±2δ\pm 2\delta_{-} and a uniform next-nearest neighbor hopping given by t1±δ+t_{1}\pm\delta_{+} Sup , which is known to possess a topologically nontrivial phase.

Refer to caption
Figure 4: (a) Sketch of the HCS-SSHH_{\text{CS-SSH}} model with cross inter-chain non-reciprocal couplings ±δab\pm\delta_{ab}. (b). OBC spectra (black dots) at N=20N=20, 3030 and 4040 unit cells and coupling δab=0.5×103\delta_{ab}=0.5\times 10^{-3}. The majority of the spectrum behaves similarly as the model in Fig. 2(b), except for a pair of topological edge states emerge within the point gap at zero energy. The OBC EE_{\infty} spectrum is given by green and red colors in the decoupled and coupled thermodynamic limit respectively. Other parameters are δa=δb=0.5\delta_{a}=-\delta_{b}=0.5, t1=0.75t_{1}=0.75, and V=1.2V=1.2. (c) κ\kappa solutions (red, blue, green, and yellow surfaces) of f(z,E)=0f(z,E)=0 as a function of the complex energy, with the same parameters in (b). Intersecting regions (green and red dotted lines) give the OBC skin solutions of the system in the thermodynamic limit. Among them, green and blue lines correspond to the skin solutions of two decoupled chains at δab=0\delta_{ab}=0. The solutions of red curves emerge at a small but nonzero δab\delta_{ab}, and the skin solutions of the weakly coupled system is given by the intersecting regions with smallest |κ||\kappa|, i.e. the red loop in the center and green lines at the two ends with large and small Re[E]{\rm Re}[E]. (d) Emergence of in-gap degenerate modes as a function of δab/δa\delta_{ab}/\delta_{a} and NN with δa=δb=0.5\delta_{a}=-\delta_{b}=0.5, t1=0.75t_{1}=0.75, V=1.2V=1.2, with the plotted boundary scaling logarithmically with NN.

When δab=0\delta_{ab}=0, the system is decoupled into two Hatano-Nelson chains which must be topologically trivial. The OBC spectrum EE_{\infty} in the decoupled case and the associated inverse decay length κ\kappa are shown in Figs. 4(b) and (c)(green curves), with positive/negative κ\kappa corresponding to skin modes accumulating population at opposite boundaries. Also shown in in Figs. 4(b) and (c)(red curves) are EE_{\infty} in the coupled case and the corresponding κ\kappa for the hybridized skin modes. With small N=20N=20 unit cells in Fig. 4(b), the finite-size OBC spectrum (gray dots) qualitatively agrees with the decoupled EE_{\infty} (green), with a real-valued gap at E=0E=0 along the Im[E]=0\text{Im}[E]=0 axis (inset). Upon the size increase to N=30N=30 and then to N=40N=40, such a gap first closes on the complex plane and then develops into a point gap with two zero-energy degenerate modes lying in its center. The topological origin of such in-gap modes is also verified in Supplementary Material. The gap closure and then the emergence of in-gap topological modes resemble the typical behavior of a topological phase transition. Yet, here it is an intriguing size-induced effect. Further, the emergence of in-gap modes only requires exponentially weaker inter-chain coupling (i.e. smaller δab/δa\delta_{ab}/\delta_{a}) for larger NN, as shown in the “phase” diagram shown in Fig. 4(d).


Discussion.- In mathematical terms, the CSE arises when the energy eigenequation exhibits an algebraic singularity that leads to inequivalent auxiliary GBZs across the transition. The CSE heralds a whole new class of discontinuous critical phase transitions with rich anomalous scaling behavior, challenging traditional associations of criticality with scale-free behavior. Even a vanishingly small coupling between dissimilar skin modes can be consequential as the system size increases. This insight is much relevant to sensing and switching applications. Beyond our two-chain models, there are other scenarios that can engineer coupling between subsystems of dissimilar NHSE length scales and hence yield CSE Sup . In particular, we anticipate fruitful investigations in various experimentally feasible settings such as electric circuits Helbig et al. ; Hofmann et al. ; Hofmann et al. (2019); Ezawa (2019), cold atom systems Li et al. ; Gou et al. (2020), photonic quantum walks Xiao et al. and metamaterials Ghatak et al. ; Brandenbourger et al. (2019).

Acknowledgements.- J.G. acknowledges support from Singapore NRF Grant No. NRF-NRFI2017-04 (WBS No. R-144-000-378-281).

C.H.L. and L.L. contributed equally to this work.

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Supplementary Materials

I I. Conditions for having discontinuous transition of GBZ solutions EE_{\infty} for the Critical Skin Effect

I.1 a. Two-chain models

The discontinuous transition induced by an infinitesimal transverse coupling in thermodynamic limit, and also the crossover in a finite system, exist only when the two decoupled chains have different κ\kappa of their OBC skin solutions. To see this, we consider a general two-chain model described by Hamiltonian

h(z)=(ga(z)+Vat0t0gb(z)+Vb),\displaystyle h(z)=\left(\begin{matrix}g_{a}(z)+V_{a}&t_{0}\\ t_{0}&g_{b}(z)+V_{b}\\ \end{matrix}\right), (S1)

where ga,b(z)g_{a,b}(z) only contain terms with nonzero order of zz. When decoupled, the two chains correspond to the polynomials ga,b(z)+Va,bg_{a,b}(z)+V_{a,b} respectively, and possess the same κ\kappa solutions when and only when gb(z)=cga(z)g_{b}(z)=cg_{a}(z), with cc a nonzero coefficient. When a nonzero transverse coupling t0t_{0} is introduced, the characteristic polynomial of the two-chain system takes the form of

Pc(z)\displaystyle P_{c}(z) =\displaystyle= (ga(z)+VaE)(gb(z)+VbE)r2\displaystyle(g_{a}(z)+V_{a}-E)(g_{b}(z)+V_{b}-E)-r^{2} (S2)
=\displaystyle= cga2(z)+[(VbE)+c(VaE)]ga+VaVb+E2r2\displaystyle cg_{a}^{2}(z)+\left[(V_{b}-E)+c(V_{a}-E)\right]g_{a}+V_{a}V_{b}+E^{2}-r^{2}
=\displaystyle= (cga(z)A)(ga(z)B),\displaystyle(cg_{a}(z)-A)(g_{a}(z)-B),

where A,BA,B are two coefficients determined by Va,bV_{a,b}, r=t0r=t_{0}, and EE. Therefore for two chains with the same κ\kappa solutions, a transverse coupling t0t_{0} only modifies the energy offset between them, without inducing a transition of skin solutions.

Nevertheless, the above factorization does not hold when the coupling term rr is zz-dependent, corresponding to inter-chain couplings between different unit cells. Under this condition, Pc(z)P_{c}(z) cannot be factorized into two sub-polynomials of ga(z)g_{a}(z) and gb(z)=cgz(a)g_{b}(z)=cg_{z}(a), meaning that the skin solution is changed for the system.

I.2 b. Dissimilar skin modes in general two-band models

In a more general picture, the critical skin effect and the size-dependent variation may exist when different parts of the system have dissimilar skin accumulation of eigenmodes. In the two-chain model, we mainly consider regime with small inter-chain couplings, thus the two energy bands (overlapped or connected in most cases) with dissimilar skin modes are mostly given by one of the two chains respectively. To unveil the condition of having dissimilar skin modes in a general two-band system, we consider an arbitrary two-band system described by a non-Bloch Hamiltonian H(z)=h0(z)𝕀+n=1,2,3hn(z)σnH(z)=h_{0}(z)\mathbb{I}+\sum_{n=1,2,3}h_{n}(z)\sigma_{n}, with z=eikeκ(k)z=e^{ik}e^{-\kappa(k)}, and κ(k)\kappa(k) a complex deformation of momentum kk describing the NHSE. Its characteristic polynomial is given by

f(z,E)=[Eh0(z)]2P(z)=0\displaystyle f(z,E)=[E-h_{0}(z)]^{2}-P(z)=0 (S3)

with P(z)=n=1,2,3hn2(z)P(z)=\sum_{n=1,2,3}h_{n}^{2}(z).NHSE can be described by a GBZ where the solutions of f(z,E)=0f(z,E)=0 satisfy Eα(zμ)=Eα(zν)E_{\alpha}(z_{\mu})=E_{\alpha}(z_{\nu}) with |zμ|=|zν||z_{\mu}|=|z_{\nu}| and α=±\alpha=\pm the band index, and κ(k)=log|z|\kappa(k)=-\log|z| gives the inverse decay length. Conventionally, NHSE is studied mostly for system with only nonzero h0(z)h_{0}(z) (i.e. a one-band model) or P(z)P(z) (e.g. the non-reciprocal SSH model), where the zeros of f(z,E)f(z,E) lead to E±=h0(z)E_{\pm}=h_{0}(z) and E±2=P(z)E_{\pm}^{2}=P(z) respectively. In either case, we can see that the two bands of E±E_{\pm} must have the same inverse skin localization depth κ(k)\kappa(k), as Eα(zμ)=Eα(zν)E_{\alpha}(z_{\mu})=E_{\alpha}(z_{\nu}) must be satisfied for α=±\alpha=\pm with the same zμ,νz_{\mu,\nu}. To have dissimilar skin modes for the two bands, h0(z)h_{0}(z) and P(z)P(z) must both be non-vanishing, and possess different skin solutions. That is, although h0(zμ)=h0(zν)h_{0}(z_{\mu})=h_{0}(z_{\nu}) and P(zμ)=h0(zν)P(z_{\mu^{\prime}})=h_{0}(z_{\nu^{\prime}}) can still be satisfied with |zμ|=|zν||z_{\mu}|=|z_{\nu}| and |zμ|=|zν||z_{\mu^{\prime}}|=|z_{\nu^{\prime}}|, we cannot have zμ=zμz_{\mu}=z_{\mu}^{\prime} and zν=zνz_{\nu}=z_{\nu}^{\prime} at the same time, otherwise the same κ(k)\kappa(k) can be obtained for the two bands.

I.3 c. Non-monotonicity of convergence towards EE_{\infty}

In Fig. S1, we illustrate the PBC-OBC spectral flow Lee and Thomale (2019) of the two-chain model with different parameters, by rescaling the amplitudes of the hopping across the boundary as t1±δa,bc(t1±δa,b)t_{1}\pm\delta_{a,b}\rightarrow c(t_{1}\pm\delta_{a,b}), and tuning cc from 11 (PBC) to 0 (OBC). We can see that in the decoupled limit, each of the two PBC bands (red or blue) merges with itself along the real axis when approaching OBC limit [Fig. S1(a,d,e)]. On the other hand, in the coupled regime of Fig. S1(b,c,f), each band first flows toward the real axis, but then ”turns back” and merges with the other band, forming a central-loop structure. In this process, the PBC bands do not necessarily go monotonically closer to OBC spectrum that reflects the GBZ solutions. A systematic study of the interplay between the switching off of boundary couplings (PBC-OBC interpolation) and subsystem coupling (t0t_{0}) is deferred to future work.

Refer to caption
Figure S1: Spectral flow of the two-chain model. (a-c) for N=60N=60 unit cells, (d-f) for N=20N=20 unit cells. From left to right, the inter-chain coupling is t0=0,2×104,0.1t_{0}=0,2\times 10^{-4},0.1 respectively. Other parameters are t1=0.75t_{1}=0.75, δa=δb=0.25\delta_{a}=-\delta_{b}=0.25, and V=0.5V=0.5. Red and blue circles are PBC spectra obtained from the Bloch Hamiltonian, black dots are OBC spectra, and blue-purple curves are the spectral flow from PBC to OBC. In the coupled regime of (b,c,f), two points of PBC bands on the real axis first flow toward zero energy, then rapidly separate along the imaginary axis, as shown by the arrows in Fig. S1(c).

I.4 d. Reciprocal realization of the two-chain model

Here, we discuss how the CSE, which requires subsystems of different NHSE decay lengths, can in fact be realized with reciprocal models that are more easily realizable in experiment. In the two-chain model, the Hamiltonian can be rewritten in the form of Pauli matrices as

h(z)\displaystyle h(z) =\displaystyle= [t(z+1/z)+δ+sink(z1/z)]σ0\displaystyle[t(z+1/z)+\delta_{+}\sin k(z-1/z)]\sigma_{0} (S4)
+t0σx+[V+δ(z1/z)]σz,\displaystyle+t_{0}\sigma_{x}+[V+\delta_{-}(z-1/z)]\sigma_{z},

with δ±=(δa±δb)/2\delta_{\pm}=(\delta_{a}\pm\delta_{b})/2. Here δ+\delta_{+} describes the equivalent part of non-Hermiticity acting on the two chains, which shall induce the same NHSE to them. The critical behavior and transition of NHSE occurs only with nonzero δ\delta_{-}, which induces band-dependent NHSE along the two chains. As shown in Fig. S2, δ±\delta_{\pm} can be divided into different couplings with a rotation of pseudospin σzσy\sigma_{z}\rightarrow\sigma_{y}, and the rotated Bloch Hamiltonian hr(k)h_{r}(k) satisfies hrT(k)=hr(k)h_{r}^{T}(k)=h_{r}(-k) at δ+=V=0\delta_{+}=V=0. Under this condition, the rotated system is reciprocal, and thus provides convenience for experimental realization such as RLC circuit lattices.

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Figure S2: The two-chain model with a rotation of the basis. The rotated lattice has only reciprocal hoppings when δ+=V=0\delta_{+}=V=0.

II II. Anomalous scaling behavior

II.1 a. Competition between skin localization and inter-chain coupling

As mentioned in the main text, if two coupling chains have inverse NHSE decay lengths (non-Hermitian localization length scales) κa,κb\kappa_{a},\kappa_{b}, a change of basis will bring their coupling to be effectively between a chain with no skin effect, and another with an effective skin depth κaκb\kappa_{a}-\kappa_{b}. Since that entails exponentially growing skin modes scaling like e(κaκb)Ne^{(\kappa_{a}-\kappa_{b})N} at one end, we expect the effect of even an infinitesimally small inter-chain coupling t0t_{0} to scale exponentially with NN, and eventually change the OBC spectrum substantially.

Consider increasing the inter-chain coupling t0t_{0} in our two-chain model (Eq. 3 of main text) from zero. At sufficiently small t0t_{0}, we have two practically independent OBC Hatano-Nelson chains with real spectra. Their infinitesimal coupling only shifts their eigenenergies slightly along the real line. But at a critical t0=tct_{0}=t_{c}, the OBC spectrum is rendered complex as one or more pairs of eigenenergies coalesece and repel along in the imaginary direction. Shown in Fig. S3(a) is the inverse exponential scaling of the critical t0=tct_{0}=t_{c} with NN. We observe that tc2e(κaκb)N𝒪(1)t_{c}^{2}e^{(\kappa_{a}-\kappa_{b})N}\sim\mathcal{O}(1), in agreement with the intuitive expectation that tct_{c} should scale inverse exponentially with NN because the effect of t0t_{0} scales exponentially with NN. Yet, the fact that tc2e(κaκb)Nt_{c}^{2}\sim e^{-(\kappa_{a}-\kappa_{b})N} signifies that the Critical Skin Effect is fundamentally a non-perturbative effect, since it differs from tce(κaκb)Nt_{c}\sim e^{-(\kappa_{a}-\kappa_{b})N} as expected from first-order perturbation theory with left and right eigenstates that are oppositely exponentially localized spatially.

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Figure S3: Inverse exponential scaling of the critical bare coupling t0=tct_{0}=t_{c} required for the OBC spectrum of H2-chainH_{\text{2-chain}} to transition from real to complex, versus the system’s size NN and effective skin depth κaκb\kappa_{a}-\kappa_{b} in (a,b) respectively. The numerical data (blue) fits very well with the predicted scaling law tce(κaκb)N/2t_{c}\sim e^{-(\kappa_{a}-\kappa_{b})N/2} (dashed lines) with κaκb=log2\kappa_{a}-\kappa_{b}=\log 2 in (a) and N=40N=40 in (b). Unless specified in the figure, the parameters are t1=0.75t_{1}=0.75, δa=δb=0.25\delta_{a}=-\delta_{b}=0.25 as in Fig. 2 of the main text. In (b), κaκb\kappa_{a}-\kappa_{b} is obtained from Eq. (S5) with δa=δb\delta_{a}=-\delta_{b} varying from 0.10.1 to 0.40.4.

The scaling behavior of e(κaκb)Ne^{(\kappa_{a}-\kappa_{b})N} also suggests that increasing NN has similar consequences as increasing the non-reciprocity in the system, the strength of which is reflected by the absolute value of (κaκb)(\kappa_{a}-\kappa_{b}). Therefore it is also expected that the critical skin effect shall emerge when we enhance the non-reciprocity but fix NN. In Fig. S3(b) we show the inverse exponential scaling of the critical t0=tct_{0}=t_{c} with κaκb\kappa_{a}-\kappa_{b}, where the inverse NHSE decay lengths are given by

eκa,b=t1+δa,bt1δa,b\displaystyle e^{\kappa_{a,b}}=\sqrt{\frac{t_{1}+\delta_{a,b}}{t_{1}-\delta_{a,b}}} (S5)

for the two decoupled chains. The scaling behavior versus κaκb\kappa_{a}-\kappa_{b} further confirms that tc2e(κaκb)Nt_{c}^{2}\sim e^{-(\kappa_{a}-\kappa_{b})N}.

In Fig. S4, we illustrate another example of our two-chain model with non-Hermitian cross inter-chain coupling δab\delta_{ab}, i.e. HCSSSHH_{\rm CS-SSH} in the main text. By increasing δ\delta_{-}, the non-reciprocity is strengthened along each chain, but toward opposite directions. Thus the effective inverse skin depth κaκb\kappa_{a}-\kappa_{b} is enhanced, and we observe a transition of OBC spectrum from a line to a central-loop structure, accompanied with a topological transition reflected by the emergence of zero-energy degenerate edge states. This behavior is similar to the transition with enlarging NN as discussed in the main text.

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Figure S4: OBC spectra (black dots) at different δ\delta_{-} for the two-chain model with non-Hermitian cross inter-chain coupling described by HCSSSHH_{\rm CS-SSH} in the main text. Red (green) dot lines indicate the OBC skin solution in the thermodynamical limit with a weak (zero) inter-chain coupling δab=0.5×103(0)\delta_{ab}=0.5\times 10^{-3}(0). Other parameters are N=40N=40, δa=δb=δ\delta_{a}=-\delta_{b}=\delta_{-}, t1=0.75t_{1}=0.75, and V=1.2V=1.2.

II.2 b. Anomalous scaling of entanglement entropy

The Fermionic entanglement entropy (EE) SS scaling behavior depends qualitatively on the nature of the phase, increasing as 13logN~{}\frac{1}{3}\log N at an ordinary critical point, decreasing possibly as a negative multiple of logN\log N at a critical exceptional point Chang et al. (2019), and saturating at a gapped or decoupled scenario. Since NN itself can drive phase transitions in our case of the Critical Skin Effect, we expect the scaling of SS to interpolate and transition through distinct behaviors.

For free Fermions in a many-body state |Ψ|\Psi\rangle, the (biorthogonal) EE Herviou et al. (2019); Mu et al. (2019) for a chosen entanglement cut can be computed via

S=j[cjlogcj+(1cj)log(1cj)],S=-\sum_{j}[c_{j}\log c_{j}+(1-c_{j})\log(1-c_{j})], (S6)

where the cjc_{j}’s are the eigenvalues of the 2-particle correlator C=PQPC=PQP Peschel (2003); Alexandradinata et al. (2011); Lee and Ye (2015). Here PP is the projector implementing the entanglement cut and Q=μocc.|ψμψμ|Q=\sum_{\mu\in occ.}|\psi_{\mu}\rangle\langle\psi_{\mu}| is the single-body biorthogonal projector onto the set of basis states |ψμ|\psi_{\mu}\rangle occupied by the many-body state |Ψ|\Psi\rangle. In a perfectly unentangled case, cj=0c_{j}=0 or 11 only, giving rise to a vanishing EE. With increased entanglement, the cjc_{j}’s encroach closer to 1/21/2, attaining the latter when the sector jj is fully entangled. In the biorthogonal setting, it is possible for cjc_{j} to take values outside of [0,1][0,1] since |ψμ|\psi_{\mu}\rangle is not the complex conjugate of ψμ|\langle\psi_{\mu}|, leading to negative or even imaginary contributions to SS Chang et al. (2019).

In Fig. S5, we observe a crossover from a decoupled regime to a critical regime when NN increases. SS also exhibits non-universal negative values for certain even NN [Fig. S5(b)], a behavior resulting from cj[0,1]c_{j}\notin[0,1] for a few of these NN. In real space, the two-Fermion correlator CC decays rapidly for small NN, but interesting decays more slowly like x1x^{-1} for larger NN when the system becomes gapless. As such, correlators generally become enhanced in larger systems where the effects of coupling become amplified by the CSE.

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(a)
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(b)
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(c)
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(d)
Figure S5: (a,b) Scaling of SS with odd/even NN (blue) for a half-filled OBC H2-chainH_{\text{2-chain}} with real-space cut at N2\lfloor\frac{N}{2}\rfloor and parameters t1=0.58t_{1}=0.58, V=1V=1, t0=0.4t_{0}=0.4 and δa=δb=0.25\delta_{a}=-\delta_{b}=0.25 (same as Fig. 3a of the main text). At small NN, SS is almost vanishing/is negative for odd/even system sizes. At larger NN, both odd and even cases display a tendency towards the expected S13logNS\sim\frac{1}{3}\log N critical behavior (yellow). (c) The corresponding correlator eigenvalues cjc_{j}, showing how the system transitions to critical behavior with a single cj=1/2c_{j}=1/2 (and other eigenvalues slowly approaching it) only beyond N10N\approx 10. Before that, the system is essentially decoupled. (d) The corresponding two-Fermion correlation at N=10,18,40,50,60N=10,18,40,50,60 (blue,brown,green,puple,red), with rapid exponential decay for small NN and power-law decay for large NN (Black dashed curve shows N1N^{-1} decay for reference).

III III. GBZ solutions EE_{\infty} for the 2-chain model

For analytic tractability, we consider the case of Eq. 3 of the main text with ta+=tb=1t^{+}_{a}=t_{b}^{-}=1 and ta=tb+=0t^{-}_{a}=t^{+}_{b}=0 (i.e. t1=δa=δb=0.5t_{1}=\delta_{a}=-\delta_{b}=0.5), but nonzero bb and VV. We obtain

H2-chain(z)=(z+Vt0t01/zV)H_{\text{2-chain}}(z)=\left(\begin{matrix}z+V&t_{0}\\ t_{0}&1/z-V\end{matrix}\right) (S7)

with characteristic polynomial given by

f(z,E)\displaystyle f(z,E) =\displaystyle= E2E(z1+z)+[(z+V)(z1V)t02]\displaystyle E^{2}-E(z^{-1}+z)+[(z+V)(z^{-1}-V)-t_{0}^{2}] (S8)
=\displaystyle= VEzz(V+E)+[E2V2t02+1]\displaystyle\frac{V-E}{z}-z(V+E)+[E^{2}-V^{2}-t_{0}^{2}+1]

To find the GBZ solutions EE_{\infty} for comparison with the actual OBC solutions, we solve for roots |z+|=|z||z_{+}|=|z_{-}| of f(z,E)=0f(z,E)=0 (with Σ=E2V2t02+1\Sigma=E^{2}-V^{2}-t_{0}^{2}+1):

z±\displaystyle z_{\pm} =\displaystyle= (Σ±Σ2+4(V2E2))2(V+E)\displaystyle\frac{\left(\Sigma\pm\sqrt{\Sigma^{2}+4(V^{2}-E^{2})}\right)}{2(V+E)} (S9)
=\displaystyle= Σ±(Σ2)24t022(V+E)\displaystyle\frac{\Sigma\pm\sqrt{(\Sigma-2)^{2}-4t_{0}^{2}}}{2(V+E)}

For |z+|=|z||z_{+}|=|z_{-}| to hold, the square root quantity must differ from Σ\Sigma by a complex argument of π/2\pi/2 Lee et al. i.e.

(Σ2)24t02=iηΣ\sqrt{(\Sigma-2)^{2}-4t_{0}^{2}}=i{\color[rgb]{0,0,0}\eta}\Sigma (S10)

where η\eta\in\mathbb{R}. Simplifying, we obtain Σ=21+η2(1±t02+η2(t021))\Sigma=\frac{2}{1+\eta^{2}}\left(1\pm\sqrt{t_{0}^{2}+\eta^{2}(t_{0}^{2}-1)}\right) or, in terms of E2E2E^{2}\rightarrow E_{\infty}^{2},

E2=1η2±2t02η2+η2t021+η2+V2+t02E_{\infty}^{2}=\frac{1-\eta^{2}\pm 2\sqrt{t_{0}^{2}-\eta^{2}+\eta^{2}t_{0}^{2}}}{1+\eta^{2}}+V^{2}+t_{0}^{2} (S11)

as in the main text, with η\eta tracing out a one-parameter continuous spectrum. The GBZ can be numerically obtained by substituting Eq. S11 into the expression for z±z_{\pm} in Eq. S9 with E=EE=E_{\infty}. From that, we obtain two momentum values k±=Re[ilogz±]k_{\pm}=\text{Re}[-i\log z_{\pm}] with κ(k+)=κ(k)=log|z+|=log|z|\kappa(k_{+})=\kappa(k_{-})=-\log|z_{+}|=-\log|z_{-}| inverse length scales. Note however that because of the proximity to the t0=0t_{0}=0 critical point, this value of κ(k±)\kappa(k_{\pm}) is significantly different from the actual inverse OBC skin depth for a large range of finite system sizes.

IV IV. Mapping between the SSH model and two non-reciprocal 1D chains

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Figure S6: Transforming the two-chain model with non-reciprocal cross couplings to a SSH model with non-reciprocal inter-cell couplings and second-nearest-neighbor couplings. The different parameters in the two panels are connected through δ±=(δa±δb)/2\delta_{\pm}=(\delta_{a}\pm\delta_{b})/2. Blue dash lines indicate a unit cell before and after the rotation, and red dash line indicates an alternative choice of unit cell with a shift of one lattice site, with which the non-reciprocal couplings of 2δ2\delta_{-} can be further transformed into on-site gain and loss.

In the main text we have considered a two-chain model with both intra-chain and inter-chain couplings being non-reciprocal, described by the Hamiltonian

HCS-SSH(z)\displaystyle H_{\text{CS-SSH}}(z) =\displaystyle= [iδab(z+1/z)]σy+[V+δ(z1/z)]σz+[t1(z+1/z)+δ+(z1/z)]𝕀\displaystyle[i\delta_{ab}(z+1/z)]\sigma_{y}+[V+\delta_{-}(z-1/z)]\sigma_{z}+[t_{1}(z+1/z)+\delta_{+}(z-1/z)]\mathbb{I} (S12)

with δ±=(δa±δb)/2\delta_{\pm}=(\delta_{a}\pm\delta_{b})/2. In the parameter regime with δab=δ\delta_{ab}=\delta_{-}, through a rotation of basis σzσx\sigma_{z}\rightarrow\sigma_{x}, this Hamiltonian becomes

Hr(z)=(t1(z+1/z)+δ+(z1/z)V+2δzV2δ/zt1(z+1/z)+δ+(z1/z)).\displaystyle H_{r}(z)=\left(\begin{matrix}t_{1}(z+1/z)+\delta_{+}(z-1/z)&V+2\delta_{-}z\\ V-2\delta_{-}/z&t_{1}(z+1/z)+\delta_{+}(z-1/z)\end{matrix}\right). (S13)

This Hamiltonian describes a SSH model with non-reciprocal inter-cell couplings and second-nearest-neighbor couplings, as illustrated in Fig. S6. In the main text we have chosen δa=δb\delta_{a}=-\delta_{b}, so that δ+=0\delta_{+}=0 and the second-nearest-neighbor couplings are Hermitian. In this parameter regime, by redefining the unit cell as the red dashed line in Fig. S6 (shifting one lattice site), we can see that the rotated model is equivalent to the non-reciprocal SSH model studied in Refs. Yao and Wang (2018); Yin et al. (2018) etc. with a uniform second-nearest-neighbor couplings, described by the Hamiltonian

Hr(z)=(t1(z+1/z)V/z+2δVz2δt1(z+1/z)).\displaystyle H^{\prime}_{r}(z)=\left(\begin{matrix}t_{1}(z+1/z)&V/z+2\delta_{-}\\ Vz-2\delta_{-}&t_{1}(z+1/z)\end{matrix}\right). (S14)

Finally, by applying another rotation of basis σyσz\sigma_{y}\rightarrow\sigma_{z}, the system can be further transformed into a ladder model with non-Hermiticity being only on-site gain and loss Song et al. (2019a); Li et al. .

Note that in the main text we have considered the case with δabδ\delta_{ab}\ll\delta_{-}. In the SSH model, this inequality corresponds to some extra longer-range couplings. Also note that the redefinition of unit cells also corresponds to a different lattice structure where the first and last lattice sites are coupled by VV instead of ±δ\pm\delta_{-}. Under OBCs, these two choices of unit cells will result in different behaviors of topological edge states.

V V. Topological edge states in a line gap

Here we consider the two-chain model with cross inter-chain couplings discussed in the main text, but with a stronger inter-chain coupling strength δab=0.15\delta_{ab}=0.15. We can see in Fig. S7 that the system has a narrow real line-gap at small N=10N=10, a point-gap at N=20N=20, and an imaginary line-gap at N=40N=40. Degenerate zero-energy edge states emerge in the later two cases. As the two OBC bands are fully separated from each others in the last case, a Berry phase can be well-defined for each non-Bloch band to characterize the topological properties in this system.

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Figure S7: (a) κ\kappa solutions (red, blue, green, and yellow surfaces) of f(z,E)=0f(z,E)=0 as a function of the complex energy. Parameters are δa=δb=0.5\delta_{a}=-\delta_{b}=0.5, t1=0.75t_{1}=0.75, V=1.2V=1.2, and δab=0.15\delta_{ab}=0.15. Different κ\kappa solutions coincide along the green and red dot lines, the later one gives the OBC skin solutions of the system in the thermodynamic limit. (b) OBC spectra (black dots) at N=10N=10, 2020 and 4040 unit cells. At small NN, the OBC spectrum mostly lies in the real axis and is partially given by the green dot lines in (a), analogous to the skin solutions in the decoupled limit. At larger |Re[E]||{\rm Re}[E]|, however, the eigenenergies obtained different complex values and form a Y-shape spectrum, matching the OBC skin solutions of the red curves. With enlarging system’s size, the spectrum continuously approaches these OBC skin solutions.