The transfer of information between topological edge states is a robust way of spatially manipulating spatial states in lattice environments. This method is particularly efficient when the edge modes are kept within the topological gap of the lattice during the transfer. In this work, we show experimentally the transfer of photonic modes between topological edge states located at opposite ends of a dimerized one-dimensional photonic lattice. We use a diamond lattice of coupled waveguides and show that the topological transfer is insensitive to the presence of a high density of states in the form of a flat band at an energy close to that of the edge states and prevails in the presence of a hopping impurity. We explore the dynamics in the waveguide lattice using a wavelength-scan method, where different input wavelengths translate into different effective lattice lengths. Our results offer an alternative way to the implementation of efficient transfer protocols based on active driving mechanisms.

Topological edge states are a remarkable resource for engineering photonic systems with isolated modes protected from the presence of disorder. In two-dimensional lattices, they can be used to fabricate topological edge mode lasers with distributed gain and quantized orbital momentum,1,2 to transfer single photons around corners in elaborated photonic circuits,3,4 and to design topological frequency combs with enhanced efficiency.5,6 One-dimensional systems such as the Su-Schrieffer-Heeger (SSH) lattice are particularly interesting because topological edges and interface modes are hosted deep into the topological gap of the lattice. This gap protection has been shown to be beneficial in preserving the quantum state of photons in boundary modes.7,8 Interestingly, the presence of topological edge modes on both sides of one-dimensional lattices can be used to transfer a state from one edge of the lattice to the other with high fidelity with the advantage of being protected from certain types of disorder due to the topological nature of the system. Such edge state transfer is a promising route to store and manipulate photonic quantum states in on-chip lattice environments.

Most topological edge transfer protocols rely on the adiabatic evolution of the lattice such that an edge mode is driven into quasi-bulk modes and again into an edge state at the other side.9–17 While these protocols present an optimized transfer rate and fidelity, they are limited by the adiabaticity condition, which requires the adiabatic passage to be slow enough to avoid the Zenner coupling of the edge state information into the bulk modes.18,19 Furthermore, the presence of disorder in the lattice would enhance this coupling. A variation of these protocols includes counter-adiabatic driving methods.20 Recently, a rather different route has been proposed based on the coherent coupling of edge modes within the gap.19,21,22 The great advantage of this approach is that edge modes are kept well into the topological gap throughout the protocol, ensuring high fidelity in reduced time. The simplest version of the coherent state transfer of topological edge states is via passive evanescent coupling of the exponential tails of edge modes at opposite sides of the finite size lattice. In this case, periodic oscillations between edge modes take place at a frequency determined by the tail overlap,23 which can be controlled by the size of the gap. Observation of such coherent oscillations was reported in a short SSH lattice for Rydberg atoms.24 

In this work, we demonstrate coherent edge-to-edge transfer of light in dimerized diamond lattices of coupled optical waveguides by employing a spectral tomographic technique. First, we show that the orthogonality of eigenmodes in our undriven protocol preserves the transfer even in the presence of a high density of states in the form of a flat band (FB) at energies close to those of the edge states. Second, we demonstrate that the transfer mechanism persists in the presence of lattice defects thanks to the underlying chiral symmetry of the system. Our results offer a purely linear transfer of light via distant edge states, in strong contrast to, for example, the nonlinear switching in between two nearby topological interface states.25 Additionally, the experimental proof of principle we report in this work can be significantly speeded up, for example, by applying a number of driven techniques based on the modulating of the hoppings in time and the use of concatenated topological lattices.19,22,26

To demonstrate the topological edge transfer, we use a diamond lattice27–29 of coupled waveguides with different intracell (t1) and intercell (t2) hoppings, as sketched in Fig. 1(a). The lattice has three sites per unit cell, denoted as A, B, and C sites. Considering a tight-binding coupled-mode approach, the evolution of the optical field at every site of the n-th unit cell is written as
izAn=t1Bn+t2Bn+1,izBn=t1(An+Cn)+t2(An1+Cn1),izCn=t1Bn+t2Bn+1.
(1)
Here, An, Bn, and Cn are the amplitudes of the optical field at the n-th unit cell. z describes the coordinate along the waveguides and the dynamical variable. Moreover, the hopping strengths among nearest-neighbor (NN) sites can be varied experimentally by adjusting the lattice distances.30 We then define the control parameter δt1/t2 to characterize the different regimes. We assume an infinite system and impose a Bloch-like ansatz in Eq. (1), obtaining the following bands:
βz(kx)=0,±t22δ2+2δcos(kxa)+1,
(2)
where βz is the propagation constant (energy), a is the lattice constant, and kx is the quasimomentum. The spectrum is composed of two dispersive and one flat band (FB) [see shaded areas and the horizontal light-blue line at βz = 0 in Fig. 1(b), respectively]. The gap in between both dispersive bands has a size equal to 22t2|δ1|. For δ = 1, this gap closes, and the three bands touch each other at the edges of the Brillouin zone.31 The diamond lattice possesses the smallest experimentally reported FB states,31–33 with an inverse participation ratio (IPR)34 of 1/2 [represented as a light-blue color in Fig. 1(b)]. Specifically, in the bases of Wannier functions in the A, B, and C sites, the FB eigenvector is given by: |vFB={1,0,1}/2, and the ones corresponding to the dispersive bands are |v±={eiϕ(kx),±2,eiϕ(kx)}/2, where ϕ(kx) = arctan(−sin(kxa)/[δ + cos(kxa)]).
FIG. 1.

(a) Sketch of a dimerized diamond lattice, with A, B, and C as the sites of the unit cell. A thick (thin) line denotes strong (weak) hopping, and t1 (t2) indicates the intra(inter)-cell coupling constant. The top (bottom) panel schematizes the trivial (topological) case t1 > t2 (t1 < t2). (b) Spectrum as a function of δ for a finite (lines) and an infinite (shaded area) lattice. The vertical dashed line denotes δ = 1. The color indicates the IPR for all the states. Inset: amplitude profiles of edge states at δ = 0.4. (c) Sketch of the fs laser writing technique. (d) Microscope image of a diamond lattice with {d1, d2} = {35, 25} μm (δ = 0.37) and dv = 32 μm. Output intensity profiles, after a propagation length of 7 cm, for (e1) a B left edge and (e2) an in-phase AC right edge site excitations. Yellow ellipses indicate the excited sites.

FIG. 1.

(a) Sketch of a dimerized diamond lattice, with A, B, and C as the sites of the unit cell. A thick (thin) line denotes strong (weak) hopping, and t1 (t2) indicates the intra(inter)-cell coupling constant. The top (bottom) panel schematizes the trivial (topological) case t1 > t2 (t1 < t2). (b) Spectrum as a function of δ for a finite (lines) and an infinite (shaded area) lattice. The vertical dashed line denotes δ = 1. The color indicates the IPR for all the states. Inset: amplitude profiles of edge states at δ = 0.4. (c) Sketch of the fs laser writing technique. (d) Microscope image of a diamond lattice with {d1, d2} = {35, 25} μm (δ = 0.37) and dv = 32 μm. Output intensity profiles, after a propagation length of 7 cm, for (e1) a B left edge and (e2) an in-phase AC right edge site excitations. Yellow ellipses indicate the excited sites.

Close modal

Even though this lattice has three sites per unit cell, it exhibits similar topological features to the SSH model35 when varying the parameter δ.36 Indeed, a quantized Zak phase of value 0 or π can be found when δ > 1 (t1 > t2) or δ < 1 (t1 < t2), respectively. In this case, the nontrivial phase is protected by inversion symmetry between An and Cn, and by chiral symmetry.36,37 Therefore, we expect the appearance of two edge states at a zero propagation constant on a lattice with open boundaries when δ < 1. These two states are chiral partners and, therefore, one must have amplitude only at A sites, while the other must possess amplitude only at B and C sites. To corroborate this, we compute the spectrum as a function of δ for dimerized diamond lattices of 9 unit cells [see full lines in Fig. 1(b)]. It can be clearly seen that two states at zero frequency (lighter blue) transform into two dispersive states (darker blue) around δ = 1. When increasing δ, the degeneracy between them is removed at around δ = 0.7 [splitting Δβze0.06, see Fig. S4(e) in the supplementary material] due to the finite size of the lattice. The flat band remains unchanged at βz = 0, for any value of δ. The IPR (denoted by color) shows very clearly the transition from localized edge states (IPR = 1 or 1/2, light blue) into extended propagating modes (IPR 1/N, black).

Figure 1(b) insets show the two edge states for δ = 0.4. They exhibit exponentially localized amplitudes at both edges. On the left edge, these states present a null amplitude at A and C sites, whereas the states have a null amplitude at B sites on the right edge. Moreover, one edge state is antisymmetric (bottom inset) and the other is symmetric (top inset) with respect to the opposite edge. They decay exponentially into the bulk as (δ)|nne| for a semi-infinite system, exhibiting a phase shift of π at consecutive B or A, C sites, depending on the specific edge (ne). For δ ≳ 0.7, the frequency of the edge states deviates from 0 to ±βze. Therefore, the excitation of sites at the edges is expected to induce an oscillatory pattern in between both surfaces with a frequency βze,23 with a long-distance state transfer occurring on a large dynamical scale ztransfer=π/βze (see supplementary material.

Experimentally, the diamond lattice exhibits an important advantage compared to the SSH lattice because the bandgap is 2 wider for the diamond lattice, considering equal hopping strengths t1,2; therefore, it reduces the possible coupling between edge and bulk modes in the presence of disorder in the couplings.

We fabricate several dimerized diamond photonic lattices of 9 unit cells each by using a femtosecond (fs) laser writing technique,30,38 as sketched in Fig. 1(c). For the first set of experiments, the diamond geometry is defined by distances d1, d2, and dv = 32 μm, as described in Fig. 1(d). For these values, the diagonal (NN) distance was swept in the interval {25.6, 43.1} μm, as d1 and d2 were varied in the interval {20, 40} μm in steps of 1 μm. The hopping coefficients (which decay exponentially on waveguide separation30) range in the interval ∼{0.03, 0.21} cm−1 at a wavelength of 640 nm. Figure 1(d) shows an output facet of a lattice with d1 = 35 and d2 = 25 μm, with t1 = 0.05 and t2 = 0.14 cm−1 (δ = 0.37). We first test the quality of the lattices by exciting them at different input positions using a 640 nm laser beam (see supplementary material for a complete characterization). For example, topological edge states can be efficiently excited by injecting light directly at the lattice boundaries.34,39,40 Figure 1(e1) shows the output profile after a B-edge site excitation, with a clear exponential decaying profile from the edge into the bulk. The excitation at the right boundary requires a more complicated input condition with two in-phase beams. The result of this is shown in Fig. 1(e2), with an output profile formed mostly by A and C sites.

We characterize the lattice dynamics by implementing a wavelength-scan method: The dynamics of a wavepacket injected into the input facet of a lattice are revealed when varying the input wavelength coming from a Supercontinuum (SC) laser source.41–43 Therefore, instead of measuring the output profiles at different z values, which implies the fabrication of a larger number of lattices, we manipulate the input beam wavelength. The lattice dynamics depend on the excitation wavelength λ: the longer the wavelength, the wider the mode profile, and the larger the coupling constants42 (see also the supplementary material). In this way, we can study the same lattice at different effective lengths by tuning the input wavelength.

We first consider a diamond lattice with d1 = d2 = 30 μm. We excite a B site at the central fifth unit cell and scan the input wavelength in the interval 600–760 nm, with a step of 10 nm. Figure 2(a) shows the output intensity for three selected λ’s (a complete sweep is shown in supplementary material). Figure 2(b) shows the second moment (width), defined as m2n(nnc)2Pn, vs the input wavelength (Pn ≡ |An|2 + |Bn|2 + |Cn|2, the unit cell power, and nc ≡ ∑nnPn, the center of mass). We observe a growing diffraction pattern33 with a width that increases almost linearly with the input wavelength [a linear fit is included in Fig. 2(b)]. m2 ∼ z corresponds to a ballistic regime,44 as expected for discrete diffraction dynamics; therefore, a λ increment produces an effectively larger lattice propagation distance z or, equivalently, a larger coupling constant t1,2.

FIG. 2.

(a) Output intensity profiles for a B-site central excitation for a lattice with d1 = d2 = 30 μm at the indicated wavelength. (b) m2 vs λ. (c) md vs δ (bottom) and d1 in μm (top). Insets in (c) show the profiles at 700 nm for the indicated cases. The bars show the standard deviation, and the orange curve shows the results obtained after numerically simulating model (1) for 9 unit cells. In (a) and (c), yellow ellipses indicate the excited sites.

FIG. 2.

(a) Output intensity profiles for a B-site central excitation for a lattice with d1 = d2 = 30 μm at the indicated wavelength. (b) m2 vs λ. (c) md vs δ (bottom) and d1 in μm (top). Insets in (c) show the profiles at 700 nm for the indicated cases. The bars show the standard deviation, and the orange curve shows the results obtained after numerically simulating model (1) for 9 unit cells. In (a) and (c), yellow ellipses indicate the excited sites.

Close modal

A dimerized diamond lattice has two hoppings that simultaneously change while λ is modified. Since we observe a linear dependence of coupling constants on wavelength, we can assume δ as a constant as a first approximation. We use the wavelength-scan method to experimentally determine nc for all the output profiles after exciting a B site at the central (fifth) unit cell of 17 dimerized lattices with different values of δ. For each lattice, we average nc over λ and obtain the averaged beam displacement md, from which the topological invariant can be inferred.45,46 A topologically trivial lattice has an md ∼ 0, as an indication of a zero Zak phase. A topological system will shift this value to md ∼ 0.5, corresponding to a non-trivial π Zak phase.45 Our collected results are shown in Fig. 2(c). We observe that for δ > 1 (d1 < 30 μm), the lattice is topologically trivial, and the propagation shows a md around zero. For δ ∼ 1 (d1 ∼ 30 μm), a transition region without a well-defined topological phase is observed. For δ < 1.0 (d1 > 30 μm), the lattices express an averaged beam displacement around 0.5, implying a clear nontrivial Zak phase (see also the supplementary material). This is in very good agreement with the direct numerical simulations shown in Fig. 2(c) by an orange curve. Therefore, the wavelength-scan method gives us valuable information about the dynamics on a specific lattice and, in addition, it becomes a key and simple method to determine its topological phase experimentally.

The number of unit cells in the lattice affects the edge state properties: the fewer unit cells, the shorter the range of δ in which the edge states keep degenerate in βz (see supplementary material). When the degeneracy is lifted, the two edge modes hybridize. Therefore, an input on one edge will coherently excite both modes and will result in periodic oscillations of the amplitude at the two edges on a very long dynamical scale. Then, an effective transfer of light from one edge to the other becomes possible.23,24 To experimentally demonstrate this, we fabricate a topological lattice with 9 unit cells and distances d1 = 18, d2 = 14, and dv = 14 μm (t1 = 0.30 and t2 = 0.42 cm−1 at 640 nm, and δ = 0.71). The trivial lattice (δ = 1.40) is obtained by inverting these distances to d1 = 14 and d2 = 18 μm. In this experiment, we decreased the distances to increase the coupling coefficients and favor faster transport in between the edges while staying in the non-degenerate situation. The inclusion of vertical next-nearest-neighbor (NNN) couplings would shift the energies for FB modes and, also, for the edge states, and the topological transfer would not be observable. The NNN hopping indeed does not destroy the edge states, but the definition of the winding number is not the same anymore47(see also supplementary material). Again, we use an SC laser source in the range of 610–740 nm and sweep the input wavelength in steps of 10 nm. We excite the system by injecting light at the B left edge waveguide, as shown in Fig. 3(a). For λ ≲ 670 nm, the intensity profiles are well localized at the left edge, with most of the light intensity at the B sublattices, with a profile resembling the edge state [Fig. 1(e1)]. The edge state splitting manifests around λ ≈ 680 nm, where we start observing a smooth population of the opposite edge with a very weak excitation of the lattice center (a weak background radiation is always observed due to the excitation of dispersive modes; see supplementary material). The connection in between both edge patterns [see Fig. 1(b) insets and (e)], with a B-site exponential decaying profile at the left surface and an A, C exponential profile at the right edge, becomes evident for 710 nm. The spectral state transfer phenomenon starts occurring at λ ≳ 720 nm: the light injected at one edge is mostly transferred to the opposite edge. This shows a very interesting transport mechanism that does not require the light to explore the bulk modes of the lattice. In this case, the light transfers suddenly from one edge mode to the other without interacting with the lattice bulk modes. Due to the topological properties of this dimerized lattice, the edge-to-edge transfer dynamics are mainly governed by the topological edge states, with only a weak leak to dispersive modes.

FIG. 3.

(a) Output profiles of a non-trivial diamond photonic lattice at different λ’s after a B-edge excitation (see yellow ellipse). (b) Fidelity vs wavelength for topological (black), trivial (gray), topological + defect (red), and trivial + defect (orange) lattices. (c) Microscope image of a topological lattice plus two coupling defects (see dashed rectangle). (d) Same as (a) for a topological lattice with a coupling defect.

FIG. 3.

(a) Output profiles of a non-trivial diamond photonic lattice at different λ’s after a B-edge excitation (see yellow ellipse). (b) Fidelity vs wavelength for topological (black), trivial (gray), topological + defect (red), and trivial + defect (orange) lattices. (c) Microscope image of a topological lattice plus two coupling defects (see dashed rectangle). (d) Same as (a) for a topological lattice with a coupling defect.

Close modal

To quantify the transfer, starting from a left edge B-site input excitation into the opposite right edge, we define the fidelity F for an edge-to-edge light transfer by measuring the normalized transferred intensity at the opposite lattice edge: F ≡ (|Aedge|2 + |Cedge|2)/∑nPn. If all the light reaches the two rightmost sites, F = 1, and F = 0 in the fully opposite case. We show our results in Fig. 3(b), where we plot the fidelity F vs λ for topological and trivial lattices. We observe how the topological (black) and trivial (gray) cases have a similar dynamical scale, i.e., both processes occur approximately at the same speed. However, the fidelity at the A, C surface is larger for the topological lattice (61%). The trivial lattice presents a standard discrete diffraction pattern,33 with the energy exploring the whole lattice while it moves from one edge into the other as the wavelength increases [similar to Fig. 2(a); see also the supplementary material]. Therefore, once the light arrives at the A, C right edge, it is reflected back due to the absence of the edge states. The fidelity in this case decreases to 40%.

A remarkable feature of the state transfer between topological edge states is the resilience to disorder in the coupling constants. Although the fabrication process can produce random on-site or inter-site defects, we fabricate a couple of lattices with a symmetric coupling defect, as shown in Fig. 3(c). We design a different distance in between the fourth and fifth cells, and inside the fifth cell [see dashed rectangle in Fig. 3(c)]. Specifically, we set this distance to 23 μm, implying a coupling constant of 0.18 cm−1. This corresponds to a strong impurity, considering the t1 and t2 values. Figure 3(d) shows a set of output images at the indicated values of λ for the topological lattice with a defect. We notice that this defect produces some reflection and trapping of energy at shorter wavelengths for 7 cm of propagation; consequently, not all the energy is edge-to-edge transferred. Despite this, a significant amount of light excites the topological right-edge state composed of A and C sites. The fidelity takes into account the effect of the defect on the transfer, which is reduced to 26% for the topological case, whereas it drops to 15% for the trivial lattice (in this case, for λ = 740 nm).

These numbers show that a trivial lattice undergoes a stronger back reflection caused by the defect because the light explores the whole lattice and interacts strongly with it. On the other hand, in the topological case, the light does not need to interact with the bulk modes across the lattice, and it excites efficiently the edge state without the need to arrive at the boundary by standard transportation mechanisms. The fidelity is not perfect in any of the topological cases because a single B-site input always excites part of the dispersive spectrum, in which the modes extend over the entire lattice. Nonetheless, the important difference between the topological and trivial cases is the key to success for a topological state transfer process, which occurs due to the excitation of exponentially localized topological edge states, which exist at both edges simultaneously and deep into the gap of the lattice spectrum.

In comparison with the photonic realization of a Heisenberg spin chain of qubits, in which a state is transferred from one edge to the other with high fidelity,48 our transfer protocol provides a more versatile tool when considering deliberate disorder in the coupling constants and a wide range of wavelengths for the incident beam. This could be a proof of concept for a long-distance photonic sensor that detects away from the interaction/excitation region and can be more robust against bulk imperfections.

In this work, we used the wavelength-scan method as an important tool for investigating the dynamics of photonic waveguide lattices. We evidenced the nontrivial topology of dimerized diamond lattices by experimentally measuring the averaged beam displacement. In addition, we demonstrated an edge-to-edge transfer of light via a strong excitation of the lattice topological edge states. This transfer is based on an undriven protocol, in contrast with the one based on a driven 1D quasicrystal,9 and is partially robust to defects across the lattice bulk. Furthermore, this lattice configuration could be used as a precise wavelength filter or as an efficient information transport mechanism. Considering very distant ports, a sequence of concatenated topological lattices could transform into a key solution for long-distance quantum communication protocols.12,14 We became aware of a recent work reporting related transport properties in a SSH chain of split resonators.49 

See supplementary material for both simulation at experimental details.

This work was supported in part by Millennium Science Initiative Program ICN17012 and FONDECYT Grants 1191205 and 3230139. A.A. acknowledges the support of the European Research Council grant EmergenTopo (Grant No. 865151), the French government through the Program Investissement d’Avenir (Grant No. I-SITE ULNE/ANR-16-IDEX-0004 ULNE) managed by the Agence Nationale de la Recherche, the Labex CEMPI (Grant No. ANR-11-LABX-0007), and the CPER Wavetech. T.O. acknowledges the support from JSPS KAKENHI Grant No. JP20H01845, JST PRESTO Grant No. JPMJPR19L2, and JST CREST Grant No. JPMJCR19T1.

The authors have no conflicts to disclose.

G.C.-A. and B.R. authors contributed equally to this work.

Gabriel Cáceres-Aravena: Conceptualization (equal); Data curation (equal); Formal analysis (equal); Investigation (equal); Visualization (equal). Bastián Real: Conceptualization (equal); Data curation (equal); Formal analysis (equal); Investigation (equal); Visualization (equal); Writing – original draft (equal); Writing – review & editing (equal). Diego Guzmán-Silva: Data curation (equal); Formal analysis (equal); Investigation (equal); Writing – original draft (equal). Paloma Vildoso: Investigation (equal). Ignacio Salinas: Investigation (equal). Alberto Amo: Formal analysis (equal); Funding acquisition (equal); Writing – original draft (equal). Tomoki Ozawa: Formal analysis (equal); Funding acquisition (equal); Writing – original draft (equal). Rodrigo A. Vicencio: Data curation (equal); Formal analysis (equal); Funding acquisition (equal); Investigation (equal); Methodology (equal); Resources (equal); Supervision (equal); Visualization (equal); Writing – original draft (equal); Writing – review & editing (equal).

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Supplementary Material