Abstract
We present strong enhancement of third harmonic generation in an amorphous silicon metasurface consisting of elliptical nano resonators. We show that this enhancement originates from a new type of multi-mode Fano mechanism. These ‘Super-Fano’ resonances are investigated numerically in great detail using full-wave simulations. The theoretically predicted behavior of the metasurface is experimentally verified by linear and nonlinear transmission spectroscopy. Moreover, quantitative nonlinear measurements are performed, in which an absolute conversion efficiency as high as ηmax ≈ 2.8 × 10−7 a peak power intensity of 1.2 GW cm−2 is found. Compared to an unpatterned silicon film of the same thickness amplification factors of up to ~900 are demonstrated. Our results pave the way to exploiting a strong Fano-type multi-mode coupling in metasurfaces for high THG in potential applications.
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Introduction
Nonlinear optics has been an active field of research over the past several decades providing us with the ground for many physical processes and phenomena such as high-harmonic generation, spontaneous parametric up/down conversion, stimulated Raman scattering, the non-linear Kerr effect, etc1. Such kind of processes form the essence of a wide range of applications which extends from ultrafast pulse characterization2,3,4 and frequency-resolved optical gating (FROG)5,6 to novel light sources7,8,9 and ultrafast nanoscale devices as optical sensors10. Recently, enhanced generation of nonlinear light on a subwavelength scale using metasurfaces has attracted booming attention due to their ultrathin compact profile and advanced functionalities relevant for modern integrated photonics11,12,13. In comparison to their bulk counterparts, nonlinear metasurfaces do not suffer from phase matching condition problems and can utilize the resonant nature of the nanoantennas they are formed of ref. 14. Initially, plasmonic metasurfaces, which support surface plasmon resonances15, have been extensively used for enhancing high-harmonic generation16,17. However, they typically possess only a relatively low nonlinear surface susceptibility, high absorption losses caused by ohmic dissipation in metals, and have low damage thresholds. As an alternative, dielectric metasurfaces have lately emerged offering many possibilities to significantly increase the light-matter interaction via tailoring optically induced Mie-type resonances hosted within nanoparticles made of high refractive index materials. The inherently rich variety of electric and magnetic multipolar resonances can be spectrally tailored by varying the size and shape of the nanoparticles, which can lead to their mutual overlap and even swap positions in the spectrum. This can give rise to the exotic phenomena, such as the excitation of Fano resonances18,19,20, nonradiative modes21,22, and resonances associated with bound states in the continuum (BIC)23,24,25,26, which possess ultra-high quality factors. High-quality modes supported by all-dielectric metasurfaces in combination with negligible ohmic losses compared to plasmonic devices, low heating, and high excitable mode volume have led to their emerging application for the efficient nonlinear light generation27,28,29.
In particular, the BIC concept is extensively exploited in the generation of enhanced third harmonic generation (THG) in metasurfaces composed of silicon nano resonators with the latest record peak power independent conversion efficiency of 3.9 × 10−4W−2 at a peak power intensity of 1 GW cm−2 reported by ref. 26. Also, in other metasurfaces consisting of materials with a very large nonlinear susceptibility component, such as germanium, gallium arsenide, aluminum gallium arsenide, or zinc oxide, a substantial enhancement of the harmonic generation processes (SHG and THG) has been demonstrated30,31,32,33. This development in the nonlinear metasurfaces opened up new ways to advance nonlinear wavefront design with a variety of exciting applications, such as nonlinear holographic imaging34,35,36,37, beam steering38,39, and generation of entangled photons by spontaneous parametric downconversion13,40,41.
In this paper, we report on theoretical and experimental demonstration of a completely new Fano-resonant all-dielectric metasurface possessing large THG. We utilize an amorphous silicon (a-Si) nanocylinder of an elliptical form as the building block of the nonlinear metasurface. By tailoring multipolar Mie resonances in these nano resonators via geometrical parameters, we achieve a THG enhancement up to ~900 compared to an unpatterned silicon film of the same thickness and a conversion efficiency of ηmax ≈ 2.8 × 10−7 at a peak power intensity of 1.2 GW cm−2. Our extremely enhanced THG is generated by the interaction of an ultra-narrow high-Q quadrupolar magnetic mode with the two broad electric dipole and electric quadrupole modes, which are spectrally brought so close together that they form what we call the ‘Super-Fano’ resonance. Our full-wave simulations are in good qualitative agreement with the experimental results obtained from linear and nonlinear transmission spectroscopy on the fabricated metasurface.
Results
Numerical analysis
Our metasurface consists of a periodic arrangement of a-Si elliptical cylinders on a glass substrate, see Fig. 1a. We used a Monte Carlo method to sample over a large ensemble of parameters and determined a range of height and lattice constant parameters leading to enhanced THG42. We selected a lattice constant of p = 916.7 nm, which we kept constant in all our calculations to exclude any undesired influence from lattice effects. For the resonator height, we chose h = 590 nm, which is expected to be thick enough to sustain dielectric mode resonances even at the fundamental frequencies. The two remaining parameters dx and dy vary in a range from 350 nm to 850 nm.
We start our analysis by studying the linear behavior of the metasurface. The result of numerical calculations of the linear transmittance is shown in Fig. 2b. This map unveils the rich structure with multiple Mie-modes, suggesting their mutual interaction when they get within close vicinity inside the parameter space. It should be noted here that the modes in the map appear as dark-blue colored valley regions, since an optical mode causes absorption of light, i.e., a low transmission value. We identified at least four resonances indicated by the contour isolines (colored curves) with corresponding labels. Figure 2d shows the electric-field amplitude maps |E(ω)| associated with these resonances in the different planes at y = 0. From the symmetry characteristics of these fields revealing 2- and 4-fold symmetries, we can assign the four main valleys in the map to the broad magnetic (MD) and electric (ED) dipolar modes as well as the magnetic (MQ) and electric (EQ) quadrupolar modes.
As a more detailed analysis of the resonances reveals (also see spectra in Supplementary Fig. S3), the narrow magnetic quadrupole mode interacts over a wide range of diameter parameters with the nearly parallel broad continuum electric dipole mode (green curve), forming a classical asymmetric Fano resonance feature indicated by the dashed curve and the MQ/Fano label in the transmittance map Fig. 2b. By adjusting the diameters of the resonator along this curve, the spectral width and thus the Q-factor and radiated THG of the Fano resonance can be easily optimized. Intriguingly, the sharpest Fano resonance feature and the strongest THG emission (approx. five orders of magnitude enhancement) is obtained at the point, we label as the Super-Fano resonance in Fig. 2b, where the MQ/Fano resonance comes in close contact with a third resonance, the electric quadrupole mode, indicated by the magenta curve. Unexpectedly, this point is slightly shifted from the supposed intersection of the three curves, ED, MQ/Fano and EQ, because the MQ mode acts in this case as a barrier for the broad ED and EQ resonances, resulting in a bending of the curves closely before the intersection (also see magnified transmittance map in Supplementary Fig. S4). The exact formation of this unique Fano resonance is schematically illustrated in Fig. 3. The plane wave excitation with the incident electric field (E) polarized as indicated by the blue arrow induces the parallel ED (p) and EQ (Qe) and perpendicular MQ moments (Qm) inside the resonators (Fig. 3a, b). The excited resonances interfere with the coupling strength κ, forming the typical asymmetric resonance profile in the resulting transmittance spectrum (Fig. 3c), which, in turn, produces a strong TH emission (Fig. 3d). The width and spectral position of the individual resonances and thus the Fano-resonance can be easily tuned by varying the elliptical diameters dx and dy. In the special case of highly fine-tuned resonances, the sharp asymmetric resonance feature in the transmission spectrum disappears and a Lorentz resonance profile is formed25,43.
We follow our analysis by investigating the nonlinear response of the metasurface in the considered range of parameters. The calculated intensity of the THG signal together with the superimposed contour isolines of the modes from the transmittance map revealed by the linear response are shown in Fig. 2c. Notably, despite the considered absorption losses in the resonator (also see the a-Si dispersion curve in Supplementary Fig. S2), the TH enhancement features found in this map follow strictly the MQ/Fano mode path, indicating their dominant impact on the generated high harmonic radiation. Furthermore, a quick glance at the electric field amplitude maps at the third harmonic, presented in Fig. 2e, shows that the enhanced TH emission is supported by the relatively outer location of the THG hotspots compared to the more inner located hotspots at the other resonances. The TH intensity spans twelve orders of magnitude with the highest magnitude being found near the intersection of the MQ/Fano with ED and EQ modes in the region, where the Super-Fano mode exists. The maximal THG is found for elliptical diameters of dx ~ 740 nm and dy ~ 550 nm. In a simplified picture, the ultra-narrow high-Q linear resonance is connected to locally enhanced fields, which lead to a THG enhancement due to the polynomial exponent of the nonlinear process.
Experimental analysis
To verify our theoretical findings of ultrahigh THG, we fabricated and analyzed 100 × 100 μm2 patches of a-Si cylinders on glass substrate using the methods described in the sections ‘Fabrication’ and ‘Experimental measurement methods’. As seen in the SEM image of the fabricated structure in Fig. 1b, the side walls of the Si nanoantennas are not perfectly vertical, but slightly slanted. This effect is often unavoidable and frequently seen in similar dielectric structures. Therefore, we numerically investigated the impact of slanted sidewalls on THG. For this, we assumed a sidewall angle of 1° and compared the results for both, the linear transmission as well as the nonlinear THG intensity. The results are shown in Fig. 4a–d. Note that in this figure, the results are plotted for a fixed y-diameter of dy = 550 nm for various dx over the fundamental/THG wavelength. From these data, it can immediately be seen that already a small sidewall angle leads to a significant blue-shift of the observed resonance. A more careful analysis of the individual spectra also reveals a broadening of the Fano resonance itself for the resonators with slanted sidewalls. Consequently, a similar effect is expected in the experimental results. Nevertheless, for both calculations, a strong enhancement of the THG signal is expected, as the THG intensity is predicted to be several orders of magnitude higher than for the non-resonant case.
Compared to the narrow resonance stripe in the theoretically calculated transmittance maps in Fig. 4a, c, the width of the resonance stripe in the experimentally measured transmittance map in Fig. 4e is much wider. This broadening is caused by losses not accounted for in the simulation model. Some of the contributions to these losses are, e.g., the two-photon absorption (TPA), manufacturing inaccuracies such as sidewall roughness and the numerical aperture, i.e., the large acceptance angle of the used Cassegrain objective in the FTIR setup. Moreover, the inserted black and white dashed line in the transmittance map is not exactly aligned with the resonance feature, like in the transmittance map in Fig. 4a, and is slightly tilted. Comparing the experimental results for the nonlinear THG intensity in Fig. 4f with the numerical simulations in Fig. 4b, d, a qualitative agreement is found. However, also here, a stronger dependence on the x-diameter dx is found than in the numerical simulations. Another interesting observation in the experimental result for the THG intensity is the fact that the THG amplification vanishes for larger values of dx and λ. But this is not the case in the numerical results, where the resonant THG enhancement is found to be strong in the entire range of dx values. A possible explanation for this might be the large excitation wavelength range used in the experiments, which causes the pulse profile and, therefore, the peak power intensities to change with varying wavelength even if the mean power is kept constant.
Finally, it should be pointed out again that the change of the resonator x-diameter theoretically leads only to a wavelength shift of the resonance and not to a change of the intensity over a large range. This behavior can also be expected from the maps in Fig. 2b, c, where a nearly horizontal resonance feature occurs without a large change in the y-diameter around the optimum labeled with Super-Fano in the parameter space map. In contrast, changing the y-diameter alone leads to a significant decrease in the generated THG, see the corresponding maps in Fig. 2 and Supplementary Fig. S5. Therefore, the x-diameter represents an excellent parameter for fine-tuning the enhancement of THG for a given wavelength. Moreover, the reduction in THG caused by the change in y-diameter can be compensated by an additional change in x-diameter. The corresponding maps are included in Supplementary Fig. S6.
In the final step of the investigation, we determine the maximum possible TH conversion efficiency of the proposed optimal metasurface. Therefore, the power of the pump beam Pin (ω) and the radiated TH signal Pout (3ω) are measured as described in the experimental measurement methods ‘Experimental measurement methods’ and shown in Fig. 5. The inset shows the achieved conversion efficiency dependent on the excitation power. A deviation in the cubic law can be observed for high peak intensities above approximately 150 mW in contrast to the as-grown thin film (see Supplementary Fig. S8) indicating that the undepleted pump approximation is not applicable anymore. This saturation can also be observed in the conversion efficiency, where its value maximizes with ηmax ≈ 2.8 × 10−7 at a peak power intensity of approx. 1.2 GW cm−2 (estimated from the excitation power assuming 80 fs long pulses at 80 MHz repetition rate). Related approaches to the enhancement of THG have been examined in refs. 44,18, where conversion efficiencies of 1 × 10−7 at 5.5 GW cm−2 and 1.2 × 10−6 at 3.2 GW cm−2 were achieved, respectively.
In comparison, we reach a similar conversion efficiency with a much lower peak power intensity. However, it should be noticed that due to the very high Q-factor, our developed Super-Fano THG process is an ultra-narrow nonlinear process, which can consequently transfer only a very small part of a general broad or ultra short input pulse into the third harmonic. Accordingly, a temporally longer pulse at the same power should significantly increase the achievable conversion efficiency. Apart from this, the designed structure is still very attractive for various applications where, for example, very little space is available, and is also capable of producing a strong light visible to the naked eye in less than a wavelength, as shown in the small photo in Fig. 5. Moreover, maximum amplification factors of up to ~900 are reached compared to an unpatterned a-Si thin film of same thickness. Polarization dependent measurements show the expected cos6 dependency of the THG intensity, as can be seen in Supplementary Fig. S7, proving the sole attribution of the Fano-resonant structure on the enhancement in THG.
Discussion
In summary, it is shown that a periodically arranged array of elliptical nanoresonators made of amorphous silicon exhibits strong light-matter interaction due to Fano resonances. Theoretical calculations reveal that these Fano resonances are the result of coupling between a high-quality magnetic quadrupole and a broad electric dipole. As predicted by theory, the strong light-matter interaction can be used to extremely enhance the generation of third harmonic light, especially if additionally interacting with the electric quadrupole mode as further constituent leading to the formation of ultra-narrow features, which we call ‘Super-Fano’. Amplification factors of up to ~900 compared to an unpatterned a-Si thin film of same thickness are achieved. A maximum conversion efficiency of ηmax ≈ 2.8 × 10−7 at a peak power intensity of approx. 1.2 GW cm−2 is measured.
Materials and methods
Fabrication
To achieve the desired enhancement of THG by Fano resonances in amorphous silicon metasurfaces the design depicted in Fig. 1a is proposed. Our fabrication process includes the following steps. First, 590nm amorphous silicon (a-Si) is deposited on a glass substrate using a plasma-enhanced chemical vapor deposition (PECVD) process with 400 sccm of SiH4/Ar mix (2%/98%) at 300 °C, 1 torr chamber pressure and 10 W rf power. Electron beam lithography (EBL) is used to define a mask for the subsequent pattern transfer. The adhesion promoter AR 300-80 is spin-coated with 400 rpm for 40 s onto the a-Si thin film and baked at 90 °C for 2 min. Then, the positive electron beam resist AR-P 679.03 (PMMA 950k) is spin-coated with 4000 rpm for 40 s and baked at 180 °C for 10 min. In order to mitigate charging effects during lithography caused by the insulating property of the glass substrate, a thin layer of the conductive protective coating Electra 92 AR-PC 5090 is spin-coated with 5500 rpm for 40 s and baked at 90 °C for 2 min. EBL is performed at 20 kV with an area dose of 220 μC cm−2. The sample is developed in subsequent baths of de-ionized water for 60 s and the developer AR 600-56 for 75 s to remove the Electra 92. Isopropyl alcohol is used to stop the development process. A lift-off procedure is then employed to fabricate a metallic hard mask. For this, electron beam evaporation is used to deposit a 20 nm thin chromium film onto the developed sample. For the lift-off process the sample is soaked in 80 °C warm acetone for 1 h before an ultrasonic cleaner is used to remove all resist and unwanted chromium from the sample. The ramaining structured chromium mask is needed for the pattern transfer into the a-Si thin film. This pattern transfer is accomplished by anisotropic inductively coupled plasma (ICP) reactive ion etching (RIE) in a gas mixture of 45 sccm C4F8 and 18 sccm SF6 with an ICP power of 900 W and rf power of 41W. Helium backside cooling is used with a helium flow of 7 sccm. The sample is etched for 2 min 5 s to expose the glass substrate in regions where no chromium hard mask is present. Finally, the strucutre is completed by wet chemical etching of the remaining chromium with a 1: 1 dilution of the chromium etchant TechniEtch Cr01 and de-ionized water for 15 min. With this technique 100 × 100 μm2 antenna fields consisting of elliptical a-Si nanoantennas arranged in a square lattice are fabricated, as sketched in Fig. 1a. The lattice parameter p = 916.7 nm is kept constant for every antenna field and the height of the antennas h = 590 nm is given by the thickness of the a-Si film. The diameters in x- and y-direction of the antennas are varied between different antenna fields. Figure 1b shows a scanning electron microscope (SEM) image of such an antenna.
Experimental measurement methods
Linear transmittance measurements are performed by FTIR-spectroscopy. Here, an adjustable rectangular aperture is used to limit the measured area to a single antenna field. As reference, the bare exposed SiO2 substrate is measured which later allows to deduce the effect of the Si nanoantenna field on the transmittance. Two customized optical setups are used for nonlinear measurements. One is shown schematically in Fig. S1 of the Supplementary Material. The used 200 fs-pulsed Ti-sapphire laser pumping an optical parametric oscillator (OPO) allows for wavelength-dependent analysis of the fabricated antenna fields. A half-wave plate and a following polarizing beam splitter (PBS) are used for controlling the laser power. For all measurements the average laser power is adjusted to P = 75 mW using an optical power meter (OPM), unless otherwise stated. A second half-wave plate is used to rotate the polarization of the laser light and thus change the excitation polarization. The laser beam is focused onto an antenna field from the backside of the sample by a lens with focal length f = 50 mm, resulting in a laser spot with a diameter of about 50 μm. The sample can be moved in two directions allowing for accurate positioning of the laser beam onto an antenna field in combination with the used camera. This guarantees that only the nonlinear signal from a single antenna field is collected by an objective with 20× magnification and a numerical aperture of NA = 0.5. A long-pass dichroic mirror is used to filter out the excitation wavelength, so only the third harmonic signal is collected by the spectrometer. An unpatterned a-Si thin film is used as reference to directly calculate the amplification of the THG signal resulting from the nanoantenna array without consideration of the nonlinear active volume.
The second nonlinear setup uses a similar measurement geometry and is employed for power dependent measurements of the investigated THG process (not shown here). It uses a fiber laser emitting monochromatic light with a wavelength of 1560 nm allowing for higher and more stable excitation powers. The power can be adjusted in software making the power control via half-wave plate and PBS obsolete. Any THG signal generated by optical components like the half-wave plate for polarization control in front of the sample is filtered by a long-pass filter. The excitation laser is filtered by a band-pass filter after the sample, to prevent distortion in the measured THG power by an OPM. With this, the THG conversion efficiency η = Pout (3ω)/Pin (ω) is readily obtained, where Pin (ω) is the power of the pump beam and Pout (3ω) the radiated TH signal power7.
Theoretical methods
For the theoretical calculations of the linear and nonlinear response from the metasurfaces, we use a commercial tool based on the finite element method (FEM)45. The general simulation model, a unit cell of the infinitely periodic surface, consists of a single elliptical cylinder made of amorphous silicon (a-Si) placed on a glass (silicon dioxide, SiO2) substrate block, as shown in Fig. 2a. The periodicity of the structure is modeled by introducing periodic boundary conditions on the sidewalls of the unit cell in the x- and y-directions, while open boundary conditions with perfectly matched layers (PML) are added above and below the resonator in z-direction. The unit cell model is excited from the air-side by a wave source port closely below the PML, which emits a vertically (z-direction) propagating plane wave linearly polarized in the x-direction at the fundamental frequency/wavelength. To account for the dispersive dielectric function of the amorphous silicon, we use experimental results obtained employing spectroscopic ellipsometry. The corresponding model parameter and dispersion curves are provided in Supplementary Table S1 and Fig. S2. For the dielectric function of the silicon dioxide, the experimentally measured values from the database by Malitson46 are used. Since silicon is a centrosymmetric material, there are no contributions to second-order nonlinear processes from the bulk crystal. Thus, third-order nonlinear processes, such as THG, are the lowest order nonlinear processes occurring in silicon. In simulations, the third-order nonlinearity is taken into account via the nonlinear polarization term \({{{\mathbf{P}}}}_{{{{\mathbf{NL}}}}}^{\left( 3 \right)}(3\omega ) = \varepsilon _0\chi ^{\left( 3 \right)}({{{\mathbf{E}}}}\left( \omega \right) \cdot {{{\mathbf{E}}}}(\omega )){{{\mathbf{E}}}}(\omega )\) with the constant value of 2.45 × 10−19m2V−2 for the nonlinear susceptibility χ(3) (ref. 47.). The back coupling of the generated third harmonic on the fundamental signal is assumed to be so small that it can be neglected. Due to this, the simulations are performed in two calculation steps, starting with the plane wave excitation at the fundamental frequency followed by an external current excitation generated by the nonlinear polarization with \({{{\mathbf{J}}}}_{{{{\mathrm{ext}}}}} = j3\omega {{{\mathbf{P}}}}_{{{{\mathbf{NL}}}}}^{\left( 3 \right)}(3\omega )\) at the third harmonic within the silicon resonator. The corresponding far-field quantities at the fundamental frequency and third harmonic are extracted with a near-field to far-field transformation (NFFFT) for periodic structures48, which resembles the integral for the two-dimensional complex Fourier series. However, only the emitted zeroth diffraction order (kx = ky = 0) in transmission or reflection direction is considered in this work.
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Acknowledgements
The authors gratefully acknowledge financial support from the Deutsche Forschungsgemeinschaft (DFG) via TRR142/3 project C05, project number 231447078, and computing time support provided by the Paderborner Center for Parallel Computing (PC2).
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C.M., J.F., and T.Z. initiated the project. D.H. performed all simulations, analyzed the numerical data, and discovered the THG enhancement. C.G. and M.A. fabricated the samples, carried out the measurements, and analyzed the experimental data. C.M., J.F., V.M., and T.Z. supervised the project. All authors discussed the results and contributed to the final manuscript.
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Hähnel, D., Golla, C., Albert, M. et al. A multi-mode super-fano mechanism for enhanced third harmonic generation in silicon metasurfaces. Light Sci Appl 12, 97 (2023). https://doi.org/10.1038/s41377-023-01134-1
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DOI: https://doi.org/10.1038/s41377-023-01134-1
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