Second harmonic generation (SHG) is forbidden for materials with inversion symmetry, such as bulk metals. Symmetry can be broken by morphological or dielectric discontinuities, yet SHG from a smooth continuous metallic surface is negligible. Using non-linear microscopy, we experimentally demonstrate enhanced SHG within an area of smooth silver film surrounded by nanocavities. Nanocavity-assisted SHG is locally enhanced by more than one order of magnitude compared to a neighboring silver surface area. Linear optical measurements and cathodoluminescence (CL) imaging substantiate these observations. We suggest that plasmonic modes launched from the edges of the nanocavities propagate onto the smooth silver film and annihilate, locally generating SHG. In addition, we show that these hotspots can be dynamically controlled in intensity and location by altering the polarization of the incoming field. Our results show that switchable nonlinear hotspots can be generated on smooth metallic films, with important applications in photocatalysis, single-molecule spectroscopy and non-linear surface imaging.
Second harmonic generation (SHG) is a process in which two photons at the fundamental frequency combine to generate a photon with a double frequency through nonlinear scattering1. SHG is forbidden in materials with inversion symmetry such as bulk metals, yet symmetry can be broken by material discontinuity2,3 or by electromagnetic (EM) field properties4,5. Significant SHG responses were observed from metallic surfaces and were attributed to nonlinear polarizability of free and bound electrons at the metal interface6.
Plasmonic structures, whether particles or cavities, increase the nonlinear response dramatically due to their enhancement of the EM fields at the interface7,8,9,10,11,12,13,14,15. Nonlinear responses of both nanoparticles and nanocavities with various sizes and shapes, including metasurfaces, were studied both in the visible and near-infrared regimes8,9,14,16,17,18,19,20,21,22. Additionally, metallic nanoparticles have been shown to increase the SHG responses of dielectric particles23,24. Typically, SHG emanating from nanostructures is enhanced when the plasmonic structure resonates with the electric field, E, either at the fundamental (ω) or harmonic frequency (2ω) or both25,26,27,28,29, since the SHG intensity is proportional to (|E(ω)|2|E(2ω)|)2 30,31,32. While most studies have focused on metallic structures with no inversion symmetry, SHG is also observed from symmetric plasmonic structures21,33. The reason for such an enhanced nonlinear conversion process has remained elusive.
Nanocavities milled in a metallic film have emerged as a promising class of optical materials19,20,34,35,36. The localized modes of the nanocavities may lead to the excitation of surface plasmon polaritons (SPPs), and long-range coupling between cavities can occur13,17,19,20,37,38. In this respect, nanocavities differ from their so-called “complementary” nanoparticle structures and they exhibit dissimilar optical behavior. Elementary SPPs excited from nanocavities can combine and emit a more energetic photon39. In this case, SPPs do not boost local fields but are rather annihilated to form a photon at double the frequency. This implies that in practice, a sub-wavelength aperture is not necessarily needed to generate enhanced SHG. This was experimentally shown by Woggon and co-workers when measuring SHG emission from silver films using a Kretschmann configuration40 and theoretically supported by Finazzi and Ciccacci39.
Here, we experimentally demonstrate enhanced SHG emission from a smooth silver film area surrounded by several nanocavities. We used triangular nanocavities milled into a silver thin film in a configuration with a base-to-base distance of 400 nm. We show that SHG emission results solely from the strong interaction between the SPP modes propagating from each cavity edge. Those SPPs, at the fundamental frequency, propagate and annihilate to form a spatially confined SHG “hotspot” on the flat surface (Fig. 1). In this geometry, SHG stemming from the inter-cavity smooth surface is dramatically enhanced, and that from the triangular plasmonic cavities is suppressed. These observations and their interpretation are further supported by spatially resolved linear transmission measurements, as well as by CL micro-spectrometry.
Materials and methods
Our sample is composed of two pairs of triangular cavities. The triangular nanocavities have a typical side length of 200 nm, and they are fabricated using a focused ion beam (FIB, Dual Beam, Helios Nano Lab 600i from FEI), in a 200-nm-thick smooth silver film deposited on a clean fused silica substrate (Fig. 1 and Fig. S1). The silver surface is covered by a 150-nm-thick polyvinyl alcohol (PVA) layer in order to match the refractive indices on both sides of the sample (average refractive index in the visible to near-infrared region on the order of 1.5) and to prevent sample oxidation and aging.
Similar triangular cavities have been thoroughly studied and were found to enhance nonlinear responses such as SHG. Their geometry with respect to the fundamental incident field plays an essential role in governing the optical response12,13,41. A triangular cavity supports several plasmonic modes, among them a broadband side-length mode, which can launch SPP modes onto the surface19,20,42,43. Based on these earlier findings, we designed a plasmonic structure in which the “bases” of two adjacent triangular cavities are face-to-face, a configuration that leads to a confinement of the EM field onto the flat surface between the cavities and the frequency of which can be adjusted by the distance between the cavities16. The SHG response from such structures was investigated using custom-fabricated two-photon microscopes (Fig. 1c and Fig. S2). The samples were excited in reflection mode at normal incidence by a tunable (700–1000 nm) Ti:Sapphire laser (Spectra-Physics Mai-Tai HP, 100 fs, 80 MHz), using a ×50 numerical aperture (NA) 0.5 air objective lens (Olympus), giving an illumination spot size of approximately 2 microns. SHG was collected through the same objective lens. The SHG images were scanned at 940 nm using a piezo stage (Piezosystem, Jena). The piezo stage spatial resolution is of a few nanometers, and our system spatial resolution is approximately 250 nm, a sub-diffraction limit resolution. The polarization-dependent measurements were performed by varying the polarization angle of the fundamental field using a rotating half-wavelength plate. Prior to the measurements, the system was carefully aligned, and the response from the silver surface was found to be negligible. In addition, each time, we ran rotational SHG measurements (polar plots) from several regions on the silver surface to verify that the fundamental field was at normal incidence and that the system was well aligned. Our results have been repeated more than ten times on different structures and samples.
Results and discussion
When the two triangular cavities are arranged in a base-to-tip configuration, an intense SHG signal emanates from them (Fig. 2a). The SHG response is half an order of magnitude stronger for the in-axis (interaction axis) polarization compared to the off-axis (orthogonal) polarization of the incoming field, in agreement with previous work13. Both cavities emit SHG in phase and are considered to be strongly coupled. They are referred to here as a sub-unit. Now, when two of these sub-units are arranged base-to-base, the overall optical response is dramatically changed as shown in (Fig. 2b, c). When the polarization of the incoming field is along the symmetry axis, the SHG is enhanced and is emitted solely from the area in between the two sub-units. In turn, the SHG response of the outer cavity pairs drops dramatically compared to the earlier case and is comparable to that of a free silver surface (see also Fig. S3). As before, when the polarization state of the incoming field is orthogonal to the symmetry axis, the SHG response of the plasmonic unit is weak and spreads uniformly across the entire unit. Clearly, the two sub-units together with the silver surface behave as a single entity, and the area from which SHG is detected is smaller than that the sum of the two sub-units (Fig. 2). The SHG emission and its dependency on the fundamental wavelength are shown in the supporting information (Fig. S3b). We note as well that the surface between the cavities is ultra-smooth and there is no sub-wavelength aperture to scatter the plasmonic modes to the free-propagating light (see S1). In fact, when the surface is rough, we do not observe this phenomenon. The SHG nature of the structure under study is confirmed by spectral analysis (Fig. S4). Finally, we measured the two sub-units in a bowtie configuration, ceteris paribus. As expected, the two sub-units behave as individual units with no coupling between them (Fig. S5), and no SHG is detected from the flat surface between them.
How large is the SHG enhancement observed between the base-to-base configurations compared to a smooth bare-silver surface? The effective nonlinear coefficient for such an arrangement is 8.9 × 10−15 W−1 (for detailed calculations, see S6 and table S1), seven-fold greater than the hyper-Rayleigh scattering (HRS) from a neighboring bare-silver film. Thus, for a laser power of 4 mW and a NA 0.5 objective, we obtain 3.5 × 104 photons at 2ω (for detailed calculations see S6 and table S1). We note that this high gain is achieved on a flat surface without a demanding fabrication. It is now clear that the nano-patterned silver surface plays an important role in achieving such a dynamic SH hotspot. To better understand the nature of the interaction between the sub-units and the surface, we run a full polarization analysis of the SHG emission generated by the structures composing the plasmonic unit. The two orthogonal polarization components of the SHG output emission are individually measured as a function of the polarization angle of the fundamental field. In this way, we directly obtain information about the second-order susceptibility tensor χ(2)ijk. Figure 3 shows the polar plots corresponding to each sub-unit composing the full studied structure. As expected, in the case of the bare-silver film, we observed two perpendicular dipolar patterns (Fig. 3a). They are due to HRS, the incoherent summation of contributions from randomly oriented dipoles, associated with symmetry-breaking silver grains and grain boundaries12,30. Next, for the pair of two equally aligned oriented triangular cavities, the off-axis shows an octupolar polarization behavior, the signature of a three-fold symmetric object11,12,43,44,45, while the in-axis reveals moderate coupling between the two triangular cavities. A highly polarized SHG emission is observed for the full structure composed of two oppositely oriented sub-units (Fig. 3c). Particularly, only the y-axis output is appreciable, whereas the x-axis is close to the noise level. The y-axis component displays a residual octupolar symmetry, indicating that the tensor element of the triangular cavity building blocks does not completely vanish. The polar plots shown in Fig. 3 are all normalized with respect to the SHG response of a flat silver film (see S7). It can be seen that the emission stemming from the flat area of the plasmonic structure is about one order of magnitude higher than that of a bare-silver surface, in agreement with the data shown in Fig. 2.
To further characterize the behavior of this plasmonic structure, we studied the linear spectral transmission of the system, using a polarized broadband light source (see supporting information S2.2 for the setup information). The results are shown in Fig. 4. For both polarizations, an 885 nm peak that is delocalized over the entire structure appears, while a weaker and broader peak at ~450–480 nm is observed only around each sub-unit. However, for the polarization parallel to the interaction axis (Fig. 4a), an additional, high-intensity peak, centered at ~500 nm, is observed. This peak is localized between the two sub-units, on the bare-silver region. This mode arises from the coupling between the triangular side length mode and the bare-silver surface, as shown recently19. The appearance of this mode gives rise to a high density of photonic states in this spectral range in accordance with the observed enhanced SHG emission. When the polarization of the incoming field is oriented perpendicularly to the interaction axis, this peak vanishes completely, and transmission occurs only from the cavities themselves rather than from the bare-silver area between the two sub-units (Fig. 4b). The linear transmission spectra taken at the level of the hotspot area for two orthogonal polarizations are shown in Fig. 4c. A double resonance behavior is observed for in-axis polarization, unlike the off-axis case, in agreement with the observed SHG results.
To further support this claim and to map these modes with increased spatial resolution, we also performed cathodoluminescence (CL) measurements on a similar plasmonic structure with identical geometrical parameters. In CL, the plasmonic modes are locally excited by an electron beam, and spatial mapping of the emitted photons at a given wavelengths directly maps the plasmonic modes of the system46,47,48 (see S 2.3 for experimental details). Hence, the radiative plasmonic response of the metallic system can be probed, and high-resolution spectral imaging can be achieved49,50,51. In contrast, the excite mechanism in CL is different from that of SHG in that both probe the plasmonic response and the optical properties of the plasmonic modes. Figure 5a shows a pseudo-colored CL image of the plasmonic structure from which the PVA layer has been removed (metal–air interface). The colors correspond to the fundamental (red) and SHG (blue) modes. The cavities show a strong response at the fundamental frequency, while a robust response at 2ω is observed in their close vicinity and in the middle of the structure19,20. The wavelength of interest in the CL measurements is 370 nm, correlated with the 470 nm in the SHG measurements due to differences in the refractive indices, i.e., PVA vs. air. Figure 5b shows the CL cross section along the structure at 370 nm alongside the SEM cross section. Beside the detected cavity modes, a confined and spectrally narrow mode is observed in the central flat area at ~370 nm (see also Fig.S6) in agreement with the transmission measurements shown above. The SHG emission from this plasmonic structure is shown in Fig. 5c. Clearly, the SHG is emanating from the smooth surface between the plasmonic cavities in accordance with the above observation. We note that such a structure is highly symmetric and that the silver surface between the cavities is smooth, with no sub-wavelength apertures. Otherwise, no CL or SHG are observed from the center (see supporting information Fig. S7).
In this study, we demonstrate an enhanced SHG response from a centrosymmetric nanostructured silver film. We observed a very strong SHG signal from the smooth surface area between the triangular cavities, where the amplitude of the SHG signal is highly dependent on the polarization state of the driving fundamental field relative to the orientation of the triangular cavities. Based on several observations, we suggest that this strong SHG response arises from SPP modes launched from adjacent sub-units and subsequent plasmon–plasmon annihilation on the flat surface area: (i) in a base-to-base configuration and for in-axis polarization of the incoming field, the SHG emission emanates from the flat surface between the cavities, whereas the signal from the subunits is dramatically reduced. Individually, those sub-units enhance SHG (Fig. 2). This observation would not be expected for a classical SHG process; (ii) a result conforming to this classical expectation is observed for the same number of subunits, but in a bow-tie configuration (Fig. S5) or when the surface is rough (Fig. S7). This indicates that the phenomenon is due to the propagation of surface plasmons rather than localized plasmonic modes of the cavities; (iii) throughout this study, we detect SHG in the far field using an objective with an NA of 0.5. Thus, we would not expect to observe SHG between the cavities unless sub-wavelength apertures were present to couple the nearfield SHG to the far-field. Even so, we observed a localized enhanced SHG signal in the absence of such sub-wavelength apertures because plasmon–plasmon annihilation creates photons propagating within our detection NA; and (iv) we note that although the main studied structure is elongated, the SHG emission is rather symmetrical, spatially spreading equally along the x- and the y-axes.
In previously studied systems8,12,13,36,41,52,53,54, nanocavities were used to boost the EM fields resulting in an enhanced nonlinear response. In stark contrast, the symmetric plasmonic systems introduced herein, with inversion symmetry, enhance SHG emission through what we believe to be a plasmon–plasmon annihilation processes.
One might consider the assembly of the cavities in the framework of the extended hybridization model. That is, the cavities are in analogous to the atoms and the SHG emanating we observed from the middle could be the probability function. However, the mode is too localized to support this explanation.
From an application point of view, our findings may further be used to produce SHG hotspots at any given location on a given metallic surface. The ability to form such a strongly confined SHG spot in the optical regime may provide a useful tool to study physical-chemical transformations occurring on surfaces, such as photocatalysis processes. Moreover, it may be useful for molecular, label-free biological sensing and imaging near surfaces55.
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This work was supported partially by the GIF grant no. 203785 and partially by the Israel Science foundation grant no. 2797/11. The authors thank Dr. Emir Haleva for fruitful discussions.
Conflict of interest
The authors declare that they have no conflict of interest.
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Galanty, M., Shavit, O., Weissman, A. et al. Second harmonic generation hotspot on a centrosymmetric smooth silver surface. Light Sci Appl 7, 49 (2018). https://doi.org/10.1038/s41377-018-0053-6