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Zinc oxide-zinc tungstate (ZnO-ZnWO

Chiral properties of plasmonic metasurfaces, especially related to different absorption of left and right circularly polarized light leading to circular dichroism (CD), are a research hot topic in nanophotonics. There is often a need to understand the physical origin of CD for different chiral metasurfaces, and to get guidelines for the design of structures with optimized and robust CD. In this work, we numerically study CD at normal incidence in square arrays of elliptic nanoholes etched in thin metallic layers (Ag, Au, Al) on a glass substrate and tilted with respect to the symmetry axes. Strong CD arises in absorption spectra at the same wavelength region of extraordinary optical transmission, indicating highly resonant coupling between light and surface plasmon polaritons at the metal/glass and metal/air interfaces. We elucidate the physical origin of absorption CD by a careful comparison of optical spectra for different polarizations (linear and circular), with the aid of static and dynamic simulations of local enhancement of the electric field. Furthermore, we optimize the CD as a function of the ellipse parameters (diameters and tilt), the thickness of the metallic layer, and the lattice constant. We find that silver and gold metasurfaces are most useful for CD resonances above 600 nm, while aluminum metasurfaces are convenient for achieving strong CD resonances in the short-wavelength range of the visible regime and in the near UV. The results give a full picture of chiral optical effects at normal incidence in this simple nanohole array, and suggest interesting applications for chiral biomolecules sensing in such plasmonic geometries.

We investigate the chiro-optical properties of the electromagnetic near-field associated with the excitation of collective optical resonances (surface lattice resonances) in achiral plasmonic lattices. These arrays are specially designed to support dispersive resonances with nontrivial, multipolar near-field distributions in the surroundings of the nanostructure, which gives rise to an enhanced chiro-optical response. The presence of these multipolar resonances in lattices without explicitly broken mirror symmetry is experimentally confirmed by far-field extinction measurements, while the angular, spectral, and spatial dependence of the associated chiral near-field are numerically simulated. In contrast with typical pseudochiral systems, the extended chiro-optical near-field response appears even at normal incidence. We believe that surface lattice resonances in achiral plasmonic lattices can be potentially utilized as a substrate for enhanced background-free enantioselectivity and tunable chiral molecule recognition over large areas.

In this work, we review the last attempts to use nanostructured materials for the enhancement of the chiro-optical effects at the nanoscale. Starting from the numerical design, we review different geometries that exhibit circular dichroic behavior in the far field; we then focus on the new branch of near-field chirality, where numerous nanostructures have been proposed for background-free chiral sensing. The next section reports on nanofabrication methods, with a special focus on self-assembling, cost- and time-efficient techniques. Finally, we review the chiro-optical experiments. Besides conventional extinction-based techniques, we are today able to reveal chiro-optical effects via photothermal behavior and photoluminescence, going down to single nanostructure chirality with sophisticated near-field techniques. We believe that the novel designs, state-of-the-art nanofabrication and modern characterization techniques have come to a stage to provide chiro-optical sensors and light components based on nanostructures.

The mimicking of chiral effects at the nanoscale usually requires complex nanostructured systems fabricated by using highly sophisticated techniques. Here, we demonstrate that low-cost diffractive metasurfaces, fabricated by nanosphere lithography, can offer a remarkably rich chiral broadband response in the near-infrared range. We measure the spin-dependent response as a function of the incident angle and wavelength. The resulting extinction maps reveal switching of the resonances governed by extrinsic chirality. We further employ numerical modeling to gain an insight into the electromagnetic behavior over the unit cell. The simulation results agree with experiments, and we further investigate the possibility of tailoring chirality by matching the refractive index below and above the metasurface. Finally, we investigate chiral emission of the ensemble of electric dipoles embedded in the refractive-index-matching layer. This approach opens alternative perspectives for chiral surface-lattice resonances and chiral emission in low-cost materials.

Plasmonic nanostructures with broken symmetry have been proposed for the control of the circular polarization at the nanoscale, important for applications spanning from chiral sensing to circularly polarized nanosources. We recently demonstrated that the low-cost self-assembling nanosphere lithography, combined with tilted metal deposition, opens new possibilities for the design and fabrication of chiral nanostructures. Starting from polystyrene nanospheres (PNS) covered by asymmetric metallic shell, we measured chirality in absorption at 633 nm [1] . We discovered that the nanohole array (NHA) formed due to the shadow, can exhibit chiral properties in a broad near-infrared range [2] , [3] .

Characterization of both natural and artificial chiral structures involves measurements of differential absorption of circularly polarized light of opposite handedness, i.e. circular dichroism (CD). Here we use a scattering-free, non-destructive photo-deflection technique [1] to detect optical chirality in diffracted orders of a metasurface.

Optical enantioselectivity of chiral molecules could be enhanced by depositing them on suitable nanostructured substrates. Different kind of chiral substrates can be developed, but chiral features are in general difficult to fabricate or costly. Self-assembled approach allows realizing plasmonic metasurfaces with a low cost reliable procedure. In this case asymmetric fabrication parameters can induce chiral optical response of the realised substrate. Self-organized polystyrene spheres deposited on glass substrate, are utilised to produce asymmetric hole array on a metal thin film. In our case the spheres (518 nm in diameter) where reduced by selective reactive ion etching and then covered by gold (and other metals), that is evaporated at a glancing angle. After the removing of the spheres an elliptical-hole array is produced forming a circular-dichroic substrate. The circular dichroic response of light interacting with the substrate can be tuned by choosing proper incidence angle and excitation wavelength, while the flat nature of the metasurface is very useful for easy molecular deposition processes. Two new enantiomers (right-handed and left-handed molecules) have been synthesized in order to present a good circular dichroism in the visible range and to be tested on the realized metasurfaces. Different tests were carried out on the samples, investigating the spectral optical properties of the structures with and without chiral molecules on top of them. The results are very promising due to the possibility of easily tuning and optimizing the optical response.

In this work, we study chiral effects in well-known 2D plasmonic nanohole arrays with a triangular unit cell. The chirality can be induced by moving from circular to elliptical nanohole shape and tilting the ellipse away from the array symmetry. This symmetry breaking induces a different absorption of the circularly polarized light of opposite handedness, i.e. circular dichroism. We numerically study circular dichroism at normal incidence in elliptic nanoholes in Au in the spectral range 400-1000 nm. CD arises in transmission and absorption spectra in the same wavelength region of extraordinary optical transmission, indicating highly resonant light-metasurface coupling mechanisms. We focus on its dependence on the elliptic nanohole tilt and further proceed with the ellipse radii optimization. The optimized CD is on the order of 80%, and it is robust with respect to the radii and rotation angle variations. Moreover, such samples could be produced by means of low-cost nanosphere lithography, which makes them interesting for applications in enhanced sensing of chiral biomolecules.

Nanophotonic component can be tuned by means of a thin phase change material (PCM) film put in its vicinity; PCM changes phases upon heat stimuli and thus provides a phase or amplitude optical contrast at the nanoscale. Vanadium dioxide (VO2) is a promising material which undergoes semiconductor-to-metal phase transition at about 68 °C. In this work we combine its transition with a metamaterial made of golden nanodiscs, in the infrared spectral range. Metamaterial dimensions can be adjusted to provide the almost unitary absorption in the desired spectral range, which can be switched to zero absorption by changing the VO2 phase. We further propose the optical switching of a large number of unitary cells by means of a near-infrared or visible laser. For given wavelength and power of the laser, we show how the spot-size can be adjusted to ensure that the whole VO2 reaches the transition temperature. We further investigate the substrate influence. We believe that this approach can be generally used to design the metamaterial for a specific application, and find optimum experimental requirements for its switching.

In this work we present an approach to induce chiral effects in well-known plasmonic nanohole arrays with triangular unit cell. Arrays with circular nanoholes in metals can exhibit interesting light-matter interaction mechanisms such as surface plasmon polaritons and extraordinary optical transmission. Moving from circular to elliptical shape and tilting the ellipse away from the lattice symmetry lines, a symmetry breaking induces a different absorption of the circularly polarized light of opposite handedness, i.e. circular dichroism. We numerically investigate circular dichroism at normal incidence in elliptic nanoholes in Au in the spectral range 400–1000 nm. We focus on its dependence on the elliptic nanohole tilt, and further proceed with the ellipse radii optimization. The optimized circular dichroism reaches 84%, and we report on the near field absorption distribution at the wavelengths of this maximum value.

A detailed structural investigation of the semiconductor-to-metal transition (SMT) in vanadium dioxide thin films deposited on sapphire substrates by pulsed laser deposition was performed by in situ temperature-dependent X-ray diffraction (XRD) measurements. The structural results are correlated with those of infrared radiometry measurements in the SWIR (2.5-5 μm) and LWIR (8-10.6 μm) spectral ranges. The main results indicate a good agreement between XRD and optical analysis, therefore demonstrating that the structural transition from monoclinic to tetragonal phases is the dominating mechanism for controlling the global properties of the SMT transition. The picture that emerges is a SMT transition in which the two phases (monoclinic and tetragonal) coexist during the transition. Finally, the thermal hysteresis, measured for thin films with different thickness, showed a clear dependence of the transition temperature and the width of the hysteresis loop on the film thickness and on the size of the crystallites.

2D metasurfaces based on periodic nanoholes in metal have been proposed in various plasmonic platforms. Specifically, their resonant features have led to applications spanning in biosensing. Here we investigate additional degree of freedom in elliptical nanohole arrays with hexagonal geometry: chiro-optical effects. Namely, the in-plane asymmetry and a slightly elliptical shape of nanoholes were previously shown to differently extinct light of opposite handedness, even at normal incidence. We now fully characterize nanoholes in Ag, fabricated by low-cost nanosphere lithography. We first measure the dependence of the transmitted intensity for opposite handedness, in a broad spectral and angle of incidence range. We then resolve the circular polarization degree of the transmitted light when the nanohole array is excited with linear polarization. Finally, we numerically investigate the origin of the chiro-optical effect at the nanoscale. We believe that circular polarization resolving of the transmitted degree could be further adapted as a highly sensitive tool in chiral sensing.

Addition of asymmetry in plasmonic nanostructures can lead to chiro-optical phenomena, usually monitored as different absorption of left and right polarization, i.e. circular dichroism. Moreover, interesting features arise when the nanostructure changes the polarization state of the input beam. In this work, we perform extrinsic chirality characterization in a widely tuneable near-infrared range, by monitoring both polarization of the input and of the transmitted beam. We characterize low-cost metasurfaces based on polystyrene nanospheres asymmetrically covered by Ag, by exciting them at different angle of incidence with left, right and linear polarization. We then resolve the circular polarization degree of the transmitted beam, demonstrating resonance-governed circular polarization degree in the output, showing the interplay of both intrinsic and extrinsic chirality.

A detailed structural investigation of the semiconductor-to-metal transition (SMT) in vanadium dioxide thin films deposited on sapphire substrates by pulsed laser deposition was performed by in situ temperature-dependent X-ray diffraction (XRD) measurements. The structural results are correlated with those of infrared radiometry measurements in the SWIR (2.5-5 μm) and LWIR (8-10.6 μm) spectral ranges. The main results indicate a good agreement between XRD and optical analysis, therefore demonstrating that the structural transition from monoclinic to tetragonal phases is the dominating mechanism for controlling the global properties of the SMT transition. The picture that emerges is a SMT transition in which the two phases (monoclinic and tetragonal) coexist during the transition. Finally, the thermal hysteresis, measured for thin films with different thickness, showed a clear dependence of the transition temperature and the width of the hysteresis loop on the film thickness and on the size of the crystallites.

Chiral optical response is an inherent property of molecules and nanostructures, which cannot be superimposed on their mirror images. In specific cases, optical chirality can be observed also for symmetric structures. This so-called extrinsic chirality requires that the mirror symmetry is broken by the geometry of the structure together with the incident or emission angle of light. From the fabrication point of view, the benefit of extrinsic chirality is that there is no need to induce structural chirality at nanoscale. This paper reports demonstration extrinsic chirality of photoluminescence emission from asymmetrically Au-coated GaAs-AlGaAs-GaAs core-shell nanowires fabricated on silicon by a completely lithography-free self-assembled method. In particular, the extrinsic chirality of PL emission is shown to originate from a strong symmetry breaking of fundamental HE

Active, ultra-fast external control of the emission properties at the nanoscale is of great interest for chip-scale, tunable and efficient nanophotonics. Here we investigated the emission control of dipolar emitters coupled to a nanostructure made of an Au nanoantenna, and a thin vanadium dioxide (VO

The light interacting on asymmetric nanostructures can give rise to the phenomenon called extrinsic chirality [1–3], even if the nanostructures are not chiral by themselves. In this cases, light can be manipulated in order to obtain interesting behaviour such as anomalous refraction [4] or circular dichroism [5].

Photoacoustic Spectroscopy (PAS) and Photothermal deflection Spectroscopy (PDS) are excellent techniques for studying the optical absorption spectra of opaque and highly light-scattering substances such as nanomaterials. In this paper we review recent advances in the methodology of PAS and its novel applications. In particular we discuss the performance of PAS to detect circular dichroism of intrinsic chiral materials [1] as well as extrinsic pseudo-chiral metasurfaces [2], showing how the selective absorption of circularly polarized light depend on the orientation of the metasurface. We also applied PAS in the VIS/IR range to measure the resonant absorption peaks related to the guided modes of GaAs-based NW on Si [3–5].

In this work, we combine the enhancement of the emitter efficiency due to the proximity of a resonant nanostructure, and the possibility to modulate it by means of a thin layer of a phase change material (PCM). PCMs have been used as active subwavelength elements that can switch between the phases that differ in electric and optical properties. The phase change results in a modulation of amplitude or phase of transmission or reflection over nanoscale propagation lengths, and it is compatible with fast optical systems [1,2]. Vanadium Dioxide (VO 2 ) is a promising candidate for nanoscale modulation since it shows dramatic contrast in its complex refractive index as it undergoes a structural phase transition from monoclinic (semiconductor) to rutile (metallic) phase at 68°C [3], induced thermally, electrically or optically.

Asymmetric nanostructures can mimic a chiral response when circular polarized light interacts with the structures under particular angle of incidence [1]. This phenomenon is called ‘extrinsic chirality’ and usually is present under linear optical investigation with low visibility. Due to the fact that optical second harmonic generation is possible only in samples with some degree of asymmetry, this can be used in order to investigate the extrinsic chirality with a background free technique, thus inducing a high visibility of the artificial circular dichroism [2,3]. Here we present the second harmonic generation (SHG) measurements obtained on samples composed by GaAs nanowires grown on silicon. The wires present resonant leaky modes around 800nm and at 400nm due to the high refractive index contrast ratio between wires and air, even if these wavelengths lie on the absorption band of GaAs [4]. The measurements performed on this sample present good SHG signal due to the second order nonlinear term of GaAs, but did not present any circular dichroism (SHG-CD). By coating the sample with a 20nm thin layer of gold deposited asymmetrically, by evaporating the metal only from one side of the nanowires, the symmetry of the structure is broken, thus induced high SHG-CD. The SHG-CD is measured by shining the sample with circular polarized pump light at the fundamental wavelength of 800nm and by revealing the second harmonic signal at 400nm in s or p polarization, as a function of sample rotation. Four samples were measured with GaAs wires of about 5 micron in length with different diameters ranging from 140nm to 200nm. In this case it is possible to explore different resonance conditions and different SHG-CD is revealed. For each sample, the measured were carried out before and after the asymmetric gold layer deposition, thus allowing direct comparison of the results. References [1] A. Belardini, M. C. Larciprete, M. Centini, E. Fazio, C. Sibilia, D. Chiappe, C. Martella, A. Toma, M. Giordano, and F. Buatier de Mongeot, Phys. Rev. Lett. 107, 257401 (2011). [2] A. Belardini, M. Centini, G. Leahu, D. C. Hooper, R. Li Voti, E. Fazio, J. W. Haus, A. Sarangan, V. K. Valev, C. Sibilia, Sci. Rep. 2016, 6, 31796. [3] G. Leahu, E. Petronijevic, A. Belardini et al., Adv. Optical Mater. 2017, 1601063 (2017). [4] G. Leahu, E. Petronijevic, A. Belardini, M. Centini, R. Li Voti, T. Hakkarainen, E. Koivusalo, M. Guina, C. Sibilia. Sci. Rep. 7, 2833 (2017).

Active, ultra-fast external control of the emission properties at the nanoscale is of great interest for chip-scale, tunable and efficient nanophotonics. Here we investigated the emission control of dipolar emitters coupled to a nanostructure made of an Au nanoantenna, and a thin vanadium dioxide (VO2) layer that changes from semiconductor to metallic state. If the emitters are sandwiched between the nanoantenna and the VO2 layer, the enhancement and/or suppression of the nanostructure's magnetic dipole resonance enabled by the phase change behavior of the VO2 layer can provide a high contrast ratio of the emission efficiency. We show that a single nanoantenna can provide high magnetic field in the emission layer when VO2 is metallic, leading to high emission of the magnetic dipoles; this emission is then lowered when VO2 switches back to semiconductor. We finally optimized the contrast ratio by considering different orientation, distribution and nature of the dipoles, as well as the influence of a periodic Au nanoantenna pattern. As an example of a possible application, the design is optimized for the active control of an Er3+ doped SiO2 emission layer. The combination of the emission efficiency increase due to the plasmonic nanoantenna resonances and the ultra-fast contrast control due to the phase-changing medium can have important applications in tunable efficient light sources and their nanoscale integration.

Today, nanophotonics still lacks components for modulation that can be easily implementable in existing siliconon-insulator (SOI) technology. Chalcogenide phase change materials (PCMs) are promising candidates for tuning in the near infrared: at the nanoscale, thin layers can provide enough contrast to control the optical response of a nanostructure. Moreover, all-dielectric metamaterials allow for resonant behavior without having ohmic losses in the telecom range. Here, a novel hybridization of a SOI-based metamaterial with PCM GeTe is experimentally investigated. A metamaterial based on Si nanorods, covered by a thin layer of GeTe, is designed and fabricated. Switching GeTe from amorphous to crystalline leads to a rather high resonance-governed reflection contrast at 1.55 mu m. Additional confocal Raman imaging is done to differentiate the crystallized zones of the metamaterials' unit cell. The findings are in good agreement with numerical analysis and show good perspectives of all-dielectric tunable near-infrared nanophotonics. (C) 2019 Optical Society of America

Arrays of nanoholes in metal are important plasmonic devices, proposed for applications spanning from biosensing to communications. In this work, we show that in such arrays the symmetry can be broken by means of the elliptical shape of the nanoholes, combined with the in-plane tilt of the ellipse axes away from the array symmetry lines. The array then differently interacts with circular polarizations of opposite handedness at normal incidence, i.e., it becomes intrinsically chiral. The measure of this difference is called circular dichroism (CD). The nanosphere lithography combined with tilted silver evaporation was employed as a low-cost fabrication technique. In this paper, we demonstrate intrinsic chirality and CD by measuring the extinction in the near-infrared range. We further employ numerical analysis to visualize the circular polarization coupling with the nanostructure. We find a good agreement between simulations and the experiment, meaning that the optimization can be used to further increase CD.

Semiconductor nanowires made of high refractive index materials can couple the incoming light to specific waveguide modes that offer resonant absorption enhancement under the bandgap wavelength, essential for light harvesting, lasing and detection applications. Moreover, the non-trivial ellipticity of such modes can offer near field interactions with chiral molecules, governed by near chiral field. These modes are therefore very important to detect. Here, we present the photo-acoustic spectroscopy as a low-cost, reliable, sensitive and scattering-free tool to measure the spectral position and absorption efficiency of these modes. The investigated samples are hexagonal nanowires with GaAs core; the fabrication by means of lithography-free molecular beam epitaxy provides controllable and uniform dimensions that allow for the excitation of the fundamental resonant mode around 800 nm. We show that the modulation frequency increase leads to the discrimination of the resonant mode absorption from the overall absorption of the substrate. As the experimental data are in great agreement with numerical simulations, the design can be optimized and followed by photo-acoustic characterization for a specific application. acceptedVersion

We report on the extrinsic chirality behavior of GaAs-based NWs asymmetrically hybridized with Au. The samples are fabricated by a recently developed, lithography-free self-organized GaAs growth, with the addition of AlGaAs shell and GaAs supershell. The angled Au flux is then used to cover three-out-of-six sidewalls with a thin layer of Au. Oblique incidence and proper sample orientation can lead to circular dichroism. We characterize this chiral behavior at $$ 532\,{\text{nm}} $$ and $$ 980\,{\text{nm}} $$ by means of photo-acoustic spectroscopy, which directly measures the difference in absorption for the circularly polarized light of the opposite headedness. For the first time to our knowledge, circular dichroism is observed in both the amplitude and the phase of the photo-acoustic signal. We strongly believe that such samples can be used for chiral applications, spanning from circularly polarized light emission, to the enantioselectivity applications.

Photothermal and photoacoustic techniques are utilized to explore the thermal properties of metal based metasurfaces. We experimentally evidence the role of the symmetry in the heat transport and its relation with the optical circular dichroism.

We demonstrate the control of enhanced chiral field distribution at the surface of hybrid metallo-dielectric nanostructures composed of self-assembled vertical hexagonal GaAs-based nanowires having three of the six sidewalls covered with Au. We show that weakly-guided modes of vertical GaAs nanowires can generate regions of high optical chirality that are further enhanced by the break of the symmetry introduced by the gold layer. Changing the angle of incidence of a linearly polarized plane wave it is possible to tailor and optimize the maps of the optical chirality in proximity of the gold plated walls. The low cost feasibility of the sample combined to the simple control by using linearly polarized light and the easy positioning of chiral molecules by functionalization of the gold plates make our proposed scheme very promising for enhanced enantioselective spectroscopy applications. publishedVersion

III–V semiconductors nanowires (NW) have recently attracted a significant interest for their potential application in the development of high efficiency, highly-integrated photonic devices and in particular for the possibility to integrate direct bandgap materials with silicon-based devices. Here we report the absorbance properties of GaAs-AlGaAs-GaAs core-shell-supershell NWs using photo-acoustic spectroscopy (PAS) measurements in the spectral range from 300 nm to 1100 nm wavelengths. The NWs were fabricated by self-catalyzed growth on Si substrates and their dimensions (length ~5 μm, diameter ~140–150 nm) allow for the coupling of the incident light to the guided modes in near-infrared (IR) part of the spectrum. This coupling results in resonant absorption peaks in the visible and near IR clearly evidenced by PAS. The analysis reveal broadening of the resonant absorption peaks arising from the NW size distribution and the interaction with other NWs. The results show that the PAS technique, directly providing scattering independent absorption spectra, is a very useful tool for the characterization and investigation of vertical NWs as well as for the design of NW ensembles for photonic applications, such as Si-integrated light sources, solar cells, and wavelength dependent photodetectors.

Electromagnetically induced transparency (EIT), a pump-induced narrow transparency window within the absorption region of a probe, had offered new perspectives in slow-light control in atomic physics. For applications in nanophotonics, the implementation on chip-scaled devices has later been obtained by mimicking this effect by metallic metamaterials. High losses in visible and near infrared range of metal-based metamaterialls have recently opened a new field of all-dielectric metamaterials; a proper configuration of high refractive index dielectric nanoresonators can mimick this effect without losses to get high Q, slow-light response. The next step would be the ability to tune their optical response, and in this work we investigate thin layers of phase change materials (PCM) for all-optical control of EIT-like all-dielectric metamaterials. PCM can be nonvolatively and reversibly switched between two stable phases that differ in optical properties by applying a visible laser pulse. The device is based on Si nanoresonators covered by a thin layer of PCM GeTe; optical and transient thermal simulations have been done to find and optimize the fabrication parameters and switching parameters such as the intensity and duration of the pulse. We have found that the EIT-like response can be switched on and off by applying the 532nm laser pulse to change the phase of the upper GeTe layer. We strongly believe that such approach could open new perspectives in all-optically controlled slow-light metamaterials.

Second-order nonlinear optical materials are used to generate new frequencies by exploiting second-harmonic generation (SHG), a phenomenon where a nonlinear material generates light at double the optical frequency of the input beam. Maximum SHG is achieved when the pump and the generated waves are in phase, for example through birefringence in uniaxial crystals. However, applying these materials usually requires a complicated cutting procedure to yield a crystal with a particular orientation. Here we demonstrate the first example of phase matching under the normal incidence of SHG in a biaxial monoclinic single crystal of zinc tungstate. The crystal was grown by the micro-pulling-down method with the (102) plane perpendicular to the growth direction. Additionally, at the same time white light was generated as a result of stimulated Raman scattering and multiphoton luminescence induced by higher-order effects such as three-photon luminescence enhanced by cascaded third-harmonic generation. The annealed crystal offers SHG intensities approximately four times larger than the as grown one; optimized growth and annealing conditions may lead to much higher SHG intensities.

In this work we report on the resonant absorption properties of GaAs-based nanowires, and on the chiral response when such nanowires are asymmetrically covered by gold. We use photo-acoustic spectroscopy which is a scattering-free, stable and highly sensitive technique that directly measures the absorption of the nanowire ensembles. Highly uniform samples were fabricated by lithography-free process of selfcatalyzed growth on Si substrates. We report on the experimental resonant absorption in the range (300÷1100) nm, which is in great agreement with simulations. We then measure the circular dichroism at 532nm, and discuss on the formation of near chiral fields for enhanced enantioselectivity applications.

We apply photo-acoustic (PA) technique to examine plasmonic properties of 2D periodic arrays of nanoholes etched in gold/chromium layer upon a glass substrate. The pitch of these arrays lies in the near IR, and this, under appropriate wave vector matching conditions in the visible region, allows for the excitation of surface plasmon polaritons (SPP) guided along a dielectric - metal surface. SPP offered new approaches in light guiding and local field intensity enhancement, but their detection is often difficult due to the problematic discrimination of their contribution from the overall scattering. Here PA measures the energy absorbed due to the non-radiative decay of SPPs. We report on the absorption enhancement by presenting the spatial mapping of absorption under the incidence angles and wavelength that correspond to the efficient excitation of SPPs. Moreover, a comparison with optical transmission measurements is carried out, underlining the applicability and sensitivity of PA technique.

We show that photo-acoustic spectroscopy allows determination of the nanowire absorbance properties including resonant peak positions and peak broadening due to collective ensemble properties. Furthermore, we demonstrate chiral optical response in asymmetrically Aucoated nanowires.