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Surface Plasmon Polaritons (SPP) are exploited due to their intriguing properties for photonic circuits fabrication and miniaturization, for surface enhanced spectroscopies and imaging beyond the diffraction limit. However, the excitation of these plasmonic modes by direct illumination is forbidden by energy/momentum conservation rules. One strategy to overcome this limitation relies on diffraction gratings to match the wavevector of the incoming photons with that of propagating SPP excitations. The main limit of the approaches so far reported in literature is that they rely on highly ordered diffraction gratings fabricated by means of demanding nano-lithographic processes. In this work we demonstrate that an innovative, fully self-organized method based on wrinkling-assisted Ion Beam Sputtering can be exploited to fabricate large area (cm^2 scale) nano-rippled soda-lime templates which conformally support ultrathin Au films deposited by physical deposition. The self-organized patterns act as quasi-1D gratings characterized by a remarkably high spatial order which matches properly the transverse photon coherence length. The gratings can thus enable the excitation of hybrid SPP modes confined at the Au/dielectric interfaces, with a resonant wavelength which can be tuned either by modifying the grating period, photon incidence angle or, potentially, the choice of the thin film conductive material. Surface Enhanced Raman Scattering experiments show promising gains in the range of 10^3 which are competitive, even before a systematic optimization of the sample fabrication parameters, with state-of-the art lithographic systems, demonstrating the potential of such templates for a broad range of optoelectronic applications aiming at plasmon-enhanced photon harvesting for molecular or bio-sensing.

Bidirectional nanoantennas are of key relevance for advanced functionalities to be implemented at the nanoscale, and in particular for color routing in an ultracompact flat-optics configuration. Here we demonstrate a novel approach avoiding complex collective geometries and/or restrictive morphological parameters, based on cross-polarized detuned plasmonic nanoantennas in a uniaxial (quasi-1D) bimetallic configuration. The nanofabrication of such a flat-optics system is controlled over a large-area (cm^2) by a novel self-organized technique exploiting ion-induced nanoscale wrinkling instability on glass templates to engineer tilted bimetallic nanostrip dimers. These nanoantennas feature broadband color routing with superior light scattering directivity figures, which are well described by numerical simulations and turn out to be competitive with the response of lithographic nanoantennas. These results demonstrate that our large-area self-organized metasurfaces can be implemented in real world applications of flat optics color routing from telecom photonics to optical nanosensing., Comment: 25+8 pages, 5+4 figures

Capabilities of highly sensitive surface-enhanced infrared absorption (SEIRA) spectroscopy are demonstrated by exploiting large-area templates ($cm^2$) based on self-organized (SO) nanorod antennas. We engineered highly dense arrays of gold nanorod antennas featuring polarization-sensitive localized plasmon resonances, tunable over a broadband near- and mid-infrared (IR) spectrum, in overlap with the so-called 'functional group' window. We demonstrate polarization-sensitive SEIRA activity, homogeneous over macroscopic areas and stable in time, by exploiting prototype self-assembled monolayers of IR-active octadecanthiol (ODT) molecules. The strong coupling between the plasmonic excitation and molecular stretching modes gives rise to characteristic Fano resonances in SEIRA. The SO engineering of the active hotspots in the arrays allows us to achieve signal amplitude improved up to 5.7%. This figure is competitive to the response of lithographic nanoantennas and is stable when the optical excitation spot varies from the micro- to macroscale, thus enabling highly sensitive SEIRA spectroscopy with cost-effective nanosensor devices., Comment: 28+8 pages, 3+5 figures