Direct programming of confined Surface Phonon Polariton Resonators using the plasmonic Phase-Change Material In3_3SbTe2_2

Tailoring light-matter interaction is essential to realize nanophotonic components. It can be achieved with surface phonon polaritons (SPhPs), an excitation of photons coupled with phonons of polar crystals, which also occur in 2d materials such as hexagonal boron nitride or anisotropic crystals. Ultra-confined resonances are observed by restricting the SPhPs to cavities. Phase-change materials (PCMs) enable non-volatile programming of these cavities based on a change in the refractive index. Recently, the new plasmonic PCM In$_3$SbTe$_2$ (IST) was introduced which can be reversibly switched from an amorphous dielectric state to a crystalline metallic one in the entire infrared to realize numerous nanoantenna geometries. However, reconfiguring SPhP resonators to modify the confined polaritons modes remains elusive. Here, we demonstrate direct programming of confined SPhP resonators by phase-switching IST on top of a polar silicon carbide crystal and investigate the strongly confined resonance modes with scanning near-field optical microscopy. Reconfiguring the size of the resonators themselves result in enhanced mode confinements up to a value of $\lambda/35$. Finally, unconventional cavity shapes with complex field patterns are explored as well. This study is a first step towards rapid prototyping of reconfigurable SPhP resonators that can be easily transferred to hyperbolic and anisotropic 2d materials.Comment: Main Manuscript 16 pages, 5 figures, SI 15 page

Probing hyperbolic polaritons using infrared attenuated total reflectance micro-spectroscopy

Hyperbolic polariton modes are highly appealing for a broad range of applications in nanophotonics, including surfaced enhanced sensing, sub-diffractional imaging and reconfigurable metasurfaces. Here we show that attenuated total reflectance micro-spectroscopy (ATR) using standard spectroscopic tools can launch hyperbolic polaritons in a Kretschmann-Raether configuration. We measure multiple hyperbolic and dielectric modes within the naturally hyperbolic material hexagonal boron nitride as a function of different isotopic enrichments and flake thickness. This overcomes the technical challenges of measurement approaches based on nanostructuring, or scattering scanning nearfield optical microscopy. Ultimately, our ATR approach allows us to compare the optical properties of small-scale materials prepared by different techniques systematicallyComment: 13 pages 4 figure

Substrate-enhanced infrared near-field spectroscopy

17 pages, 8 figures.-- OCIS codes: 240.6490, 300.6340, 180.4243, 290.5825.-- © 2008 Optical Society of America.We study the amplitude and phase signals detected in infrared scattering-type near field optical microscopy (s-SNOM) when probing a thin sample layer on a substrate. We theoretically describe this situation by solving the electromagnetic scattering of a dipole near a planar sample consisting of a substrate covered by thin layers. We perform calculations to describe the effect of both weakly (Si and SiO2) and strongly (Au) reflecting substrates on the spectral s-SNOM signal of a thin PMMA layer. We theoretically predict, and experimentally confirm an enhancement effect in the polymer vibrational spectrum when placed on strongly reflecting substrates. We also calculate the scattered fields for a resonant tip-substrate interaction, obtaining a dramatic enhancement of the signal amplitude and spectroscopic contrast of the sample layer, together with a change of the spectral line shape. The enhanced contrast opens the possibility to perform ultra-sensitive near field infrared spectroscopy of monolayers and biomolecules.We wish to acknowledge financial support from the Department of Industry of the Basque Country (ETORTEK project NANOTRON), from Gipuzkoa Foru Aldundia (nanoGUNE), from the Spanish MEC (NAN2004-08843-C05- 05 and MAT2007-66050), from BMBF grant no. 03N8705, and from the Bavarian California Technology Center (BaCaTec). T.T. was supported by a fellowship within the Postdoc-Programme of the German Academic Exchange Service (DAAD).Peer reviewe

Nanostructured In3SbTe2 antennas enable switching from sharp dielectric to broad plasmonic resonances

Phase-change materials (PCMs) allow for non-volatile resonance tuning of nanophotonic components. Upon switching, they offer a large dielectric contrast between their amorphous and crystalline phases. The recently introduced “plasmonic PCM” In3SbTe2 (IST) additionally features in its crystalline phase a sign change of its permittivity over a broad infrared spectral range. While optical resonance switching in unpatterned IST thin films has been investigated before, nanostructured IST antennas have not been studied, yet. Here, we present numerical and experimental investigations of nanostructured IST rod and disk antennas. By crystallizing the IST with microsecond laser pulses, we switched individual antennas from narrow dielectric to broad plasmonic resonances. For the rod antennas, we demonstrated a resonance shift of up to 1.2 µm (twice the resonance width), allowing on/off switching of plasmonic resonances with a contrast ratio of 2.7. With the disk antennas, we realized an increase of the resonance width by more than 800% from 0.24 µm to 1.98 µm while keeping the resonance wavelength constant. Further, we demonstrated intermediate switching states by tuning the crystallization depth within the resonators. Our work empowers future design concepts for nanophotonic applications like active spectral filters, tunable absorbers, and switchable flat optics

All‐Dielectric Programmable Huygens' Metasurfaces

Low‐loss nanostructured dielectric metasurfaces have emerged as a breakthrough platform for ultrathin optics and cutting‐edge photonic applications, including beam shaping, focusing, and holography. However, the static nature of their constituent materials has traditionally limited them to fixed functionalities. Tunable all‐dielectric infrared Huygens' metasurfaces consisting of multi‐layer Ge disk meta‐units with strategically incorporated non‐volatile phase change material Ge3Sb2Te6 are introduced. Switching the phase‐change material between its amorphous and crystalline structural state enables nearly full dynamic light phase control with high transmittance in the mid‐IR spectrum. The metasurface is realized experimentally, showing post‐fabrication tuning of the light phase within a range of 81% of the full 2π phase shift. Additionally, the versatility of the tunable Huygen's metasurfaces is demonstrated by optically programming the spatial light phase distribution of the metasurface with single meta‐unit precision and retrieving high‐resolution phase‐encoded images using hyperspectral measurements. The programmable metasurface concept overcomes the static limitations of previous dielectric metasurfaces, paving the way for “universal” metasurfaces and highly efficient, ultracompact active optical elements like tunable lenses, dynamic holograms, and spatial light modulators

Mid infrared near-field fingerprint spectroscopy of the 2D electron gas in LaAlO3_3/SrTiO3_3 at low temperatures

Confined electron systems, such as 2D electron gases (2DEGs), 2D materials, or topological insulators show great technological promise but their susceptibility to defects often results in nanoscale inhomogeneities with unclear origins. Scattering-type scanning near-field optical microscopy (s-SNOM) is useful to investigate buried confined electron systems non-destructively with nanoscale resolution, however, a clear separation of carrier concentration and mobility was often impossible in s-SNOM. Here, we predict a previously inaccessible characteristic "fingerprint" response of the prototypical LaAlO$_3$/SrTiO$_3$ 2DEG, and verify this using a state-of-the-art tunable narrow-band laser in mid-infrared cryo-s-SNOM at 8 K. Our modelling allows us to separate the influence of carrier concentration and mobility on fingerprint spectra and to characterize 2DEG inhomogeneities on the nanoscale. This spatially resolved information about the local electronic properties can be used to identify the origin of inhomogeneities in confined electron systems, making the s-SNOM fingerprint response a valuable tool for nanoelectronics and quantum technology

Corrections

Surface phonon polaritons (SPhP) and surface plasmon polaritons (SPP), evanescent modes supported by media with negative permittivity, are a fundamental building block of nanophotonics. These modes are unmatched in terms of field enhancement and spatial confinement, and dynamical all-optical control can be achieved e.g. by employing phase-change materials (PCMs). However, the excitation of surface polaritons in planar structures is intrinsically limited to p-polarization. On the contrary, waveguide modes in high-permittivity films can couple to both p- and s-polarized light, and in thin films, their confinement can become comparable to surface polaritons. Here we demonstrate that the s-polarized waveguide mode in a thin Ge3Sb2Te6 (GST) film features a similar dispersion, confinement, and electric field enhancement as the SPhP mode of the silicon carbide (SiC) substrate, while even expanding the allowed frequency range. Moreover, we experimentally show that switching the GST film grants non-volatile control over the SPhP and the waveguide mode dispersions. We provide an analytical model for the description of the GST/SiC waveguide mode and show that our concept is applicable to the broad variety of polar crystals throughout the infrared spectral range. As such, complementarily to the polarization-limited surface polaritons, the s-polarized PCM waveguide mode constitutes a promising additional building block for nanophotonic applications