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An acoustic plasmon mode in a graphene-dielectric-metal structure has recently been spotlighted as a superior platform for strong light-matter interaction. It originates from the coupling of graphene plasmon with its mirror image and exhibits the largest field confinement in the limit of a sub-nm-thick dielectric. Although recently detected in the far-field regime, optical near-fields of this mode are yet to be observed and characterized. Here, we demonstrate a direct optical probing of the plasmonic fields reflected by the edges of graphene via near-field scattering microscope, revealing a relatively small propagation loss of the mid-infrared acoustic plasmons in our devices that allows for their real-space mapping at ambient conditions even with unprotected, large-area graphene grown by chemical vapor deposition. We show an acoustic plasmon mode that is twice as confined and has 1.4 times higher figure of merit in terms of the normalized propagation length compared to the graphene surface plasmon under similar conditions. We also investigate the behavior of the acoustic graphene plasmons in a periodic array of gold nanoribbons. Our results highlight the promise of acoustic plasmons for graphene-based optoelectronics and sensing applications. Acoustic graphene plasmons are superior to the graphene surface plasmons in field confinement and normalized propagation length, thus promising for applications. Here, the authors report near-field imaging of acoustic plasmons in high-quality CVD graphene, measure the AGP dispersion and propagation loss, and investigate their behavior in a periodic structure.

Active metasurfaces have been proposed as one attractive means of achieving high-resolution spatiotemporal control of optical wavefronts, having applications such as LIDAR and dynamic holography. However, achieving full, dynamic phase control has been elusive in metasurfaces. In this paper, we unveil an electrically tunable metasurface design strategy that operates near the avoided crossing of two resonances, one a spectrally narrow, over-coupled resonance and the other with a high resonance frequency tunability. This strategy displays an unprecedented upper limit of 4π range of dynamic phase modulation with no significant variations in optical amplitude, by enhancing the phase tunability through utilizing two coupled resonances. A proof-of-concept metasurface is justified analytically and verified numerically in an experimentally accessible platform using quasi-bound states in the continuum and graphene plasmon resonances, with results showing a 3π phase modulation capacity with a uniform reflection amplitude of ~0.65. Though active metasurfaces have been attractive for applications requiring control of optical wavefronts, realizing metasurfaces with full phase control remains a challenge. Here, the authors report a metasurface design strategy for enhanced dynamic phase modulation and tunability.

Controlling the wavefront of light, especially on a subwavelength scale, is pivotal in modern optics. Metasurfaces present a unique platform for realizing flat lenses, called metalenses, with thicknesses on the order of the wavelength. Despite substantial effort, however, suppressing the chromatic aberrations over large operational bandwidths of metalenses still remains a challenge. Here, we develop a systematic design method enabling a simultaneous, polarization-insensitive control of the phase and the group delay of a light beam based on libraries of transmission-mode dielectric meta-elements. Mid-infrared achromatic metalenses are designed and theoretically analyzed to have diffraction-limited focal spots with vanishing chromatic aberrations in the operating wavelength range of 6–8.5 μm, while maintaining high focusing efficiencies of 41% on average. The proposed methodology, which can be used as a general design rule for all spectra, also provides a versatile design scheme for ultrashort pulse focusing and achromatic vortex-beam generation (orbital angular momentum), representing a major advance toward practical implementations of functional metalenses.

Polaritonic crystals – periodic structures where the hybrid light–matter waves called polaritons can form Bloch states – promise a deeply subdiffractional nanolight manipulation and enhanced light-matter interaction. In particular, polaritons in van der Waals materials boast extreme field confinement and long lifetimes allowing for the exploitation of wave phenomena at the nanoscale. However, in conventionally patterned nanostructures, polaritons are prone to severe scattering loss at the sharp material edges, making it challenging to create functional polaritonic crystals. Here, we introduce a concept of a polaritonic Fourier crystal based on a harmonic modulation of the polariton momentum in a pristine polaritonic waveguide with minimal scattering. We employ hexagonal boron nitride (hBN) and near-field imaging to reveal a neat and well-defined band structure of phonon-polaritons in the Fourier crystal, stemming from the dominant excitation of the first-order Bloch mode. Furthermore, we show that the fundamental Bloch mode possesses a polaritonic bandgap even in the relatively lossy naturally abundant hBN. Thus, our work provides an alternative paradigm for polaritonic crystals essential for enhanced light-matter interaction, dispersion engineering, and nanolight guiding. Polaritonic Fourier crystal provides harmonic modulation of the polariton momentum in a pristine polaritonic waveguide. Authors employ hexagonal boron nitride and near-field imaging to probe Bloch waves of phonon-polaritons in the Fourier crystal.

Polaritonic modes in low-dimensional materials enable strong light–matter interactions and the manipulation of light on nanometer length scales. Very recently, a new class of polaritons has attracted considerable interest in nanophotonics: image polaritons in van der Waals crystals, manifesting when a polaritonic material is in close proximity to a highly conductive metal, so that the polaritonic mode couples with its mirror image. Image modes constitute an appealing nanophotonic platform, providing an unparalleled degree of optical field compression into nanometric volumes while exhibiting lower normalized propagation loss compared to conventional polariton modes in van der Waals crystals on nonmetallic substrates. Moreover, the ultra-compressed image modes provide access to the nonlocal regime of light–matter interaction. In this review, we systematically overview the young, yet rapidly growing, field of image polaritons. More specifically, we discuss the dispersion properties of image modes, showcase the diversity of the available polaritons in various van der Waals materials, and highlight experimental breakthroughs owing to the unique properties of image polaritons.

The recently suggested concept of a polaritonic Fourier crystal (PFC) is based on a harmonically-corrugated mirror substrate for a thin pristine polaritonic crystal layer. The propagating polaritons in PFC experience a harmonic and mode-selective momentum modulation leading to a manifestation of Bloch modes with practically zero inter-mode scattering. PFC was first demonstrated for the hyperbolic phonon-polaritons in hexagonal boron nitride (hBN) within its Type II Reststrahlen band (RB-II) where the in-plane components of the dielectric permittivity tensor are isotropic and negative, while the out-of-plane component is positive. By contrast, a Type I Reststrahlen band (RB-I) is characterized by negative out-of-plane and positive in-plane permittivity components, and consequently, the inversion of field symmetry of phonon-polaritons compared to RB-II. Behavior of such RB-I modes in a polaritonic crystal is yet to be explored. Here, we employ a biaxial crystal alpha-phase molybdenum trioxide ({\\alpha}-MoO3) and near-field imaging to study polaritonic Bloch modes in a one-dimensional PFC within the RB-I where the mid-infrared phonon-polaritons in {\\alpha}-MoO3 have anomalous dispersion and negative phase velocity. Surprisingly, we observe a manifestation of Bloch waves as a dispersionless near-field pattern across the first Brillouin zone, in contrast to RB-II case demonstrated with in-plane isotropic hBN. We attribute this difference to the opposite field symmetry of the lowest-order phonon-polariton mode in the two RBs, leading to a different momentum modulation regime in the polaritonic Fourier crystal. Our results reveal the importance of mode symmetry for polaritonic crystals in general and for the emerging field of Fourier crystals in particular, which promise new ways to manipulate the nanolight.

Topological insulators generally have dielectric bulk and conductive surface states. Consequently, some of these materials have been shown to support polaritonic modes at visible and THz frequencies. At the same time, the optical properties of topological insulators in the mid-infrared (IR) remain poorly investigated. We employ near-field imaging to probe the mid-IR response from the exfoliated flakes of bismuth (Bi) / selenide (Se) / telluride (Te) / antimony (Sb) crystals with varying stoichiometry - Bi2Se3, Bi2Te2Se, and Bi1.5Sb0.5Te1.7Se1.3 - in pristine form as well as covered by thin flakes of hexagonal boron nitride (hBN). Contrary to theoretical expectations, all three materials exhibit a dielectric response with a high refractive index and with a loss below the experimental detection limit. Particularly, the near-field mapping of propagating phonon-polaritons in hBN demonstrates that these van der Waals crystals act as a practically lossless dielectric substrate with an ultra-high refractive index of up to 7.5 in Bi2Te2Se. Such a unique dielectric crystal would be of great advantage for numerous nanophotonic applications in the mid-IR.

Electromagnetic design relies on an accurate understanding of light-matter interactions, yet often overlooks electronic length scales. Under extreme confinement, this omission can lead to nonclassical effects, such as nonlocal response. Here, we use mid-infrared phonon-polaritons in hexagonal boron nitride (hBN) screened by monocrystalline gold flakes to push the limits of nanolight confinement unobstructed by nonlocal phenomena, even when the polariton phase velocity approaches the Fermi velocities of electrons in gold. We employ near-field imaging to probe polaritons in nanometre-thin crystals of hBN on gold and extract their complex propagation constant, observing effective indices exceeding 90. We further show the importance of sample characterisation by revealing a thin low-index interfacial layer naturally forming on monocrystalline gold. Our experiments address a fundamental limitation posed by nonlocal effects in van der Waals heterostructures and outline a pathway to bypass their impact in high-confinement regimes.

Scattering-type scanning near-field optical microscope (s-SNOM) has become an essential tool to study polaritons - quasiparticles of light coupled to collective charge oscillations - via direct probing of their near field with a spatial resolution far beyond the diffraction limit. However, extraction of the polariton complex propagation constant from the near-field images requires subtle considerations that have not received necessary attention so far. In this study, we discuss important yet overlooked aspects of the near-field analysis. First, we experimentally demonstrate that the sample orientation inside the s-SNOM may significantly affect the near-field interference pattern of mid-infrared polaritons, leading to an error in momentum measurement up to 7.7% even for the modes with effective index of 12.5. Second, we establish a methodology to correctly extract the polariton damping rate from the interference fringes depending on their origin - the s-SNOM nano-tip or the material edge. Overall, our work provides a unified framework for the accurate extraction of the polariton momentum and damping from the near-field interference fringes.

Polaritonic modes in low-dimensional materials enable strong light-matter interactions and provide a platform for light manipulation at nanoscale. Very recently, a new class of polaritons has attracted considerable interest in nanophotonics: image polaritons in van der Waals crystals, manifesting when a polaritonic material is in close proximity to a highly conductive metal, so that the polaritonic mode couples with its mirror image. Image modes constitute an appealing nanophotonic platform, providing an unparalleled degree of optical field compression into nanometric volumes while exhibiting lower normalized propagation loss compared to conventional polariton modes in van der Waals crystals on non-metallic substrates. Moreover, the ultra-compressed image modes provide access to the nonlocal regime of light-matter interaction. In this Review, we systematically overview the young yet rapidly growing field of image polaritons. We discuss their dispersion properties, showcase the diversity of image modes in various van der Waals materials, and highlight the experimental breakthroughs owing to the unique properties of image polaritons.