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Layered van der Waals (vdW) materials have emerged as a promising platform for nanophotonics due to large refractive indexes and giant optical anisotropy. Unlike conventional dielectrics and semiconductors, the absence of covalent bonds between layers allows for novel degrees of freedom in designing optically resonant nanophotonic structures down to the atomic scale, from the precise stacking of vertical heterostructures to controlling the twist angle between crystallographic axes. Specifically, while transition metal dichalcogenides monolayers exhibit giant second order nonlinear responses, their bulk counterparts with 2H stacking have zero second order response. In this work, we show second harmonic generation (SHG) arising from the interface of WS$_2$/MoS$_2$ hetero-bilayer thin films with an additional SHG enhancement in nanostructured optical antennas mediated by both the excitonic resonances and the anapole condition. When both conditions are met, we observe up to $10^2$ SHG signal enhancement. Our results highlights vdW materials as a platform for designing unique multilayer optical nanostructures and metamaterial, paving the way for advanced applications in nanophotonics and nonlinear optics., Comment: Manuscript + Supplementary (21 pages, 3 Main figures 8 supplementary figures)

Metasurfaces offer a powerful platform for effective light manipulation, which is crucial for advanced optical technologies. While designs of polarization-independent structures have reduced the need for polarized illumination, they are often limited by either low Q factors or low resonance modulation. Here, we design and experimentally demonstrate a metasurface with polarization-independent quasi-bound state in the continuum (quasi-BIC), where the unit cell consists of four silicon squares arranged in a two-dimensional array and the resonance properties can be controlled by adjusting the edge length difference between different squares. Our metasurface experimentally achieves a Q factor of approximately 100 and a resonance modulation of around 50%. This work addresses a common limitation in previous designs, which either achieved high Q factors exceeding 200 with a resonance modulation of less than 10%, leading to challenging signal-to-noise ratio requirements, or achieved strong resonance modulation with Q factors of only around 10, limiting light confinement and fine-tuning capabilities. In contrast, our metasurface ensures that the polarization-independent signal is sharp and distinct within the system, reducing the demands on signal-to-noise ratio and improving robustness. Experiments show the consistent performance across different polarization angles. This work contributes to the development of versatile optical devices, enhancing the potential for the practical application of BIC-based designs in areas such as optical filtering and sensing.

In the strong-coupling regime, the interaction between light and matter reaches a hybridization state where the photonic and material components become inseparably linked. Using tailored states of light to break symmetries in such systems can underpin the development of novel non-equilibrium quantum materials. Chiral optical cavities offer a promising way for this, enabling either temporal or spatial symmetry-breaking, both of which are unachievable with conventional mirror cavities. For spatial symmetry-breaking a cavity needs to discriminate the handedness of circularly polarized light, a functionality that can only be achieved with metamaterials. Here, we suggest and demonstrate experimentally a chiral transition metal dichalcogenide (TMDC) metasurface with broken out-of-plane symmetry, allowing for a selective formation of self-hybridized exciton-polaritons with specific chirality. Our metasurface cavity maintains maximum chirality for oblique incidence up to 20{\deg}, significantly outperforming all previously known designs, thereby turning the angle of incidence from a constraint to a new degree of freedom for sub-nanometer precise control of resonance wavelengths. Moreover, we study the chiral strong-coupling regime in nonlinear experiments and show the polariton-driven nature of chiral third-harmonic generation. Our results demonstrate a clear pathway towards novel quantum material engineering with implications in a wide range of photonics research, such as superconductivity and valleytronics., Comment: 34 pages, 4 figures, and 12 supporting figures

Photonics has been revolutionized by breakthroughs in optical metasurfaces and layered two-dimensional materials. Yet, integrating these two fields in a singular system has remained challenging. Here, we introduce the concept of van der Waals (vdW) heterostructure metasurfaces, where ultrathin multilayer vdW material stacks are shaped into precisely engineered resonant nanostructures for boosting light-matter interactions. By leveraging quasi-bound states in the continuum to create intrinsic cavities from WS$_2$ monolayers encapsulated in hexagonal boron nitride, we observe room-temperature strong coupling and polaritonic luminescence, which further unveils a saturation of the strong-coupling regime at ultralow fluences <1 nJ/cm2, more than three orders of magnitude smaller than in previous 2D-cavity systems. Our approach, seamlessly merging metasurfaces and vdW materials, unlocks new avenues for ultrathin optical devices with atomic-scale precision and control., Comment: main + supplementary (28 pages, 4 main figures, 9 supplementary figures)

Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions and with minimal interference is crucial for advancing nanomedicine, photopharmacology, drug delivery, nanotheranostics and synthetic biology. Yet, analytical methods struggle to combine precise chemical imaging and measurements without perturbative labeling. This challenge is exemplified for azobenzene-based photoswitchable lipids, which are intriguing reagents for controlling nanocarrier properties on fast timescales, enabling, e.g., precise light-induced drug release processes. Here, we leverage the chemical recognition and high spatio-temporal resolution of scattering-type scanning near-field optical microscopy (s-SNOM) to demonstrate non-destructive, label-free mid-infrared (MIR) imaging and spectroscopy of photoswitchable liposomes below the diffraction limit and the tracking of their dynamics down to 50 ms resolution. The vesicles are adsorbed on an ultrathin 10-nm SiN membrane, which separates the sample space from the tip space for stable and hour-long observations. By implementing a transient nanoscopy approach, we accurately resolve, for the first time, photoinduced changes in both the shape and the MIR spectral signature of individual vesicles and reveal abrupt change dynamics of the underlying photoisomerization process. Our findings highlight the methods potential for future studies on the complex dynamics of unlabeled nanoscale soft matter, as well as, in a broader context, for host-guest systems, energy materials or drugs., Comment: 4 figures, 10 supplementary figures

Photonic metasurfaces offer exceptional control over light at the nanoscale, facilitating applications spanning from biosensing, and nonlinear optics to photocatalysis. Many metasurfaces, especially resonant ones, rely on periodicity for the collective mode to form, which makes them subject to the influences of finite size effects, defects, and edge effects, all of which have considerable negative impact at the application level. These aspects are especially important for quasi-bound state in the continuum (BIC) metasurfaces, for which the collective mode is highly sensitive to perturbations due to high quality factors and strong near-field enhancement. Here, we quantitatively investigate the mode formation in quasi-BIC metasurfaces on the individual resonator level using scattering scanning near-field optical microscopy (s-SNOM) in combination with a new image processing technique. We find that the quasi-BIC mode is formed at a minimum size of 10 x 10-unit cells much smaller than expected from far-field measurements. Furthermore, we show that the coupling direction of the resonators, defects and edge states have pronounced influence on the quasi-BIC mode. This study serves as a link between the far-field and near-field responses of metasurfaces, offering crucial insights for optimizing spatial footprint and active area, holding promise for augmenting applications such as catalysis and biospectroscopy., Comment: 30 pages, 6 figures, 8 supplementary figures

In the rapidly evolving field of nanophotonics, achieving precise spectral and temporal light manipulation at the nanoscale remains a critical challenge. While photonic bound states in the continuum (BICs) have emerged as a powerful means of controlling light, their common reliance on geometrical symmetry breaking for obtaining tailored resonances makes them highly susceptible to fabrication imperfections and fundamentally limits their maximum resonance quality factor. Here, we introduce the concept of environmental symmetry breaking by embedding identical resonators into a surrounding medium with carefully placed regions of contrasting refractive indexes, activating permittivity-driven quasi-BIC resonances without any alterations of the underlying resonator geometry and unlocking an additional degree of freedom for light manipulation through actively tuning the surrounding refractive index contrast. We demonstrate this concept by integrating polyaniline (PANI), an electro-optically active polymer, to achieve electrically reconfigurable qBICs. This integration not only demonstrates rapid switching speeds, and exceptional durability but also significantly boosts the system's optical response to environmental perturbations. Our strategy significantly expands the capabilities of resonant light manipulation through permittivity modulation, opening avenues for on-chip optical devices, advanced sensing, and beyond., Comment: 35 pages, 4 figures, and 11 supporting figures

Scattering scanning near-field optical microscopy (s-SNOM) is a powerful technique for mid-infrared spectroscopy at nanometer length scales. By investigating objects in aqueous environments through ultrathin membranes, s-SNOM has recently been extended towards label-free nanoscopy of the dynamics of living cells and nanoparticles, assessing both the optical and the mechanical interactions between the tip, the membrane and the liquid suspension underneath. Here, we report that the tapping AFM tip induces a reversible nanometric deformation of the membrane manifested as either an indentation or protrusion. This mechanism depends on the driving force of the tapping cantilever, which we exploit to minimize topographical deformations of the membrane to improve optical measurements. Furthermore, we show that the tapping phase, or phase delay between driving signal and tip oscillation, is a highly sensitive observable for quantifying the mechanics of adhering objects, exhibiting highest contrast for low tapping amplitudes where the membrane remains nearly flat. We correlate mechanical responses with simultaneously recorded spectroscopy data to reveal the thickness of nanometric water pockets between membrane and adhering objects. Besides a general applicability of depth profiling, our technique holds great promise for studying mechano-active biopolymers and living cells, biomaterials that exhibit complex behaviors when under a mechanical load., Comment: 31 pages, 7 figures, 7 supplementary figures

Squeezing light into subwavelength dimensions is vital for on-chip integration of photonic technologies. One approach to overcome the diffraction limit is coupling light to material excitations, leading to polariton states. Here, we showcase how low-loss mid-infrared surface phonon polaritons enable metasurfaces supporting quasi-bound states in the continuum (qBICs) with deeply subwavelength unit cells. Utilizing 100 nm thick free-standing silicon carbide membranes, we achieve highly confined qBIC states with a unit cell volume ~ 10^4 times smaller than the diffraction limit. This results in remarkable robustness of the platform against the incident angle that is unique among qBIC systems. We also demonstrate vibrational strong coupling with a thin layer of spin-coated molecules, leveraging the small mode volume. This work introduces phononic qBICs as a novel ultra-confined nanophotonic platform, paving a way for the miniaturization of mid-infrared devices for molecular sensing and thermal radiation engineering.

Resonances are usually associated with finite systems - the vibrations of clamped strings in a guitar or the optical modes in a cavity defined by mirrors. In optics, resonances may be induced in infinite continuous media via periodic modulations of their optical properties. Here we demonstrate that periodic modulations of the permittivity of a featureless thin film can also act as a symmetry breaking mechanism, allowing the excitation of photonic $\textit{quasi}$-bound states in the continuum ($\textit{q}$BICs). By interfering two ultrashort laser pulses in the unbounded film, transient resonances can be tailored through different parameters of the pump beams. We show that the system offers resonances tunable in wavelength and quality-factor, and spectrally selective enhancement of third harmonic generation. Due to a fast decay of the permittivity asymmetry, we observe ultrafast dynamics, enabling time-selective near-field enhancement with picosecond precision. Optically-induced permittivity asymmetries may be exploited in on-demand weak to ultrastrong light-matter interaction regimes and light manipulation at dynamically chosen wavelengths in lithography-free metasurfaces.

The development of nanoscale nonlinear elements in photonic integrated circuits is hindered by the physical limits to the nonlinear optical response of dielectrics, which requires that the interacting waves propagate in transparent volumes for distances much longer than their wavelength. Here we present experimental evidence that optical nonlinearities in doped semiconductors are due to free-electron and their efficiency could exceed by several orders of magnitude that of conventional dielectric nonlinearities. Our experimental findings are supported by comprehensive computational results based on the hydrodynamic modeling, which naturally includes nonlocal effects, of the free-electron dynamics in heavily doped semiconductors. By studying third-harmonic generation from plasmonic nanoantenna arrays made out of heavily n-doped InGaAs with increasing levels of free-carrier density, we discriminate between hydrodynamic and dielectric nonlinearities. As a result, the value of maximum nonlinear efficiency as well as its spectral location can now be controlled by tuning the doping level. Having employed the common material platform InGaAs/InP that supports integrated waveguides, our findings pave the way for future exploitation of plasmonic nonlinearities in all-semiconductor photonic integrated circuits.

Enhancing and controlling light-matter interactions is crucial in nanotechnology and material science, propelling research on green energy, laser technology, and quantum cryptography. Central to enhanced light-matter coupling are two parameters: the spectral overlap between an optical cavity mode and the material's spectral features (e.g., excitonic or molecular absorption lines), and the quality factor of the cavity. Controlling both parameters simultaneously is vital, especially in complex systems requiring extensive data to uncover the numerous effects at play. However, so far, photonic approaches have focused solely on sampling a limited set of data points within this 2D parameter space. Here we introduce a nanophotonic approach that can simultaneously and continuously encode the spectral and quality factor parameter space of light-matter interactions within a compact spatial area. Our novel dual-gradient metasurface design is composed of a 2D array of smoothly varying subwavelength nanoresonators, each supporting a unique mode. This results in 27,500 distinct modes within one array and a resonance density approaching the theoretical upper limit for metasurfaces. By applying our dual-gradient to surface-enhanced molecular sensing, we demonstrate the importance of coupling tailoring and unveil an additional coupling-based dimension of spectroscopic data. Our metasurface design paves the way for generalized light-matter coupling metasurfaces, leading to advancements in the field of photocatalysis, chemical sensing, and entangled photon generation., Comment: 5 figures, 5 supplementary notes, 14 supplementary figures

Metasurfaces have unlocked significant advancements across photonics, yet their efficient active control remains challenging. The active materials required often lack continuous tunability, exhibit inadequate refractive index (RI) changes, or suffer from high losses. These aspects pose an inherent limitation for resonance-shifting based switching: when RI changes are small, the resulting shift is also minor. Conversely, high RI changes typically come with high intrinsic losses necessitating broad modes because narrow ones cannot tolerate such losses. Therefore, larger spectral shifts are required to effectively detune the modes. This paper introduces a novel active metasurface approach that converts the constraint of high intrinsic losses into a beneficial feature. This is achieved by controlling the losses in a hybrid vanadium dioxide (VO$_{2}$) - silicon metasurface, supporting symmetry-protected bound states in the continuum (BICs) within the infrared spectrum. By leveraging the temperature-controlled losses in VO$_{2}$ and combining them with the inherent far-field-coupling tunability of BICs, we gain unprecedented precision in independently controlling both the radiative and nonradiative losses of the resonant system. Our dual-control mechanism allows us to optimize our metasurfaces and we experimentally demonstrate quality factors above 200, a maximum reflectance amplitude of 90%, a relative switching contrast of 78%, and continuous tuning from under- to over-coupling within the infrared spectral range. This study provides a foundation for experimentally and technologically simple, fine-tunable, active metasurfaces for applications ranging from molecular sensors to filters and optical modulators., Comment: 25 pages, 4 figures, 4 supplementary figures

The technological requirements of low-power and high-fidelity color displays have been instrumental in driving research into advanced coloration technologies. At the forefront of these developments is the implementation of dye-free coloration techniques, which overcome previous constraints related to insufficient resolution and color fading. In this context, resonant dielectric nanostructures have emerged as a promising paradigm, showing great potential for high efficiency, remarkably high color saturation, wide gamut palette, and realistic image reproduction. However, they still face limitations related to color accuracy, purity, and simultaneous brightness tunability. Here, we demonstrate an all-dielectric metasurface empowered by photonic bound states in the continuum (BICs), which supports sharp resonances throughout the visible spectral range, ideally suited for producing a wide range of structural colors. The metasurface design consists of titanium dioxide (TiO2) ellipses with carefully controlled sizes and geometrical asymmetry, allowing versatile and on-demand variation of the brightness and hue of the output colors, respectively.

Semiconductor-based surface-enhanced Raman spectroscopy (SERS) substrates, as a new frontier in the field of SERS, are hindered by their poor electromagnetic field confinement, and weak light-matter interaction. Metasurfaces, a class of 2D artificial materials based on the electromagnetic design of nanophotonic resonators, enable strong electromagnetic field enhancement and optical absorption engineering for a wide range of semiconductor materials. However, the engineering of semiconductor substrates into metasurfaces for improving SERS activity remains underexplored. Here, we develop an improved SERS metasurface platform that leverages the combination of titanium oxide (TiO2) and the emerging physical concept of optical bound states in the continuum (BICs) to boost the Raman emission. Moreover, fine-tuning of BIC-assisted resonant absorption offers a pathway for maximizing the photoinduced charge transfer effect (PICT) in SERS. We achieve ultrahigh values of BIC-assisted electric field enhancement (|E/E0|^2 ~ 10^3), challenging the preconception of weak electromagnetic (EM) field enhancement on semiconductor SERS substrates. Our BIC-assisted TiO2 metasurface platform offers a new dimension in spectrally-tunable SERS with earth-abundant and bio-compatible semiconductor materials, beyond the traditional plasmonic ones.

Nanophotonic devices excel at confining light into intense hot spots of the electromagnetic near fields, creating unprecedented opportunities for light-matter coupling and surface-enhanced sensing. Recently, all-dielectric metasurfaces with ultrasharp resonances enabled by photonic bound states in the continuum have unlocked new functionalities for surface-enhanced biospectroscopy by precisely targeting and reading out molecular absorption signatures of diverse molecular systems. However, BIC-driven molecular spectroscopy has so far focused on endpoint measurements in dry conditions, neglecting the crucial interaction dynamics of biological systems. Here, we combine the advantages of pixelated all-dielectric metasurfaces with deep learning-enabled feature extraction and prediction to realize an integrated optofluidic platform for time-resolved in-situ biospectroscopy. Our approach harnesses high-Q metasurfaces specifically designed for operation in a lossy aqueous environment together with advanced spectral sampling techniques to temporally resolve the dynamic behavior of photoswitchable lipid membranes. Enabled by a software convolutional neural network, we further demonstrate the real-time classification of the characteristic cis and trans membrane conformations with 98% accuracy. Our synergistic sensing platform incorporating metasurfaces, optofluidics, and deep learning opens exciting possibilities for studying multi-molecular biological systems, ranging from the behavior of transmembrane proteins to the dynamic processes associated with cellular communication., Comment: 22 pages, 5 Figures

Surface-enhanced spectroscopy techniques are the method-of-choice to characterize adsorbed intermediates occurring during electrochemical reactions, which are crucial in realizing a green sustainable future. Characterizing species with low coverages or short lifetimes have so far been limited by low signal enhancement. Recently, metasurface-driven surface-enhanced infrared absorption spectroscopy (SEIRAS) has been pioneered as a promising narrowband technology to study single vibrational modes of electrochemical interfaces during CO oxidation. However, many reactions involve several species or configurations of adsorption that need to be monitored simultaneously requiring reproducible and broadband sensing platforms to provide a clear understanding of the underlying electrochemical processes. Here, we experimentally realize multi-band metasurface-driven SEIRAS for the in-situ study of electrochemical CO2 reduction on a Pt surface. We develop an easily reproducible and spectrally-tunable platinum nano-slot metasurface. Two CO adsorption configurations at 2030 cm-1 and 1840 cm-1 are locally enhanced as a proof of concept that can be extended to more vibrational bands. Our platform provides a 41-fold enhancement in the detection of characteristic absorption signals compared to conventional broadband electrochemically roughened platinum films. A straightforward methodology is outlined starting by baselining our system in CO saturated environment and clearly detecting both configurations of adsorption, in particular the hitherto hardly detectable CO bridge configuration. Then, thanks to the signal enhancement provided by our platform, we find that the CO bridge configuration on platinum does not play a significant role during CO2 reduction in an alkaline environment. We anticipate that our technology will guide researchers in developing similar sensing platforms., Comment: 21 pages, 4 figures

Van der Waals (vdW) materials, including hexagonal boron nitride (hBN), are layered crystalline solids with appealing properties for investigating light-matter interactions at the nanoscale. hBN has emerged as a versatile building block for nanophotonic structures, and the recent identification of native optically addressable spin defects has opened up exciting possibilities in quantum technologies. However, these defects exhibit relatively low quantum efficiencies and a broad emission spectrum, limiting potential applications. Optical metasurfaces present a novel approach to boost light emission efficiency, offering remarkable control over light-matter coupling at the sub-wavelength regime. Here, we propose and realise a monolithic scalable integration between intrinsic spin defects in hBN metasurfaces and high quality (Q) factor resonances leveraging quasi-bound states in the continuum (qBICs). Coupling between spin defect ensembles and qBIC resonances delivers a 25-fold increase in photoluminescence intensity, accompanied by spectral narrowing to below 4 nm linewidth facilitated by Q factors exceeding $10^2$. Our findings demonstrate a new class of spin based metasurfaces and pave the way towards vdW-based nanophotonic devices with enhanced efficiency and sensitivity for quantum applications in imaging, sensing, and light emission., Comment: accepted version

Bound states in the continuum (BICs) are localized electromagnetic modes within the continuous spectrum of radiating waves. Due to their infinite lifetimes without radiation losses, BICs are driving research directions in lasing, non-linear optical processes, and sensing. However, conventional methods for converting BICs into leaky resonances, or quasi-BICs, with high-quality factors typically rely on breaking the in-plane inversion symmetry of the metasurface and often result in resonances that are strongly dependent on the angle of the incident light, making them unsuitable for many practical applications. Here, we numerically analyze and experimentally demonstrate an emerging class of BIC-driven metasurfaces, where the coupling to the far field is controlled by the displacement of individual resonators. In particular, we investigate both all-dielectric and metallic as well as positive and inverse displacement-mediated metasurfaces sustaining angular-robust quasi-BICs in the mid-infrared spectral region. We explore their behavior with changes in the incidence angle of illumination and experimentally show their superior performance compared to two conventional alternatives: silicon-based tilted ellipses and cylindrical nanoholes in gold. We anticipate our findings to open exciting perspectives for bio-sensing, conformal optical devices, and photonic devices using focused light., Comment: 27 pages, 7 figures, 1 table

Active metasurfaces provide unique advantages for on-demand light manipulation at a subwavelength scale for emerging applications of 3D displays, augmented/virtual reality (AR/VR) glasses, holographic projectors and light detection and ranging (LiDAR). These applications put stringent requirements on switching speed, cycling duration, controllability over intermediate states, modulation contrast, optical efficiency and operation voltages. However, previous demonstrations focus only on particular subsets of these key performance requirements for device implementation, while the other performance metrics have remained too low for any practical use. Here, we demonstrate an active Huygens' metasurface based on in-situ grown conductive polymer with holistic switching performance, including switching speed of 60 frames per second (fps), switching duration of more than 2000 switching cycles without noticeable degradation, hysteresis-free controllability over intermediate states, modulation contrast of over 1400%, optical efficiency of 28% and operation voltage range within 1 V. Our active metasurface design meets all foundational requirements for display applications and can be readily incorporated into other metasurface concepts to deliver high-reliability electrical control over its optical response, paving the way for compact and robust electro-optic metadevices., Comment: Main text and supplementary information, 36 pages, 4 manuscript Figures + 8 supplementary Figures

Electrocatalysis plays a crucial role in realizing the transition towards green energy, driving research directions from hydrogen generation to carbon dioxide reduction. Understanding electrochemical reactions is crucial to improve their efficiency and to bridge the gap toward a sustainable zero-carbon future. Surface-enhanced infrared absorption spectroscopy (SEIRAS) is a suitable method for investigating these processes because it can monitor with chemical specificity the mechanisms of the reactions. However, it remains difficult to detect many relevant aspects of electrochemical reactions such as short-lived intermediates. Here, we develop and experimentally realize an integrated nanophotonic-electrochemical SEIRAS platform for the in situ investigation of molecular signal traces emerging during electrochemical experiments. Specifically, we implement a platinum nano-slot metasurface featuring strongly enhanced electromagnetic near fields and spectrally target it at the weak vibrational bending mode of adsorbed CO at ~2033 cm-1. Crucially, our platinum nano-slot metasurface provides high molecular sensitivity. The resonances can be tuned over a broad range in the mid-infrared spectrum. Compared to conventional unstructured platinum layers, our nanophotonic-electrochemical platform delivers a substantial improvement of the experimentally detected characteristic absorption signals by a factor of 27, enabling the detection of new species with weak signals, fast conversions, or low surface concentrations. By providing a deeper understanding of catalytic reactions, we anticipate our nanophotonic-electrochemical platform to open exciting perspectives for electrochemical SEIRAS, surface-enhanced Raman spectroscopy, and the study of reactions in other fields of chemistry such as photoelectrocatalysis., Comment: Main text and supporting information, 28 pages, 4 figures + 1 supporting figure

Tailoring critical light-matter coupling is a fundamental challenge of nanophotonics, impacting diverse fields from higher harmonic generation and energy conversion to surface-enhanced spectroscopy. Plasmonic perfect absorbers (PAs), where resonant antennas couple to their mirror images in adjacent metal films, have been instrumental for obtaining different coupling regimes by tuning the antenna-film distance. However, for on-chip uses, the ideal PA gap size can only match one wavelength, and wide range multispectral approaches remain challenging. Here, we introduce a new paradigm for plasmonic PAs by combining mirror-coupled resonances with the unique loss engineering capabilities of plasmonic bound states in the continuum (BICs). Our BIC-driven PA platform leverages the asymmetry of the constituent meta-atoms as an additional degree of freedom for reaching the critical coupling (CC) condition, delivering resonances with unity absorbance and high quality factors approaching 100 in the mid-infrared. Such a platform holds flexible tuning knobs including asymmetry parameter, dielectric gap, and geometrical scaling factor to precisely control the coupling condition, resonance frequency, and selective enhancement of magnetic and electric fields while maintaining CC. We demonstrate a pixelated PA metasurface with optimal absorption over a broad range of mid-infrared frequencies (950 ~ 2000 1/cm) using only a single spacer layer thickness and apply it for multispectral surface-enhanced molecular spectroscopy in tailored coupling regimes. Our concept greatly expands the capabilities and flexibility of traditional gap-tuned PAs, opening new perspectives for miniaturized sensing platforms towards on-chip and in-situ detection., Comment: Main text and supporting information, 31 pages, 5 Figures manuscript + 11 Supporting Figures

Broken symmetries lie at the heart of nontrivial physical phenomena. Breaking the in-plane geometrical symmetry of optical systems allows to access a set of electromagnetic states termed symmetry-protected quasi-bound states in the continuum (qBICs). Here we demonstrate, theoretically, numerically and experimentally, that such optical states can also be accessed in metasurfaces by breaking the in-plane symmetry in the permittivity of the comprising materials, showing a remarkable equivalence to their geometrically-asymmetric counterparts. However, while the physical size of atoms imposes a limit on the lowest achievable geometrical asymmetry, weak permittivity modulations due to carrier doping and electro-optical Pockels and Kerr effects, usually considered insignificant, open up the possibility of infinitesimal permittivity asymmetries for on-demand, and dynamically tuneable optical resonances of extremely high quality factors. We probe the excitation of permittivity-asymmetric qBICs (${\varepsilon}$-qBICs) using a prototype Si/TiO$_{2}$ metasurface, in which the asymmetry in the unit cell is provided by the refractive index contrast of the dissimilar materials, surpassing any unwanted asymmetries from nanofabrication defects or angular deviations of light from normal incidence. ${\varepsilon}$-qBICs can also be excited in 1D gratings, where quality-factor enhancement and tailored interference phenomena via the interplay of geometrical and permittivity asymmetries are numerically demonstrated. The emergence of ${\varepsilon}$-qBICs in systems with broken symmetries in their permittivity may enable to test time-energy uncertainties in quantum mechanics, and lead to a whole new class of low-footprint optical and optoelectronic devices, from arbitrarily narrow filters and topological sources, biosensing and ultrastrong light-matter interaction platforms, to tuneable optical switches., Comment: Manuscript and Supplementary Information, 27 pages, 4 Figures manuscript + 4 Supplementary Figures

All-dielectric optical metasurfaces with high quality (Q) factors have so far been hampered by the lack of simultaneously lossless and high refractive index (RI) materials over the full visible spectrum. To achieve broad spectral coverage, the use of low-index materials is, in fact, unavoidable due to the inverse correlation between the band-gap energy (and therefore the optical losses) and the RI. However, for Mie resonant photonics, smaller RIs are associated with reduced Q factors and mode volume confinement. In this work, we leverage symmetry-broken bound states in the continuum (BICs) to efficiently suppress radiation losses from the low-index (n~2) van der Waals material hexagonal boron nitride (hBN), realizing metasurfaces with high-Q resonances over the complete visible spectrum. In particular, we analyze the rational use of low and high RI materials as resonator components and harness our insights to experimentally demonstrate sharp BIC resonances with Q factors above 300, spanning wavelengths between 400 nm and 1000 nm from a single hBN flake. Moreover, we utilize the enhanced electric near-fields to demonstrate second harmonic generation (SHG) with enhancement factors above 102. Our results provide a theoretical and experimental framework for the implementation of low RI materials as photonic media for metaoptics., Comment: Main text and supporting information, 23 pages, 4 Figures manuscript + 4 Supporting Figures

The realization of lossless metasurfaces with true chirality crucially requires the fabrication of three-dimensional structures, constraining their feasibility for experiments and hampering practical implementations. Even though the three-dimensional assembly of metallic nanostructures has been demonstrated previously, the resulting plasmonic resonances suffer from high intrinsic and radiative losses. The concept of photonic bound states in the continuum (BICs) is instrumental for tailoring radiative losses in diverse geometries, especially when implemented using lossless dielectrics, but applications have so far been limited to planar and intrinsically achiral structures. Here, we introduce a novel nanofabrication approach to unlock the height of generally flat all-dielectric metasurfaces as an accessible parameter for efficient resonance and functionality control. In particular, we realize out-of-plane symmetry breaking in quasi-BIC metasurfaces and leverage this design degree of freedom to demonstrate, for the first time, an optical all-dielectric quasi-BIC metasurface with maximum intrinsic chirality that responds selectively to light of a particular circular polarization depending on the structural handedness. Our experimental results not only open a new paradigm for all-dielectric BICs and chiral nanophotonics but also promise advances in the realization of efficient generation of optical angular momentum, holographic metasurfaces, and parity-time symmetry-broken optical systems., Comment: Main text and supporting information, 35 pages, 3 Figures manuscript + 13 Supporting Figures

Photonic bound states in the continuum (BICs) are a standout nanophotonic platform for strong light-matter coupling with transition metal dichalcogenides (TMDCs), but have so far mostly been employed as all-dielectric metasurfaces with adjacent TMDC layers, incurring limitations related to strain, mode overlap, and material integration. In this work, we experimentally demonstrate for the first time asymmetry-dependent BIC resonances in 2D arrays of monolithic metasurfaces composed solely of the nanostructured bulk TMDC WS$_2$ with BIC modes exhibiting sharp and tailored linewidths, ideal for selectively enhancing light-matter interactions. Geometrical variation enables the tuning of the BIC resonances across the exciton resonance in bulk WS$_2$, revealing the strong-coupling regime with an anti-crossing pattern and a Rabi splitting of 116 meV. The precise control over the radiative loss channel provided by the BIC concept is harnessed to tailor the Rabi splitting via a geometrical asymmetry parameter of the metasurface. Crucially, the coupling strength itself can be controlled and is shown to be independent of material-intrinsic losses. Our BIC-driven monolithic metasurface platform can readily incorporate other TMDCs or excitonic materials to deliver previously unavailable fundamental insights and practical device concepts for polaritonic applications., Comment: Main text and supporting information, 31 pages, 4 Figures manuscript + 8 Supporting Figures

Plasmon resonances play a pivotal role in enhancing light-matter interactions in nanophotonics, but their low-quality factors have hindered applications demanding high spectral selectivity. Even though symmetry-protected bound states in the continuum with high-quality factors have been realized in dielectric metasurfaces, impinging light is not efficiently coupled to the resonant metasurfaces and is lost in the form of reflection due to low intrinsic losses. Here, we demonstrate a novel design and 3D laser nanoprinting of plasmonic nanofin metasurfaces, which support symmetry-protected bound states in the continuum up to 4th order. By breaking the nanofins out-of-plane symmetry in parameter space, we achieve high-quality factor (up to 180) modes under normal incidence. We reveal that the out-of-plane symmetry breaking can be fine-tuned by the triangle angle of the 3D nanofin meta-atoms, opening a pathway to precisely control the ratio of radiative to intrinsic losses. This enables access to the under-, critical-, and over-coupled regimes, which we exploit for pixelated molecular sensing. Depending on the coupling regime we observe negative, no, or positive modulation induced by the analyte, unveiling the undeniable importance of tailoring light-matter interaction. Our demonstration provides a novel metasurface platform for enhanced light-matter interaction with a wide range of applications in optical sensing, energy conversion, nonlinear photonics, surface-enhanced spectroscopy, and quantum optics., Comment: 33 pages, 4 figures, 9 supplementary figures

All-dielectric nanophotonics underpinned by the physics of bound states in the continuum (BICs) have demonstrated breakthrough applications in nanoscale light manipulation, frequency conversion and optical sensing. Leading BIC implementations range from isolated nanoantennas with localized electromagnetic fields to symmetry-protected metasurfaces with controllable resonance quality (Q) factors. However, they either require structured light illumination with complex beam-shaping optics or large, fabrication-intense arrays of polarization-sensitive unit cells, hindering tailored nanophotonic applications and on-chip integration. Here, we introduce radial quasi bound states in the continuum (radial BICs) as a new class of radially distributed electromagnetic modes controlled by structural asymmetry in a ring of dielectric rod pair resonators. The radial BIC platform provides polarization-invariant and tunable high-Q resonances with strongly enhanced near fields in an ultracompact footprint as low as 2 $\mu$m$^2$. We demonstrate radial BIC realizations in the visible for sensitive biomolecular detection and enhanced second-harmonic generation from monolayers of transition metal dichalcogenides, opening new perspectives for compact, spectrally selective, and polarization-invariant metadevices for multi-functional light-matter coupling, multiplexed sensing, and high-density on-chip photonics., Comment: Accepted version and supporting information, 4 Figures manuscript + 14 Supporting Figures

Dielectric metasurfaces supporting quasi-bound states in the continuum (quasi-BICs) exhibit very high quality factor resonances and electric field confinement. However, accessing the high-Q end of the quasi-BIC regime usually requires marginally distorting the metasurface design from a BIC condition, pushing the needed nanoscale fabrication precision to the limit. This work introduces a novel concept for generating high-Q quasi-BICs, which strongly relaxes this requirement by incorporating a relatively large perturbative element close to high-symmetry points of an undistorted BIC metasurface, acting as a coupler to the radiation continuum. We validate this approach by adding a $\sim$100 nm diameter cylinder between two reflection-symmetry points separated by a 300 nm gap in an elliptical disk metasurface unit cell, using gallium phosphide as the dielectric. We find that high-Q resonances emerge when the cylindrical coupler is placed at any position between such symmetry points. We further explore this metasurface's second harmonic generation capability in the optical range. Displacing the coupler as much as a full diameter from a BIC condition produces record-breaking normalized conversion efficiencies >10$^{2}$ W$^{-1}$. The strategy of enclosing a disruptive element between multiple high-symmetry points in a BIC metasurface could be applied to construct robust high-Q quasi-BICs in many geometrical designs., Comment: 21 pages, 8 figures