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Structural coloration takes inspiration from the bright hues found in nature to control the reflection and transmission of light from artificially structured materials. Combining them with active electrical tuning heralds breakthrough applications in optical displays.

Metasurfaces based on resonant subwavelength photonic structures enable novel ways of wavefront control and light focusing, underpinning a new generation of flat-optics devices1. Recently emerged all-dielectric asymmetric metasurfaces, composed of arrays of metaunits with broken in-plane inversion symmetry2–7, exhibit high-quality resonances originating from the intriguing physics of bound states in the continuum. Here, we combine dielectric metasurfaces and hyperspectral imaging to develop an ultrasensitive label-free analytical platform for biosensing. Our technique can acquire spatially resolved spectra from millions of image pixels and use smart data-processing tools to extract high-throughput digital sensing information at the unprecedented level of less than three molecules per μm2. We further show spectral data retrieval from a single image without using spectrometers, enabled by our unique sensor design, paving the way for portable diagnostic applications. This combination of nanophotonics and imaging optics extends the capabilities of dielectric metasurfaces to analyse biological entities and atomic-layer-thick two-dimensional materials over large areas.Spatially resolved spectra from millions of pixels and information extraction from three molecules per μm2 is now possible using dielectric metasurfaces.

Although mid-infrared (mid-IR) spectroscopy is a mainstay of molecular fingerprinting, its sensitivity is diminished somewhat when looking at small volumes of sample. Nanophotonics provides a platform to enhance the detection capability. Tittl et al. built a mid-IR nanophotonic sensor based on reflection from an all-dielectric metasurface array of specially designed scattering elements. The scattering elements could be tuned via geometry across a broad range of wavelengths in the mid-IR. The approach successfully detected and differentiated the absorption fingerprints of various molecules. The technique offers the prospect of on-chip molecular fingerprinting without the need for spectrometry, frequency scanning, or moving mechanical parts. Science , this issue p. 1105 A pixelated dielectric metasurface is used for the mid-infrared detection of molecular fingerprints. Metasurfaces provide opportunities for wavefront control, flat optics, and subwavelength light focusing. We developed an imaging-based nanophotonic method for detecting mid-infrared molecular fingerprints and implemented it for the chemical identification and compositional analysis of surface-bound analytes. Our technique features a two-dimensional pixelated dielectric metasurface with a range of ultrasharp resonances, each tuned to a discrete frequency; this enables molecular absorption signatures to be read out at multiple spectral points, and the resulting information is then translated into a barcode-like spatial absorption map for imaging. The signatures of biological, polymer, and pesticide molecules can be detected with high sensitivity, covering applications such as biosensing and environmental monitoring. Our chemically specific technique can resolve absorption fingerprints without the need for spectrometry, frequency scanning, or moving mechanical parts, thereby paving the way toward sensitive and versatile miniaturized mid-infrared spectroscopy devices.

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 µm 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. In their work on radial BICs, the authors realize a nanophotonic platform with high resonance Q factors and drastically reduced spatial footprint ideally suited for enhanced on-chip biomolecular sensing and nonlinear light generation.

Achieving precise spectral and temporal light manipulation at the nanoscale remains a critical challenge in nanophotonics. While photonic bound states in the continuum (BICs) have emerged as a powerful means of controlling light, their reliance on geometrical symmetry breaking for obtaining tailored resonances makes them highly susceptible to fabrication imperfections, and their generally fixed asymmetry factor fundamentally limits applications in reconfigurable metasurfaces. 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 (ε- q BICs) without altering the underlying resonator geometry and unlocking an additional degree of freedom for light manipulation through active tuning of the surrounding dielectric environment. We demonstrate this concept by integrating polyaniline (PANI), an electro-optically active polymer, to achieve electrically reconfigurable ε- q BICs. This integration not only demonstrates rapid switching speeds and exceptional durability but also 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. Achieving precise spectral and temporal light manipulation at the nanoscale remains a challenge. Here, authors develop the concept of permittivity-asymmetric bound states in the continuum metasurfaces, achieving fast electrical switching performance by integrating the polyaniline.

A multitude of biological processes are enabled by complex interactions between lipid membranes and proteins. To understand such dynamic processes, it is crucial to differentiate the constituent biomolecular species and track their individual time evolution without invasive labels. Here, we present a label-free mid-infrared biosensor capable of distinguishing multiple analytes in heterogeneous biological samples with high sensitivity. Our technology leverages a multi-resonant metasurface to simultaneously enhance the different vibrational fingerprints of multiple biomolecules. By providing up to 1000-fold near-field intensity enhancement over both amide and methylene bands, our sensor resolves the interactions of lipid membranes with different polypeptides in real time. Significantly, we demonstrate that our label-free chemically specific sensor can analyze peptide-induced neurotransmitter cargo release from synaptic vesicle mimics. Our sensor opens up exciting possibilities for gaining new insights into biological processes such as signaling or transport in basic research as well as provides a valuable toolkit for bioanalytical and pharmaceutical applications. Complex protein-lipid interactions are difficult to study in real-time without labels. Here, Rodrigo et al . introduce a multimodal plasmonic infrared biosensor to simultaneously distinguish multiple analytes with high sensitivity.

The realization of lossless metasurfaces with true chirality crucially requires the fabrication of three-dimensional structures, constraining experimental feasibility 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 structures. Here, we introduce a novel nanofabrication approach to unlock the height of individual resonators within all-dielectric metasurfaces as an accessible parameter for the efficient control of resonance features and nanophotonic functionalities. In particular, we realize out-of-plane symmetry breaking in quasi-BIC metasurfaces and leverage this design degree of freedom to demonstrate 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. We unlock the height as accessible parameter of all-dielectric metasurfaces, allowing polarization-selective interaction of their high-Q eigenstates with light of different helicity and promoting ultra-narrow maximally chiral optical resonances.

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, exceeding 10 2 , leveraging quasi-bound states in the continuum (qBICs). Coupling between defect ensembles and qBIC resonances delivers a 25-fold increase in photoluminescence intensity, accompanied by spectral narrowing to below 4 nm linewidth and increased narrowband spin-readout efficiency. Our findings demonstrate a new class of metasurfaces for spin-defect-based technologies and pave the way towards vdW-based nanophotonic devices with enhanced efficiency and sensitivity for quantum applications in imaging, sensing, and light emission. Previous research reported enhanced emission from spin defects in hBN by coupling to optical resonators; however, this approach has limited scalability. Here the authors use a monolithic metasurface featuring quasi bound states fabricated from hBN to enhance photoemission and optical spin-readout efficiency of defects in the same material.

All-dielectric metasurfaces supporting photonic bound states in the continuum (BICs) are an exciting toolkit for achieving resonances with ultranarrow linewidths. However, the transition from theory to experimental realization can significantly reduce the optical performance of BIC-based nanophotonic systems, severely limiting their application potential. Here, we introduce a combined numerical/experimental methodology for predicting how unavoidable tolerances in nanofabrication such as random geometrical variations affect the performance of different BIC metasurface designs. We compare several established all-dielectric BIC unit cell geometries with broken in-plane inversion symmetry including tilted ellipses, asymmetric double rods, and split rings. Significantly, even for low fabrication-induced geometrical changes, both the BIC resonance amplitude and its quality factor (Q-factor) are significantly reduced. We find that the all-dielectric ellipses maintain the highest Q-factors throughout the geometrical variation range, whereas the rod and split ring geometries fall off more quickly. The same behavior is confirmed experimentally, where geometrical variation values are derived from automated processing of sets of scanning electron microscopy (SEM) images. Our methodology provides crucial insights into the performance degradation of BIC metasurfaces when moving from simulations to fabricated samples and will enable the development of robust, high-Q, and easy to manufacture nanophotonic platforms for applications ranging from biomolecular sensing to higher harmonic generation.

Bound states in the continuum (BICs) provide exceptional light confinement due to their inherent decoupling from radiative channels. Small symmetry breaking transforms BIC into quasi-BIC (qBIC) that couples to free-space radiation enabling ultra-high-quality-factor (Q-factor) resonances desirable for refractive index (RI) sensing. In practical implementations, geometric asymmetry is typically employed. However, since the radiative loss remains fixed once fabricated, such metasurfaces exhibit only a horizontal shift of the resonance spectrum in RI sensing, without modification of its overall shape. Here, we demonstrate a permittivity-asymmetric qBIC (ε-qBIC) metasurface, which encodes environmental refractive index variations directly into the asymmetry factor, resulting in an index response involving both resonance wavelength shift and modulation variation. In addition to exhibiting a competitive transmittance sensitivity of ∼5,300 %/RIU under single-wavelength conditions, the -qBIC design provides a substantially improved linear response. Specifically, the linear window area of its sensing data distribution, calculated as the integrated wavelength region where the linearity parameter remains above the preset threshold, is 104 times larger than that of the geometry-asymmetric qBIC (g-qBIC), enabling more robust and reliable single-wavelength signal readout. Additionally, numerical results reveal that environmental permittivity asymmetry can optically restore the g-qBIC to a state with ultra-high-Q (over 10 ), approaching the BIC condition. Unlike traditional BICs, which are typically inaccessible once perturbed, the permittivity-restored BIC becomes accessible through environmental perturbations. These findings suggest an alternative design strategy for developing high-performance photonic devices for practical sensing applications.