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Register a new userUltimate Phase Sensitivity in Surface Plasmon Resonance Sensors by Tuning Critical Coupling with Phase Change Materials
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Plasmonic sensing is an established technology for real-time biomedical diagnostics and air-quality monitoring. While intensity and wavelength tracking are the most commonly used interrogation methods for Surface Plasmon Resonance (SPR), several works indicate the potential superiority of phase interrogation in detection sensitivity. Here, we theoretically and numerically establish the link between ultra-high sensitivities in phase interrogation SPR sensors and the critical coupling condition. However, reaching this condition requires a technically infeasible angstrom-level precision in the metal layer thickness. We propose a robust solution to overcome this limitation by coupling the SPR with a phase-change material (PCM) thin film. By exploiting the multilevel reconfigurable phase states of PCM, we theoretically demonstrate ultra-high phase sensitivities with a limit of detection as low as $10^{-10}$ refractive index unit (RIU). Such a PCM-assisted SPR sensor platform paves the way for unprecedented sensitivity sensors for the detection of trace amounts of low molecular weight species in biomedical sensing and environmental monitoring.
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Structural colors generated due to light scattering from static all-dielectric metasurfaces have successfully enabled high-resolution, high-saturation and wide-gamut color printing applications. Despite recent advances, most demonstrations of these structure-dependent colors lack post-fabrication tunability that hinders their applicability for front-end dynamic display technologies. Phase-change materials (PCMs), with significant contrast of their optical properties between their amorphous and crystalline states, have demonstrated promising potentials in reconfigurable nanophotonics. Herein, we leverage a tunable all-dielectric reflective metasurface made of a newly emerged class of low-loss optical PCMs with superb characteristics, i.e., antimony trisulphide (Sb$_2$S$_3$), antimony triselenide (Sb$_2$Se$_3$), and binary germanium-doped selenide (GeSe$_3$), to realize switchable, high-saturation, high-efficiency and high-resolution structural colors. Having polarization sensitive building blocks, the presented metasurface can generate two different colors when illuminated by two orthogonally polarized incident beams. Such degrees of freedom (i.e., structural state and polarization) enable a single reconfigurable metasurface with fixed geometrical parameters to generate four distinct wide-gamut colors suitable for a wide range of applications, including tunable full-color printing and displays, information encryption, and anti-counterfeiting.
We propose a nonvolatile, reconfigurable, and narrowband mid-infrared bandpass filter based on surface lattice resonance in phase-change material Ge2Sb2Te5 (GST). The proposed filter is composed of a two-dimensional gold nanorod array embedded in a thick GST film. Results show that when GST transits from the amorphous state to the crystalline state, the narrowband reflection spectrum of the proposed filter is tuned from 3.197 {mu}m to 4.795 {mu}m, covering the majority of the mid-infrared regime, the peak reflectance decreases from 72.6% to 25.8%, and the corresponding Q-factor decreases from 19.6 to 10.3. We show that the spectral tuning range can be adjusted by varying the incidence angle or the lattice period. By properly designing the gold nanorod sizes, we also show that the Q-factor can be greatly increased to 70 at the cost of relatively smaller peak reflection efficiencies, and that the peak reflection efficiency can be further increased to 80% at the cost of relatively smaller Q-factors. We expect this work will advance the engineering of GST-based nonvalatile tunable surface lattice resonances and will promote their applications especially in reconfigurable narrowband filters.
The ability to engineer nonlinear optical processes in all-dielectric nanostructures is both of fundamental interest and highly desirable for high-performance, robust, and miniaturized nonlinear optical devices. Herein, we propose a novel paradigm for the efficient tuning of second-harmonic generation (SHG) process in dielectric nanoantennas by integrating with chalcogenide phase change material. In a design with Ge$_{2}$Sb$_{2}$Te$_{5}$ (GST) film sandwiched between the AlGaAs nanoantennas and AlO$_{x}$ substrate, the nonlinear SHG signal from the AlGaAs nanoantennas can be boosted via the resonantly localized field induced by the optically-induced Mie-type resonances, and further modulated by exploiting the GST amorphous-to-crystalline phase change in a non-volatile, multi-level manner. The tuning strategy originates from the modulation of resonant conditions by changes in the refractive index of GST. With a thorough examination of tuning performances for different nanoantenna radii, a maximum modulation depth as high as 540$%$ is numerically demonstrated. This work not only reveals out the potential of GST in optical nonlinearity control, but also provides promising strategy in smart designing tunable and reconfigurable nonlinear optical devices, e.g., light emitters, modulators, and sensors.
The functionalities of a wide range of optical and opto-electronic devices are based on resonance effects and active tuning of the amplitude and wavelength response is often essential. Plasmonic nanostructures are an efficient way to create optical resonances, a prominent example is the extraordinary optical transmission (EOT) through arrays of nanoholes patterned in a metallic film. Tuning of resonances by heating, applying electrical or optical signals has proven to be more elusive, due to the lack of materials that can induce modulation over a broad spectral range and/or at high speeds. Here we show that nanopatterned metals combined with phase change materials (PCMs) can overcome this limitation due to the large change in optical constants which can be induced thermally or on an ultrafast timescale. We demonstrate resonance wavelength shifts as large as 385 nm - an order of magnitude higher than previously reported - by combining properly designed Au EOT nanostructures with Ge2Sb2Te5 (GST). Moreover, we show, through pump probe measurements, repeatable and reversible, large amplitude modulations in the resonances, especially at telecommunication wavelengths, over ps time scales and at powers far below those needed to produce a permanent phase transition. Our findings open a pathway to the design of hybrid metal PCM nanostructures with ultrafast and widely tuneable resonance responses, which hold potential impact on active nanophotonic devices such as tuneable optical filters, smart windows, biosensors and reconfigurable memories.
Since the invention of the laser, adoption of new gain media and device architectures has provided solutions to a variety of applications requiring specific power, size, spectral, spatial, and temporal tunability. Here we introduce a fundamentally new type of tunable semiconductor laser based on a phase-change perovskite metasurface that acts simultaneously as gain medium and optical cavity. As a proof of principle demonstration, we fabricate a subwavelength-thin perovskite metasurface supporting bound states in the continuum (BICs). Upon the perovskite structural phase transitions, both its refractive index and gain vary substantially, inducing fast (1.35 nm/K rate) and broad spectral tunability (>15 nm in the near-infrared), deterministic spatial mode hopping between polarization vortexes, and hysteretic optical bistability of the microlaser. These features highlight the uniqueness of phase-change perovskite tunable lasers, which may find wide applications in compact and low-cost optical multiplexers, sensors, memories, and LIDARs.
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