Light, science & applications最新文献

An optical vortex beam has attracted significant attention across diverse applications, including optical manipulation, phase-contrast microscopy, optical communication, and quantum photonics. To utilize vortex generators for integrated photonics, researchers have developed ultra-compact vortex generators using fork gratings, metasurfaces, and integrated microcombs. However, those devices depend on costly, time-consuming nanofabrication and are constrained by the low signal-to-noise ratio due to the fabrication error. As an alternative maneuver, spin-orbit coupling has emerged as a method to obtain the vortex beam by converting spin angular momentum (SAM) without nanostructures. Here, we demonstrate the creation of an optical vortex beam using van der Waals (vdW) materials. The significantly high birefringence of vdW materials allows the generation of optical vortex beams, even with materials of sub-wavelength thickness. In this work, we utilize an 8 µm-thick hexagonal boron nitride (hBN) crystal for the creation of optical vortices carrying topological charges of ±2. We also present the generation of an optical vortex beam in a 320 nm-thick MoS₂ crystal with a conversion efficiency of 0.09. This study paves the way for fabrication-less and ultra-compact optical vortex generators, which can be applied for integrated photonics and large-scale vortex generator arrays.

Combining bright-field and edge-enhanced imaging affords an effective avenue for extracting complex morphological information from objects, which is particularly beneficial for biological imaging. Multiplexing meta-lenses present promising candidates for achieving this functionality. However, current multiplexing meta-lenses lack spectral modulation, and crosstalk between different wavelengths hampers the imaging quality, especially for biological samples requiring precise wavelength specificity. Here, we experimentally demonstrate the nonlocal Huygens' meta-lens for high-quality-factor spin-multiplexing imaging. Quasi-bound states in the continuum (q-BICs) are excited to provide a high quality factor of 90 and incident-angle dependence. The generalized Kerker condition, driven by Fano-like interactions between q-BIC and in-plane Mie resonances, breaks the radiation symmetry, resulting in a transmission peak with a geometric phase for polarization-converted light, while unconverted light exhibits a transmission dip without a geometric phase. Enhanced polarization conversion efficiency of 65% is achieved, accompanied by a minimal unconverted value, surpassing the theoretical limit of traditional thin nonlocal metasurfaces. Leveraging these effects, the output polarization-converted state exhibits an efficient wavelength-selective focusing phase profile. The unconverted counterpart serves as an effective spatial frequency filter based on incident-angular dispersion, passing high-frequency edge details. Bright-field imaging and edge detection are thus presented under two output spin states. This work provides a versatile framework for nonlocal metasurfaces, boosting biomedical imaging and sensing applications.

In recent years, the demand for optical imaging and detection in hypersonic aircraft has been on the rise. The high-temperature and high-pressure compressed flow field near airborne optoelectronic devices creates significant interference with light transmission, known as hypersonic aero-optical effects. This effect has emerged as a key technological challenge, limiting hypersonic optical imaging and detection capabilities. This article focuses on introducing the thermal effects and optical transmission effects of hypersonic aero-optical effects, as along with corresponding suppression techniques. In addition, this article critically reviews and succinctly summarizes the advancements made in hypersonic aero-optical effects testing technology, while also delineating avenues for future research needs in this field. In conclusion, there is an urgent call for further exploration into the study of aero-optical effects under conditions characterized by high Mach, high enthalpy, and high Reynolds number in the future.

This paper demonstrates the novel approach of sub-micron-thick InGaAs broadband photodetectors (PDs) designed for high-resolution imaging from the visible to short-wavelength infrared (SWIR) spectrum. Conventional approaches encounter challenges such as low resolution and crosstalk issues caused by a thick absorption layer (AL). Therefore, we propose a guided-mode resonance (GMR) structure to enhance the quantum efficiency (QE) of the InGaAs PDs in the SWIR region with only sub-micron-thick AL. The TiO_x/Au-based GMR structure compensates for the reduced AL thickness, achieving a remarkably high QE (>70%) from 400 to 1700 nm with only a 0.98 μm AL InGaAs PD (defined as 1 μm AL PD). This represents a reduction in thickness by at least 2.5 times compared to previous results while maintaining a high QE. Furthermore, the rapid transit time is highly expected to result in decreased electrical crosstalk. The effectiveness of the GMR structure is evident in its ability to sustain QE even with a reduced AL thickness, simultaneously enhancing the transit time. This breakthrough offers a viable solution for high-resolution and low-noise broadband image sensors.

The ultimate aim of fluorescence microscopy is to achieve high-resolution imaging of increasingly larger biological samples. Extended depth of field presents a potential solution to accelerate imaging of large samples when compression of information along the optical axis is not detrimental to the interpretation of images. We have implemented an extended depth of field (EDF) approach in a random illumination microscope (RIM). RIM uses multiple speckled illuminations and variance data processing to double the resolution. It is particularly adapted to the imaging of thick samples as it does not require the knowledge of illumination patterns. We demonstrate highly-resolved projective images of biological tissues and cells. Compared to a sequential scan of the imaged volume with conventional 2D-RIM, EDF-RIM allows an order of magnitude improvement in speed and light dose reduction, with comparable resolution. As the axial information is lost in an EDF modality, we propose a method to retrieve the sample topography for samples that are organized in cell sheets.

Conventional hyperspectral cameras cascade lenses and spectrometers to acquire the spectral datacube, which forms the fundamental framework for hyperspectral imaging. However, this cascading framework involves tradeoffs among spectral and imaging performances when the system is driven toward miniaturization. Here, we propose a spectral singlet lens that unifies optical imaging and computational spectrometry functions, enabling the creation of minimalist, miniaturized and high-performance hyperspectral cameras. As a paradigm, we capitalize on planar liquid crystal optics to implement the proposed framework, with each liquid-crystal unit cell acting as both phase modulator and electrically tunable spectral filter. Experiments with various targets show that the resulting millimeter-scale hyperspectral camera exhibits both high spectral fidelity ( > 95%) and high spatial resolutions ( ~1.7 times the diffraction limit). The proposed "two-in-one" framework can resolve the conflicts between spectral and imaging resolutions, which paves a practical pathway for advancing hyperspectral imaging systems toward miniaturization and portable applications.

Pyroelectric (PE) detection technologies have attracted extensive attention due to the cooling-free, bias-free, and broadband properties. However, the PE signals are generated by the continuous energy conversion processes from light, heat, to electricity, normally leading to very slow response speeds. Herein, we design and fabricate a PE detector which shows extremely fast response in near-infrared (NIR) band by combining with the inhomogeneous plasmonic metasurface. The plasmonic effect dramatically accelerates the light-heat conversion process, unprecedentedly improving the NIR response speed by 2-4 orders of magnitude to 22 μs, faster than any reported infrared (IR) PE detector. We also innovatively introduce the concept of time resolution into the field of PE detection, which represents the detector's ability to distinguish multiple fast-moving targets. Furthermore, the spatially inhomogeneous design overcomes the traditional narrowband constraint of plasmonic systems and thus ensures a wideband response from visible to NIR. This study provides a promising approach to develop next-generation IR PE detectors with ultrafast and broadband responses.

In cutting-edge optical technologies, polarization is a key for encoding and transmitting vast information, highlighting the importance of selectively switching and modulating polarized light. Recently, anisotropic two-dimensional materials have emerged for ultrafast switching of polarization-multiplexed optical signals, but face challenges with low polarization ratios and limited spectral ranges. Here, we apply strain to quasi-one-dimensional layered ZrSe₃ to enhance polarization selectivity and tune operational energies in ultrafast all-optical switching. Initially, transient absorption on unstrained ZrSe₃ reveals a sub-picosecond switching response in polarization along a specific crystal axis, attributed to shifting-recovery dynamics of an anisotropic exciton. However, its polarization selectivity is weakened by a slow non-excitonic response in the perpendicular polarization. To overcome this limitation, we apply strain to ZrSe₃ by bending its flexible substrate. The compressive strain spectrally decouples the excitonic and non-excitonic components, doubling the polarization selectivity of the sub-picosecond switching and tripling it compared to that in the tensile-strained ZrSe₃. It also effectively tunes the switching energy at a shift rate of ~93 meV %^-1. This strain-tunable switching is repeatable, reversible, and robustly maintains the sub-picosecond operation. First-principles calculations reveal that the strain control is enabled by momentum- and band-dependent modulations of the electronic band structure, causing opposite shifts in the excitonic and non-excitonic transitions. Our findings offer a novel approach for high-performance, wavelength-tunable, polarization-selective ultrafast optical switching.