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Optical metasurfaces are regular quasi-planar nanopatterns that can apply diverse spatial and spectral transformations to light waves. However, metasurfaces are no longer adjustable after fabrication, and a critical challenge is to realise a technique of tuning their optical properties that is both fast and efficient. We experimentally realise an ultrafast tunable metasurface consisting of subwavelength gallium arsenide nanoparticles supporting Mie-type resonances in the near infrared. Using transient reflectance spectroscopy, we demonstrate a picosecond-scale absolute reflectance modulation of up to 0.35 at the magnetic dipole resonance of the metasurfaces and a spectral shift of the resonance by 30 nm, both achieved at unprecedentedly low pump fluences of less than 400 μJ cm –2 . Our findings thereby enable a versatile tool for ultrafast and efficient control of light using light. Metasurfaces are not adjustable after fabrication, and a critical challenge is to realise a technique of tuning their optical properties that is both fast and efficient. Here, Shcherbakov et al. realise an ultrafast tunable metasurface with picosecond-scale large absolute reflectance modulation at low pump fluences.

Entangled photon-pair sources are at the core of quantum applications like quantum key distribution, sensing, and imaging. Operation in space-limited and adverse environments such as in satellite-based and mobile communication requires robust entanglement sources with minimal size and weight requirements. Here, we meet this challenge by realizing a cubic micrometer scale entangled photon-pair source in a 3R-stacked transition metal dichalcogenide crystal. Its crystal symmetry enables the generation of polarization-entangled Bell states without additional components and provides tunability by simple control of the pump polarization. Remarkably, generation rate and state tuning are decoupled, leading to equal generation efficiency and no loss of entanglement. Combining transition metal dichalcogenides with monolithic cavities and integrated photonic circuitry or using quasi-phasematching opens the gate towards ultrasmall and scalable quantum devices. Spontaneous parametric down-conversion in thin films should allow to realise extremely compact entangled photon sources. Here, the authors generate entangled photon pairs from a 3R-MoS2 flake, characterize them via quantum state tomography, and show how to tune between different Bell state outputs by changing the pump polarization.

Microscopy with extreme ultraviolet (EUV) radiation holds promise for high-resolution imaging with excellent material contrast, due to the short wavelength and numerous element-specific absorption edges available in this spectral range. At the same time, EUV radiation has significantly larger penetration depths than electrons. It thus enables a nano-scale view into complex three-dimensional structures that are important for material science, semiconductor metrology, and next-generation nano-devices. Here, we present high-resolution and material-specific microscopy at 13.5 nm wavelength. We combine a highly stable, high photon-flux, table-top EUV source with an interferometrically stabilized ptychography setup. By utilizing structured EUV illumination, we overcome the limitations of conventional EUV focusing optics and demonstrate high-resolution microscopy at a half-pitch lateral resolution of 16 nm. Moreover, we propose mixed-state orthogonal probe relaxation ptychography, enabling robust phase-contrast imaging over wide fields of view and long acquisition times. In this way, the complex transmission of an integrated circuit is precisely reconstructed, allowing for the classification of the material composition of mesoscopic semiconductor systems.The combination of a state-of-the-art high harmonic source, structured EUV light, and advanced ptychography reconstruction algorithms enables material-specific high-contrast and high-resolution imaging on the nanoscale.

We experimentally demonstrate frequency non-degenerate photon-pair generation via spontaneous four-wave mixing from a novel CS 2 -filled microstructured optical fiber. CS 2 has high nonlinearity, narrow Raman lines, a broad transmission spectrum, and also has a large index contrast with the microstructured silica fiber. We can achieve phase matching over a large spectral range by tuning the pump wavelength, allowing the generation of idler photons in the infrared region, which is suitable for applications in quantum spectroscopy. Moreover, we demonstrate a coincidence-to-accidental ratio of larger than 90 and a pair generation efficiency of about 10 - 2 per pump pulse, which shows the viability of this fiber-based platform as a photon-pair source for quantum technology applications.

Optical communication can be revolutionized by encoding data into the orbital angular momentum of light beams. However, state-of-the-art approaches for dynamic control of complex optical wavefronts are mainly based on liquid crystal spatial light modulators or miniaturized mirrors, which suffer from intrinsically slow (µs-ms) response times. Here, we experimentally realize a hybrid meta-optical system that enables complex control of the wavefront of light with pulse-duration limited dynamics. Specifically, by combining ultrafast polarization switching in a WSe 2 monolayer with a dielectric metasurface, we demonstrate second harmonic beam deflection and structuring of orbital angular momentum on the femtosecond timescale. Our results pave the way to robust encoding of information for free space optical links, while reaching response times compatible with real-world telecom applications. Enhancing the data encoding into the orbital angular momentum of light beams could enable faster and more efficient optical communications. This work demonstrates complex control of the second harmonic wavefront with dynamics solely limited by the pulse duration.

The valley degree of freedom in atomically thin transition metal dichalcogenides, coupled with valley-contrasting optical selection rules, holds great potential for future electronic and optoelectronic devices. Resonant optical nanostructures emerge as promising tools for controlling this degree of freedom at the nanoscale. However, their impact on the circular polarization of valley-selective emission remains poorly understood. In our study, we explore a hybrid system where valley-specific emission from a molybdenum disulfide monolayer interacts with a resonant plasmonic nanosphere. Contrary to the simple intuition that a centrosymmetric nanoresonator mostly preserves the degree of circular polarization, our cryogenic experiments reveal significant depolarization of the photoluminescence scattered by the nanoparticle. This striking effect presents an ideal platform for studying the mechanisms governing light-matter interactions in such hybrid systems. Our full-wave numerical analysis provides insights into the key physical mechanisms affecting the polarization response, offering a pathway toward designing novel valleytronic devices. The authors investigate spin-valley polarization in hybrid systems of Au nanoparticles and monolayer MoS 2 and observe a nearly complete quenching of the far-field circular polarization state of emission from MoS 2 at the position of the nanoparticle. This highlights the need to consider an ensemble, rather than just a single rotating dipole emitter, for precise predictions of polarization responses in these hybrid systems.

The field of nonlinear optics is a well-established discipline that relies on macroscopic media and employs propagation distances longer than a wavelength of light. Recent progress with electromagnetic metamaterials has allowed for the expansion of this field into new directions of new phenomena and novel functionalities. In particular, nonlinear effects in thin, artificially structured materials such as metasurfaces do not rely on phase-matching conditions and symmetry-related selection rules of natural materials; they may be substantially enhanced by strong local and collective resonances of fields inside the metasurface nanostructures. Consequently, nonlinear processes may extend beyond simple harmonic generation and spectral broadening due to electronic nonlinearities. This article provides a brief review of basic concepts and recent results in the field of nonlinear optical metasurfaces.

All-optical tunability of semiconductor metasurfaces offers unique opportunities for novel time-varying effects, including frequency conversion and light trapping. However, the all-optical processes often induce optical absorption that fundamentally limits the possible dynamic increase of their quality factor (Q-boosting). Here, we propose and numerically demonstrate the concept of large Q-boosting in a single-material metasurface by dynamically reducing its structural anisotropy on a femtosecond timescale. This balance is achieved by excitation with a structured pump and takes advantage of the band-filling effect in a GaAs direct-bandgap semiconductor to eliminate the free-carrier-induced loss. We show that this approach allows a dynamic boosting of the resonance quality factor over orders of magnitude, only limited by the free-carrier relaxation processes. The proposed approach offers complete dynamic control over the resonance bandwidth and opens applications in frequency conversion and light trapping.

Nonlinear metasurfaces have recently been established as a new platform for generating photon pairs via spontaneous parametric down-conversion. While for classical harmonic generation in metasurfaces a high level of control over all degrees of freedom of light has been reached, this capability is yet to be developed for photon-pair generation. In this work, we theoretically and experimentally demonstrate for the first time precise control of the emission angle of photon pairs generated from a nonlinear metasurface. Our measurements show angularly tunable pair generation with high coincidence-to-accidental ratio for both co- and counterpropagating emission. The underlying principle is the transverse phase matching of guided-mode resonances with strong angular dispersion in a nonlinear metasurface consisting of a silicon dioxide grating on a nonlinear lithium niobate guiding layer. We provide a straightforward design strategy for photon-pair generation in such a device and find very good agreement between the calculations and experimental results. Here, we use all-optical emission angle tuning by means of the pump wavelength; however, the principle could be extended to modulation via the electro-optic effect in lithium niobate. In sum, this work provides an important addition to the toolset of subwavelength thickness photon-pair sources.

Table-top extreme ultraviolet (EUV) microscopy offers unique opportunities for label-free investigation of biological samples. Here, we demonstrate ptychographic EUV imaging of two dried, unstained model specimens: germlings of a fungus ( Aspergillus nidulans ), and bacteria ( Escherichia coli ) cells at 13.5 nm wavelength. We find that the EUV spectral region, which to date has not received much attention for biological imaging, offers sufficient penetration depths for the identification of intracellular features. By implementing a position-correlated ptychography approach, we demonstrate a millimeter-squared field of view enabled by infrared illumination combined with sub-60 nm spatial resolution achieved with EUV illumination on selected regions of interest. The strong element contrast at 13.5 nm wavelength enables the identification of the nanoscale material composition inside the specimens. Our work will advance and facilitate EUV imaging applications and enable further possibilities in life science.