Volume 9, Issue 11

We review the recent progress regarding the physics and applications of boron nitride bulk crystals and its epitaxial layers in various fields. First, we highlight its importance from optoelectronics side, for simple devices operating in the deep ultraviolet, in view of sanitary applications. Emphasis will be directed towards the unusually strong efficiency of the exciton–phonon coupling in this indirect band gap semiconductor. Second, we shift towards nanophotonics, for the management of hyper-magnification and of medical imaging. Here, advantage is taken of the efficient coupling of the electromagnetic field with some of its phonons, those interacting with light at 12 and 6 µm in vacuum. Third, we present the different defects that are currently studied for their propensity to behave as single photon emitters, in the perspective to help them becoming challengers of the NV centres in diamond or of the double vacancy in silicon carbide in the field of modern and developing quantum technologies.

Optical metasurfaces, planar subwavelength nanoantenna arrays with the singular ability to sculpt wavefront in almost arbitrary manners, are poised to become a powerful tool enabling compact and high-performance optics with novel functionalities. A particularly intriguing research direction within this field is active metasurfaces, whose optical response can be dynamically tuned postfabrication, thus allowing a plurality of applications unattainable with traditional bulk optics. Designing reconfigurable optics based on active metasurfaces is, however, presented with a unique challenge, since the optical quality of the devices must be optimized at multiple optical states. In this article, we provide a critical review on the active meta-optics design principles and algorithms that are applied across structural hierarchies ranging from single meta-atoms to full meta-optical devices. The discussed approaches are illustrated by specific examples of reconfigurable metasurfaces based on optical phase-change materials.

Cavity optomechanics has recently emerged as a new paradigm enabling the manipulation of mechanical motion via optical fields tightly confined in deformable cavities. When driving an optomechanical (OM) crystal cavity with a laser blue-detuned with respect to the optical resonance, the mechanical motion is amplified, ultimately resulting in phonon lasing at MHz and even GHz frequencies. In this work, we show that a silicon OM crystal cavity performs as an OM microwave oscillator when pumped above the threshold for self-sustained OM oscillations. To this end, we use an OM cavity designed to have a breathing-like mechanical mode at 3.897 GHz in a full phononic bandgap. Our measurements show that the first harmonic of the detected signal displays a phase noise of ≈−100 dBc/Hz at 100 kHz. Stronger blue-detuned driving leads eventually to the formation of an OM frequency comb, whose lines are spaced by the mechanical frequency. We also measure the phase noise for higher-order harmonics and show that, unlike in Brillouin oscillators, the noise is increased as corresponding to classical harmonic mixing. Finally, we present real-time measurements of the comb waveform and show that it can be fitted to a theoretical model recently presented. Our results suggest that silicon OM cavities could be relevant processing elements in microwave photonics and optical RF processing, in particular in disciplines requiring low weight, compactness and fiber interconnection.

We report on the numerical demonstration of enhanced second harmonic generation (SHG) originating from collective resonances in plasmonic nanoparticle arrays. The nonlinear optical response of the metal nanoparticles is modeled by employing a hydrodynamic nonlinear Drude model implemented into Finite-Difference Time-Domain (FDTD) simulations, and effective polarizabilities of nanoparticle multipoles in the lattice are analytically calculated at the fundamental wavelength by using a coupled dipole–quadrupole approximation. Excitation of narrow collective resonances in nanoparticle arrays with electric quadrupole (EQ) and magnetic dipole (MD) resonant coupling leads to strong linear resonance enhancement. In this work, we analyze SHG in the vicinity of the lattice resonance corresponding to different nanoparticle multipoles and explore SHG efficiency by varying the lattice periods. Coupling of electric quadrupole and magnetic dipole in the nanoparticle lattice indicates symmetry breaking and the possibility of enhanced SHG under these conditions. By varying the structure parameters, we can change the strength of electric dipole (ED), EQ, and MD polarizabilities, which can be used to control the linewidth and magnitude of SHG emission in plasmonic lattices. Engineering of lattice resonances and associated magnetic dipole resonant excitations can be used for spectrally narrow nonlinear response as the SHG can be enhanced and controlled by higher multipole excitations and their lattice resonances. We show that both ED and EQ–MD lattice coupling contribute to SHG, but the presence of strong EQ–MD coupling is important for spectrally narrow SHG and, in our structure, excitation of narrow higher-order multipole lattice resonances results in five times enhancement.

Due to small optical mode volumes and linear polarizations of surface-plasmon-polariton (SPP) resonant modes in metallic antennas, it is very difficult to obtain complex emission patterns and polarizations for single-photon emitters. Herein, nonresonant enhancement in a silver nanowire is used to both enhance emission rates and extract a z -oriented dipole, and then the symmetry of metallic nanostructures is proposed to tailor the patterns and polarizations of single-photon emission. The emission pattern of a quantum dot located close to a metallic nanostructure with a symmetric axis is split into multiple flaps. The number of splitting flaps is equal to the order of the symmetric axis. Moreover, the electric vectors of the emitted photons become centrally symmetric about the symmetric axis. The above phenomena are well explained by both a simulation and an image dipole model. The structural-symmetry-tailoring mechanism may open up a new avenue in the design of multifunctional and novel quantum-plasmonic devices.

Ultrathin metal films emerge as an innovative category of transparent electrodes in recent decades, holding great promises enabling the next-generation flexible organic light-emitting devices (OLEDs). Although metal thin films with polymer nucleation inducers have been extensively studied in OLEDs, satisfying the requirements of both superior optoelectrical and high optical outcoupling characteristics is still challenging. Here, we demonstrate a metal oxide/ultrathin Ag/polymer (MAP) composite electrode with low sheet resistance of 15.1 Ω/sq, high transmittance of 87.4% at 550 nm, and smooth morphology with surface roughness of 0.768 nm. Besides, the composite electrodes significantly enhance the outcoupling of the light trapped in OLEDs due to the relatively high-refractive index polymer. Flexible OLEDs with the MAP anodes exhibit over 2.3 times enhancement in efficiency to that of indium tin oxide (ITO)-based OLEDs. The flexible OLEDs can survive 1000 bending cycles at a bending radius of 8 mm with negligible decrease in electroluminescent performance.

Second harmonic generation (SHG) with a material of large transparency is an attractive way of generating coherent light sources at exotic wavelength range such as VUV, UV and visible light. It is of critical importance to improve nonlinear conversion efficiency in order to find practical applications in quantum light source and high resolution nonlinear microscopy, etc. Here an enhanced SHG with conversion efficiency up to 10 −2 % at SH wavelength of 282.7 nm under 11 GW/cm 2 pump intensity via the excitation of anapole in lithium niobite (LiNbO 3 , or LN) nanodisk through the dominating d 33 nonlinear coefficient is investigated. The anapole has advantages of strongly suppressing far-field scattering and well-confined internal field which helps to boost the nonlinear conversion. Anapoles in LN nanodisk is facilitated by high index contrast between LN and substrate with properties of near-zero-index via hyperbolic metamaterial structure design. By tailoring the multi-layers structure of hyperbolic metamaterials, the anapole excitation wavelength can be tuned at different wavelengths. It indicates that an enhanced SHG can be achieved at a wide range of pump light wavelengths via different design of the epsilon-near-zero (ENZ) hyperbolic metamaterials substrates. The proposed nanostructure in this work might hold significances for the enhanced light–matter interactions at the nanoscale such as integrated optics.

The Fano and Rabi models represent remarkably common effects in optics. Here we study the coherent time dynamics of plasmonic systems exhibiting Fano and Rabi spectral responses. We demonstrate that these systems show fundamentally different dynamics. A plasmonic system with a Fano resonance displays at most one temporal beat under pulsed excitation, whereas a plasmonic system in the Rabi-like regime may have any number of beats. Remarkably, the Fano-like systems show time dynamics with very characteristic coherent tails despite the strong decoherence that is intrinsic for such systems. The coherent Fano and Rabi dynamics that we predicted can be observed in plasmonic nanocrystal dimers in time-resolved experiments. Our study demonstrates that such coherent temporal plasmonics includes non-trivial and characteristic relaxation behaviors and presents an interesting direction to develop with further research.

Hydrogen peroxide (H 2 O 2 ) is an important product generated in the body and related to many pathophysiological processes and glucose metabolism disorder can cause many fatal diseases in living bodies. Therefore, the sensing of H 2 O 2 and glucose is of great significance in disease diagnostics and treatment. Fluorescent carbon dots (CDs) are one new class of nanoprobes for H 2 O 2 and glucose. Nevertheless, the CD-based sensor is always based on its fluorescence response, which is influenced by the auto-fluorescent interference. Herein, efficient fluorescent CDs were synthesized by one-pot solvothermal method, and the CDs exhibit bright and persistent deep-red (DR) chemiluminescence (CL) in bis(2,4,6-trichlorophenyl) oxalate and H 2 O 2 solution with a CL quantum yield of (8.22 ± 0.30) × 10 −3 , which is amongst the highest values in ever reported nanomaterials for chemical analysis. Employing the CDs as CL nanoprobes, sensitive sensing for H 2 O 2 has been achieved with a detection limit of 11.7 μM, and further for glucose detection with a detection limit of 12.6 μM. The DR CL CDs is promising to be applied in blood glucose analysis or in vivo biosensor.

In this paper, a novel method is proposed to achieve two distinct information channels by simultaneously manipulating both the transmitted cross- and co-polarized components of a 1-bit coding metasurface under linearly polarized incidence. Compared to previously demonstrated incidence-switchable or position multiplexed holograms, our proposed coding meta-hologram can simultaneously project two independent holographic images without inevitable change of the incidence state and can at the same time also avoid crosstalk between different channels. Moreover, the orientation of the double-layered split ring (SR) apertures is specially designed to be 45° or 135° to achieve identical multiplexed functionality for both x -polarized and y -polarized incidences. The proof-of-concept experimental demonstrations present total transmittance efficiency above 30% for the dual linearly polarized incidences at 15 GHz, and good imaging performances with 53.98%/48.18% imaging efficiency, 1.55%/1.46% RMSE, and 29.9/28.72 peak signal-to-noise ratio for the cross-/co-polarized channels under y -polarized incidence, and 47.27%/45.75% imaging efficienc y , 1.55%/1.43% RMSE, and 18.74/25.93 peak signal-to-noise ratio under x -polarized incidence, demonstrating great potential of the proposed multiplexed coding meta-hologram in practical applications such as data storage and information processing.

Various technological and biomedical applications rely on the ability of materials to emit light (photoluminescence [PL]), and, among them, metal nanoparticles (NPs) and semi-conductor Quantum Dots (QDs) represent ideal candidates as sensing probes and imaging tools, portraying better PL features than conventional organic dyes. However, the knowledge of PL behavior of semiconductor NPs – i.e., selenium; SeNPs – is still in its infancy, especially for those synthesized by microorganisms. Considering the essential role played by biogenic SeNPs as antimicrobial, anticancer, and antioxidant agents, or food supplements, their PL properties must be explored to take full advantage of them as eco-friendly and versatile tools. Here, PL features of SeNPs produced by the Se-tolerant Stenotrophomonas maltophilia SeITE02 strain, compared with chemogenic ones, are investigated, highlighting the PL dependency on the NP size. Indeed, PL emission shifted from indigo-blue (emission wavelength λ em 400–450 nm) to green-yellow ( λ em 480–570 nm) and orange-red ( λ em 580–700 nm) for small (ca. 50 nm) and big (ca. 100 nm) SeNPs respectively, revealing the versatility of an environmental bacterial isolate to synthesize diverse PL probes. Besides, biogenic SeNPs show PL lifetime comparable to those of the most used fluorophores, supporting their potential application as markers for (bio)imaging.

Sub wavelength all-dielectric structures processing simultaneously electric and magnetic resonances provide a new horizon for tailoring magnetic light–matter interaction that is often overlooked in optical spectrum. In general, the magnetic field enhancement can be boosted by utilizing the magnetic resonances of dielectric resonators where structural disorder effect is considered as a parasitic negative effect for the targeted response. Here, in contrast, we theoretically propose and experimentally demonstrate that compact disordered dielectric resonators with substantial enhancement of free-space magnetic field can be automatically designed by the combination of simulated annealing algorithm and numerical solution of Maxwell’s equations, providing an alternative for tailoring magnetic light–matter interaction. The functionality and reliability of the proposed concept are further verified by microwave experiment. Our results might facilitate the application of compact disordered magnetic resonators in enhancing magnetic dipole transition of quantum emitter, magnetic resonance imaging, wireless power transfer and beyond.

Localized plasmon resonance of a metal nanoantenna is determined by its size, shape and environment. Here, we diminish the size dependence by using multilayer metamaterials as epsilon-near-zero (ENZ) substrates. By means of the vanishing index of the substrate, we show that the spectral position of the plasmonic resonance becomes less sensitive to the characteristics of the plasmonic nanostructure and is controlled mostly by the substrate, and hence, it is pinned at a fixed narrow spectral range near the ENZ wavelength. Moreover, this plasmon wavelength can be adjusted by tuning the ENZ region of the substrate, for the same size nanodisk (ND) array. We also show that the difference in the phase of the scattered field by different size NDs at a certain distance is reduced when the substrate is changed to ENZ metamaterial. This provides effective control of the phase contribution of each nanostructure. Our results could be utilized to manipulate the resonance for advanced metasurfaces and plasmonic applications, especially when precise control of the plasmon resonance is required in flat optics designs. In addition, the pinning wavelength can be tuned optically, electrically and thermally by introducing active layers inside the hyperbolic metamaterial.

Germanium phosphide (GeP), a rising star of novel two-dimensional (2D) material composed of Group IV–V elements, has been extensively studied and applied in photonics thanks to its broadband optical absorption, strong light–matter interaction and flexible bandgap structure. Here, we show the strong nonlinear optical (NLO) properties of 2D GeP nanoflakes in the broadband range with open-aperture Z-scan technique to explore the performance of 2D GeP microfiber photonic devices (GMPDs) in near-infrared (near-IR) and mid-infrared (mid-IR) ultrafast photonics. Our results suggest that employing the GMPD as an optical device in an erbium-doped fiber laser (EDFL) system results in ultrashort pulses and rogue waves (RWs) at 1.55 μm. Likewise, by the incorporation of GMPD into a thulium-doped fiber laser (TDFL) system, stable ultrashort pulse operation is also achieved at 2.0 μm. We expect these findings to be an excellent GMPD that can be applied in mode-locked fiber lasers to open up new avenues for its development and application in ultrafast photonics.

Hybrid quantum photonics combines classical photonics with quantum emitters in a postprocessing step. It facilitates to link ideal quantum light sources to optimized photonic platforms. Optical cavities enable to harness the Purcell-effect boosting the device efficiency. Here, we postprocess a free-standing, crossed-waveguide photonic crystal cavity based on Si 3 N 4 with SiV − center in nanodiamonds. We develop a routine that optimizes the overlap with the cavity electric field utilizing atomic force microscope (AFM) nanomanipulation to attain control of spatial and dipole alignment. Temperature tuning further gives access to the spectral emitter-cavity overlap. After a few optimization cycles, we resolve the fine-structure of individual SiV − centers and achieve a Purcell enhancement of more than 4 on individual optical transitions, meaning that four out of five spontaneously emitted photons are channeled into the photonic device. Our work opens up new avenues to construct efficient quantum photonic devices.

The hybrid structures of graphene with semiconductor materials based on photogating effect have attracted extensive interest in recent years due to the ultrahigh responsivity. However, the responsivity (or gain) was increased at the expense of response time. In this paper, we devise a mechanism which can obtain an enhanced responsivity and fast response time simultaneously by manipulating the photogating effect (MPE). This concept is demonstrated by using a graphene/silicon-on-insulator (GSOI) hybrid structure. An ultrahigh responsivity of more than 10 7  A/W and a fast response time of 90 µs were obtained. The specific detectivity D * was measured to be 1.46 ⨯ 10 13  Jones at a wavelength of 532 nm. The Silvaco TCAD modeling was carried out to explain the manipulation effect, which was further verified by the GSOI devices with different doping levels of graphene in the experiment. The proposed mechanism provides excellent guidance for modulating carrier distribution and transport, representing a new route to improve the performance of graphene/semiconductor hybrid photodetectors.

A novel metallic nanostructure for efficient plasmon-enhanced fluorescence readout of biomolecular binding events on the surface of a solid sensor chip is reported. It is based on gold multiperiod plasmonic grating (MPG) that supports spectrally narrow plasmonic resonances centered at multiple distinct wavelengths. They originate from diffraction coupling to propagating surface plasmons (SPs) forming a delocalized plasmonic hotspot associated with enhanced electromagnetic field intensity and local density of optical states at its surface. The supported SP resonances are tailored to couple with the excitation and emission transitions of fluorophores that are conjugated with the biomolecules and serve as labels. By the simultaneous coupling at both excitation and emission wavelengths, detected fluorescence intensity is enhanced by the factor of 300 at the MPG surface, which when applied for the readout of fluorescence immunoassays translates to a limit of detection of 6 fM within detection time of 20 min. The proposed approach is attractive for parallel monitoring of kinetics of surface reactions in microarray format arranged on a macroscopic footprint. The readout by epi-fluorescence geometry (that inherently relies on low numerical aperture optics for the imaging of the arrays) can particularly take advantage of the reported MPG. In addition, the proposed MPG nanostructure can be prepared in scaled up means by UV-nanoimprint lithography for future practical applications.

Multi-channel information encryption technology has been implemented by optical metasurfaces owing to their superior ability to control the phase, amplitude, wavelength and polarization of incident light. However, current metasurface-based multi-channel encryption technologies suffer from information leakage in non-full channel decoding processes. To better increase the security of the encrypted information, we develop a secret shared phase encoding scheme by combining a visual secret sharing scheme with a metasurface-based phase-encoding technique. Our method achieves its high-concealment through mapping the target image into a set of unrecognizable phase-only keys that are subsequently encoded by a multi-wavelength metasurface. In the decryption process, the secret information can be reconstructed only by decoding and stacking all the wavelength channels of the metasurface. At the same time, chaotic images can be extracted from the other channels without revealing any original information. The simulated results and the theoretical analysis show the strong robustness and high security of our encryption setup, which is sure to find applications in emerging optical encryption schemes.