All‐optical signal processing on nonlinear photonic chips is a burgeoning field. These processes include light generation, optical regeneration and pulse metrology. Nonlinear photonic chips offer the benefits of small footprints, significantly larger nonlinear parameters and flexibility in generating dispersion. The nonlinear compression of optical pulses relies on a delicate balance of a material's nonlinearity and optical dispersion. Recent developments in dispersion engineering on a chip are proving to be key enablers of high‐efficiency integrated optical pulse compression. We review the recent advances made in optical pulse compression based on nonlinear photonic chips, as well as the future outlook and challenges that remain to be solved.
Hyperbolic metamaterials comprised of an array of plasmonic nanorods provide a unique platform for designing optical sensors and integrating nonlinear and active nanophotonic functionalities. In this work, the waveguiding properties and mode structure of planar anisotropic metamaterial waveguides are characterized experimentally and theoretically. While ordinary modes are the typical guided modes of the highly anisotropic waveguides, extraordinary modes, below the effective plasma frequency, exist in a hyperbolic metamaterial slab in the form of bulk plasmon‐polaritons, in analogy to planar‐cavity exciton‐polaritons in semiconductors. They may have very low or negative group velocity with high effective refractive indices (up to 10) and have an unusual cut‐off from the high‐frequency side, providing deep‐subwavelength (λ0/6–λ0/8 waveguide thickness) single‐mode guiding. These properties, dictated by the hyperbolic anisotropy of the metamaterial, may be tuned by altering the geometrical parameters of the nanorod composite.
The interaction of light with nanostructured materials provides exciting new opportunities for investigating classical wave analogies of quantum phenomena. A topic of particular interest forms the interplay between wave physics and chaos in systems where a small perturbation can drive the behavior from the classical to chaotic regime. Here, we report an all‐optical laser‐driven transition from order to chaos in integrated chips on a silicon photonics platform. A square photonic crystal microcavity at telecom wavelengths is tuned from an ordered into a chaotic regime through a perturbation induced by ultrafast laser pulses in the ultraviolet range. The chaotic dynamics of weak probe pulses in the near infrared is characterized for different pump‐probe delay times and at various positions in the cavity, with high spatial accuracy. Our experimental analysis, confirmed by numerical modelling based on random matrices, demonstrates that nonlinear optics can be used to control reversibly the chaotic behavior of light in optical resonators.
Open‐access microcavities are emerging as a new approach to confine and engineer light at mode volumes down to the λ3 regime. They offer direct access to a highly confined electromagnetic field while maintaining tunability of the system and flexibility for coupling to a range of matter systems. This article presents a study of coupled cavities, for which the substrates are produced using Focused Ion Beam milling. Based on experimental and theoretical investigation the engineering of the coupling between two microcavities with radius of curvature of 6 m is demonstrated. Details are provided by studying the evolution of spectral, spatial and polarisation properties through the transition from isolated to coupled cavities. Normal mode splittings up to 20 meV are observed for total mode volumes around . This work is of importance for future development of lab‐on‐a‐chip sensors and photonic open‐access devices ranging from polariton systems to quantum simulators.
We demonstrate a high optoelectronic performance and application potential of our random network, with subwavelength diameter, ultralong, and high‐quality silver nanowires, stabilized on a substrate with a UV binder. Our networks show very good optoelectronic properties, with the single best figure of merit of ∼1686, and excellent stability under harsh mechanical strain, as well as thermal, and chemical challenge. Our network transparency strongly exceeds the simple shading limit. We show that this transmission enhancement is due to plasmonic refraction, which in an effective medium picture involves localized plasmons, and identify the inhomogeneous broadening as the key factor in promoting this mechanism. Such networks could become a basis for a next generation of ultrahigh‐performance transparent conductors.
Recently, metasurfaces have received increasing attention due to their ability to locally manipulate the amplitude, phase and polarization of light with high spatial resolution. Transmissive metasurfaces based on high‐index dielectric materials are particularly interesting due to the low intrinsic losses and compatibility with standard industrial processes. Here, it is demonstrated numerically and experimentally that a uniform array of silicon nanodisks can exhibit close‐to‐unity transmission at resonance in the visible spectrum. A single‐layer gradient metasurface utilizing this concept is shown to achieve around 45% transmission into the desired order. These values represent an improvement over existing state‐of‐the‐art, and are the result of simultaneous excitation and mutual interference of magnetic and electric‐dipole resonances in the nanodisks, which enables directional forward scattering with a broad bandwidth. Due to CMOS compatibility and the relative ease of fabrication, this approach is promising for creation of novel flat optical devices.
Due to the broad scattering spectral profiles, localized surface plasmon resonances (LSPRs) of Pd nanoparticles have low resolution and limited sensitivity for hydrogen detection. In this work, we use a simple light‐irradiation method to demonstrate that free‐space light can be efficiently coupled into and from the microfiber whispering‐gallery modes (WGMs) by the Pd nanoantennas. The nanoantenna–microfiber cavity system provides strong intermodal coupling between LSPRs and WGMs, and induces significant modulation of the scattering spectra. A measured full width at half‐maximum of 3.2 nm at 622.7 nm is obtained, which is the narrowest in Pd nanoparticle‐based LSPR structures reported up to now. The ultranarrow resonances offer enhanced sensitivity to hydrogen gas detection with a figure of merit reaching ∼2.22. Other advantages of the Pd nanoantenna–microfiber cavity system including independence of precise alignment of excitation light, large tunability of the resonant wavelengths, easy and low‐cost fabrication of the system, have also been demonstrated.
We report on the realisation of ultra‐small‐mode‐volume tunable dye lasers based on hemispherical open microcavities. The cavity mode volume is of the order of cubic micrometers, such that self‐diffusion of the dye molecules allows continuous wave operation over several minutes without the need for driven circulation. Such micro lasers could be integrated into lab‐on‐a‐chip devices. A rate‐equation model that incorporates the diffusion mechanism is used to predict the effect of the microcavity parameters on the lasing threshold.
Dynamic charge carriers play a vital role in active photonic quantum/nanodevices, such as electrically pumped semiconductor lasers. Here we present a systematic experimental study of gain‐providing charge‐carrier distribution in a lasing interband cascade laser. The unique charge‐carrier distribution profile in the quantum‐well active region is quantitatively measured at nanometer scales by using a noninvasive scanning voltage microscopy technique. Experimental results clearly confirm the accumulation and spatial segregation of holes and electrons in the beating heart of the device. The measurement also shows that the charge‐carrier density is essentially clamped in the presence of stimulated emission at low temperatures. The threshold charge‐carrier density exhibits a linear but fairly weak temperature dependence, in contrast to the exponential temperature dependence of the threshold current. The experimental approach will lead to a deeper understanding of fundamental processes that govern the operation and performance of nanoelectronic devices, quantum devices and optoelectronic devices.
An analytical model is presented describing the temporal intensity contrast determined by amplified spontaneous emission in high‐intensity laser systems which are based on the principle of chirped pulse amplification. The model describes both the generation and the amplification of the amplified spontaneous emission for each type of laser amplifier. This model is applied to different solid state laser materials which can support the amplification of pulse durations . The results are compared to intensity and fluence thresholds, e.g. determined by damage thresholds of a certain target material to be used in high‐intensity applications. This allows determining if additional means for contrast improvement, e.g. plasma mirrors, are required for a certain type of laser system and application. Using this model, the requirements for an optimized high‐contrast front‐end design are derived regarding the necessary contrast improvement and the amplified “clean” output energy for a desired focussed peak intensity. Finally, the model is compared to measurements at three different high‐intensity laser systems based on Ti:Sapphire and Yb:glass. These measurements show an excellent agreement with the model.
Near‐field optical microscopy techniques provide information on the amplitude and phase of local fields in samples of interest in nanooptics. However, the information on the near field is typically obtained by converting it into propagating far fields where the signal is detected. This is the case, for instance, in polarization‐resolved scattering‐type scanning near‐field optical microscopy (s‐SNOM), where a sharp dielectric tip scatters the local near field off the antenna to the far field. Up to now, basic models have interpreted S‐ and P‐polarized maps obtained in s‐SNOM as directly proportional to the in‐plane ( or ) and out‐of‐plane () near‐field components of the antenna, respectively, at the position of the probing tip. Here, a novel model that includes the multiple‐scattering process of the probing tip and the nanoantenna is developed, with use of the reciprocity theorem of electromagnetism. This novel theoretical framework provides new insights into the interpretation of s‐SNOM near‐field maps: the model reveals that the fields detected by polarization‐resolved interferometric s‐SNOM do not correlate with a single component of the local near field, but rather with a complex combination of the different local near‐field components at each point (, and ). Furthermore, depending on the detection scheme (S‐ or P‐polarization), a different scaling of the scattered fields as a function of the local near‐field enhancement is obtained. The theoretical findings are corroborated by s‐SNOM experiments which map the near field of linear and gap plasmonic antennas. This new interpretation of nanoantenna s‐SNOM maps as a complex‐valued combination of vectorial local near fields is crucial to correctly understand scattering‐type near‐field microscopy measurements as well as to interpret the signals obtained in field‐enhanced spectroscopy.
Surface‐plasmon‐polariton waves are two‐dimensional electromagnetic surface waves that propagate at the interface between a metal and a dielectric. These waves exhibit unusual and attractive properties, such as high spatial confinement and enhancement of the optical field, and are widely used in a variety of applications, such as sensing and subwavelength optics. The ability to precisely control the spatial and spectral properties of the surface‐plasmon wave is required in order to support the growing interest in both research and applications of plasmonic waves, and to bring it to the next level. Here, we review the challenges and methods for shaping the wavefront and spectrum of plasmonic waves. In particular, we present the recent advances in plasmonic spatial and spectral shaping, which are based on the realization of plasmonic holograms for the optical nearfield.
Photoconductive antennas are promising sources of terahertz radiation that is widely used for spectroscopy, characterization, and imaging of biological objects, deep space studies, scanning of surfaces, and detection of potentially hazardous substances. These antennas are compact and allow for generation of both ultrabroadband pulses and tunable continuous wave terahertz signals at room temperatures, with no need for high‐power optical sources. However, such antennas have relatively low energy conversion efficiency of femtosecond laser pulses or two close pump wavelengths (photomixers) into the pulsed and continuous terahertz radiation, correspondingly. Recently, an approach to solving this problem that involves known methods of nanophotonics applied to terahertz photoconductive antennas and photomixers has been proposed. This approach comprises the use of optical nanoantennas for enhancing the absorption of pump laser radiation in the antenna gap, reducing the lifetime of photoexcited carriers, and improving the antenna thermal efficiency. This Review is intended to systematize the main results obtained by researchers in this promising field of hybrid optical‐to‐terahertz photoconductive antennas and photomixers. We summarize the main results on hybrid THz antennas, compare the approaches to their implementation, and offer further perspectives of their development including an application of all‐dielectric nanoantennas instead of plasmonic ones.
The ability of generating arbitrary surface plasmon (SP) profiles in a controllable manner is of particular interest in designing plasmonic imaging, lithography and forcing devices. During the past decades, holography has gained enormous interest and achievements in free‐space three‐dimensional displays. Here, by applying a two‐dimensional version of holography, we experimentally demonstrate a generic method to control the SP profiles. Through controlling the orientation angles of two separated slits under circular polarization incidence, the amplitude and phase of the excited SPs can be freely manipulated, which allows direct generation of the desired SP profiles. A series of controllable SP holography schemes are theoretically and experimentally demonstrated, where the holographic SP profiles with high imaging quality can be dynamically modulated by varying the circular polarization handedness or orientation angle of linear polarization. The universality and simplicity of the proposed design strategies would offer promising opportunities for practical plasmonic applications.
The realization of an ultra‐fast source of heralded single photons emitted at the wavelength of 1540 nm is reported. The presented strategy is based on state‐of‐the‐art telecom technology, combined with off‐the‐shelf fiber components and waveguide non‐linear stages pumped by a 10 GHz repetition rate laser. The single photons are heralded at a rate as high as 2.1 MHz with a heralding efficiency of 42%. Single‐photon character of the source is inferred by measuring the second‐order autocorrelation function. For the highest heralding rate, a value as low as 0.023 is found. This not only proves negligible multi‐photon contributions but also represents one of the best measured values reported to date for heralding rates in the MHz regime. These performances, associated with a device‐like configuration, are key ingredients for both fast and secure quantum communication protocols.
Branched photonic structures have served as paramount important components for nanophotonic integration and circuitry. However, these structures are generally constructed with photonic and plasmonic nanowires, which are nonbiomaterials and often need to be specially engineered to interface with cells and biological system. For bionanophotonics, photonic components assembled with self‐adaptive biomaterials are highly desirable to be directly interfaced with the dynamic biological system. In this work, branched structures for bionanophotonics assembled with natural living biomaterials, i.e., nanorod‐shaped Escherichia coli bacteria are reported. The E. coli cells were orderly trapped using a specially desired tapered optical fiber, forming structures with different branches and lengths. Light‐propagation performances along these branched structures were investigated, and the robustness property of the structures were demonstrated. The results show that the bacteria‐based branched structures provide different promising self‐sustainable and evolvable components, such as multidirectional waveguides and beam splitters, for bionanophotonics by connecting the biological and optical worlds with a seamless interface.
Rectangular arrays of pyramidal recesses coated by silver film are investigated by means of polarization‐resolved nonlinear microscopy at 900 nm fundamental wavelength, demonstrating strong dependence of the dipole‐allowed SHG upon the lattice parameters. The plasmonic band gap causes nearly complete SHG suppression in arrays of 650 nm periodicity, whereas a sharp resonance at 550 nm periodicity is observed due to excitation of band edge Bloch states at fundamental frequency, accompanied by symmetry‐constrained interactions with similar modes at the second‐harmonic frequency. Additionally, coupling with modes at the bottom side of the silver film may lead to extraordinary optical transmission, opening a channel for SHG from the highly nonlinear GaAs substrate. Changing the lattice geometry enables SHG intensity modulation over three orders of magnitude, while the effective nonlinear anisotropy can be continuously switched between the two lattice directions, reaching values as high as ±0.96.
We report a high‐repetition‐rate picosecond fiber‐based source at 2.1 µm offering exceptional performance capabilities over existing lasers near this wavelength, providing high average power and efficiency together with excellent spectral, power and beam pointing stability, in high spatial beam quality. This new source is based on a near‐degenerate MgO:PPLN optical parametric oscillator (OPO) pumped by an Yb‐fiber laser at 1064 nm, and incorporating a diffraction grating for spectral control. The device provides as much as 7.1 W of average power at 2.1 µm for a pump power of 18 W at an extraction efficiency of 39.4% in pulses of 20 ps at 79.3 MHz. The output exhibits passive power stability better than 1% rms over 15 hours, and a beam pointing stability ∼40 µrad over 1 hour, in high spatial quality with M2 ∼ 3.5. The output beam is linearly polarized and the pulse train has an amplitude stability better than 3.4% rms over 2 µsec. Radio‐frequency measurements of the output pulse train also confirm high temporal stability and low timing jitter, indicating that the source is ideal for variety of applications including pumping long‐wavelength mid‐infrared OPOs. Photograph shows the temperature‐controlled, 50‐mm‐long MgO:PPLN crystal inside the cavity, used as nonlinear gain medium in the picosecond source operating at 2.1 µm. The visible light is the result of non‐phase‐matched second harmonic generation of the pump beam in the MgO:PPLN crystal.
We uncover that the breaking point of the ‐symmetry in optical waveguide arrays has a dramatic impact on light localization induced by the off‐diagonal disorder. Specifically, when the gain/loss control parameter approaches a critical value at which ‐symmetry breaking occurs, a fast growth of the coupling between neighboring waveguides causes diffraction to dominate to an extent that light localization is strongly suppressed and the statistically averaged width of the output pattern substantially increases. Beyond the symmetry‐breaking point localization is gradually restored, although in this regime the power of localized modes grows upon propagation. The strength of localization monotonically increases with disorder at both broken and unbroken ‐symmetry. Our findings are supported by statistical analysis of parameters of stationary eigenmodes of disordered‐symmetric waveguide arrays and by analysis of dynamical evolution of single‐site excitations in such structures.
Two hundred years after Malus' discovery of optical anisotropy, the study of polarization‐driven optical effects is as active as ever, generating interest in new phenomena and potential applications. However, in ultrafast optics, the influence of polarization is frequently overlooked being considered as either detrimental or negligible. Here we demonstrate that spatio‐temporal couplings, which are inherent for ultrafast laser systems with chirped‐pulse amplification, accumulate in multi‐pulse irradiation and lead to a strongly anisotropic light‐matter interaction. Our results identify angular dispersion in the focus as the origin for the polarization dependence in modification, yielding an increase in modification strength. With tight focusing (NA ≥ ∼0.4), this non‐paraxial effect leads to a manifestation of spatio‐temporal couplings in photo‐induced modification. We devise a practical way to control the polarization dependence and exploit it as a new degree of freedom in tailoring laser‐induced modification in transparent material. A near‐focus, non‐paraxial field structure analysis of an optical beam provides insight on the origin of the polarization dependent modification. However, single pulse non‐paraxial corrected calculations are not sufficient to explain the phenomena confirming the experimental observations and exemplifying the need for multi‐pulse analysis.
