We present a general theory of circular dichroism in planar chiral nanostructures with rotational symmetry. It is demonstrated, analytically, that the handedness of the incident field's polarization can control whether a nanostructure induces either absorption or scattering losses, even when the total optical loss (extinction) is polarization‐independent. We show that this effect is a consequence of modal interference so that strong circular dichroism in absorption and scattering can be engineered by combining Fano resonances with planar chiral nanoparticle clusters.
The so‐called ‘flat optics’ that shape the amplitude and phase of light with high spatial resolution are presently receiving considerable attention. Numerous journal publications seemingly offer hope for great promises for ultra‐flat metalenses with high efficiency, high numerical aperture, broadband operation… We temperate the expectation by referring to the current status of metalenses against their historical background, assessing the technical and scientific challenges recently solved and critically identifying those that still stand in the way.
We investigate the fractional Schrödinger equation with a periodic ‐symmetric potential. In the inverse space, the problem transfers into a first‐order nonlocal frequency‐delay partial differential equation. We show that at a critical point, the band structure becomes linear and symmetric in the one‐dimensional case, which results in a nondiffracting propagation and conical diffraction of input beams. If only one channel in the periodic potential is excited, adjacent channels become uniformly excited along the propagation direction, which can be used to generate laser beams of high power and narrow width. In the two‐dimensional case, there appears conical diffraction that depends on the competition between the fractional Laplacian operator and the ‐symmetric potential. This investigation may find applications in novel on‐chip optical devices.
This work presents analytical, numerical and experimental demonstrations of light diffracted through a logarithmic spiral (LS) nanoslit, which forms a type of switchable and focus‐tunable structure. Owing to a strong dependence on the incident photon spin, the proposed LS‐nanoslit converges incoming light of opposite handedness (to that of the LS‐nanoslit) into a confined subwavelength spot, while it shapes light with similar chirality into a donut‐like intensity profile. Benefitting from the varying width of the LS‐nanoslit, different incident wavelengths interfere constructively at different positions, i.e., the focal length shifts from 7.5 μm (at λ = 632.8 nm) to 10 μm (at λ = 488 nm), which opens up new opportunities for tuning and spatially separating broadband light at the micrometer scale.
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.
About twenty years ago, in the autumn of 1996, the first white light‐emitting diodes (LEDs) were offered for sale. These then‐new devices ushered in a new era in lighting by displacing lower‐efficiency conventional light sources including Edison's venerable incandescent lamp as well as the Hg‐discharge‐based fluorescent lamp. We review the history of the conception, improvement, and commercialization of the white LED. Early models of white LEDs already exceeded the efficiency of low‐wattage incandescent lamps, and extraordinary progress has been made during the last 20 years. The review also includes a discussion of advances in blue LED chips, device architecture, light extraction, and phosphors. Finally, we offer a brief outlook on opportunities provided by smart LED technology.
Surface plasmon polaritons (SPPs) have sparked enormous interest on nanophotonics beyond the diffraction limit for their remarkable capabilities of subwavelength confinements and strong enhancements. Due to the inherent polarization sensitivity of the SPPs [transverse‐magnetic (TM) polarization], it is a great challenge to couple the s‐polarized free‐space light to the SPPs. Here, an ultrasmall defect aperture (<λ2/2) is designed to directionally couple both the p‐ and s‐polarized incident beams to the single SPP mode in a broad bandwidth, which is guided by a subwavelength plasmonic waveguide. Simulations show that hot spots emerge at the sharp corners of the defect aperture when the incident beams illuminate it from the back side. The strong radiative fields from the hot spots are directionally coupled to the SPP mode because of the symmetry breaking of the defect aperture. By adjusting the structural parameters, both the unidirectional and bidirectional SPP coupling from the two orthogonal linear‐polarization incident beams are experimentally demonstrated. The polarization‐free coupling of the SPPs is of importance in circuits for fully optical processing of information with a deep‐subwavelength footprint.
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.
Microresonator‐based Kerr frequency comb (microcomb) generation can potentially revolutionize a variety of applications ranging from telecommunications to optical frequency synthesis. However, phase‐locked microcombs have generally had low conversion efficiency limited to a few percent. Here we report experimental results that achieve conversion efficiency ( on‐chip comb power excluding the pump) in the fiber telecommunication band with broadband mode‐locked dark‐pulse combs. We present a general analysis on the efficiency which is applicable to any phase‐locked microcomb state. The effective coupling condition for the pump as well as the duty cycle of localized time‐domain structures play a key role in determining the conversion efficiency. Our observation of high efficiency comb states is relevant for applications such as optical communications which require high power per comb line.
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.
This article reviews the state of the art of ultrafast transient absorption microscopy, discusses current experimental concepts and highlights future challenges. The advantages of transient absorption microscopy over other micro‐spectroscopic techniques are its high optical resolution combined with high temporal resolution as well as its ability to study non‐fluorescent and weakly fluorescent molecular species and to probe excited‐state processes. In conventional transient absorption spectroscopy the spectroscopic information usually presents a spatial average over the focal spot of the typically weakly focused probe beam. Transient absorption microscopy, however, enables investigations of the excited state dynamics in individual microscopic areas of a sample. Hence, the technique does not only yield detailed morphological information based on a label‐free molecular contrast, but also gives insight into the ultrafast morphology‐dependent photoinduced processes in heterogeneous samples. Different variations of transient absorption microscopy have found a number of applications ranging from material sciences to biology, which are discussed in this review together with different setup modifications and approaches towards transient absorption spectroscopy with spatial resolution below the diffraction limit.
Detecting the optical vortices of darkness hidden in an ultra‐weak background is a difficult task. Here we report an experiment demonstrating that the optical vortices can be directly visualized and identified with a smaller number of photons. Our method is based on the extension of the spiral phase contrast technique to incorporate vortex phase plates (VPP) of high‐order topological charges. In our experiment, we prepare optical vortex arrays of interesting structures such as Arabic numerals and the wings carrying various topological charges. By placing various VPP filters in the Fourier plane of a 4f imaging system, the embedded vortices of an incident ultra‐weak light field can be visualized, revealing both their positions and topological charges. It is found that a higher order vortex generally requires a smaller number of photons to be detected. Our method may find potential application in the fields of astronomical optics and biosensing in an ultra‐weak light environment.
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.
We report complete spatial shaping (both phase and amplitude) of the second‐harmonic beam generated in a nonlinear photonic crystal. Using a collinear second‐order process in a nonlinear computer generated hologram imprinted on the crystal, the desired beam is generated on‐axis and in the near field. This enables compact and efficient one‐dimensional beam shaping in comparison to previously demonstrated off‐axis Fourier holograms. We experimentally demonstrate the second‐harmonic generation of high‐order Hermite–Gauss, top hats and arbitrary skyline‐shaped beams.
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.
Nonlinear dynamics of continuous‐wave pumped regenerative amplifiers operating at 2 μm are investigated. At repetition rates near 1 kHz, three different operation regimes are observed, including stable regular, chaotic, and subharmonic dynamics. Numerical simulations reproduce this behavior in a quantitative way. In particular, we find stable periodic doubling regimes in which every other seed pulse experiences high gain. Exploiting a narrow parameter window beyond the onset of chaos enables operation of a high‐gain picosecond Ho:YLF regenerative amplifier which delivers up to 16 mJ picosecond pulses at 2050 nm. Energy fluctuations of the 700 Hz pulse train are as low as 0.9% rms.
This work proves the feasibility of a novel concept of differential absorption lidar based on the Scheimpflug principle. The range‐resolved atmospheric backscattering signal of a laser beam is retrieved by employing a tilted linear sensor with a Newtonian telescope, satisfying the Scheimpflug condition. Infinite focus depth is achieved despite employing a large optical aperture. The concept is demonstrated by measuring the range‐resolved atmospheric oxygen concentration with a tunable continuous‐wave narrow‐band laser diode emitting around 761 nm over a path of one kilometer during night time. Laser power requirements for daytime operation are also investigated and validated with single‐band atmospheric aerosol measurements by employing a broad‐band 3.2‐W laser diode. The results presented in this work show the potential of employing the continuous‐wave differential absorption lidar (CW‐DIAL) technique for remote profiling of atmospheric gases in daytime if high‐power narrow‐band continuous‐wave light sources were to be employed.
One of the challenges of the modern photonics is to develop all‐optical devices enabling increased speed and energy efficiency for transmitting and processing information on an optical chip. It is believed that the recently suggested Parity‐Time (PT) symmetric photonic systems with alternating regions of gain and loss can bring novel functionalities. In such systems, losses are as important as gain and, depending on the structural parameters, gain compensates losses. Generally, PT systems demonstrate nontrivial non‐conservative wave interactions and phase transitions, which can be employed for signal filtering and switching, opening new prospects for active control of light. In this review, we discuss a broad range of problems involving nonlinear PT‐symmetric photonic systems with an intensity‐dependent refractive index. Nonlinearity in such PT symmetric systems provides a basis for many effects such as the formation of localized modes, nonlinearly‐induced PT‐symmetry breaking, and all‐optical switching. Nonlinear PT‐symmetric systems can serve as powerful building blocks for the development of novel photonic devices targeting an active light control.
The newly engineered ternary CdZnS/ZnS colloidal quantum dots (CQDs) are found to exhibit remarkably high photoluminescence quantum yield and excellent optical gain properties. However, the underlying mechanisms, which could offer the guidelines for devising CQDs for optimized photonic devices, remain undisclosed. In this work, through comprehensive steady‐state and time‐resolved spectroscopy studies on a series of CdZnS‐based CQDs, we unambiguously clarify that CdZnS‐based CQDs are inherently superior optical gain media in the blue spectral range due to the slow Auger process and that the ultralow threshold stimulated emission is enabled by surface/interface engineering. Furthermore, external cavity‐free high‐Q quasitoroid microlasers were produced from self‐assembly of CdZnS/ZnS CQDs by facile inkjet printing technique. Detailed spectroscopy analysis confirms the whispering gallery mode lasing mechanism of the quasitoroid microlasers. This tempting microlaser fabrication method should be applicable to other solution‐processed gain materials, which could trigger broad research interests.
