Band 10, Heft 2

Carbon nanotubes (CNTs) possess remarkable nonlinear optical properties; a particular application is to function as a mode locker used in ultrafast fiber lasers to produce ultrashort optical pulses. Various types of CNT saturable absorbers (SAs) and ultrafast fiber lasers have been demonstrated. In this review, typical fabrication process and development of CNT SAs are discussed and we highlight the recent investigation and progress of state-of-the-art ultrafast fiber lasers covering GHz, bidirectional ultrafast fiber lasers, vectorial mode fiber lasers, comb systems, and mode-locking dynamics. Our perspectives of ultrafast fiber lasers based on CNT SAs are given finally.

Using in situ ultrafast laser spectroscopic techniques to monitor the charge dynamics of semiconductor photocatalysts under operating conditions is essential for digging out the veritable interactions between charge carriers and the reactive species. This real-time observation is desirable for optimizing individual components and their integration in advanced photoelectrochemical (PEC) and photocatalytic systems, which can achieve the “Holy Grail” of solar energy harvesting and solar fuel generation. This Review summarizes the recent developments of employing transient absorption spectroscopy for in situ measurements of charge dynamics on semiconductor nanostructures. The implications in the PEC and photocatalytic reactions toward hydrogen production and carbon dioxide reduction will be discussed, along with future outlooks and perspectives.

Chirality is one of the most fascinating occurrences in the natural world and plays a crucial role in chemistry, biochemistry, pharmacology, and medicine. Chirality has also been envisaged to play an important role in nanotechnology and particularly in nanophotonics, therefore, chiral and chiroptical active nanoparticles (NPs) have attracted a lot of interest over recent years. Optical activity can be induced in NPs in several different ways, including via the direct interaction of achiral NPs with a chiral molecule. This results in circular dichroism (CD) in the region of the intrinsic absorption of the NPs. This interaction in turn affects the optical properties of the chiral molecule. Recently, studies of induced chirality in quantum dots (QDs) has deserved special attention and this phenomenon has been explored in detail in a number of important papers. In this article, we review these important recent advances in the preparation and formation of chiral molecule–QD systems and analyze the mechanisms of induced chirality, the factors influencing CD spectra shape and the intensity of the CD, as well as the effect of QDs on chiral molecules. We also consider potential applications of these types of chiroptical QDs including sensing, bioimaging, enantioselective synthesis, circularly polarized light emitters, and spintronic devices. Finally, we highlight the problems and possibilities that can arise in research areas concerning the interaction of QDs with chiral molecules and that a mutual influence approach must be taken into account particularly in areas, such as photonics, cell imaging, pharmacology, nanomedicine and nanotoxicology.

Electrochromism, an emerging energy conversion technology, has attracted immense interest due to its various applications including bistable displays, optical filters, variable optical attenuators, optical switches, and energy-efficient smart windows. Currently, the major drawback for the development of electrochromism is the slow switching speed, especially in inorganic electrochromic materials. The slow switching speed is mainly attributed to slow reaction kinetics of the dense inorganic electrochromic films. As such, an efficient design of nanostructured electrochromic materials is a key strategy to attain a rapid switching speed for their real-world applications. In this review article, we summarize the classifications of electrochromic materials, including inorganic materials (e.g., transition metal oxides, Prussian blue, and polyoxometalates), organic materials (e.g., polymers, covalent organic frameworks, and viologens), inorganic-organic hybrids, and plasmonic materials. We also discuss the electrochromic properties and synthesis methods for various nanostructured inorganic electrochromic materials depending on structure/morphology engineering, doping techniques, and crystal phase design. Finally, we outline the major challenges to be solved and discuss the outlooks and our perspectives for the development of high-performance nanostructured electrochromic materials.

Advances in lighting and quantum computing will require new degrees of control over the emission of photons, where localized defects and the quantum confinement of carriers can be utilized. In this contribution, recent developments in the controlled redistribution of energy in rare earth (RE)–doped nanosystems, such as quantum dots or within bulk insulating and semiconducting hosts, will be reviewed. In their trivalent form, RE ions are particularly useful dopants because they retain much of their atomic nature regardless of their environment; however, in systems such as GaN and Si, the electronic states of the RE ions couple strongly to those of the host material by forming nanocomplexes. This coupling facilities fast energy transfer (ET) (<100 ps) and a carrier-mediate energy exchange between the host and the various states of the RE ions, which is mediated by the presence of carriers. A model has been developed using a set of rate equations, which takes into consideration the various ET pathways and the lifetimes of each state within the nanocomplex, which can be used to predict the nature of the emitted photons given an excitation condition. This model will be used to elucidate recent experimental observations in Eu-doped GaN.

Heavy metal (HM) pollution is a major global concern. Carbon dots (CDs) have demonstrated unique properties as sensing platforms for HMs detection. This review summarizes the progress made in recent years in fluorescence methods to determine HMs and their species using CDs. First, the strategies to synthesize and purify CDs are reviewed. The photoluminescence principles of CDs and their sensing mechanisms as HMs sensors are then summarized. The binding strategies between CDs and HMs are proposed to provide salient principles to design desirable CD-based HMs sensors. The preparation and merits of “turn-on” and ratiometric CDs for HMs detection with higher accuracy are discussed compared with commonly used “turn-off” sensors. Subsequently, the progress on detecting single HM ions, multi-HMs, and different metal species in solution, and the development of gel/solid-state sensor platforms such as paper-based devices, sensor arrays, hydrogels, polymer films, and ion-imprinted polymers are critically accessed. Furthermore, the advances in the cell, bacterial, plant, and animal bioimaging of HMs with CDs as promising bioimaging reagents are presented. Finally, the challenges and prospects of CDs as HMs sensors in future investigations are discussed.

Active metasurfaces, in which the optical property of a metasurface device can be controlled by external stimuli, have attracted great research interest recently. For optical switching and modulation applications, high-performance active metasurfaces need to show high transparency, high power efficiency, as well as ultrafast switching and large-scale fabrication capability. This paper reports Au/VO 2 -based active metasurfaces meeting the requirements above. Centimeter-scale Au/VO 2 metasurfaces are fabricated by polystyrene sphere colloidal crystal self-assembly. The devices show optical modulation on-off ratio up to 12.7 dB and insertion loss down to 3.3 dB at 2200 nm wavelength in the static heating experiment, and Δ T / T of 10% in ultrafast pump-probe experiments. In particular, by judiciously aligning the surface plasmon resonance wavelength to the pump wavelength of the femtosecond laser, the enhanced electric field at 800 nm is capable to switch off the extraordinary optical transmission effect at 2200 nm in 100 fs time scale. Compared to VO 2 thin-film samples, the devices also show 50% power reduction for all-optical modulation. Our work provides a practical way to fabricate large-scale and power-efficient active metasurfaces for ultrafast optical modulation.

Structural coloration using metasurfaces has been steadily researched to overcome the limitations of conventional color printing using pigments by improving the resolution, lowering the toxicity, and increasing the durability. Many metasurfaces have been demonstrated for dynamic structural coloration to convert images at the visible spectrum. However, the previous works cannot reach near-zero scattering when colors are turned-off, preventing it from being cryptographic applications. Herein, we propose a completely on/off switchable structural coloration with polarization-sensitive metasurfaces, enabling full-colored images to be displayed and hidden through the control of the polarization of incident light. It is confirmed that the nanostructure exhibits the polarization-dependent magnetic field distributions, and near-zero scattering is realized when the polarization of incident light is perpendicular to the long axis of the nanofins. Also, the metasurfaces are made up of triple-nanofin structures whose lengths affect locations of resonance peaks, resulting in full-color spectrum coverages. With such advantages, a QR code image, a two-color object image, and an overlapped dual-portrait image are obtained with the metasurfaces. Such demonstrations will provide potential applications in the fields of high-security information encryption, security tag, multichannel imaging, and dynamic displays.

Van der Waals heterostructures are composed of stacked atomically thin two-dimensional (2D) crystals to provide unprecedented functionalities and novel physics. Franckeite, a naturally occurring van der Waals heterostructure consisting of superimposed SnS 2 -like and PbS-like layers alternately, shows intriguing potential in versatile optoelectronic applications. Here, we have prepared the few-layer franckeite via liquid-phase exfoliation method and characterized its third-order nonlinearity and ultrafast dynamics experimentally. We have found that the layered franckeite shows low saturable intensity, large modulation depth and picosecond ultrafast response. We have designed the passive photonic diodes based on the layered franckeite/C 60 cascaded film and suspension configuration and found that the passive photonic diodes exhibit stable nonreciprocal transmission of light. The experimental results show the excellent nonlinear optical performance and ultrafast response of the layered franckeite, which may make inroad for the cost effective and reliable high-performance optoelectronic devices.

Ultracompact and low-power-consumption optical switches are desired for high-performance telecommunication networks and data centers. Here, we demonstrate an on-chip power-efficient 2 × 2 thermo-optic switch unit by using a suspended photonic crystal nanobeam structure. A submilliwatt switching power of 0.15 mW is obtained with a tuning efficiency of 7.71 nm/mW in a compact footprint of 60 μm × 16 μm. The bandwidth of the switch is properly designed for a four-level pulse amplitude modulation signal with a 124 Gb/s raw data rate. To the best of our knowledge, the proposed switch is the most power-efficient resonator-based thermo-optic switch unit with the highest tuning efficiency and data ever reported.

Plasmonic Fano resonance (FR) that contributes to multitudinous potential applications in subwavelength nanostructures can facilitate the realization of tunable wavelength selectivity for controlling light–matter interactions in metasurfaces. However, the plasmonic FR can be generated in metasurfaces with simple or complex geometries, and few of them can support flexible amplitude modulation and multiwavelength information transfer and processing. Here, we study the near-infrared plasmonic FR in a hybrid metasurface composed of concentrically hybridized parabolic-hole and circular-ring-aperture unit cells, which can induce polarization-dependent dual-wavelength passive plasmonic switching (PPS) and digital metasurface (DM). It is shown that the designable plasmonic FR can be realized by changing the geometric configurations of the unit cells. In particular, owing to the polarization-dependent characteristic of FR, it is possible to fulfill a compact dual-wavelength PPS with high ON/OFF ratios in the related optical communication bands. Moreover, such PPS that manipulates the amplitude response of the transmitted spectrum is an efficient way to reveal a 1-bit DM, which can also be rationally extended to a 2-bit DM or more. Our results suggest a pathway for studying polarization-dependent PPS and programmable metasurface devices, yielding possibilities for subwavelength nanostructures in optical communication and information processing.

We demonstrate control over the spatial and temporal properties of surface plasmon polaritons (SPPs) launched from nanohole arrays in silver. The arrays provide wave vector matching to allow the conversion of free-space photons into counter-propagating SPPs. SPPs launched from multiple arrays interfere at well-defined spatial positions, and the interference fringes form an all-SPP periodic nano-optical grating which evolves in space and time as the SPPs propagate. The spatio-temporal characteristics of the optical grating can be tuned through various nanohole array parameters such as tilt angle, separation, and array width. In addition, we examine multiperiodic arrays (MPAs) consisting of arrays with different pitches placed adjacent to one another. This platform allows the temporal interference of SPPs with different central wavelengths to be tailored through the MPA geometric and structural parameters. The temporal interference serves as an encoded signal, whereby the frequency components can be controlled by the array properties.

Splitting the spectrum of incident light at nanoscale has been of great scientific and practical interest due to its potential application in various optical sensors. For many years, researchers have been striving to realize the full-color sorting of light at subwavelength scale, while keeping the loss of incident photons to a minimum. In this article, we present semiconductor-based metasurfaces that facilitate the efficient sorting of full-color by inducing anti-Hermitian coupling between multiple nanoantenna arrays. To achieve this, we first explore how the coherent interactions between maximally crafted nanoantennas in the metasurfaces can be effectively controlled by judiciously positioning them in both lateral and vertical directions, which leads to the switched coupling of light at each target position. Based on the analysis, we demonstrate a metasurface-based absorber that features efficient, spectropolarimetric detections over the entire visible spectrum, ranging from 470 to 630 nm. In addition, the metasurface detects relatively narrow spectral linewidth of 60 nm and shows the sensitivity up to 70%, which surpasses the previous works on subwavelength photon sorting or color filter-based detection system. We envision that our approach provides guidelines for realizing the metasurfaces with enhanced functionalities, that is the increase of spectral channels for detection in a given subwavelength-scaled unit cell.

Plasmonic nanostructures have garnered tremendous interest in enhanced light–matter interaction because of their unique capability of extreme field confinement in nanoscale, especially beneficial for boosting the photoluminescence (PL) signals of weak light–matter interaction materials such as transition metal dichalcogenides atomic crystals. Here we report the surface plasmon polariton (SPP)-assisted PL enhancement of MoS 2 monolayer via a suspended periodic metallic (SPM) structure. Without involving metallic nanoparticle–based plasmonic geometries, the SPM structure can enable more than two orders of magnitude PL enhancement. Systematic analysis unravels the underlying physics of the pronounced enhancement to two primary plasmonic effects: concentrated local field of SPP enabled excitation rate increment (45.2) as well as the quantum yield amplification (5.4 times) by the SPM nanostructure, overwhelming most of the nanoparticle-based geometries reported thus far. Our results provide a powerful way to boost two-dimensional exciton emission by plasmonic effects which may shed light on the on-chip photonic integration of 2D materials.