Strong Light-matter Interaction Research Articles

Eco-friendly and biocompatible gelatin plasmonic filters for UV-vis-NIR light

The quest for environmentally sustainable materials spans many fields and applications including optical materials. Here, we present the development of light filters using a gelatin-based nanocomposite. Owing to the plasmonic properties of metallic nanoparticles (NPs), strong light-matter interactions, these filters can be customized across the UV-Visible-NIR spectrum. The filters are designed for modular use, allowing for the addition or removal of desired spectral ranges. Moreover, the nanocomposites are composed of biodegradable and biocompatible materials which highlight the intersection of chemistry and ecological awareness for the exploration of new eco-friendly alternatives. These plasmonic gelatin-based filters block light due to the Localized Surface Plasmon Resonance (LSPR) of the NPs and can be tailored to meet various requirements, akin to a diner selecting options from a menu. This approach is inspired by culinary techniques, and we anticipate it will stimulate further exploration of biomaterials for applications in optics, materials science or electronics.

Highly tunable ground and excited state excitonic dipoles in multilayer 2H-MoSe2

The fundamental properties of an exciton are determined by the spin, valley, energy, and spatial wavefunctions of the Coulomb-bound electron and hole. In van der Waals materials, these attributes can be widely engineered through layer stacking configuration to create highly tunable interlayer excitons with static out-of-plane electric dipoles, at the expense of the strength of the oscillating in-plane dipole responsible for light-matter coupling. Here we show that interlayer excitons in bi- and tri-layer 2H-MoSe2 crystals exhibit electric-field-driven coupling with the ground (1s) and excited states (2s) of the intralayer A excitons. We demonstrate that the hybrid states of these distinct exciton species provide strong oscillator strength, large permanent dipoles (up to 0.73 ± 0.01 enm), high energy tunability (up to ~200 meV), and full control of the spin and valley characteristics such that the exciton g-factor can be manipulated over a large range (from −4 to +14). Further, we observe the bi- and tri-layer excited state (2s) interlayer excitons and their coupling with the intralayer excitons states (1s and 2s). Our results, in good agreement with a coupled oscillator model with spin (layer)-selectivity and beyond standard density functional theory calculations, promote multilayer 2H-MoSe2 as a highly tunable platform to explore exciton-exciton interactions with strong light-matter interactions.

Photodetectors Based on ZrS3/MoS2 Heterostructures.

High-performance photodetectors with the detection capability of linearly polarized light have broad applications in both military and civilian fields. Quasi-one-dimensional ZrS3 as an emerging anisotropic two-dimensional material has come under the spotlight owing to its intriguing properties. However, the performance of the ZrS3 photodetector is seriously restricted by its low responsivity. Herein, a novel high-performance photodetector based on the van der Waals ZrS3/MoS2 heterostructure is proposed. Attributed to the charge trapping-assisted photogating effect, interlayer carrier transitions, and fast spatial separation of the photogenerated electron-hole pairs, the device displays superior photoresponse characteristics ranging from the ultraviolet to the visible spectrum in terms of high responsivity up to 212 A/W, an extraordinary external quantum efficiency of 8.5 × 104%, and a prompt rise/decay time of 0.19/0.38 ms. In addition, owing to the profound birefringence and dichroism effects in ZrS3 together with strong light-matter interactions in the heterostructure, profound linear-polarization sensitivity is demonstrated with a dichroic ratio of about 2.8. Overall, this photodetector not only is integrated with the excellent properties of ZrS3 and monolayer MoS2 but also further enhances the advantages through interlayer couplings, which demonstrate the strong potential of the ZrS3-based devices for high-performance, ultrafast, and polarization-sensitive photodetection.

Plasmon-assisted boosting of strong self-hybrid exciton–anapole coupling in bulk transition metal dichalcogenides nanoresonators

Intrinsic strong coupling between excitons and anapole mode in self-hybridizing transition metal dichalcogenide (TMD) nanostructures has recently attracted much attention for their capability of improving exciton–anapole interactions as a consequence of the nonradiative feature of anapole mode and the excellent mode overlap in the self-hybridizing geometry. Here, we propose a strategy for further enhancing exciton–anapole coupling. By embedding Au dimers as plasmonic components in slotted bulk WS2 nanodisks, a plasmon-induced electric field strength enhancement over nearly 140 times is achieved compared to that of the bulk WS2 nanodisk, boosting the strong exciton–anapole hybridization with greatly enhanced Rabi splitting up to 532 meV. Importantly, we demonstrate not only the effect of the plasmon mode on the initial Rabi phase of the anapole mode but also the great reduction of the ultrafast energy transfer time by the constructed full-quantum model. The plasmon-assisted hybrid system proposed in this paper provides a promising approach for enhancing strong light–matter interactions and may pave the way for the development of high-performance TMD-based photonic devices.

High-Q silicon microring resonator with ultrathin sub-wavelength thicknesses for sensitive gas sensing

Microring resonators, due to their ability to enable robust strong light–matter interactions within their structures, have garnered substantial interest for their utility in sensing applications, particularly in the realm of gas detection. However, there is an inherent trade-off between a microring resonator's quality factor and confinement factor in the air, making it difficult to balance them. Here, we demonstrate a novel solution with a suspended nanomembrane silicon (SNS) microring resonator. This resonator has ultrathin sub-wavelength thicknesses (0.02–0.03λ), which breaks the trade-off, offering not only a high intrinsic quality factor of 6 × 105 but also an extraordinarily large confinement factor of ∼80% in the air at mid-infrared wavelengths. As a proof-of-concept demonstration, we applied the SNS microring resonator for CO2 gas sensing, exhibiting a sensitivity over 10 times higher than conventional silicon resonators and a large dynamic sensing range spanning from 0% to 100% with a high resolution of better than 4% and chemical specificity. By virtue of its excellent properties, the SNS microring resonator has the potential to open new possibilities for the development of unprecedented nanophotonic integrated circuits, with a broad range of applications in on-chip sensing scenarios.

Ultralow-threshold dual-wavelength optical bistability from a perovskite hyperbolic metasurface and its application in a photonic neural network

In a hyperbolic metamaterial or metasurface (HMM or HMS), strong light-matter interaction occurs at the phase transition wavelength where the material behavior changes from metal to dielectric. As a result, the enhanced electric field can generate non-linear phenomena, such as optical bistability. In this work, we numerically investigate polarization-dependent dual-wavelength optical bistability from perovskite HMS consisting of alternating layers of MAPbBr3 perovskite and Au. Benefiting from the anisotropic property, the bistable operation wavelength for TE and TM polarizations are different. In particular, for TE polarization, strong light matter interaction resulting from the increment of incident light power not only shifts the phase transition wavelength but also enhances the transmission. Consequently, the bistable on-off contrast ratio is unprecedentedly enlarged. For TM polarization, strong light-matter interaction gives rise to an ultra-low bistable threshold. The proposed optical bistable states can serve as an activation function for optical neurons in a photonic neural network, with similar prediction accuracy across a variety of learning tasks as the classic activation functions ReLU and Sigmoid. Our work suggests a novel avenue towards the insertion of perovskite HMS into optical computing networks.

Topologically protected subradiant cavity polaritons through linewidth narrowing enabled by dissipationless edge states

Cavity polaritons derived from strong light–matter interaction provide a basis for efficient manipulation of quantum states via cavity field. Polaritons with narrow linewidth and long lifetime are appealing in applications, such as quantum sensing and storage. Here, we propose a prototypical arrangement to implement a whispering-gallery-mode resonator with one-dimensional topological atom mirror, which allows to boost the lifetime of cavity polaritons over an order of magnitude. This considerable enhancement attributes to the coupling of polaritonic states to dissipationless edge states protected by the topological bandgap of atom mirror that suppresses the leakage of cavity modes. When exceeding the width of Rabi splitting, topological bandgap can further reduce the dissipation from polaritonic states to bulk states, giving arise to subradiant cavity polaritons with extremely sharp linewidth. The resultant Rabi oscillation experiences decay rate lower than the free-space decay of a single quantum emitter. Inheriting from the topologically protected properties of edge states, the subradiance of cavity polaritons can be preserved in disordered atom mirror with moderate perturbations involving the atomic frequency, interaction strengths and location fluctuations. Our work opens up a new paradigm of topology-engineered quantum states with robust quantum coherence for future applications in quantum computing and network.

All-optical high-contrast femtosecond switching using nonlinearity from an epsilon-near-zero effect in plasmonic metamaterials.

Metamaterials opened a new realm to control light-matter interactions at sub-wavelength scale by engineering meta-atoms. Recently, the integration of several emerging nonlinear materials with metamaterial structures enables ultra-fast all-optical switching at the nanoscale and thus brings enormous possibilities to realize next-generation optical communication systems. This Letter presents a novel, to the best of our knowledge, design of plasmonic metamaterials for high-contrast femtosecond all-optical switching. We leverage magnetic plasmon (MP) resonance combined with the nonlinear effects of an epsilon-near-zero (ENZ)-material. The proposed design comprises a periodic array of two closely spaced Au-nanogratings deposited on an optically thick Au-substrate to excite MP-resonance. To enable a dynamically tunable resonance, the nanogrooves in meta-atoms are filled with an ENZ-material, cadmium-oxide (CdO). The intraband transition-induced optical nonlinearities in the ENZ-medium are studied using a two-temperature model. The MP-resonance ensures strong light-matter interactions enabling enhancement of the nonlinearities of the proposed structure. We observe that the pump-induced refractive index change in the CdO layer causes a redshift of the MP-resonance dip wavelength in the reflectance spectrum, leading to a high modulation depth of 0.83 at 1.55 µm. With an ultra-fast response time of 776 fs while maintaining a low pump-fluence of 75 µJ/cm2, the proposed metamaterial could help in realizing switches for next-generation optical computation systems.

Band Alignment Transition and Enhanced Performance in Vertical SnS2/MoS2 van der Waals Photodetectors.

The strong light-matter interaction and naturally passivated surfaces of van der Waals materials make heterojunctions of such materials ideal candidates for high-performance photodetectors. In this study, we fabricated SnS2/MoS2 van der Waals heterojunctions and investigated their photoelectric properties. Using an applied gate voltage, we can effectively alter the band arrangement and achieve a transition in type II and type I junctions. It is found that the SnS2/MoS2 van der Waals heterostructures are type II heterojunctions when the gate voltage is above -25 V. Below this gate voltage, the heterojunctions become type I. Photoelectric measurements under various wavelengths of incident light reveal enhanced sensitivity in the ultraviolet region and a broadband sensing range from 400 to 800 nm. Moreover, due to the transition from type II to type I band alignment, the measured photocurrent saturates at a specific gate voltage, and this value depends crucially on the bias voltage and light wavelength, providing a potential avenue for designing compact spectrometers.

Temperature-Dependent Excitonic Light Manipulation with Atomically Thin Optical Elements.

Monolayer 2D semiconductors, such as WS2, exhibit uniquely strong light-matter interactions due to exciton resonances that enable atomically thin optical elements. Similar to geometry-dependent plasmon and Mie resonances, these intrinsic material resonances offer coherent and tunable light scattering. Thus far, the impact of the excitons' temporal dynamics on the performance of such excitonic metasurfaces remains unexplored. Here, we show how the excitonic decay rates dictate the focusing efficiency of an atomically thin lens carved directly out of exfoliated monolayer WS2. By isolating the coherent exciton radiation from the incoherent background in the focus of the lens, we obtain a direct measure of the role of exciton radiation in wavefront shaping. Furthermore, we investigate the influence of exciton-phonon scattering by characterizing the focusing efficiency as a function of temperature, demonstrating an increased optical efficiency at cryogenic temperatures. Our results provide valuable insights into the role of excitonic light scattering in 2D nanophotonic devices.

Active strong coupling of exciton and nanocavity based on GSST-WSe2 hybrid nanostructures

The strong coupling between optical resonance microcavity and matter excitations provides a practical path for controlling light-matter interactions. However, conventional microcavity, whose functions are fixed at the fabrication stage, dramatically limits the modulation of light-matter interactions. Here, we investigate the active strong coupling of resonance mode and exciton in GSST-WSe2 hybrid nanostructures. It is demonstrated that significant spectral splitting is observed in single nanostructures, tetramers, and metasurfaces. We further confirm the strong coupling by calculating the enhanced fluorescence spectra. The coupling effect between the excited resonance and exciton is dramatically modulated during the change of GSST from amorphous to crystalline, thus realizing the strong coupling switching. This switching property has been fully demonstrated in several systems mentioned earlier. Our work is significant in guiding the study of actively tunable strong light-matter interactions at the nanoscale.

Ultrafast wavelength sweeping of surface plasmon lasing in planar metal grating with semiconductor gain

Surface plasmon (SP) lasing, characterized by strong light–matter interaction at a metal interface, can derive from SP cavities coupled with a semiconductor gain material. With this setup, we demonstrate ultrafast wavelength sweeping of SP lasing in a metal grating. When the device was optically pumped by ultrashort pulses with sufficient power, a wavelength sweep over 10 nm within 50 ps was obtained in the telecom band of 1550 nm. Based on the pump-power-dependent lasing wavelength change in combination with finite-difference time-domain simulation, we attribute the wavelength sweep to a modulation of the SP cavity that induces changes in the refractive index from changes in the carrier density. Such a refractive index change is a critical factor in determining SP cavity resonance.

Unveiling the potential of vanadium-doped CVD-grown p-type MoS2 in vertical homojunction UV–Vis photodiodes

2D materials are a popular choice for the fabrication of p-n diodes for applications in integrated optoelectronics owing to their outstanding properties such as strong light-matter interactions, high mobility, and tunable band gap. The synthesis of monolayer and few-layer 2D materials with both p-type and n-type behavior is thus essential for the design and fabrication of such devices. However, the large-scale direct synthesis of p-type 2D materials is still a challenge as most of these materials are either n-type or ambipolar. Here, we report the successful synthesis of large-area, p-type MoS2 layers doped with vanadium on SiO2/Si substrates, achieving flake sizes >100 μm. By varying the concentration of the vanadium precursor, we precisely controlled the doping level, achieving vanadium atomic percentages ranging from 0.70 % to 1.57 %. Back gate field-effect transistors (FETs) were fabricated, enabling the tuning of device characteristics to exhibit ambipolar or p-type behavior. Moreover, a vertical p-n MoS2 homojunction was fabricated for rectification and optoelectronic applications, demonstrating a high responsivity of up to 978.1 A/W and a specific detectivity (D*) of 1.06 × 1012 Jones at λ = 365 nm with varied powers of the incident light source. This work demonstrates the role of vanadium as a dopant for tunable electrical transport behavior as well as for the fabrication of a photodiode, which can be used for high-performance optoelectronic devices in the future.

Strong light–matter interactions based on excitons and the abnormal all-dielectric anapole mode with both large field enhancement and low loss

The room temperature strong coupling between the photonic modes of micro/nanocavities and quantum emitters (QEs) can bring about promising advantages for fundamental and applied physics. Improving the electric fields (EFs) by using plasmonic modes and reducing their losses by applying dielectric nanocavities are widely employed approaches to achieve room temperature strong coupling. However, ideal photonic modes with both large EFs and low loss have been lacking. Herein, we propose the abnormal anapole mode (AAM), showing both a strong EF enhancement of ∼70-fold (comparable to plasmonic modes) and a low loss of 34 meV, which is much smaller than previous records of isolated all-dielectric nanocavities. Besides realizing strong coupling, we further show that by replacing the normal anapole mode with the AAM, the lasing threshold of the AAM-coupled QEs can be reduced by one order of magnitude, implying a vital step toward on-chip integration of nanophotonic devices.

A WGM-FP hybrid microcavity for simultaneous measurement of NaCl concentration and temperature

Whispering gallery mode (WGM) resonator is sensitive to the external medium change due to its strong light-matter interaction. However, the temperature sensitivity of silica-based WGM resonators would cause crosstalk, which is a fatal shortcoming for those high-quality (Q) resonators. In this paper, a hybrid microcavity including WGM resonance and Fabry–Pérot (FP) interference is proposed for simultaneous measurement of NaCl concentration and temperature, using the same microcavity in the same system to obtain two types of optical signals. The experimental results indicate that the maximum measurement error of NaCl concentration and temperature without compensation is about ± 0.026 % and ± 1.1 °C, while they would be ± 0.012 % and ± 0.3 °C after compensation. Sharing one microcavity enables temperature compensation to achieve temperature synchronization, and sharing of one system ensures the simplicity and stability of the sensing platform.

Strong Coupling of Two-Dimensional Excitons and Plasmonic Photonic Crystals: Microscopic Theory Reveals Triplet Spectra.

Monolayers of transition metal dichalcogenides (TMDCs) are direct-gap semiconductors with strong light-matter interactions featuring tightly bound excitons, while plasmonic crystals (PCs), consisting of metal nanoparticles that act as meta-atoms, exhibit collective plasmon modes and allow one to tailor electric fields on the nanoscale. Recent experiments show that TMDC-PC hybrids can reach the strong-coupling limit between excitons and plasmons, forming new quasiparticles, so-called plexcitons. To describe this coupling theoretically, we develop a self-consistent Maxwell-Bloch theory for TMDC-PC hybrid structures, which allows us to compute the scattered light in the near- and far-fields explicitly and provide guidance for experimental studies. One of the key findings of the developed theory is the necessity to differentiate between bright and originally momentum-dark excitons. Our calculations reveal a spectral splitting signature of strong coupling of more than 100 meV in gold-MoSe2 structures with 30 nm nanoparticles, manifesting in a hybridization of the plasmon mode with momentum-dark excitons into two effective plexcitonic bands. The semianalytical theory allows us to directly infer the characteristic asymmetric line shape of the hybrid spectra in the strong coupling regime from the energy distribution of the momentum-dark excitons. In addition to the hybridized states, we find a remaining excitonic mode with significantly smaller coupling to the plasmonic near-field, emitting directly into the far-field. Thus, hybrid spectra in the strong coupling regime can contain three emission peaks.

Cavity Catalysis of an Enantioselective Reaction under Vibrational Strong Coupling.

Strong light-matter interaction is emerging as an exciting tool for controlling chemical reactions. Here, we demonstrate an L-proline-catalyzed direct asymmetric Aldol reaction under vibrational strong coupling. Both the reactants (4-nitrobenzaldehyde and acetone) carbonyl bands are coupled to an infrared photon and react in the presence of L-proline. The reaction mixture is eluted from the cavity, and the conversion yields and enantiomeric excess are quantified using NMR and chiral HPLC. The conversion yields increase by up to 90 % in ON-resonance conditions. Interestingly, a large increase in the conversion yield does not affect the enantiomeric excess. Further control experiments were carried out by varying the temperature, and we propose that the rate-limiting step may not be the deciding factor in enantioselectivity. Whereas the formation of the enamine intermediate is modified by cavity coupling experiments. For this class of enantioselective reactions, strong coupling does not change the enantiomeric excess, possibly due to the large energy difference in chiral transition states. Strong coupling can boost the formation of enamine intermediate, thereby favouring the product yield. This gives more hope to test polaritonic chemistry based on enantioselective reactions in which the branching ratios can be controlled.

Tunable optoelectronic response in van der Waals heterojunction transistors for artificial visual recognition

Optoelectronic synaptic transistors are advantageous in in-memory light sensing for artificial neural networks. Herein, optoelectronic synaptic junction field-effect transistors (JFETs) based on a Ga2O3/MoS2 heterojunction are fabricated. The devices exhibit robust electrical performances, including a high on/off ratio of 108, a low subthreshold swing of 69 mV dec−1, and a high output current of 3.4 μA μm−1. An inverter and a NAND gate are constructed based on the dual-gated configuration, with the inverter showing a high voltage gain of 28 and the near-ideal noise margin of 90.4%. Additionally, the devices demonstrate outstanding optoelectronic performances benefiting from the strong light–matter interactions of MoS2. Typical synaptic plasticities, including short-term plasticity, long-term plasticity, and spiking-rate-dependent plasticity, are simulated by applying the light pulses. Furthermore, metaplastic excitatory postsynaptic current, metaplastic facilitation of long-term potentiation and transition from potentiation to depression are also readily demonstrated. The artificial neural network, in which neurons are interconnected through our proposed optoelectronic synaptic transistors, achieves a high accuracy of 89.8% in recognizing handwritten digits. This work provides insight into the design of an optoelectronic synapse based on JFETs.

Time-of-flight detection of terahertz phonon-polariton

A polariton is a fundamental quasiparticle that arises from strong light-matter interaction and as such has attracted wide scientific and practical interest. When light is strongly coupled to the crystal lattice, it gives rise to phonon-polaritons (PPs), which have been proven useful in the dynamical manipulation of quantum materials and the advancement of terahertz technologies. Yet, current detection and characterization methods of polaritons are still limited. Traditional techniques such as Raman or transient grating either rely on fine-tuning of external parameters or complex phase extraction techniques. To overcome these inherent limitations, we propose and demonstrate a technique based on a time-of-flight measurement of PPs. We resonantly launch broadband PPs with intense terahertz fields and measure the time-of-flight of each spectral component with time-resolved second harmonic generation. The time-of-flight information, combined with the PP attenuation, enables us to resolve the real and imaginary parts of the PP dispersion relation. We demonstrate this technique in the van der Waals magnets NiI2 and MnPS3 and reveal a hidden magnon-phonon interaction. We believe that this approach will unlock new opportunities for studying polaritons across diverse material systems and enhance our understanding of strong light-matter interaction.

Chemical Vapor Deposition Growth of Atomically Thin SnSb2Te4 Single Crystals Toward Fast Photodetection

AbstractSnSb2Te4 (SST), a ternary van der Waals (vdW) material, has been widely investigated during last decades for potential applications in superconductivity, thermoelectricity, and optoelectronics. Recently, atomically thin SST has been predicted to show abnormal electronic band structure evolutions, high carrier mobility, and strong light–matter interaction. However, controllable synthesis of such SST crystals has been a huge challenge. Herein, atomically thin SST flakes are prepared via a chemical vapor deposition (CVD) method by using SbCl3, SnCl4·5H2O, and Te as the precursors. Multiple structural characterizations reveal that the SST flakes are single crystals with high crystallinity. Due to the narrow bandgap of 0.42 eV, SST‐based photodetectors have a broadband spectrum detection range from visible light through communication bands (480–1550 nm). More importantly, benefiting from a high room‐temperature carrier mobility over 300 cm2 V−1 s−1, the SST photodetectors demonstrate a response/recovery time of tens of tens of microseconds, which exceeds most typical transition metal dichalcogenide (TMDC) flakes. In addition, the photodetector maintains high performance after being exposed to the air for 2 months, suggesting good environmental stability. These excellent performances suggest that the SST flakes are promising for next‐generation optoelectronics.