Plasmonic Interactions Research Articles

Numerical study of a D-shaped optical fiber SPR biosensor for monitoring refractive index variations in biological tissue via a thin layer of gold coated with titanium dioxide

This study aims to explore the numerical analysis of the impact of integrating titanium oxide (TiO2) into a D-shaped optical fiber biosensor based on surface plasmon resonance (SPR). A thin layer of gold (Au) is applied to the flat section of the fiber, which is also coated with a thin layer of titanium dioxide (TiO2). The behavior and performance of the proposed biosensor for use in biological environments are evaluated using the finite element method (FEM). The optical response of SPR-based biosensors is highly dependent on the analyzed medium, enabling the detection of pathogenic cells and abnormalities in biological tissues. This provides high sensitivity and selectivity, as well as real-time detection accuracy and speed. In this study, the biosensor is incorporated into a biological medium with a refractive index that varies with wavelength. A series of simulations have been conducted to plot the spectra of transmissions, absorptions, and dielectric losses obtained in the output of the sensor instrument. From these spectra, the corresponding surface plasmon resonance (SPR) wavelength (λSPR) within the visible-near-infrared band can be determined. Taking into account the various parameters that influence plasmonic interactions, the biosensor's performance parameters, in particular sensitivity and refractive index resolution have been optimized. Our results show that the presence of the TiO2 layer improves the performance of the proposed sensor and offers the possibility of adjusting the resonance wavelength (λSPR). In addition, our proposed sensor can achieve a better resolution of 7.50×10-6[RIU] in 1.34-143 range of analyte refractive index, which notably exceeds that of current technologies. This opens up new prospects in the field of chemical and biological detection.

Microlens-Assisted Light-Scattering Imaging of Plasmonic Nanoparticles at the Single Particle Level.

We present a microlens-assisted imaging approach to record the scattering light of plasmonic nanoparticles at the single particle level. The microlens can significantly enhance the backscattering of visible light from individual plasmonic nanoparticles by several dozen folds, and single gold nanoparticles with a diameter as low as 60 nm can be imaged under a conventional optical microscope. This can benefit from a significant increase in the scattering intensity afforded by the microlens, meaning that the imaging of gold nanoparticles at a high temporal resolution (up to 5000 Hz) can be achieved, which is fast enough to record single particle adhesion events on the substrate. This research presents a fast and efficient means of acquiring scattering light from plasmonic nanoparticles, which has great potential to develop plasmonic nanoparticle-based biosensors and investigate a wide range of plasmonic nanoparticle-based fast interaction processes.

Stereoselective Plasmonic Interaction in Peptide-tethered Photopolymerizable Diacetylenes Doped with Chiral Gold Nanoparticles.

Designing polymeric systems with ultra-high optical activity is instrumental in the pursuit of smart artificial chiroptical materials, including the fundamental understanding of structure/property relations. Herein, we report a diacetylene (DA) moiety flanked by chiral D- and L-FF dipeptide methyl esters that exhibits efficient topochemical photopolymerization in the solid phase to furnish polydiacetylene (PDA) with desired control over the chiroptical properties. The doping of the achiral gold nanoparticles provides plasmonic interaction with the PDAs to render asymmetric shape to the circular dichroism bands. With the judicious design of the chiral amino acid ligand appended to the AuNPs, we demonstrate the first example of selective chiral amplification mediated by stereo-structural matching of the polymer-plasmonic AuNP hybrid pairs. Such ordered self-assembly aided by topochemical polymerization in peptide-tethered PDA provides a smart strategy to produce soft responsive materials for applications in chiral photonics.

Stereoselective Plasmonic Interaction in Peptide‐tethered Photopolymerizable Diacetylenes Doped with Chiral Gold Nanoparticles

AbstractDesigning polymeric systems with ultra‐high optical activity is instrumental in the pursuit of smart artificial chiroptical materials, including the fundamental understanding of structure/property relations. Herein, we report a diacetylene (DA) moiety flanked by chiral D‐ and L‐FF dipeptide methyl esters that exhibits efficient topochemical photopolymerization in the solid phase to furnish polydiacetylene (PDA) with desired control over the chiroptical properties. The doping of the achiral gold nanoparticles provides plasmonic interaction with the PDAs to render asymmetric shape to the circular dichroism bands. With the judicious design of the chiral amino acid ligand appended to the AuNPs, we demonstrate the first example of selective chiral amplification mediated by stereo‐structural matching of the polymer‐plasmonic AuNP hybrid pairs. Such ordered self‐assembly aided by topochemical polymerization in peptide‐tethered PDA provides a smart strategy to produce soft responsive materials for applications in chiral photonics.

Collectively Enhanced Giant Circular Dichroism of Germanium Nanohelix Square Lattice Arrays

Circular dichroism is a unique chiroptical signature of the chirality of a system and is a prevalent way to characterize and distinguish systems on a fundamental level and for their technological applicability. Thus, engineering and maximizing the chiroptical response of a single chiral object or a metasurface composed of chiral entities is a formidable task. Current efforts strongly focus on individual metallic nanostructures and their periodic ensembles to harvest on (resonant) plasmonic properties and interactions. This route, however, waives the advantages of high‐refractive‐index nanoscale materials embracing low dissipative losses at optical wavelengths and electromagnetic fields penetrating and propagating in such materials. Herein, a strong circular dichroism is demonstrated in square lattices of nanohelices made of the high‐refractive‐index semiconductor germanium, with dissymmetry factors outperforming metal‐based ensembles. The observation of a much higher dissymmetry emerges for illumination with spatially coherent light, in comparison to spatially incoherent light. High dissymmetry is attributed to cooperative coupling between single helices, resulting from the combination of dielectric resonances of both the individual helical building blocks and the highly ordered lattice.

Componential and molecular-weight-dependent effects of natural organic matter on the colloidal behavior, transformation, and toxicity of MoS2 nanoflakes

The potential widespread applications in water processing have rendered the necessity for investigations of the fate and hazard of molybdenum disulfide (MoS2) nanosheets. Herein, it was found that humic acid (HA) had better performances toward stabilizing pure 2H phase MoS2 and chemical-exfoliated MoS2 (ce-MoS2) in electrolyte solutions than fulvic acid (FA), and molecular weight (MW)-dependent manners were disclosed due to steric repulsions. Compared with darkness, the extent to which the aggregation and sedimentation of ce-MoS2 facilitated by visible light irradiation was greater in the presence of HA and FA fractions, likely due to the introduction of stronger plasmonic dipole-dipole interaction and Van der Waals attraction forces. HA-triggered structural disintegration of nanosheets was performed after irradiation and it was observed to be more significant with the increase in MWs, whereas the MW-dependent dissolution of MoS2 caused by FA was much quicker than that by HA owing to the higher generation of singlet oxygen. Moreover, FA lowered the bioavailability of MoS2 and relieved its toxicity to zebrafish more effectively than HA. Our findings boost the insights into the effects of organic molecules on the fates and hazards of MoS2, providing guidance for the MoS2-based nanotechnological development on environment.

On the Surface Plasmonic Waves Excited by a Dipole Above Anisotropic and Spatially Dispersive Two-Dimensional Surfaces of Infinite Extent in Planarly Layered Media

The surface plasmonic waves excited by a vertical or horizontal oriented Hertzian dipole above anisotropic and spatially dispersive two-dimensional surfaces of infinite extent embedded in planarly layered uniaxial media are investigated using the dyadic Green function approach. The spectral-domain transmission line analogy Green function formulation and iso-frequency-contour equations are derived. The methods to accurately and efficiently evaluate the two-dimensional Fourier integral arising from the spatial-domain Green function computation are also developed. To resolve the numerical inefficiency due to the highly oscillatory integrand and singularities of surface plasmonic waves that possess large wavenumber, the methods of extrapolating the real-axis integration combined with singularity subtraction are proposed and found to be applicable to a wide range of observation distances. As an application example of the proposed formulation, we compute the scattered fields of a vertical dipole above the graphene biased by drift current which exhibits significant spatial dispersion. It is shown that the light-matter interaction of graphene plasmons can be significantly reinforced when placed above uniaxially anisotropic epsilon-near-zero substrates. The proposed formulation may provide the methodology for the computational analysis of two-dimensional materials and surface plasmonic waves.

Sustainable chemistry with plasmonic photocatalysts

Abstract There is a pressing global need to increase the use of renewable energy sources and limit greenhouse gas emissions. Towards this goal, highly efficient and molecularly selective chemical processes that operate under mild conditions are critical. Plasmonic photocatalysis uses optically-resonant metallic nanoparticles and their resulting plasmonic, electronic, and phononic light-matter interactions to drive chemical reactions. The promise of simultaneous high-efficiency and product-selective reactions with plasmon photocatalysis provides a compelling opportunity to rethink how chemistry is achieved. Plasmonic nanoparticles serve as nanoscale ‘antennas’ that enable strong light–matter interactions, surpassing the light-harvesting capabilities one would expect purely from their size. Complex composite structures, combining engineered light harvesters with more chemically active components, are a focal point of current research endeavors. In this review, we provide an overview of recent advances in plasmonic catalysis. We start with a discussion of the relevant mechanisms in photochemical transformations and explain hot-carrier generation and distributions from several ubiquitous plasmonic antennae. Then we highlight three important types of catalytic processes for sustainable chemistry: ammonia synthesis, hydrogen production and CO2 reduction. To help elucidate the reaction mechanism, both state-of-art electromagnetic calculations and quantum mechanistic calculations are discussed. This review provides insights to better understand the mechanism of plasmonic photocatalysis with a variety of metallic and composite nanostructures toward designing and controlling improved platforms for green chemistry in the future.

Optical Binding-Driven Micropatterning and Photosculpting with Silver Nanorods.

Controlling the nano- and micropatterning of metal structures is an important requirement for various technological applications in photonics and biosensing. This work presents a method for controllably creating silver micropatterns by laser-induced photosculpting. Photosculpting is driven by plasmonic interactions between pulsed laser radiation and silver nanorods (AgNRs) in aqueous suspension; this process leads to optical binding forces transporting the AgNRs in the surroundings, while electronic thermalization results in photooxidation, melting, and ripening of the AgNRs into well-defined 3D structures. This work call these structures Airy castles due to their structural similarity with a diffraction-limited Airy disk. The photosculpted Airy castles contain emissive Ag nanoclusters, allowing for the visualization and examination of the aggregation process using luminescence microscopy. This work comprehensively examines the factors that define the photosculpting process, namely, the concentration and shape of the AgNRs, as well as the energy, power, and repetition rate of the laser. Finally, this work investigates the potential applications by measuring the metal-enhanced luminescence of a europium-based luminophore using Airy castles.

High-efficiency plasmonic luminescent solar concentrators based on thiol-ene polymer

Advances in solar energy harvesting technology require innovative approaches to meet the growing energy demand. In this work, we exploit the plasmonic interaction of metal nanoparticles with fluorophores to improve the optical performance of luminescent solar concentrators (LSCs). The plasmonic luminescent solar concentrators (PLSCs) with dimensions of 5 cm × 5 cm × 0.5 cm containing CsPbBr3 quantum dots (QDs) and gold nanoparticles (Au NPs) are fabricated, characterized, and evaluated systematically. As the Au NPs concentration increases, the optical performance of PLSCs exhibits, first enhancement, and then diminishment. When the Au NPs concentration is 2 × 10−4 wt%, the optimal external quantum efficiency, optical conversion efficiency, and power conversion efficiency of the PLSC reach 1.58%, 2.90%, and 0.437%, respectively. At higher concentrations of Au NPs, the non-radiative energy transfer from the CsPbBr3 QDs to the Au NPs leads to a decrease of the emission, which can be confirmed by the decreasing lifetime of the QDs. The overall optical performance of PLSCs depends on two competing effects, excitation rate and non-radiative energy transfer efficiency. Furthermore, the PLSC demonstrate the good aesthetic quality as an excellent substitute for commercial glass. We anticipate that the high optical conversion efficiency of PLSCs based on thiol-ene polymer would shed light on future application in LSCs.

THE INFLUENCE OF A POTENTIAL BARRIER ON THE MECHANISMS OF EXCITATION OF OWN FLUCTUATIONS IN RADIO PRODUCTS IN CONDITIONS OF EXPOSURE TO ELECTROMAGNETIC RADIATION

The subject matter is the processes of analysis and the mechanisms of the emergence of their own fluctuations in the semiconductor complex electro -radio devices (communications equipment), if there are currents and voltages entrusted with pulsed electromagnetic radiation, the results obtained in the work of the potential barrier on the border of the semi -conductive structure on the border of the semiconductor (voltage ampere) characteristics of a electro -radio device. The aim is model of transforming the energy of the flow of charged particles, induced by external electromagnetic radiation, into the energy of its own fluctuations in the semiconductor structure, taking into account the properties of the structure itself (heterogeneity of potential at the border). The implementation of this model is due to the effect of transitional radiation of moving charges, when the particle flow crosses the boundary of the media section with various electromagnetic properties (dielectric permeability) and part of its energy is transformed into the energy of its own fluctuations in the semiconductor structure. The objectives are: mechanisms of the strengthening (instability) mode of semiconductor components of semiconductor devices under conditions of impulse electromagnetic radiation in the presence of a potential barrier on the boundary of the media of the media. The methods used are the method of theory of small disturbances, which allows you to determine the spectrum of the own vibrations of the system: the current fluctuations of the semiconductor device in electromagnetic radiation. The following results are obtained: The interaction of surface plasmons with the flow was considered charged particles in the presence of a potential barrier based on energy principle. Kinetic equations have been obtained that determine the change in the number superficial plasmons, expressions for the increments of their instability with taking into account the size of a potential barrier on the border, which leads to the appearance of a beam reflected from the border. The results of the work allow you to take into account the contribution of the reflected and completed component of the energy flow energy into the total energy of the radiation of surface vibrations. The mechanisms of interaction between the flow of charged particles with the own electromagnetic fluctuations of two -dimensional electronic gas, the occurrence of which is due to the presence of a potential barrier on the border of the media section. Conclusion. Determination of the amplification (generation) modes of electro -radio products that distort their volt are ampere characteristics (reversible failures) depending on the parameters of external electromagnetic radiation. An analysis of the routes obtained in the work can be used in the development of radio emergency for working in a millimeter and submilimeter range (amplifiers, generators and frequency converters). Assessment of indicators of the exponential growth of amplitudes of the own fluctuations of semiconductor components (increement of instability as a criterion of reversible failures) show that the magnitude of the energy of radiation lies within the sensitivity of modern receivers of the radiation of the submilimeter range and is the reason for the failure.

Terahertz inner and outer edge modes in a tetramer of strongly coupled spoof localized surface plasmons.

Photonic edge mode confining light in cavities of surface plasmons is beneficial in image and biosensor applications. In the terahertz band, however, the edge mode in a cavity of spoof localized surface plasmons has not matured sufficiently. Herein, a cost-effective strategy to achieve a terahertz photonic edge mode using a metasurface of strongly coupled fourfold spoof localized surface plasmons in a tetramer layout is demonstrated. The quality factors of edge modes decrease when the tetramer shrinks, as revealed by the terahertz dielectric functions. The edge modes that emerge can be categorized as inner and outer edge modes, as deduced from the simulated electric field distribution. Our results show that the edge modes are due to the interaction of spoof localized surface plasmons in the terahertz band.

Strong Plasmon-Mie Resonance in Si@Pd Core-Ω Shell Nanocavity.

The surface plasmon resonance (SPR) and localized surface plasmon resonance (LSPR) can be used to enhance the generation of the hot electrons in plasmon metal nanocavity. In this paper, Pd nanomembrane (NMB) is sputtered on the surface of Si nanosphere (NS) on glass substrate to form the Si@Pd core-Ω shell nanocavity. A plasmon-Mie resonance is induced in the nanocavity by coupling the plasmon resonance with the Mie resonance to control the optical property of Si NS. When this nanocavity is excited by near-infrared-1 (NIR-1, 650 nm-900 nm) femtosecond (fs) laser, the luminescence intensity of Si NS is dramatically enhanced due to the synergistic interaction of plasmon and Mie resonance. The generation of resonance coupling regulates resonant mode of the nanocavity to realize multi-dimensional nonlinear optical response, which can be utilized in the fields of biological imaging and nanoscale light source.

Polygonal gold nanocrystal induced efficient phase transition in 2D-MoS2 for enhancing photo-electrocatalytic hydrogen generation

Plasmonic nanocrystals (NCs) assisted phase transition of two-dimensional molybdenum disulfide (2D-MoS2) unlashes numerous opportunities in the fields of energy harvesting via electrocatalysis and photoelectrocatalysis by enhancing electronic conductivity, increasing catalytic active sites, lowering Gibbs free energy for hydrogen adsorption and desorption, etc. Here, we report the synthesis of faceted gold pentagonal bi-pyramidal (Au-PBP) nanocrystals (NC) for efficient plasmon-induced phase transition (from 2 H to 1 T phase) in chemical vapor deposited 2D-MoS2. The as-developed Au-PBP NC with the increased number of corners and edges showed an enhanced multi-modal plasmonic effect under light irradiations. The overpotential of hydrogen evolution reaction (HER) was reduced by 61 mV, whereas the Tafel slope decreased by 23.7 mV/dec on photoexcitation of the Au-PBP@MoS2 hybrid catalyst. The enhanced performance can be attributed to the light-induced 2H to 1 T phase transition of 2D-MoS2, increased active sites, reduced Gibbs free energy, efficient charge separation, change in surface potential, and improved electrical conductivity of 2D-MoS2 film. From density functional theory (DFT) calculations, we obtain a significant change in the electronic properties of 2D-MoS2 (i.e. work function, surface chemical potential, and the density of states), which was primarily due to the plasmonic interactions and exchange-interactions between the Au-PBP nanocrystals and monolayer 2D-MoS2, thereby enhancing the phase transition and improving the surface properties. This work would lay out finding assorted routes to explore more complex nanocrystals-based multipolar plasmonic NC to escalate the HER activity of 2D-MoS2 and other 2D transition metal dichalcogenides.

Surface plasmon mediated harmonically resonant effects on third harmonic generation from Au and CuS nanoparticle films

Abstract A growing class of nonlinear materials employ the localized surface plasmonic resonance (LSPR) of nanoparticles to enhance harmonic generation. Material systems containing harmonically coupled metallic and semiconductor plasmonic nanoparticles have been shown to further increase performance. Here, we explore the effect of dual plasmonic interactions in bilayer CuS and Au nanoparticle films on third harmonic generation (THG). Detuning the CuS LSPR away from the excitation frequency changes the dominant upconversion pathway from THG to multiple photon photoluminescence (MPPL). Changing the size of the Au nanoparticle red shifts the LSPR from the second harmonic of the pump frequency and also eliminates the enhancement effect. When both LSPRs satisfy the harmonic condition, simultaneous excitation of CuS-Au nanoparticle films at the resonant frequency of each nanoparticle species enhances the generation of third harmonic light by sum-frequency generation, suggesting that the enhancement of THG in dually plasmonic nanoparticle films is the result of a cascaded nonlinear mechanism. An analytic model of the interaction between the plasmonic nanoparticles due to incoherent dipolar interactions is also presented. Understanding these processes opens a pathway for developing ultrafast, high-efficiency upconversion thin-film devices by clarifying the conditions that efficiently produce third harmonic generation without background MPPL or additional harmonics.

Plasmonic photothermal therapy in the near-IR region using gold nanostars.

Photothermal therapy using nanoparticles is a prominent technique for cancer treatment. The principle is to maximize the heat conversion efficiency using plasmonic nanoparticle-light interaction. Due to their unique optical characteristics derived from their anisotropic structure, gold nanostars (GNSs) have gotten significant attention in photothermal therapy. To design a proper cancer treatment, it is vital to study the thermal effect induced close to the gold nanoparticles, in the vicinity, and the cancerous tissue. A temperature-dependent 2D model based on finite element method models is commonly used to simulate near-IR tumor ablation. The bioheat equation describes the photothermal effect within the GNSs and the environment. Surface cooling and heating strategies, such as the periodical heating method and a reduced laser irradiation area, were investigated to address surface overheating problems. We also determined that the optimal laser radius depends on tumor aspect ratio and laser intensity. Our results provide guidelines to evaluate a safe and feasible temperature range, treatment time, optimal laser intensity, and laser radius to annihilate a tumor volume.

Probing Bidirectional Plasmon-Plasmon Coupling-Induced Hot Charge Carriers in Dual Plasmonic Au/CuS Nanocrystals.

Heterostructured Au/CuS nanocrystals (NCs) exhibit localized surface plasmon resonance (LSPR) centered at two different wavelengths (551 and 1051nm) with a slight broadening compared to respective homostructured Au and CuS NC spectra. By applying ultrafast transient absorption spectroscopyweshow that a resonant excitation at the respective LSPR maxima of the heterostructured Au/CuS NCs leads to the characteristic hot charge carrier relaxation associated with both LSPRs in both cases. A comparison of the dual plasmonic heterostructure with a colloidal mixture of homostructured Au and CuS NCs shows that the coupled dual plasmonic interaction is only active in the heterostructured Au/CuS NCs. By investigating the charge carrier dynamics of the process,wefind that the observed interaction is faster than phononic or thermal processes (< 100fs). The relaxation of the generated hot charge carriers is faster for heterostructured nanocrystals and indicates that the interaction occurs as an energy transfer (we propose Landau damping or interaction via LSPR beat oscillations as possible mechanisms) or charge carrier transfer between both materials.Ourresults strengthen the understanding of multiplasmonic interactions in heterostructured Au/CuS NCs and will significantly advance applications where these interactions are essential, such as catalytic reactions.

Hybrid Image Graphene Polaritons with Extremely Confined Mode and Field Enhancement in the Terahertz Regime

AbstractGuiding terahertz waves below the diffraction limit of light typically excite graphene plasmons (GPs). However, the mode confinements of conventional GPs using graphene–dielectric interfaces are limited. To further squeeze the optical mode sizes, a graphene–dielectric–metal (GDM) configuration supporting an image graphene plasmon (IGP) has been reported recently through the plasmon interactions in a graphene sheet and its mirror image inside a metal with out‐of‐phase charge oscillations. This study proposes a waveguide structure consisting of a cylindrical dielectric wire over a GDM to achieve an ultraconfined mode area by coupling a dielectric waveguide and an IGP mode. Furthermore, this work examines the dependence of waveguide dimensions and material properties on the mode characteristics of the proposed hybrid IGP (HIGP). This HIGP achieves plasmon wavelengths 20 times shorter and normalized propagation lengths twice longer than GPs, accompanying a mode size of 3 × 10−8A0, where A0 is the diffraction‐limited mode area. Moreover, the simple structure makes the HIGP easy to be verified experimentally. This work demonstrates that the HIGP delivering strong light–matter interactions at extremely compact dimensions can be exploited for building highly integrated, enhanced nonlinear, high‐resolution sensing and imaging THz devices.

Titanium carbide MXenes-initiated plasmonic metal-support interaction for effective photocatalysis on uncoated Ag nanoparticles

Localized surface plasmon resonances enable the effective harvesting of visible-light photons and yield energetic electrons and holes on short timescale in plasmonic nanoparticles (NPs). However, the balance between the higher stability (which requires stabilizing ligands) and the higher photocatalytic activity (which prefers a clean surface for adsorbing reactant molecules and diminishing the charge-recombination rate) is still a challenge, limiting the efficiency of light utilization. Herein, we show that by forming uncoated Ag-Ti3C2 nanohybrids via in situ reduction, the photocatalytic performance of plasmonic Ag NPs is promoted with the benefit of plasmonic metal-support interaction with Ti3C2 MXenes. The photodegradation efficiency of the organic pollutant methyl orange is elevated from 1.0% to 96.5% due to the excellent metal-like conductivity of Ti3C2 and Schottky barriers of interfacial Ag-TiO2-x. This work reveals the assistance of MXenes for stabilizing the illuminated Ag NPs and boosting efficient hot charge carrier separations in direct plasmonic photocatalysis.

Ultra-confined Propagating Exciton–Plasmon Polaritons Enabled by Cavity-Free Strong Coupling: Beating Plasmonic Trade-Offs

Hybrid coupling systems consisting of transition metal dichalcogenides (TMD) and plasmonic nanostructures have emerged as a promising platform to explore exciton–plasmon polaritons. However, the requisite cavity/resonator for strong coupling introduces extra complexities and challenges for waveguiding applications. Alternatively, plasmonic nano-waveguides can also be utilized to provide a non-resonant approach for strong coupling, while their utility is limited by the plasmonic confinement-loss and confinement-momentum trade-offs. Here, based on a cavity-free approach, we overcome these constraints by theoretically strong coupling of a monolayer TMD to a single metal nanowire, generating ultra-confined propagating exciton–plasmon polaritons (PEPPs) that beat the plasmonic trade-offs. By leveraging strong-coupling-induced reformations in energy distribution and combining favorable properties of surface plasmon polaritons (SPPs) and excitons, the generated PEPPs feature ultra-deep subwavelength confinement (down to 1-nm level with mode areas ~ 10–4 of λ2), long propagation length (up to ~ 60 µm), tunable dispersion with versatile mode characters (SPP- and exciton-like mode characters), and small momentum mismatch to free-space photons. With the capability to overcome the trade-offs of SPPs and the compatibility for waveguiding applications, our theoretical results suggest an attractive guided-wave platform to manipulate exciton–plasmon interactions at the ultra-deep subwavelength scale, opening new horizons for waveguiding nano-polaritonic components and devices.