Plasmonic Interactions Research Articles

Ultrafast Infrared Plasmonics.

Ultrafast plasmonics represents a cutting-edge frontier in light-matter interactions, providing a unique platform to study electronic interactions and collective motions across femtosecond to picosecond timescales. In the infrared regime, where energy aligns with the rearrangements of low-energy electrons, molecular vibrations, and thermal fluctuations, ultrafast plasmonics can be a powerful tool for revealing ultrafast electronic phase transitions, controlling molecular reactions, and driving subwavelength thermal processes. Here, the evolution of ultrafast infrared plasmonics, discussing the recent progress in their manipulation, detection, and applications is reviewed. The future opportunities, including their potential to probe electronic correlations, investigate intrinsic ultrafast plasmonic interactions, and enable advanced applications in quantum information are highlighted, which may be promoted by multi-physical field integrated ultrafast techniques.

Surface plasmon resonance excitation and imaging in circular gratings: a study of non-polarized, radial and azimuthal polarization effects

Abstract This study explores the effects of various polarization states on Surface Plasmon Resonance (SPR) in circular gratings, emphasizing their potential in sensing technologies. We present a mathematical modeling framework alongside experimental investigations involving the fabrication and characterization of circular gratings using linearly polarized, radially polarized, and non-polarized light. Our findings demonstrate stable SPR responses across multiple polarization angles, with strong signals achievable even with non-polarized light, minimizing reliance on polarizers. Additionally, we analyze spatial intensity responses and the influence of polarization on excitation patterns, enhancing our understanding of plasmonic interactions. Through Surface Plasmon Resonance imaging (SPRi), we highlight the capability to capture topographical information, further contributing to advancements in plasmonics and the development of improved sensing devices.

Polarization-Dependent Plasmon-Induced Doping and Strain Effects in MoS2 Monolayers on Gold Nanostructures.

Monolayers of transition-metal dichalcogenides, such as MoS2, have attracted significant attention for their exceptional electronic and optical properties, positioning them as ideal candidates for advanced optoelectronic applications. Despite their strong excitonic effects, the atomic-scale thickness of these materials limits their light absorption efficiency, necessitating innovative strategies to enhance light-matter interactions. Plasmonic nanostructures offer a promising solution to overcome those challenges by amplifying the electromagnetic field and also introducing other mechanisms, such as hot electron injection. In this study, we investigate the vibrational and optical properties of MoS2 monolayer deposited on gold substrates and gratings, emphasizing the role of strain and plasmonic effects using conventional spectroscopic techniques. Our results reveal significant biaxial strain in the supported regions and a uniaxial strain gradient in the suspended ones, showing a strain-induced exciton and carrier funneling effect toward the center of the nanogaps. Moreover, we observed an additional polarization-dependent doping mechanism in the suspended regions. This effect was attributed to localized surface plasmons generated within the slits, as confirmed by numerical simulations, which may decay nonradiatively into hot electrons and be injected into the monolayer. Photoluminescence measurements further demonstrated a polarization-dependent trion-to-A exciton intensity ratio, supporting the hypothesis of additional plasmon-induced doping. These findings provide a comprehensive understanding of the strain-mediated funneling effects and plasmonic interactions in hybrid MoS2/Au nanostructures, offering valuable insights for developing high-efficiency photonic devices and quantum technologies, including polarization-sensitive detectors and excitonic circuits.

Electrically Tunable Metasurface Reflector based on Graphene–Metal Plasmon Interactions on a Silver Grating

Electrically Tunable Metasurface Reflector based on Graphene–Metal Plasmon Interactions on a Silver Grating

High-Throughput Multiplexed Plasmonic Color Encryption of Microgel Architectures via Programmable Dithering-Mask Flow Microlithography.

Silver nanoparticles (AgNPs) are known for their unique plasmonic colors and interaction with light, making them ideal for color printing and data encoding. Traditional methods like electron beam lithography (EBL) and focused ion beam (FIB) milling, however, suffer from low throughput and high costs. In this paper, a scalable and cost-efficient method is introduced for producing multiplexed plasmonic colors by in situ photoreducing AgNPs within microgel architectures with controlled porosity. Utilizing a digital micro-mirror device (DMD)-based flow microlithography system combined with a programmable dithering-mask technique, the high-throughput synthesis of shape or barcoded microparticles is facilitated, along with large-scale, high-resolution images embedded with hidden multiplexed plasmonic colors. This approach allows for a hidden multiplexed plasmonic color code library, significant enhancing the encoding capacity of barcode microparticles from 33 to 303 (a 1000-fold increase). Additionally, quantitative agreement is achieved between chemically encrypted and optically decrypted plasmonic colors using a deep learning classifier. Moreover, the method also supports the production of large scale (>5.6 × 5.6cm2), high-resolution (>300 dpi) microgel arrays encrypted with multiple plasmonic colors in under 30min. The multiplexed plasmonic coloration strategy in microgel architectures paves a new way for hidden data storage, secure optical labeling, and anti-counterfeiting technologies.

Engineering the plasmonic activities of copper nanostructures for SERS and photocatalysis

Nanoparticles of plasmonic metals such as gold (Au), silver (Ag) and copper (Cu) have numerous applications due to their localized surface plasmon resonance. Among these, nanoparticles of Cu remain underexplored when compared to Au and Ag, although the former is much cheaper. Here we report the surface enhanced Raman spectroscopy (SERS), interaction of molecule with a plasmonics and photocatalysis applications of Cu nanostructures. Hexagonal and cubic shaped Cu nanostructures were successfully synthesized by varying the reaction conditions in a polyol synthesis method. Rapid nucleation at an elevated temperature (140 °C) and subsequent slow growth at lower temperature (80 °C) in presence of PVP polymeric stabilizer resulted in the formation of uniform cube shaped Cu nanoparticles (Cucube). Whereas polyol synthesis at a low temperature (80 °C) resulted in hexagonal Cu nanoparticles (Cuhex). Cuhex exhibited higher SERS enhancement compared to Cucube. Specifically, Using 532, 633 and 785 nm lasers, Cuhex showed enhancement factor 9.0×105. The detection limit as low as 10-10 M for RhB using Cuhex. Moreover, based on emission and time-dependent measurements, strong molecular and plasmonic interactions reveal energy transfer from RhB molecules to the Cu nanostructures. Additionally, Cuhex showed very good catalytic and visible light plasmonic photocatalytic activities for the para-nitrophenol (p-NP) reduction reaction.

Using polarization sensitive SMLM to infer the interaction strength of dye-plasmonic nanosphere systems

Single-molecule microscopy is an effective tool for the characterization of fluorophore–plasmonic structure interaction. However, sophisticated evaluation is required as specific information is hidden in the emission. Here, we theoretically and experimentally investigated the emission polarization of rotationally mobile fluorophores near plasmonic Au–Ag alloy nanospheres. We developed an elaborate calculation based on the Mie theory, which considers the rotational mobility of dyes near spherical plasmonic nanoparticles of any size. Furthermore, we have created a simplified model that describes the emission’s degree of polarization within 10% accuracy in the case of small nanoparticles, when dipole approximation is valid. Our results indicate the close relation of the polarization degree of the emission, which can reach up to be ∼0.8 in the resonant case, to fluorescence scattering. DNA-PAINT single-molecule localization microscopy experiments conducted using AF488 and Atto647N dyes revealed that the measured polarization degree distribution followed the tendency predicted by calculations.

Bimodal functionality of highly conductive nanostructured silver film towards improved performance of photosystem I-based graphene photocathode

We present the novel design of photosystem I (PSI)-based biosolar cell, whereby conductive transparent electrode materials, such as ITO or FTO, are replaced with glass covered with silver island film. This nanostructured metallic layer combines high electric conductance with enhancing the absorption efficiency of the PSI biocatalyst via the plasmonic effect. We demonstrate strong enhancement of the photocurrent generated in the biohybrid electrode composed of oriented layers of PSI reaction centers due to plasmonic interactions of the PSI fluorophores and redox centres with the conductive silver island film.

Plasmonic coupling dependent sensitivity in localized surface plasmon resonance based optical sensors

This paper investigates the impact of environmental changes on silver nanoparticles (AgNp) immobilized sensor probe within strong and weak plasmonic coupling regimes. To monitor these interaction regimes, evanescent wave absorption based on fiber optic and attenuated total reflection techniques have been employed. In the weak coupling regime, variations in refractive index (RI) primarily affect intensity rather than wavelength. Conversely, in the strong coupling regime, intensity decreases, while wavelength sensitivity increases with changes in RI. Our findings qualitatively agree with a theoretical framework based on the discrete dipole approximation (DDA) for two-particle interacting systems, providing valuable insights for optimizing plasmonic interactions to enhance sensitivity. This information will aid the scientific and industrial community in understanding the plasmonic interaction region for maximizing sensitivity of Localized surface plasmon resonance (LSPR) based photonic devices.

Multi-wavelength and broadband plasmonic switching with V-shaped plasmonic nanostructures on a VO2 coated plasmonic substrate

In this paper, periodic arrays of identical V-shaped gold nanostructures and variable V-shaped gold nanostructures are designed on top of a gold-coated silicon dioxide (SiO2) substrate with a thin spacer layer of vanadium dioxide (VO2) to realize multi-wavelength and broadband plasmonic switches, respectively. The periodic array of identical V-shaped nanostructures (IVNSs) with small inter-particle separation leads to coupled interactions of the elementary plasmons of a V-shaped nanostructure (VNS), resulting in a hybridized plasmon response with two longitudinal plasmonic modes in the reflectance spectra of the proposed switches when the incident light is polarized in the x-direction. The x-direction is oriented along the axis that joins the V-junctions of all VNSs in one unit cell of the periodic array. On exposure to temperature, electric field, or optical stimulus, the VO2 layer transforms from its monoclinic semiconducting state to its rutile metallic state, leading to an overall change in the reflectance spectra obtained from the proposed nanostructures and resulting in an efficient multi-wavelength switching action. Finite difference time domain modelling is employed to demonstrate that an extinction ratio (ER) >12 dB at two wavelengths can be achieved by employing the proposed switches based on periodic arrays of IVNSs. Further, plasmonic switches based on variable V-shaped nanostructures—i.e. multiple VNSs with variable arm lengths in one unit cell of a periodic array—are proposed for broadband switching. In the broadband operation mode, we report an ER >5 dB over an operational wavelength range >1400 nm in the near-IR spectral range spanning over all optical communication bands, i.e. the O, E, S, C, L and U bands. Further, it is also demonstrated that the wavelength of operation for these switches can be tuned by varying the geometrical parameters of the proposed switches. These switches have the potential to be employed in communication networks where ultrasmall and ultrafast switches with multi-wavelength operation or switching over a wide operational bandwidth are inevitably required.

Pongamia pinnata seed extract-mediated green synthesis of silver nanoparticle loaded nanogel for estimation of their antipsoriatic properties.

This research describes the eco-friendly green synthesis of silver nanoparticles employing Pongamia pinnata seed extracts loaded with nanogel formulations (AgNPs CUD NG) to improve the retention, accumulation, and the penetration of AgNPs into the epidermal layer of psoriasis. AgNPs were synthesized using the Box-Behnken design. Optimized AgNPs and AgNPs CUD NG were physico-chemically evaluated using UV-vis spectroscopy, SEM, FT-IR, PXRD, viscosity, spreadability, and retention studies. It was also functionally assessed using an imiquimod-induced rat model. The entrapment efficiency of AgNPs revealed ~ 79.35%. Physico-chemical parameters announced the formation of AgNPs via surface plasmon resonance and interaction between O-H, C = O, and amide I carbonyl group of protein extract and AgNO3. Optimized AgNPs showed spherical NPs ~ 116nm with better physical stability and suitability for transdermal applications. AgNPs CUD NG revealed non-Newtonian, higher spreadability, and better extrudability, indicating its suitability for a transdermal route. AgNPs CUD NG enhanced the retention of AgNPs on the psoriatic skin compared to normal skin. Optimized formulations exhibit no irritation by the end of 72h, indicating formulation safety. AgNPs CUD NG at a dose of 1 FTU showed significant recovery from psoriasis with a PASI score of ~ 0.8 compared to NG base and marketed formulations. Results indicated that seed extract-assisted AgNPs in association with CUD-based NG formulations could be a promising nanocarrier for psoriasis and other skin disorders.

Giant Plasmonic Enhancement of Chiroptical Properties by Anisotropic Gold Nanocrystals Grown In Situ in a Chiral Polymer

AbstractPolymer‐based chiral materials with exceptional optical activity can dramatically impact integrated chiral photonics due to the tunability of their optical responses coupled with ease of fabrication. Realizing these applications requires increasing the absorbance dissymmetry factor. Here, in situ, the synthesis of gold nanostars is introduced in a chiral polymer medium to produce chiral polymer‐anisotropic plasmonic nanocrystal nanocomposites. The optimized nanocomposite shows a tenfold enhancement of dissymmetry factor, gabs (up to 0.64) and a corresponding 46‐fold augmented circular dichroism (CD) value upon annealing, relative to the annealed pure chiral polymer film. Moreover, the enhancement relative to the non‐annealed polymer‐gold nanostar nanocomposite is strikingly higher: a 35‐fold increase in gabs and a 4272‐fold increase in CD. Based on computational analysis, it is concluded that the local plasmon field enhancement around the crevices and tips of nanostars is mainly responsible for the observed effect which is further supported by a signal enhancement in Surface Enhanced Raman Scattering (SERS). Thus, this study underscores the significant role of close‐range plasmon interactions in altering the chiroptical response of nanocomposite materials and a practical pathway toward the realization of next‐generation integrated photonics and optoelectronic circuitry with photon spin control.

Plasmonically engineered nitrogen-vacancy spin readout.

Ultra-precise readout of single nitrogen-vacancy (NV) spins holds promise for major advancements in quantum sensing, computing, and communication technologies. Here we present a rigorous open quantum theory capable of simultaneously capturing the optical, vibronic, and spin interactions of the negatively charged NV center, both in the presence and absence of plasmonic interaction. Our theory is verified against existing experiments in the literature. We predict orders of magnitude brightness and contrast enhancements in optically detected magnetic resonance (ODMR) and NV spin qubit readout arising from plasmonic interaction. Such optimal enhancements occur in carefully engineered parameter regions, necessitating rigorous modelling prior to experimentation. Our theory equips the community with a tool to identify such regions.

Plasmonic Interaction of Gold Nanoparticles with the Anti-hypoglycemic Medicament Metformin

Plasmonic Interaction of Gold Nanoparticles with the Anti-hypoglycemic Medicament Metformin

Precise regulation of surface plasmonic hotspots in an Au split nanoring coupled system

The signal enhancement in plasmon-enhanced spectroscopy is primarily contributed by hotspots generated through the surface plasmon resonance effect. Precise control of hotspot positions within nanostructures is of great significance in surface-enhanced Raman spectroscopy (SERS) and high spatial resolution imaging. However, predicting the positions of hotspots is challenging due to the small nanogaps and complex plasmonic interactions. In this study, we theoretically investigate the localized surface plasmonic properties of split ring nanostructure. The effects of variations in the inner radius, gap distance and thickness of the split ring on the hotspot distribution at the nanogaps are systematically analyzed using a three-dimensional finite element method. The results demonstrate that precise control over the positions and quantities of hotspots can be achieved by choosing the excitation wavelength and the gap size of the split rings. The calculated maximum Raman enhancement obtained at the hotspots can reach nine orders of magnitude. Our findings not only contribute to a deeper understanding of the SERS enhancement mechanism, but also provide theoretical insights for further development of surface-enhanced fluorescence, plasmonic sensors, and super-resolution imaging in the field of interface spectroscopy.

Ni-based plasmonic photocatalysts for solar to energy conversion: A review

Plasmonic-based semiconductors are compelling contenders of current research endeavors to drive chemical reactions via plasmonic and phononic light-matter interactions. Among various plasmonic metals, Ni as a non-precious metal has been extensively studied due to its ability to participate in interband excitation and comparable metal-hydrogen binding energy to that of noble metals including Pt and Ag. The phenomenally high charge-carrier density in photoexcited Ni-based plasmonic nanomaterials offers photochemical conversion of high-energy chemical bonds accompanied by thermal effect. Since the research on the plasmonic activity of the non-precious metal is still emerging, no comprehensive review has addressed the significance of Ni as a plasmonic photocatalyst to the best of our knowledge. This review article sums up the recent progress in the field of plasmonic photocatalysis focusing on Ni-based photocatalysts. The basic principles of the plasmonic effect have been presented, along with an explanation of why Ni may be a viable option. Ni has been investigated for use as a co-catalyst and plasmonic photocatalyst in composite photocatalysis to achieve an accelerated process. After the energy transfer mechanism has been assessed, the review covers the state-of-the-art of two significant effects—plasmon energy transfer and the localized heating effect that are responsible for increased efficiency in energy production. In conclusion, we have included a synopsis of the assessment and emphasized the problems that must be resolved before the technology can be made available for purchase. In a nutshell, the chemistry of plasmonic photocatalysis is promising; but acquiring a detailed mechanism of charge transfer and utilization of charge carriers is still a roadblock in apprehending the full potential of plasmonic photocatalysis. Therefore, this study aims to motivate the scientific community to envision impactful work in the creation of next-generation plasmonic photocatalysts.

Plasmonic hybridized modes empowered by strong plasmon interaction in the nanograting-dielectric-metal stacked structure

Abstract The coupling between surface plasmon polaritons (SPPs) and waveguide (WG) modes has been widely investigated by using prism-coupled structures and has demonstrated a large number of interesting physical phenomena. However, these conventional structures mainly rely on the angle-dependent total internal reflection excitation. This is not conducive to their further development due to the large volume and the requirement of oblique incidence. In this paper, we theoretically propose a three-layer nanograting-dielectric-metal (NDM) plasmonic structure. Within this structure, a thickness-dependent plasmonic WG (PWG) mode in the middle dielectric cavity strongly couples with SPPs on the top surface, resulting in two new hybridized PWG-SPPs modes. This hybridization coupling phenomenon is analyzed in detail by using plasmonic hybridization and two coupled oscillator models. Besides, a thorough investigation is conducted on the sensing performance of these two PWG-SPPs hybridized modes. The difference in sensing characteristics between these two hybridized modes can be well explained by their coupling strength variation. This NDM plasmonic nanostructure owns unparalleled advantages in the generation and modulation of a variety of new modes, effectively promoting the development of miniaturized optoelectronic devices.

Investigation of a highly-sensitive aluminum-based plasmonic device using antimonene for sensing applications

Aluminum (Al) has gained popularity for surface plasmon resonance-based applications due to its affordability and compatibility with CMOS technology at the nanoscale. Over angle-interrogation mode, plasmonic interactions occurring at the metal-dielectric junction, are the outcomes of the attenuated total internal reflection phenomenon. Modified Al-based Kretschmann configuration results in phase-matching conditions that are seen as resonant points in the reflection characteristics. In our work, we have engineered an Al-based plasmonic device utilizing Antimonene as a 2D nanomaterial for bio-sensing purposes in the Near-Infrared (NIR) spectral domain. The study investigates the performance of Surface Plasmon Resonance (SPR) based refractive index sensor using different 2D nanomaterials with an optimized Al thickness of 30 nm. A comparative analysis of Al-based Kretschmann configurations in the presence of Graphene, Black Phosphorus, MXene, and Antimonene is presented using engineered intermediate layers. It is observed that the Al-antimonene-based plasmonic device exhibits improved sensing parameters in the NIR optical window.

Plasmon induced hot carrier distribution in Ag20 -CO composite.

The interaction between plasmons and the molecules leads to the transfer of plasmon-induced hot carriers, presenting innovative opportunities for controlling chemical reactions on sub-femtosecond timescales. Through real-time time-dependent density functional theory simulations, we have investigated the enhancement of the electric field due to plasmon excitation and the subsequent generation and transfer of plasmon-induced hot carriers in a linear atomic chain of Ag20 and an Ag20 -CO composite system. By applying a Gaussian laser pulse tuned to align with the plasmon frequency, we observe a plasmon-induced transfer of hot electrons from the occupied states of Ag to the unoccupied molecular orbitals of CO. Remarkably, there is a pronounced accumulation of hot electrons and hot holes on the C and O atoms. This phenomenon arises from the electron migration from the inter-nuclear regions of the C-O bond towards the individual C and O atoms. The insights garnered from our study hold the potential to drive advancements in the development of more efficient systems for catalytic processes empowered by plasmonic interactions.

Theoretical research on a broadband terahertz absorber for thermally controlled radiation emission based on the epsilon-near-zero mode.

In this paper, a tunable and ultra-broadband terahertz (THz) absorber is proposed. The absorber, which is built upon the conventional metal-dielectric-metal tri-layer configuration, incorporates a KCl thin film within the dielectric gap situated between the top resonator and the middle dielectric layer. The simulation indicates that the absorber effectively captures more than 90% of terahertz waves between 3.6 and 7.3 THz, achieving absorption of over 99% within the 5.8-6.9 THz range. This unique broadband absorber is enabled by the interaction of plasmon and epsilon-near-zero (ENZ) modes. Additionally, due to the utilization of VO2 in the top resonator, the designed absorber holds potential to function as a thermally controlled radiation emitter, exhibiting a high emissivity of 90.5% at high temperatures while maintaining a low emissivity of 8.2% at low temperatures. The absorber is uncomplicated and adjustable, offering great potential for use in thermal management, terahertz camouflage, and engineering insulation.