Silver Nanodisks Research Articles

Controlling directional emission of ions attached on the surface of nanoparticles

Abstract The interaction between lasers and nanoparticles holds significant theoretical and practical importance. Here, we investigate the near-field enhancement effects on silver nanotriangles and nanodiscs under ultrafast laser pulses, as well as the dynamics of protons and ions attached to the nanoparticle surfaces. By adjusting the size parameters of the nanoparticles, we explore the near-field enhancement effects and proton emission dynamics at different laser wavelengths. The results demonstrate that nanoparticles with varying morphologies substantially impact the proton momentum spectrum. The directional proton emission of nanotriangle structures is more pronounced compared to that of nanodiscs, and this effect can be further enhanced by adjusting the laser wavelength. Additionally, manipulating the thickness of particles also controls the Mie scattering phenomenon of light. Finally, we qualitatively discuss the emission processes of alpha particles and 9C6+ heavy ions. This research has important implications for proton and heavy ion radiotherapy in cancer treatment and targeted drug delivery, while providing theoretical foundations for understanding, characterizing, and controlling experimental studies of nanosystems with significant potential for expanding research into microdynamic behavior in complex nanomaterial superstructures.

Tunable Plasmon Resonance in Silver Nanodisk-on-Mirror Structures and Scattering Enhancement by Annealing.

In this study, we evaluated the surface plasmon characteristics of periodic silver nanodisk structures fabricated on a dielectric thin-film spacer layer on a Ag mirror substrate (NanoDisk on Mirror: NDoM) through finite difference time domain (FDTD) simulations and experiments involving actual sample fabrication. Through FDTD simulations, it was confirmed that the NDoM structure exhibits two sharp peaks in the visible range, and by adjusting the thickness of the spacer layer and the size of the nanodisk structure, sharp peaks can be obtained across the entire visible range. Additionally, we fabricated the NDoM structure using electron beam lithography (EBL) and experimentally confirmed that the obtained peaks matched the simulation results. Furthermore, we discovered that applying annealing at an appropriate temperature to the fabricated structure enables the adjustment of the resonance peak wavelength and enhances the scattering intensity by approximately five times. This enhancement is believed to result from changes in the shape and size of the nanodisk structure, as well as a reduction in grain boundaries in the metal crystal due to annealing. These results have the potential to contribute to technological advancements in various application fields, such as optical sensing and emission enhancement.

Optical theorem in the 3-D scattering from a locally perturbed lossless or lossy thin dielectric plate: silver disk-sealed hole analysis

This paper is aimed at devising a new optical theorem formulation for the 3-D plane-wave scattering from an infinite resistive plane and, more generally, a thin dielectric plate with a finite-size inhomogeneity shaped as a hollow or sealed hole. This formulation is further modified to cover the case of the plane guided wave scattering from the same inhomogeneity. For the lossless plane, the diffracted field combines a classical outgoing spherical wave, satisfying the Silver-Muller radiation condition, with an outgoing cylindrical guided wave supported by the plane; the power absorbed in the lossy filling is finite. When a lossy plane is involved, a complication appears: the total absorbed power is infinite. However, a change in the inhomogeneity characteristics perturbs the absorbed power density, thus suggesting the perturbative absorption analysis. After developing the analytical procedure for the resistive plane case and the corresponding generalization to the thin dielectric plate case, we illustrate the significance of the new optical theorem by the numerical analysis of the visible-light scattering from a dielectric plate with a circular nanosize hole sealed with a silver disk. Our analysis uses the in-house code having mathematically guaranteed convergence; it reveals the scattering and absorption resonances on the plasmon modes of the silver nanodisk. The derived optical theorem allows us to see that, in the resonances, the power carried by the guided waves can be comparable to the power scattered into the free space.

Effect of thermal annealing on the surface plasmon properties of gold and silver nanodisk structures fabricated by electron beam lithography

This study investigates the effect of thermal annealing on the surface plasmon resonance properties of gold and silver nanodisk structures fabricated by electron beam lithography. Despite no significant size change due to a nickel adhesion layer, thermal annealing at 500 °C notably altered surface plasmon resonance properties, especially in gold nanodisks, which showed peak blue-shifts and narrowing, indicating improved crystallinity. We fitted the peak shift by using an electromagnetic field analysis and discussed the changes in the dielectric function. The dielectric function of the simple Drude model was adopted, which was fitted to the values of the Lorentz Drude model in a limited wavelength region. While both silver and gold exhibited increased oscillation strength, only gold nanodisk structures showed a decrease in damping frequency. Increased oscillation strength indicated that these structures should be useful for selective enhancement of the light at specific wavelengths by a very simple heat treatment.

Photoluminescence Enhancement and Carrier Dynamics of Charged Biexciton in Monolayer WS2 Coupled with Plasmonic Nanocavity

Monolayer two-dimensional transition metal dichalcogenide (TMD)-based materials have become one of the ideal platforms for the study of multibody interactions due to their rich excitonic complexes. The coupling between optical nanocavity and material has become an important means for manipulating the optical properties of materials, but there are few studies on the coupling of nanocavities and the multi-body effect in materials. In this study, we investigate the optical properties of silver nanodisk (Ag ND) arrays covering a monolayer WS2. In the experimental sample, we observed a ~114.3-fold photoluminescence enhancement of charged biexciton in the heterostructure region, as compared to the monolayer WS2 region, a value which is much higher than those for exciton (~2.2-fold) and trion (~16.4-fold), a finding which is attributed to the Fano resonant coupling between monolayer WS2 and the Ag ND. By means of time-resolved spectroscopy, we studied the carrier dynamics in the hybrid system. Our findings reveal that resonant coupling promotes the formation and radiation recombination processes of the charged biexciton, significantly reducing the radiative recombination lifetime by ~15-fold, which is much higher than the measurement in exciton (~2-fold). Our results provide an opportunity to understand the multibody physics of coupling with nanocavities, which could facilitate the application of multi-body excitons in the fields of light-emitting devices and lasers, etc.

Realizing the diffraction coupling of silver nanodisk pair array for high-quality sensing

We report a novel approach to enhance the local electromagnetic fields of silver nanodisk pair arrays to achieve high-quality sensing. It is found that through lifting metallic nanodisk pair array by dielectric nanopillars to decrease the effects of substrates, the strong diffraction coupling of metallic nanodisk pair array can be achieved, which will result in a mixed localized surface plasmon resonance (LSPR) with huge electric field enhancement. More importantly, we also demonstrate that for such a diffraction coupling, the electric field component of the lattice resonance mode of periodic arrays must be parallel to the induced electric moment in the silver nanodisk pair array. Due to ultra-narrow linewidth and great electric field enhancement at the LSPR, the metallic nanodisk pair array performs high sensitivity (S = 760 nm RIU−1, S* = 89.5 RIU−1) and figure of merit (FOM = 492, FOM* = 6147), which holds important applications in high-efficiency biomedical sensing.

Dual light-responsive shape transformations of a nanocomposite hydrogel sheet enabled by in situ etching shaped plasmonic nanoparticles.

We report here on dual shape transformations of the same thermo-responsive hybrid hydrogel sheet under irradiation of a laser with two different wavelengths (808 nm and 450 nm). By in situ etching the silver nanoprisms in the sheet to silver nanodiscs by using chloride ions (Cl-), two areas with distinct light extinction properties are integrated in a single sheet. The conversion of photon energy to thermal energy in local areas by the silver nanoprisms or nanodiscs under laser irradiation with an appropriate wavelength heats up the sheet locally and causes a local volumetric shrinkage, and hence a volumetric mismatch in different areas in the sheet. The sheet then transforms in a specific way to accommodate this volumetric mismatch. Different patterns of silver nanoprisms and nanodiscs in the sheet are achieved by controlling the delivery patterns of the etchant Cl-. We demonstrate that by designing the distribution pattern of silver nanoprisms and nanodiscs in the sheet, the same hybrid sheet transforms either to a saddle or to a helical twisted shape, while with another type of distribution pattern, it transforms either to a hoof-like or to a boat-like shape under the irradiation of a laser with a wavelength of either 808 nm or 450 nm. We point out that to program arbitrary curvature of the transformed shape of our sheet, the pattern size of silver nanoprisms and nanodiscs (i.e. actuation area) in the sheet needs to be largely reduced, which however limits the heat generated and hence the shape transformations. Factors that affect the sheet's shape transformations are discussed and solutions are suggested to enhance its performance. The hybrid sheet may find applications in soft robotics, for example, as a robotic finger.

Plasmon-induced hot carrier distribution in a composite nanosystem: role of the adsorption site.

The generation of hot carriers (HCs) through the excitation of localized surface plasmon resonance (LSPR) in metal nanostructures is a fascinating phenomenon that fuels both fundamental and applied research. However, gaining insights into HCs at a microscopic level has posed a complex challenge, limiting our ability to create efficient nanoantennas that utilize these energized carriers. In this investigation, we employ real-time time-dependent density functional theory (rt-TDDFT) calculations to examine the creation and distribution of HCs within a model composite system consisting of a silver (Ag) nanodisk and a carbon monoxide (CO) molecule. We find that the creation and distribution of HCs are notably affected by the CO adsorption site. Particularly, when the CO molecule adsorbs onto the hollow site of the Ag nanodisk, it exhibits the highest potential among various composite systems in terms of structural stability, enhanced orbital hybridization, and HC generation and transfer. Utilizing a Gaussian laser pulse adjusted to match the LSPR frequency, we observe a marked buildup of hot electrons and hot holes on the C and O atoms. Conversely, the region encompassing the C-O bond exhibits a depletion of hot electrons and hot holes. We believe that these findings could have significant implications in the field of HC photocatalysis.

Revealing the high efficiency of fluorescence quenching of rhodamine B by triangular silver nanodisks due to the inner filter effect mechanism.

Performing effective fluorescence quenching based on a metal nanomaterial is essential to construct fluorescence sensors. Silver nanomaterials are well known as an excellent candidate for an absorber in fluorescence sensing systems. Herein, we investigated the fluorescence quenching of rhodamine B (RhB) in the presence of triangular silver nanodisks in which perfect overlap between the absorption of the absorber and the fluorescence of the fluorophore was observed. The fluorescence quenching mechanism of RhB was investigated under various excitation wavelengths, together with measurement of the fluorescence lifetime. The quenching efficiency of RhB was proportional to the wavelength excitation. Remarkably, the highest efficiency of fluorescence quenching of RhB was achieved (∼60%). The quenching mechanism was investigated and revealed to be mostly due to the inner filter effect (IFE) mechanism, without the contribution of energy transfer. This result shows a completely different story from most previous studies based on silver nanoparticles, where energy transfer was reported to play a significant role.

Simulation of a Transparent Wood-Based Surface Plasmon Resonance Sensor with Silver Nano Disks for Measuring the Refractive Index of Crude Oil

Simulation of a Transparent Wood-Based Surface Plasmon Resonance Sensor with Silver Nano Disks for Measuring the Refractive Index of Crude Oil

Bandwidth-tunable absorption enhancement of visible and near-infrared light in monolayer graphene by localized plasmon resonances and their diffraction coupling

Bandwidth-tunable light absorption enhancement in monolayer graphene is practically important for graphene-based photoelectric devices. Especially, it is still a huge challenge to achieve high-efficiency graphene absorption with extremely narrow sub-nanometer bandwidth much smaller than one nanometer. In this work, both broadband and narrowband absorption peaks of monolayer graphene are numerically achieved in visible and near-infrared wavelength ranges. The broadband absorption peak is ascribed to localized dipolar plasmon resonances in individual silver nanodisks, and the narrowband absorption peak arises from collective first-order diffraction coupling effect in periodic array of silver nanodisks. By changing the array period, the full width at half maximum (FWHM) of the broadband absorption peak can vary from 100 nm to 50 nm. Correspondingly, the FWHM of the narrowband absorption peak is tuned from about 6.4 nm to only 0.25 nm, thus realizing an ultra-narrow sub-nanometer bandwidth.

Numerical Analysis of Three-dimensional Nanodisk Array-based Surface Plasmon Resonance Biosensors for SARS-CoV-2 Detection.

The online version contains supplementary material available at 10.1007/s11468-023-01802-3.

Color Transferability from Solution to Solid Using Silica Coated Silver Nanoparticles.

The interpretation of color change in sensors and tests can be linked to incorrect conclusions if the intrinsic color changes are not accounted for. In this work, we study the intrinsic color change associated with the process of embedding nanoparticles in a polymer to create nanocomposite films. We present a safer, faster method to coat silver nanoparticles with silica and employ a seven-factor Plackett-Burman design to identify critical factors in the synthesis. Silver nanodisks with increasing thicknesses of the silica shell showed a decreasing sensitivity of their localized surface plasmon resonance (LSPR) toward changes in the refractive index surrounding the nanoparticle. A color shift of up to 72 nm was observed when bare nanoparticles were embedded in poly(vinyl alcohol), but no color change was perceived when nanoparticles were coated with a 25-nm-thick silica shell. Understanding the origin of color changes intrinsic to the preparation of polymeric nanocomposites aids in the design and correct use of plasmonic sensors.

Synergistic effects of dual-optical-nanocavity resonance and localized surface plasmons to enhance light absorption in organic solar cells

For organic solar cells, it is a vital issue to effectively confine more light in a thin photoactive layer to guarantee both efficient light absorption and effective collection for photogenerated carriers. Herein, a simple but high-performance composite structure consisting of a front indium tin oxide hemisphere (ITO-HS) array and a silver nanodisk (Ag-ND) array embedded in the photoactive layer is proposed. Benefiting from antireflection and light scattering induced by the ITO-HS array, dual-optical-nanocavity resonances formed by the ITO-HS array, Ag-ND array and Ag electrode, together with the secondary scattering and localized surface plasmons caused by the Ag-ND array, significantly enhanced light absorption can be achieved in a broad range from 300 to 800 nm. Simulation results indicate that the short-circuit current density and power conversion efficiency can be remarkably enhanced by 43.58% and 46.03%, respectively, through introducing the optimal composite light management structure into the normal inverted device architecture of ITO/ZnO/PTB7:PC 71 BM (100 nm)/MoO 3 /Ag, as compared to the control device. Furthermore, this composite light management structure exhibits excellent omnidirectional light confinement. Considering the notable device performance enhancement and the simple structure, this study may provide a guideline for designing and fabricating high-performance light management structures applicable in thin film-based optoelectronic devices. • A simple and efficient light management structure consisting of a front ITO-HS array and an Ag-ND array is proposed. • The enhancement of 43.58% and 46.03% for J sc and PCE is achieved for the device with the optimized light management structure. • Excellent omnidirectional light management is delivered for the proposed optical structure.

NIR band-pass filters for CMOS image sensors constructed with NIR absorbing dyes and plasmonic nanoparticles.

Two NIR band-pass filters for CMOS image sensors are developed by incorporating NIR absorption dye and silver nanodisks simultaneously in a transparent polymer, one of which blocks the NIR near the wavelength of 750 nm and the other near 950 nm. They offer low NIR transmittance while maintaining high visible light transparency even at a thin film thickness of 500 nm. By superimposing the proposed NIR band-pass filters, an NIR cutoff filter with a thickness of 1 µm is formed that shields the NIR at wavelengths longer than 680 nm while remaining transparent in the visible range.

Angle robust transmitted plasmonic colors with different surroundings utilizing localized surface plasmon resonance

Color filters in different surroundings inherently suffer from angular sensitivity, which hinders their practical applications. Here, we present an angle-insensitive plasmonic filter that can produce different color responses to different surrounding environments. The color filters are based on a two-dimensional periodically and randomly distributed silver nanodisk array on a silica substrate. The proposed plasmonic color filters not only produce bright colors by altering the diameter of the Ag nanodisk, but also achieve continuous color palettes by changing the surrounding environment. Due to the weak coupling between the metallic nanodisks, the plasmonic color filters can enable good incident angle-insensitive properties (up to 30°). The strategy presented here could exhibit robust and promising applicability in anti-counterfeiting and imaging technologies.

Ferric Chloride-Induced Synthesis of Silver Nanodisks with Considerable Activity for the Reduction of 4-Nitrophenol.

Silver nanodisks (AgNDs) have been successfully synthesized by using ferric chloride as an auxiliary agent in the presence of polyvinylpyrrolidone and N,N-dimethylformamide as both a solvent and a reducing agent. The mass ratio of reactants, temperature, and time were demonstrated to be the key factors determining the morphology of the product, and the conversion of Fe3+/Fe2+ ions played an important role in increasing the ratio of silver nanosheets (AgNSs). As the reaction prolonged, the etching effect of Cl– ions on the tips of AgNSs became more and more obvious, which made the obtained typical polygonal AgNSs turn into AgNDs eventually. In addition, the prepared AgNDs exhibited a considerable catalytic activity in the reduction of 4-nitrophenol.

Compact multispectral photodetectors based on nanodisk arrays atop optical cavity substrates.

It is challenging for the multi-spectral photodetector to have a compact structure, high spectral resolution, and high detection efficiency. This paper reports on a new approach for compact multi-spectral visible light detecting based on the hexagonal lattice silver nanodisk arrays atop optical cavity substrates. Through numerical calculations and optimizations of experiments, we verified that the narrow band responsivity of the photodetector was caused by coupling the surface plasmonic resonances and cavity mode. The multi-spectral photodetector exhibited that the minimum FWHM and the maximum responsivity of was achieved to be 80 nm and 91.5 mA·W-1, respectively. Besides, we also analyzed the influence of the proposed structure on the energy wastage by numerical comparison. The proposed way for multi-spectral photodetector is promising to be an excellent design for the narrow band spectral detection. The design can also be easily integrated with CMOS devices and applied to other spectral regimes for different applications.

Paper Biosensor for the Detection of NT-proBNP Using Silver Nanodisks as Electrochemical Labels.

We report on the use of silver nanodisks (AgNDs), having a diameter of 50 ± 8 nm and a thickness of 8 ± 2 nm, as electrochemical labels for the detection of a model metalloimmunoassay for the heart failure biomarker NT-proBNP. The detection method is based on an electrochemically activated galvanic exchange (GE) followed by the detection of Ag using anodic stripping voltammetry (ASV). The AgNDs labels are superior to Ag nanocubes and Ag nanospheres in terms of the dynamic range for both the model and NT-proBNP metalloimmunoassays. The linear dynamic range for the model composite is 1.5 to 30.0 pM AgNDs. When AgND labels are used for the NT-proBNP assay, the dynamic range is 0.03–4.0 nM NT-proBNP. The latter range fully overlaps the risk stratification range for heart failure from 53 pM to 590 pM. The performance improvement of the AgNDs is a result of the specific GE mechanism for nanodisks. Specifically, GE is complete across the face of the AgNDs, leaving behind an incompletely exchanged ring structure composed of both Ag and Au.

Optical nonlinearity goes ultrafast in 2D semiconductor-based nanocavities.

Hybrid systems of silver nanodisks strongly coupled to monolayer tungsten-disulfide (WS2) show giant room-temperature nonlinearity due to their deeply sub-wavelength localized nature, resulting in ultrafast modifications of nonlinear absorption in a solid-state system.