Plasmonic Properties of Silver Nanoparticles on Two Substrates

In this paper, we examine the plasmonic properties of silver nanoparticles, with an emphasis on the sensitivity of the extinction spectra on the supporting substrate: silica (SiO₂) microsphere and indium tin oxide (ITO) coated glass slide, on which silver particles are deposited electroless and electrochemically, respectively. The microstructures and phases of these nanoparticles are characterized by transmission electron microscopy, field emission electron microscopy and X-ray diffraction analysis. The surface plasmon resonance (SPR) properties which are experimentally measured in the ultraviolet-visible-near infrared spectral region are compared to electrodynamics calculations based on the discrete dipole approximation. A wide SPR band ranging from 400 to 800 nm is observed for the silver nanoparticles on a silica microsphere, which is similar to the plasmon resonance characteristics of metal nanoshells. The SPR of a conducting substrate, however, has an effect on the plasmonic properties of silver nanoparticles at longer wavelength.      

Shape-Controlled Synthesis of Silver Nanoparticles for Plasmonic and Sensing Applications

The localized surface plasmon resonance of a silver nanoparticle is responsible for its ability to strongly absorb and scatter light at specific wavelengths. The absorption and scattering spectra (i.e., plots of cross sections as a function of wavelength) of a particle can be predicted using Mie theory (for a spherical particle) or the discrete dipole approximation method (for particles in arbitrary shapes). In this review, we briefly discuss the calculated spectra for silver nanoparticles with different shapes and the synthetic methods available to produce these nanoparticles. As validated in recent studies, there is good agreement between the theoretically calculated and the experimentally measured spectra. We conclude with a discussion of new plasmonic and sensing applications enabled by the shape-controlled nanoparticles.     

Enhanced and Selective Photodetection Using Graphene-Stabilized Hybrid Plasmonic Silver Nanoparticles

We report the fabrication and characteristics of a novel graphene-Ag⁰ hybrid plasmonic nanostructure-based photodetector exhibiting moderately high responsivity (～28 mA/W) and spectral selectivity (～510 nm) in the visible wavelength. The formation of highly stable Ag⁰ nanoparticles with an average size of 40 nm is observed within the graphene layers, resulting in n-type doping of hybrid material. The absorption peak of graphene-Ag⁰ hybrid is redshifted to the visible wavelength (～510 nm) from the plasmonic Ag peak (～380 nm) in agreement with the optical simulation results for embedded metal nanoparticles. The study demonstrates the synergistic effect of the graphene-metal nanocomposite, which appears attractive for applications in graphene-based photonic devices.     

Investigation of the Plasmonic Interaction of Gold Nanoparticles Toward Plasmonic Photothermal Therapeutics

Plasmonic interaction of nanoparticles located in close proximity, embedded in breast tissue, is simulated for estimating the optical characteristics like optical absorption cross-section, plasmonic wavelength as well as full-width half maxima (FWHM). The computations are done for the monomers, homodimers, and heterodimers of spherical and rod-shaped gold nanoparticles considering various interparticle spacings for gold nanospheres and the interparticle spacing as well as the orientation for gold nanorods (GNRs). The results indicate that for the spherical dimer, with the change in interparticle spacing from 1 to 20 nm, the peak absorption cross-section decreases by 43%. Whereas for the GNRs, the absorption cross-section increases/decreases, within 9–18%, depending on the homodimer or heterodimer configuration. Furthermore, secondary peaks for the absorption cross-section are obtained within wavelengths of 630–940 nm due to antibonding modes for GNR heterodimers. For GNR heterodimer located end-to-end, this secondary peak for the absorption cross-section appears at 780 nm irrespective of interparticle spacing within 1–5 nm. The absorption coefficient is considerably dependent on the configuration and proximity of GNRs located within the tissue. While FWHM is not significantly influenced by GNRs configuration and interparticle spacing. For interparticle spacing from 1 to 20 nm, the plasmonic wavelength shifts by 38 nm for the spherical dimer and by 35–86 nm for various GNR dimers. The findings of this study are useful for plasmonic photothermal therapeutics as the heat generation is governed by the resulting absorption cross-section due to plasmonic coupling of the closely spaced and different orientations of the nanoparticles.

     

Plasmonic Sensor Based on Silver Nanoparticles for the Detection of Glucose

Plasmonics - Sensors for detecting glucose concentrations are crucial to medical testing. Here, we introduce silver nanoparticles (Ag NPs) uniformly distributed in space to investigate the sensing...     

Fabrication of Monodispersed Silver Nanoparticles and their Collective Sharp Plasmonic Response

Monodispersed silver (Ag) nanoparticles (NPs) were obtained by applying an electric field on unipolar-charged Ag NPs fabricated using a heterogeneous condensation technique in gas media. Well defined and charged Ag NPs were separated based on their sizes and were collected on quartz substrates. Thin films consisting of monodispersed Ag NPs with size ranging from 35 to 120 nm were prepared by varying an applied electric field during the fabrication process. Scanning electron microscope results showed that the samples have uniform size distribution. Coherent oscillations of conduction band electrons in gas medium induced by electromagnetic field and coupling of all similar plasmon resonances due to uniform Ag NPs size produced unique and interesting optical properties. Narrow extinction widths (～41 to ～69 nm) were observed compared to the width of polydispersed Ag sample. The ability to prepare samples in gas media and tune the plasmon resonance by merely varying an electric field during fabrication makes the method simple, fast, and highly economical.     

Investigation of the Growth Kinetics and Multipolar Plasmonic Properties of Silver Nanoparticle Cluster by Experiment and Numerical Simulations

Silver nanoparticle (AgNP) has wide-spread applications in photovoltaic cell, biological sensors, biomedical devices, surface enhanced Raman scattering (SERS) etc. which are intricately dependent on AgNP shape, size, concentration and aggregation states. Here, the particle size, shape and aggregation dependent dipole and quadrupole surface plasmon resonances are spectroscopically investigated by preparing AgNPs (diameter 10–110nm) using silver nitrate (AgNO₃) and sodium borohydride (NaBH₄ as reducing agent) in aqueous environment at 0 ^∘C. The AgNP UV-Visible spectra showing plasmon-induced dipole and quadrupole modes are corroborated by the theoretical framework of Mie-Gans model and discrete dipole scattering model DDSCAT and different particle sizes, shapes and possible aggregation or clusterization are predicted. All the samples show presence of spherical and nonspherical distribution of AgNP. However, the concentration of nonspherical particle is more for higher concentration of reducing agent as is evidenced by the appearance of quadrapole absorption maxima. The minimum particle size is found at a particular ratio of concentration of AgNO₃ and NaBH₄. The day variation of AgNP kinetics also signalled the onset of quadrupole deformation of clusters.

     

Impact of Nonuniform Electron Density on Plasmonic Properties of Metal Nanoparticles

The interfacial nonuniformity of the electron density that occurs in metals as a result of atomic imperfections can strongly affect the plasmonic properties of metallic nanostructures. Under certain conditions, it induces the bulk plasmon resonance in the transition area and can significantly change scattering and absorption of light by metallic nanostructures in a broad frequency range. This effect is numerically demonstrated for radially nonuniform spherical silver nanoparticles and analytically investigated with respect to the resonant coupling with the dipolar surface plasmons of the metal core.     

Influence of Plasmonic Silver Nanoparticles on Fluorescence Quenching of 1,4-dihydroxy-3-methylanthracene-9,10-dione

Optical absorption and fluorescence emission techniques were employed to investigate the size effects of silver nanoparticles (Ag NPs) on 1,4-dihydroxy-3-methylanthracene-9,10-dione (DHMAD). Silver nanoparticles of different sizes were prepared by Creighton method under microwave irradiation. The prepared Ag NPs show the surface plasmon band around 400 nm. Fluorescence quenching of DHMAD by Ag NPs was found to increase with an increase in the size of Ag NPs. The fluorescence quenching is explained by resonant energy transfer mechanism between DHMAD and Ag NPs, orientation of DHMAD on silver nanoparticles through chemisorptions. The Stern–Volmer quenching constant and Benesi–Hildebrand association constant for the above system were calculated. DFT calculations were also performed to study the ground and excited state behavior of DHMAD and DHMAD + Ag system.     

Comparative Study of Plasmonic Properties of Cysteine-Functionalized Gold and Silver Nanoparticle Aggregates

The absorptance spectra of gold and silver nanoparticle (NP) aqueous dispersions were measured by UV–visible spectroscopy and computed numerically by finite element method. Both NPs were functionalized by l-cysteine amino acid (Cys) in order to develop aggregate-based localized surface plasmon resonance biosensors. Absorptance spectra measured at an analogous pH value of ～4.9 were compared, where Au-Cys conjugates have moderately split spectra with two commensurate maxima, while Ag-Cys conjugates exhibit the most pronounced secondary peak according to the highest degree of aggregation. The purpose of our theoretical study was to determine the simplest linear chain-like and wavy aggregate geometries, which result in maxima matching the measured peaks. The aggregates were characterized by N number and d diameter of NPs, g gap between the NPs, and t thickness of the l-cysteine covering. By tuning the angle of incidence and E -field oscillation direction in p-polarized light with respect to the aggregates, the contribution of longitudinal and transversal modes was varied. The comparison of measurements and computations revealed that spectra measured on bioconjugate dispersions include effects of numerous aggregates with various geometries, illuminated from different directions and are influenced by inter-aggregate coupling. Inspecting the normalized E -field distribution surrounding the aggregates, it was shown that fundamentally different multipolar modes can be identified at primary and secondary absorptance maxima, due to coupled plasmonic resonances on NPs.     

Synthesis and Optical Properties of Highly Stabilized Peptide-Coated Silver Nanoparticles

The interaction between peptide and silver nanoparticle surfaces has been increasingly of interest for bionanotechnology applications. To fully understand how to control such interactions, we have studied the optical properties of peptide-modified silver nanoparticles. However, the impacts of peptide binding motif upon the surface characteristics and physicochemical properties of nanoparticles remain not yet fully understood. Here, we have prepared sodium citrate-stabilized silver nanoparticles and coated with peptide IVD (ID₃). These nanomaterials were characterized by UV-visible, transmission electron microscopy (TEM), and z-potential measurement. The results indicate that silver nanoparticles (AgNP)-peptide interface is generated using ID₃ peptide and suggested that the reactivity of peptide is governed by the conformation of the bound peptide on the nanoparticle surface. The peptide-nanoparticle interactions could potentially be used to make specific functionality into the peptide capped nanomaterials and antibacterial applications.     

Theoretical Investigation of an Interferometer-type Plasmonic Biosensor Using a Metal-insulator-silicon Waveguide

This work proposes and investigates theoretically a biosensor that is an integrated plasmonic Mach–Zehnder interferometer. The biosensor consists of three sections. The first and third sections are input and output dielectric waveguides whose core is a silicon film. The second section is a combination of a surface plasmon polariton waveguide and a metal-insulator-silicon waveguide, which are separated by a thick gold film. The former and the latter function as sensing and reference arms, respectively. The latter supports a mode whose fields are highly enhanced in a thin insulator, silicon nitride film, and it has relatively small propagation loss. It is shown that the biosensor has insertion loss lower than 2 dB, and that it is very compact since the length of its second section for sensing is shorter than 6 μm. In addition, it is discussed that it can be easily implemented by using simple fabrication processes. Analyzed are the characteristics of sensing a refractive index change of liquid covering the biosensor. Despite its compactness, they are similar to those of previous surface plasmon interferometers. Also, its characteristics as a DNA sensor are analyzed. The analysis demonstrates that the biosensor can detect sensitively target single-stranded DNAs whose total weight is smaller than 10 fg.     

Predicting the Size of Silver Nanoparticles from Their Optical Properties

Plasmonics - In this study, localized surface plasmon resonance (LSPR) of the spherical silver nanoparticles (AgNPs) was evaluated based on experimental and theoretical viewpoints. In the...     

Antiviral Properties of Silver Nanoparticles on a Magnetic Hybrid Colloid

Silver nanoparticles (AgNPs) are considered to be a potentially useful tool for controlling various pathogens. However, there are concerns about the release of AgNPs into environmental media, as they may generate adverse human health and ecological effects. In this study, we developed and evaluated a novel micrometer-sized magnetic hybrid colloid (MHC) decorated with variously sized AgNPs (AgNP-MHCs). After being applied for disinfection, these particles can be easily recovered from environmental media using their magnetic properties and remain effective for inactivating viral pathogens. We evaluated the efficacy of AgNP-MHCs for inactivating bacteriophage ϕX174, murine norovirus (MNV), and adenovirus serotype 2 (AdV2). These target viruses were exposed to AgNP-MHCs for 1, 3, and 6 h at 25°C and then analyzed by plaque assay and real-time TaqMan PCR. The AgNP-MHCs were exposed to a wide range of pH levels and to tap and surface water to assess their antiviral effects under different environmental conditions. Among the three types of AgNP-MHCs tested, Ag30-MHCs displayed the highest efficacy for inactivating the viruses. The ϕX174 and MNV were reduced by more than 2 log₁₀ after exposure to 4.6 × 10⁹ Ag30-MHCs/ml for 1 h. These results indicated that the AgNP-MHCs could be used to inactivate viral pathogens with minimum chance of potential release into environment.     

Preparation of Luminescent Plasmonic Silver Nanoparticles for Electrochemical Detection of Sulphide and Thiourea in Aqueous Solution and Ab Initio DFT Study of the Chemical Affinity Towards Silver Nanoparticles

Plasmonics - A changing of the mole ratio of L-ascorbic acid: citrate is used to synthesize coloured luminescent silver nanoparticles (AgNPs) such as AgNPs green (G), reddish green (RG) and reddish...     

Colloidal Synthesis of Plasmonic Metallic Nanoparticles

Solutions of Ag and Au nanoparticles are strongly colored because of localized surface plasmon resonance in the UV/visible spectral region. The optical properties of these nanoparticles may be tuned to suit the needs of the application. This article summarizes our work in recent years on the solution synthesis of nanoparticles with tunable optical properties. The systems of interest include zero-dimensional bimetallic Ag–Au nanoparticles with different structures, one-, two-, and three-dimensional anisotropic monometallic Ag or Au nanoparticles. All of these nanosystems were prepared from colloidal synthesis through simple changes in the synthesis conditions. This is a demonstration of the versatility of colloidal synthesis as a convenient scalable technique for tuning the properties of metallic nanoparticles. Zhang, Tan, and Xie contributed equally to this article     

Near-Field-Induced Femtosecond Breakdown of Plasmonic Nanoparticles

Plasmonics - We studied the evolution of femtosecond breakdown in lithographically produced plasmonic nanoparticles with increasing laser intensity. Localized plasmons were generated with 40-fs...     

Fano Resonance-Assisted Plasmonic Trapping of Nanoparticles

Plasmonic optical trapping is widely applied in the field of bioscience, microfluidics, and quantum optics. It can play a vital role to extend optical manipulation tools from micrometer to nanometer scale level. Currently, it is a challenge to obtain the highly stable optical trapping with low power and less damage. In this paper, we propose Fano resonance-assisted self-induced back-action (FASIBA) method, through which a single 40-nm gold particle can be trapped in hole-slit nano-aperture milled on metallic film. It is used to achieve ultra-accurate positioning of nanoparticle, metallic nanostructures at wide infrared wavelength range, quite effectively and evidently. The stable plasmonic trapping is achieved by tuning the transmission wavelengths and modifications of nanoslit, indicating that the depth of potential well can be increased from minus 8KT to 12KT, with the input power of 10⁹ W/m². This can be attributed to great modifications in Fano resonance transmissions according to self-induced back-action (SIBA) theory. The results are basically helpful to facilitate the trapping with lower power and less damage to the objects, which enables new scenario for the treatment of undesirable spread of a single nanoscale creature, such as virus.