Dielectric Nanocup Coating Effect on the Resonant Optical Properties of Individual Au Nanosphere

By finite element method (FEM), dielectric nanocup coating effect on the resonant optical properties of individual Au nanosphere was investigated. It is demonstrated not deleterious to the sensing signals of the nanosphere. The proposed nanocomposite provides an interesting localized surface plasmon resonance (LSPR) sensor with quadratic response, which refractive index (RI) sensitivity is revealed to increase with the RI both of its surrounding and local environment. The differences between the LSPR peak positions of the nanocomposite measured from far-field and near-field spectra are discussed, too. It is believed to shed light on the future applications in surface enhanced Raman spectroscopy, biochemical sensing, and detections.     

Optical Fiber-Based Surface-Enhanced Raman Scattering Sensor Using Au Nanovoid Arrays

Plasmonic properties of gold nanovoid array substrates for fiber-based surface-enhanced Raman scattering (SERS) sensing are studied numerically and experimentally. In the nanovoid arrays, each void has openings on both sides, bottom hole facing the fiber tip for introducing incident light and collecting scattered light and the top hole exposed to the analyte solution for interrogating analyte molecules in the voids. Electromagnetic field modes are confined strongly in and around these nanovoids, acting as localized plasmon resonators. The enhanced electric field extends hundreds of nanometers into the voids, resulting in a large SERS-active zone several orders of magnitude larger than nanoparticle-based structures. The effect of structural parameters of the nanovoid arrays, including void diameter, Au film thickness, and bottom hole diameter, on electric field confinement in the voids is investigated using three-dimensional finite difference time domain simulation. Au nanovoid arrays are fabricated using a scalable, inexpensive nanosphere lithography fabrication method. The largest SERS signal is realized by tuning the localized plasmon resonance peak of Au nanovoid arrays to the laser excitation wavelength. Multiplexed detection capability with the fiber-based SERS sensor using Au nanovoid arrays is demonstrated by measuring the Raman spectrum of a mixture solution of diethylthiatricarbocyanine and crystal violet.     

Localized Surface Plasmon Resonance in Gold Nanocluster Arrays on Opaque Substrates

Plasmonics - We report on the investigation of the localized surface plasmon resonance (LSPR) in periodical Au nanostructures. The arrays of Au nanoclusters and dimers were fabricated on Si and...     

Morphology Dependence on Surface-Enhanced Raman Scattering Using Gold Nanorod Arrays Consisting of Agglomerated Nanoparticles

Plasmonics - Highly ordered arrays of vertically aligned Au nanorod arrays consisting of agglomerated nanoparticles are fabricated by porous anodic aluminum oxide (AAO) template-assisted...     

Tunable Plasmonic Resonances in Hexagonally Ordered Gold Nanostructure Arrays with Increasing Interstice Size

Plasmonics - Gold nanostructure arrays were fabricated by combining colloidal lithography with inclined reactive ion etching and inclinded sputtering. Field emission scanning electron microscopy...     

The Effect of Ag Nanoparticles on Surface-Enhanced Luminescence from Au Nanovoid Arrays

Studies comparing the effect of adding two different nanoparticle compositions on the plasmonic properties of Au nanovoid arrays were undertaken. Surface-enhanced resonance luminescence and surface-enhanced resonance Raman studies comparing dispersed Ag nanoparticles and Ag nanoparticle aggregates on gold nanovoid arrays were undertaken. These studies showed that using Ag nanoparticle aggregates increased both luminescence and Raman efficiency relative to when dispersed nanoparticles were used; in addition, these studies also showed that adding dispersed Ag nanoparticles supported a more reproducible enhancement in luminescence and Raman across the substrate compared to using Ag nanoparticle aggregates. Finite element analysis simulations indicated that surface plasmon polariton distribution in the sample was affected by the presence of the Ag nanoparticles on the Au nanovoid array.     

Surface Plasmon-Enhanced Spontaneous Emission from InGaN/GaN Multiple Quantum Wells by Indium Nanoparticles Fabricated Using Nanosphere Lithography

Economic nanofabrication of Ag, Al, Au nanotriangle arrays and In nanoparticle arrays are demonstrated using nanosphere lithography. The sizes of the nanoparticles are precisely tuned when nanospheres with different diameters are used. Localized surface plasmon resonances (LSPR) of the nanoparticle arrays are observed to be strongly dependent on their sizes and the LSPR of In nanoparticle arrays with various sizes cover the whole visible spectrum. By placing In nanoparticle arrays near the InGaN/GaN multiple quantum wells (MQWs), enhanced spontaneous emission is observed when the LSPR of the In nanoparticles matches the emission wavelength of InGaN/GaN MQWs.     

Ordered Hexagonal Nanoplasmonic Au Nanoparticle Arrays: AAO-Assisted Thermal Treatment Synthesis and Application as Surface-Enhanced Raman Scattering Substrates

We have reported on the synthesis of ordered hexagonal Au nanoparticle (NPs) arrays by anodic alumina oxide templates (AAO)-assisted thermal treatment. This simple process has led to the formation of an ordered hexagonal array of Au NPs on the surface of AAO. SERS properties of the ordered hexagonal Au NPs could be obtained by varying the size of Au NPs. Compared with the Au thin film on AAO, the SERS intensity of rhodamine adsorbed on the ordered hexagonal Au NPs was about 1000 times stronger. And the hexagonal Au NPs array films have had stronger Raman-enhanced signal compared to the disorder Au NPs films. Simulations according to the three-dimensional finite-difference time domain (3D-FDTD) have displayed that these electric field enhancements of the ordered hexagonal Au NPs are strongly dependent on the gap distance. Plasmonic ordered hexagonal Au NPs could provide us new platforms to realize novel optoelectronic devices.

     

Systematic Study on the Self-Assembled Hexagonal Au Voids,Nano-Clusters and Nanoparticles on GaN (0001)

Au nano-clusters and nanoparticles (NPs) have been widely utilized in various electronic, optoelectronic, and bio-medical applications due to their great potentials. The size, density and configuration of Au NPs play a vital role in the performance of these devices. In this paper, we present a systematic study on the self-assembled hexagonal Au voids, nano-clusters and NPs fabricated on GaN (0001) by the variation of annealing temperature and deposition amount. At relatively low annealing temperatures between 400 and 600°C, the fabrication of hexagonal shaped Au voids and Au nano-clusters are observed and discussed based on the diffusion limited aggregation model. The size and density of voids and nano-clusters can systematically be controlled. The self-assembled Au NPs are fabricated at comparatively high temperatures from 650 to 800°C based on the Volmer-Weber growth model and also the size and density can be tuned accordingly. The results are symmetrically analyzed and discussed in conjunction with the diffusion theory and thermodynamics by utilizing AFM and SEM images, EDS maps and spectra, FFT power spectra, cross-sectional line-profiles and size and density plots.     

Study of Implosion of Twisted Nested Arrays at the Angara-5-1 Facility

Results are presented from experimental studies of the implosion of twisted nested arrays in which the wires of the outer and inner arrays are twisted about the array axis in opposite directions (clockwise and counterclockwise). Experiments with twisted arrays were carried out at the Angara-5-1 facility at currents of up to 4 MA. The currents through the arrays were switched either simultaneously or the current pulse through the outer array was delayed by 10–15 ns with the help of an anode spark gap. It is shown that, in such arrays, the currents flow along the inclined wires and, accordingly, there are both the azimuthal and axial components of the discharge current. The process of plasma implosion in twisted arrays depends substantially on the value of the axial (longitudinal) magnetic field generated inside the array by the azimuthal currents. Two-dimensional simulations of the magnetic field in twisted nested arrays were performed in the (r, z) geometry with allowance for the skin effect in the discharge electrodes. It is shown that, depending on the geometry of the discharge electrodes, different configurations of the magnetic field can be implemented inside twisted nested arrays. The calculated magnetic configurations are compared with the results of measurements of the magnetic field inside such arrays. It is shown that the configuration of the axial magnetic field inside a twisted nested array depends substantially on the distribution of the azimuthal currents between the inner and outer arrays.     

Tunable Mid-Infrared Optical Properties of Monolayer Black Phosphorus Through Au Nanotriangle Arrays via Electric Field Reflection and Surface Plasmon Polaritons

A metamaterial system composed of monolayer black phosphorus and Au triangle arrays is designed. Absorptivity, transmittivity, and reflectivity are investigated in mid-infrared regime. A low transmissivity and high absorptivity can be obtained via surface plasmon polaritons at the black phosphorus and Au triangle array interface. By changing the geometrical parameters, such as angle magnitude and slit width of Au triangle, we can modulate the transmissivity, reflectivity and absorptivity properties. Different from other previous work, it is found the zigzag direction has a better photoresponse than that armchair by changing the slit width. The electric field of the external radiation field is reflected at the Au triangle edges. Thus, electric field component perpendicular to the polarization direction generates, which can also lead to surface plasmon polaritons and is not researched in others’ work. With increase in the angle of Au triangle, transmittivity (or absorptivity) for armchair direction has a blue shift and for zigzag direction has a red shift. The transmittivity decrease ( or absorptivity increase ) for special wavelength caused by the surface plasmon polaritons may be applied to design filter devices.

     

Structure and bonding of gold(I) and gold(III) nucleosides studied by 197Au Mössbauer spectroscopy

¹⁹⁷Au Mössbauer spectra of the series of complexes of gold(I), Au(nucl)₂Cl and gold(III), Au(nucl)Cl₃, Au(nucl - H⁺)Cl₂ and Au(nucl)₂Cl₃ were measured at 4.2 K, (nucl = nucleoside, e.g. guanosine(guo), inosine(ino), triacetylguanosine-(trguo) and triacetylinosine(trino)). It is concluded from the spectra that the gold(I) nucleosides have linear ClAuN coordination, with one coordinated nucleoside molecule per gold(I) ion, bound via the N(7) atom. The σ-donor strength of the guo ligand is somewhat higher than that of the ino ligand. The complexes Au(ino)Cl₃ and Au(guo)Cl₃, in the series Au(nucl)Cl₃, have significantly higher IS and QS values than the corresponding complexes with the triacetylnucleosides, Au(trino)Cl₃ and Au(trguo)Cl₃. This may be explained by a weak O(6)-interaction with gold(III), in a nearly trigonal bipyramidal configuration in the former case and by the presence of the strongly electron withdrawing acetyl groups in the latter, which reduces the donor strength of their N(7) atoms. The complexes of the Au(nucl - H⁺)Cl₂ series all appear to have a polymeric structure. The gold(III) ion is bound to the N(7) atom and the O(6) or the N(1) atom of the nucleosides. Finally, the Mössbauer spectra of the series Au(nucl)₂)Cl₃ can only be explained by assuming approximately octahedral AuN₂Cl₄ structures, with bridging chlorine atoms.     

Plasmon-Enhanced Second Harmonic Generation: from Individual Antennas to Extended Arrays

We analyze the emission yield of the second harmonic generation (SHG) from dense ordered arrays of L-shaped Au nanoantennas within a well-defined collection angle and compare it to that of the isolated nanostructures designed with the same geometrical parameters. Thanks to the high antenna surface density, arrays display one order of magnitude higher SHG yield per unit surface with respect to isolated nanoantennas. The difference in the collected nonlinear signals becomes even more pronounced by reducing the collection angle, because of the efficient angular filtering that can be attained in dense arrays around the zero order. Albeit this key-enabling feature allows envisioning application of these platforms to nonlinear sensing, a normalization of the SHG yield to the number of excited antennas in the array reveals a reduced nonlinear emission from each individual antenna element. We explain this potential drawback in terms of resonance broadening, commonly observed in densely packed arrays, and angular filtering of the single antenna emission pattern provided by the array 0th order.

     

Localized Surface Plasmon Enhanced Organic Light-Emitting Diodes

Current work demonstrates enhanced efficiencies in organic light-emitting diodes by using the localized surface plasmons originated from Au nanoclusters deposited using thermal evaporation technique. The effect of localized surface plasmons on organic emitter was studied using UV–vis absorption spectra, steady state and time-resolved photoluminescence spectra. These studies have revealed that the optical properties like absorption, emission have been greatly modified by the localized surface plasmon. These effects were found to be dependent on the distance between the emitter and Au layer. Further, efficiencies of the OLEDs were also found to be dependent on this distance.     

Formation of Self-organized Silver Nanocup-Type Structures and Their Plasmonic Absorption

The present work reports on the formation of extremely low volume, silver nanocup-type structures on the surface by annealing of ultra-thin silver film on quartz in inert environment. Atomic force microscopy studies together with scanning electron microscopy confirmed the formation of Ag nanocup-type structures at the surface. A basic physical model for the formation of nanocups in terms of buckling and Oswald ripening due to surface-induced morphological instability and diffusional mass transport under thermal treatment is demonstrated. Surface plasmon resonance absorptions of nanocup structures are studied and preliminary experiment for observing the surface-enhanced Raman scattering of fullerene C₇₀ molecules has been shown.     

Inhibitiory effects of gold(III) ions on ribonuclease and deoxyribonuclease

Inhibitory effects of gold(III) ions (Au(III)) on ribonuclease A (RNase A) and deoxyribonuclease I (DNase I) were investigated at neutral pH. RNase A was completely inhibited by 3 molar equivalents of Au(III) ions. DNase I was inhibited by 10 molar equivalents of Au(III) ions. Stoichiometric analyses suggest that Au(III) ions were coordinated to RNase A molecules. The Au(III)-inhibited RNase A and DNase I were renatured to exhibit 80% and 60% of their intrinsic activity, when the bound Au(III) ions were eliminated from the nucleases by addition of thiourea, which forms a strong complex with gold ions. This suggests that RNase A and DNase I were not oxidized to lose their activity, but reversibly complexed with Au(III) ions to lose their activity. Au(III) ions were probably considered to be bound to histidine and methionine residues in the nucleases, resulting in the inhibition of their activity. CD spectra revealed that the Au(III)-induced inhibition caused a conformational change in RNase A molecules and that the addition of thiourea induced refolding of the Au(III)-inhibited RNase A.     

Fabrication and Characterization of Large, Perfectly Periodic Arrays of Metallic Nanocups

Fabrication of plasmonic resonance devices composed of large arrays of highly ordered gold nanocups is presented. The nanostructures are generated from periodic photoresist templates created by interference lithography and subsequent reflow, deposition, and dislodging. The nanocups are hemispherical in shape and arranged in both rectangular and hexagonal arrays with periods of ~500?nm. Their ability to support surface plasmonic resonances is manifested experimentally by reflectance spectroscopy. Theoretical modeling to ascertain the plasmonic spectra of these nanostructures is performed. The computed spectra of the rectangular structure are in qualitative agreement with the measurements. A weaker correlation observed for the hexagonal structure is explained by its more intricate symmetry which complicates the spectral response.     

The antitumor effect of magnetic nanodisks and DNA aptamer conjugates

Here we describe a method of forming large arrays (up to 10⁹ pieces) of free magnetic Ni-nanodisks 50 nm thick coated on both sides with layers of 5 nm thick Au. The antitumor effect of the magnetic nickel gold-coated nanodisks and DNA aptamer conjugates was evaluated in vivo and in vitro. Under the influence of rotating magnetic field, the studied nanodisks can cause the death of Ehrlich ascites carcinoma cells.     

Exceptional Visible‐Light‐Driven Cocatalyst‐Free Photocatalytic Activity of g‐C3N4 by Well Designed Nanocomposites with Plasmonic Au and SnO2

In this work, plasmonic Au/SnO₂/g‐C₃N₄ (Au/SO/CN) nanocomposites have been successfully synthesized and applied in the H₂ evolution as photocatalysts, which exhibit superior photocatalytic activities and favorable stability without any cocatalyst under visible‐light irradiation. The amount‐optimized 2Au/6SO/CN nanocomposite capable of producing approximately 770 μmol g^?1 h^?1 H₂ gas under λ > 400 nm light illumination far surpasses the H₂ gas output of SO/CN (130 μmol g^?1), Au/CN (112 μmol g^?1 h^?1), and CN (11 μmol g^?1 h^?1) as a contrast. In addition, the photocatalytic activity of 2Au/6SO/CN maintains unchanged for 5 runs in 5 h. The enhanced photoactivity for H₂ evolution is attributed to the prominently promoted photogenerated charge separation via the excited electron transfer from plasmonic Au (≈520 nm) and CN (470 nm > λ > 400 nm) to SO, as indicated by the surface photovoltage spectra, photoelectrochemical I–V curves, electrochemical impedance spectra, examination of formed hydroxyl radicals, and photocurrent action spectra. Moreover, the Kelvin probe test indicates that the newly aligned conduction band of SO in the fabricated 2Au/6SO/CN is indispensable to assist developing a proper energy platform for the photocatalytic H₂ evolution. This work distinctly provides a feasible strategy to synthesize highly efficient plasmonic‐assisted CN‐based photocatalysts utilized for solar fuel production.