Martin G. Blaber

Structure Enhancement Factor Relationships in Single Gold Nanoantennas by Surface-Enhanced Raman Excitation Spectroscopy

Determining the existence of any direct spectral relationship between the far-field scattering properties and the near-field Raman-enhancing properties of surface-enhanced Raman spectroscopy (SERS) substrates has been a challenging task with only a few significant results to date. Here, we prove that hot spot dominated systems show little dependence on the far-field scattering properties because of differences between near- and far-field localized surface plasmon resonance (LSPR) effects as well as excitation of new plasmon modes via a localized emitter. We directly probe the relationship between the near- and far-field light interactions using a correlated LSPR-transmission electron microscopy (TEM) surface-enhanced Raman excitation spectroscopy (SERES) technique. Fourteen individual SERS nanoantennas, Au nanoparticle aggregates ranging from dimers to undecamers, coated in a reporter molecule and encased in a protective silica shell, were excited using eight laser wavelengths. We observed no correlation between the spectral position of the LSPR maxima and the maximum enhancement factor (EF). The single nanoantenna data reveal EFs ranging from (2.5 ± 0.6) × 10(4) to (4.5 ± 0.6) × 10(8) with maximum enhancement for excitation wavelengths of 785 nm and lower energy. The magnitude of maximum EF was not correlated to the number of cores in the nanoantenna or the spectral position of the LSPR, suggesting a separation between near-field SERS enhancement and far-field Rayleigh scattering. Computational electrodynamics confirms the decoupling of maximum SERS enhancement from the peak of the scattering spectrum. It also points to the importance of a localized emitter for radiating Raman photons to the far-field which, in nonsymmetric systems, allows for the excitation of radiative plasmon modes that are difficult to excite with plane waves. Once these effects are considered, we are able to fully explain the hot spot dominated SERS response of the nanoantennas.

A review of the optical properties of alloys and intermetallics for plasmonics

Alternative materials are required to enhance the efficacy of plasmonic devices. We discuss the optical properties of a number of alloys, doped metals, intermetallics, silicides, metallic glasses and high pressure materials. We conclude that due to the probability of low frequency interband transitions, materials with partially occupied d states perform poorly as plasmonic materials, ruling out many alloys, intermetallics and silicides as viable. The increased probability of electron-electron and electron-phonon scattering rules out many doped and glassy metals.

Tailorable plasmonic circular dichroism properties of helical nanoparticle superstructures.

We utilize a peptide-based methodology to prepare a diverse collection of double-helical gold nanoparticle superstructures having controllable handedness and structural metrics. These materials exhibit well-defined circular dichroism signatures at visible wavelengths owing to the collective dipole-dipole interactions between the nanoparticles. We couple theory and experiment to show how tuning the metrics and structure of the helices results in predictable and tailorable chirooptical properties. Finally, we experimentally and theoretically demonstrate that the intensity, position, and nature of the chirooptical activity can be carefully adjusted via silver overgrowth. These studies illustrate the utility of peptide-based nanoparticle assembly platforms for designing and preparing complex plasmonic materials with tailorable optical properties.

Immobilized Nanorod Assemblies: Fabrication and Understanding of Large Area Surface-Enhanced Raman Spectroscopy Substrates

We describe the fabrication of optimized plasmonic substrates in the form of immobilized nanorod assemblies (INRA) for surface-enhanced Raman spectroscopy (SERS). Included are high-resolution scanning electron micrograph (SEM) images of the surface structures, along with a mechanistic description of their growth. It is shown that, by varying the size of support microspheres, the surface plasmon resonance is tuned between 330 and 1840 nm. Notably, there are predicted optimal microsphere sizes for each of the commonly used SERS laser wavelengths of 532, 633, 785, and 1064 nm.

Using DNA to design plasmonic metamaterials with tunable optical properties.

Abstract : Due to their potential for creating designer materials, the 3D assembly of nanoparticle building blocks into macroscopic structures with well-defined order and symmetry remains one of the most important challenges in materials science. [ 1 5 ] Furthermore, superlattices consisting of noble-metal nanoparticles have emerged as a new platform for the bottom-up design of plasmonic metamaterials. [ 6 8 ] The allure of optical metamaterials is that they provide a means for altering the temporal and spatial propagation of electromagnetic fields, resulting in materials that exhibit many properties that do not exist in nature. [ 9 13 ] With the vast array of nanostructures now synthetically realizable, computational methods play a crucial role in identifying the assemblies that exhibit the most exciting properties. [ 14 ] Once target assemblies are identified, the synthesis of nanometer-scale structures for use at optical and IR wavelengths must be taken into account. Many of the current methods to fabricate metamaterials in the optical range use serial lithographic-based approaches. [ 6 ] The challenge of controlled assembly into well-defined architectures has kept bottom-up methods that rely on the self-organization of colloidal metal nanoparticles from being fully explored for metamaterial applications. [ 8 ] DNA-mediated assembly of nanoparticles has the potential to help overcome this challenge. The predictability and programmability of DNA makes it a powerful tool for the rational assembly of plasmonic nanoparticles with tunable nearest-neighbor distances and symmetries. [ 1,15 18 ] Herein, we combine theory and experiment to study a new class of plasmonic superlattices first using electrodynamics simulations to identify that superlattices of spherical silver nanoparticles (Ag NPs) have the potential to exhibit emergent metamaterial properties, including epsilon-near-zero (ENZ) behavior, [ 13 ] and a region with an optically metallic response.

Correlating nanorod structure with experimentally measured and theoretically predicted surface plasmon resonance

The extinction spectra of Au nanorods electrochemically synthesized using anodic aluminum oxide templates are reported. Homogeneous suspensions of nanorods with average diameters of 35, 55, 80, and 100 nm and varying lengths were synthesized, and their resultant surface plasmon resonances were probed by experimental and theoretical methods. Experimental extinction spectra of the nanoparticles exhibit good overall agreement with those calculated using the discrete dipole approximation. We determine the dependence of the dipole plasmon wavelength on both rod length and diameter, and we then utilize these results to derive an equation for predicting longitudinal dipole resonance wavelength for nanorod dimensions beyond the quasistatic limit. On average, the equation allows one to predict plasmon resonance maxima within 25 nm of the experimentally measured values. An analysis of factors that are important in determining the plasmon width is also provided. For long rods, the width decreases with increasing length in spite of increased radiative damping due to increased frequency dispersion in the real part of the metal dielectric function.

Plasmonic Resonances of Closely Coupled Gold Nanosphere Chains

The optical properties of an ordered array of gold nanospheres have been calculated using the T-matrix method in the regime where the near-fields of the particles are strongly coupled. The array consists of a one-dimensional chain of spheres of 15 nm diameter where the number of spheres in the chain and interparticle spacing is varied. Calculations have been performed with chains up to 150 particles in length and with an interparticle spacing between 0.5 and 30 nm. Incident light polarized along the axis of the chain (longitudinal) and perpendicular (transverse) to it are considered, and in the latter case for wavevectors along and perpendicular to the chain axis. For fixed chain length the longitudinal plasmon resonance red shifts, relative to the resonance of an isolated sphere, as the interparticle spacing is reduced. The shift in the plasmon resonance does not appear to follow an exponential dependence upon gap size for these extended arrays of particles. The peak shift is inversely proportional to th...

Optical performance and metallic absorption in nanoplasmonic systems

Optical metrics relating to metallic absorption in representative plasmonic systems are surveyed, with a view to developing heuristics for optimizing performance over a range of applications. We use the real part of the permittivity as the independent variable; consider strengths of particle resonances, resolving power of planar lenses, and guiding lengths of planar waveguides; and compare nearly-free-electron metals including Al, Cu, Ag, Au, Li, Na, and K. Whilst the imaginary part of metal permittivity has a strong damping effect, field distribution is equally important and thus factors including geometry, real permittivity and frequency must be considered when selecting a metal. Al performs well at low permittivities (e.g. sphere resonances, superlenses) whereas Au & Ag only perform well at very negative permittivities (shell and rod resonances, LRSPP). The alkali metals perform well overall but present engineering challenges.

Extending SERS into the infrared with gold nanosphere dimers

Here we discuss some of the challenges of using dimers of spheres for SERS at long wavelengths. We show that the field enhancement in the gap between two spheres scales with a local surface plasmon metric, effectively limiting the range of wavelengths for which the largest SERS enhancements can be obtained for this class of structures to the near-IR.

Using nanoscale and mesoscale anisotropy to engineer the optical response of three-dimensional plasmonic metamaterials

The a priori ability to design electromagnetic wave propagation is crucial for the development of novel metamaterials. Incorporating plasmonic building blocks is of particular interest due to their ability to confine visible light. Here we explore the use of anisotropy in nanoscale and mesoscale plasmonic array architectures to produce noble metal-based metamaterials with unusual optical properties. We find that the combination of nanoscale and mesoscale anisotropy leads to rich opportunities for metamaterials throughout the visible and near-infrared. The low volume fraction (<5%) plasmonic metamaterials explored herein exhibit birefringence, a skin depth approaching that of pure metals for selected wavelengths, and directionally confined waves similar to those found in optical fibres. These data provide design principles with which the electromagnetic behaviour of plasmonic metamaterials can be tailored using high aspect ratio nanostructures that are accessible via a variety of synthesis and assembly methods.