Coinage metals, such as Au, Ag, and Cu, have been important materials throughout history.1 While in ancient cultures they were admired primarily for their ability to reflect light, their applications have become far more sophisticated with our increased understanding and control of the atomic world. Today, these metals are widely used in electronics, catalysis, and as structural materials, but when they are fashioned into structures with nanometer-sized dimensions, they also become enablers for a completely different set of applications that involve light. These new applications go far beyond merely reflecting light, and have renewed our interest in maneuvering the interactions between metals and light in a field known as plasmonics.2–6

In plasmonics, the metal nanostructures can serve as antennas to convert light into localized electric fields (E-fields) or as waveguides to route light to desired locations with nanometer precision. These applications are made possible through a strong interaction between incident light and free electrons in the nanostructures. With a tight control over the nanostructures in terms of size and shape, light can be effectively manipulated and controlled with unprecedented accuracy.3,7 While many new technologies stand to be realized from plasmonics, with notable examples including superlenses,8 invisible cloaks,9 and quantum computing,10,11 conventional technologies like microprocessors and photovoltaic devices could also be made significantly faster and more efficient with the integration of plasmonic nanostructures.12–15 Of the metals, Ag has probably played the most important role in the development of plasmonics, and its unique properties make it well-suited for most of the next-generation plasmonic technologies.16–18

1.1. What is Plasmonics?
Plasmonics is related to the localization, guiding, and manipulation of electromagnetic waves beyond the diffraction limit and down to the nanometer length scale.4,6 The key component of plasmonics is a metal, because it supports surface plasmon polariton modes (indicated as surface plasmons or SPs throughout this review), which are electromagnetic waves coupled to the collective oscillations of free electrons in the metal.

While there are a rich variety of plasmonic metal nanostructures, they can be differentiated based on the plasmonic modes they support: localized surface plasmons (LSPs) or propagating surface plasmons (PSPs).5,19 In LSPs, the time-varying electric field associated with the light (Eo) exerts a force on the gas of negatively charged electrons in the conduction band of the metal and drives them to oscillate collectively. At a certain excitation frequency (w), this oscillation will be in resonance with the incident light, resulting in a strong oscillation of the surface electrons, commonly known as a localized surface plasmon resonance (LSPR) mode.20 This phenomenon is illustrated in Figure 1A. Structures that support LSPRs experience a uniform Eo when excited by light as their dimensions are much smaller than the wavelength of the light.



Figure 1

Schematic illustration of the two types of plasmonic nanostructures discussed in this article as excited by the electric field (Eo) of incident light with wavevector (k). In (A) the nanostructure is smaller than the wavelength of light and the free electrons ...



In contrast, PSPs are supported by structures that have at least one dimension that approaches the excitation wavelength, as shown in Figure 1B.4 In this case, the Eo is not uniform across the structure and other effects must be considered. In such a structure, like a nanowire for example, SPs propagate back and forth between the ends of the structure. This can be described as a Fabry-Perot resonator with resonance condition l=nλsp, where l is the length of the nanowire, n is an integer, and λsp is the wavelength of the PSP mode.21,22 Reflection from the ends of the structure must also be considered, which can change the phase and resonant length. Propagation lengths can be in the tens of micrometers (for nanowires) and the PSP waves can be manipulated by controlling the geometrical parameters of the structure.23

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Controlling the synthesis and assembly of silver nanostructures for plasmonic applications

When light interacts with a metal nanoparticle (NP), its conduction electrons can be driven by the incident electric field in collective oscillations known as localized surface plasmon resonances (LSPRs). These give rise to a drastic alteration of the incident radiation pattern and to striking effects such as the subwavelength localization of electromagnetic (EM) energy, the formation of high intensity hot spots at the NP surface, or the directional scattering of light out of the structure. LSPRs can also couple to the EM fields emitted by molecules, atoms, or quantum dots placed in the vicinity of the NP, leading in turn to a strong modification of the radiative and nonradiative properties of the emitter. Since LSPRs enable an efficient transfer of EM energy from the near to the far-field of metal NPs and vice versa, we can consider plasmonic nanostructures as nanoantennas, because they operate in a similar way to radio antennas but at higher frequencies. Typically, plasmonic nanoantennas at optical frequencies are made of gold and silver due to their goodmetallic properties and low absorption. Controlling and guiding light has been one of science’s most influential achievements. It affects everyday life in many ways, such as the development of telescopes, microscopes, spectrometers, and optical fibers, to name but a few. These examples exploit the wave nature of light and are based on the reflection, refraction and diffraction of light by optical elements such as mirrors, lenses or gratings. However, the wave nature of light limits the resolution to which an object can be imaged, as well as the size of the transverse cross section of efficient guiding structures to the wavelength dimension. Plasmonic resonances in nanoantennas overcome these constraints, allowing unprecedented control of light-matter interactions within subwavelength volumes (i.e., within the nanoscale at optical frequencies). Such properties have attracted much interest lately, due to the implications they have both in fundamental research and in technological applications. Metal NPs have been used since antiquity. Due to their strong scattering properties in the visible range, they show attractive colors. One of their first applications, dating back to the Roman Empire more than 2000 years ago, was as a colorant for clothing. In art, they were used to stain window glass and ceramics. Obviously, it was not known then that the colorants being used contained metal NPs or that the spectacular colors were due to the excitation of LSPRs. The first reported intentional production of metal NPs dates from 1857, when Faraday synthesized gold colloids. However, at the time there was not much interest in understanding the physics behind the optical properties of colloids due to the impossibility of synthesizing NPs with well-controlled shapes and sizes, as well as the lack of accurate detection techniques. The first theoretical work on the scattering of light by particles smaller than the incident wavelength was carried out by Lord Rayleigh at the end of the 19th century. He analyzed the diffusion of light by diluted gases, and his theory explained physical phenomena such as the blueness of the sky, the redness of the sunset, or the yellow color of the sun. Mie took the next step forward by deriving an analytical solution to Maxwell’s equations to describe the interaction of light with spheres of arbitrary radius and composition. Subsequently, based on the results of Rayleigh and Mie, Gans considered elliptical geometries. He demonstrated that the optical response of metal NPs is

Plasmonic nanoantennas: fundamentals and their use in controlling the radiative properties of nanoemitters.

This review discusses how low-energy, valence excitations created by swift electrons can render information on the optical response of structured materials with unmatched spatial resolution. Electron microscopes are capable of focusing electron beams on sub-nanometer spots and probing the target response either by analyzing electron energy losses or by detecting emitted radiation. Theoretical frameworks suited to calculate the probability of energy loss and light emission (cathodoluminescence) are revisited and compared with experimental results. More precisely, a quantum-mechanical description of the interaction between the electrons and the sample is discussed, followed by a powerful classical dielectric approach that can be in practice applied to more complex systems. We assess the conditions under which classical and quantum-mechanical formulations are equivalent. The excitation of collective modes such as plasmons is studied in bulk materials, planar surfaces, and nanoparticles. Light emission induced by the electrons is shown to constitute an excellent probe of plasmons, combining sub-nanometer resolution in the position of the electron beam with nanometer resolution in the emitted wavelength. Both electron energy-loss and cathodoluminescence spectroscopies performed in a scanning mode of operation yield snap shots of plasmon modes in nanostructures with fine spatial detail as compared to other existing imaging techniques, thus providing an ideal tool for nanophotonics studies.

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Optical excitations in electron microscopy

Nanoparticles of noble metals belong to the most extensively studied colloidal systems in the field of nanoscience and nanotechnology. Due to continuing progress in the synthesis of nanoparticles with controlled morphologies, the exploration of unique morphology-dependent properties has gained momentum. Anisotropic features in nonspherical nanoparticles make them ideal candidates for enhanced chemical, catalytic, and local field related applications. Nonspherical plasmon resonant nanoparticles offer favorable properties for their use as analytical tools, or as diagnostic and therapeutic agents. This Review highlights morphology-dependent properties of nonspherical noble metal nanoparticles with a focus on localized surface plasmon resonance and local field enhancement, as well as their applications in various fields including Raman spectroscopy, fluorescence enhancement, analytics and sensing, photothermal therapy, (bio-)diagnostics, and imaging.

Properties and Applications of Colloidal Nonspherical Noble Metal Nanoparticles

Nanoantennas for visible and infrared radiation can strongly enhance the interaction of light with nanoscale matter by their ability to efficiently link propagating and spatially localized optical fields. This ability unlocks an enormous potential for applications ranging from nanoscale optical microscopy and spectroscopy over solar energy conversion, integrated optical nanocircuitry, opto-electronics and density-of-states engineering to ultra-sensing as well as enhancement of optical nonlinearities. Here we review the current understanding of metallic optical antennas based on the background of both well-developed radiowave antenna engineering and plasmonics. In particular, we discuss the role of plasmonic resonances on the performance of nanoantennas and address the influence of geometrical parameters imposed by nanofabrication. Finally, we give a brief account of the current status of the field and the major established and emerging lines of investigation in this vivid area of research.

https://iopscience.iop.org/article/10.1088/0034-4885/75/2/024402/pdf

Nanoantennas for visible and infrared radiation.

The optical local-field enhancement on nanometer length scales provides the basis for plasmonic metal nanostructures to serve as molecular sensors and as nanophotonic devices. However, particle morphology and the associated surface plasmon resonance alone do not uniquely reflect the important details of the local field distribution. Here, we use interferometric homodyne tip-scattering near-field microscopy for plasmonic near-field imaging of crystalline triangular silver nanoprisms. Strong spatial field variation on lengths scales as short as 20 nm are observed sensitively depending on structural details and environment. The poles of the dipole and quadrupole plasmon modes, as identified by phase-sensitive probing and calculations performed in the discrete dipole approximation (DDA), reflect the particle symmetry. Together with the observation that the largest enhancement is not necessarily found to be associated with the tips of the nanoprisms, our results provide critical information for the selection of particle geometries as building blocks for plasmonic device applications.

Optical near-field mapping of plasmonic nanoprisms.

In addition to the electric field $\mathbit{E}(\mathbit{r})$, the associated magnetic field $\mathbit{H}(\mathbit{r})$ and current density $\mathbit{J}(\mathbit{r})$ characterize any electromagnetic device, providing insight into antenna coupling and mutual impedance. We demonstrate the optical analogue of the radio frequency vector network analyzer implemented in interferometric homodyne scattering-type scanning near-field optical microscopy for obtaining $\mathbit{E}(\mathbit{r})$, $\mathbit{H}(\mathbit{r})$, and $\mathbit{J}(\mathbit{r})$. The approach is generally applicable and demonstrated for the case of a linear coupled-dipole antenna in the midinfrared spectral region. The determination of the underlying 3D vector electric near-field distribution $\mathbit{E}(\mathbit{r})$ with nanometer spatial resolution and full phase and amplitude information is enabled by the design of probe tips with selectivity with respect to ${E}_{\ensuremath{\parallel}}$ and ${E}_{\ensuremath{\perp}}$ fabricated by focused ion-beam milling and nano-chemical-vapor-deposition methods.

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Determination of Electric-Field, Magnetic-Field, and Electric-Current Distributions of Infrared Optical Antennas: A Near-Field Optical Vector Network Analyzer

We demonstrate molecular radiative infrared vibrational free-induction decay on the nano-scale and its control via near-field coupling between the transient molecular polarization and optical antenna properties of the metallic scanning near-field probe tip. This allows for pushing the sensitivity of infrared vibrational spectroscopy into the single molecule regime.

/pdf/ultrafast-infrared-near-field-molecular-nano-spectroscopy-22f8vskrb8.pdf

Matthias Rang

Papers

Optical near-field mapping of plasmonic nanoprisms.

Determination of Electric-Field, Magnetic-Field, and Electric-Current Distributions of Infrared Optical Antennas: A Near-Field Optical Vector Network Analyzer

Ultrafast infrared near-field molecular nano-spectroscopy