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The energy point of view in plasmonics

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 Added by Antoine Moreau
 Publication date 2019
  fields Physics
and research's language is English




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The group velocity of a plasmonic guided mode can be written as the ratio of the flux of the Poynting to the integral of the energy density along the profile of the mode. This theorem, linking the way energy propagates in metals to the properties of guided modes and Bloch modes in a multilayer, provides a unique physical insight in plasmonics. It allows to better understand the link between the negative permittivity of metals and the wide diversity of exotic phenomenon that occur in plasmonics -- like the slowing down of guided modes, the high wavevector and the negative refraction.



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Unlike conventional optics, plasmonics enables unrivalled concentration of optical energy well beyond the diffraction limit of light. However, a significant part of this energy is dissipated as heat. Plasmonic losses present a major hurdle in the development of plasmonic devices and circuits that can compete with other mature technologies. Until recently, they have largely kept the use of plasmonics to a few niche areas where loss is not a key factor, such as surface enhanced Raman scattering and biochemical sensing. Here, we discuss the origin of plasmonic losses and various approaches to either minimize or mitigate them based on understanding of fundamental processes underlying surface plasmon modes excitation and decay. Along with the ongoing effort to find and synthesize better plasmonic materials, optical designs that modify the optical powerflow through plasmonic nanostructures can help in reducing both radiative damping and dissipative losses of surface plasmons. Another strategy relies on the development of hybrid photonic-plasmonic devices by coupling plasmonic nanostructures to resonant optical elements. Hybrid integration not only helps to reduce dissipative losses and radiative damping of surface plasmons, but also makes possible passive radiative cooling of nano-devices. Finally, we review emerging applications of thermoplasmonics that leverage Ohmic losses to achieve new enhanced functionalities. The most successful commercialized example of a loss-enabled novel application of plasmonics is heat-assisted magnetic recording. Other promising technological directions include thermal emission manipulation, cancer therapy, nanofabrication, nano-manipulation, plasmon-enabled material spectroscopy and thermo-catalysis, and solar water treatment.
We present a comprehensive overview of chirality and its optical manifestation in plasmonic nanosystems and nanostructures. We discuss top-down fabricated structures that range from solid metallic nanostructures to groupings of metallic nanoparticles arranged in three dimensions. We also present the large variety of bottom-up synthesized structures. Using DNA, peptides, or other scaffolds, complex nanoparticle arrangements of up to hundreds of individual nanoparticles have been realized. Beyond this static picture, we also give an overview of recent demonstrations of active chiral plasmonic systems, where the chiral optical response can be controlled by an external stimulus. We discuss the prospect of using the unique properties of complex chiral plasmonic systems for enantiomeric sensing schemes.
Evanescent light can be localized at the nanoscale by resonant absorption in a plasmonic nanoparticle or taper or by transmission through a nanohole. However, a conventional lens cannot focus free-space light beyond half of the wavelength {lambda}. Nevertheless, precisely tailored interference of multiple waves can form a hotspot in free space of arbitrarily small size known as superoscillation. Here, we report a new type of integrated metamaterial interferometry that allows for the first time mapping of fields with deep subwavelength resolution ~ {lambda}/100. It reveals that electromagnetic field near the superoscillatory hotspot has many features similar to those found near resonant plasmonic nanoparticles or nanoholes: the hotspots are surrounded by nanoscale phase singularities (~ {lambda}/50 in size) and zones where the phase of the wave changes more than tenfold faster than in a standing wave. These areas with high local wavevectors are pinned to phase vortices and zones of energy backflow (~ {lambda}/20 in size) that contribute to tightening of the main focal spot size beyond the Abbe-Rayleigh limit. Our observations reveal the analogy between plasmonic nano-focusing of evanescent waves and superoscillatory nano-focusing of free-space waves, and prove the fundamental link between superoscillations and superfocusing offering new opportunities for nanoscale metrology and imaging.
We study theoretically the photoelectron emission in noble gases using plasmonic enhanced near-fields. We demonstrate that these fields have a great potential to generate high energy electrons by direct mid-infrared laser pulses of the current femtosecond oscillator. Typically, these fields appear in the surroundings of plasmonic nanostructures, having different geometrical shape such as bow-ties, metallic waveguides, metal nanoparticles and nanotips, when illuminated by a short laser pulse. In here, we consider metal nanospheres, in which the spatial decay of the near-field of the isolated nanoparticle can be approximated by an exponential function according to recent attosecond streaking measurements. We establish that the strong nonhomogeneous character of the enhanced near-field plays an important role in the above threshold ionization (ATI) process and leads to a significant extension in the photoelectron spectra. In this work, we employ the time dependent Schrodinger equation in reduced dimensions to calculate the photoelectron emission of xenon atoms in such enhanced near-field. Our findings are supported by classical calculations.
Harnessing the optical properties of noble metals down to the nanometer-scale is a key step towards fast and low-dissipative information processing. At the 10-nm length scale, metal crystallinity and patterning as well as probing of surface plasmon (SP) properties must be controlled with a challenging high level of precision. Here, we demonstrate that ultimate lateral confinement and delocalization of SP modes are simultaneously achieved in extended self-assembled networks comprising linear chains of partially fused gold nanoparticles. The spectral and spatial distributions of the SP modes associated with the colloidal superstructures are evidenced by performing monochromated electron energy loss spectroscopy with a nanometer-sized electron probe. We prepare the metallic bead strings by electron beam-induced interparticle fusion of nanoparticle networks. The fused superstructures retain the native morphology and crystallinity but develop very low energy SP modes that are capable of supporting long range and spectrally tunable propagation in nanoscale waveguides.
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