Quantum Plasmonics

Quantum plasmonics is an exciting subbranch of nanoplasmonics where the laws of quantum theory are used to describe light–matter interactions on the nanoscale. Plasmonic materials allow extreme subdiffraction confinement of (quantum or classical) light to regions so small that the quantization of both light and matter may be necessary for an accurate description. State-of-the-art experiments now allow us to probe these regimes and push existing theories to the limits which opens up the possibilities of exploring the nature of many-body collective oscillations as well as developing new plasmonic devices, which use the particle quality of light and the wave quality of matter, and have a wealth of potential applications in sensing, lasing, and quantum computing. This merging of fundamental condensed matter theory with application-rich electromagnetism (and a splash of quantum optics thrown in) gives rise to a fascinating area of modern physics that is still very much in its infancy. In this review, we discuss and compare the key models and experiments used to explore how the quantum nature of electrons impacts plasmonics in the context of quantum size corrections of localized plasmons and quantum tunneling between nanoparticle dimers. We also look at some of the remarkable experiments that are revealing the quantum nature of surface plasmon polaritons

Vaccinations, infections and antibacterials in the first grass pollen season of life and risk of later hayfever

Published source: Bremner, S. A., Carey, I. M., DeWilde, S., Richards, N., Maier, W. C., Hilton, S. R., Strachan, D. P. and Cook, D. G. (2007), Vaccinations, infections and antibacterials in the first grass pollen season of life and risk of later hayfever. Clinical & Experimental Allergy, 37: 512–517. doi: 10.1111/j.1365-2222.2007.02697.

Double blind ultrafast pulse characterization by mixed frequency generation in a gold antenna

Ultrafast pulse characterization requires the analysis of correlation functions generated by frequency mixing of optical pulses in a nonlinear medium. In this work, we use a gold optical nanoantenna to generate simultaneously Four Wave Mixing and Sum Frequency Generation across the tuning range of a Ti: Sapphire and Optical Parametric Oscillator (OPO) system. Since metal nanoparticles create remarkably strong nonlinear responses for their size without the need for phase matching, this allows us to simultaneously characterize the unknown OPO pulse and its pump pulse using a single spectrogram. The nonlinear mixing is efficient enough to retrieve pulses with energies in the picojoule range

Broadband spin-controlled focusing via logarithmic-spiral nanoslits of varying width

This work presents analytical, numerical and experimental demonstrations of light diffracted through a logarithmic spiral (LS) nanoslit, which forms a type of switchable and focus-tunable structure. Owing to a strong dependence on the incident photon spin, the proposed LS-nanoslit converges incoming light of opposite handedness (to that of the LS-nanoslit) into a confined subwavelength spot, while it shapes light with similar chirality into a donut-like intensity profile. Benefitting from the varying width of the LS-nanoslit, different incident wavelengths interfere constructively at different positions, i.e., the focal length shifts from 7.5 μm (at λ = 632.8 nm) to 10 μm (at λ = 488 nm), which opens up new opportunities for tuning and spatially separating broadband light at the micrometer scale

Generating, probing and utilising photo-induced surface oxygen vacancies for trace molecular detection

Metal oxide semiconductors (MOS) are extensively used for a wide range of industrial applications [1] – [3] , where defects states in MOS can strongly affect their overall performance, even at very low concentrations [4] , [5] . The functionality of MOS has been reported to be significantly altered through the addition of defects, whereby the materials can become more/less chemically active or the electronic properties are altered. Surface defects, in particular, are often one of the most reactive sites on the surface, greatly influencing MOS photocatalytic activity. Under UV irradiation conditions, interactions with photo- induced charge carriers can generate temporary oxygen vacancies, VO, defect states on the surface of MOS [6] , affecting the material properties during the defects’ lifetime

Optically-Triggered Nanoscale Memory Effect in a Hybrid Plasmonic-Phase Changing Nanostructure

Nanoscale devices, such as all-optical modulators and electro-optical transducers, can be implemented in heterostructures that integrate plasmonic nanostructures with functional active materials. Here we demonstrate all-optical control of a nanoscale memory effect in such a heterostructure by coupling the localized surface plasmon resonance (LSPR) of gold nanodisk arrays to a phase-changing material (PCM), vanadium dioxide (VO<inf>2</inf>). By latching the VO<inf>2</inf> in a distinct correlated metallic state during the insulator-to-metal transition (IMT), while concurrently exciting the hybrid nanostructure with one or more ultraviolet optical pulses, the entire phase space of this correlated state can be accessed optically to modulate the plasmon response. We find that the LSPR modulation depends strongly but linearly on the initial latched state, suggesting that the memory effect encoded in the plasmon resonance wavelength is linked to the strongly correlated electron states of the VO<inf>2</inf>. The continuous, linear variation of the electronic and optical properties of these model heterostructures opens the way to multiple design strategies for hybrid devices with novel optoelectronic functionalities, which can be controlled by an applied electric or optical field, strain, injected charge, or temperature.Department of Applied Physic