Landau Damping in Hybrid Plasmonics.

The Landau damping (LD) mechanism of the localized surface plasmon (LSP) decay is studied for the hybrid nanoplasmonic (metal core/dielectric shell) structures. It is shown that LD in hybrid structures is strongly affected by the permittivity and the electron effective mass in the dielectric shell in accordance with previous observations by Kreibig, and the strength of LD can be enhanced by an order of magnitude for some combinations of permittivity and effective mass. The physical reason for this effect is identified as an electron spillover into the dielectric where the electric field is higher than that in the metal and the presence of quasi-discrete energy levels in the dielectric. The theory indicates that the transition absorption at the metal-dielectric interface is a dominant contribution to LD in such hybrid structures. Thus, by judicious selection of dielectric material and its thickness, one can engineer decay rates and hot carrier production for important applications, such as photodetection and photochemistry.

Resonance photogeneration of hot electrons through Tamm surface states.

Internal surface photoemission of electrons from 1D crystal into a barrier with participation of Tamm state (TS) at the interface crystal barrier is considered theoretically for the first time, to the best of our knowledge. It is shown that resonant tunneling of electrons through a TS could lead to substantial enhancement of the quantum efficiency and lowering the red border to a value defined by the TS. In contrast to the Fowler quadratic law, the photocurrent scales linearly with photon energy near the red border. The results suggest that the efficiency of hot electron generation with plasmonic metal nanoparticles could reach several tens of percent, which is very attractive for application in energy conversion technologies such as water splitting.

Luminescence and energy transfer mechanisms in photo-thermo-refractive glasses co-doped with silver molecular clusters and Eu3.

Silver molecular clusters were synthesized in photo-thermo-refractive glasses using the Na+-Ag+ ion exchange technique followed by heat treatment. Comprehensive study of cluster emission reveals the presence of spectrally separated fluorescence and phosphorescence with nanosecond and microsecond lifetime. Co-doping of glasses with Eu3+ was shown to results in quenching of cluster luminescence caused by energy transfer. The monitoring of silver cluster luminescence quantum yield and lifetime in the presence of Eu3+ indicates the presence of two different mechanisms of energy transfer. The first one affects the decay kinetics of cluster fluorescence and manifests at long distances, while the second one leads to static quenching of cluster emission at shorter distances and becomes prominent at higher doping Eu3+ concentration.

Linear self-focusing of continuous UV laser beam in photo-thermo-refractive glasses.

The experimental and theoretical study of continuous UV laser beam propagation through thick silver-containing photo-thermo-refractive glass is presented. It is shown for the first time that self-action of UV Gaussian beam in glass results in its self-focusing. The observed linear effect is non-reversible and is caused by the transformation of subnanosized charged silver molecular clusters to neutral state under UV laser radiation. Such transformation is accompanied by the increase of molecular clusters polarizability and the refractive index increase in irradiated area. As a result, an extended positive lens is formed in glass bulk. In a theoretical study of linear self-focusing effect, the "aberration-free" approximation was used, taking into account spatial distribution of induced absorption.