Nonradiative limitations to plasmon propagation in chains of metallic nanoparticles

We investigate the collective plasmonic modes in a chain of metallic nanoparticles that are coupled by near-field interactions. The size- and momentum-dependent nonradiative Landau damping and radiative decay rates are calculated analytically within an open quantum system approach. These decay rates determine the excitation propagation along the chain. In particular, the behavior of the radiative decay rate as a function of the plasmon wavelength leads to a transition from an exponential decay of the collective excitation for short distances to an algebraic decay for large distances. Importantly, we show that the exponential decay is of a purely nonradiative origin. Our transparent model enables us to provide analytical expressions for the polarization-dependent plasmon excitation profile along the chain and for the associated propagation length. Our theoretical analysis constitutes an important step in the quest for the optimal conditions for plasmonic propagation in nanoparticle chains.Comment: 14 pages, 6 figures; v2: published versio

Exciton decay dynamics in individual carbon nanotubes at room temperature

We studied the exciton decay dynamics of individual semiconducting single-walled carbon nanotubes at room temperature using time-resolved photoluminescence spectroscopy. The photoluminescence decay from nanotubes of the same (n,m) type follows a single exponential decay function, however, with lifetimes varying between about 1 and 40 ps from nanotube to nanotube. A correlation between broad photoluminescence spectra and short lifetimes was found and explained by defects promoting both nonradiative decay and vibronic dephasing

Enhancing infrared emission of mercury telluride (HgTe) quantum dots by plasmonic structures

The coupling of HgTe quantum dots to a gold nanobump plasmonic array can enhance the spontaneous infrared emission by a factor of five and reduce the influence of nonradiative decay channels

Spontaneous decay of excited atomic states near a carbon nanotube

Spontaneous decay process of an excited atom placed inside or outside (near the surface) a carbon nanotube is analyzed. Calculations have been performed for various achiral nanotubes. The effect of the nanotube surface has been demonstrated to dramatically increase the atomic spontaneous decay rate -- by 6 to 7 orders of magnitude compared with that of the same atom in vacuum. Such an increase is associated with the nonradiative decay via surface excitations in the nanotube.Comment: 8 pages, 3 figure