Demetra Psiachos | Searcharxiv

arXiv2014

${\cal PT}-$Symmetric Dimers with Time-Periodic Gain/Loss Function

${\mathcal PT}-$symmetric dimers with a time-periodic gain/loss function in a balanced configuration where the amount of gain equals that of loss are investigated analytically and numerically. Two prototypical dimers in the linear regime are investigated: a system of coupled classical oscillators, and a Schrödinger dimer representing the coupling of field amplitudes; each system representing a wide class of physical models. Through a thorough analysis of their stability behaviour, we find that turning on the coupling parameter in the classical dimer system, leads initially to decreased stability but then to re-entrant transitions from the exact to the broken ${\mathcal PT}-$phase and vice versa, as it is increased beyond a critical value. On the other hand, the Schrödinger dimer behaves more like a single oscillator with time-periodic gain/loss. In addition, we are able to identify the conditions under which the behaviour of the two dimer systems coincides and/or reduces to that of a single oscillator.

cond-mat.other↗

arXiv2008

Electron-electron interaction effects on the photophysics of metallic single-walled carbon nanotubes

Single-walled carbon nanotubes are strongly correlated systems with large Coulomb repulsion between two electrons occupying the same $p_z$ orbital. Within a molecular Hamiltonian appropriate for correlated $π$-electron systems, we show that optical excitations polarized parallel to the nanotube axes in the so-called metallic single-walled carbon nanotubes are to excitons. Our calculated absolute exciton energies in twelve different metallic single-walled carbon nanotubes, with diameters in the range 0.8 - 1.4 nm, are in nearly quantitative agreement with experimental results. We have also calculated the absorption spectrum for the (21,21) single-walled carbon nanotube in the E$_{22}$ region. Our calculated spectrum gives an excellent fit to the experimental absorption spectrum. In all cases our calculated exciton binding energies are only slightly smaller than those of semiconducting nanotubes with comparable diameters, in contradiction to results obtained within the {\it ab initio} approach, which predicts much smaller binding energies. We ascribe this difference to the difficulty of determining the behavior of systems with strong on-site Coulomb interactions within theories based on the density functional approach. As in the semiconducting nanotubes we predict in the metallic nanotubes a two-photon exciton above the lowest longitudinally polarized exciton that can be detected by ultrafast pump-probe spectroscopy. We also predict a subgap absorption polarized perpendicular to the nanotube axes below the lowest longitudinal exciton, blueshifted from the exact midgap by electron-electron interactions.

cond-mat.mtrl-sci↗