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Emission spectra of quantum dot arrays in zero-dimensional microcavities are studied theoretically, and it is shown that they are determined by the competition between the formation of the collective superradiant mode and inhomogeneous broadening. The random sources method for the calculation of photoluminescence spectra under a non-resonant pumping is developed, and a microscopic justification of the random sources method within a framework of the standard diagram technique is given. The emission spectra of a microcavity are analyzed with allowance for the spread of exciton states energies caused by an inhomogeneous distribution of quantum dots and a tunneling between them. It is demonstrated that in the case of a strong tunneling coupling the luminescence spectra are sensitive to the geometric positions of the dots, and the collective mode can, under certain conditions, be stabilized by the random tunnel junctions.
Collective behavior is one of the most intriguing aspects of the hydrodynamic approach to electronic transport. Here we provide a consistent, unified calculation of the dispersion relations of the hydrodynamic collective modes in graphene. Taking int
We compare the response of five different models of two interacting electrons in a quantum dot to an external short lived radial excitation that is strong enough to excite the system well beyond the linear response regime. The models considered descr
Dislocations are ubiquitous in three-dimensional solid-state materials. The interplay of such real space topology with the emergent band topology defined in reciprocal space gives rise to gapless helical modes bound to the line defects. This is known
Interference of a single photon generated from a single quantum dot is observed between two photon polarization modes. Each emitted single photon has two orthogonal polarization modes associated with the solid-state single photon source, in which two
The excitation spectrum and the collective modes of graphene antidot lattices (GALs) are studied in the context of a $pi$-band tight-binding model. The dynamical polarizability and dielectric function are calculated within the random phase approximat