No Arabic abstract
In this article we perform the quantization of graphene plasmons using both a macroscopic approach based on the classical average electromagnetic energy and a quantum hydrodynamic model, in which graphene charge carriers are modeled as a charged fluid. Both models allow to take into account the dispersion of graphenes optical response, with the hydrodynamic model also allowing for the inclusion of non-local effects. Using both methods, the electromagnetic field mode-functions, and the respective frequencies, are determined for two different graphene structures. we show how to quantize graphene plasmons, considering that graphene is a dispersive medium, and taking into account both local and nonlocal descriptions. It is found that the dispersion of graphenes optical response leads to a non-trivial normalization condition for the mode-functions. The obtained mode-functions are then used to calculate the decay of an emitter, represented by a dipole, via the excitation of graphene surface plasmon-polaritons. The obtained results are compared with the total spontaneous decay rate of the emitter and a near perfect match is found in the relevant spectral range. It is found that non-local effects in graphenes conductivity, become relevant for the emission rate for small Fermi energies and small distances between the dipole and the graphene sheet.
Electrostatic gating and optical pumping schemes enable efficient time modulation of graphenes free carrier density, or Drude weight. We develop a theory for plasmon propagation in graphene under temporal modulation. When the modulation is on the timescale of the plasmonic period, we show that it is possible to create a backwards-propagating or standing plasmon wave and to amplify plasmons. The theoretical models show very good agreement with direct Maxwell simulations.
The two-dimensionality of graphene and other layered materials can be exploited to simplify the theoretical description of their plasmonic and polaritonic modes. We present an analytical theory that allows us to simulate these excitations in terms of plasmon wave functions (PWFs). Closed-form expressions are offered for their associated extinction spectra, involving only two real parameters for each plasmon mode and graphene morphology, which we calculate and tabulate once and for all. Classical and quantum-mechanical formulations of this PWF formalism are introduced, in excellent mutual agreement for armchaired islands with $>10,$nm characteristic size. Examples of application are presented to predict both plasmon-induced transparency in interacting nanoribbons and excellent sensing capabilities through the response to the dielectric environment. We argue that the PWF formalism has general applicability and allows us to analytically describe a wide range of 2D polaritonic behavior, thus facilitating their use for the design of actual devices.
The optical response of a heavily doped quantum well, with two occupied subbands, has been investigated as a function of the electronic density. It is shown that the two optically active transitions are mutually coupled by dipole-dipole Coulomb interaction, which strongly renormalizes their absorption amplitude. In order to demonstrate this effect, we have measured a set of optical spectra on a device in which the electronic density can be tuned by the application of a gate voltage. Our results show that the absorption spectra can be correctly described only by taking into account the Coulomb coupling between the two transitions. As a consequence, the optical dipoles originating from intersubband transitions are not independent, but rather coupled oscillators with an adjustable strength.
We present a quantum model to calculate the dipole-dipole coupling between electronic excitations in the conduction band of semiconductor quantum wells. We demonstrate that the coupling depends on a characteristic length, related to the overlap between microscopic current densities associated with each electronic excitation. As a result of the coupling, a macroscopic polarization is established in the quantum wells, corresponding to one or few bright collective modes of the electron gas. Our model is applied to derive a sum rule and to investigate the interplay between tunnel coupling and Coulomb interaction in the absorption spectrum of a dense electron gas.
Graphene has raised high expectations as a low-loss plasmonic material in which the plasmon properties can be controlled via electrostatic doping. Here, we analyze realistic configurations, which produce inhomogeneous doping, in contrast to what has been so far assumed in the study of plasmons in nanostructured graphene. Specifically, we investigate backgated ribbons, co-planar ribbon pairs placed at opposite potentials, and individual ribbons subject to a uniform electric field. Plasmons in backgated ribbons and ribbon pairs are similar to those of uniformly doped ribbons, provided the Fermi energy is appropriately scaled to compensate for finite-size effects such as the divergence of the carrier density at the edges. In contrast, the plasmons of a ribbon exposed to a uniform field exhibit distinct dispersion and spatial profiles that considerably differ from uniformly doped ribbons. Our results provide a road map to understand graphene plasmons under realistic electrostatic doping conditions.