Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userTemporal control of graphene plasmons
262
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
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.
rate research
Read More
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.
In this paper we analyze the effects of nonlocality on the optical properties of a system consisting of a thin metallic film separated from a graphene sheet by a hexagonal boron nitride (hBN) layer. We show that nonlocal effects in the metal have a strong impact on the spectrum of the surface plasmon-polaritons on graphene. If the graphene sheet is shaped into a grating, we show that the extinction curves can be used to shed light on the importance of nonlocal effects in metals. Therefore, graphene surface plasmons emerge as a tool for probing nonlocal effects in metallic nanostructures, including thin metallic films. As a byproduct of our study, we show that nonlocal effects lead to smaller losses for the graphene plasmons than what is predicted by a local calculation. We show that these effects can be very well mimicked using a local theory with an effective spacer thickness larger than its actual value.
We study localized plasmons at the nanoscale (nano-plasmons) in graphene. The collective excitations of induced charge density modulations in graphene are drastically changed in the vicinity of a single impurity compared to graphenes bulk behavior. The dispersion of nano-plasmons depends on the number of electrons and the sign, strength and size of the impurity potential. Due to this rich parameter space the calculated dispersions are intrinsically multidimensional requiring an advanced visualization tool for their efficient analysis, which can be achieved with parallel rendering. To overcome the problem of analyzing thousands of very complex spatial patterns of nano-plasmonic modes, we take a combined visual and quantitative approach to investigate the excitations on the two-dimensional graphene lattice. Our visual and quantitative analysis shows that impurities trigger the formation of localized plasmonic excitations of various symmetries. We visually identify dipolar, quadrupolar and radial modes, and quantify the spatial distributions of induced charges.
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.
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.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
