No Arabic abstract
A residual disorder in the gate system is the main problem on the way to create artificial graphene based on two-dimensional electron gas. The disorder can be significantly screened/reduced due to the many-body effects. To analyse the screening/disorder problem we consider AlGaAs/GaAs/AlGaAs heterostructure with two metallic gates. We demonstrate that the design least susceptible to the disorder corresponds to the weak coupling regime (opposite to tight binding) which is realised via system of quantum anti-dots. The most relevant type of disorder is the area disorder which is a random variation of areas of quantum anti-dots. The area disorder results in formation of puddles. Other types of disorder, the position disorder and the shape disorder, are practically irrelevant. The formation/importance of puddles dramatically depends on parameters of the nanopatterned heterostructure. A variation of the parameters by 20--30% can change the relative amplitude of puddles by orders of magnitude. Based on this analysis we formulate criteria for the acceptable design of the heterostructure aimed at creation of the artificial graphene.
Electromagnetic fields bound tightly to charge carriers in a two-dimensional sheet, namely surface plasmons, are shielded by metallic plates that are a part of a device. It is shown that for epitaxial graphenes, the propagation velocity of surface plasmons is suppressed significantly through a partial screening of the electron charge by the interface states. On the basis of analytical calculations of the electron lifetime determined by the screened Coulomb interaction, we show that the screening effect gives results in agreement with those of a recent experiment.
We study the transport of charge carriers through finite graphene structures. The use of numerical exact kernel polynomial and Green function techniques allows us to treat actual sized samples beyond the Dirac-cone approximation. Particularly we investigate disordered nanoribbons, normal-conductor/graphene interfaces and normal-conductor/graphene/normal-conductor junctions with a focus on the behavior of the local density of states, single-particle spectral function, optical conductivity and conductance. We demonstrate that the contacts and bulk disorder will have a major impact on the electronic properties of graphene-based devices.
Majorana zero modes in a superconductor-semiconductor nanowire have been extensively studied during the past decade. Disorder remains a serious problem, preventing the definitive observation of topological Majorana bound states. Thus, it is worthwhile to revisit the simple model, the Kitaev chain, and study the effects of weak and strong disorder on the Kitaev chain. By comparing the role of disorder in a Kitaev chain with that in a nanowire, we find that disorder affects both systems but in a nonuniversal manner. In general, disorder has a much stronger effect on the nanowire than the Kitaev chain, particularly for weak to intermediate disorder. For strong disorder, both the Kitaev chain and nanowire manifest random featureless behavior due to universal Anderson localization. Only the vanishing and strong disorder regimes are thus universal, manifesting respectively topological superconductivity and Anderson localization, but the experimentally relevant intermediate disorder regime is nonuniversal with the details dependent on the disorder realization in the system.
We present a proof of concept for a spectrally selective thermal mid-IR source based on nanopatterned graphene (NPG) with a typical mobility of CVD-grown graphene (up to $3000$ cm$^2$V$^{-1}$s$^{-1}$), ensuring scalability to large areas. For that, we solve the electrostatic problem of a conducting hyperboloid with an elliptical wormhole in the presence of an in-plane electric field. The localized surface plasmons (LSPs) on the NPG sheet allow for the control and tuning of the thermal emission spectrum in the wavelength regime from 3 $mu$m to 12 $mu$m. The LSPs along with an optical cavity increase the emittance of graphene from about 2.3% for pristine graphene to 80% for NPG, thereby outperforming state-of-the-art pristine graphene light sources operating in the near-infrared (NIR) by a factor of 100. A maximum emission power per area of 11x10^3 W/m$^2$ at $T=2000$ K for a bias voltage of $V=23$ V is achieved by Joule heating. By generalizing Plancks theory and considering the nonlocal fluctuation-dissipation theorem with nonlocal response of surface plasmons in graphene in RPA, we show that the coherence length of the graphene plasmons and the thermally emitted photons can be as large as 13 $mu$m and 150 $mu$m, respectively, providing the opportunity to create phased arrays. The spatial phase variation of the coherence allows for beamsteering of the thermal emission in the range between $12^circ$ and $80^circ$ by tuning the Fermi energy. Our analysis of the nonlocal hydrodynamic response leads to the conjecture that the diffusion length and viscosity in graphene are frequency-dependent. Using finite-difference time domain (FDTD) calculations, coupled mode theory, and RPA, we develop the model of a mid-IR light source based on NPG, which will pave the way to graphene-based optical mid-IR communication, mid-IR color displays, mid-IR spectroscopy, and virus detection.
Flat bands near M points in the Brillouin zone are key features of honeycomb symmetry in artificial graphene (AG) where electrons may condense into novel correlated phases. Here we report the observation of van Hove singularity doublet of AG in GaAs quantum well transistors, which presents the evidence of flat bands in semiconductor AG. Two emerging peaks in photoluminescence spectra tuned by backgate voltages probe the singularity doublet of AG flat bands, and demonstrate their accessibility to the Fermi level. As the Fermi level crosses the doublet, the spectra display dramatic stability against electron density, indicating interplays between electron-electron interactions and honeycomb symmetry. Our results provide a new flexible platform to explore intriguing flat band physics.