Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userMicroscopic theory for electron hydrodynamics in monolayer and bilayer graphene
140
0
0.0
(
0
)
Authors
Derek Y. H. Ho
Ask ChatGPT about the research
No Arabic abstract
Electrons behave like a classical fluid with a momentum distribution function that varies slowly in space and time when the quantum mechanical carrier-carrier scattering dominates over all other scattering processes. Recent experiments in monolayer and bilayer graphene have reported signatures of such hydrodynamic electron behavior in ultra-clean devices. In this theoretical work, starting from a microscopic treatment of electron-electron, electron-phonon and electron-impurity interactions within the Random Phase Approximation, we demonstrate that monolayer and bilayer graphene both host two different hydrodynamic regimes. We predict that the hydrodynamic window in bilayer graphene is stronger than in monolayer graphene, and has a characteristic `v-shape as opposed to a `lung-shape. Finally, we collapse experimental data onto a universal disorder-limited theory, thereby proving that the observed violation of Wiedemann-Franz law in monolayers occurs in a regime dominated by impurity-induced electron-hole puddles.
rate research
Read More
We describe the weak localization correction to conductivity in ultra-thin graphene films, taking into account disorder scattering and the influence of trigonal warping of the Fermi surface. A possible manifestation of the chiral nature of electrons in the localization properties is hampered by trigonal warping, resulting in a suppression of the weak anti-localization effect in monolayer graphene and of weak localization in bilayer graphene. Intervalley scattering due to atomically sharp scatterers in a realistic graphene sheet or by edges in a narrow wire tends to restore weak localization resulting in negative magnetoresistance in both materials.
The electron gas hosted in a two-dimensional solid-state matrix, such as a quantum well or a two-dimensional van der Waals heterostructure, supports the propagation of plasma waves. Nonlinear interactions between plasma waves, due to charge conservation and current convection, generate a constant density gradient which can be detected as a dc potential signal at the boundaries of the system. This phenomenon is at the heart of a plasma-wave photodetection scheme which was first introduced by Dyakonov and Shur for electronic systems with a parabolic dispersion and then extended to the massless Dirac fermions in graphene. In this work, we develop the theory of plasma-wave photodetection in bilayer graphene, which has the peculiarity that the dispersion relation depends locally and dynamically on the intensity of the plasma wave. In our analysis, we show how quantum capacitance effects, arising from the local fluctuations of the electronic dispersion, modify the intensity of the photodetection signal. An external electrical bias, e.g. induced by top and bottom gates, can be used to control the strength of the quantum capacitance corrections, and thus the photoresponse.
We prepare twist-controlled resonant tunneling transistors consisting of monolayer (Gr) and Bernal bilayer (BGr) graphene electrodes separated by a thin layer of hexagonal boron nitride (hBN). The resonant conditions are achieved by closely aligning the crystallographic orientation of the graphene electrodes, which leads to momentum conservation for tunneling electrons at certain bias voltages. Under such conditions, negative differential conductance (NDC) can be achieved. Application of in-plane magnetic field leads to electrons acquiring additional momentum during the tunneling process, which allows control over the resonant conditions.
Hydrodynamic behavior in electronic systems is commonly accepted to be associated with extremely clean samples such that electron-electron collisions dominate and total momentum is conserved. Contrary to this, we show that in monolayer graphene the presence of disorder is essential to enable an unconventional hydrodynamic regime which exists near the charge neutrality point and is characterized by a large enhancement of the Wiedemann-Franz ratio. Although the enhancement becomes more pronounced with decreasing disorder, the very possibility of observing the effect depends crucially on the presence of disorder. We calculate the maximum extrinsic carrier density $n_c$ below which the effect becomes manifest, and show that $n_c$ vanishes in the limit of zero disorder. For $n>n_c$ we predict that the Wiedemann-Franz ratio actually decreases with decreasing disorder. We complete our analysis by presenting a transparent picture of the physical processes that are responsible for the crossover from conventional to disorder-enabled hydrodynamics. Recent experiments on monolayer graphene are discussed and shown to be consistent with this picture.
Band structure determines the motion of electrons in a solid, giving rise to exotic phenomena when properly engineered. Drawing an analogy between electrons and photons, artificially designed optical lattices indicate the possibility of a similar band modulation effect in graphene systems. Yet due to the fermionic nature of electrons, modulated electronic systems promise far richer categories of behaviors than those found in optical lattices. Here, we uncovered a strong modulation of electronic states in bilayer graphene subject to periodic potentials. We observed for the first time the hybridization of electron and hole sub-bands, resulting in local band gaps at both primary and secondary charge neutrality points. Such hybridization leads to the formation of flat bands, enabling the study of correlated effects in graphene systems. This work may also offer a viable platform to form and continuously tune Majorana zero modes, which is important to the realization of topological quantum computation.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
