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Register a new userAngular momentum anisotropy of Dirac carriers: A new twist in graphene
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Authors
Marta Prada
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Dirac carriers in graphene are commonly characterized by a pseudospin degree of freedom, arising from the degeneracy of the two inequivalent sublattices. The inherent chirality of the quasiparticles leads to a topologically non-trivial band structure, where the in-plane component of sublattice spin and momentum are intertwined. Equivalently, sublattice imbalance is intimately connected with angular momentum, inducing a torque of opposite sign at each Dirac point. In this work we develop an intuitive picture that associates sublattice spin and winding number with angular momentum. We develop a microscopic perturbative model to obtain the finite angular momentum contributions along the main crystallographic directions. Our results can be employed to determine the angular dependence of the g-factor and of light absorption in honeycomb bipartite structures.
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We show that the conductivity of a two-dimensional electron gas can be intrinsically anisotropic despite isotropic Fermi surface, energy dispersion, and disorder configuration. In the model we study, the anisotropy stems from the interplay between Dirac and Schrodinger features combined in a special two-band Hamiltonian describing the quasiparticles similar to the low-energy excitations in phosphorene. As a result, even scalar isotropic disorder scattering alters the nature of the carriers and results in anisotropic transport. Solving the Boltzmann equation exactly for such carriers with point-like random impurities we find a hidden knob to control the anisotropy just by tuning either the Fermi energy or temperature. Our results are expected to be generally applicable beyond the model studied here, and should stimulate further search for the alternative ways to control electron transport in advanced materials.
Pseudospin, an additional degree of freedom inherent in graphene, plays a key role in understanding many fundamental phenomena such as the anomalous quantum Hall effect, electron chirality and Klein paradox. Unlike the electron spin, the pseudospin was traditionally considered as an unmeasurable quantity, immune to Stern-Gerlach-type experiments. Recently, however, it has been suggested that graphene pseudospin is a real angular momentum that might manifest itself as an observable quantity, but so far direct tests of such a momentum remained unfruitful. Here, by selective excitation of two sublattices of an artificial photonic graphene, we demonstrate pseudospin-mediated vortex generation and topological charge flipping in otherwise uniform optical beams with Bloch momentum traversing through the Dirac points. Corroborated by numerical solutions of the linear massless Dirac-Weyl equation, we show that pseudospin can turn into orbital angular momentum completely, thus upholding the belief that pseudospin is not merely for theoretical elegance but rather physically measurable.
Dirac electrons in graphene are to lowest order spin 1/2 particles, owing to the orbital symmetries at the Fermi level. However, anisotropic corrections in the $g$-factor appear due to the intricate spin-valley-orbit coupling of chiral electrons. We resolve experimentally the $g$-factor along the three orthogonal directions in a large-scale graphene sample. We employ a Hall bar structure with an external magnetic field of arbitrary direction, and extract the effective $g$-tensor via resistively-detected electron spin resonance. We employ a theoretical perturbative approach to identify the intrinsic and extrinsic spin orbit coupling and obtain a fundamental parameter inherent to the atomic structure of $^{12}$C, commonly used in ab-initio models.
We investigate the polarization dependence of the carrier excitation and relaxation in epitaxial multilayer graphene. Degenerate pump-probe experiments with a temporal resolution of 30 fs are performed for different rotation angles of the pump-pulse polarization with respect to the polarization of the probe pulse. A pronounced dependence of the pump-induced transmission on this angle is found. It reflects a strong anisotropy of the pump-induced occupation of photogenerated carriers in momentum space even though the band structure is isotropic. Within 150 fs after excitation an isotropic carrier distribution is established. Our observations imply the predominant role of collinear scattering preserving the initially optically generated anisotropy in the carrier distribution. The experiments are well described by microscopic time-, momentum, and angle-resolved modelling, which allows us to unambiguously identify non-collinear carrier-phonon scattering to be the main relaxation mechanism giving rise to an isotropic distribution in the first hundred fs after optical excitation.
The diffusion of electron-hole pairs, which are excited in an intrinsic graphene by the ultrashort focused laser pulse in mid-IR or visible spectral region, is described for the cases of peak-like or spread over the passive region distributions of carriers. The spatio-temporal transient optical response on a high-frequency probe beam appears to be strongly dependent on the regime of diffusion and can be used for verification of the elasic relaxation mechanism. Sign flip of the differential transmission coefficient takes place due to interplay of the carrier-induced contribution and weak dynamic conductivity of undoped graphene.
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