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Register a new userHidden Anisotropy in the Drude Conductivity of Charge Carriers with Dirac-Schrodinger Dynamics
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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.
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We consider the problem of confining the famously elusive Dirac-like quasiparticles, as found in some recently discovered low-dimensional systems. After briefly surveying the existing theoretical proposals for creating bound states in Dirac materials, we study relativistic excitations with a position-dependent mass term. With the aid of an exactly-solvable model, we show how bound states begin to emerge after a critical condition on the size of the mass term is met. We also reveal some exotic properties of the unusual confinement discovered, including an elegant chevron structure of the bound state energies as a function of the size of the mass.
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.
The optical conductivity of charge carriers coupled to quantum phonons is studied in the framework of the one-dimensional spinless Holstein model. For one electron, variational diagonalisation yields exact results in the thermodynamic limit, whereas at finite carrier density analytical approximations based on previous work on single-particle spectral functions are obtained. Particular emphasis is put on deviations from weak-coupling, small-polaron or one-electron theories occurring at intermediate coupling and/or finite carrier density. The analytical results are in surprisingly good agreement with exact data, and exhibit the characteristic polaronic excitations observed in experiments on manganites.
Graphene, a monolayer of carbon atoms arranged in a hexagonal pattern, provides a unique two-dimensional (2D) system exhibiting exotic phenomena such as quantum Hall effects, massless Dirac quasiparticle excitations and universal absorption & conductivity. The linear energy-momentum dispersion relation in graphene also offers the opportunity to mimic the physics of far-away relativistic particles like neutron stars and white dwarfs. In this letter, we perform a counterintuitive ultrafast pump-probe experiment with high photon energies to isolate the Drude-like intraband dynamics of photoexcited carriers. We directly demonstrate the relativistic nature of the photoexcited Dirac quasiparticles by observing a nonlinear scaling of the response with the density of photoexcited carriers. This is in striking contrast to the linear scaling that is usually observed in conventional materials. Our results also indicate strong electron-phonon coupling in graphene, leading to a sub-100 femtosecond thermalization between high energy photoexcited carriers and optical phonons.
When the excitation of carriers in real space is focused down to the nanometer scale, the carrier system can no longer be viewed as homogeneous and ultrafast transport of the excited carrier wave packets occurs. In state-of-the-art semiconductor structures like low-dimensional heterostructures or monolayers of transition metal dichalcogenides, the Coulomb interaction between excited carriers becomes stronger due to confinement or reduced screening. This demands a fundamental understanding of strongly interacting electrons and holes and the influence of Coulomb correlations. To study the corresponding particle dynamics in a controlled way we consider a system of up to two electron-hole pairs exactly within a wave function approach. We show that the excited wave packets contain a non-trivial mixture of free particle and excitonic states. We further scrutinize the influence of Coulomb interaction on the wave packet dynamics revealing its different role for below and above band-gap excitation.
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