Emergence of massless Froḧlich polarons in two-dimensional semi-metals on polar substrates

• Published in: Journal of physics communications Vol. 5; no. 1; p. 15009
• Main Author: Banerjee, Swapnonil
• Format: Journal Article
• Language: English
• Published: 01.01.2021
• ISSN: 2399-6528; 2399-6528
• DOI: 10.1088/2399-6528/abd69a

Abstract We consider the polaron dynamics driven by Froḧlich type, long wavelength dominated electron-phonon interaction at zero temperature, for three different semi-metals: single and bilayer graphene, and semi-Dirac, all grown on polar substrates such as, SiC . Single layer graphene (henceforth called SL graphene), bilayer graphene (henceforth called BL graphene), and semi-Dirac have two dimensional band-structures with point Fermi surfaces in their natural undoped conditions. When these materials are grown on polar substrates, their electrons can interact with the optical phonons (LO) at the surface of the substrates. That gives rise to the possibility of polaron formation in the context of these semi-metals, although they themselves are non-polar. Starting from the Froḧlich type electron-phonon interaction Hamiltonian, perturbation theory is employed to calculate the self energy of the electron due to polaron formation for the three aforementioned systems. The electron self energy, or the polaron energy, calculated analytically for BL graphene, is shown to vary linearly with the electron momentum for small electron momenta. Whereas for ordinary polar crystals (both two and three dimensional), for small electron momentum, the polaron energy is quadratic leading to the mass correction of the electron, for BL graphene the polaron energy disperses linearly, rendering the massive BL graphene electrons effectively massless. Energies for Froḧlich polarons in SL graphene and semi-Dirac on polar substrates, are numerically evaluated. Also, the electron relaxation rate, related to the imaginary part of the analytically continued electron self energy expression, is calculated for the three systems.