Relaxation of electrons in quantum-confined states in Pb/Si(111) thin films from master equation with first-principles-derived rates

Author:

Kratzer Peter,Zahedifar Maedeh

Abstract

Abstract Atomically thin films of Pb on Si(111) provide an experimentally tunable system comprising a highly structured electronic density of states. The lifetime of excited electrons in these states is limited by both electron–electron (e–e) and electron–phonon (e–ph) scattering. We employ the description by a master equation for the electronic occupation numbers to analyze the relative importance of both scattering mechanisms. The electronic and phononic band structures, as well as the matrix elements for electron–phonon coupling within deformation potential theory were obtained from density functional calculations, thus taking into account quantum confinement effects. For the relaxation dynamics, the contribution of impact ionization processes to the lifetime is estimated from the imaginary part of the electronic self-energy calculated in the GW approximation. By numerically solving rate equations for the occupations of the Pb-derived electronic states coupled to a phononic heat bath, we are able to follow the distribution of the electronic excitation energy to the various modes of Pb lattice vibrations. While e–e scattering is the dominant relaxation mechanism, we demonstrate that the e–ph scattering is highly phonon-mode-specific, with a large contribution from surface phonons. At electron energies of about 0.3 eV above the Fermi surface, a ‘phonon bottleneck’ characteristic of relaxation in nanostructures with well-separated electronic states is observed. The time scales extracted from the simulations are compared to data from pump-probe experiments using time-resolved two-photon photoemission.

Funder

Deutsche Forschungsgemeinschaft

Publisher

IOP Publishing

Subject

General Physics and Astronomy

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