4.6 Article

Charge-carrier thermalization in bulk and monolayer CdTe from first principles

Journal

PHYSICAL REVIEW B
Volume 103, Issue 12, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.103.125113

Keywords

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Funding

  1. Carl Zeiss Foundation
  2. Collaborative Research Center of the German Research Foundation (DFG) at University of Konstanz [(SFB) 767]
  3. CA2DM at NUS (Singapore NRF Medium Sized Centre Programme) [R-723-000-001-281]

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The study presents theoretical predictions on photocarrier dynamics in extremely thin CdTe slabs, revealing a significant reduction in photocarrier thermalization time as the CdTe crystal is thinned down to a monolayer. The electron thermalization time becomes independent of excess energy up to 0.5 eV from the conduction band minimum in 2D limit, which is attributed to the degenerate and nearly parabolic lowest conduction band in CdTe. These findings could be valuable for designing novel optoelectronic devices based on CdTe with improved performance using non-equilibrium photoexcited carriers.
While cadmium telluride (CdTe) thin films are being used in solar cell prototyping for decades, the recent advent of two-dimensional (2D) materials challenges the fundamental limit for thickness of conventional CdTe layers. Here, we report our theoretical predictions on photocarrier dynamics in an ultimately thin (about 1 nm) CdTe slab. It corresponds to a layer that is just a single unit cell thick, when the bulk parent crystal in the zinc blende phase is cleaved along the [110] facet. Using an ab initio method based on density functional theory (DFT) and the Boltzmann equation in the relaxation time approximation (RTA), we determine the thermalization time for charge carriers excited to a certain energy for instance through laser irradiation. Our calculations include contributions arising from all phonon branches in the first Brillouin zone (BZ), thus capturing all relevant interand intraband carrier transitions due to electron-phonon scattering. We find that the photocarrier thermalization time is strongly reduced, by one order of magnitude for holes and by three orders of magnitude for electrons, once the CdTe crystal is thinned down from the bulk to a monolayer. Most surprisingly, the electron thermalization time becomes independent of the electron excess energy up to about 0.5 eV, when counted from the conduction band minimum (CBM). We relate this peculiar behavior to the degenerate and nearly parabolic lowest conduction band that yields a constant density of states (DOS) in the 2D limit. Our findings may be useful for designing novel CdTe-based optoelectronic devices, which employ nonequilibrium photoexcited carriers to improve the performance.

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