Exfoliation energy, quasi-particle bandstructure, and excitonic properties of selenium and tellurium atomic chains
Eesha Andharia, Thaneshwor P. Kaloni, Gregory J. Salamo, Shui-Qing Yu,, Hugh O. H. Churchill, Salvador Barraza-Lopez

TL;DR
This study investigates the exfoliation energy, electronic bandstructure, and excitonic properties of selenium and tellurium atomic chains using advanced many-body perturbation theories, revealing their potential for optoelectronic applications.
Contribution
It provides non-empirical van der Waals corrected exfoliation energies and detailed GW and Bethe-Salpeter calculations of electronic and optical properties of selenium and tellurium chains, which were previously unexplored.
Findings
Exfoliation energies range from 0.547 to 0.926 eV/u.c.
GW bandgaps are between 4.44 and 5.47 eV.
Excitonic energies are within the visible spectrum, suitable for LED applications.
Abstract
Effects that are not captured by the generalized-gradient density-functional theory play a prominent effect on the structural binding, and on the electronic and optical properties of reduced-dimensional and weakly-bound materials. Here, we report the exfoliation energy of selenium and tellurium atomic chains with non-empirical van der Waals corrections, and their electronic and optical properties with the GW and Bethe-Salpeter formalisms. The exfoliation energy is found to be within 0.547 to 0.719 eV/u.c. for the selenium atomic chain, and 0.737 to 0.926 eV/u.c. for the tellurium atomic chain (u.c. stands for unit cell), depending on the approximation for the van der Waals interaction and the numerical tool chosen. The GW electronic bandgap turned out to be 5.22--5.47 (4.44--4.59) eV for the Se (Te) atomic chains, with the lowest bound obtained with the Godby-Needs (GB), and the upper…
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