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Flexoelectric radial polarization of single-walled nanotubes from first-principles

Published version
Peer-reviewed

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Authors

Bennett, Daniel 

Abstract

Flexoelectricity is the polar response of an insulator to strain gradients such as bending. While the size dependence of this effect makes it weak in bulk systems in comparison to piezoelectricity, it suggests that it plays a bigger role in nanoscale systems such as thin films and nanotubes (NTs). In this paper we demonstrate using first-principles calculations that the walls of carbon nanotubes (CNTs) and transition metal dichalcogenide nanotubes (TMD NTs) are polarized in the radial direction, the strength of the polarization increasing as the size of the NT decreases. For CNTs and TMD NTs with chiral indices (n,m), the radial polarization of the walls PR starts to diverge below $ C(n,m)/a = \sqrt{n^2 +nm + m^2} \sim 10$, where C(n,m) is the circumference of the NT and a is the lattice constant of the 2D monolayer. For CNTs, PR drops to zero above this value but for TMD NTs there is a non-zero polarization above this value, which is an ionic rather than electronic effect. The size dependence of PR in the TMD NTs is interesting: it increases gradually and reaches a maximum of PR∼100 C/cm2 at C(n,m)/a∼15, then decreases until C(n,m)/a∼10 where it starts to diverge. Measurements of the radial strain on the chalcogen atoms with respect to the 2D monolayers shows that this polarization is the result of a significantly larger strain on the outer bonds than the inner bonds, but did not offer an explanation for the peculiar size dependence. These results suggest that while the walls of smaller CNTs and TMD NTs are polarized, the walls of larger TMD NTs are also polarized due to a difference in strain on the inner and outer atoms in the walls. This result may prove useful for the application of NTs for screening in liquid or biological systems.

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Keywords

Journal Title

Electronic Structure

Conference Name

Journal ISSN

2516-1075
2516-1075

Volume Title

3

Publisher

IOP
Sponsorship
EPSRC (EP/L015552/1)
The author acknowledges support from the EPSRC Centre for Doctoral Training in Computational Methods for Materials Science under Grant No. EP/L015552/1.