Unraveling the Surface Stability and Chemical Reactivity of Aza-Triphenylene Monolayer under O$_2$ and H$_2$O Exposure

TL;DR

This study uses first principles calculations to analyze how aza-triphenylene monolayers interact with O$_2$ and H$_2$O, revealing weak adsorption, high energy barriers for dissociation, and stability against environmental oxidation for potential device use.

Contribution

First systematic investigation of O$_2$ and H$_2$O interactions with aza-triphenylene monolayers, revealing their stability and dissociation barriers through advanced computational methods.

Findings

Weak adsorption energies for O$_2$ and H$_2$O (-0.16 eV and -0.37 eV)

High energy barriers for dissociation (up to 2.3 eV)

Enhanced band gap after dissociation indicating stability

Abstract

Environmental oxidation has a great impact in tuning the physical, chemical and electronic properties of two-dimensional (2D) monolayers which can affect their practical applications in nanoscale engineering devices under ambient conditions. aza-triphenylene is a recently synthesized 2D materials whose practcal applications have not been systematically studied yet. In this study, we report for the first time, the adsorption and dissociation of O$_2$ and H$_2$O molecules on the surface of 2D aza-triphenylene monolayer through first principles calculations in combination with climbing image nudged elastic band (CINEB) method. The results indicates that both the O$_2$ and H$_2$O molecules weakly interact over the monolayer surface with an adsorption energy -0.16 eV and -0.37 eV respectively. In contrast, both the molecules exhibit resistance for dissociation due to the formation of energy barriers. The transition path indicates that molecular oxygen experience two energy barriers (0.16 ev and 1.22 eV) before getting dissociated atomic oxygen. However, the dissociation of H$_2$O requires larger energy barrier (2.3 eV and 0.86 eV) due to breaking of covalent bonds and transfer of hydrogen. The strong chemical adsorption of atomic oxygen and H$^+$/OH$^-$ ions is due to the significant charge transfer from monolayer to the adsorbate as evidenced from the charge density difference and Bader charge analysis. Moreover, the dissociated configuration exhibit a larger band gap as compared to the pristine aza-triphenylene due to the strong hybridization between the p states of carbon and oxygen. our work predicts the robustness of azatriphylene monolayer against oxygen/water exposer thus ensuring their stability for device applications using these materials.