Gas sensing potential of stacked graphene/h-BN structures: a DFT-based investigation

TL;DR

This study uses density functional theory to explore how graphene/h-BN heterostructures interact with various gas molecules, revealing their potential for sensitive and selective gas sensing applications.

Contribution

It provides a detailed theoretical analysis of gas adsorption behaviors on different graphene/h-BN configurations, highlighting their sensing capabilities and electronic property changes.

Findings

NO2 binds strongly to h-BN islands, forming chemical bonds.

O3 dissociates on h-BN islands but remains intact on bilayers.

Graphene/h-BN structures can significantly alter conductivity upon gas adsorption.

Abstract

Using periodic DFT, we examined the adsorption of NO2, NH3, and O3 on the h-BN side of a graphene/h-BN heterostructure designed as a model gas sensor material. The h-BN overlayer serves both as an active adsorption surface and as protection that may reduce irreversible processes such as graphene oxidation. Two model systems were considered: an extended graphene/h-BN bilayer (B36N36C72) and a graphene sheet partially covered by a smaller h-BN island (B11N11C72). Their electronic structures differ strongly near the Dirac point. In the extended bilayer, the Fermi level remains aligned with that of pristine graphene, indicating negligible charge transfer. In the island-covered system, the Fermi level shifts to lower energies, reflecting electron transfer from graphene to h-BN. These differences lead to distinct adsorption behavior. NO2 binds much more strongly to B11N11C72, forming a chemical bond, while O3 dissociates on this surface but remains intact on the extended bilayer. NH3 unusually acts as an electron acceptor in the island system. Overall, NO2 and O3 substantially increase graphene conductivity, whereas NH3 induces much weaker changes. These results highlight the potential of graphene/h-BN heterostructures for gas sensing.