Theoretical insights into the methane catalytic decomposition on graphene nanoribbons edges

Neubi F Xavier Jr; Anthony J R Payne; Glauco F Bauerfeldt; Marco Sacchi

doi:10.3389/fchem.2023.1172687

Theoretical insights into the methane catalytic decomposition on graphene nanoribbons edges

Front Chem. 2023 Jun 1:11:1172687. doi: 10.3389/fchem.2023.1172687. eCollection 2023.

Authors

Neubi F Xavier Jr¹, Anthony J R Payne¹, Glauco F Bauerfeldt², Marco Sacchi¹

Affiliations

¹ School of Chemistry and Chemical Engineering, University of Surrey, Guildford, United Kingdom.
² Instituto de Química, Universidade Federal Rural Do Rio de Janeiro, Seropédica, Brazil.

Abstract

Catalytic methane decomposition (CMD) is receiving much attention as a promising application for hydrogen production. Due to the high energy required for breaking the C-H bonds of methane, the choice of catalyst is crucial to the viability of this process. However, atomistic insights for the CMD mechanism on carbon-based materials are still limited. Here, we investigate the viability of CMD under reaction conditions on the zigzag (12-ZGNR) and armchair (AGRN) edges of graphene nanoribbons employing dispersion-corrected density functional theory (DFT). First, we investigated the desorption of H and H₂ at 1200 K on the passivated 12-ZGNR and 12-AGNR edges. The diffusion of hydrogen atom on the passivated edges is the rate determinant step for the most favourable H₂ desorption pathway, with a activation free energy of 4.17 eV and 3.45 eV on 12-ZGNR and 12-AGNR, respectively. The most favourable H₂ desorption occurs on the 12-AGNR edges with a free energy barrier of 1.56 eV, reflecting the availability of bare carbon active sites on the catalytic application. The direct dissociative chemisorption of CH₄ is the preferred pathway on the non-passivated 12-ZGNR edges, with an activation free energy of 0.56 eV. We also present the reaction steps for the complete catalytic dehydrogenation of methane on 12-ZGNR and 12-AGNR edges, proposing a mechanism in which the solid carbon formed on the edges act as new active sites. The active sites on the 12-AGNR edges show more propensity to be regenerated due lower free energy barrier of 2.71 eV for the H₂ desorption from the newly grown active site. Comparison is made between the results obtained here and experimental and computational data available in the literature. We provide fundamental insights for the engineering of carbon-based catalysts for the CMD, showing that the bare carbon edges of graphene nanoribbons have performance comparable to commonly used metallic and bi-metallic catalysts for methane decomposition.

Keywords: DFT; carbon catalysis; graphene edges and nanoribbons; hydrogen; methane.

Grants and funding

The authors acknowledge the Royal Society for funding through the grants URF\R\191029 and RF\ERE\210215. We are grateful for computational support from the UK national high-performance computing service, ARCHER2, for which access was obtained via the UKCP consortium and funded by EPSRC grant ref EP/P022561/1.