The Activation of Methane on Ru, Rh, and Pd Decorated Carbon Nanotube and Boron Nitride Nanotube: A DFT Study

• Published in: Catalysts 2018-05, Vol.8 (5), p.190
• Main Authors: Boekfa, Bundet, Treesukol, Piti, Injongkol, Yuwanda, Maihom, Thana, Maitarad, Phornphimon, Limtrakul, Jumras
• Format: Article
• Language: English
• Subjects: Activation energy; Adsorption; Alternative energy sources; Atoms & subatomic particles; Boron; Boron nitride; boron nitride nanotubes; Carbon; Carbon nanotubes; Catalysts; Catalytic activity; Chemical reactions; Decomposition; Decoration; Density functional theory; Graphene; Methane; methane decomposition reaction; Nitrogen; Palladium; Rhodium; Ruthenium
• ISSN: 2073-4344; 2073-4344
• DOI: 10.3390/catal8050190

Methane decomposition catalyzed by an Ru, Rh, or Pd atom supported on a carbon or boron nitride nanotubes was analyzed by means of the density functional theory with the M06-L hybrid functional. The results suggested that the dissociative reaction of methane was a single-step mechanism. Based on the calculated activation energy, the Ru-decorated carbon nanotube showed superior catalytic activity with an activation barrier of 14.5 kcal mol−1, followed by the Rh-decorated carbon nanotube (18.1 kcal mol−1) and the Pd-decorated carbon nanotube (25.6 kcal mol−1). The catalytic performances of metals supported on a boron nitride nanotube were better than those on a carbon nanotube. The total activation barrier for the Ru, Rh, and Pd atoms on boron nitride nanotube was 10.2, 14.0, and 20.5 kcal mol−1, respectively. Dissociative adsorption complexes on the Ru–boron nitride nanotube were the most stable. The anionic state of the supported metal atom was responsible for decreasing the activation energy of methane decomposition. Our finding provides a crucial point for further investigation.