Density functional theory study on the catalytic dehydrogenation of methane on MoO<sub>3</sub> (0 1 0) surface

<p dir="ltr">Methane conversion offers hydrocarbon building blocks of high market value, which are easier to transport than natural gas. Under non-oxidative conditions, the process can also produce clean hydrogen fuel. In this study, we explored the catalytic dehydrogenation of metha...

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Main Author: Ismail Badran (1989553) (author)
Other Authors: Najamus Sahar Riyaz (17563272) (author), Amjad M. Shraim (14156922) (author), Nashaat N. Nassar (1308663) (author)
Published: 2022
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Summary:<p dir="ltr">Methane conversion offers hydrocarbon building blocks of high market value, which are easier to transport than natural gas. Under non-oxidative conditions, the process can also produce clean hydrogen fuel. In this study, we explored the catalytic dehydrogenation of methane on molybdenum oxide (MoO<sub>3</sub>) surface. Periodic density functional theory calculations were performed to study the adsorption of CH<sub>4</sub> on two different supercells of the MoO<sub>3</sub> (010) surface. It was found that CH<sub>4</sub> adsorption was more favorable on a smooth surface constructed of Mo and O network, rather than a surface made with dangling O atoms as thought before. A reaction mechanism for hydrogen formation was then proposed. The first energy barrier for the H-abstraction step was calculated to be 66.4 kJ/mol, which is lower than previously reported values obtained for simple Mo<sub>x</sub>Oy clusters. The reactions were discussed using the two-state reactivity approach, where different electronic states can play a role in the H-abstraction step. The mechanism also showed the formation of methyl radicals and ethylene, in addition to molecular hydrogen.</p><h2>Other Information</h2><p dir="ltr">Published in: Computational and Theoretical Chemistry<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1016/j.comptc.2022.113689" target="_blank">https://dx.doi.org/10.1016/j.comptc.2022.113689</a></p>