CH4 decomposition over carbon for CO2-free hydrogen production: A combined DFT and experimental investigation on the role of carbon

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CH4 decomposition over carbon for CO2-free hydrogen production: A combined DFT and experimental investigation on the role of carbon
Title:
CH4 decomposition over carbon for CO2-free hydrogen production: A combined DFT and experimental investigation on the role of carbon
Journal Title:
ACS Catalysis
Keywords:
Publication Date:
09 September 2025
Citation:
Zhao, P., Poh, C. K., Gao, J., Zeng, J., Abubakar, S., Cao, G., Zhang, L., & Zhang, J. (2025). CH4 decomposition over carbon for CO2-free hydrogen production: A combined DFT and experimental investigation on the role of carbon. ACS Catalysis, 15(18), 16333–16343. https://doi.org/10.1021/acscatal.5c04541
Abstract:
Carbon-based self-catalysis for methane pyrolysis is of great interest for producing H2 and carbon materials without CO2 emissions and the need for catalyst regeneration, but atomic-level insights into this process remain limited. Here, building on experimental observations of layered graphite synthesis during CH4 pyrolysis and the catalytic role of carbon in accelerating CH4 decomposition, we employ density functional theory (DFT) and ab initio atomistic thermodynamics to systematically investigate the adsorption, dehydrogenation, and reaction mechanisms involved in CH4 pyrolysis on armchair-edged graphene (Gr_arm). Our study highlights the unique catalytic properties of Gr_arm under varying temperature, pressure, and radical partial pressures. Equilibrium analyses of adsorption-desorption and dehydrogenation-desorption revealed the unique ability of Gr_arm to stabilize and activate key intermediates across varying conditions. The initial dehydrogenation of CH4 is a critical step, where the presence of carbon markedly enhances the reaction rate under low-temperature and high-pressure conditions. The reaction mechanism study indicates that the CH* + H* co-adsorption species corresponds to the most stable state in the overall CH4(g) → 2H2(g) + C* reaction, with CH* dehydrogenation requiring the highest activation free energy (Ga = 3.65 eV), suggesting potential for CH*−CH* coupling reactions. Moreover, varying CHx· and H· radical partial pressures alters the thermodynamic preference between dehydrogenation and desorption, reshaping the most favorable reaction pathways. These findings underscore indispensable role of carbon in methane pyrolysis, offering critical insights for designing efficient carbon-based catalysts and advancing their practical applications.
License type:
Publisher Copyright
Funding Info:
This research / project is supported by the ExxonMobil joint Singapore Corporate Lab through its partnership with Agency for Science, Technology and Research (A*STAR) and Nanyang Technological University - Industry Alignment Fund – Industry Collaboration Projects
Grant Reference no. : I2301E0025
Description:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see 10.1021/acscatal.5c04541.
ISSN:
2155-5435
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