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Breaking Simple Scaling Relations Through Metal-Oxide Interactions: Understanding Room Temperature Activation of Methane on M-CeO2 (M= Pt, Ni or Co) Interfaces

preprint
submitted on 26.08.2020 and posted on 27.08.2020 by Pablo Lustemberg, Feng Zhang, Ramón A. Gutiérrez, Pedro J. Ramírez, Sanjaya D. Senanayake, José A. Rodriguez, M. V. Ganduglia-Pirovano
The clean activation of methane at low temperatures remains an eminent challenge and a field of competitive research. In particular, on late transition metal surfaces such as Pt(111) or Ni(111), elevated temperatures are necessary to activate the hydrocarbon molecule, but a massive deposition of carbon makes the metal surface useless for catalytic activity. However, on very low-loaded M/CeO2 (M= Pt, Ni, or Co) surfaces, the dissociation of methane occurs at room temperature, which is unexpected considering simple linear scaling relationships. This intriguing phenomenon has been studied using a combination of experimental techniques (ambient-pressure X-ray photoelectron spectroscopy, time-resolved X-ray diffraction and X-ray absorption spectroscopy) and density functional theory-based calculations. The experimental and theoretical studies show that the size and morphology of the supported nanoparticles together with strong metal-support interactions are behind the deviations from the scaling relations. These findings point toward a possible strategy to circumvent scaling relations, producing active and stable catalysts which can be employed for methane activation and conversion.

History

Email Address of Submitting Author

lustemberg@gmail.com

Institution

Instituto de Catálisis y Petroleoquímica

Country

SPAIN

ORCID For Submitting Author

0000-0003-4058-4023

Declaration of Conflict of Interest

No conflict of interest

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