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Bifunctional Mechanism of CO2 Methanation on Pd-MgO/SiO2 Catalyst: Independent Roles of MgO and Pd on CO2 Methanation

Kim, Hyun You, Lee, Hyuck Mo, Park, Jung-Nam·2010·The Journal of Physical Chemistry C

Abstract

We scrutinized the reaction mechanism of CO 2 methanation catalyzed by a Pd-MgO/SiO 2 catalyst. Density functional theory studies showed that MgO and Pd nanoparticles play completely different roles. We found that MgO initiates the reaction by binding a CO 2 molecule, forming a magnesium carbonate species on the surface, and that a supply of atomic H is essential for further hydrogenation of magnesium carbonate to methane. A CO 2 temperature-programmed desorption study gives credence to our findings on the role of MgO. Our results confirm the bifunctional mechanism of CO 2 methanation by a Pd-MgO/SiO 2 catalyst.

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Metadata

Authors
Kim, H. Y., Lee, H. M., & Park, J.-N.
Venue
The Journal of Physical Chemistry C
Published
2010-03-26
Volume
114
Issue
15
Pages
7128-7131
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W2041771687
Cited by
186
References
2
FWCI
2.39
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Bifunctional Mechanism of CO2 Methanation on Pd-MgO/SiO2 Catalyst: Independent Roles of MgO and Pd on CO2 Methanation. https://app.cochat.ai/papers/10.1021/jp100938v
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Kim, H. Y., Lee, H. M., & Park, J.-N. (2010). Bifunctional Mechanism of CO2 Methanation on Pd-MgO/SiO2 Catalyst: Independent Roles of MgO and Pd on CO2 Methanation. The Journal of Physical Chemistry C. https://doi.org/10.1021/jp100938v

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