2015
DOI: 10.1016/j.jcat.2015.01.018
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Methane, formaldehyde and methanol formation pathways from carbon monoxide and hydrogen on the (0 0 1) surface of the iron carbide χ-Fe5C2

Abstract: a b s t r a c tFormation of CH x (O) monomers and C 1 products (CH 4 , CH 2 O, and CH 3 OH) on C-terminated v-Fe 5 C 2 (0 0 1) (Hägg carbide) surfaces of different carbon contents was investigated using periodic DFT simulations. Methane (CH 4 ) as well as monomer (CH x ) formation follows a Mars-van Krevelen-like cycle starting with the hydrogenation of surface carbidic carbon, which is regenerated by subsequent CO dissociation, while oxygen is removed as H 2 O. In cases where surface carbon is readily availab… Show more

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Cited by 45 publications
(49 citation statements)
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References 73 publications
(117 reference statements)
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“…4 indicate that CO can in fact play a crucial role in steering the selectivity of, in particular, hydrocarbon surface reactions, and hence it is of crucial importance to further explore this in a systematic manner to further test the hypotheses brought forward in the present article. For the case of FT on iron it should be realized that catalysts are active in carbidic form, and recent computational work [13][14][15] has been based on the assumption that lattice carbidic carbon can be involved in the reaction, while C-vacancies would enable dissociation of CO without the need for explicit surface step sites, making the situation distinctly different from the proposed reaction sequence on the metallic surfaces…”
Section: Discussionmentioning
confidence: 99%
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“…4 indicate that CO can in fact play a crucial role in steering the selectivity of, in particular, hydrocarbon surface reactions, and hence it is of crucial importance to further explore this in a systematic manner to further test the hypotheses brought forward in the present article. For the case of FT on iron it should be realized that catalysts are active in carbidic form, and recent computational work [13][14][15] has been based on the assumption that lattice carbidic carbon can be involved in the reaction, while C-vacancies would enable dissociation of CO without the need for explicit surface step sites, making the situation distinctly different from the proposed reaction sequence on the metallic surfaces…”
Section: Discussionmentioning
confidence: 99%
“…As a consequence, the influx of monomer species into the smaller ensembles that do exist is comparatively smaller. Assuming that the residence time of a growing chain is not affected by particle size the consequence is that selectivity, defined as: ␣ = r growth r growth + r term (14) goes down. This is even worsened when the activity of active sites drops as well, for example because it becomes progressively more difficult to remove oxygen from the surface.…”
Section: Consequences For a Growth Ensemblementioning
confidence: 99%
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“…This adsorption is thought to facilitate the hydrogenation reaction. There have been several studies on the kinetics of hydrogenation on various catalytic surfaces such as platinum, nickel, palladium, ruthenium, cobalt, rhodium, osmium, iridium, and iron [31][32], copper [33], iron carbides [34], copper-zinc [35], etc. All surfaces show significant catalytic activity with the activation barrier dropping, for example, to 107 kJ mol -1 on copper [33] or to 125 kJ mol -1 on nickel(111) [32].…”
Section: Methanol Formation Kineticsmentioning
confidence: 99%
“…Therefore, studies on methane oxidation show that methane with significant amount under 600 °C does not oxidize, while, as already mentioned, formaldehyde begins to decompose at temperatures below this. Formaldehyde is used because of elimination of bacteria as an antiseptic solution [16][17][18][19].…”
Section: Introductionmentioning
confidence: 99%