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• W2005368109 abstract "Using density functional theory (DFT) together with periodic slab models, the adsorption and dehydrogenation mechanisms of methane on clean and oxygen-covered Pd (1 0 0) surfaces have been studied systematically. Different adsorption geometries were investigated for CH4 and related intermediates (CH3, CH2, CH, C, H, O and OH). It was found that CH4 and CH3 prefer to adsorb on the top site, CH2 and OH are favorable on the bridge site, while CH, C, O and H species adsorb preferentially on the hollow site. In addition, this work identified the stable co-adsorption configurations for the relevant co-adsorption groups. It was concluded that the effect of co-adsorbed oxygen atom tends to weaken the adsorbate–substrate interaction on the Pd (1 0 0) surface. Finally, transition states, energy barriers and reaction energies were determined to confirm the mechanism of dehydrogenation of CH4 on clean and oxygen-covered Pd (1 0 0) surfaces. The existence of oxygen atom increases the energy barriers obviously and inhibits the dissociation of CHx (x = 1, 2 and 4) except for CH3 group." @default.
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• W2005368109 date "2014-11-01" @default.
• W2005368109 modified "2023-10-16" @default.
• W2005368109 title "Adsorption and dehydrogenation mechanism of methane on clean and oxygen-covered Pd (1 0 0) surfaces: A DFT study" @default.
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• W2005368109 doi "https://doi.org/10.1016/j.apsusc.2014.08.195" @default.
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