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231223s2008 xx |||||o 00| ||eng c |
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|a 10.1021/la802295x
|2 doi
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|a pubmed24n0610.xml
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|a DE-627
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|a eng
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|a Pan, Yunxiang
|e verfasserin
|4 aut
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|a Adsorption and protonation of CO2 on partially hydroxylated gamma-Al2O3 surfaces
|b a density functional theory study
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|c 2008
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 01.12.2008
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|a Date Revised 30.10.2008
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Adsorption and protonation of CO2 on the (110) and (100) surfaces of gamma-Al2O3 have been studied using density functional theory slab calculations. On the dry (110) and (100) surfaces, the O-Al bridge sites were found to be energetically favorable for CO2 adsorption. The adsorbed CO2 was bound in a bidentate configuration across the O-Al bridge sites, forming a carbonate species. The strongest binding with an adsorption energy of 0.80 eV occurs at the O3c-Al5c bridge site of the (100) surface. Dissociation of water across the O-Al bridge sites resulted in partially hydroxylated surfaces, and the dissociation is energetically favorable on both surfaces. Water dissociation on the (110) surface has a barrier of 0.42 eV, but the same process on the (100) surface has no barrier with respect to the isolated water molecule. On the partially hydroxylated gamma-Al2O3 surfaces, a bicarbonate species was formed by protonating the carbonate species with the protons from neighboring hydroxyl groups. The energy difference between the bicarbonate species and the coadsorbed bidentate carbonate species and hydroxyls is only 0.04 eV on the (110) surface, but the difference reaches 0.97 eV on the (100) surface. The activation barrier for forming the bicarbonate species on the (100) surface, 0.42 eV, is also lower than that on the (110) surface (0.53 eV)
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|a Journal Article
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|a Liu, Chang-jun
|e verfasserin
|4 aut
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|a Ge, Qingfeng
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 24(2008), 21 vom: 04. Nov., Seite 12410-9
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|x 1520-5827
|7 nnns
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|g volume:24
|g year:2008
|g number:21
|g day:04
|g month:11
|g pages:12410-9
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|u http://dx.doi.org/10.1021/la802295x
|3 Volltext
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