Modification of active sites on YSZ(111) by yttria segregation

dc.contributor.author Lahiri, Jayeeta
dc.contributor.author Mayernick, Adam
dc.contributor.author Morrow, Suzanne L.
dc.contributor.author Koel, Bruce E.
dc.contributor.author Van Duin, Adri C.T.
dc.contributor.author Janik, Michael J.
dc.contributor.author Batzill, Matthias
dc.date.accessioned 2022-03-27T11:46:16Z
dc.date.available 2022-03-27T11:46:16Z
dc.date.issued 2010-04-08
dc.description.abstract The surface properties of YSZ (111) have been investigated by X-ray photoemission spectroscopy (XPS), scanning tunneling microscopy (STM), temperature programmed desorption (TPD) of adsorbed formate, and computational studies using the ReaxFF reactive force field approach. XPS and computer simulations showed enrichment of the surface with yttria. STM studies indicated that a high density of step edges are readily formed with ∼35% of the surface sites located at steps. Step edges are identified as the primary adsorption sites for formate. The formate oxidizes in a dehydration reaction producing carbon monoxide and water at ∼600 K. This is contrasted to the reaction of formate on pure zirconia where formate reacts by both dehydration and dehydrogenation reactions. This shift in the selectivity between pure zirconia and yttria-doped zirconia is attributed to the modification of the active step edge sites by yttria segregation. Therefore, the modification of active sites by minority species in a mixed oxide can control the chemical surface functionality. © 2010 American Chemical Society.
dc.identifier.citation Journal of Physical Chemistry C. v.114(13)
dc.identifier.issn 19327447
dc.identifier.uri 10.1021/jp9109964
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jp9109964
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/14687
dc.title Modification of active sites on YSZ(111) by yttria segregation
dc.type Journal. Article
dspace.entity.type
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