Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/76422
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dc.titleKinetic Constraints in the Phase Transitions of Chemisorbed Carbon Monoxide on Co{1010} at High Coverages
dc.contributor.authorGu, J.
dc.contributor.authorYeo, Y.Y.
dc.contributor.authorSim, W.S.
dc.contributor.authorKing, D.A.
dc.date.accessioned2014-06-23T05:42:35Z
dc.date.available2014-06-23T05:42:35Z
dc.date.issued2000-05-18
dc.identifier.citationGu, J.,Yeo, Y.Y.,Sim, W.S.,King, D.A. (2000-05-18). Kinetic Constraints in the Phase Transitions of Chemisorbed Carbon Monoxide on Co{1010} at High Coverages. Journal of Physical Chemistry B 104 (19) : 4684-4689. ScholarBank@NUS Repository.
dc.identifier.issn10895647
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76422
dc.description.abstractThe high-coverage structures of CO on Co{1010} have been investigated in detail using reflection - absorption infrared spectroscopy (RAIRS) and low-energy electron diffraction (LEED) over the temperature range from 100 to 250 K. This has revealed a curious anomaly. As the coverage is increased above 0.5 monolayer (ML) at temperatures below 250 K, a p(2x1) phase, with atop CO, is incompletely converted to a p(2x1)g phase with a local coverage of 1 ML and CO in bridge sites. At temperatures below 180 K, one-third of the surface is converted into the energetically most stable structure, c(2x6), with CO in two types of bridge sites, local coverage 1.17 ML, and the remaining two-thirds remains in the p(2x1)g phase. On cooling to 100 K, the stable c(2x6) phase is unchanged, still occupying one-third of the surface, and the p(2x1)g phase is transformed to a p(6x1)g phase, driven by vibrational entropy. At these low temperatures, this phase transition occurs between two ordered phases that are both metastable with respect to the high-coverage c(2x6) phase. This is attributed to kinetic constraints within the close-packed adsorbed overlayer associated with frozen-in antiphase domains.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleJournal of Physical Chemistry B
dc.description.volume104
dc.description.issue19
dc.description.page4684-4689
dc.description.codenJPCBF
dc.identifier.isiutNOT_IN_WOS
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