Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/94241
DC Field | Value | |
---|---|---|
dc.title | Migration of H-atoms from metal interface to adsorbed metal carbonyl layers | |
dc.contributor.author | Huang, H.H. | |
dc.contributor.author | Seet, C.S. | |
dc.contributor.author | Sreekanth, C.S. | |
dc.contributor.author | Xu, G.Q. | |
dc.date.accessioned | 2014-10-16T08:33:46Z | |
dc.date.available | 2014-10-16T08:33:46Z | |
dc.date.issued | 1996-03-01 | |
dc.identifier.citation | Huang, H.H.,Seet, C.S.,Sreekanth, C.S.,Xu, G.Q. (1996-03-01). Migration of H-atoms from metal interface to adsorbed metal carbonyl layers. Surface Science 348 (1-2) : 192-196. ScholarBank@NUS Repository. | |
dc.identifier.issn | 00396028 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/94241 | |
dc.description.abstract | The interaction of Fe(CO)5 with H-adatoms was studied on a Ru(001) surface by thermal desorption spectroscopy. The desorption spectra showed, in addition to the normal hydrogen desorption peak from the Ru(001) surface, two low temperature sharp peaks at 160 and 190 K coinciding with the peaks due to the molecular desorption of Fe(CO)5, This is explained by a model suggesting the migration of H-adatoms into the multilayers of Fe(CO)5 due to either the repulsive interaction between H-adatoms and CO formed by the decomposition of Fe(CO)5 on Ru(001) or the attractive interaction between H-adatoms and Fe(CO)5 molecules. | |
dc.source | Scopus | |
dc.subject | Diffusion and migration | |
dc.subject | Hydrogen | |
dc.subject | Iron pentacarbonyl | |
dc.subject | Ruthenium | |
dc.subject | Single crystal surfaces | |
dc.subject | Thermal desorption spectroscopy | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.sourcetitle | Surface Science | |
dc.description.volume | 348 | |
dc.description.issue | 1-2 | |
dc.description.page | 192-196 | |
dc.description.coden | SUSCA | |
dc.identifier.isiut | NOT_IN_WOS | |
Appears in Collections: | Staff Publications |
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