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dc.contributor.authorShih, YTen_US
dc.contributor.authorChunu, DSen_US
dc.contributor.authorMei, WNen_US
dc.date.accessioned2014-12-08T15:02:22Z-
dc.date.available2014-12-08T15:02:22Z-
dc.date.issued1996-09-01en_US
dc.identifier.issn0038-1098en_US
dc.identifier.urihttp://dx.doi.org/10.1016/0038-1098(96)00300-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/1045-
dc.description.abstractA finite conical well was proposed to model the surface hindering potential to which a horizontally adsorbed molecule is subjected. Eigenfunctions and eigenvalues for this model were presented. In addition to the hindering rotation, the external electric field effect on the rotational states of a horizontally adsorbed dipole molecule was also investigated by variational calculation. We found that, as with our previous result of the vertical configuration, the rotational energy Levels of the horizontally adsorbed molecule exhibit oscillatory behavior when plotted as functions of the hindrance angle. On the other hand, our result showed that the Stark shifts of the rotational energies were suppressed by the conical well if the field strength is not comparable with the hindering potential. However, when the applied held is strong, large negative shifts were found. Furthermore, the plotted angular distributions of wave function showed that a very strong electric field will enduce a change of adsorption configuration from horizontal to vertical. Copyright (C) 1996 Published by Elsevier Science Ltden_US
dc.language.isoen_USen_US
dc.subjectmetalsen_US
dc.subjectsurfaces and interfacesen_US
dc.titleHindered rotation and external electric field effect of adsorbed diatomic moleculesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0038-1098(96)00300-6en_US
dc.identifier.journalSOLID STATE COMMUNICATIONSen_US
dc.citation.volume99en_US
dc.citation.issue11en_US
dc.citation.spage819en_US
dc.citation.epage824en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:A1996VE35600011-
dc.citation.woscount5-
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