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dc.contributor.authorFerng, SSen_US
dc.contributor.authorLin, CTen_US
dc.contributor.authorYang, KMen_US
dc.contributor.authorLin, DSen_US
dc.contributor.authorChiang, TCen_US
dc.date.accessioned2014-12-08T15:19:07Z-
dc.date.available2014-12-08T15:19:07Z-
dc.date.issued2005-05-20en_US
dc.identifier.issn0031-9007en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevLett.94.196103en_US
dc.identifier.urihttp://hdl.handle.net/11536/13702-
dc.description.abstractScanning tunneling microscopy is employed to investigate the recombinative desorption of H(2) from hydrogenated Si(100) surfaces consisting of dihydride (SiH(2)) and monohydride (SiH) surface species organized in (1x1), (3x1), and (2x1) configurations. The results show that desorption from dihydrides involves a pair of neighboring dihydrides linked along the tetrahedral bond direction. Dihydrides in (3x1) domains are separated in the same direction by monohydrides, and desorption from a pair is geometrically impossible. The same desorption mechanism nevertheless applies via first a position switching of dihydrides with neighboring monohydrides.en_US
dc.language.isoen_USen_US
dc.titleAtomistic view of the recombinative desorption of H(2) from H/Si(100)en_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevLett.94.196103en_US
dc.identifier.journalPHYSICAL REVIEW LETTERSen_US
dc.citation.volume94en_US
dc.citation.issue19en_US
dc.citation.spageen_US
dc.citation.epageen_US
dc.contributor.department物理研究所zh_TW
dc.contributor.departmentInstitute of Physicsen_US
Appears in Collections:Articles