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dc.contributor.authorLin, DSen_US
dc.contributor.authorKu, TSen_US
dc.contributor.authorChen, RPen_US
dc.date.accessioned2019-04-03T06:39:34Z-
dc.date.available2019-04-03T06:39:34Z-
dc.date.issued2000-01-15en_US
dc.identifier.issn1098-0121en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.61.2799en_US
dc.identifier.urihttp://hdl.handle.net/11536/30802-
dc.description.abstractIn this paper, we investigate the interaction of phosphine (PH3) on the Si(100)-2 x 1 surface at temperatures between 635 and 900 K. The hydrogen desorption, growth mode, surface morphology, and chemical composition and ordering of the surface layer are examined by synchrotron radiation core-level photoemission and real-time high-temperature scanning tunneling microscopy. The P 2p core-level spectra indicate that decomposition of PHn is complete above similar to 550 K and the maximum P coverage is strongly influenced by the growth temperature, which governs the coverage of H-terminated sites. The scanning tunneling microscopy (STM) images taken at real time during PH3 exposure indicate that a surface phosphorus atom readily and randomly displaces one Si atom from the substrate. The ejected Si diffuses, nucleates, and incorporates itself into islands or step edges, leading to similar growth behavior as that found in Si chemical vapor deposition. Line defects both perpendicular and parallel to the dimer rows are observed on the nearly P-saturated surface. Perpendicular line defects act as a strain relief mechanism. Parallel line defects result from growth kinetics. STM images also indicate that incorporating a small amount of phosphorus eliminates the line defects in the Si(100)-2 x n surface.en_US
dc.language.isoen_USen_US
dc.titleInteraction of phosphine with Si(100) from core-level photoemission and real-time scanning tunneling microscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.61.2799en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume61en_US
dc.citation.issue4en_US
dc.citation.spage2799en_US
dc.citation.epage2805en_US
dc.contributor.department物理研究所zh_TW
dc.contributor.departmentInstitute of Physicsen_US
dc.identifier.wosnumberWOS:000085348300063en_US
dc.citation.woscount32en_US
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