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dc.contributor.authorWu, JLen_US
dc.contributor.authorPan, SYen_US
dc.contributor.authorLin, DSen_US
dc.date.accessioned2019-04-03T06:37:21Z-
dc.date.available2019-04-03T06:37:21Z-
dc.date.issued2004-01-01en_US
dc.identifier.issn2469-9950en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.69.045308en_US
dc.identifier.urihttp://hdl.handle.net/11536/27158-
dc.description.abstractThis work investigates the effect of chlorine termination on the stability and the etching of ultra thin Ge layers on a Si(100) surface, using scanning tunneling microscopy (STM) and synchrotron radiation photoemission spectroscopy. The initial growth of Ge on the Si(100) surface is known to occur layer by layer. The intensities of the Ge 3d, Si 2p, and Cl 2p core levels, after the chlorine passivation of Ge/Si(100) surfaces, together with the STM images reveal that most of the deposited Ge atoms have been randomly dispersed on the surface layer during initial submonolayer growth. They occupy only similar to90% of the surface after a 2-ML (monolayer) coverage. Chlorine termination drastically alters the atomic composition of the surface (dimer) layer and in the thin films when annealing at elevated temperatures occurs. Specifically, Cl termination of the Ge/Si(100) surfaces causes Ge, which initially form Cl-Ge bonds in the surface layer, to move into the subsurface layers after annealing at 650-750 K. Silicon is extracted from the subsurface layers to form Cl-Si bonds. Above 900 K, chlorine is desorbed in the form of SiCl2, leaving the initial thin Ge films on the Si(100) surface almost intact.en_US
dc.language.isoen_USen_US
dc.titleStability and mechanism of selective etching of ultrathin Ge films on the Si(100) surface upon chlorine adsorptionen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.69.045308en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume69en_US
dc.citation.issue4en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department物理研究所zh_TW
dc.contributor.departmentInstitute of Physicsen_US
dc.identifier.wosnumberWOS:000189075200053en_US
dc.citation.woscount3en_US
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