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dc.contributor.authorChang, TFen_US
dc.contributor.authorChang, Len_US
dc.date.accessioned2014-12-08T15:37:24Z-
dc.date.available2014-12-08T15:37:24Z-
dc.date.issued2004-11-01en_US
dc.identifier.issn0925-9635en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.diamond.2004.06.004en_US
dc.identifier.urihttp://hdl.handle.net/11536/25716-
dc.description.abstractHighly oriented (100) diamond films have been successfully grown on SixGe1-x(100) thin films by bias enhanced nucleation (BEN) in microwave plasma chemical vapor deposition (MPCVD) system. Raman spectra show the 1332 cm(-1) peak which proves the formation of diamond. Diamond nucleation density on SixGe1-x substrate estimated by scanning electron microscopy is higher than 10(9) cm(-2). The interface between diamond and SixGe1-x substrate was characterized by transmission electron microscopy (TEM). About 20 nm decrease in thickness of the SixGe1-x film. was observed after bias enhanced nucleation step. TEM shows the existence of silicon carbide and heteroepitaxial diamond grains grown on SixGe1-x substrate. Characterization from high-resolution TEM on the specimen of short time deposition reveals that a number of epitaxial diamond grains were directly nucleated on SixGe1-x with {111} interplanar spacing ratio of diamond and SixGe1-x of 2:3. The diamond nucleation is found to be preferred on the ridge position of the rough substrate surface. Diamond {100} facets were quickly developed in the early stage of growth. (C) 2004 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectdiamonden_US
dc.subjectSixGe1-xen_US
dc.subjectnucleationen_US
dc.subjecttransmission electron microscopyen_US
dc.titleHighly oriented diamond growth on SixGe1-x (100) thin filmsen_US
dc.typeArticle; Proceedings Paperen_US
dc.identifier.doi10.1016/j.diamond.2004.06.004en_US
dc.identifier.journalDIAMOND AND RELATED MATERIALSen_US
dc.citation.volume13en_US
dc.citation.issue11-12en_US
dc.citation.spage2088en_US
dc.citation.epage2091en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000225057300031-
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