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dc.contributor.authorChen, CFen_US
dc.contributor.authorLi, YWen_US
dc.date.accessioned2014-12-08T15:38:47Z-
dc.date.available2014-12-08T15:38:47Z-
dc.date.issued2004-08-01en_US
dc.identifier.issn0021-4922en_US
dc.identifier.urihttp://dx.doi.org/10.1143/JJAP.43.5545en_US
dc.identifier.urihttp://hdl.handle.net/11536/26545-
dc.description.abstractAmorphous hydrogenated silicon carbide (a-SiC:H) films were deposited using plasma-enhanced chemical vapor deposition (PECVD) process. Reducing silane flow rate increased the carbon concentration and optical band gap in the a-SiC:H films, but decreased the refractive index and dielectric constant. X-ray photoelectron spectroscopy (XPS) data revealed that the carbon concentration decreased as the methane flow rate increased, but the silicon concentration increased. Increasing the carbon concentration in the a-SiC:H film reduces the dielectric constant of the film. The carbon-rich a-Si0.24C0.68:H,, films treated with hydrogen plasma for various periods, were converted into films with more silicon content. Increasing the hydrogen plasma treatment period gradually roughened the surface even though the original film had a smooth surface, with a roughness <0.231 nm. The leakage current density of the hydrogen plasma treated a-Si0.24C0.68:1-1, films declined as the duration of the hydrogen plasma treatment period decreased.en_US
dc.language.isoen_USen_US
dc.subjecta-SiC : Hen_US
dc.subjectPECVDen_US
dc.subjecthydrogen plasmaen_US
dc.subjectleakage currenten_US
dc.subjectdielectric constanten_US
dc.titleThe effects of hydrogen plasma treatment on the plasma-enhanced chemical vapor deposition a-SiC : H filmsen_US
dc.typeArticleen_US
dc.identifier.doi10.1143/JJAP.43.5545en_US
dc.identifier.journalJAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERSen_US
dc.citation.volume43en_US
dc.citation.issue8Aen_US
dc.citation.spage5545en_US
dc.citation.epage5549en_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:000224841400091-
dc.citation.woscount3-
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