完整後設資料紀錄
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dc.contributor.authorFang, Yu-Siangen_US
dc.contributor.authorChiu, Kun-Anen_US
dc.contributor.authorDo, Hienen_US
dc.contributor.authorChang, Lien_US
dc.date.accessioned2019-12-13T01:10:01Z-
dc.date.available2019-12-13T01:10:01Z-
dc.date.issued2019-11-15en_US
dc.identifier.issn0257-8972en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.surfcoat.2019.07.087en_US
dc.identifier.urihttp://hdl.handle.net/11536/153091-
dc.description.abstractHighly oriented cubic (100) HfN films were grown on Si (100) substrates by direct current magnetron reactive sputtering of a metallic Hf target in an Ar/N-2 gas environment. The influence of N-2 flow ratio on the (100) preferred orientation and crystallinity of the HfN films is investigated. X-ray diffraction shows that not only HEN but also orthorhombic HfSi2 forms in the sputtered films. Increasing the N-2 flow ratio is unfavorable for the formation of HfSi2 while the deposition rate of HfN is decreased. X-ray diffraction and cross-sectional scanning transmission electron microscopy (STEM) reveal that epitaxial orthorhombic HfSi2 can form on the Si substrate, and (100) HfN is in epitaxy with the epitaxial HfSi2. As a result, a (100) oriented HfN film can grow on Si. The epitaxial relationships are shown to be HfN (100)[01 (1) over bar] // HfSi2 (020)[001] // Si (100)[01 (1) over bar] and HfN (100)[01 (1) over bar] // HfSi2 (020)[100] // Si (100)[01 (1) over bar]. Atomically resolved STEM images also show the bonding characteristics across the HfN/HfSi2 and HfSi2/Si interfaces.en_US
dc.language.isoen_USen_US
dc.subjectHfNen_US
dc.subjectHfSi2en_US
dc.subjectEpitaxial growthen_US
dc.subjectReactive magnetron sputteringen_US
dc.titleReactive sputtering for highly oriented HfN film growth on Si (100) substrateen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.surfcoat.2019.07.087en_US
dc.identifier.journalSURFACE & COATINGS TECHNOLOGYen_US
dc.citation.volume377en_US
dc.citation.spage0en_US
dc.citation.epage0en_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:000488417800007en_US
dc.citation.woscount0en_US
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