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dc.contributor.authorHao, OYen_US
dc.contributor.authorWu, YCSen_US
dc.contributor.authorChiou, HHen_US
dc.contributor.authorLiu, CCen_US
dc.contributor.authorCheng, JHen_US
dc.contributor.authorWen, OYen_US
dc.contributor.authorChiou, SHen_US
dc.contributor.authorShiue, STen_US
dc.contributor.authorChueh, YLen_US
dc.contributor.authorChou, LJen_US
dc.date.accessioned2014-12-08T15:17:05Z-
dc.date.available2014-12-08T15:17:05Z-
dc.date.issued2006-03-13en_US
dc.identifier.issn0003-6951en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.2185611en_US
dc.identifier.urihttp://hdl.handle.net/11536/12489-
dc.description.abstractElectrical performance was found to be closely related to the variation of nanosized interface morphology in previous studies. This work investigated in detail the microstructural development of in- and anti-phase bonded interfaces for n-type (100) GaAs wafers treated at 500, 600, 700 and 850 degrees C. The interfacial energy of anti-phase bonding is higher than that of in-phase bonding based on the first-principles calculations. The higher interface energy tends to stabilize the interfacial oxide layer. The continuous interfacial oxide layer observed below 700 degrees C can deteriorate the electrical property due to its insulating property. However, the existence of nanoscaled oxide at anti-phase bonded interfaces can improve the electrical conductivity at 700 degrees C. This is due to the suppression of the evaporation of As atom by the interfacial nanoscaled oxides based on the analysis of autocorrelation function and energy dispersive x-ray spectroscopy. (c) 2006 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleAnomalous electrical performance of nanoscaled interfacial oxides for bonded n-GaAs wafersen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.2185611en_US
dc.identifier.journalAPPLIED PHYSICS LETTERSen_US
dc.citation.volume88en_US
dc.citation.issue11en_US
dc.citation.epageen_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:000236062700048-
dc.citation.woscount1-
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