完整後設資料紀錄
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dc.contributor.authorHuang, Yu-Jenen_US
dc.contributor.authorChen, Yen-Chouen_US
dc.contributor.authorHsieh, Tsung-Eongen_US
dc.date.accessioned2014-12-08T15:09:03Z-
dc.date.available2014-12-08T15:09:03Z-
dc.date.issued2009-08-01en_US
dc.identifier.issn0021-8979en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.3194787en_US
dc.identifier.urihttp://hdl.handle.net/11536/6894-
dc.description.abstractPhase-change behaviors of Ge(2)Sb(2)Te(5) (GST) thin films doped with molybdenum (Mo) or nitrogen (N) were investigated by utilizing in situ electrical property measurement, x-ray diffraction (XRD), transmission electron microscopy (TEM), and x-ray photoelectron spectroscopy. It was found that the Mo doping mainly reduces the resistivity level of amorphous GST while the N-doping raises both the resistivity levels of amorphous and crystalline GSTs. XRD and TEM analyses revealed that the element doping stabilizes the amorphous state of GST and suppresses the grain growth in GST films. This resulted in the increase in recrystallization temperature (T(m)) and activation energy (E(a)) of amorphous-to-crystalline phase transition in GST layers, as revealed by the calculation in terms of Kissinger's theory. The results of data fitting into various percolation models and Johnson-Mehl-Avrami analysis indicated the heterogeneous feature of phase transition process in GST layers that the nucleation first occurs at the atmosphere/sample interface and the recrystallization front advances into the interior of sample in a layer-by-layer manner along the direction of surface normal.en_US
dc.language.isoen_USen_US
dc.titlePhase transition behaviors of Mo- and nitrogen-doped Ge(2)Sb(2)Te(5) thin films investigated by in situ electrical measurementsen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.3194787en_US
dc.identifier.journalJOURNAL OF APPLIED PHYSICSen_US
dc.citation.volume106en_US
dc.citation.issue3en_US
dc.citation.spageen_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
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