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dc.contributor.authorWang, Hongtao
dc.contributor.authorGordon, Roy Gerald
dc.contributor.authorAlvis, Roger
dc.contributor.authorUlfig, Robert M.
dc.date.accessioned2009-10-14T12:49:42Z
dc.date.issued2009-10-14
dc.identifier.citationWang, Hongtao, Roy G. Gordon, Roger Alvis, and Robert M. Ulfig. Forthcoming. Atomic layer deposition of ruthenium thin films from an amidinate precursor. Chemical Vapor Deposition.en_US
dc.identifier.issn0948-1907en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:3347576
dc.description.abstractRuthenium thin films were deposited by atomic layer deposition from bis(N,N’-di-tert-butylacetamidinato)ruthenium(II) dicarbonyl and O2. Highly conductive, dense and pure thin films can be deposited when oxygen exposure EO approaches a certain threshold ( Emax ). When EO > Emax, the film peels off due to the recombinative desorption of O2 at the film/substrate interface. Analysis by an atomic probe microscope shows that the crystallites are nearly free of carbon impurity (<0.1 at.%), while a low level of carbon (<0.5 at.%) is segregated near the grain boundaries. The atom probe microscope also shows that a small amount of O impurity (0.3 at.%) is distributed uniformly between the crystallites and the grain boundaries.en_US
dc.description.sponsorshipChemistry and Chemical Biologyen_US
dc.description.sponsorshipEngineering and Applied Sciencesen_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.relation.isversionofhttp://www3.interscience.wiley.com/journal/10003226/homeen_US
dash.licenseOAP
dc.subjectO2 exposureen_US
dc.subjectatomic layer depositionen_US
dc.subjectruthenium thin filmsen_US
dc.titleAtomic Layer Deposition of Ruthenium Thin Films From an Amidinate Precursoren_US
dc.typeJournal Articleen_US
dc.description.versionAccepted Manuscripten_US
dc.relation.journalChemical Vapor Depositionen_US
dash.depositing.authorGordon, Roy Gerald
dc.date.available2009-10-14T12:49:42Z
dc.identifier.doi10.1002/cvde.200906789
dash.contributor.affiliatedGordon, Roy


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