Low Temperature Two-Step Atomic Layer Deposition of Tantalum Nitride for Cu Diffusion Barrier

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dc.contributor.authorKwon J.-D.ko
dc.contributor.authorJeong S.-J.ko
dc.contributor.authorKang J.-W.ko
dc.contributor.authorKim D.-G.ko
dc.contributor.authorKim J.-K.ko
dc.contributor.authorRha J.-J.ko
dc.contributor.authorNam K.-S.ko
dc.contributor.authorKwon S.-H.ko
dc.date.accessioned2013-03-08T21:14:50Z-
dc.date.available2013-03-08T21:14:50Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-
dc.identifier.citationJOURNAL OF THE ELECTROCHEMICAL SOCIETY, v.156, no.11, pp.H832 - H835-
dc.identifier.issn0013-4651-
dc.identifier.urihttp://hdl.handle.net/10203/94317-
dc.description.abstractA cubic delta-TaN thin film with an electrical resistivity of 400 mu Omega cm was successfully obtained by suppressing the formation of Ta(3)N(5) using two-step atomic layer deposition independent of NH(3) dosage. The deposition cycle involved two chemical reaction steps: The formation of elemental tantalum (Ta) by reducing tantalum pentafluoride (TaF(5)) with hydrogen plasma and the subsequent nitridation of the preformed Ta with NH(3) at 200-350 degrees C. The microstructure of the preformed Ta was beta-Ta phase with an electrical resistivity of 220 mu Omega cm, which was formed without regard to the deposition temperature. At a deposition temperature of less than 250 degrees C, cubic delta-TaN with a Ta/N ratio of 1 was achieved independent of the NH(3) dosage. However, at a deposition temperature of greater than 300 degrees C, the resistivity of Ta-N-based thin film increased abruptly as the NH(3) dosage exceeded 16.08 x 10(19) molecules/cm(3) due to the formation of Ta(3)N(5). (C) 2009 The Electrochemical Society. [DOI:10.1149/1.3223989] All rights reserved.-
dc.languageEnglish-
dc.publisherELECTROCHEMICAL SOC INC-
dc.subjectCHEMICAL-VAPOR-DEPOSITION-
dc.subjectTHIN-FILMS-
dc.subjectCOPPER METALLIZATION-
dc.subjectGROWTH-
dc.titleLow Temperature Two-Step Atomic Layer Deposition of Tantalum Nitride for Cu Diffusion Barrier-
dc.typeArticle-
dc.identifier.wosid000270457600063-
dc.identifier.scopusid2-s2.0-70349745544-
dc.type.rimsART-
dc.citation.volume156-
dc.citation.issue11-
dc.citation.beginningpageH832-
dc.citation.endingpageH835-
dc.citation.publicationnameJOURNAL OF THE ELECTROCHEMICAL SOCIETY-
dc.identifier.doi10.1149/1.3223989-
dc.contributor.localauthorJeong S.-J.-
dc.contributor.nonIdAuthorKwon J.-D.-
dc.contributor.nonIdAuthorKang J.-W.-
dc.contributor.nonIdAuthorKim D.-G.-
dc.contributor.nonIdAuthorKim J.-K.-
dc.contributor.nonIdAuthorRha J.-J.-
dc.contributor.nonIdAuthorNam K.-S.-
dc.contributor.nonIdAuthorKwon S.-H.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCHEMICAL-VAPOR-DEPOSITION-
dc.subject.keywordPlusTHIN-FILMS-
dc.subject.keywordPlusCOPPER METALLIZATION-
dc.subject.keywordPlusGROWTH-
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