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Anisotropic crystallization of orthorhombic ScSi on Si(001) substrates

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cris.virtual.orcid0000-0003-3663-8842
cris.virtual.orcid0000-0002-4561-348X
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dc.contributor.authorPollefliet, Bert
dc.contributor.authorPorret, Clement
dc.contributor.authorEveraert, Jean-Luc
dc.contributor.authorSankaran, Kiroubanand
dc.contributor.authorRichard, Olivier
dc.contributor.authorHan, Han
dc.contributor.authorLoo, Roger
dc.contributor.authorDetavernier, Christophe
dc.contributor.authorVantomme, André
dc.contributor.authorMerckling, Clement
dc.date.accessioned2026-07-27T13:18:40Z
dc.date.available2026-07-27T13:18:40Z
dc.date.createdwos2026
dc.date.issued2026
dc.description.abstractScandium-based silicides have attracted attention as new contact materials for ultimately scaled CMOS devices. Excellent contact properties in combination with P-doped Si have been demonstrated. However, unlike conventional Ti, Co, and Ni silicides, little is known about the formation mechanisms and properties of Sc silicides. This manuscript, therefore, reports on the formation and structural properties of orthorhombic ScSi silicide formed by solid state reaction between a sputter deposited 15 nm Sc film and a Si(001) substrate. Synchrotron x-ray diffraction (XRD) pole figures, in combination with cross-sectional transmission electron microscopy, are leveraged to determine the texture of ScSi. An epitaxial texture with two different components is evidenced. Large (≳20 nm) grains, having a minimal defectivity originating from the lattice mismatch between the silicide and the substrate, are distinguished from small (≲5 nm) nanotwinned grains. The formation of these two sets of grains is investigated by in situ XRD. Due to a solid state amorphization reaction between Sc and Si, the formation of orthorhombic ScSi is preceded by the formation of an amorphous ScSi phase. Orthorhombic ScSi formation is initiated at ∼320 °C by the crystallization of small nuclei at the interface with Si, as evidenced for the first time by cross-sectional transmission electron microscopy. These nuclei share a singular epitaxial orientation, corresponding to the one of the large grains in the final ScSi film. Further crystallization occurs anisotropically in the lateral direction. Along the c axis, the initial epitaxial orientation is maintained. However, along the a axis, twin defects are generated, resulting in the small grain size.
dc.description.wosFundingTextThis work has been enabled in part by the NanoIC pilot line. The acquisition and operation are jointly funded by the Chips Joint Undertaking, through the European Union's Digital Europe (Grant No. 101183266) and Horizon Europe programs (Grant No. 101183277), as well as by the participating states Belgium (Flanders), France, Germany, Finland, Ireland, and Romania. For more information, visit nanoic-project.eu. Views and opinions expressed are, however, those of the author(s) only and do not necessarily reflect those of the European Union or Chips Joint Undertaking. Neither the European Union nor the granting authority can be held responsible for them. Elettra Sincrotrone Trieste is acknowledged for beamtime allocation on the MCX beamline (Proposal No. 20230227). The excellent support of beamline responsible J. Plaisier is acknowledged. Soleil synchrotron is acknowledged for beamtime allocation on the DiffAbs beamline (Proposal No. 20240142). The excellent support of beamline scientist C. Mocuta is acknowledged. The authors thank A. Akula and D. Schippers for assisting the measurements. In the supplementary material, results obtained at the ESRF DUBBLE BM26 beamline are included. The authors acknowledge the ESRF for beamtime allocation under Proposal No. A26-2-1005. Beamline scientist M. Rosenthal is acknowledged for his excellent support. The authors thank T. Dursap for assisting the measurements.
dc.identifier.doi10.1063/5.0326525
dc.identifier.issn2166-532X
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/59991
dc.language.isoeng
dc.provenance.editstepusergreet.vanhoof@imec.be
dc.publisherAIP Publishing
dc.source.beginpage041103
dc.source.issue4
dc.source.journalAPL MATERIALS
dc.source.numberofpages9
dc.source.volume14
dc.subject.keywordsTHIN-FILMS
dc.subject.keywordsELECTRICAL-PROPERTIES
dc.subject.keywordsYTTRIUM SILICIDE
dc.subject.keywordsTEMPERATURE
dc.subject.keywordsDIFFUSION
dc.subject.keywordsTEXTURE
dc.subject.keywordsNUCLEATION
dc.subject.keywordsSCANDIUM
dc.subject.keywordsPHASE
dc.title

Anisotropic crystallization of orthorhombic ScSi on Si(001) substrates

dc.typeJournal article
dspace.entity.typePublication
imec.internal.crawledAt2026-04-11
imec.internal.sourcecrawler
imec.internal.wosCreatedAt2026-07-14
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