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dc.contributor.authorHefty, Robert C.
dc.contributor.authorHolt, Judson
dc.contributor.authorTate, Matthew R.
dc.contributor.authorCeyer, Sylvia
dc.date.accessioned2011-06-30T15:21:39Z
dc.date.available2011-06-30T15:21:39Z
dc.date.issued2009-04
dc.date.submitted2008-12
dc.identifier.issn0021-9606
dc.identifier.issn1089-7690
dc.identifier.urihttp://hdl.handle.net/1721.1/64720
dc.description.abstractXenon difluoride is observed to react with Si–Si σ-dimer and σ-lattice bonds of Si(100)2×1 at 150 K by single and two atom abstraction at F coverages above 1 ML. As in the limit of zero F coverage, a measurable fraction of the scattered, gas phase product of single atom abstraction, XeF, is sufficiently internally excited to dissociate into F and Xe atoms before detection. Using the XeF internal energy and orientation distributions determined in the limit of zero coverage, the laws of conservation of momentum, energy, and mass are applied to the measured F velocity and angular distributions at higher coverage to simulate the Xe atom velocity and angular distributions and their intensities at higher coverage. The simulation predicts the observed Xe atom velocity and angular distributions at high coverage reasonably well, largely because the exothermicity channeled to XeF remains approximately constant as the coverage increases. This constancy is an opportune consequence of the trade-off between the attractiveness of the potential energy surface as the coverage is increased and the dynamics of the XeF product along the potential surface. The energy, momentum, and mass conservation analysis is also used to distinguish between Xe atoms that arise from XeF gas phase dissociation and Xe atoms that are produced by two atom abstraction. This distinction enables the calculation of percentages of the single and two atom abstraction pathways, as well as the percentages of the two pathways available to the Xe atom produced by two atom abstraction, inelastic scattering, and desorption. Finally, the simulation reveals that between 9% and 12% of F atoms produced by gas phase dissociation of XeF are scattered back toward the surface. These F atoms likely react readily with Si to form the higher fluorides that ultimately lead to etching. Gas phase dissociation of the scattered product of a surface reaction is a novel mechanism to explain the unique reactivity of XeF2 to etch Si in the absence of a plasma.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant CHE-0517786)en_US
dc.language.isoen_US
dc.publisherAmerican Institute of Physicsen_US
dc.relation.isversionofhttp://dx.doi.org/10.1063/1.3118629en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Ceyer via Erja Kajosaloen_US
dc.titleMechanism and dynamics of the reaction of XeF2 with fluorinated Si(100): Possible role of gas phase dissociation of a surface reaction product in plasmaless etchingen_US
dc.typeArticleen_US
dc.identifier.citationHefty, R. C. et al. “Mechanism and Dynamics of the Reaction of XeF[sub 2] with Fluorinated Si(100): Possible Role of Gas Phase Dissociation of a Surface Reaction Product in Plasmaless Etching.” The Journal of Chemical Physics 130.16 (2009) : 164714-13. © 2009 American Institute of Physicsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverCeyer, Sylvia
dc.contributor.mitauthorHefty, Robert C.
dc.contributor.mitauthorHolt, Judson
dc.contributor.mitauthorTate, Matthew R.
dc.contributor.mitauthorCeyer, Sylvia T.
dc.relation.journalJournal of Chemical Physicsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHefty, R. C.; Holt, J. R.; Tate, M. R.; Ceyer, S. T.en
dc.identifier.orcidhttps://orcid.org/0000-0002-9989-6622
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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