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dc.contributor.authorOrava, J
dc.contributor.authorGreer, AL
dc.date.accessioned2017-08-09T15:26:27Z
dc.date.available2017-08-09T15:26:27Z
dc.date.issued2017-10-15
dc.identifier.issn1359-6454
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/266142
dc.description.abstractThe chalcogenide Ge2Sb2Te5 (GST) is of interest for use in phase-change memory. Crystallization is the rate-limiting step for memory operation, and can be accelerated by the prior application of a “priming” heating pulse. There is characteristic fading of the priming effect if there is a time interval between the priming pulse and the main heating pulse to achieve crystallization. We apply classical nucleation theory to interpret these effects, based on a fitting of nucleation kinetics (steady-state and transient) over the full temperature range of the supercooled liquid. The input data come from both physical experiments and atomistic simulations. Prior studies of conventional glass-formers such as lithium disilicate preclude any possibility of fading; the present study shows, however, that fading can be expected with the particular thermodynamic parameters relevant for GST and, possibly, other phase-change chalcogenides. We also use the nucleation analysis to highlight the distinction between GST and the other archetypical chalcogenide system (Ag,In)-doped Sb2Te. Classical nucleation theory appears to be applicable to phase-change chalcogenides, and to predict performance consistent with that of actual memory cells. Nucleation modeling may therefore be useful in optimizing materials selection and performance in device applications.
dc.description.sponsorshipWe acknowledge financial support by the World Premier International Research Center Initiative (WPI), MEXT, Japan, and from the European Research Council under the European Union's Horizon 2020 research and innovation program (grant ERC-2015-AdG-695487: ExtendGlass).
dc.language.isoen
dc.publisherElsevier
dc.rightsAttribution 4.0 International
dc.rightsAttribution 4.0 International
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectamorphous materials
dc.subjectclassical nucleation theory
dc.subjectphase-change chalcogenides
dc.subjectphase transformation kinetics
dc.subjectrapid solidification
dc.titleClassical-nucleation-theory analysis of priming in chalcogenide phase-change memory
dc.typeArticle
prism.endingPage235
prism.publicationDate2017
prism.publicationNameActa Materialia
prism.startingPage226
prism.volume139
dc.identifier.doi10.17863/CAM.12463
dcterms.dateAccepted2017-08-07
rioxxterms.versionofrecord10.1016/j.actamat.2017.08.013
rioxxterms.versionAM
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/
rioxxterms.licenseref.startdate2017-10-15
dc.contributor.orcidOrava, Jiri [0000-0002-4036-5069]
dc.contributor.orcidGreer, Alan [0000-0001-7360-5439]
dc.identifier.eissn1873-2453
rioxxterms.typeJournal Article/Review
pubs.funder-project-idEuropean Research Council (695487)
cam.issuedOnline2017-08-08
cam.orpheus.successThu Jan 30 13:04:38 GMT 2020 - The item has an open VoR version.
rioxxterms.freetoread.startdate2100-01-01


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