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dc.contributor.authorShin, Taeho
dc.contributor.authorCheng, Yu-Hsiang
dc.contributor.authorTeitelbaum, Samuel Welch
dc.contributor.authorWolfson, Johanna W.
dc.contributor.authorPorter, Ilana J.
dc.contributor.authorKandyla, Maria
dc.contributor.authorNelson, Keith Adam
dc.date.accessioned2018-10-01T19:52:23Z
dc.date.available2018-10-01T19:52:23Z
dc.date.issued2018-09
dc.date.submitted2018-03
dc.identifier.issn2160-3308
dc.identifier.urihttp://hdl.handle.net/1721.1/118327
dc.description.abstractExcursions far from their equilibrium structures can bring crystalline solids through collective transformations including transitions into new phases that may be transient or long-lived. The direct spectroscopic observation of far-from-equilibrium rearrangements provides fundamental mechanistic insight into chemical and structural transformations and a potential route to practical applications, including ultrafast optical control over material structure and properties. However, in many cases, photoinduced transitions are irreversible or only slowly reversible, or the light fluence required exceeds material damage thresholds. This requirement precludes conventional ultrafast spectroscopy, in which optical excitation and probe pulses irradiate the sample many times, each measurement providing information about the sample response at just one probe delay time following excitation, with each measurement at a high repetition rate and with the sample fully recovering its initial state in between measurements. Using a single-shot, real-time measurement method, we are able to observe the photoinduced phase transition from the semimetallic, low-symmetry phase of crystalline bismuth into a high-symmetry phase whose existence at high electronic excitation densities is predicted based on earlier measurements at moderate excitation densities below the damage threshold. Our observations indicate that coherent lattice vibrational motion launched upon photoexcitation with an incident fluence above 10  mJ/cm[superscript 2] in bulk bismuth brings the lattice structure directly into the high-symmetry configuration for several picoseconds, after which carrier relaxation and diffusion restore the equilibrium lattice configuration. Subject Areas: Condensed Matter Physics, Materials Science, Physical Chemistryen_US
dc.description.sponsorshipUnited States. Office of Naval Research (Grant N00014-12-1- 0530)en_US
dc.description.sponsorshipUnited States. Office of Naval Research (Grant N00014-16-1-2090)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant CHE-1111557)en_US
dc.publisherAmerican Physical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1103/PhysRevX.8.031081en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0en_US
dc.sourceAmerican Physical Societyen_US
dc.titleReal-Time Observation of a Coherent Lattice Transformation into a High-Symmetry Phaseen_US
dc.typeArticleen_US
dc.identifier.citationTeitelbaum, Samuel W., et al. “Real-Time Observation of a Coherent Lattice Transformation into a High-Symmetry Phase.” Physical Review X, vol. 8, no. 3, Sept. 2018. © 2018 American Physical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorTeitelbaum, Samuel Welch
dc.contributor.mitauthorWolfson, Johanna W.
dc.contributor.mitauthorPorter, Ilana J.
dc.contributor.mitauthorKandyla, Maria
dc.contributor.mitauthorNelson, Keith Adam
dc.relation.journalPhysical Review Xen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-09-26T18:00:20Z
dc.language.rfc3066en
dspace.orderedauthorsTeitelbaum, Samuel W.; Shin, Taeho; Wolfson, Johanna W.; Cheng, Yu-Hsiang; Porter, Ilana J.; Kandyla, Maria; Nelson, Keith A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0812-9832
dc.identifier.orcidhttps://orcid.org/0000-0001-7804-5418
mit.licensePUBLISHER_CCen_US


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