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dc.contributor.authorProvencher, F.en
dc.contributor.authorBérubé, N.en
dc.contributor.authorParker, A. W.en
dc.contributor.authorGreetham, G. M.en
dc.contributor.authorTowrie, M.en
dc.contributor.authorHellmann, C.en
dc.contributor.authorCôté, M.en
dc.contributor.authorStingelin, N.en
dc.contributor.authorSilva, C.en
dc.contributor.authorHayes, Sophia C.en
dc.creatorProvencher, F.en
dc.creatorBérubé, N.en
dc.creatorParker, A. W.en
dc.creatorGreetham, G. M.en
dc.creatorTowrie, M.en
dc.creatorHellmann, C.en
dc.creatorCôté, M.en
dc.creatorStingelin, N.en
dc.creatorSilva, C.en
dc.creatorHayes, Sophia C.en
dc.date.accessioned2019-11-21T06:22:30Z
dc.date.available2019-11-21T06:22:30Z
dc.date.issued2014
dc.identifier.issn2041-1723
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56062
dc.description.abstractIn polymeric semiconductors, charge carriers are polarons, which means that the excess charge deforms the molecular structure of the polymer chain that hosts it. This results in distinctive signatures in the vibrational modes of the polymer. Here, we probe polaron photogeneration dynamics at polymer:fullerene heterojunctions by monitoring its time-resolved resonance-Raman spectrum following ultrafast photoexcitation. We conclude that polarons emerge within 300 fs. Surprisingly, further structural evolution on ≤50-ps timescales is modest, indicating that the polymer conformation hosting nascent polarons is not significantly different from that near equilibrium. We interpret this as suggestive that charges are free from their mutual Coulomb potential because we would expect rich vibrational dynamics associated with charge-pair relaxation. We address current debates on the photocarrier generation mechanism at molecular heterojunctions, and our work is, to our knowledge, the first direct probe of molecular conformation dynamics during this fundamentally important process in these materials. © 2014 Macmillan Publishers Limited. All rights reserved.en
dc.sourceNature Communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84903774827&doi=10.1038%2fncomms5288&partnerID=40&md5=4e01cc1859694009e6aa6753bb472198
dc.subjectarticleen
dc.subjectcovalent bonden
dc.subjectelectronen
dc.subjectsemiconductoren
dc.subjectRaman spectroscopyen
dc.subjectabsorptionen
dc.subjectchemical structureen
dc.subjectdensity functional theoryen
dc.subjectpolymeren
dc.subjectcopolymeren
dc.subjectconformationen
dc.subjectmolecular analysisen
dc.subjectfullereneen
dc.subjectRaman spectrometryen
dc.subjectvibrationen
dc.subjectCoulomb criterionen
dc.subjectelectric currenten
dc.subjectresonanceen
dc.subjecttimescaleen
dc.titleDirect observation of ultrafast long-range charge separation at polymer-fullerene heterojunctionsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1038/ncomms5288
dc.description.volume5
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :56</p>en
dc.source.abbreviationNat.Commun.en
dc.contributor.orcidHayes, Sophia C. [0000-0002-2809-6193]
dc.gnosis.orcid0000-0002-2809-6193


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