Unraveling the Metastability of C-n(2+) (n=2-4) Clusters

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dc.contributor.authorPeng, Zirongko
dc.contributor.authorZanuttini, Davidko
dc.contributor.authorGervais, Benoitko
dc.contributor.authorJacquet, Emmanuelleko
dc.contributor.authorBlum, Ivanko
dc.contributor.authorChoi, Pyuck-Pako
dc.contributor.authorRaabe, Dierkko
dc.contributor.authorVurpillot, Francoisko
dc.contributor.authorGault, Baptisteko
dc.date.accessioned2019-03-19T01:25:32Z-
dc.date.available2019-03-19T01:25:32Z-
dc.date.created2019-03-04-
dc.date.created2019-03-04-
dc.date.created2019-03-04-
dc.date.issued2019-02-
dc.identifier.citationJOURNAL OF PHYSICAL CHEMISTRY LETTERS, v.10, no.3, pp.581 - 588-
dc.identifier.issn1948-7185-
dc.identifier.urihttp://hdl.handle.net/10203/251626-
dc.description.abstractPure carbon clusters have received considerable attention for a long time. However, fundamental questions, such as what the smallest stable carbon cluster dication is, remain unclear. We investigated the stability and fragmentation behavior of C-n(2+) (n = 2-4) dications using state-of-the-art atom probe tomography. These small doubly charged carbon cluster ions were produced by laser-pulsed field evaporation from a tungsten carbide field emitter. Correlation analysis of the fragments detected in coincidence reveals that they only decay to C-n-1(+) + C+. During C-2(2+) -> C+ + C+ significant kinetic energy release (similar to 5.75-7.8 eV) is evidenced. Through advanced experimental data processing combined with ab initio calculations and simulations, we show that the field-evaporated diatomic C-12(2)2+ dications are either in weakly bound (3)Pi(u) and (3)Sigma(-)(g) states, quickly dissociating under the intense electric field, or in a deeply bound electronic (5)Sigma(-)(u) state with lifetimes >180 ps.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleUnraveling the Metastability of C-n(2+) (n=2-4) Clusters-
dc.typeArticle-
dc.identifier.wosid000458704800041-
dc.identifier.scopusid2-s2.0-85060796675-
dc.type.rimsART-
dc.citation.volume10-
dc.citation.issue3-
dc.citation.beginningpage581-
dc.citation.endingpage588-
dc.citation.publicationnameJOURNAL OF PHYSICAL CHEMISTRY LETTERS-
dc.identifier.doi10.1021/acs.jpclett.8b03449-
dc.contributor.localauthorChoi, Pyuck-Pa-
dc.contributor.nonIdAuthorPeng, Zirong-
dc.contributor.nonIdAuthorZanuttini, David-
dc.contributor.nonIdAuthorGervais, Benoit-
dc.contributor.nonIdAuthorJacquet, Emmanuelle-
dc.contributor.nonIdAuthorBlum, Ivan-
dc.contributor.nonIdAuthorRaabe, Dierk-
dc.contributor.nonIdAuthorVurpillot, Francois-
dc.contributor.nonIdAuthorGault, Baptiste-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusATOM-PROBE TOMOGRAPHY-
dc.subject.keywordPlusFIELD EVAPORATION-
dc.subject.keywordPlusCARBON CLUSTERS-
dc.subject.keywordPlusIONS-
dc.subject.keywordPlusC-60-
dc.subject.keywordPlusIONIZATION-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusFRAGMENTATION-
dc.subject.keywordPlusWAVELENGTH-
dc.subject.keywordPlusFULLERENES-
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