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hal.structure.identifierDepartamento de Quımica Fısica [Alicante]
hal.structure.identifierUniv Castilla La Mancha, Renewable Energy Res Inst
dc.contributor.authorMORAL, Monica
hal.structure.identifierUniv Castilla La Mancha, Fac Pharm
dc.contributor.authorGARZON, Andres
hal.structure.identifierUniv Mons, Lab Chem Novel Mat, Belgium
dc.contributor.authorOLIVIER, Yoann
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorMUCCIOLI, Luca
hal.structure.identifierDepartamento de Quımica Fısica [Alicante]
dc.contributor.authorSANCHO-GARCIA, Juan-Carlos
hal.structure.identifierUniversidad de Jaén [UJA]
dc.contributor.authorGRANADINO-ROLDAN, Jose M.
hal.structure.identifierUniversidad de Jaén [UJA]
dc.contributor.authorFERNANDEZ-GOMEZ, Manuel
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn1932-7447
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20160
dc.description.abstractEnWe theoretically describe in this work the n-type semiconducting behavior of a set of bis(arylene-ethynylene)-s-tetrazines ((ArCC)(2)Tz), by comparing their electronic properties with those of their parent diaryl-s-tetrazines (Ar(2)Tz) after the introduction of ethynylene bridges. The significantly reduced internal reorganization energy for electron transfer is ascribed to an extended delocalization of the LUMO for (ArCC)(2)Tz as opposite to that for Ar(2)Tz, which was described mostly localized on the s-tetrazine ring. The largest electronic coupling and the corresponding electron transfer rates found for bis(phenyl-ethynylene)-s-tetrazine, as well as for some halogenated derivatives, are comparable to those reported for the best performing n-type organic semiconductor materials such as diimides and perylenes. The theoretical mobilities for the studied compounds turn out to be in the range 0.3-1.3 cm(2) V-1 s(-1), close to values experimentally determined for common n-type organic semiconductors used in real devices. In addition, ohmic contacts can be expected when these compounds are coupled to metallic cathodes such as Na, Ca, and Sm. For these reasons, the future application of semiconducting bis(phenyl-ethynylene)-s-tetrazine and its fluorinated and brominated derivatives in optoelectronic devices is envisioned.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enCHARGE-TRANSPORT PROPERTIES
dc.subject.enDENSITY-FUNCTIONAL THEORY
dc.subject.enFIELD-EFFECT TRANSISTORS
dc.subject.enTHIN-FILM TRANSISTORS
dc.subject.enPERYLENE BISIMIDE SEMICONDUCTORS
dc.subject.enPI-CONJUGATED OLIGOMERS
dc.subject.enMOLECULAR MATERIALS
dc.subject.enS-TETRAZINES
dc.subject.enNONCOVALENT INTERACTIONS
dc.subject.enELECTRON-TRANSFER
dc.title.enBis(arylene-ethynylene)-s-tetrazines: A Promising Family of n-Type Organic Semiconductors?
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.jpcc.5b05015
dc.subject.halChimie/Polymères
bordeaux.journalJournal of Physical Chemistry C
bordeaux.page18945-18955
bordeaux.volume119
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue33
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01415464
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01415464v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Physical%20Chemistry%20C&rft.date=2015&rft.volume=119&rft.issue=33&rft.spage=18945-18955&rft.epage=18945-18955&rft.eissn=1932-7447&rft.issn=1932-7447&rft.au=MORAL,%20Monica&GARZON,%20Andres&OLIVIER,%20Yoann&MUCCIOLI,%20Luca&SANCHO-GARCIA,%20Juan-Carlos&rft.genre=article


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