Bis(arylene-ethynylene)-s-tetrazines: A Promising Family of n-Type Organic Semiconductors?
dc.rights.license | open | |
hal.structure.identifier | Departamento de Quımica Fısica [Alicante] | |
hal.structure.identifier | Univ Castilla La Mancha, Renewable Energy Res Inst | |
dc.contributor.author | MORAL, Monica | |
hal.structure.identifier | Univ Castilla La Mancha, Fac Pharm | |
dc.contributor.author | GARZON, Andres | |
hal.structure.identifier | Univ Mons, Lab Chem Novel Mat, Belgium | |
dc.contributor.author | OLIVIER, Yoann | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies | |
dc.contributor.author | MUCCIOLI, Luca | |
hal.structure.identifier | Departamento de Quımica Fısica [Alicante] | |
dc.contributor.author | SANCHO-GARCIA, Juan-Carlos | |
hal.structure.identifier | Universidad de Jaén [UJA] | |
dc.contributor.author | GRANADINO-ROLDAN, Jose M. | |
hal.structure.identifier | Universidad de Jaén [UJA] | |
dc.contributor.author | FERNANDEZ-GOMEZ, Manuel | |
dc.date.accessioned | 2020 | |
dc.date.available | 2020 | |
dc.date.issued | 2015 | |
dc.identifier.issn | 1932-7447 | |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/20160 | |
dc.description.abstractEn | We 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.iso | en | |
dc.publisher | American Chemical Society | |
dc.subject.en | CHARGE-TRANSPORT PROPERTIES | |
dc.subject.en | DENSITY-FUNCTIONAL THEORY | |
dc.subject.en | FIELD-EFFECT TRANSISTORS | |
dc.subject.en | THIN-FILM TRANSISTORS | |
dc.subject.en | PERYLENE BISIMIDE SEMICONDUCTORS | |
dc.subject.en | PI-CONJUGATED OLIGOMERS | |
dc.subject.en | MOLECULAR MATERIALS | |
dc.subject.en | S-TETRAZINES | |
dc.subject.en | NONCOVALENT INTERACTIONS | |
dc.subject.en | ELECTRON-TRANSFER | |
dc.title.en | Bis(arylene-ethynylene)-s-tetrazines: A Promising Family of n-Type Organic Semiconductors? | |
dc.type | Article de revue | |
dc.identifier.doi | 10.1021/acs.jpcc.5b05015 | |
dc.subject.hal | Chimie/Polymères | |
bordeaux.journal | Journal of Physical Chemistry C | |
bordeaux.page | 18945-18955 | |
bordeaux.volume | 119 | |
bordeaux.hal.laboratories | Laboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629 | * |
bordeaux.issue | 33 | |
bordeaux.institution | Bordeaux INP | |
bordeaux.institution | Université de Bordeaux | |
bordeaux.peerReviewed | oui | |
hal.identifier | hal-01415464 | |
hal.version | 1 | |
hal.origin.link | https://hal.archives-ouvertes.fr//hal-01415464v1 | |
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