Difluorinated 6,13-Bis(triisopropylsilylethynyl)pentacene: Synthesis, Crystallinity, and Charge-Transport Properties - École polytechnique Accéder directement au contenu
Article Dans Une Revue ChemPhysChem Année : 2015

Difluorinated 6,13-Bis(triisopropylsilylethynyl)pentacene: Synthesis, Crystallinity, and Charge-Transport Properties

Résumé

Fluorination has been demonstrated to improve stability and processing in thiophene-containing small-molecule semiconductors. Here, the impact of partial fluorination on these parameters in a pentacene derivative is examined. Although the improvement in photostability is not as dramatic, there is a clear improvement in the stability of the chromophore upon fluorination. The improvement in processability is more dramatic; devices formed by spin-coating with the fluorinated derivative perform substantially better than those formed from the nonfluorinated compound.

Dates et versions

hal-01144565 , version 1 (22-04-2015)

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Citer

Chang-Hyun Kim, Htay Hlaing, Marcia Payne, Sean Parkin, John E. Anthony, et al.. Difluorinated 6,13-Bis(triisopropylsilylethynyl)pentacene: Synthesis, Crystallinity, and Charge-Transport Properties. ChemPhysChem, 2015, 16 (6), pp.1251-1257. ⟨10.1002/cphc.201402750⟩. ⟨hal-01144565⟩
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