Yayın: Epindolidiones-Versatile and Stable Hydrogen-Bonded Pigments for Organic Field-Effect Transistors and Light-Emitting Diodes
| dc.contributor.author | Glowacki, Eric Daniel | |
| dc.contributor.author | Romanazzi, Giuseppe | |
| dc.contributor.author | Yumusak, Cigdem | |
| dc.contributor.author | Coskun, Halime | |
| dc.contributor.author | Monkowius, Uwe | |
| dc.contributor.author | Voss, Gundula | |
| dc.contributor.author | Burian, Max | |
| dc.contributor.author | Lechner, Rainer T. | |
| dc.contributor.author | Demitri, Nicola | |
| dc.contributor.author | Redhammer, Guenther J. | |
| dc.contributor.author | Sunger, Nevsal | |
| dc.contributor.author | Suranna, Gian Paolo | |
| dc.contributor.author | Sariciftci, Serdar | |
| dc.date.accessioned | 2026-06-27T13:38:47Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | Hydrogen-bonded pigments are remarkably stable high-crystal lattice energy organic solids. Here a lesser-known family of compounds, the epindolidiones, which demonstrates electronic transport with extraordinary stability, even in highly demanding aqueous environments, is reported. Hole mobilities in the range 0.05-1 cm(2) V-1 s(-1) can be achieved, with lower electron mobilities of up to 0.1 cm(2) V-1 s(-1). To help understand charge transport in epindolidiones, X-ray diffraction is used to solve the crystal structure of 2,8-difluoroepindolidione and 2,8-dichloroepindolidione. Both derivatives crystallize with a linear-chain H-bonding lattice featuring two-dimensional - stacking. Powder diffraction indicates that the unsubstituted epindolidione has very similar crystallinity. All types of epindolidiones measured here display strong low-energy optical emission originating from excimeric states, which coexists with higher-energy fluorescence. This can be exploited in light-emitting diodes, which show the same hybrid singlet and low-energy excimer electroluminescence. Low-voltage FETs are fabricated with epindolidione, which operate reliably under repeated cyclic tests in different ionic solutions within the pH range 3-10 without degradation. Finally, in order to overcome the insolubility of epindolidiones in organic solvents, a chemical procedure is devised to allow solution-processing via the introduction of suitable thermolabile solubilizing groups. This work shows the versatile potential of epindolidione pigments for electronics applications. | en |
| dc.description.sponsorship | Austrian Science Foundation, FWF [Z222-N19, TRP 294-N19] | |
| dc.description.sponsorship | Italian MIUR - PON project Molecular Nanotechnologies for Health and Environment-MAAT [PON02_005633316357 - CUP B31C12001230005] | |
| dc.description.sponsorship | Austrian Science Fund (FWF) [TRP 294] Funding Source: researchfish | |
| dc.description.uri | https://doi.org/10.1002/adfm.201402539 | |
| dc.identifier.doi | 10.1002/adfm.201402539 | |
| dc.identifier.eissn | 1616-3028 | |
| dc.identifier.endpage | 787 | |
| dc.identifier.issn | 1616-301X | |
| dc.identifier.issue | 5 | |
| dc.identifier.startpage | 776 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14981/54130 | |
| dc.identifier.volume | 25 | |
| dc.identifier.wos | 000349225400014 | |
| dc.language.iso | eng | |
| dc.publisher | WILEY-V C H VERLAG GMBH | |
| dc.relation.ispartof | ADVANCED FUNCTIONAL MATERIALS | |
| dc.subject | hydrogen-bonds | |
| dc.subject | organic semiconductors | |
| dc.subject | indigoids | |
| dc.subject | organic electronics | |
| dc.subject | organic field-effect transistors | |
| dc.subject | organic pigments | |
| dc.subject | OPTICAL PROBES | |
| dc.subject | FILMS | |
| dc.subject | INDIGO | |
| dc.subject | QUINACRIDONES | |
| dc.subject | STATES | |
| dc.subject | Chemistry | |
| dc.subject | Science & Technology - Other Topics | |
| dc.subject | Materials Science | |
| dc.subject | Physics | |
| dc.title | Epindolidiones-Versatile and Stable Hydrogen-Bonded Pigments for Organic Field-Effect Transistors and Light-Emitting Diodes | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.import.source | WOS |