6533b861fe1ef96bd12c4f29

RESEARCH PRODUCT

Flexible diphenylsulfone versus rigid dibenzothiophene-dioxide as acceptor moieties in donor-acceptor-donor TADF emitters for highly efficient OLEDs

Tien-lung ChiuDmytro VolyniukJuozas V. GrazuleviciusChia-hsun ChenHans ÅGrenHans ÅGrenOleksandr BezvikonnyiBoris F. MinaevDalius GudeikaDalius GudeikaJiun-haw LeeGleb V. BaryshnikovPei-hsi Lee

subject

Electron mobilityPhotoluminescenceMaterials science02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiomaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculeMoietySinglet stateDibenzothiophene dioxideElectrical and Electronic Engineeringdi-tert-butyldimethyldihydroacridineGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsDiphenylsulfoneAcceptor0104 chemical sciencesElectronic Optical and Magnetic MaterialsThermally activated delayed fluorescencQuantum efficiency0210 nano-technologyBipolar charge transport

description

DG acknowledges funding from the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177 . This research is/was funded by the European Regional Development Fund according to the supported activity ‘ Research Projects Implemented by World-class Researcher Groups ’ under Measure No. 01.2.2-LMT-K-718 . Ministry of Science and Technology (MOST), Taiwan , Grant No. MOST 106-2923-E-155-002-MY3 . This work was also supported by the Ministry of Education and Science of Ukraine (projects no. 0117U003908 and 0118U003862 ), and by the Olle Engkvist Byggmästare foundation (contract No. 189-0223 ). The quantum-chemical calculations were performed with computational resources provided by the High Performance Computing Center North (HPC2N) in Umeå, Sweden, through the project ‘‘Multiphysics Modeling of Molecular Materials” SNIC 2018-2-38.

10.1016/j.orgel.2020.105733http://dx.doi.org/10.1016/j.orgel.2020.105733