Multifunctional donor–acceptor compound 4,4′-bis(dibenzothiophene-S,S-dioxide-2-yl)triphenylamine (DSTPA) was obtained by linking a strongly electron-withdrawing core and a strongly electron-donating core with a biphenyl bridge in linear spatial alignment. DSTPA not only has suitable HOMO and LUMO levels for easily accepting both holes and electrons, it was also demonstrated to have a high fluorescence quantum yield of 0.98 and a high triplet energy level of 2.39 eV. Versatile applications of DSTPA for bipolar transport, green fluorescent emission, and sensitizing a red phosphor were systematically investigated in a series of multi- and single-layer organic light-emitting devices. In traditional multilayer devices, it shows excellent performance both in an undoped fluorescent device (used as a green emitter and achieving maximum current and power efficiencies (CE and PE) of 12.6 cd A−1 and 9.4 Lm W−1, respectively) and in a red phosphorescent device (used as a host and achieving maximum CE and PE of 26.4 cd A−1 and 26.3 Lm W−1, respectively). Furthermore, DSTPA was also simultaneously used as an emitter, a hole transporter, and an electron transporter in a single-layer device showing CE and PE of 5.1 cd A−1 and 4.7 Lm W−1, respectively. A single-layer red phosphorescent device with efficiencies of 11.7 cd A−1 and 12.6 Lm W−1 was obtained by doping DSTPA with a red phosphor. The performances of all of the devices in this work are comparable to the best of their corresponding classes in the literature.
Chemistry - A European Journal, 2014 Calculated electronic HOMO and LUMO distributions of DSTPA. |
