Recently, various host materials have been developed for solution-processed thermally activated delayed fluorescent organic light-emitting diodes (TADF-OLEDs). Compared with small-molecule hosts, polymeric hosts are advantageous for inducing a uniform distribution and segregation of dopant molecules in the emissive layer without undesired large-scale phase separation. In this study, new polymer hosts were demonstrated, in which a bipolar conjugative moiety consisting of a carbazole (Cz) donor and an α-carboline (α-Cb) acceptor was bound to the polystyrene backbone through a non-conjugated linker. They exhibited high triplet energies of >2.8 eV, and their emission spectra overlapped with the absorption spectrum of a green TADF emitter, which allowed facile energy transfer from the polymeric host to the small-molecule dopants. High device performance was observed, with external quantum efficiencies (EQEs) of 13.65, 17.09, and 17.48% for solution-processed green TADF-OLEDs using PSCzCz, PSCzCb, and PSCbCz, respectively, as hosts for the EML. The EQEs of bipolar host (PSCzCb and PSCbCz)-based devices were higher than those of unipolar host (poly(N-vinylcarbazole) and PSCzCz)-based devices owing to the well-balanced charge-carrier transport. According to these results, the polymeric host bearing a bipolar Cz and α-Cb coupled moiety is a promising material for solution-processable TADF-OLEDs.
Keywords: carbazole; carboline; polymer light-emitting diode; polymeric host; solution process; thermally activated delayed fluorescent.