High-efficiency solution-processed green thermally activated delayed fluorescence OLEDs using a polymer-small molecule mixed host
Literature Information
Seunguk Cho, Na Yeon Kwon, Chai Won Kim, Hyoseong Lee, Jung Min Ha, Hyung Jong Kim, Han Young Woo, Sungnam Park, Min Ju Cho, Dong Hoon Choi
The development of suitable host materials for application to an emitter is of significant importance for high-efficiency organic light-emitting diodes (OLEDs). In this study, we successfully synthesized poly(9,9-diphenyl-10-(4-vinylbenzyl)-9,10-dihydroacridine) (P(Bn-DPAc)) as a polymer donor and 2-(4′-(tert-butyl)-[1,1′-biphenyl]-4-yl)-4,6-diphenyl-1,3,5-triazine (tPTRZ) as a small-molecule acceptor. A blend of P(Bn-DPAc) and tPTRZ was used as the host material in solution-processed green thermally activated delayed fluorescence OLEDs (TADF-OLEDs). The P(Bn-DPAc)–tPTRZ blend showed a new red-shifted peak in the photoluminescence spectrum, suggesting the possibility of exciplex formation. The polymer-mixed host film showed a fine surface morphology, a well-formed exciplex in the bulk state, and good charge balance. The OLED fabricated with the as-prepared mixed host (P(Bn-DPAc) : tPTRZ = 1 : 1 wt ratio) and 2,4,5,6-tetra(3,6-di-tert-butylcarbazol-9-yl)-1,3-dicyanobenzene (t4CzIPN) emitter exhibited a high current efficiency of 107.3 cd A−1 and a maximum external quantum efficiency (EQE) of 31.2%. The OLED fabricated with the mixed host demonstrated better performance compared to the device with a unipolar host P(Bn-DPAc).
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