Two pyridine-containing bipolar host materials with high
triplet energy, 9,10-dihydro-9,9-dimethyl-10-(3-(6-(3-(9,9-dimethylacridin-10(9H)-yl)phenyl)pyridin-2-yl)phenyl acridin (DDMACPy) and N-(3-(6-(3-(diphenyl amino)phenyl)pyridin-2-yl)phenyl)-N-phenylbenzenamine (DTPAPy), are synthesized from the modification
of the commonly adapted host material 2,6-bis(3-(9H-carbazol-9-yl)phenyl)pyridine (DCzPPy). The highest occupied molecular
orbital levels of DDMACPy (5.50 eV) and DTPAPy (5.60 eV) are found
to be shallower than that of DCzPPy (5.90 eV) that leads to the improvement
in hole injection from the hole transport layer PEDOT:PSS (WF = 5.10
eV). These host materials are used in the emitting layer of bluish-green
organic light-emitting diode (OLED) with the thermally activated delayed
fluorescence (TADF) emitter, 9,9-dimethyl-9,10-dihydroacridine-2,4,6-triphenyl-1,3,5-triazine,
as the guest. The DDMACPy-based device shows the highest performance
among them, with the maximum external quantum efficiency (EQEmax), current efficiency (CEmax), and power efficiency
(PEmax) of 21.0%, 53.1 cd A–1, and 44.0
lm W–1 at CIE (0.17, 0.42), respectively. By further
doping with the red-emitting phosphor iridium(III) bis(2-phenylquinoline)(2,2,6,6-tetramethylheptane-3,5-ionate)
[Ir(dpm)PQ2] and yellow-emitting phosphor iridium(III)
bis(4-(4-t-butylphenyl)thieno[3,2-c]pyridinato-N,C20)acetylacetonate (PO-01-TB) emitters into the bluish-green
emitting layer, a TADF–phosphor hybrid white OLED (T–P
WOLED) is obtained with excellent EQEmax, CEmax, and PEmax of 17.4%, 48.7 cd A–1, and
44.5 lm W–1 at CIE (0.35, 0.44), respectively. Moreover,
both the bluish-green and WOLED show a low efficiency roll-off with
external quantum efficiencies at the brightness of 1000 cd m–2 (EQE1000) of 18.7 and 16.2%, respectively, which are
the highest performance records among the solution-processed TADF
bluish-green and T–P WOLEDs.