A series of bipolar hosts, namely,
5-(2-(9H-carbazol-9-yl)-phenyl)-1,3-dipyrazolbenzene
(o-CzDPz), 5-(3-(9H-carbazol-9-yl)-phenyl)-1,3-dipyrazolbenzene
(m-CzDPz), 5-(9-phenyl-9H-carbazol-3-yl)-1,3-dipyrazolbenzene
(3-CzDPz), and 5-(3,5-di(9H-carbazol-9-yl)-phenyl)-1,3-dipyrazolbenzene
(mCPDPz), are developed for phosphorescent and thermally
activated delayed fluorescence (TADF) organic light-emitting diodes
(OLEDs). They are designed by selecting pyrazole as n-type unit and
carbazole as p-type one. The triplet energy (ET), the frontier molecular orbital level, and charge transporting
abilities, are adjusted by varying the molar ratio of pyrazole to
carbazole and the linking mode between them. They have high ET values of 2.76–3.02 eV. Their electroluminescence
performance is evaluated by fabricating both phosphorescent and TADF
devices with blue or green emitters. The m-CzDPz
hosted blue phosphorescent OLEDs achieves high efficiency of 48.3
cd A–1 (26.8%), the 3-CzDPz hosted green phosphorescent
device exhibits 91.2 cd A–1 (29.0%). The blue and
green TADF devices with 3-CzDPz host also reach high efficiencies
of 26.2 cd A–1 (15.8%) and 41.1 cd A–1 (13.3%), respectively. The excellent performance of all these OLEDs
verifies that these pyrazole-based bipolar compounds are capable of
being universal host materials for OLED application. The influence
of molar ratio of n-type unit to p-type one and the molecular conformation
of these hosts on their device performance is discussed and interpreted.