Developing high-performance host
materials is one of the biggest
challenges for blue and white thermally activated delayed-fluorescence
(TADF) organic light-emitting diode (OLED) technology due to the rigorous
requirements of both efficient carrier flux ability and high triplet
energy (E
T) levels in static donor–acceptor
molecules. Here, with the aid of a dual-resonance strategy, a host
molecule showing dynamic adaption features in the acceptor–resonance–donor–resonance–acceptor
(A–r–D–r–A) molecular configuration has
been successfully developed through the implantation of two acceptors
of diphenylphosphine oxide into electron-donating 5,10-dihydrophenazine
with N–PO resonance linkages. Owing to the dual enantiotropic
N+P–O– resonances, the
designed A–r–D–r–A molecule exhibits an
extraordinarily balanced charge flux transportation attribute at high E
T (2.96 eV). Excitingly, blue and warm-white
TADF OLEDs hosted by the A–r–D–r–A molecule
exhibit outstanding external quantum efficiencies of 14.7 and 20.3%,
respectively. Our studies not only broaden the scope of resonance
molecules but also indicate that a resonance structure is an effective
linkage to develop optoelectronic materials with dynamically adaptive
properties.