Improving power efficiency (PE) and reducing roll-off are of significant importance for the commercialization of white organic light-emitting diodes (WOLEDs) in consideration of energy conservation. Herein, record-beating PE of 130.7 lm W−1 and outstanding external quantum efficiency (EQE) of 31.1% are achieved in all-fluorescence two-color WOLEDs based on a simple sandwich configuration of emitting layer consisting of sky-blue and orange delayed fluorescence materials. By introducing a red fluorescence dopant, all-fluorescence three-color WOLEDs with high color rendering index are constructed based on an interlayer sensitization configuration, furnishing ultrahigh PE of 110.7 lm W−1 and EQE of 30.8%. More importantly, both two-color and three-color WOLEDs maintain excellent PEs at operating luminance with smaller roll-offs than the reported state-of-the-art WOLEDs, and further device optimization realizes outstanding comprehensive performances of low driving voltages, large luminance, high PEs and long operational lifetimes. The underlying mechanisms of the impressive device performances are elucidated by host-tuning effect and electron-trapping effect, providing useful guidance for the development of energy-conserving all-fluorescence WOLEDs.
As promising luminescent materials for organic light-emitting diodes (OLEDs), thermally activated delayed fluorescence materials are booming vigorously in recent years, but robust blue ones still remain challenging. Herein, we report three highly efficient blue and deep-blue delayed fluorescence materials comprised of a weak electron acceptor chromeno[3,2-c]carbazol-8(5H)-one with a rigid polycyclic structure and a weak electron donor spiro[acridine-9,9’-xanthene]. They hold distinguished merits of excellent photoluminescence quantum yields (99%), ultrahigh horizontal transition dipole ratios (93.6%), and fast radiative transition and reverse intersystem crossing, which furnish superb blue and deep-blue electroluminescence with Commission Internationale de I’Eclairage coordinates (CIEx,y) of (0.14, 0.18) and (0.14, 0.15) and record-beating external quantum efficiencies (ηexts) of 43.4% and 41.3%, respectively. Their efficiency roll-offs are successfully reduced by suppressing triplet-triplet and singlet-singlet annihilations. Moreover, high-performance deep-blue and green hyperfluorescence OLEDs are achieved by utilizing these materials as sensitizers for multi-resonance delayed fluorescence dopants, providing state-of-the-art ηexts of 32.5% (CIEx,y = 0.14, 0.10) and 37.6% (CIEx,y = 0.32, 0.64), respectively, as well as greatly advanced operational lifetimes. These splendid results can surely inspire the development of blue and deep-blue luminescent materials and devices.
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