SummaryThe design of blue fluorescent materials combining both deep-blue emission (CIEy<0.06) and high-efficiency climbing over the typically limited exciton production efficiency of 25% is a challenge for organic light-emitting diodes (OLEDs). In this work, we have synthesized two blue luminogens, trans-9,10-bis(2-butoxyphenyl)anthracene (BBPA) and trans-9,10-bis (2,4-dimethoxyphenyl)anthracene with high photoluminescence quantum yields (PLQYs) of 89.5% and 87.0%, respectively. Intriguingly, we have proposed a strategy to avoid aggregation-caused quenching, which can effectively reduce the undesirable excimeric emission by introducing two host matrices with twisted molecular structure, 9,10-di(naphth-2-yl) anthracene and 10,10′-bis-(4-fluorophenyl)-3,3′-dimethyl-9,9′-bianthracene (MBAn-(4)-F), in the BBPA emission layer. The device containing the EML of BBPA-doped MBAn-(4)-F exhibited a high external quantum efficiency of 10.27% for deep-blue emission with the Commission International de L'Eclairage CIE coordinates of (0.15, 0.05) via the steric effect. Importantly, this represents an advance in deep-blue-emitting fluorescent OLED architectures and materials that meet the requirements of high-definition display.

A common obstacle of many organic semiconductors is that they show highly unipolar charge transport. This unipolarity is caused by trapping of either electrons or holes by extrinsic impurities, such as water or oxygen. For devices that benefit from balanced transport, such as organic light-emitting diodes, organic solar cells and organic ambipolar transistors, the energy levels of the organic semiconductors are ideally situated within an energetic window with a width of 2.5 eV where charge trapping is strongly suppressed. However, for semiconductors with a band gap larger than this window, as used in blue-emitting organic light-emitting diodes, the removal or disabling of charge traps poses a longstanding challenge. Here we demonstrate a molecular strategy where the highest occupied molecular orbital and lowest unoccupied molecular orbital are spatially separated on different parts of the molecules. By tuning their stacking by modification of the chemical structure, the lowest unoccupied molecular orbitals can be spatially protected from impurities that cause electron trapping, increasing the electron current by orders of magnitude. In this way, the trap-free window can be substantially broadened, opening a path towards large band gap organic semiconductors with balanced and trap-free transport.

The application of exciplex energy has become a unique way to achieve organic light-emitting diodes (OLEDs) with high efficiencies, low turn-on voltage, and low roll-off. Novel δ-carboline derivatives with high triplet energy (T ≈ 2.92 eV) and high glass transition temperature (T ≈ 153 °C) were employed to manipulate exciplex emissions in this paper. Deep blue (peak at 436 nm) and pure blue (peak at 468 nm) thermally activated delayed fluorescence (TADF) of exciplex OLEDs were demonstrated by utilizing them as emitters with the maximum current efficiency (CE) of 4.64 cd A, power efficiency (PE) of 2.91 lm W, and external quantum efficiency (EQE) of 2.36%. Highly efficient blue phosphorescent OLEDs doped with FIrpic showed a maximum CE of 55.6 cd A, PE of 52.9 lm W, and EQE of 24.6% respectively with very low turn on voltage at 2.7 V. The devices still remain high CE of 46.5 cd A at 100 cd m, 45.4 cd A at 1000 cd m and 42.3 cd A at 5000 cd m with EQE close to 20% indicating low roll-off. Manipulating blue exciplex emissions by chemical structure gives an ideal strategy to fully utilize all exciton energies for lighting of OLEDs.

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