期刊
DYES AND PIGMENTS
卷 219, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2023.111568
关键词
Dibenzo[ a; c ]phenazine; Orange-red emitter; Isomer; Thermally activated delayed fluorescence; Organic light-emitting diodes
In this study, two pairs of asymmetric isomers based on electron-donor units and electron-deficient moieties were designed and synthesized. Their photophysical properties were finely modulated by changing the position and number of certain groups. The results showed that the asymmetric and isomeric molecular design is a potential strategy for promoting the development of highly efficient long-wavelength thermally activated delayed fluorescence materials.
It is an immense challenge to develop efficient long-wavelength (orange-to-red) thermally activated delayed fluorescence (TADF) materials due to the increasing nonradiative decay rates following the energy-gap law. Herein, two pairs of asymmetric isomers; DPyPzTPA and TPAPzDPy, and PyPzDTPA and DTPAPzPy based on electron-deficient moieties dibenzo[a,c]phenazine (Pz) and pyridine (Py) combined with electron-donor units of triphenylamine (TPA) were designed and synthesized. Their photophysical properties could be finely modulated by changing the position and number of Py groups as well as TPA fragments onto Pz cores. DPyPzTPA and DTPAPzPy possess much more rigidity and thus less geometry relaxation and non-radiative decay between ground states and excited states than those of PyPzDTPA and TPAPzDPy. Intriguingly, DPyPzTPA exhibits the highest relative photoluminescence quantum yield (& phi;PL) and the fastest reverse intersystem crossing (rISC) rate among them owing to relatively stronger rigidity and spin-orbit coupling (SOC) interactions between the lowest singlet (S1) and energetically close-lying excited triplet state and therefore, the device showed the highest maximum external quantum efficiency (EQEmax) of 16.6% (60.9 lm/W, 53.3 cd/A) with Commission Internationale de I'Eclairage (CIE) coordinates of (0.43, 0.55), peak wavelength 556 nm. In stark contrast, due to its lower rigidity and extremely weak delayed fluorescence (DF) characteristic and thus the much lower & phi;PL, TPAPzDPy-based devices are only half as efficient (30.8 lm/W, 27.5 cd/A, 8.3% EQE) despite the isomers possessing equal singlet-triplet energy gaps (& UDelta;EST) of 0.43 eV. On the other hand, the device based on DTPAPzPy also demonstrated a strongly enhanced performance (59.1 lm/W, 52.7 cd/A, 16.1% EQE) than its isomer PyPzDTPA-based device (39.5 lm/W, 35.2 cd/A, 10.3% EQE). This work explicitly implicates that the asymmetric and isomeric molecular design is a potential strategy for promoting the development of highly efficient long-wavelength TADF materials.
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