Thermally activated delayed fluorescence (TADF) polymer has great potential for the construction of flexible solution-processed organic light-emitting diodes (OLEDs). However, the relationship between polymerization engineering and device functions has rarely been reported. Here, two novel TADF polymers, P-Ph4CzCN and P-Ph5CzCN, with a small energy gap between the first excited singlet and triplet states (ΔEST; <0.16 eV) were newly developed by both solvent and in situ polymerization of a styrene component. Detailed device performance testing indicates that both polymerization strategies ensure that the TADF polymer achieves comparable high efficiencies in commonly rigid devices, and the maximum external quantum efficiencies (EQEmax) were 11.9%, 14.1%, and 16.2% for blue, green, and white OLEDs, respectively. Although in situ polymerization provides a simplified device fabrication process, which avoids the complicated synthesis and purification of the polymer, the inevitable high-temperature annealing makes it fail in a plastic substrate device. In contrast, P-Ph5CzCN achieved by solvent polymerization enables the successful fabrication of a flexible device on a poly(ethylene terephthalate) (PET) substrate, which was the first reported flexible OLED based on a TADF polymer. This work provides a strong guideline for the simple fabrication of TADF polymer devices and the application of TADF polymer materials in OLED flexible panels and flexible lighting.
Keywords: TADF; flexible WOLEDs; in situ polymerization; polymer; solution-processed OLEDs.