Charge Transport in Organic Semiconducting Crystals Exhibiting TADF: Insight from Quantum Chemical Calculations

Luminophores featuring thermally activated delayed fluorescence (TADF) are the workhorses of the third- and fourth-generation OLEDs. While these compounds have usually been used as dopants embedded in the host, non-doped TADF OLEDs have recently shown significant progress as well and have attained performances comparable to those of the host-dopant systems. For efficient operation of non-doped OLEDs, the charge transport in neat films and single crystals of TADF luminophores is important; however, this issue was nearly unexplored theoretically. In the current study, we calculated the charge-carrier mobilities in four single crystals of TADF luminophores that have different molecular packing motifs. Specifically, in one of them both the donor and acceptor moieties form uniform pi-stacks, while in the others the donors (acceptors) show alternating lateral shifts along the stacks; the difference in the molecular packing resulted in the difference in the transfer integrals between the molecules. The reorganization energies differed as well by up to four times for the studied crystals. As a result, the charge mobilities varied from 0.001 to similar to 0.3 cm(2)/(V center dot s), with the largest being predicted for the crystal of the luminophore that consisted of a rigid donor and acceptor. We anticipate that the results obtained will be useful in the design of TADF luminophores for non-doped OLEDs, OLETs, and other organic light-emitting devices.

Automated summary

In this study, the charge-carrier mobilities in four single crystals of TADF luminophores with different molecular packing motifs were calculated. The results show that the molecular packing affects the transfer integrals between the molecules, leading to different charge mobilities.