“…In particular, Dexter energy transfer between the triplet states of the TADF and fluorescent molecules must be largely precluded in order to avoid the generation of nonradiative triplet excitons (T 1 FE ) on the fluorescent emitters. − The important question that then arises is whether Dexter energy transfer could be minimized by a rational choice of the fluorescent emitter. Here, in order to address this question, we have investigated the electronic structure of a series of fluorescent emitters (see Figure ) that were recently used in hyperfluorescence-based OLED devices: 2,5,8,11-tetra- tert -butylperylene (TBPe), ,,,, 9,10-bis[ N , N -di( p -tolyl)-amino]anthracene (TTPA), ,− 2,8-di- tert -butyl-5,11-bis(4- tert -butylphenyl)-6,12-diphenyltetracene (TBRb), ,,,,− 5,6,11,12-tetraphenyltetracene (rubrene), − and tetraphenyldibenzoperiflanthene (DBP), ,, and terrylene …”