Abstract
Donor-acceptor (D-A) conjugated polymers often possess a significant frontier molecular orbital overlap because of the conjugation elongation, leading to no thermally activated delayed fluorescence (TADF) caused by a large singlet-triplet energy splitting (▵EST ). Herein a novel steric locking strategy is proposed by incorporating methyl groups into D-A conjugated polymers. Benefitting from the methyl hindrance, the torsion between the donor and acceptor can be well tuned to form a sterically-locked conformation, so that the unwanted relaxation toward planarity and thus conjugation elongation is prevented to boost hole-electron separation. The resultant D-A conjugated polymer achieves an extremely low ΔEST of 0.09 eV to enable efficient TADF. The corresponding doped and non-doped devices are fabricated via a solution process, revealing a record-high external quantum efficiency (EQE) of 24.0 % (79.4 cd A-1 , 75.0 lm W-1 ) and 15.3 % (50.9 cd A-1 , 47.3 lm W-1 ).
Published Version
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