Thermally-activated delayed fluorescence (TADF) materials have emerged as next-generation emitters for organic light-emitting diodes (OLEDs).The donor-σ-acceptor mol. is a promising paradigm for developing TADF, but its radiative decay rate (kr,s) and photoluminescent efficiency (ΦPL) require large improvements, due to weak intramol. charge-transfer (CT).Here, efficient donor-σ-acceptor emitters (1-3) with strengthened intramol. CT are developed by directly linking the donor and acceptor with a short alkyl chain. 9,9-dimethyl-9,10-dihydroacridine and 2,4,6-triphenyl-1,3,5-triazine are employed as the donor and acceptor, resp., and -CH2- (for 1), -CH2CH2- (for 2) and -CH2CH2CH2- (for 3) are employed as the σ-linkers.The chem. structures of 1-3 have been verified by X-ray crystallog.In dilute solution and lightly doped films, emitters 1-3 show considerably strong intramol. CT, due to the σ-π hyperconjugation between the donor/acceptor and the alkyl σ-linker.In the 20 weight% doped films, emitters 1-3 show green-blue TADF with combined intra- and inter-mol. CT, with high ΦPLkr,s and reverse intersystem crossing rates up to 0.91, 8.5 x 106 s-1 and 2.6 x 106 s-1, resp.OLEDs based on emitters 1-3 show green-blue emission with high external quantum efficiencies (EQEs) over 20 %.A hyperfluorescent OLED with emitter 3 as the sensitizer and a typical multiple resonance emitter (DtBuCzB) as the terminal emitter shows narrowband blue-green emission with a high EQE of 28.1 %.