We designed novel thermally activated delayed fluorescence (TADF) host molecules for blue electrophosphorescence by combining electron donor acridine derivatives and the electron acceptor 3,4,5-triphenyl-1,2,4-triazole (TPT) unit into a single molecule based on density functional theory (DFT). We obtain the energies of the first singlet (S1) and first triplet (T1) excited states of TADF materials by performing DFT and time-dependent DFT (TD-DFT) calculations on the ground state using dependence on charge transfer amounts for the optimal Hartree-Fock percentage in the exchange-correlation of TD-DFT. The host molecules retained high triplet energy and showed great potential for use in blue phosphorescent organic light-emitting diodes. The results showed that these molecules are promising TADF host materials because they have a low barrier to hole and electron injection, a balanced charge transport for both holes and electrons, and a small energy difference (ΔEST) between the S1 and T1 states.