Focusing on the photoinduced electron transfer properties of the D-D-A molecule ((TPA-TT)-BODIPY-C 60 ) in an external electric field (F ext ), the excited-state properties in which the double-donor molecule is excited to form three chargeseparated states were simulated. The charge-transfer processes of these three charge-separated states were investigated by considering the two donors as a whole ((TPA-TT-BODIPY)• + -C 60 • − ) as a comparison object. The electronic coupling (V DA ), reorganization energy (λ), and free energy (ΔG) of the different charge-separated states in F ext were calculated and simulated. The calculated results show that the λ of (TPA-TT-BODIPY)• + -C 60 • − ranges from 0.576 to 0.51 eV, and the calculated ΔG of exciton dissociation ranges from −1.402 to −1.143 eV, indicating that exciton dissociation occurs in the Marcus inverted region. In the range of F ext = −10 × 10 −5 to 10 × 10 −5 au, the trend of the charge-transfer rate is gradually increasing, and the rate increase is mainly from the V DA and ΔG changes. Moreover, the rapid formation of the (TPA-TT)-BODIPY• + -C 60 • − charge-separated state and the formation of the long-lived (TPA-TT)• + -BODIPY-C 60 • − are indicated by the exciton dissociation rate. By studying the charge-transfer parameters under different electric field directions, it is found that the regulation of electric field strength on the charge-transfer rate is consistent. These results provide a feasible method for the rational design of a new type of electron transfer process with high efficiency of the D-D-A system.