We have investigated, by means of steady-state and time-resolved optical spectroscopies, the excited-state dynamics of the luminescent europium complex Eu-III(tta)(3)dpbt (ua = henoyltrifluoroacetonate; dbpt = 2-(N,N-diethylanilin-4-yl)-4,6-bis(3,5-dimethylpyrazol-1-yl)-1,3,5-triaz ine) with Gd-III(tta)(3)dpbt and Tb-III(tta)(3)dpbt as the reference complexes that cannot be photosensitized. In the Eu-III(tta)(3)dpbt complex, the ligand dpbt exhibited biphasic fluorescence decay kinetics; the faster component (decay time constant, 8.5 ps) is ascribed to the rapid conversion of the lowest-lying singlet excited state of dpbt (S-1 or (1)dpbt*) to a ligand-to-metal charge transfer singlet state of the complex ((LMCT)-L-1*), whereas the slower one (1.8 ns) is shown by temperature-dependent luminescence spectroscopy to be delayed fluorescence due to the LMCT-to-dpbt backward energy transfer and represents the time scale of efficient excitation energy flow from the (LMCT)-L-1* state to the state of Eu-III. On the basis of the spectroscopic results of the Ln(III)(tta)(3)dpbt complexes (Ln = Eu, Gd, and Tb), the crucial role of the (LMCT)-L-1* state in photosensitization of the Eu-III(tta)(3)dpbt complex is established, and a LMCT-mediated nontriplet sensitization mechanism is proposed, which is advantageous in high efficiency and low excitation photon energy as well as in low susceptibility against oxygen quenching.