Abstract
Trivalent europium (Eu(III)) complexes emit narrow-band luminescence as a result of energy transfer following the photoexcitation of antenna ligands. Bidentate β-diketonates are typically used as antenna ligands; however, their entire energy transfer mechanism to Eu(III) remains unknown. We used time-resolved photoluminescence spectroscopy and femtosecond transient absorption spectroscopy to map the complete intramolecular energy transfer process in the [Eu(hfa)(3)(TPPO)(2)] (hfa = hexafluoroacetylacetonate, TPPO = triphenylphosphine oxide) complex; hfa is a β-diketonate antenna ligand. Our analysis provides a "full picture" of energy transfer, tracing each step from initial photoexcitation to final relaxation: intersystem crossing in the ligands, energy transfer from the ligands to the metal center, and multiple internal conversion of Eu(III). We demonstrated that the direct bonds of the bidentate ligands enabled a quick and near-unity-efficiency energy transfer from the triplet state of the ligand to the (5)D(2) state of Eu(III). We also revealed that the loss of the ligand-centered intersystem crossing process reduces the overall sensitization efficiency. Our findings provide a foundation for the rational design of advanced luminescent materials, paving the way for advances in lanthanide-based luminescence research.