Luminescence properties of lanthanide(III) ions in concentrated carbonate solution

Abstract

Luminescence properties of lanthanide(III) ions (Ln = Nd, Sm, Eu, Gd, Tb, Dy and Tm) were investigated by measuring the excitation and emission spectra, and emission lifetimes in H2O and D2O solutions of 3 moll−1 K2CO3, where anionic tetra-carbonate complexes, [Ln(CO3)4]5- were the predominant species. Electronic transitions of the carbonato complex corresponding to both the excitation and emission spectra were assigned from the energy level diagrams of Ln(III) and compared with those of the aqua ion. Enhancement of emission intensity of the complex was observed at particular excitation transitions of Eu(III), Gd(III) and Tb(III), and at particular emission transitions of Sm(III), Eu(III), Dy(III) and Tm(III). The enhancement at the emission transition was estimated quantitatively as a branching ratio from the lowest emitting state of Ln(III), and discussed in terms of hypersensitivity. Emission lifetimes of the carbonato complexes were all longer than those of aqua ions in H2O solution, while the lifetimes of the complexes for Eu(III) and Tb(III) shorter than those in D2O solution. The difference in non-radiative decay constants for the excited complex in H2O and D2O solutions was found to be proportional to an exponential of the energy gap of Ln(III). The lifetime ratio between the H2O and D2O solutions showed the order of Sm > Dy > Eu > Tb, corresponding to the opposite order of the energy gap. These were discussed in terms of an energy gap law, i.e. a relationship between the energy gap of Ln(III) and vibration energies of the ligand or water molecules.