Hydrated europium(III) orthophosphates EuPO 4 × n H 2 O (rhabdophane) of a nanocrystalline particle size ranging from 5 to 40 nm were precipitated from aqueous solution at neutral pH. The hexagonal crystal structure of the synthesized phase remained stable up to a calcination temperature of 600 °C according to X-ray diffraction (XRD) analysis. The complete loss of water at temperatures exceeding 600 °C caused the transformation into monoclinic nonhydrated EuPO 4 isomorphous to monazite. The typical Eu 3+ luminescence emissions excited at 396 nm for hexagonal EuPO 4 × n H 2 O as well as for the monoclinic nonhydrated EuPO 4 were attributed to magnetic-dipole and vibronic as well as forced electric-dipole 5 D 0 → 7 F J ( J = 1, 2, 3, 4) transitions. If the trivalent europium ion lies on an inversion center, the hypersensitivity is absent. The intensity ratio of the magnetic-dipole 5 D 0 → 7 F 1 transition to the electric-dipole 5 D 0 → 7 F 2 transition decreased with increasing calcination temperature up to 600 °C, indicating the presence of a hypersensitive, forced electric-dipole 5 D 0 → 7 F 2 transition due to the lack of inversion symmetry sites. The loss of water during heating up to 600 °C was considered to be responsible for the variations in the emission characteristics of the EuPO 4 × n H 2 O.
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Zollfrank et al. (2008) studied this question.
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