Fluorine-substituted CaTiO₃:Pr phosphors were prepared by a solid-state reaction. Rietveld refinements of powder X-ray diffraction patterns revealed that increasing fluorine-substitution leads to the gradual shrinkage of the unit-cell. Enhanced afterglow intensities were observed with fluorine-substitution. Furthermore, the effect of annealing atmosphere was investigated by thermochemical treatment in different atmospheres (Ar, air and NH₃). UV-Vis diffuse reflectance spectra and photoluminescence excitation spectra revealed that Pr⁴⁺ in the pristine CaTi(O,F)₃:Pr phosphor was partially reduced to Pr³⁺ under NH₃ flow leading to an intensity improvement of ca. 450% compared to CaTiO₃:Pr. The substantial improvement of afterglow intensity by fluorine substitution and annealing in NH₃ is considered to be connected with the generation of oxygen vacancies and the partial reduction of Pr⁴⁺ to Pr³⁺.

The phosphor CaTiO₃:Pr³⁺ was synthesized via a solid-state reaction in combination with a subsequent annealing under flowing NH₃. Comparatively large off-center displacements of Ti in the TiO₆ octahedra were confirmed for as-synthesized CaTiO₃:Pr³Â by XANES. Raman spectroscopy showed that the local crystal structure becomes highly symmetric when the powders are ammonolyzed at 400 °C. Rietveld refinement of powder X-ray diffraction data revealed that the samples ammonolyzed at 400 °C have the smallest lattice strain and at the same time the largest average Ti-O-Ti angles were obtained. The samples ammonolyzed at 400 °C also showed the smallest mass loss during the thermal re-oxidation in thermogravimetric analysis (TGA). Enhanced photolumincescence brightness and an improved decay curve as well as the highest reflectance were obtained for the samples ammonolyzed at 400 °C. The improved photoluminescence and afterglow by NH₃ treatment are explained as a result of the reduced concentration of oxygen excesses with simultaneous relaxation of the lattice strain.

Red emitting CaTiO₃:Pr phosphors with a nominal composition of Ca_0.998+xPr_0.002TiO_3+δ (0.02≤x≤0.04) were prepared by solid state reactions with different thermal post treatments and characterized by X-ray diffraction, transmission electron microscopy and photoluminescence. The Ca excess exhibited complete solubility up to 4% in the samples treated at 1400 °C but segregation in the form of Ruddlesden-Popper phases (Ca₃Ti₂O₇ - Ca₄Ti₃O₁₀) was observed in samples prepared at 1500 °C. The increase in temperature for stoichiometric samples showed a monotonic increase of decay time due to the reduction of non-radiative recombination defects. It was found that the Ca excess favored the formation of oxygen vacancies which are known to act as trap. In the samples treated at 1400 °C, 3% of Ca excess showed to be the best concentration to increase the decay time of persistent luminescence. For the samples treated at 1500 °C, the segregation of Ruddlesden-Popper phases left a constant amount of Ca soluble in all the CaTiO₃ samples. This constant concentration of Ca caused the same density of defects and, consequently, the same decay time in all samples.