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A succession of Ce3+ and Tb3+ co-doped BaF2 nanoparticles were synthesized by co-precipitation and hydrothermal methods. The structure, morphology, elemental composition and photoluminescence characteristics of the doped samples were studied by X-ray diffractometry (XRD), transmission electron microscopy (TEM), X-ray energy spectrometry (EDX), photoluminescence emission spectroscopy (PL) and photoluminescence excitation spectroscopy (PLE). The phosphor has a cubic structure. According to the energy level relationship between Ce3+ and Tb3+, the energy transfer mechanism of Ce3+ and Tb3+ co-doped BaF2 samples was analyzed. Ce3+, Tb3+ co-doped BaF2 shows a strong green emission, and its fluorescence emission intensity is about 9 times higher than that of Tb3+ single doped BaF2. The energy transfer efficiency from Ce3+ to Tb3+ was calculated using a formula, and it was found that the energy transfer efficiency could reach up to 88.22%. The detection solution was prepared by uniformly dispersing the phosphor in absolute ethanol. Through a comparative study of a series of metal ions, it was found that the detection solution has a peculiar sensitivity to aqueous solutions containing Cu2+. At the same time, the relationship between the fluorescence intensity of the detection solution and the concentration of Cu2+ was studied, and the cause of fluorescence quenching caused by Cu2+ ions was analyzed from the perspective of energy transfer. From this work, it is considered that the phosphor has a great potential application in the determination of Cu2+ in practical wastewater. [ABSTRACT FROM AUTHOR]

Phase pure BaF2 doped with Ce3+ (0.1%) nanocrystals are synthesized using an ionic liquid (IL) ([C4mim][BF4]) assisted solvothermal method where the IL is not only used as a reaction medium and a capping agent, but also as a reaction partner. Subsequently, upon calcining the as-prepared nanocrystals at various temperatures (200, 400, 600 and 800 °C), athough the crystal phase remains the same, however, a significant change in the lattice strain and morphology is observed. Tensile strain appears in the nanocrystals calcined at temperatures up to 400 °C, but a reversal of the strain, i.e. compressive strain, takes place when calcination is performed at 600 °C and onwards. Nanoflakes are obtained until calcination at 400 °C. However on calcination at 600 °C and beyond, a drastic modification in the morphology is observed. Layer or step-like structures appear due to secondary nucleation of nanoparticles. Meanwhile, the photoluminescence (PL) intensity of Ce3+ ions gradually decreases with the calcination temperature and finally vanishes at 600 °C/800 °C. To investigate the reasons for the quenching of the PL intensity, thermally stimulated luminescence (TSL) and thermally stimulated exoelectron emission (TSEE) measurements are performed. The TSL and TSEE results indicate that in addition to the domination of deeper electron traps that appear as a high-temperature shift of TSEE glow peaks for both 600 °C and 800 °C, some new types of defects like F vacancies (F-centers) can be present, especially in the 800 °C calcined sample. The conditions leading to the quenching of Ce3+ luminescence in the nanoparticles are analyzed and discussed. [ABSTRACT FROM AUTHOR]