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To evaluate the effect of flux, activator and co‐activator on solid state synthesis of SrAl₂O₄: Eu^2 +, Dy^3 + phosphor, where boric oxide, europium oxide and dispersium oxide were used, respectively.

To optimise synthesis condition of long lasting phosphorescence SrAl₂O₄ phosphor, boric oxide was used as a flux. To improve relative intensity of SrAl₂O₄: Eu^2 + phosphor, the critical concentration of Eu^2 + was determined. The effect of various concentration of co‐activator on afterglow properties, the effect of Dy^3 + ion on the emission and excitation spectra were examined.

The SrAl₂O₄: Eu^2 +, Dy^3 + phosphor powders have been synthesised by solid state reaction method. The result of XRD patterns indicated that, addition of 5 mol% B₂O₃ enhanced the formation of SrAl₂O₄ at 1,200°C. Investigation on the variation of emission intensity of different phosphors containing different amounts of Eu^2 + revealed that after 6 mol% of Eu^2 + concentration, quenching process occurred. Dy^3 + formed trap levels and results demonstrated that increasing concentration of Dy^3 + up to 5 mol% reduced the relative intensity and increased the decay time.

Using B₂O₃ as a flux and solid state reaction method for preparation of this phosphor is in good agreement with industrial production and make it economic, because of reduced sintering temperature.

The purpose of this paper is to evaluate the effect of copolymer and starting material concentrations in homogeneous precipitation synthesis of Yttria nanoparticles and red‐emitting nanophosphors Y₂O₃:Eu³⁺. N‐isopropylacrylamide and acrylic acid (NIPAM/AAc) and urea are used.

To optimise synthesis condition of Y₂O₃:Eu³⁺ nanophosphor NIPAM/AAc copolymer was used as a modifier and the effect of various concentration of yttrium ions, urea and precipitation time on size, morphology and emission spectra were investigated.

Using NIPAM/AAc copolymer shows significant improvement on size and dispersion of nanoparticles. It is found that yttrium concentration, varying between 0.006 and 0.03 M, has a profound impact on the average size of particles, which systematically increases from 65 to over 165 nm. The rate of precipitation reaction, however, is shown to be independent of yttrium concentration. In contrast, as urea concentration increases from 0.2 to 5 M, the average particle size exhibits a gradual decrease from 183 to 70 nm. At extremely high urea concentration such as 5 M, a significant level of inter‐particle agglomeration is observed.

Based on this paper, the authors have successfully prepared some promising nanophosphors. The nanoparticles are studied by X‐ray diffraction, transmission electronic microscopy, zeta sizer, Infra red and photoluminescence spectroscopy.