A solid-state reaction method was used to synthesize Ca2+x MgSi2Eu0.025O7+x (x = 0-1.0) powders in the air atmosphere and in a reduction atmosphere (95% N2 + 5% H2) at 1350 °C and 4 h, and the reduction atmosphere was removed at 800 °C. Only the Ca2MgSi2O7 phase was found in the XRD pattern of the synthesized Ca2MgSi2Eu0.025O7 powder. The first important discovery was that when the x value of Ca2+x MgSi2Eu0.025O7+x powders was increased from 0.2 to 0.8, both Ca2MgSi2O7 and Ca3MgSi2O8 phases coexisted in the synthesized Ca2+x MgSi2Eu0.025O7+x powders, and the diffraction intensity of the Ca2MgSi2O7 (Ca3MgSi2O8) phase decreased (increased) with the x value. The second important discovery was that the Ca2MgSi2Eu0.025O7 phosphor exhibited stronger photoluminescence excitation (PLE), photoluminescence (PL), and decay curve properties than the Ca2.2MgSi2Eu0.025O7.2 phosphor, and the Ca3MgSi2Eu0.025O8 phosphor exhibited stronger PLE, PL, and decay curve properties than the Ca2+x MgSi2Eu0.025O7+x phosphors for x = 0.4, 0.6, and 0.8. For x = 0.2-0.8, the PL spectra of the Ca2+x MgSi2Eu0.025O7+x phosphors were a combination of the PL spectra of Ca2MgSi2Eu0.025O7 and Ca3MgSi2Eu0.025O8 phosphors. The third important discovery was that as the x value was increased, the maximum emission peak wavelengths of the Ca2+x MgSi2Eu0.025O7+x phosphors shifted to a lower value, the maximum emission intensity of the PL spectra increased, and the emission light changed from green and cyan to blue.
© 2022 The Authors. Published by American Chemical Society.