In a series of (Ca2–x/2–yEuy□x/2)(Si1–xPx)O4 (x = 0.06, 0.02 ≤ y ≤0.5), various color-emitting phosphors were successfully synthesized by a solid-state reaction. These phosphors were characterized by photoluminescence (PL) spectroscopy, X-ray powder diffractometry, transmission electron microscopy, and X-ray absorption fine structure spectroscopy. We evaluated the effect of heat treatment on PL properties with various annealing temperatures at 1373–1773 K for 4 h before/after reduction treatment from Eu3+ to Eu2+. In the red-emitting (Ca1.95Eu3+0.02□0.03)(Si0.94P0.06)O4+δ phosphor, the highest PL intensity exhibited when it was annealed at 1773 K. On the other hand, in the green-emitting (Ca1.95Eu2+0.02□0.03)(Si0.94P0.06)O4 phosphor, the highest PL intensity was realized when it was annealed at 1473 K and consequently treated under a reductive atmosphere. With increasing annealing temperature, the emission peak wavelength steadily decreased. Furthermore, with increasing Eu2+ content, the emission peak wavelength increased, with the color of emitting light becoming yellowish. Thus, the PL properties of the phosphors were affected by both the structural change from β to α’L, which occurred by heat treatment, and the amount of doped Eu ions.

We prepared four types of Eu 2 O 3 -and P 2 O 5 -doped Ca 2 SiO 4 phosphors with different phase compositions but identical chemical composition, the chemical formula of which was (Ca 1.950 Eu 3+ 0.013 0.037 )(Si 0.940 P 0.060 )O 4 ( denotes vacancies in Ca sites). One of the phosphors was composed exclusively of the incommensurate (IC) phase with superspace group Pnma(0β0)00s and basic unit-cell dimensions of a = 0.68004(2) nm, b = 0.54481(2) nm, and c = 0.93956(3) nm (Z = 4). The crystal structure was made up of four types of β-Ca 2 SiO 4 -related layers with an interlayer. The incommensurate modulation with wavelength of 4.110 × b was induced by the long-range stacking order of these layers. When increasing the relative amount of the IC-phase with respect to the coexisting β-phase, the red light emission intensity, under excitation at 394 nm, steadily decreased to reach the minimum, at which the specimen was composed exclusively of the IC-phase. The coordination environments of Eu 3+ ion in the crystal structures of βand IC-phases might be closely related to the photoluminescence intensities of the phosphors.

We first successfully synthesized Li1+x−yNb1−x−3yTix+4yO3 (LNT) solid solutions (0.13 ≤ x ≤ 0.18, 0 ≤ y ≤ 0.06) rapidly at 1373 K for one hour under 0.35 MPa by the controlling of air pressure using an air-pressure control atmosphere furnace. The composition is a formation area of a superstructure for LNT, in which the periodical intergrowth layer was formed in the matrix, and where it can be controlled by Ti content. Therefore, the sintering time depended on Ti content, and annealing was repeated for over 24 h until a homogeneous structure was formed using a conventional electric furnace. We clarified the mechanism of the rapid sintering using various microscale to nanoscale characterization techniques: X-ray diffraction, a scanning electron microscope, a transmission electron microscope (TEM), a Cs-corrected scanning TEM equipped with electron energy-loss spectroscopy, and X-ray absorption fine structure spectroscopy.

In this work, we investigated the crystal structure and photoluminescence (PL) property of Ca 2 (Si,P)O 4 :Eu 2+ phosphor doped with Al 3+ ions. Changes in the crystal structure were evaluated via X-ray diffraction and X-ray absorption fine structure measurements. With increasing concentrations of Al and P ions, the crystal structure transforms from β to α' L phase. The emission color of phosphor changes from green to blue. However, Al ions exerted only a modest effect on the crystal structure and PL property of the material compared with the absence of Al ions.