Phosphor, light-emitting device using same, image display and illuminating device
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example 1
[0086]Raw material powders were measured out such that CeO2 as M1 source compound, CaCO3 as M2 source compound and Sc2O3 as M3 source compound were incorporated in an amount of 0.01 mols, 0.99 mols and 1 mol, respectively, based on 1 mol of phosphor to give a phosphor chemical composition Ce0.01Ca0.99Sc2O4. These raw material powders were wet-ground and mixed with ethanol as a dispersion medium in a powder mixer, and the dispersion medium was then evaporated away to obtain a dried mixture of ground raw material powders. The dried ground mixture thus obtained was heated at 1,600° C. at maximum in a nitrogen atmosphere containing 4% of hydrogen in a platinum crucible for 3 hours so that it was calcined, and then subsequently subjected to washing with water, drying and classification to produce a phosphor powder.
[0087]The median diameter of the thus obtained phosphor measured by a Type LA-300 laser diffraction particle size distribution meter (produced by HORIBA, Ltd.) was 14 μm. The o...
examples 2 to 6
[0091]Phosphors were produced in the same manner as in Example 1 except that the material of the crucible and the calcining temperature during the production of the phosphor were changed as set forth in Table 1.
[0092]The phosphors thus obtained were each identified comprising CaSc2O4 as a host crystal and having trivalent Ce as an activator element in said host crystal by the analysis of powder X-ray diffraction, emission spectrum, and excitation spectrum. The emission peak wavelength and the emission intensity of the phosphors thus obtained are also set forth in Table 1. For the measurement of the emission spectrum of the phosphors of Example 2 and after, a high speed phosphor evaluation device produced by JASCO Corporation was used. This device comprises a Xe lamp as a light source and a Type C7041 multi-channel detector produced by Hamamatsu Photonics K.K. as a light-receiving element.
[0093]The phosphors produced using a platinum crucible showed a high emission intensity, and the...
examples 7 to 11
[0094]Phosphors were produced in the same manner as in Example 1 except that the formulation of mixing of raw materials Ce and Ca of phosphor were changed as set forth in Table 2. The phosphors thus obtained were each identified comprising CaSc2O4 as a host crystal and having trivalent Ce as an activator element in said host crystal by the analysis of powder X-ray diffraction, emission spectrum, and excitation spectrum. The emission peak wavelength and the emission intensity of the phosphors thus obtained are also set forth in Table 2. The phosphors obtained by adjusting the Ce mixing molar ratio to 0.01 showed the highest emission intensity. Further, as the concentration of Ce increased, the emission peak wavelength shifted toward a longer wavelength and a higher color purity green emission was shown.
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