Complex oxynitride phosphor, light-emitting device using same, image display, illuminating device, phosphor-containing composition and complex oxynitride
a technology of complex oxynitride and phosphor, which is applied in the direction of discharge tube/lamp details, luminescent compositions, and discharge tubes luminescnet screens, etc., can solve the problems of low emission efficiency decrease, insufficient conversion efficiency of blue or near-ultraviolet light, and insufficient green phosphors. , to achieve the effect of high power, low emission efficiency and high efficiency
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[0562]In the following, the present invention will be explained in more detail using Examples. It is to be understood that the present invention is by no means limited by the following examples insofar as they do not depart from the intent of the invention.
[1. Method for Measurement and Evaluation of Phosphor]
[0563]Various evaluations of phosphor particles were carried out by the following methods in each Example and Comparative Example to be described later.
[0564][Method for Measuring Emission Spectrum]
[0565]The emission spectrum was measured by using a fluorescence measurement apparatus (manufactured by JASCO corporation) equipped with an excitation light source of 150-W xenon lamp and a spectrum measurement apparatus of multichannel CCD detector, C7041 (manufactured by Hamamatsu Photonics K.K.). The light from an excitation light source was passed through a grating monochromator with focal length of 10 cm to separate a light having wavelength of 340 nm, 400 nm or 455 nm, and the ...
production examples 1 to 12
[0617]Each of BaCO3, SiO2, Si3N4 and Eu2O3 was used in the amount shown in Table 1, in order to realize a nominal chemical composition ratio shown in Table 2, and mixing and firing were performed.
TABLE 1[Table 1: Amounts of materials used]Production ExampleBaCO3SiO2Si3N4Eu2O313.08 g1.89 g0.00 g0.03 g22.83 g1.74 g0.41 g0.03 g32.62 g1.61 g0.75 g0.02 g42.52 g1.55 g0.91 g0.02 g52.43 g1.49 g1.05 g0.02 g62.27 g1.40 g1.31 g0.02 g72.14 g1.31 g1.53 g0.02 g82.01 g1.24 g1.73 g0.02 g91.90 g1.17 g1.91 g0.02 g101.80 g1.11 g2.070.02 g111.71 g1.05 g2.22 g0.02 g121.63 g1.01 g2.25 g0.02 g
TABLE 2[Table 2: Nominal chemical composition ratio]Nominal chemical compositionFiring conditionProduction Example 1B0.99Eu0.01Si2O51600° C. 2 hr + 1800° C. 2 hrProduction Example 2B0.99Eu0.01Si2.6N0.4O51600° C. 2 hr + 1800° C. 2 hrProduction Example 3B0.99Eu0.01Si3.2N1.6O51600° C. 2 hr + 1800° C. 2 hrProduction Example 4B0.99Eu0.01Si3.5N2O51600° C. 2 hr + 1800° C. 2 hrProduction Example 5B0.99Eu0.01Si3.8N2.4O51600° ...
examples 1 to 13 , 18 and examples 35 to 38
Examples 1 to 13, 18 and Examples 35 to 38
[0620]Each of BaCO3, SrCO3 (manufactured by Hakushin Chemical Laboratory Co, Ltd.), CaCO3 (manufactured by Hakushin Chemical Laboratory Co, Ltd.), SiO2, Si3N4 and Eu2O3 was weighed out so as to give a nominal chemical composition ratio shown in Table 3, and mixing / firing was performed in the same manner as described for Production Examples 1 to 12. Namely, in Example 1, 2.52 g of BaCO3, 1.55 g of SiO2, 0.91 g of Si3N4 and 0.02 g of Eu2O3 were used. In Example 2, 2.29 g of BaCO3, 0.10 g of SrCO3, 1.57 g of SiO2, 0.91 g of Si3N4 and 0.14 g of Eu2O3 were used. In each of other Examples, according to each composition ratio, the proportion was varied based on the above-mentioned charge amount.
[0621]X-ray diffraction patterns of the fired products obtained are shown in FIG. 7. In each of Examples 1 to 7, 8 to 12 and 18, BSON crystal phase was detected as the main phase. It is evident that, when 40 atom % or more of Ba is replaced with Ca, BSON-pha...
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