Ultraviolet light-emitting phosphor, light-emitting element, and light-emitting device
11015119 · 2021-05-25
Assignee
Inventors
Cpc classification
H01L33/00
ELECTRICITY
A61L2202/11
HUMAN NECESSITIES
International classification
A61L2/00
HUMAN NECESSITIES
H01L33/00
ELECTRICITY
H05B33/14
ELECTRICITY
Abstract
An ultraviolet light-emitting phosphor having excellent degradation resistance and emission intensity is provided. The ultraviolet light-emitting phosphor is a phosphor comprising yttrium element, scandium element, aluminum element and oxygen element, which is excited by irradiation of vacuum ultraviolet rays or electron beams to emit ultraviolet rays.
Claims
1. An ultraviolet light-emitting phosphor consisting of a yttrium element, a scandium element, an aluminum element and an oxygen element, wherein the ultraviolet light-emitting phosphor is excited by irradiation of vacuum ultraviolet rays or electron beams to emit ultraviolet rays, wherein the ultraviolet light-emitting phosphor is represented by a general formula (Y.sub.1-xSc.sub.x)AlO.sub.3 (wherein 0<x<1).
2. The ultraviolet light-emitting phosphor according to claim 1, wherein 0.007≤x≤0.50.
3. A light-emitting element, comprising the ultraviolet light-emitting phosphor according to claim 1.
4. A light-emitting device, comprising the light-emitting element according to claim 3.
5. A light-emitting element, comprising the ultraviolet light-emitting phosphor according to claim 2.
6. A light-emitting device, comprising the light-emitting element according to claim 5.
Description
BRIEF DESCRIPTION OF DRAWINGS
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DESCRIPTION OF EMBODIMENTS
(7) As long as the ultraviolet light-emitting phosphor disclosed in the present application is a phosphor comprising yttrium element, scandium element, aluminum element and oxygen element, wherein the ultraviolet light-emitting phosphor is excited by the irradiation of vacuum ultraviolet rays or electron beams to emit ultraviolet rays, it is not particularly limited.
(8) Although the excitation source is not particularly limited, vacuum ultraviolet rays or electron beams can be used. Vacuum ultraviolet rays means ultraviolet rays with a wavelength of 200 nm or less, and, for example, ultraviolet rays with a wavelength of 147 nm, ultraviolet rays with a wavelength of 172 nm or the like can be used.
(9) The ultraviolet light-emitting phosphor disclosed in the present application can emit ultraviolet rays in various wavelength regions by the irradiation of such vacuum ultraviolet rays or electron beams. Since firing in a reducing atmosphere is not required, by far higher durability is obtained than that of the conventional ultraviolet light-emitting phosphors.
(10) The ultraviolet light-emitting phosphor disclosed in the present application is not particularly limited, and can be represented as a general formula (Y.sub.1-xSc.sub.x)AlO.sub.3 (wherein 0<x<1) as an example as long as the ultraviolet light-emitting phosphor is a phosphor comprising yttrium element (Y), aluminum element (Al) and scandium element (Sc).
(11) Strong emission intensity is easily obtained from this ultraviolet light-emitting phosphor (Y.sub.1-xSc.sub.x)AlO.sub.3 when the fractional content of scandium element (Sc) is smaller, and meanwhile it tends to become difficult that sufficient emitted light is obtained when the fractional content of scandium element (Sc) is too small. From such a viewpoint, it is more preferable that 0.007≤x≤0.50. From a viewpoint that emitted light having the wavelength of a still stronger peak is easily obtained, it is more preferable that 0.007≤x≤0.40.
(12) The present inventors have actually confirmed that the integrated emission intensity (a.u.) as to ultraviolet light emission is improved dramatically when the fractional content of yttrium element (Y) (1-x) exceeds 0.60 (namely, when x is smaller than 0.40) (refer to the below-mentioned Examples). Additionally, the present inventors have also confirmed that the peak wavelength of the ultraviolet light-emitting phosphor according to the present application is shortened gradually from around 300 nm when the fractional content of yttrium element (Y) (1-x) exceeds 0.60. More specifically, it is more preferable that 0.007≤x≤0.40. In the case, this ultraviolet light-emitting phosphor (Y.sub.1-xSc.sub.x)AlO.sub.3 can exhibit the excellent characteristics of ultraviolet light with a shorter wavelength being obtained than around 300 nm and its integrated emission intensity being also improved dramatically.
(13) The use of the ultraviolet light-emitting phosphor according to the present application is not particularly limited as long as its use is a use in which emitted ultraviolet light is used, but the ultraviolet light-emitting phosphor can be used as, for example, the use of disinfection (bactericidal lamp or the like) in terms of ultraviolet light with such a short wavelength being obtained with a high emission intensity. From this, the ultraviolet light-emitting phosphor according to the present application can function as a light source that can replace mercury lamps mainly used until now as a disinfection use.
(14) For example, when this ultraviolet light-emitting phosphor (Y.sub.1-xSc.sub.x)AlO.sub.3 is used, specializing in the above-mentioned disinfection use, it is preferable that 0.007≤x≤0.4 in terms of a suitable peak wavelength for the disinfection use being obtained at a short wavelength of around 300 nm or less. Additionally, it is more preferable that 0.007≤x≤0.25 in terms of a more suitable peak wavelength for the disinfection use being obtained at a short wavelength of around 290 nm or less. For example, in a use in which a strong disinfection capability is required, it is still more preferable that 0.007≤x≤0.10 in terms of a peak wavelength being obtained at a short wavelength of around 260 nm to around 270 nm or less. That is, the ultraviolet light-emitting phosphor according to the present application has the excellent characteristic of being capable of emitting ultraviolet light that is suitable for a disinfection use and exhibits an emission peak at around 300 nm or less (especially 260 nm to 270 nm).
(15) Thus, the ultraviolet light-emitting phosphor disclosed in the present application enables obtaining not only the excellent effect of high emission intensity being obtained by irradiating vacuum ultraviolet rays but also additionally by far higher durability than that of the conventional ultraviolet light-emitting phosphors due to firing in a reducing atmosphere not being required. The excellent characteristic of being hardly subject to in-process degradation has been also confirmed actually (refer to the below-mentioned Examples).
(16) The mechanism in which the ultraviolet light-emitting phosphor according to the present application exhibits the above-mentioned excellent effect is not clarified in detail yet. However, presumably there has happened such an organization that scandium element is preferably adapted to the physical configuration of atoms making up elements of yttrium, aluminum and oxygen constituting the phosphor to form an emission center capable of significantly promoting light emission and a structural factor allowing strong ultraviolet light emission has thus been incorporated. In other words, it is presumed that the phosphor is transferred more easily to an energy level allowing light emission in the specific ultraviolet band at the atomic level by irradiating vacuum ultraviolet rays or electron beams.
(17) It is considered that scandium element maintains a state difficult to change in valence at the atomic level due to the physical configuration of atoms making up the elements of yttrium, aluminum and oxygen constituting the phosphor. It is therefore presumed that the phosphor forms a state difficult to deteriorate by external heat and chemical change.
(18) In a method for obtaining the ultraviolet light-emitting phosphor according to the present application, respective compounds (for example, oxides) containing constituent elements are used as raw materials and mixed at a stoichiometric proportion that forms the composition of a desired phosphor. For example, as these materials, powders of aluminum oxide (Al.sub.2O.sub.3), yttrium oxide (Y.sub.2O.sub.3), and scandium oxide (Sc.sub.2O.sub.3) can be used.
(19) The ultraviolet light-emitting phosphor according to the present application is obtained by firing a powder obtained by mixing these materials at a high temperature in the air atmosphere. The ultraviolet light-emitting phosphor can be obtained by performing this high temperature firing in the air atmosphere at 1000° C. to 1350° C. for 30 minutes to 10 hours.
(20) The uses of the ultraviolet light-emitting phosphor thus obtained are various. For example, clean disinfection by ultraviolet rays with residues and environmental damage suppressed can be performed by disinfecting various organisms to be disinfected using ultraviolet light emitted by the ultraviolet light-emitting phosphor according to the present application. The decomposition treatment of hardly decomposed substances (such as formaldehyde and PCB) and the synthesis of new chemical substances (for example, photocatalyst substance or the like) can also be performed by using this ultraviolet light. The ultraviolet light-emitting phosphor can also be applied to various medical fields such as the medical treatment of intractable diseases (such as atopic dermatitis) and the prevention of hospital infection by using this ultraviolet light.
(21) The ultraviolet light-emitting phosphor can be used as various light-emitting elements comprising such an ultraviolet light-emitting phosphor. The phosphor can also be used for light-emitting devices, comprising the light-emitting element.
EXAMPLES
(22) In order to clarify the characteristics of the present invention further, Examples are shown below, but the present invention is not limited by these Examples.
Example 1
(23) (1-1) Manufacturing of Phosphors
(24) Aluminum oxide (Al.sub.2O.sub.3), yttrium oxide (Y.sub.2O.sub.3) and scandium oxide (Sc.sub.2O.sub.3) were used as raw materials and mixed at stoichiometric proportions that were identical to the compositions of desired phosphors, respectively. The mixed powders were fired in the air atmosphere at 1300° C. for 5 hours.
(25) (1-2) Identification of Phosphors
(26) X-ray diffraction results acquired by an X-ray diffraction device a radiation source of which is FeKα regarding sintered bodies (the fractional content of Sc x: 0.007, 0.02, 0.10, 0.25, 0.30, 0.40, 0.50, 0.75) obtained above are shown in
(27) (1-3) Measurement of Emission Intensity
(28) The phosphors obtained above were irradiated with vacuum ultraviolet rays emitted using a deuterium lamp L1835 (manufactured by Hamamatsu Photonics K.K.) having an excitation wavelength of 146 nm as a light source. Results of emission intensity spectra as to emitted light obtained by this irradiation is shown in
(29) It was confirmed from the results of
(30) It was also confirmed from the results of
(31) To summarize, the ultraviolet light-emitting phosphors (Y.sub.1-xSc.sub.x)AlO.sub.3 in this Example, not particularly limited to, but with 0.007≤x≤0.50 was observed to have the wavelengths of stronger peaks. Further, it was confirmed that the ultraviolet light-emitting phosphors with 0.007≤x≤0.40 exhibited the excellent characteristics that strong ultraviolet light having peak wavelengths at shorter wavelengths than around 300 nm was emitted and the integrated emission intensities thereof were also improved dramatically at the same time.
Example 2
(32) (2-1) Evaluation of Deterioration Resistance
(33) The evaluation of degradation resistance (evaluation of durability) was performed on the ultraviolet light-emitting phosphors (Y.sub.1-xSc.sub.x)AlO.sub.3 obtained in the above-mentioned Example 1. The evaluation of durability was also performed on phosphors ZnAl.sub.2O.sub.4 and YAlO.sub.3:Pr, which were known conventionally, as a Comparative Examples. (Samples: Comparative Example (ZnAl.sub.2O.sub.4), Comparative Example (YAlO.sub.3:Pr), the present Example (Y.sub.1-xSc.sub.x)(AlO.sub.3))
(34) The mixing ratio of a phosphor to a solvent was set at 1:1. The phosphor and the solvent were mixed in a glass bottle by stirring for 5 minutes. The obtained mixed solution was poured into an alumina dish and spread. The obtained mixed solution was fired in the air atmosphere at 700° C. for 30 minutes, and the obtained powder was then collected by a medicine spoon. The collected powder was filled in a holder for measurement. Emission spectra were measured and evaluated at an excitation wavelength of 146 nm using a deuterium lamp L1835 (manufactured by Hamamatsu Photonics K.K.) for a light source and using a vacuum ultraviolet spectroscopic system for excitation (manufactured by JASCO Corporation) as a measuring device.
(35) The obtained emission spectra are shown in
(36) TABLE-US-00001 TABLE 1 Change in Sample intensity ZnAl.sub.2O.sub.4 97.1 YAlO.sub.3:Pr 97.7 The present 100.8 Example
(37) As is apparent from the obtained results, the intensities of Comparative Examples ZnAl.sub.2O.sub.4 and YAlO.sub.3:Pr were found to decrease, but the intensity of the present Example (Y.sub.1-xSc.sub.x)AlO.sub.3 was not found to decrease, and it was confirmed that the intensity of the present Example (Y.sub.1-xSc.sub.x)AlO.sub.3 was rather heighten. The ease of being subject to the influence of heat and an organic solvent can be considered as a cause of this difference. Specifically, it was shown that the present Example (Y.sub.1-xSc.sub.x)AlO.sub.3 was by far more stable also as to heat and an organic solvent than the phosphors of Comparative Examples. From another viewpoint, in the phosphor (Y.sub.1-xSc.sub.x)AlO.sub.3 according to the present Example, it is presumed that Sc forms a state difficult to change in valence, and it is therefore considered that the degradation resistance is enhanced as to various external factors.