Patent Application
20250002781
This application claims priority to Japanese Patent Application No. 2023-105243, filed on Jun. 27, 2023, the disclosure of which is hereby incorporated by reference in its entirety.
The present disclosure relates to an oxide fluorescent material and a light emitting device using the same.
Light emitting devices having light emission intensity in a wavelength range from red light to near-infrared light are desired for use in, for example, infrared cameras, infrared communication, light sources for plant growth and cultivation, vein authentication, which is a type of biometric authentication, food composition analyzers for non-destructive measurement of sugar content and other parameters in food or agricultural products such as fruits and vegetables, and analyzers for non-destructive measurement of foreign substances in pharmaceutical products. Light emitting devices that emit light in the wavelength range from red light to near-infrared light as well as in a wavelength range of visible light are also desired.
Examples of such light emitting devices include a light emitting device in which a light emitting diode (LED) and a fluorescent material are combined.
Examples of the fluorescent material combined in the light emitting device include a fluorescent material having a light emission spectrum with a relatively large light emission intensity in the wavelength range from red light to near-infrared light (hereinafter, also referred to as “near-infrared light emitting fluorescent material”).
As the near-infrared light emitting fluorescent material, Japanese Translation of PCT International Application Publication No. 2020-528486 discloses a fluorescent material having a light emission peak wavelength that is 680 nm or more and 760 nm or less and having a composition represented by, for example, CaYAlO4:Mn4+. Near-infrared light emitting fluorescent materials having a light emission spectrum with a wider full width at half maximum and with a light emission peak wavelength in a longer wavelength range, which are suitable for each application described above, may be needed.
The present disclosure has an object to provide an oxide fluorescent material having a light emission spectrum with a light emission peak wavelength in a wavelength range from red light to near-infrared light and with a wider full width at half maximum, and a light emitting device using the same.
A first aspect of the present disclosure relates to an oxide fluorescent material having a composition represented by the following formula (1).
(Mg1-sM1s)2(Al1-tM2t)u(Ge1-vM3v)wOx:Cry,M4z (1)
A second aspect of the present disclosure relates to a light emitting device including the oxide fluorescent material and a light emitting element emitting light having a light emission peak wavelength that is 365 nm or more and 650 nm or less and irradiating the oxide fluorescent material.
The present disclosure provides an oxide fluorescent material having a light emission spectrum with a light emission peak wavelength in a wavelength range from red light to near-infrared light and with a wider full width at half maximum, and a light emitting device using the same.
The oxide fluorescent material according to the present disclosure, the light emitting device using the same, and the method for producing an oxide fluorescent material are described below. The embodiments described below are intended to embody the technical idea of the present disclosure, and the present disclosure is not limited to the following oxide fluorescent material and the light emitting device. For visible light, the relationship between color names and chromaticity coordinates, and the relationship between wavelength ranges of light and color names of monochromatic light are in accordance with Japanese Industrial Standard (JIS) Z8110. In this specification, the “fluorescent material” is used in the same meaning as a “fluorescent phosphor”.
Light emitting devices using a fluorescent material are required to emit light in an appropriate wavelength range according to a visual object and conditions of use. For example, in the medical field, there may be a need to easily obtain information inside a living body. The living body includes light absorbers such as water, hemoglobin, and melanin. For example, hemoglobin has a high light absorptance in a visible light wavelength range of less than 650 nm, and with a light emitting device that emits light in the visible light wavelength range, the light in the visible light wavelength range is less easily transmitted through the living body, which makes it difficult to obtain information inside the living body. If it is possible to irradiate light in a wavelength range where absorption and scattering of light in living tissues are reduced, it becomes easier to obtain information deep inside the living body. Therefore, there is a need for a light emitting device that can emit light in a wavelength range referred to as a “biological window” where light easily transmits through the living body. The “biological window” may be referred to as a “first biological window” in a wavelength range from around 650 nm to 950 nm, may be referred to as a “second biological window” in a wavelength range from around 1,000 nm to 1,350 nm, and may be referred to as a “third biological window” in a wavelength range from around 1,500 nm to 1,800 nm. For example, if the increase or decrease of oxygen concentration in the blood in the living body can be measured by measuring the increase or decrease of light absorption due to hemoglobin that binds to oxygen, the information inside the living body can be easily obtained by irradiation with the light emitted from the light emitting device. If the information deep inside the living body can be obtained by irradiation with the light emitted from the fluorescent material and the light emitting element, instead of irradiating X-rays or others, it is possible to obtain the information inside the living body more safely. Therefore, the fluorescent material used in the light emitting device may be required to have a light emission peak wavelength in a wavelength range from red light to near-infrared light. The fluorescent material used in the light emitting device may be required to have a light emission peak wavelength that is 680 nm or more and 1,000 nm or less, or a light emission peak wavelength that is 840 nm or more and 970 nm or less. Recently, there is a need for a light emitting device that emits light in a wavelength range from red light to near-infrared light, which allow for more clearly visualizing deep inside the living body and is highly safe. When a light emitting device including a light emitting element and a fluorescent material is configured to allow a high current to flow into the light emitting device and can emit light with high output power, detection capability can be improved, making it easier to obtain information inside the living body.
In the agricultural and food fields, there is a need for non-destructive sugar content meters for non-destructively measuring the sugar content of agricultural products and fruits and vegetables, and non-destructive taste meters for rice. Near-infrared spectroscopy may be used as a non-destructive method for measuring internal quality such as sugar content, acidity, ripeness, and internal damage of fruits and vegetables, and the outer-layer quality such as abnormal drying appearing on the skin surface of fruits and vegetables or in the outer layer near the skin surface. In the near-infrared spectroscopy, fruits and vegetables are irradiated with light in the near-infrared light wavelength range, and the transmitted light that is transmitted through the fruits and vegetables and the reflected light that is reflected by the fruits and vegetables are received, and the quality of the fruits and vegetables is measured by measuring the decrease in light intensity (light absorption). Light sources such as tungsten or xenon lamps are used in near-infrared spectroscopy analysis devices used in such food fields. The general rules for near-infrared spectrophotometric analysis in JIS K0134 state that near-infrared rays have a wavelength range of 700 nm or more and 2,500 nm or less.
In the face of environmental changes such as climate change, it is also desirable to stably supply plants such as vegetables and to increase the production efficiency of plants. Plant factories that can be artificially controlled can stably supply safe vegetables to the market, and are expected to be a next-generation industry. Such plant factories require a light emitting device that emits light capable of promoting the growth of plants. Reactions of plants to light can be grouped into photosynthesis and photomorphogenesis. Photosynthesis is a reaction that uses light energy to decompose water, generate oxygen, and fix carbon dioxide to organic materials, which is a necessary reaction for the growth of plants. Photomorphogenesis is a morphogenetic reaction that uses light as a signal for seed germination, differentiation (germ formation, leaf formation), movement (pore opening and closing, chloroplast movement), and photorefraction. In the photomorphogenesis reaction, it has been found that light with the wavelength of 690 nm or more and 800 nm or less affects the photoreceptors of plants. Therefore, light emitting devices used in plant factories may be required to be capable of emitting light in the wavelength range that affects plant photoreceptors (chlorophyll a, chlorophyll b, carotenoids, phytochromes, cryptochromes, and phototropins) and promotes the growth of plants.
For use in the light emitting device using a light emitting element such as a light emitting diode (LED) or laser diode (LD) configured to emit light in a range of purple to blue as an excitation light source, the above-mentioned near-infrared light emitting fluorescent material has room for improvement in the light emission characteristics of the fluorescent material such that the light emitting device can emit light suitable for intended use.
Light emitting devices that emit light in the red light to near-infrared light wavelength range as well as in the wavelength range of 365 nm or more and less than 700 nm may be required. For example, it may be necessary to emit light in the visible light wavelength range not only to obtain internal information on living bodies or fruits and vegetables, but also to enhance the visibility of objects.
The oxide fluorescent material has a composition represented by the following formula (1).
(Mg1-sM1s)2(Al1-tM2t)u(Ge1-vM3v)wOx:Cry,M4z (1)
When the parameter y in the formula (1), which represents the molar ratio of the activating element Cr, is of 0.005 or more and 1.0 or less (0.005≤y≤1.0) in 1 mol of the composition of the oxide fluorescent material, the oxide fluorescent material has a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, and with a relatively wide full width at half maximum. In the oxide fluorescent material, the parameter y in the formula (1) may be 0.01 or more and 0.90 or less (0.01≤y≤0.90), may be 0.015 or more and 0.80 or less (0.015≤y≤0.80), may be 0.02 or more and 0.70 or less (0.02≤y≤0.70), may be 0.025 or more and 0.60 or less (0.025≤y≤0.60), may be 0.03 or more and 0.50 or less (0.03≤y≤0.50), may be 0.035 or more and 0.50 or less (0.035≤y≤0.50), or may be 0.04 or more and 0.40 or less (0.04≤y≤0.40), in 1 mol of the composition of the oxide fluorescent material. In order for the oxide fluorescent material to obtain a light emission spectrum with a light emission peak wavelength on the longer wavelength side in the wavelength range from red light to near-infrared light and with a relatively wide full width at half maximum, the parameter y in the formula (1) may be 0.05 or more and 0.50 or less (0.05≤y≤0.50), may be 0.10 or more and 0.45 or less (0.10≤y≤0.45), or may be 0.20 or more and 0.40 or less (0.20≤y≤0.40), in 1 mol of the composition of the oxide fluorescent material. In the present specification, in the composition formulae representing the compositions of the fluorescent materials including the oxide fluorescent material, the part before the colon (:) represents elements and the molar ratio constituting a host crystal, and the part after the colon (:) represents an activating element.
In the oxide fluorescent material, the first element M1 included as necessary is at least one element selected from the group consisting of Ca, Sr, Ba, and Zn, or may be two or more elements selected from the group consisting of Ca, Sr, Ba, and Zn in the composition represented by the formula (1). In one example, the oxide fluorescent material does not contain the first element M1, but contains Mg. In the oxide fluorescent material a part of Mg may be replaced by the first element M1, or two or more elements may be contained as the first element M1. In the oxide fluorescent material, Mg may be entirely replaced by the first element M1 in the composition represented by the formula (1). When the first element M1 is Ca or Zn, Mg may be entirely replaced by Ca, or Mg may be entirely replaced by Zn. In one example, the oxide fluorescent material does not contain Mg, and contain Ca as an essential element and Mg may be replaced by at least one first element M1 selected from the group consisting of Sr, Ba, and Zn, or two or more elements may be contained as the first element M1 in the composition represented by the formula (1). In one example, the oxide fluorescent material does not contain Mg, and contain Zn as an essential element and Mg may be replaced by at least one first element M1 selected from the group consisting of Ca, Sr, and Ba, or two or more elements may be contained as the first element M1 in the composition represented by the formula (1).
In the oxide fluorescent material, the molar ratio of the first element M1 is represented by a product of 2 and the parameter s in the formula (1), wherein the parameter s is 0 or more and 1.0 or less (0≤s≤1.0), in 1 mol of the composition of the oxide fluorescent material. In order for the oxide fluorescent material to obtain a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, the parameter s in the formula (1) may be 0 or more and less than 1.0 (0≤s≤1.0), may be more than 0 and 1.0 or less (0≤s≤1.0), may be 0.05 or more and 0.95 or less (0.05≤s≤0.95), may be 0.10 or more and 0.90 or less (0.10≤s≤0.90), may be 0.15 or more and 0.85 or less (0.15≤s≤0.85), or may be 0.20 or more and 0.80 or less (0.20≤s≤0.80). When Mg is entirely replaced by the first element M1, the parameter s is 1 (s=1.0) in 1 mol of the composition of the oxide fluorescent material, and when the parameter s is 1, the oxide fluorescent material may contain two or more elements may be contained as the first element M1. The oxide fluorescent material need not substantially contain the first element M1, and the parameter s may be substantially 0 (s=0) in the composition represented by the formula (1). In the present specification, when the numerical value of the parameter representing the molar ratio of the element in the composition is “substantially 0”, it means that the element is not intentionally contained. The numerical value of the parameter representing the molar ratio of the element in the composition being substantially 0 specifically means the case where the content is 1,000 ppm by mass or less, 500 ppm by mass or less, or 1 ppm by mass or more.
In the oxide fluorescent material, the second element M2 included as necessary is at least one element selected from the group consisting of Ga, Sc, and In, or may be two or more elements thereof in the composition represented by the formula (1). The oxide fluorescent material may contain part or all of Al replaced by the second element M2 in the composition represented by the formula (1). Even when the oxide fluorescent material contains part or all of Al replaced by the second element M2 in the composition represented by the formula (1), the oxide fluorescent material has a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use. In the oxide fluorescent material, a part of Al may be replaced by the second element M2, and the second element M2 may be either Sc or In, in the composition represented by the formula (1). In the oxide fluorescent material, Al may be entirely replaced by the second element M2, wherein the second element M2 may be either Ga or In, in the composition represented by the formula (1).
When the parameter u in the formula (1), which represents the total molar ratio of Al and the second element M2, is 1.5 or more and 2.5 or less (1.5≤u≤2.5) in 1 mol of the composition of the oxide fluorescent material, the oxide fluorescent material has a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, and with a wider full width at half maximum. In the oxide fluorescent material, the parameter u in the formula (1) may be 1.8 or more and 2.2 or less (1.8≤u≤2.2), may be 1.9 or more and 2.1 or less (1.8≤u≤2.1), or may be 2 (u=2). In the oxide fluorescent material, the parameter u in the formula (1), which represents the total molar ratio of Al and the second element M2, may have the same value as the total molar ratio of Mg and the first element M1 in 1 mol of the composition of the oxide fluorescent material. In the oxide fluorescent material, the parameter u, which represents the total molar ratio of Al and the second element M2, may be smaller or larger than 2, which represents the total molar ratio of Mg and the first element M1, as long as the parameter u is 1.5 or more and 2.5 or less, in 1 mol of the composition of the oxide fluorescent material.
In the oxide fluorescent material, the molar ratio of the second element M2 included as necessary is represented by a product of the parameter t and the parameter u in the formula (1), wherein the parameter t is 0 or more and 1.0 or less (0≤t≤1.0), in 1 mol of the composition of the oxide fluorescent material. In the oxide fluorescent material, Al may be entirely replaced by the second element M2 in the formula (1), wherein the parameter u may be 1.0 (u=1.0), in 1 mol of the composition of the oxide fluorescent material. The oxide fluorescent material contains the second element M2 as a part of Al in the formula (1), wherein the parameter t in the formula (1) may be more than 0 and 1.0 or less (0≤t≤1.0), may be more than 0 and less than 1.0 (0≤t≤1.0), may be 0.1 or more and 0.9 or less (0.1<t≤0.9), may be 0.2 or more and 0.8 or less (0.2≤t≤0.8), may be 0.3 or more and 0.7 or less (0.3≤t≤0.7), or may be 0.4 or more and 0.6 or less (0.4≤t≤0.6), in 1 mol of the composition of the oxide fluorescent material. The oxide fluorescent material need not substantially contain the second element M2, and the parameter t may be substantially 0 (t=0) in the composition represented by the formula (1).
In the oxide fluorescent material, the third element M3 included as necessary is at least one element selected from the group consisting of Si, Ti, Zr, Sn, and Hf in the composition represented by the formula (1). In order for the oxide fluorescent material to obtain a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, and with a wider full width at half maximum, the third element M3 included as necessary may be either Si or Hf, or may be Si in the composition represented by the formula (1).
When the parameter w in the formula (1), which represents the total molar ratio of Ge and the third element M3, is 3.0 or more and 6.0 or less (3.0≤w≤6.0) in 1 mol of the composition of the oxide fluorescent material, the oxide fluorescent material has a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, and with a wider full width at half maximum. In the oxide fluorescent material, the parameter w in the formula (1) may be 3.5 or more and 6.0 or less (3.5≤w≤6.0), or may be 4.0 or more and 6.0 or less (4.0≤w≤6.0). In order to obtain an oxide fluorescent material having a light emission spectrum with a light emission peak wavelength in a desired wavelength range depending on the purpose of use, and with a wider full width at half maximum, when the parameter x in the formula (1), which represents the molar ratio of oxygen, is less than 15 in the oxide fluorescent material, the parameter w in the formula (1) may be 3.5 or more and 4.5 or less (3.5≤w≤4.5) in 1 mol of the composition of the oxide fluorescent material.
In the oxide fluorescent material, the molar ratio of the third element M3 included as necessary is represented by a product of the parameter v and the parameter w in the formula (1), wherein the parameter v is 0 or more and 0.5 or less (0≤v≤0.5), may be 0 or more and 0.4 or less (0≤v≤0.4), or may be 0 or more and 0.3 or less (0≤v≤0.3) in 1 mol of the composition of the oxide fluorescent material. The oxide fluorescent material need not contain substantially the third element M3, and the parameter v may be substantially 0 (v=0) in the composition represented by the formula (1).
In order for the oxide fluorescent material to obtain a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light depending on the purpose of use, and with a wider full width at half maximum, the parameter x in the formula (1), which represents the molar ratio of oxygen, is 11.0 or more and 17.0 or less (11.0≤x≤17.0), may be 12.0 or more and 17.0 or less (12.0≤x≤17.0), may be 13.0 or more and 17.0 or less (13.0≤x≤17.0), may be 16.0 or less (x≤16.0), may be 15.0 or less (x≤15.0), may be less than 15.0 (x≤15.0), or may be 14.0 or less (x≤14.0), in 1 mol of the composition of the oxide fluorescent material.
In the oxide fluorescent material, the fourth element M4 included as necessary is at least one element selected from the group consisting of Ni, Ce, Eu, Fe, Mn, Nd, Tm, Ho, Er, and Yb, or may be at least one element selected from the group consisting of Ni, Ce, Eu, Fe, Mn, and Nd, in the composition represented by the formula (1).
In the oxide fluorescent material, the parameter z representing the molar ratio of the fourth element M4, which is the same activating element as Cr and is included as necessary, in the formula (1) is 0 or more and 0.5 or less (0≤z≤0.5), may be 0 or more and 0.4 or less (0≤z≤0.4), may be 0 or more and 0.3 or less (0≤z≤0.3), may be 0 or more and 0.2 or less (0 K z≤0.2), may be 0 or more and 0.1 or less (0≤z≤0.1), or may be 0.001 or more (0.001≤z), in 1 mol of the composition of the oxide fluorescent material. The oxide fluorescent material need not contain substantially the fourth element M4, and the parameter z may be substantially 0 (z=0) in the composition represented by the formula (1).
The oxide fluorescent material preferably has a light emission spectrum in which a light emission intensity at 1,000 nm is 5% or more relative to the light emission intensity at the light emission peak wavelength as 100%. When the oxide fluorescent material has a light emission spectrum in which a light emission intensity at 1,000 nm is 5% or more relative to the light emission intensity at the light emission peak wavelength as 100%, the oxide fluorescent material emits light having a light emission intensity required for analysis in a wavelength range of 900 nm or more and 1,100 nm or less, which facilitates obtaining information inside living bodies or information on agricultural products, foods, and pharmaceutical products in a non-destructive manner, and it can be used in light emitting devices for analysis in place of a tungsten or xenon lamp. In the light emission spectrum of the oxide fluorescent material, the ratio of the light emission intensity at 1,000 nm of the light emission intensity of the light emission peak wavelength as 100% is preferably high. However, even when the ratio of the light emission intensity at 1,000 nm is low, if the light emission spectrum has a relatively wide full width at half maximum, it is possible for the oxide fluorescent material to emit light having a light emission intensity required for analysis for obtaining information inside living bodies or information on agricultural products, foods, and pharmaceutical products in a non-destructive manner. In the light emission spectrum of the oxide fluorescent material, the light emission intensity at 1,000 nm relative to the light emission intensity of the light emission peak wavelength as 100% may be 10% or more, may be 20% or more, may be 30% or more, may be 40% or more, and more preferably 50% or more.
The oxide fluorescent material preferably has a light emission spectrum with a full width at half maximum that is 90 nm or more and 250 nm or less. The oxide fluorescent material preferably converts the wavelength of excitation light emitted from an excitation light source such as a light emitting element to thereby emit light having a light emission spectrum with a light emission peak wavelength in a desired wavelength range from red light to near-infrared light, with a wider full width at half maximum, and with a light emission intensity required for analysis or other purposes.
When light having a light emission spectrum with a wider full width at half maximum can be irradiated in the wavelength range where information inside living bodies and on agricultural products can be obtained in a non-destructive manner, it is easier to obtain information inside living bodies and on agricultural products. It is also desirable for the color appearance of an object when irradiated with light (hereinafter, also referred to as “color rendering property”) to have a light emission spectrum in a wider wavelength range, and the wider the full width at half maximum, the better the color rendering property of light can be emitted. For example, when emitting light in a wavelength range that affects the growth of plants in a plant factory, it may be necessary to emit light that does not disturb the spectral balance of the light so that workers can work comfortably. The full width at half maximum in the light emission spectrum of the oxide fluorescent material may be 100 nm or more, may be 110 nm or more, may be 115 nm or more, may be 120 nm or more, may be 130 nm or more, may be 140 nm or more, or may be 150 nm or more; and may be 245 nm or less, may be 240 nm or less, or may be 230 nm or less. The full width at half maximum in the light emission spectrum of the oxide fluorescent material may be 150 nm or more and 250 nm or less. In the present specification, the full width at half maximum refers to a wavelength width where the light emission intensity is 50% of the maximum light emission intensity in the light emission spectrum at the light emission peak wavelength.
The oxide fluorescent material preferably has a light emission spectrum with a light emission peak wavelength 680 nm or more and 1,000 nm or less. The oxide fluorescent material converts the wavelength of excitation light emitted from an excitation light source such as a light emitting element, and emits light in a wavelength range from red light to near-infrared light. A light emitting device including the oxide fluorescent material that emits light in the wavelength range from red light to near-infrared light can be an alternative light source to a tungsten or xenon lamp. The oxide fluorescent material preferably has a light emission spectrum in which the light emission intensity required for analysis can be obtained in a wavelength range that facilitates obtaining information inside living bodies and on agricultural products. When the oxide fluorescent material has a light emission spectrum with a light emission peak wavelength in the range of 680 nm or more and 1,000 nm or less, a light emission spectrum having a light emission intensity required for analysis can be obtained in a wavelength range that facilitates obtaining information inside living bodies or information on agricultural products, foods, and pharmaceutical products in a non-destructive manner. The oxide fluorescent material preferably has a light emission peak wavelength 690 nm or more and 990 nm or less, may have a light emission peak wavelength 700 nm or more and 990 nm or less, may have a light emission peak wavelength of 750 nm or more and 990 nm or less, or may have a light emission peak wavelength of 770 nm or more and 980 nm or less, in the light emission spectrum. The oxide fluorescent material may have a light emission peak wavelength that is 800 nm or more and 980 nm or less, may have a light emission peak wavelength that is 820 nm or more and 970 nm or less, or may have a light emission peak wavelength that is 840 nm or more and 970 nm or less, in a wavelength range from red light to near-infrared light depending on the purpose of use.
The light emitting device includes an oxide fluorescent material having a composition represented by the formula (1) and a light emitting element having a light emission peak wavelength of 365 nm or more and 650 nm or less and irradiating the oxide fluorescent material. The oxide fluorescent material can be used as a member constituting a wavelength conversion member together with a light-transmissive material.
A semiconductor element can be used as the light emitting element for irradiating the oxide fluorescent material. For example, a nitride semiconductor can be selected as the material for the light emitting element that emits green or blue light. Materials such as InXAlYGa1-X-YN (0≤X≤1, 0≤Y≤1, X+Y≤1) can be used as the material for the semiconductor structure constituting the light emitting element. For example, a gallium-aluminum-arsenic semiconductor or an aluminum-indium-gallium-phosphorus semiconductor can be selected as the material for the light emitting element that emits red light. For example, an LED chip or an LD chip is preferably used for the light emitting element.
The light emitting element has a light emission peak wavelength of 365 nm or more and 650 nm or less, may have a light emission peak wavelength of 365 nm or more and 500 nm or less, may have a light emission peak wavelength of 370 nm or more and 490 nm or less, or may have a light emission peak wavelength of 375 nm or more and 480 nm or less. The light emitting element may have a light emission peak wavelength of more than 500 nm and 650 nm or less, may have a light emission peak wavelength of 510 nm or more and 650 nm or less, or may have a light emission peak wavelength of 520 nm or more and 650 nm or less. By using the light emitting element as the excitation light source of the oxide fluorescent material, a light emitting device that emits mixed color light of light emitted from the light emitting element and fluorescence emitted from the fluorescent material containing the oxide fluorescent material in a desired wavelength range can be constituted. The full width at half maximum of the light emission peak in the light emission spectrum of the light emitting element can be, for example, 30 nm or less. For example, a light emitting element using a nitride-based semiconductor is preferably used as the light emitting element. By using a light emitting element using a nitride-based semiconductor as the excitation light source, a stable light emitting device having high efficiency, high input-output linearity, and high resistance to mechanical impacts can be obtained.
The light emitting device necessarily includes a first fluorescent material containing the oxide fluorescent material described above, and may further include a fluorescent material having a different composition. The light emitting device preferably includes, in addition to the first fluorescent material, at least one fluorescent material selected from the group consisting of a second fluorescent material having a light emission peak wavelength of 455 nm or more and less than 495 nm, a third fluorescent material having a light emission peak wavelength of 495 nm or more and less than 610 nm, a fourth fluorescent material having a light emission peak wavelength of 610 nm or more and less than 700 nm, and a fifth fluorescent material having a light emission peak wavelength of 700 nm or more and 1,050 nm or less, in the light emission spectrum of each fluorescent material. The light emitting device includes a light emitting element, a first fluorescent material containing the oxide fluorescent material described above, and at least one fluorescent material selected from the group consisting of a second fluorescent material, a third fluorescent material, a fourth fluorescent material, and a fifth fluorescent material, so that the light emitting device can be used as a light source that emits light having a light emission spectrum in a wavelength range from visible light to a part of near-infrared light. The light emitting device can be used as a light source that has a light emission spectrum similar to that of conventionally used tungsten and xenon lamps and can be downsized compared to tungsten and xenon lamps. A small light emitting device can be mounted on small mobile devices such as smartphones and smartwatches to obtain information in a living body, which can be used to manage physical conditions.
The light emitting device can be used, for example, in a reflection spectroscopic measuring device, and a lighting device capable of non-destructively measuring a living body, fruits and vegetables, and the like, and requiring light with a good in color rendering property.
The second fluorescent material, which has a composition different from that of the first fluorescent material containing the oxide fluorescent material described above, preferably contains at least one fluorescent material selected from the group consisting of a phosphate fluorescent material having a composition represented by the following formula (2a), an aluminate fluorescent material having a composition represented by the following formula (2b), and an aluminate fluorescent material having a composition represented by the following formula (2c); and may contain two or more fluorescent materials of these.
(Ca,Sr,Ba,Mg)10(PO4)6(F,Cl,Br,I)2:Eu (2a)
(Ba,Sr,Ca)MgAl10O17:Eu (2b)
Sr4Al14O25:Eu (2c)
In the present specification, plural elements sectioned by comma (,) in the composition formulae mean that at least one of these plural elements is contained in the composition.
The third fluorescent material preferably contains at least one fluorescent material selected from the group consisting of a silicate fluorescent material having a composition represented by the following formula (3a), an aluminate fluorescent material or a gallate fluorescent material having a composition represented by the following formula (3b), a β-SiAlON fluorescent material having a composition represented by the following formula (3c), a cesium lead halide fluorescent material having a composition represented by the following formula (3d), and a nitride fluorescent material having a composition represented by the following formula (3e); and may contain two or more fluorescent materials of these. In the case where the third fluorescent material contains two or more fluorescent materials, the two or more third fluorescent materials preferably have light emission peak wavelengths in different ranges within a range of 495 nm or more and less than 610 nm.
(Ca,Sr,Ba)8MgSi4O16(F,Cl,Br)2:Eu (3a)
(Lu,Y,Gd,Tb)3(Al,Ga)5O12:Ce (3b)
Si6-zAlzOzN8-z:Eu (0≤z≤4.2) (3c)
CsPb(F,Cl,Br)3 (3d)
(La,Y,Gd)3Si6N11:Ce (3e)
The fourth fluorescent material preferably contains at least one fluorescent material selected from the group consisting of a nitride fluorescent material having a composition represented by the following formula (4a), a fluoro-germanate fluorescent material having a composition represented by the following formula (4b), an oxynitride fluorescent material having a composition represented by the following formula (4c), a fluoride fluorescent material having a composition represented by the following formula (4d), a fluoride fluorescent material having a composition represented by the following formula (4e), a nitride fluorescent material having a composition represented by the following formula (4f), and a nitride fluorescent material having a composition represented by the following formula (4g); and may contain two or more fluorescent materials of these. In the case where the fourth fluorescent material contains two or more fluorescent materials, the two or more fourth fluorescent materials preferably have light emission peak wavelength in different ranges within a range of 610 nm or more and less than 700 nm.
(Sr,Ca)AlSiN3:Eu (4a)
3.5MgO·0.5MgF2·GeO2:Mn (4b)
(Ca,Sr,Mg)kSi12-(m+n)Alm+nOnN16-n:Eu (4c)
A1c1[M51-b1Mn4+b1Fd1] (4d)
A2c2[M61-b2Mn4+b2Fd2] (4e)
(Ba,Sr,Ca)2Si5N8:Eu (4f)
(Sr,Ca)LiAl3N4:Eu (4g)
The fifth fluorescent material preferably contains at least one fluorescent material selected from the group consisting of a gallate fluorescent material having a composition represented by the following formula (5a), an aluminate fluorescent material having a composition represented by the following formula (5b), a gallate fluorescent material having a composition represented by the following formula (5c), an aluminate fluorescent material having a composition represented by the following formula (5d), a fluorescent material having a composition represented by the following formula (5e) different from those of the above oxide fluorescent materials, a fluorescent material having a composition represented by the following formula (5f) different from those of the above oxide fluorescent materials, a fluorescent material having a composition represented by the following formula (5g) different from those of the above oxide fluorescent materials, a fluorescent material having a composition represented by the following formula (5h) different from those of the above oxide fluorescent materials, and a fluorescent material having a composition represented by the following formula (5i) different from those of the above oxide fluorescent materials; and may contain two or more fluorescent materials of these.
Ga2O3:Cr (5a)
Al2O3:Cr (5b)
ZnGa2O4:Cr (5c)
(Lu,Y,Gd,Tb)3(Al,Ga)5O12:Ce,Cr (5d)
M7gM8hM9iM105Oj:Cre,M11f (5e)
(Mg1-t1M12t1)u1(Ga1-v1-x1-y1M13v1)2Ow1:Crx1,M14y1 (5f)
(Li1-t2M15t2)u2(Ga1-v2M16v2)5Ow2:Crx2,Niy2,M17z2 (5g)
(Ga1-u3M18u3)2(Ge1-v3M19v3)w3Ox3:Cry3,M20z3 (5h)
(Mg1-p4M21p4)q4(Li1-r4M12r4)s4(In1-t4M23t4)u4(Ge1-v4M24v4)w4Ox4:Cry4,M25z4 (5i)
An example of the light emitting device is described with reference to the drawings.
As shown in
Examples of the light transmissive material constituting the wavelength conversion body together with the fluorescent material include at least one selected from the group consisting of resin, glass, and inorganic substances. The resin can use at least one resin selected from the group consisting of a silicone resin, an epoxy resin, a phenol resin, a polycarbonate resin, an acrylic resin, and modified resins thereof. Among them, a silicone resin and a modified silicone resin are preferred because of their good heat and light resistance. The wavelength conversion member may optionally contain a filler, a colorant, and a light diffusing material in addition to the fluorescent material and the light transmissive material. Examples of the filler include silicon oxide, barium titanate, titanium oxide, and aluminum oxide.
The light transmissive body can use a plate-shaped body formed of a light transmissive material such as glass or resin. Examples of the glass include borosilicate glass and quartz glass. Examples of the resin include a silicone resin and an epoxy resin. When the wavelength conversion member includes a substrate, the substrate is preferably formed of an insulating material that is difficult to transmit light from the light emitting element and external light. Examples of the material of the substrate include ceramics such as aluminum oxide and aluminum nitride, and resins such as a phenol resin, an epoxy resin, a polyimide resin, a bismaleimide triazine resin (BT resin), and a polyphthalamide (PPA) resin. When an adhesive layer is interposed between the light emitting element and the wavelength conversion member, the adhesive constituting the adhesive layer is preferably formed of a material capable of optically connecting the light emitting element and the wavelength conversion member. The material constituting the adhesive layer is preferably at least one resin selected from the group consisting of an epoxy resin, a silicone resin, a phenol resin, and a polyimide resin. The light transmissive body does not have to be disposed on the wavelength conversion member.
Examples of the semiconductor element optionally disposed in the light emitting device include a transistor for controlling the light emitting element and a protective element for suppressing the destruction and the performance deterioration of the light emitting element due to excessive voltage application. Examples of the protective element include a Zener diode. When the light emitting device includes a covering member, it is preferable to use an insulating material as the material of the covering member. More specific examples thereof include a phenol resin, an epoxy resin, a bismaleimide triazine resin (BT resin), a polyphthalamide (PPA) resin, and a silicone resin. A colorant, a fluorescent material, and a filler may be optionally added to the covering member. The light emitting device may use bumps as conductive members. Examples of the material of the bumps include Au and an alloy thereof, and examples of the other conductive member include eutectic solder (Au—Sn), Pb—Sn, and lead-free solder.
An example of the method for producing an exemplary light emitting device according to the first embodiment is described below. For the details, for example, the disclosure of Japanese Unexamined Patent Publication No. 2010-062272 may be referred to. The method for producing a light emitting device preferably includes a step of providing a formed body, a step of disposing a light emitting element, a step of disposing a wavelength conversion member-forming composition, and a step of forming a resin package. When using a block of a plurality of formed bodies each having a recessed portion, the production method may include an individualizing step of separating each resin package in each unit region after the step of forming a resin package.
In the step of providing a formed body, a plurality of leads are monolithically formed using a thermosetting resin or a thermoplastic resin to provide a formed body having a recessed portion with lateral surface(s) and a bottom surface. The formed body may be formed from a block substrate including a plurality of recessed portions.
In the step of disposing a light emitting element, a light emitting element is disposed on the bottom surface of the recessed portion of the formed body, and the positive and negative electrodes of the light emitting element are connected to the first lead and the second lead, respectively, by a wire.
In the step of disposing a wavelength conversion member-forming composition, a wavelength conversion member-forming composition is disposed in the recessed portion of the formed body.
In the step of forming a resin package, the wavelength conversion member-forming composition disposed in the recessed portion of the formed body is cured to form a resin package, thereby producing a light emitting device. When using a plurality of formed bodies formed from a block substrate having a plurality of recessed portions, in the individualizing step after the step of forming a resin package, the resin package is separated for each resin package in each unit region from the block substrate having a plurality of recessed portions, thereby producing individual light emitting devices. As described above, the light emitting devices shown in
An example of the method for producing an exemplary light emitting device according to the second embodiment is described below. For the details, for example, the disclosure of Japanese Unexamined Patent Publication No. 2014-112635 or Japanese Unexamined Patent Publication No. 2017-117912 may be referred to. The method for producing a light emitting device preferably includes a step of disposing a light emitting element, a discretionary step of disposing a semiconductor element, a step of forming a wavelength conversion member including a wavelength conversion body, a step of adhering a light emitting element and a wavelength conversion member, and a step of forming a covering member.
For example, in the step of disposing a light emitting element, a light emitting element is disposed on a substrate. The light emitting element and a semiconductor element are flip-chip mounted, for example, on the substrate. Subsequently, in the step of forming a wavelength conversion member including a wavelength conversion body, a wavelength conversion body may be obtained by forming a plate-shaped, sheet-shaped, or layered wavelength conversion body on one surface of a light transmissive body by a printing method, an adhesive method, a compression molding method, or an electrodeposition method. For example, in the printing method, a wavelength conversion body composition containing a fluorescent material and a resin serving as a binder or a solvent can be printed on one surface of the light transmissive body to form a wavelength converter member including a wavelength conversion body. Subsequently, in the step of adhering a light emitting element and a wavelength conversion member, the wavelength conversion member is allowed to face to the light emitting surface of the light emitting element, and the wavelength conversion member is adhered onto the light emitting element by an adhesive layer. Subsequently, in the step of forming a covering member, the lateral surfaces of the light emitting element and the wavelength conversion member are covered with the composition for a covering member. The covering member is intended to reflect light emitted from the light emitting element, and when the light emitting device includes a semiconductor element, it is preferable to form the covering member such that the semiconductor element is embedded by the covering member. As described above, the light emitting device shown in
The method for producing an oxide fluorescent material includes: providing a first compound containing Mg and/or a second compound containing at least one first element M1 selected from the group consisting of Ca, Sr, Ba, and Zn, a third compound containing Al and/or a fourth compound containing at least one second element M2 selected from the group consisting of Ga, Sc, and In, a fifth compound containing Ge, a sixth compound containing Cr, optionally a seventh compound containing at least one third element M3 selected from the group consisting of Si, Ti, Zr, Sn, and Hf, and optionally an eighth compound containing at least one fourth element M4 selected from the group consisting of Ni, Ce, Eu, Fe, Mn, Nd, Tm, Ho, Er, and Yb; adjusting and mixing the first compound and/or the second compound, the third compound and/or the fourth compound, the fifth compound, the sixth compound, optionally the seventh compound, and optionally the eighth compound to provide a raw material mixture such that, when the total molar ratio of Mg and/or the at least one first element M1 in 1 mol of the composition of the oxide fluorescent material is 2, the molar ratio of the at least one first element M1 is a product of the parameter s and 2, the parameter s is a numerical value of 0 or more and 1.0 or less, and the molar ratio of Mg is a product of 1 minus the parameter s and 2, when the total molar ratio of Al and/or the at least one second element M2 is the parameter u, the molar ratio of the at least one second element M2 is a product of the parameter t and the parameter u, the parameter t is a numerical value of 0 or more and 1.0 or less, the parameter u is a numerical value of 1.5 or more and 2.5 or less, and the molar ratio of Al is a product of 1 minus the parameter t and the parameter u, and when the total molar ratio of Ge and/or the at least one third element M3 is the parameter w, the molar ratio of the at least one third element M3 is a product of the parameter v and the parameter w, the parameter v is a numerical value of 0 or more and 0.5 or less, the parameter w is a numerical value of 3.0 or more and 6.0 or less, the molar ratio of Ge is a product of 1 minus the parameter v and the parameter w, the molar ratio of Cr is the parameter y, the parameter y is a numerical value of 0.005 or more and 1.0 or less, the molar ratio of the at least one fourth element M4 is the parameter z, and the parameter z is a numerical value of 0 or more and 0.5 or less; and heat-treating the raw material mixture at a temperature of 800° C. or higher and 1,400° C. or lower in an atmosphere containing oxygen to obtain an oxide fluorescent material, wherein at least one selected from the group consisting of the first compound, the second compound, the third compound, the fourth compound, the fifth compound, and the sixth compound preferably uses an oxide. The oxide fluorescent material to be obtained preferably has a molar ratio of each element of the oxide fluorescent material in the same or similar range as the supplied composition for obtaining the raw material mixture in 1 mol of the composition of the oxide fluorescent material.
The raw materials for producing an oxide fluorescent material include a first compound containing Mg and/or a second compound containing the first element M1, a third compound containing Al and/or a fourth compound containing the second element M2, a fifth compound containing Ga, a sixth compound containing Cr; and may include a seventh compound containing the third element M3 included as necessary, and an eighth compound containing the fourth element M4 included as necessary. The raw materials for producing an oxide fluorescent material may include at least one compound selected from the group consisting of a first compound containing Mg and a second compound containing the first element M1. The raw materials for producing an oxide fluorescent material may include at least one compound selected from the group consisting of a third compound containing Al and a fourth compound containing the second element M2. Examples of the first compound, the second compound, the third compound, the fourth compound, the fifth compound, the sixth compound, the seventh compound, and the eighth compound include oxides, carbonates, and chlorides, and hydrates of these, respectively. At least one compound selected from the group consisting of the first compound, the second compound, the third compound, the fourth compound, the fifth compound, and the sixth compound is an oxide, and two or more compounds may be oxides. The seventh compound containing the third element M3 included as necessary or the eighth compound containing the fourth element M4 included as necessary may be an oxide. The first compound, the second compound, the third compound, the fourth compound, the fifth compound, and the sixth compound are preferably in the form of powder. The seventh compound and the eighth compound may be in the form of powder.
Examples of the first compound include MgO, MgCO3, and MgCl2. Examples of the second compound include CaO, CaCO3, CaCl2, SrO, SrCO3, SrCl2, BaO, BaCO3, BaCl2, ZnO, ZnCO3, and ZnCl2. Examples of the third compound include Al2O3 and AlCl3. Examples of the fourth compound include Ga2O3, GaCl3, Sc2O3, ScCl3, In2O3, and InCl3. Examples of the fifth compound include GeO2 and GeCl4. Examples of the sixth compound include Cr2O3, Cr2(CO3)3, and CrCl3. The first compound, the second compound, the third compound, the fourth compound, the fifth compound, and the sixth compound may be hydrates.
Examples of the seventh compound include SiO2, TiO2, TiCl4, ZrO2, ZrCl4, SnO2, SnCl2, HfO2, and HfCl4. The seventh compound may be a hydrate.
Examples of the eighth compound include NiO, NiCl2, CeO2, CeCl3, Ce2(CO3)3, Eu2O3, EuCl3, Fe2O3, Fe3O4, FeCl2, FeCl3, FeCO3, Fe2(CO3)3, MnO, MnO2, Mn2O3, Mn3O4, Nd2(CO3)3, Nd2O3, NdCl3, Tm2O3, TmCl3, Ho2O3, HoCl3, Er2O3, ErCl3, Yb2O3, and YbCl3. The eighth compound may be a hydrate.
The raw material mixture is preferably provided by adjusting and mixing raw materials so as to have a composition represented by the following formula (1). The oxide fluorescent material obtained by the production method preferably has a composition in which each element of the oxide fluorescent material is the same as or similar to the composition represented by the following formula (1) for obtaining the raw material mixture in 1 mol of the composition of the oxide fluorescent material.
(Mg1-sM1s)2(Al1-tM2t)u(Ge1-vM3v)wOx:Cry,M4z (1)
In the raw material mixture, in the composition represented by the formula (1), a part of Mg may be replaced by the at least one first element M1; or Mg may entirely be replaced by Ca or Zn of the first elements M1, by two or more first elements M1, that are Ca and at least one selected from the group consisting of Sr, Ba, and Zn, or by two or more first elements M1, that are Zn and at least one selected from the group consisting of Ca, Sr, and Ba. In the composition represented by the formula (1), the raw material mixture may have part of Al replaced by the at least one second element M2, or the second element M2 may be either Sc or In. In the composition represented by the formula (1), the raw material mixture may have all of Al replaced by the at least one second element M2, or the second element M2 may be either Ga or In. In the raw material mixture, in the composition represented by the formula (1), the third element M3 may be either Si or Hf, and the fourth element M4 may be at least one element selected from the group consisting of Ni, Ce, Eu, Fe, Mn, and Nd.
In the raw material mixture, the raw materials containing each element are preferably mixed such that s, t, u, and w satisfy 0≤s≤1.0, 0≤t≤1.0, 1.8≤u≤2.2, and 3.5≤w≤4.5, respectively, in the composition represented by the formula (1). The raw material mixture is preferably mixed with the compound containing Cr such that y satisfies 0.04≤y≤0.40 or 0.20≤y≤0.40 in the composition represented by the formula (1).
The first compound and/or the second compound, the third compound and/or the fourth compound, the fifth compound, the sixth compound, the seventh compound included as necessary, and the eighth compound included as necessary, which are weighed such that the elements contained in each compound of the raw material satisfy the aforementioned composition, can be mixed in wet or in dry to obtain a raw material mixture. The weighed compounds may be mixed using a mixing machine. As the mixing machine, for example, a ball mill, a vibration mill, a roll mill, and a jet mill, which are industrially commonly used, can be used.
The raw material mixture may contain a flux. When the raw material mixture contains a flux, the reaction between the raw materials is promoted more and the solid-phase reaction proceeds more uniformly, so that a fluorescent material having a large particle diameter and good light emission characteristics can be obtained. When the temperature of the heat treatment for obtaining a fluorescent material is similar to the temperature at which the liquid phase of the compound used as the flux is formed, the flux promotes the reaction between the raw materials. As a flux, boric acid, a borate containing at least one element selected from the group consisting of alkaline earth metal elements and alkali metal elements, or a halide containing at least one element selected from the group consisting of alkaline earth metal elements and alkali metal elements can be used. Among the halides, fluoride can be used as a flux. For example, boric acid (H3BO3) and lithium fluoride (LiF) can be used as fluxes.
The raw material mixture can be placed in a crucible or a boat formed of a material such as graphite or other carbon, boron nitride (BN), alumina (Al2O3), tungsten (W), or molybdenum (Mo), and heat-treated in a furnace.
The raw material mixture is heat-treated in an atmosphere containing oxygen. The content of oxygen in the atmosphere is not particularly limited. The content of oxygen in the atmosphere containing oxygen is preferably 5% by volume or more, more preferably 10% by volume or more, and even more preferably 15% by volume or more. The heat treatment is preferably performed in an air atmosphere (oxygen content of 20% by volume or more). When the atmosphere does not contain oxygen, such as an oxygen content of less than 1% by volume, an oxide fluorescent material having a desired composition need not be obtained.
The temperature at which the raw material mixture is heat-treated is 800° C. or higher and 1,400° C. or lower, preferably 850° C. or higher and 1,300° C. or lower, more preferably 870° C. or higher and 1,290° C. or lower, and even more preferably 900° C. or higher and 1,280° C. or lower. When the heat treatment temperature is of 800° C. or higher and 1,400° C. or lower, decomposition by heat is suppressed, and a fluorescent material having a desired composition and a stable crystal structure can be obtained.
In the heat treatment, a maintaining time at a predetermined temperature may be set up. The maintaining time may be, for example, 0.5 hour or more and 48 hours or less, may be 1 hour or more and 40 hours or less, may be 2 hours or more and 30 hours or less, may be 3 hours or more and 20 hours or less, and may be 5 hours or more and 10 hours or less. By setting the maintaining time in the range of 0.5 hour or more and 48 hours or less, the crystal growth can be promoted.
The pressure in the heat treatment atmosphere may be standard atmospheric pressure (0.101 MPa, air atmosphere), and may be 0.101 MPa or more; and the heat treatment may be performed in a pressurized atmosphere range of 0.11 MPa or more and 200 MPa or less. In the heat-treated product obtained by the heat treatment, the crystal structure is more easily decomposed at a higher heat treatment temperature, but in a pressurized atmosphere, the decomposition of the crystal structure can be suppressed.
The heat treatment time can be appropriately selected depending on the heat treatment temperature and the pressure of the atmosphere during the heat treatment, and is preferably of 0.5 hour or more and 20 hours or less. Even in the case of performing two or more stages of heat treatment, the time for one heat treatment is preferably in a range of 0.5 hour or more and 20 hours or less. When the heat treatment time is of 0.5 hour or more and 20 hours or less, the decomposition of the heat-treated product obtained is suppressed, and a fluorescent material having a stable crystal structure and a desired light emission intensity can be obtained. In addition, the production cost can be reduced and the production time can be relatively shortened. The heat treatment time is more preferably 1 hour or more and 10 hours or less, and even more preferably 1.5 hours or more and 9 hours or less.
The heat-treated product obtained by the heat treatment may be subjected to post-treatments such as pulverization, dispersion, solid-liquid separation, and drying. The solid-liquid separation may be performed by a method generally used industrially, such as filtration, suction filtration, pressure filtration, centrifugal separation, and decantation. The drying may be performed with an apparatus generally used industrially, such as a vacuum dryer, a hot air dryer, a conical dryer, and a rotary evaporator.
The present disclosure is hereunder specifically described by reference to the following Examples. The present disclosure is not limited to the following Examples.
For raw materials, 1.61 g of a first compound MgO, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.06 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.04 in the supplied composition. Using an agate mortar and an agate pestle, the raw materials were mixed for 10 minutes to obtain a raw material mixture. The resulting raw material mixture was placed in an alumina crucible and heat-treated at 1,250° C. for 8 hours in an air atmosphere (20% by volume of oxygen) with standard air pressure (0.101 MPa). After the heat treatment, the resulting heat-treated product was pulverized to obtain an oxide fluorescent material of Example 1 having the composition shown in Table 1, which has the molar ratios in the supplied composition. In the compositions of the oxide fluorescent materials of Examples shown in Table 1, the parameter u in the formula (1) is 2.0 (u=2.0), and the parameter w is in the range of 4.0 or more and 6.0 or less (4.0≤w≤6.0). In the compositions of the oxide fluorescent materials of Examples shown in Table 1, the third element M3 and the fourth element M4 are substantially not contained, and the parameter v is substantially 0 (v=0) and the parameter z is substantially 0 (z=0).
The raw materials were weighed and used in the same manner as in Example 1, except that 0.09 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.06 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 2 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
The raw materials were weighed and used in the same manner as in Example 1, except that 0.18 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.12 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 3 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
The raw materials were weighed and used in the same manner as in Example 1, except that 0.27 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.18 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 4 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
The raw materials were weighed and used in the same manner as in Example 1, except that 0.36 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.24 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 5 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
The raw materials were weighed and used in the same manner as in Example 1, except that 0.45 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.31 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 6 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
The raw materials were weighed and used in the same manner as in Example 1, except that 0.60 g of the sixth compound Cr2O3 was weighed. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge4O13:Cr0.40 in the supplied composition. The other procedures were the same as in Example 1 to obtain an oxide fluorescent material of Example 7 having the composition shown in Table 1, which has the molar ratios in the supplied composition.
For raw materials, 1.61 g of a first compound MgO, 3.75 g of Ga2O3, which is a fourth compound containing Ga as the second element M2, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Ga2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 8 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,275° C.
For raw materials, 1.61 g of a first compound MgO, 5.56 g of In2O3, which is a fourth compound containing In as the second element M2, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2In2Ge4O13:Cr0.12 in the supplied composition. In the compositional formula, the molar ratio of elements without numerical values is 1. An oxide fluorescent material of Example 9 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,275° C.
For raw materials, 1.61 g of a first compound MgO, 1.53 g of a third compound Al2O3, 1.39 g of In2O3, which is a fourth compound containing In as the second element M2, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al1.5In0.5Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 10 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,275° C.
For raw materials, 1.61 g of a first compound MgO, 1.53 g of a third compound Al2O3, 0.69 g of Sc2O3, which is a fourth compound containing Sc as the second element M2, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al1.5Sc0.5Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 11 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,275° C.
For raw materials, 0.81 g of a first compound MgO, 1.63 g of ZnO, which is a second compound containing Zn as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg1Zn1Al2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 12 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C. In the compositional formula, the molar ratio of elements without numerical values is 1.
For raw materials, 1.21 g of a first compound MgO, 0.81 g of ZnO, which is a second compound containing Zn as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg1.5Zn0.5Al2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 13 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C.
For raw materials, 1.21 g of a first compound MgO, 1.00 g of CaCO3, which is a second compound containing Ca as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg1.5Ca0.5Al2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 14 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C.
For raw materials, 1.21 g of a first compound MgO, 1.48 g of SrCO3, which is a second compound containing Sr as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg1.5Sr0.5Al2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 15 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C.
For raw materials, 1.21 g of a first compound MgO, 1.97 g of BaCO3, which is a second compound containing Ba as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.18 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg1.5Ba0.5Al2Ge4O13:Cr0.12 in the supplied composition. An oxide fluorescent material of Example 16 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,200° C.
For raw materials, 4.00 g of CaCO3, which is a second compound containing Ca as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.12 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Ca2Al2Ge4O13:Cr0.08 in the supplied composition. An oxide fluorescent material of Example 17 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,200° C.
For raw materials, 4.00 g of CaCO3, which is a second compound containing Ca as the first element M1, 5.56 g of In2O3, which is a fourth compound containing In as the second element M2, 8.37 g of a fifth compound GeO2, and 0.12 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Ca2In2Ge4O13:Cr0.08 in the supplied composition. An oxide fluorescent material of Example 18 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,200° C.
For raw materials, 3.26 g of ZnO, which is a second compound containing Zn as the first element M1, 2.04 g of a third compound Al2O3, 8.37 g of a fifth compound GeO2, and 0.09 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Zn2Al2Ge4O13:Cr0.06 in the supplied composition. An oxide fluorescent material of Example 19 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,180° C.
For raw materials, 1.61 g of a first compound MgO, 2.04 g of a third compound Al2O3, 10.5 g of a fifth compound GeO2, and 0.12 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge5O13:Cr0.08 in the supplied composition. An oxide fluorescent material of Example 20 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C.
For raw materials, 1.61 g of a first compound MgO, 2.04 g of a third compound Al2O3, 12.6 g of a fifth compound GeO2, and 0.12 g of a sixth compound Cr2O3 were weighed and used. The raw materials were weighed such that the molar ratio of each element in 1 mol of the composition of the oxide fluorescent material to be obtained was Mg2Al2Ge6O17:Cr0.08 in the supplied composition. An oxide fluorescent material of Example 21 having the composition shown in Table 1, which has the molar ratios in the supplied composition, was obtained in the same manner as in Example 1, except that the heat treatment temperature was 1,220° C.
For the oxide fluorescent material in each of Examples, the light emission spectrum was measured using a quantum efficiency measurement system (QE-2000, manufactured by Otsuka Electronics Co., Ltd.). The light emission peak wavelength of the excitation light of the light emitting element, which is a semiconductor element, used in the quantum efficiency measurement system was 450 nm. From the obtained light emission spectrum of each fluorescent material, the relative light emission intensity, light emission peak wavelength, and full width at half maximum were determined as light emission characteristics. Specifically, the light emission peak wavelength (nm) in the light emission spectrum of each fluorescent material and the full width at half maximum (FWHM) (nm) in the light emission spectrum were determined. Furthermore, in the light emission spectrum of each oxide fluorescent material, the light emission intensity (%) at 1,000 nm was determined relative to 100% of the light emission intensity of the light emission peak wavelength. The light emission intensity of the oxide fluorescent material according to Example 1 was defined as 100%, and the light emission intensity of the oxide fluorescent material according to each of Examples other than Example 1 was determined as the relative light emission intensity (%). The results are shown in Table 1.
As shown in Table 1 and
The oxide fluorescent materials according to Examples 1 to 7 each contained Mg, Al, Ge, and Cr in 1 mol of the composition of the oxide fluorescent material, and did not contain the first element M1, the second element M2, the third element M3, and the fourth element M4. The oxide fluorescent materials according to Examples 1 to 7 each had a light emission spectrum with a light emission peak wavelength on the longer wavelength side in the wavelength range from red light to near-infrared light, as the molar ratio of the activating element Cr increased, and with a relatively wide full width at half maximum range of 150 nm or more and 250 nm or less. The oxide fluorescent materials according to Examples 1 to 7 each had a parameter y representing the molar ratio of the activating element Cr in the formula (1) in the range of 0.04 or more and 0.40 or less (0.04≤y≤0.40) in 1 mol of the composition of the oxide fluorescent material. The oxide fluorescent materials according to Examples 1 to 7 each having a light emission intensity at 1,000 nm is 5% or more relative to the light emission intensity of the light emission peak wavelength as 100%, and thus emitted light required for analysis in the wavelength range of 900 nm or more and 1,100 nm or less in the wavelength range of near-infrared light.
The oxide fluorescent materials according to Examples 5 to 7 each had a light emission spectrum with a light emission peak wavelength in the wavelength range of more than 900 nm and 1,000 nm or less, and with a wide full width at half maximum range of 200 nm or more and 250 nm or less. The oxide fluorescent materials according to Examples 5 to 7 each having a light emission intensity at 1,000 nm is 50% or more relative to the light emission intensity of the light emission peak wavelength as 100%, and thus emitted light having a high light emission intensity required for analysis in the wavelength range of near-infrared light.
The oxide fluorescent materials according to Examples 8 to 11 each had all or part of Al replaced by the second element M2 in the composition of the oxide fluorescent material, and the second element M2 was at least one selected from the group consisting of Ga, Sc, and In. The oxide fluorescent materials according to Examples 8 to 11 each had a parameter u of 2.0 (u=0) and a parameter t in the range of more than 0 and 1.0 or less (0≤t≤1.0) in the formula (1). The oxide fluorescent materials according to Examples 8 to 11 each had a light emission spectrum with a light emission peak wavelength in the wavelength range of 899 nm or more and 1,000 nm or less, which is close to 900 nm, and with a relatively wide full width at half maximum range of 150 nm or more and 250 nm or less. The oxide fluorescent materials according to Examples 8 to 11 each having a light emission intensity at 1,000 nm is 30% or more relative to the light emission intensity of the light emission peak wavelength as 100%, and thus emitted light having a high light emission intensity required for analysis in the wavelength range of near-infrared light.
The oxide fluorescent materials according to Examples 12 to 16 each had part of Mg replaced by the first element M1 in the composition of the oxide fluorescent material, and the first element M1 was at least one selected from the group consisting of Ca, Sr, Ba, and Zn. The oxide fluorescent materials according to Examples 12 to 16 each had a parameter s in the range of more than 0 and less than 1.0 (0<s<1.0) in the formula (1). The oxide fluorescent materials according to Examples 12 to 16 each had a light emission spectrum with a light emission peak wavelength in the wavelength range of 820 nm or more and 1,000 nm or less, and with a relatively wide full width at half maximum range of 150 nm or more and 250 nm or less. The oxide fluorescent materials according to Examples 14 to 16 each having a light emission intensity at 1,000 nm is 40% or more relative to the light emission intensity of the light emission peak wavelength as 100%, and thus emitted light having a high light emission intensity required for analysis in the wavelength range of near-infrared light.
The oxide fluorescent materials according to Examples 17 to 19 each had all of Mg replaced by the first element M1 in the composition of the oxide fluorescent material, and the first element M1 was at least one selected from the group consisting of Ca and Zn. The oxide fluorescent material according to Example 18 had all of Al replaced by the second element M2 in the composition of the oxide fluorescent material, and the second element M2 was In. The oxide fluorescent materials according to Examples 17 to 19 each had a parameter s of 1.0 (s=1.0) in the formula (1). The oxide fluorescent material according to Example 18 had a parameter u of 2.0 (u=2.0) and a parameter t of 1.0 (t=1.0) in the formula (1). The oxide fluorescent materials according to Examples 17 to 19 each had a light emission spectrum with a light emission peak wavelength in the wavelength range of 680 nm or more and 1,000 nm or less, and with a relatively wide full width at half maximum range of 90 nm or more and 250 nm or less.
The oxide fluorescent materials according to Examples 20 and 21 each contained Mg, Al, and Ge in the composition of the oxide fluorescent material, and did not contain the first element M1, the second element M2, the third element M3, and the fourth element M4. The oxide fluorescent materials according to Examples 20 and 21 each had a parameter x in the range of 13.0 or more and 17.0 or less (13.0≤x≤17.0) in the formula (1). The oxide fluorescent materials according to Examples 20 and 21 each had a light emission spectrum with a light emission peak wavelength in the wavelength range of 830 nm or more and 1,000 nm or less, and with a relatively wide full width at half maximum range of 180 nm or more and 250 nm or less. The oxide fluorescent materials according to Examples 20 and 21 each having a light emission intensity at 1,000 nm is 20% or more relative to the light emission intensity of the light emission peak wavelength as 100%, and thus emitted light having a light emission intensity required for analysis in the wavelength range of near-infrared light.
Embodiments according to the present disclosure include the following oxide fluorescent material and the light emitting device using the same. Embodiments according to the present disclosure preferably include the following method for producing an oxide fluorescent material.
The oxide fluorescent material according to the present disclosure can be used in light emitting devices for medical use to obtain information inside living bodies, light emitting devices to be mounted on small mobile devices such as smartphones and smartwatches to manage physical conditions, light emitting devices used in medical devices, light emitting devices for analyzers to non-destructively measure the internal information of agricultural products such as fruits, vegetables, rice, foods, and pharmaceutical products, light emitting devices for plant cultivation to affect the photoreceptors of plants, and light emitting devices for reflection spectroscopic measuring devices used for measuring film thickness or the like.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2023-105243 | Jun 2023 | JP | national |
