KR20110004915A - Red phosphor and its forming method for use in solid state lighting - Google Patents
Red phosphor and its forming method for use in solid state lighting Download PDFInfo
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Abstract
Description
The present invention relates to a red phosphor and a method for producing the same, and more particularly, to a red phosphor for a solid state lighting and a method for producing the same.
In general, white LEDs using semiconductors have longer life, smaller size, and lower voltage than incandescent lamps such as 60W low-end lamps. The possibility of the light source is recognized.
As a method of manufacturing the white LED, there is a method of using all three color (red, green, blue) light emitting diodes, but there is a disadvantage in that the size of the product is increased because the manufacturing cost is high and the driving circuit is complicated. In addition, white LEDs combining YAG: Ce phosphors with InGaN-based blue LEDs having a wavelength of 460 nm have been put to practical use, and part of the blue light generated from the blue LEDs excites the YAG: Ce phosphors to generate yellow-green fluorescence. In addition, these blue and yellow-green are synthesized on the principle of emitting white light.
However, since the light of a white LED, which combines a blue LED with a YAG: Ce phosphor, has only a part of the spectrum of visible light, a color rendering index is low, and thus color rendering is not properly performed.
In order to solve the above problems of white LED, efforts are actively underway to develop white LEDs that emit white light close to natural colors by using ultraviolet (“UV”) LEDs as excitation light sources and combining red, green, and blue phosphors. It is becoming. In order to manufacture such a white LED, it is essential to develop a fluorescent material having a particularly good luminous efficiency, particularly a red fluorescent material, in an excitation light source having a wavelength of about 400 nm, which has the best chip efficiency. That is, although blue and green have satisfactory luminous efficiency at present, the red fluorescent material has the worst characteristics. Therefore, it is urgent to develop a red fluorescent material having excellent luminous efficiency in the UV excitation source.
In addition, fluorescent materials having good efficiency in the near ultraviolet are also very important in the development of active light emitting liquid crystal displays. Active emission type liquid crystal display means that the light irradiated from the rear light source passes through the polarizer through the liquid crystal layer, and the liquid crystal layer acts to block or prevent the back light from passing through the rear light through its orientation. The light forms a predetermined display form, and the back light passing through the liquid crystal layer is configured to implement an image through the windshield by exciting the corresponding phosphor. The active light-emitting liquid crystal display device has an advantage that the structure is simple and easy to manufacture compared to the conventional color liquid crystal display device, but it is evaluated as not practical because of the low luminance of the red phosphor among the phosphors used.
In particular, the active light-emitting liquid crystal display device should use near-ultraviolet rays of 390 nm or more as a rear light source for protecting the liquid crystal. The most promising candidate for this rear light source is a UV LED having a wavelength of 390 nm or more. Therefore, the development of such a efficient red fluorescent material for near ultraviolet rays is very important in the development of an active light emitting liquid crystal display device as in the development of red and white LED.
Conventional white LEDs use a combination of a blue LED and a yellow phosphor (YAG: Ce), but the red component lacks the emitted light to have a blue white color. In addition, the use of red phosphors has problems such as low luminous efficiency, deterioration with time and temperature, and impossibility of excitation of visible light.
CaAlSiN 3 has been developed as a red phosphor for the purpose of solving the above problems. This red phosphor uses a blue LED light source having a wavelength of 450 nm to 490 nm as excitation light, and it is reported that there is no degradation in the temperature range from room temperature to 100 ° C. However, this phosphor is manufactured by mixing aluminum nitride, calcium nitride and europium in a glove box where water and air are blocked, and reacting at about 10 atm and at about 1,800 ° C in a nitrogen atmosphere. Prepare the phosphor. Such a method for producing a red phosphor containing CaAlSiN 3 has a fairly complicated process and a very expensive raw material. In addition, such a conventional red phosphor is known to have a low near ultraviolet excitation efficiency.
Accordingly, it is an object of the present invention to provide a red phosphor for solid-state illumination that can be excited by any of near ultraviolet light, blue light, and green light as a red phosphor that can be produced in atmospheric air, and a method of manufacturing the same.
In order to achieve the above object, according to the present invention there is provided a red phosphor for solid-state illumination, comprising La and Ti oxide and a rare earth element.
There is provided a red phosphor for solid-state illumination, characterized in that the rare earth element has one or more combinations selected from the group consisting of Eu, Er, Dy, Sm, Tb, Ce, Gd, Nd, Dy, Ho. Eu is representative as the rare earth element. According to the present invention, a red phosphor for solid-state illumination, which is prepared by mixing 'La oxide', 'Ti oxide' and 'Eu oxide' at a predetermined molar ratio, may be provided. In the present invention, La and Ti oxides may be selected from La 2 TiO 5 , LaTi 2 O 9 and La 4 Ti 9 O 24 . The red phosphor for solid state lighting according to the present invention can be produced in a temperature range of 1,000 ° C. to 1,500 ° C. using a solid state sintering method in the atmosphere.
The conventional red phosphor has a problem in that the phosphor manufacturing cost is high due to a complicated manufacturing facility and the ultraviolet excitation is not efficient because it is manufactured under a high temperature, high pressure nitrogen atmosphere. In contrast, the red phosphor for solid-state illumination according to the present invention can be produced at low cost in atmospheric air, and is a red phosphor containing La oxide and Ti oxide as a main component and containing rare earth elements, and is excited by any of near ultraviolet light, blue light, and green light. Is an efficient red phosphor.
The red phosphor according to the present invention shows an excellent effect in improving the color rendering of the conventional white LED. In addition, the red phosphor according to the present invention is excellent in thermal stability.
1 is a diagram showing an XRD diffraction pattern of a La 2 TiO 5 red phosphor according to a first embodiment of the present invention.
FIG. 2 is La excited from 395 nm near ultraviolet when LaO 2 , TiO 2 and Eu 2 O 3 form a La 2 TiO 5 red phosphor at a molar ratio of 0.8: 1.0: 0.2 according to the first embodiment of the present invention. Figure 2 shows the luminescence intensity of 2 TiO 5 red phosphor and Y 2 O 2 S phosphor.
FIG. 3 is La excited according to a first embodiment of the present invention when LaO 2 , TiO 2 and Eu 2 O 3 are made of La 2 TiO 5 red phosphor at a molar ratio of 0.8: 1.0: 0.2 2 shows the luminescence intensity of TiO 5 and Y 2 O 2 S red phosphors.
FIG. 4 shows the luminescence intensity of La 2 TiO 5 red phosphors excited at 395 nm near ultraviolet light according to the first embodiment of the present invention, and shows three emission peaks according to the change amount of Eu 2 O 3 (mixed molar ratio). (peak) (594 nm, 610 nm, 628 nm).
FIG. 5 shows the light emission intensity of the La 2 TiO 5 red phosphor that is excited in 465 nm blue light according to the first embodiment of the present invention, and shows three emission peaks according to the change amount of Eu 2 O 3 (mixed molar ratio). peak) (594 nm, 610 nm, 628 nm).
Figure 6 is according to the first embodiment of the present invention, La 2 TiO 5 red phosphor has a molar ratio of 0.8: 1.0: time been made to 0.2 of LaO 2, TiO 2, Eu 2
7 is a diagram showing an XRD diffraction pattern of a LaTi 2 O 9 red phosphor according to a second embodiment of the present invention.
FIG. 8 is LaTi excited at 395 nm near ultraviolet when LaO 2 , TiO 2 and Eu 2 O 3 form a LaTi 2 O 9 red phosphor at a molar ratio of 0.8: 2.0: 0.2 according to the second embodiment of the present invention. Figure showing emission intensity of 2 0 9 red phosphor and conventional Y 2 O 2 S phosphor.
9 is according to a second embodiment of the present invention is LaO 2, TiO 2, and Eu 2 O 3 0.8: LaTi 2 O which is excited in, 465nm blue light as achieved by LaTi 2 O 9, the red phosphor in a molar ratio of 0.2: 2.0 9 shows the luminescence intensity of red phosphor and conventional Y 2 O 2 S phosphor.
FIG. 10 is a view showing the luminescence intensity of LaTi 2 O 9 red phosphor excited at 395 nm near ultraviolet light according to the change amount of Eu 2 O 3 (mixed molar ratio) according to the second embodiment of the present invention.
FIG. 11 is a view showing the luminescence intensity of LaTi 2 O 9 red phosphor excited at 465 nm blue light according to the change amount of Eu 2 O 3 (mixed molar ratio) according to the second embodiment of the present invention.
12 is a LaTi 2 O 9 red phosphor and conventionally, when LaO 2 , TiO 2 and Eu 2 O 3 form a LaTi 2 O 9 red phosphor at a molar ratio of 0.8: 2.0: 0.2 according to the second embodiment of the present invention. Excitation spectrum of Y 2 O 2 S phosphor.
13 is an XRD diffraction pattern of a La 4 Ti 9 O 24 red phosphor obtained by mixing and heating LaO 2 , TiO 2, and Eu 2 O 3 in a molar ratio of 0.8: 3.0: 0.2 according to a third embodiment of the present invention. Figure shown.
FIG. 14 illustrates a La 4 Ti 9 O 24 red phosphor at an optimal mixing ratio (mixing molar ratio of LaO 2 , TiO 2, and Eu 2 O 3 is 0.8: 3.0: 0.2) according to the third embodiment of the present invention. A diagram showing the luminescence intensity of La 4 Ti 9 O 24 red phosphors excited in 395 nm near ultraviolet and conventional Y 2 O 2 S phosphors.
FIG. 15 illustrates a La 4 Ti 9 O 24 red phosphor at an optimum mixing ratio (mixing molar ratio of LaO 2 , TiO 2, and Eu 2 O 3 is 0.8: 3.0: 0.2) according to the third embodiment of the present invention. A diagram showing the luminescence intensities of a La 4 Ti 9 O 24 red phosphor excited at 465 nm blue light and a conventional Y 2 O 2 S phosphor.
FIG. 16 is a graph showing the luminescence intensity of a La 4 Ti 9 O 24 red phosphor excited at 395 nm near ultraviolet light according to a change amount of Eu 2 O 3 (mixed molar ratio) according to a third embodiment of the present invention.
FIG. 17 is a graph showing the luminescence intensity of La 4 Ti 9 O 24 red phosphor excited at 465 nm blue light according to the change amount of Eu 2 O 3 (mixed molar ratio) according to the third embodiment of the present invention.
FIG. 18 is a La 4 Ti 9 O 24 red phosphor formed by LaO 2 , TiO 2 and Eu 2 O 3 depending on a change in temperature in a molar ratio of 0.8: 3.0: 0.2 according to a third embodiment of the present invention. Figure showing the luminous intensity of La 4 Ti 9 O 24 red phosphor.
19 is La 4 Ti 9 O 24 red in a molar ratio of 0.8: 3.0: 0.2 (optimal mixing molar ratio of Eu 2 O 3 ) of LaO 2 , TiO 2 and Eu 2 O 3 according to the third embodiment of the present invention. Excitation spectra of La 4 Ti 9 O 24 red phosphors and conventional Y 2 O 2 S phosphors when formed into phosphors.
20 is a La-Ti oxide red phosphor and a conventional Y 2 O 2 S phosphor when each of the La-Ti oxide red phosphors according to a preferred embodiment of the present invention is composed of the corresponding optimal mole fraction of Eu 2 O 3 . Shows excitation spectra of a wave.
FIG. 21 illustrates a La-Ti oxide red phosphor excited in 395 nm near ultraviolet light, when each of the La-Ti oxide red phosphors according to a preferred embodiment of the present invention is composed of a corresponding optimal Eu 2 O 3 mixture. Figure showing the luminescence intensity of Y 2 O 2 S phosphor.
FIG. 22 shows a La-Ti oxide red phosphor excited in 465 nm blue light and a conventional Y when each of the La-Ti oxide red phosphors according to a preferred embodiment of the present invention consist of a corresponding optimal Eu 2 O 3 mixed mole fraction. Figure 2 shows the luminescence intensity of 2 O 2 S phosphors.
According to one embodiment of the present invention in order to solve the above technical problem of the conventional red phosphor, as a raw material 'La oxide' and 'Ti oxide' and 'Eu oxide' by mixing in an optimal molar ratio of 1,000 in the air The red phosphor, which is mainly composed of La and Ti oxides (hereinafter also referred to as 'La-Ti' oxides) as a main component, may be prepared by heat treatment at a temperature of 1 ° C. to 1500 ° C. Here, La and Ti oxide is a compound containing La, Ti, and oxygen (O) as an element, such as La 2 TiO 5 , LaTi 2 O 9 and La 4 Ti 9 O 24 , which are compounds, and a formula of La x Ti y O z . Refers to the substance represented by
In the following, the red phosphor for solid-state lighting prepared according to the preferred embodiment of the present invention will be mainly described for the red phosphor for white LED, for example, the red phosphor for solid-state lighting according to the present invention is not limited to the white LED for various other solid It should be noted that it can be applied to a variety of uses.
In addition, in the following examples of the present invention, Eu will be described as an example of the rare earth element, but a person having ordinary knowledge in the relevant field ('who is skilled in the art') can add and modify various rare earth elements in addition to the Eu. There will be. That is, the rare earth element may have one or more combinations selected from the group consisting of Eu, Er, Dy, Sm, Tb, Ce, Gd, Nd, Dy, Ho.
[First Embodiment] La 2 TiO 5 : Preparation of Eu Phosphor
Using a mortar and pestle, the raw materials LaO 2 , TiO 2 and Eu 2 O 3 were mixed well in an appropriate amount of alcohol solvent, and the slurry formed was mixed until the alcohol evaporated. Alternatively, the raw material was weighed in an appropriate stoichiometric ratio and properly mixed with an alcohol solvent using an yttria stabilized zirconia ball. Then, the raw material mixed in an alcohol solvent was mixed with a ball mill for 24 hours, dried in an oven at 95 ° C., and then mixed with a mortar and then formed into a pellet or powder. Thereafter, heat treatment was performed in the air at a temperature range of 1,000 ° C to 1500 ° C. At this time, according as the mixture of Eu 2 O 3, the mixture fraction of Eu 2 O 3 to the total of the raw materials it was tested by changing from 0.005 to 0.4.
Table 1 shows the raw materials at the time the first embodiment TiO 2 is from 1.0 mole depending according to the present invention, La 2 O 3, TiO 2, Eu 2 O to the total raw materials in the mixing molar ratio of the respective mixture ratio of Eu 2 O 3 3 The mixing fraction of is shown.
The optimum mixing fraction of Eu 2 O 3 was confirmed by changing the mixing fraction. Here, the optimum mixing fraction represents the mixing fraction of Eu 2 O 3 which maximizes the extubation intensity of the red phosphor, which is used in the same sense throughout the specification of the present invention.
1 is a La 2 TiO 5 red phosphor prepared by mixing a mixture ratio of each of La 2 O 3 , TiO 2 and Eu 2 O 3 in a ratio of 0.8: 1.0: 0.2 and heat-treating them according to the first embodiment of the present invention ( In other words, La and Ti oxides are XRD diffraction patterns of a red phosphor in the form of La 2 TiO 5 ). Referring to Figure 1 it can be seen that substantially a single phase of the La 2 TiO 5 compound was formed. In FIG. 1, three numbers indicated as 08_1_02 after LTE indicate a case where a mixed molar ratio of La 2 O 3 , TiO 2, and Eu 2 O 3 is 0.8: 1.0: 0.2, but also in FIGS. 7, 13, 14, and 15. It is the same.
Observation of the emission spectrum
FIG. 2 shows excitation at 395 nm near ultraviolet light when La 2 O 3 , TiO 2 and Eu 2 O 3 form a La 2 TiO 5 red phosphor at a molar ratio of 0.8: 1.0: 0.2 according to the first embodiment of the present invention. FIG. 3 is a view showing luminescence intensity of La 2 TiO 5 red phosphor and Y 2 O 2 S phosphor, and FIG. 3 is an optimal mole fraction of Eu 2 O 3 according to the first embodiment of the present invention (LaO 2 , TiO 2 and Eu Molar ratio of 2 O 3 = 0.8: 1.0: 0.2), showing the emission intensity of La 2 TiO 5 and Y 2 O 2 S red phosphors excited at 465 nm blue light when the La 2 TiO 5 red phosphor was formed.
Referring to FIG. 2, the maximum tube strength value of the red phosphor prepared at the optimum mixing ratio through the experiment of the first embodiment obtained by being excited at 395 nm near ultraviolet ray is smaller than the Y 2 O 2 S red tube intensity. However, in FIG. 3, the maximum tube strength value of the red phosphor prepared at the optimum mixing ratio through the experiment of the first embodiment obtained by being excited at 465 nm blue light is much larger than the Y 2 O 2 S red tube intensity.
2 and 3, three emission peak values such as 594 nm, 610 nm and 628 nm are observed in La 2 TiO 5 secreted at the optimum mixing fraction of Eu 2 O 3 according to the first embodiment of the present invention. Here, as shown in FIGS. 2 and 3, the optimum mixing mole fraction of Eu 2 O 3 relative to the entire raw material is 0.1 (corresponding to the mixing mole ratio 0.2 of Eu 2 O 3 ) as shown in FIGS. 4 and 5. It is derived based on experimental results.
Eu 2 O 3 Of optimum mixing mole fractions
FIG. 4 shows the light emission intensity of a La 2 TiO 5 red phosphor excited at 395 nm near ultraviolet light according to the first embodiment of the present invention, and shows three light emission levels depending on the amount of Eu 2 O 3 added (mixed molar ratio). peak (peak) (594nm, 610nm, 628nm) , showing a diagram, and Fig. 5 is that showing the light intensity of the La 2 TiO 5, a red phosphor which is excited at 465nm blue light according to the first embodiment of the present invention, Eu 2 O It is a figure which shows three light emission peaks (594 nm, 610 nm, 628 nm) according to the addition amount of 3 (mixed molar ratio).
As shown in Figs. 4 and 5, in any case excited with 395 nm near ultraviolet or 465 nm blue light, the La 2 TiO 5 red phosphor emission intensity corresponds to 0.2 (mole fraction 0.1 of Eu 2 O 3 relative to the entire raw material). An optimal mixing molar ratio of Eu 2 O 3 is observed. In other words, the optimal mixing molar ratio of Eu 2 O 3 is about 0.2. In this case, the luminescence intensity decreases at concentrations of 0.2 or more due to excess concentration and at concentrations of 0.2 or less due to activator deficiency concentration, respectively. 4 and 5, the optimum heat treatment temperature is about 1470 ℃.
Observation of the excitation spectrum
6 is a La 2 TiO 5 red phosphor according to the first embodiment of the present invention when LaO 2 , TiO 2 , Eu 2 O 3 having a molar ratio of 0.8: 1.0: 0.2 (that is, an optimal mixing ratio), Excitation spectra of La 2 TiO 5 red phosphors and conventional Y 2 O 2 S phosphors are shown. Referring to FIG. 6, when compared with the Y 2 O 2 S red phosphor used as a conventional UV phosphor, a red phosphor prepared at an optimal mixing ratio has a small excitation peak for near ultraviolet rays and a larger one for 465 nm blue light. It is observed to have an excitation peak.
Second Embodiment LaTi 2 O 9 : Preparation of Eu Phosphor
LaTi oxide and LaTi 2 O 9 as a rare-earth element for use in a solid-state light emitting body including the main raw materials for the production of Eu La 2 (i.e., Li and Ti oxide is a red phosphor which is represented in the form of LaTi 2 O 9) O 3 , TiO 2 and Eu 2 O 3 are mixed in a stoichiometric ratio.
Using a mortar and pestle, the raw materials LaO 2 , TiO 2 and Eu 2 O 3 were mixed well in an appropriate amount of alcohol solvent, and the slurry formed was mixed until the alcohol evaporated. Alternatively, the raw material was weighed in an appropriate stoichiometric ratio and properly mixed with an alcohol solvent using an yttria stabilized zirconia ball. Then, the raw material mixed in an alcohol solvent was mixed with a ball mill for 24 hours, dried in an oven at 95 ° C., and then mixed with a mortar and then formed into a pellet or powder. Thereafter, heat treatment was performed in the air at a temperature range of 1,000 ° C to 1500 ° C. At this time, according as the mixture of Eu 2 O 3, the mixture fraction of Eu 2 O 3 to the total of the raw materials it was tested by changing to 0.0033 to 0.267. Table 2 raw material at the time the second embodiment TiO 2 is from 1.0 mole depending according to the present invention, La 2 O 3, TiO 2, Eu 2 O to the total raw materials in the mixing molar ratio of the respective mixture ratio of Eu 2 O 3 3 The mixing fraction of is shown.
7 is a diagram illustrating an XRD diffraction pattern of a LaTi 2 O 9 red phosphor according to a second embodiment of the present invention. Referring to FIG. 7, when the mixed molar ratio of La 2 O 3 , TiO 2, and Eu 2 O 3 is 0.8: 2.0: 0.2 (LTE_08_2_02) and 0.5: 2.0: 0.5 (LTE_05_2_05), the LaTi 2 O 9 compound may be substantially It can be seen that a single phase has been formed. It should be noted here that the single phase of the LaTi 2 O 9 compound is obtained from a mixed fraction of 0.002 to 0.1667 of Eu 2 O 3 .
Observation of the emission spectrum
8 illustrates a LaTi 2 O 9 red phosphor at a molar ratio of LaO 2 : TiO: Eu 2 O 3 = 0.8: 2.0: 0.2 according to the second embodiment of the present invention.
As a rule, the luminescence intensity of the LaTi 2 O 9 red phosphor and the conventional Y 2 O 2 S phosphor excited at 395 nm near ultraviolet is shown, and FIG. 9 shows LaO 2 : TiO: according to the second embodiment of the present invention. A diagram showing the luminescence intensity of LaTi 2 O 9 red phosphors excited by 465 nm blue light and conventional Y 2 O 2 S phosphors when formed into LaTi 2 O 9 red phosphors at a molar ratio of Eu 2 O 3 = 0.8: 2.0: 0.2.
The maximum luminous intensity of the LaTi 2 O 9 red phosphor prepared at the optimum mixing molar ratio of the second embodiment and excited to near-ultraviolet light of 395 nm is similar to that of the conventional Y 2 O 2 S phosphor, but considering the emission range, the conventional Y It is much stronger than the luminescence intensity of 2O 2 S phosphor. As shown in Fig. 9, when using 465 nm blue light as the excitation source, the emission intensity of the LaTi 2 O 9 red phosphor according to the optimum mixing mole ratio of the second embodiment is much larger than that of the conventional Y 2 O 2 S phosphor. .
Eu 2 O 3 Of optimum mixing mole fractions
FIG. 10 is a graph showing the luminescence intensity of LaTi 2 O 9 red phosphor excited at 395 nm near ultraviolet ray according to the change in the amount of Eu 2 O 3 (mixed molar ratio) according to the second embodiment of the present invention. The emission intensity of the LaTi 2 O 9 red phosphor excited by 465 nm blue light according to the addition amount (mixed molar ratio) of Eu 2 O 3 according to the second embodiment of the present invention is shown.
As shown in FIGS. 10 and 11, the optimum mixing molar ratio of Eu 2 O 3 is 0.2 (corresponding to a mole fraction of Eu 2 O 3 relative to the entire raw material of 0.067), at a concentration of at least 0.2 due to excess concentration and The luminescence intensity decreases at concentrations of 0.2 or less due to activator deficiency concentrations, respectively. 10 and 11, the optimum heat treatment temperature is about 1440 ℃.
Observation of the excitation spectrum
12 is a LaTi 2 O 9 red phosphor and conventionally, when LaO 2 , TiO 2 and Eu 2 O 3 form a LaTi 2 O 9 red phosphor at a molar ratio of 0.8: 2.0: 0.2 according to the second embodiment of the present invention. of Y 2 O 2 S phosphor exciting a view showing the spectrum. Referring to FIG. 12, it is observed that the LaTi 2 O 9 red phosphor prepared at the optimum mixing ratio has a larger excitation peak at near ultraviolet of 395 nm and blue light of 465 nm when compared with the conventional Y 2 O 2 S phosphor.
Third Embodiment La
4
Ti
9
O
24
Preparation of Eu Phosphor
Using a mortar and pestle, the raw materials LaO 2 , TiO 2 and Eu 2 O 3 were mixed well in an appropriate amount of alcohol solvent, and the slurry formed was mixed until the alcohol evaporated. Alternatively, the raw material was weighed in an appropriate stoichiometric ratio and properly mixed with an alcohol solvent using an yttria stabilized zirconia ball. Then, the raw material mixed in an alcohol solvent was mixed with a ball mill for 24 hours, dried in an oven at 95 ° C., and then mixed with a mortar and then formed into a pellet or powder. Thereafter, heat treatment was performed in the air at a temperature range of 1,000 ° C to 1500 ° C. At this time, according as the mixture of Eu 2 O 3, the mixture fraction of Eu 2 O 3 to the total of the raw materials it was tested by changing from 0.0025 to 0.2. Table 3 raw material when the third embodiment is TiO 2 3.0 mole depending according to the present invention, La 2 O 3, TiO 2, Eu 2 O to the total raw materials in the mixing molar ratio of the respective mixture ratio of Eu 2 O 3 3 The mixing fraction of is shown.
13 is an XRD diffraction pattern of a La 4 Ti 9 O 24 red phosphor obtained by mixing and heating LaO 2 , TiO 2, and Eu 2 O 3 in a molar ratio of 0.8: 3.0: 0.2 according to a third embodiment of the present invention. Figure is shown. Referring to FIG. 13, when the mixed molar ratio of La 2 O 3 , TiO 2, and Eu 2 O 3 is 0.5: 5.0: 0.5 (LTE_05_3_05) and 0.8: 3.0: 0.2 (LTE_08_3_02), the LaTi 2 O 9 compound may be substantially It can be seen that a single phase has been formed. It should be noted here that the single phase of the La 4 Ti 9 O 24 compound is obtained from a mixed fraction of 0.0025 to 0.125 of Eu 2 O 3 .
Observation of the emission spectrum
FIG. 14 illustrates a La 4 Ti 9 O 24 red phosphor at an optimal mixing ratio (mixing molar ratio of LaO 2 , TiO 2, and Eu 2 O 3 is 0.8: 3.0: 0.2) according to the third embodiment of the present invention. The emission intensity of the La 4 Ti 9 O 24 red phosphor and the conventional Y 2 O 2 S phosphor excited at 395 nm near ultraviolet ray is shown. FIG. 15 is an optimal mixing ratio (LaO) according to the third embodiment of the present invention. 2, TiO 2, and Eu mixing molar ratio of the 2 O 3 is 0.8: 3.0: 0.2) to La 4 Ti 9 O 24 when achieve a red phosphor, La which is excited at 465nm blue light 4 Ti 9 O 24 red phosphor and the conventional Y 2 O It is a figure which shows the light emission intensity of 2S fluorescent substance.
In FIGS. 14 and 15, LTE_08_3_02 represents an extubation spectrum of a red phosphor prepared at an optimal mixing fraction of Eu 2 O 3 according to the third embodiment of the present invention. La 4 Ti 9 O 24, the red phosphor is La 4 Ti 9 O emission amount of 24 red phosphor is prepared in the optimum mixing ratio of the excited by near ultraviolet and blue LED is much larger emission intensity of a conventional Y 2 O 2 S phosphor .
Eu 2 O 3 Of optimum mixing mole fractions
FIG. 16 is a graph showing the luminescence intensity of La 4 Ti 9 O 24 red phosphor excited at 395 nm near ultraviolet ray according to the change in the amount of Eu 2 O 3 (mixed molar ratio) according to the third embodiment of the present invention. FIG. 17 is a graph showing the luminescence intensity of La 4 Ti 9 O 24 red phosphors excited at 465 nm blue light according to the change in the amount of Eu 2 O 3 (mixed molar ratio) according to the third embodiment of the present invention.
As shown in Figures 16 and 17, the optimal mixing molar ratio of Eu 2 O 3 is 0.2 (corresponding to a mole fraction of Eu 2 O 3 relative to the entire raw material of 0.05), at concentrations of at least 0.2 due to excess concentration and The luminescence intensity decreases at concentrations of 0.2 or less due to activator deficiency concentrations, respectively.
18 shows LaO 2 , TiO 2 and Eu 2 O 3 formed of La 4 Ti 9 O 24 red phosphors depending on the change in temperature at a molar ratio of 0.8: 3.0: 0.2 according to the third embodiment of the present invention. It is a figure which shows the light emission intensity of La 4 Ti 9 O 24 red phosphor. 16 and 17 degrees, the optimum heat treatment temperature is about 1,340 ℃.
Observation of the excitation spectrum
19 is a La 4 Ti 9 O in a molar ratio of LaO 2 , TiO 2 and Eu 2 O 3 0.8: 3.0: 0.2 (that is, the optimum mixing molar ratio of Eu 2 O 3 ) according to a third embodiment of the present invention 24 is achieved when a red phosphor, La Ti 4 O 9 24 a red phosphor and a view showing the excitation spectra of a conventional Y 2 O 2 S phosphor. Referring to FIG. 19, it was observed that the La 4 Ti 9 O 24 red phosphor prepared at the optimum mixing ratio had a larger excitation peak at near ultraviolet of 395 nm and blue light of 465 nm, compared with the conventional Y 2 O 2 S phosphor. do. In FIG. 19, LTE_1_3_614nm represents an excitation spectrum of a red phosphor prepared in Eu 2 O 3 of an optimal mixing fraction according to the third embodiment of the present invention.
Hereinafter, on the basis of the results of the first to third embodiments as described above, a detailed description of the invention will be described with reference to FIGS. 20 to 22. 20 is a La-Ti oxide red phosphor and a conventional Y 2 O 2 S phosphor when La-Ti oxide is composed of an optimal Eu 2 O 3 mixed molar ratio according to the first to third embodiments of the present invention Is an illustration of the excitation spectrum of?
In Fig. 20, LTE_1_1_610 nm shows the excitation spectrum (measured at the maximum value of 610 nm) of the red phosphor prepared in Eu 2 O 3 of the optimum mixing fraction according to the first embodiment of the present invention; LTE_1_2_614 nm represents the excitation spectrum (measured at the maximum value of 614 nm) of the red phosphor prepared in Eu 2 O 3 of the optimum mixing fraction according to the second embodiment of the present invention; LTE_1_3_614 nm represents the excitation spectrum (measured at the maximum value of 614 nm) of the red phosphor prepared in Eu 2 O 3 of the optimum mixing fraction according to the third embodiment of the present invention.
In Figure 20, the horizontal axis represents the wavelength of photo-luminescence and the vertical axis represents the intensity of the photoluminescence. As shown in FIG. 20, the red phosphor according to the embodiment of the present invention may be effectively excited to any one of near ultraviolet light, blue light, and green light. Referring to FIG. 20, according to the first embodiment (LTE_1_1), the second embodiment (LTE_1_2), and the third embodiment (LTE_1_3) of the present invention, optimal mixing of Eu 2 O 3 including La-Ti oxide as a main component The red phosphor prepared at the fraction is compared with a conventional Y 2 O 2 S phosphor which has been used as a red phosphor for UV excitation of a conventional fluorescent lamp.
As shown in FIG. 20, the conventional Y 2 O 2 S phosphor spectrum mainly has an excitation band in the UV region, but has a much smaller excitation band in the visible region than the red phosphor of the present invention. Therefore, the conventional Y 2 O 2 S phosphor cannot be effectively excited in blue light and green light. According to the present invention, the red phosphor comprising La-Ti oxide as a main component has higher excitation intensity than any of the conventional Y 2 O 2 S phosphor in any of near ultraviolet, blue light and green light.
FIG. 21 shows La-Ti oxide red phosphors according to the first embodiment (LTE_1_1), the second embodiment (LTE_1_2), and the third embodiment (LTE_1_3) (where PL represents emission intensity). The emission intensity of La-Ti oxide red phosphors and conventional Y 2 O 2 S phosphors excited at 395 nm near ultraviolet, when made with the corresponding optimal Eu 2 O 3 mixed mole fraction, is shown. As shown in FIG. 21, the luminescence intensity of the La-Ti oxide red phosphor prepared according to the present invention is three times higher than that of the conventional Y 2 O 2 S phosphor which has been used as a red phosphor for UV of a conventional fluorescent lamp. It is clearly shown.
FIG. 22 shows La-Ti oxide red phosphors according to the first embodiment (LTE_1_1), the second embodiment (LTE_1_2), and the third embodiment (LTE_1_3) (where PL represents emission intensity). The emission intensity of La-Ti oxide red phosphors and conventional Y 2 O 2 S phosphors excited at 465 nm blue light, when made at the corresponding optimal mixing ratio of Eu 2 O 3 , is shown.
Referring to Figure 22, the luminous intensity of the La-Ti oxide red phosphor prepared according to the present invention has a seven times the intensity of the conventional Y 2 O 2 S phosphor that has been used as a red phosphor for UV of a conventional fluorescent lamp, It is clearly shown that the La-Ti oxide red phosphor is excited more effectively in blue light. It should be noted here that any one of near ultraviolet light, blue light and green tube source may be the excitation source.
In the above, various embodiments of the production of a red phosphor for solid-state lighting containing La oxide and Ti oxide as a main raw material and rare earth such as Eu as a secondary component and La and Ti oxide and rare earth elements have been described. In summary.
On the other hand, according to another aspect of the present invention, in the manufacture of a solid phosphor red phosphor, the solid phosphor red phosphor containing La and Ti oxide as a main component from a raw material such as chlorides, nitrides, sulfides, hydroxides of La and Ti Can be provided. In this case, the chlorides, nitrides, sulfides, and hydroxides of La and / or Ti may be mixed with each other with a suitable raw material of the rare earth element and heat treated.
In the above manufacturing process, the chlorides, nitrides, sulfides, and hydroxides of La and / or Ti are decomposed by heat treatment, and as a result, La and Ti combine with oxygen (O) to form La-Ti oxide as a main component. It contains a rare earth element such as Eu to obtain the desired red phosphor for solid illumination. The specific manufacturing method may be variously designed by those skilled in the art with reference to the first to third embodiments, and thus a detailed description thereof will be omitted.
Claims (12)
La and Ti oxides; And
A red phosphor for solid state illumination comprising a rare earth element.
Main component La and Ti oxides; And
Including rare earth elements,
The red phosphor for solid state lighting is a red phosphor for solid state lighting, characterized in that the mixture of any one or more of La and / or chlorides, nitrides, sulfides and hydroxides and the rare earth raw material and heat-treated at atmospheric pressure.
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| PCT/KR2008/004994 WO2010024480A1 (en) | 2008-08-26 | 2008-08-26 | Red phosphor and forming method thereof for use in solid state lighting |
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| KR101072576B1 KR101072576B1 (en) | 2011-10-11 |
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| JP (1) | JP5583670B2 (en) |
| KR (1) | KR101072576B1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2017039200A1 (en) * | 2015-08-28 | 2017-03-09 | 부경대학교 산학협력단 | Functionally graded composite for energy conversion, manufacturing method therefor, and sensor using same |
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| CN104059648B (en) * | 2014-06-28 | 2016-05-11 | 吉林大学 | A kind of one dimension TiO2:Eu3+The preparation method of nano particle and nanometer rods luminescent material |
| CN104745188B (en) * | 2015-01-17 | 2017-06-16 | 东北大学 | A kind of Sm3+Lanthanium titanate red fluorescence material for the centre of luminescence and preparation method thereof |
| CN104830334B (en) * | 2015-04-26 | 2017-07-07 | 东北大学 | A kind of preparation method and applications of dysprosium doped blue colour fluorescent powder |
| CN104861973B (en) * | 2015-04-26 | 2017-01-25 | 东北大学 | Preparation method for green fluorescent powder applicable to white-light LED with lanthanum titanate serving as substrate and application of method |
| CN104861974B (en) * | 2015-05-15 | 2017-01-25 | 东北大学 | Fluorescent compound using pyrochlore structure metatitanic acid lanthanum as substrate and preparation method and application |
| CN105038790B (en) * | 2015-06-13 | 2017-08-29 | 东北大学 | The preparation method and applications of the upper and lower changing luminous material of holmium doping |
| CN104910909B (en) * | 2015-06-15 | 2017-01-25 | 东北大学 | Erbium-doped lanthanum titanate fluorescent compound, and preparation method and application thereof |
| CN105385446B (en) * | 2015-11-16 | 2018-03-23 | 沈阳工业大学 | A kind of preparation method and applications of thulium doped titanate blue colour fluorescent powder |
| CN115058246B (en) * | 2022-06-29 | 2023-09-22 | 江西理工大学 | High-brightness high-color-purity titanate up-conversion green fluorescent powder and preparation method thereof |
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| JPS6014056B2 (en) * | 1980-01-14 | 1985-04-11 | 株式会社東芝 | fluorescent material |
| JPH10279935A (en) * | 1997-04-10 | 1998-10-20 | Kasei Optonix Co Ltd | Fluorescent substance |
| CN1239673C (en) * | 2003-10-23 | 2006-02-01 | 北京有色金属研究总院 | Red luminescent powder in use for LED, preparing method and electric light source produced |
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2008
- 2008-08-26 JP JP2011524875A patent/JP5583670B2/en not_active Expired - Fee Related
- 2008-08-26 WO PCT/KR2008/004994 patent/WO2010024480A1/en active Application Filing
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| WO2017039200A1 (en) * | 2015-08-28 | 2017-03-09 | 부경대학교 산학협력단 | Functionally graded composite for energy conversion, manufacturing method therefor, and sensor using same |
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| Publication number | Publication date |
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| KR101072576B1 (en) | 2011-10-11 |
| JP5583670B2 (en) | 2014-09-03 |
| WO2010024480A1 (en) | 2010-03-04 |
| JP2012501365A (en) | 2012-01-19 |
| TW201009050A (en) | 2010-03-01 |
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