The present application relates to a compound of phosphor and the manufacturing method thereof, and particularly to a metal oxonitridosilicate phosphor and the manufacturing method thereof.
This application claims the right of priority based on TW application Serial No. 101138832, filed on Oct. 18, 2012, and the content of which is hereby incorporated by reference in its entirety.
There are many manufacturing methods of making white light emitting diodes (WLEDs), such as applying yellow phosphors to a blue light-emitting diode chip, applying red and green phosphors to a blue light-emitting diode chip, mixing red, green, and blue light-emitting diode chips and applying tricolor blue/green/red phosphors or applying different phosphors with different colors to a light-emitting diode emitting in the UV spectral range.
Compared to a traditional incandescent light bulb, a white light-emitting diode has some advantages, e.g. long lifetime, low power consumption, small volume, fast response time and good shake-resistance, and thus light-emitting diodes are gradually replacing traditional lighting products. However, current white light emitting diodes still need to overcome the problems such as heat dissipation, inadequate brightness and relatively high price in its development. As a result, in the lighting market, auxiliary lighting, including flash lights, car interior lights, architectural decorative lighting products, is still the main market of white light-emitting diodes, while still white light-emitting diodes are expected to replace traditional lighting products in the future to become the mainstream of the global lighting market.
Besides package techniques, the chosen phosphor is also an important factor in affecting luminous efficiency of a light source. Thus, one of the research directions that solid state lighting companies are devoted to is modifying phosphor compositions to increase phosphor conversion efficiency. The color render index of the white light generated by a yellow phosphor excited by a traditional single blue chip is not good and thus the color saturation of an object illuminated by such white light is poor, thereby lowering the commercial lighting market value. After many years of research and development, it is found that using a high efficient UV-light-emitting diode (UV-LED) as an excitation light source is another way of white light emitting diodes to become lighting devices. Because the UV-LED technique is gradually mature, the phosphor development of the UV-LED excitation light source is more and more important, so as to develop phosphors matching the emission wavelength of UV-LEDs and thus manufacture white light emitting diodes with high efficiency and high brightness.
A metal oxonitridosilicate phosphor has a general formula M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a:Euz,Mnb, wherein M is one or more alkaline earth metals; 0≦x≦7; 0≦a≦1; 0<z≦0.3; and 0<b≦0.3.
A metal oxonitridosilicate phosphor has a composition of M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a as a host lattice, Eu as a first active center and Mn as a second active center.
A metal oxonitridosilicate phosphor has a general formula M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a:Euz,Mnb, wherein when M is Sr, x=2, a=0, z=0.1, 0.02≦b≦0.1, the phosphor emits a fluorescence with a wavelength ranging from 480 nm to 700 nm when excited by a light source with a wavelength ranging from 300 nm to 460 nm.
The light source with the wavelength ranging from 300 nm to 460 nm of the present application is from a light-emitting diode or plasma.
Exemplary embodiments of the present application will be described in detail with reference to the accompanying drawings hereafter. The following embodiments are given by way of illustration to help those skilled in the art fully understand the spirit of the present application. Hence, it should be noted that the present application is not limited to the embodiments herein and can be realized by various forms. Further, the drawings are not precise scale and components may be exaggerated in view of width, height, length, etc. Herein, the similar or identical reference numerals will denote the similar or identical components throughout the drawings.
The embodiments of the present application provide a phosphor having a general formula M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a:Euz,Mnb, wherein M is one or more alkaline earth metals; 0≦x≦7; 0≦a≦1; 0<z≦0.3; and 0<b≦0.3. M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a of the phosphor is a host lattice, Eu is a first active center, and Mn is a second active center.
The present embodiment is a comparative embodiment of the metal oxonitridosilicate phosphor (a), wherein M is Sr, x=2, a=0, z=0.1, b=0, namely, the phosphor is Sr4.9Al5Si21N35O2:Eu0.1. The phosphor is prepared by solid-state reaction at high pressure, and the method is shown as follows.
First, a stoichiometric first reactant comprising Sr, such as Sr3N2; a stoichiometric second reactant comprising Al, such as AlN; a stoichiometric third reactant comprising Si, such as Si3N4 or SiO2; and a stoichiometric fourth reactant comprising Eu, such as EuN are provided to form a mixture having a formula Sr4.9Al5Si21N35O2:Eu0.1.
Second, a pestle is used to grind and mix the mixture uniformly, and subsequently the uniform mixture is put into a boron nitride crucible, and then the boron nitride crucible is put into a high-temperature sintering furnace to carry out a sintering step under a temperature ranging from 1700° C. to 2300° C. for 3 to 8 hours, so as to form the metal oxonitridosilicate phosphor. More specifically, the mixture is heated to the temperature ranging from 1700° C. to 2300° C. at a heating rate of 35° C./minute under nitrogen atmosphere at a pressure ranging from 0.5 to 1.5 Mpa, and then the mixture is kept for 3 to 8 hours, and subsequently the mixture was cooled down to room temperature at a cooling rate of 15° C./minute. After the sintering step, a pestle is used again to grind the metal oxonitridosilicate phosphor into powders having uniform particle sizes after the metal oxonitridosilicate phosphor is taken out from the high-temperature sintering furnace.
The reactants can be oxides or nitrides comprising corresponding element respectively.
In the present embodiment, five metal oxonitridosilicate phosphors (b) to (f) having the general formula M5−z−a−bAl3+xSi23−xN37−x−2aOx+2a:Euz,Mnb are prepared, wherein M of each phosphor is Sr, x of each phosphor is 2, a of each phosphor is 0, z of each phosphor is 0.1, namely the five phosphors having a formula Sr4.9−bAl5Si21N35O2:Eu0.1,Mnb, and wherein b is 0.02, 0.04, 0.06, 0.08, 0.1 respectively. Each of the phosphor is prepared by solid-state reaction at high pressure, and the method is shown as follows.
First, a stoichiometric first reactant comprising Sr, such as Sr3N2; a stoichiometric second reactant comprising Al, such as AlN; a stoichiometric third reactant comprising Si, such as Si3N4 or SiO2; a stoichiometric fourth reactant comprising Eu, such as EuN; and a stoichiometric fifth reactant comprising Mn, such as MnO2 are provided to form a mixture having a formula Sr4.9−bAl5Si21N35O2:Eu0.1,Mnb.
Second, a pestle is used to grind and mix the mixture uniformly, and subsequently the uniform mixture is put into a boron nitride crucible, and then the boron nitride crucible is put into a high-temperature sintering furnace to carry out a sintering step under a temperature ranging from 1700° C. to 2300° C. for 3 to 8 hours. More specifically, the mixture is heated to the temperature ranging from 1700° C. to 2300° C. at a heating rate of 35° C./minute under nitrogen atmosphere at a pressure ranging from 0.5 to 1.5 Mpa, and then the mixture is kept for 3 to 8 hours, and subsequently the mixture was cooled down to room temperature at a cooling rate of 15° C./minute. After the sintering step, a pestle is used again to grind the sintered mixture into powders having uniform particle sizes after the sintered mixture is taken out from the high-temperature sintering furnace.
The reactants can be oxides or nitrides comprising corresponding element respectively.
The crystal phase purity and crystal structure of the phosphors of the embodiments are determined by an X-ray diffractometer.
Referring to
Referring to
Table 1 shows chromaticity coordinates of the phosphor (a) in accordance with the first embodiment having a formula Sr4.9Al5Si21N35O2:Eu0.1, the phosphors (b) to (f) in accordance with the second embodiment having a formula Sr4.9−bAl5Si21N35O2:Eu0.1, Mnb, wherein b of the phosphor (b) to (f) is 0.02, 0.04, 0.06, 0.08, 0.1 respectively. The chromaticity coordinates are obtained by converting the data by the equation standardized by Commission internationale de l'éclairage (CIE), wherein the data are obtained from the emission spectrum. Furthermore,
The foregoing description of preferred and other embodiments in the present disclosure is not intended to limit or restrict the scope or applicability of the inventive concepts conceived by the Applicant. In exchange for disclosing the inventive concepts contained herein, the Applicant desires all patent rights afforded by the appended claims. Therefore, it is intended that the appended claims include all modifications and alterations to the full extent that they come within the scope of the following claims or the equivalents thereof.
Number | Date | Country | Kind |
---|---|---|---|
101138832 A | Oct 2012 | TW | national |
Number | Name | Date | Kind |
---|---|---|---|
7351356 | Delsing | Apr 2008 | B2 |
8153025 | Schmidt | Apr 2012 | B2 |
8679367 | Liu | Mar 2014 | B2 |
20060197439 | Sakane | Sep 2006 | A1 |
20070194685 | Hirosaki | Aug 2007 | A1 |
20090236963 | Nagatomi | Sep 2009 | A1 |
20100102707 | Fukuda | Apr 2010 | A1 |
20100244076 | Schmidt | Sep 2010 | A1 |
Number | Date | Country |
---|---|---|
101883835 | Nov 2010 | CN |
Entry |
---|
Liu. Enhanced luminescence of SrSi2O2N2 :Eu2+ phosphors by codoping with Ce3+, Mn2+, and Dy3+ ions. App. Phys. Lett. 91 061119 (2007. |
Liu, “Phosphors, Up Converison Nano Particles, Quantum Dots and Their Applications”,Springer, vol. 1, 13 pages. |
Number | Date | Country | |
---|---|---|---|
20140110632 A1 | Apr 2014 | US |