Patent Application
20140217447
The present disclosure relates to phosphor compositions and, more specifically, to phosphor compositions used in white light-emitting diode (LED) devices.
With the recent trend of rising demand for slimness and high performance in image display devices, liquid crystal displays (LCD) have been widely used in a wide array of consumer products, including televisions, computer monitors and smart-phone displays. A LCD panel cannot emit light by itself, thus requiring a separate light source unit, e.g., a backlight unit. Choosing a backlight unit for LCDs is a major consideration since the backlight unit significantly affects the brightness, the contrast, and many other aspects of the viewing experience. White LEDs have recently gained popularity as the backlight units due to their low power consumption, high reliability, and long operating lifetime.
A white LED is typically composed of a blue LED and a yellow phosphor. A part of the blue light emitted by the blue LED excites the yellow phosphor causing it to emit yellow light; and the yellow color mixes with another part of the blue light from the blue LED to create the white light. In addition, the LED can use a mixture of green and red phosphors which convert the blue light of the LED at least partially into green and red luminescent radiation. Owing to the resultant additive color mixing of the colors blue, red and green, white light can therefore be produced. Generally, the phosphor determines luminescence efficiency, color rendering, color temperature, and lifespan of the white LEDs.
To lower manufacturing cost, the number of white LEDs per backlight unit needs to be reduced. In turn, the white LEDs have to be driven at a much higher voltage so that the brightness of the backlight unit can remain the same. This would require utilizing phosphors with high thermal stability in the white LEDs.
In the field, the most commonly used yellow light-emitting phosphor is Ce doped yttrium aluminum garnet (YAG:Ce) which shows unsurpassed efficiency. Silicate-based phosphors have been developed as an alternative to YAG. However, silicate-based phosphors have poor stability in high temperature and high humidity environments. Therefore, while these phosphors are efficient at room temperature, they suffer relatively strong quenching at elevated temperature. Accordingly, there remains a need to develop a new phosphor composition that has an emission and thermal stability similar to YAG phosphor, as a viable alternative to YAG phosphor.
The present disclosure provides a phosphor composition as well as a highly reliable white LED device using such phosphor composition to address the aforementioned problems.
In one aspect, a phosphor composition is provided. The phosphor composition may comprise a first oxynitride-based phosphor that emits green light; and a second nitride-based phosphor that emits red light. The phosphor composition may have an emission with CIE color coordinates satisfying an equation expressed as: y=0.0805x3−154.06x2+97017x−2E+07.
In one embodiment, the first oxynitride-based phosphor may be represented by a general formula of M(II)aSibOcNdCe:A. In M(II)aSibOcNdCe:A, M(II) may comprises Be, Mg, Ca, Sr, Ba, Cu, Co, Ni, Pd, Zn, Cd, or a combination thereof. A may comprises a luminescence activator selected from the group consisting of Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Mn, Bi, and Sb. Additionally, the following conditions may exist: 6<a<8, 8<b<14, 13<c<17, 5<d<9, and 0<e<2.
In one embodiment, the second nitride-based phosphor may be represented by a formula of CaAlSiN3:Eu.
In one embodiment, a weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be from about 8:2 to about 9:1.
In one embodiment, the weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be about 8.04:1.95.
In one embodiment, the CIE color coordinates of the phosphor composition may fall within a region defined by points having coordinates of (0.30, 0.25), (0.30, 0.43), (0.39, 0.25), and (0.39, 0.43).
In one embodiment, the CIE color coordinates of the emission of the phosphor composition may be at (0.365, 0.372).
In another aspect, a phosphor composition is provided. The phosphor composition may comprise a first oxynitride-based phosphor, represented by a general formula of M(II)aSibOcNdCe:A; and a second nitride-based phosphor, represented by a formula of CaAlSiN3:Eu. In M(II)aSibOcNdCe:A, M(II) may comprise at least one divalent cation selected from the group consisting of Be, Mg, Ca, Sr, Ba, Cu, Co, Ni, Pd, Zn, and Cd. A may comprise a luminescence activator selected from the group consisting of Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Mn, Bi, and Sb. Additionally, the following conditions may exist: 6<a<8, 8<b<14, 13<c<17, 5<d<9, and 0<e<2. A weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be from about 8:2 to about 9:1.
In one embodiment, the weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be about 8.04:1.95.
In one embodiment, the phosphor composition may have an emission with CIE color coordinates satisfying an equation expressed as: y=0.0805x3−154.06x2+97017x−2E+07.
In one embodiment, the CIE color coordinates of the emission of the phosphor composition may fall within a region defined by points having coordinates of (0.30, 0.25), (0.30, 0.43), (0.39, 0.25), and (0.39, 0.43).
In another aspect, a phosphor composition is provided. The phosphor composition may comprise a first oxynitride-based phosphor, represented by a general formula of M(II)aSibOcNdCe:A; and a second nitride-based phosphor, represented by a formula of CaAlSiN3:Eu. In M(II)aSibOcNdCe:A, M(II) may comprise at least one divalent cation selected from the group consisting of Be, Mg, Ca, Sr, Ba, Cu, Co, Ni, Pd, Zn, and Cd. A may comprise a luminescence activator selected from the group consisting of Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Mn, Bi, and Sb. Additionally, the following conditions may exist: 6<a<8, 8<b<14, 13<c<17, 5<d<9, and 0<e<2. The phosphor composition may have an emission with CIE color coordinates in a range of 0.356≦x≦0.365 and 0.372≦y≦0.380.
In one embodiment, the weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be about 8.04:1.95.
In one embodiment, the phosphor composition may have an emission with CIE color coordinates satisfying an equation expressed as: y=0.0805x3−154.06x2+97017x−2E+07.
In yet another aspect, a light-emitting diode (LED) device is provided. The LED device may comprise a blue LED having a peak emission wavelength in a range of 450 nm-460 nm, and a phosphor composition disposed on or over the LED. The phosphor composition may comprise a first oxynitride-based phosphor having a peak emission wavelength in a range of 550 nm-560 nm; and a second nitride-based phosphor having a peak emission wavelength in a range of 570 nm-600 nm. The phosphor composition may have an emission with CIE color coordinates satisfying an equation expressed as: y=0.0805x3−154.06x2+97017x−2E+07.
In one embodiment, the first oxynitride-based phosphor may be represented by a general formula of M(II)aSibOcNdCe:A. In M(II)aSibOcNdCe:A, M(II) may comprise Be, Mg, Ca, Sr, Ba, Cu, Co, Ni, Pd, Zn, Cd, or a combination thereof, and A may comprise a luminescence activator selected from the group consisting of Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Mn, Bi, and Sb. Additionally, the following conditions may exist: 6<a<8, 8<b<14, 13<c<17, 5<d<9, and 0<e<2.
In one embodiment, the second nitride-based phosphor may be represented by a formula of CaAlSiN3:Eu.
In one embodiment, a weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be from about 8:2 to about 9:1.
In one embodiment, the weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be about 8.04:1.95.
In one embodiment, the CIE color coordinates of the emission of the phosphor composition may be fall with a region defined by points having coordinates of (0.30, 0.25), (0.30, 0.43), (0.39, 0.25), and (0.39, 0.43).
In one embodiment, the CIE color coordinates of the emission of the phosphor composition are in a range of 0.356≦x≦0.365 and 0.372≦y≦0.380.
In one embodiment, the CIE color coordinates of emission of the LED device are in a range of 0.28≦x≦0.39 and 0.25≦y≦0.35.
In one embodiment, the LED device may additionally comprise a diffuser.
In one embodiment, the diffuser may comprise ZnO2, SiO2, TiO2, Al2O3, or a combination thereof.
Detailed description of various embodiments are provided below, with reference to the attached figures, to promote better understanding of the characteristics and benefits of the various embodiments of the present disclosure.
The present disclosure provides phosphor compositions with emission and thermal stability similar to the yttrium aluminum garnet (YAG) phosphor for high reliability white LED devices.
In the above-described phosphor composition 111 of the white LED device 100, in order to produce emission similar to that of the YAG phosphor, a first oxynitride-based green-emitting phosphor and a second nitride-based red-emitting phosphor are mixed in an appropriate proportion. The first oxynitride-based phosphor emits in the green region with an emission peak ranging from about 550 nm to 560 nm when excited by blue or ultraviolet light. The second nitride-based phosphor emits in the red region with an emission peak ranging from about 570 nm to 600 nm when excited by blue or ultraviolet light.
In the above-described phosphor composition 111, the first oxynitride-based phosphor is represented by a general formula of M(II)aSibOcNdCe:A, wherein 6<a<8, 8<b<14, 13<c<17, 5<d<9, and 0<e<2; preferably 6.5<a<7.5, 8.5<b<12.5, 14<c<16, 6<d<7.5, and 0<e<1. M(II) comprises at least one divalent cation, and may be selected from the group consisting of Be, Mg, Ca, Sr, Ba, Cu, Co, Ni, Pd, Zn, and Cd. A comprises a luminescence activator doped in the host crystal of the first oxynitride-based phosphor at a concentration from about 0.001 mol % to about 20 mol %, preferably from about 0.1 mol % to about 10 mol %, relative to M(II). In one embodiment, A may be selected from the group consisting of Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Mn, Bi, and Sb, and preferably Eu2+, Ce3+, Tb3+, Yb2+ and Mn2+.
The second nitride-based phosphor is represented by a formula of CaAlSiN3:Eu.
The mixing weight ratio of the first oxynitride-based phosphor to the second nitride-based phosphor may be preferably from about 9:1 to about 8:2, and more preferably about 8.04:1.95. The CIE color coordinates of the emission of the phosphor compositions satisfy the following equation: y=0.0805x3−154.06x2+97017x−2E+07. The CIE color coordinates of the emission of the phosphor compositions fall within a region defined by points having coordinates of (0.30, 0.25), (0.30, 0.43), (0.39, 0.25), and (0.39, 0.43).
Table 1 summarizes the CIE color coordinates of example embodiments of phosphor compositions according to the present disclosure.
The above-described phosphor composition 111 may include a diffuser (5−15% (w/w) with particle size D50 of 1-10 μm) to increase the brightness of the white LED device 100. The diffuser may comprise, for example, ZnO2, SiO2, TiO2, Al2O3, or a combination thereof.
It is worth mentioning that, to enhance the excitation efficiency of the phosphor composition 111 in the white LED device 100, the concentration of the phosphor composition 111 may be gradually increased from the surface of the encapsulant layer 109 towards the surface of the blue LED 101. The blue LED 101 may be covered by the phosphor composition 111 of a common form, and in such case the phosphor composition 111 of a common form may be formed by spraying, molding, printing, etc. Alternatively, the blue LED 101 may be indirectly covered by the phosphor composition 111. The phosphor composition 111 may be disposed a distance away from the blue LED 101 and still be excited by the blue LED 101. For example, the phosphor composition 111 may be mixed with resin to form a phosphor plate or light guide plate, or may be spread over a resin plate or disposed above a light guide plate. This way, the light uniformity, as well as the thermal tolerance of the phosphor composition 111 with respect to the high heat generated by the blue LED 101, may be enhanced.
In summary, the phosphor compositions used in the white LED device of the present disclosure have the emission in the yellow region similar to that of a yellow YAG phosphor, and do not have the thermal instability problem of the silicate-based phosphors. Therefore, the phosphor compositions of the present disclosure can effectively replace the conventional YAG phosphor and silicate-based phosphors to provide white LEDs with high reliability.
A number of embodiments of the present disclosure are described herein. However, as those skilled in the art would appreciate, the scope of the present disclosure is not and cannot be limited to the disclosed embodiments. More specifically, one ordinarily skilled in the art may make various deviations and improvements based on the disclosed embodiments, and such deviations and improvements are still within the scope of the present disclosure. Accordingly, the scope of protection of a patent issued from the present disclosure is determined by the claims provided below.
This application is the non-provisional of, and claims the priority benefit of, U.S. Patent Application No. 61/761,924, filed on 7 Feb. 2013, which is incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61761924 | Feb 2013 | US |
