This application claims the benefit, under 35 U.S.C. §365 of International Application PCT/US2006/024812, filed Jun. 23, 2006 which was published in accordance with PCT Article 21(2) on Jan. 3, 2008 in English.
1. Field of the Invention
The invention relates to a carbon nanotube(CNT)/field emission device (FED) displays and, more particularly to luminescent materials therefor.
2. Description of the Background Art
Carbon nanotube(CNT)/field emission device (FED) displays typically include a cathode with CNT emitters thereon, a metal gate, insulating spacers and a phosphor screen. The metal gate is interposed between the cathode and the phosphor screen. The phosphor screen is located on an inner surface of a faceplate of the display. The metal gate functions to direct electron beams generated from the CNT emitters toward appropriate color-emitting phosphors on the screen of the display.
The screen may be a luminescent screen. Luminescent screens typically comprise an array of three different color-emitting phosphors (e.g., green, blue and red) formed thereon. Each of the color-emitting phosphors is separated from another by a matrix line. The matrix lines are typically formed of a light-absorbing black, inert material.
In order to achieve displays with good color bightness and color gamut levels, CNT/FEDs should be operated between about 4-10 kV. CNT/FED displays operating below 4 kV are not competitive from a brightness standpoint and suffer additional degradation from electron stimulated surface reactions of the color-emitting phosphors.
Thus, a need exists for a phosphor system for a CNT/FED display with good color bightness and color gamut levels when operated between about 4-10 kV.
The present invention relates to a RGB phosphor system for a carbon nanotube (CNT)/field emission device (FED) display operated between about 4-10 kV. The RGB phosphor system is formed on an interior surface of a screen of the CNT/FED display. The RGB phosphor system includes ZnS:Cu, Al (green phosphor), ZnS:Ag,Cl (blue phosphor) and Y2O2S:Eu+3 (red phosphor). The average particle size for each of the green, blue and red phosphors should be about 3-4 microns.
The invention will now be described in greater detail, with relation to the accompanying drawings, in which:
The screen 10 of a CNT/FED display comprises a viewing surface 18 and an interior surface 15, shown in cross-section in
The RGB phosphor system is formed on an interior surface of the screen 10 of the CNT/FED display. The RGB phosphor system includes ZnS:Cu, Al (green phosphor), ZnS:Ag,Cl (blue phosphor) and Y2O2S:Eu+3 (red phosphor). This RGB phosphor system is suitable for a carbon nanotube (CNT)/field emission device (FED) display operated between about 4-10 kV.
The average particle size for each of the green, blue and red phosphors should be about 3-4 microns. Such a particle size is suited for filling the phosphor openings in the light absorbing matrix 23 with minimum overlap and good packing density for planarizing layers. Phosphors in this size range have efficiencies of >95% of standard cathode ray tube (CRT) materials with particle sizes of between 6-9 microns. RGB phosphor systems with average particle sizes below 3 microns display decreased efficiency.
The screen 10 is manufactured according to the process steps represented schematically in
The interior surface 15 of the screen 10 is then provided with the light-absorbing matrix 23, as indicated by reference numeral 302, preferably using a wet matrix process in a manner well known in the art.
The light-absorbing matrix 23 is uniformly provided over the interior viewing surface 15 of the screen 12. Rectangular openings are formed between in the light-absorbing matrix 23 and typically have dimensions of about 0.7 mm2. Referring to
As indicated by reference numeral 304 in
The photosensitive material layer 46 should have a viscosity within a range of about 10 centipoise (cps) to about 25 cps. The photosensitive material layer 46 may include sodium dichromate within a range of about 6 weight % to about 12 weight % and the polymer (e.g., PVA) within a range of about 88 weight % to about 94 weight %.
After the photosensitive material layer 46 is deposited on interior surfaces of the faceplate panel 12, portions of the photosensitive material layer 46 may be irradiated using, for example, actinic radiation to cross-link the photosensitive material of the photosensitive material layer 46 in the first and second sets of fields 40, 42. Cross-linking the photosensitive material in the photosensitive material layer 46 in the first and second sets of fields 40, 42 hardens the photosensitive material in such fields.
Referring to
After the unhardened portions of the irradiated photosensitive material layer 46 are removed, a first color phosphor layer 60 is applied over the interior surface 15 of the screen 10 in the third set of fields 44 and over the hardened photosensitive material in the first and second fields 40, 42. The first color phosphor layer 60 may be one of ZnS:Cu, Al (green phosphor), ZnS:Ag,Cl (blue phosphor) and Y2O2S:Eu+3 (red phosphor).
After the first color phosphor layer 60 is applied over the interior surface 15 of the screen 10, the screen 10 is heated. The screen 10 may be heated to a temperature of about 50° C. to about 100° C. and then cooled to a temperature of about 40° C. Thereafter, as shown in
The first color phosphor layer formation process described above with reference to
Although an exemplary luminescent screen for a carbon nanotube (CNT)/field emission display (FED) which incorporates the teachings of the present invention has been shown and described in detail herein, those skilled in the art can readily devise many other varied embodiments that still incorporate these teachings.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2006/024812 | 6/23/2006 | WO | 00 | 12/19/2008 |
Publishing Document | Publishing Date | Country | Kind |
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WO2008/002288 | 1/3/2008 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2785331 | Donahue | Mar 1957 | A |
4204136 | Phillips | May 1980 | A |
5906771 | Watkins et al. | May 1999 | A |
6005342 | Morton | Dec 1999 | A |
6379583 | Gray et al. | Apr 2002 | B1 |
6875372 | Hampden-Smith et al. | Apr 2005 | B1 |
6882099 | Yamaguchi | Apr 2005 | B2 |
20010008363 | Sanghera et al. | Jul 2001 | A1 |
20030102797 | Kajiwara | Jun 2003 | A1 |
20050012447 | Komatsu et al. | Jan 2005 | A1 |
20080265743 | Yokosawa et al. | Oct 2008 | A1 |
Number | Date | Country |
---|---|---|
1422320 | Jun 2003 | CN |
1273645 | Jan 2003 | EP |
1555306 | Jul 2005 | EP |
05251023 | Sep 1993 | JP |
2004055385 | Feb 2004 | JP |
WO0012649 | Mar 2000 | WO |
WO2005080528 | Jan 2005 | WO |
Number | Date | Country | |
---|---|---|---|
20100164366 A1 | Jul 2010 | US |