Patent Application
20090153019
This application makes reference to, incorporates the same herein, and claims all benefits accruing under 35 U.S.C. §119 from an application for PROTECTING LAYER HAVING MAGNESIUM OXIDE PARTICLES AT ITS SURFACE, METHOD OF PREPARING THE SAME, AND PLASMA DISPLAY PANEL COMPRISING THE PROTECTING LAYER earlier filed in the Korean Intellectual Property Office on the Dec. 14, 2007 and there duly assigned Serial No. 10-2007-0130978.
1. Field of the Invention
The present invention relates to a protecting layer of a plasma display panel, a method of preparing the protecting layer, and a plasma display panel including the protecting layer, and more particularly, to a protecting layer comprising a magnesium oxide-containing layer having a surface to which magnesium oxide-containing particles having a magnesium vacancy-impurity center (VIC) are attached, a method of preparing the protecting layer, and a plasma display panel (PDP) including the protecting layer. This protecting layer having magnesium oxide particles at its surface is hardly damaged by plasma ions and has excellent electron emission performance, and thus, a PDP including the protecting layer has high reliability.
2. Description of the Related Art
Plasma display panels (PDPs) are self-emission devices that can be easily manufactured in a large size, and have good display quality and rapid response time. PDPs can also be manufactured to be thin, and thus, like LCDs, are suitable for wall displays.
Meanwhile, an address electrode 11 is formed on a second substrate 10, and the address electrode 11 is covered by a second dielectric layer 12. The first substrate 14 and the second substrate 10 face each other, and are separated from each other by a predetermined distance. Barrier ribs 19 are interposed between the first substrate 14 and the second substrate 10 to define a discharge cell. A phosphor layer 13 is formed in the discharge cell. A gaseous mixture which generates ultraviolet rays is filled in the discharge cell. The gaseous mixture can be a mixture of Ne and Xe, or a gaseous mixture of He, Ne, and Xe at a predetermined pressure, for example, 450 Torr, in which Xe generates vacuum ultraviolet (VUV) rays (Xe ion: 147 nm of atomic rays; and Xe2: 173 nm of molecular rays), Ne reduces and stabilizes a discharge initiation voltage, and He increases mobility of Xe and increases emission of the molecular rays of Xe of 173 nm.
Generally, a protective layer of a PDP performs the following three functions.
First, a protecting layer protects an electrode and a dielectric layer. Discharging occurs even when only an electrode or a dielectric layer and an electrode are used. When only an electrode is used, it may be difficult to control a discharge current. When only a dielectric layer and an electrode are used, damage to the dielectric layer by sputtering may occur. Thus, the dielectric layer must be coated with a protective layer resistant to plasma ions.
Second, a protecting layer reduces a discharge initiation voltage. A discharge initiation voltage is directly correlated with the coefficient of secondary electron emission from a material constituting the protective layer against plasma ions. As more secondary electrons are emitted from the protecting layer, the discharge initiation voltage is reduced. In this regard, it is preferable to form a protective layer using a material with a high secondary electron emission coefficient.
Finally, a protecting layer reduces a discharge delay time. The discharge delay time refers to time needed to initiate discharge after a voltage is applied. The discharge delay time is the sum of a formation delay time Tf and a statistic delay time Ts. The formation delay time Tf is a time interval between the time when a voltage is applied and the time when a discharge current is generated, and the statistical delay time Ts is a statistical distribution of the formation delay time. The shorter the discharge delay time Tf is, the faster addressing is performed for a single scan method. Further, a shorter discharge delay time Tf can reduce scan drive costs, increase the number of sub-fields, and improve brightness and image quality.
A conventional protecting layer for a PDP can be formed by depositing a mono-crystalline magnesium oxide or a polycrystalline magnesium oxide on a substrate (see KR 2005-0073531). However, a PDP having such a conventional protecting layer has a high operating voltage, high power consumption, and long discharge delay time, and thus the conventional protecting layer is unsuitable for a HD PDP using a single scan method. Therefore, there is a need to develop a protecting layer with improved characteristics.
The present invention provides a protecting layer that substantially prevents damages caused by plasma ions and has excellent electron emission effects, a method of preparing the same, and a plasma display panel (PDP) including the protecting layer.
According to an aspect of the present invention, there is provided a protecting layer for a PDP, the protecting layer including a magnesium oxide-containing layer, and magnesium oxide-containing particles formed on a surface of the magnesium oxide-containing layer. The magnesium oxide-containing particles have a magnesium vacancy-impurity center (VIC).
A cathodoluminescence (CL) emission spectrum of the magnesium oxide containing particles may have a peak from VIC in the range of 3.1 eV to 6 eV. The cathodoluminescence (CL) emission spectrum of the magnesium oxide containing particles may have a peak from VIC in the range of 3.1 eV to 4.2 eV. The cathodoluminescence (CL) emission spectrum of the magnesium oxide containing particles may have a peak from VIC in the range of 3.35 eV to 3.87 eV The magnesium oxide containing layer may further include a rare earth element. The magnesium oxide containing layer may further include Al, Ca, or Si. The magnesium oxide containing particles may further include a rare earth element. The magnesium oxide containing particles may further include Al, Ca, or Si. The magnesium oxide containing particles further comprise scandium (Sc).
According to another aspect of the present invention, there is provided a method of forming a protecting layer for a PDP, the method including forming a magnesium oxide-containing layer on a substrate, preparing magnesium oxide-containing particles, and attaching the magnesium oxide-containing particles to a surface of the magnesium oxide-containing layer.
According to another aspect of the present invention, there is provided a PDP including the protecting layer having magnesium oxide particles at its surface.
The protecting layer having magnesium oxide particles at its surface is substantially not damaged by a plasma ion and has excellent electron emission performances. Therefore, the PDP including the protecting layer has high reliability.
A more complete appreciation of the invention, and many of the attendant advantages thereof, will be readily apparent as the same becomes better understood by reference to the following detailed description when considered in conjunction with the accompanying drawings in which like reference symbols indicated the same or similar components, wherein:
The present invention will now be described more fully with reference to the accompanying drawings, in which exemplary embodiments of the invention are shown.
A protecting layer for a PDP according to the present invention includes a magnesium oxide-containing layer having a surface to which magnesium oxide-containing particles are attached.
The magnesium oxide-containing particles at the surface of the magnesium oxide-containing layer have a magnesium vacancy-impurity center (VIC). As a result, more secondary electrons can be emitted when a PDP including the protecting layer is operated. The magnesium vacancy-impurity center (VIC) may be generally understood to indicate an excited state made by an interaction between a donor state formed in a band gap of magnesium oxide (impurity) and an acceptor state (magnesium vacancy).
Unlike a magnesium oxide layer, VIC-containing magnesium oxide particles have VIC. The structural difference between magnesium oxide particles and a magnesium oxide layer can be identified through a cathodoluminescence (CL) emission spectrum. In a CL spectrum of a magnesium oxide layer, an emission peak related to an F center or F+ center appears between 2.3 eV and 3.1 eV. F center or F+ center is formed as a result of vacancy of oxygen. When there are two trap electrons, an F center (about 2.3 eV) emission occurs; on the other hand, when there is only one trap electron, an F+ center (about 3.1 eV) emission occurs. In general, in an emission spectrum of a magnesium oxide layer, an emission peak related to the magnesium VIC is not shown. Although not limited to a specific principle, such result may be due to the fact that the magnesium oxide layer is formed using a deposition method such as an e-beam deposition method or a plasma deposition method, which is performed under oxygen-poor conditions, and thus, VIC is not formed in the magnesium oxide layer.
On the other hand, a CL spectrum of VIC-containing magnesium oxide particles is different from that of a magnesium oxide layer which has been described above.
As shown in
In VIC-containing magnesium oxide particles described above, the vacancy of VIC generates an acceptor level and a hole is formed, and the impurity of VIC generates a donor level and an electron is formed. Therefore, through the transition between the acceptor level and the donor level, the magnesium oxide particles can have many electrons. Therefore, when a PDP is operated, more secondary electrons can be emitted, unlike a protecting layer formed of a magnesium oxide layer (without VIC) alone. Such secondary electron emission mechanism can be understood, for example, according to the Auger neutralization principle although not limited one principle.
E
k
=E
l−2Eg+χ Equation 1
where Ek is energy generated when an electron is emitted from a solid when it collides with a gaseous ion; El is ionization energy of the gas; Eg is energy of the band gap of the solid; and χ is an electron affinity of the solid.
The Auger neutralization principle and Equation 1 can be applied to a protecting layer for a PDP and a discharge gas. When a voltage is applied to a pixel for a PDP, a seed electron generated by a cosmic ray or an ultraviolet ray collides with a discharge gas to generate a discharge gaseous ion and the discharge gaseous ion collides with the protecting layer to emit a secondary electron.
Table 1 below shows the resonance emission wavelength and dissociation voltage of an inert gas acting as a discharge gas, that is, ionization energy of the discharge gas. When a protecting layer is formed of magnesium oxide, the band gap energy of the solid, that is, Eg of Equation 1 is 7.7 eV that is the band gap energy of magnesium oxide, and the electron affinity χ is 0.5 that is the electron affinity of magnesium oxide.
In the meantime, Xe gas that can generate a vacuum ultraviolet ray having the longest possible wavelength is suitable for improving light conversion efficiency of a phosphor for a PDP. However, Xe has a dissociation voltage, that is, ionization energy El of 12.13 eV, and thus energy generated when an electron is emitted from a protecting layer formed of magnesium oxide, that is, Ek of Equation 1, is less than 0. Therefore, a very high discharge voltage is required. Accordingly, there is a need to use a gas having a high dissociation voltage El to reduce the discharge voltage. According to Equation 1, with respect to the magnesium oxide protecting layer, when He is used, Ek is 8.19 eV; and when Ne is used, Ek is 5.17 eV. Therefore, it can be shown that He or Ne is suitable for low discharge initiation voltage. However, when He gas is used for PDP discharging, the protecting layer can be damaged by plasma etching due to high mobility of He.
Therefore, it is more desirable to obtain easy emission of secondary electrons from the protecting layer, rather than modification of a discharge gas. As described in this specification, when magnesium oxide-containing particles having VIC exist at the surface of a magnesium oxide-containing layer, secondary electrons can be efficiently emitted since magnesium oxide-containing particles, unlike a magnesium oxide-containing layer, have many electrons, and thus, the discharge voltage can be reduced. Therefore, a PDP using such a protecting layer can have a low operating voltage and low power consumption.
Magnesium oxide-containing particles can be uniformly or non-uniformly attached to the surface of the magnesium oxide-containing layer.
On the other hand,
A magnesium oxide-containing layer according to the present invention, that is, a layer represented by reference numeral 33 in
The magnesium oxide-containing layer can include, in addition to magnesium oxide, a rare-earth element. The rare-earth element can be Sc (scandium), Y (yttrium), La (lanthan), Ce (cerium), Pr (praseodymium), Nd (neodymium), Pm (promethium), Sm (samarium), Eu (europium), Gd (gadolinium), Tb (terbium), Dy (dysprosium), Ho (holmium), Er (erbium), Tm (thulium), Yb (ytterbium), or Lu (lutetium). Furthermore, the magnesium oxide-containing layer can include one or more of the above elements. For example, the magnesium oxide-containing layer can further include Sc.
The amount of the rare-earth element may be in the range of 5.0×10−5 parts by weight to 6.0×10−4 parts by weight, preferably, 5.0×10−5 parts by weight to 5.0×10−4 parts by weight, and more preferably, 1.5×10−4 parts by weight to 4.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide in the magnesium oxide-containing layer. When the amount of the rare-earth element is outside the above range, a reduction in discharge delay time and in temperature dependency of the discharge delay time may be unsatisfactory.
The magnesium oxide-containing layer can further include one or more elements selected from Ca, Si and Al.
When the magnesium oxide-containing layer further includes Al, the discharge delay time at low temperature can be more reduced. The amount of Al may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the layer.
When the magnesium oxide-containing layer further includes Ca, a discharge delay time can be more independent with respect to temperature. That is, the discharge delay time may not substantially vary according to temperature. The amount of Ca may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically, 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the layer.
When the magnesium oxide-containing layer further includes Si, the discharge delay time at low temperature can be more reduced. The amount of Si may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically, 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the layer. In particular, when the amount of Si is outside this range, a glass phase can be formed in the layer.
The magnesium oxide-containing layer can further include, in addition to the rare-earth element, Al, Ca, and Si, one or more elements selected from the group consisting of Mn, Na, K, Cr, Fe, Zn, B, Ni and Zr in a small amount as determined to be as an impurity.
Magnesium oxide-containing particles which are attached to the surface of the magnesium oxide-containing layer can include, in addition to magnesium oxide, a rare-earth element. The rare-earth element can be Sc (scandium), Y (yttrium), La (lanthan), Ce (cerium), Pr (praseodymium), Nd (neodymium), Pm (promethium), Sm (samarium), Eu (europium), Gd (gadolinium), Tb (terbium), Dy (dysprosium), Ho (holmium), Er (erbium), Tm (thulium), Yb (ytterbium), or Lu (lutetium). The magnesium oxide-containing particles can include one or more elements selected from the above elements. For example, magnesium oxide-containing particles can contain Sc.
The amount of the rare-earth element may be in the range of 5.0×10−5 parts by weight to 6.0×10−4 parts by weight, preferably, 5.0×10−5 parts by weight to 5.0×10−4 parts by weight, and more preferably, 1.5×10−4 parts by weight to 4.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the magnesium oxide-containing particles. When the amount of the rare-earth element is outside this range, a reduction in discharge delay time and in temperature dependency of the discharge delay time may be unsatisfactory.
The magnesium oxide-containing particles may further include one or more elements selected from Ca, Si and Al.
When the magnesium oxide-containing particles further include Al, the discharge delay time at low temperature can be more reduced. The amount of Al may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of magnesium oxide-containing particles.
When the magnesium oxide-containing particles further include Ca, the discharge delay time can be more independent upon temperature. That is, the discharge delay time may not substantially vary according to temperature. The amount of Ca may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically, 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the magnesium oxide-containing particles.
When the magnesium oxide-containing particles further include Si, the discharge delay time at low temperature can be more reduced. The amount of Si may be in the range of 5.0×10−5 parts by weight to 4.0×10−4 parts by weight, specifically, 6.0×10−5 parts by weight to 3.0×10−4 parts by weight, based on 1 part by weight of magnesium oxide of the magnesium oxide-containing particles. In particular, when the amount of Si is outside this range, a glass phase can be formed in the magnesium oxide-containing particles.
The magnesium oxide-containing particles can further include, in addition to the rare-earth element and one or more elements selected from Al, Ca, and Si, one or more elements selected from the group consisting of Mn, Na, K, Cr, Fe, Zn, B, Ni and Zr in a small amount as determined to be as an impurity.
The magnesium oxide-containing particles attached to the magnesium oxide-containing layer may have an average diameter of 50 nm to 2 μm, specifically 100 nm to 1 μm. When the average diameter of the magnesium oxide-containing particles is less than 50 nm, a secondary electron emission effect may be too small. On the other hand, when the average diameter of the magnesium oxide-containing particles is greater than 2 μm, magnesium oxide-containing particles may be agglomerated together, which can cause distribution of a process.
A method of forming a protecting layer for a PDP according to an embodiment of the present invention includes forming a magnesium oxide-containing layer on a substrate, preparing magnesium oxide-containing particles, and attaching the magnesium oxide-containing particles to the surface of the magnesium oxide-containing layer.
First, a magnesium oxide-containing layer is formed on a substrate. The magnesium oxide-containing layer is to be formed on various kinds of a substrate according to the structure for a PDP. For example, the substrate can be a dielectric layer of a PDP. The magnesium oxide-containing layer can be formed using a conventional thin layer forming method, such as an E-beam evaporation method, a plasma evaporation method, a sputtering method, or a chemical vapor deposition method. The magnesium oxide-containing layer may be formed using mono-crystalline magnesium oxide pellets or polycrystalline magnesium oxide pellets. The mono-crystalline magnesium oxide pellets or polycrystalline magnesium oxide pellets can include a rare-earth element, Ca, Si, or Al. Therefore, the magnesium oxide-containing layer can include, in addition to magnesium oxide, a rare-earth element, Ca, Si, or Al.
Meanwhile, magnesium oxide-containing particles to be attached to the magnesium oxide-containing layer are prepared. Magnesium oxide-containing particles to be attached to the magnesium oxide-containing layer can be prepared using any known precipitation method, a chemical vapor oxidation (CVO) method, or a pellet milling method.
Then, magnesium oxide-containing particles are attached to the magnesium oxide-containing layer. Specifically, the magnesium oxide-containing particles can be uniformly attached to the magnesium oxide-containing layer as illustrated in
A conventional photolithography method can be used to uniformly attach the magnesium oxide particles to the magnesium oxide-containing layer as illustrated in
Meanwhile, in order to non-uniformly attach the magnesium oxide-containing particles to the magnesium oxide-containing layer as illustrated in
The solvent of such mixture can be ethanol or isopropanol, but is not limited thereto. The heat treatment temperature may vary according to the boiling point and evaporating properties of the solvent used and the kind of magnesium oxide-containing layer. For example, the heat treatment temperature may be in the range of about 80° C. to about 350° C. When the heat treatment temperature is less than 80° C., the solvent may be inefficiently evaporated. On the other hand, when the heat treatment temperature is greater than 350° C., the magnesium oxide-containing layer can be damaged.
The protecting layer having a magnesium oxide-containing layer having a surface to which magnesium oxide-containing particles are attached according to the present invention can be used in a gas discharge display device, specifically, a PDP.
Referring to
The PDP according to the current embodiment of the present invention further includes a second panel 220 including a second substrate 221, address electrodes 222 formed on a top (or inner) surface 221a of the second substrate 221 to cross the sustain electrode pairs 214, a second dielectric layer 223 covering the address electrode 222, a plurality of barrier ribs 224 which are formed on the second dielectric layer 223 and define discharge cells 226, and a phosphor layer 225 disposed inside the discharge cells 226. The discharge cells 226 can be filled with a gaseous mixture of Ne and at least one type of gas selected from Xe, N2 and Kr2, or with a gaseous mixture of Ne and at least two types of gas selected from Xe, He, N2, and Kr.
The protecting layer according to the present invention can be used in a two-component gaseous mixture of Ne and Xe as the discharge gas, in which an amount of Xe is increased in order to improve brightness. A protecting layer according to the present invention can provide a high sputtering resistance and can prevent a decrease in the lifetime for a PDP in a three-component gaseous mixture of Ne, Xe, and He as the discharge gas. Therefore, a decrease in the lifetime for a PDP can be prevented. The present invention provides a protective layer capable of reducing an increase in discharge voltage due to an increase in Xe content and satisfying a discharge delay time required for a single scan method.
The present invention will be described in further detail with reference to the following examples. These examples are for illustrative purposes only and are not intended to limit the scope of the present invention.
A discharge cell substrate was prepared such that an φ8 mm Ag electrode, a connection pad, and a 30 μm-thick PbO-containing SiO2 dielectric layer were formed on a 2.8 mm-thick glass panel for a PDP, in which the 30 μm-thick PbO-containing SiO2 dielectric layer was formed on the φ8 mm Ag electrode.
Then, a magnesium oxide-containing layer was formed on the PbO-containing SiO2 dielectric layer to a thickness of about 0.7 μm using an e-beam evaporation method. In the e-beam evaporation method, the temperature of the discharge cell substrate was 250° C., and the pressure was adjusted to 6×10−4 torr using oxygen and argon gases through a gas flow controller. The magnesium oxide-containing layer was formed from a polycrystalline magnesium oxide.
Meanwhile, magnesium oxide-containing particles having an average particle diameter of 500 nm and containing Sc in an amount of 4.0×10−4 parts by weight based on 1 part by weight of magnesium oxide of the magnesium oxide-containing particles were prepared. Such magnesium oxide-containing particles having Sc were obtained in such a manner that a Sc nitrate solution and MgCl2 aqueous solution were mixed in ethanol and NH4OH was added thereto to precipitate a Mg(OH)2 having Sc, the precipitated product was collected and heat-treated at 1000° C. to obtain magnesium oxide-containing particles having Sc, and then the obtained magnesium oxide-containing particles having Sc were milled using a plasma milling method to obtain magnesium oxide particles having an average particle diameter of 500 nm and containing Sc in an amount of 4.0×10−4 parts by weight based on 1 part by weight of the magnesium oxide of the magnesium oxide-containing particles having Sc (hereinafter, referred to as “Sc-containing magnesium oxide particles”).
1 g of the Sc-containing magnesium oxide particles was added to 15 ml of ethanol, and the obtained mixture was stirred. The stirred product was sprayed onto the magnesium oxide-containing layer. Then, the obtained structure was heat treated at 150° C. so as to attach the Sc-containing magnesium oxide particles onto the magnesium oxide-containing layer.
A 120 μm-thick quartz sieve was interposed between the two discharge cell substrates to form a facing discharge cell. The facing discharge cell was placed in a high-vacuum chamber and the high-vacuum chamber was sufficiently evacuated and purged with Ar gas to remove moisture therein. Then, a gaseous mixture of Ne and Xe in a mixture ratio of 9:1 as a discharge gas was added to the high-pressure chamber. As a result, a discharge measurement cell (Sample 1) was prepared.
A discharge cell (Sample A) for evaluation was prepared in the same manner as in Example 1, except that the Sc-containing magnesium oxide particles were not attached to the magnesium oxide-containing layer.
A bus electrode comprising copper was formed on a 2.8 mm-thick glass substrate using a photolithography method. PbO glass was coated on the bus electrode to form a front dielectric layer having a thickness of 20 μm.
Then, a magnesium oxide-containing layer was formed to a thickness of about 0.7 μm on the PbO dielectric layer using an e-beam evaporation method. In the e-beam evaporation method, the temperature of the substrate was 250° C., and the pressure was adjusted to 6×10−4 torr using oxygen and argon gases through a gas flow controller. The magnesium oxide-containing layer was formed from a polycrystalline magnesium oxide.
Meanwhile, magnesium oxide-containing particles having an average particle diameter of 500 nm and containing Sc in an amount of 4.0×10−4 parts by weight based on 1 part by weight of magnesium oxide of the magnesium oxide-containing particles were prepared. Such Sc-containing magnesium oxide particles was obtained in such a manner that a Sc nitrate solution and MgCl2 aqueous solution were mixed in ethanol and NH4OH was added thereto to precipitate Mg(OH)2 having Sc, the precipitated product was collected and heat-treated at 1000° C. to obtain Sc-containing magnesium oxide-containing particles, and then the obtained Sc-containing magnesium oxide-containing particles were milled using a plasma milling method to obtain magnesium oxide-containing particles having an average particle diameter of 500 nm and containing Sc in an amount of 4.0×10−4 parts by weight based on 1 part by weight of magnesium oxide of the Sc-containing magnesium oxide-containing particles.
1 g of the Sc-containing magnesium oxide particles was added to 15 ml of ethanol and the mixture was stirred. The stirred product was sprayed onto the magnesium oxide-containing layer. Then, the obtained structure was heat treated at 150° C. so as to attach the Sc-containing magnesium oxide particles onto the magnesium oxide-containing layer.
The substrate prepared as described above and a rear substrate were disposed to face each other with a distance of 120 μm, thereby forming a discharge cell. Then, the discharge cell was filled with a gaseous mixture of Ne and Xe in a mixture ratio of 9:1 acting as a discharge gas. As a result, 42-inch SD V4 PDP (Sample 2) was produced.
A PDP (Sample B) was prepared in the same manner as in Example 2, except that the Sc-containing magnesium oxide particles were not attached to the magnesium oxide-containing layer.
Measurement 1: Discharge Initiation Voltages of Samples 1 and A
The discharge initiation voltages of Samples 1 and A were measured. The results are shown in
The discharge initiation voltage was measured using a Tektronix oscilloscope, a trek amplifier, an NF function generator, a high-vacuum chamber, a peltier device, a I-V power source, and a LCR meter. First, Sample A was connected to the trek amplifier and the NF function generator, and then a 2 kHz sinuous wave was applied thereto to measure a discharge initiation voltage. Such process was also performed on Sample 1.
The results are shown in
Measurement 2: Secondary Electron Emission Coefficients of Samples 1 and A
Secondary electron emission coefficients of Samples 1 and A were measured. The results are shown in
The secondary electron emission coefficients were measured by irradiating an accelerated focused ion beam (FIB) onto Samples 1 and A. Specifically, the protecting layer of Sample A was collided with a Ne+ ion, and electrons emitted from Sample A were collected by applying a positive voltage (+15V) to a Faraday cup. Ions entering Sample A were collected using a Faraday cup and the amount of the collected ions was mathematically computed to obtain a secondary electron emission coefficient of Sample A. Such process was also performed on Sample 1.
Referring to
Measurement 3: Discharge Delay Time of Samples 2 and B
A discharge delay time (unit: ns) of Samples 2 and B with respect to temperature was measured. The results are shown in
Therefore, Sample 2 that is a PDP including the protecting layer of the present invention has a short discharge delay time and thus, is suitable for increase in Xe content and single scan.
A protecting layer according to the present invention includes a magnesium oxide-containing layer having a surface to which magnesium oxide-containing particles having Mg vacancy impurity center (VIC) are attached, and specifically, magnesium oxide particles form the surface of the protecting layer. Therefore, the protecting layer of the present invention can emit more secondary electrons and can be resistant to the plasma ion, and a PDP including the protecting layer has low discharge voltage and low power consumption.
While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2007-0130978 | Dec 2007 | KR | national |
