TW200407938A - Method of growing isomeric carbon emitters onto triode structure of field emission display - Google Patents
Method of growing isomeric carbon emitters onto triode structure of field emission display Download PDFInfo
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- TW200407938A TW200407938A TW91133488A TW91133488A TW200407938A TW 200407938 A TW200407938 A TW 200407938A TW 91133488 A TW91133488 A TW 91133488A TW 91133488 A TW91133488 A TW 91133488A TW 200407938 A TW200407938 A TW 200407938A
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- 238000000034 method Methods 0.000 title claims abstract description 74
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 29
- 229910052799 carbon Inorganic materials 0.000 title abstract description 11
- 239000000758 substrate Substances 0.000 claims abstract description 44
- 229910052751 metal Inorganic materials 0.000 claims abstract description 42
- 239000002184 metal Substances 0.000 claims abstract description 42
- 239000003054 catalyst Substances 0.000 claims abstract description 36
- 238000004519 manufacturing process Methods 0.000 claims abstract description 23
- 238000005516 engineering process Methods 0.000 claims description 23
- 229910021392 nanocarbon Inorganic materials 0.000 claims description 17
- 150000001721 carbon Chemical class 0.000 claims description 16
- 229910021393 carbon nanotube Inorganic materials 0.000 claims description 14
- 239000002041 carbon nanotube Substances 0.000 claims description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 11
- 238000007650 screen-printing Methods 0.000 claims description 11
- 238000005488 sandblasting Methods 0.000 claims description 10
- 238000000059 patterning Methods 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 4
- 239000004917 carbon fiber Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 229910002804 graphite Inorganic materials 0.000 claims description 4
- 239000010439 graphite Substances 0.000 claims description 4
- 239000002121 nanofiber Substances 0.000 claims description 4
- 229910052723 transition metal Inorganic materials 0.000 claims description 4
- 150000003624 transition metals Chemical class 0.000 claims description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 238000007639 printing Methods 0.000 claims description 2
- 239000002002 slurry Substances 0.000 abstract description 4
- 239000003989 dielectric material Substances 0.000 description 10
- 239000011521 glass Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 229920002120 photoresistant polymer Polymers 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 239000007772 electrode material Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 150000000921 Gadolinium Chemical class 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002071 nanotube Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000001259 photo etching Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
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Abstract
Description
200407938 五、發明說明(1) 發明領域 本發明係關於場發射顯示器(f i e 1 d e m i s s i ο η display,FED)。特別是關於一種在三極結構 (triode structure)場發射顯示器上成長碳類異構物場發射電子源 (isomeric carbon emitters)的方法。 發明背景 近年來場發射顯示器被廣泛地研發,以製作大尺寸的 平面顯示器(f 1 a t p a n e 1 d i s p 1 a y )。場發射顯示器利用冷 陰極發射益尖端(cold cathode emitter tip)作為電子的 來源’以取代傳統的陰極射線管(cath〇de ray tube,CRT )中的熱.陰極電子搶(hot cathode electron gun)。當場 發射顯示器置於電場時,冷陰極發射器尖端(t i p)瞄準場 考χ射顯示裔内塗上螢光粉的陽極基板(an〇deSubstrate) 而射出電子束’打在螢光粉(ph〇sph〇r)上。 圖1為傳統之二極結構奈米碳管(carbon nano-tube C N T)%發射顯示裔的結構示意圖。利用電場將陰極玻璃 基板1 0 1上的冷陰極發射器尖端3的電子吸出,在真空環 境下離開陰極板的場發射電子受陽極破璃基板i 〇4上正電 壓的加速吸引,撞擊至陽極105的螢光粉1〇6而發光。奈米 碳管冷陰極發射器尖端103形成在介電層1〇7的空隙内,豆200407938 V. Description of the invention (1) Field of the invention The present invention relates to a field emission display (f i e 1 d e m i s s i o η display, FED). In particular, it relates to a method for growing carbon isomer field emitters on a triode structure field emission display. BACKGROUND OF THE INVENTION Field emission displays have been extensively developed in recent years to make large size flat displays (f 1 a t p a n e 1 d p s p 1 a y). The field emission display uses a cold cathode emitter tip as a source of electrons' to replace the heat in a conventional cathode ray tube (CRT). Hot cathode electron gun. When the field emission display is placed in an electric field, the tip of the cold cathode emitter is aimed at the field test, and the anode substrate (an〇deSubstrate) coated with fluorescent powder is emitted and the electron beam is emitted to hit the fluorescent powder (ph〇 sph0r). FIG. 1 is a schematic diagram of the structure of a traditional carbon nano-tube CNT% emission display. The electrons of the cold cathode emitter tip 3 on the cathode glass substrate 101 are extracted by an electric field, and the field emission electrons leaving the cathode plate in a vacuum environment are attracted by the acceleration of the positive voltage on the anode glass substrate i 04, and hit the anode. 105 phosphor 106 emits light. The carbon nanotube cold cathode emitter tip 103 is formed in the gap of the dielectric layer 107.
200407938 五、發明說明(2) 中介電層1 0 7係形成在玻璃基板1 0 1上方的冷陰極層1 〇 2。 冷陰極層1 0 2和閘層1 〇 8的交界處形成開口( 〇 p e n i n g s ),作 為電子的匯集(e m e r g e t h r o u g h )。 圖2A至圖2D說明奈米碳管場發射顯示器的陰極板的製 作方法。如圖2A所示,首先塗佈並圖樣化導電漿料 (conductive paste)於透明基板(transparent substrate )201上,以形成底電極層 (cathode electrode layer) 2 0 2,再於透明基板2 〇 1和底電極層2 0 2的上方全面性塗佈 一層可蝕刻的介電材料2 0 3,如圖2 B所示。再將一層導電 的閘極材料2 0 4塗佈在介電層2 0 3之上,並以圖樣化的光阻 層2 0 5定義閘極圖樣(gate pattern),如圖2 0所示。再以 嘴砂(sand blasting)和在空氣中燃燒(fired in air)法 將閘極材料和介電材料去除。最後,以網印製程(s c r e e η printing process)將奈米碳管層2 0 6塗佈在底電極層202 上’如圖2 D戶斤示。 圖2中所示的場發射顯示器2 〇 6係以網印技術製作,及 利用刮刀將事先調製好的漿料刮過已圖樣化的網板,使圖 案印製在玻璃基板上,如此逐層將圖案堆疊。由於此方法 受限於網板之網目與網結大小,使印製圖案的解析無法提 幵’導致必須提供較高的場發射起始電壓,才能使顯示器 達到要求的亮度。此外會受網板張力不均的影響,造成膜 厚均勻性不佳與印製圖案失真,產生電場強度分佈不均與200407938 V. Description of the invention (2) The dielectric layer 107 is a cold cathode layer 102 formed on a glass substrate 101. An opening is formed at the junction of the cold cathode layer 102 and the gate layer 108 (〇 p en n g s) as a collection of electrons (emer g e t h r o u g h). 2A to 2D illustrate a method of manufacturing a cathode plate of a nano carbon tube field emission display. As shown in FIG. 2A, a conductive paste is first coated and patterned on a transparent substrate 201 to form a cathode electrode layer 2 0 2 and then a transparent substrate 2 0 1 An overall layer of an etchable dielectric material 230 is coated on the bottom electrode layer 202, as shown in FIG. 2B. Then, a layer of conductive gate material 204 is coated on the dielectric layer 203, and a gate pattern is defined by a patterned photoresist layer 205, as shown in FIG. The gate and dielectric materials were removed by sand blasting and fired in air. Finally, the nano carbon tube layer 2 06 is coated on the bottom electrode layer 202 by a scre printing process, as shown in FIG. 2D. The field emission display 2 shown in FIG. 2 is produced by screen printing technology, and the pre-adjusted paste is scraped across the patterned screen using a doctor blade, so that the pattern is printed on the glass substrate, so as to layer by layer Stack the patterns. Because this method is limited by the mesh and knot size of the screen, the analysis of the printed pattern cannot be improved. As a result, a higher field emission starting voltage must be provided in order to achieve the required brightness of the display. In addition, it will be affected by uneven screen tension, resulting in poor film thickness uniformity and distortion of printed patterns, resulting in uneven electric field intensity distribution and
第6頁 200407938 五、發明說明(3) 後續製程中對位困難的缺點。 〇為了克服傳統奈米碳管場發射顯示器的缺點 1 。"’尚有其他利用厚膜網印技術製作陰極板的方::二 以匕係1利:h導電Ϊ料和可钱刻的介電材料結:土 先I牙王(photo lithography)與蝕刻處理 。汽 管場發射顯示器的陰極板。 衣乍不米碳 圖3A至圖3E說明利用厚膜網印技術製作奈 射顯示器陰極板的方法。如圖3A所〒 .^ g贫發 導電漿料於透明基板30 1上,以形忐、i先塗佈並圖樣化 明基板301和底電極層30 2的上方I面&生汾極層一3〇2’再於透 介電材料3 0 3,如圖3B所示。再將一 、/"佈一層可蝕刻的 塗佈在介電層3 0 3之上,並以黃朵制曰冷電的閘極材料3 0 4 (Wnter)後形成閘電極層3 0 4,、如出圖樣及燒結 用來當作保護膜(protecting fn C所不。閘極圖樣係 極圖樣覆蓋的部份介電材料,如m二以,刻-掉沒有被閘 極層3 0 2的上方填入奈米碳管發"所不。最後,在底電 構,如圖3E所示。 射層以形成陰極板結 如圖3D所示 程,將一層感光的奈米碳管漿二 、衣私可用黃光製 並以對位曝光方式定義奈米碳管二,在陰極板的表面上, ’在氮氣氣氛下燒結。“碳30 5的圖樣。然後 号X射層3 0 5的製作也可利Page 6 200407938 V. Description of the invention (3) Disadvantages of difficult alignment in subsequent processes. In order to overcome the shortcomings of traditional nano carbon tube field emission displays 1. " 'There are other recipes for making cathode plates using thick film screen printing technology :: two, one, two, one, one, one, h, conductive materials, and dielectric materials that can be engraved; junction: soil first, photo lithography, and Etching. The cathode plate of a steam field emission display. Clothes Carbon Figures 3A to 3E illustrate a method for fabricating a cathode plate of a nanometer display using a thick film screen printing technique. As shown in FIG. 3A, a thin conductive conductive paste is applied on the transparent substrate 301, and the upper surface of the substrate 301 and the bottom electrode layer 302 are coated and patterned in a pattern, i. A 302 ′ is then permeable to the dielectric material 303, as shown in FIG. 3B. A layer of etchable coating is applied over the dielectric layer 3 0, and a gate electrode layer 3 0 4 (Wnter) made of cold electricity is used as the gate electrode material 3 0 4 made of yellow flower. , Such as patterning and sintering are used as protective films (not for protecting fn C. The gate pattern is part of the dielectric material covered by the electrode pattern, such as m2, engraved-without the gate layer 3 0 2 Fill the top of the nano carbon tube with "No." Finally, at the bottom of the electrical structure, as shown in Figure 3E. Shoot the layer to form the cathode junction as shown in Figure 3D, a layer of photosensitive nano carbon tube slurry Second, the clothing can be made of yellow light and define the carbon nanotubes in the form of a counter-exposure method. On the surface of the cathode plate, 'sinter in a nitrogen atmosphere.' Making
200407938 五、發明說明(4) 用電泳法(electrical deposition),其步驟包含在底電 極層3 0 2和閘電極層3 0 4的上方全面性塗佈一層正型或負型 光阻(positive or negative photoresist),如圖 3D戶斤示 ’且以對位曝光方式利用一光罩定義光阻圖樣。在閘電極 層3 0 4之上形成光阻圖樣後,以電泳法(e 1 e c t r i ca 1 1 y depositing)將奈米碳管漿料塗佈在底電極層3〇2之上,並 在氮氣氣壓(nitrogen atmosphere)下,於爐中燒結以形 成奈米碳管發射層3 0 5。 如上所述,在奈米碳管場發射顯示器的三極結構上的 奈米碳管發射層的製程要求在閘極開口與奈米碳管圖案間 作嚴格的對位,使得其製程成本及製程難度皆較高。因此 ’要里產奈米碳管場發射顯示器仍有很多技術上的障礙亟 待克服。 與其他技術相比較之下,使用觸媒金屬.(catalytic metals)的化學蒸發濺渡(chemicai vap〇]r deposition, C V D)製程具有更多優點,已被證明為製作大面積奈米碳管 時’其製程成本較低。然而溫控CVD的反應溫度通常高達 攝氏700-100 0度,遠超過一般平面顯示器的玻璃基板6〇〇 度的溶點。目前已有文獻及專利指出低溫成長場發射電子 源的可行性,係在攝氏5 5 0度使用C2Η2氣體CVD將鎳觸媒 (Ni catalyst)塗佈在s〇da-lime玻璃基板上以成長奈米碳 管。故開發一套能量產奈米碳管場發射顯示器的整合厚膜200407938 V. Description of the invention (4) The method of electrical deposition includes the steps of comprehensively coating a positive or negative photoresistor on the bottom electrode layer 3 02 and the gate electrode layer 3 0 4 (positive or negative photoresist), as shown in FIG. 3D, and a photomask is used to define the photoresist pattern in a counter-exposure manner. After forming a photoresist pattern on the gate electrode layer 3 0 4, the nano carbon tube slurry was coated on the bottom electrode layer 3 2 by electrophoresis (e 1 ectri ca 1 1 y depositing), and under nitrogen Under a nitrogen atmosphere, it is sintered in a furnace to form a nano-carbon tube emission layer 3 05. As described above, the manufacturing process of the carbon nanotube emission layer on the triode structure of the carbon nanotube field emission display requires strict alignment between the gate opening and the carbon nanotube pattern, making its process cost and process The difficulty is high. Therefore, there are still many technical obstacles in the field of carbon nanotube field emission display to be overcome. Compared with other technologies, the chemical vapor deposition (chemicai vapor) deposition (CVD) process using catalytic metals has more advantages and has been proven to be used for the production of large-area carbon nanotubes. 'Its process cost is lower. However, the reaction temperature of temperature-controlled CVD is usually as high as 700-100 ° C, which is much higher than the melting point of 600 ° C of the glass substrate of a general flat panel display. At present, there are literatures and patents that point out the feasibility of emitting electron sources in a low-temperature growth field. A nickel catalyst was coated on a soda-lime glass substrate using C2Η2 gas CVD at 50 ° C. Meter carbon tube. Therefore, the development of a set of integrated thick film of energy-producing nano carbon tube field emission display
200407938 五、發明說明(5) 三極結構製程搭配低溫CVD技術是極為需要的。 發明概要 本發明克服上述之傳統場發射顯示器製程上的缺點。 其主要目的疋’ k供一種低製程成本之在三極結構場發射 顯示器上成長碳類異構物場發射電子源的製作方法。^主 要原理疋利用厚膜技術製作三極結構場發射顯示器之後再 以CVD製程在三極結構場發射顯示器上成長碳類異構物場 發射電子源。 本發明的另一目的是,提供一三極結構之陰電極層 (cathode electrode layer),使碳類異構物場發射電子 源得以C V D製程在此三極結構上成長。根據本發明,首先 將金屬觸媒與導電金屬粉末混合,以形成陰電X極層,再將 此導電金屬粉末调製成導電金屬漿料,在經厚膜製程將導 電金屬漿料成形為陰電極層於透明基板上。然後在陰電極 層之上沉積介電層和閘電極層,圖樣化後形成三極結構。 由於陰電極層包含金屬觸媒,故碳類異構物場發射電子源 極易成長在三極結構之上。 本發明的另一目的是,提供一層在三極結構中的金屬 觸媒層使得場發射顯示器的碳類異構物場發射電子源易於 成長。其係在底電極層上形成一金屬觸媒層,以取代將金200407938 V. Description of the invention (5) A three-pole structure process with low-temperature CVD technology is extremely needed. SUMMARY OF THE INVENTION The present invention overcomes the shortcomings of the conventional field emission display process described above. The main purpose of the method is to provide a method for producing a carbon isomer field emission electron source on a tripolar field emission display with low process cost. ^ Main principle: After producing a triode structure field emission display using thick film technology, a carbon isomer field emission electron source is grown on the tripolar structure field emission display by a CVD process. Another object of the present invention is to provide a cathode electrode layer with a tripolar structure, so that the carbon isomer field emission electron source can grow on this tripolar structure by the CVD process. According to the present invention, a metal catalyst is first mixed with a conductive metal powder to form a negative electrode X pole layer, and then the conductive metal powder is prepared into a conductive metal paste, and the conductive metal paste is formed into a cathode through a thick film process The electrode layer is on a transparent substrate. A dielectric layer and a gate electrode layer are then deposited on the cathode electrode layer, and a tripolar structure is formed after patterning. Because the cathode electrode layer contains a metal catalyst, the carbon isomer field emission electron source can easily grow on the tripolar structure. Another object of the present invention is to provide a metal catalyst layer in a tripolar structure so that the carbon isomer field emission electron source of the field emission display is easy to grow. It forms a metal catalyst layer on the bottom electrode layer to replace the gold
第9頁 200407938 五'發明說明(6) 屬觸媒與導電金屬漿料混合後在透明基板上形成底電極層 的方式。然後,在金屬觸媒層和陰電極層以及透明基板之 上方形成介電層和閘電極層。將介電層和閘電極層圖樣化 後,遂完成了三極結構。最後,利用CVD製程,在金屬觸 媒層上成長碳類異構物場發射電子源。 根據本發明,三極結構的形成可利用網印技術,乾式 蝕刻-喷砂法及厚膜黃光製程等方法來製作。而陰電極層 或金屬觸媒層的圖樣化可利用網印技術或厚膜黃光製程等 方法來製作。金屬觸媒可使用的材料包含鐵(Fe),鈷(Co) ,鎳(N i )等過渡金屬。碳類異構物場發射電子源可使用的 材料包含奈米碳管,碳纖維(c a r b ο n f i b e r )或石墨奈米纖 維(graphite nano-fiber)0 茲配合下列圖式、實施例之詳細說明及專利申請範 圍,將上述及本發明之其他目的與優點詳述於后。 發明之詳細說明 圖4詳細說明本發明的第一實施例中奈米碳管場發射 顯示器利用厚膜製程搭配CVD技術的製程步驟。首先,如 圖4A所示,準備一透明基板401。圖4B說明在透明基板401 之上形成陰電極層402。Page 9 200407938 Five 'invention description (6) It is a method for forming a bottom electrode layer on a transparent substrate after the catalyst is mixed with the conductive metal paste. Then, a dielectric layer and a gate electrode layer are formed over the metal catalyst layer, the cathode electrode layer, and the transparent substrate. After patterning the dielectric layer and the gate electrode layer, the tripolar structure is completed. Finally, a CVD process was used to grow a carbon isomer field emission electron source on the metal catalyst layer. According to the present invention, the formation of the tripolar structure can be made by screen printing technology, dry etching-sandblasting method, and thick film yellow light process. The patterning of the cathode electrode layer or the metal catalyst layer can be made by screen printing technology or thick film yellow light process. Materials that can be used for the metal catalyst include transition metals such as iron (Fe), cobalt (Co), and nickel (N i). Carbon isomers field emission electron source can use materials including carbon nanotubes, carbon fibers (carb ο nfiber) or graphite nano-fiber (0) with the following drawings, detailed description of the examples and patents The scope of the application details the above and other objects and advantages of the present invention. Detailed Description of the Invention FIG. 4 illustrates in detail the process steps of the nano-carbon tube field emission display using the thick film process and the CVD technology in the first embodiment of the present invention. First, as shown in Fig. 4A, a transparent substrate 401 is prepared. FIG. 4B illustrates forming a cathode electrode layer 402 on the transparent substrate 401.
第10頁 200407938 五、發明說明(7) 首先,在透明基板4 0 1上沉積一層導電漿料。導電漿 料以黃光製程圖樣化後’經過退火燒結後形成陰電極層 4 0 2。黃光製程包括預烤後以光罩定義圖樣,以及曝光和 顯影的步騍。圖4β說明顯影後陰電極層4 0 2圖樣的一個剖 面結構示意圖。陰電極層4 0 2也可利用網印技術使其圖樣 化。、 在本發明的第一實施例中,陰電極層4 0 2包含一觸媒 導電材料以輔助後置CVD製程中的長成。首先將金屬觸媒 混合導電金屬粉末以形成導電 是鐵,鎳或始。然後將介電層 層40 2的上方。介電層40 3的上 用噴砂法或黃光製程製作出閘 構的一剖面結構不意圖。 漿料。金屬觸媒的材料可以 方再沉積閜& 搞处桃1電極層404,利 極結構。縢 _ 4C說明此閘極結 陰電極層40 2包含複數條相互平行的 電層4 0 3包含複數條介電材料且相互平二長線條電極。介 閘電極層4 0 4包含複數條相互平行的手仃的長線條電極。 層的每一長線條電極位於介雷W緩條電極。閘電極 電極層的長線條電極垂直交又。問電極%電極之上且與陰 條電極與底電極層的長線條曾托二 > 層和介電層的長線 八丨來电極於交又虚 (circular openings/cirrni 义形成圓洞開口 cuiar cavities、 4 0 5於低温以C V D技術填於茈圓 s )。奈米碳管層 、'此W洞開口内。Page 10 200407938 V. Description of the invention (7) First, a layer of conductive paste is deposited on the transparent substrate 401. After the conductive paste is patterned in a yellow light process, the negative electrode layer 4 02 is formed after annealing and sintering. The yellow light process includes a mask definition pattern after pre-baking, and steps for exposure and development. FIG. 4β illustrates a cross-sectional structure of the cathode electrode layer 402 pattern after development. The cathode electrode layer 4 2 can also be patterned using screen printing technology. In the first embodiment of the present invention, the cathode electrode layer 402 includes a catalyst conductive material to assist the growth in the post-CVD process. The metal catalyst is first mixed with a conductive metal powder to form a conductive material such as iron, nickel or metal. The dielectric layer is then layered over the layer 40 2. It is not intended that a cross-sectional structure of the gate structure is fabricated on the dielectric layer 403 by a sand blasting method or a yellow light process. Slurry. The material of the metal catalyst can be redeposited 閜 & Peach 1 electrode layer 404, a polar structure. 4 _ 4C illustrates this gate junction. The cathode electrode layer 40 2 includes a plurality of parallel electrical layers 4 0 3 and a plurality of dielectric materials and is a long flat electrode. The gate electrode layer 404 includes a plurality of long-line electrodes that are parallel to each other. Each of the long-line electrodes of the layer is located on the dielectric W-strip electrode. Gate electrode The long-line electrodes in the electrode layer intersect vertically. The long lines above the electrode% electrode and the cathode electrode and the bottom electrode layer have been supported by two long lines of the > layer and the dielectric layer. The circular electrodes / circular openings / cirrni mean circular openings. cavities, 405 are filled at the low temperature by CVD technology at low temperature). Nano carbon tube layer, 'this W hole opening.
200407938 五、發明說明(8) 圖5說明本發明之第二實施例的奈米碳管場發射顯示 器的製作流程。參考圖5 A,與第一實施例同樣地,首先準 備一透明基板50 1。圖5B說明在透明基板50 1的上方形成陰 電極層5 0 2。之後,在陰電極層5〇2的上方形成一金屬觸媒 層5 0 6以辅助後置CVD製程中奈米碳管的長成。 第二實施例中,首先在透明基板5 0 1上沉積一層導電 漿料。導電漿料以黃光製程圖樣化後,經過退火燒結後形 成陰電極層5 0 2。圖5B說明顯影後陰電極層5 0 2圖樣的一個 剖面結構示意圖。金屬觸媒層5 〇 6係形成在陰電極層之上 而不是將金屬觸媒與導電漿料混合。如圖5 c所示,金屬觸 媒詹5 0 6用來辅助後置CVD製程中奈米碳管的長成。金屬觸 媒的材質可以是過渡金屬(transition metal),如鐵、始 、鎳等。 第二實施例接下來的製程與第一實施例完全相同。在 基板5 0 1、底電極層5 0 2和金屬觸媒層5 0 6的上方全面沉積 一介電層503。介電層50 3的上方再沉積一閘電極層5〇4。 然後利用喷砂法或黃光製程製作閘極結構。圖51)說明閘極 結構的一剖面結構示意圖。第二實施例的介電材料可使用 與第一實施例相同的介電材料。奈米碳管層5 〇 5係利用CV]) 技術成長在金屬觸媒層5 0 6之上。 圖6說明根據本發明之製程製作的碳類異構物場發射200407938 V. Description of the invention (8) FIG. 5 illustrates a manufacturing process of a nano carbon tube field emission display according to a second embodiment of the present invention. Referring to Fig. 5A, as in the first embodiment, a transparent substrate 501 is first prepared. Fig. 5B illustrates the formation of a cathode electrode layer 502 over the transparent substrate 501. After that, a metal catalyst layer 506 is formed on the cathode electrode layer 502 to assist the growth of the carbon nanotubes in the post-CVD process. In the second embodiment, a layer of conductive paste is first deposited on the transparent substrate 501. The conductive paste was patterned in a yellow light process, and then annealed and sintered to form a negative electrode layer 502. Fig. 5B illustrates a schematic cross-sectional structure of the pattern of the cathode electrode layer 502 after development. The metal catalyst layer 506 is formed on the cathode layer instead of mixing the metal catalyst with the conductive paste. As shown in Fig. 5c, the metal catalyst Zan 506 is used to assist the growth of the carbon nanotubes in the post-CVD process. The material of the metal catalyst can be a transition metal, such as iron, iron, and nickel. The subsequent processes of the second embodiment are exactly the same as those of the first embodiment. A dielectric layer 503 is entirely deposited on the substrate 501, the bottom electrode layer 502, and the metal catalyst layer 506. A gate electrode layer 504 is further deposited on the dielectric layer 503. Then the gate structure is made by sandblasting or yellow light process. Fig. 51) A cross-sectional structure diagram illustrating the gate structure. As the dielectric material of the second embodiment, the same dielectric material as that of the first embodiment can be used. Nano-carbon tube layer 505 uses CV]) technology to grow on metal catalyst layer 506. Figure 6 illustrates the field emission of carbon isomers made according to the process of the present invention
第12頁 200407938 五、發明說明(9) ---- 電子源的SEM影像。其中閘極結構係以喷砂法製作,而碳 類異構物場發射電子源層係以CVD技術沉積而成。圖6A和 圖6 B分別以5 0 0倍和5 0 0 0倍的放大倍率說明在奈米碳管成 長在陰極上之後的閘極洞(Sated —electrode hole)的SEM 剖面示意圖。 根據本發明,奈米碳管層4 0 5或5 0 5係以CVD技術在底 電極層4 0.2或金屬觸媒層5 0 6之上製作。含有金屬觸媒或金 屬觸媒層5 0 6的底電極層4 0 2係利用厚膜技術,例如網印技 術或厚膜黃光製程製作。三極結構的形成更包含噴砂法。 而本發明的碳類異構物場發射電子源可為奈米碳管,碳纖 維或石墨奈米纖維。 綜上所述,本發明利用厚膜技術在含金屬觸媒或金屬 觸媒層底電極層上,來製作三極結構。然後利用CVD製程 直接在底電極層或金屬觸媒層製作碳類異構物場發射電子 源層。厚膜技術結合CVD製程提供一低製程成本的技術以 製作大面積的場發射顯示器。 唯,以上所述者’僅為本發明之較佳實施例而已,當 不能以此限定本發明實施之範圍。即大凡依本發明申請專 利範圍所作之均等變化與修飾,皆應仍屬本發明專利涵蓋 之範圍内。Page 12 200407938 V. Description of Invention (9) ---- SEM image of electron source. The gate structure is made by sandblasting, and the carbon isomer field emission electron source layer is deposited by CVD technology. Figures 6A and 6B illustrate the SEM cross-section diagrams of the gated hole (Sated-electrode hole) after the nano-carbon tube has grown on the cathode at 500x and 5000x magnifications, respectively. According to the present invention, the carbon nanotube layer 405 or 505 is fabricated on the bottom electrode layer 4 0.2 or the metal catalyst layer 506 by a CVD technique. The bottom electrode layer 402 containing a metal catalyst or a metal catalyst layer 506 is produced by using a thick film technology, such as a screen printing technology or a thick film yellow light process. The formation of the tripolar structure further includes a sandblasting method. The carbon isomer field emission electron source of the present invention may be a nano carbon tube, carbon fiber or graphite nano fiber. In summary, the present invention uses a thick film technology to make a three-pole structure on a metal-containing catalyst or a bottom layer of a metal catalyst layer. Then, a carbon isomer field emission electron source layer is directly formed on the bottom electrode layer or the metal catalyst layer by a CVD process. The thick film technology combined with the CVD process provides a low process cost technology to fabricate a large area field emission display. However, the above-mentioned ones are merely preferred embodiments of the present invention, and the scope of implementation of the present invention cannot be limited by this. That is to say, all equal changes and modifications made in accordance with the scope of the patent application of the present invention shall still fall within the scope of the patent of the present invention.
第13頁 200407938 圖式簡單說明 圖1為一傳統之三極結構奈米碳管場發射顯示器的結構示 意圖。 圖2A至圖2D說明奈米碳管場發射顯示器的陰極板的製作方 法。 用厚膜網印技術製作奈米破管場發射顯 圖4詳細說明本發明的第一實施例中奉 押 ^ 丁、木石厌官%發射顯不 态,利用厚膜製程搭配CVD技術的製程+ V 〇 圖5說明本發明之第二實施例的奈米硝 制价^ # 官場發射顯示器的 製作流程。 圖6 A和圖6 B分別以5 0 0倍和5 0 0 0倍的於丄 ^大倍率今、明為泰+ 碳管成長在陰極上之後的閘極洞的π _立®r ^ it7 J面不思圖。 圖7說明根據本發明,利用CVD成長之砝#田* , 妷類異構物場發射電 子源的11V曲線。 圖號說明 101陰極玻璃基板 1 〇2 冷陰極層Page 13 200407938 Brief description of the drawings Fig. 1 is a schematic diagram showing the structure of a conventional triode structured carbon nanotube field emission display. 2A to 2D illustrate a method for fabricating a cathode plate of a nano carbon tube field emission display. Using thick film screen printing technology to produce nano tube breaking field emission display Figure 4 details the first embodiment of the present invention Feng Ding ^ Ding, Mu Shigangan% emission display state, using a thick film process with CVD technology + V 〇 FIG. 5 illustrates the fabrication process of the nanometer nitrate production price of the second embodiment of the present invention. Figure 6A and Figure 6B are respectively 500 and 5000 times the magnification of Yu 丄 ^, and Ming Weitai + π_ 立 ®r ^ it7 of the gate hole after the carbon tube grows on the cathode J face is not thinking. Fig. 7 illustrates an 11V curve of a field emission electron source of a gadolinium isomer according to the present invention using a CVD growth weight. Drawing number description 101 cathode glass substrate 1 〇2 cold cathode layer
1 m ΪΙ1 m ΪΙ
第14頁 200407938 圖式簡單說明 1 0 3奈米碳管冷陰極發射器尖端 1 0 4陽極玻璃基板 1 0 5陽極 1 07介電層 2 0 1透明基板 2 0 3介電材料,介電層 2 0 5光阻層 3 0 1透明基板 3 0 3介電材料,介電層 3 0 5奈米碳管發射層 4 0 1透明基板 4 0 3介電層 4 0 5奈米碳管層 5 0 1透明基板 5 0 3介電層 505奈米碳管層 1 0 6螢光粉 1 0 8閘層 2 0 2陰電極層 2 0 4閘極材料 2 0 6奈米碳管層 3 0 2電極層 3 0 4閘極材料,閘電極層 40 2陰電極層 4 0 4閘電極層 5 0 2陰電極層 5 0 4閘電極層 5 0 6金屬觸媒層Page 14 200407938 Brief description of the drawings 1 0 3 Nano carbon tube cold cathode emitter tip 1 0 4 anode glass substrate 1 0 5 anode 1 07 dielectric layer 2 0 1 transparent substrate 2 0 3 dielectric material, dielectric layer 2 0 5 photoresist layer 3 0 1 transparent substrate 3 0 3 dielectric material, dielectric layer 3 0 5 nanometer carbon tube emitting layer 4 0 1 transparent substrate 4 0 3 dielectric layer 4 0 5 nanometer carbon tube layer 5 0 1 transparent substrate 5 0 3 dielectric layer 505 nanometer carbon tube layer 1 0 6 fluorescent powder 1 0 8 gate layer 2 0 2 cathode electrode layer 2 0 4 gate electrode material 2 0 6 nanometer carbon tube layer 3 0 2 Electrode layer 3 0 4 gate electrode material, gate electrode layer 40 2 cathode electrode layer 4 0 4 gate electrode layer 5 0 2 cathode electrode layer 5 0 4 gate electrode layer 5 0 6 metal catalyst layer
第15頁Page 15
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| Application Number | Title | Priority Date | Filing Date |
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| TW91133488A TWI220265B (en) | 2002-11-15 | 2002-11-15 | Method of growing isomeric carbon emitters onto triode structure of field emission display |
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| TW (1) | TWI220265B (en) |
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| Publication number | Publication date |
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| TWI220265B (en) | 2004-08-11 |
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