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TWI276135B - Field emission lamp and method for making the same - Google Patents

Field emission lamp and method for making the same Download PDF

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Publication number
TWI276135B
TWI276135B TW95111399A TW95111399A TWI276135B TW I276135 B TWI276135 B TW I276135B TW 95111399 A TW95111399 A TW 95111399A TW 95111399 A TW95111399 A TW 95111399A TW I276135 B TWI276135 B TW I276135B
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TW
Taiwan
Prior art keywords
field emission
emission lamp
cathode
anode
glass tube
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Application number
TW95111399A
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Chinese (zh)
Other versions
TW200737263A (en
Inventor
Li Qian
Liang Liu
Peng Liu
Jie Tang
Yang Wei
Original Assignee
Hon Hai Prec Ind Co Ltd
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Priority to TW95111399A priority Critical patent/TWI276135B/en
Application granted granted Critical
Publication of TWI276135B publication Critical patent/TWI276135B/en
Publication of TW200737263A publication Critical patent/TW200737263A/en

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Abstract

A field emission lamp is provided, including a glass pipe with at least one opening end, an anode, at least one sealing member disposed on the at least one opening end, and a cathode disposed in the pipe. The anode has a conductive layer formed on inner wall of the pipe and a fluorescent layer formed on the conductive layer. The cathode has an electron emission layer formed on a surface thereof. The electron emission layer includes a number of getter particles, metallic conductive particles and nano-scale material, and glass. A method for making the above-mentioned field emission lamp is also provided.

Description

1276135 " 九、發明說明: 【發明所屬之技術領域】 本發明係涉及一種場發射燈管及其製造方法,尤其 涉及一種藉由吸氣劑有效保持其内部具有正常工作下 所需真空度之場發射燈管及其製造方法' 【先前技術】 曰光燈管係日常生活之必需品,其包括/透明玻璃 管’該玻璃管内壁塗覆有白色或彩色螢光材料,内部充 _ 有水祭。該日光燈管之工作原理係利用熱陰極發射電 子激發汞蒸汽發出紫外光,而紫外光照射於螢光材料上 發出白色光或彩色光。該曰光燈管係一種熱陰極光源, 發光效率較高,惟,其内部使用之汞蒸汽有毒,當燈管 被打破後,汞蒸汽流出外面將對環境以及人體有害。 爲解決上述問題,一種冷陰極之場發射燈管被提 供,其包括陰極以及與陰極對應設置之陽極。該陰極表 面没有電子發射層,陽極與電子發射層對應設置有螢光 層。當於陰極與陽極之間施加一定電壓時,陰極之電子 _ 發射層發射電子,陽極之螢光層於電子之轟擊下發光。 該種場發射燈管能耗低,發光效率高,對環境及人體無 危害。惟,對於場發射燈管來說,其内部需要高真空密 封封裝,即,内部真空度越高,燈管之場發射性能也就 越好。 ^先如技術中,場發射燈管爲獲得長壽命玎靠工作所 採用維持真空之措施主要係於其内部安裝吸氣劑,大致 有兩種類型,即蒸散式及集中非蒸散式。 對於蒸散式吸氣劑,需於場發射燈管内部設置一平 面結構用以藉由預先之蒸散過程形成吸氣劑層,故會增 1276135 加製造成本,亦可引起電極引線間短路或漏電’從而導 致燈管失效。對於集中非蒸散式吸氣劑,通常集中設置 於場發射燈管之一端因而場發射燈管内真空度較不均 勻,即於場發射燈管内部靠近吸氣劑之位置真空度較 好,而遠離吸氣劑之位置真空度較差從而影響場發射燈 管之場發射性能。 有鑒於此,確有必要提供一種場發射燈管,其能有 效地維持其内部具有正常工作下所需之真空度。 【發明内容】[1276135 " IX. Description of the invention: [Technical field] The present invention relates to a field emission lamp and a method of manufacturing the same, and more particularly to a method for effectively maintaining the required vacuum under normal working conditions by a getter. Field emission lamp and its manufacturing method 'Prior Art】 The lamp is a necessity for daily life, including / transparent glass tube. The inner wall of the glass tube is coated with white or colored fluorescent material, and the interior is filled with water. . The working principle of the fluorescent tube is to use the hot cathode to emit electrons to excite the mercury vapor to emit ultraviolet light, and the ultraviolet light to illuminate the fluorescent material to emit white light or colored light. The neon lamp is a hot cathode light source with high luminous efficiency. However, the mercury vapor used inside is poisonous. When the lamp is broken, the mercury vapor flows out of the outside and is harmful to the environment and the human body. In order to solve the above problems, a cold cathode field emission lamp is provided which includes a cathode and an anode disposed corresponding to the cathode. The cathode surface has no electron-emitting layer, and the anode and the electron-emitting layer are provided with a phosphor layer. When a certain voltage is applied between the cathode and the anode, the electron-emitting layer of the cathode emits electrons, and the phosphor layer of the anode emits light under the bombardment of electrons. The field emission lamp has low energy consumption, high luminous efficiency, and no harm to the environment and the human body. However, for a field emission lamp, a high vacuum sealed package is required inside, that is, the higher the internal vacuum, the better the field emission performance of the lamp. ^ First, as in the technology, the field emission lamp is used to obtain a long life. The vacuum is mainly used to install the getter inside. There are roughly two types, namely, evapotranspiration and concentrated non-evaporable. For the evapotranspiration getter, a planar structure is required inside the field emission lamp to form the getter layer by the pre-evaporation process, which increases the manufacturing cost by 1276135 plus the short circuit or leakage between the electrode leads. This causes the lamp to fail. For the concentrated non-evaporable getter, it is usually disposed at one end of the field emission lamp, so that the vacuum in the field emission lamp is less uniform, that is, the vacuum inside the field emission lamp near the getter is better, and The vacuum away from the position of the getter is poor and affects the field emission performance of the field emission lamp. In view of this, it is indeed necessary to provide a field emission lamp that effectively maintains the vacuum required for normal operation inside. [Summary of the Invention]

以下將藉由實施例說明一種場發射燈管及其製造 方法,該場發射燈管可有效地維持其内部具有正常工作 下所需之真空度從而確保其良好之工作品質。 一種場發射燈管,係包括一密封透明玻璃管、形成 於玻璃管内壁上之陽極、至少一封裝件以及設置於玻璃 管内之陰極。該玻璃管具有至少一開口端,封裝件配套 安裝於玻璃管之開口端並於玻璃管内部形成一密封空 間。該陽極包括形成於玻璃管内壁上之陽極導電層、形 成於陽極導電層上螢光層以及連接陽極導電層並延伸 1極接線頭之至少-陽極電極。該陰極包 通r/及至少—延伸出封裝件形成陰極接線 舻矣=。該陰極發射體包括導電體及形成於導電 射層。其中,該電子發射層含有吸氣劑 =料、導電金屬微粒及玻璃。 驟:%又射燈官之製造方法,該方法係包括以下步 姑料提微粒、導電金屬微粒、玻璃微粒及奈米 開口端之玻璃管、至少-陽極電極、 夕丢’極、導電體以及至少一封裝件,該玻璃管 12761^5 内璧形成有陽極導電層及形成於陽極導電層上之螢光 層; 將吸氣劑微粒、導電金屬微粒、玻璃微粒及奈米材 科於有機載體中進行充分混合形成漿料; 將上述漿料塗敷於導電體表面; 將塗敷有漿料之導電體於300〜60(rc下進行烘乾與 跨燒從而於‘電體表面上形成電子發射層以得到陰極 發射體,該陰極發射體及陰極電極形成陰極;Hereinafter, a field emission lamp and a method of manufacturing the same will be described by way of an embodiment, which can effectively maintain the vacuum required for normal operation inside the inside to ensure its good working quality. A field emission lamp comprises a sealed transparent glass tube, an anode formed on an inner wall of the glass tube, at least one package, and a cathode disposed in the glass tube. The glass tube has at least one open end, and the package is mounted on the open end of the glass tube to form a sealed space inside the glass tube. The anode includes an anode conductive layer formed on the inner wall of the glass tube, a phosphor layer formed on the anode conductive layer, and at least an anode electrode connected to the anode conductive layer and extending the 1-pole terminal. The cathode package r/ and at least - extends out of the package to form a cathode connection 舻矣 =. The cathode emitter includes an electrical conductor and is formed on the electrically conductive layer. The electron emission layer contains a getter, a conductive metal particle, and a glass. Step: % is a method of manufacturing a lamp, which includes the following steps: picking up particles, conductive metal particles, glass particles, and glass tubes at the open end of the nanometer, at least - an anode electrode, a smattering pole, an electrical conductor, and At least one package, the glass tube 12761^5 is internally formed with an anode conductive layer and a phosphor layer formed on the anode conductive layer; the getter particles, the conductive metal particles, the glass particles and the nanometer material are used in the organic carrier Fully mixing to form a slurry; applying the above slurry to the surface of the conductor; drying the conductive body coated with the slurry at 300 to 60 (bc under rc to form electrons on the surface of the electric body) Emitting a layer to obtain a cathode emitter, the cathode emitter and the cathode electrode forming a cathode;

組裝玻璃管、陽極電極、陰極及封裝件,於玻璃管 與封裝件之間加上您封材料,一併加熱至40Q〜5〇〇, 密封材料熔融以固定玻璃管與封裝件並於玻璃管内部 形成一密封空間,從而得到場發射燈管。 上述場發射燈管中吸氣劑微粒係分散於陰極電子 發射層中’其I有效地吸收螢光層發出之氣體或由其他 各禮原因進入場發射燈管内部之氣體,從而保持場發射 燈管内部具有較好之真空度進而提高其使用品質。 [實施方式】 以下將結合附圖詳細說明本發明場發射燈管及 其製造方法之實施例。 清參閱,1,本發明實施例場發射燈管10包括一密 封透明破璃=20、形成於玻璃管2〇内壁上之陽極3〇、 安裝官20端部之封裝件40以及設置於玻璃管20 中之陰極50。 玻璃官20爲條形管狀結構,其直徑爲2〜4〇毫米, 據實^要進行設計。該玻璃管20具有一半 =、°之封閉端22及一與封閉端22對應設置之開口 與封穿^開24與封裝件40配套安裝且開口端24 ' 40之間填充有密封材料(圖中未顯示),從 9 1276135 而於玻璃管20内部形成一密封空間。 陽極30包括形成於玻璃管内壁上之陽極導電層 32、設置於陽極導電層32上之螢光層34以及與陽極導 電層32連接導通之陽極電極36。該陽極導電層32覆蓋 玻璃管20内壁之多數區域,其一邊緣與玻璃管2〇開口 _ 端24之邊緣相平齊,另一邊緣遠離玻璃管2〇封閉端22 之頂部從而與該頂部之間形成一定距離。該陽極導電層 32爲透明導電膜,優選地,採用透明氧化銦錫膜作爲陽 極導電層32。該螢光層34靠近玻璃管20封閉端22之 籲邊緣與陽極導電層32之邊緣平齊,其另一邊緣與玻璃 管20開口端24之邊緣間形成一定距離從而於陽極導電 層32靠近玻璃管20開口端24之區域形成一裸露導電 部分320。該螢光層34選用高光電轉換效率、低應用電 壓及長餘輝之螢光層,螢光層34之螢光物質根據實際 需要可選用白色螢光物質或彩色螢光物質。可選擇地, 螢光層34表面可設置一鋁膜(圖中未顯示),該鋁膜可 -防止螢光物質過早老化,亦可提高光源亮度。 φ 陽極電極36包括一設置於陽極導電層32之陽極引 線環360、陽極引線柱362以及連接.陽極引線環360與 陽極引線柱362之陽極連接引線364。該陽極引線環360 設置於陽極導電層32之導電部分320上。陽極引線柱 362+與玻璃管2〇之軸線平行設置,並藉由封裝件4〇被 ^疋該喊極引線柱362設置於玻璃管20内部之端部 陽極連接引線364與陽極引線環360連接導通,另 卩由玻璃管20向外延伸形成可與外界電連接之陽 1接線頭366。該陽極引線環36〇、陽極引線柱362及 極^連接引線364均由導電材料製成,如銅。陽極電極 叹置之目的在於提供陽極30與外界電性導接之陽極Assembling the glass tube, the anode electrode, the cathode and the package, and adding the sealing material between the glass tube and the package, and heating it to 40Q~5〇〇, the sealing material is melted to fix the glass tube and the package and the glass tube A sealed space is formed inside to obtain a field emission lamp. The getter particles in the field emission lamp are dispersed in the cathode electron emission layer 'I effectively absorb the gas emitted from the phosphor layer or enter the gas inside the field emission lamp by other reasons, thereby maintaining the field emission lamp The inside of the tube has a good degree of vacuum to improve its quality of use. [Embodiment] Hereinafter, embodiments of a field emission lamp of the present invention and a method of manufacturing the same will be described in detail with reference to the accompanying drawings. 1. In the embodiment of the present invention, the field emission lamp 10 includes a sealed transparent glass=20, an anode 3〇 formed on the inner wall of the glass tube 2, a package 40 at the end of the mounting member 20, and a glass tube disposed on the glass tube. Cathode 50 in 20. The glass officer 20 is a strip-shaped tubular structure having a diameter of 2 to 4 mm, which is designed according to the actual situation. The glass tube 20 has a closed end 22 of half =, °, and an opening corresponding to the closed end 22, and the sealing member 24 is mounted with the package 40 and the opening end 24' 40 is filled with a sealing material (in the figure) Not shown), a sealed space is formed inside the glass tube 20 from 9 1276135. The anode 30 includes an anode conductive layer 32 formed on the inner wall of the glass tube, a phosphor layer 34 disposed on the anode conductive layer 32, and an anode electrode 36 connected to the anode conductive layer 32. The anode conductive layer 32 covers a plurality of regions of the inner wall of the glass tube 20, one edge of which is flush with the edge of the opening/end 24 of the glass tube 2, and the other edge is away from the top of the closed end 22 of the glass tube 2 and the top portion Form a certain distance. The anode conductive layer 32 is a transparent conductive film, and preferably, a transparent indium tin oxide film is used as the anode conductive layer 32. The edge of the phosphor layer 34 near the closed end 22 of the glass tube 20 is flush with the edge of the anode conductive layer 32, and the other edge forms a distance from the edge of the open end 24 of the glass tube 20 so that the anode conductive layer 32 is close to the glass. The area of the open end 24 of the tube 20 forms a bare conductive portion 320. The phosphor layer 34 is provided with a high photoelectric conversion efficiency, a low application voltage and a long afterglow phosphor layer. The phosphor material of the phosphor layer 34 may be white phosphor or color phosphor according to actual needs. Alternatively, an aluminum film (not shown) may be disposed on the surface of the phosphor layer 34. The aluminum film may prevent premature aging of the phosphor material and increase the brightness of the light source. The φ anode electrode 36 includes an anode lead ring 360 disposed on the anode conductive layer 32, an anode lead post 362, and an anode connection lead 364 connecting the anode lead ring 360 and the anode lead post 362. The anode lead ring 360 is disposed on the conductive portion 320 of the anode conductive layer 32. The anode lead post 362+ is disposed in parallel with the axis of the glass tube 2〇, and is connected to the anode lead ring 360 by the package member 4's end portion of the shim electrode lead post 362 disposed inside the glass tube 20. Turning on, the other is extended outward from the glass tube 20 to form a male 1 terminal 366 that can be electrically connected to the outside. The anode lead ring 36A, the anode lead post 362, and the pole connecting leads 364 are each made of a conductive material such as copper. The purpose of the anode electrode is to provide an anode for electrically connecting the anode 30 to the outside.

1276135 如故而’陽極電極36之結構可採用龙他步式, 線頭_^ct延λ件4g作爲陽極接 作爲陽極接^ ΐ 另—端延伸4封裝件4〇 〇穷從钱線碩366之導電柱或導電絲。 陰極50包括陰極發射體52及陰極電極5 一 i於ί 該陰極發射體52包括—狹長導電體52°ί及形 係柱表面之電子發射層522。該導電體52^0 SI:金製成,優選地,由銀製成。該Ϊ電= 二=,—陰極固定柱524與玻璃管2〇封閉端π之 5乂二,另一端與陰極電@ 54固定。該陰極電極 爲 V電柱,其一端與陰極發射體52相連,另一端 ,伸出^裝件40作爲陰極接線頭540。可選擇地,一彈 簧56設置於陰極發射體52與陰極電極54之間,當陰 極發射體52於接通或關閉電源從而受熱或冷卻時,吟 極,射體52將産生熱脹或冷縮,此時,彈簧%可起二 =節與平衡之作用。該彈簧56之高度以低於陽極引線 環360爲較佳。該陰極電極54之作用在於提供陰極5〇 與外界電性導接之陰極接線頭540,該陰極電極54之結 構可採用其他形式,如陰極發射體52之末端可直接作 爲陰極電極54,其延伸出封裝件40之外作爲陰極接線 頭 540 〇 陰極發射體52之外表面上形成有電子發射層522 , 該電子發射層522包含有奈米材料530、玻璃532、導 電金屬微粒534及吸氣劑微粒536。其中,該吸氣劑微 粒536係非蒸散型吸氣劑材料,直徑爲1〜10微米。非 11 1276135 蒸散型吸氣劑係靠表面吸氣或體擴散吸氣,以鈦、錯、 給、鉦、稀土金屬或者其合金等成分爲主,如锆鋁合金、 電子漿料級鈦粉、錯鈒鐵。該導電金屬微粒534選用銀 或氧化姻錫,其可確保奈米材料530與導電體520間電 性連接,優選地,導電金屬微粒534由銀製成。奈米材 料530包括能用於場發射之奈米碳管或其他材料之奈米 管、奈米線、奈米棒或奈米級微粒,其長度爲5〜15微 米,直徑爲1〜100奈米。優選地,該奈米材料53〇之至 少一端露出電子發射層522之表面。 _ 爲確保陽極30及陰極50間絕緣,可進一步於陰極 固定柱524與陽極導電層32之間設置一絕緣介質58。 該絕緣介質58由絕緣材料製成,如破璃或陶曼。 使用時,電子發射層522於電場作用下發射電子, 電子撞擊陽極30之螢光層34,當螢光層34採用彩色螢 光物質時,會發出彩色光,當螢光層34採用白色螢光 物質時,會發出白色光。此過程中,吸氣劑微粒536由 於均勻分散於電子發射層522之内,其可有效地吸收榮 _ 光層34發出之氣體或由其他各種原因進入場發射燈管 10内部之氣體,保持場發射燈管1 〇内部具有較好之真 空度。 可選擇地,場發射燈管10可設置一排氣管6〇,其 固定安裝於封裝件40上,一端與玻璃管20内部接通, 另一端延伸出封裝件40之外並密封。該排氣管60可外 接真空泵(圖中未顯示),用以場發射燈管1〇抽真空。 請參閱圖3,本發明揭示之另一實施例場發射燈管 10結構與上述實施例場發射燈管10結構之不同之處 在於:於另一實施例場發射燈管1〇’中,玻璃管2〇, 具有兩個開口端24,,該二開口端24,均與封裝件40, 12 1276135 ΓΛ安於兩開口端24’處均設有分別與陽極導電層 相ί之陽極接線頭縦以及與陰極發射體52, 相v通之陰極接線頭540,。 10、Γη㈣f、4/’纟發明實施例製造上述場發射燈管 、10之方法係包括以下步驟·· 屬與)’提供一定量吸氣劑微粒536、導電金 玻璃微,奈米材料530、具有至少一開 2()'2()’、至少-陽極電極36、 40, 54、導電體52以及至少-封裝件40、 於,、口:官2〇、2〇’内壁形成有陽極導電層32、 32以及形成於陽極導電層32、32,上之螢光層34; 吸氣劑微粒536與導電金屬微粒534均可預s先採用 球磨機分別球磨,使吸氣劑微粒536 導電金屬微粒534直徑爲〇丨〜1(1 = 微 m 7 微米。優選地,選用 激活/皿度為300〜500 C之吸氣劑,如鍅鋁合金吸氣劑。 玻璃微粒選用低熔點玻璃,i / ’、 ⑽…直徑爲奈V溶;=係四氧r 不不化點爲350〜600 C。车米 材料53G可預先藉由化學氣相沈積法 或1276135 For example, the structure of the anode electrode 36 can be used in the form of a dragon step, the wire head _^ct extension λ piece 4g as the anode connection as the anode connection ΐ the other end extension 4 package 4 〇〇 poor from the money line 366 Conductive column or conductive wire. The cathode 50 includes a cathode emitter 52 and a cathode electrode 5 - i. The cathode emitter 52 includes an elongated conductor 52 and an electron-emitting layer 522 on the surface of the pillar. The conductor 52^0 SI: made of gold, preferably made of silver. The xenon = two =, the cathode fixed post 524 and the closed end of the glass tube 2 are π 5 乂, and the other end is fixed to the cathode electric @ 54. The cathode electrode is a V-electrode, one end of which is connected to the cathode emitter 52, and the other end of which extends the mounting member 40 as a cathode terminal 540. Optionally, a spring 56 is disposed between the cathode emitter 52 and the cathode electrode 54. When the cathode emitter 52 is heated or cooled by turning on or off the power source, the emitter 52, the emitter 52 will be thermally expanded or contracted. At this time, the spring % can function as two = knots and balance. The height of the spring 56 is preferably lower than the anode lead ring 360. The cathode electrode 54 functions to provide a cathode terminal 540 for electrically connecting the cathode 5 〇 to the outside. The cathode electrode 54 can be formed in other forms. For example, the end of the cathode emitter 52 can directly serve as the cathode electrode 54 and extend. An electron emission layer 522 is formed on the outer surface of the cathode emitter 540 outside the package 40. The electron emission layer 522 includes a nano material 530, a glass 532, conductive metal particles 534, and a getter. Particle 536. Among them, the getter particles 536 are non-evaporable getter materials having a diameter of 1 to 10 μm. Non-11 1276135 Evaporable getter is based on surface gettering or bulk diffusion, and is mainly composed of titanium, wrong, feed, antimony, rare earth metals or alloys thereof, such as zirconium aluminum alloy, electronic paste grade titanium powder, Wrong iron. The conductive metal particles 534 are made of silver or sulphur oxide, which ensures electrical connection between the nanomaterial 530 and the conductor 520. Preferably, the conductive metal particles 534 are made of silver. The nanomaterial 530 comprises a nanotube, a nanowire, a nanorod or a nanometer particle which can be used for field emission of carbon nanotubes or other materials, and has a length of 5 to 15 micrometers and a diameter of 1 to 100 nanometers. Meter. Preferably, at least one end of the nanomaterial 53 is exposed to the surface of the electron-emitting layer 522. _ In order to ensure insulation between the anode 30 and the cathode 50, an insulating medium 58 may be further disposed between the cathode fixing post 524 and the anode conductive layer 32. The insulating medium 58 is made of an insulating material such as a glass or a ceramic. In use, the electron emission layer 522 emits electrons under the action of an electric field, and the electrons strike the phosphor layer 34 of the anode 30. When the phosphor layer 34 is colored with a fluorescent material, color light is emitted, and when the phosphor layer 34 is white fluorescent. When it is a substance, it emits white light. During this process, the getter particles 536 are uniformly dispersed in the electron-emitting layer 522, which can effectively absorb the gas emitted from the light-emitting layer 34 or enter the gas inside the field emission lamp 10 by various other reasons, and maintain the field. The inside of the emission lamp 1 has a good vacuum inside. Alternatively, the field emission lamp 10 may be provided with an exhaust pipe 6〇 fixedly mounted on the package member 40, one end of which is connected to the inside of the glass tube 20, and the other end extending beyond the package member 40 and sealed. The exhaust pipe 60 can be externally connected to a vacuum pump (not shown) for vacuuming the field emission lamp. Referring to FIG. 3, another embodiment of the field emission lamp 10 of the present invention is different from the structure of the field emission lamp 10 of the above embodiment in another embodiment of the field emission lamp 1', glass. The tube 2 has two open ends 24, and the two open ends 24 are provided with an anode terminal respectively connected to the anode conductive layer at the two open ends 24' of the package 40, 12 1276135. And a cathode terminal 540 that is in phase with the cathode emitter 52. 10. Γη(四)f, 4/' 纟Invention Example The method for manufacturing the above field emission lamp, 10 includes the following steps: · Providing a certain amount of getter particles 536, conductive gold glass micro, nano material 530, Having at least one opening 2 () '2 () ', at least - anode electrode 36, 40, 54, electrical conductor 52 and at least - package 40, the mouth: the official 2 〇, 2 〇 ' inner wall formed with anode conduction The layers 32, 32 and the phosphor layer 34 formed on the anode conductive layers 32, 32; the getter particles 536 and the conductive metal particles 534 can be ball-milled separately by a ball mill to make the getter particles 536 conductive metal particles The diameter of 534 is 〇丨~1 (1 = microm 7 μm. Preferably, a getter with an activation/dishness of 300~500 C, such as a bismuth aluminum alloy getter, is selected. The glass particles are selected from low melting glass, i / ', (10)... diameter is Nai V dissolved; = system is four oxygen r not point is 350~600 C. Car rice material 53G can be pre-chemical vapor deposition or

射蒸發法等習知技術製備,.其長M .. con 八负度爲5〜15微米,過短 會減弱奈未材料530之場發射特性, 料530相互纏繞結團。 长谷易使/丁、未材 陽極導電層32、32’藉由蒸鍍 於玻璃管20、20’内壁上,1責、“、★手奴預先形成 24,之邊緣與玻璃管開口端24、、工破璃J開口端24、 本场之邊緣相平齊。營 光層34藉由沈積或/、他手段於陽極導 9、 形成,其靠近玻璃管開口端24、 ΓΤ破%、夕、嘉络目士 之邊緣與玻璃管開 卩9,土 i涔卩^、 一疋距離從而於陽極導電層 32、32罪近玻璃&開口端24、24,之區域形成至少一 13It is prepared by a conventional technique such as the ejection evaporation method, and its length M.. con eight degrees of negativeness is 5 to 15 μm. Too short will weaken the field emission characteristics of the nanomaterial 530, and the material 530 is entangled with each other. The long valley easy / butyl, uncoated anode conductive layer 32, 32' by evaporation on the inner wall of the glass tube 20, 20', 1 responsibility, ", ★ hand slave pre-formed 24, the edge and the open end of the glass tube 24 , the edge of the open glass 24, the edge of the field is flush. The camping layer 34 is formed by deposition or /, he is guided by the anode, which is close to the open end of the glass tube 24, smashed%, eve , the edge of the Jialuo man and the glass tube open 9, the soil i 涔卩 ^, a distance between the anode conductive layer 32, 32 sin near the glass & open end 24, 24, the area forms at least a 13

該烘乾與料係於真空環境下進減者於烘乾與 =、:?程中通入惰性氣體加以保護防止烘乾與焙燒時 X生礼化反應亦防止吸氣劑飽和。烘乾之目的在於使有 1276135 裸露導電部分320。 封裝件40、40’ 、陽極電極36及陰極電極54之數 量與破璃管開口端24、24’之數量一致,當玻璃管20 具有一開口端24時分別需要一封裝件40、一陽極電極 36及一陰極電極54,當玻璃管20,具有兩開口端24、 24’時分別需要兩封裝件40、40’ 、兩陽極電極36及 兩陰極電極54。 步驟(二),將吸氣劑微粒536、導電金屬微粒534、 玻璃微粒及奈米材料530於有機載體中進行充分混合形 成漿料; 有機載體係由作爲溶劑之松油醇、作爲增塑劑之少 里部位本^一甲^一 丁 S曰及作爲穩定劑之少量乙基纖維素 形成之混合劑。該漿料中吸氣劑微粒536之質量百分比 濃度為40〜80%,混合過程優選於60〜8(TC混合3〜5小 時。爲更好分散奈米材料530並得到奈米材料530直徑 均勻之漿料,可進一步使用低功率之超聲波對含有奈米 材料530之有機溶劑進行超聲波震蕩,後再對其進行離 心處理。 步驟(三),將上述漿料塗敷於導電體52〇表面; 塗敷過程應於潔淨環境内進行,優選地,環境内之 灰塵度應小於1000/m3。 步驟(四),將塗敷有漿料之導電體520於300〜600°C 2行烘乾與、錢從而於導㈣52g表面上形成電子發 f/ 522以得到陰極發射體52、52,,該陰極發射體 、52與陰極電極54形成陰極5〇 ; 1276135 機載體從導電體520上揮發。焙燒之目的在於使玻璃微 粒熔融從而將吸氣劑微粒536、導電金屬微粒534與太 米材料530粘結於導電體520之上形成電子發射^ 522。另、,炫融玻璃532可調節整體之熱膨脹係“以; 止所形成之電子發射層522産生裂紋或發生斷裂。 爲進一步增強電子發射層522之場發射特^,於經 過烘乾與焙燒過程之後,可對電子發射層522之表面進 行摩擦,部分奈米材料530之末端經摩擦後露出 射層522表面。 " 步驟(五),組裝玻璃管20、20,、陽極電極36、 陰極50及封裝件40、40,,於玻璃管2〇、20,與封裝 件40、40間加上密封材料,一併加熱至4〇〇〜5〇〇°c, 密封材料熔融以固定玻璃管2〇、2(Τ與封裝件4〇、4〇, 並於玻璃管20、20,内部形成一密封空間,從而得到場 發射燈管10、10,。 陽極電極36 —端與陽極導電層32、32,之導電部 分320相連,另一端延伸出封裝件形成陽極接線頭加6、 ) 366 。陰極電極54之一端部延伸出封裝件4〇、4〇,形 成陰極接線頭54〇、540’ 。加熱過程通常於真空環境下 $行或者於加熱過程中通入惰性氣體加以保護。加熱過 程中吸氣劑微粒536被激活。密封材料可選用習知密 2料如,選用溶點為350〜600。C之低熔點玻璃粉作 爲饴封材料。由於玻璃粉微粒直徑較小,其實際熔點低 =6〇〇°C。當加熱至400〜50(Γ(:時,玻璃粉熔融,冷卻 後’溶融坡璃凝固從而將封裝件4〇、4〇,固定於玻璃管 、20端部並於玻璃管之内部形成一密封空間。 當場發射燈管具有排氣管60時,於玻璃管20、20, 與封裴件40、40,密封之前,可先藉由排氣管60外接 15 1276135 真空泵使玻璃官20、20,内部具有一定真空度,然後密 封排氣官60之端部再將玻璃管2〇、2〇,與封裝件40、 4〇’進行密封。 〃 綜上所述,本發明確已符合發明專利要件,爰依法 提出專利申請。惟,以上所述者僅為本發明之較佳實施 例,舉凡熟悉本案技藝之人士,於援依本案發明精神所 作之等效修飾或變化,皆應包含於以下之申請專利範 之内。 m 【圖式簡單說明】 圖1係本發明一實施例場發射燈管之剖視示意圖。 圖2係圖1沿11 -11線之剖視放大圖。 圖3係本發明另一實施例場發射燈管之剖視示意 圖4係本發明實施例場發射燈管製造方法之步驟示 意圖。 【主要元件符號說明】 場發射燈管 10、10, 玻璃管 20、20, 封閉端 22 開口端 24、24, 1¼極 .30 陽極導電層 32 導電部分 320 螢光層 34 1%極電極 36 陽極引線環 360 陽極引線柱 362 陽極連接引線 364 陽極接線頭 366、366’ 封裝件 40、40, 陰極 50 陰極發射體 52、52, 導電體 520 電子發射層 522 陰極固定柱 524 奈米材料 530 玻璃 532 導電金屬微粒 534 吸氣劑微粒 536 陰極電極 54 16 1276135 彈簧 56 陰極接線頭 540、540’ 絕緣介質 58The drying and the material are in the vacuum environment, and the drying and the drying are combined with =, :? The inert gas is passed through the process to prevent drying and roasting. The X-raying reaction also prevents the getter from saturating. The purpose of drying is to have 1276135 bare conductive portion 320. The number of the packages 40, 40', the anode electrode 36 and the cathode electrode 54 is the same as the number of the open ends 24, 24' of the glass tube. When the glass tube 20 has an open end 24, a package 40 and an anode electrode are respectively required. 36 and a cathode electrode 54, when the glass tube 20 has two open ends 24, 24', two packages 40, 40', two anode electrodes 36 and two cathode electrodes 54 are required, respectively. In the step (2), the getter particles 536, the conductive metal particles 534, the glass particles and the nano-material 530 are thoroughly mixed in an organic vehicle to form a slurry; the organic carrier is a terpineol as a solvent, and is used as a plasticizer. A mixture of a small amount of ethyl cellulose as a stabilizer and a mixture of a small amount of ethyl cellulose as a stabilizer. The mass percentage of the getter particles 536 in the slurry is 40 to 80%, and the mixing process is preferably 60 to 8 (TC mixing for 3 to 5 hours. For better dispersion of the nano material 530 and obtaining a uniform diameter of the nano material 530) The slurry may further ultrasonically oscillate the organic solvent containing the nano material 530 by using low-power ultrasonic waves, and then centrifuge the same. Step (3), applying the slurry to the surface of the conductor 52; The coating process should be carried out in a clean environment. Preferably, the degree of dust in the environment should be less than 1000/m3. In step (4), the conductive body 520 coated with the slurry is dried at 300 to 600 ° C for 2 lines. The money thus forms an electron emission f/522 on the surface of 52g to obtain a cathode emitter 52, 52, and the cathode emitter 52 and the cathode electrode 54 form a cathode 5〇; 1276135 the carrier is volatilized from the conductor 520. The purpose is to melt the glass particles to bond the getter particles 536, the conductive metal particles 534 and the rice material 530 onto the conductor 520 to form an electron emission 522. In addition, the glazing glass 532 can adjust the overall thermal expansion. system" The electron-emitting layer 522 formed is cracked or broken. To further enhance the field emission of the electron-emitting layer 522, after the drying and baking process, the surface of the electron-emitting layer 522 may be rubbed. The end of the rice material 530 is rubbed to expose the surface of the shot layer 522. " Step (5), assembling the glass tube 20, 20, the anode electrode 36, the cathode 50, and the package members 40, 40, in the glass tube 2, 20 And a sealing material is applied between the packages 40 and 40, and is heated to 4 〇〇 5 〇〇 ° C, and the sealing material is melted to fix the glass tubes 2 〇, 2 (Τ and the package 4 〇, 4 〇, and In the glass tubes 20, 20, a sealed space is formed inside, thereby obtaining field emission lamps 10, 10. The anode electrode 36 is connected to the conductive portions 320 of the anode conductive layers 32, 32, and the other end extends out of the package. The anode terminal is provided with 6, 366. One end of the cathode electrode 54 extends out of the package 4〇, 4〇 to form a cathode terminal 54〇, 540'. The heating process is usually performed in a vacuum environment or in a heating process. Inert gas is added for protection. During the process, the getter particles 536 are activated. The sealing material may be selected from the conventional materials such as a low melting point glass powder having a melting point of 350 to 600° C. The glass frit particles have a small diameter and a low actual melting point. =6〇〇°C. When heated to 400~50 (Γ(:, when the glass frit melts, after cooling, the molten glass solidifies to seal the package 4〇, 4〇, fixed to the glass tube, 20 end and The inside of the glass tube forms a sealed space. When the field emission lamp has the exhaust pipe 60, the glass tube 20, 20, and the sealing member 40, 40 can be externally connected to the exhaust pipe 60 by a 15 1276135 vacuum pump. The glass doors 20, 20 have a certain degree of vacuum inside, and then the ends of the exhaustors 60 are sealed and the glass tubes 2, 2, and sealed with the packages 40, 4'.综 In summary, the present invention has indeed met the requirements of the invention patent, and has filed a patent application in accordance with the law. However, the above description is only the preferred embodiment of the present invention, and those skilled in the art will be able to include the equivalent modifications or variations of the invention in the spirit of the invention. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a cross-sectional view showing a field emission lamp of an embodiment of the present invention. Figure 2 is an enlarged cross-sectional view of Figure 1 taken along line 11-11. Fig. 3 is a cross-sectional view showing a field emission lamp according to another embodiment of the present invention. Fig. 4 is a view showing the steps of a method of manufacturing a field emission lamp according to an embodiment of the present invention. [Main component symbol description] Field emission lamp 10, 10, glass tube 20, 20, closed end 22 open end 24, 24, 11⁄4 pole. 30 anode conductive layer 32 conductive portion 320 fluorescent layer 34 1% electrode 36 anode Lead ring 360 anode lead post 362 anode connection lead 364 anode terminal 366, 366' package 40, 40, cathode 50 cathode emitter 52, 52, conductor 520 electron emission layer 522 cathode fixed column 524 nano material 530 glass 532 Conductive metal particles 534 getter particles 536 cathode electrode 54 16 1276135 spring 56 cathode terminal 540, 540' insulating medium 58

1717

Claims (1)

1276135 十、申請專利範圍 1 · 一種場發射燈管,係包括: 密封之透明玻璃管,其具有裏少一開口端; 至少一封裝件,與玻璃管開口端配套安裝; 陽極,其包括形成於玻璃管内壁上之陽極導電層、 形成於陽極導電層上之螢光層以及連接陽極導電層並 延伸出封裝件之至少一陽極電極;以及 陰極,安裝於玻璃管内,其包括陰極發射體及至少 一延伸出封裝件之陰極電極,該陰極發射體包括導電體 及形成於導電體表面之電子發射層; 其中,該電子發射層含有吸氟劑微粒、奈米材料、 導電金屬微粒及玻璃。 2·如申請專利範圍第1項所述之場發射燈管,其中, 該吸氣劑微粒係非蒸散型吸氣劑。 3·如申請專利範圍第2項所述之場發射燈管,其中, 該吸氣劑微粒直徑爲1〜1〇微米。 4·如申請專利範圍第3項所述i場發射燈管,其中, 該奈米材料之長度爲5〜15微米,直徑爲1〜100奈米。 5·如申請專利範圍第3項所述之場發射燈管,其中, 該玻璃管具有一開口端及與開口端相對應之封閉端,該 封閉端爲半圓形結構,該陽極電極、陰極電極及封閉件 各爲一件。 6.如申請專利範圍第3項所述之場發射燈管,其中, 該玻璃管具有兩開口端,該陽極電極、陰極電極及封閉 件各爲兩件。 7·如申請專利範圍第5或6項所述之場發射燈管,其 中,該陰極電極爲一導電柱,其一端與導電體相連,另 一端延伸出封裝件外作爲陰極接線頭。 18 1276135 8·如申請專利範圍第7項所述之場發射燈管,其中, 該陰極亦包括至少一彈簧,其設置於陰極電極與導電體 之間。 _ 9·如申請專利範圍第5或6項所述之場發射燈管,其 中,該陰極電極由導電體末端形成,其延伸出封裝件外 '作爲陰極接線頭。 10·如申請專利範圍第3項所述之場發射燈管,其中, 該導電金屬微粒選用銀或氧化銦錫,其直徑爲〇·1〜10 微米。 I 11·如申請專利範圍第3項所述之場發射燈管,其中, 該陽極亦包括一鋁膜設置於螢光層外表面。 12.如申請專利範圍第3項所述之場發射燈管,亦包括 一排氣管,其一端設置於玻璃管内部,另一端延伸出封 裝件外。 13·—種場發射燈管之製造方法,包括以下步驟: (一)提供吸氣劑微粒、導電金屬微粒、玻璃微粒 及奈米材料、具有至少^一開口端之玻璃管、至少一陽極 電極、至少一陰極電極、導電體以及至少一封裝件,該 * - 玻璃管内壁形成有陽極導電層及形成於陽極導電層上 之螢光層; (-Ο將吸氣劑微粒、導電金屬微粒、玻璃微粒及 奈米材料於有機載體中進行充分混合形成漿料; (三) 將上述漿料塗敷於導電體表面; (四) 將塗敷有漿料之導電體於3〇〇〜6〇〇°C下進行 烘乾與焙燒從而於導電體表面上形成電子發射層以得 到陰極發射體,該陰極發射體與陰極電極形成陰極; (五) 組裝玻璃管、陽極電極、陰極及封裝件,並 於玻璃管内部形成一密封空間,從而得到場發射燈管。 19 1276135 14. 如申請專利範圍第13項所述場發射燈管之製造方 法,其中,於步驟(一)中,該吸氣劑微粒係非蒸散型 吸氣劑,其激活溫度爲300〜500°C。 15. 如申請專利範圍第14項所述場發射燈管之製造方 法,其中,於步驟(一)中,該玻璃微粒爲低熔點玻璃 微粒,其熔點為350〜600 °C,微粒直徑爲10〜100奈米。 16. 如申請專利範圍第15項所述場發射燈管之製造方 法,其中,於步驟(一)中,該陽極導電層係藉由蒸鍍 之方法於玻璃外殼内壁上形成,該螢光層係藉由沈積之 . 方法於陽極導電層上形成。 17. 如申請專利範圍第16項所述場發射燈管之製造方 法,其中,於步驟(二)中,該有機載體係松油醇、鄰 位苯二甲二丁酯及乙基纖維素之混合劑。 18. 如申請專利範圍第17項所述場發射、燈管之製造方 法,其中,於步驟(二)中,該漿料中吸氣劑微粒之質 量百分比濃度為40〜80°/〇。 19. 如申請專利範圍第18項所述場發射燈管之製造方 法,其中,於步驟(二)中,該混合過程係於60〜80°C B 下進行3〜5小時。 20. 如申請專利範圍第19項所述場發射燈管之製造方 法,其中,於步驟(三)中,該塗敷過程係於灰塵度小 於1000/m3之環境内進行。 21. 如申請專利範圍第20項所述場發射燈管之製造方 法,其中,於步驟(四)中,該烘乾與焙燒過程於真空 或惰性氣體保護下進行。 22. 如申請專利範圍第21項所述場發射燈管之製造方 法,其中,於實施步驟(五)之前,可預先對陰極之電 子發射層表面進行摩擦,部分奈米材料末端經摩擦後露 1276135 出電子發射層表面。 23.如申請專利範圍第22項所述場發射燈管之製造方 法,其中,於步驟(五)中,該玻璃管之密封空間係藉 由於玻璃管與封裝件之間加上密封材料,加熱至 400〜500°C,密封材料熔融而形成。 211276135 X. Patent application scope 1 · A field emission lamp comprising: a sealed transparent glass tube having one less open end; at least one package for mounting with an open end of the glass tube; an anode comprising: An anode conductive layer on the inner wall of the glass tube, a phosphor layer formed on the anode conductive layer, and at least one anode electrode connecting the anode conductive layer and extending out of the package; and a cathode mounted in the glass tube, including the cathode emitter and at least A cathode electrode extending from the package, the cathode emitter comprising an electrical conductor and an electron emission layer formed on the surface of the electrical conductor; wherein the electron emission layer comprises fluorine absorbing agent particles, a nano material, conductive metal particles and glass. 2. The field emission lamp of claim 1, wherein the getter particles are non-evaporable getters. 3. The field emission lamp of claim 2, wherein the getter particles have a diameter of 1 to 1 micron. 4. The i field emission lamp of claim 3, wherein the nano material has a length of 5 to 15 micrometers and a diameter of 1 to 100 nanometers. 5. The field emission lamp of claim 3, wherein the glass tube has an open end and a closed end corresponding to the open end, the closed end is a semicircular structure, the anode electrode and the cathode The electrode and the closure are each a piece. 6. The field emission lamp of claim 3, wherein the glass tube has two open ends, and the anode electrode, the cathode electrode and the closure are each two pieces. 7. The field emission lamp of claim 5, wherein the cathode electrode is a conductive post having one end connected to the electrical conductor and the other end extending out of the package as a cathode terminal. 18 1276135. The field emission lamp of claim 7, wherein the cathode further comprises at least one spring disposed between the cathode electrode and the electrical conductor. The field emission lamp of claim 5, wherein the cathode electrode is formed by an end of a conductor that extends out of the package as a cathode terminal. 10. The field emission lamp of claim 3, wherein the conductive metal particles are silver or indium tin oxide having a diameter of 〇1 to 10 μm. The field emission lamp of claim 3, wherein the anode further comprises an aluminum film disposed on an outer surface of the phosphor layer. 12. The field emission lamp of claim 3, further comprising an exhaust pipe having one end disposed inside the glass tube and the other end extending outside the package. 13·—The method for manufacturing a field emission lamp comprises the following steps: (1) providing getter particles, conductive metal particles, glass particles and nano materials, a glass tube having at least one open end, and at least one anode electrode At least one cathode electrode, a conductor and at least one package, the inner wall of the glass tube is formed with an anode conductive layer and a phosphor layer formed on the anode conductive layer; (-Ο a getter particle, a conductive metal particle, The glass particles and the nano material are thoroughly mixed in an organic carrier to form a slurry; (3) applying the slurry to the surface of the conductor; (4) applying the slurry coated with the conductor at 3〇〇6〇6〇 Drying and baking at 〇°C to form an electron emission layer on the surface of the conductor to obtain a cathode emitter, the cathode emitter and the cathode electrode forming a cathode; (5) assembling a glass tube, an anode electrode, a cathode and a package, And forming a sealed space inside the glass tube to obtain a field emission lamp. 19 1276135 14. The method for manufacturing a field emission lamp according to claim 13 of the patent application, wherein In the first step, the getter particles are non-evaporable getters, and the activation temperature is 300 to 500 ° C. 15. The method for manufacturing a field emission lamp according to claim 14 , wherein In the step (1), the glass particles are low-melting glass particles having a melting point of 350 to 600 ° C and a particle diameter of 10 to 100 nm. 16. The field emission lamp of claim 15 The manufacturing method, wherein in the step (1), the anode conductive layer is formed on the inner wall of the glass envelope by evaporation, and the phosphor layer is formed on the anode conductive layer by deposition. The method for producing a field emission lamp according to claim 16, wherein in the step (2), the organic carrier is a mixture of terpineol, ortho-dibutyl dibutylate and ethyl cellulose. 18. The method for manufacturing a field emission and a lamp according to claim 17, wherein in the step (2), the mass percentage of the getter particles in the slurry is 40 to 80°/〇. 19. For the field emission lamp as described in claim 18 The manufacturing method, wherein, in the step (2), the mixing process is carried out at 60 to 80 ° C for 3 to 5 hours. 20. The method for manufacturing a field emission lamp according to claim 19, wherein In the step (3), the coating process is carried out in an environment in which the degree of dust is less than 1000/m3. 21. The method for manufacturing a field emission lamp according to claim 20, wherein in the step (4) The drying and calcining process is carried out under the protection of a vacuum or an inert gas. 22. The method for manufacturing a field emission lamp according to claim 21, wherein before the step (5), the cathode can be preliminarily The surface of the electron-emitting layer is rubbed, and the end of the portion of the nano-material is rubbed to expose 1276135 to the surface of the electron-emitting layer. The method of manufacturing the field emission lamp of claim 22, wherein in the step (5), the sealing space of the glass tube is heated by adding a sealing material between the glass tube and the package. The sealing material is formed by melting to 400 to 500 ° C. twenty one
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