TW200828621A - Method for manufacturing light-emitting diode - Google Patents
Method for manufacturing light-emitting diode Download PDFInfo
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- TW200828621A TW200828621A TW95149056A TW95149056A TW200828621A TW 200828621 A TW200828621 A TW 200828621A TW 95149056 A TW95149056 A TW 95149056A TW 95149056 A TW95149056 A TW 95149056A TW 200828621 A TW200828621 A TW 200828621A
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- 238000000034 method Methods 0.000 title claims abstract description 92
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 36
- 239000000758 substrate Substances 0.000 claims abstract description 78
- 229910052751 metal Inorganic materials 0.000 claims abstract description 35
- 239000002184 metal Substances 0.000 claims abstract description 35
- 238000004140 cleaning Methods 0.000 claims abstract description 11
- 239000010410 layer Substances 0.000 claims description 84
- 239000000463 material Substances 0.000 claims description 36
- 239000004065 semiconductor Substances 0.000 claims description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 229910045601 alloy Inorganic materials 0.000 claims description 10
- 239000000956 alloy Substances 0.000 claims description 10
- 238000005498 polishing Methods 0.000 claims description 10
- 238000001312 dry etching Methods 0.000 claims description 9
- 239000011241 protective layer Substances 0.000 claims description 9
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052737 gold Inorganic materials 0.000 claims description 8
- 239000010931 gold Substances 0.000 claims description 8
- 239000013078 crystal Substances 0.000 claims description 7
- 229910052738 indium Inorganic materials 0.000 claims description 7
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 7
- 238000001039 wet etching Methods 0.000 claims description 7
- 229910002601 GaN Inorganic materials 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000004332 silver Substances 0.000 claims description 5
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052733 gallium Inorganic materials 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 150000004767 nitrides Chemical class 0.000 claims description 4
- 229910052594 sapphire Inorganic materials 0.000 claims description 4
- 239000010980 sapphire Substances 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 238000000407 epitaxy Methods 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 239000011368 organic material Substances 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 229910005540 GaP Inorganic materials 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 238000005520 cutting process Methods 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims description 2
- HZXMRANICFIONG-UHFFFAOYSA-N gallium phosphide Chemical compound [Ga]#P HZXMRANICFIONG-UHFFFAOYSA-N 0.000 claims description 2
- 229910003437 indium oxide Inorganic materials 0.000 claims description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000004943 liquid phase epitaxy Methods 0.000 claims description 2
- 125000002524 organometallic group Chemical group 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- -1 turn Substances 0.000 claims description 2
- 238000007740 vapor deposition Methods 0.000 claims description 2
- RNQKDQAVIXDKAG-UHFFFAOYSA-N aluminum gallium Chemical group [Al].[Ga] RNQKDQAVIXDKAG-UHFFFAOYSA-N 0.000 claims 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 6
- NWAIGJYBQQYSPW-UHFFFAOYSA-N azanylidyneindigane Chemical compound [In]#N NWAIGJYBQQYSPW-UHFFFAOYSA-N 0.000 claims 5
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 claims 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 2
- 229910001218 Gallium arsenide Inorganic materials 0.000 claims 2
- GPXJNWSHGFTCBW-UHFFFAOYSA-N Indium phosphide Chemical compound [In]#P GPXJNWSHGFTCBW-UHFFFAOYSA-N 0.000 claims 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 239000010949 copper Substances 0.000 claims 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical group Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 claims 2
- 238000009713 electroplating Methods 0.000 claims 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical group O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 claims 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical group [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 claims 2
- 238000009616 inductively coupled plasma Methods 0.000 claims 2
- 229910052750 molybdenum Inorganic materials 0.000 claims 2
- 239000011733 molybdenum Substances 0.000 claims 2
- 238000001020 plasma etching Methods 0.000 claims 2
- 230000008646 thermal stress Effects 0.000 claims 2
- 229910052684 Cerium Inorganic materials 0.000 claims 1
- 229910000530 Gallium indium arsenide Inorganic materials 0.000 claims 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
- GHZFPSVXDWJLSD-UHFFFAOYSA-N chromium silver Chemical compound [Cr].[Ag] GHZFPSVXDWJLSD-UHFFFAOYSA-N 0.000 claims 1
- 210000001268 chyle Anatomy 0.000 claims 1
- 239000007772 electrode material Substances 0.000 claims 1
- 238000001962 electrophoresis Methods 0.000 claims 1
- 229910052732 germanium Inorganic materials 0.000 claims 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims 1
- 229940119177 germanium dioxide Drugs 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 239000007791 liquid phase Substances 0.000 claims 1
- 230000004807 localization Effects 0.000 claims 1
- 239000000395 magnesium oxide Substances 0.000 claims 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
- 239000012071 phase Substances 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 238000000992 sputter etching Methods 0.000 claims 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 claims 1
- 239000011135 tin Substances 0.000 claims 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims 1
- 229910001887 tin oxide Inorganic materials 0.000 claims 1
- 239000011787 zinc oxide Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910000673 Indium arsenide Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- RPQDHPTXJYYUPQ-UHFFFAOYSA-N indium arsenide Chemical compound [In]#[As] RPQDHPTXJYYUPQ-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000001451 molecular beam epitaxy Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 238000002207 thermal evaporation Methods 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
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Abstract
Description
200828621 九、發明說明 【發明所屬之技術領域】 本發明是有關於一種發光二極體(LED)之製造方法,且特 別是有關於一種具有可重複使用之成長基板的發光二極體之 製造方法。 【先前技術】 一般金屬基板氮化物(Ill-Nitride)發光二極體的製作方 式’大多係先磊晶成長於由藍寶石或半導體所組成之成長基 板上’接著再利用接合方式將發光磊晶結構與金屬基板接 合’再將成長基板自發光蠢晶結構上剝除,而完成發光二極 體之製作。 在金屬基板氮化物發光二極體的製作過程中,於發光二 極體磊晶片之成長基板剝除後,此一成長基板即無法再使 用。如此一來,在金屬基板發光二極體之製程中,大量耗用 的成長基板將成為量產金屬基板發光二極體產品中無法降低 的成本的重要因素之一。因此,將造成資源的浪費,也產生 大量廢棄物,不符經濟效益與環保需求。 【發明内容】 因此,本發明之目的就是在提供一種發光二極體之製造 方法’透過乾式、濕式、或搭配使用乾式與濕式蝕刻的 方式,清潔自遙晶結構域離之成長基板。經清潔後之成長 基板可再回收使用,以供下—蠢晶結構成長。因此,可節省 200828621 成長基板的耗用,兼具環保及降低成本,而可大大地提升經 濟效益。 根據本發明之上述目的,提出一種發光二極體之製造方 法,至少包括··提供一成長基板;形成一第一發光二極體於 成長基板上’其中形成第一發光二極體之步驟至少包括··形 成一第一緩衝層於成長基板之上;形成一第一發光磊晶結構 於第一緩衝層之上;形成一第一金屬基板於第一發光磊晶結 構之上;以及剝離成長基板,以暴露出第一發光磊晶結構·, 對成長基板進行一清潔步驟;以及形成一第二發光二極體於 上述成長基板上。 依照本發明一較佳實施例,進行上述之清潔步驟時,可 利用乾式蝕刻法、濕式蝕刻法、機械研磨法或高溫烘烤法。 【實施方式】 為了使本發明之敘述更加詳盡與完備,可參照下列描述 並配合第1圖至第5圖之圖式。 請參照第i圖至第3圖’其繪示依照本發明_較佳實施 ::的m::體之製程剖面圖。首先’提供成長基板 100’其中成長基板100之材料可例如為藍寶石、砷化 ^ 化銦或磷化鎵。再於成長隸⑽上製作發光二極體、。製: 發光二極體時,先利用例如低溫磊晶法形成緩衝 在成長基板H)〇之表面上,其中緩衝層1〇2之 二 氮化铭或氣化鎵。接下來,利用例如有機金屬氣相沉 法、液相磊晶法或分子束磊晶法於緩衝岸丨〇 貝曰日 9 上成長發光磊 6 200828621 °在本示範實施例中,發光蟲晶結構包括依序堆疊在 拿由上之弟電性半導體層104、第一電性侷限層 :第:電性揭限層11〇以及第二電性接觸層 二弟—電性與第二電性為不同電性。當第—電性為Ν - 弟-電性為Ρ型;而當第-電性為Ρ型時,第二電性 -則為Ν型。在本示範實施例中’第-電性為Ν型,且第二電 性為Ρ,。在一實施例中,第一電性半導體層刚之材料可 Γ例如為氮化紹; OSd, osg u,第 Μ*性偈限層 10 6 之好祖-ρ 丨、斤 UAlx〇a,,yIni.yN;0,x" —=1,〇Sy$i],主動層1〇8可為雙昱 =、、=構或多重量子井結構,且主動層1G8之材料可例如包含 鼠化链鎵銦[(AlxGai.x)yIni_yN; e g l ^ 013,第二電性 =限層11G之材料可例如為氮化紹鎵銦[(AlxGai x)yin 〇 且第二電性接觸層112之材料 化銘鎵銦UAUGUySLkded]。 為乱 、接著,可於發光磊晶結構之第二電性接觸層112上直 形成金屬基板12G’或者可先選擇性地對發光蟲晶結構進行— -处理例如疋義發光磊晶結構之圖案,及/或於發光磊曰 :之第二電性議112上額外形成一些結構層,例如:: 電極與金屬反射層。在本示範實施例中,先利用例如微事逝 蝕f或切割技術對發光磊晶結構進行圖案定義,以移除:二 之第二電性接觸層112、部分之第二電性侷限層11〇、部^刀 主動層108、部分之第一電性侷限層1〇6 ’而在發光磊晶結: 中形成溝渠122,其中溝渠暴露出部分之第一電性半導體層 200828621 1〇4。在發光磊晶結構中形成溝渠122時,可利 濕式蝕刻法或機械切割研磨法。接著 ::法、 方式形成介電保護層118覆蓋在溝渠122之侧==佈 隻霉木122所暴露出之發光磊晶結構的部分。i 人 _電保護層118之材料可為高介電有機材料、切之氧" 或切之氮化物,例如二氧切或氮㈣。夕之減物、 再利用例如熱蒸鍍(The_l Evap〇ra =eam Eva_iGn)或離子濺物utt =電蓋在第二電性接觸層⑴上,以提:=: 錫、氧化錮、氧化:、=:之材料可例如為氧化銦 μ或錢鎂。隨後,_例如熱 .二'、、、鍍或離子濺鍍方式形成金屬反射層116覆蓋 在第二電性透明電極114Ji,以將 = Π6之方向發射之“ 肝主動層1〇8朝金屬反射層 先予以反射,其中金屬反射層116之材料可 用、鋁、銀、鉑、鉻、鎳或這些金屬之合金。接著,利 c = 形成金屬基板12G覆蓋在介電保護層 之晨/部一Λ 114之暴露部分以及金屬反射層116 全屬:板刀120纟填滿溝渠122,而形成如第1圖所示之結構。 Ϊ = 材料可例如為鋼、錮、鎳、金、銀、鈾、銘 或這些金屬之合金。 待元成金屬基板〗2 Ω夕制祕 <.I 加熱應力差異方 衣乍後,利用例如雷射剝除法或 ^^ 4弋將成長基板100自發光磊晶結構剝離。由 合遭到^ [ 1〇0與發光蟲晶結構分離時,部分之緩衝層102 曰 $ ’而另―部分之緩_ 102則可能殘留在成長基 8 200828621 板100之表面上,如第 102a。將成長基板100 電性半導體層104。 斤示之成長基板100上的緩衝層 剝除後,暴露出發光磊晶結構之第一 性電==100剝除後,利用例如沉積方式形成第-電 ㈣^覆盖在暴露出之第—電性半導體1104上,200828621 IX. Description of the Invention [Technical Field] The present invention relates to a method of manufacturing a light-emitting diode (LED), and more particularly to a method of manufacturing a light-emitting diode having a reusable growth substrate . [Prior Art] A general metal substrate nitride (Ill-Nitride) light-emitting diode is formed by a plurality of epitaxial growth on a growth substrate composed of sapphire or a semiconductor, and then a bonding epitaxial structure is used. Bonding to the metal substrate', the growth substrate is stripped from the light-emitting amorphous structure to complete the fabrication of the light-emitting diode. In the process of fabricating a metal substrate nitride light-emitting diode, the growth substrate can no longer be used after the growth substrate of the light-emitting diode epitaxial wafer is removed. As a result, in the process of the metal substrate light-emitting diode, a large amount of the grown substrate is one of the important factors that cannot be reduced in the mass production of the metal substrate light-emitting diode product. Therefore, it will result in waste of resources and a large amount of waste, which is inconsistent with economic benefits and environmental protection needs. SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a method for fabricating a light-emitting diode that cleans a substrate grown from a remote crystal domain by dry, wet, or a combination of dry and wet etching. After cleaning, the substrate can be recycled for use in the growth of the next-stack structure. Therefore, the consumption of the 200828621 growth substrate can be saved, and the environmental protection and cost reduction can be greatly improved, and the economic benefit can be greatly improved. According to the above object of the present invention, a method for fabricating a light emitting diode includes at least providing a growth substrate, and forming a first light emitting diode on the growth substrate, wherein the step of forming the first light emitting diode is at least Forming a first buffer layer on the growth substrate; forming a first light-emitting epitaxial structure on the first buffer layer; forming a first metal substrate on the first light-emitting epitaxial structure; and stripping growth a substrate for exposing the first luminescent epitaxial structure, performing a cleaning step on the grown substrate, and forming a second luminescent diode on the grown substrate. According to a preferred embodiment of the present invention, the dry etching method, the wet etching method, the mechanical polishing method or the high temperature baking method may be employed in the above cleaning step. [Embodiment] In order to make the description of the present invention more detailed and complete, reference is made to the following description in conjunction with the drawings of Figs. 1 to 5. Referring to Figures i through 3, a cross-sectional view of a m: body process in accordance with the present invention is illustrated. First, the growth substrate 100 is provided. The material of the growth substrate 100 may be, for example, sapphire, indium arsenide or gallium phosphide. Then, a light-emitting diode is produced on the growth (10). System: In the case of a light-emitting diode, first, for example, by low-temperature epitaxy, a buffer is formed on the surface of the growth substrate H), wherein the buffer layer is 〇2 or galvanized. Next, using, for example, an organometallic vapor deposition method, a liquid phase epitaxy method, or a molecular beam epitaxy method to grow the luminescent ray on the buffered 丨〇 曰 9 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 2008 The method includes sequentially stacking the upper semiconductor layer 104, the first electrical limiting layer: the first electrical limiting layer 11 and the second electrical contact layer, the second electrical property and the second electrical property are Different electrical properties. When the first electrical property is Ν-di-electricity is Ρ-type; and when the first electrical property is Ρ-type, the second electrical property- is Ν-type. In the present exemplary embodiment, the 'first electrical property is a Ν type, and the second electrical property is Ρ. In an embodiment, the material of the first electrical semiconductor layer may be, for example, nitrided; OSd, osg u, the ancestor of the first layer 10 偈 丨, U UAlx〇a, yIni.yN;0,x" —=1,〇Sy$i], the active layer 1〇8 may be a double 昱=, ,= structure or multiple quantum well structure, and the material of the active layer 1G8 may include, for example, a mouse chain Gallium indium [(AlxGai.x) yIni_yN; egl ^ 013, the second electrical property = the material of the confinement layer 11G may be, for example, a gallium nitride indium [(AlxGai x) yin 〇 and a materialization of the second electrical contact layer 112 Ming gallium indium UAUGUySLkded]. For the disorder, the metal substrate 12G' may be formed directly on the second electrical contact layer 112 of the luminescent epitaxial structure or the luminescent crystal structure may be selectively processed, for example, a pattern of a sinusoidal luminescent epitaxial structure. And/or additional structural layers are formed on the second electrical reflector 112, such as: an electrode and a metal reflective layer. In the exemplary embodiment, the luminescent epitaxial structure is first patterned by using, for example, a micro-destruction f or a dicing technique to remove: a second electrical contact layer 112, a portion of the second electrical limiting layer 11 The trenches 122 are formed in the luminescent epitaxial layer, wherein the trenches expose a portion of the first electrical semiconductor layer 200828621 1〇4. When the trench 122 is formed in the luminescent epitaxial structure, the wet etching method or the mechanical cutting polishing method can be used. Then, the method of forming a dielectric protective layer 118 over the side of the trench 122 == the portion of the luminescent epitaxial structure exposed by the mold wood 122. i The material of the electrical protection layer 118 may be a high dielectric organic material, a cut oxygen or a nitride, such as a dioxate or a nitrogen (four). Subtracting, reusing, for example, thermal evaporation (The_l Evap〇ra = eam Eva_iGn) or ion splash utt = electric cover on the second electrical contact layer (1) to: =: tin, yttrium oxide, oxidation: The material of =, : can be, for example, indium oxide or magnesium. Subsequently, a metal reflective layer 116 is formed over the second electrically transparent electrode 114Ji to illuminate the liver active layer 1 〇 8 toward the metal in the direction of = Π6. The layer is first reflected, wherein the material of the metal reflective layer 116 can be made of aluminum, silver, platinum, chromium, nickel or an alloy of these metals. Then, the c=forming metal substrate 12G covers the morning/part of the dielectric protective layer. The exposed portion of 114 and the metal reflective layer 116 are all: the plate cutter 120 纟 fills the trench 122 to form the structure as shown in Fig. 1. Ϊ = the material may be, for example, steel, tantalum, nickel, gold, silver, uranium, Ming or alloy of these metals. To be a metal substrate 〗 2 Ω 制 秘 & . . . 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热 加热Peeling. When the combination is [^〇0 separated from the luminescent crystal structure, part of the buffer layer 102 曰$ ' and the other part of the buffer _ 102 may remain on the surface of the growth substrate 8 200828621 board 100, such as 102a. The substrate 100 will be grown as an electrical semiconductor layer 104. After the buffer layer on the growth substrate 100 is stripped, the first electric charge of the luminescent epitaxial structure is exposed ==100 stripping, and the first electric (four) is formed by, for example, deposition to cover the exposed first electric semiconductor 1104. on,
第一電性電極124之;bf斗沐也丨丄上 ’、T 么… 枓可例如為導電金屬氧化物,或者可 為鈦、鋁、金或這些金屬之合金。接著,利 形成第一電性電極墊126位於部 _ /儿積方式The first electrical electrode 124; bf is also ’, T? 枓 can be, for example, a conductive metal oxide, or can be titanium, aluminum, gold or an alloy of these metals. Then, the first electrical electrode pad 126 is formed in the portion _ / 儿
々、口丨刀之苐一電性電極124 F =發光二極體128之製作。其中,第-電性電極墊126 之材料可例如為鈦、銘、金或這些金屬的合金。墊电, 丨 苐 苐 电 an electric electrode 124 F = the production of the light-emitting diode 128. The material of the first-electrode electrode pad 126 may be, for example, titanium, inscription, gold or an alloy of these metals. pad
請參照第4圖與第5圖’其係綠示依照本發 施例的-種成長基板之清潔流程剖面 I 成長基板100剝除下來後,由於成長基板1〇〇 ^ 殘留有緩衝層l〇2a與其他污染4勿。此時,可對:可此 進行清潔步驟’以移除殘留在成長基板1〇〇 "土,100 102a與其他污染物’以使成長基板1〇〇可供;:緩衝層 製乍。^成長基板Η)()時,可採用乾心刻法、 刻法、機械研磨法或高溫供烤法。利用乾式飿刻法時^ 用反應性離子㈣技術(RIE)或感應輕合電襞料㈣技來 (ICP)。在一乾式蝕刻製程的示範例中,可 > / X ,τ 來清潔成長基板1GG。利用濕式㈣法時,用=系列孔體 氧化鉀作為_液,來清潔成長基板i⑽。硝酸或氫 時’可運用拋光墊和拋光液。利用高温棋烤法時, 溫來裂解殘留在成長基板100上之殘留物,例如緩衝層:a 200828621 與一些污染物,再將裂解後之殘留物清除。經清潔後之成長 基板100如第5圖所示,可再回收使用,而供下一發光二極 體於其上製作。 由上述本發明較佳實施例可知,本發明之一優點就是因 為本發明之發光二極體之製造方法係透過乾式、濕式、咬於 配使用乾式與濕式蝕刻的方式,清潔自磊晶結構上剝離之成 長基板。經清潔後之成長基板可再回收使用,以供下一蠢晶 結構成長。因此,可節省成長基板的耗用,兼具環保及降低 成本’而可大大地提升經濟效益。 雖然本發明已以一較佳實施例揭露如上,然其並非用以 限定本發明,任何在此技術領域中具有通常知識者,在不脫 離本發明之精神和範圍内,當可作各種之更動與潤飾,因此 本發明之保護範圍當視後附之申請專利範圍所界定者為準。 【圖式簡單說明】 第1圖至第3圖係繪示依照本發明一較佳 發光二極體之製程剖面圖。、]的 、第4圖至第5圖係繪示依照本發明一較佳實施例的一種 成長基板之清潔流程剖面圖。 【主要元件符號說明】 100 ·成長基板 102 :緩衝層 1()4:第一電性半導體層 •第—電性侷限層 108:主動層 200828621 110 : 第二電性侷限層 112 114 : 第二電性透明電極 116 118 : 介電保護層 120 122 : 溝渠 124 126 : 第一電性電極墊 128 第二電性接觸層 金屬反射層 金屬基板 第一電性電極 發光二極體 11Referring to FIG. 4 and FIG. 5 'the green color is removed according to the cleaning process profile I of the growth substrate of the present embodiment, after the growth substrate 100 is removed, the buffer layer l remains on the growth substrate 1〇〇. 2a and other pollution 4 do not. At this time, it is possible to: perform a cleaning step to remove the residual substrate 1 " soil, 100 102a and other contaminants' to make the grown substrate 1 ;; ^ When growing the substrate Η) (), dry heart engraving, engraving, mechanical grinding or high temperature baking can be used. When using the dry engraving method, use reactive ion (four) technology (RIE) or induction light (4) technology (ICP). In an example of a dry etching process, the growth substrate 1GG can be cleaned with > / X , τ . When the wet type (four) method is used, the growth substrate i (10) is cleaned by using the = series of pores of potassium oxide as the liquid. Polishing pads and polishing fluids are available for nitric acid or hydrogen. When the high temperature chess baking method is used, the residue remaining on the growth substrate 100 is tempered, for example, a buffer layer: a 200828621 with some contaminants, and the residue after the cleavage is removed. After cleaning, the substrate 100 can be recycled for use as shown in Fig. 5, and the next light-emitting diode can be fabricated thereon. According to the preferred embodiment of the present invention, one of the advantages of the present invention is that the manufacturing method of the light-emitting diode of the present invention is cleaned and self-expanded by means of dry, wet, bite, dry and wet etching. A structurally exfoliated growth substrate. The cleaned growth substrate can be recycled for use in the growth of the next stupid structure. Therefore, the consumption of the growth substrate can be saved, and the environment can be environmentally friendly and the cost can be reduced, which can greatly improve the economic efficiency. Although the present invention has been described above in terms of a preferred embodiment, it is not intended to limit the invention, and it is intended that various modifications may be made without departing from the spirit and scope of the invention. And the scope of the present invention is defined by the scope of the appended claims. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 through Fig. 3 are cross-sectional views showing a process of a preferred light emitting diode in accordance with the present invention. 4 to 5 are cross-sectional views showing a cleaning process of a growth substrate in accordance with a preferred embodiment of the present invention. [Description of main component symbols] 100 · Growth substrate 102 : Buffer layer 1 () 4: First electrical semiconductor layer • First—Electrical confinement layer 108: Active layer 200828621 110 : Second electrical confinement layer 112 114 : Second Electrically transparent electrode 116 118 : dielectric protective layer 120 122 : trench 124 126 : first electrical electrode pad 128 second electrical contact layer metal reflective layer metal substrate first electrical electrode light emitting diode 11
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| TW523939B (en) * | 2001-11-07 | 2003-03-11 | Nat Univ Chung Hsing | High-efficient light emitting diode and its manufacturing method |
| TWI222756B (en) * | 2002-11-12 | 2004-10-21 | Epitech Corp Ltd | Lateral current blocking light emitting diode and method of making the same |
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