TW476990B - Semiconductor device - Google Patents
Semiconductor device Download PDFInfo
- Publication number
- TW476990B TW476990B TW090104917A TW90104917A TW476990B TW 476990 B TW476990 B TW 476990B TW 090104917 A TW090104917 A TW 090104917A TW 90104917 A TW90104917 A TW 90104917A TW 476990 B TW476990 B TW 476990B
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- Prior art keywords
- film
- point metal
- melting point
- high melting
- intermediate layer
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 46
- 150000004767 nitrides Chemical class 0.000 claims abstract description 53
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229910052802 copper Inorganic materials 0.000 claims abstract description 44
- 239000010949 copper Substances 0.000 claims abstract description 44
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 36
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000000758 substrate Substances 0.000 claims abstract description 11
- 239000003870 refractory metal Substances 0.000 claims abstract 4
- 229910052751 metal Inorganic materials 0.000 claims description 146
- 239000002184 metal Substances 0.000 claims description 145
- 238000002844 melting Methods 0.000 claims description 101
- 230000008018 melting Effects 0.000 claims description 88
- 229910052719 titanium Inorganic materials 0.000 claims description 11
- 229910052720 vanadium Inorganic materials 0.000 claims description 11
- 230000002079 cooperative effect Effects 0.000 claims description 10
- 229910052758 niobium Inorganic materials 0.000 claims description 9
- 229910052715 tantalum Inorganic materials 0.000 claims description 9
- 150000002739 metals Chemical class 0.000 claims 1
- 239000010408 film Substances 0.000 description 224
- 239000010410 layer Substances 0.000 description 111
- 238000000034 method Methods 0.000 description 23
- 230000004888 barrier function Effects 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 238000004544 sputter deposition Methods 0.000 description 13
- 229910052581 Si3N4 Inorganic materials 0.000 description 12
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000011229 interlayer Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 229910052681 coesite Inorganic materials 0.000 description 5
- 230000000875 corresponding effect Effects 0.000 description 5
- 229910052906 cristobalite Inorganic materials 0.000 description 5
- 229910052682 stishovite Inorganic materials 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- 229910052905 tridymite Inorganic materials 0.000 description 5
- 238000009413 insulation Methods 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000001020 plasma etching Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229910052814 silicon oxide Inorganic materials 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- DAZWMJDZEPDDGO-UHFFFAOYSA-N [O].[O].[Cu] Chemical compound [O].[O].[Cu] DAZWMJDZEPDDGO-UHFFFAOYSA-N 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920002120 photoresistant polymer Polymers 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 241000446313 Lamella Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000005477 sputtering target Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
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- H01L23/53238—Additional layers associated with copper layers, e.g. adhesion, barrier, cladding layers
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- H01L2924/0495—5th Group
- H01L2924/04953—TaN
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- H—ELECTRICITY
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- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/049—Nitrides composed of metals from groups of the periodic table
- H01L2924/0504—14th Group
- H01L2924/05042—Si3N4
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/19—Details of hybrid assemblies other than the semiconductor or other solid state devices to be connected
- H01L2924/1901—Structure
- H01L2924/1904—Component type
- H01L2924/19043—Component type being a resistor
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Description
476990 經濟部智慧財產局員工消費合作社印制衣 A7 B7 五、發明說明(1 ) 發明説明 本發明是有關以LSI爲代表之半導體裝置,特別是與配 線(wring)用之銅膜層及墊層用之鋁膜之接續有關。 圖10是具有銅膜層及墊層用之鋁膜構造之以往之半導裝 置之斷面圖。 、 如圖10所示,第1層區(由層間絕緣膜interlayer insulating film 11、能障層(barrier layer )12、及配線用金 屬膜13所組成),其上形成第2層區(由層間絕緣膜2 1、能障 層22、及配線用金屬膜23所組成),在第2層區之上又形成 第3層區(由矽氮化膜silicon nitride film 31、上層絕緣膜32 、能障層33、及墊襯用鋁膜34所組成)。 如圖所示,配線用之銅膜23及墊襯用鋁膜34之間設有能 障層33。此能障層33是防止銅膜23及塾襯用鋁膜34之間相 互擴散。能障層33之能障金屬有TaN、NbN、TiN、VN等高 溶點金屬氮化物(refactory metal nitride )。 然而如上述以往技術鋁膜3 4是用濺鍍等方法形成,銘膜 34含有之鋁和能障層33含有之氮反應成絕緣物氮化鋁ΑιΝχ ’因這Α1ΝΧ使電阻上升(特別是接觸孔Via電阻)而產生問題 。又上層絕緣膜32用的矽氧化膜(silicon oxcide film )和能 障層33用的高熔點金屬氮化物膜之接著性不佳,在兩者之 間的空隙滲入氧氣氧化銅膜23也產生問題。 如此爲防止配線用銅膜23及墊襯用鋁膜34之間相互擴散 ,以往在兩者之間設有高熔點金屬氮化物膜之能障層,然 而銘和氮之間反應產生A1NX使電阻上升,又上層絕緣膜和 -4- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) — — — — — — — — ----· I I I # (請先閱讀背面之注意事項再填寫本頁) 訂---------
經濟部智慧財產局員工消費合作社印制农 旎障層之接著性不佳使銅膜氧化。這是造成半導體裝置之 特性或信賴不良的原因。 發明之簡單説明 針對以上問題,提高具有配線用銅膜及和此接續墊襯用 鋁膜之半導體裝置之特性或信賴性是本發明之目的。 本發明之第一個重點是針對在半導體基板主面上形成構 成配線層(wiring layer)之銅膜,至少在銅膜上形成中間層 ,及在中間層上形成構成墊層之鋁膜之半導體裝置,而中 間層是在高熔點金屬氮化物膜及高熔點金屬氮化物膜上形 成之高熔點金屬膜。 依本發明方法在鋁膜和鬲溶點金屬氮化物膜之間置入一 層高熔點金屬膜。因此可防止鋁膜含有之鋁和高熔點金屬 氮化物膜含有之氮反應生成絕緣物A1NX。因此可防止因 A1NX造成之電阻上升問題,得到特性優良之半導體裝置。 本發明之第二個重點是針對在半導體基板主面上形成構 成配線層之銅膜,至少在銅膜上形成中間層,及在中間層 上形成構成墊層之鋁膜之半導體裝置,而中間層是在高溶 點金屬膜及高熔點金屬物膜上形成之高熔點金屬氮化物膜。 依本發明方法在鬲熔點金屬氮化物膜之下形成一層比高 少谷”:、占至屬氮化物膜對、纟巴緣膜(特別是石夕氧化膜系絕緣膜)接 著性好之高熔點金屬膜,提高中間層和絕緣膜之接著性。 因此可防止因接著不良產生間隙滲入氧氣氧化銅膜等問題 ,得到信賴性優良之半導體裝置。 在%述第一及第二重點提及含於高溶點金屬膜之高溶點 金屬和含於高熔點金屬氮化物膜之高熔點金屬最好是同一 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) ·裝--------訂--------- (請先閱讀背面之注音?事項再填寫本頁) 476990 A7 B7 經 濟 部 智 慧 財 產 局 員 工 消 費 合 作 社 印 製 五、發明說明(3 ) 種金屬。因使用同一種金屬在濺鍍高熔點金屬氮化物膜和 高溶點金屬膜時用同一藏鍍革巴,可同時縮減工時及成本。 在前述第一及第二重點提及含於高熔點金屬膜之高溶點 金屬可在Ta(銥)、Nb(說)、Ti(鈦)、V(釩)擇一使用,又前述 含於尚溶點金屬氮》化物fl吴之南 '丨容點金屬最好在、Nb、τι 、V擇一使用。 在前述第一及第二重點提及高熔點金屬膜之厚度最好在 5nm以下。 本發明之第三個重點是針對在半導體基板主面上形成構 成配線層之銅膜,至少在銅膜上形成中間層,及在中間層 上形成構成墊層之鋁膜之半導體裝置,而中間層是由第一 高熔點金屬膜及前述第一高熔點金屬物膜上形成之高熔點 金屬氮化物膜及前述高熔點金屬氮化物膜上形成之第二高 溶點金屬膜所組成。 在前述第三重點提及含^第―高以金屬膜之高溶點金 屬和含於高熔點金屬氮化物膜之高熔點金屬及含於第二高 溶點金屬膜之高熔點金屬最好是同一種金屬。口、 问 在前述第三重點提及含於第一高烷 、丄 U金屬腰1鬲溶點金 屬可在Ta、Nb、Ti、V擇一使用,又4丄人 卜 文〗又則述含於高熔點金屬 鼠化物膜之高熔點金屬最好在丁&、Nb、τ· 人、,. b、Τι、V擇一使用, έ於第二高熔點金屬膜之高熔點金屬 /旬 J 在 Ta、Nb、Ti、ν 擇一使用。 在前述第三重點提及高炫點金相之厚度最好在5n_ 下0 (請先閱讀背面之注意事項再填寫本頁) --------訂--------- -6 - 經濟部智慧財產局員工消費合作社印制衣 476990 A7 B7 ------—---— 五、發明說明(4 ) 在前述第一、第二、及第三重點提及高熔點金屬氮化物 膜是指高熔點金屬及氮爲主成分之化合物。 在前述第一、第二、及第三重點提及之中間層包本和前 述銅膜接觸之第一部分及不和銅膜接觸之第二部分,最好 於前述第二部分和絕緣膜接觸。 在前述第一、第二、及第三重點提及由鋁膜構成之塾層 最好和接合配線(bonding wire)接續。 發明之實施形態 以下參照圖面説明本發明之實施形態。 (實施形態1) 圖1是與本發明第一實施形態有關半導體裝置構成之斷 面圖。 如圖1所示’半導體基板1 〇上形成第1層區(由層間絕緣 膜11、能障層12、及配線用金屬膜13所組成),在其上形成 第2層區(由層間絕緣膜21、能障層22、及配線用銅膜23所 組成),在第2層區之上又形成第3層區(由矽氮化膜3丨、上層 絕緣膜32、能障層33、及墊襯用鋁膜34所組成)。又在半導 體基板10和第一層區之間·亦可再加一下層區。 圖2A〜圖2G是與本發明第一實施形態有關半導體裝置製 造万法工程之斷面圖。又將如圖丨所示半導體基板1〇之圖示 省略。 首先如圖2A所不電晶體等半導體元件(未圖示)形成之半 導to基板(未圖tf )之主表面上形成包括層間絕緣膜丨丨、能障 (請先閱讀背面之注意事項再填寫本頁) · ϋ n I n ϋ 一· n n ϋ I ϋ ϋ
476990 A7 B7 五、發明說明(5 ) 層12、及配線用金屬膜13所組成之第1層區。在其上形成第 一層區之層間絕緣膜21 (例TEOS -Si〇2膜或Low-k膜(低電容 率膜)、或這些層積膜)。 其次如圖2B所示,將層間絕緣膜21加工形成接觸孔、 配線用或墊襯用溝糟。 其次如圖2C所示,全面形成TaN、NbN等高溶點金屬氮 化物構成之能障層(能障金屬層)22。在能障層22上形成銅膜 23。此銅膜23是在能障層22上形成之薄片層銅膜,以電解 鍍敷法(electroplating)形成之銅膜。 其次如圖 2D 所示,以 CMP(chemical mechanical polishing)法平坦化處理,只允許能障層22及銅膜23在接觸 孔、配線用或墊襯用溝糟内部殘留。以此處理方法形成第 二層區之接觸孔、配線及塾襯。 之後形成TE0S-Si02膜構成之保護膜或Low-k膜(低電容 率膜)之絕緣膜,在此絕緣膜上形成墊襯用孔使銅墊部之表 面呈露出狀態。因此不僅銅墊部氧化,經過一段時間銅配 線全部氧化。 在此爲防止銅墊部氧化在上層再形成鋁墊區構成之第三 層區。本例在此形成鋁墊區如圖2E〜圖2G所示,以雙鑲金 (dual damascene)法處理。 如圖2E所示,爲防止銅膜23之銅擴散全面形成矽氮化 膜31(電漿SiN膜)。然後在矽氮化膜上形成上層絕緣膜32(例 TEOS-Si〇2膜或Low-k膜(低電容率膜)、或這些層積膜)。之 後對矽氮化膜3 1及上層絕緣膜32加工形成接觸孔及墊襯用 -8- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) ------------裝--- (請先閱讀背面之注意事項再填寫本頁) 訂 經濟部智慧財產局員工消費合作社印制衣 476990 石 _I__ 經濟部智慧財產局員工消費合作社印製 A7 B7 發明說明(6) 溝。 ’ 其次如圖2F所示,全面形成中間層其構造容後再述。 又在中間層33上以濺鍍法(最好是長擲濺鍍i〇ng thr〇w spattering或反射流濺鍍reflow )等形成銘膜34。 其次如圖2G所示,以CMP法平坦化處理,只允許中間 層3 3及鋁膜3 4在接觸孔、配線用或塾襯用溝糟内部殘留。 以此處理方法形成第三層區之接觸孔、配線及墊襯。如此 得到和接合配線(未圖示)連接之錯整。 圖3 A〜圖3C説明上述中間層33之幾種構造例。 圖3A其中間層33是由高熔點金屬氮化物膜33b(例TaN膜 等之能障金屬膜)及高溶點金屬膜3 3 c(例Ta膜等)之層積構 造。如此在銘膜34和高熔點金屬氮化物膜33b之間夾有高熔 點金屬膜33c,得以防止以往的問題。即含有鋁之鋁膜34和 含有氮之高熔點金屬氮化物膜33b反應形成絕緣物A1NX,得 以防止因A1NX產生之電阻(特別是接孔電阻)上升問題。 圖3B其中間層33是由高熔點金屬膜33 a (例Ta膜等)及高 熔點金屬氮化物膜33b(例TaN膜等)之層積構造。如此在高 溶點金屬氮化物膜33b和上層絕緣膜32(矽氧化膜系膜)之間 炎有接著性良好的高熔點金屬膜33a(例Ta膜等),得以提高 中間層33和上層絕緣膜32之接著性。因此可防止因上層絕 緣膜3 2和中間層3 3接著不良產生間隙滲入氧氣氧化銅膜3 2 寺問題。 圖3C其中間層是由高熔點金屬膜33 a(例Ta膜等)及高熔 點金屬氮化物膜33b(例TaN膜等)及高熔點金屬膜33c(例Ta 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) ·裝 476990 A7 --------- -B7__ 五、發明細(7 ) 膜等)之層積構造。如此得到如圖从及圖3B之構造兼得兩 者之效果。 (請先閱讀背面之注意事項再填寫本頁) 又高熔點金屬膜33&及高熔點金屬膜33〇可在^膜、Nb 、TiM、V膜中擇_使用,又高溶點金屬氮化物膜说可 在 TaN、NbN、TiN、VN 中擇一使用。 在圖3A〜圖3C中之各構造其含於統點金屬膜内之高溶 點金屬7L素及高熔點金屬氮化物膜内之高熔點金屬元素可 以是兩種不同的金屬元素,但最好是選用同一種金屬元素 。在圖3C之構造中高熔點金屬膜33a、高熔點金屬氮化物膜 33b、及高熔點金屬膜33c最好選用同一種高熔點金屬元素 ,因使用同一種金屬在濺鍍各高熔點金屬膜時用同一濺鍍 靶,可同時縮減工時及成本。 經濟部智慧財產局員工消費合作社印制衣 又以能障性的觀點高熔點金屬氮化物膜是愈厚愈好,但 從電阻(特別是接觸孔電阻)及CMp的觀點是愈薄愈好。圖4 疋改變回火條件,不同TaN膜厚和薄層電阻關係實驗結果。 如圖所不’將鋼配線做Em試驗時之條件(450°C4min(相當反 射泥漱鍵時間)+400°C 30min(相當燒結sinter時間)+ 350°C 6h(相當EM試驗時間),TaN膜最好在20nm以上。若考慮加 上熱壓(相當增加EM試驗時間),TaN膜最好在40nm以上。 但Ta膜太厚時CMP處理困難最好在5nm以下。 又在第三層區之上層絕緣膜32形成之接觸孔圖樣伸到在 第二層區形成之墊襯用溝槽圖樣之外側區時,如圖5所示產 生不良情形。即如圖2E所示步驟中使上層絕緣膜32及矽氮 化膜3 1過餘刻時第二層區之層間絕緣膜2 1也被蝕刻。如圖5 本紙張尺度_+國國家規格⑽ X 297公爱) 476990 A7 B7 五、發明說明(8 ) 所示產生凹陷。因此在圖2F步驟中堆積中間層33及鋁膜34 時這些膜無法完全填入這凹陷部分。因此位於第三層區所 有接觸孔用之孔洞圖樣最好是位於第二層區墊襯用溝槽圖 樣之内側。 又鋁墊部最好是分割墊構造。因分割墊構造可減少因能 障金屬等和矽氧化膜系絕緣膜之膨脹係數不同降低接著性 等問題。 圖6是提鬲接合配線時耐性之構造。即使由铭膜3 4及中 間層33構成之墊部延伸,在這延伸區連接接合配線4〇。這 種構造縱使在接合配線時接合之配線突到中間層33也不會 影響銅膜23和鋁膜34之間的連接。 (實施形態2) 圖7A〜圖7C是與本發明第二實施形態有關半導體裝置製 造方法步驟之剖面圖。在本實施形態形成第三層區之鋁塾 邵時是用單鑲金法。到圖2D以前的步驟和第一實施形態相 同,以下説明其後之步驟。 圖2 D所示步驟後係如圖7 A所示,和第一實施形態一樣 全面形成矽氮化膜(電漿SiN膜)31。接著在矽氮化膜3 1上形 成上層絕緣膜32(例TE0S-Si02膜或Low-k膜(低電容率膜)、 或這些層積膜)。之後對矽氮化膜3 1及上層絕緣膜32加工形 成墊襯用溝槽。 其次如圖7B所示,全面形成中間層3 3。在中間層3 3上 以濺鏡法(最好是長擲濺鍍或反射流濺鍍)形成鋁膜34。中間 層33和第一實施形態相同,即如圖3 A〜圖3C所示層積構造 -11 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁)
· 1— 11 1·— ϋ I ·1 ϋ 一:0雩 I 1_1 ^1 ^1 1_1 1 ϋ I 經濟部智慧財產局員工消費合作社印製 經濟部智慧財產局員工消費合作社印製 476990 A7 B7___ 五、發明說明(9 ) 。具體説就是高熔點金屬膜/高熔點金屬氮化物膜之層積構 造、高熔點金屬氮化物膜/高熔點金屬膜之層積構造、或是 向溶點金屬膜/高熔點金屬氮化物膜/高熔點金屬膜之層積構 造。又高溶點金屬氮膜及高熔點金屬氮化物膜所使用的材 料和其組合也和第一實施形態相同。 其次如圖7C所示,以CMP法平坦化處理,只允許中間 層3 3及銘膜3 4在塾襯用溝糟内部殘留。以此處理方法形成 第三層區之墊襯。 圖7D是對應於圖7C之主要部分構造之斷面圖。在第三 層區之上層絕緣膜32形成之墊襯用圖樣伸到在第二層區形 成之塾襯用溝槽圖樣之外側區時,如第一實施形態所述產 生不良情形。如圖7D所示,因此位於第三層區所有整襯用 溝槽圖樣最好是位第二層區墊襯用溝槽圖樣之内側。 (實施形態3) 圖8A〜圖8C是與本發明第三實施形態有關半導體裝置製 造方法工程之斷面圖。在本實施形態形成第三層區之鋁墊
邵時是用穿孔程序及RIE(reactive ion etching)法。到圖2D 以前的步驟和第一實施形態相同,以下説明其後之步驟。 圖2 D所示’步驟後、如圖8 A所示,和第一實施形態一 樣全面形成矽氮化膜(電漿SiN膜)31。接著在矽氮化膜31上 形成上層絕緣膜32(例TEOS-Si〇2膜或Low-k膜(低電容率膜) 、或這些層積膜)。之後對矽氮化膜3丨及上層絕緣膜32加工 形成接觸孔。 其次如圖8B所示,全面形成中間層33。在中間層33上 -12· 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公爱) " --- (請先閱讀背面之注意事項再填寫本頁) * n n I B·— n ϋ ϋ 訂--------- 脅 4/()990 、發明說明(10 以表鍍法(最好是長擲濺鍍或反射流濺鍍)形成鋁膜34。中間 層33和第一貫施形態相同。即中間層33之構造如圖3A〜圖 3C所不層積構造,具體説就是高熔點金屬膜/高熔點金屬氮 化物膜之層積構造、高熔點金屬氮化物膜/高熔點金屬膜之 層積構造、或是高熔點金屬膜/高熔點金屬氮化物膜/高熔點 金屬膜之層積構造。又高熔點金屬氮膜及高熔點金屬氮化 物膜所使用的材料和其組合也和第一實施形態相同。 其次如圖7C所示,以光阻罩(未圖示)蝕刻鋁膜34及中間 層33形成第三區之墊襯。 圖8D是對應於圖8C之主要部分構造之斷面圖。在第三 層區 < 上層絕緣膜32形成之接觸孔圖樣伸到在第二層區形 成足塾襯用溝槽圖樣之外側區時,如第一實施形態所述產 生不良情形。如圖8D所示,因此位於第三層區所有接觸孔 用圖樣最好是位第二層區墊襯用溝槽圖樣之内側。 (實施形態4) 圖9A及圖9C是與本發明第四實施形態有關半導體裝置 製造方法工程之斷面圖。在本實施形態形成第三層區之鋁 整邵時是用RIE法。到圖2D以前的步驟和第一實施形態相同 ’以下説明其後之步驟。. 圖2D所示之步驟後,其次如圖9A所示,全面形成中間 層33。在中間層33上以濺鍍法(最好是長擲濺鍍或反射流濺 鐘)开^成銘膜3 4。中間層3 3和第一實施形態相同。即中間層 33之構造如圖3A〜圖3C所示層積構造,具體説就是高熔點 金屬膜/高熔點金屬氮化物膜之層積構造、高熔點金屬氮化 -13 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) · I Ml· IW 囉 — Ο··· I ΜΜ I > 經濟部智慧財產局員工消費合作社印製 476990 A7 . —— B7 五、發明說明(”) 物fe/鬲熔點金屬膜之層積構造、或是高熔點金屬膜/高熔點 金屬氮化物膜/高熔點金屬膜之層積構造。又高熔點金屬氮 月吴及鬲熔點金屬氮化物膜所使用的材料和其組合也 實施形態相同。 其次如9B所示,以光阻罩(未圖示)蝕刻鋁膜34及中間層 33形成第三區之墊襯。 日 圖9C是對應於圖9B之主要部分構造之斷面圖。以第三 層區之鋁墊的圖樣不能覆蓋在第二層區形成之銅墊的圖樣 襯用溝槽圖樣時在第二層上形成之銅墊會產生氧化等不良 情形。如圖9C所示,因此位於第三層區墊襯圖樣最好是可 完全覆蓋全部第二層區墊襯圖樣。換這之最好將全部第二 層區塾襯圖樣置於第三層區墊襯圖樣内側。 圖式之簡單説明 圖1是與本發明第一實施形態有關半導體裝置構成之斷 面圖。 圖2A〜圖2G是與本發明第一實施形態有關半導體裝置製 造方法工程之斷面圖。 圖3A〜圖3C是與本發明第一實施形態有關半導體裝置之 主要邵分構造之斷面圖。 圖4是TaN膜和薄膜電姐關係圖。 圖5是有關墊層間接續不良情形。 圖6是本發明實施形態配線接合(wire b〇nding)時爲提高 耐性構造之斷面圖。 圖7A〜圖7C是與本發明第二實施形態有關半導體裝置製 造方法工程之斷面圖。圖7D是對應於圖7C之主要部分構造 -14- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注意事項再填寫本頁) 裝 訂· 經濟部智慧財產局員工消費合作社印製 476990 A7 B7 五、發明說明(12 ) 之斷面圖。 (請先閱讀背面之注意事項再填寫本頁) 圖8A〜圖8C是是與本發明第三實施形態有關半導體裝置 製造方法工程之斷面圖。圖8D是對應於圖8C之主要部分構 造之斷面圖。 圖9A及圖9B是與本發明第四實施形態有關半導體裝置 製造方法工程之斷面圖。圖9C是對應於圖9B之主要部分構 造之斷面圖。 圖10是與以往技術有關半導體裝置構造之斷面圖。 經濟部智慧財產局員工消費合作社印製 -15- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
Claims (1)
- 經濟部智慧財產局員工消費合作社印製 476990六、申請專利範圍 種半導f豆裝置(semiconductor device),其特徵爲具有 在半導體基板主面上形成構成配線層之銅膜;至少在銅 膜上形成中間層;及在中間層上形成構成墊層之鋁膜; 这中間層包含咼溶點金屬氮化物膜 rntride film)及於前述高熔點金屬氮化物膜上形成之高熔 點金屬膜(refractory metal film)。 2. 如申請專利範圍第1項之半導體裝置,其中中間層包含和 前j銅膜接觸之第一部分及不和銅膜接觸之第二部;, 於前述第二部分和絕緣膜接觸。 3. 如申請專利範圍第丨項之半導體裝置,其中包含於前述高 熔點金屬膜之高熔點金屬和包含於前述高熔點金屬氮化 物膜之高熔點金屬是同一種金屬。 人 4. 如申請專利範圍第1項之半導體裝置,其中包含於前述高 熔點金屬膜之高熔點金屬可在Ta、Nb、Ti、V擇一使用 二又前述包含於前述高熔點金屬氮化物膜之高熔點金屬 最好在Ta、Nb、Ti、V擇一使用。 5· 一種半導體裝置’其特徵爲具有在半導體基板主面上形 成構成配線層之銅膜;至少在銅膜上形成中間層;及在 中間層上形成構成墊層之鋁膜;前述中間層包含高熔點 金屬膜及於前述高熔點金屬膜上形成之高熔點:屬氮化 物膜。 6.如申請專利範圍第5項之半導體裝置,其中中間層包含和 岫述銅膜接觸之第一部分及不和銅膜接觸之第二部分, 於則述第二邵分和絕緣膜接觸。 本紙張尺度適財_家鮮χ挪公爱) (請先閱讀背面之注意事項再填寫本頁)&8 ^/0990 &8 ^/0990 經濟部智慧財產局員工消費合作社印製 ----— _ D8_ 六、申請專利範圍 7·如申請專利範圍第5項之半導體裝置,其中包含於前述高 燦點金屬膜之高熔點金屬和包含於前述高熔點金屬氮化 物膜之高熔點金屬是同一種金屬。 8·如申請專利範圍第5項之半導體裝置,其中包含於前述高 溶點金屬膜之高熔點金屬可在Ta、Nb、Ti、V擇—使用 ,又前述包含於前述高熔點金屬氮化物膜之高燦點金屬 最好在Ta、Nb、Ti、V擇一使用。 9· 一種半導體裝置,其特徵爲具有在半導體基板主面上形 成構成配線層之銅膜;至少在銅膜上形成中間層;及在 中間層上形成構成墊層之鋁膜;前述中間層包含第一言 溶點金屬膜、在前述第一高溶點金屬膜上形成之高燦點 金屬氮化物膜及前述高熔點金屬氮化物膜上形成之第一 高熔點金屬膜。 — W·如申請專利範圍第9項之半導體裝置,其中中間層包含和 别述銅膜接觸之第一部分及不和銅膜接觸之第二部分 於前述第二部分和絕緣膜接觸。 11·如申請專利範圍第9項之半導體裝置,其中包含於前述第 一高熔點金屬膜之高熔點金屬、包含於前述高熔點 氮化物膜之南溶點金屬及包含於前述第二高溶點金屬月L 之南溶點金屬是同一種金屬。 12.如申請專利範圍第9項之半導體裝置,其中含於前述第一 咼谷點金屬膜之南溶點金屬可在Ta、Nb、Ti、V擇 用,前述含於前述高熔點金屬氮化物膜之高熔點金屬最 好在Ta、Nb、Ti、V擇—使用,及含於前述第二高 -17- 本紙張尺度適用中國國家標準(CNS)A4規格(21〇 X 297公愛) --------訂--------- (請先閲讀背面之注意事項再填寫本頁} 476990 A8B8C8D8 六、申請專利範圍 金屬膜之高熔點金屬可在Ta、Nb、Ti、V擇一使用 (請先閱讀背面之注意事項再填寫本頁) 濟 部 智 慧 財 產 局 員 工 消 費 合 作 社 -18 印 製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
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JP2000086383A JP3651765B2 (ja) | 2000-03-27 | 2000-03-27 | 半導体装置 |
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JP (1) | JP3651765B2 (zh) |
KR (1) | KR100426555B1 (zh) |
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TW (1) | TW476990B (zh) |
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2001
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- 2001-03-22 CN CNB011118695A patent/CN1230901C/zh not_active Expired - Fee Related
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- 2001-03-26 US US09/816,177 patent/US6909191B2/en not_active Expired - Lifetime
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US6909191B2 (en) | 2005-06-21 |
JP3651765B2 (ja) | 2005-05-25 |
KR100426555B1 (ko) | 2004-04-08 |
CN1230901C (zh) | 2005-12-07 |
CN1377082A (zh) | 2002-10-30 |
US20010023988A1 (en) | 2001-09-27 |
KR20010090729A (ko) | 2001-10-19 |
JP2001274162A (ja) | 2001-10-05 |
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