TW541599B - Single c-axis PGO thin film electrodes having good surface smoothness and uniformity and methods for making the same - Google Patents
Single c-axis PGO thin film electrodes having good surface smoothness and uniformity and methods for making the same Download PDFInfo
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- TW541599B TW541599B TW091105726A TW91105726A TW541599B TW 541599 B TW541599 B TW 541599B TW 091105726 A TW091105726 A TW 091105726A TW 91105726 A TW91105726 A TW 91105726A TW 541599 B TW541599 B TW 541599B
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- 239000010409 thin film Substances 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims abstract description 25
- 239000000758 substrate Substances 0.000 claims abstract description 43
- 238000000151 deposition Methods 0.000 claims abstract description 27
- 229910052741 iridium Inorganic materials 0.000 claims abstract description 24
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 21
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 16
- 239000002131 composite material Substances 0.000 claims abstract description 11
- HTXDPTMKBJXEOW-UHFFFAOYSA-N iridium(IV) oxide Inorganic materials O=[Ir]=O HTXDPTMKBJXEOW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000010408 film Substances 0.000 claims description 33
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 19
- 230000008021 deposition Effects 0.000 claims description 17
- 238000000137 annealing Methods 0.000 claims description 16
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052709 silver Inorganic materials 0.000 claims description 12
- 239000004332 silver Substances 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 10
- 229910052681 coesite Inorganic materials 0.000 claims description 9
- 229910052906 cristobalite Inorganic materials 0.000 claims description 9
- 238000004544 sputter deposition Methods 0.000 claims description 9
- 229910052682 stishovite Inorganic materials 0.000 claims description 9
- 229910052905 tridymite Inorganic materials 0.000 claims description 9
- 229910052786 argon Inorganic materials 0.000 claims description 7
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- -1 V02 Inorganic materials 0.000 claims description 5
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 5
- 239000012159 carrier gas Substances 0.000 claims description 5
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 5
- 238000000224 chemical solution deposition Methods 0.000 claims description 5
- 229910052735 hafnium Inorganic materials 0.000 claims description 5
- 239000002243 precursor Substances 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 claims description 4
- ZKATWMILCYLAPD-UHFFFAOYSA-N niobium pentoxide Inorganic materials O=[Nb](=O)O[Nb](=O)=O ZKATWMILCYLAPD-UHFFFAOYSA-N 0.000 claims description 4
- PBCFLUZVCVVTBY-UHFFFAOYSA-N tantalum pentoxide Inorganic materials O=[Ta](=O)O[Ta](=O)=O PBCFLUZVCVVTBY-UHFFFAOYSA-N 0.000 claims description 4
- YRAJNWYBUCUFBD-UHFFFAOYSA-N 2,2,6,6-tetramethylheptane-3,5-dione Chemical compound CC(C)(C)C(=O)CC(=O)C(C)(C)C YRAJNWYBUCUFBD-UHFFFAOYSA-N 0.000 claims description 3
- KQNKJJBFUFKYFX-UHFFFAOYSA-N acetic acid;trihydrate Chemical compound O.O.O.CC(O)=O KQNKJJBFUFKYFX-UHFFFAOYSA-N 0.000 claims description 3
- 229910052593 corundum Inorganic materials 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 229940046892 lead acetate Drugs 0.000 claims description 3
- 238000005546 reactive sputtering Methods 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- 239000006200 vaporizer Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 3
- GXMNGLIMQIPFEB-UHFFFAOYSA-N tetraethoxygermane Chemical compound CCO[Ge](OCC)(OCC)OCC GXMNGLIMQIPFEB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- VVTSZOCINPYFDP-UHFFFAOYSA-N [O].[Ar] Chemical compound [O].[Ar] VVTSZOCINPYFDP-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 229910052715 tantalum Inorganic materials 0.000 claims 1
- 150000002503 iridium Chemical class 0.000 abstract 3
- 229910018516 Al—O Inorganic materials 0.000 abstract 1
- 229910003077 Ti−O Inorganic materials 0.000 abstract 1
- 229910007746 Zr—O Inorganic materials 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 229910044991 metal oxide Inorganic materials 0.000 description 6
- 150000004706 metal oxides Chemical class 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 5
- 239000013078 crystal Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- XKENYNILAAWPFQ-UHFFFAOYSA-N dioxido(oxo)germane;lead(2+) Chemical compound [Pb+2].[O-][Ge]([O-])=O XKENYNILAAWPFQ-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000010897 surface acoustic wave method Methods 0.000 description 2
- 238000007736 thin film deposition technique Methods 0.000 description 2
- 238000000427 thin-film deposition Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
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- H01L28/40—Capacitors
- H01L28/60—Electrodes
- H01L28/65—Electrodes comprising a noble metal or a noble metal oxide, e.g. platinum (Pt), ruthenium (Ru), ruthenium dioxide (RuO2), iridium (Ir), iridium dioxide (IrO2)
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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
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
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- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
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- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
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- H01L21/314—Inorganic layers
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Description
541599 A7 B7 五、發明説明( 發明領域 本發明有關FeRAM與DRAM積體電路,更明確地說,有 關具有 Ir-Ta-〇、Ir-Ti-0、Ir-Nb-0、Ir-Al-0、Ir-Hf-〇、 Ir-V-〇或Ir-Zr-0作為底電極,以及位於在此等電極上面的 PGO薄膜以供應用之結構。 發明背景 PGO薄膜係指鐵電相。雖然c^^pG〇經常顯示 層狀微結構,但是於沈積過程,其很難形成具有非常平滑 與均勻表面的單相c-軸PG〇薄膜。其原因之一係,該pG〇 相是多晶相。不過,有許多鉛鍺氧化物化合物,其在組成 與形成溫度兩方面都非常接近朴…以…々,而且其更容 易於相似條件下形成。若同時在底電極表面上形成具有不 同微結構的多相鍺酸鉛,則很難製得平滑且均勻之c-軸 PGO薄膜。有許多因素影響該單相レ軸pGo薄膜的形成, 其中之一係該底電極的表面狀態。晶袼常數相配是形成層 狀c-軸PGO薄膜的重要因素。該pG〇相之微結構是六邊形 結構,其晶格常數為a= 1〇·251 A,而c=l0.685 A。至於純 銀(Ir)與翻(Pt)底電極,其係面心立方(17(:(::)結構,晶格常 數分別為a=3.83 A與a=3.92 A。理論上,很難在這兩種電 極上製得該c-軸PGO單相。然而,雖然對鉑基板而言如此 ,但是在銥基板上較容易形成(:_軸1>(}〇膜。這可能是 薄層的緣故,該薄層於沈積與退火過程,在Ir表面上於原 位形成,而且可促進該c-軸PG〇核晶作用與晶粒生長。 Ir02 的晶格常數係 a=4.498 A,c = 3.154A。
裝 訂
線 -6- 541599 A7 B7
該底電極定向對於該PGO薄膜的相形成也非常重要。已 發現,非晶相與多晶相基板有助於形成平滑與均勻pG〇薄 膜。具有不相配晶格常數的強定向基板容易促使形成具有 其他第一相之多晶相鐵電PGO薄膜,其中該膜顯示粗輪表 面0 圖1表不藉由MOCVD在一形成圖案基板上形成PG〇薄膜 。圖la的焭區係經磨光鉑基板區,而較暗區是§丨〇2基板。 這兩種基板均經磨光與平面化。圖115表示在鉑(左)與Si〇2 (右)基板上形成之PGO薄膜的結晶結構。很清楚地看出, 在該鉑基板上形成的PGO薄膜係多晶相,而且顯示粗糙表 面。在該Si〇2基板上形成的pg〇薄膜顯示出層狀單相結構 。在該Si〇2基板上形成的PG0薄膜係單相^轴?〇〇薄膜。 為了形成均勻單相c-軸PGO薄膜,該電極的熱安定性亦 很重要。已發現,鉑與銥二者可能於高溫退火(例如高於 500 C )期間形成小丘,其會影響pg〇薄膜的核晶作用與定 向。不過,即使在氧環境中以非常高溫退火,^複合物電 極仍然很安定。 該底部氧化物電極中存在的氧亦扮演一重要角色。由於 該PGO與電極二者均是金屬氧化物,介於該界面處氧化物 之間的有利結合條件可以提高核晶密度,有助於形成平滑 c-轴PGO薄膜。
Fengyan Zhang、Tingkai Li、Douglas J. Tweet與 Sheng
Teng Hsu之以金屬有機化學氣相沈積法沈積之鍺酸鉛薄膜 的相與数結填分析(Pfjase and rnicrostructure analysis of lead 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公爱) 541599 A7 B7 五、發明説明(3 ) germanate thin film deposited by metalorganic chemical vapor deposition), Jpn. J. Appl. Phys. Vol. 38,pp59-61 1999,討論形成薄膜之鍺酸鉛的各種相。
Fengyan Zhang、Jer-shen Maa、Sheng Teng Hsu、Shigeo Ohnish與Wendong Zhen之以Ir-Ta-0作為高溫安定電極材 料之研究及其作為鐵電Si:Bi2Ta209薄膜沈積之應用(A以 of Ir-Ta-O as high temperature stable electrode Material and its application for ferroelectric SrBi2Ta2〇9 thin film deposition), Jpn. J. Appl. Phys. Vol. 38, ppl447-1449, 1999,描述使用一種Ta障層與一種Ir-Ta-0電極。
Fengyan Zhang、Tingkai Li、Tue Nguyen、Sheng Teng Hsu之鐵電鍺酸鉛薄膜之MOCVD法及底電極效用(MOCFD process of ferroelectric lead germanate thin films and bottom electrode effects), Mat. Res. Soc. Symp. Proc. Vol· 541, pp549-554,1998,描述c-軸PGO薄膜之生長。 發明總論 一種形成電極與其上之鐵電薄膜的方法,包括:製備一 基板;在該基板上沈積一電極,其中該電極係由一種選自 由銥與銥複合物所組成的材料群組的材料形成;以及於其 上形成一單相c-軸PGO鐵電薄膜,其中該鐵電薄膜顯示表 面平滑度與均勻厚度。一種積體電路,其包括一基板;在 該基板上沈積之電極’其中電極係由一種選自由錶與銀複 合物所組成的材料群組的材料形成,其中該銥複合物係選 自由 Ir02 ' Ir-Ta-0、Ir-Ti-〇、ir-Nb-0、Ir-Al-0、ir-Hf-〇 • 8 - 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公釐) 裝 訂
-線 541599 A7 B7 五、發明説明(4 )
Ir-V-Ο、1]>21>〇與Ir-〇組成之複合物群組;以及在該電 極上形成的單相軸PG〇鐵電薄膜,其中該鐵電薄膜顯示 表面平滑度與均勻厚度。 本發明目的係在一金屬電極上提供一層均句單相心軸 PGO薄膜。 本發明另一目的係提供一銀複合物電極,諸如卜〇2、
Ir-Ta-0、Ir-Ti-0、Ir-Nb-0、Ir-A卜0、Ir-Hf-0、ir-V-Ο、
Ir-Zr-0或Ir-〇,作為FeRAM與DRAM應用之底電極。 本發明另一目的係提供一種在金屬電極上形成PG〇薄膜 之方法,該PGO薄膜可用於積體電路,諸如電容器、熱電 紅外線感應器、光學顯示器、光學開關、壓電轉換器與表 面聲波裝置。 ^ 本發明另外目的係提供一種沈積PG〇薄膜之方法,其係 藉由化學溶液沈積(CSD)、濺鍍、MOCVD或其他薄膜沈積 方法進行,其會顯示製造積體電路中所需要的平滑度與均 一性0 本發明另一目的係提供一種銥複合物電極,以改善PG〇 薄膜之表面特徵與晶格結構。 本發明總論與目的係用以快速理解本發明性質。參考下 列本發明較佳具體實施例與圖式,可以更完整理解本發明。 圖太簡i本 圖la係沈積PGO薄膜前之基板SEM相片。 圖lb係上面形成PGO薄膜之圖ia基板的SEM相片。 圖2a至2f係顯示在叙、銀與ir-Ta—Q基板上形成之pG〇薄 -9 _ 本紙張尺度適用中國國家標準(CNS) A4規格(210 X 297公爱) ----- 541599 A7 B7 五、發明説明( 膜的表面形態之SEM相片,其係俯視圖與橫切面圖。 圖3係在一 PG0上旋轉iXRD光譜,其中該p(}〇係沈積 於一 Ir-Ta-Ο底電極上,並於氧氣團中以8〇〇。〇退火十分鐘。 圖4係一 SEM相片,其顯示以m〇CVD沈積在ΙΓ〇2上之 PGO薄膜形態。 敫jj:具體實施例詳細說明 本發明提供一種銥(Ir)複合物電極,其係由Ir〇2、Ir_Ta_〇 、Ir-Ti-〇、lr-Nb-〇、ΙΓ-Α1-〇、Ir-Hf-〇、lr-V-0、Ir-Zr-〇 或Ir 0中任何一者形成,以該電極作為製造積體電路的底 電極’此等積體電路係諸如FeRAM、DRAM應用,以及作 為電容器、熱電紅外線感應器、光學顯示器、光學開關、 壓電轉換器與表面聲波裝置。該PGO薄膜可由任何一種化 學溶液沈積(CSD)作用,包括旋壓沈積,或藉由濺鍍作用 、MOCVD或其他薄膜沈積方法形成。該銥複合物電極改 善所形成之PGO薄膜之表面粗糙度與厚度均一性,而且有 助於形成單相C-軸p GO薄膜。 供沈積PG0薄膜之銥複合物電極之優點說明如下:a)促 使核晶岔度提高;b)形成顯示平滑度與均勻厚度表面之 PG〇薄膜;c)形成純c-軸PGO薄膜;以及d)提供供沈積與 退火處理用之更安定基板。 蒼考圖2,說明沈積於各種基板上之PGO薄膜形態。如 圖2c與2f所示,由沈積於Ir_Ta_〇基板上之pG〇形成最平滑 表面。 該電極的處理條件包括在一基板(諸如矽、Si〇2、siGe -10- ^張尺度適用中®國家標規格(21Q X 297公釐)
訂
線 、多晶矽、组、鈦、鈮、鋁、铪、鍅與任一者及其氮化物 或氧化物任一者之基板)上,藉由反應濺鍍作用沈積一 Ir-Ta-Ο電極。氬:氧的載體氣體/反應性氣體混合物為u ,其負景塵力約5 · 1 0托耳。該濺鍍塵力設於約1 〇毫托耳 。在約3 0 0瓦之功率下濺錢四英忖直徑鉉與麵乾材。所形 成之Ir-Ta-Ο電極之厚度在約1〇〇〇 A至5000 A範圍内。 為了在純金屬電極上製得與銥複合物電極相似之表面狀 態’可在諸如上述之基板上形成銀電極,並於其上沈積非 常薄之金屬或金屬氧化物層。該金屬或金屬氧化物的厚度 介於約1〇Α至300A間。該金屬可為欽、叙、錯、給、銳 、釩中任一者;該金屬氧化物可為Ti02、Ta205、Zr〇2、 Hf02、Nb205、V02、Ce02、Al2〇3與 Si02 中任一者。在沈 積PGO薄膜之前,必須於氧中進行後電極退火處理。較佳 之退火條件係於氧氣團中,介於約500 °C至1000。(:下進行 約十秒至三個小時。 圖3係藉由旋轉沈積於一 ir-Ta-Ο基板以及一經退火 Ir-Ta-Ο基板上之pg〇薄膜的XRD光譜。該Ir-Ta-Ο電極之 退火溫度係約800 °C約10分鐘。所使用之前趨體係醋酸鉛 三水合物、Pb(CH3C00)2.3H20與乙氧化鍺,以及Ge(OC2H5)4 ,其Pb/Ge之莫耳比為4-6:3,其中藉由蒸餾作用去除附在 Pb(CH3C00)2.3H20上之水。於約l〇〇°c至30〇°c之間烘烤 該膜,並於氧中以5〇〇°C結晶退火。在氧氣團中,以500°C 進行15分鐘退火處理之後,沈積在該剛沈積Ir-Ta-Ο電極 上的P G Ο薄膜為非晶相。於相同退火之後’沈積在5亥經退 -11 - 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公釐) 541599 A7 -------B7 五、發明説明(7 ) ~ 火Ir-Ta-Ο電極上的PG0薄膜顯示出強c_車由pG〇尖峰。比較 違剛沈積與退火後之I卜Ta_〇電極之XRD光譜尖彳,發現該 強結晶Ir〇2與TaA尖峰存在該經退火Ιγ_τ&_〇電極中,而且 該純銥金屬強度變底。此意味著表面之在形 成平滑〇軸PGO薄膜時扮演重要角色。 亦觀察藉由MOC VD沈積在Ir〇2基板上之pG〇薄膜的相似 微結構。該PGO薄膜的膜表面亦非常光滑,如圖4所示。 形成Ir〇2基板的條件係在1:1比率之Ar/〇2氣團中反應濺鍍 ,濺鍍溫度介於約20(TC至3〇(rc。該四英吋銥靶材上的功 率約500瓦。該背景壓力也是約5.1〇·7托耳,而且該濺鍍壓 力約10笔托耳。用於MOCVD的前趨體係Pb(TMHD)2與 Ge(ETO)4 ’其莫耳比為5:3,汽化器溫度介於約15〇至18〇。〔 間,而基板溫度介於約45(TC至550°C。該室中之壓力為5 托耳。該氬載體氣體與氧反應載體的流速分別約4〇〇〇 sccm 與 2000 seem 〇 該銥複合物電極必須在沈積PG0薄膜之前於氧氣團中退 火。該退火溫度介於約500°C至1000°C,而退火時間介於 十私至二小%•’視該ir〇2膜的厚度而定。亦可藉由沈積一 層金屬或金屬氧化物薄層,然後於氧氣團中退火該結構, 在Ir基板上形成一具有優良表面平滑度與均一性之pG〇單 相c-軸薄膜。該金屬可為鈦、组、錯、給、銳、鈒中任_ 者,而該金屬氧化物可為Ti〇2、丁a205、Zr〇2、Hf〇2、 Hb2〇5、V〇2、Ce〇2、AI2O3與Si〇2中任一者由本發明方法 形成的電極可以改善PGO薄膜四表面粗彳造度,並且促進形 -12 - 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公釐)
線 541599 A7 B7 五、發明説明(8 ) 成單c-軸PGO薄膜。 因此,已揭示一種具有優良表面平滑度與均一性之單相 c-轴PGO薄膜電極,以及彼之製造方法。應暸解在附錄申 請專利範圍所界定的本發明範圍内,可以製得另外之變化 與修正。 -13- 本紙張尺度適用中國國家標準(CNS) A4規格(210 X 297公釐)
Claims (1)
- 541599L一種形成電極與其上之鐵電薄膜之方法,包括: 製備一基板; 在該基板上沈積一電極,其中該電極係由一種選自包 括銀與銀之複合物組成的材料群組之材料所形成;以及 在其上形成一鐵電薄膜,其中該鐵電薄膜顯示表面平 滑度與均勻厚度。 2.根據申請專利範圍第丨項之方法,其中該沈積作用包括 沈積一銀複合物電極,其係選自由Ir〇2、Ir-Ta-〇、Ir-丁i 〇、Ir-Nb-0、Ir-Al-〇、Ir-Hf-0、Ir-V-0、Ir-Zr-0與 Ir-0所組成之複合物群組。 3 ·根據申請專利範圍第2項之方法,其中該沈積作用包括 使用氬:氧之比率為1:1的載體氣體/反應性氣體混合物 月景壓力約5 · 1 〇 7托耳,以沈積該電極,其中該濺鍍 壓力设為約1 0毫托耳,而且其中以約3〇〇瓦之功率濺鍍 該四英吋直徑銥與鈕靶材,而且其中形成的電極厚度介 於約1000 A與5000 A之間。 4·根據申請專利範圍第丨項之方法,其中該沈積作用包括 銀層’以及沈積一層材料,其厚度介於約1〇 A與3〇〇 a 之間’其中該材料係選自由丁丨、丁a、Zr、Hf、Nb、V、 Ti02、Ta205、Zr02、Hf02、Nb205、V02、Ce〇2、 Ah〇3與Si〇2所組成的材料群組,而且其另外包括於該 形成作用之前’於氧氣團中退火該結構。 5 ·根據申請專利範圍第4項之方法,其中該退火作用包括 在介於約500°C與1〇〇〇。〇間之溫度下,退火該結構約… -14- 本纸張尺歧财g g家㈣(CNS) A4規格Τ21〇Χ297公董) 541599 圍範利專 請中 A B c D 秒至3小時。 6.根據申請專利範圍第丨項之方法,其中該形成作用包括 以Pb/Ge莫耳比為4-6:3混合醋酸鉛三水合物前趨體與乙 氧化鍺,蒸餾該混合物以去除水;藉由化學溶液沈積作 用沈積PGO薄膜;以及在介於1〇〇。(:至3〇〇。(:之烘烤該枯 構;並於氧氣團中,以約500。〇之溫度結晶退火。 7·根據申請專利範圍第i項之方法,其中該沈積作用包括 沈積一 ΙΓ〇2電極,其係藉由在比率為1:1的氬:氧氣團 中進行反應性藏鑛而沈積,其錢錢溫度約2⑽π〜3⑼。^ ’該四英吋銥靶材上的功率約5〇〇瓦,背景壓力約51 〇_7 托耳,而且該濺鍍壓力約1 〇毫托耳。 8. 根據申請專利範圍第7項之方法,其中該形成作用包括 藉由MOCVD沈積一 PGO薄膜,其係使用Pb(TMHD)2與 Ge(ETO)4之前趨體,其莫耳比為5:3,汽化器溫度介於 約1 5 0至1 8 0 C間,而基板溫度介於約4 5 0。〇至5 5 0。〇;室 壓為5托耳;氬載體氣體的流速約40〇〇 sccm,而氧反應 載體的流速約2000 seem。 9. 一種形成電極與其上之鐵電薄膜的方法,包括·· 製備一基板; 在該基板上沈積一電極’其中該電極係由一種材料形 成,該材料係選自由銥與銥複合物所組成的群組,其中 該銀複合物係選自由Ir〇2、Ir-Ta-〇、ιΓ-τ卜〇、Ir-Nb、〇 、Ir-Al-〇、lr-Hf-〇、Ir-V-〇、Ir-Zr-0與 ir-〇所組成的 複合物群組;以及 -15- 本紙張尺度適用中國國家標準(CNS) A4規格(210 X 297公釐) 541599申请專利範圍 在八上形成一 PG〇鐵電薄胺 #而丞、典由t #膜其中該鐵電薄膜顯示出 表面平滑度與均勾厚度。 i〇.根據申請專利範圍第9項 I; . ^ ^ ^ 、、方法’其中該沈積作用使用 氬·氧比率為1:1之載體裹轉 Ψ ^ # % 〃収反應性氣體混合物沈積該 電極,其背景壓力約5·1(Γ7 古k π 托耳’其中該濺鍍壓力約K 笔托耳,而且其中以约 、 瓦之功率錢鍍直徑四英叶之 銀與ί旦乾材,呈中所形# + /、〒所形成電極的厚度介於約1〇〇〇人與 5000 Α之間。 U.根據巾請專利範圍第9項之方法,#中該沈積作用包括 一銥層,以及沈積一層材料,其厚度介於約1〇人與3〇〇 A 之間’其中該材料係選自由丁丨、Ta、Zr、Hf、Nb、v、 Ti〇2、Ta205、Zr02、Hf〇2、Nb2〇5、v〇2、Ce〇2、 Al2〇3與Si〇2所組成的材料群組,而且其另外包括於該 形成作用之前,於氧氣團中退火該結構。 12·根據申請專利範圍第11項之方法,其中該退火作用包括 在介於約500°c與1000°c之溫度下退火該結構約10秒至 約3小時。 1 3·根據申請專利範圍第9項之方法,其中該形成作用包括 以Pb/Ge莫耳比為4-6:3混合醋酸鉛三水合物前趨體與乙 氧化錯’蒸館該混合物以去除水;以及在介於1 至 3 0 0 C之溫度烘烤該結構;並於氧氣團中,以約5 〇 〇之 溫度結晶退火。 14 ·根據申請專利範圍第9項之方法,其中該沈積作用包括 沈積一 Ir02電極,其係藉由在比率為1:1的氬:氧氣團 -16- 本紙張尺度適用中國國家標準(CNS) A4規格(210X297公爱) 541599 A B c D 申請專利範圍 中進行反應性濺鍍而沈積,其濺鍍溫度約2〇〇。〇至3〇〇。(: ’該四英吋銥靶材上的功率約5〇〇瓦,背景壓力約5 ·丨〇_·7 托耳’而且該濺鐘壓力約1 〇毫托耳。 15·根據申請專利範圍第14項之方法,其中該形成作用包括 藉由MOCVD沈積一 PG0薄膜,其係使用pb(TMHD)2與 Ge(ETO)4之前趨體,其莫耳比為4_6:3,汽化器溫度介 於約150°C至180°C間,而基板溫度介於約45〇。(:至55〇。〇 ;室壓為5托耳;氬載體氣體的流速約4〇〇〇 sccm,而氧 反應載體的流速約2000 sccm。 16.—種積體電路,其包括: 一基板; 一沈積於該基板之電極,其中該電極係由一種選自包 括銥與銀之複合物組成的材料群組之材料形成,其中該 銥複合物係選自由Ir〇2、Ir-Ta-〇、Ir 丁丨_〇、〇 ' ΙΓ-Α1-0、、Ir_v_0、匕2卜0與 Ir 〇所組成的複 合物群組;以及 —在該電極上形成單相C,PG〇鐵電薄膜,纟中該鐵電 薄膜顯示出表面平滑度與均勻厚度。 其中該電極厚^ 其中該電極包} 該材料層厚度 1 7·根據申請專利範圍第16項之積體電路 介於約1000 A與5000 A之間。 1 8.根據申請專利範圍第1 6項之積體電路 一層銥層與一種沈積於其上的材料層 於約10 A至300 A,其中該材料係選自由Ti、Ta、 Hf、Nb、V、Ti02、Ta205、Zr02、Hf〇2、Nb2〇5、v( Ce〇2、Al2〇3與Si〇2所組成的材料群組。 -17- 本紙張尺度適财國时鮮(CNS) A4規格Τ^ιοχ撕公釐)
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US7101720B2 (en) * | 2004-03-15 | 2006-09-05 | Sharp Laboratories Of America, Inc. | Mixed noble metal/noble metal oxide bottom electrode for enhanced PGO c-axis nucleation and growth |
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