TW200406831A - Method for fabricating silicide - Google Patents
Method for fabricating silicide Download PDFInfo
- Publication number
- TW200406831A TW200406831A TW92133444A TW92133444A TW200406831A TW 200406831 A TW200406831 A TW 200406831A TW 92133444 A TW92133444 A TW 92133444A TW 92133444 A TW92133444 A TW 92133444A TW 200406831 A TW200406831 A TW 200406831A
- Authority
- TW
- Taiwan
- Prior art keywords
- forming
- metal
- patent application
- scope
- item
- Prior art date
Links
- 229910021332 silicide Inorganic materials 0.000 title claims abstract description 13
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims description 41
- 229910052751 metal Inorganic materials 0.000 claims abstract description 52
- 239000002184 metal Substances 0.000 claims abstract description 52
- 239000004065 semiconductor Substances 0.000 claims abstract description 35
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 6
- 238000003672 processing method Methods 0.000 claims abstract 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 22
- 229910052710 silicon Inorganic materials 0.000 claims description 22
- 239000010703 silicon Substances 0.000 claims description 22
- 239000000758 substrate Substances 0.000 claims description 14
- 125000006850 spacer group Chemical group 0.000 claims description 7
- 239000004575 stone Substances 0.000 claims description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
- 239000013078 crystal Substances 0.000 claims description 5
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims description 5
- 239000010936 titanium Substances 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 238000001312 dry etching Methods 0.000 claims description 3
- 238000005530 etching Methods 0.000 claims description 3
- 238000001039 wet etching Methods 0.000 claims description 3
- 238000002955 isolation Methods 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 229910052709 silver Inorganic materials 0.000 claims 1
- 239000004332 silver Substances 0.000 claims 1
- 238000009413 insulation Methods 0.000 abstract description 4
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 239000012212 insulator Substances 0.000 description 11
- 238000010586 diagram Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 6
- 238000005496 tempering Methods 0.000 description 5
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005192 partition Methods 0.000 description 3
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000002019 doping agent Substances 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 210000004013 groin Anatomy 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910021341 titanium silicide Inorganic materials 0.000 description 1
Landscapes
- Electrodes Of Semiconductors (AREA)
- Insulated Gate Type Field-Effect Transistor (AREA)
Abstract
Description
200406831 五、發明說明(1) 一、【發明所屬技術領域 本發明係有關於半導體梦鞋 〒股衣%的方法,特別 改進矽化金屬製程的方法。 J疋關於一種 二、【先前技術】 由於半導體製程尺寸的縮小,則寄生 以及片電阻會增加。而為了減少寄生電阻★二:電阻 Silicide)製程是廣受注意以及歡。 五屬( 化金屬中,二…(C〇Sl2)以及二梦化在二=同厂 =重視以及學習的。它們可以被應用到自“1 準:夕: 衣釭(SALICIDE)中以及在不同矽化金屬中以顯干出 ”取低的電阻率。且對於改進熱穩定,以及磊晶地成 化金屬都是被需要的。 θθ 、 第一Α圖至第一D圖顯示習知技術製程的順序。第一α 圖顯示-基本半導體結構1〇1,它包含一具有兩推雜區 103Α,103Β之底材1〇2,一具有向上表面以及多數個側面 之閘極電極104,一間隙壁][05位於閘極電極1〇4的每一個 側面上及留有一部份摻雜區1〇3Α,1〇3Β曝露出來,以及隔 離元件(isolation device)或稱數個絕緣物ι〇6Α,106Β以 阻隔其它半導體結構。第一 B圖顯示沉積一磊晶矽(200406831 V. Description of the invention (1) 1. [Technical field to which the invention belongs] The present invention relates to a method for semiconductor dream shoes and a groin coat method, in particular to a method for improving the process of silicided metal. J 疋 About a type II. [Prior art] Due to the reduction in the size of the semiconductor process, parasitics and chip resistance will increase. In order to reduce parasitic resistance ★ Second: resistance Silicide) process is widely noticed and enjoyed. Five genus (chemical metals, two ... (CoS12) and two dreams in two = same factory = value and learning. They can be applied to "1 standard: evening: clothing (SALICIDE) and in different The silicidated metal has a low resistivity with "significantly dry out". It is also required for improving thermal stability and epitaxial formation of chemically formed metals. Θθ, the first A to D graphs show the conventional technology process Sequence. The first alpha diagram shows a basic semiconductor structure 101, which includes a substrate 10 with two doped regions 103A, 103B, a gate electrode 104 with an upward surface and a plurality of sides, and a spacer. ] [05 is located on each side of the gate electrode 104 and a part of the doped region 103A is left, and 103B is exposed, and an isolation device or a number of insulators ι〇6Α, 106B to block other semiconductor structures. Figure B shows the deposition of an epitaxial silicon (
Epi taxial Si 1 icon ) 111,在摻雜區 ι〇3Α,103B 曝露出來Epi taxial Si 1 icon) 111, exposed in the doped region ι〇3Α, 103B
的部份以及閘極電極1 〇 4的向上表面;同時,一部份的磊 晶矽以及致污物112附著在間隙壁1〇5以及數.個絕緣物106APart and the upward surface of the gate electrode 104; at the same time, a part of the epitaxial silicon and the contaminant 112 are attached to the spacer 105 and several insulators 106A
第5頁 200406831 五、發明說明(2) ,106B上。第一C圖顯示沉積一金屬鈷(c〇b 在蟲晶石夕m上。最後,第一D圖顯示一加熱過,)121 熱回火(RTA )是被廣泛地使用在矽化金王、,且快速 矽化金屬1 3 1步驟中。 衣以及形成 參閱第一D圖,一厚的矽化金起一 漏電流以及低可靠性。而厚的欲仆入Y ~起—向的接合 底材的結晶矽’就像厚的矽化金屬接近就會—亡¥體 合漏電流。還有在間隙壁上的矽化 :的接 電流,此漏電流會由閑極電極到摻雜區而造;;=漏 使該半導體失效。 i战决動作甚至 三、【發明内容】 鑒於上述之發明背景中,功υ β 絕緣物上造成諸多缺點。本# 曰於'纟巴緣間隙壁以及 上之雜質,進而改善製程緣間隙壁以及絕緣物 一石夕化金屬製造的方法已揭雨 首先,一半導體結構具有一:接下來的實施例中, 結構,其中,該處理步: = ; =著,,理該半導體 對該遙晶層之移除速率,缺後巴、面之私除速率大於 晶層之該半導體結構上,最J ”-金屬層於形成該蟲 取俊’加熱以使該磊晶層與該金Page 5 200406831 V. Description of the Invention (2), 106B. The first picture C shows the deposition of a metallic cobalt (c0b on the worm crystal stone m. Finally, the first picture D shows a heating,) 121 Thermal Tempering (RTA) is widely used in the King of Silicon Silicide, , And fast silicidating metal 1 3 1 steps. Clothing and formation Refer to the first D figure, a thick silicon silicide causes a leakage current and low reliability. The thick crystalline silicon that is to be joined from the substrate to the substrate will be like a thick silicided metal, and the leakage current will be combined. There is also a silicidation on the gap wall: the leakage current will be caused by the idler electrode to the doped region;; = leakage causes the semiconductor to fail. i-decision action even 3. [Summary of the invention] In view of the above-mentioned background of the invention, there are many shortcomings caused by the work β insulator. Ben # 于 于 纟 巴 缘边 边墙 and impurities on it, thereby improving the process edge spacer and insulators. A method for manufacturing petrochemical metal has been unveiled. First, a semiconductor structure has one: In the following embodiments, the structure Wherein, the processing step: =; = The reason, the removal rate of the semiconductor to the remote crystal layer, the removal rate of the missing bar and surface is greater than that of the semiconductor structure of the crystal layer, the most J ”-metal layer In the formation of the worm take Jun 'heating to make the epitaxial layer and the gold
第6頁 五、發明說明(3) 屬層作用而形成 # 在該絕緣表面,以二降低該處理步驟避免矽化金屬形成 工丨+低元件的特性。 四、【實施方式】 以下對製程與方牛 。本發明所沿用的現有枯:包含積體電路製造的完整流程 助本發明的敘述。而且下=,在此僅作重點式的引用,以 製,其作用僅在 =内文中相關圖示並未依比例繪 衣現本發明之方法特徵。 而揭本明的内容可經由下述實施例盘复相 而揭不。首先,— Λ a 1…、相關圖示的敘述 表面。其次,形成ί石::構具有一半導體表面與-絕緣 該半導體結構,:中=於該半導體表面”妾著,處理 J =於對該“層之;;驟該::表::移除 層’與= = 冓上,最後,力:熱 金屬形成L 切化金屬。該處理步驟避免砍化 巴、、彖表面,以至於降低元件的特性。 本务明的一貫施例顯示在繁— 圖表示一可用任何、商」』不在第—Α圖至弟二Ε圖。第二A 甘a人了用任付適虽的方法產生的基本半導體社構20 1 ,^ ^ ^ , 203A , 2〇3B „ ;2"2 於Η =二多數個側面的閘極電極204,-間隙壁20 5位 J . ° " ^ 4側面上且留有一部份摻雜區203A , 203B暴 路在卜,以及多數個絕緣物2〇6Α,2〇6β用以隔絕其它半導 200406831 五、發明說明(4) 體結構。對於本發明而言,底材2 〇 2可為任何適當的半導 體材料,如像石夕(S i )、鍺(Ge )以及矽鍺(S i Ge )且此 實施例為石夕。摻雜區2〇3A,2 0 3B可分為N型或P型摻雜物於 底材2 0 2内,而N型摻雜物用於此實施例。閘極電極2 〇 4可 為多晶體且此實施例為使用多晶矽(p〇ly-si丨ic〇n )。間 隙壁2 0 5以及絕緣物2〇64,2 0 66可為氧化矽類或氮化矽類 ’於此實施例是二氧化矽(S i 〇2 )。在此實施例中,需注 意摻雜區2 0 3A,20 3B暴露的區域以及閘極電極2〇4向上的 表面,形成一半導體表面,而且間隙壁2 〇 5暴露的區域以 及絕緣物2 0 6 A,2 0 6B暴露的部分形成一絕緣表面。 ;苐一 B圖中,一蠢晶層211如蠢晶石夕(Epitaxiai SU^C0n)層形成於半導體表面上。在選擇性的沉積磊晶 一些片段的磊晶矽及致污物2 1 2可能沉積形成於絕 、’、面上。為了避免磊晶矽及致污物2丨2附著於絕緣表面 ^,下面的步驟提供一方法以移除磊晶矽及致污物212。 1二C圖中顯示移除附著於絕緣表面上的磊 2。其中在此移除的過程中是使用稀釋氯氣酸(Du = 而蝕刻過程於此實施例中,移除 面墙晶…污刪已被移…二A I ,现日日矽表面的磊晶矽被移除少於1 0 A。換句話士兒, 在本發明^層的移除速率是慢於絕緣表面的移除速率。 在這個具體實施例中,移除速率如钱刻速率是要被考 200406831 五、發明說明(5) ~ _- 慮的。對於濕蝕刻(Wet etching)的方法,選擇稀釋氫 f酸是因為它具有對二氧化石夕(絕緣表面)以及磊晶矽較 高的移除率。在另一具體實施例中緩衝氧化矽蝕刻液(b〇e ,Buffer Onde etcher)也被使用於濕蝕刻的方法中。 而還有許多種不同的調劑可針對不同的絕緣表面以及半導 體表面。又另一方面說,對於乾蝕刻(Dry etching )的 方法中,氫化合物也可被應用於本發明之中。總之,無論 何種凋劑被選用,只要符合對絕緣表面的移除率快於磊晶 層的移除率即可。 第二D圖顯示經一適當方法(如沉積方法)形成一金 _ 屬層231 (如错金屬層)於磊晶矽211上,最後第二e圖是 一加熱過程於半導體結構上。在此發明中快速熱回火( RTA )是一種被普遍使用於矽化金屬製程以及形成矽化金 屬的步驟。一符合此實施例快速熱回火的步驟是溫度接近 攝氏650度大約20分鐘以形成矽化金屬矽化鈷(c〇si 2 ), 對於其他的貫施例如鈦金屬,它的快速熱回火有兩個步驟 。第一步驟是回火(A n n e a 1 i n g ),舉例說明,溫度接近 攝氏6 5 0度大約2 〇分鐘在氮(n 2 )氣體中,其中氮氣和鈦 金屬反應成氮化鈦(TiN2 )於金屬表面,同時鈦金屬和磊 _ 晶矽反應形成矽化金屬,於與磊晶矽直接接觸的區域。溫 度方面如介於攝氏6 5 〇至7 5 0度,一高阻值相位的矽化鈦形 成的速度快於氮化鈦在磊晶矽暴露的區域,同時無關磊晶 石夕的反應發生在有金屬覆蓋的二氧化矽層或氮化矽層。與Page 6 V. Description of the invention (3) Formed by the action of the metal layer # On the insulating surface, the processing step is reduced by two to avoid the formation of silicided metal and the characteristics of low components. 4. [Implementation] The following processes and Fang Niu. The existing dry circuit used in the present invention includes a complete process for manufacturing integrated circuits to assist the description of the present invention. Moreover, the following = is only used as a key reference here to control, and its role is only in the context. The related diagrams in the text are not drawn to scale to show the features of the method of the present invention. The contents of the disclosure can be uncovered through the following embodiments. First, — Λ a 1 ..., the related narrative surface. Secondly, a lithium :: structure has a semiconductor surface and-insulates the semiconductor structure, and: the middle = on the semiconductor surface ", processing J = on the" layer; ": the table :: removed Layer 'and = = 冓, and finally, the force: hot metal forms the L-cut metal. This processing step avoids cutting the surface of the bar, and the surface, so as to reduce the characteristics of the component. The consistent example of this matter is shown in the traditional Chinese-English diagram, which shows that any one can be used, and the "quotient" is not in the first-second diagram to the second-second diagram. The second method is to use the basic semiconductor structures 20 1, ^ ^ ^, 203A, and 203B produced by the method of arbitrarily, and 2 " 2 Yu Η = two majority side gate electrodes 204,- Spacer 20 5 digits J. ° " ^ 4 on the side with a part of the doped regions 203A, 203B blunders, and most insulators 206A, 206β to isolate other semiconductors 200406831 5 4. Description of the invention (4) bulk structure. For the present invention, the substrate 200 may be any suitable semiconductor material, such as Shi Xi (Si), germanium (Ge), and silicon germanium (Si Ge), and This embodiment is Shi Xi. The doped regions 203A and 203B can be divided into N-type or P-type dopants in the substrate 202, and N-type dopants are used in this embodiment. Gate The electrode 2 04 may be polycrystalline, and in this embodiment, polycrystalline silicon (poly-silicon) is used. The partition wall 2 05 and the insulator 2064, 2 0 66 may be silicon oxide or nitride. Silicon type 'in this embodiment is silicon dioxide (Si02). In this embodiment, it is necessary to pay attention to the exposed areas of the doped regions 230A, 203B and the upward surface of the gate electrode 204 to form A semiconductor surface In addition, the exposed area of the partition wall 205 and the exposed portions of the insulators 206A and 206B form an insulating surface. In the first figure, a stupid layer 211 is like stupid stone (Epitaxiai SU ^ C0n). ) Layer is formed on the semiconductor surface. Epitaxial silicon and contaminants 2 1 2 may be deposited and deposited on the surface of selective epitaxial silicon. In order to avoid epitaxial silicon and contaminants 2 丨2 is attached to the insulating surface ^, the following steps provide a method to remove epitaxial silicon and contaminants 212. Figure 2C shows the removal of the epitaxial 2 attached to the insulating surface. During this removal process It is the use of dilute chlorine acid (Du = and the etching process in this embodiment, removing the wall crystal ... the dirty has been moved ... two AI, the epitaxial silicon on the silicon surface today is removed less than 10 A. In other words, the removal rate of the layer in the present invention is slower than the removal rate of the insulating surface. In this specific embodiment, the removal rate, such as the rate of money engraving, is to be considered 200406831 V. Description of the invention (5 ) ~ _- Concerned. For the wet etching method, the dilute hydrogen f acid was chosen because it has The high removal rate of stone dioxide (insulating surface) and epitaxial silicon. In another embodiment, a buffered silicon oxide etching solution (boe, Buffer Onde etcher) is also used in the wet etching method. There are many different kinds of regulators that can target different insulation surfaces and semiconductor surfaces. On the other hand, for dry etching, hydrogen compounds can also be used in the present invention. In short, no matter what kind of wither is selected, as long as the removal rate of the insulating surface is faster than that of the epitaxial layer. The second diagram D shows that a metal layer 231 (such as a wrong metal layer) is formed on the epitaxial silicon 211 by an appropriate method (such as a deposition method). Finally, the second diagram e is a heating process on the semiconductor structure. In this invention, Rapid Thermal Tempering (RTA) is a step that is commonly used in the process of forming silicided metals and forming silicided metals. One step for rapid thermal tempering in accordance with this embodiment is to form a silicide metal cobalt silicide (cosi 2) at a temperature close to 650 degrees Celsius for about 20 minutes. For other applications such as titanium, its rapid thermal tempering has two Steps. The first step is tempering (A nnea 1 ing). For example, the temperature is close to 650 degrees Celsius for about 20 minutes in a nitrogen (n 2) gas, where nitrogen and titanium react to form titanium nitride (TiN 2). On the metal surface, at the same time titanium reacts with epitaxial silicon to form silicided metal in the area directly contacting epitaxial silicon. If the temperature is between 650 and 750 degrees Celsius, titanium silicide with a high resistance phase is formed faster than titanium nitride in the epitaxial silicon exposed area. At the same time, the reaction that has nothing to do with epitaxial silicon occurs at the same time. Metal-covered silicon dioxide or silicon nitride. versus
200406831 五、發明說明(6) 絕緣表面接觸的金屬沉積主要包含了氮化鈦以及未反應的 鈦。使用過氧化物即可移除上述之氮化鈦以及未反應的鈥 ,而留下矽化金屬區。 比較第一D圖(習知技藝)以及第二E圖,在第二E圖 我們可以看出,已經沒有殘留物附著於暴露的絕緣表面上 而且石夕化金屬也只變薄一點。此意味著橋接漏電流已被改 善以及此半導體結構變得更有可信度。 揭露本發明技藝的例子是從此規格的考量,以及本發 明的應用。而此處也只是顯示考慮規格的典型例子,對於 實際請求的範圍以及本發明的精神是條列在隨後的專利請 求範圍内。200406831 V. Description of the invention (6) The metal deposit in contact with the insulating surface mainly contains titanium nitride and unreacted titanium. The use of peroxide removes the titanium nitride and unreacted ”mentioned above, leaving the silicided metal region. Comparing the first D picture (known technique) and the second E picture, in the second E picture, we can see that there is no residue attached to the exposed insulating surface and the petrified metal has only become thinner. This means that the bridge leakage current has been improved and the semiconductor structure has become more reliable. Examples of revealing the technology of the present invention are from the consideration of this specification and the application of the present invention. And here is only a typical example of considering the specifications. The scope of the actual request and the spirit of the present invention are listed in the scope of the subsequent patent claims.
第10頁 200406831 圖式簡單說明 第一 A圖至第一 D圖顯示對於習知矽化金屬結構製造的 代表性圖示;以及 第二A圖至第二E圖顯示對於本發明矽化金屬結構製造 的代表性圖示; 主要部分之代表符號: 101 半導體結構 102 底材 103A 摻雜區 1 0 3 β摻雜區 104 閘極電極 105 間隙壁 1 0 6 Α 絕緣物 10 6B 絕緣物 111 蠢晶碎 112 磊晶矽及致污物 121 金屬層 1 3 1 矽化金屬 201 半導體結構 2 0 2 底材 2 0 3A摻雜區 20 3B摻雜區 204 閘極電極Page 10 200406831 Schematic illustrations Figures A through D show representative representations of conventional silicidated metal structure manufacturing; and Figures A through E show second Representative diagram; Representative symbols of main parts: 101 semiconductor structure 102 substrate 103A doped region 1 0 3 β doped region 104 gate electrode 105 spacer 1 0 6 Α insulator 10 6B insulator 111 Epitaxial silicon and contaminants 121 metal layer 1 3 1 silicided metal 201 semiconductor structure 2 0 2 substrate 2 0 3A doped region 20 3B doped region 204 gate electrode
第11頁 200406831 圖式簡單說明 2 0 5 間隙壁 2 0 6 A 絕緣物 2 0 6 B 絕緣物 211 蠢晶石夕 212 磊晶矽及致污物 231 金屬層 2 41 石夕化金屬Page 11 200406831 Brief description of the drawing 2 0 5 Partition wall 2 0 6 A Insulator 2 0 6 B Insulator 211 Stupid stone 212 Epitaxial silicon and contaminants 231 Metal layer 2 41 Petrochemical metal
第12頁Page 12
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW92133444A TWI232507B (en) | 2003-11-27 | 2003-11-27 | Method for fabricating silicide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW92133444A TWI232507B (en) | 2003-11-27 | 2003-11-27 | Method for fabricating silicide |
Publications (2)
Publication Number | Publication Date |
---|---|
TW200406831A true TW200406831A (en) | 2004-05-01 |
TWI232507B TWI232507B (en) | 2005-05-11 |
Family
ID=36320045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW92133444A TWI232507B (en) | 2003-11-27 | 2003-11-27 | Method for fabricating silicide |
Country Status (1)
Country | Link |
---|---|
TW (1) | TWI232507B (en) |
-
2003
- 2003-11-27 TW TW92133444A patent/TWI232507B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
TWI232507B (en) | 2005-05-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6905922B2 (en) | Dual fully-silicided gate MOSFETs | |
TWI415174B (en) | Method for forming self-aligned metal silicide contacts | |
CN100505168C (en) | Uni-directional diffusion of metal silicide in semiconductor devices | |
JP5090173B2 (en) | Method of manufacturing a semiconductor device having a high dielectric constant gate dielectric layer and a silicide gate electrode | |
JP5361128B2 (en) | Control method of gate electrode height | |
US7649263B2 (en) | Semiconductor device | |
JP4531068B2 (en) | Method for selective removal of unsilicided metal | |
JP2008527743A (en) | Self-formed metal silicidation gate for CMOS devices | |
CN105529253B (en) | The forming method of semiconductor devices | |
TWI337390B (en) | Method for semiconductor device performance enhancement | |
JP3873008B2 (en) | Method for forming silicide film of semiconductor device | |
TW200406831A (en) | Method for fabricating silicide | |
US9412861B2 (en) | Semiconductor device having structure capable of suppressing oxygen diffusion and method of manufacturing the same | |
JP2006352127A (en) | Method of forming self-aligned silicide film by using multiple heat treatment processes | |
JP4882287B2 (en) | Semiconductor device | |
JP2007067229A (en) | Method for manufacturing insulating gate field effect transistor | |
CN103794561A (en) | Manufacturing method of semiconductor device | |
US7595264B2 (en) | Fabrication method of semiconductor device | |
TW432510B (en) | Method for producing device having wavy titanium silicide | |
TW558759B (en) | Method of forming and etching resistor protection oxide layer | |
TWI292928B (en) | Manufacturing method of semiconductor device | |
KR100823707B1 (en) | Method of manufacturing a semiconductor device | |
JP2019110211A (en) | Manufacturing method of semiconductor device | |
TWI222141B (en) | Semiconductor devices having a metal silicide bi-layer and the method for fabricating the same | |
TWI267949B (en) | Method of reducing current-degradation of NMOS device |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK4A | Expiration of patent term of an invention patent |