TWI487037B - The manufacturing method for forming mosfet having the stable threshold voltage - Google Patents
The manufacturing method for forming mosfet having the stable threshold voltage Download PDFInfo
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- 238000004519 manufacturing process Methods 0.000 title description 6
- 238000000034 method Methods 0.000 claims description 56
- 229910052751 metal Inorganic materials 0.000 claims description 52
- 239000002184 metal Substances 0.000 claims description 51
- 229910044991 metal oxide Inorganic materials 0.000 claims description 33
- 239000004065 semiconductor Substances 0.000 claims description 28
- 150000004706 metal oxides Chemical class 0.000 claims description 26
- 229910052732 germanium Inorganic materials 0.000 claims description 14
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 14
- 238000000151 deposition Methods 0.000 claims description 12
- 238000005530 etching Methods 0.000 claims description 12
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 claims description 9
- 238000005229 chemical vapour deposition Methods 0.000 claims description 8
- 238000004544 sputter deposition Methods 0.000 claims description 8
- 150000004767 nitrides Chemical class 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 7
- 238000000137 annealing Methods 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 238000005468 ion implantation Methods 0.000 claims description 3
- 238000005289 physical deposition Methods 0.000 claims description 3
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- 125000002524 organometallic group Chemical group 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 5
- 239000010953 base metal Substances 0.000 claims 1
- 230000008020 evaporation Effects 0.000 claims 1
- 229910052707 ruthenium Inorganic materials 0.000 claims 1
- 230000000694 effects Effects 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000000295 complement effect Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000007547 defect Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000005240 physical vapour deposition Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000000231 atomic layer deposition Methods 0.000 description 2
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 229910052735 hafnium Inorganic materials 0.000 description 2
- -1 oxygen ions Chemical class 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- 229910052691 Erbium Inorganic materials 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- CFJRGWXELQQLSA-UHFFFAOYSA-N azanylidyneniobium Chemical compound [Nb]#N CFJRGWXELQQLSA-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 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
- 230000005693 optoelectronics Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
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Description
本發明係有關於一種形成電晶體的方法,特別是一種形成具有穩定臨限電壓之電晶體的方法。The present invention relates to a method of forming a transistor, and more particularly to a method of forming a transistor having a stable threshold voltage.
互補式金屬氧化層半導體(Complementary Metal Oxide Semiconductor,CMOS)具有僅在電晶體需要切換啟閉時才需耗能的優點,因此非常省電且其所產生的發熱較少。在傳統上製造電子半導體元件(或光電半導體元件)的互補式金屬氧化層半導體製造程序指的是能夠在矽晶圓上製作出(P-channel MOSFET,PMOS)元件以及(N-channel MOSFET,NMOS)元件,由於PMOS元件與NMOS元件具有互補的特性,因此稱為互補式金屬氧化層半導體製程。而該互補式金屬氧化層半導體製程可應用在包括微處理器(Microprocessor),微控制器(Microcontroller),靜態隨機存取記憶體(SRAM)與其他數位邏輯電路等半導體積體電路的製程。Complementary Metal Oxide Semiconductor (CMOS) has the advantage of requiring energy only when the transistor needs to be switched on and off, so it is very power-saving and generates less heat. A complementary metal oxide semiconductor fabrication process that traditionally manufactures electronic semiconductor components (or optoelectronic semiconductor components) refers to the ability to fabricate (P-channel MOSFET, PMOS) components and (N-channel MOSFETs, NMOS) on germanium wafers. The device, because of its complementary nature to the PMOS device, is referred to as a complementary metal oxide semiconductor process. The complementary metal oxide semiconductor process can be applied to a process including a semiconductor integrated circuit such as a microprocessor, a microcontroller, a static random access memory (SRAM), and other digital logic circuits.
在目前半導體互補式金屬氧化層半導體的製程技術中,已發展至目前的32奈米(nm)線寬(gate length)等級,故而其製程要求越來越嚴苛,更無法容忍所謂的製程不穩定以及缺陷等因素而影響產品的良率。故而在前述半導體互補式金屬氧化層半導體製程技術中所謂的製程不穩定以及缺陷等因素包括了會產生臨限電壓不穩定性以及偶極效應等製程缺陷,而臨限電壓不穩定性的三個原因主要包括了如下列所述的:In the current process technology of semiconductor complementary metal oxide semiconductors, the current 32 nanometer (nm) line length grade has been developed, so the process requirements are more and more stringent, and the so-called process is not tolerated. Factors such as stability and defects affect the yield of the product. Therefore, the so-called process instability and defects in the semiconductor complementary metal oxide semiconductor process technology include process defects such as threshold voltage instability and dipole effect, and three threshold voltage instability. The reasons mainly include the following:
1. 於金屬/閘極氧化層(Metal/gate oxide)介面的費米能階鎖定效應(Fermi-level pinning effect)。1. The Fermi-level pinning effect of the metal/gate oxide interface.
2. 於閘極氧化層(Gate oxide)中的電荷效應。2. The charge effect in the gate oxide.
3. 於閘極氧化層與矽(Si)基板基本之間產生了介面偶極效應(Interface dipole effect),該介面偶極效應係由於兩種材料間的單位面積的氧密度不相同(Areal oxygen density difference)而造成,而單位面積氧密度可以σ值表示。當氧離子會從σ值較高的材料擴散至σ值較低的材料時,在高σ值的材料中會留下氧空缺(Oxygen vacancy),而在低σ的材料中會產生額外的氧原子,故而會在該介面中形成一個偶極效應。3. An interface dipole effect is generated between the gate oxide layer and the bismuth (Si) substrate. The interface dipole effect is due to the difference in oxygen density per unit area between the two materials (Areal oxygen). The density difference is caused by the σ value. Oxygen vacancy is left in materials with high σ values when oxygen ions diffuse from materials with higher σ values to materials with lower σ values, while extra oxygen is produced in materials with low σ. The atom, therefore, forms a dipole effect in the interface.
故而為了能產生更有效率的現象,提供產業界掌握更佳的生產製程,且可運用於電晶體半導體元件的製造上,需要研發新式方法,藉以提高生產良率且能降低電晶體半導體元件的製造成本。Therefore, in order to produce a more efficient phenomenon, to provide the industry with a better production process, and to be applied to the manufacture of transistor semiconductor components, it is necessary to develop a new method to improve the production yield and reduce the transistor semiconductor components. manufacturing cost.
本發明係一種形成具有穩定臨限電壓之電晶體的方法,該電晶體具有雙極濺鍍高介電係數(High-k gate dielectric)絕緣層,故而所產生的電晶體係為不會產生費米能階釘紮效應(Fermi-level pinning effect)的場效電晶體。The invention is a method for forming a transistor having a stable threshold voltage, the transistor having a bipolar sputtering high-k gate dielectric insulating layer, so that the generated electro-crystalline system does not generate a fee Field effect transistor with Fermi-level pinning effect.
本發明係一種形成具有穩定臨限電壓之電晶體的方法,首先提供正型矽半導體層,接著沉積成長第一氧化層於正型矽半導體層的上方表面上;再進行第一光罩與第一蝕刻製程以形成場氧化層於正型矽半導體層的上方表面上;繼續進行沉積選擇性閘極氧化層於正型矽半導體層與場氧化層的上方表面上且施以退火製程;沉積選擇性閘極金屬層於選擇性閘極氧化層的上方表面上;再進行第二光罩與第二蝕刻製程以形成閘極;接著進行離子植入法以形成源極與汲極;再沉積第二氧化層於場氧化層,閘極,源極與汲極的上方表面上;再進行第三光罩與第三蝕刻製程以形成閘極的接觸孔;繼續形成金屬層以形成金屬導線於場氧化層,閘極金屬層,源極與汲極的上方表面上;最後進行第四光罩與第四蝕刻製程以形成金屬導線於場氧化層,閘極,源極與汲極的上方表面上。The present invention is a method of forming a transistor having a stable threshold voltage, first providing a positive-type germanium semiconductor layer, followed by depositing a first oxide layer on an upper surface of the positive-type germanium semiconductor layer; and performing a first mask and a first mask An etching process to form a field oxide layer on the upper surface of the positive-type germanium semiconductor layer; continuing to deposit a selective gate oxide layer on the upper surface of the positive-type germanium semiconductor layer and the field oxide layer and applying an annealing process; deposition selection a gate metal layer on the upper surface of the selective gate oxide layer; a second mask and a second etching process to form a gate; followed by ion implantation to form a source and a drain; The dioxide layer is on the field oxide layer, the gate, the upper surface of the source and the drain; the third mask and the third etching process are performed to form a contact hole of the gate; the metal layer is continuously formed to form the metal wire. An oxide layer, a gate metal layer, an upper surface of the source and the drain; and finally a fourth mask and a fourth etching process to form a metal wire on the field oxide layer, the gate, the source and the drain Surface.
本發明提出能產生高穩定性臨限電壓的場效電晶體製程,故而能夠減除高介電係數絕緣層(High-k gate dielectrics)與二氧化矽基板介面的偶極(Interface dipole)效應。The present invention proposes a field effect transistor process capable of generating a high stability threshold voltage, thereby reducing the interface dipole effect of the high-k gate dielectrics and the ceria substrate interface.
本發明可產生無費米能階釘紮效應(Fermi-level pinning effect)的金屬閘極(Metal gate electrode),故可使電晶體產生有效地穩定臨限電壓飄移的現象(Threshold voltage instability)。The present invention can produce a metal gate electrode without a Fermi-level pinning effect, so that the transistor can effectively stabilize the threshold voltage instability.
為讓本發明的上述和其他目的、特徵和優點能更明顯易懂,下文特舉較佳實施例,並配合附圖以詳細說明如下。The above and other objects, features, and advantages of the invention will be apparent from
如第1A圖所示係本發明一種形成具有穩定臨限電壓之電晶體的方法的圖示,首先提供一正型(P-type)矽半導體層101。As shown in Fig. 1A, there is shown a diagram of a method of forming a transistor having a stable threshold voltage, first providing a positive (P-type) germanium semiconductor layer 101.
續如第1B圖所示,沉積成長5奈米厚度的二氧化矽(SiO2 )層(第一氧化層)101於該正型矽半導體層101的上方表面上。Subsequently, as shown in FIG. 1B, a ceria (SiO 2 ) layer (first oxide layer) 101 having a thickness of 5 nm is deposited on the upper surface of the positive-type germanium semiconductor layer 101.
如第1C圖所示,進行光罩與蝕刻製程後形成場氧化(Field Oxide)層102於該正型矽半導體層101的上方表面上。As shown in FIG. 1C, a field oxide (Field Oxide) layer 102 is formed on the upper surface of the positive-type germanium semiconductor layer 101 after the mask and the etching process.
再如第1D圖所示,沉積一選擇性閘極氧化層103,10奈米於該正型矽半導體層101與該場氧化層102的上方表面上。其中該沉積的方法包括了物理沉積(PVD)法,如濺鍍(Sputtering)法,蒸鍍(Evaporation)法等方法;以及化學氣相沉積(CVD)法,如電漿輔助化學氣相沈積(PECVD)法以及有機金屬化學氣相沉積(MOCVD)法等方法。且在形成該選擇性閘極氧化層103後,接著再進行退火製程,係於攝氏溫度700℃、800℃、900℃等的溫度中進行退火。Further, as shown in FIG. 1D, a selective gate oxide layer 103 is deposited on the upper surface of the positive-type germanium semiconductor layer 101 and the field oxide layer 102. The method of depositing includes a physical deposition (PVD) method such as a sputtering method, an evaporation method, and a chemical vapor deposition (CVD) method such as plasma-assisted chemical vapor deposition ( Methods such as PECVD) and organometallic chemical vapor deposition (MOCVD). After the selective gate oxide layer 103 is formed, an annealing process is further performed, and annealing is performed at temperatures of 700 ° C, 800 ° C, and 900 ° C.
而如第2圖所示之金屬氧化物的組成表,於第1D圖所示之該選擇性閘極氧化層103係由不同的金屬氧化物以特定的比例所混合而成,其中包括了兩組金屬氧化物的組成表,第1組元素組成包括了鉿(Hafnium,Hf)金屬氧化物,鋁(Aluminium,Al)金屬氧化物,鉬(Molybdenum,Mo)金屬氧化物,以及鋯(Zirconium,Zr)金屬氧化物等所組成,且以M1為所組成的百分比,其範圍由0.1%~99.9%。而第2組元素的組成包括了釤(Samarium,Sm)金屬氧化物,釔(Yttrium,Y)金屬氧化物,釓(Gadolinium,Gd)金屬氧化物,以及鉺(Erbium,Er)金屬氧化物所組成,且以M2為所組成的百分比,其範圍由99.9%~0.1%。故而推導出下列的百分比數學式,由M1與M2的:M1+M2=100%As shown in FIG. 2, the selective gate oxide layer 103 shown in FIG. 1D is formed by mixing different metal oxides in a specific ratio, including two. The composition of the group of metal oxides, the first group of elements consists of hafnium (Hf) metal oxides, aluminum (Aluminium, Al) metal oxides, molybdenum (Mo) metal oxides, and zirconium (Zirconium, Zr) is composed of a metal oxide or the like and has a percentage of M1 as a composition, and ranges from 0.1% to 99.9%. The composition of the second group of elements includes Samarium (Sm) metal oxides, Yttrium (Y) metal oxides, Gadolinium (Gd) metal oxides, and Erbium (Er) metal oxides. The composition, and the percentage of M2, which ranges from 99.9% to 0.1%. Therefore, the following percentage mathematical formula is derived, from M1 and M2: M1+M2=100%
其中M1以及M2均是M1M2Ox中的金屬元素,其計算方式如:倘M1的比例是10%,則M2的比例就是90%。該金屬混合的方式包括利用雙極濺鍍(Dual Sputtering)或是以物理氣相沉積法(PVD)進行蒸鍍,以及利用原子層沉積技術(ALD)以及金屬有機氣相沉積技術(MOCVD)中的化學氣相沉積法(CVD)。而調整混合比例的方式,則可以藉由沉積時所使用的原料進行以調整。此外,其組成的比例為原子組成比例,即該化合物中M1及M2所佔的原子個數比例。Among them, M1 and M2 are metal elements in M1M2Ox, and the calculation method is as follows: If the ratio of M1 is 10%, the ratio of M2 is 90%. The metal mixing method includes double layer sputtering (Dual Sputtering) or vapor deposition by physical vapor deposition (PVD), and using atomic layer deposition (ALD) and metal organic vapor deposition (MOCVD). Chemical vapor deposition (CVD). The manner in which the mixing ratio is adjusted can be adjusted by the raw materials used in the deposition. Further, the proportion of the composition is the atomic composition ratio, that is, the ratio of the number of atoms occupied by M1 and M2 in the compound.
續如第1E圖所示,沉積一選擇性閘極金屬層104於該選擇性閘極氧化層103的上方表面上。其中該選擇性閘極金屬層104包括了氮化金屬閘極層,亦或是多層金屬閘極層。其中該氮化金屬層包括了氮化鉭(TaN),氮化鈦(TiN),以及氮化鉿(HfN);而多層金屬閘極層則包括了氮化鉭/鈦(TaN/Ti),氮化鉿/鈦(HfN/Ti),以及氮化鉿/鉭(HfN/Ta)。而通入氮氣的比例為:Continued as shown in FIG. 1E, a selective gate metal layer 104 is deposited on the upper surface of the selective gate oxide layer 103. The selective gate metal layer 104 includes a metal nitride gate layer or a multilayer metal gate layer. The metal nitride layer includes tantalum nitride (TaN), titanium nitride (TiN), and hafnium nitride (HfN); and the multilayer metal gate layer includes tantalum nitride/titanium (TaN/Ti). Niobium nitride/titanium (HfN/Ti), and tantalum nitride/niobium (HfN/Ta). The ratio of nitrogen gas is:
氮氣(N2 )/氬氣(Ar)+氮氣=0%~20%Nitrogen (N 2 ) / Argon (Ar) + Nitrogen = 0% ~ 20%
於沉積該選擇性閘極金屬層104時,其中的氮化金屬閘極層經由濺鍍的方式沉積,此時沉積時的製程壓力將控制在20毫托耳(mtorr),濺鍍時的能量則控制在150瓦。而濺鍍時的氬氣比例會控制在20 sccm,氮氣則會從0標準狀態毫升/分(sccm)調變至20標準狀態毫升/分。而當沉積多層金屬閘極層時,則是於前述的氮化金屬層下方,預先沉積一層純金屬層(如Ti、Ta、或是La),其中該純金屬層介於氮化金屬閘極層以及高介電係數氧化層中間。When the selective gate metal layer 104 is deposited, the metal nitride gate layer is deposited by sputtering, and the process pressure during deposition is controlled at 20 mTorr, and the energy during sputtering. Then control at 150 watts. The argon ratio at the time of sputtering is controlled at 20 sccm, and the nitrogen is adjusted from 0 standard state cc/min (sccm) to 20 standard cc/min. When depositing a plurality of metal gate layers, a layer of pure metal (such as Ti, Ta, or La) is deposited in advance under the metal nitride layer, wherein the pure metal layer is interposed between the metal gates. The layer and the middle of the high dielectric constant oxide layer.
又如第1F圖所示,進行光罩與蝕刻製程後,而形成包含有選擇性閘極氧化層103與閘極金屬層104的閘極500。Further, as shown in FIG. 1F, after the mask and the etching process are performed, the gate 500 including the selective gate oxide layer 103 and the gate metal layer 104 is formed.
再如第1G圖所示,進行離子植入法(implantion)以形成源極(Source)105與汲極(Drain)106。Further, as shown in FIG. 1G, ion implantation is performed to form a source 105 and a drain 106.
續如第1H圖所示,沉積一第二氧化層107於該場氧化層102,該閘極金屬層104,該源極105與該汲極106的上方表面上。Continued as shown in FIG. 1H, a second oxide layer 107 is deposited on the field oxide layer 102, the gate metal layer 104, the source electrode 105 and the upper surface of the drain 106.
又如第1I圖所示,進行光罩與蝕刻製程以形成閘極金屬層104的接觸孔(Contact hole)。Further, as shown in FIG. 1I, a mask and an etching process are performed to form a contact hole of the gate metal layer 104.
再如第1J圖所示,形成一金屬層以形成一金屬導線於該場氧化層,該閘極金屬層104,該源極105與該汲極106的上方表面上(圖中未示),並進行光罩與蝕刻製程後以形成一金屬導線108於該場氧化層102,該閘極金屬層104,該源極105與該汲極106的上方表面上。Further, as shown in FIG. 1J, a metal layer is formed to form a metal wire on the field oxide layer, the gate metal layer 104, the source electrode 105 and the upper surface of the drain electrode 106 (not shown). After the mask and the etching process, a metal wire 108 is formed on the field oxide layer 102, the gate metal layer 104, the source electrode 105 and the upper surface of the drain 106.
本發明係使用金屬閘極與氮化金屬閘極的功函數,藉由不同的氮氣流量和雙層金屬結構以調整金屬的功函數,可同時求得費米能階釘紮效應之數值(電子伏特),即本發明使用物理性分析,可將原始金屬材料功函數(initial metal work function)與以電性分析所萃取的等效金屬功函數(effective metal work function)進行比對,其如下關係式所表示:The invention uses the work function of the metal gate and the metal nitride gate, and the value of the Fermi level pinning effect can be simultaneously obtained by adjusting the work function of the metal by different nitrogen flow rates and double metal structures. Volt, ie, the physical analysis of the present invention, the original metal work function can be compared with the equivalent metal work function extracted by electrical analysis, as follows Expressed by:
Φm(initial) -Φm(effective) =Fermi-level pinning effectΦ m(initial) -Φ m(effective) =Fermi-level pinning effect
而經運算後即可得到費米能階釘紮效應之數值;故相較於傳統電晶體的效果,本發明可具有較好的效果。After the operation, the value of the Fermi level pinning effect can be obtained; therefore, the present invention can have a better effect than the effect of the conventional transistor.
以上所述僅為本發明之較佳實施例而已,並非用以限定本發明之申請專利範圍;凡其它未脫離本發明所揭示之精神下所完成之等效改變或修飾,均應包含在下述之申請專利範圍內。The above is only the preferred embodiment of the present invention, and is not intended to limit the scope of the present invention; all other equivalent changes or modifications which are not departing from the spirit of the present invention should be included in the following. Within the scope of the patent application.
101...正型矽半導體層101. . . Positive 矽 semiconductor layer
102...場氧化層102. . . Field oxide layer
103...選擇性閘極氧化層103. . . Selective gate oxide
104...閘極金屬層104. . . Gate metal layer
105...源極105. . . Source
106...汲極106. . . Bungee
107...第二氧化層107. . . Second oxide layer
108...金屬導線108. . . Metal wire
500...閘極500. . . Gate
第1A~1J圖所示係本發明一種形成具有穩定臨限電壓之電晶體的方法的連續示意圖。1A-1J is a continuous schematic diagram of a method of forming a transistor having a stable threshold voltage.
第2圖所示係本發明金屬氧化物的組成表。Fig. 2 is a table showing the composition of the metal oxide of the present invention.
101...正型矽半導體層101. . . Positive 矽 semiconductor layer
102...場氧化層102. . . Field oxide layer
103...選擇性閘極氧化層103. . . Selective gate oxide
104...閘極金屬層104. . . Gate metal layer
105...源極105. . . Source
106...汲極106. . . Bungee
107...第二氧化層107. . . Second oxide layer
108...金屬導線108. . . Metal wire
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