TW201508841A - Method for improving the electrical conductivity of metal oxide semiconductor layers - Google Patents
Method for improving the electrical conductivity of metal oxide semiconductor layers Download PDFInfo
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- 238000000034 method Methods 0.000 title claims abstract description 69
- 239000004065 semiconductor Substances 0.000 title claims abstract description 27
- 229910044991 metal oxide Inorganic materials 0.000 title abstract description 12
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- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
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- 230000001939 inductive effect Effects 0.000 claims description 3
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- 230000000694 effects Effects 0.000 description 5
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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- 229910052720 vanadium Inorganic materials 0.000 description 4
- 229910005191 Ga 2 O 3 Inorganic materials 0.000 description 3
- 229910052732 germanium Inorganic materials 0.000 description 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 238000000059 patterning Methods 0.000 description 3
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- 229920001621 AMOLED Polymers 0.000 description 2
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- 229910000449 hafnium oxide Inorganic materials 0.000 description 2
- WIHZLLGSGQNAGK-UHFFFAOYSA-N hafnium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Hf+4] WIHZLLGSGQNAGK-UHFFFAOYSA-N 0.000 description 2
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- 238000004528 spin coating Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- JUPQTSLXMOCDHR-UHFFFAOYSA-N benzene-1,4-diol;bis(4-fluorophenyl)methanone Chemical compound OC1=CC=C(O)C=C1.C1=CC(F)=CC=C1C(=O)C1=CC=C(F)C=C1 JUPQTSLXMOCDHR-UHFFFAOYSA-N 0.000 description 1
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- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- OFIYHXOOOISSDN-UHFFFAOYSA-N tellanylidenegallium Chemical compound [Te]=[Ga] OFIYHXOOOISSDN-UHFFFAOYSA-N 0.000 description 1
- 238000002207 thermal evaporation Methods 0.000 description 1
- RGGPNXQUMRMPRA-UHFFFAOYSA-N triethylgallium Chemical compound CC[Ga](CC)CC RGGPNXQUMRMPRA-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/66007—Multistep manufacturing processes
- H01L29/66075—Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials
- H01L29/66227—Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials the devices being controllable only by the electric current supplied or the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched, e.g. three-terminal devices
- H01L29/66409—Unipolar field-effect transistors
- H01L29/66477—Unipolar field-effect transistors with an insulated gate, i.e. MISFET
- H01L29/66742—Thin film unipolar transistors
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/78606—Thin film transistors, i.e. transistors with a channel being at least partly a thin film with supplementary region or layer in the thin film or in the insulated bulk substrate supporting it for controlling or increasing the safety of the device
- H01L29/78618—Thin film transistors, i.e. transistors with a channel being at least partly a thin film with supplementary region or layer in the thin film or in the insulated bulk substrate supporting it for controlling or increasing the safety of the device characterised by the drain or the source properties, e.g. the doping structure, the composition, the sectional shape or the contact structure
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/7869—Thin film transistors, i.e. transistors with a channel being at least partly a thin film having a semiconductor body comprising an oxide semiconductor material, e.g. zinc oxide, copper aluminium oxide, cadmium stannate
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- Computer Hardware Design (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Thin Film Transistor (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
Description
本揭示內容關於局部改善金氧半導體層之導電性的方法。 The present disclosure is directed to a method of locally improving the conductivity of a MOS layer.
本揭示內容進一步關於製作以金氧半導體為基礎的薄膜電晶體的方法。 The present disclosure further relates to a method of fabricating a metal oxide based thin film transistor.
非晶金氧半導體薄膜電晶體(Thin Film Transistor,TFT)(例如,舉例來說,非晶氧化銦鎵鋅(Amorphous Indium-Gallium-Zinc Oxide,a-IGZO)薄膜電晶體)已經被研究成為平板顯示器應用中以矽為基礎的TFT的潛在替代品,因為它們有更高的移動係數及較大區域均勻性。 Amorphous GaN thin film transistor (TFT) (for example, Amorphous Indium-Gallium-Zinc Oxide (a-IGZO) thin film transistor) has been studied as a flat panel. Potential replacements for germanium-based TFTs in display applications because of their higher mobility and greater area uniformity.
被當作主動式矩陣液晶顯示器中的切換裝置的習知非晶矽TFT的優點為具有大區域均勻性。然而,它們的場效移動係數(<1cm2/V.s)太低而無法驅動有機發光二極體(Organic Light-Emitting Diode,OLED)。 A conventional amorphous germanium TFT which is regarded as a switching device in an active matrix liquid crystal display has an advantage of having a large area uniformity. However, their field effect mobility coefficients (<1 cm 2 /Vs) are too low to drive an Organic Light-Emitting Diode (OLED).
相反地,目前被當作AMOLED顯示器中的切換裝置的高移動係數(>50cm2/V.s)的結晶p-Si TFT則在大尺寸的AMOLED顯示器中有場效移動係數與臨界電壓不均勻性的缺點。 Conversely, a high mobility factor is currently used as the switching device in an AMOLED display (> 50cm 2 / Vs) of the crystalline p-Si TFT have the threshold voltage of the field effect movement of non-uniformity coefficient AMOLED display a large size Disadvantages.
已知的底部閘極TFT結構和頂端閘極TFT結構並不適合使用在高解析度顯示器之中,因為它們有高寄生電容及不良的可縮性 (scalability)(大覆蓋範圍)。此些TFT結構中的高寄生電容和源極與閘極之間及/或汲極與閘極之間有重疊存在有關。此重疊係因為使用的電晶體閘極長度大於通道長度的關是,用以避免或限制在該閘極與源極和汲極之間有對齊偏差的負面結果。 Known bottom gate TFT structures and top gate TFT structures are not suitable for use in high resolution displays because of their high parasitic capacitance and poor shrinkability. (scalability) (large coverage). The high parasitic capacitance in such TFT structures is related to the presence of overlap between the source and the gate and/or between the drain and the gate. This overlap is due to the use of a transistor gate length greater than the channel length to avoid or limit the negative consequences of alignment misalignment between the gate and the source and drain.
所以,目前正在研發用於製造自我對齊頂端閘極氧化物TFT的方法,其中,源極與汲極會對齊閘極,且其中,該些TFT會有良好的電氣效能及很高的穩定性。已經有人記述過數種具有一氧化物半導體主動層的自我對齊頂端閘極結構,其中,該金氧半導體的導電性會在源極區與汲極區中局部地提高。 Therefore, a method for fabricating a self-aligned top gate oxide TFT is currently being developed in which a source and a drain are aligned with a gate, and wherein the TFTs have good electrical efficiency and high stability. Several self-aligned top gate structures having an active layer of an oxide semiconductor have been described in which the conductivity of the MOS is locally increased in the source and drain regions.
已經有數種方法被提出用以(局部地)提高金氧半導體材料的導電性。其中一種方式係藉由雜質(例如,硼、磷、或是砷)的離子植入達成的摻雜所組成。然而,在撓性基板上進行離子植入可能有困難,因為需要實施退火步驟以進行摻雜物活化,其通常係在高於450℃的溫度處進行。 Several methods have been proposed to (locally) increase the conductivity of oxy-semiconductor materials. One of these methods consists of doping by ion implantation of impurities such as boron, phosphorus, or arsenic. However, ion implantation on a flexible substrate can be difficult because an annealing step is required to perform dopant activation, which is typically performed at temperatures above 450 °C.
另一種方式係由實施氬電漿處置、氫電漿處置、或是NH3電漿處置所組成。然而,已經觀察到,此些經過電漿處置的源極區與汲極區的穩定性不佳,並且電漿處置的效應可能會因為整合OLED所需要的進一步處理步驟的結果而消失。 Another method consists of performing argon plasma treatment, hydrogen plasma treatment, or NH 3 plasma treatment. However, it has been observed that the stability of the source and drain regions of such plasma treatment is poor, and the effects of plasma treatment may disappear as a result of further processing steps required to integrate the OLED.
在US 2012/0001167中說明一種用以製作自我對齊金氧半導體薄膜電晶體的方法,其中,使用一種替代方法來局部地提高金氧半導體層的導電性。在沉積一金氧半導體層、一閘極絕緣體與一閘極電極之後會提供一由金屬(例如,Ti、Al、或是In)製成的金屬膜,該金屬膜的厚度為10nm或更小。接著,會在含氧的環境中實施熱處置,舉例來說,在300℃的溫度 處。由於此熱處置的關是,該金屬膜會被氧化。於該金屬膜的氧化反應中,該金氧半導體層的一源極區與一汲極區之中所包含的氧的一部分會被傳輸至該金屬膜。因為該源極區與該汲極區之中的氧濃度下降的關是,其會導致在該金氧半導體層的一上方部分中形成低阻區。該金屬膜的厚度較佳的係10nm或更小,俾使得該金屬膜可以在該熱處置期間於該含氧的環境中被完全氧化。依此方式,可以不需要實施蝕刻步驟來移除未被氧化的金屬。 A method for fabricating a self-aligned MOS film transistor is described in US 2012/0001167, wherein an alternative method is used to locally increase the conductivity of the MOS layer. After depositing a MOS layer, a gate insulator and a gate electrode, a metal film made of a metal (for example, Ti, Al, or In) having a thickness of 10 nm or less is provided. . Then, heat treatment is carried out in an oxygen-containing environment, for example, at a temperature of 300 ° C. At the office. Due to the thermal shutdown, the metal film is oxidized. In the oxidation reaction of the metal film, a portion of the oxygen contained in a source region and a drain region of the MOS layer is transferred to the metal film. Because of the decrease in oxygen concentration in the source region and the drain region, it results in the formation of a low resistance region in an upper portion of the MOS layer. The thickness of the metal film is preferably 10 nm or less, so that the metal film can be completely oxidized in the oxygen-containing environment during the heat treatment. In this manner, an etching step may not be required to remove the metal that is not oxidized.
在US 2012/0001167中所述的方法需要至少200℃的溫度, 舉例來說,300℃的大小。所以,此方法不相容於某些低成本的撓性基板,例如,舉例來說,PET(聚乙烯對苯二甲酸酯)、PEN(聚萘二甲酸乙二酯)、以及PC(聚碳酸酯),並且可能需要用到有高熱穩定性及/或化學穩定性之較高價格的塑膠薄片,例如,PI(聚亞醯胺)、PES(聚醚碸)、或是PEEK(聚醚醚酮)。 該方法還需要良好、精確的控制該金屬層的厚度,以便避免需要實施蝕刻步驟來移除未被氧化的金屬。 The method described in US 2012/0001167 requires a temperature of at least 200 ° C, For example, the size of 300 ° C. Therefore, this method is not compatible with certain low cost flexible substrates such as, for example, PET (polyethylene terephthalate), PEN (polyethylene naphthalate), and PC (poly) Carbonate) and may require the use of higher quality plastic sheets with high thermal stability and/or chemical stability, for example, PI (polyimide), PES (polyether oxime), or PEEK (polyether) Ether ketone). The method also requires good and precise control of the thickness of the metal layer in order to avoid the need to perform an etching step to remove the unoxidized metal.
本揭示內容的目的係提供一種局部地提高金氧半導體層的導電性的方法,其中,該高導電性有良好的溫度穩定性,且其中,該方法能夠在低於200℃的溫度處被實施。 It is an object of the present disclosure to provide a method of locally improving the electrical conductivity of a MOS layer, wherein the high conductivity has good temperature stability, and wherein the method can be implemented at a temperature lower than 200 ° C .
本揭示內容的進一步目的係提供一種製作具有良好源極接點與汲極接點、良好場效移動係數(舉例來說,高於10cm2/Vs)、良好熱穩定性、以及良好偏壓穩定性的自我對齊頂端閘極金氧半導體薄膜電晶體的方法,其中,該些電晶體能夠在低於200℃的溫度處被製作。 A further object of the present disclosure is to provide a good source contact and drain contact, good field effect shift coefficient (for example, above 10 cm 2 /Vs), good thermal stability, and good bias stability. A method of self-aligning a top gate MOS thin film transistor, wherein the transistors can be fabricated at temperatures below 200 °C.
本揭示內容關於一種在預設位置處改善金氧半導體層的導 電性的方法。該方法包括:在一基板上提供一金氧半導體層;以及藉由原子層沉積(Atomic Layer Deposition,ALD)在該金氧半導體層的頂端提供一金氧層,其中,該金氧層在該些預設位置處物理性接觸(也就是,藉由一直接物理性介面來介接)該金氧半導體層。 The present disclosure relates to a guide for improving a MOS layer at a predetermined position Electrical method. The method includes: providing a MOS layer on a substrate; and providing a gold oxide layer on top of the MOS layer by Atomic Layer Deposition (ALD), wherein the MOS layer is The MOS layer is physically contacted (ie, by a direct physical interface).
驚人的發現是,藉由ALD來沉積此金氧層會導致該金氧半導體層在該金氧層直接物理性接觸該金氧半導體層的位置處有高導電性。 It has been surprisingly discovered that depositing the gold oxide layer by ALD results in the gold oxide semiconductor layer having high conductivity at a location where the gold oxide layer is in direct physical contact with the gold oxide semiconductor layer.
於本揭示內容的實施例中,舉例來說,該金氧半導體層的厚度可以在10nm與100nm之間的範圍中,或者在11nm與99nm之間的範圍中,本揭示內容並不受限於此。 In an embodiment of the present disclosure, for example, the thickness of the MOS layer may be in a range between 10 nm and 100 nm, or in a range between 11 nm and 99 nm, the disclosure is not limited this.
於本揭示內容的實施例中,藉由原子層沉積來提供(舉例來說,沉積)金氧層可以在150℃與200℃之間的範圍中的某一溫度處進行。 In an embodiment of the present disclosure, providing (for example, depositing) a gold oxide layer by atomic layer deposition may be performed at a temperature in a range between 150 ° C and 200 ° C.
於本揭示內容的實施例中,該方法可以在該金氧半導體層的頂端提供該金氧層之前進一步包括:提供一包括鹼金屬(舉例來說,Li、Na、K、Rb、Cs、或是Fr之中的任一者或任何組合)或鹼土金屬(舉例來說,Be、Mg、Ca、Sr、Ba、或是Ra之中的任一者或任何組合)的還原層在該些預設位置處物理性接觸該金氧半導體層;在該還原層與該金氧半導體層之間誘發化學還原反應,舉例來說,藉由在20℃與200℃之間的範圍中的某一溫度處實施退火步驟;以及移除該還原層與該還原反應中的反應副產物,舉例來說,藉由在水或是酒精之中沖洗。 In an embodiment of the present disclosure, the method may further include: providing an alkali metal (for example, Li, Na, K, Rb, Cs, or a reduction layer of any one or any combination of Fr or alkaline earth metals (for example, any one or any combination of Be, Mg, Ca, Sr, Ba, or Ra) Setting a physical contact with the MOS layer; inducing a chemical reduction reaction between the reducing layer and the MOS layer, for example, by a temperature in a range between 20 ° C and 200 ° C An annealing step is performed; and the reducing layer and the reaction by-products in the reduction reaction are removed, for example, by rinsing in water or alcohol.
於本揭示內容的實施例中,舉例來說,該金氧半導體層可以包括氧化鎵銦鋅(GIZO或IGZO);以及舉例來說,該金氧層可以包括Al2O3。然而,本揭示內容並不受限於此。亦可以使用其它金氧半導體,例如,舉 例來說,ZnO、ZnSnO、InO、InZnSnO、LaInZnO、GaInO、HfInZnO、MgZnO、LaInZnO、TiO、TiInSnO、ScInZnO、以及SiInZnO與ZrInZnO、或是ZrZnSnO。亦可以使用其它金氧層,例如,舉例來說,HfO2、Ta2O5、ZrO2、或是Ga2O3。 In an embodiment of the present disclosure, for example, the MOS layer may include gallium indium zinc oxide (GIZO or IGZO); and, for example, the gold oxide layer may include Al 2 O 3 . However, the disclosure is not limited thereto. Other MOS semiconductors can also be used, such as, for example, ZnO, ZnSnO, InO, InZnSnO, LaInZnO, GaInO, HfInZnO, MgZnO, LaInZnO, TiO, TiInSnO, ScInZnO, and SiInZnO and ZrInZnO, or ZrZnSnO. Other gold oxide layers can also be used, such as, for example, HfO 2 , Ta 2 O 5 , ZrO 2 , or Ga 2 O 3 .
於該金氧層係一Al2O3層的本揭示內容的實施例中,該金氧層可以三甲基鋁和水(H2O)當作前軀體來沉積,或者,舉例來說,以三乙基鋁和水當作前軀體或是以三異丁基鋁和水當作前軀體來沉積。 In an embodiment of the present disclosure in which the gold oxide layer is an Al 2 O 3 layer, the gold oxide layer may be deposited as a precursor of trimethylaluminum and water (H 2 O), or, for example, Triethylaluminum and water are used as precursors or are deposited with triisobutylaluminum and water as precursors.
於本揭示內容的實施例中,當形成該金氧層時,不同的前軀體可以被混合或者可以交替使用不同的前軀體。 In embodiments of the present disclosure, when forming the gold oxide layer, different precursors may be mixed or different precursors may be used alternately.
本揭示內容還進一步關於一種製作自我對齊(其意義為源極與汲極會自我對齊閘極)頂端閘極(該閘極被提供在該金氧半導體層的頂端)金氧半導體薄膜電晶體的方法。該方法包括:提供一金氧半導體層於一基板上;沉積一閘極介電層於該金氧半導體層的頂端;沉積一閘極電極層於該閘極介電層上;圖樣化該閘極電極層與該閘極絕緣層,用以形成一閘極電極與一閘極絕緣體,從而在該金氧半導體層之中定義一通道區;圖樣化該金氧半導體層,從而在該金氧半導體層之中定義一源極區與一汲極區;以及藉由原子層沉積來沉積一金氧層,舉例來說,至少在該源極區與該汲極區之中,從而在該源極區之中與該汲極區之中該金氧層直接物理性接觸(也就是,藉由一直接物理性介面來介接)該金氧半導體層的地方提高該金氧半導體層的導電性。 The present disclosure is further directed to a fabrication of a self-aligned (meaning that the source and drain will self-align the gate) a top gate (the gate is provided at the top of the MOS layer) of a MOS film transistor method. The method includes: providing a MOS layer on a substrate; depositing a gate dielectric layer on top of the MOS layer; depositing a gate electrode layer on the gate dielectric layer; patterning the gate a pole electrode layer and the gate insulating layer for forming a gate electrode and a gate insulator, thereby defining a channel region in the MOS layer; patterning the MOS layer to thereby form the gold oxide Defining a source region and a drain region in the semiconductor layer; and depositing a gold oxide layer by atomic layer deposition, for example, at least in the source region and the drain region, thereby at the source The direct contact of the gold oxide layer in the polar region with the gold oxide layer (that is, the interface through a direct physical interface) increases the conductivity of the gold oxide semiconductor layer. .
該方法可以進一步包括:提供一介電層於該金氧層的頂端;形成通孔貫穿該介電層與該金氧層;以及以一金屬來填充該些通孔,用以形成一源極接點與一汲極接點。 The method may further include: providing a dielectric layer to the top of the gold oxide layer; forming a via hole penetrating the dielectric layer and the gold oxide layer; and filling the via holes with a metal to form a source The contact is connected to a bungee.
於本揭示內容的實施例中,該方法可以在該金氧半導體層的 頂端提供該金氧層之前進一步包括:提供一包括鹼金屬(舉例來說,Li、Na、K、Rb、Cs、或是Fr之中的任一者或任何組合)或鹼土金屬(舉例來說,Be、Mg、Ca、Sr、Ba、或是Ra之中的任一者或任何組合)的還原層在該些預設位置處物理性接觸該金氧半導體層;在該還原層與該金氧半導體層之間誘發化學還原反應,舉例來說,藉由在20℃與200℃之間的範圍中的某一溫度處實施退火步驟;以及移除該還原層與該還原反應中的反應副產物,舉例來說,藉由在水或是酒精之中沖洗。 In an embodiment of the present disclosure, the method may be in the MOS layer Further providing the gold oxide layer before the top portion further comprises: providing an alkali metal (for example, any one or any combination of Li, Na, K, Rb, Cs, or Fr) or an alkaline earth metal (for example, a reducing layer of any one or any combination of Be, Mg, Ca, Sr, Ba, or Ra) physically contacting the oxynitride layer at the predetermined positions; at the reducing layer and the gold Inducing a chemical reduction reaction between the oxygen semiconductor layers, for example, by performing an annealing step at a temperature in a range between 20 ° C and 200 ° C; and removing the reduced layer and the reaction pair in the reduction reaction The product, for example, is rinsed in water or alcohol.
本揭示內容的方法的優點是,能夠在低於200℃、或是低於 199℃、或是低於190℃、或是低於180℃、或是低於170℃、或是低於160℃的溫度處被實施。所以,該些方法相容於低成本的撓性基板,例如,舉例來說,PET(聚乙烯對苯二甲酸酯)、PEN(聚萘二甲酸乙二酯)、以及PC(聚碳酸酯)。 An advantage of the method of the present disclosure is that it can be below 200 ° C or below A temperature of 199 ° C, or less than 190 ° C, or less than 180 ° C, or less than 170 ° C, or less than 160 ° C is carried out. Therefore, the methods are compatible with low cost flexible substrates such as, for example, PET (polyethylene terephthalate), PEN (polyethylene naphthalate), and PC (polycarbonate). ).
本揭示內容的方法的優點是,比較不需要或是完全不需要如同在某些先前技術方式的情況般精確地控制層厚度。 An advantage of the method of the present disclosure is that it is relatively unnecessary or not necessary to precisely control the layer thickness as is the case with certain prior art approaches.
本揭示內容的方法的優點是,沉積該金氧層不僅造成下方的金氧半導體層有改善的導電性;此外,沉積該金氧層還會導致下方的金氧半導體層的鈍化與囊封(舉例來說,該金氧半導體層會完全被覆蓋或囊封,也就是,不再曝露於環境中)。 An advantage of the method of the present disclosure is that depositing the gold oxide layer not only results in improved conductivity of the underlying gold oxide semiconductor layer; in addition, depositing the gold oxide layer results in passivation and encapsulation of the underlying gold oxide semiconductor layer ( For example, the MOS layer will be completely covered or encapsulated, that is, no longer exposed to the environment).
本揭示內容的方法的優點是,它們會導致該金氧半導體層的高導電性的良好穩定性;該高導電性不會隨著時間經過而改變。 An advantage of the methods of the present disclosure is that they result in good stability of the high electrical conductivity of the MOS layer; this high conductivity does not change over time.
本揭示內容的方法的優點是,它們允許製作具有良好偏壓穩 定性且具有良好熱穩定性的自我對齊頂端閘極金氧半導體薄膜電晶體。 An advantage of the method of the present disclosure is that they allow for good bias stability Self-aligned top gate MOS thin film transistor that is qualitative and has good thermal stability.
本文中已於上面說明本發明的各種創新觀點的特定目的與 優點。當然,應該瞭解的是,未必所有此些目的或優點皆可根據本揭示內容的任何特殊實施例來達成。因此,舉例來說,熟習本技術的人士便會明瞭,本揭示內容可以達成或最佳化如本文中所教示之其中一項優點或一群優點但未必達成可能如本文中所教示或建議之其它目的或優點的方式來具現或實現。進一步言之,應該瞭解的是,【發明內容】僅為範例而沒有限制本揭示內容之範疇的用意。參考下面的詳細說明,在閱讀時配合隨附的圖式,可以最佳瞭解本揭示內容(組織及其運作方法)及其特點與優點。 The specific objects and advantages of various innovative aspects of the present invention have been described hereinabove. It should be understood, of course, that not necessarily all such objects or advantages may be achieved in accordance with any particular embodiment of the present disclosure. Thus, for example, those skilled in the art will appreciate that the present disclosure may achieve or optimize one of the advantages or a group of advantages as taught herein, but does not necessarily achieve other possibilities that may be as taught or suggested herein. The purpose or advantage of the way to achieve or achieve. Further, it should be understood that the summary is merely exemplary and not intended to limit the scope of the disclosure. With reference to the detailed description below, it is best to understand the disclosure (organization and its method of operation) and its features and advantages when reading with the accompanying drawings.
10‧‧‧基板 10‧‧‧Substrate
11‧‧‧主動層 11‧‧‧Active layer
12‧‧‧金氧半導體層 12‧‧‧Gold-oxide semiconductor layer
13‧‧‧閘極介電層 13‧‧‧ gate dielectric layer
14‧‧‧閘極電極層 14‧‧‧ gate electrode layer
15‧‧‧金氧層 15‧‧‧Gold oxygen layer
16‧‧‧介電層 16‧‧‧Dielectric layer
21‧‧‧源極電極 21‧‧‧Source electrode
22‧‧‧汲極電極 22‧‧‧汲electrode
101‧‧‧矽基板 101‧‧‧矽 substrate
102‧‧‧介電層 102‧‧‧ dielectric layer
110‧‧‧通道區 110‧‧‧Channel area
111‧‧‧源極區 111‧‧‧ source area
112‧‧‧汲極區 112‧‧‧Bungee Area
131‧‧‧閘極絕緣體 131‧‧‧gate insulator
141‧‧‧閘極電極 141‧‧‧gate electrode
圖1(a)至圖1(f)所示的係根據本揭示內容的一種方法來製作金氧半導體薄膜電晶體的方法。 1(a) to 1(f) show a method of fabricating a gold oxide semiconductor thin film transistor according to a method of the present disclosure.
圖2所示的係根據本揭示內容的一種方法所製作的a-IGZO薄膜電晶體的轉換特徵曲線(IDS-VGS)。 2 is a conversion characteristic curve (I DS -V GS ) of an a-IGZO thin film transistor fabricated according to a method of the present disclosure.
圖3所示的係根據本揭示內容的一種方法所製作的a-IGZO薄膜電晶體的輸出特徵曲線(IDS-VDS)。 Figure 3 shows an output characteristic curve (I DS - V DS ) of an a-IGZO thin film transistor fabricated according to a method of the present disclosure.
圖4所示的係根據本揭示內容的一種方法所製作的a-IGZO TFT(W/L=30/10μm/μm)在不同的偏壓應力(bias stress)時間中的轉換特徵曲線(IDS-VGS):圖4(a)為-1MV/cm(VGS=-12V且VDS=0V)的負偏壓應力;圖4(b)為+1MV/cm(VGS=+12V且VDS=+12V)的正偏壓應力。 4 is a conversion characteristic curve (I DS ) of a-IGZO TFT (W/L=30/10 μm/μm) produced according to a method of the present disclosure at different bias stress times. -V GS ): Figure 4(a) is the negative bias stress of -1 MV/cm (V GS = -12 V and V DS =0 V); Figure 4 (b) is +1 MV/cm (V GS = +12 V and Positive bias stress of V DS = +12 V).
圖5所示的係根據本揭示內容的一種方法所製作的a-IGZO TFT的VTH 偏移在正向與負向中以應力時間為函數的關係圖。 Figure 5 is a graph of the VTH shift of an a-IGZO TFT fabricated in accordance with a method of the present disclosure as a function of stress time in the forward and negative directions.
圖6所示的係一a-IGZO TFT(W/L=30/10μm/μm)的初始轉換特徵曲線(空心圓)以及在150℃處於氮氣中進行2小時退火之後的轉換特徵曲線(實心方形)。 Figure 6 shows the initial conversion characteristic curve (open circles) of an a-IGZO TFT (W/L = 30/10 μm/μm) and the conversion characteristic curve after a 2 hour annealing at 150 ° C in nitrogen (solid square) ).
申請專利範圍中的任何元件符號皆不被視為限至本揭示內容的範疇。 Any component symbols in the scope of the patent application are not considered to be limited to the scope of the present disclosure.
在不同的圖式中,相同的元件符號表示相同或類似的元件。 In the different figures, the same element symbols indicate the same or similar elements.
在下面的詳細說明中會提出許多明確的細節,以便透澈理解本揭示內容以及如何在特殊實施例中實行本揭示內容。然而,應該瞭解的是,即使沒有此些特定細節仍可實行本揭示內容。於其它實例中不會詳細說明眾所熟知的方法、程序、以及技術,以免混淆本揭示內容。 In the following detailed description, numerous specific details are set forth However, it should be understood that the present disclosure may be practiced without such specific details. The methods, procedures, and techniques that are well known will not be described in detail in other examples, so as not to obscure the present disclosure.
雖然本揭示內容配合特殊實施例並且參考特定圖式來作說明;但是,本揭示內容並不受限於此。本文中所包含及說明的圖式為略圖並且沒有限制本揭示內容的範疇。還應該注意的是,在圖式中,為達解釋之目的,某些元件的大小可能會被放大,且所以並未依照比例繪製。 The disclosure is described with respect to particular embodiments and with reference to specific drawings; however, the disclosure is not limited thereto. The drawings contained and illustrated herein are illustrative and not limiting of the scope of the disclosure. It should also be noted that in the drawings, the size of some of the elements may be exaggerated for the purpose of explanation and are not drawn to scale.
再者,說明中的第一、第二、第三、以及類似詞係用來區分雷同的元件而未必依照等級或任何其它方式來說明時間或空間的順序。應該瞭解的是,所使用的該些術語可在適當的情況下交換使用而且本文中所述之揭示內容的實施例能夠以本文中所述或所示以外的其它順序來運作。 Furthermore, the first, second, third, and similar words in the description are used to distinguish the same elements and do not necessarily indicate the order of time or space according to the level or any other manner. It will be appreciated that the terms used may be used interchangeably, where appropriate, and that the embodiments of the disclosure described herein can operate in other sequences than those described or illustrated herein.
又,說明中的頂端、底部、之上、之下、以及類似詞係作為說明的用途而未必說明相對的位置。應該瞭解的是,所使用的該些術語可在適當的情況下交換使用而且本文中所述之揭示內容的實施例能夠以本文 中所述或所示以外的其它方位來運作。 Further, the top, bottom, over, under, and similar words in the description are for illustrative purposes and do not necessarily indicate relative positions. It will be appreciated that the terms used may be used interchangeably where appropriate and that embodiments of the disclosure described herein can be used herein. Operates in other orientations than those described or illustrated.
本揭示內容提供一種改善(提高)金氧半導體層之導電性的方法,舉例來說,在一金氧半導體薄膜電晶體的源極接點與汲極接點的位置處局部改善此些層的導電性。導電性的提高可以很明顯,舉例來說,至少提高1個大小等級,舉例來說,高達3個大小等級。 The present disclosure provides a method of improving (improving) the conductivity of a MOS layer, for example, locally improving the layers at a source contact and a drain contact of a MOS film transistor Electrical conductivity. The increase in conductivity can be significant, for example, by at least one size rating, for example, up to three size classes.
根據本揭示內容的一項觀點,提供一種在預設位置處提高金氧半導體層的導電性的方法,其中,該方法包括:藉由原子層沉積在該些預設位置處沉積一金氧層於該金氧半導體層的頂端並且物理性接觸(因而介接)該金氧半導體層。 According to an aspect of the present disclosure, there is provided a method of improving conductivity of a MOS layer at a predetermined position, wherein the method comprises: depositing a gold oxide layer at the predetermined locations by atomic layer deposition At the top end of the MOS layer and physically contacting (and thus interposing) the MOS layer.
驚人的發現是,藉由ALD來沉積此金氧層會導致該金氧半導體層在該金氧層直接物理性接觸該金氧半導體層的位置處有高導電性。 It has been surprisingly discovered that depositing the gold oxide layer by ALD results in the gold oxide semiconductor layer having high conductivity at a location where the gold oxide layer is in direct physical contact with the gold oxide semiconductor layer.
舉例來說,該金氧層會包括Al2O3、HfO2、Ta2O5、ZrO2、或是Ga2O3,但是本發明並不受限於此。 For example, the gold oxide layer may include Al 2 O 3 , HfO 2 , Ta 2 O 5 , ZrO 2 , or Ga 2 O 3 , but the invention is not limited thereto.
於本揭示內容的實施例中,舉例來說,該金氧層可以為一Al2O3層。舉例來說,其可以三甲基鋁(TMA,Al(CH3)3)和水(H2O)當作前軀體來沉積。然而,亦可以使用其它前軀體,例如,舉例來說,以三乙基鋁和水當作前軀體或是以三異丁基鋁和水當作前軀體來形成一Al2O3層。 In an embodiment of the present disclosure, for example, the gold oxide layer may be an Al 2 O 3 layer. For example, it can be deposited as a precursor of trimethylaluminum (TMA, Al(CH 3 ) 3 ) and water (H 2 O). However, other precursors may also be used, such as, for example, triethylaluminum and water as precursors or triisobutylaluminum and water as precursors to form an Al 2 O 3 layer.
於本揭示內容的實施例中,舉例來說,該金氧層可以為一Ga2O3層。舉例來說,可用於此層的前軀體包括三乙基鎵和水、三甲基鎵和水、三異丙基鎵和水、或是三-第三丁基鎵和水,但是本發明並不受限於此。 In an embodiment of the present disclosure, for example, the gold oxide layer may be a Ga 2 O 3 layer. For example, precursors useful in this layer include triethylgallium and water, trimethylgallium and water, triisopropylgallium and water, or tri-tertiary butylgallium and water, but the present invention Not limited to this.
於本揭示內容的實施例中,當形成該金氧層時,不同的前軀體可以被混合或者可以交替使用不同的前軀體。 In embodiments of the present disclosure, when forming the gold oxide layer, different precursors may be mixed or different precursors may be used alternately.
舉例來說,該金氧層的厚度可以在10nm與100nm之間的範圍中,而且舉例來說,其可以在150℃與200℃之間的範圍中的某一溫度處被沉積,舉例來說,在150℃與170℃之間,但是本發明並不受限於此。 For example, the thickness of the gold oxide layer may be in the range between 10 nm and 100 nm, and for example, it may be deposited at a temperature in the range between 150 ° C and 200 ° C, for example , between 150 ° C and 170 ° C, but the invention is not limited thereto.
本揭示內容的方法能夠有利地使用在具有一金氧半導體主動層的薄膜電晶體的製作過程中,用以局部地提高對應於源極區與汲極區的預設位置處的導電性,從而改善來自該些源極接點與汲極接點的電荷射出。該方法能夠有利地使用在自我對齊頂端閘極薄膜電晶體的製作過程中。 The method of the present disclosure can be advantageously used in the fabrication of a thin film transistor having a MOS active layer to locally increase the conductivity at a predetermined position corresponding to the source region and the drain region, thereby The charge emission from the source contacts and the drain contacts is improved. This method can be advantageously used in the fabrication of self-aligned top gate thin film transistors.
該方法亦可以使用在其它以金氧半導體為基礎的裝置(舉例來說,二極體或電晶體-二極體)的製作過程中,用以改善來自接點處的電荷射出。 The method can also be used in the fabrication of other MOS-based devices (for example, diodes or transistor-diodes) to improve charge emission from the contacts.
舉例來說,該金氧半導體層能夠包括氧化鎵銦鋅(GIZO或者亦稱為IGZO),或是以其它金屬氧化物為基礎的半導體,舉例來說,下面的組合物(其並沒有理想配比指示):ZnO、ZnSnO、InO、InZnSnO、LaInZnO、GaInO、HfInZnO、MgZnO、LaInZnO、TiO、TiInSnO、ScInZnO、SiInZnO、以及ZrInZnO、ZrZnSnO。然而,本揭示內容並不受限於此,而且該方法能夠用於熟習本技術的人士已知的其它合宜金氧半導體。具有介於5nm與50nm之間,或是介於6nm與49nm之間,的典型厚度的半導體層能夠藉由許多方法來提供,例如,舉例來說,濺鍍、熱蒸發、脈衝式雷射沉積、以及旋鑄(spin casting)、噴墨印刷、或是滴鑄(drop casting)前軀體溶液。 For example, the MOS layer can include gallium indium zinc oxide (GIZO or IGZO), or a semiconductor based on other metal oxides, for example, the following composition (which is not ideal) Ratio indication): ZnO, ZnSnO, InO, InZnSnO, LaInZnO, GaInO, HfInZnO, MgZnO, LaInZnO, TiO, TiInSnO, ScInZnO, SiInZnO, and ZrInZnO, ZrZnSnO. However, the present disclosure is not limited thereto, and the method can be applied to other suitable gold oxide semiconductors known to those skilled in the art. A semiconductor layer having a typical thickness between 5 nm and 50 nm, or between 6 nm and 49 nm, can be provided by a number of methods such as, for example, sputtering, thermal evaporation, pulsed laser deposition. And spin casting, inkjet printing, or drop casting of the precursor solution.
本文進一步說明一種用於製作自我對齊頂端閘極金氧半導體薄膜電晶體的方法,其中,本揭示內容的方法被用來局部改善源極區與汲極區之中的金氧半導體層的導電性。於此裝置結構中,該ALD金氧層會 改變下方源極區與汲極區的導電性,並且其還具有一鈍化與囊封層的功能。 Further described herein is a method for fabricating a self-aligned top gate MOS thin film transistor, wherein the method of the present disclosure is used to locally improve the conductivity of the MOS layer in the source and drain regions. . In the structure of the device, the ALD metal oxide layer The conductivity of the lower source region and the drain region is changed, and it also has a function of passivation and encapsulation layer.
在圖1(a)至圖1(f)中概略圖解根據本揭示內容的一種用於製作金氧半導體薄膜電晶體的示範性製程流程。 An exemplary process flow for fabricating a MOS thin film transistor in accordance with the present disclosure is schematically illustrated in FIGS. 1(a) through 1(f).
在圖1(a)中所示的第一步驟中,一金氧半導體層12(例如,一GIZO層)被提供在一基板10上,舉例來說,藉由從一前軀體溶液中進行濺鍍、雷射燒蝕、或是旋塗。於圖1(a)中所示的範例中,基板10雖然包括一矽基板101與一介電層102(舉例來說,氧化矽層);然而,亦可以使用其它合宜的基板。舉例來說,GIZO層12的厚度大小為約10nm或約15nm至20nm,舉例來說,介於10nm與20nm之間,或是介於11nm與19nm之間;但是,亦能夠使用其它合宜的厚度。 In the first step shown in Fig. 1(a), a oxynitride layer 12 (e.g., a GIZO layer) is provided on a substrate 10, for example, by sputtering from a precursor solution. Plating, laser ablation, or spin coating. In the example shown in FIG. 1(a), the substrate 10 includes a germanium substrate 101 and a dielectric layer 102 (for example, a hafnium oxide layer); however, other suitable substrates may be used. For example, the thickness of the GIZO layer 12 is about 10 nm or about 15 nm to 20 nm, for example, between 10 nm and 20 nm, or between 11 nm and 19 nm; however, other suitable thicknesses can also be used. .
接著,如圖1(b)中所示,一閘極介電層13(例如,舉例來說,二氧化矽層)被沉積在該金氧半導體層12的頂端,舉例來說,藉由電漿增強化學氣相沉積。其後會沉積一閘極電極層14(例如,舉例來說,Mo層)於該閘極介電層13的頂端(圖1(b))。 Next, as shown in FIG. 1(b), a gate dielectric layer 13 (for example, a hafnium oxide layer) is deposited on top of the MOS layer 12, for example, by electricity. Slurry enhanced chemical vapor deposition. Thereafter, a gate electrode layer 14 (for example, a Mo layer) is deposited on the top end of the gate dielectric layer 13 (Fig. 1(b)).
閘極電極層14與閘極絕緣層13接著會被圖樣化,舉例來說,藉由乾式蝕刻,用以形成一閘極電極141與一閘極絕緣體131,如圖1(c)中所示。 The gate electrode layer 14 and the gate insulating layer 13 are then patterned, for example, by dry etching to form a gate electrode 141 and a gate insulator 131, as shown in FIG. 1(c). .
接著,該金氧半導體層12會被圖樣化,從而定義該薄膜電晶體的主動層11(圖1(d))。舉例來說,該金氧半導體層能夠藉由濕式蝕刻被圖樣化,舉例來說,利用緩衝式HF或草酸。在主動層圖樣化中使用草酸的優點係其對下方的層有良好的選擇性。經圖樣化的閘極電極141會在主動層11之中定義一通道區110、一源極區111、以及一汲極區112,如圖1(d) 中概略顯示。該些源極區與汲極區直接相鄰於該通道區並且自我對齊。 Next, the MOS layer 12 is patterned to define the active layer 11 of the thin film transistor (Fig. 1 (d)). For example, the MOS layer can be patterned by wet etching, for example, using buffered HF or oxalic acid. The advantage of using oxalic acid in active layer patterning is that it has good selectivity for the underlying layer. The patterned gate electrode 141 defines a channel region 110, a source region 111, and a drain region 112 among the active layers 11, as shown in FIG. 1(d). The outline is shown. The source and drain regions are directly adjacent to the channel region and self-aligned.
於圖1中所示的範例中,該金氧半導體層雖然係在該閘極電極層與該閘極介電層圖樣化之後才被圖樣化;然而,本揭示內容並不受限於此。舉例來說,該金氧半導體層亦能夠在該閘極製作過程之前先被圖樣化,或是在該閘極製作過程之後的某一較晚階段中才被圖樣化。 In the example shown in FIG. 1, the MOS layer is patterned after the gate electrode layer and the gate dielectric layer are patterned; however, the disclosure is not limited thereto. For example, the MOS layer can also be patterned prior to the gate fabrication process or patterned at a later stage after the gate fabrication process.
接著,一金氧層15(例如,舉例來說,Al2O3層)會藉由ALD(舉例來說,利用三甲基鋁(TMA,Al(CH3)3)和水(H2O)當作前軀體)被沉積(如圖1(e)中所示)。驚人的發現是,沉積此層會導致該金氧半導體層在該Al2O3層15直接物理性接觸該金氧半導體層11的位置處有高導電性。所以,在該金氧半導體層11的源極區111與汲極區112中會達成強化的導電性,至少在該金氧半導體層的一上方部分中。相信,因為該些ALD前軀體與該金氧半導體層表面之間的相互作用的關係會有一種摻雜效應或還原反應。舉例來說,在Al2O3中作為ALD前軀體的TMA和H2O可以和IGZO表面反應。舉例來說,倘若在該反應中有H2O、O2、O3的話,摻雜效應便會發生。該上方部分較佳的係具有數nm上至10或約10nm的深度/厚度。倘若該ALD金氧沉積結合額外的摻雜的話(舉例來說,利用Ca,參見上文),那麼,該增強的導電性預期會更深入延伸至該金氧半導體層之中,舉例來說,上至數十nm,舉例來說,上至20nm或是上至30nm。 Next, a gold oxide layer 15 (for example, an Al 2 O 3 layer) will be formed by ALD (for example, using trimethylaluminum (TMA, Al(CH 3 ) 3 )) and water (H 2 O). ) is deposited as a precursor (as shown in Figure 1(e)). A surprising finding is that depositing this layer results in a high conductivity of the MOS layer at the location where the Al 2 O 3 layer 15 is in direct physical contact with the MOS layer 11. Therefore, enhanced conductivity is achieved in the source region 111 and the drain region 112 of the MOS layer 11, at least in an upper portion of the MOS layer. It is believed that there is a doping effect or a reduction reaction due to the interaction between the ALD precursors and the surface of the oxynitride layer. For example, TMA and H 2 O, which are ALD precursors in Al 2 O 3 , can react with the IGZO surface. For example, if H 2 O, O 2 , O 3 are present in the reaction, a doping effect will occur. The upper portion preferably has a depth/thickness of from several nanometers up to 10 or about 10 nm. If the ALD gold oxide is combined with additional doping (for example, using Ca, see above), then the enhanced conductivity is expected to extend deeper into the MOS layer, for example, Up to tens of nm, for example, up to 20 nm or up to 30 nm.
接著,一介電層16(例如,舉例來說,氮化矽層)會被提供在該金氧層15的頂端,接著會在要形成源極接點與汲極接點的位置處形成通孔貫穿此介電層16與下方的金氧層15。接著會以一合宜的金屬(例如,舉例來說,Mo)來填充該些通孔,用以形成一源極電極21與一汲極電極22。 所生成的結構概略地顯示在圖1(f)中。 Next, a dielectric layer 16 (for example, a tantalum nitride layer) is provided on the top end of the gold oxide layer 15 and then formed at a position where the source contact and the drain contact are to be formed. A hole penetrates through the dielectric layer 16 and the underlying gold oxide layer 15. The vias are then filled with a suitable metal (e.g., Mo) for forming a source electrode 21 and a drain electrode 22. The resulting structure is schematically shown in Figure 1 (f).
圖2所示的係根據如上面所述的本揭示內容的一種方法所製作的a-IGZO薄膜電晶體的轉換特徵曲線(IDS-VGS),其具有一ALD Al2O3金氧層15。圖3所示的係此電晶體的輸出特徵曲線(IDS-VDS)。 2 is a conversion characteristic curve (I DS -V GS ) of an a-IGZO thin film transistor fabricated according to a method of the present disclosure as described above, having an ALD Al 2 O 3 gold oxide layer 15. Figure 3 shows the output characteristic curve (I DS - V DS ) of this transistor.
該a-IGZO TFT呈現高熱穩定性及良好的電氣效能。從圖中會觀察到14.82cm2/V.S的場效移動係數,3.6V的臨界電壓,0.42V/dec的次臨界擺動,以及約108的導通/不導通電流比。 The a-IGZO TFT exhibits high thermal stability and good electrical performance. From the figure, a field effect shift coefficient of 14.82 cm 2 /VS, a threshold voltage of 3.6 V, a subcritical swing of 0.42 V/dec, and a turn-on/non-conduction current ratio of about 10 8 are observed.
本發明已研究過偏壓應力對TFT電氣效能的影響。一對應於正向與負向中+/-1.0MV/cm的閘極電場在黑暗的室溫中被施加長達104秒的應力時間。倘若為正閘極偏壓應力的話,其對應於完全導通條件(VDS=12V且VGS=12V),會觀察到0.8V的臨界電壓偏移。倘若為負偏壓應力的話(VDS=0V且VGS=-12V),會觀察到1.0V的臨界電壓偏移。圖4(a)與圖4(b)顯示負閘極偏壓應力(圖4(a))與正閘極偏壓應力(圖4(b))兩者在下面不同的偏壓應力時間中的轉換特徵曲線:0s(也就是,沒有偏壓應力)、100s、300s、1000s、3000s、以及10000s。圖5所示的係在正向與負向中以應力時間為函數的VTH偏移。從此些結果中得到的結論為,在各種應力條件下的穩定性非常好。 The effect of bias stress on the electrical performance of a TFT has been studied in the present invention. Corresponding to a positive and negative / cm gate electric field is applied for up to 104 seconds of stress at the time in a dark room temperature to +/- 1.0MV. In the case of a positive gate bias stress, which corresponds to a full turn-on condition (V DS = 12 V and V GS = 12 V), a threshold voltage shift of 0.8 V is observed. If it is a negative bias stress (V DS =0V and V GS = -12V), a critical voltage offset of 1.0V is observed. Figure 4(a) and Figure 4(b) show that both the negative gate bias stress (Figure 4(a)) and the positive gate bias stress (Figure 4(b)) are in different bias stress times below. Conversion characteristic curve: 0s (that is, no bias stress), 100s, 300s, 1000s, 3000s, and 10000s. Figure 5 shows the VTH offset as a function of stress time in the positive and negative directions. The conclusions obtained from these results are that the stability under various stress conditions is very good.
圖6所示的係一a-IGZO TFT(W/L=30/10μm/μm)的初始轉換特徵曲線(空心圓)以及在150℃處於氮氣中進行2小時退火之後的轉換特徵曲線(實心方形)。從此些結果中可以得到的結論為,退火步驟對裝置特徵曲線的效應可以忽略,其表示有良好的熱穩定性。 Figure 6 shows the initial conversion characteristic curve (open circles) of an a-IGZO TFT (W/L = 30/10 μm/μm) and the conversion characteristic curve after a 2 hour annealing at 150 ° C in nitrogen (solid square) ). It can be concluded from these results that the effect of the annealing step on the characteristic curve of the device is negligible, which indicates good thermal stability.
前面的說明雖然詳述本揭示內容的特定實施例;然而,應該明白的是,不論前面的文字敘述如何詳細,本揭示內容皆可以許多方式來 實行。應該注意的是,當說明本揭示內容的特定特點與觀點時使用特殊的術語不應被視為隱喻該術語於本文中被重新定義為僅限包含本揭示內容中和該術語相關聯的特點或觀點的特定特徵。 The foregoing description details specific embodiments of the present disclosure; however, it should be understood that the present disclosure may be in many ways, no matter how detailed the preceding text is. Implemented. It should be noted that the use of specific terms when describing specific features and aspects of the present disclosure should not be considered as a metaphor. The term is redefined herein to include only the features associated with the term in this disclosure or Specific characteristics of the point of view.
雖然上面的詳細說明已經顯示、說明、並且指出套用於各種實施例中之本發明的觀點的新穎特點;但是,應該瞭解的是,熟習本技術的人士便可以對文中所示的裝置或製程的形式與細節進行各種省略、替換、以及改變,其並沒有脫離本發明的觀點的上位概念。 Although the above detailed description has shown, illustrated, and pointed out the novel features of the aspects of the present invention in various embodiments, it should be understood that those skilled in the art can The form and details are subject to various omissions, substitutions, and changes,
10‧‧‧基板 10‧‧‧Substrate
11‧‧‧主動層 11‧‧‧Active layer
15‧‧‧金氧層 15‧‧‧Gold oxygen layer
16‧‧‧介電層 16‧‧‧Dielectric layer
21‧‧‧源極電極 21‧‧‧Source electrode
22‧‧‧汲極電極 22‧‧‧汲electrode
101‧‧‧矽基板 101‧‧‧矽 substrate
102‧‧‧介電層 102‧‧‧ dielectric layer
131‧‧‧閘極絕緣體 131‧‧‧gate insulator
141‧‧‧閘極電極 141‧‧‧gate electrode
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TWI613706B (en) * | 2015-07-03 | 2018-02-01 | 友達光電股份有限公司 | Oxide semiconductor thin film transistor and manufacturing method thereof |
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EP3136446A1 (en) | 2015-08-28 | 2017-03-01 | Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO | Tft device and manufacturing method |
US20200035717A1 (en) * | 2018-07-26 | 2020-01-30 | Sharp Kabushiki Kaisha | Thin film transistor substrate and method of producing thin film transistor substrate |
JP2021128978A (en) * | 2020-02-12 | 2021-09-02 | 株式会社ジャパンディスプレイ | Semiconductor device and manufacturing method for the same |
KR20230061713A (en) | 2021-10-29 | 2023-05-09 | (주) 예스티 | High pressure annealing process for metal oxides |
KR102697352B1 (en) * | 2021-12-06 | 2024-08-21 | 연세대학교 산학협력단 | Method for manufacturing oxide thin film transistor |
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KR100858821B1 (en) * | 2007-05-11 | 2008-09-17 | 삼성에스디아이 주식회사 | Thin film transistor, method of manufacturing the same, organic light emitting display apparatus comprising the thin film transistor and method of manufacturing the same |
US20090230389A1 (en) * | 2008-03-17 | 2009-09-17 | Zhizhang Chen | Atomic Layer Deposition of Gate Dielectric Layer with High Dielectric Constant for Thin Film Transisitor |
JP5584960B2 (en) * | 2008-07-03 | 2014-09-10 | ソニー株式会社 | Thin film transistor and display device |
JP5708910B2 (en) * | 2010-03-30 | 2015-04-30 | ソニー株式会社 | THIN FILM TRANSISTOR, MANUFACTURING METHOD THEREOF, AND DISPLAY DEVICE |
JP5604938B2 (en) * | 2010-03-31 | 2014-10-15 | 凸版印刷株式会社 | Thin film transistor and manufacturing method thereof |
JP2012015436A (en) | 2010-07-05 | 2012-01-19 | Sony Corp | Thin film transistor and display device |
JP2014507794A (en) * | 2010-12-30 | 2014-03-27 | ジュスン エンジニアリング カンパニー リミテッド | Thin film transistor and manufacturing method thereof |
US8716073B2 (en) * | 2011-07-22 | 2014-05-06 | Semiconductor Energy Laboratory Co., Ltd. | Method for processing oxide semiconductor film and method for manufacturing semiconductor device |
CN102969362B (en) * | 2011-09-01 | 2016-03-30 | 中国科学院微电子研究所 | high stability amorphous metal oxide TFT device |
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TWI613706B (en) * | 2015-07-03 | 2018-02-01 | 友達光電股份有限公司 | Oxide semiconductor thin film transistor and manufacturing method thereof |
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CN105409003A (en) | 2016-03-16 |
CN105409003B (en) | 2019-03-08 |
JP2016527719A (en) | 2016-09-08 |
WO2015010825A1 (en) | 2015-01-29 |
TWI660432B (en) | 2019-05-21 |
KR20160034262A (en) | 2016-03-29 |
JP6426177B2 (en) | 2018-11-21 |
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