JP2021002633A - Oxide semiconductor processing method and thin film transistor manufacturing method - Google Patents
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 274
- 238000003672 processing method Methods 0.000 title claims abstract description 14
- 239000010409 thin film Substances 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 claims abstract description 45
- 239000000758 substrate Substances 0.000 claims abstract description 29
- 238000012545 processing Methods 0.000 claims abstract description 24
- 238000000992 sputter etching Methods 0.000 claims abstract description 17
- 238000002441 X-ray diffraction Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 7
- 238000003475 lamination Methods 0.000 claims description 6
- 238000005259 measurement Methods 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 139
- 239000010408 film Substances 0.000 description 104
- 238000004544 sputter deposition Methods 0.000 description 30
- 239000007789 gas Substances 0.000 description 18
- 238000005530 etching Methods 0.000 description 17
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 9
- 229910001882 dioxygen Inorganic materials 0.000 description 9
- 229910007541 Zn O Inorganic materials 0.000 description 8
- 238000001039 wet etching Methods 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 238000003486 chemical etching Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000010030 laminating Methods 0.000 description 5
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- 229910052786 argon Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000009616 inductively coupled plasma Methods 0.000 description 2
- 238000010884 ion-beam technique Methods 0.000 description 2
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- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
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- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical class N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229910019092 Mg-O Inorganic materials 0.000 description 1
- 229910019395 Mg—O Inorganic materials 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 229920012266 Poly(ether sulfone) PES Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 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
- 238000000465 moulding Methods 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
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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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- 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
- H01L29/66969—Multistep manufacturing processes of devices having semiconductor bodies not comprising group 14 or group 13/15 materials
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- C—CHEMISTRY; METALLURGY
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- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/08—Oxides
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
- H01L21/3065—Plasma etching; Reactive-ion etching
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- 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
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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
- H01L29/78693—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 the semiconducting oxide being amorphous
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Abstract
Description
本発明は、酸化物半導体の加工方法及び薄膜トランジスタの製造方法に関するものである。 The present invention relates to a method for processing an oxide semiconductor and a method for manufacturing a thin film transistor.
近年、In−Ga−Zn−O系(IGZO)等の酸化物半導体層をチャネル層に用いた薄膜トランジスタ(TFT)の開発が活発に行われている。酸化物半導体層をチャネル層に用いた薄膜トランジスタの製造方法として、例えば特許文献1には、スパッタリングによりゲート絶縁層の上に酸化物半導体層を形成した後、酸化物半導体層の上に金属膜を形成し、この金属膜をエッチングすることによりソース電極及びドレイン電極を形成する方法が開示されている。この特許文献1では、優れた膜質の酸化物半導体層を大きな成膜速度で形成するため、スパッタリングを行う際に、スパッタリングガスとしてアルゴンのみを供給することで結晶性の低い第1の酸化物半導体層をまず形成し、その上に、スパッタリングガスとしてアルゴンと酸素の混合ガスを供給することで結晶性の高い第2の酸化物半導体層を形成することが記載されている。 In recent years, a thin film transistor (TFT) using an oxide semiconductor layer such as an In-Ga-Zn-O system (IGZO) as a channel layer has been actively developed. As a method for manufacturing a thin film transistor using an oxide semiconductor layer as a channel layer, for example, in Patent Document 1, after forming an oxide semiconductor layer on a gate insulating layer by sputtering, a metal film is formed on the oxide semiconductor layer. A method of forming and etching the metal film to form a source electrode and a drain electrode is disclosed. In Patent Document 1, in order to form an oxide semiconductor layer having an excellent film quality at a high film forming rate, a first oxide semiconductor having low crystallinity is supplied by supplying only argon as a sputtering gas when sputtering is performed. It is described that a layer is first formed, and then a second oxide semiconductor layer having high crystallinity is formed by supplying a mixed gas of argon and oxygen as a sputtering gas.
ところで、上記したような結晶性の異なる複数の酸化物半導体層を積層したものに対してウェットエッチング等の化学エッチングにより加工を行う場合、積層方向(膜厚方向)における膜質の違いに起因して、所望の形状を得ることが難しいことがある。すなわち、結晶性が低い酸化物半導体層では、結晶性がより高い酸化物半導体層に比べて化学エッチングに対するエッチング速度が大きいため、これらに対して化学エッチングを行うと、エッチング速度の違いによって2つの酸化物半導体層の境界で段差が生じてしまうことがある。特に、上記したように、結晶性が低い酸化物半導体層の上に結晶性が高い酸化物半導体層を積層した場合には、これらに対して化学エッチングを行うと、上層の酸化物半導体層に比べて下層の酸化物半導体層が、積層方向に垂直な方向に深く削られてしまい、その加工断面が奥まってしまうことがある。そのため、後工程で例えば保護膜等を塗布する場合、下層の酸化物半導体層の加工断面にまで保護膜が行き渡りにくいことがある。 By the way, when processing is performed by chemical etching such as wet etching on a laminated product of a plurality of oxide semiconductor layers having different crystallinity as described above, it is caused by the difference in film quality in the stacking direction (film thickness direction). , It may be difficult to obtain the desired shape. That is, since the oxide semiconductor layer having low crystallinity has a higher etching rate for chemical etching than the oxide semiconductor layer having higher crystallinity, when chemical etching is performed on these, there are two differences due to the difference in etching rate. A step may occur at the boundary of the oxide semiconductor layer. In particular, as described above, when the oxide semiconductor layer having high crystallinity is laminated on the oxide semiconductor layer having low crystallinity, when chemical etching is performed on these, the oxide semiconductor layer in the upper layer is formed. In comparison, the lower oxide semiconductor layer may be deeply scraped in the direction perpendicular to the stacking direction, and the processed cross section may be deepened. Therefore, for example, when a protective film or the like is applied in a subsequent process, it may be difficult for the protective film to reach the processed cross section of the oxide semiconductor layer underneath.
本発明はこのような問題に鑑みてなされたものであり、結晶性の異なる2つの酸化物半導体が積層された酸化物半導体層の加工において、所望の形状を得やすい加工方法を提供することを主たる課題とするものである。 The present invention has been made in view of such a problem, and provides a processing method for easily obtaining a desired shape in the processing of an oxide semiconductor layer in which two oxide semiconductors having different crystallinities are laminated. This is the main issue.
本発明は上記課題を解決するために鋭意検討した結果、エッチングの手法としてイオンミリング法を用いた場合には、結晶性の異なる2つの酸化物半導体が積層されたものであっても、その酸化物半導体の結晶性の違いによらず、同程度のエッチング速度でエッチングを行うことができることを見出した。すなわち、イオンミリング法であれば、化学的な反応を伴わない物理的なエッチングであるので、結晶性の違いによってエッチング速度に大きな差異が出ないことを見出し、本発明に想到したのである。 As a result of diligent studies to solve the above problems, the present invention, when the ion milling method is used as the etching method, oxidizes even if two oxide semiconductors having different crystallinities are laminated. It has been found that etching can be performed at the same etching rate regardless of the difference in crystallinity of the physical semiconductor. That is, since the ion milling method is a physical etching that does not involve a chemical reaction, it was found that the etching rate does not differ greatly depending on the difference in crystallinity, and the present invention was conceived.
すなわち本発明の酸化物半導体の加工方法は、酸化物半導体から成る第1半導体層と、前記第1半導体層を構成する酸化物半導体よりも結晶性が高い酸化物半導体から成る第2半導体層とが基板側から順に積層された半導体積層体を、イオンミリング法により加工して成形することを特徴とする。 That is, the method for processing an oxide semiconductor of the present invention includes a first semiconductor layer made of an oxide semiconductor and a second semiconductor layer made of an oxide semiconductor having a higher crystallinity than the oxide semiconductor constituting the first semiconductor layer. Is characterized in that semiconductor laminates laminated in order from the substrate side are processed and formed by an ion milling method.
このような加工方法であれば、イオンミリング法により半導体積層体の加工を行うので、結晶性の異なる第1半導体層と第2半導体層とに対して同程度の速度でエッチングを行うことができる。そのため、ウェットエッチングを行った場合に生じ得る、結晶性が比較的低い第1半導体層だけが積層方向に垂直な方向に深く削られてしまうといった事態を防止でき、所望の断面形状を得やすくなる。
また、第1半導体層と第2半導体層とに対して同程度の速度でエッチングを行うことができるので、第1半導体層と第2半導体層のそれぞれの加工断面の境界における段差を小さくすることができる。そのため、後工程で例えば保護膜等を塗布した場合に、第1半導体層と第2半導体層のいずれの加工断面にも、保護膜を行き渡らせやすくできる。
With such a processing method, the semiconductor laminate is processed by the ion milling method, so that the first semiconductor layer and the second semiconductor layer having different crystallinities can be etched at the same speed. .. Therefore, it is possible to prevent a situation in which only the first semiconductor layer having relatively low crystallinity is deeply scraped in the direction perpendicular to the stacking direction, which may occur when wet etching is performed, and it becomes easy to obtain a desired cross-sectional shape. ..
Further, since the first semiconductor layer and the second semiconductor layer can be etched at the same speed, the step at the boundary between the processed cross sections of the first semiconductor layer and the second semiconductor layer should be reduced. Can be done. Therefore, when a protective film or the like is applied in a subsequent step, the protective film can be easily spread over any of the processed cross sections of the first semiconductor layer and the second semiconductor layer.
前記した本発明の効果を顕著にする前記半導体積層体の態様として、前記加工方法により加工する半導体積層体が、前記第1半導体層が非晶質の酸化物半導体から成り、前記第2半導体層が結晶質の酸化物半導体から成るものを挙げることができる。 As an aspect of the semiconductor laminate that makes the effect of the present invention remarkable, the semiconductor laminate processed by the processing method comprises the first semiconductor layer made of an amorphous oxide semiconductor and the second semiconductor layer. Can be mentioned as being composed of a crystalline oxide semiconductor.
前記した本発明の効果を顕著にする前記半導体積層体の態様として、前記第1半導体層を構成する酸化物半導体の組成と、前記第2半導体層を構成する酸化物半導体の組成とが同じであるものを挙げることができる。 As an aspect of the semiconductor laminate that makes the effect of the present invention remarkable, the composition of the oxide semiconductor constituting the first semiconductor layer and the composition of the oxide semiconductor constituting the second semiconductor layer are the same. Some can be mentioned.
前記酸化物半導体の加工方法における半導体積層体の具体的態様として、前記第1半導体層及び前記第2半導体層を構成する酸化物半導体がIGZOであるものを挙げることができる。 As a specific embodiment of the semiconductor laminate in the method for processing an oxide semiconductor, the oxide semiconductor constituting the first semiconductor layer and the second semiconductor layer may be IGZO.
前記酸化物半導体の加工方法における半導体積層体の具体的態様として、前記第2半導体層に対するCu‐Kα線を用いたθ−2θ法によるX線回折測定における回折角2θ=31°近傍において確認されるピークの半値全幅が、前記第1半導体層に対する前記X線回折測定における回折角2θ=31°近傍において確認されるピークの半値全幅よりも小さいことが好ましい。 As a specific aspect of the semiconductor laminate in the method for processing an oxide semiconductor, it was confirmed at a diffraction angle of 2θ = 31 ° in the X-ray diffraction measurement by the θ-2θ method using Cu—Kα rays for the second semiconductor layer. It is preferable that the half-value full width of the peak is smaller than the half-value full width of the peak confirmed in the vicinity of the diffraction angle 2θ = 31 ° in the X-ray diffraction measurement with respect to the first semiconductor layer.
また本発明の薄膜トランジスタの製造方法は、基板上に、ゲート電極と、ゲート絶縁層と、酸化物半導体層と、ソース電極及びドレイン電極とが順に配置された薄膜トランジスタの製造方法であって、酸化物半導体から成る第1半導体層と、前記第1半導体層を構成する酸化物半導体よりも結晶性が高い酸化物半導体から成る第2半導体層と、を前記基板側から順に積層する半導体積層工程と、積層された前記第1半導体層及び前記第2半導体層をイオンミリング法により加工して前記酸化物半導体層を形成する半導体加工工程と、を有することを特徴とする。 Further, the method for manufacturing a thin film of the present invention is a method for manufacturing a thin film in which a gate electrode, a gate insulating layer, an oxide semiconductor layer, a source electrode and a drain electrode are sequentially arranged on a substrate, and is an oxide. A semiconductor lamination step of laminating a first semiconductor layer made of a semiconductor and a second semiconductor layer made of an oxide semiconductor having a higher crystallinity than the oxide semiconductor constituting the first semiconductor layer in order from the substrate side. It is characterized by having a semiconductor processing step of processing the laminated first semiconductor layer and the second semiconductor layer by an ion milling method to form the oxide semiconductor layer.
このような薄膜トランジスタの製造方法であれば、前記した酸化物半導体の加工方法と同様の効果を得ることができる。 With such a method for manufacturing a thin film transistor, the same effect as the above-mentioned method for processing an oxide semiconductor can be obtained.
このように構成した本発明によれば、結晶性の異なる2つの酸化物半導体が積層された酸化物半導体層の加工において、所望の形状を得やすい加工方法を提供することができる。 According to the present invention configured in this way, it is possible to provide a processing method that makes it easy to obtain a desired shape in the processing of an oxide semiconductor layer in which two oxide semiconductors having different crystallinities are laminated.
以下に、本発明の一実施形態に係る薄膜トランジスタおよびその製造方法について説明する。 The thin film transistor and the manufacturing method thereof according to the embodiment of the present invention will be described below.
<1.薄膜トランジスタ>
本実施形態の薄膜トランジスタ1は所謂ボトムゲート型のものである。具体的には図1に示すように、基板2と、ゲート電極3と、ゲート絶縁層4と、チャネル層たる酸化物半導体層5と、ソース電極6及びドレイン電極7とを有しており、基板2側からこの順に配置(形成)されている。以下、各部について詳述する。
<1. Thin film transistor>
The thin film transistor 1 of the present embodiment is a so-called bottom gate type. Specifically, as shown in FIG. 1, it has a substrate 2, a gate electrode 3, a gate insulating layer 4, an oxide semiconductor layer 5 as a channel layer, a source electrode 6, and a drain electrode 7. They are arranged (formed) in this order from the substrate 2 side. Each part will be described in detail below.
基板2は光を透過できるような材料から構成されており、例えば、ポリエチレンテレフタレート(PET)、ポリエチレンナフタレート(PEN)、ポリエーテルサルフォン(PES)、アクリル、ポリイミド等のプラスチック(合成樹脂)やガラス等によって構成されてよい。 The substrate 2 is made of a material capable of transmitting light, for example, polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyether sulfone (PES), acrylic, polyimide and other plastics (synthetic resin). It may be composed of glass or the like.
基板2の表面にはゲート電極3が設けられている。ゲート電極3は高い導電性を有する材料から構成されており、例えばSi、Al、Mo、Cr、Ta、Ti、Pt、Au、Ag等から選択される1種以上の金属から構成されてよい。また、Al−Nd、Ag合金、酸化錫、酸化亜鉛、酸化インジウム、酸化インジウム錫(ITO)、酸化亜鉛インジウム(IZO)、In−Ga−Zn−O(IGZO)等の金属酸化物の導電性膜から構成されてよい。ゲート電極3は、これらの導電性膜の単層構造又は2層以上の積層構造から構成されてもよい。 A gate electrode 3 is provided on the surface of the substrate 2. The gate electrode 3 is made of a material having high conductivity, and may be made of one or more metals selected from, for example, Si, Al, Mo, Cr, Ta, Ti, Pt, Au, Ag and the like. Further, the conductivity of metal oxides such as Al-Nd, Ag alloy, tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO), and In-Ga-Zn-O (IGZO). It may be composed of a membrane. The gate electrode 3 may be composed of a single-layer structure of these conductive films or a laminated structure of two or more layers.
ゲート電極3の上にはゲート絶縁層4が配置されている。ゲート絶縁層4は高い絶縁性を有する材料から構成されており、例えば、SiO2、SiNx、SiON、Al2O3、Y2O3、Ta2O5、Hf2等から選択される1つ以上の酸化物を含む絶縁膜であってよい。ゲート絶縁層4は、これらの導電性膜を単層構造又は2層以上の積層構造としたものであってよい。 A gate insulating layer 4 is arranged on the gate electrode 3. The gate insulating layer 4 is made of a material having high insulating properties, and is selected from, for example, SiO 2 , SiN x , SiON, Al 2 O 3 , Y 2 O 3 , Ta 2 O 5 , Hf 2 and the like 1 It may be an insulating film containing one or more oxides. The gate insulating layer 4 may have a single-layer structure or a laminated structure of two or more layers of these conductive films.
ゲート絶縁層4の上には酸化物半導体層5が配置されている。酸化物半導体層5は、いずれも酸化物半導体から成る第1半導体層5aと第2半導体層5bとが基板2側から順に配置された二層構造を成している。 An oxide semiconductor layer 5 is arranged on the gate insulating layer 4. The oxide semiconductor layer 5 has a two-layer structure in which a first semiconductor layer 5a and a second semiconductor layer 5b made of an oxide semiconductor are arranged in order from the substrate 2 side.
第1半導体層5aと第2半導体層5bは、互いに同一の組成の酸化物半導体から構成されており、互いに同一の構成元素及び不可避的な不純物から成る酸化物半導体から構成されていることが好ましい。本実施形態では、第1半導体層5aと第2半導体層5bはいずれも、Inを含む酸化物を主成分とする酸化物半導体から成る。Inを含む酸化物とは、例えばIn−Ga−Zn−O、In−Al−Mg−O、In−Al−Zn−O又はIn−Hf−Zn−O等の酸化物である。 The first semiconductor layer 5a and the second semiconductor layer 5b are preferably composed of oxide semiconductors having the same composition as each other, and preferably composed of oxide semiconductors composed of the same constituent elements and unavoidable impurities. .. In the present embodiment, both the first semiconductor layer 5a and the second semiconductor layer 5b are made of an oxide semiconductor containing an oxide containing In as a main component. The oxide containing In is, for example, an oxide such as In-Ga-Zn-O, In-Al-Mg-O, In-Al-Zn-O or In-Hf-Zn-O.
第1半導体層5aと第2半導体層5bは、結晶性の高さ(度合)が互いに異なる酸化物半導体から構成されている。具体的には、第2半導体層5bを構成する酸化物半導体の結晶性は、第1半導体層5aを構成する酸化物半導体の結晶性よりも高くなるように構成されている。 The first semiconductor layer 5a and the second semiconductor layer 5b are composed of oxide semiconductors having different crystallinities (degrees) from each other. Specifically, the crystallinity of the oxide semiconductor constituting the second semiconductor layer 5b is configured to be higher than the crystallinity of the oxide semiconductor constituting the first semiconductor layer 5a.
第1半導体aは、その結晶性が低いほど、後述する第1成膜工程における成膜速度を早くし、生産性を向上することができる。そのため第1半導体層aを構成する酸化物半導体は、その結晶性が低いほど好ましく、非晶質(アモルファス)であることがより好ましい。 The lower the crystallinity of the first semiconductor a, the faster the film forming speed in the first film forming step described later, and the higher the productivity. Therefore, the oxide semiconductor constituting the first semiconductor layer a is preferably as low as its crystallinity, and more preferably amorphous.
ソース電極6及びドレイン電極7との間で界面を形成する第2半導体層5bは、その結晶性が高いほど界面における酸素欠陥を低減でき、薄膜トランジスタ1のゲート閾値電圧Vth(ドレイン電流Id=1nAにおけるゲート電圧Vg)を大きくすることができる。そのため第2半導体層5bは、結晶性の酸化物半導体から成り、その結晶性は高いほど好ましい。 The higher the crystallinity of the second semiconductor layer 5b forming the interface between the source electrode 6 and the drain electrode 7, the more oxygen defects can be reduced at the interface, and the gate threshold voltage Vth of the thin film transistor 1 (drain current Id = it is possible to increase the gate voltage V g) in 1 nA. Therefore, the second semiconductor layer 5b is made of a crystalline oxide semiconductor, and the higher the crystallinity, the more preferable.
第1半導体層5aと第2半導体層5bを構成する酸化物半導体の結晶性の高さ(度合)は、例えばCu光源(Cu−Kα線)を用いたθ−2θ法によるXRD(X線回折)測定によって観測できるピークの半値全幅(FWHM)により確認することができる。具体的には、第1半導体層5a及び第2半導体層5bがIn−Ga−Zn−O(IGZO)等のInを含む酸化物を主成分(体積分率で90%以上含むことを言う)とする酸化物半導体から成る場合には、X線回折測定において2θ=31°近傍(例えば30°〜32°)で確認できるピークの半値全幅の大きさにより評価することができる。より具体的には当該ピークの半値全幅が小さいほど結晶性が高いと評価できる。 The high crystallinity (degree) of the oxide semiconductors constituting the first semiconductor layer 5a and the second semiconductor layer 5b is determined by, for example, XRD (X-ray diffraction) by the θ-2θ method using a Cu light source (Cu—Kα ray). ) It can be confirmed by the half-value full width (FWHM) of the peak that can be observed by measurement. Specifically, the first semiconductor layer 5a and the second semiconductor layer 5b contain an oxide containing In such as In-Ga-Zn-O (IGZO) as a main component (meaning that it contains 90% or more in volume fraction). In the case of an oxide semiconductor, it can be evaluated by the size of the half-value full width of the peak that can be confirmed in the vicinity of 2θ = 31 ° (for example, 30 ° to 32 °) in the X-ray diffraction measurement. More specifically, it can be evaluated that the smaller the full width at half maximum of the peak, the higher the crystallinity.
第2半導体層5bを構成する酸化物半導体の結晶性が、第1半導体層5aを構成する酸化物半導体の結晶性よりも高いことは、第2半導体層5bに対するX線回折測定における回折角2θ=31°近傍において確認されるピークの半値全幅が、第1半導体層5aに対するX線回折測定における回折角2θ=31°近傍において確認されるピークの半値全幅よりも小さいことにより確認することができる。 The fact that the crystallinity of the oxide semiconductor constituting the second semiconductor layer 5b is higher than the crystallinity of the oxide semiconductor constituting the first semiconductor layer 5a is that the diffraction angle 2θ in the X-ray diffraction measurement with respect to the second semiconductor layer 5b It can be confirmed that the half-value full width of the peak confirmed near = 31 ° is smaller than the half-value full width of the peak confirmed near the diffraction angle 2θ = 31 ° in the X-ray diffraction measurement with respect to the first semiconductor layer 5a. ..
第1半導体層5aが非晶質の酸化物半導体であることは、第1半導体層5aがIn−Ga−Zn−O(IGZO)からなる酸化物半導体である場合、上記したXRD(X線回折)による測定において2θ=31°近傍にピークが現れないことにより確認できる。 The fact that the first semiconductor layer 5a is an amorphous oxide semiconductor means that when the first semiconductor layer 5a is an oxide semiconductor made of In-Ga-Zn-O (IGZO), the above-mentioned XRD (X-ray diffraction) ) Does not appear in the vicinity of 2θ = 31 °.
薄膜トランジスタ1のゲート閾値電圧Vthを大きくする観点から、第2半導体層5bは、XRD(X線回折)による測定において2θ=31°近傍(例えば30°〜32°)で確認できるピークの半値全幅が4.5°以下であることが好ましく、3.0°以下であることがより好ましく、2.5°以下であることがさらに好ましい。 From the viewpoint of increasing the gate threshold voltage Vth of the thin film transistor 1, the second semiconductor layer 5b has the full width at half maximum of the peak that can be confirmed in the vicinity of 2θ = 31 ° (for example, 30 ° to 32 °) in the measurement by XRD (X-ray diffraction). Is preferably 4.5 ° or less, more preferably 3.0 ° or less, and even more preferably 2.5 ° or less.
酸化物半導体層5の上には、ソース電極6およびドレイン電極7が配置されている。ソース電極6及びドレイン電極7はそれぞれ、電極として機能するように高い導電性を有する材料から構成されている。例えばゲート電極2と同様の材料により構成されてもよく、異なる材料により構成されてもよい。ソース電極6及びドレイン電極7は、金属や導電性酸化物の単層構造から構成されてもよく、2層以上の積層構造から構成されてもよい。 A source electrode 6 and a drain electrode 7 are arranged on the oxide semiconductor layer 5. The source electrode 6 and the drain electrode 7 are each made of a material having high conductivity so as to function as an electrode. For example, it may be made of the same material as the gate electrode 2, or it may be made of a different material. The source electrode 6 and the drain electrode 7 may be composed of a single-layer structure of a metal or a conductive oxide, or may be composed of a laminated structure of two or more layers.
必要に応じて、酸化物半導体5、ソース電極6およびドレイン電極7の上には、これらを保護するための保護膜が配置されていてもよい。保護膜は、例えばシリコン酸化膜(SiO2)、シリコン窒化膜中にフッ素を含有するフッ素化シリコン窒化膜(SiN:F)等によって構成されてもよい。 If necessary, a protective film for protecting the oxide semiconductor 5, the source electrode 6, and the drain electrode 7 may be arranged. The protective film may be composed of, for example, a silicon oxide film (SiO 2 ), a fluorinated silicon nitride film (SiN: F) containing fluorine in the silicon nitride film, or the like.
<2.薄膜トランジスタの製造方法>
次に、上述した構造の薄膜トランジスタ1の製造方法を、図2及び図3を参照して説明する。
本実施形態の薄膜トランジスタ1の製造方法は、ゲート電極形成工程、ゲート絶縁層形成工程、半導体層形成工程、ソース・ドレイン電極形成工程を含む。以下、各工程について説明する。
<2. Thin film transistor manufacturing method>
Next, a method for manufacturing the thin film transistor 1 having the above-mentioned structure will be described with reference to FIGS. 2 and 3.
The method for manufacturing the thin film transistor 1 of the present embodiment includes a gate electrode forming step, a gate insulating layer forming step, a semiconductor layer forming step, and a source / drain electrode forming step. Hereinafter, each step will be described.
(1)ゲート電極形成工程
まず図2(a)に示すように、例えば石英ガラスからなる基板2を準備し、基板2の表面にゲート電極3を形成する。ゲート電極3の形成方法は特に制限されず、例えば真空蒸着法、DCスパッタリング法等の既知の方法により形成してよい。
(1) Gate Electrode Forming Step First, as shown in FIG. 2A, a substrate 2 made of, for example, quartz glass is prepared, and a gate electrode 3 is formed on the surface of the substrate 2. The method for forming the gate electrode 3 is not particularly limited, and the gate electrode 3 may be formed by a known method such as a vacuum vapor deposition method or a DC sputtering method.
(2)ゲート絶縁層形成工程
次に、図2(b)に示すように、基板2及びゲート電極3の表面を覆うようにゲート絶縁層4を形成する。ゲート絶縁層4の形成方法は特に限定されず、既知の方法により形成してよい。
(2) Gate Insulating Layer Forming Step Next, as shown in FIG. 2B, the gate insulating layer 4 is formed so as to cover the surfaces of the substrate 2 and the gate electrode 3. The method for forming the gate insulating layer 4 is not particularly limited, and the gate insulating layer 4 may be formed by a known method.
(3)半導体層形成工程
次に、図2(c)〜図3(f)に示すように、ゲート絶縁層4上にチャネル層としての酸化物半導体層5を形成する。半導体層形成工程は、2種類の酸化物半導体膜を基板2側から順に積層する半導体積層工程と、積層した酸化物半導体膜を加工する半導体加工工程と、を含む。
(3) Semiconductor Layer Forming Step Next, as shown in FIGS. 2 (c) to 3 (f), an oxide semiconductor layer 5 as a channel layer is formed on the gate insulating layer 4. The semiconductor layer forming step includes a semiconductor laminating step of laminating two types of oxide semiconductor films in order from the substrate 2 side, and a semiconductor processing step of processing the laminated oxide semiconductor film.
(3−1)半導体積層工程
半導体積層工程では、ゲート絶縁層4上に第1酸化物半導体膜S1を形成し、この上に、第1酸化物半導体膜S1よりも結晶性が高い第2酸化物半導体膜S2を形成する。半導体積層工程は、第1酸化物半導体膜S1を形成する第1成膜工程と、第2酸化物半導体膜S2を形成する第2成膜工程とを含む。
(3-1) In the semiconductor lamination process semiconductor lamination step, the first to form an oxide semiconductor film S 1 on the gate insulating layer 4, on the crystalline than the first oxide semiconductor film S 1 is higher the forming a second oxide semiconductor film S 2. The semiconductor laminating step includes a first film forming step of forming the first oxide semiconductor film S 1 and a second film forming step of forming the second oxide semiconductor film S 2 .
本実施形態において、第1成膜工程及び第2成膜工程はいずれも、プラズマを用いてターゲットをスパッタリングすることにより酸化物半導体膜を成膜する。具体的には、図4に示すような、誘導結合型のプラズマPを用いてターゲットTをスパッタリングするスパッタリング装置100を用いて行われる。スパッタリング装置100は、真空容器20と、真空容器20内において基板2を保持する基板保持部30と、真空容器20内において基板2と対向してターゲットTを保持するターゲット保持部40と、基板保持部30に保持された基板2の表面に沿って配列され、プラズマPを発生させる複数のアンテナ50とを備える。スパッタリング装置100を使用することにより、アンテナ50に供給する高周波電圧とターゲットTのバイアス電圧との設定を独立して行うことができる。そのため、バイアス電圧をプラズマPの生成とは独立してプラズマ中のイオンをターゲットに引き込んでスパッタさせる程度の低電圧に設定することができ、スパッタリング時にターゲットTに印加する負のバイアス電圧を−1kV以上(すなわち絶対値が1kV以下)の負電圧に設定することが可能になる。第1成膜工程及び第2成膜工程では、ターゲット保持部40にターゲットTを配置し、基板保持部30に基板2を配置して行われる。ここではターゲットTとして、酸化物半導体層5の原料となるInGaZnO等の導電性酸化物焼結体が用いられる。 In the present embodiment, both the first film forming step and the second film forming step form an oxide semiconductor film by sputtering the target using plasma. Specifically, it is performed by using a sputtering apparatus 100 that sputters the target T using an inductively coupled plasma P as shown in FIG. The sputtering apparatus 100 includes a vacuum vessel 20, a substrate holding portion 30 that holds the substrate 2 in the vacuum vessel 20, a target holding portion 40 that holds the target T facing the substrate 2 in the vacuum vessel 20, and a substrate holding unit. A plurality of antennas 50 arranged along the surface of the substrate 2 held by the portion 30 and generating the plasma P are provided. By using the sputtering apparatus 100, the high frequency voltage supplied to the antenna 50 and the bias voltage of the target T can be set independently. Therefore, the bias voltage can be set to a low voltage such that ions in the plasma are drawn into the target and sputtered independently of the generation of the plasma P, and the negative bias voltage applied to the target T during sputtering is -1 kV. It is possible to set the negative voltage to the above (that is, the absolute value is 1 kV or less). In the first film forming step and the second film forming step, the target T is arranged in the target holding portion 40, and the substrate 2 is arranged in the substrate holding portion 30. Here, as the target T, a conductive oxide sintered body such as InGaZnO, which is a raw material for the oxide semiconductor layer 5, is used.
(3−1−1)第1成膜工程
第1成膜工程ではまず、図2(c)に示すように、ゲート絶縁層4上に第1酸化物半導体膜S1を形成する。具体的には、スパッタリング装置100の真空容器20を3×10−6Torr以下に真空排気した後、50sccm以上200sccm以下でスパッタリングガスを導入しつつ、真空容器内20の圧力を0.5Pa以上3.1Pa以下に調整する。そして複数のアンテナ50に1kW以上10kW以下の高周波電力を供給し、誘導結合型のプラズマを生成し、これを維持する。ターゲットに直流電圧パルスを印加して、ターゲットのスパッタリングを行う。酸素が脱離したスパッタ粒子の生成を抑制し、膜中の酸素欠陥が少ない酸化物半導体膜を形成する観点から、ターゲットTに印加する電圧を−1kV以上0V未満の負電圧とする。なお、真空容器20内の圧力、スパッタリングガスの流量、アンテナに供給する電力量は適宜変更されてもよい。
In (3-1-1) the first film-forming step the first film forming step First, as shown in FIG. 2 (c), to form the first oxide semiconductor film S 1 on the gate insulating layer 4. Specifically, after the vacuum vessel 20 of the sputtering apparatus 100 is evacuated to 3 × 10-6 Torr or less, the pressure inside the vacuum vessel 20 is 0.5 Pa or more and 3 while introducing the sputtering gas at 50 sccm or more and 200 sccm or less. .Adjust to 1 Pa or less. Then, high-frequency power of 1 kW or more and 10 kW or less is supplied to the plurality of antennas 50 to generate and maintain inductively coupled plasma. A DC voltage pulse is applied to the target to sputter the target. From the viewpoint of suppressing the formation of sputtered particles desorbed from oxygen and forming an oxide semiconductor film having few oxygen defects in the film, the voltage applied to the target T is set to a negative voltage of -1 kV or more and less than 0 V. The pressure in the vacuum vessel 20, the flow rate of the sputtering gas, and the amount of electric power supplied to the antenna may be changed as appropriate.
(3−1−2)第2成膜工程
第1成膜工程の後、図2(d)に示すように、第1酸化物半導体膜S1の上に第2酸化物半導体膜S2を形成する。具体的には、第1成膜工程と同様に、スパッタリング装置100を用いて、ターゲットTのスパッタリングを行うことにより第2酸化物半導体膜S2を形成する。第1成膜工程と同様に、第2成膜工程においても、ターゲットTに印加する電圧を−1kV以上0V未満の負電圧とすることが好ましい。第2成膜工程における真空容器20内の圧力、スパッタリングガスの流量、アンテナに供給する電力量等の条件は第1成膜工程と同じであってよく、適宜変更してもよい。
(3-1-2) after the second film-forming step the first film forming step, as shown in FIG. 2 (d), the second oxide semiconductor film S 2 on the first oxide semiconductor film S 1 Form. Specifically, similarly to the first film forming step, by using the sputtering apparatus 100, a second oxide semiconductor film S 2 by performing sputtering of the target T. Similar to the first film forming step, in the second film forming step, it is preferable that the voltage applied to the target T is a negative voltage of -1 kV or more and less than 0 V. Conditions such as the pressure in the vacuum vessel 20, the flow rate of the sputtering gas, and the amount of power supplied to the antenna in the second film forming step may be the same as those in the first film forming step, and may be changed as appropriate.
(3−1−3)スパッタリングガス中の酸素ガス濃度
本実施形態では、第2成膜工程において供給するスパッタリングガスに含まれる酸素ガス濃度を、第1成膜工程において供給するスパッタリングガスに含まれる酸素ガス濃度よりも高くする。これにより第2成膜工程では、第1成膜工程に比べて、酸素が脱離したスパッタ粒子の生成をより抑えて、ターゲットの酸化状態をより維持したまま成膜することができる。そのため、第2酸化物半導体膜S2の結晶性を、第1酸化物半導体膜S1の結晶性よりも高くすることができる。
(3-1-3) Oxygen Gas Concentration in Sputtering Gas In the present embodiment, the oxygen gas concentration contained in the sputtering gas supplied in the second film forming step is included in the sputtering gas supplied in the first forming step. Make it higher than the oxygen gas concentration. As a result, in the second film forming step, as compared with the first film forming step, the generation of sputtered particles desorbed from oxygen can be further suppressed, and the film can be formed while maintaining the oxidized state of the target. Therefore, the crystallinity of the second oxide semiconductor film S 2 can be made higher than the crystallinity of the first oxide semiconductor film S 1 .
第1成膜工程において供給されるスパッタリングガス中の酸素ガス濃度は、第2成膜工程において供給されるスパッタリングガス中の酸素ガス濃度よりも低ければよい。第1成膜工程において、非晶質の第1酸化物半導体膜S1を形成する観点から、スパッタリングガスに含まれる酸素ガス濃度は体積分率で2vоl%以下が好ましく、スパッタリングガスとしてアルゴンガスのみが供給されることが好ましい。 The oxygen gas concentration in the sputtering gas supplied in the first film forming step may be lower than the oxygen gas concentration in the sputtering gas supplied in the second film forming step. In the first film forming step, from the viewpoint of forming a first oxide semiconductor film S 1 of amorphous, preferably less 2Vol% oxygen gas concentration the volume fraction contained in the sputtering gas as a sputtering gas of argon gas only Is preferably supplied.
第2酸化物半導体膜S2の結晶性を高くする観点から、第2成膜工程において供給されるスパッタリングガスに含まれる酸素ガス濃度は、体積分率で20vоl%以上であることが好ましく、50vоl%以上であることがより好ましい。スパッタリングガスとして酸素ガスのみ(すなわち、体積分率が99.999vоl%以上)が供給されることが最も好ましい。 From the viewpoint of increasing the crystallinity of the second oxide semiconductor film S 2, the oxygen gas concentration in the sputtering gas supplied in the second film forming step is preferably at least 20Vol% in volume fraction, 50Vol More preferably, it is% or more. Most preferably, only oxygen gas (that is, a volume fraction of 99.999vоl% or more) is supplied as the sputtering gas.
(3−2)半導体加工工程
次に、半導体加工工程において、積層した第1酸化物半導体膜S1及び第2酸化物半導体膜S2を加工して、酸化物半導体層5を形成する。
(3-2) semiconductor processing step Next, in a semiconductor processing step, by processing the first oxide semiconductor film S 1 and the second oxide semiconductor film S 2 laminated to form the oxide semiconductor layer 5.
具体的にはまず、第2酸化物半導体膜S2上にレジストR1を塗布する。その後露光・現像等を行い、図3の(e)に示すように、後に酸化物半導体層5とする部位にのみレジストR1を残すようにする。そして、図3の(f)に示すように、第1酸化物半導体膜S1及び第2酸化物半導体膜S2をエッチング加工し、第1半導体層5a及び第2半導体層5bが基板2側から順に積層した酸化物半導体層5を形成する。 Specifically first, the resist R 1 is coated on the second oxide semiconductor film S 2. Perform subsequent exposure and development or the like, as shown in (e) of FIG. 3, so as to leave the resist R 1 only site with the oxide semiconductor layer 5 later. Then, as shown in (f) of FIG. 3, the first oxide semiconductor film S 1 and the second oxide semiconductor film S 2 is etched, the first semiconductor layer 5a and the second semiconductor layer 5b is the substrate 2 side The oxide semiconductor layer 5 laminated in order from the first is formed.
ここで、実施形態の製造方法では、イオンミリング法による物理的エッチングによって第2酸化物半導体膜S2及び第1酸化物半導体膜S1を加工する。具体的には、イオンミリング装置を用いて、第2酸化物半導体膜S2及び第1酸化物半導体膜S1に対して、第2酸化物半導体膜S2側からイオンビームを照射することにより行われる。 Here, in the manufacturing method of the embodiment, processing the physical second oxide by etching the semiconductor film S 2 and the first oxide semiconductor film S 1 by ion milling method. Specifically, using an ion milling apparatus, the second oxide semiconductor film S 2 and the first oxide semiconductor film S 1, by the second oxide semiconductor film S 2 side is irradiated with the ion beam Will be done.
イオンビームは、第2酸化物半導体膜S2及び第1酸化物半導体膜S1に対して、その積層方向(膜厚方向)に平行な方向に照射されることが好ましい。このようにすることで、形成された第1半導体層5a及び第2半導体層5bの加工断面を積層方向に対して平行にできる。第1半導体層5a及び第2半導体層5bの加工断面の形状はこれに限らず、基板2に向かって広がるようテーパ状になるように形成されてもよい。 Ion beam, the second oxide semiconductor film S 2 and the first oxide semiconductor film S 1, are preferably irradiated in a direction parallel to the lamination direction (thickness direction). By doing so, the processed cross sections of the formed first semiconductor layer 5a and second semiconductor layer 5b can be made parallel to the stacking direction. The shape of the processed cross section of the first semiconductor layer 5a and the second semiconductor layer 5b is not limited to this, and may be formed so as to be tapered so as to spread toward the substrate 2.
イオンミリング法において使用されるイオン材は特に限定されず、例えばNe、Ar、Kr、Xe等が挙げられる。またその他イオンミリング法の実施条件は特に限定されず、例えば次のように例示できる
・イオン加速電圧:230eV
・加速電流:100mA
・ビーム照射角度:0°〜±30°
The ionic material used in the ion milling method is not particularly limited, and examples thereof include Ne, Ar, Kr, and Xe. In addition, the implementation conditions of other ion milling methods are not particularly limited and can be exemplified as follows: ・ Ion acceleration voltage: 230 eV
・ Acceleration current: 100mA
・ Beam irradiation angle: 0 ° to ± 30 °
(4)ソース・ドレイン電極形成工程
次に、酸化物半導体層5上のレジストR1を除去した後、酸化物半導体層5上にソース電極6およびドレイン電極7を形成する。ソース電極6およびドレイン電極7の形成は、例えば、RFマグネトロンスパッタリング等を用いた既知の方法により形成することができる。
(4) the source and drain electrode formation step Next, after removing the resist R 1 on the oxide semiconductor layer 5, a source electrode 6 and drain electrode 7 is formed on the oxide semiconductor layer 5. The source electrode 6 and the drain electrode 7 can be formed by, for example, a known method using RF magnetron sputtering or the like.
(5)その他
その後、必要に応じて、形成された酸化物半導体層5、ソース電極6及びドレイン電極7の上面を覆うように、例えばプラズマCVD法を用いて保護膜を形成してもよい。また必要に応じて、酸素を含む大気圧下の雰囲気中で熱処理を行ってもよい。
(5) Others After that, if necessary, a protective film may be formed so as to cover the upper surfaces of the formed oxide semiconductor layer 5, the source electrode 6, and the drain electrode 7, for example, by using a plasma CVD method. If necessary, the heat treatment may be performed in an atmosphere containing oxygen under atmospheric pressure.
以上により、本実施形態の薄膜トランジスタ1を得ることができる。 From the above, the thin film transistor 1 of the present embodiment can be obtained.
<3.酸化物半導体層の断面の観測>
上記した半導体加工工程における加工方法の違いによる、酸化物半導体層5(第1半導体層5a及び第2半導体層5b)の断面形状への影響について評価した。
<3. Observation of cross section of oxide semiconductor layer>
The influence on the cross-sectional shape of the oxide semiconductor layer 5 (first semiconductor layer 5a and second semiconductor layer 5b) due to the difference in the processing method in the above-mentioned semiconductor processing process was evaluated.
(1.サンプル作製)
シリコン基板を2つ準備し、前記した製造方法の半導体積層工程に基づいて、In−Ga−Zn−O(IGZO1114)から成る酸化物半導体膜をシリコン基板上に成膜し、2つのサンプルを作製した。
(1. Sample preparation)
Two silicon substrates are prepared, and an oxide semiconductor film made of In-Ga-Zn-O (IGZO1114) is formed on the silicon substrate based on the semiconductor lamination process of the manufacturing method described above to prepare two samples. did.
具体的には、スパッタリング装置100を用いて、真空容器内の圧力を0.9Pa以下まで減圧し、複数のアンテナに7kWの高周波電力を供給し、ターゲットに−400Vの直流パルス電圧を印加してターゲットのスパッタリングを行った。そして供給するスパッタリングガス中の酸素ガス濃度を変化させることで、シリコン基板上に非晶質の第1酸化物半導体膜S1(a−IGZO)を成膜し、第1酸化物半導体膜S1上に結晶質の第2酸化物半導体膜S2(c−IGZO)を成膜した。 Specifically, using the sputtering apparatus 100, the pressure in the vacuum vessel is reduced to 0.9 Pa or less, high-frequency power of 7 kW is supplied to a plurality of antennas, and a DC pulse voltage of −400 V is applied to the target. The target was sputtered. Then, by changing the oxygen gas concentration in the supplied sputtering gas, an amorphous first oxide semiconductor film S 1 (a-IGZO) is formed on the silicon substrate, and the first oxide semiconductor film S 1 is formed. and forming the second oxide crystalline semiconductor film S 2 (c-IGZO) above.
(2.加工及び成形)
次に、作成した2つのサンプルに対して、第2酸化物半導体膜側から第1酸化物半導体膜側へ向けてエッチング加工を行った。
(2. Processing and molding)
Next, the two prepared samples were etched from the second oxide semiconductor film side to the first oxide semiconductor film side.
具体的には2つのサンプルの第2酸化物半導体膜S2の表面の所定領域にレジストを施した後、一方のサンプルに対してはウェットエッチング(化学的エッチング)を行い、他方のサンプルに対してはイオンミリング(物理的エッチング)を行った。行ったウェットエッチング及びイオンミリングの具体的な条件は、次のとおりである。 Specifically, after resisting a predetermined region on the surface of the second oxide semiconductor film S2 of the two samples, wet etching (chemical etching) is performed on one sample and the other sample is subjected to wet etching. Ion milling (physical etching) was performed. The specific conditions of the wet etching and ion milling performed are as follows.
(ウェットエッチングの条件)
・エッチング液:HCl(0.05M)
・エッチング時間:210秒
・温度:25℃
(Conditions for wet etching)
・ Etching solution: HCl (0.05M)
・ Etching time: 210 seconds ・ Temperature: 25 ° C
(イオンミリングの条件)
・イオン加速電圧:230eV
・加速電流:100mA
・基板回転:12rpm
・エッチング時間:360秒
・ビーム照射角度:0°
(Conditions for ion milling)
・ Ion acceleration voltage: 230eV
・ Acceleration current: 100mA
・ Board rotation: 12 rpm
・ Etching time: 360 seconds ・ Beam irradiation angle: 0 °
(3.エッチング加工及び加工断面の観察)
各サンプルにおける、エッチングによる第1酸化物半導体膜S1及び第2酸化物半導体膜S2の加工断面をSEM(走査型電子顕微鏡)により観察した。その結果を図5に示す。
(3. Etching process and observation of processed cross section)
In each sample was observed first processing section of the oxide semiconductor film S 1 and the second oxide semiconductor film S 2 by etching by SEM (scanning electron microscope). The result is shown in FIG.
図5(a)に示すように、ウェットエッチングにより加工を行ったサンプルでは、第1酸化物半導体膜S1と第2酸化物半導体膜S2との境界において大きな段差が生じていた。具体的には、第2半導体膜S2よりも結晶性が低くエッチング速度が高い第1半導体膜S1では、第2半導体膜S2との境界付近において、積層方向に対して横方向に向けてのエッチングが進行していた。 As shown in FIG. 5 (a), the sample was processed by wet etching, a large step at the boundary between the first oxide semiconductor film S 1 and the second oxide semiconductor film S 2 has occurred. Specifically, first the semiconductor film S 1 is high low etch rate crystallinity than the second semiconductor film S 2, in the vicinity of the boundary between the second semiconductor film S 2, oriented transversely to the stacking direction Etching was in progress.
一方で図5(b)に示すように、イオンミリングにより加工を行ったサンプルでは、第1酸化物半導体膜S1と第2酸化物半導体膜S2との境界において大きな段差が生じず、滑らかな一続きの断面が形成されていた。 On the other hand, as shown in FIG. 5 (b), in the samples was processed by ion milling, a large step does not occur at the boundary between the first oxide semiconductor film S 1 and the second oxide semiconductor film S 2, smooth A series of cross sections was formed.
<4.本実施形態の効果>
このようにした本実施形態の薄膜トランジスタ1の製造方法によれば、
半導体加工工程において、イオンミリング法によって第2酸化物半導体膜S2及び第1酸化物半導体膜S1を加工するので、結晶性の異なる第2酸化物半導体膜S2と第1酸化物半導体膜S1とに対して同程度の速度でエッチングを行うことができる。そのため、ウェットエッチングを行った場合に生じ得るような、非晶質の第1酸化物半導体膜S1だけが積層方向に垂直な方向に深く削られてしまうといった事態を防止でき、結晶質の第2酸化物半導体膜S2とともに所望の断面形状を得やすくなる。
<4. Effect of this embodiment>
According to the manufacturing method of the thin film transistor 1 of the present embodiment as described above,
In semiconductor processing step, the processing the second oxide semiconductor film S 2 and the first oxide semiconductor film S 1 by ion milling, crystallinity different second oxide semiconductor film S 2 and the first oxide semiconductor film etching can be performed at comparable rates for the S 1. Therefore, as may occur when performing the wet etching, can be prevented a situation only the first oxide semiconductor film S 1 of amorphous resulting in scraped deep in a direction perpendicular to the stacking direction, the crystalline with second oxide semiconductor film S 2 becomes easy to obtain a desired cross-sectional shape.
また、第2酸化物半導体膜S2と第1酸化物半導体膜S1とに対して同程度の速度でエッチングを行うことができるので、得られた第1半導体層5aと第2半導体層5bのそれぞれの加工断面の境界における段差を小さくすることができる。そのため、後工程であるソース・ドレイン電極形成工程において、スパッタリング等により酸化物半導体層5を覆うように導電性膜を製膜した際に、第1半導体層と第2半導体層のいずれの加工断面にも、導電性膜を成膜しやすくなる。 Further, since the second oxide semiconductor film S 2 and the first oxide semiconductor film S 1 can be etched at the same speed, the obtained first semiconductor layer 5a and second semiconductor layer 5b can be etched. It is possible to reduce the step at the boundary of each processed cross section of. Therefore, in the source / drain electrode forming step, which is a subsequent step, when the conductive film is formed so as to cover the oxide semiconductor layer 5 by sputtering or the like, either the processed cross section of the first semiconductor layer or the second semiconductor layer is processed. In addition, it becomes easy to form a conductive film.
<その他の変形実施形態>
なお、本発明は前記実施形態に限られるものではない。
<Other modified embodiments>
The present invention is not limited to the above embodiment.
前記実施形態では、第1半導体層5aと第2半導体層5bは組成が同一の酸化物半導体から構成されていたが、これに限らない。他の実施形態では、第1半導体層5aと第2半導体層5bとは組成が異なる酸化物半導体から構成されてもよい。 In the above embodiment, the first semiconductor layer 5a and the second semiconductor layer 5b are composed of oxide semiconductors having the same composition, but the present invention is not limited to this. In another embodiment, the first semiconductor layer 5a and the second semiconductor layer 5b may be composed of oxide semiconductors having different compositions.
前記実施形態では、第1成膜工程及び第2成膜工程において、スパッタリングガス中の酸素濃度を変化させることにより、第1酸化物半導体膜S1及び第2酸化物半導体膜S2の結晶性を変化させていたが、これに限らない。第1酸化物半導体膜S1を成膜し、その上により結晶性の高い第2酸化物半導体膜S2を成膜できるものであれば、他の方法により第1成膜工程及び第2成膜工程を行ってもよい。 In the above embodiment, the first film forming step and the second deposition step, by changing the oxygen concentration in the sputtering gas, the crystallinity of the first oxide semiconductor film S 1 and the second oxide semiconductor film S 2 Was changed, but it is not limited to this. A first oxide semiconductor film S 1 is formed, if on the second oxide semiconductor film S 2 with high crystallinity as it can be formed by the first film forming process by another method and the second formation A membrane step may be performed.
第1半導体層5aは、非晶質のものに限らず、結晶質の酸化物半導体から構成されてもよい。第2半導体層5bを構成する酸化物半導体よりも結晶性が低いものであればよい。 The first semiconductor layer 5a is not limited to an amorphous one, and may be made of a crystalline oxide semiconductor. Any semiconductor having lower crystallinity than the oxide semiconductor constituting the second semiconductor layer 5b may be used.
前記実施形態の酸化物半導体層5は、結晶性の異なる2つの酸化物半導体層が積層されたものであったが、これに限らない。他の実施形態の酸化物半導体層5は、結晶性の異なる3つ以上の酸化物半導体層が積層されたものであってもよい。 The oxide semiconductor layer 5 of the above embodiment is obtained by laminating two oxide semiconductor layers having different crystallinities, but the present invention is not limited to this. The oxide semiconductor layer 5 of the other embodiment may be one in which three or more oxide semiconductor layers having different crystallinities are laminated.
前記実施形態では、複数のターゲット保持部40を有する構成であったが、1つのターゲット保持部40を有する構成であってもよい。この場合であっても、複数のアンテナ50を有する構成が望ましいが、1つのアンテナ50を有する構成であってもよい。 In the above embodiment, the configuration has a plurality of target holding units 40, but a configuration having one target holding unit 40 may be used. Even in this case, a configuration having a plurality of antennas 50 is desirable, but a configuration having one antenna 50 may be used.
その他、本発明は前記実施形態に限られず、その趣旨を逸脱しない範囲で種々の変形が可能であるのは言うまでもない。 In addition, the present invention is not limited to the above-described embodiment, and it goes without saying that various modifications can be made without departing from the spirit of the present invention.
1 ・・・薄膜トランジスタ
2 ・・・基板
3 ・・・ゲート電極
4 ・・・ゲート絶縁層
5 ・・・酸化物半導体層
5a ・・・第1半導体層
5b ・・・第2半導体層
6 ・・・ソース電極
7 ・・・ドレイン電極
1 ・ ・ ・ Thin film transistor 2 ・ ・ ・ Substrate 3 ・ ・ ・ Gate electrode 4 ・ ・ ・ Gate insulating layer 5 ・ ・ ・ Oxide semiconductor layer 5a ・ ・ ・ First semiconductor layer 5b ・ ・ ・ Second semiconductor layer 6 ・ ・・ Source electrode 7 ・ ・ ・ Drain electrode
Claims (6)
酸化物半導体から成る第1半導体層と、前記第1半導体層を構成する酸化物半導体よりも結晶性が高い酸化物半導体から成る第2半導体層と、を前記基板側から順に積層する半導体積層工程と、
積層された前記第1半導体層及び前記第2半導体層をイオンミリング法により加工して前記酸化物半導体層を形成する半導体加工工程と、
を有する薄膜トランジスタの製造方法。 A method for manufacturing a thin film transistor in which a gate electrode, a gate insulating layer, an oxide semiconductor layer, a source electrode, and a drain electrode are arranged in this order on a substrate.
A semiconductor lamination step in which a first semiconductor layer made of an oxide semiconductor and a second semiconductor layer made of an oxide semiconductor having a higher crystallinity than the oxide semiconductor constituting the first semiconductor layer are laminated in order from the substrate side. When,
A semiconductor processing step of processing the laminated first semiconductor layer and the second semiconductor layer by an ion milling method to form the oxide semiconductor layer.
A method for manufacturing a thin film transistor having.
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JP2019116880A JP2021002633A (en) | 2019-06-25 | 2019-06-25 | Oxide semiconductor processing method and thin film transistor manufacturing method |
PCT/JP2020/024450 WO2020262322A1 (en) | 2019-06-25 | 2020-06-22 | Method for processing oxide semiconductor and method for manufacturing thin film transistor |
KR1020217039350A KR20220003603A (en) | 2019-06-25 | 2020-06-22 | Oxide semiconductor processing method and thin film transistor manufacturing method |
CN202080042357.XA CN114008752A (en) | 2019-06-25 | 2020-06-22 | Method for processing oxide semiconductor and method for manufacturing thin film transistor |
TW109121527A TWI739491B (en) | 2019-06-25 | 2020-06-24 | Method for processing oxide semiconductor and method for manufacturing thin film transistor |
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JP2004335712A (en) * | 2003-05-07 | 2004-11-25 | Sharp Corp | Oxide semiconductor light emitting element and its processing method |
JP2011187506A (en) * | 2010-03-04 | 2011-09-22 | Sony Corp | Thin-film transistor, method of manufacturing the thin-film transistor, and display device |
JP2011254003A (en) * | 2010-06-03 | 2011-12-15 | Fujitsu Ltd | Semiconductor device and method for manufacturing the same |
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JP2004335712A (en) * | 2003-05-07 | 2004-11-25 | Sharp Corp | Oxide semiconductor light emitting element and its processing method |
JP2011187506A (en) * | 2010-03-04 | 2011-09-22 | Sony Corp | Thin-film transistor, method of manufacturing the thin-film transistor, and display device |
JP2011254003A (en) * | 2010-06-03 | 2011-12-15 | Fujitsu Ltd | Semiconductor device and method for manufacturing the same |
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