KR20150057377A - High mobility oxide sintered body and novel thin film transistor comprising the same - Google Patents
High mobility oxide sintered body and novel thin film transistor comprising the same Download PDFInfo
- Publication number
- KR20150057377A KR20150057377A KR1020130140677A KR20130140677A KR20150057377A KR 20150057377 A KR20150057377 A KR 20150057377A KR 1020130140677 A KR1020130140677 A KR 1020130140677A KR 20130140677 A KR20130140677 A KR 20130140677A KR 20150057377 A KR20150057377 A KR 20150057377A
- Authority
- KR
- South Korea
- Prior art keywords
- oxide
- thin film
- film transistor
- layer
- channel layer
- Prior art date
Links
- 239000010409 thin film Substances 0.000 title claims abstract description 58
- 239000004065 semiconductor Substances 0.000 claims abstract description 43
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 claims abstract description 18
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 18
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910001887 tin oxide Inorganic materials 0.000 claims abstract description 16
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 15
- 229910003437 indium oxide Inorganic materials 0.000 claims abstract description 15
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 15
- 239000011787 zinc oxide Substances 0.000 claims abstract description 9
- 239000000758 substrate Substances 0.000 claims description 42
- 239000010408 film Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 27
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- 238000004544 sputter deposition Methods 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 239000012298 atmosphere Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052750 molybdenum Inorganic materials 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910001182 Mo alloy Inorganic materials 0.000 claims description 7
- 229910044991 metal oxide Inorganic materials 0.000 claims description 7
- 150000004706 metal oxides Chemical class 0.000 claims description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 6
- 239000011733 molybdenum Substances 0.000 claims description 6
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- 239000004033 plastic Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 17
- 239000011701 zinc Substances 0.000 abstract description 8
- 239000010410 layer Substances 0.000 description 94
- 239000000843 powder Substances 0.000 description 28
- 239000002002 slurry Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 10
- 239000011324 bead Substances 0.000 description 9
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 8
- 238000000151 deposition Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000012212 insulator Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 229910006404 SnO 2 Inorganic materials 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 238000005530 etching Methods 0.000 description 5
- 229910052738 indium Inorganic materials 0.000 description 5
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000011241 protective layer Substances 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 229910052581 Si3N4 Inorganic materials 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 238000003486 chemical etching Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 238000007733 ion plating Methods 0.000 description 4
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 239000011268 mixed slurry Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 4
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 4
- 229910052814 silicon oxide Inorganic materials 0.000 description 4
- 239000002210 silicon-based material Substances 0.000 description 4
- 238000005477 sputtering target Methods 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 229910001882 dioxygen Inorganic materials 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000001039 wet etching Methods 0.000 description 3
- 229910004541 SiN Inorganic materials 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000001451 molecular beam epitaxy Methods 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 238000000053 physical method Methods 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- 108091006149 Electron carriers Proteins 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- -1 Si 3 N 4 Inorganic materials 0.000 description 1
- 229910004205 SiNX Inorganic materials 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910009367 Zn M Inorganic materials 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 238000001182 laser chemical vapour deposition Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 229910001512 metal fluoride Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005546 reactive sputtering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000002230 thermal chemical vapour deposition Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- 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
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02518—Deposited layers
- H01L21/02521—Materials
- H01L21/02565—Oxide semiconducting materials not being Group 12/16 materials, e.g. ternary compounds
-
- 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
-
- 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
Landscapes
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Ceramic Engineering (AREA)
- Thin Film Transistor (AREA)
Abstract
(M + Sn) / (M + Sn + In + Zn) atomic ratio of indium oxide, tin oxide, and zinc oxide to an oxide containing metal ions M (Hf, V, The present invention also provides a thin film transistor formed from the oxide sintered body and having high mobility characteristics and stability, and a method of manufacturing the same.
In the present invention, by optimizing the composition of a semiconductor target used as a channel layer of a thin film transistor, characteristics of a high mobility thin film transistor of 20 cm / Vs or more can be secured.
Description
The present invention relates to a novel oxide sintered body having a composition optimized so as to exhibit excellent mobility characteristics of the element even if the size of the display is increased, a thin film transistor formed from the oxide sintered body and realizing high mobility and stability and a method for manufacturing the same .
Among the elements of a liquid crystal-based display, thin film transistors which drive a device by displaying a driving voltage are widely used. The thin film transistor is composed of a gate electrode, an insulating film, a semiconductor layer, and a source / drain electrode. The semiconductor layer must be electrically stable and excellent in etching property. The silicon-based material has an advantage of excellent electrical stability and processability, but has a disadvantage in that it may cause malfunction of the thin film transistor due to generation of carriers due to light incidence due to absorption of a visible light region. Further, in the case of a silicon-based material, since a high-temperature process of about 200 ° C or more is required in forming amorphous silicon, the production cost is increased and deposition on a polymer substrate is difficult.
Accordingly, thin film transistors using transparent oxide semiconductors instead of the silicon-based materials have been actively developed. Transparent oxide semiconductors can be formed on a substrate without heating, exhibit a mobility of about 10 cm 2 / Vs or more, and the structure of a thin film transistor can be simply changed compared to the case of using a conventional silicon-based material. As a material of the transparent oxide semiconductor, an InGaZnO-based material including indium, gallium, zinc, and oxygen as a constituent element is typical. InGaZnO can be formed by a vapor phase method such as a sputtering method, a pulse laser vapor deposition method, or an electron beam vapor deposition method by making a polycrystalline sintered body of InGaO 3 (ZnO) x target as a target. In the case of dual mass productivity, the sputtering method is most suitable.
On the other hand, the InGaZnO oxide thin film transistor can realize stable device characteristics, but as the size of the display becomes larger, it is difficult to drive the display of the InGaZnO. Therefore, a high mobility oxide semiconductor of 20 cm / Vs or more is required for application to a device that can be mounted on a large display.
SUMMARY OF THE INVENTION The present invention has been made in order to solve the above-mentioned problems, and it is an object of the present invention to provide a method of manufacturing a semiconductor device including an oxide containing indium oxide, tin oxide, zinc oxide and specific metal ions (M = Al, Hf, V) It is an object of the present invention to provide an oxide sintered body having high resistance to chemical etching and excellent environmental resistance characteristics and high mobility by constituting the composition of the high mobility oxide semiconductor
It is another object of the present invention to provide a thin film transistor in which a channel layer of a thin film transistor is formed using an oxide sintered body of the above-mentioned composition and a method of manufacturing the same.
(M + Sn) / (M + Sn + In), wherein the oxide contains indium oxide, tin oxide, zinc oxide and metal ions M + Zn) atomic ratio of 10 to 45 at%. The present invention also provides an oxide sintered body for forming a thin film transistor channel layer.
In addition, the present invention provides a semiconductor device including at least a gate electrode, an insulating film, a channel layer made of an oxide semiconductor, an etch stop layer (ESL), a source electrode and a drain electrode on a substrate, and an etch stop layer (ESL) A source electrode and a drain electrode are formed on the etch stop layer (ESL), and the channel layer is formed from the oxide sintered body for forming the channel layer described above. Preferably, the etch stop layer etch stop layer type thin film transistor.
In addition, the present invention provides a method of manufacturing the above-described thin film transistor.
As a preferable example of the above-described manufacturing method, there are a step of forming a gate electrode on a substrate; Forming an insulating layer on the gate electrode; Forming a channel layer made of an oxide semiconductor of the above composition on the gate insulating layer; Forming an etch stop layer (ESL) on the channel layer, the etch stop layer (ESL) comprising at least one selected from the group consisting of SiO, SiN and Al 2 O 3 ; Forming a drain electrode and a source electrode on the etch stop layer; And a step of bringing the drain electrode and the source electrode into contact with both ends of the channel layer.
Furthermore, the present invention provides a flat panel display device including the thin film transistor described above. Here, the flat panel display device may be a liquid crystal display device or an organic light emitting display device.
In the present invention, the oxide sintered body used as the channel layer of the thin film transistor includes a specific metal ion M (Al, Hf, V) as well as an optimized composition of the atomic ratio thereof. It is possible to exhibit a strong resistance to chemical etching and a significant improvement in element stability characteristics.
BRIEF DESCRIPTION OF DRAWINGS FIG. 1 is a diagram showing mobility characteristics of a transistor manufactured according to Example 1. FIG.
2 is a diagram showing mobility characteristics of a transistor manufactured according to the second embodiment.
3 is a diagram showing mobility characteristics of the transistor manufactured by the third embodiment.
4 is a diagram showing mobility characteristics of the transistor manufactured by Comparative Example 1. FIG.
Hereinafter, the present invention will be described in detail.
The conventional InGaZnO oxide thin film transistor realizes stable device characteristics, but as the display becomes larger, the driving of the InGaZnO oxide is difficult to drive the display.
Accordingly, in order to manufacture an oxide device having a high mobility of 20 cm / Vs or more, the present invention provides an oxide semiconductor having a composition including not only specific metal ions M (Al, Hf, V) but also their atomic ratio .
Such an oxide semiconductor is an amorphous oxide having a high electron carrier concentration. Therefore, the thin film transistor using the amorphous oxide as a channel layer can exhibit a high mobility of 20 cm / Vs or more.
Also, since the oxide semiconductor is a sputtering target that exhibits little change in characteristics of the thin film transistor even when forming a long time, it is possible to manufacture an excellent thin film transistor which simultaneously improves the high mobility characteristics and the element stability when the thin film transistor is formed.
≪ Sintered body for oxide semiconductor film formation &
The oxide semiconductor layer used as the channel layer of the thin film transistor according to the present invention can be formed by forming an oxide sintered body as a sputtering target.
In the present invention, the oxide-sintered body for oxide semiconductor film formation comprises an oxide containing indium oxide, tin oxide, zinc oxide and metal ions M (Hf, V, Al), wherein (M + Sn) / + In + Zn) atomic ratio of 10 to 45 atomic%.
For example, when the oxide specified by the metal ion M (Hf, V, Al) is added to the indium oxide powder, the tin oxide powder and the zinc oxide powder in the ratio of (M + Sn) / (M + Sn + In + Zn) Oxides in the range of 10 to 45 atomic% can be used.
Here, the ratio of the metal ion M means a ratio based on the total amount of Sn + In + Zn.
The oxide-sintered body has the above-described composition and has a relative density of 95% or more and a specific resistance of 1 x 10 < -2 > At this time, when the relative density of the oxide-sintered body is less than 95%, there is a high possibility that an abnormal discharge occurs due to generation of nodules when the film is used as a sputtering target.
Here, the relative density is a value calculated by (actual density / theoretical density) x 100 of the sintered body. For the actual density, the density is calculated by measuring the sintered body at 1 atm and 4 ° C water.
In the case where the oxide-sintered body has 10 to 45 atomic% of (M + Sn) / (M + Sn + In + Zn) Stabilization and adsorption of oxygen in the sintered body to slightly decrease in mobility, which is a device characteristic of the transistor, but excellent characteristics can be observed from the viewpoint of optical reliability. However, when the atomic ratio of (M + Sn) / (M + Sn + In + Zn) is less than 10 atomic%, the influence of the added element is small.
In the present invention, an oxide-sintered body can be produced by a conventional method known in the art, except that the metal oxide of the above-mentioned composition is used. In one preferred embodiment of the method, a slurry is prepared by mixing indium oxide powder, tin oxide powder, zinc oxide powder, and oxides containing the above metal ions M (Hf, V, Al), followed by milling, drying and pulverizing , A step of molding the pulverized material, and a step of sintering the shaped material.
The indium oxide, tin oxide, and zinc oxide may be used without limitation in the conventional components known in the art. For example, they may be In 2 O 3, SnO 2 or ZnO.
When mixing the above-mentioned powders, additives such as binders, dispersants, defoamers, etc., which are known in the art, may be added as needed.
The dispersant is added in order to satisfy the purpose of finely pulverizing the particles while maintaining a stable dispersion evenly in the solution for a long time in the pulverized raw material particles. Nonlimiting examples of usable dispersing agents include organic acid-based ones having a carboxyl group such as citric acid, polyacrylic acid (PAA) or a salt thereof, a copolymer, or a combination thereof. The dispersant may be used in an amount of 0.5 to 3% by weight based on the weight of the powder in the slurry.
The binder is added in order to maintain the molding strength of the formed body in the process of drying the slurry after the powder is dried. Non-limiting examples thereof include polymers such as polyvinyl alcohol and polyethylene glycol. The amount of the binder used may be in the range of 0.01 to 5% by weight based on the powder in the slurry.
The antifoaming agent is used for removing bubbles in the slurry, and silicone oil, octyl alcohol, boric acid and the like can be usually used. The amount of the antifoaming agent used may be in the range of 0.001 to 0.01% by weight relative to the powder in the slurry.
The slurry prepared by mixing the above indium oxide powder, tin oxide powder, zinc oxide powder, metal oxide containing metal ion (M), water and additives is milled and dried to prepare a dry powder.
The milling may be carried out using a conventional ball mill, bead mill or the like known in the art. The viscosity of the slurry obtained through milling is preferably adjusted to 100 cps or less.
The milled slurry is spray-dried using a spray dryer or the like to obtain a dry powder.
Thereafter, the dried powder is subjected to a molding step of producing a molded body having a predetermined shape. It is preferable to use a cold isostatic press (CIP) in consideration of the convenience of the process at the time of manufacturing the molded article.
After the above-described molding step, an oxide sintered body for forming an oxide semiconductor film is produced through a sintering step. The sintering step may be performed in an oxygen gas atmosphere, an inert gas atmosphere, or an oxygen-inert gas mixed atmosphere. The sintering step may be carried out at a temperature in the range of 1000 to 1650 ° C under an atmosphere of oxygen gas or inert gas, or by sintering the shaped body at 900 to 1600 ° C under a pressurized condition of an oxygen or inert gas atmosphere. The pressure conditions may be using the CIP 2 to 3 ton / cm 2 range.
In the present invention, a sintered body for forming an oxide semiconductor film having the above-described composition and physical properties is formed on a substrate by a sputtering method, and the formed amorphous oxide thin film is used as a channel layer of the thin film transistor. For example, the manufactured sintered body is processed into a predetermined size and shape and attached to a cooling metal plate or a backing plate to be used as a sputtering target. In this case, an oxide semiconductor thin film used as a channel layer of the thin film transistor can be manufactured by supplying argon gas mixed with oxygen gas in the range of 0 to 1% in a vacuum tank at a rate of 80 sccm.
<Thin Film Transistor>
A thin film transistor (TFT) according to the present invention includes at least a gate electrode, an insulating film, a channel layer made of an oxide semiconductor, an etch stop layer (ESL), a source electrode and a drain electrode on a substrate.
Such a thin film transistor is an active element having a function of applying a voltage to a gate electrode, controlling a current flowing to a channel layer, and switching a current between a source electrode and a drain electrode.
The thin film transistor is fabricated by depositing an oxide thin film on a substrate by sputtering an oxide sintered body having the above composition and using an amorphous oxide as a channel layer. The fabricated thin film transistor is utilized in a polarization display device.
In the thin film transistor of the present invention, an ESL layer may be formed on the channel layer, and a source electrode and a drain electrode may be formed on the ESL layer. Preferably, the gate electrode is disposed under the channel layer, the source electrode and the drain electrode are located on the etch stop layer, and the both electrodes are provided in contact with both ends of the channel layer, (Etch Stop Layer) type. At this time, the source electrode and the drain electrode are brought into contact with the channel layer through a via hole or the like according to a conventional method known in the art.
The substrate can be any material used for a substrate of a conventional semiconductor device. For example, silicon (Si), glass, inorganic materials, organic materials or metals may be used without limitation.
In this case, the thickness of the substrate is not particularly limited, and when the flexible substrate is used, the thickness is preferably in the range of 50 to 500 mu m. If the thickness of the flexible substrate is less than 50 mu m, it is difficult to maintain sufficient flatness of the substrate itself. If the thickness of the flexible substrate exceeds 500 mu m, flexibility of the substrate itself becomes insufficient and it is difficult to bend the substrate itself It is because.
The substrate may have a moisture barrier layer (gas barrier layer) formed on its surface or back surface to prevent permeation of water vapor and oxygen. As the material of the moisture permeation preventing layer (gas barrier layer), an inorganic material such as silicon nitride and silicon oxide is suitably used. The moisture barrier layer (gas barrier layer) can be formed by, for example, high-frequency sputtering. When a thermoplastic substrate is used, a hard coat layer, an undercoat layer, or the like may be further formed as necessary.
The gate electrode is for applying a voltage to turn on / off the thin film transistor. The gate electrode may be formed using a conductive material such as a metal or a metal oxide. For example, the gate electrode may be formed of a metal such as Pt, Ru, Au, Ag, Mo, Al, W, or Cu or an alloy thereof, IZO (InZnO) A metal such as AZO (AlZnO) or a conductive oxide may be used, or an organic conductive compound such as polyaniline, polythiophene, and polypyrrole, or a mixture thereof may be used.
As the gate electrode, it is preferable to use Mo, Mo alloy or Cr from the viewpoint of reliability of TFT characteristics. The thickness of the gate electrode may be in the range of, for example, 10 nm to 1000 nm.
The method of forming the gate electrode is not particularly limited. For example, the gate electrode is formed by a physical method such as a wet method such as a printing method or a coating method, a vacuum evaporation method, a sputtering method, and an ion plating method, or a chemical method such as CVD or plasma CVD. Of these, the formation method can be appropriately selected in consideration of suitability with the material constituting the gate electrode. For example, when a gate electrode is formed using Mo or Mo alloy, a DC sputtering method is used. When an organic conductive compound is used for the gate electrode, a wet film-forming method may be used.
The gate insulating film can be formed using an insulating material used in a typical semiconductor device, and silicon oxide or nitride can be used. For example, HfO 2 , Al 2 O 3 , Si 3 N 4 , SiNx, YsO 3 , Ta 2 O 5 , or a mixture thereof can be used as the high-K material having a dielectric constant higher than that of SiO 2 or SiO 2 . Or a double layer film made of these materials, or a polymer insulator such as polyimide may also be used.
The thickness of the gate insulating film is not particularly limited, and is preferably in the range of 10 nm to 10 mu m. The gate insulating film needs to have a certain thickness to some extent in order to increase the voltage resistance in order to reduce the leakage current. However, if the film thickness of the gate insulating film is increased, the driving voltage of the TFT is increased. Therefore, the thickness of the gate insulating film is more preferably 50 nm to 1000 nm in the case of the inorganic insulator, and more preferably 0.5 to 5 mu m in the case of the polymer insulator.
In addition, when a high dielectric constant insulator such as HfO 2 is used for the gate insulating film, it is preferable to use a high dielectric constant insulator for the gate insulating film because the transistor can be driven at a low voltage even if the film thickness is increased.
In the present invention, the oxide semiconductor layer constituting the channel layer is produced by using the sintered body for forming an oxide semiconductor described above as a target.
At this time, the oxide semiconductor layer may be formed by sputtering using the sintered body for oxide semiconductor film formation as a target, although the difference in the composition may occur depending on the deposition atmosphere. Therefore, the oxide semiconductor layer has substantially the same composition as the target. Therefore, a metal oxide thin film having substantially the same composition as the above-described sintered body can be formed.
For example, the oxide semiconductor layer includes an oxide containing indium oxide, tin oxide, zinc oxide, and a metal ion M (Hf, V, Al), wherein (M + Sn) / (M + Sn + And is preferably contained in an amount of 10 to 45 atomic%
In the present invention, an etch stop layer (ESL) is provided to effectively protect the channel layer.
The etch stop layer may be formed using an inorganic insulating material, and may be at least one selected from the group consisting of SiO, SiN, Al 2 O 3 , and TiO 2 , for example. The etch stop layer may typically be patterned by dry etching.
The source electrode and the drain electrode may be formed using a conductive material. A metal such as Pt, Ru, Au, Ag, Mo, Al, W, Cu, Cr, Ta and Ti or an alloy thereof, an alloy such as Al-Nd and APC, tin oxide, And may be formed using a metal oxide conductive material such as indium tin oxide (ITO), indium zinc oxide (IZO), or AZO (AlZnO). It is preferable to use molybdenum (Mo) or molybdenum (Mo) alloy as the material of the source electrode and the drain electrode in view of the reliability of the TFT characteristic and the etching rate with respect to the sacrificial layer. The thickness of the source electrode and the drain electrode may be, for example, in the range of 10 nm to 1000 nm.
The source electrode and the drain electrode may be formed according to a conventional method known in the art. For example, the source electrode and the drain electrode are formed by forming a film, forming a resist pattern on the film by photolithography, and etching the film.
The method of forming the film constituted by the source electrode and the drain electrode is not particularly limited. For example, a physical method such as a wet method such as a printing method or a coating method, a vacuum evaporation method, a sputtering method, an ion plating method, A chemical method such as a plasma CVD method, or the like.
In the present invention, when the source electrode and the drain electrode are formed of Mo or a Mo alloy, for example, a Mo film or an Mo alloy film is formed using DC sputtering, and then a Mo film or a Mo alloy film is coated with a resist pattern And the Mo film or the Mo alloy film is etched by the etching solution to form the source electrode and the drain electrode.
In addition to the above-described configuration, the present invention includes a protective layer for protecting a channel layer, an etch stop layer (ESL), a source electrode and a drain electrode, and isolating the device from an electronic device fabricated on the transistor.
The protective layer may be formed by curing a conventional photosensitive or thermosetting resin composition known in the art or a resin composition containing a metal oxide, a metal nitride, a metal fluoride, or the like.
The method of forming the protective layer is not particularly limited and examples of the protective layer include vacuum vapor deposition, sputtering, reactive sputtering, MBE (molecular beam epitaxy), cluster ion beam, ion plating, plasma polymerization (high frequency excitation ion plating) , A plasma CVD method, a laser CVD method, a thermal CVD method, a gas source CVD method, a coating method, a printing method, or a transfer method.
<Thin Film Transistor Manufacturing Method>
Hereinafter, a method of manufacturing a thin film transistor according to the present invention will be described. However, the present invention is not limited to the following production methods, and the steps of each process may be modified or selectively mixed if necessary.
The thin film transistor of the present invention can be manufactured by a conventional method known in the art. According to a preferred embodiment thereof, there is provided a method of manufacturing a semiconductor device, comprising: forming a gate electrode on a substrate; Forming an insulating layer on the gate electrode; Forming a channel layer made of an oxide semiconductor on the gate insulating layer; Forming an etch stop layer on the channel layer; Forming a source electrode and a drain electrode on the etch stop layer; And a step of bringing the source electrode and the source electrode into contact with both ends of the channel layer.
First, a substrate is prepared, and then a gate electrode is formed on the substrate.
As the substrate, a silicon substrate is generally used, but in addition, a glass substrate, a metal substrate, or a plastic substrate can be used.
The gate electrode may be formed by depositing a metal material on the substrate and patterning the metal material.
Next, a gate insulator is formed on the substrate so as to cover the gate electrode. Here, the gate insulating layer may be made of, for example, silicon oxide or silicon nitride.
Then, a channel layer made of an oxide semiconductor is formed on the gate insulating layer.
At this time, the channel layer includes oxides of metal ions M (Hf, V, Al) in indium oxide powder, tin oxide powder and zinc oxide powder, and the ratio of (M + Sn) / (M + Sn + An amorphous oxide thin film can be formed by depositing an oxide semiconductor sintered body containing 10 to 45 atomic% by the sputtering method.
Thereafter, an etch stop layer (ESL) is formed on the channel layer.
The etch stop layer (ESL) may be formed by depositing one of Al 2 O 3 , SiO 2 , SiN, and TiO 2 by plasma CVD, CVD, or ALD. The thickness of the ESL thin film may be, for example, in the range of 10 nm to 1000 nm, and preferably in the range of 50 to 500 nm (500 to 5000 ANGSTROM).
Here, it is preferable that after subjected to the channel layer formed on the substrate, the atmosphere in the proportion of the additional O 2 / (Ar + O 2 ) to contain oxygen of 10 to 40% of heat-treating at 100 ~ 400 ℃.
Then, a drain electrode and a source electrode are formed on the formed ESL layer according to a conventional method known in the art, and both electrodes are formed to be in contact with both ends of the channel layer. As an example, a molybdenum film can be prepared using a DC sputtering method to a thickness of 100 nm.
Thereafter, a resist film is formed on the molybdenum film, and a resist pattern is formed by photolithography. After the molybdenum film is etched with the wet etching solution, the resist film is peeled off. As a result, a source electrode and a drain electrode formed so as to cover the surface of the ESL layer and a part of the surface of the channel layer are obtained.
In the wet etching step, the etching rate of the sacrificial layer is not particularly limited, and is preferably in the range of 1 to 10 Å / sec. The etchant used for the wet etching may be any conventional etchant known in the art.
Then, a protective layer covering the channel layer, the ESL layer, the source electrode, and the drain electrode is formed, thereby completing the manufacture of the thin film transistor according to the present invention.
The thin film transistor according to the present invention can be applied as a switching device or a driving device to a flat panel display device such as a liquid crystal display device and an organic light emitting display device.
As described above, since the transistor according to the present invention has a mobility of 20 cm 2 / vs or more, and is stable and has little change in characteristics due to light, when applied to a flat panel display device, reliability of the flat panel display device can be improved have. In particular, even if the display size is increased, it can be used stably.
Here, the structures of the above-described liquid crystal display device and organic light emitting display device are well known, and a detailed description thereof will be omitted. The transistor according to the present invention can be applied to various fields of electronic devices such as a memory device and a logic device as well as a flat panel display device.
Hereinafter, the present invention will be described in more detail with reference to Examples. However, the following Examples and Experimental Examples are merely illustrative of the present invention, and the scope of the present invention is not limited by the following Examples and Experimental Examples.
[Example 1]
1-1. Manufacture of transparent oxide sintered body
Each oxide powder of indium oxide (In 2 O 3 ), 1.5 탆 tin oxide (SnO 2 ), zinc oxide (ZnO) and metal ion M having an average particle size of powder of 1.0 탆 was mixed with indium 44 (Hf, V, Al) of 0.32 atomic%, and then mixed to obtain a wet mixed slurry having a concentration of 55%, which was dispersed in a bead mill medium of 0.1 mm in thickness Zirconia beads. The dispersed slurry was spray-dried, and the obtained granulated powder was pressure-molded and sintered at a flow rate of 25 L / min at 1100 to 1500 ° C for 10 hours. The oxide semiconductor target thus obtained had a relative density of 98% and a specific resistance of 3 x 10 < -3 > [Omega] cm. The sintered body was used as an oxide layer.
1-2. Thin Film Transistor Manufacturing
The thin film transistor may have a gate electrode G1 formed on a substrate (glass) B. The substrate B is any of various substrates that can be used in a general semiconductor device process such as a glass substrate, a metal substrate, a plastic substrate, and a plastic film. The gate electrode G1 may be generally formed of an electrode material. A gate insulating layer GI1 may be formed on the substrate B so as to cover the gate electrode G1.
The gate insulating layer GI1 may be a silicon oxide layer or a silicon nitride layer. In the ESL structure, the gate electrode G1 is provided under the channel layer A1, and the source electrode S1 and the drain electrode D1 are in contact with the upper surface of the channel layer A1. The power density was 0.5 to 3.6 W / cm 2 using a high frequency (RF) sputter during the formation of the channel layer (A1) using a mixed gas of argon and oxygen. After the channel layer A1 was formed, the ESL layer A2 was deposited, and a pattern was formed, followed by chemical etching. Thereafter, a source electrode (S1) and a drain electrode (D1) were deposited and a pattern was formed. Then, the source electrode and the drain electrode were separated through chemical etching.
After the sputtering film was formed on the substrate B, the post-heat treatment temperature was further raised at 100 to 400 ° C in an atmosphere containing oxygen having a ratio of O 2 / (Ar + O 2 ) of 10 to 40%.
As a method of measuring the device characteristics, a voltage of 0.1 V and 10 V was applied to the drain electrode D 1 and the source electrode S 1 of the transistor to observe a change in the characteristics of the transistor . As a result of measuring the characteristics of the transistor, the results shown in Table 1 and Fig. 1 were obtained.
[Example 2]
Each oxide powder of indium oxide (In 2 O 3 ), 1.5 탆 tin oxide (SnO 2 ), zinc oxide (ZnO) and metal ion M having an average particle size of powder of 1.0 탆 was mixed with indium 15 (Hf, V, Al) of 0.32 atomic%, and then mixed to obtain a wet mixed slurry having a concentration of 55%, which was dispersed in a bead mill medium of 0.1 mm in thickness Zirconia beads. The dispersed slurry was spray-dried, and the obtained granulated powder was pressure-molded and sintered at a flow rate of 25 L / min at 1100 to 1500 ° C for 10 hours. The relative density of the oxide semiconductor target thus obtained was 98%, the resistivity was measured to be 1 10 -3 ? Cm, and the sintered body was used as an oxide layer. A thin film transistor was fabricated in the same manner as in Example 1.
Using the sintered body, a transistor was fabricated as in Example 1 and the device was measured. As a result, the results shown in Table 1 and FIG. 2 were obtained.
[Example 3]
Each oxide powder of indium oxide (In 2 O 3 ), 1.5 탆 tin oxide (SnO 2 ), zinc oxide (ZnO) and metal ion M having an average particle size of powder of 1.0 탆 was mixed with indium 20 (Hf, V, Al) of 0.32 atomic%, and then mixed to obtain a wet mixed slurry having a concentration of 55%, which was dispersed in a bead mill medium of 0.1 mm in thickness Zirconia beads. The dispersed slurry was spray-dried, and the obtained granulated powder was pressure-molded and sintered at a flow rate of 25 L / min at 1100 to 1500 ° C for 10 hours. The relative density of the oxide semiconductor target thus obtained was 98%, the resistivity was measured to be 1 10 -3 ? Cm, and the sintered body was used as an oxide layer. A thin film transistor was fabricated in the same manner as in Example 1.
The sintered body was used to fabricate a transistor as in Example 1, and the device was measured. As a result, the results shown in Table 1 and FIG. 3 were obtained.
[Comparative Example 1]
Each oxide powder of indium oxide (In 2 O 3 ), 1.5 탆 tin oxide (SnO 2 ), zinc oxide (ZnO) and metal ion M having an average particle size of the powder of 1.0 탆 was mixed with indium 92 (Hf, V, Al) of 0.32 atomic%, and then mixed to obtain a wet mixed slurry having a concentration of 55%, which was dispersed in a bead mill medium of 0.1 mm in thickness Zirconia beads. The dispersed slurry was spray-dried, and the obtained granulated powder was pressure-molded and sintered at a flow rate of 25 L / min at 1100 to 1500 ° C for 10 hours. The relative density of the oxide semiconductor target thus obtained was 98%, the resistivity was measured to be 1 10 -3 ? Cm, and the sintered body was used as an oxide layer. A thin film transistor was fabricated in the same manner as in Example 1. Using this sintered body, a transistor was fabricated as in Example 1 and the device was measured. As a result, the results shown in Table 1 and FIG. 4 were obtained.
Table 1 below is a table showing mobility characteristics of the transistors manufactured in Examples 1 to 3 and Comparative Example 1.
As a result of the experiment, in the present invention, not only the specific metal ions M (Al, Hf, V) are included in the composition of the oxide-sintered body but also the atomic ratio of them is optimized to exhibit a high mobility of 20 cm / Vs or more, (See Table 1).
Claims (10)
An etch stop layer (ESL) is formed on the channel layer, a source electrode and a drain electrode are formed on the etch stop layer (ESL)
Wherein the channel layer is formed from the oxide-sintered body of claim 1.
Wherein the source electrode and the drain electrode are etch stop layers disposed on the etch stop layer so as to be in contact with both ends of the channel layer.
Forming a gate insulating layer on the gate electrode;
Forming a channel layer from the oxide semiconductor sintered body of claim 1 on the gate insulating layer;
Forming an etch stop layer (ESL) on the channel layer, the etch stop layer (ESL) comprising at least one selected from the group consisting of SiO, SiN and Al 2 O 3 ;
Forming a drain electrode and a source electrode on the etch stop layer; And
A step of bringing the drain electrode and the source electrode into contact with both ends of the channel layer
The method of manufacturing a thin film transistor according to claim 3,
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020130140677A KR20150057377A (en) | 2013-11-19 | 2013-11-19 | High mobility oxide sintered body and novel thin film transistor comprising the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020130140677A KR20150057377A (en) | 2013-11-19 | 2013-11-19 | High mobility oxide sintered body and novel thin film transistor comprising the same |
Publications (1)
Publication Number | Publication Date |
---|---|
KR20150057377A true KR20150057377A (en) | 2015-05-28 |
Family
ID=53392259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020130140677A KR20150057377A (en) | 2013-11-19 | 2013-11-19 | High mobility oxide sintered body and novel thin film transistor comprising the same |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR20150057377A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019117363A1 (en) * | 2017-12-13 | 2019-06-20 | 엘티메탈 주식회사 | High-mobility oxide sintered body and thin-film transistor comprising same |
-
2013
- 2013-11-19 KR KR1020130140677A patent/KR20150057377A/en not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019117363A1 (en) * | 2017-12-13 | 2019-06-20 | 엘티메탈 주식회사 | High-mobility oxide sintered body and thin-film transistor comprising same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5724157B2 (en) | Oxide semiconductor target and method of manufacturing oxide semiconductor device using the same | |
KR101518091B1 (en) | Field effect transistor using oxide semiconductor and method for manufacturing the same | |
KR101538283B1 (en) | Field-effect transistor, method for manufacturing same, and sputtering target | |
TWI453915B (en) | Thin film transistor | |
KR101516034B1 (en) | Oxide semiconductor field effect transistor and method for manufacturing the same | |
TWI517409B (en) | Thin film transistor and method for manufacturing the same | |
WO2010021106A1 (en) | Semiconductor device, method for manufacturing semiconductor device, transistor substrate, light emitting device and display device | |
JP6414946B2 (en) | Thin film transistor and zinc oxide sputtering target therefor | |
WO2014181777A1 (en) | Thin-film transistor and method for manufacturing same | |
KR20090122391A (en) | Sputtering target, oxide semiconductor film and semiconductor device | |
KR20080069607A (en) | Semiconductor thin film, method for producing same, thin film transistor and active-matrix-driven display panel | |
CN103855194A (en) | Semiconductor materials, transistors including the same, and electronic devices including transistors | |
US20040222089A1 (en) | Sputtering target and transparent electroconductive film | |
WO2015119385A1 (en) | Thin-film transistor having active layer made of molybdenum disulfide, method for manufacturing same, and display device comprising same | |
CN104798205A (en) | Oxide semiconductor thin film, method for producing same, and thin film transistor | |
CN103325842A (en) | Oxide semiconductor thin film and thin film transistor | |
KR102486098B1 (en) | Oxide sintered body and thin film transistor comprising the same | |
KR20150057377A (en) | High mobility oxide sintered body and novel thin film transistor comprising the same | |
KR20190070732A (en) | High mobility oxide sintered body and thin film transistor comprising the same | |
TW201936951A (en) | Oxide semiconductor thin film, thin film transistor, and sputtering target | |
TWI767186B (en) | Oxide semiconductor thin films, thin film transistors and sputtering targets | |
WO2012124408A1 (en) | Method for producing oxide semiconductor thin film | |
KR101500175B1 (en) | High density oxide sintered body and novel thin film transistor comprising the same | |
KR101512819B1 (en) | ZnO BASED SPUTTERING TARGET, METHOD OF FABRICATING THEREOF AND THIN FILM TRANSISTOR HAVING SHIELDING LAYER DEPOSITED BY THE SAME | |
JP6252903B2 (en) | Thin film transistor and manufacturing method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E902 | Notification of reason for refusal | ||
E601 | Decision to refuse application |