Manufacturing method of gallium oxide single crystal

Information

  • Patent Grant
  • 8900362
  • Patent Number
    8,900,362
  • Date Filed
    Tuesday, March 8, 2011
    13 years ago
  • Date Issued
    Tuesday, December 2, 2014
    10 years ago
Abstract
A method of growing a single crystal of gallium oxide at a lower temperature than the melting point (1900° C.) of gallium oxide is provided. A compound film (hereinafter referred to as “gallium oxide compound film”) containing Ga atoms, O atoms, and atoms or molecules that easily sublimate, is heated to sublimate the atoms or molecules that easily sublimate from inside the gallium oxide compound film, thereby growing a single crystal of gallium oxide with a heat energy that is lower than a binding energy of gallium oxide.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates to a manufacturing method of a metal oxide single crystal, for example, a gallium oxide single crystal, and specifically relates to a method of obtaining a gallium oxide single crystal layer by growing a gallium oxide single crystal over a single crystal substrate that is not gallium oxide.


2. Description of the Related Art


Because gallium oxide single crystals (β type) have excellent light transmittance and have a large bandgap of about 5 eV (see Non-Patent Document 1, Non-Patent Document 2, and Non-Patent Document 3), they are expected as application materials for devices that operate stably under a high temperature, deep ultraviolet sensors, light-emitting devices, or the like. Also, manufacturing of a gallium oxide single crystal is described in Patent Document 1 and Patent Document 2.


[Reference]


[Patent Document]




  • [Patent Document 1] Japanese Published Patent Application No. 2008-37725

  • [Patent Document 2] Japanese Published Patent Application No. 2002-93243


    [Non-Patent Document]


    [Non-Patent Document 1]

  • H. H. Tippins, “Optical Absorption and Photoconductivity in the Band Edge of β-Ga2O3” Physical Review, 4 Oct. 1965, Vol. 140, A316-A319


    [Non-Patent Document 2]

  • Masahiro Orita et al., Appl. Phys. Lett., 2000, Vol. 77 No. 25, p. 4166-4168


    [Non-Patent Document 3]

  • T. Takagi et al., Jpn. J. Appl. Phys., 2003, Vol. 42, p. L401



SUMMARY OF THE INVENTION

A gallium oxide single crystal is manufactured by a Czochralski method (CZ method), a floating zone method (FZ method), or the like. However, since a melting point of gallium oxide is at a high temperature of 1900° C., a lot of heat energy is necessary to grow a single crystal, and a manufacturing apparatus that can withstand the high temperature is also necessary.


Consequently, there is a problem that cost of manufacturing gallium oxide is high. An object of an embodiment of the present invention is to provide a method of growing a single crystal of gallium oxide at a lower temperature than the melting point (1900° C.) of gallium oxide.


To form a crystal lattice of gallium oxide from an amorphous state, it is necessary to break bonds between oxygen atoms and gallium atoms and then rearrange the oxygen atoms and the gallium atoms. Therefore, it is necessary to add energy for breaking the bonds between the oxygen atoms and the gallium atoms from the outside. Gallium oxide has a large bandgap of about 5 eV, which originates from the atoms of gallium oxide having high binding energy. Consequently, heat energy for breaking the atomic bonds of gallium oxide is high.


However, in a gallium oxide compound containing atoms or molecules that easily sublimate, if oxygen atoms or gallium atoms are bonded to the atoms or molecules that easily sublimate, the atoms or molecules sublimate easily from inside the gallium oxide by adding from the outside a heat energy that is lower than the binding energy, and after they sublimate, a dangling bonds of the oxygen atoms and the gallium atoms occur. With this, rearrangement of the oxygen atoms and the gallium atoms becomes easy, and it is possible to generate crystallization of gallium oxide with lower energy than the binding energy.


In an embodiment of the present invention, a compound film (hereinafter referred to as “gallium oxide compound film”) containing Ga atoms, O atoms, and atoms or molecules that easily sublimate, is heated to sublimate the atoms or molecules that easily sublimate from inside the gallium oxide compound film, thereby growing a single crystal of gallium oxide with a heat energy that is lower than a binding energy of gallium oxide. Note that the atoms and molecules that easily sublimate refer to elements that easily sublimate from inside the gallium oxide compound film, typically indium, zinc, or a halogen element such as fluorine.


In one aspect of the present invention disclosed in this specification, two single crystal substrates that are the same are used, and a method thereof is a manufacturing method of a gallium oxide single crystal, including the steps of forming a first metal oxide film over a first single crystal substrate and forming a first gallium oxide compound film over the first metal oxide film; forming a second metal oxide film over a second single crystal substrate and forming a second gallium oxide compound film over the second metal oxide film; and performing a heating treatment while the second single crystal substrate is positioned over the first gallium oxide compound film in a manner that the first gallium oxide compound film and the second gallium oxide compound film face each other with space between the first gallium oxide compound film and the second gallium oxide compound film, to sublimate a metal that is contained in the first gallium oxide compound film, and obtain a gallium oxide single crystal layer over the first single crystal substrate. Note that, the second metal oxide film is not always necessary. Furthermore, in the case that the first gallium oxide compound film is easily crystallized, the first metal oxide film is not always necessary.


With the above structure, a temperature of the heating treatment for obtaining the gallium oxide single crystal can be less than 1900° C., and the above problem is solved.


In the above structure, each of the first metal oxide film and the second metal oxide film that are formed on their respective single crystal substrates so as to be in contact thereto, is a zinc oxide film or an oxide film containing zinc oxide and one or both of indium and gallium, and is a thin film that becomes a nucleus for crystal growth when the heating treatment is performed, or a thin film that promotes crystal growth.


In the above structure, each of the first gallium oxide compound film and the second gallium oxide compound film is a film containing one or both of indium and zinc. Film thicknesses of the first gallium oxide compound film and the second gallium oxide compound film are made to be thicker than at least the first metal oxide film and the second metal oxide film, respectively.


In the above structure, by performing a heating treatment at about 1400° C. for example on a lamination of the first metal oxide film and the first gallium oxide compound film, there is crystal growth of a gallium oxide single crystal and sublimation of zinc or indium contained in the first gallium oxide compound film, and a gallium oxide single crystal layer is obtained. As a result, the film thickness of the gallium oxide single crystal layer obtained after the heat treatment is thinner than the thickness of the first gallium oxide compound film before the heating treatment.


Also, if the heating treatment at about 1400° C. is performed on the lamination of the first metal oxide film and the first gallium oxide compound film without placing the second single crystal substrate, the first gallium oxide compound film is sublimated and there is concern that the film itself will be lost. In preventing the loss of the first gallium oxide compound film, the second single crystal substrate for covering over the first gallium oxide compound film fulfills an important role.


A single crystal of gallium oxide can be grown over a single crystal substrate at a lower temperature than a melting point (1900° C.) of gallium oxide.





BRIEF DESCRIPTION OF THE DRAWINGS

In the accompanying drawings:



FIGS. 1A to 1D are a perspective view and cross-sectional views showing one aspect of the present invention;



FIG. 2 is a graph showing a condition of a heating treatment;



FIG. 3 is a cross-sectional TEM image of a single crystal layer;



FIG. 4 is a graph showing a result of an EDX analysis of a single crystal layer;



FIG. 5 is a figure showing an electron beam diffraction pattern of a single crystal layer;



FIG. 6 is a cross-sectional TEM image of a single crystal layer;



FIG. 7 is a graph showing a result of an EDX analysis of a single crystal layer; and



FIG. 8 is a figure showing an electron beam diffraction pattern of a single crystal layer.





DETAILED DESCRIPTION OF THE INVENTION

Hereinafter, an embodiment of the present invention will be described in detail with reference to the accompanying drawings. However, the present invention is not limited to the description below, and it is easily understood by those skilled in the art that modes and details disclosed herein can be modified in various ways without departing from the spirit and the scope of the present invention. Therefore, the present invention is not construed as being limited to description of the embodiment.


(Embodiment 1)


In this embodiment, an example of a method of obtaining a single crystal of gallium oxide will be described below with reference to FIGS. 1A to 1D.


First, a first metal oxide film 101 and a first gallium oxide compound film 102 are formed and laminated over a first single crystal substrate 100.


As the first metal oxide film 101, a zinc oxide film that is obtained by a sputtering method is used, and the film thickness is to be 1 nm or more and 10 nm or less.


As the first gallium oxide compound film 102, an InGaO film, an InGaZnO film, a GaZnO film, or the like that is obtained by a sputtering method can be used, and the film thickness is to be 10 nm or more and 500 nm or less.


Then, spacing materials 103, 104, 105, and 106 are placed at four corners of the first gallium oxide compound film 102 over the first single crystal substrate 100, to maintain substrate spacing. A perspective view at this stage corresponds to FIG. 1A, and a corresponding cross-sectional view is shown in FIG. 1B. Each of the spacing materials 103, 104, 105, and 106 may be formed of the same material as that of the first single crystal substrate 100, or of a different material from that of the single crystal substrate as long as it has a high melting point that is higher than the melting point of the single crystal substrate.


Furthermore, a second single crystal substrate 200 is prepared, which is to be placed over the first single crystal substrate 100.


Over the second single crystal substrate 200 also, a second metal oxide film 201 and a second gallium oxide compound film 202 are formed and laminated. Note that the second metal oxide film 201 is not always necessary. Furthermore, in the case that the first gallium oxide compound film 102 is easily crystallized, the first metal oxide film 101 is not always necessary. Also, compositions of the first gallium oxide compound film 102 and the second gallium oxide compound film 202 are preferably equivalent.


As the second metal oxide film 201, a zinc oxide film that is obtained by a sputtering method is used, and the film thickness is to be 1 nm or more and 10 nm or less.


As the second gallium oxide compound film 202, an InGaO film, an InGaZnO film, a GaZnO film, or the like that is obtained by a sputtering method can be used, and the film thickness is to be 10 nm or more and 500 nm or less.


Then, as shown in FIG. 1C, the second single crystal substrate 200 is positioned over the first single crystal substrate 100 so that the first gallium oxide compound film 102 and the second gallium oxide compound film 202 face each other with certain space therebetween created by the spacing materials 103 and 104.


Next, a heating treatment is performed at 1000° C. or higher and lower than 1900° C. However, after maintaining the temperature at 1000° C. or higher and lower than 1900° C. for a predetermined time period, cooling to room temperature is to be done naturally. Note that, for each of the first single crystal substrate 100 and the second single crystal substrate 200, a single crystal substrate that can withstand this heating treatment is to be used.


By performing the heating treatment, crystal growth occurs while a metal (zinc or indium) contained in the first gallium oxide compound film 102 is removed (for example, sublimated) from inside the film, and a gallium oxide single crystal layer 107 that is in contact with the first single crystal substrate 100 can be obtained. Note that in FIG. 1D, a dotted line shows the first gallium oxide compound film before the heating treatment, and it is shown that the gallium oxide single crystal layer 107 with a thinner film thickness than the first gallium oxide compound film can be obtained after the heating treatment.


Note that by the above heating treatment, there are cases in which the second gallium oxide compound film 202 provided over the second single crystal substrate 200 is lost.


An embodiment of the present invention having the above structure will be explained in more detail in the example below.


Example 1

In this example, as each of the first single crystal substrate and the second single crystal substrate, an yttria-stabilized zirconia substrate with a plane orientation of (1 1 1), which is a so-called YSZ substrate (substrate size of 10 mm×10 mm, thickness of 0.5 mm), is used.


Over each of the first single crystal substrate and the second single crystal substrate, a zinc oxide film with a film thickness of 2 nm and an InGaZnO film with a film thickness of 100 nm were laminated.


Formation of the zinc oxide film was performed with a film formation pressure of 0.4 Pa, a power of 0.5 kW, an argon flow rate of 10 sccm, and an oxygen flow rate of 5 sccm.


Formation of the InGaZnO film was performed using an oxide target of In2O3:Ga2O3:ZnO=1:1:1 [molar ratio], with a film formation pressure of 0.4 Pa, a power of 0.5 kW using a DC power source, an argon flow rate of 10 sccm, and an oxygen flow rate of 5 sccm. The InGaZnO film immediately after being formed is an amorphous film.


Furthermore, the spacing materials had a height of 0.5 mm, and the first single crystal substrate 100 and the second single crystal substrate 200 were arranged in a manner shown in FIG. 1C.


Then, a heating treatment was performed, and a single crystal layer of gallium oxide with a film thickness of about 70 nm was obtained in a manner that was in contact with the first single crystal substrate.


Conditions of the heating treatment were use of a high speed heating electric furnace (Product Name: NHA-3045F), and performing the heating treatment in the atmosphere at a temperature of 1400° C. for 1 hour. Note that, details of the heating treatment conditions are shown in FIG. 2.



FIG. 3 shows a cross-sectional TEM image of a crystallized region. Lattice images are lined up neatly and horizontally in a film thickness direction of about 70 nm, and it is apparent that there is growth of a single crystal.



FIG. 4 shows a result of an energy dispersive X-ray (EDX) analysis of the obtained crystal layer. From this, it is apparent that a concentration ratio of Ga atoms to O atoms is about 2:3. That is, it indicates that Ga2O3 was formed.



FIG. 5 shows an electron beam diffraction pattern of a cross section of a single crystal layer, and analysis results thereof are shown in Table 1 and Table 2









TABLE 1







lattice plane distance
















d value
measured


point
h
k
l
(nm)
d value (nm)















1
1
2
1
0.4686
0.468


2
4
−1
−1
0.2111
0.208


3
5
−1
0
0.1873
0.184
















TABLE 2







plane angle










calculated
measured



(°)
(°)





∠ 102
85.7
85.4


∠ 103
62.2
62.1









With this, it was also confirmed from the analysis result of electron beam diffraction that the obtained single crystal was Ga2O3. Furthermore, it was confirmed that the plane orientation of a surface of Ga2O3 was (1 0 1), and that there was perpendicular growth with respect to a substrate surface with this plane orientation. It was also confirmed from a result of X-ray diffraction (XRD) analysis that a crystal structure of the obtained Ga2O3 was base-centered monoclinic and β-Ga2O3. That is, Ga2O3 (1 0 1) grows with respect to the YSZ (1 1 1) substrate.


Also, as a comparative example, when the same experiment was performed using a sapphire substrate as the second single crystal substrate, a film over the YSZ substrate serving as the first single crystal substrate was lost, and a single crystal layer of gallium oxide was not obtained. From this experiment result, it can be said that the same material is preferably used for the first single crystal substrate and the second single crystal substrate. As each of the single crystal substrates, a sapphire (Al2O3) substrate, an aluminum nitride (AlN) substrate, or the like which can withstand a heat treatment at a high temperature can be used alternatively to an yttria-stabilized zirconia (YSZ) substrate.


Also, as a comparative example, when an InGaZnO film with a film thickness of 100 nm formed over the first single crystal substrate and an InGaZnO film with a film thickness of 100 nm formed over the second single crystal substrate were made to be in contact with each other by not providing spacing materials, and then subjected to the same heating treatment, Zn and In remained in the film, and a single crystal layer of gallium oxide was not obtained. From this experiment result, it can be said that in forming a single crystal layer of gallium oxide, it is necessary that there is space between the pair of substrates by providing the spacing materials between the first single crystal substrate and the second single crystal substrate.


Example 2

In this example, a result of performing an experiment under conditions with different target composition ratio and heat treatment temperature from those in Example 1 will be described. Note that, other conditions are the same as those in Example 1; therefore, descriptions there will be omitted.


In this example, an InGaZnO film was formed using an oxide target of In2O3:Ga2O3:ZnO=1:1:10 [molar ratio], with a film formation pressure of 0.4 Pa, a power of 0.5 kW using a DC power source, an argon flow rate of 10 sccm, and an oxygen flow rate of 5 sccm. Note that the InGaZnO film immediately after being formed is an amorphous film.


Also, a maintained temperature of the heating treatment was set at 1350° C. A cross-sectional TEM image of a single crystal layer of gallium oxide obtained by the heating treatment is shown in FIG. 6. It can be observed that lattice images are lined up horizontally and that a single crystal is growing.



FIG. 7 shows a result of an EDX analysis of the obtained crystal layer. It was indicated from a concentration ratio of Ga atoms and O atoms that Ga2O3 was formed.



FIG. 8 shows an electron beam diffraction pattern of a cross section of a single crystal layer, and analysis results thereof are shown in Table 3 and Table 4.









TABLE 3







lattice plane distance


















d value
measured



point
h
k
l
(nm)
d value (nm)

















1
−2
0
1
0.4687
0.467



2
1
1
1
0.2550
0.255



3
1
1
2
0.2101
0.209
















TABLE 4







plane angle










calculated
measured



(°)
(°)





∠ 102
80.6
80.8


∠ 103
54.4
55.2









With this, it was also confirmed from the analysis results of the electron beam diffraction that the obtained single crystal was Ga2O3. Also, it was confirmed that the plane orientation of a surface of Ga2O3 was (−2 0 1), and that there was perpendicular growth with this plane orientation with respect to the substrate. However, it was confirmed that this crystal growth plane orientation was different from the plane orientation (1 0 1) of single crystal Ga2O3 that was crystallized using a target of In2O3:Ga2O3:ZnO=1:1:1 [molar ratio]. Furthermore, it was confirmed from a result of X-ray diffraction (XRD) analysis that a crystal structure of the obtained Ga2O3 was base-centered monoclinic and β-Ga2O3. That is, Ga2O3 (−2 0 1) grows with respect to the YSZ (1 1 1) substrate.


Furthermore, as a comparative example, when the maintained temperature of the heating treatment was changed from 1350° C. to 1400° C., the film remaining on the first single crystal substrate became patchy and sparse. Since Ga2O3 is to be manufactured by sublimating In and Zn from the InGaZnO film, it is thought that density of Zn and In inside the InGaZnO film to be formed is preferably low. This is because it can be thought that the higher the density of In and Zn inside the InGaZnO film, the lower the film density will be after they are sublimated.


This application is based on Japanese Patent Application serial no. 2010-056118 filed with Japan Patent Office on Mar. 12, 2010, the entire contents of which are hereby incorporated by reference.

Claims
  • 1. A manufacturing method of a gallium oxide single crystal, comprising the steps of: forming a first metal oxide film over a first single crystal substrate;forming a first gallium oxide compound film comprising a metal, over the first metal oxide film;forming a second metal oxide film over a second single crystal substrate;forming a second gallium oxide compound film over the second metal oxide film; andperforming a heating treatment while the second single crystal substrate is positioned over the first gallium oxide compound film in a manner that the first gallium oxide compound film and the second gallium oxide compound film face each other with space between the first gallium oxide compound film and the second gallium oxide compound film, to obtain a gallium oxide single crystal over the first single crystal substrate from at least a part of the first gallium oxide compound film.
  • 2. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein each of the first metal oxide film and the second metal oxide film is a zinc oxide film or an oxide film containing zinc oxide and one or both of indium and gallium.
  • 3. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein the metal is at least one of indium and zinc.
  • 4. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein the second gallium oxide compound film comprises at least one of indium and zinc.
  • 5. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein the first single crystal substrate and the second single crystal substrate are formed using the same material.
  • 6. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein compositions of the first gallium oxide compound film and the second gallium oxide compound film are the same.
  • 7. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein each of the first single crystal substrate and the second single crystal substrate is an yttria-stabilized zirconia substrate, a sapphire substrate, or an aluminum nitride substrate.
  • 8. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein the gallium oxide single crystal is obtained by sublimating the metal in the first gallium oxide compound film by the heating treatment.
  • 9. The manufacturing method of a gallium oxide single crystal according to claim 1, wherein the heating treatment is performed at a temperature of equal to or higher than 1000° C. to lower than 1900° C.
  • 10. A manufacturing method of a gallium oxide single crystal, comprising the steps of: forming a first metal oxide film over a first single crystal substrate;forming a first gallium oxide compound film comprising a metal, over the first metal oxide film;forming a second gallium oxide compound film over a second single crystal substrate; andperforming a heating treatment while the second single crystal substrate is positioned over the first gallium oxide compound film in a manner that the first gallium oxide compound film and the second gallium oxide compound film face each other with space between the first gallium oxide compound film and the second gallium oxide compound film, to obtain a gallium oxide single crystal over the first single crystal substrate from at least a part of the first gallium oxide compound film.
  • 11. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the first metal oxide film is a zinc oxide film or an oxide film containing zinc oxide and one or both of indium and gallium.
  • 12. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the metal is at least one of indium and zinc.
  • 13. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the second gallium oxide compound film comprises at least one of indium and zinc.
  • 14. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the first single crystal substrate and the second single crystal substrate are formed using the same material.
  • 15. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein compositions of the first gallium oxide compound film and the second gallium oxide compound film are the same.
  • 16. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein each of the first single crystal substrate and the second single crystal substrate is a yttria-stabilized zirconia substrate, a sapphire substrate, or an aluminum nitride substrate.
  • 17. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the gallium oxide single crystal is obtained by sublimating the metal in the first gallium oxide compound film by the heating treatment.
  • 18. The manufacturing method of a gallium oxide single crystal according to claim 10, wherein the heating treatment is performed at a temperature of equal to or higher than 1000° C. to lower than 1900° C.
  • 19. A manufacturing method of a gallium oxide single crystal comprising the steps of: forming a first gallium oxide compound film comprising a metal, over a first single crystal substrate;forming a second gallium oxide compound film over a second single crystal substrate; andperforming a heating treatment while the second single crystal substrate is positioned over the first gallium oxide compound film in a manner that the first gallium oxide compound film and the second gallium oxide compound film face each other with space between the first gallium oxide compound film and the second gallium oxide compound film, to obtain a gallium oxide single crystal over the first single crystal substrate from at least a part of the first gallium oxide compound film.
  • 20. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein the metal is at least one of indium and zinc.
  • 21. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein the second gallium oxide compound film comprises at least one of indium and zinc.
  • 22. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein the first single crystal substrate and the second single crystal substrate are formed using the same material.
  • 23. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein compositions of the first gallium oxide compound film and the second gallium oxide compound film are the same.
  • 24. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein each of the first single crystal substrate and the second single crystal substrate is an yttria-stabilized zirconia substrate, a sapphire substrate, or an aluminum nitride substrate.
  • 25. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein the gallium oxide single crystal is obtained by removing the metal in the first gallium oxide compound film by the heating treatment.
  • 26. The manufacturing method of a gallium oxide single crystal according to claim 25, wherein the removing of the metal is performed by sublimating the metal.
  • 27. The manufacturing method of a gallium oxide single crystal according to claim 19, wherein the heating treatment is performed at a temperature of equal to or higher than 1000° C. to lower than 1900° C.
Priority Claims (1)
Number Date Country Kind
2010-056118 Mar 2010 JP national
US Referenced Citations (105)
Number Name Date Kind
4873833 Pfeiffer et al. Oct 1989 A
5731856 Kim et al. Mar 1998 A
5744864 Cillessen et al. Apr 1998 A
5869363 Yamazaki et al. Feb 1999 A
6204101 Yamazaki et al. Mar 2001 B1
6294274 Kawazoe et al. Sep 2001 B1
6563174 Kawasaki et al. May 2003 B2
6727522 Kawasaki et al. Apr 2004 B1
6897560 Ota et al. May 2005 B2
7049190 Takeda et al. May 2006 B2
7061014 Hosono et al. Jun 2006 B2
7064346 Kawasaki et al. Jun 2006 B2
7105868 Nause et al. Sep 2006 B2
7211825 Shih et al May 2007 B2
7282782 Hoffman et al. Oct 2007 B2
7297977 Hoffman et al. Nov 2007 B2
7323356 Hosono et al. Jan 2008 B2
7385224 Ishii et al. Jun 2008 B2
7402506 Levy et al. Jul 2008 B2
7411209 Endo et al. Aug 2008 B2
7445671 Sunkara et al. Nov 2008 B2
7453065 Saito et al. Nov 2008 B2
7453087 Iwasaki Nov 2008 B2
7462862 Hoffman et al. Dec 2008 B2
7468304 Kaji et al. Dec 2008 B2
7501293 Ito et al. Mar 2009 B2
7619301 Nishiura et al. Nov 2009 B2
7674650 Akimoto et al. Mar 2010 B2
7732819 Akimoto et al. Jun 2010 B2
20010026964 Yamazaki et al. Oct 2001 A1
20010046027 Tai et al. Nov 2001 A1
20020056838 Ogawa May 2002 A1
20020132454 Ohtsu et al. Sep 2002 A1
20030183832 Ishida et al. Oct 2003 A1
20030189401 Kido et al. Oct 2003 A1
20030218222 Wager et al. Nov 2003 A1
20040038446 Takeda et al. Feb 2004 A1
20040127038 Carcia et al. Jul 2004 A1
20050017302 Hoffman Jan 2005 A1
20050199959 Chiang et al. Sep 2005 A1
20060035452 Carcia et al. Feb 2006 A1
20060043377 Hoffman et al. Mar 2006 A1
20060091793 Baude et al. May 2006 A1
20060108529 Saito et al. May 2006 A1
20060108636 Sano et al. May 2006 A1
20060110867 Yabuta et al. May 2006 A1
20060113536 Kumomi et al. Jun 2006 A1
20060113539 Sano et al. Jun 2006 A1
20060113549 Den et al. Jun 2006 A1
20060113565 Abe et al. Jun 2006 A1
20060115962 Maeda Jun 2006 A1
20060169973 Isa et al. Aug 2006 A1
20060170111 Isa et al. Aug 2006 A1
20060197092 Hoffman et al. Sep 2006 A1
20060208977 Kimura Sep 2006 A1
20060228974 Thelss et al. Oct 2006 A1
20060231882 Kim et al. Oct 2006 A1
20060238135 Kimura Oct 2006 A1
20060244107 Sugihara et al. Nov 2006 A1
20060284171 Levy et al. Dec 2006 A1
20060284172 Ishii Dec 2006 A1
20060292777 Dunbar Dec 2006 A1
20070024187 Shin et al. Feb 2007 A1
20070046191 Saito Mar 2007 A1
20070052025 Yabuta Mar 2007 A1
20070054507 Kaji et al. Mar 2007 A1
20070090365 Hayashi et al. Apr 2007 A1
20070108446 Akimoto May 2007 A1
20070152217 Lai et al. Jul 2007 A1
20070172591 Seo et al. Jul 2007 A1
20070187678 Hirao et al. Aug 2007 A1
20070187760 Furuta et al. Aug 2007 A1
20070194379 Hosono et al. Aug 2007 A1
20070252928 Ito et al. Nov 2007 A1
20070272922 Kim et al. Nov 2007 A1
20070287296 Chang Dec 2007 A1
20080006877 Mardilovich et al. Jan 2008 A1
20080038882 Takechi et al. Feb 2008 A1
20080038929 Chang Feb 2008 A1
20080050595 Nakagawara et al. Feb 2008 A1
20080073653 Iwasaki Mar 2008 A1
20080083950 Pan et al. Apr 2008 A1
20080106191 Kawase May 2008 A1
20080128689 Lee et al. Jun 2008 A1
20080129195 Ishizaki et al. Jun 2008 A1
20080166834 Kim et al. Jul 2008 A1
20080182358 Cowdery-Corvan et al. Jul 2008 A1
20080224133 Park et al. Sep 2008 A1
20080254569 Hoffman et al. Oct 2008 A1
20080258139 Ito et al. Oct 2008 A1
20080258140 Lee et al. Oct 2008 A1
20080258141 Park et al. Oct 2008 A1
20080258143 Kim et al. Oct 2008 A1
20080296568 Ryu et al. Dec 2008 A1
20090068773 Lai et al. Mar 2009 A1
20090073325 Kuwabara et al. Mar 2009 A1
20090114910 Chang May 2009 A1
20090134399 Sakakura et al. May 2009 A1
20090152506 Umeda et al. Jun 2009 A1
20090152541 Maekawa et al. Jun 2009 A1
20090278122 Hosono et al. Nov 2009 A1
20090280600 Hosono et al. Nov 2009 A1
20100065844 Tokunaga Mar 2010 A1
20100092800 Itagaki et al. Apr 2010 A1
20100109002 Itagaki et al. May 2010 A1
Foreign Referenced Citations (26)
Number Date Country
1737044 Dec 2006 EP
2226847 Sep 2010 EP
60-198861 Oct 1985 JP
63-210022 Aug 1988 JP
63-210023 Aug 1988 JP
63-210024 Aug 1988 JP
63-215519 Sep 1988 JP
63-239117 Oct 1988 JP
63-265818 Nov 1988 JP
05-251705 Sep 1993 JP
08-264794 Oct 1996 JP
09-223669 Aug 1997 JP
11-505377 May 1999 JP
2000-044236 Feb 2000 JP
2000-150900 May 2000 JP
2002-076356 Mar 2002 JP
2002-093243 Mar 2002 JP
2002-289859 Oct 2002 JP
2003-086000 Mar 2003 JP
2003-086808 Mar 2003 JP
2004-103957 Apr 2004 JP
2004-273614 Sep 2004 JP
2004-273732 Sep 2004 JP
2008-037725 Feb 2008 JP
2008-156141 Jul 2008 JP
WO-2004114391 Dec 2004 WO
Non-Patent Literature Citations (72)
Entry
Fortunato.E et al., “Wide-Bandgap High-Mobility ZNO Thin-Film Transistors Produced at Room Temperature,”, Appl. Phys. Lett. (Applied Physics Letters) , Sep. 27, 2004, vol. 85, No. 13, pp. 2541-2543.
Dembo.H et al., “RFCPUS on Glass and Plastic Substrates Fabricated by TFT Transfer Technology,”, IEDM 05: Technical Digest of International Electron Devices Meeting, Dec. 5, 2005, pp. 1067-1069.
Ikeda.T et al., “Full-Functional System Liquid Crystal Display Using CG-Silicon Technology,”, SID Digest '04 : SID International Symposium Digest of Technical Papers, 2004, vol. 35, pp. 860-863.
Nomura.K et al., “Room-Temperature Fabrication of Transparent Flexible Thin-Film Transistors Using Amorphous Oxide Semiconducters,”, Nature, Nov. 25, 2004, vol. 432, pp. 488-492.
Park.J et al., “Improvements in the Device Characteristics of Amorphous Indium Gallium Zinc Oxide Thin-Film Transistors By Ar Plasma Treatment,”, Appl. Phys. Lett. (Applied Physics Letter) , Jun. 26, 2007, vol. 90, No. 26, pp. 262106-1-262106-3.
Takahashi.M et al., “Theoretical Analysis of IGZO Transparent Amorphous Oxide Semiconductor,”, IDW '08 : Proceedings of the 15th International Display Workshops, Dec. 3, 2008, pp. 1637-1640.
Hayashi.R et al., “42.1: Invited Paper: Improved Amorphous In-Ga-Zn-O TFTS,”, SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008 vol. 39, pp. 621-624.
Prins.M et al., “A Ferroelectric Transparent Thin-Film Transistor,”, Appl. Phys. Lett. (Applied Physics Letters) , Jun. 17, 1996, vol. No. 25, pp. 3650-3652.
Nakamura.M et al., “The phase relations in the In2O3-Ga2ZnO4-ZnO system at 1350°C,”, Journal of Solid State Chemistry, Aug. 1, 1991, vol. 93, No. 2 pp. 298-315.
Kimizuka.N. et al., “Syntheses and Single-Crystal Data of Homologous Compounds, In2O3(ZnO)m (m=3, 4, and 5), InGaO3(ZnO)3, and Ga2O3(ZnO)m (m=7, 8, 9, and 16) in the In2O3-ZnGa2O4-ZnO System,”, Journal of Solid State Chemistry, Apr. 1, 1995, vol. 116, No. 1, pp. 170-178.
Nomura.K et al., “Thin-Film Transistor Fabricated in Single-Crystalline Transparent Oxide Semiconductor,”, Science, May 23, 2003, vol. 300, No. 5623, pp. 1269-1272.
Masuda.S et al., “Transparent thin film transistors using ZnO as an active channel layer and their electrical properties,”, J. Appl. Phys. (Journal of Applied Physics) , Feb. 1, 2003, vol. 93, No. 3, pp. 1624-1630.
Asakuma.N. et al., “Crystallization and Reduction of Sol-Gel-Derived Zinc Oxide Films by Irradiation with Ultaviolet Lamp,”, Journal of Sol-Gel Science and Technology, 2003, vol. 26, pp. 181-184.
Osada.T et al., “15.2: Development of Driver-Integrated Panel using Amorphous In-Ga-Zn-Oxide TFT,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 184-187
Nomura.K et al., “Carrier transport in transparent oxide semiconductor with intrinsic structural randomness probed using single-crystalliine InGaO3(ZnO)5 films,”, Appl. Phys. Lett. (Applied Physics Letters) , Sep. 13, 2004 vol. No. 11, pp. 1993-1995.
Li.C et al., “Modulated Structures of Homologous Compounds InMO3(ZnO)m (M=In,Ga; m=Integer) Described by Four-Dimensional Superspace Group,”, Journal of Solid State Chemistry , 1998 vol. 139, pp. 347-355.
Son.K et al., “42.4L: Late-News Paper: 4 Inch QVGA AMOLED Driven by the Threshold Voltage Controlled Amorphous GIZO (Ga2O3-In2O3-ZnO) TFT,”, SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, pp. 633-636.
Lee.J et al., “World's Largest (15-Inch) XGA AMLCD Panel Using IGZO Oxide TFT,”, SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 38, pp. 625-628.
Nowatari.H et al., “60.2: Intermediate Connector With Suppressed Voltage Loss for White Tandem OLEDS,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, vol. 40, pp. 899-902.
Kanno.H et al., “White Stacked Electrophosphorecent Organic Light-Emitting Devices Employing MOO3 as a Charge-Generation Layer,”, Adv. Mater. (Advanced Materials), 2006, vol. 18, No. 3, pp. 339-342.
Tsuda.K et al., “Ultra Low Power Consumption Technologies for Mobile TFT-LCDs ,”, IDW '02 : Proceedings of the 9th International Display Workshops, Dec. 4, 2002, pp. 295-298.
Van de Walle.C, “Hydrogen as a Cause of Doping in Zinc Oxide,”, Phys. Rev. Lett. (Physical Review Letters), Jul. 31, 2000, vol. 85, No. 5, pp. 1012-1015.
Fung.T et al., “2-D Numerical Simulation of High Performance Amorphous In-Ga-Zn-O TFTs for Flat Panel Displays,”, AM-FPD '08 Digest of Technical Papers, Jul. 2, 2008, pp. 251-252, The Japan Society of Applied Physics.
Jeong.J et al., “3.1: Distinguished Paper: 12.1-Inch WXGA AMOLED Display Driven by Indium-Gallium-Zinc Oxide TFTs Array,”, SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, No. 1, pp. 1-4.
Park.J et al., “High performance amorphous oxide thin film transistors with self-aligned top-gate structure,”, IEDM 09: Technical Digest of International Electron Devices Meeting, Dec. 7, 2009, pp. 191-194.
Kurokawa.Y et al., “UHF RFCPUS on Flexible and Glass Substrates for Secure RFID Systems,”, Journal of Solid-State Circuits , 2008, vol. 43, No. 1, pp. 292-299.
Ohara.H et al., “Amorphous In-Ga-Zn-Oxide TFTs with Suppressed Variation for 4.0 inch QVGA AMOLED Display,”, AM-FPD '09 Digest of Technical Papers, Jul. 1, 2009, pp. 227-230, The Japan Society of Applied Physics.
Coates.D et al., “Optical Studies of the Amorphous Liquid-Cholesteric Liquid Crystal Transition:The “Blue Phase”,”, Physics Letters, Sep. 10, 1973, vol. 45A, No. 2, pp. 115-116.
Cho.D et al., “21.2:AL and SN-Doped Zinc Indium Oxide Thin Film Transistors for AMOLED Back-Plane,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 280-283.
Lee.M et al., “15.4:Excellent Performance of Indium-Oxide-Based Thin-Film Transistors by DC Sputtering,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 191-193.
Jin.D et al., “65.2:Distinguished Paper:World-Largest (6.5″) Flexible Full Color Top Emission AMOLED Display on PLastic Film and its Bending Properties,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 983-985.
Sakata.J et al., “Development of 4.0-IN. AMOLED Display With Driver Circuit Using Amorphous In-Ga-Zn-Oxide TFTs, ”, IDW '09 : Proceedings of the 16th International Display Workshop, 2009, pp. 689-692.
Park.J et al., “Amorphous Indium-Gallium-Zinc Oxide Tfts and Their Application for Large Size AMOLED,”, AM-FPD '08 Digest of Technical Papers, Jul. 2, 2008, pp. 275-278.
Park.S et al., “Challenge to Future Displays: Transparent AM-OLED Driven by Peald Grown ZNO TFT,”, IMID '07 Digest, 2007, pp. 1249-1252.
Godo.H et al., “Temperature Dependence of Characteristics and Electronic Structure for Amorphous In-Ga-Zn-Oxide TFT,”,AM-FDP '09 Digest of Technical Papers, Jul. 1, 2009, pp. 41-44.
Osada.T et al., “Development of Driver-Integrated Panel Using Amorphous In-Ga-Zn-Oxide TFT,”, AM-FPD '09 Digest of Technical Papers, Jul. 1, 2009, pp. 33-36.
Hirao.T et al., “Novel Top-Gate Zinc Oxide Thin-Film Transistors (ZNO TFTS) for AMLCDS,”, Journal of the SID, 2007, vol. 15, No. 1, pp. 17-22.
Hosono.H, “68.3:Invited Paper:Transparent Amorphous Oxide Semiconductors for High Performance TFT,”, SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1830-1833.
Godo.H et al., “P-9:Numerical Analysis on Temperature Dependence of Characteristics of Amorphous In-Ga-Zn-Oxide TFT,”, SID '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 1110-1112.
Ohara.H et al., “21.3:4.0 in. QVGA AMOLED Display Using In-Ga-Zn-Oxide TFTs With a Novel Passivation Layer,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 284-287.
Miyasaka.M, “Suftla Flexible Microelectronics on Their Way to Business,”, SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1673-1676.
Chern.H et al., “An Analytical Model for the Above-Threshold Characteristics of Polysilicon Thin-Film Transistors,”, IEEE Transactions on Electron Devices, Jul. 1, 1995, vol. 42, No. 7, pp. 1240-1246.
Kikuchi.H et al., “39.1:Invited Paper:Optically Isotropic Nano-Structured Liquid Crystal Composites for Display Applications,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 578-581.
Asaoka.Y et al., “29.1: Polarizer-Free Reflective LCD Combined With Ultra Low-Power Driving Technology,”, SID Digest '09 : SID International Symposium Digest of Technical Papers, May 31, 2009, pp. 395-398.
Lee.H et al., “Current Status of, Challenges to, and Perspective View of AM-OLED ,”, IDW '06 : Proceedings of the 13TH International Display Workshops, Dec. 7, 2006, pp. 663-666.
Kikuchi.H et al., “62.2:Invited Paper:Fast Electro-Optical Switching in Polymer-Stabilized Liquid Crystalline Blue Phases for Display Application,”, SID Digest '07 : SID International Symposium Digest of Technical Papers, 2007, vol. 38, pp. 1737-1740.
Nakamura.M, “Synthesis of Homologous Compound with New Long-Period Structure,”, Nirim Newsletter, Mar. 1, 1995, vol. 150, pp. 1-4.
Kikuchi.H et al., “Polymer-Stabilized Liquid Crystal Blue Phases,”, Nature Materials, Sep. 1, 2002, vol. 1, pp. 64-68.
Kimizuka.N. et al., “Spinel,YBFE204, and YB2FE3O7 Types of Structures for Compounds in the IN2O3 and SC2O3-A2O3-BO Systems [A; FE, GA, or AL; B: MG, MN, FE, NI, CU,or ZN] at Temperatures Over 1000°C,”, Journal of Solid State Chemistry, 1985, vol. 60, pp. 382-384.
Kitzerow.H et al., “Observation of Blue Phases in Chiral Networks,”, Liquid Crystals, 1993, vol. 14, No. 3, pp. 911-916.
Costello.M et al., “Electron Microscopy of a Cholesteric Liquid Crystal and Its Blue Phase,”, Phys. Rev. A (Physical Review. A.), May 1, 1984, vol. 29, No. 5, pp. 2957-2959.
Meiboom.S et al., “Theory of the Blue Phase of Cholesteric Liquid Crystals,”, Phys. Rev. Lett. (Physical Review Letters), May 4, 1981, vol. 46, No. 18, pp. 1216-1219.
Park.Sang-Hee et al., “42.3: Transparent ZnO Thin Film Transistor for the Application of High Aperture Ratio Bottom Emission AM-OLED Display,”, SID Digest '08 : SID International Symposium Digest of Technical Papers, May 20, 2008, vol. 39, pp. 629-632.
Orita.M et al., “Mechanism of Electrical Conductivity of Transparent InGaZn04,”, Phys. Rev. B. (Physical Review. B), Jan. 15, 2000, vol. No. 3, pp. 1811-1816.
Nomura.K et al., “Amorphous Oxide Semiconductors for High-Performance Flexible Thin-Film Transistors,”, Jpn. J. Appl. Phy. (Japanese Journal of Applied Physics) , 2006, vol. 45, No. 5B, pp. 4303-4308.
Janotti.A et al., “Native Point Defects in ZnO,”, Phys. Rev. B (Physical Review. B), Oct. 4, 2007, vol. 76, No. 16, pp. 165202-1-165202-22.
Park.J et al., “Electronic Transport Properties of Amorphous Indium-Gallium-Zinc Oxide Semiconductor Upon Exposure to Water,”, Appl. Phys. Lett. (Applied Physics Letters) , 2008, vol. 92, pp. 072104-1-072104-3.
Hsieh.H et al., “P-29:Modeling of Amorphous Oxide Semiconductor Thin Film Transistors and Subgap Density of States.”, SID Digest '08 : SID International Symposium Digest of Technical Papers, 2008, vol. 39, pp. 1277-1280.
Janotti.A et al., “Oxygen Vacancies in ZnO,”, Appl. Phys. Lett. (Applied Physics Letters) , 2005, vol. 87, pp. 122102-1-122102-3.
Oba.F et al., “Defect energetics in ZnO: A hybrid Hartree-Fock density functional study,”, Phys. Rev. B. (Physical Review. B), 2008, vol. 77, pp. 245202-1-245202-6.
Orita.M et al., “Amorphous transparent conductive oxide InGaO3(ZnO)m (m<4):a Zn4s conductor,”, Philosophical Magazine, 2001 vol. 81, No. 5, pp. 501-515.
Hosono.H et al., “Working hypothesis to explore novel wide band gap electrically conducting amorphous oxides and examples,”, J. Non-Cryst. Solids (Journal of Non-Crystalline Solids), 1996, vol. 198-200, pp. 165-169.
Mo.Y et al., “Amorphous Oxide TFT Backplanes for Large Size AMOLED Displays,”, IDW '08 : Proceedings of the 6TH International Display Workshops, Dec. 3, 2008, pp. 581-584.
Kim.S et al., “High-Performance oxide thin film transistors passivated by various gas plasmas,”, 214th ECS Meeting, 2008, No. 2317.
Clark.S et al., “First Principles Methods Using CASTEP,”, Zeitschrift fur Kristallographie, 2005, vol.220, pp. 567-570.
Lany.S et al., “Dopability, Intrinsic Conductivity, and Nonstoichiometry of Transparent Conducting Oxides,”, Phys. Rev. Lett. (Physical Review Letters), Jan. 26, 2007, vol. 98, pp. 045501-1-045501-4.
Park.J et al., “Dry etching of ZnO films and plasma-induced damage to optical properties,”, J. Vac. Sci. Technol. B (Journal of Vacuum Science & Technology B), Mar. 1, 2003, vol. 21, No. 2, pp. 800-803.
Oh.M et al., “Improving the Gate Stability of ZNO Thin-Film Transistors With Aluminum Oxide Dielectric Layers,”, J. Electrochem. Soc. (Journal of the Electrochemical Society), 2008, vol. 155, No. 12, pp. H1009-H1014.
Ueno.K et al., “Field-Effect Transistor on SrTiO3 With Sputtered AI2O3 Gate Insulator,”, Appl. Phys. Lett. (Applied Physics Letters), Sep. 1, 2003, vol. 83, No. 9, pp. 1755-1757.
Tippins.H, “Optical Absorption and Photoconductivity in the Band Edge of (β-Ga203,”, Phys. Rev. (Physical Review), Oct. 4, 1965, vol. 140, No. 1A, pp. A316-A319.
Orita.M et al., “Deep-ultraviolet transparent conductive β-Ga203 thin films,”, Appl. Phys. Lett. (Applied Physics Letters) , Dec. 18, 2000, vol. 77, No. 25, pp. 4166-4168.
Takagi.T et al., “Molecular Beam Epitaxy of High Magnesium Content Single-Phase Wurzite MgxZni-xO Alloys (x =0.5) and Their Application to Solar-Blind Region Photodetectors,”, JPN. J. Appl. Phys. (Japanese Journal of Applied Physics) , 2003, vol. 42, Part 2, No. 4B, pp. L401-L403.
Related Publications (1)
Number Date Country
20110220011 A1 Sep 2011 US