LAYERED BODY HAVING FUNCTION AS TRANSPARENT ELECTROCONDUCTIVE FILM AND METHOD FOR PRODUCING SAME, AND OXIDE SPUTTERING TARGET FOR SAID LAYERED BODY PRODUCTION

Information

  • Patent Application
  • 20240183022
  • Publication Number
    20240183022
  • Date Filed
    April 21, 2022
    2 years ago
  • Date Published
    June 06, 2024
    22 days ago
Abstract
Provided is a layered body having lower resistivity (higher conductivity) and higher transmittance than conventional ITO films. A layered body obtained by layering an ITO film and an oxide film, wherein the layered body has a surface resistance of 40 Ω/sq. or less and a visible light average transmittance of 90% or higher, and a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15. A layered body obtained by layering an ITO film and an oxide film, wherein R2/R1≤1.0 is satisfied when a surface resistance of the layered body that underwent atmosphere annealing at 220° C. is R1, and a surface resistance of the layered body that underwent atmosphere annealing at 550° C. is R2.
Description
TECHNICAL FIELD

The present invention relates to a layered body having a function as a transparent electroconductive film, a method for producing the layered body, and an oxide sputtering target for producing the layered body.


BACKGROUND ART

ITO (Indium-Tin-Oxide) films are used across a broad range of fields, including display electrodes for flat panel displays, since they exhibit characteristics such as low resistivity, high transmittance and ease of microfabrication, and these characteristics are superior to those of other transparent electroconductive films. Today, since many of the ITO films for industrial use have superior large-area uniformity and can be produced with favorable productivity, they are produced based on the so-called sputter deposition method of depositing films using an ITO sintered body as the sputtering target.


Since an ITO film will become a low-resistant, transparent film by being crystallized, annealing is performed at roughly 220 to 250° C. after deposition. Meanwhile, films having low resistivity and high transmittance are desired, and annealing at a temperature of 300° C. or higher is also being attempted. Nevertheless, when annealing is performed, while transmittance will improve, resistivity will increase, and, as it stands now, films comprising both lower resistivity and higher transmittance have not been realized. The present applicant has previously proposed a technology capable of forming low resistance ITO films at a low temperature (for example, Patent Document 1).


PRIOR ART DOCUMENTS
Patent Documents

[Patent Document 1] Japanese Unexamined Patent Application Publication No. 2020-16493


DISCLOSURE OF THE INVENTION
Problems to Be Solved by the Invention

An object of the present invention is to provide a layered body having lower resistivity (surface resistance) and higher transmittance than ITO films.


Means for Solving the Problems

In order to achieve the foregoing object, as a result of intense study, the present inventors discovered that, by preparing a layered body by layering a specific oxide film on an ITO film, high transmittance can be maintained while preventing the increase in resistivity (surface resistance) caused by annealing. Based on this kind of discovery, the present disclosure provides the following modes of the present invention.


One mode of the present invention is a layered body obtained by layering an oxide film on an ITO film, wherein the layered body has a surface resistance of 40 Ωcm/sq. or less and a visible light average transmittance of 90% or higher, and a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15.


Another mode of the present invention is a layered body obtained by layering an ITO film and an oxide film, wherein R2/R1≤1.0 is satisfied when a surface resistance of the layered body that underwent atmosphere annealing at 220° C. is R1, and a surface resistance of the layered body that underwent atmosphere annealing at 550° C. is R2.


Moreover, another mode of the present invention is a layered body obtained by layering an ITO film and an oxide film, wherein the oxide film contains Zn in an amount of 0 mol % or more and less than 69 mol % in terms of ZnO, Ga in an amount of 9 mol % or more and 100 mol % or less in terms of Ga2O3, and Si in an amount of 0 mol % or more and less than 60 mol % in terms of SiO2, a film thickness of the oxide film is less than 90 nm, and a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15.


Furthermore, another mode of the present invention is an oxide sputtering target containing Zn in an amount of more than 10 mol % and less than 60 mol % in terms of ZnO, Ga in an amount of 10 mol % or more and 60 mol % or less in terms of Ga2O3, and Si in an amount of 25 mol % or more and less than 50 mol % in terms of SiO2.


Effect of the Invention

The layered body according to the present invention comprises superior characteristics, specifically lower resistivity (surface resistance) and higher high transmittance, than ITO films. Moreover, by layering a specific oxide film on an ITO film, a transparent electroconductive film (layered body) comprising favorable characteristics can be provided easily.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is an assembly drawing showing the relationship of the composition corresponding to the oxide film (Zn—Ga—Si—O) in the layered body of this embodiment and the effect of the present invention.





BEST MODE FOR CARRYING OUT THE INVENTION

ITO films having indium (In), tin (Sn), and oxygen (O) as their main components are used for a broad range of applications, including use in flat panel displays, since they exhibit characteristics such as low resistivity, high transmittance and ease of microfabrication, and these characteristics are superior to those of other transparent electroconductive films. Meanwhile, lower resistivity and higher transmittance of ITO films are demanded, and attempts for improving characteristics, such as adding other elements, are being performed continuously.


Since an ITO film will become a low-resistant, transparent film by being crystallized, annealing is performed at roughly 220 to 250° C. after deposition. Here, while transmittance can be improved by performing annealing at a higher temperature (300° C. or higher), the resistivity will increase. This is considered to be because the carrier concentration of the ITO film will deteriorate during the high temperature annealing. Accordingly, the present inventors considered that it may be possible to prevent the increase of resistivity by layering an oxide film on an ITO film in order to suppress the deterioration in the carrier concentration caused by the high temperature annealing.


As a result of intense study, the present inventors discovered that, by forming a specific oxide film on an ITO film, it is possible to maintain high transmittance while suppressing the deterioration in the carrier concentration and prevent the increase in the resistivity caused by annealing. Embodiments of the present invention are now explained in detail.


In the present specification, an ITO film is composed of oxides containing In and Sn, and, while there is no particular limitation to the composition range thereof, for example, it is possible to use ITO containing Sn in an amount of 50 wt % (approximately 65 mol %) or less in terms of SnO2, and the remainder being In and unavoidable impurities.


The first embodiment is a layered body obtained by layering an oxide film on an ITO film, wherein the layered body has a surface resistance of 40 Ω/sq. or less and a visible light average transmittance of 90% or higher. The layered body of this embodiment yields a superior effect of being able to achieve lower resistivity and higher transmittance in comparison to ITO films (single films). The surface resistance is preferably 30 Ω/sq. or less, and more preferably 20 Ω/sq. or less. Moreover, the visible light average transmittance is preferably 93% or higher. Note that, since the surface resistance and transmittance will change depending on the annealing temperature, so as long as the foregoing surface resistance and transmittance can be attained irrespective of the annealing temperature of the layered body, they are covered by the layered body of this embodiment.


In the first embodiment, a film thickness of the oxide film layered on the ITO is less than 90 nm, preferably 70 nm or less, and more preferably 50 nm or less. If the film thickness is too thick, the resistivity of the layered body may increase. Meanwhile, if the film thickness is too thin, it may not be possible to sufficiently suppress the deterioration in the carrier concentration of the ITO film, and thus the film thickness is preferably 10 nm or more. Since the effect of suppressing the deterioration in the carrier concentration and the transmittance will be affected by the composition of the oxide film, the film thickness may be adjusted by giving consideration to the composition of the oxide film.


In the first embodiment, a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15, and preferably 10 or less. While the surface roughness of the ITO film will increase when the ITO film is crystallized, the surface roughness will increase as the film thickness becomes thicker. This is because, when the film thickness of the oxide film is too thin relative to the surface roughness of the ITO film, it may not be possible to sufficiently suppress the deterioration in the carrier concentration of the ITO film.


The layered body according to the second embodiment is a layered body obtained by layering an ITO film and an oxide film, wherein R2/R1≤1.0 is satisfied when a surface resistance of the layered body that underwent atmosphere annealing at 220° C. is R1, and a surface resistance of the layered body that underwent atmosphere annealing at 550° C. is R2. The layered body of this embodiment yields a superior effect of being able to achieve lower resistivity and higher transmittance in comparison to ITO films (single films). Preferably, R2/R1≤0.5 is satisfied. In the case of an ITO single film (film thickness of 100 nm), R2/R1 is roughly 1.53, and the layered body of this embodiment yields a superior effect of being able to suppress the increase of the resistivity even when the annealing temperature is increased.


The layered body according to this embodiment can be used as a transparent electroconductive film and, in such a case, high transmittance is demanded. The layered body according to this embodiment preferably has a visible light average transmittance of 85% or higher when it is annealed at 220° C. in the atmosphere, and preferably has a visible light average transmittance of 90% or higher when it is annealed at 550° C. in the atmosphere.


The layered body according to this embodiment preferably satisfies n1>n2 when a refractive index of the ITO film is n1, and a refractive index of the oxide film is n2. By layering an oxide film, which has a lower refractive index than an ITO film, on an ITO film, it is possible to reduce the reflectance and improve the transmittance. It is thereby possible to obtain a layered body suitable for use as a transparent electroconductive film.


In the layered body according to this embodiment, while there is no particular limitation to the oxide film to be layered on the ITO film so as long as it is a film that can prevent the deterioration in the carrier concentration of the ITO film, it preferably contains one or more types among Zn, Ga, and Si. While it could be said that the ITO film is in itself an oxide film, the oxide film in the present specification does not include an ITO film having the same composition as the base film.


The layered body according to the third embodiment is a layered body obtained by layering an ITO film and an oxide film, wherein the oxide film contains Zn in an amount of 0 mol % or more and less than 69 mol % in terms of ZnO, Ga in an amount of 9 mol % or more and 100 mol % or less in terms of Ga2O3, and Si in an amount of 0 mol % or more and less than 60 mol % in terms of SiO2. The layered body of this embodiment yields a superior effect of being able to achieve lower resistivity and higher transmittance in comparison to ITO films (single films).


Preferably, the layered body of this embodiment contains Zn in an amount of more than 10 mol % and less than 60 mol % in terms of ZnO, Ga in an amount of 10 mol % or more and 60 mol % or less in terms of Ga2O3, and Si in an amount of 25 mol % or more and less than 50 mol % in terms of SiO2.


In the layered body according to this embodiment, the oxide film is preferably in an amorphous state. When the layered body of this embodiment is annealed, the ITO film will become crystallized, but the layered oxide film will maintain its amorphous state, and it is considered that the maintenance of this amorphous state considerably contributes to suppressing the increase of the resistivity.


The method of producing the layered body according an embodiment of the present invention is now specifically explained. The following is merely an exemplification, and there is no intention of limiting the production method to the following example, and other methods may also be adopted as the method of producing the layered body itself. In order to avoid the disclosed production method from becoming unclear unnecessarily, the detailed explanation of known production processes and handling operations is omitted.


An ITO sputtering target composed of oxides containing In and Sn, and a Zn—Ga—Si—O sputtering target composed of oxides containing Zn, Ga, and Si, are prepared. Foremost, the ITO sputtering target is mounted in a vacuum chamber of a sputtering system, and a film is deposited on a substrate facing the sputtering target. Subsequently, the Zn—Ga—Si—O sputtering target is used to form an oxide film on the ITO film deposited on the substrate. The film thickness of the ITO film and the oxide film can be adjusted based on the sputtering power and the sputtering time.


With the sputtering method, since deposition is performed in a vacuum, under normal circumstances, the composition of the sputtering target is reflected in the composition of the film without any loss of metal components configuring the sputtering target or inclusion of other metal compositions during the deposition process. As described later, the composition of the sputtering target is indicated in the Examples and Comparative Examples as a matter of convenience.


The sputtering conditions may be set, for example, as follows. The sputtering conditions may be changed as needed depending on the intended film thickness and composition.


Sputtering Conditions





    • Sputtering system: C-7500L manufactured by ANELVA

    • Sputtering power: DC500 to 1000 W





Targets That Cannot Undergo DC Sputtering are RF500 to 1000 W





    • Gas pressure: 0.5 Pa

    • Substrate heating: Room temperature

    • Oxygen concentration: 0%, 1%, 2%





Subsequently, after removing the layered body obtained by forming a prescribed oxide film on an ITO film from the sputtering system, annealing is performed at 200 to 600° C. in the atmosphere to crystallize the ITO film. The annealing temperature can be decided as needed by giving consideration to the intended resistivity and transmittance, and the heatproof temperature of the base material. The annealing atmosphere is not limited to the atmosphere, and it may also be a vacuum or a nitrogen atmosphere. The layered body according to this embodiment can thereby be produced.


As the sputtering target to be used for forming the oxide film, while a sputtering target having the same composition as the oxide film may be used, a film may also be deposited based on co-sputtering by using two or more types of sputtering targets. While a Zn—Ga—Si—O sputtering target was illustrated above, it is also possible to use a Zn—Ga—O sputtering target, a Zn—Si—O— sputtering target, a Ga—Si—O sputtering target, a ZnO sputtering target, a Ga2O3 sputtering target, a SiO2 sputtering target or the like. Moreover, while sputtering is a method suitable for the deposition of an oxide film, other chemical or physical deposition methods may also be used.


Moreover, the sputtering target to be used in forming the oxide film may also include, as a sintering additive, B2O3, P2O5, V2O5, Sb2O3, TeO2, Tl2O3, PbO, Bi2O3, or MoO3. These sintering additives are low-melting point oxides, and a dense sintered body (sputtering target) can be produced even when the sintering temperature is lowered. While there is no particular limitation to the additive amount of the sintering additive, the additive amount of the sintering additive is preferably 0.5 wt % or higher and 3.0 wt % or less relative to the basic composition of the target to be used for forming the oxide film. This is because, when the additive amount of the sintering additive is less than 0.5 wt %, the effect of addition as the sintering additive will be weak, and when the additive amount of the sintering additive exceeds 3.0 wt %, it may influence the characteristics of the oxide film. When the additive amount of the sintering additive is 0.5 wt % or higher and 3.0 wt % or less, low temperature sintering is enabled while maintaining the favorable characteristics of the oxide film.


In the present specification, the characteristics of the layered body were evaluated in the following manner.


Surface Resistance of the Film





    • The surface resistance of the layered body, which was obtained by layering an oxide film on an ITO film, was measured from the oxide film side.

    • System: Constant current application system

    • Device: Resistivity meter Σ−5+ manufactured by NPS

    • Method: DC 4-point probe method

    • In the case of high resistivity (100 k Ω/sq. or more)

    • System: Constant voltage application system

    • Device: High resistivity meter Hiresta-UX manufactured by Mitsubishi Chemical Analytech

    • Method: MCC-A method (JISK6911)

    • Ring electrode probe: URS

    • Measuring voltage: 1 to 1000 V





Transmittance of the Film





    • The transmittance of the layered body, which was obtained by layering an oxide film on an ITO film, was measured from the oxide film side.

    • Visible light average transmittance

    • Device: Spectrophotometer UV-2450, UV-2600 manufactured by SHIMADZU

    • Reference: Undeposited glass substrate (EagleXG)

    • Measuring wavelength: 380 to 780 nm

    • Step: 5 nm





Film Thickness





    • Device: Stylus profiler DektakXT manufactured by BRUKER





Refractive Index of the Film





    • Device: Spectrophotometer UV-2450 manufactured by SHIMADZU

    • Method: Calculated from transmittance and back-surface reflectance





Carrier Concentration and Carrier Mobility of the Film

The carrier concentration and the carrier mobility of the layered body, which was obtained by layering an oxide film on an ITO film, was measured from the oxide film side.

    • Principle: Hall measurement
    • Device: LakeShore 8400 Series


Crystallinity, Amorphous State of the Film

In the X-ray diffraction spectrum, the film was determined to be a crystalline film when a clear diffraction peak resulting from the film material was confirmed, and the film was determined to be an amorphous film when a clear diffraction peak could not be observed, and only a halo pattern was visible.

    • Principle: X-ray diffraction method
    • Device: UltimalV manufactured by Rigaku
    • Tube: Cu-Kα rays
    • Tube voltage: 40 kV
    • Tube current: 30 mA
    • Measuring method: 2θ-θ reflection method
    • Measuring range: 20 to 90°
    • Scanning speed: 8°/min
    • Sampling interval: 0.02°
    • Measurement sample: Film surface of a single film having a film thickness of 300 nm or more was measured.


EXAMPLES

The present invention is now explained based on the following Examples and Comparative Examples. Note that the following Examples are merely representative examples, and the present invention is not limited to these Examples in any way. In other words, the present invention is limited only based on the scope of its claims, and covers various modifications other than the Examples included in the present invention.


Reference Example

An ITO sintered body sputtering target configured from In2O3:90 wt % (83 mol %), SnO2:10 wt % (17 mol %) was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an ITO film having a film thickness of 100 nm was formed on a substrate. Subsequently, annealing was performed for 30 minutes in the atmosphere at different temperatures of 220° C. and 550° C. The surface resistance and the visible light average transmittance of the thus obtained ITO film were measured. The results are shown in Table 1. Note that “as-depo” in Table 1 indicates that the film was not annealed after deposition.


From Table 1, it can be understood that, when the ITO film is annealed at 220° C., the ITO film became crystallized and the surface resistance deteriorated drastically, but when the ITO film is annealed at 550° C., the surface resistance increased. With this ITO film, R2/R1 is exceeding 1.0, and, when compared to low temperature annealing (220° C.), the surface resistance has increased in the case of high temperature annealing (550° C.). Meanwhile, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher.


Example 1

A sputtering target configured from a Zn—Ga—Si—O sintered body was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an oxide film (Zn—Ga—Si—O) having a film thickness of 20 nm was layered on an ITO film (film thickness of 100 nm) that was prepared based on the same conditions as the Reference Example. The composition (in terms of oxide) of the sputtering target was set to be ZnO:Ga2O3, SiO2=40:20:40 (mol %). Subsequently, annealing was performed for 30 minutes in the atmosphere at different temperatures of 220° C. and 550° C. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 1.


As shown in Table 1, when the layered body is annealed at 220° C., the ITO film became crystallized and the resistivity deteriorated drastically. Meanwhile, unlike the ITO film (single film), the resistivity deteriorated when the layered body was annealed at 550° C. R2/R1 exceeded 1.0 considerably, and it can be understood that the surface resistance deteriorates considerably with high temperature annealing (550° C.). Moreover, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher. By producing a layered body obtained by layering an ITO film and an oxide film in the manner described above, low resistivity and high transmittance, which could not be obtained with conventional ITO films, can be realized.


Examples 2 to 23

As with Example 1, an oxide film (Zn—Ga—Si—O) having a film thickness of 20 nm was layered on an ITO film (film thickness of 100 nm). In each of the Examples, as shown in Table 1, the composition (in terms of oxide) of the sputtering target and the oxygen concentration at the time of deposition were adjusted. Moreover, in Examples 22 and 23, 1.0 wt % of B2O3 was added as a sintering additive to the sputtering target. Subsequently, annealing was performed for 30 minutes in the atmosphere at different temperatures of 220° C. and 550° ° C. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 1.


As shown in Table 1, when the layered body is annealed at a certain temperature or higher, the ITO film became crystallized and the surface resistance deteriorated drastically. Meanwhile, unlike the ITO film (single film), the surface resistance deteriorated when the layered body was annealed at 550° C. R2/R1 exceeded 1.0 considerably, and it can be understood that the surface resistance deteriorates considerably with high temperature annealing (550° C. Moreover, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher. Furthermore, in all of the layered bodies, the oxide film maintained its amorphous state. By producing a layered body obtained by layering an ITO film and an oxide film in the manner described above, low resistivity and high transmittance, which could not be obtained with ITO films (single films), can be realized.


Comparative Examples 1 to 4

As with Example 1, an oxide film (Zn—Ga—Si—O) having a film thickness of 20 nm was layered on an ITO film (film thickness of 100 nm). In each of the Comparative Examples, as shown in Table 1, the composition (in terms of oxide) of the sputtering target and the oxygen concentration at the time of deposition were adjusted. Subsequently, annealing was performed for 30 minutes in the atmosphere at different temperatures of 220° C. and 550° C. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 1.


As shown in Table 1, when the layered body is annealed at 220° C., the ITO film became crystallized and the surface resistance deteriorated drastically. Meanwhile, the surface resistance increased when the layered body was annealed at 550° C. In the Comparative Example, R2/R1 exceeded 1.0 in all cases, and, in comparison to low temperature annealing (220° C.), it can be understood that the surface resistance increases with high temperature annealing (550° C. Meanwhile, when annealing is performed at 550° C., the transmittance improved to 90% or higher.


The composition diagram showing the relationship of the composition of the sputtering target (corresponds to the composition of the oxide film) and the effect of the present invention (low resistance and high transmittance) in Examples 1 to 21 and Comparative Examples 1 to 4 is shown in FIG. 1.
















TABLE 1









ITO/Oxide film
Oxygen content
















Composition of target (mol %)
thickness
during deposition
Surface resistance (Ω/sq)


















Oxide film
ZnO
Ga2O3
SiO2
(nm)
ITO/Oxide film
as-depo
220° C.
550° C.
550° C./220° C.





Reference
ITO single film



100/—
1%
177
32
49
1.53


Example


Example1
Zn-Ga-Si-O
40
20
40
100/20
1%/0%
127
35
1text missing or illegible when filed
0.4text missing or illegible when filed


Example2
Zn-Ga-Si-O
40
20
40
100/20
1%/2%
15text missing or illegible when filed
43
1text missing or illegible when filed
0.42


Example3
Zn-Ga-Si-O

text missing or illegible when filed

16
12
100/20
1%/2%
173
4text missing or illegible when filed
30
0.text missing or illegible when filed 5


Example4
Zn-Ga-Si-O
10
60
30
100/20
1%/2%
15text missing or illegible when filed
44
21
0.48


Example5
En-Ga-Si-O
30
20
50
100/20
1%/2%
130
45
1text missing or illegible when filed
0.42


Example6
Zn-Ga-Si-O
20
50
30
100/20
1%/2%
15text missing or illegible when filed
44
20
0.4text missing or illegible when filed


Example7
Zn-Ga-Si-O
52
23
25
100/20
1%/2%
1text missing or illegible when filed 4
41
19
0.46


Example8
Zn-Ga-Si-O
59
15
26
100/20
1%/2%
1text missing or illegible when filed
41
20
0.49


Example9
Zn-Ga-Si-O
40
28
32
100/20
1%/2%
160
41
1text missing or illegible when filed
0.44


Example10
Zn-Ga-Si-O
50
10
40
100/20
1%/2%
143
34
1text missing or illegible when filed
0.53


Example11
Zn-Ga-Si-O
44
13
4text missing or illegible when filed
100/20
1%/2%
155
4text missing or illegible when filed
17
0.43


Example12
Zn-Ga-Si-O
40
50
10

1%/2%
162
41
2text missing or illegible when filed
0.68


Example13
Zn-Ga-Si-O
10
70
20
100/20
1%/2%
15text missing or illegible when filed
41
27
0.68


Example14
Zn-Ga-Si-O
20

text missing or illegible when filed 0

20
100/20
1%/2%
204

text missing or illegible when filed 2

23
0.28


Example15
Zn-Ga-Si-O
50
30
20
100/20
1%/2%
154
40
32
0.text missing or illegible when filed 0


Example16
Zn-Ga-Si-O

text missing or illegible when filed

19
21
100/20
1%/2%
130
38
27
0.75


Example17
Zn-Ga-Si-O

text missing or illegible when filed


text missing or illegible when filed

23
100/20
1%/2%
153
42
3text missing or illegible when filed
0.90


Example18
Zn-Ga-Si-O
56
21
23
100/20
1%/2%
152
39
21
0.54


Example19
Zn-Ga-Si-O
10
50
40
100/20
1%/2%
125
34
22
0.65


Example20
Zn-Ga-Si-O
10
40
50
100/20
1%/2%
146
36
35
0.97


Example21
Zn-Ga-Si-O
20
30
50
100/20
1%/2%
148
36
21
0.58


Example22
Zn-Ga-Si-O +
40
20
40
100/20
1%/2%
158
39
18
0.4text missing or illegible when filed




text missing or illegible when filed (1 wt %)



Example23
Zn-Ga-Si-O +
40
20
40
100/20
1%/0%
171
42
18
0.43




text missing or illegible when filed (1 wt %)



Comparative
Zn-Ga-Si-O

text missing or illegible when filed 3


text missing or illegible when filed

9
100/20
1%/2%
167
42
54
1.29


Example1


Comparative
Zn-Ga-Si-O
69
15
16
100/20
1%/2%
133
39
60
1.54


Example2


Comparative
Zn-Ga-Si-O
63

text missing or illegible when filed

29
100/20
1%/2%
140
35
37
1.0text missing or illegible when filed


Example3


Comparative
Zn-Ga-Si-O
20
20
6O
100/20
1%/2%
147
38
47
1.24


Example4


















Refractive




















Visible light average transmittence (%)
index *
Crystallinitytext missing or illegible when filed
Mobility (text missing or illegible when filed /V · s)

Carrier concentration (text missing or illegible when filed )



















as-depo
220° C.
550° C.
550 nm
550° C.
as-depo
220° C.
550° C.
as-depo
220° C.
550° C.





Reference
75.0

text missing or illegible when filed .0

90.5
1.99
Crystalline
0.text missing or illegible when filed
13.3
33.1
4.5E+20
1.5E+21
3.7E+20


Example


Example1

text missing or illegible when filed 3.0


text missing or illegible when filed 9.4

95.0
1.70
Amorphous
10.4
14.3
29.0
5.6E+20
1.3E+21
1.3E+21


Example2

text missing or illegible when filed 0.text missing or illegible when filed


text missing or illegible when filed

95.6
1.69
Amorphous
8.7
12.text missing or illegible when filed
2text missing or illegible when filed .5
5.3E+20
1.2E+21
1.3E+21


Example3
20.2

text missing or illegible when filed

94.0
1.83
Amorphous
8.2
11.6
3text missing or illegible when filed
4.9E+20
1.2E+21
5.text missing or illegible when filed E+20


Example4
7text missing or illegible when filed .text missing or illegible when filed

text missing or illegible when filed 7.6

93.text missing or illegible when filed
1.77
Amorphous
8.4
12.7
37.text missing or illegible when filed
4.9E+20
1.3E+21

text missing or illegible when filed .1E+20



Example5
81.8
83.4
94.6
1.66
Amorphous
7.0
11.2
32.4
4.6E+20
1.2E+21
1.0E+21


Example6
7text missing or illegible when filed .4
87.5
94.8
1.79
Amorphous
7.text missing or illegible when filed
9.8
37.text missing or illegible when filed
5.2E+20
1.5E+21
8.6E+20


Example7
8text missing or illegible when filed .text missing or illegible when filed
87.5
94.9
1.79
Amorphous
7.2
12.3
34.7
5.5E+20
1.3E+21

text missing or illegible when filed .4E+20



Example8
7text missing or illegible when filed .2
8text missing or illegible when filed .5
94.6
1.79
Amorphous
7.3
10.6
39.4
5.0E+20
1.4E+21
7.8E+20


Example9
8text missing or illegible when filed .4
87.4
94.5
1.77
Amorphous
8.4
11.4
31.5
5.1E+20
1.4E+21
1.text missing or illegible when filed E+21


Example10
80.0
88.9
95.1
1.73
Amorphous
8.9
11.text missing or illegible when filed
33.text missing or illegible when filed
5.2E+20
1.6E+21
1.vE+21


Example11
81.4
88.5
95.2
1.69
Amorphous
7.7
11.text missing or illegible when filed
29.2
5.text missing or illegible when filed E +20
1.3E+21
1.3E+21


Example12

text missing or illegible when filed

87.3
93.8
1.86
Amorphous
8.6
12.1
32.3
5.0E+20
1.3E+21
7.3E+20


Example13

text missing or illegible when filed .3

87.4
94.0
1.81
Amorphous
8.9
12.6
3text missing or illegible when filed .0
4.7E+20
1.2E+21

text missing or illegible when filed .3E+20



Example14
77.4
83.text missing or illegible when filed
94.5
1.81
Amorphous
8.5

text missing or illegible when filed .5

3text missing or illegible when filed
4.text missing or illegible when filed E+20
1.2E+21

text missing or illegible when filed .3E+20



Example15

text missing or illegible when filed 1.0

87.6
94.2
1.82
Amorphous
7.6
13.3
35.7
5.9E+20
1.2E+21
7.0E+20


Example16

text missing or illegible when filed 2.5

89.0
94.0
1.7text missing or illegible when filed
Amorphous
10.0
10.1
37.2
5.0E+20
9.4E+20
6.6E+20


Example17
79.9

text missing or illegible when filed 9.4

93.6
1.82
Amorphous
8.4
10.5
32.2
4.9E+20
1.5E+21
4.7E+20


Example18
82.7

text missing or illegible when filed 9.0

94.7
1.80
Amorphous
9.4
15.1
35.8
4.7E+20
1.1E+21
9.2E+20


Example19
81.8

text missing or illegible when filed .6

94.6
1.77
Amorphous
9.0
12.3
29.7
5.text missing or illegible when filed E+20
1.6E+21
1.1E+21


Example20
80.3

text missing or illegible when filed 9.0

93.3
1.66
Amorphous
9.5
34.text missing or illegible when filed
13.5
5.2E+20
5.7E+20
1.3E+21


Example21
80.0

text missing or illegible when filed 9.0

93.text missing or illegible when filed
1.64
Amorphous
9.4
35.9
12.8
5.1E+20
8.4E+20
1.4E+21


Example22
80.4
88.3
94.8
1.71
Amorphous
9.4
11.text missing or illegible when filed
35.3
5.2E+20
1.4E+21
9.3E+20


Example23
79.5
8text missing or illegible when filed .9
94.8
1.text missing or illegible when filed 9
Amorphous
7.text missing or illegible when filed
11.1
31.0
5.5E+20
1.4E+21
1.2E+21


Comparative
80.1
87.1
92.8
1.89
Crystalline
8.0
13.2
33.0
5.2E+20
1.2E+21
3.5E+20


Example1


Comparative
80.9
89.7
92.7
1.83
Amorphous
9.text missing or illegible when filed
12.0
31.text missing or illegible when filed
5.0E+20
1.4E+21
3.3E+20


Example2


Comparative
81.7
89.5
93.4
1.74
Amorphous

text missing or illegible when filed

15.4
35.4
4.8E+20
1.1E+21
4.9E+20


Example3


Comparative
99.4
89.5
92.6
1.62
Amorphous

text missing or illegible when filed

29.7
1text missing or illegible when filed .0
4.7E+20
3.0E+20
1.0E+21


Example4






text missing or illegible when filed The refractive index and crystallinity of the Reference Example show the properties of an ITO single film, and the refractive index and crystallinity of the Examples and Comparative Examples show the properties of the oxide film.




text missing or illegible when filed indicates data missing or illegible when filed







Examples 24 and 25

A sputtering target configured from the various oxide sintered bodies of Table 2 was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an oxide film having a film thickness of 20 nm was layered on an ITO film (film thickness of 100 nm) that was prepared based on the same conditions as the Reference Example. Here, the composition (in terms of oxide) of the sputtering target was changed as shown in Table 2. Subsequently, annealing was performed for 30 minutes in the atmosphere by changing the temperature. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 2. Note that “as-depo” in Table 1 indicates that the film was not annealed after deposition.


As shown in Table 2, when the layered body is annealed at 220° C., the ITO film became crystallized and the resistivity deteriorated drastically. Meanwhile, unlike the ITO film (single film), the surface resistance deteriorated when the layered body was annealed at 550° C. R2/R1 exceeded 1.0 considerably, and it can be understood that the surface resistance deteriorates considerably with high temperature annealing (550° C.). Moreover, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher. Furthermore, in all of the layered bodies, the oxide film maintained its amorphous state. By producing a layered body obtained by layering an ITO film and an oxide film in the manner described above, low resistivity and high transmittance, which could not be obtained with ITO films (single films), can be realized.


Comparative Examples 5 to 10

A sputtering target configured from the various oxide sintered bodies [of Table 2] was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an oxide film having a film thickness of 20 nm was layered on an ITO film (film thickness of 100 nm) that was prepared based on the same conditions as the Reference Example. Here, the composition (in terms of oxide) of the sputtering target was changed as shown in Table 2. Subsequently, annealing was performed for 30 minutes in the atmosphere by changing the temperature. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 2.


As shown in Table 2, when the layered body is annealed at 220° C., the ITO film became crystallized and the surface resistance deteriorated drastically. Meanwhile, the surface resistance increased when the layered body was annealed at 550° C. In the Comparative Example, R2/R1 exceeded 1.0 in all cases, and, in comparison to low temperature annealing (220° C., it can be understood that the surface resistance increases with high temperature annealing (550° C.). Meanwhile, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher.















TABLE 2










ITO/Oxide
ITO/Oxide
Oxygen





Composition of
film
film
content
Surface resistance



Oxide
target (mol %)
thickness
thickness
during
(Ω/text missing or illegible when filed )





















film
2nO
Ga2O3
SiO2
TiO2

text missing or illegible when filed
3O3

(nm)
ratio
deposition
as-depo
220° C.
550° C.
550° C./220° C.





Example24
Ga2O3

100



100/20

text missing or illegible when filed

1%/1%

text missing or illegible when filed

42
27
0.text missing or illegible when filed 4


Example25
Zn-Ga-O

text missing or illegible when filed


text missing or illegible when filed




100/20

text missing or illegible when filed

1%/2%

text missing or illegible when filed

47

text missing or illegible when filed

0.text missing or illegible when filed 4


Comparative
Zn-Si-O

text missing or illegible when filed


50


100/20

text missing or illegible when filed

1%/2%
143
40
45
1.13


Example5


Comparative

text missing or illegible when filed n-Zn-O


text missing or illegible when filed




71
100/20

text missing or illegible when filed

1%/2%
119
37
7text missing or illegible when filed

text missing or illegible when filed .11



Example6


Comparative
SiOtext missing or illegible when filed


1text missing or illegible when filed


100/20

text missing or illegible when filed

1%/1%

text missing or illegible when filed

35
57
1.text missing or illegible when filed


Example7


Comparative

text missing or illegible when filed n2O3





100
100/20

text missing or illegible when filed

1%/2%

text missing or illegible when filed

47
58
1.4text missing or illegible when filed


Example8


Comparative
TiO2



100

100/20

text missing or illegible when filed

1%/1%
174
4text missing or illegible when filed

text missing or illegible when filed

1.text missing or illegible when filed


Example9


Comparative
ZnO
100




100/20

text missing or illegible when filed

1%/2%
113

text missing or illegible when filed 7

4text missing or illegible when filed
1.24


Example10


















Visible light average



Carrier




transmittance
Refractive

Mobility
concentration




(%)
index n2
Crystallinitytext missing or illegible when filed
(cm2/V · s)
(text missing or illegible when filed )





















as-depo
220° C.
550° C.

text missing or illegible when filed  = 550 nm

550° C.
as-depo
220° C.
550° C.
as-dego
220° C.
550° C.







Example24
77.9
8text missing or illegible when filed .8
93.3
1.88
Amorphous

text missing or illegible when filed

10.text missing or illegible when filed
3text missing or illegible when filed .2
5.1E+20
1.4E+21

text missing or illegible when filed E+20




Example25
7text missing or illegible when filed

text missing or illegible when filed

93.2
1.80
Amorphous
7.text missing or illegible when filed
10.1
37.text missing or illegible when filed

text missing or illegible when filed E+20

1.3E+21
5.text missing or illegible when filed E+20



Comparative
80.5
88.5

text missing or illegible when filed 3.1

1.7text missing or illegible when filed
Amorphous
9.2
10.1
29.8
4.7E+20
1.7E+21

text missing or illegible when filed E+20




Example5



Comparative
79.0

text missing or illegible when filed .4

88.6
1.17
Crystalline
12.5

text missing or illegible when filed .9

51.4
4.4E+20
1.3E+21
2.7E+20



Example6



Comparative
79.0

text missing or illegible when filed


text missing or illegible when filed 2.2

1.46

8.6
11.1
54.0

text missing or illegible when filed E+20

1.1E+21
2.7E+20



Example7



Comparative
76.2
83.5

text missing or illegible when filed 1.3

1.9text missing or illegible when filed
Crystalline
10.9
10.4

text missing or illegible when filed

4.4E+20
1.3E+21
2.text missing or illegible when filed E+20



Example8



Comparative
76.0
80.2
87.3
1.37
Crystalline
7.8
13.4

text missing or illegible when filed

4.text missing or illegible when filed E+20
1.2E+21
2.5E+20



Example9



Comparative
76.9
88.7
91.3
1.97
Crystalline
7.0
13.2

text missing or illegible when filed .2

4.text missing or illegible when filed E+20
1.2E+21
4.3E+20



Example10








text missing or illegible when filed Crystallinity shows the crystallinity of the oxide film.





text missing or illegible when filed indicates data missing or illegible when filed







Examples 26 to 34

A sputtering target configured from a Zn—Ga—Si sintered body was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an oxide film was layered on an ITO film that was prepared based on the same conditions as the Reference Example. Here, in each of the Examples, the film thickness of the ITO film and the film thickness of the oxide film were changed. The composition (in terms of oxide) of the sputtering target was set to be ZnO:Ga2O3, SiO2=40:20:40 (mol %). Subsequently, annealing was performed for 30 minutes in the atmosphere by changing the temperature. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 3. Note that “as-depo” in Table 1 indicates that the film was not annealed after deposition.


As shown in Table 3, when the layered body is annealed at 220° C., the ITO film became crystallized and the surface resistance deteriorated drastically. Meanwhile, unlike the ITO film (single film), the surface resistance deteriorated when the layered body was annealed at 550° C. R2/R1 exceeded 1.0 considerably, and it can be understood that the resistivity deteriorates considerably with high temperature annealing (550° C.). Moreover, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher. Furthermore, in all of the layered bodies, the oxide film maintained its amorphous state. By producing a layered body obtained by layering an ITO film and an oxide film in the manner described above, low resistivity and high transmittance, which could not be obtained with ITO films (single films), can be realized.


Comparative Examples 11 and 12

A sputtering target configured from a Zn—Ga—Si sintered body was mounted on a sputtering system, sputtering was performed based on the conditions described above, and an oxide film was layered on an ITO film that was prepared based on the same conditions as the Reference Example. Here, in each of the Comparative Examples, the film thickness of the ITO film and the film thickness of the oxide film were changed. Note that the composition (in terms of oxide) of the sputtering target was set to be ZNO:Ga2O3, SiO2=40:20:40 (mol %). Subsequently, annealing was performed for 30 minutes in the atmosphere by changing the temperature. The surface resistance and the visible light average transmittance of the thus obtained layered body were measured. The results are shown in Table 3.


As shown in Table 3, when the layered body is annealed at 220° C., the ITO film became crystallized and the surface resistance deteriorated drastically. Meanwhile, the surface resistance increased when the layered body was annealed at 550° C. In the Comparative Example, R2/R1 exceeded 1.0 in all cases, and, in comparison to low temperature annealing (220° C., it can be understood that the surface resistance increases with high temperature annealing (550° C.). Meanwhile, when the annealing temperature is set to 550° C., the transmittance improved to 90% or higher.















TABLE 3










ITO/Oxide film







Composition of target (mol %)
thickness
ITO/Oxide film
Oxygen content
Surface resistance (Ω/sq)

















Oxide film
ZnO
Ga2O3
SiO2
(nm)
thickness ratio
during deposition
as-depo
220° C.





Example26
Zn-Ga-Si-O
40
20
40
100/10
10.0
1%/2%
167
41


Example27
Zn-Ga-Si-O
40
20
40
100/20
5.0
1%/2%
158
43


Example28
Zn-Ga-Si-O
40
20
40
100/30
3.3
1%/2%
173
39


Example29
Zn-Ga-Si-O
40
20
40
100/40
2.5
1%/2%
164
4.7E+10


Example30
Zn-Ga-Si-O
40
20
40
150/30
5.0
1%/0%
14text missing or illegible when filed
35


Example31
Zn-Ga-Si-O
40
20
40
200/20
10.0
1%/0%
120
25


Example32
Zn-Ga-Si-O
40
20
40
200/40
5.0
1%/0%
113
28


Example33
Zn-Ga-Si-O
40
20
40
300/40
7.5
1%/0%

text missing or illegible when filed 6

19


Example34
Zn-Ga-Si-O
40
20
40
 50/20
2.5
1%/0%
295
82


Comparative
Zn-Ga-Si-O
40
20
40
100/90
1.1
1%/2%
2.text missing or illegible when filed E+08
3.6E+10


Example11


Comparative
Zn-Ga-Si-O
40
20
40
300/20
15.0
1%/0%
104
21


Example12















Surface resistance (Ω/sq)
Visible light average transmittance (%)
Refractive index n2
Crystallinity*

















550° C.
550° C./220° C.
as-depo
220° C.
550° C.

text missing or illegible when filed  = 550 nm

550° C.







Example26
22
0.54
78.4

text missing or illegible when filed 7.0

93.6
1.69
Amorphous



Example27
18
0.42

text missing or illegible when filed 0.9


text missing or illegible when filed 8.0

95.6
1.69
Amorphous



Example28
17
0.44
79.2
86.3
95.1
1.69
Amorphous



Example29
17
0.00
81.7
87.2
95.7
1.69
Amorphous



Example30
11
0.31

text missing or illegible when filed .2

79.8
93.3
1.70
Amorphous



Example31
13
0.52
88.1
73.3
91.9
1.70
Amorphous



Example32

text missing or illegible when filed

0.32
70.2
76.2
91.8
1.70
Amorphous



Example33
18
0.text missing or illegible when filed 5
70.0
77.1
93.8
1.70
Amorphous



Example34
35
0.43
77.7
85.9
90.2
1.70
Amorphous



Comparative
5.3E+06

82.9
85.9
94.3
1.69
Amorphous



Example11



Comparative
31
1.4text missing or illegible when filed

text missing or illegible when filed .7

7text missing or illegible when filed
90.1
1.70
Amorphous



Example12







*Crystallinity shows the crystallinity of the oxide film.




text missing or illegible when filed indicates data missing or illegible when filed







INDUSTRIAL APPLICABILITY

The layered body of the present invention can obtain superior characteristics, specifically lower resistivity and higher transmittance, in comparison to ITO films (single films). Moreover, the present invention yields a superior effect of being able to provide a transparent electroconductive film (layered body) comprising favorable characteristics easily by layering [an oxide film] on an ITO film. The layered body according to the present invention is particularly useful as a transparent electroconductive film in a device (flat panel display, micro LED or the like) using a glass substrate or a Si substrate that can be annealed at a high temperature.

Claims
  • 1: A layered body obtained by layering an ITO film and an oxide film, wherein the layered body has a surface resistance of 40 Ω/sq. or less and a visible light average transmittance of 90% or higher, and a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15.
  • 2: A layered body obtained by layering an ITO film and an oxide film, wherein R2/R1≤1.0 is satisfied when a surface resistance of the layered body that underwent atmosphere annealing at 220° C. is R1, and a surface resistance of the layered body that underwent atmosphere annealing at 550° C. is R2.
  • 3: The layered body according to claim 2, wherein a ratio of the surface resistance R1 and the surface resistance R2 is R2/R1≤0.5.
  • 4: The layered body according to claim 2, wherein the visible light average transmittance of the layered body that underwent atmosphere annealing at 220° C. is 85% or higher.
  • 5: The layered body according to claim 2, wherein the visible light average transmittance of the layered body that underwent atmosphere annealing at 550° C. is 90% or higher.
  • 6: The layered body according to claim 2, wherein n1>n2 is satisfied when a refractive index of the ITO film is n1, and a refractive index of the oxide film is n2.
  • 7: The layered body according to claim 2, wherein the oxide film includes one of more types among Zn, Ga, and Si.
  • 8: A layered body obtained by layering an ITO film and an oxide film, wherein the oxide film contains Zn in an amount of 0 mol % or more and less than 69 mol % in terms of ZnO, Ga in an amount of 9 mol % or more and 100 mol % or less in terms of Ga2O3, and Si in an amount of 0 mol % or more and less than 60 mol % in terms of SiO2, a film thickness of the oxide film is less than 90 nm, and a ratio of a film thickness of the ITO film and a film thickness of the oxide film (film thickness of the ITO film/film thickness of the oxide film) is less than 15.
  • 9: The layered body according to claim 8, wherein the oxide film contains Zn in an amount of more than 10 mol % and less than 60 mol % in terms of ZnO, Ga in an amount of 10 mol % or more and 60 mol % or less in terms of Ga2O3, and Si in an amount of 25 mol % or more and less than 50 mol % in terms of SiO2.
  • 10: The layered body according to claim 8, wherein the oxide film is amorphous.
  • 11: A method of producing the layered body according to claim 8, wherein an oxide film is layered on an ITO film, and the obtained layered body is annealed at 200° C. or higher.
  • 12: An oxide sputtering target for producing the layered body according to claim 8, wherein the oxide sputtering target contains Zn in an amount of 0 mol % or more and less than 69 mol % in terms of ZnO, Ga in an amount of 9 mol % or more and 100 mol % or less in terms of Ga2O3, and Si in an amount of 0 mol % or more and less than 60 mol % in terms of SiO2.
  • 13: The oxide sputtering target according to claim 12, wherein the oxide sputtering target contains Zn in an amount of more than 10 mol % and less than 60 mol % in terms of ZnO, Ga in an amount of 10 mol % or more and 60 mol % or less in terms of Ga2O3, and Si in an amount of 25 mol % or more and less than 50 mol % in terms of SiO2.
  • 14: The oxide sputtering target according to claim 12, wherein the oxide sputtering target contains, as a sintering additive, one or more types among B2O3, P2O5, V2O5, Sb2O3, TeO2, Tl2O3, PbO, Bi2O3, and MoO3.
  • 15: The layered body according to claim 2, wherein the oxide film is amorphous.
  • 16: The layered body according to claim 1, wherein the oxide film is amorphous.
  • 17: A method of producing the layered body according to claim 1, wherein an oxide film is layered on an ITO film, and the obtained layered body is annealed at 200° ° C. or higher.
  • 18: The layered body according to claim 1, wherein n1>n2 is satisfied when a refractive index of the ITO film is n1, and a refractive index of the oxide film is n2.
  • 19: The layered body according to claim 1, wherein the oxide film includes one of more types among Zn, Ga, and Si.
Priority Claims (2)
Number Date Country Kind
2021-074650 Apr 2021 JP national
2022-014394 Feb 2022 JP national
PCT Information
Filing Document Filing Date Country Kind
PCT/JP2022/018417 4/21/2022 WO