TW201714855A - Sintered body and sputtering target composed of the sintered body, and thin film formed using the sputtering target characterized in that the sintered body contains 40 to 70 mol% of ZnS, and the oxide in the sintered body contains at least a composite oxide containing Zn, Ga, and O - Google Patents

Abstract

A sintered body or film containing ZnS and an oxide, characterized in that the sintered body contains 40 to 70 mol% of ZnS, and the oxide in the sintered body contains at least a composite oxide containing Zn, Ga, and O. The composition of the sintered body or film satisfies the relationship of 4at% ≤ Ga (Ga + Zn-S) ≤ 18 at%. The present invention aims to provide a sputtering target having a low bulk resistance and capable of performing stable DC sputtering. Further, the object of this invention is to provide a film which has excellent optical properties or high temperature and high moisture resistance, and used as a transparent conductive film in various displays or a protective film for optical disk, and an optical adjustment film.

Description

a sintered body, a sputtering target composed of the sintered body, and a film formed using the sputtering target

The present invention relates to a sintered body, a sputtering target composed of the sintered body, and a film formed using the sputtering target, and more particularly to a sputtering target capable of performing DC sputtering and a film having desired characteristics.

In the case of using visible light in various optical devices such as organic EL, liquid crystal display, touch panel, and optical disc, the material used must be transparent, and in particular, it is desirable to have high transmittance in the entire region of the visible light region. For example, ZnS-SiO ₂ has been used as a protective film for optical discs because of its high transmittance and softness. However, since this material is insulative, there is a problem that DC sputtering cannot be performed.

In view of such a situation, there is a technique in which DC sputtering is made possible by reducing the resistance of the ZnS-added conductive material. For example, Patent Document 1 discloses that zinc sulfide (ZnS) is used as a main component and further contains a conductive oxide, thereby reducing the bulk resistance value and making DC sputtering possible. As the conductive oxide, indium oxide, tin oxide, and zinc oxide are disclosed.

Further, Patent Document 2 discloses a sputtering target in which a ZnS-based dielectric material (in the case where ITO is also contained) is mainly composed, and 0 to 5 mol% of Al ₂ is dispersed in the material. 5 to 30 mol% of ZnO of O ₃ . Further, it is described that the target has a resistance value of 500 Ω or less and can be subjected to DC sputtering, and further, the dielectric film obtained by using the target is amorphous.

However, when indium oxide (In ₂ O ₃ ) is added as a conductive material, there is a problem that absorption occurs in a short-wavelength region of visible light, and transmittance is lowered. In this respect, although it is not particularly problematic in the use of a disc (DVD) using light having a wavelength of 650 nm, when it is used in a display device such as a touch panel or a display, it is required to be in the entire visible light region. It is transparent (high transmittance), so there is a problem that it is not suitable for such a device. Further, when aluminum oxide (Al ₂ O ₃ ) is added, there is also a problem that Al is more likely to form a stable sulfide than Zn, and Al is bonded to sulfur (S), and the excellent characteristics of ZnS cannot be maintained.

Further, in the case of use as a protective layer, since some devices are also used in a large amount in the presence of a metal which is in contact with water, it is also required to be protected from water (humidity) as one of its characteristics. In particular, record-keeping media such as optical discs must have water resistance due to long-term preservation of data, and in the case of organic EL, because of the fear of oxygen or water, the material is required to have particularly high water resistance.

In addition, the above-mentioned technique, which is used to control optical characteristics and the like (an optical adjustment film, a protective film, etc.), is different from the use as a general transparent conductive film (electrode) which requires conductivity. In addition to the optical properties such as the refractive index and the transmittance, such a film requires an increase in several properties in order to improve the moisture resistance or the amorphous film.

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2003-242684

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2011-8912

An object of the present invention is to provide a sintered body sputtering target which is low in bulk resistivity and can be subjected to DC sputtering. Further, an object of the present invention is to provide a film having desired optical characteristics and the like. The film has high transmittance and high refractive index in the entire visible light region, and is an amorphous film, and has good moisture resistance, so that it can be used as an optical device for an organic EL, a liquid crystal display, a touch panel, or an optical device. film.

In order to solve the above problems, the present inventors conducted intensive studies, and as a result, obtained the following findings: by using the material system described below, it is possible to perform stable and highly productive film formation by DC sputtering, and obtain desired optical fibers. A film of a characteristic or the like can achieve improvement in characteristics or productivity of an optical device using the film.

Based on this finding, the inventors provided the following invention.

1) A sintered body containing ZnS and an oxide, characterized in that the sintered body contains 40 to 70 mol% of ZnS, and the oxide contains at least an oxide composed of Zn, Ga, and O, and the composition of the sintered body The relationship of 4at% ≦Ga/(Ga+Zn-S)≦18at% is satisfied.

2) The sintered body according to the above 1), which has a volume resistivity of 10 Ω‧ cm or less.

The sintered body according to the above 1) or 2), which is characterized in that the relative density is 90% or more.

4) A sputtering target comprising the sintered body according to any one of the above 1) to 3).

5) A film containing Zn, Ga, S, and O, which is characterized by containing 40 to 70 mol% of S in terms of ZnS, and satisfying a relationship of 4 at% ≦Ga/(Ga+Zn-S)≦18 at%.

6) The film according to the above 5), characterized in that the refractive index at a wavelength of 550 nm is 2.10. on.

7) The film according to the above 5) or 6), wherein the extinction coefficient at a wavelength of 405 nm is 0.1 or less.

The film according to any one of the above 5), wherein the film is amorphous.

According to the present invention, by using the material system shown above, the resistivity is low, and stable film formation can be performed by DC sputtering, whereby productivity improvement becomes possible. Moreover, according to the present invention, it is possible to secure good optical characteristics (transmittance or refractive index) of a film for an optical device such as an organic EL, a liquid crystal display, a touch panel, or an optical disk, and to secure good water resistance and the like.

Fig. 1 is a view showing an EPMA image of the targets of Examples 1 and 2.

2 is a view showing X-ray diffraction spectra of the films of Example 2 and Comparative Example 5.

The sintered body (sputter target) of the present invention contains ZnS and an oxide, and the oxide contains at least an oxide composed of Zn, Ga, and O. Examples of the oxide composed of Zn, Ga, and O include a ZnO solid solution of Ga (GZO) in which solid solution is dissolved, or a composite oxide such as ZnGa ₂ O ₄ . Thereby, the bulk resistivity is low, DC (direct current) sputtering can be performed, and it can be formed into an organic EL, a liquid crystal display or a touch panel, which has good optical characteristics (transmittance, refractive index, etc.) and water resistance. An amorphous film of an optical device such as an optical disc.

Compared to RF (high frequency) sputtering, DC sputtering has a faster film formation rate and sputtering Excellent features with better efficiency. Moreover, the DC sputtering apparatus has the advantages of being inexpensive, easy to control, and having a small amount of power consumption. Therefore, by using the sputtering target of the present invention, the film can be produced at a low cost and stably, and productivity can be improved.

The content of zinc sulfide (ZnS) in the sputtering target is set to 40 mol% or more and 70 mol% or less. The reason why the content of ZnS is 40 to 70 mol% is that if the content is less than 40 mol%, the excellent characteristics of ZnS cannot be maintained, that is, the oxide film is soft and suitable for the characteristics of the soft component, and the formed The film is not amorphous and has poor water resistance (water resistance). On the other hand, when the content exceeds 70 mol%, the conductivity of the sputtering target is lowered, and DC sputtering cannot be performed.

As described above, the oxide constituting the sintered body of the present invention contains at least a solid solution or a composite oxide composed of Zn, Ga, and O, and may also contain an oxide of Zn (ZnO or the like) or Ga. Oxide (Ga ₂ O _{3 ,} etc.). Further, the composition of the sintered body of the present invention is characterized by satisfying the relationship of 4 at% ≦Ga/(Ga+Zn-S)≦18 at%. In addition, the element symbol in the above relationship means the concentration (atomic ratio) of each element in the sintered body.

When the content of the Ga oxide is small, the film properties (especially the moisture resistance) are lowered, which is not preferable. On the other hand, when the content of the Ga oxide is large, the conductivity is lowered, and stable DC sputtering is difficult to be performed. The comparison between Ga and Zn is preferably set within the above range. Further, since ZnS also contains Zn, the amount of Zn(S) in ZnS is subtracted from the above relationship.

As the conductive oxide, In ₂ O ₃ , SnO ₂ , ZnO, or the like is known, and it is known that Al ₂ O ₃ , Ga ₂ O _{3 ,} or the like is further added. Previously, the resistance of the target was lowered by the addition of such a conductive oxide. On the other hand, the optical properties of the film may be deteriorated due to the type or amount of the added material, especially as the entire visible light region. A film for a display device requiring high transmittance does not have sufficient characteristics.

For example, in the case of using a material containing In ₂ O ₃ , absorption occurs in a short wavelength region. Further, in the case of using a material containing SnO ₂ , in order to obtain sufficient conductivity, it is necessary to increase the amount of addition, and as a result, the amount of ZnS is reduced, and excellent characteristics of ZnS cannot be obtained. Further, similarly to In ₂ O ₃ , SnO ₂ also has a problem that absorption is likely to occur in a short-wavelength region. Therefore, in order to obtain a film having high transmittance in the entire visible light region, it is effective to use a ZnO-based material. Further, by adding an oxide having a different valence to the ZnO-based material, conductivity and the like can be improved.

As oxides having different valences, Al ₂ O ₃ , B ₂ O ₃ , Ga ₂ O ₃ and the like are known. However, in the case where Al ₂ O ₃ is used, a Zn-stabilized sulfide is formed to lower the excellent characteristics of ZnS. Further, since the added Al ₂ O ₃ does not function as an n-type dopant in ZnO due to the formation of a sulfide, the conductivity is lowered. Further, B ₂ O ₃ has low water resistance and may have an adverse effect on the reliability of the device. On the other hand, in the case of Ga ₂ O ₃ , since the sulfide stability is inferior to that of Zn, the characteristics and conductivity of ZnS are not hindered. Therefore, it is preferable to add Ga ₂ O ₃ as an oxide having a different valence. As described above, in the present invention, by strictly adjusting the type and amount of the additive material, it is possible to ensure good optical characteristics and perform DC sputtering.

When the sintered body of the present invention is used as a sputtering target, the relative density is preferably 90% or more, and further 95% or more. Such a high-density sputtering target has the effects of improving the uniformity of the film thickness and suppressing the generation of particles (dust) or noodles during sputtering. Thereby, the variation in quality can be made small, and mass production can be improved.

Further, when the sintered body of the present invention is used as a sputtering target, the volume resistivity is preferably 10 Ω‧ cm or less. Film formation can be performed by DC sputtering by lowering the volume resistivity. Compared to RF sputtering, DC sputtering has a high film formation rate and excellent sputtering efficiency, which can increase productivity. Furthermore, Depending on the manufacturing conditions, there is also a case where RF sputtering is also performed, but even in this case, the film formation speed is improved.

In the case of use as an optical adjustment film, generally, in order to resist reflection or reduce optical loss, a material having a specific refractive index is required. The required refractive index differs depending on the device configuration (the refractive index of the peripheral layer of the optical adjustment film). The film obtained by the present invention can control the refractive index n at a wavelength of 550 nm to be in the range of 2.10 or more. Furthermore, the composition of the film formed using the sputtering target can be controlled to substantially the same level as the composition of the target. In other words, it contains Zn, Ga, S, and O, and contains 40 to 70 mol% of S in terms of ZnS, and satisfies the relationship of 4 at% ≦Ga/(Ga+Zn-S)≦18 at%.

It is preferable that the optical adjustment film itself has a high transmittance (small extinction coefficient), and according to the present invention, a film having an extinction coefficient of 405 nm at a wavelength of 0.1 or less and having a small absorption in a short-wavelength region of visible light can be obtained. Furthermore, the extinction coefficient is a value that does not depend on the film thickness. Moreover, since the film of the present invention is amorphous, it is excellent in workability, and has high temperature and high humidity resistance, so that deterioration of film quality can be prevented.

The sintered body of the present invention can be produced by weighing and mixing each raw material powder, and then subjecting the mixed powder to pressure sintering (hot pressing) in an inert gas atmosphere or a vacuum atmosphere, or by subjecting the raw material powder to The formed body was subjected to normal pressure sintering after press forming. At this time, the sintering temperature is preferably set to 800 ° C or more and 1400 ° C or less. When the temperature is less than 800 ° C, a sintered body having a high density cannot be obtained. When the temperature is more than 1400 ° C, the composition variation due to evaporation of the raw material or the decrease in density is not preferable. Further, the pressing pressure is preferably set to 150 to 500 kgf/cm ² .

In order to further increase the density, it is effective to prepare a synthetic powder which is mixed with a ZnS powder and used as a powder for sintering, which is obtained by weighing and mixing a Ga ₂ O ₃ raw material powder and a ZnO raw material powder. The mixed powder was calcined (synthesized), and then it was finely pulverized. Thus, by performing synthesis and fine pulverization in advance, a uniform fine raw material powder can be obtained, and a dense sintered body can be produced. The particle diameter after the fine pulverization is set to have an average particle diameter of 5 μm or less, and preferably an average particle diameter of 2 μm or less. Further, the calcination temperature is preferably 800 ° C or more and 1200 ° C or less. By setting it as such a range, sinterability becomes favorable, and it can carry out higher density.

The evaluation methods and the like of the present invention, including the examples and comparative examples described below, are as follows.

(for composition)

Device: SPS3500DD manufactured by SII

Method: ICP-OES (high frequency inductively coupled plasma luminescence analysis method)

(for density determination)

Dimensional measurement (caliper), weight measurement

(for relative density)

The following calculation was performed using the theoretical density.

Relative density (%) = size density / theoretical density × 100

The theoretical density is calculated based on the blend ratio of the compounds of the respective metal elements.

When the ZnS conversion weight of Zn is a (wt%), the Ga ₂ O ₃ conversion weight of Ga is b (wt%), and the ZnO ZnO conversion weight is c (wt%).

Theoretical density = 100 / (a / 4.06 + b / 5.95 + c / 5.61)

Moreover, the following values were used for the compound density of each metal element.

ZnS: 4.06 g/cm ³ , Ga ₂ O ₃ : 5.95 g/cm ³ ,

ZnO: 5.61 g/cm ³

(for body resistance)

Device: manufactured by NPS Corporation Resistivity meter Σ-5+

Method: DC four-probe method

(for film formation methods and conditions)

Device: ANELVA SPL-500

target: 6 inch×5mmt

Substrate: 4 inch

Substrate temperature: room temperature

(for refractive index, extinction coefficient)

Device: manufactured by Shimadzu Corporation, spectrophotometer UV-2450

Measurement sample: film-forming sample on a glass substrate having a film thickness of 500 nm or more, and an unformed glass substrate

Measurement data:

(film formation sample): reflectance and transmittance from the film surface and reflectance from the substrate surface (both back reflection)

(glass substrate): reflectance and transmittance of back reflection, no reflectance of back reflection

Calculation method: Calculated based on the measurement data and based on the following data (Otaruyama Shinsuke, Basic Theory of Optical Films, OPTRONICS Co., Ltd., (2006), 126-131)

(for the amorphous nature of the film)

It is judged based on whether or not the film-forming sample has a diffraction peak generated by X-ray diffraction. Under the following conditions When the diffraction peak due to the film material was not observed in the measurement, it was judged to be an amorphous film.

In addition, the absence of a diffraction peak means that the maximum peak intensity of 2 θ=10° to 60° is I _max , and the average peak intensity of 2 θ=40° to 50° is I _BG . I _max /I _BG <5 case.

Device: Ultima IV manufactured by Rigaku Corporation

Tube: Cu-K α-ray

Tube voltage: 40kV

Current: 30mA

Determination method: 2 θ-θ reflection method

Scanning speed: 8.0 ° / min

Sampling interval: 0.02°

Measuring range: 10°~60°

Measurement sample: film-forming sample on glass substrate (Eagle 2000) (film thickness: 500 nm or more)

(for high temperature and high humidity resistance)

High temperature and high humidity resistance (weather resistance) test: Store at a temperature of 80 ° C and a humidity of 80% for 48 hours. Then, the optical constant and resistance measurement were performed, and the difference in characteristics before and after the high temperature and high humidity test was less than 10%. ○, the case of 10% or more is judged as ×.

[Examples]

Hereinafter, description will be made based on examples and comparative examples. Furthermore, this embodiment is merely an example and is not limited by this example. That is, the present invention is limited only by the scope of the patent application, and includes various modifications other than the embodiments included in the present invention.

(Example 1)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot pressed and sintered at a temperature of 1,100 ° C and a pressure of 200 kgf / cm ² in an Ar atmosphere.

Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and the relative density of the obtained target were measured. As shown in Table 1, the relative density was 97.7%, and the volume resistance was 0.02 Ω ‧ cm, and stable DC sputtering was possible. Regarding the composition of the components of the target, the results of the analysis confirmed that the blending ratio with the raw material powder was the same. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), as shown in Fig. 1, it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Sputtering is performed using the final processed target described above. The sputtering condition was set to DC sputtering, the sputtering power was 500 W, the pressure of argon containing 2.0 vol% of oxygen was 0.5 Pa, and the film formation was 5000 to 7000 Å. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 mm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the film formed by sputtering had a refractive index of 2.35 and an extinction coefficient of 0.02, and the desired optical characteristics were obtained. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Example 2)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and relative density of the obtained target were measured. As shown in Table 1, the relative density was 96.7%, and the volume resistance was 0.003 Ω ‧ cm, which was stable DC sputtering. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), as shown in Fig. 1, it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.24, and the extinction coefficient was 0.04. , obtained the desired optical properties. Moreover, the amorphous property (see FIG. 2) and the high temperature and high humidity resistance (weather resistance) are good.

(Example 3)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and the relative density of the obtained target were measured. As shown in Table 1, the relative density was 98.2%, and the volume resistance was 0.001 Ω ‧ cm, and stable DC sputtering was possible. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.22, and the extinction coefficient was 0.001. , obtained the desired optical properties. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Example 4)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and relative density of the obtained target were measured. As shown in Table 1, the relative density was 98.5%, and the volume resistance was 0.2 Ω ‧ cm, which was stable DC sputtering. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.23. The optical coefficient was 0.03, and the desired optical characteristics were obtained. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Example 5)

The Ga ₂ O ₃ powder, the ZnO powder, and the ZnS powder were mixed at the blending ratios shown in Table 1. This mixed powder was subjected to hot press sintering in the same manner as in Example 1 (wherein the sintering temperature was 1150 ° C). Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and the relative density of the obtained target were measured. As shown in Table 1, the relative density was 97.5%, and the volume resistance was 0.01 Ω ‧ cm, and stable DC sputtering was possible. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.23, and the extinction coefficient was 0.05. , obtained the desired optical properties. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Example 6)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in a vacuum at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and relative density of the obtained target were measured. As shown in Table 1, the relative density was 96.6%, and the volume resistance was 0.5 Ω ‧ cm, which was stable DC sputtering. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.31, and the extinction coefficient was 0.05. Obtained the desired optical properties. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Example 7)

Ga. ₂ O ₃ powder and ZnO powder were prepared in such a manner as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in a vacuum at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The bulk resistance and relative density of the obtained target were measured. As shown in Table 1, the relative density was 96.8%, and the volume resistance was 3 Ω ‧ cm, and stable DC sputtering was possible. Further, when the target structure was observed using an EPMA (electron beam microanalyzer), it was confirmed that an oxide composed of Ga, Zn, and O was formed.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength: 550 nm), extinction coefficient (wavelength: 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.32, and the extinction coefficient was 0.04. , obtained the desired optical properties. Moreover, amorphousness, high temperature and high humidity resistance (weather resistance) are good.

(Comparative Example 1)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Furthermore, the amount of ZnS is made more than specified. Then, the sintered body is finally processed into a sputtering target shape by machining. The body resistance of the obtained target was measured. As shown in Table 1, the bulk resistance became more than 500 kΩ ‧ cm, making it difficult to perform stable DC sputtering.

(Comparative Example 2)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. At this time, the amount of Ga ₂ O _{3 is made} less than the regulation. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1. Then, the sintered body is finally processed into a sputtering target shape by machining. The body resistance of the obtained target was measured, and as shown in Table 1, the relative density was 98.5%, and the volume resistance was 0.01 Ω ‧ cm, and stable DC sputtering was possible.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.32, and the extinction coefficient was 0.02. , obtained the desired optical properties. On the other hand, high temperature and high humidity resistance (weathering resistance) Sex) is poor.

(Comparative Example 3)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. At this time, the amount of Ga ₂ O ₃ is made more than a predetermined value. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1 (wherein the sintering temperature was 1,150 ° C). Then, the sintered body is finally processed into a sputtering target shape by machining. The body resistance of the obtained target was measured. As shown in Table 1, the bulk resistance became more than 500 kΩ ‧ cm, making it difficult to perform stable DC sputtering.

(Comparative Example 4)

The Al ₂ O ₃ powder and the ZnO powder were prepared in such a manner as to have an atomic ratio shown in Table 1, and they were mixed. At this time, Al ₂ O ₃ powder was used instead of Ga ₂ O ₃ powder. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1 (wherein the sintering temperature was 1,150 ° C). Then, the sintered body is finally processed into a sputtering target shape by machining. The body resistance of the obtained target was measured, and as shown in Table 1, the relative density was 96.9%, and the volume resistance was 0.3 Ω ‧ cm, and stable DC sputtering was possible.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. Refractive index (wavelength 550 nm), extinction coefficient (wavelength 405 nm), volume resistance of film-forming samples The results were measured. As a result, as shown in Table 1, the film formed by sputtering had a refractive index of 2.28 and an extinction coefficient of 0.03, and the desired optical characteristics were obtained. On the other hand, high temperature and high humidity resistance (weather resistance) are poor.

(Comparative Example 5)

The Ga ₂ O ₃ powder and the ZnO powder were prepared so as to have an atomic ratio shown in Table 1, and they were mixed. Then, the mixed powder was calcined in the air at a temperature of 1,050 ° C, and then pulverized into an average particle diameter of 2 μm or less by wet fine pulverization (using ZrO ₂ beads), dried, and then sieved using a sieve having a mesh size of 150 μm. Then, the finely pulverized powder and the ZnS powder were mixed at the blending ratios shown in Table 1, and then hot press sintering was carried out in the same manner as in Example 1 (wherein the sintering temperature was 1,150 ° C). Furthermore, the amount of ZnS is made less than the regulation. Then, the sintered body is finally processed into a sputtering target shape by machining. The body resistance of the obtained target was measured, and as shown in Table 1, the relative density was 96.4%, and the volume resistance was 0.8 Ω ‧ cm, and stable DC sputtering was possible.

Then, the final processed target is used for sputtering. The sputtering conditions were set to be the same as in the first embodiment. The refractive index (wavelength: 550 nm), extinction coefficient (wavelength: 405 nm), and volume resistivity of the film-forming sample were measured. As shown in Table 1, the refractive index of the film formed by sputtering was 2.18, and the extinction coefficient was 0.07. Obtained the desired optical properties. On the other hand, the amorphous film (see FIG. 2) is not inferior in high-temperature and high-humidity resistance (weather resistance).

[Industrial availability]

Since the sputtering target of the present invention has a low bulk resistance value and a high density of 90% or more, stable DC sputtering can be performed. Moreover, it has the following significant effects: the DC sputtering feature, that is, the controllability of sputtering, is easier, the film formation speed is increased, and the sputtering efficiency is improved. Rise. Further, at the time of film formation, fine particles (dust) or nodules generated during sputtering can be reduced, and the variation in quality can be made small, thereby improving mass productivity. Further, the film formed by using the sputtering target of the present invention is a transparent conductive film or a protective film for an optical disk and a film for optical adjustment in various displays, and has extremely excellent characteristics in terms of optical characteristics or high-temperature and high-humidity resistance.

Claims (9)

A sintered body containing ZnS and an oxide, characterized in that the sintered body contains 40 to 70 mol% of ZnS, and the oxide contains at least a composite oxide composed of Zn, Ga, and O, and the composition of the sintered body satisfies 4 att The relationship between %≦Ga/(Ga+Zn-S)≦18at%. The sintered body of the first aspect of the patent application has a volume resistivity of 10 Ω‧ cm or less. The sintered body of claim 1 or 2 has a relative density of 90% or more. A sputtering target comprising the sintered body of any one of claims 1 to 3. A film containing Zn, Ga, S, and O, which is characterized by containing 40 to 70 mol% of S in terms of ZnS, and satisfying a relationship of 4 at% ≦Ga/(Ga+Zn-S)≦18 at%. The film of the fifth aspect of the patent application has a refractive index of 2.10 or more at a wavelength of 550 nm. The film of the fifth or sixth aspect of the patent application has an extinction coefficient of 0.1 or less at a wavelength of 405 nm. The film of claim 5 or 6 is amorphous. The film of claim 7 is amorphous.