Phase shift mask blank, phase shift mask, and production method of phase shift mask

Abstract

To provide a phase shift mask blank capable of sufficiently suppressing the occurrence of haze on a mask, to provide a phase shift mask with less haze defect, and to provide a production method of the phase shift mask.SOLUTION: A phase shift mask blank 10 according to the embodiment is used for making a phase shift mask to which exposure light with a wavelength of 200nm or less is applied, and comprises a base plate 11 and a phase shift film 14 formed on the base plate 11. The phase shift film 14 comprises a phase layer 12 enabling adjustment of a phase of a predetermined quantity and a transmissivity to exposure light to be transmitted, and a protective layer 13 formed on the phase layer 12 and inhibiting gas transmission to the phase layer 12. The phase layer 12 is positioned at a base plate 11 side. When a film thickness of the phase layer 12 is d1 and a film thickness of the protective layer 13 is d2, the film thickness d1 of the phase layer 12 is thicker than the film thickness d2 of the protective layer 13, and the film thickness d2 of the protective layer 13 is 15 nm or less.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] The present invention relates to a phase shift mask blank, a phase shift mask, and a method for manufacturing a phase shift mask, which are used in the manufacture of semiconductor devices and the like. [Background technology]

[0002] In recent years, in semiconductor processing, particularly with the increasing integration of large-scale integrated circuits, finer circuit patterns have become necessary, and there is an increasing demand for finer technology for the wiring patterns and contact hole patterns that make up the circuits. As a result, the exposure light source used in the manufacture of semiconductor devices, etc. is becoming shorter in wavelength, from KrF excimer lasers (wavelength 248 nm) to ArF excimer lasers (wavelength 193 nm).

[0003] As another example of a mask with improved wafer transfer characteristics, there is a phase shift mask. In a phase shift mask, both the phase difference and the transmittance are adjusted so that the phase difference (hereinafter simply referred to as "phase difference") between the ArF excimer laser light passing through the transparent substrate and the ArF excimer laser light passing through both the transparent substrate and the phase shift film is 180 degrees, and the ratio of the amount of ArF excimer laser light passing through both the transparent substrate and the phase shift film to the amount of ArF excimer laser light passing through the transparent substrate (hereinafter simply referred to as "transmittance") is 6%. It is possible.

[0004] For example, when manufacturing a phase shift mask with a phase difference of 180 degrees, a known method is to set the thickness of the phase shift film so that the phase difference is around 177 degrees, and then dry etch the phase shift film with a fluorine-based gas while simultaneously processing the transparent substrate by about 3 nm, thereby finally adjusting the phase difference to around 180 degrees.

[0005] In phase shift masks that use exposure light with a wavelength of 200 nm or less, foreign matter called "haze" gradually forms, grows, and becomes evident on the mask as a result of exposure, which can make the mask unusable. In particular, when the phase shift film is made of silicon, transition metals, and light elements such as oxygen and nitrogen, foreign matter can form on the surface of the phase shift film. Techniques for suppressing haze are described in, for example, Patent Documents 1 and 2. However, the techniques described in Patent Documents 1 and 2 may not be effective enough in suppressing the above-mentioned haze. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] JP 2018-173621 A [Patent Document 2] Patent No. 4579728 Summary of the Invention [Problem to be solved by the invention]

[0007] The present invention has been made in light of the above circumstances, and aims to provide a phase shift mask blank that can sufficiently suppress the occurrence of haze on the surface of a phase shift film, a phase shift mask with few haze defects, and a method for manufacturing such a phase shift mask. [Means for solving the problem]

[0008] The present invention has been made to solve the above-mentioned problems. A phase shift mask blank according to one embodiment of the present invention is a phase shift mask blank used for producing a phase shift mask to which exposure light having a wavelength of 200 nm or less is applied, comprising a transparent substrate and a phase shift film formed on the transparent substrate, the phase shift film comprising a phase difference transmittance adjusting layer capable of adjusting a predetermined amount of phase and transmittance for the transmitted exposure light, and a gas permeable protective layer formed on the phase difference transmittance adjusting layer and preventing gas from permeating into the phase difference transmittance adjusting layer, the phase difference transmittance adjusting layer being located on the transparent substrate side, and wherein when the thickness of the phase difference transmittance adjusting layer is d1 and the thickness of the gas permeable protective layer is d2, d1 is thicker than d2 and d2 is 15 nm or less.

[0009] In addition, a phase shift mask according to one embodiment of the present invention is a phase shift mask having a circuit pattern and is applied to exposure light having a wavelength of 200 nm or less, the phase shift mask comprising: a transparent substrate; and a phase shift film formed on the transparent substrate. The phase shift film comprises a phase difference transmittance adjusting layer capable of adjusting a predetermined amount of phase and transmittance for the transmitted exposure light, and a gas permeable protective layer formed on the phase difference transmittance adjusting layer and preventing gas from permeating into the phase difference transmittance adjusting layer. The phase difference transmittance adjusting layer is located on the transparent substrate side, and when the thickness of the phase difference transmittance adjusting layer is d1 and the thickness of the gas permeable protective layer is d2, d1 is thicker than d2 and d2 is 15 nm or less.

[0010] Furthermore, a method for manufacturing a phase shift mask according to one embodiment of the present invention is a method for manufacturing a phase shift mask using the above-mentioned phase shift mask blank, and is characterized in that it includes the steps of forming a light-shielding film on the phase shift film, forming a resist pattern on the light-shielding film formed on the phase shift film, forming a pattern on the light-shielding film by oxygen-containing chlorine-based etching (Cl / O-based) after forming the resist pattern, forming a pattern on the light-shielding film by fluorine-based etching (F-based) after forming the pattern on the light-shielding film, removing the resist pattern after forming the pattern on the phase shift film, and removing the light-shielding film from above the phase shift film by oxygen-containing chlorine-based etching (Cl / O-based) after removing the resist pattern. Effect of the Invention

[0011] By using a phase shift mask blank according to one embodiment of the present invention, the occurrence of haze on a mask can be sufficiently suppressed. [Brief description of the drawings]

[0012] [Figure 1] 1 is a schematic cross-sectional view showing a configuration of a phase shift mask blank according to an embodiment of the present invention. [Diagram 2] 1 is a schematic cross-sectional view showing a configuration of a phase shift mask according to an embodiment of the present invention. [Diagram 3] 1A to 1C are schematic cross-sectional views showing a manufacturing process of a phase shift mask using a phase shift mask blank according to an embodiment of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] The inventors of the present application considered that the occurrence of haze in a mask blank or mask can be reduced if all three elements, namely, the constituent material of a phase adjustment film (a phase difference transmittance adjusting layer described later) constituting a phase shift mask blank or a phase shift mask, an oxidizing gas such as water or oxygen, and exposure energy, are present, and therefore configured a phase shift mask blank or a phase shift mask as follows. That is, the phase shift mask blank, phase shift mask, and manufacturing method thereof according to this embodiment are based on the technical idea of ​​reducing the occurrence of haze by providing a gas protection layer (a so-called gas barrier layer) on the phase adjustment film to prevent the oxidizing gas from coming into contact with the constituent material of the phase adjustment film.

[0014] Hereinafter, an embodiment of the present invention will be described with reference to the drawings. Note that the schematic cross-sectional views do not accurately reflect the actual dimensional ratio or the number of patterns, and the amount of engraving in the transparent substrate and the amount of damage to the film are omitted. Suitable embodiments of the phase shift mask blank of the present invention include the following.

[0015] (Overall structure of phase shift mask blank) FIG. 1 is a schematic cross-sectional view showing the configuration of a phase shift mask blank according to an embodiment of the present invention. The phase shift mask blank 10 shown in FIG. 1 is a phase shift mask blank used to prepare a phase shift mask to which exposure light having a wavelength of 200 nm or less is applied, and includes a substrate (hereinafter, also simply referred to as "substrate") 11 transparent to the exposure wavelength, and a phase shift film 14 formed on the substrate 11. The phase shift film 14 includes at least a phase difference transmittance adjusting layer (hereinafter, also simply referred to as "phase layer") 12 that can adjust a predetermined amount of phase and transmittance to the transmitted exposure light, and a gas permeable protective layer (hereinafter, also simply referred to as "protective layer") 13 that is formed on the phase difference transmittance adjusting layer 12 and prevents gas from permeating into the phase difference transmittance adjusting layer 12, and the phase layer 12 is located on the substrate 11 side. When the thickness of the phase layer 12 is d1 and the thickness of the protective layer 13 is d2, d1 is thicker than d2, and d2 is 15 nm or less. Each layer constituting the phase shift mask blank 10 according to the embodiment of the present invention will now be described in detail.

[0016] (substrate) There is no particular limitation on the substrate 11, and as the substrate 11, for example, quartz glass, CaF2, aluminosilicate glass, or the like is generally used.

[0017] (Phase shift film) The phase shift film 14 comprises a phase layer 12 and a protective layer 13 in this order, and is formed on the substrate 11 with or without other films interposed therebetween. The phase shift film 14 is, for example, a film that is resistant to oxygen-containing chlorine-based etching (Cl / O-based) and can be etched with fluorine-based etching (F-based).

[0018] The transmittance value of the phase shift film 14 is, for example, within a range of 3% to 80% relative to the transmittance of the substrate 11, and an optimal transmittance can be appropriately selected according to a desired wafer pattern. The phase difference value of the phase shift film 14 is, for example, within a range of 160 degrees to 220 degrees, and more preferably within a range of 175 degrees to 190 degrees. That is, the phase shift film 14 may have a transmittance to the exposure light within a range of 3% to 80% and a phase difference within a range of 160 degrees to 220 degrees. When the transmittance of the phase shift film 14 to the exposure light is less than 3%, good exposure performance may not be obtained. When the phase difference is within a range of 160 degrees to 220 degrees, the required exposure performance can be easily maintained.

[0019] <Phase layer> The phase layer 12 is formed on the substrate 11 with or without other films, and is a layer that can adjust the phase and transmittance of the transmitted exposure light by a predetermined amount. Here, "adjusting the phase" means, for example, inverting the phase. Also, "transmittance" means the transmittance of the exposure light. The phase layer 12 is, for example, a single layer film containing silicon and at least one selected from a transition metal, nitrogen, oxygen, and carbon, or a multilayer film or gradient film thereof, and the transmittance and phase difference for the exposure wavelength are adjusted by appropriately selecting the composition and film thickness.

[0020] The phase layer 12 preferably contains silicon in the range of 20 atomic % to 60 atomic % in the element ratio of the entire phase layer 12, preferably contains transition metals in the range of 0 atomic % to 20 atomic % in the element ratio of the entire phase layer 12, preferably contains nitrogen in the range of 30 atomic % to 80 atomic % in the element ratio of the entire phase layer 12, preferably contains oxygen in the range of 0 atomic % to 30 atomic % in the element ratio of the entire phase layer 12, and preferably contains carbon in the range of 0 atomic % to 10 atomic % in the element ratio of the entire phase layer 12. The more preferable content range of each element in the phase layer 12 is 30 atomic % to 50 atomic % in the element ratio of silicon, 0 atomic % to 10 atomic % in the element ratio of the entire phase layer 12, 40 atomic % to 70 atomic % in the element ratio of the entire phase layer 12, 0 atomic % to 20 atomic % in the element ratio of the entire phase layer 12, and 0 atomic % to 5 atomic % in the element ratio of the entire phase layer 12. If the content of each element in the phase layer 12 is within the above numerical range, the phase difference as well as the transmittance of the phase layer 12 can be easily controlled. The phase layer 12 may contain at least one of oxide, carbide, and nitride of a metal silicide. In this case, the metal constituting the metal silicide may be the above-mentioned transition metal.

[0021] The transition metal contained in the phase layer 12 is preferably at least one selected from molybdenum, titanium, vanadium, cobalt, nickel, zirconium, niobium, and hafnium, and more preferably molybdenum. If the transition metal contained in the phase layer 12 is at least one selected from molybdenum, titanium, vanadium, cobalt, nickel, zirconium, niobium, and hafnium, the processing of the phase layer 12 becomes easy, and if it is molybdenum, the processing of the phase layer 12 such as etching becomes even more excellent.

[0022] When the thickness of the phase layer 12 is d1 and the thickness of the protective layer 13 is d2, the thickness d1 of the phase layer 12 is thicker than the thickness d2 of the protective layer 13, and the thickness d2 of the protective layer 13 is 15 nm or less. If the thickness d2 of the protective layer 13 is made thicker than 15 nm, the optical characteristics and correction characteristics may be affected. Furthermore, the thickness d1 of the phase layer 12 may be greater than 15 nm. When the thickness d1 of the phase layer 12 is greater than 15 nm, it becomes easier to adjust the phase and transmittance. The total thickness of the phase layer 12 and the protective layer 13 is preferably 50 nm or more, and more preferably 70 nm or more. If the total thickness of the phase layer 12 and the protective layer 13 is within the above-mentioned numerical range, the function of the phase shift film 14 can be easily set to a desired value.

[0023] <Protective layer> The protective layer 13 is formed on the phase layer 12 with or without another film interposed therebetween, and is a layer for preventing or suppressing gas permeation (particularly, permeation of oxidizing gases such as water and oxygen) into the phase layer 12, i.e., a gas barrier layer. This embodiment can prevent or suppress the intrusion of gas, which is considered to be one of the factors that cause haze, into the phase layer 12, and therefore, when the mask is used for a long period of time (for example, when the dose on the mask is 100 kJ / cm 2 Even if the exposure temperature exceeds 100° C., the generation of haze on the surface of the phase shift mask can be prevented or suppressed. The gas (atmospheric gas) whose permeation is prevented or suppressed by the protective layer 13 is an oxidizing gas, specifically, oxygen-containing molecules, and more specifically, water molecules.

[0024] The protective layer 13 is preferably a layer that is resistant to oxygen-containing chlorine-based (Cl / O-based) gas etching, can be etched with a fluorine-based gas (F-based), and can be repaired by an EB (electron beam) repair method. The protective layer 13 is preferably a single layer film made of one or more compounds selected from tantalum metal, tantalum compounds, tungsten metal, tungsten compounds, tellurium metal, and tellurium compounds, or a mixed film or multi-layer film of these compounds. The composition of the layer is not particularly limited as long as it can be formed. Note that the above-mentioned tantalum metal, tungsten metal, and tellurium metal refer to the individual metals.

[0025] The protective layer 13 made of a tantalum compound is a single layer film containing tantalum and one or more elements selected from oxygen, nitrogen, and carbon, or a multilayer film or gradient film thereof. The protective layer 13 made of a tantalum compound preferably contains tantalum in the range of 10 atomic % to 90 atomic % in the entire element ratio of the protective layer 13, preferably contains oxygen in the range of 0 atomic % to 90 atomic % in the entire element ratio of the protective layer 13, preferably contains nitrogen in the range of 0 atomic % to 70 atomic % in the entire element ratio of the protective layer 13, and preferably contains carbon in the range of 0 atomic % to 20 atomic % in the entire element ratio of the protective layer 13. More preferable content ranges of each element in the protective layer 13 made of a tantalum compound are tantalum in the range of 20 atomic % to 80 atomic % in the entire element ratio of the protective layer 13, oxygen in the range of 0 atomic % to 80 atomic % in the entire element ratio of the protective layer 13, nitrogen in the range of 0 atomic % to 60 atomic % in the entire element ratio of the protective layer 13, and carbon in the range of 0 atomic % to 10 atomic % in the entire element ratio of the protective layer 13. If the content of each element in the protective layer 13 made of a tantalum compound is within the above numerical range, the barrier property of the protective layer 13 against gas permeation into the phase layer 12 is improved.

[0026] Moreover, the protective layer 13 made of a tungsten compound is a single layer film containing tungsten and one or more elements selected from oxygen, nitrogen, and carbon, or a multilayer film or gradient film thereof. The protective layer 13 made of a tungsten compound preferably contains tungsten in the range of 10 atomic % to 70 atomic % in the element ratio of the entire protective layer 13, preferably contains oxygen in the range of 30 atomic % to 90 atomic % in the element ratio of the entire protective layer 13, preferably contains nitrogen in the range of 0 atomic % to 20 atomic % in the element ratio of the entire protective layer 13, and preferably contains carbon in the range of 0 atomic % to 20 atomic % in the element ratio of the entire protective layer 13. More preferable content ranges of each element in the protective layer 13 made of a tungsten compound are tungsten in the range of 20 atomic % to 60 atomic % in the element ratio of the entire protective layer 13, oxygen in the range of 50 atomic % to 80 atomic % in the element ratio of the entire protective layer 13, nitrogen in the range of 0 atomic % to 10 atomic % in the element ratio of the entire protective layer 13, and carbon in the range of 0 atomic % to 10 atomic % in the element ratio of the entire protective layer 13. If the content of each element in the protective layer 13 made of a tungsten compound is within the above numerical range, the barrier property of the protective layer 13 against gas permeation to the phase layer 12 is improved.

[0027] The protective layer 13 made of a tellurium compound is a single layer film containing tellurium and one or more elements selected from oxygen, nitrogen, and carbon, or a multilayer film or gradient film thereof. The protective layer 13 made of a tellurium compound preferably contains tellurium in the range of 20 atomic % to 70 atomic % in the element ratio of the entire protective layer 13, preferably contains oxygen in the range of 30 atomic % to 90 atomic % in the element ratio of the entire protective layer 13, preferably contains nitrogen in the range of 0 atomic % to 20 atomic % in the element ratio of the entire protective layer 13, and preferably contains carbon in the range of 0 atomic % to 20 atomic % in the element ratio of the entire protective layer 13. More preferable content ranges of each element in the protective layer 13 made of a tellurium compound are 30 atomic % to 60 atomic % in the element ratio of the entire protective layer 13, 50 atomic % to 80 atomic % in the element ratio of the entire protective layer 13, 0 atomic % to 10 atomic % in the element ratio of the entire protective layer 13, and 0 atomic % to 10 atomic % in the element ratio of the entire protective layer 13. If the content of each element in the protective layer 13 made of a tellurium compound is within the above numerical range, the barrier property of the protective layer 13 against gas permeation to the phase layer 12 is improved.

[0028] As described above, if the protective layer 13 is a single layer film made of one or more compounds selected from tantalum metal, tantalum compounds, tungsten metal, tungsten compounds, tellurium metal, and tellurium compounds, or a mixed film or multi-layer film of these compounds, it can effectively prevent gas permeation into the phase layer 12. As described above, the thickness d2 of the protective layer 13 is 15 nm or less. If the thickness d2 of the protective layer 13 is within the above-mentioned numerical range, the barrier properties against gas permeation into the phase layer 12 can be maintained while maintaining the optical characteristics and correction characteristics.

[0029] (Overall structure of phase shift mask) The configuration of a phase shift mask 100 according to an embodiment of the present invention will now be described. 2 is a schematic cross-sectional view showing the configuration of a phase shift mask according to an embodiment of the present invention. The phase shift mask 100 shown in FIG. 2 is a phase shift mask (i.e., a patterned phase shift mask) to which exposure light having a wavelength of 200 nm or less is applied and which has a circuit pattern, and includes a substrate 11 transparent to the exposure wavelength and a phase shift film 14 formed on the substrate 11. The phase shift film 14 includes at least a phase layer 12 that can adjust a predetermined amount of phase and transmittance for the transmitted exposure light, and a protective layer 13 formed on the phase layer 12 to prevent gas from passing through the phase layer 12, and the phase layer 12 is located on the substrate 11 side. When the thickness of the phase layer 12 is d1 and the thickness of the protective layer 13 is d2, d1 is thicker than d2, and d2 is 15 nm or less.

[0030] Phase shift mask 100 includes a phase shift film pattern 17 formed by removing a portion of phase shift film 14 to expose the surface of substrate 11 . The composition of each layer constituting the phase shift mask 100 according to an embodiment of the present invention is the same as the composition of each layer constituting the phase shift mask blank 10 according to the embodiment of the present invention described above, and therefore detailed explanations of the composition of each layer will be omitted.

[0031] (Method of manufacturing phase shift mask blank) A method for manufacturing a phase shift mask 100 using the phase shift mask blank 10 of this embodiment includes the steps of forming a light-shielding film 15 on a phase shift film 14, forming a resist pattern 16 on the light-shielding film 15 formed on the phase shift film 14, forming a pattern in the light-shielding film 15 by oxygen-containing chlorine-based etching (Cl / O-based) after forming the resist pattern 16, forming a pattern in the light-shielding film 15 by fluorine-based etching (F-based) after forming the pattern in the light-shielding film 15, removing the resist pattern 16 after forming the pattern in the phase shift film 14, and removing the light-shielding film 15 from above the phase shift film 14 by oxygen-containing chlorine-based etching (Cl / O-based) after removing the resist pattern 16. Here, the light-shielding film 15 according to the embodiment of the present invention will be described.

[0032] <Light-shielding film> The light-shielding film 15 is a layer formed on the phase shift mask blank 10 (protective layer 13) according to the embodiment of the present invention described above. The light-shielding film 15 is, for example, a single layer film made of chromium alone or a chromium compound, or a multilayer film or gradient film thereof. More specifically, the light-shielding film 15 made of a chromium compound is a single layer film containing chromium and one or more elements selected from nitrogen and oxygen, or a multilayer film or gradient film thereof.

[0033] The light-shielding film 15 made of a chromium compound preferably contains chromium in the range of 30 atomic % to 100 atomic % inclusive, oxygen in the range of 0 atomic % to 50 atomic % inclusive, nitrogen in the range of 0 atomic % to 50 atomic % inclusive, and carbon in the range of 0 atomic % to 10 atomic % inclusive, in terms of the element ratio of the entire light-shielding film 15. More preferred content ranges of each element in the light-shielding film 15 made of a chromium compound are 50 atomic % to 100 atomic % inclusive for chromium, 0 atomic % to 40 atomic % inclusive for oxygen, 0 atomic % to 40 atomic % inclusive for nitrogen, and 0 atomic % to 5 atomic % inclusive for carbon, in terms of the element ratio of the entire light-shielding film 15. If the content of each element in the light-shielding film 15 made of a chromium compound is within the above numerical range, the light-shielding property of the light-shielding film 15 is enhanced.

[0034] The thickness of the light-shielding film 15 is preferably, for example, in the range of 35 nm to 80 nm, particularly in the range of 40 nm to 75 nm. The light-shielding film 15 can be formed by a known method. A preferred method for obtaining a film with excellent uniformity most easily is a sputtering film formation method, but the present embodiment is not limited to the sputtering film formation method.

[0035] The target and the sputtering gas are selected according to the film composition. For example, a method for forming a film containing chromium can be exemplified by using a target containing chromium and performing reactive sputtering in only an inert gas such as argon gas, only a reactive gas such as oxygen, or a mixed gas of an inert gas and a reactive gas. The flow rate of the sputtering gas can be adjusted according to the film characteristics, and may be constant during film formation, or may be changed according to the desired composition when the amount of oxygen or nitrogen is to be changed in the thickness direction of the film. In addition, the power applied to the target, the distance between the target and the substrate, and the pressure in the film formation chamber may be adjusted.

[0036] Each step of the method for manufacturing the phase shift mask 100 according to the embodiment of the present invention will now be described in detail. FIG. 3 is a schematic cross-sectional view showing a manufacturing process of a phase shift mask 100 using the phase shift mask blank 10 shown in FIG. 1. FIG. 3(a) shows a process of forming a light-shielding film 15 on a phase shift film 14. FIG. 3(b) shows a process of applying a resist film on the light-shielding film 15, drawing, and then performing a development process to form a resist pattern 16. FIG. 3(c) shows a process of patterning the light-shielding film 15 by oxygen-containing chlorine-based dry etching (Cl / O-based) along the resist pattern 16. FIG. 3(d) shows a process of patterning the phase shift film 14 by fluorine-based etching (F-based) along the pattern of the light-shielding film 15 to form a phase shift film pattern 17. FIG. 3(e) shows a process of peeling and removing the resist pattern 16 and then cleaning it. FIG. 3(f) shows a process of removing the light-shielding film 15 by oxygen-containing chlorine-based etching (Cl / O-based) from above the phase shift film 14 on which the phase shift film pattern 17 has been formed. In this way, the phase shift mask 100 according to this embodiment is manufactured.

[0037] The phase shift mask 100 according to the present embodiment is a phase shift mask to which exposure light having a wavelength of 200 nm or less is applied, and includes a substrate 11 and a phase shift film 14 formed on the substrate 11 with or without other films. The phase shift film 14 includes a phase layer 12 that can adjust a predetermined amount of phase and transmittance for the transmitted exposure light, and a protective layer 13 that is formed on the phase layer 12 and prevents gas from passing through the phase layer 12, and the phase layer 12 is located on the substrate 11 side. The phase shift mask 100 includes a phase shift film pattern 17 formed by removing a part of the phase shift film 14 so that a part of the substrate 11 is exposed. When the thickness of the phase layer 12 is d1 and the thickness of the protective layer 13 is d2, the thickness d1 of the phase layer 12 is thicker than the thickness d2 of the protective layer 13, and the thickness d2 of the protective layer 13 is 15 nm or less.

[0038] In the step of FIG. 3(b), either a positive resist or a negative resist can be used as the material for the resist film, but it is preferable to use a chemically amplified resist for electron beam writing, which enables the formation of highly accurate patterns. The thickness of the resist film is, for example, within the range of 50 nm to 250 nm. In particular, when producing a phase shift mask which requires the formation of fine patterns, in order to prevent pattern collapse, it is necessary to thin the resist film so that the aspect ratio of the resist pattern 16 does not become large, and a thickness of 200 nm or less is preferable. On the other hand, the lower limit of the thickness of the resist film is determined by comprehensively taking into consideration conditions such as the etching resistance of the resist material used, and is preferably 60 nm or more. As a resist film When using a chemically amplified type for electron beam lithography, the energy density of the electron beam during lithography is 35 μC / cm 2 to 100μC / cm 2 After this drawing, a heat treatment and a development treatment are performed to obtain a resist pattern 16.

[0039] In the step of FIG. 3(e), the resist pattern 16 may be removed by wet stripping using a stripping liquid, or by dry stripping using dry etching. 3(c), the conditions of the oxygen-containing chlorine-based dry etching (Cl / O-based) for patterning the light-shielding film 15 made of simple chromium or a chromium compound may be known conditions used for removing chromium compound films, and in addition to chlorine gas and oxygen gas, an inert gas such as nitrogen gas or helium gas may be mixed as necessary. The underlying phase shift film 14 is resistant to the oxygen-containing chlorine-based dry etching (Cl / O-based), and therefore remains without being removed or patterned in this process.

[0040] In the step of FIG. 3(d), the conditions of the fluorine-based dry etching (F-based) for patterning the phase shift film 14 may be known conditions that have been used when dry etching a silicon-based compound film, a tantalum compound film, a molybdenum compound film, or the like. The fluorine-based gas is generally CF4, C2F6, or SF6, and may be mixed with an active gas such as oxygen, or an inert gas such as nitrogen gas or helium gas, as necessary. In the case of FIG. 3(d), the upper light-shielding film 15 or resist pattern 16 is resistant to the fluorine-based dry etching (F-based), so it is not removed or patterned in this step and remains. In FIG. 3(d), the substrate 11 is generally recessed by about 1 nm to 3 nm at the same time to prevent the phase shift film 14 from being removed and to fine-tune the phase difference.

[0041] 3(f), the conditions for the oxygen-containing chlorine-based dry etching (Cl / O-based) for removing the light-shielding film 15 may be known conditions that have been used for removing chromium compound films, and in addition to chlorine gas and oxygen gas, an inert gas such as nitrogen gas or helium gas may be mixed as necessary. The underlying phase shift film 14 and substrate 11 are both resistant to the oxygen-containing chlorine-based dry etching (Cl / O-based), and therefore remain without being removed or patterned in this process.

[0042] [Example] The embodiments of the present invention will be described in more detail below with reference to examples, but the present invention is not limited to the following examples.

[0043] Example 1 A phase layer consisting of silicon, molybdenum, oxygen, and nitrogen was deposited to a thickness of 65 nm on a quartz substrate using a DC sputtering device with two targets. The targets used were molybdenum and silicon, and the sputtering gases used were argon, oxygen, and nitrogen. The composition of this phase layer was analyzed by ESCA and found to be Si:Mo:O:N=30:5:20:45 (atomic percentage). A protective layer made of tantalum and oxygen was deposited on this phase layer with a thickness of 8 nm using a DC sputtering device. The target was tantalum, and the sputtering gas was argon and oxygen. The composition of this protective layer was analyzed by ESCA and found to be Ta:O=30:70 (atomic percentage).

[0044] The phase shift film composed of the thus formed phase layer and protective layer had a transmittance of 6% for the exposure light and a phase difference of 180 degrees. Next, a light-shielding film made of chromium, oxygen, and nitrogen was deposited on the protective layer to a thickness of 50 nm using a DC sputtering device. Chromium was used as the target, and argon was used as the sputtering gas. The composition of this light-shielding film was analyzed by ESCA and found to be Cr:O:N=55:35:10 (atomic percentage ratio).

[0045] Next, a negative chemically amplified electron beam resist was spin-coated on the light-shielding film to a thickness of 200 nm, and a pattern was formed with a dose of 35 μC / cm 2 The resist was patterned by electron beam drawing at 800 .ANG., heat-treated at 110.degree. C. for 10 minutes, and developed by paddle development for 90 seconds to form a resist pattern. Next, the light-shielding film was patterned using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. Overetching was performed to 100%. Next, a dry etching device was used to pattern the phase shift film consisting of the protective layer and the phase layer. CF4 and oxygen were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. The dry etching was stopped when the quartz substrate was dug to an average depth of 3 nm.

[0046] Next, the resist pattern was stripped and cleaned by washing with sulfuric acid and water. Next, the light-shielding film was removed using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 10 mTorr, the ICP power to 500 W, and the bias power to 10 W. Overetching was performed by 200%. During this process, no damage was caused to the underlying phase shift film and the quartz substrate. In this manner, the phase shift mask of Example 1 was obtained. Next, the dose at which haze occurred due to accelerated exposure was measured for this phase shift mask, and it was found to be 135 kJ / cm 2 It was.

[0047] The "dose at which haze occurs due to accelerated exposure" means that the larger the value, the less likely haze is to occur. 2 If the dose is more than 100 kJ / cm, there is no problem in using a phase shift mask. 2 If the above is true, the phase shift mask is extremely unlikely to produce haze. From the above measurement results, in the case of the phase shift mask of Example 1, the dose is 135 kJ / cm 2 Therefore, it was confirmed that the occurrence of haze can be reduced.

[0048] Example 2 A phase layer consisting of silicon, molybdenum, oxygen, and nitrogen was deposited to a thickness of 67 nm on a quartz substrate using a DC sputtering device with two targets. The targets used were molybdenum and silicon, and the sputtering gases used were argon, oxygen, and nitrogen. The composition of this phase layer was analyzed by ESCA and found to be Si:Mo:O:N = 35:5:15:45 (atomic percentage). A protective layer made of tungsten and oxygen was deposited on this phase layer with a thickness of 5 nm using a DC sputtering device. The target was tungsten, and the sputtering gas was argon and oxygen. The composition of this protective layer was analyzed by ESCA and found to be W:O=25:75 (atomic %).

[0049] The phase shift film composed of the thus formed phase layer and protective layer had a transmittance of 6% for the exposure light and a phase difference of 180 degrees. Next, a light-shielding film made of chromium, oxygen, and nitrogen was deposited on this protective layer with a thickness of 50 nm using a DC sputtering device. Chromium was used as the target, and argon, oxygen, and nitrogen were used as the sputtering gas. The composition of this light-shielding film was analyzed by ESCA and found to be Cr:O:N=55:35:10 (atomic percentage). Next, a negative chemically amplified electron beam resist was spin-coated on the light-shielding film to a thickness of 200 nm, and a pattern was formed with a dose of 35 μC / cm 2 The resist was patterned by electron beam drawing at 800 .ANG., heat-treated at 110.degree. C. for 10 minutes, and developed by paddle development for 90 seconds to form a resist pattern.

[0050] Next, the light-shielding film was patterned using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. Overetching was performed to 100%. Next, a dry etching device was used to pattern the phase shift film consisting of the protective layer and the phase layer. CF4 and oxygen were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. The dry etching was stopped when the quartz substrate was dug to an average depth of 3 nm.

[0051] Next, the resist pattern was stripped and cleaned by washing with sulfuric acid and water. Next, the light-shielding film was removed using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 10 mTorr, the ICP power to 500 W, and the bias power to 10 W. Overetching was performed by 200%. During this process, no damage was caused to the underlying phase shift film and the quartz substrate. In this manner, the phase shift mask according to the second embodiment was obtained. Next, the dose at which haze occurred due to accelerated exposure was measured for this phase shift mask, and it was found to be 92 kJ / cm 2 It was. From the above results, in the case of the phase shift mask of Example 2, the dose is 92 kJ / cm 2 Therefore, it was confirmed that the occurrence of haze can be reduced.

[0052] Example 3 A phase layer consisting of silicon, molybdenum, oxygen, and nitrogen was deposited to a thickness of 67 nm on a quartz substrate using a DC sputtering device with two targets. The targets used were molybdenum and silicon, and the sputtering gases used were argon, oxygen, and nitrogen. The composition of this phase layer was analyzed by ESCA and found to be Si:Mo:O:N=40:8:7:45 (atomic percentage). A protective layer consisting of tellurium and oxygen was deposited on this phase layer with a thickness of 3 nm using a DC sputtering device. Tellurium was used as the target, and argon and oxygen were used as the sputtering gas. The composition of this protective layer was analyzed by ESCA and found to be Te:O=35:65 (atomic percentage).

[0053] The phase shift film composed of the thus formed phase layer and protective layer had a transmittance of 6% for the exposure light and a phase difference of 180 degrees. Next, a light-shielding film made of chromium, oxygen, and nitrogen was deposited on this protective layer with a thickness of 50 nm using a DC sputtering device. Chromium was used as the target, and argon, oxygen, and nitrogen were used as the sputtering gas. The composition of this light-shielding film was analyzed by ESCA and found to be Cr:O:N=55:35:10 (atomic percentage). Next, a negative chemically amplified electron beam resist was spin-coated on the light-shielding film to a thickness of 200 nm, and a pattern was formed with a dose of 35 μC / cm 2 The resist was patterned by electron beam drawing at 800 .ANG., heat-treated at 110.degree. C. for 10 minutes, and developed by paddle development for 90 seconds to form a resist pattern.

[0054] Next, the light-shielding film was patterned using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. Overetching was performed to 100%. Next, a dry etching device was used to pattern the phase shift film consisting of the protective layer and the phase layer. CF4 and oxygen were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. The dry etching was stopped when the quartz substrate was dug to an average depth of 3 nm.

[0055] Next, the resist pattern was stripped and cleaned by washing with sulfuric acid and water. Next, the light-shielding film was removed using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 10 mTorr, the ICP power to 500 W, and the bias power to 10 W. Overetching was performed by 200%. During this process, no damage was caused to the underlying phase shift film and the quartz substrate. In this manner, the phase shift mask of Example 3 was obtained. Next, the dose at which haze occurred due to accelerated exposure was measured for this phase shift mask, and it was found to be 87 kJ / cm 2 It was. From the above results, in the case of the phase shift mask of Example 3, the dose amount is 87 kJ / cm 2 Therefore, it was confirmed that the occurrence of haze can be reduced.

[0056] Example 4 A phase layer consisting of silicon, molybdenum, oxygen, and nitrogen was deposited to a thickness of 70 nm on a quartz substrate using a DC sputtering device with two targets. The targets used were molybdenum and silicon, and the sputtering gases used were argon, oxygen, and nitrogen. The composition of this phase layer was analyzed by ESCA and found to be Si:Mo:O:N = 35:5:15:45 (atomic percentage). A protective layer consisting of tantalum, oxygen, and nitrogen was deposited on this phase layer with a thickness of 2 nm using a DC sputtering device. The target was tantalum, and the sputtering gas was argon, oxygen, and nitrogen. The composition of this protective layer was analyzed by ESCA and found to be Ta:O:N=65:5:30 (atomic percentage).

[0057] The phase shift film composed of the thus formed phase layer and protective layer had a transmittance of 6% for the exposure light and a phase difference of 180 degrees. Next, a light-shielding film made of chromium, oxygen, and nitrogen was deposited on this protective layer with a thickness of 50 nm using a DC sputtering device. Chromium was used as the target, and argon, oxygen, and nitrogen were used as the sputtering gas. The composition of this light-shielding film was analyzed by ESCA and found to be Cr:O:N=55:35:10 (atomic percentage). Next, a negative chemically amplified electron beam resist was spin-coated on the light-shielding film to a thickness of 200 nm, and a pattern was formed with a dose of 35 μC / cm 2 The resist was patterned by electron beam drawing at 800 .ANG., heat-treated at 110.degree. C. for 10 minutes, and developed by paddle development for 90 seconds to form a resist pattern.

[0058] Next, the light-shielding film was patterned using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. Overetching was performed to 100%. Next, a dry etching device was used to pattern the phase shift film consisting of the protective layer and the phase layer. CF4 and oxygen were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. The dry etching was stopped when the quartz substrate was dug to an average depth of 3 nm.

[0059] Next, the resist pattern was stripped and cleaned by washing with sulfuric acid and water. Next, the light-shielding film was removed using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 10 mTorr, the ICP power to 500 W, and the bias power to 10 W. Overetching was performed by 200%. During this process, no damage was caused to the underlying phase shift film and the quartz substrate. In this manner, the phase shift mask of Example 4 was obtained. Next, the dose at which haze occurred due to accelerated exposure was measured for this phase shift mask, and it was found to be 110 kJ / cm 2 It was. From the above results, in the case of the phase shift mask of Example 4, the dose amount is 110 kJ / cm 2 Therefore, it was confirmed that the occurrence of haze can be reduced.

[0060] Comparative Example 1 A phase layer consisting of silicon, molybdenum, oxygen, and nitrogen was deposited to a thickness of 70 nm on a quartz substrate using a DC sputtering device with two targets. The targets used were molybdenum and silicon, and the sputtering gases used were argon, oxygen, and nitrogen. The composition of this phase layer was analyzed by ESCA and found to be Si:Mo:O:N=40:8:7:45 (atomic percentage). Next, a light-shielding film consisting of chromium, oxygen, and nitrogen was deposited on the phase layer with a thickness of 50 nm using a DC sputtering device. Chromium was used as the target, and argon, oxygen, and nitrogen were used as the sputtering gas. The composition of this light-shielding film was analyzed by ESCA and found to be Cr:O:N = 55:35:10 (atomic percentage).

[0061] Next, a negative chemically amplified electron beam resist was spin-coated on the light-shielding film to a thickness of 200 nm, and a pattern was formed with a dose of 35 μC / cm 2 The resist was patterned by electron beam drawing at 800 .ANG., heat-treated at 110.degree. C. for 10 minutes, and developed by paddle development for 90 seconds to form a resist pattern. Next, the light-shielding film was patterned using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. Overetching was performed to 100%.

[0062] Next, a dry etching device was used to pattern the phase shift film consisting of only the phase layer. CF4 and oxygen were used as the etching gas, and the gas pressure was set to 5 mTorr, the ICP power to 400 W, and the bias power to 40 W. The dry etching was stopped when the quartz substrate was dug to an average depth of 3 nm. Next, the resist pattern was stripped and cleaned by washing with sulfuric acid and water. Next, the light-shielding film was removed using a dry etching device. Chlorine, oxygen, and helium were used as the etching gas, and the gas pressure was set to 10 mTorr, the ICP power to 500 W, and the bias power to 10 W. Overetching was performed by 200%. During this process, no damage was caused to the underlying phase shift film and the quartz substrate.

[0063] In this way, there was obtained the phase shift mask of Comparative Example 1. That is, the phase shift mask of Comparative Example 1 is a phase shift mask that does not include the protective layer formed in Examples 1-4. Next, the dose at which haze occurred due to accelerated exposure was measured for this phase shift mask, and it was found to be 58 kJ / cm 2 It was. From the above results, in the phase shift mask of Comparative Example 1, the dose was 58 kJ / cm 2 Therefore, it was confirmed that the generation of haze could not be sufficiently reduced. As described above, it is understood that forming a protective layer on a phase layer is effective in reducing the amount of haze generated in a phase shift mask.

[0064] The phase shift mask blank of the present invention and the phase shift mask produced using the same have been described above using the above examples, but the above examples are merely examples for carrying out the present invention, and the present invention is not limited to these. Furthermore, modifications of these examples are within the scope of the present invention, and it is self-evident from the above description that various other embodiments are possible within the scope of the present invention. [Industrial Applicability]

[0065] In the present invention, the composition, film thickness, and layer structure of the phase shift mask blank, as well as the manufacturing process and conditions for a phase shift mask using the same are selected within appropriate ranges, making it possible to provide a phase shift mask in which fine patterns are formed with high precision and which is suitable for the manufacture of logic devices of 28 nm or less, or memory devices of 30 nm or less. [Explanation of symbols]

[0066] 10. Phase shift mask blank 11... Substrate (substrate) transparent to the exposure wavelength 12...Phase layer (phase difference transmittance adjustment layer) 13 Protective layer (gas permeable protective layer) 14. Phase shift film 15. Light-shielding film 16. Resist pattern 17 Phase shift film pattern 100 Phase shift mask d1: Phase layer thickness d2: Thickness of protective layer

Claims

1. A phase shift mask blank used to fabricate a phase shift mask to which exposure light with a wavelength of 200 nm or less is applied, The device comprises a transparent substrate and a phase-shift film formed on the transparent substrate, The phase shift film comprises a phase difference transmittance adjustment layer that allows for adjustment of predetermined amounts of phase and transmittance with respect to transmitted exposure light, and a gas permeability protection layer formed on the phase difference transmittance adjustment layer to prevent gas permeation into the phase difference transmittance adjustment layer. The phase difference transmittance adjustment layer is located on the transparent substrate side, When the thickness of the phase difference transmittance adjustment layer is d1 and the thickness of the gas permeability protection layer is d2, d1 is thicker than d2, and d2 is 15 nm or less. The phase difference transmittance adjustment layer contains silicon, a transition metal, and carbon. The transition metal is at least one selected from titanium, vanadium, cobalt, nickel, zirconium, niobium, and hafnium. The phase-shift mask blank is characterized in that the gas permeable protective layer contains at least one selected from tantalum metal, tantalum compounds, tellurium metal, and tellurium compounds.

2. The phase-shift mask blank according to claim 1, characterized in that the phase-shift film is resistant to oxygen-containing chlorine-based etching (Cl / O system) and can be etched with fluorine-based etching (F system).

3. The gas permeable protective layer contains the tantalum compound, The tantalum compound is characterized by containing tantalum and at least one selected from oxygen, nitrogen, and carbon, as described in claim 1 or 2.

4. The phase shift mask blank according to any one of claims 1 to 3, characterized in that the phase difference transmittance adjustment layer has a single-layer structure.

5. The phase shift mask blank according to any one of claims 1 to 4, characterized in that the phase difference transmittance adjustment layer contains a carbide of metal silicide.

6. The phase shift mask blank according to any one of claims 1 to 5, characterized in that the total thickness of the phase difference transmittance adjustment layer and the gas permeability protection layer is 50 nm or more.

7. The phase shift mask blank according to any one of claims 1 to 6, characterized in that the transition metal is at least one selected from cobalt, nickel, zirconium, and hafnium.

8. A phase shift mask to which exposure light with a wavelength of 200 nm or less is applied, and which has a circuit pattern, The device comprises a transparent substrate and a phase-shift film formed on the transparent substrate, The phase shift film comprises a phase difference transmittance adjustment layer that allows for adjustment of predetermined amounts of phase and transmittance with respect to transmitted exposure light, and a gas permeability protection layer formed on the phase difference transmittance adjustment layer to prevent gas permeation into the phase difference transmittance adjustment layer. The phase difference transmittance adjustment layer is located on the transparent substrate side, When the thickness of the phase difference transmittance adjustment layer is d1 and the thickness of the gas permeability protection layer is d2, d1 is thicker than d2, and d2 is 15 nm or less. The phase difference transmittance adjustment layer contains silicon, a transition metal, and carbon. The transition metal is at least one selected from titanium, vanadium, cobalt, nickel, zirconium, niobium, and hafnium. The phase shift mask is characterized in that the gas permeable protective layer contains at least one selected from tantalum metal, tantalum compounds, tellurium metal, and tellurium compounds.

9. The phase shift mask according to claim 8, characterized in that the phase shift film is resistant to oxygen-containing chlorine-based etching (Cl / O system) and can be etched with fluorine-based etching (F system).

10. The gas permeable protective layer contains the tantalum compound, The phase shift mask according to claim 8 or 9, characterized in that the tantalum compound contains tantalum and at least one selected from oxygen, nitrogen, and carbon.

11. The phase shift mask according to any one of claims 8 to 10, characterized in that the phase difference transmittance adjustment layer has a single-layer structure.

12. The phase shift mask according to any one of claims 8 to 11, characterized in that the phase difference transmittance adjustment layer contains a carbide of a metal silicide.

13. The phase shift mask according to any one of claims 8 to 12, characterized in that the total thickness of the phase difference transmittance adjustment layer and the gas permeability protection layer is 50 nm or more.

14. The phase shift mask according to any one of claims 8 to 13, characterized in that the transition metal is at least one selected from cobalt, nickel, zirconium, and hafnium.

15. A method for manufacturing a phase shift mask using a phase shift mask blank according to any one of claims 1 to 7, A step of forming a light-shielding film on the phase-shift film, A step of forming a resist pattern on the light-shielding film formed on the phase-shift film, After forming the resist pattern, the process involves forming a pattern on the light-shielding film by oxygen-containing chlorine etching (Cl / O system), The process involves forming a pattern on the light-shielding film, followed by forming a pattern on the phase-shift film using fluorine-based etching (F-based), The steps include: forming a pattern on the phase-shift film, followed by removing the resist pattern; A method for manufacturing a phase shift mask, characterized by comprising the step of removing the resist pattern, and then removing the light-shielding film from the phase shift film by oxygen-containing chlorine-based etching (Cl / O system).

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