WO2025053592A1 - Substrate processing apparatus and method - Google Patents
Substrate processing apparatus and method Download PDFInfo
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- WO2025053592A1 WO2025053592A1 PCT/KR2024/013285 KR2024013285W WO2025053592A1 WO 2025053592 A1 WO2025053592 A1 WO 2025053592A1 KR 2024013285 W KR2024013285 W KR 2024013285W WO 2025053592 A1 WO2025053592 A1 WO 2025053592A1
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- WIPO (PCT)
- Prior art keywords
- surface treatment
- gas
- substrate
- process chamber
- treatment process
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- H10P72/0406—
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/4401—Means for minimising impurities, e.g. dust, moisture or residual gas, in the reaction chamber
- C23C16/4405—Cleaning of reactor or parts inside the reactor by using reactive gases
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- H10P14/6336—
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- H10P14/6339—
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- H10P14/668—
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- H10P70/12—
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- H10P72/00—
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- H10P95/00—
Definitions
- the present invention relates to a substrate processing device and method, and more particularly, to a substrate processing device and method that prevents deposition of an iodine component from being formed on the inner wall of a process chamber.
- Chemical vapor deposition (CVD) or atomic layer deposition (ALD) can be used to deposit a thin film on a substrate.
- a source gas causes a chemical reaction on the surface of the substrate to form a thin film.
- atomic layer deposition since one layer of the source gas attached to the surface of the substrate forms a thin film, it is possible to form a thin film with a thickness similar to the diameter of an atom.
- PECVD plasma enhanced chemical vapor deposition
- PEALD plasma enhanced atomic layer deposition
- the process gas for depositing a thin film on a substrate may include a source gas and a reaction gas.
- a thin film may be deposited on the substrate by injecting the reaction gas after the source gas is injected onto the substrate.
- a precursor containing iodine may be used for the deposition of a silicon nitride thin film. Meanwhile, if a precursor containing iodine is used and the thin film deposition process is performed, iodine may attach to the inner wall of the process chamber to form a deposit. This deposit may act as a particle in the subsequent thin film deposition process and deteriorate the quality of the thin film.
- the problem to be solved by the present invention is to provide a substrate processing device and method that prevents deposition of an iodine component from being formed on the inner wall of a process chamber.
- a substrate processing device includes a process chamber that provides a process processing space for a process on a substrate, and a control unit that controls the process on the substrate, wherein the control unit causes a surface treatment process to be performed on an internal space of the process chamber before a thin film deposition process on the substrate is performed, a process material used in the thin film deposition process includes iodine, and the surface treatment process includes a process of controlling a nitrogen concentration in a surface area of the process chamber.
- the surface area of the process chamber where the surface treatment process is completed includes first to third surface areas sequentially formed in a direction in which the depth of the surface of the process chamber decreases.
- the nitrogen concentration in each of the first surface area and the second surface area increases.
- the nitrogen concentration in the third surface area decreases.
- a substrate treatment method includes a step of performing a surface treatment process on a substrate, and a step of performing a thin film deposition process on the substrate on which the surface treatment process has been completed, wherein a process material used in the thin film deposition process includes iodine, and the surface treatment process includes a process of controlling a nitrogen concentration in a surface area of a process chamber that provides a process treatment space for the process on the substrate.
- the above surface treatment process includes a first surface treatment process in which a first surface treatment gas is sprayed onto the substrate, a second surface treatment process in which a second surface treatment gas is sprayed onto the substrate, and a third surface treatment process in which a third surface treatment gas is sprayed onto the substrate.
- the first surface treatment gas includes a first gas and a second gas
- the second surface treatment gas includes the first gas and a third gas
- the third surface treatment gas includes the first gas
- the above first surface treatment process includes a process of converting the first surface treatment gas into a plasma state with a first RF power
- the second surface treatment process includes a process of converting the second surface treatment gas into a plasma state with a second RF power
- the third surface treatment process includes a process of converting the third surface treatment gas into a plasma state with a third RF power, wherein among the first to third RF powers, the second RF power is formed to be the largest.
- the first surface treatment process is performed for a first time
- the second surface treatment process is performed for a second time
- the third surface treatment process is performed for a third time
- the second time is formed to be longer than the first time and the third time.
- the above surface treatment process includes a process of preventing bonding between the process material and the surface of a surface treatment target existing in the internal space of the process chamber.
- iodine is prevented from being attached to the inner wall of the process chamber during the thin film deposition process by forming a nitrogen layer on the inner wall of the process chamber before the thin film deposition process using a precursor containing iodine is performed.
- Figure 1 is a drawing showing a substrate processing device according to an embodiment of the present invention.
- Figure 2 is a drawing showing that the substrate support has moved into the process processing space.
- Figure 3 is a drawing showing that a deposit has been formed in the internal space of a process chamber.
- Figure 4 is a graph showing the components included in the thin film.
- Figure 5 is a drawing showing that a surface treatment process is performed in the internal space of a process chamber.
- Figure 6 is a drawing to explain the difference in electronegativity between the inner wall of the process chamber and iodine.
- Figure 7 is a diagram to explain the electronegativity difference between the surface area and iodine.
- Figure 8 is a drawing for explaining the process cycle.
- Figure 9 is a drawing for explaining the surface treatment process.
- Figure 10 is a drawing showing the surface area.
- Figure 11 is a graph showing the nitrogen concentration of the surface area shown in Figure 10.
- Figure 12 is a table showing the process conditions of the surface treatment process.
- Figure 13 is a flow chart showing a substrate processing method according to an embodiment of the present invention.
- FIG. 1 is a drawing showing a substrate processing device according to an embodiment of the present invention
- FIG. 2 is a drawing showing that a substrate support part has moved into a process processing space
- FIG. 3 is a drawing showing that a deposit has been formed in the internal space of a process chamber
- FIG. 4 is a graph showing components included in a thin film.
- a substrate processing device (10) is configured to include a process chamber (100), a substrate support unit (200), an elevator unit (300), a gas supply unit (400), a gas injection unit (500), a power supply unit (600), and a control unit (700).
- the substrate processing device (10) can deposit a thin film on a substrate (W). Specifically, the substrate processing device (10) can deposit a thin film on the substrate (W) using a plasma enhanced chemical vapor deposition (PECVD) method or a plasma enhanced atomic layer deposition (PEALD) method. Alternatively, the substrate processing device (10) can deposit a thin film on the substrate (W) using a chemical vapor deposition (CVD) method or an atomic layer deposition (ALD) method.
- PECVD plasma enhanced chemical vapor deposition
- PEALD plasma enhanced atomic layer deposition
- CVD chemical vapor deposition
- ALD atomic layer deposition
- the process chamber (100) may include a chamber body (110) and a chamber lid (120).
- the chamber body (110) may provide a space for receiving various components for processing a substrate (W).
- the chamber lid (120) may seal an upper opening of the chamber body (110).
- the chamber lid (120) may support a gas injection unit (500).
- the gas injection unit (500) may be fixed to a lower surface of the chamber lid (120).
- the process chamber (100) can provide a process processing space (SP1) and a substrate placement space (SP2).
- the process processing space (SP1) represents a space for a process on a substrate (W)
- the substrate placement space (SP2) represents a space for placement and movement of the substrate (W).
- the process processing space (SP1) and the substrate placement space (SP2) can be formed by combining the chamber body (110) and the chamber lid (120).
- an upper space can correspond to the process processing space (SP1)
- a lower space can correspond to the substrate placement space (SP2).
- a substrate entrance (130) for entrance and exit of a substrate (W) may be formed on one side of the process chamber (100).
- a substrate entrance (130) may be formed on one side of the chamber body (110).
- the substrate (W) may be brought into or taken out of the process chamber (100) through the substrate entrance (130).
- the process chamber (100) may be equipped with a shutter (140).
- the shutter (140) may open or close the substrate entrance (130).
- the shutter (140) opens the substrate entrance (130)
- the substrate (W) may be brought in or taken out through the substrate entrance (130).
- the shutter (140) may close the substrate entrance (130) to block the inside of the process chamber (100) from the outside.
- the substrate support (200) can provide a mounting surface on which the substrate (W) can be mounted. A process can be performed on the substrate (W) mounted on the mounting surface of the substrate support (200).
- the substrate support (200) can heat the substrate (W).
- a heater (not shown) can be provided inside the substrate support (200). Heat emitted from the heater can be transferred to the substrate (W) through the body of the substrate support (200).
- the heater can serve as an electrode for forming an electric field. As described below, when RF power is supplied to the showerhead (520), an electric field can be formed between the showerhead (520) and the heater.
- the substrate support member (200) can be raised to a process processing space (SP1) where a process for a substrate (W) is performed, or lowered to a substrate placement space (SP2) where placement and movement of the substrate (W) are performed.
- the elevating member (300) can generate a driving force to move the substrate support member (200) in an up-and-down direction.
- FIG. 1 illustrates that the substrate support member (200) is lowered to the substrate placement space (SP2)
- FIG. 2 illustrates that the substrate support member (200) is raised to the process processing space (SP1).
- the gas supply unit (400) serves to supply process gas to the process chamber (100). Specifically, the gas supply unit (400) can supply process gas to the gas injection unit (500) provided in the process chamber (100).
- a gas transfer line (410) can be connected to the gas supply unit (400).
- a plurality of gas transfer lines (410) can be provided, and the plurality of gas transfer lines (410) can provide transfer paths for different process gases.
- the gas injection unit (500) performs the role of injecting process gas to the substrate (W).
- the gas injection unit (500) is configured to include a diffusion unit (510) and a showerhead (520).
- the diffusion unit (510) performs the role of providing a diffusion space (530) for the process gas supplied to the process chamber (100).
- a diffusion space (530) can be formed between the diffusion unit (510) and the showerhead (520).
- the diffusion unit (510) can diffuse the process gas supplied from the gas supply unit (400) and supply it to the diffusion space (530).
- the diffusion unit (510) can supply the process gas to a plurality of different points in the diffusion space (530).
- the showerhead (520) is coupled to the diffusion unit (510) and serves to inject the process gas diffused in the diffusion space (530).
- the showerhead (520) can inject the process gas with a uniform distribution over the entire surface area of the substrate (W).
- the process gas may include a source gas, a source purge gas, a reaction gas, and a reaction purge gas.
- the source gas, the source purge gas, the reaction gas, and the reaction purge gas may be sequentially injected from the showerhead (520), or at least some of them may be injected simultaneously.
- the source gas and the reaction gas may collide with each other and react after being injected from the showerhead (520).
- the source gas activated by the reaction gas may come into contact with the substrate (W) to perform a process treatment on the substrate (W).
- the activated source gas may be deposited as a thin film on the substrate (W).
- the showerhead (520) may be provided with a plurality of injection holes (540) for injecting process gas.
- the plurality of injection holes (540) may be distributed over a certain range of the showerhead (520).
- the power supply unit (600) can supply RF power for generating plasma to the process chamber (100). Specifically, the power supply unit (600) can supply RF power to the showerhead (520).
- the showerhead (520) may have a separate electrode plate (not shown) that receives RF power, or may serve as an electrode that receives RF power on its own.
- the substrate support unit (200) may include a heater that serves as an electrode.
- RF power is supplied to the showerhead (520)
- an electric field may be formed between the showerhead (520) and the heater of the substrate support unit (200).
- the process gas introduced into the process chamber (100) is converted into particles in a plasma state by the electric field formed by the supply of RF power, and the plasma particles react with the surface of the substrate (W) so that process processing can be performed on the substrate (W).
- the process chamber (100) may be equipped with an exhaust port (150).
- the exhaust port (150) may be arranged on the inner lower surface of the chamber body (110).
- the exhaust port (150) may be arranged in an area vertically overlapping the substrate support member (200) to effectively discharge process byproducts.
- the exhaust port (150) is arranged on the inner lower surface of the chamber body (110), and according to some embodiments of the present invention, the exhaust port (150) may be arranged on the inner side surface of the chamber body (110).
- the exhaust port (150) may be arranged in an area between the substrate support member (200) and the gas injection member (500).
- the exhaust port (150) is arranged on the inner lower surface of the chamber body (110) will be mainly described.
- the exhaust port (150) may provide an exhaust path for process byproducts.
- the process byproducts may include all substances that must be exhausted from the process chamber (100), such as remaining gases that are not used for forming a thin film among the process gases supplied to the process chamber (100).
- the process byproducts may include source gas, reaction gas, source purge gas, and reaction purge gas.
- An exhaust line (160) may be connected to the exhaust port (150).
- the exhaust line (160) may provide a transport path for process byproducts introduced through the exhaust port (150).
- An exhaust pump (170) may be provided in the exhaust line (160). The exhaust pump (170) may pressurize the internal space of the exhaust line (160) so that process byproducts introduced into the exhaust port (150) may be transported through the exhaust line (160). The process byproducts transported through the exhaust line (160) may be discharged from the process chamber (100).
- the control unit (700) can perform overall control of the substrate processing device (10). For example, the control unit (700) can operate the shutter (140) to open and close the substrate entrance (130), or control the lifting unit (300) to move the substrate support unit (200). In addition, the control unit (700) can control the supply of RF power by the power supply unit (600) or the supply of process gas to the process chamber (100).
- control unit (700) can control the process for the substrate (W). Specifically, the control unit (700) can cause the surface treatment process for the internal space of the process chamber (100) to be performed before the thin film deposition process for the substrate (W) is performed.
- the surface treatment process can include a process for preventing bonding between a process material used for thin film deposition and a surface of a surface treatment target existing in the internal space of the process chamber (100).
- the surface treatment process can include a process for controlling the nitrogen concentration in the surface area of the process chamber (100).
- the source gas may be generated using a precursor containing iodine.
- the precursor may be SiH 2 I 2 .
- a deposit (800) may be formed in the internal space of the process chamber (100), as illustrated in FIG. 3.
- the component of the deposit (800) may include iodine.
- a plurality of process cycles may be repeated for deposition of the thin film, and as the process cycles are repeated, the amount of the deposit (800) formed in the internal space of the process chamber (100) may increase.
- the iodine component of the deposit (800) may deteriorate the quality of the thin film. Therefore, it is desirable to prevent the formation of the deposit (800) of the iodine component in the internal space of the process chamber (100).
- FIG. 4 is data according to X-ray photoelectron spectroscopy (XPS) that shows the types of elements and the concentration of atoms included in a thin film, where the horizontal axis represents the etching time of the thin film and the vertical axis represents the concentration of atoms.
- the etching time of the thin film can be understood as corresponding to the depth of the thin film. For example, 0 seconds (0s) means information about the surface of the thin film (900), and a specific etching time means information about the types of elements and the concentration of atoms at the corresponding time depth according to the etching rate.
- the amount of iodine contained in the thin film is not large.
- the iodine contained in the source gas does not remain in the thin film but is only combined in the internal space of the process chamber (100).
- the iodine component deposit (800) formed in the internal space of the process chamber (100) is formed because the bonding force between the internal space of the process chamber (100) and iodine is relatively large.
- the control unit (700) can cause a surface treatment process to be performed to reduce the bonding force between the internal space of the process chamber (100) and iodine before the thin film deposition process is performed.
- a surface treatment process By performing the surface treatment process, the formation of a deposit (800) of an iodine component in the internal space of the process chamber (100) can be prevented.
- Figure 5 is a drawing showing that a surface treatment process is performed in the internal space of a process chamber.
- a surface treatment process can be performed on the internal space of the process chamber.
- the interior of the process chamber (100) may include various components.
- the interior of the process chamber (100) may include a substrate support (200) and a gas injection unit (500).
- the surface treatment process may be performed on at least one of the inner wall of the process chamber (100), the substrate support (200), the gas injection unit (500), and the substrate (W).
- the surface area (900) of a surface treatment target, such as the inner wall of the process chamber (100), the substrate support (200), the gas injection unit (500), and the substrate (W) may be transformed by the surface treatment process.
- the surface area (900) where the surface treatment process is completed may have a relatively high nitrogen concentration.
- the nitrogen concentration of the surface area (900) is formed high, bonding between the process material and the surface area (900) may be prevented.
- the process material may be prevented from being attached to the surface area (900).
- the process material used in the thin film deposition process may include iodine.
- the surface area (900) of the surface treatment target may include a component having a weaker bonding force with the process material than other parts of the surface treatment target.
- the difference in electronegativity between the process material and the surface area (900) may be formed to be smaller than the difference in electronegativity between the process material and other parts. The greater the difference in electronegativity between different materials, the greater the bonding force of the corresponding materials. Since the surface area (900) is formed with a component having a low electronegativity difference with respect to the process material, the process material is prevented from being bonded to the surface area (900), and the process material can be easily discharged from the process chamber (100).
- Figure 6 is a drawing for explaining the electronegativity difference between the inner wall of the process chamber and iodine
- Figure 7 is a drawing for explaining the electronegativity difference between the surface area and iodine.
- the electronegativity difference between the surface area (900) and iodine (I) can be formed smaller than the electronegativity difference between the inner wall of the process chamber (100) and iodine (I).
- the inner wall of the process chamber (100) may be composed of a material of aluminum oxide. That is, the inner wall of the process chamber (100) may include aluminum (Al) and oxygen (O).
- the electronegativity of aluminum (Al) is 1.61
- the electronegativity of oxygen (O) is 3.44
- the electronegativity of iodine (I) is 2.66.
- the electronegativity difference between aluminum (Al) and iodine (I) may be 1.05
- the electronegativity difference between oxygen (O) and iodine (I) may be 0.78.
- the surface region (900) may include nitrogen (N).
- the inner wall of the process chamber (100) may include a surface region (900) including nitrogen (N).
- iodine (I) may be blocked from bonding with the inner wall of the process chamber (100).
- the electronegativity of nitrogen (N) may be 3.04, and the electronegativity difference between nitrogen (N) and iodine (I) may be 0.38.
- the electronegativity difference between nitrogen (N) and iodine (I) may be formed to be smaller than the electronegativity difference between aluminum (Al) and iodine (I) and the electronegativity difference between oxygen (O) and iodine (I). Since the electronegativity difference between nitrogen (N) and iodine (I) is relatively small, the bond between nitrogen (N) and iodine (I) is formed to be small, and thus, when the thin film deposition process is completed, iodine (I) may be discharged from the process chamber (100) without being bound to nitrogen (N).
- FIG. 7 illustrates that the surface of the inner wall of the process chamber (100) is surface-treated to form a surface area (900), but as described above, the surface area (900) may also be formed by surface-treating the surfaces of various surface treatment targets, such as a gas injection unit (500), a substrate support unit (200), and a substrate (W).
- various surface treatment targets such as a gas injection unit (500), a substrate support unit (200), and a substrate (W).
- Figure 8 is a drawing for explaining the process cycle.
- multiple processes can be sequentially performed to deposit a thin film (900) on a substrate (W).
- a surface treatment process may be performed before deposition of a thin film (900) on a substrate (W).
- a surface treatment gas may be injected into a process chamber (100) for the surface treatment process.
- the surface treatment gas may contain nitrogen.
- RF power can be supplied to the process chamber (100) by the power supply unit (600).
- the surface treatment gas can be converted into a plasma state.
- the surface treatment gas in the plasma state can react with the surface of the surface treatment target to form a surface area (900).
- the control unit (700) can adjust the size of RF power while the surface treatment process is being performed.
- the surface treatment process can be performed in multiple stages, and the control unit (700) can supply RF power of individual sizes for each stage.
- the surface of the surface treatment target may be damaged.
- a relatively small amount of RF power may be supplied to the process chamber (100) at the beginning of the surface treatment process, and then the RF power may be increased.
- the surface treatment process may be performed in three stages, and a larger RF power may be supplied in the second stage compared to the first stage.
- the amount of RF power in the third stage may be the same as the amount of RF power in the first stage, or may be smaller than the amount of RF power in the second stage, and larger than the amount of RF power in the first stage.
- a thin film deposition process may be performed.
- a source gas may be injected into the process chamber (100) to deposit a thin film (900) on the substrate (W).
- the source purge gas may be continuously supplied to pressurize the source gas while the process for the substrate (W) is in progress.
- the source gas may be sprayed onto the surface of the substrate (W) through the showerhead (520). Some of the source gas sprayed onto the substrate (W) may be adsorbed onto the surface of the substrate (W), and some may not be adsorbed.
- the non-adsorbed source gas may be deposited on the adsorbed source gas or may float inside the process chamber (100).
- the step of purging the source gas in the process chamber (100) may include a step of discharging the source gas and the surface treatment gas that are not adsorbed on the surface of the substrate (W) from the process chamber (100). That is, when the source gas is purged in the process chamber (100), only the source gas adsorbed on the substrate (W) remains, and the source gas and the surface treatment gas that are laminated on the adsorbed source gas or floated in the process chamber (100) may be discharged to the outside of the process chamber (100). Accordingly, a single source gas layer may be formed on the surface of the substrate (W).
- a reaction gas may be injected into the process chamber (100).
- the reaction purge gas may be continuously supplied while the process for the substrate (W) is in progress to pressurize the reaction gas.
- the reaction gas may be sprayed onto the surface of the substrate (W) through the showerhead (520).
- the reaction gas may react with the source gas adsorbed on the substrate (W) to form a thin film (900).
- RF power may be applied to the process chamber (100) so that the reaction gas may be converted into a plasma state.
- the source gas may also be converted into a plasma state by the RF power.
- a source gas and a reaction gas in a plasma state can react to form a thin film (900) with high reaction efficiency.
- the reaction gas can be purged from the process chamber (100). That is, RF power is applied for a certain period of time to convert the reaction gas into plasma, and when the period of time has elapsed, the supply of RF power is stopped, and then the reaction gas can be purged.
- the step of purging the reaction gas from the process chamber (100) includes the step of discharging process byproducts such as reaction gas, surface treatment gas, and plasma that are not used to form a thin film (900) on the surface of the substrate (W) from the process chamber (100).
- the process of supplying source gas and reaction gas to the process chamber (100) to form a thin film (900) forms one process cycle, and multiple layers of thin films (900) can be deposited on the substrate (W) through multiple process cycles.
- the thin film deposition process is performed after the surface treatment process, the formation of a deposition product (800) of an iodine component on the surface of the surface treatment target can be prevented.
- Figure 9 is a drawing for explaining the surface treatment process.
- the surface treatment process may include a first surface treatment process, a second surface treatment process, and a third surface treatment process.
- the first surface treatment process, the second surface treatment process, and the third surface treatment process are performed sequentially, and a surface treatment gas may be injected into the internal space of the process chamber (100) through each process.
- the flow rates (sccm) of the first gas and the second gas included in the first surface treatment gas may be different from each other.
- the flow rate of the first gas when the first surface treatment process is performed, the flow rate of the first gas may be formed to be greater than the flow rate of the second gas.
- the flow rate of the first gas used in the third surface treatment process may be different from the flow rates of the first gas used in each of the first surface treatment process and the second surface treatment process.
- the flow rate of the first gas used in the third surface treatment process may be formed to be less than the flow rates of the first gas used in each of the first surface treatment process and the second surface treatment process.
- the first surface treatment process may include a process in which a first RF power is supplied and a first surface treatment gas provided to the substrate (W) is converted into a plasma state
- the second surface treatment process may include a process in which a second RF power is supplied and a second surface treatment gas provided to the substrate (W) is converted into a plasma state
- the third surface treatment process may include a process in which a third RF power is supplied and a third surface treatment gas provided to the substrate (W) is converted into a plasma state.
- Fig. 10 is a drawing showing a surface area
- Fig. 11 is a graph showing the nitrogen concentration of the surface area shown in Fig. 10.
- the surface region (900) on which the surface treatment process is completed includes a first surface region (910), a second surface region (920), and a third surface region (930), and each surface region (910, 920, 930) may have a different nitrogen concentration.
- FIG. 10 illustrates a surface region (900) formed on an inner wall of a process chamber (100).
- the first to third surface regions (910, 920, 930) may be sequentially formed in a direction in which the depth of the surface of the process chamber (100) decreases.
- the first surface treatment process represents a preliminary step for forming a first surface region (910) containing nitrogen (N) on the surface of a surface treatment target.
- first gas and the second gas included in the first surface treatment gas only the first gas may contain nitrogen (N), and the first surface treatment gas may be converted into a plasma state by first RF power having a relatively low magnitude. Accordingly, the nitrogen concentration of the first surface region (910) may be formed to be relatively low.
- the nitrogen concentration in the first surface region may increase.
- the second surface treatment process represents a step for forming a second surface region (920) containing a relatively high density of nitrogen (N) to reduce the reactivity with iodine.
- both the first gas and the third gas contained in the second surface treatment gas may contain nitrogen (N), and the second surface treatment gas may be converted into a plasma state by a second RF power that is greater than the first RF power. Accordingly, the nitrogen concentration of the second surface region (920) may be formed relatively high.
- the nitrogen concentration in the second surface region may increase.
- the third surface treatment process represents a step of forming a third surface region (930) that protects the surface of the surface treatment target.
- the third surface treatment gas may include only a first gas containing nitrogen (N), and the third surface treatment gas may be converted into a plasma state by a third RF power that is smaller than the second RF power.
- the third RF power may be the same as the first RF power. Accordingly, the nitrogen concentration of the third surface region (930) may be formed to be higher than that of the first surface region (910) and lower than that of the second surface region (920).
- the nitrogen concentration may be maximum at the boundary between the second surface region and the third surface region, and the nitrogen concentration in the third surface region may decrease as the depth of the surface of the process chamber (100) decreases.
- the nitrogen concentration in the third surface region may be formed to be generally larger than that of the first surface.
- the first surface treatment process, the second surface treatment process, and the third surface treatment process may be performed for a preset time.
- the first surface treatment process may be performed for a first time
- the second surface treatment process may be performed for a second time
- the third surface treatment process may be performed for a third time.
- the first to third times may be the same.
- the first time, the second time, and the third time may be different.
- the second time may be longer than the first time and the third time
- the first time and the third time may be the same.
- the third time may be longer than the first time.
- Figure 12 is a table showing the process conditions of the surface treatment process.
- a process condition table (1000) specifies the type of surface treatment gas, the flow rate of surface treatment gas, the size of RF power, the supply time of RF power, and the substrate spacing.
- the surface treatment process includes a first surface treatment process, a second surface treatment process, and a third surface treatment process.
- nitrogen and hydrogen are sprayed into the internal space of the process chamber (100)
- nitrogen and ammonia are sprayed into the internal space of the process chamber (100)
- nitrogen is sprayed into the internal space of the process chamber (100).
- the size of RF power can be formed larger in the second surface treatment process compared to the first surface treatment process, and smaller in the third surface treatment process compared to the second surface treatment process.
- the supply of surface treatment gas and plasma conversion of the surface treatment gas can be performed while the substrate support (200) is raised to the process treatment space (SP1).
- Figure 13 is a flow chart showing a substrate processing method according to an embodiment of the present invention.
- a substrate treatment method may include a step (S1110) in which a surface treatment process is performed on a surface of a surface treatment target and a step (S1120) in which a thin film deposition process is performed on a substrate (W) on which the surface treatment process has been completed.
- the surface treatment process may include a first surface treatment process, a second surface treatment process, and a third surface treatment process. Since the first surface treatment process, the second surface treatment process, and the third surface treatment process have been described above, a detailed description thereof will be omitted.
- the surface treatment process may include a process for preventing bonding between a process material used for deposition of a thin film and a surface treatment target existing in the internal space of the process chamber (100).
- the surface treatment process may include a process for controlling the nitrogen concentration in a surface area of a process chamber (100) that provides a process treatment space for a process for a substrate (W).
- the process material used in the thin film deposition process may include iodine (I), and the surface region (900) may include a component that is formed to have a relatively small difference in electronegativity with respect to the process material.
- the surface region (900) may be configured to include nitrogen (N), and the difference in electronegativity between the process material and the surface region (900) may be formed to be small compared to the difference in electronegativity between the process material and other parts of the surface treatment target.
- the process material is prevented from attaching to the surface area (900), and the process material can be easily discharged from the process chamber (100).
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Abstract
Description
본 발명은 기판 처리 장치 및 방법에 관한 것으로서, 더욱 상세하게는 요오드 성분의 증착물이 공정 챔버의 내벽에 형성되는 것을 방지하는 기판 처리 장치 및 방법에 관한 것이다.The present invention relates to a substrate processing device and method, and more particularly, to a substrate processing device and method that prevents deposition of an iodine component from being formed on the inner wall of a process chamber.
기판에 박막을 증착시키기 위하여 화학 기상 증착법(CVD; Chemical Vapor Deposition) 또는 원자층 박막 증착법(ALD; Atomic Layer Deposition) 등이 이용될 수 있다. 화학 기상 증착법 또는 원자층 박막 증착법에 의한 경우 소스 가스가 기판의 표면에서 화학 반응을 일으켜 박막이 형성될 수 있다. 특히, 원자층 박막 증착법에 의한 경우 기판의 표면에 부착된 원료 기체의 한 층이 박막을 형성하기 때문에 원자의 직경과 유사한 두께의 박막을 형성하는 것이 가능하다.Chemical vapor deposition (CVD) or atomic layer deposition (ALD) can be used to deposit a thin film on a substrate. In the case of chemical vapor deposition or atomic layer deposition, a source gas causes a chemical reaction on the surface of the substrate to form a thin film. In particular, in the case of atomic layer deposition, since one layer of the source gas attached to the surface of the substrate forms a thin film, it is possible to form a thin film with a thickness similar to the diameter of an atom.
공정 온도의 범위를 확장하기 위하여 플라즈마 화학 기상 증착법(PECVD; Plasma Enhanced Chemical Vapor Deposition) 또는 플라즈마 원자층 박막 증착법(PEALD; Plasma Enhanced Atomic Layer Deposition)이 이용될 수 있다. 플라즈마 화학 기상 증착법 및 플라즈마 원자층 박막 증착법은 화학 기상 증착법 및 원자층 박막 증착법에 비하여 낮은 온도에서 공정 처리가 가능하기 때문에 박막의 물성이 향상될 수 있다.To extend the range of process temperatures, plasma enhanced chemical vapor deposition (PECVD) or plasma enhanced atomic layer deposition (PEALD) can be used. Since plasma enhanced chemical vapor deposition and plasma enhanced atomic layer deposition can be processed at lower temperatures than chemical vapor deposition and atomic layer deposition, the properties of the thin film can be improved.
기판에 박막을 증착시키기 위한 공정 가스는 소스 가스 및 반응 가스를 포함할 수 있다. 기판으로 소스 가스가 분사된 이후에 반응 가스가 분사됨으로써 기판에 박막이 증착될 수 있다.The process gas for depositing a thin film on a substrate may include a source gas and a reaction gas. A thin film may be deposited on the substrate by injecting the reaction gas after the source gas is injected onto the substrate.
실리콘 질화물 박막의 증착을 위하여 요오드가 포함된 전구체가 이용될 수 있다. 한편, 요오드가 포함된 전구체가 이용되어 박막 증착 공정이 진행된 경우 요오드가 공정 챔버의 내벽에 부착되어 증착물을 형성할 수 있다. 이러한 증착물은 이후의 박막 증착 공정에서 파티클로 작용하여 박막의 품질을 저해할 수 있다.A precursor containing iodine may be used for the deposition of a silicon nitride thin film. Meanwhile, if a precursor containing iodine is used and the thin film deposition process is performed, iodine may attach to the inner wall of the process chamber to form a deposit. This deposit may act as a particle in the subsequent thin film deposition process and deteriorate the quality of the thin film.
따라서, 요오드가 포함된 전구체가 이용되어 박막 증착 공정이 진행되더라도 요오드 성분의 증착물이 공정 챔버의 내벽에 형성되지 않도록 하는 발명의 등장이 요구된다.Therefore, there is a need for an invention that prevents iodine-containing deposits from being formed on the inner wall of a process chamber even when a thin film deposition process is performed using a precursor containing iodine.
본 발명이 해결하고자 하는 과제는 요오드 성분의 증착물이 공정 챔버의 내벽에 형성되는 것을 방지하는 기판 처리 장치 및 방법을 제공하는 것이다.The problem to be solved by the present invention is to provide a substrate processing device and method that prevents deposition of an iodine component from being formed on the inner wall of a process chamber.
본 발명의 과제들은 이상에서 언급한 과제로 제한되지 않으며, 언급되지 않은 또 다른 과제들은 아래의 기재로부터 당업자에게 명확하게 이해될 수 있을 것이다.The tasks of the present invention are not limited to the tasks mentioned above, and other tasks not mentioned will be clearly understood by those skilled in the art from the description below.
본 발명의 실시예에 따른 기판 처리 장치는 기판에 대한 공정을 위한 공정 처리 공간을 제공하는 공정 챔버, 및 상기 기판에 대한 공정을 제어하는 제어부를 포함하되, 상기 제어부는 상기 기판에 대한 박막 증착 공정이 수행되기 이전에 상기 공정 챔버의 내부 공간에 대한 표면 처리 공정이 수행되도록 하고, 상기 박막 증착 공정에서 사용되는 공정 물질은 요오드를 포함하고, 상기 표면 처리 공정은 상기 공정 챔버의 표면 영역의 질소 농도를 제어하는 공정을 포함한다.A substrate processing device according to an embodiment of the present invention includes a process chamber that provides a process processing space for a process on a substrate, and a control unit that controls the process on the substrate, wherein the control unit causes a surface treatment process to be performed on an internal space of the process chamber before a thin film deposition process on the substrate is performed, a process material used in the thin film deposition process includes iodine, and the surface treatment process includes a process of controlling a nitrogen concentration in a surface area of the process chamber.
상기 표면 처리 공정이 완료된 상기 공정 챔버의 표면 영역은 상기 공정 챔버의 표면의 깊이가 작아지는 방향으로 순차적으로 형성된 제1 내지 제3 표면 영역을 포함한다.The surface area of the process chamber where the surface treatment process is completed includes first to third surface areas sequentially formed in a direction in which the depth of the surface of the process chamber decreases.
상기 공정 챔버의 표면의 깊이가 작아지는 방향으로 진행할수록 상기 제1 표면 영역 및 상기 제2 표면 영역 각각에서의 질소 농도는 증가한다.As the depth of the surface of the process chamber decreases, the nitrogen concentration in each of the first surface area and the second surface area increases.
상기 공정 챔버의 표면의 깊이가 작아지는 방향으로 진행할수록 상기 제3 표면 영역에서의 질소 농도는 감소한다.As the depth of the surface of the above process chamber progresses toward decreasing, the nitrogen concentration in the third surface area decreases.
본 발명의 실시예에 따른 기판 처리 방법은 기판에 대한 표면 처리 공정이 수행되는 단계, 및 상기 표면 처리 공정이 완료된 기판에 대한 박막 증착 공정이 수행되는 단계를 포함하되, 상기 박막 증착 공정에서 사용되는 공정 물질은 요오드를 포함하고, 상기 표면 처리 공정은 상기 기판에 대한 공정을 위한 공정 처리 공간을 제공하는 공정 챔버의 표면 영역의 질소 농도를 제어하는 공정을 포함한다.A substrate treatment method according to an embodiment of the present invention includes a step of performing a surface treatment process on a substrate, and a step of performing a thin film deposition process on the substrate on which the surface treatment process has been completed, wherein a process material used in the thin film deposition process includes iodine, and the surface treatment process includes a process of controlling a nitrogen concentration in a surface area of a process chamber that provides a process treatment space for the process on the substrate.
상기 표면 처리 공정은, 제1 표면 처리 가스가 상기 기판에 분사되는 제1 표면 처리 공정과, 제2 표면 처리 가스가 상기 기판에 분사되는 제2 표면 처리 공정, 및 제3 표면 처리 가스가 상기 기판에 분사되는 제3 표면 처리 공정을 포함한다.The above surface treatment process includes a first surface treatment process in which a first surface treatment gas is sprayed onto the substrate, a second surface treatment process in which a second surface treatment gas is sprayed onto the substrate, and a third surface treatment process in which a third surface treatment gas is sprayed onto the substrate.
상기 제1 표면 처리 가스는 제1 가스 및 제2 가스를 포함하고, 상기 제2 표면 처리 가스는 상기 제1 가스 및 제3 가스를 포함하고, 상기 제3 표면 처리 가스는 상기 제1 가스를 포함한다.The first surface treatment gas includes a first gas and a second gas, the second surface treatment gas includes the first gas and a third gas, and the third surface treatment gas includes the first gas.
상기 제1 표면 처리 공정은 제1 RF 전력으로 상기 제1 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함하고,The above first surface treatment process includes a process of converting the first surface treatment gas into a plasma state with a first RF power,
상기 제2 표면 처리 공정은 제2 RF 전력으로 상기 제2 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함하고, 상기 제3 표면 처리 공정은 제3 RF 전력으로 상기 제3 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함하고, 상기 제1 내지 제3 RF 전력 중 제2 RF 전력이 가장 크게 형성된다.The second surface treatment process includes a process of converting the second surface treatment gas into a plasma state with a second RF power, and the third surface treatment process includes a process of converting the third surface treatment gas into a plasma state with a third RF power, wherein among the first to third RF powers, the second RF power is formed to be the largest.
상기 제1 표면 처리 공정은 제1 시간 동안 진행되고, 상기 제2 표면 처리 공정은 제2 시간 동안 진행되고, 상기 제3 표면 처리 공정은 제3 시간 동안 진행되고, 상기 제2 시간은 상기 제1 시간 및 제3 시간에 비하여 길게 형성된다.The first surface treatment process is performed for a first time, the second surface treatment process is performed for a second time, the third surface treatment process is performed for a third time, and the second time is formed to be longer than the first time and the third time.
상기 표면 처리 공정은 상기 공정 물질과 상기 공정 챔버의 내부 공간에 존재하는 표면 처리 대상물의 표면 간의 결합을 방지하는 공정을 포함한다.The above surface treatment process includes a process of preventing bonding between the process material and the surface of a surface treatment target existing in the internal space of the process chamber.
기타 실시예들의 구체적인 사항들은 상세한 설명 및 도면들에 포함되어 있다.Specific details of other embodiments are included in the detailed description and drawings.
상기한 바와 같은 본 발명의 실시예에 따른 기판 처리 장치 및 방법에 따르면 요오드가 포함된 전구체를 이용한 박막 증착 공정이 수행되기 이전에 공정 챔버의 내벽에 질소층을 형성함으로써 박막 증착 공정 중 요오드가 공정 챔버의 내벽에 부착되는 것을 방지하는 장점이 있다.According to the substrate processing device and method according to the embodiment of the present invention as described above, there is an advantage in that iodine is prevented from being attached to the inner wall of the process chamber during the thin film deposition process by forming a nitrogen layer on the inner wall of the process chamber before the thin film deposition process using a precursor containing iodine is performed.
도 1은 본 발명의 실시예에 따른 기판 처리 장치를 나타낸 도면이다.Figure 1 is a drawing showing a substrate processing device according to an embodiment of the present invention.
도 2는 기판 지지부가 공정 처리 공간으로 이동한 것을 나타낸 도면이다.Figure 2 is a drawing showing that the substrate support has moved into the process processing space.
도 3은 공정 챔버의 내부 공간에 증착물이 형성된 것을 나타낸 도면이다.Figure 3 is a drawing showing that a deposit has been formed in the internal space of a process chamber.
도 4는 박막에 포함된 성분을 나타낸 그래프이다.Figure 4 is a graph showing the components included in the thin film.
도 5는 공정 챔버의 내부 공간에 표면 처리 공정이 수행된 것을 나타낸 도면이다.Figure 5 is a drawing showing that a surface treatment process is performed in the internal space of a process chamber.
도 6은 공정 챔버의 내측벽과 요오드 간의 전기 음성도 차이를 설명하기 위한 도면이다.Figure 6 is a drawing to explain the difference in electronegativity between the inner wall of the process chamber and iodine.
도 7은 표면 영역과 요오드 간의 전기 음성도 차이를 설명하기 위한 도면이다.Figure 7 is a diagram to explain the electronegativity difference between the surface area and iodine.
도 8은 공정 사이클을 설명하기 위한 도면이다.Figure 8 is a drawing for explaining the process cycle.
도 9는 표면 처리 공정을 설명하기 위한 도면이다.Figure 9 is a drawing for explaining the surface treatment process.
도 10은 표면 영역을 나타낸 도면이다.Figure 10 is a drawing showing the surface area.
도 11은 도 10에 도시된 표면 영역의 질소 농도를 나타낸 그래프이다.Figure 11 is a graph showing the nitrogen concentration of the surface area shown in Figure 10.
도 12는 표면 처리 공정의 공정 조건을 나타낸 테이블이다.Figure 12 is a table showing the process conditions of the surface treatment process.
도 13은 본 발명의 실시예에 따른 기판 처리 방법을 나타낸 흐름도이다.Figure 13 is a flow chart showing a substrate processing method according to an embodiment of the present invention.
이하, 첨부된 도면을 참조하여 본 발명의 바람직한 실시예를 상세히 설명한다. 본 발명의 이점 및 특징, 그리고 그것들을 달성하는 방법은 첨부되는 도면과 함께 상세하게 후술되어 있는 실시 예들을 참조하면 명확해질 것이다. 그러나 본 발명은 이하에서 게시되는 실시 예들에 한정되는 것이 아니라 서로 다른 다양한 형태로 구현될 수 있으며, 단지 본 실시 예들은 본 발명의 게시가 완전하도록 하고, 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 발명의 범주를 완전하게 알려주기 위해 제공되는 것이며, 본 발명은 청구항의 범주에 의해 정의될 뿐이다. 명세서 전체에 걸쳐 동일 참조 부호는 동일 구성 요소를 지칭한다.Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. The advantages and features of the present invention, and the methods for achieving them, will become apparent with reference to the embodiments described in detail below together with the accompanying drawings. However, the present invention is not limited to the embodiments disclosed below, but may be implemented in various different forms, and the present embodiments are provided only to make the disclosure of the present invention complete and to fully inform those skilled in the art of the scope of the invention, and the present invention is defined only by the scope of the claims. Like reference numerals refer to like elements throughout the specification.
다른 정의가 없다면, 본 명세서에서 사용되는 모든 용어(기술 및 과학적 용어를 포함)는 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 공통적으로 이해될 수 있는 의미로 사용될 수 있을 것이다. 또 일반적으로 사용되는 사전에 정의되어 있는 용어들은 명백하게 특별히 정의되어 있지 않는 한 이상적으로 또는 과도하게 해석되지 않는다.Unless otherwise defined, all terms (including technical and scientific terms) used in this specification may be used with a meaning that can be commonly understood by a person of ordinary skill in the art to which the present invention belongs. In addition, terms defined in commonly used dictionaries shall not be ideally or excessively interpreted unless explicitly specifically defined.
도 1은 본 발명의 실시예에 따른 기판 처리 장치를 나타낸 도면이고, 도 2는 기판 지지부가 공정 처리 공간으로 이동한 것을 나타낸 도면이고, 도 3은 공정 챔버의 내부 공간에 증착물이 형성된 것을 나타낸 도면이며, 도 4는 박막에 포함된 성분을 나타낸 그래프이다.FIG. 1 is a drawing showing a substrate processing device according to an embodiment of the present invention, FIG. 2 is a drawing showing that a substrate support part has moved into a process processing space, FIG. 3 is a drawing showing that a deposit has been formed in the internal space of a process chamber, and FIG. 4 is a graph showing components included in a thin film.
도 1 및 도 2를 참조하면, 본 발명의 실시예에 따른 기판 처리 장치(10)는 공정 챔버(100), 기판 지지부(200), 승강부(300), 가스 공급부(400), 가스 분사부(500), 전력 공급부(600) 및 제어부(700)를 포함하여 구성된다.Referring to FIGS. 1 and 2, a substrate processing device (10) according to an embodiment of the present invention is configured to include a process chamber (100), a substrate support unit (200), an elevator unit (300), a gas supply unit (400), a gas injection unit (500), a power supply unit (600), and a control unit (700).
본 발명의 실시예에 따른 기판 처리 장치(10)는 기판(W)에 박막을 증착할 수 있다. 구체적으로, 기판 처리 장치(10)는 플라즈마 화학 기상 증착법(PECVD; Plasma Enhanced Chemical Vapor Deposition) 또는 플라즈마 원자층 박막 증착법(PEALD; Plasma Enhanced Atomic Layer Deposition)을 이용하여 기판(W)에 박막을 증착할 수 있다. 또는, 기판 처리 장치(10)는 화학 기상 증착법(CVD; Chemical Vapor Deposition) 또는 원자층 박막 증착법(ALD; Atomic Layer Deposition)을 이용하여 기판(W)에 박막을 증착할 수도 있다.The substrate processing device (10) according to an embodiment of the present invention can deposit a thin film on a substrate (W). Specifically, the substrate processing device (10) can deposit a thin film on the substrate (W) using a plasma enhanced chemical vapor deposition (PECVD) method or a plasma enhanced atomic layer deposition (PEALD) method. Alternatively, the substrate processing device (10) can deposit a thin film on the substrate (W) using a chemical vapor deposition (CVD) method or an atomic layer deposition (ALD) method.
공정 챔버(100)는 챔버 본체(110) 및 챔버 리드(120)를 포함할 수 있다. 챔버 본체(110)는 기판(W)의 공정을 위한 각종 부품의 수용 공간을 제공할 수 있다. 챔버 리드(120)는 챔버 본체(110)의 상부 개구를 밀폐시킬 수 있다. 챔버 리드(120)는 가스 분사부(500)를 지지할 수 있다. 가스 분사부(500)는 챔버 리드(120)의 하측면에 고정될 수 있다.The process chamber (100) may include a chamber body (110) and a chamber lid (120). The chamber body (110) may provide a space for receiving various components for processing a substrate (W). The chamber lid (120) may seal an upper opening of the chamber body (110). The chamber lid (120) may support a gas injection unit (500). The gas injection unit (500) may be fixed to a lower surface of the chamber lid (120).
공정 챔버(100)는 공정 처리 공간(SP1) 및 기판 배치 공간(SP2)을 제공할 수 있다. 공정 처리 공간(SP1)의 기판(W)에 대한 공정을 위한 공간을 나타내고, 기판 배치 공간(SP2)은 기판(W)의 배치 및 이동을 위한 공간을 나타낸다. 챔버 본체(110) 및 챔버 리드(120)가 결합됨으로써 공정 처리 공간(SP1) 및 기판 배치 공간(SP2)이 형성될 수 있다. 공정 챔버(100)의 내부 공간 중 상부 공간이 공정 처리 공간(SP1)에 대응되고, 하부 공간이 기판 배치 공간(SP2)에 대응될 수 있다.The process chamber (100) can provide a process processing space (SP1) and a substrate placement space (SP2). The process processing space (SP1) represents a space for a process on a substrate (W), and the substrate placement space (SP2) represents a space for placement and movement of the substrate (W). The process processing space (SP1) and the substrate placement space (SP2) can be formed by combining the chamber body (110) and the chamber lid (120). Among the internal spaces of the process chamber (100), an upper space can correspond to the process processing space (SP1), and a lower space can correspond to the substrate placement space (SP2).
공정 챔버(100)의 일측에는 기판(W)의 출입을 위한 기판 출입구(130)가 형성될 수 있다. 예를 들어, 챔버 본체(110)의 일측에 기판 출입구(130)가 형성될 수 있다. 기판(W)은 기판 출입구(130)를 통해 공정 챔버(100)의 내부로 반입되거나 공정 챔버(100)의 외부로 반출될 수 있다.A substrate entrance (130) for entrance and exit of a substrate (W) may be formed on one side of the process chamber (100). For example, a substrate entrance (130) may be formed on one side of the chamber body (110). The substrate (W) may be brought into or taken out of the process chamber (100) through the substrate entrance (130).
공정 챔버(100)에는 셔터(140)가 구비될 수 있다. 셔터(140)는 기판 출입구(130)를 개방하거나 폐쇄할 수 있다. 셔터(140)가 기판 출입구(130)를 개방한 경우 기판 출입구(130)를 통해 기판(W)이 반입되거나 반출될 수 있다. 기판(W)에 대한 공정이 진행되는 경우에는 셔터(140)가 기판 출입구(130)를 폐쇄하여 공정 챔버(100)의 내부를 외부에 대하여 차단할 수 있다.The process chamber (100) may be equipped with a shutter (140). The shutter (140) may open or close the substrate entrance (130). When the shutter (140) opens the substrate entrance (130), the substrate (W) may be brought in or taken out through the substrate entrance (130). When a process for the substrate (W) is in progress, the shutter (140) may close the substrate entrance (130) to block the inside of the process chamber (100) from the outside.
기판 지지부(200)는 기판(W)이 안착 가능한 안착면을 제공할 수 있다. 기판 지지부(200)의 안착면에 안착된 기판(W)에 대하여 공정이 수행될 수 있다. 기판 지지부(200)는 기판(W)을 가열할 수 있다. 이를 위하여. 기판 지지부(200)의 내부에는 히터(미도시)가 구비될 수 있다. 히터에서 발산된 열은 기판 지지부(200)의 몸체를 통해 기판(W)으로 전달될 수 있다. 히터는 전계의 형성을 위한 전극의 역할을 수행할 수 있다. 후술하는 바와 같이, 샤워헤드(520)에 RF 전력이 공급되는 경우 샤워헤드(520)와 히터의 사이에 전계가 형성될 수 있다.The substrate support (200) can provide a mounting surface on which the substrate (W) can be mounted. A process can be performed on the substrate (W) mounted on the mounting surface of the substrate support (200). The substrate support (200) can heat the substrate (W). To this end, a heater (not shown) can be provided inside the substrate support (200). Heat emitted from the heater can be transferred to the substrate (W) through the body of the substrate support (200). The heater can serve as an electrode for forming an electric field. As described below, when RF power is supplied to the showerhead (520), an electric field can be formed between the showerhead (520) and the heater.
기판 지지부(200)는 기판(W)에 대한 공정이 수행되는 공정 처리 공간(SP1)으로 상승하거나 기판(W)의 배치 및 이동이 수행되는 기판 배치 공간(SP2)으로 하강할 수 있다. 승강부(300)는 구동력을 발생시켜 기판 지지부(200)를 상하 방향으로 이동시킬 수 있다. 도 1은 기판 지지부(200)가 기판 배치 공간(SP2)으로 하강한 것을 도시하고 있고, 도 2는 기판 지지부(200)가 공정 처리 공간(SP1)으로 상승한 것을 도시하고 있다.The substrate support member (200) can be raised to a process processing space (SP1) where a process for a substrate (W) is performed, or lowered to a substrate placement space (SP2) where placement and movement of the substrate (W) are performed. The elevating member (300) can generate a driving force to move the substrate support member (200) in an up-and-down direction. FIG. 1 illustrates that the substrate support member (200) is lowered to the substrate placement space (SP2), and FIG. 2 illustrates that the substrate support member (200) is raised to the process processing space (SP1).
가스 공급부(400)는 공정 챔버(100)로 공정 가스를 공급하는 역할을 수행한다. 구체적으로, 가스 공급부(400)는 공정 챔버(100)에 구비된 가스 분사부(500)로 공정 가스를 공급할 수 있다. 가스 공급부(400)에는 가스 이송 라인(410)이 연결될 수 있다. 가스 이송 라인(410)은 복수 개가 구비될 수 있고, 복수의 가스 이송 라인(410)은 서로 다른 공정 가스의 이송 경로를 제공할 수 있다.The gas supply unit (400) serves to supply process gas to the process chamber (100). Specifically, the gas supply unit (400) can supply process gas to the gas injection unit (500) provided in the process chamber (100). A gas transfer line (410) can be connected to the gas supply unit (400). A plurality of gas transfer lines (410) can be provided, and the plurality of gas transfer lines (410) can provide transfer paths for different process gases.
가스 분사부(500)는 기판(W)으로 공정 가스를 분사하는 역할을 수행한다. 가스 분사부(500)는 확산부(510) 및 샤워헤드(520)를 포함하여 구성된다. 확산부(510)는 공정 챔버(100)로 공급된 공정 가스의 확산 공간(530)을 제공하는 역할을 수행한다. 확산부(510)와 샤워헤드(520)가 결합됨으로써 확산부(510)와 샤워헤드(520)의 사이에 확산 공간(530)이 형성될 수 있다. 또한, 확산부(510)는 가스 공급부(400)로부터 공급된 공정 가스를 확산시켜 확산 공간(530)으로 공급되도록 할 수 있다. 예를 들어, 확산부(510)는 확산 공간(530)의 서로 다른 복수의 지점으로 공정 가스가 공급되도록 할 수 있다.The gas injection unit (500) performs the role of injecting process gas to the substrate (W). The gas injection unit (500) is configured to include a diffusion unit (510) and a showerhead (520). The diffusion unit (510) performs the role of providing a diffusion space (530) for the process gas supplied to the process chamber (100). When the diffusion unit (510) and the showerhead (520) are combined, a diffusion space (530) can be formed between the diffusion unit (510) and the showerhead (520). In addition, the diffusion unit (510) can diffuse the process gas supplied from the gas supply unit (400) and supply it to the diffusion space (530). For example, the diffusion unit (510) can supply the process gas to a plurality of different points in the diffusion space (530).
샤워헤드(520)는 확산부(510)에 결합되고, 확산 공간(530)에서 확산된 공정 가스를 분사하는 역할을 수행한다. 샤워헤드(520)는 기판(W)의 표면 전체 영역에 걸쳐 균일한 분포로 공정 가스가 분사되도록 할 수 있다. 본 발명에서 공정 가스는 소스 가스, 소스 퍼지 가스, 반응 가스 및 반응 퍼지 가스를 포함할 수 있다. 소스 가스, 소스 퍼지 가스, 반응 가스 및 반응 퍼지 가스는 샤워헤드(520)에서 순차적으로 분사되거나 적어도 일부가 동시에 분사될 수 있다. 소스 가스 및 반응 가스는 샤워헤드(520)에서 분사된 이후에 서로 충돌하여 반응할 수 있다. 그리고, 반응 가스에 의하여 활성화된 소스 가스가 기판(W)에 접촉하여 기판(W)에 대한 공정 처리가 수행될 수 있다. 예를 들어, 활성화된 소스 가스가 기판(W)에 박막으로 증착될 수 있다.The showerhead (520) is coupled to the diffusion unit (510) and serves to inject the process gas diffused in the diffusion space (530). The showerhead (520) can inject the process gas with a uniform distribution over the entire surface area of the substrate (W). In the present invention, the process gas may include a source gas, a source purge gas, a reaction gas, and a reaction purge gas. The source gas, the source purge gas, the reaction gas, and the reaction purge gas may be sequentially injected from the showerhead (520), or at least some of them may be injected simultaneously. The source gas and the reaction gas may collide with each other and react after being injected from the showerhead (520). Then, the source gas activated by the reaction gas may come into contact with the substrate (W) to perform a process treatment on the substrate (W). For example, the activated source gas may be deposited as a thin film on the substrate (W).
샤워헤드(520)는 공정 가스의 분사를 위한 복수의 분사홀(540)을 구비할 수 있다. 복수의 분사홀(540)은 샤워헤드(520)의 일정 범위에 걸쳐 분포될 수 있다.The showerhead (520) may be provided with a plurality of injection holes (540) for injecting process gas. The plurality of injection holes (540) may be distributed over a certain range of the showerhead (520).
전력 공급부(600)는 플라즈마의 발생을 위한 RF 전력을 공정 챔버(100)로 공급할 수 있다. 구체적으로, 전력 공급부(600)는 샤워헤드(520)로 RF 전력을 공급할 수 있다. 샤워헤드(520)는 RF 전력을 공급받는 별도의 전극 플레이트(미도시)를 구비하거나, 자체적으로 RF 전력을 공급받는 전극의 역할을 수행할 수 있다. 전술한 바와 같이, 기판 지지부(200)는 전극의 역할을 수행하는 히터를 포함할 수 있다. 샤워헤드(520)로 RF 전력이 공급되는 경우 샤워헤드(520)와 기판 지지부(200)의 히터의 사이에 전계가 형성될 수 있다. RF 전력의 공급으로 형성된 전계에 의해 공정 챔버(100)로 유입된 공정 가스가 플라즈마 상태의 입자로 변환되고, 플라즈마 입자가 기판(W)의 표면과 반응하여 기판(W)에 대한 공정 처리가 수행될 수 있다.The power supply unit (600) can supply RF power for generating plasma to the process chamber (100). Specifically, the power supply unit (600) can supply RF power to the showerhead (520). The showerhead (520) may have a separate electrode plate (not shown) that receives RF power, or may serve as an electrode that receives RF power on its own. As described above, the substrate support unit (200) may include a heater that serves as an electrode. When RF power is supplied to the showerhead (520), an electric field may be formed between the showerhead (520) and the heater of the substrate support unit (200). The process gas introduced into the process chamber (100) is converted into particles in a plasma state by the electric field formed by the supply of RF power, and the plasma particles react with the surface of the substrate (W) so that process processing can be performed on the substrate (W).
공정 챔버(100)에는 배기 포트(150)가 구비될 수 있다. 배기 포트(150)는 챔버 본체(110)의 내부 하면에 배치될 수 있다. 예를 들어, 배기 포트(150)는 공정 부산물을 효과적으로 배출하기 위해 기판 지지부(200)에 수직 방향으로 중첩되는 영역에 배치될 수 있다. 한편, 배기 포트(150)가 챔버 본체(110)의 내부 하면에 되는 것은 예시적인 것으로서, 본 발명의 몇몇 실시예에 따르면 배기 포트(150)는 챔버 본체(110)의 내부 측면에 배치될 수도 있다. 예를 들어, 기판 지지부(200)가 공정 처리 공간(SP1)으로 상승한 경우 배기 포트(150)는 기판 지지부(200) 및 가스 분사부(500)의 사이 영역에 배치될 수 있다. 이하, 배기 포트(150)가 챔버 본체(110)의 내부 하면에 배치된 것을 위주로 설명하기로 한다.The process chamber (100) may be equipped with an exhaust port (150). The exhaust port (150) may be arranged on the inner lower surface of the chamber body (110). For example, the exhaust port (150) may be arranged in an area vertically overlapping the substrate support member (200) to effectively discharge process byproducts. Meanwhile, it is exemplary that the exhaust port (150) is arranged on the inner lower surface of the chamber body (110), and according to some embodiments of the present invention, the exhaust port (150) may be arranged on the inner side surface of the chamber body (110). For example, when the substrate support member (200) is raised to the process processing space (SP1), the exhaust port (150) may be arranged in an area between the substrate support member (200) and the gas injection member (500). Hereinafter, the case where the exhaust port (150) is arranged on the inner lower surface of the chamber body (110) will be mainly described.
배기 포트(150)는 공정 부산물의 배출 경로를 제공할 수 있다. 여기서, 공정 부산물은 공정 챔버(100)로 공급된 공정 가스 중 박막의 형성에 이용되지 않은 나머지 가스 등 공정 챔버(100)에서 배출되어야 하는 모든 물질을 포함할 수 있다. 예를 들어, 공정 부산물에는 소스 가스, 반응 가스, 소스 퍼지 가스 및 반응 퍼지 가스가 포함될 수 있다.The exhaust port (150) may provide an exhaust path for process byproducts. Here, the process byproducts may include all substances that must be exhausted from the process chamber (100), such as remaining gases that are not used for forming a thin film among the process gases supplied to the process chamber (100). For example, the process byproducts may include source gas, reaction gas, source purge gas, and reaction purge gas.
배기 포트(150)에는 배기 라인(160)이 연결될 수 있다. 배기 라인(160)은 배기 포트(150)를 통해 유입된 공정 부산물의 이송 경로를 제공할 수 있다. 배기 라인(160)에는 배기 펌프(170)가 구비될 수 있다. 배기 펌프(170)는 배기 라인(160)의 내부 공간을 가압하여 배기 포트(150)로 유입된 공정 부산물가 배기 라인(160)을 통해 이송되도록 할 수 있다. 배기 라인(160)을 통해 이송된 공정 부산물은 공정 챔버(100)에서 배출될 수 있게 된다.An exhaust line (160) may be connected to the exhaust port (150). The exhaust line (160) may provide a transport path for process byproducts introduced through the exhaust port (150). An exhaust pump (170) may be provided in the exhaust line (160). The exhaust pump (170) may pressurize the internal space of the exhaust line (160) so that process byproducts introduced into the exhaust port (150) may be transported through the exhaust line (160). The process byproducts transported through the exhaust line (160) may be discharged from the process chamber (100).
제어부(700)는 기판 처리 장치(10)에 대한 전반적인 제어를 수행할 수 있다. 예를 들어, 제어부(700)는 셔터(140)를 동작시켜 기판 출입구(130)를 개폐하거나, 승강부(300)를 제어하여 기판 지지부(200)를 이동시킬 수 있다. 또한, 제어부(700)는 전력 공급부(600)에 의해 RF 전력이 공급되는 것을 제어하거나 공정 챔버(100)로 공정 가스가 공급되는 것을 제어할 수도 있다.The control unit (700) can perform overall control of the substrate processing device (10). For example, the control unit (700) can operate the shutter (140) to open and close the substrate entrance (130), or control the lifting unit (300) to move the substrate support unit (200). In addition, the control unit (700) can control the supply of RF power by the power supply unit (600) or the supply of process gas to the process chamber (100).
또한, 제어부(700)는 기판(W)에 대한 공정을 제어할 수 있다. 구체적으로, 제어부(700)는 기판(W)에 대한 박막 증착 공정이 수행되기 이전에 공정 챔버(100)의 내부 공간에 대한 표면 처리 공정이 수행되도록 할 수 있다. 본 발명에서 표면 처리 공정은 박막의 증착에 이용되는 공정 물질과 공정 챔버(100)의 내부 공간에 존재하는 표면 처리 대상물의 표면 간의 결합을 방지하는 공정을 포함할 수 있다. 예를 들어, 표면 처리 공정은 공정 챔버(100)의 표면 영역의 질소 농도를 제어하는 공정을 포함할 수 있다.In addition, the control unit (700) can control the process for the substrate (W). Specifically, the control unit (700) can cause the surface treatment process for the internal space of the process chamber (100) to be performed before the thin film deposition process for the substrate (W) is performed. In the present invention, the surface treatment process can include a process for preventing bonding between a process material used for thin film deposition and a surface of a surface treatment target existing in the internal space of the process chamber (100). For example, the surface treatment process can include a process for controlling the nitrogen concentration in the surface area of the process chamber (100).
본 발명에서 소스 가스는 요오드가 포함된 전구체가 이용되어 생성된 것일 수 있다. 예를 들어, 전구체는 SiH2I2일 수 있다.In the present invention, the source gas may be generated using a precursor containing iodine. For example, the precursor may be SiH 2 I 2 .
요오드가 포함된 소스 가스가 이용되어 박막 증착 공정이 수행되는 경우 도 3에 도시된 바와 같이 공정 챔버(100)의 내부 공간에 증착물(800)이 형성될 수 있다. 증착물(800)의 성분은 요오드를 포함할 수 있다. 박막의 증착을 위하여 복수의 공정 사이클이 반복될 수 있는데, 공정 사이클이 반복될수록 공정 챔버(100)의 내부 공간에 형성되는 증착물(800)의 양이 증가할 수 있다. 요오드 성분은 증착물(800)은 박막의 품질을 저해할 수 있다. 따라서, 공정 챔버(100)의 내부 공간에 요오드 성분의 증착물(800)의 형성이 방지되도록 하는 것이 바람직하다.When a thin film deposition process is performed using a source gas containing iodine, a deposit (800) may be formed in the internal space of the process chamber (100), as illustrated in FIG. 3. The component of the deposit (800) may include iodine. A plurality of process cycles may be repeated for deposition of the thin film, and as the process cycles are repeated, the amount of the deposit (800) formed in the internal space of the process chamber (100) may increase. The iodine component of the deposit (800) may deteriorate the quality of the thin film. Therefore, it is desirable to prevent the formation of the deposit (800) of the iodine component in the internal space of the process chamber (100).
도 4는 박막에 포함된 원소의 종류 및 원자의 농도를 나타내는 X선 원소 분석법(XPS; X-ray Photoelectron Spectroscopy)에 따른 데이터로서, 가로축은 박막의 에칭 시간을 나타내고, 세로축은 원자의 농도를 나타낸다. 여기서, 박막의 에칭 시간은 박막의 깊이에 대응되는 것으로 이해될 수 있다. 예를 들어, 0초(0s)는 박막(900)의 표면에 대한 정보를 의미하고, 특정 에칭 시간은 에칭률(etching rate)에 따른 해당 시간 깊이에서의 원소의 종류 및 원자의 농도에 대한 정보를 의미한다.FIG. 4 is data according to X-ray photoelectron spectroscopy (XPS) that shows the types of elements and the concentration of atoms included in a thin film, where the horizontal axis represents the etching time of the thin film and the vertical axis represents the concentration of atoms. Here, the etching time of the thin film can be understood as corresponding to the depth of the thin film. For example, 0 seconds (0s) means information about the surface of the thin film (900), and a specific etching time means information about the types of elements and the concentration of atoms at the corresponding time depth according to the etching rate.
도 4를 참조하면, 요오드가 포함된 소스 가스가 이용되어 기판(W)에 박막이 증착되더라도 박막에 포함된 요오드의 양이 크기 않은 것이 확인될 수 있다. 소스 가스에 포함된 요오드는 박막에 잔류하지 않고 공정 챔버(100)의 내부 공간에만 결합되는 것이다. 이를 통하여, 공정 챔버(100)의 내부 공간에 형성되는 요오드 성분의 증착물(800)은 공정 챔버(100)의 내부 공간과 요오드 간의 결합력이 상대적으로 크게 형성되기 때문인 것으로 판단될 수 있다.Referring to FIG. 4, it can be confirmed that even if a source gas containing iodine is used to deposit a thin film on a substrate (W), the amount of iodine contained in the thin film is not large. The iodine contained in the source gas does not remain in the thin film but is only combined in the internal space of the process chamber (100). Through this, it can be determined that the iodine component deposit (800) formed in the internal space of the process chamber (100) is formed because the bonding force between the internal space of the process chamber (100) and iodine is relatively large.
제어부(700)는 박막 증착 공정이 수행되기 이전에 공정 챔버(100)의 내부 공간과 요오드 간의 결합력을 감소시키기 위한 표면 처리 공정이 수행되도록 할 수 있다. 표면 처리 공정이 수행됨으로써 공정 챔버(100)의 내부 공간에 요오드 성분의 증착물(800)이 형성되는 것이 방지될 수 있다.The control unit (700) can cause a surface treatment process to be performed to reduce the bonding force between the internal space of the process chamber (100) and iodine before the thin film deposition process is performed. By performing the surface treatment process, the formation of a deposit (800) of an iodine component in the internal space of the process chamber (100) can be prevented.
도 5는 공정 챔버의 내부 공간에 표면 처리 공정이 수행된 것을 나타낸 도면이다.Figure 5 is a drawing showing that a surface treatment process is performed in the internal space of a process chamber.
도 5를 참조하면, 공정 챔버의 내부 공간에 대하여 표면 처리 공정이 수행될 수 있다.Referring to Fig. 5, a surface treatment process can be performed on the internal space of the process chamber.
공정 챔버(100)의 내부에는 다양한 부품이 포함될 수 있다. 예를 들어, 공정 챔버(100)의 내부에는 기판 지지부(200) 및 가스 분사부(500)가 구비될 수 있다. 표면 처리 공정은 공정 챔버(100)의 내측벽, 기판 지지부(200), 가스 분사부(500) 및 기판(W) 중 적어도 하나에 대하여 수행될 수 있다. 표면 처리 공정에 의해 공정 챔버(100)의 내측벽, 기판 지지부(200), 가스 분사부(500) 및 기판(W)과 같은 표면 처리 대상물의 표면 영역(900)이 변환될 수 있다.The interior of the process chamber (100) may include various components. For example, the interior of the process chamber (100) may include a substrate support (200) and a gas injection unit (500). The surface treatment process may be performed on at least one of the inner wall of the process chamber (100), the substrate support (200), the gas injection unit (500), and the substrate (W). The surface area (900) of a surface treatment target, such as the inner wall of the process chamber (100), the substrate support (200), the gas injection unit (500), and the substrate (W), may be transformed by the surface treatment process.
표면 처리 공정이 완료된 표면 영역(900)은 상대적으로 높은 질소 농도를 가질 수 있다. 표면 영역(900)의 질소 농도가 높게 형성됨에 따라 공정 물질과 표면 영역(900) 간의 결합이 방지될 수 있다. 예를 들어, 박막 증착 공정이 수행되기 이전에 표면 처리 공정이 수행됨에 따라 박막 증착 공정이 수행되더라도 공정 물질이 표면 영역(900)에 부착되는 것이 방지될 수 있다. 여기서, 박막 증착 공정에서 사용되는 공정 물질은 요오드를 포함한 것일 수 있다.The surface area (900) where the surface treatment process is completed may have a relatively high nitrogen concentration. As the nitrogen concentration of the surface area (900) is formed high, bonding between the process material and the surface area (900) may be prevented. For example, since the surface treatment process is performed before the thin film deposition process is performed, even if the thin film deposition process is performed, the process material may be prevented from being attached to the surface area (900). Here, the process material used in the thin film deposition process may include iodine.
표면 처리 대상물의 표면 영역(900)은 표면 처리 대상물의 다른 부분에 비하여 공정 물질과의 결합력이 약한 것을 성분으로 포함할 수 있다. 이를 구체적으로 설명하면, 공정 물질과 다른 부분 간의 전기 음성도의 차이에 비하여 공정 물질과 표면 영역(900) 간의 전기 음성도의 차이가 작게 형성될 수 있다. 서로 다른 물질의 전기 음성도 차이가 클수록 해당 물질의 결합력이 증가할 수 있다. 공정 물질에 대하여 낮은 전기 음성도 차이를 갖는 성분으로 표면 영역(900)이 형성됨에 따라 공정 물질이 표면 영역(900)에 결합되는 것이 방지되고, 공정 물질이 공정 챔버(100)에서 용이하게 배출될 수 있다.The surface area (900) of the surface treatment target may include a component having a weaker bonding force with the process material than other parts of the surface treatment target. Specifically, the difference in electronegativity between the process material and the surface area (900) may be formed to be smaller than the difference in electronegativity between the process material and other parts. The greater the difference in electronegativity between different materials, the greater the bonding force of the corresponding materials. Since the surface area (900) is formed with a component having a low electronegativity difference with respect to the process material, the process material is prevented from being bonded to the surface area (900), and the process material can be easily discharged from the process chamber (100).
도 6은 공정 챔버의 내측벽과 요오드 간의 전기 음성도 차이를 설명하기 위한 도면이고, 도 7은 표면 영역과 요오드 간의 전기 음성도 차이를 설명하기 위한 도면이다.Figure 6 is a drawing for explaining the electronegativity difference between the inner wall of the process chamber and iodine, and Figure 7 is a drawing for explaining the electronegativity difference between the surface area and iodine.
도 6 및 도 7을 참조하면, 표면 영역(900)과 요오드(I) 간의 전기 음성도 차이는 공정 챔버(100)의 내측벽과 요오드(I) 간의 전기 음성도 차이에 비하여 작게 형성될 수 있다.Referring to FIGS. 6 and 7, the electronegativity difference between the surface area (900) and iodine (I) can be formed smaller than the electronegativity difference between the inner wall of the process chamber (100) and iodine (I).
공정 챔버(100)의 내측벽은 산화 알루미늄의 재질로 구성될 수 있다. 즉, 공정 챔버(100)의 내측벽은 알루미늄(Al) 및 산소(O)를 포함할 수 있다. 알루미늄(Al)의 전기 음성도는 1.61이고, 산소(O)의 전기 음성도는 3.44이며, 요오드(I)의 전기 음성도는 2.66이다. 이러한 경우 알루미늄(Al)과 요오드(I) 간의 전기 음성도 차이는 1.05이고, 산소(O)와 요오드(I) 간의 전기 음성도 차이는 0.78일 수 있다.The inner wall of the process chamber (100) may be composed of a material of aluminum oxide. That is, the inner wall of the process chamber (100) may include aluminum (Al) and oxygen (O). The electronegativity of aluminum (Al) is 1.61, the electronegativity of oxygen (O) is 3.44, and the electronegativity of iodine (I) is 2.66. In this case, the electronegativity difference between aluminum (Al) and iodine (I) may be 1.05, and the electronegativity difference between oxygen (O) and iodine (I) may be 0.78.
본 발명에서 표면 영역(900)은 질소(N)를 포함할 수 있다. 도 7에 도시된 바와 같이, 공정 챔버(100)의 내측벽이 질소(N)를 포함하는 표면 영역(900)을 포함할 수 있다. 이러한 경우 요오드(I)는 공정 챔버(100)의 내측벽과의 결합이 차단될 수 있다. 또한, 질소(N)의 전기 음성도는 3.04이고, 질소(N)와 요오드(I) 간의 전기 음성도 차이는 0.38일 수 있다.In the present invention, the surface region (900) may include nitrogen (N). As shown in FIG. 7, the inner wall of the process chamber (100) may include a surface region (900) including nitrogen (N). In this case, iodine (I) may be blocked from bonding with the inner wall of the process chamber (100). In addition, the electronegativity of nitrogen (N) may be 3.04, and the electronegativity difference between nitrogen (N) and iodine (I) may be 0.38.
도 6 및 도 7에 도시된 바와 같이, 질소(N)와 요오드(I) 간의 전기 음성도 차이는 알루미늄(Al)과 요오드(I) 간의 전기 음성도 차이 및 산소(O)와 요오드(I) 간의 전기 음성도 차이에 비하여 작게 형성될 수 있다. 질소(N)와 요오드(I) 간의 전기 음성도 차이가 상대적으로 작기 때문에 질소(N)와 요오드(I) 간의 결합이 작게 형성되고, 이로 인하여 박막 증착 공정이 완료된 경우 요오드(I)는 질소(N)에 결합되지 않고 공정 챔버(100)에서 배출될 수 있다.As illustrated in FIGS. 6 and 7, the electronegativity difference between nitrogen (N) and iodine (I) may be formed to be smaller than the electronegativity difference between aluminum (Al) and iodine (I) and the electronegativity difference between oxygen (O) and iodine (I). Since the electronegativity difference between nitrogen (N) and iodine (I) is relatively small, the bond between nitrogen (N) and iodine (I) is formed to be small, and thus, when the thin film deposition process is completed, iodine (I) may be discharged from the process chamber (100) without being bound to nitrogen (N).
도 7은 공정 챔버(100)의 내측벽의 표면이 표면 처리되어 표면 영역(900) 이 형성된 것을 설명하였으나, 전술한 바와 같이 표면 영역(900)은 가스 분사부(500), 기판 지지부(200) 및 기판(W)과 같은 다양한 표면 처리 대상물의 표면이 표면 처리되어 형성될 수도 있다.FIG. 7 illustrates that the surface of the inner wall of the process chamber (100) is surface-treated to form a surface area (900), but as described above, the surface area (900) may also be formed by surface-treating the surfaces of various surface treatment targets, such as a gas injection unit (500), a substrate support unit (200), and a substrate (W).
도 8은 공정 사이클을 설명하기 위한 도면이다.Figure 8 is a drawing for explaining the process cycle.
도 8을 참조하면, 기판(W)에 박막(900)을 증착하기 위하여 복수의 공정이 순차적으로 수행될 수 있다.Referring to FIG. 8, multiple processes can be sequentially performed to deposit a thin film (900) on a substrate (W).
기판(W)에 대한 박막(900)의 증착이 수행되기 이전에 표면 처리 공정이 수행될 수 있다. 표면 처리 공정을 위하여 공정 챔버(100)로 표면 처리 가스가 주입될 수 있다. 표면 처리 가스는 질소를 포함한 것일 수 있다.A surface treatment process may be performed before deposition of a thin film (900) on a substrate (W). A surface treatment gas may be injected into a process chamber (100) for the surface treatment process. The surface treatment gas may contain nitrogen.
표면 처리 가스가 공정 챔버(100)로 주입되면서 전력 공급부(600)에 의해 RF 전력이 공정 챔버(100)로 공급될 수 있다. RF 전력의 공급에 의해 표면 처리 가스는 플라즈마 상태로 변환될 수 있다. 플라즈마 상태의 표면 처리 가스는 표면 처리 대상물의 표면에 반응하여 표면 영역(900)을 형성할 수 있다.As the surface treatment gas is injected into the process chamber (100), RF power can be supplied to the process chamber (100) by the power supply unit (600). By supplying the RF power, the surface treatment gas can be converted into a plasma state. The surface treatment gas in the plasma state can react with the surface of the surface treatment target to form a surface area (900).
제어부(700)는 표면 처리 공정이 수행되는 도중에 RF 전력의 크기를 조절할 수 있다. 표면 처리 공정은 복수의 단계에 걸쳐 수행될 수 있는데, 제어부(700)는 각 단계별로 개별적인 크기의 RF 전력이 공급되도록 할 수 있는 것이다.The control unit (700) can adjust the size of RF power while the surface treatment process is being performed. The surface treatment process can be performed in multiple stages, and the control unit (700) can supply RF power of individual sizes for each stage.
표면 처리 공정의 초기에 지나치게 큰 RF 전력이 공급되는 경우 표면 처리 대상물의 표면이 손상될 수 있다. 표면 처리 공정의 초기에 상대적으로 작은 크기의 RF 전력이 공정 챔버(100)로 공급되고, 이어서 RF 전력이 증가할 수 있다. 예를 들어, 표면 처리 공정은 3개의 단계에 걸쳐 수행될 수 있으며, 제1 단계에 비하여 제2 단계에서 보다 큰 RF 전력이 공급될 수 있다. 제3 단계의 RF 전력의 크기는 제1 단계의 RF 전력의 크기와 동일하거나, 제2 단계의 RF 전력의 크기보다는 작고, 제1 단계의 RF 전력의 크기보다는 클 수 있다.If an excessively large RF power is supplied at the beginning of the surface treatment process, the surface of the surface treatment target may be damaged. A relatively small amount of RF power may be supplied to the process chamber (100) at the beginning of the surface treatment process, and then the RF power may be increased. For example, the surface treatment process may be performed in three stages, and a larger RF power may be supplied in the second stage compared to the first stage. The amount of RF power in the third stage may be the same as the amount of RF power in the first stage, or may be smaller than the amount of RF power in the second stage, and larger than the amount of RF power in the first stage.
표면 처리 공정이 수행된 이후에 박막 증차 공정이 수행될 수 있다. 기판(W)에 박막(900)을 증착하기 위하여 공정 챔버(100)로 소스 가스가 주입될 수 있다. 소스 퍼지 가스는 기판(W)에 대한 공정이 진행되는 도중에 지속적으로 이송되어 소스 가스를 가압할 수 있다. 소스 가스는 샤워헤드(520)를 통해 기판(W)의 표면으로 분사될 수 있다. 기판(W)으로 분사된 소스 가스 중 일부는 기판(W)의 표면에 흡착되고, 다른 일부는 흡착되지 않을 수 있다. 흡착되지 않은 소스 가스는 흡착된 소스 가스에 적층되거나 공정 챔버(100)의 내부에서 부유할 수 있다.After the surface treatment process is performed, a thin film deposition process may be performed. A source gas may be injected into the process chamber (100) to deposit a thin film (900) on the substrate (W). The source purge gas may be continuously supplied to pressurize the source gas while the process for the substrate (W) is in progress. The source gas may be sprayed onto the surface of the substrate (W) through the showerhead (520). Some of the source gas sprayed onto the substrate (W) may be adsorbed onto the surface of the substrate (W), and some may not be adsorbed. The non-adsorbed source gas may be deposited on the adsorbed source gas or may float inside the process chamber (100).
기판(W)으로 소스 가스가 분사된 이후에 공정 챔버(100)에서 소스 가스가 퍼지될 수 있다. 공정 챔버(100)에서 소스 가스가 퍼지되는 단계는 기판(W)의 표면에 흡착되지 않은 소스 가스 및 표면 처리 가스가 공정 챔버(100)에서 배출되는 단계를 포함할 수 있다. 즉, 공정 챔버(100)에서 소스 가스가 퍼지되면, 기판(W)에 흡착된 소스 가스만이 잔류하고, 흡착된 소스 가스에 적층되거나 공정 챔버(100)에서 부유한 소스 가스 및 표면 처리 가스는 공정 챔버(100)의 외부로 배출될 수 있다. 이에, 기판(W)의 표면에는 하나의 소스 가스층 형성될 수 있다.After the source gas is sprayed onto the substrate (W), the source gas may be purged in the process chamber (100). The step of purging the source gas in the process chamber (100) may include a step of discharging the source gas and the surface treatment gas that are not adsorbed on the surface of the substrate (W) from the process chamber (100). That is, when the source gas is purged in the process chamber (100), only the source gas adsorbed on the substrate (W) remains, and the source gas and the surface treatment gas that are laminated on the adsorbed source gas or floated in the process chamber (100) may be discharged to the outside of the process chamber (100). Accordingly, a single source gas layer may be formed on the surface of the substrate (W).
소스 가스가 퍼지된 이후에 공정 챔버(100)로 반응 가스가 주입될 수 있다. 반응 퍼지 가스는 기판(W)에 대한 공정이 진행되는 도중에 지속적으로 이송되어 반응 가스를 가압할 수 있다. 반응 가스는 샤워헤드(520)를 통해 기판(W)의 표면으로 분사될 수 있다. 반응 가스는 기판(W)에 흡착된 소스 가스와 반응하여 박막(900)을 형성할 수 있다. 반응 가스와 소스 가스와의 반응도를 향상시키기 위하여 공정 챔버(100)에 반응 가스가 주입되면서, 공정 챔버(100)에 RF 전력이 인가되어 반응 가스가 플라즈마 상태로 변환될 수 있다. RF 전력에 의해 소스 가스가 플라즈마 상태로 변환될 수도 있다.After the source gas is purged, a reaction gas may be injected into the process chamber (100). The reaction purge gas may be continuously supplied while the process for the substrate (W) is in progress to pressurize the reaction gas. The reaction gas may be sprayed onto the surface of the substrate (W) through the showerhead (520). The reaction gas may react with the source gas adsorbed on the substrate (W) to form a thin film (900). In order to improve the reactivity between the reaction gas and the source gas, when the reaction gas is injected into the process chamber (100), RF power may be applied to the process chamber (100) so that the reaction gas may be converted into a plasma state. The source gas may also be converted into a plasma state by the RF power.
플라즈마 상태의 소스 가스 및 반응 가스가 반응하여 높은 반응 효율로 박막(900)이 형성될 수 있다.A source gas and a reaction gas in a plasma state can react to form a thin film (900) with high reaction efficiency.
RF 전력이 인가된 이후에 공정 챔버(100)에서 반응 가스가 퍼지될 수 있다. 즉, 반응 가스를 플라즈마로 변환시키기 위하여 RF 전력이 일정 시간동안 인가되고, 해당 시간이 경과되어 RF 전력의 공급이 중단되며, 이어서 반응 가스가 퍼지될 수 있는 것이다.After RF power is applied, the reaction gas can be purged from the process chamber (100). That is, RF power is applied for a certain period of time to convert the reaction gas into plasma, and when the period of time has elapsed, the supply of RF power is stopped, and then the reaction gas can be purged.
공정 챔버(100)에서 반응 가스가 퍼지되는 단계는 기판(W)의 표면에 박막(900)을 형성하는데 이용되지 않은 반응 가스, 표면 처리 가스 및 플라즈마 등의 공정 부산물이 공정 챔버(100)에서 배출되는 단계를 포함한다.The step of purging the reaction gas from the process chamber (100) includes the step of discharging process byproducts such as reaction gas, surface treatment gas, and plasma that are not used to form a thin film (900) on the surface of the substrate (W) from the process chamber (100).
소스 가스 및 반응 가스가 공정 챔버(100)로 공급되어 박막(900)을 형성하는 과정이 하나의 공정 사이클을 형성하고, 복수의 공정 사이클을 통하여 복수 층의 박막(900)이 기판(W)에 증착될 수 있다.The process of supplying source gas and reaction gas to the process chamber (100) to form a thin film (900) forms one process cycle, and multiple layers of thin films (900) can be deposited on the substrate (W) through multiple process cycles.
표면 처리 공정이 수행된 이후에 박막 증착 공정이 수행됨에 따라 표면 처리 대상물의 표면에 요오드 성분의 증착물(800)이 형성되는 것이 방지될 수 있다.Since the thin film deposition process is performed after the surface treatment process, the formation of a deposition product (800) of an iodine component on the surface of the surface treatment target can be prevented.
도 9는 표면 처리 공정을 설명하기 위한 도면이다.Figure 9 is a drawing for explaining the surface treatment process.
도 9를 참조하면, 표면 처리 공정은 제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정을 포함할 수 있다.제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정은 순차적으로 수행되고, 각 공정을 통하여 표면 처리 가스가 공정 챔버(100)의 내부 공간으로 분사될 수 있다.Referring to FIG. 9, the surface treatment process may include a first surface treatment process, a second surface treatment process, and a third surface treatment process. The first surface treatment process, the second surface treatment process, and the third surface treatment process are performed sequentially, and a surface treatment gas may be injected into the internal space of the process chamber (100) through each process.
제1 표면 처리 공정은 제1 표면 처리 가스가 공정 챔버(100)의 내부 공간으로 분사되는 공정을 포함하고, 제2 표면 처리 공정은 제2 표면 처리 가스가 공정 챔버(100)의 내부 공간으로 분사되는 공정을 포함하며, 제3 표면 처리 공정은 제3 표면 처리 가스가 공정 챔버(100)의 내부 공간으로 분사되는 공정을 포함할 수 있다.The first surface treatment process may include a process in which a first surface treatment gas is sprayed into the internal space of the process chamber (100), the second surface treatment process may include a process in which a second surface treatment gas is sprayed into the internal space of the process chamber (100), and the third surface treatment process may include a process in which a third surface treatment gas is sprayed into the internal space of the process chamber (100).
제1 표면 처리 가스는 혼합 가스일 수 있다. 이를 자세히 설명하면, 제1 표면 처리 가스는 제1 가스 및 제2 가스를 포함하는 혼합 가스일 수 있다. 제1 가스 및 제2 가스 중 하나는 질소(N)를 포함하고, 나머지 하나는 질소(N)를 포함하지 않을 수 있다. 예를 들어, 제1 가스는 질소(N2)를 포함하고, 제2 가스는 수소(H2)를 포함할 수 있다.The first surface treatment gas may be a mixed gas. To be more specific, the first surface treatment gas may be a mixed gas including a first gas and a second gas. One of the first gas and the second gas may include nitrogen (N), and the other may not include nitrogen (N). For example, the first gas may include nitrogen (N 2 ) and the second gas may include hydrogen (H 2 ).
제1 표면 처리 가스에 포함된 제1 가스 및 제2 가스의 유량(sccm)은 서로 상이할 수 있다. 이를 자세히 설명하면, 제1 표면 처리 공정이 수행되는 경우 제1 가스의 유량은 제2 가스의 유량에 비하여 많게 형성될 수 있다.The flow rates (sccm) of the first gas and the second gas included in the first surface treatment gas may be different from each other. To explain this in detail, when the first surface treatment process is performed, the flow rate of the first gas may be formed to be greater than the flow rate of the second gas.
제2 표면 처리 가스는 혼합 가스일 수 있다. 이를 자세히 설명하면, 제2 표면 처리 가스는 제1 가스 및 제3 가스를 포함하는 혼합 가스일 수 있다. 제1 가스와 마찬가지로 제3 가스는 질소(N)를 포함할 수 있다. 예를 들어, 제3 가스는 암모니아(NH3)를 포함할 수 있다.The second surface treatment gas may be a mixed gas. To be more specific, the second surface treatment gas may be a mixed gas containing the first gas and the third gas. Like the first gas, the third gas may contain nitrogen (N). For example, the third gas may contain ammonia (NH 3 ).
제2 표면 처리 가스에 포함된 제1 가스 및 제3 가스의 유량(sccm)은 동일할 수 있다. 한편, 본 발명의 몇몇 실시예에 따르면 제2 표면 처리 가스에 포함된 제1 가스 및 제3 가스의 유량(sccm)은 서로 상이할 수도 있다. 이를 자세히 설명하면, 제2 표면 처리 공정이 수행되는 경우 제1 가스의 유량은 제3 가스의 유량에 비하여 많게 형성될 수 있다.The flow rates (sccm) of the first gas and the third gas included in the second surface treatment gas may be the same. Meanwhile, according to some embodiments of the present invention, the flow rates (sccm) of the first gas and the third gas included in the second surface treatment gas may be different from each other. To explain this in detail, when the second surface treatment process is performed, the flow rate of the first gas may be formed to be greater than the flow rate of the third gas.
제3 표면 처리 가스는 단독 가스일 수 있다. 이를 자세히 설명하면, 제3 표면 처리 가스는 제1 가스를 포함하는 단독 가스일 수 있다.The third surface treatment gas may be a single gas. To elaborate, the third surface treatment gas may be a single gas containing the first gas.
제3 표면 처리 공정에서 이용되는 제1 가스의 유량은 제1 표면 처리 공정 및 제2 표면 처리 공정에서 각각 이용되는 제1 가스의 유량에 대하여 상이할 수 있다. 이를 자세히 설명하면, 제3 표면 처리 공정에서 이용되는 제1 가스의 유량은 제1 표면 처리 공정 및 제2 표면 처리 공정에서 각각 이용되는 제1 가스의 유량에 비하여 적게 형성될 수 있다.The flow rate of the first gas used in the third surface treatment process may be different from the flow rates of the first gas used in each of the first surface treatment process and the second surface treatment process. To explain this in detail, the flow rate of the first gas used in the third surface treatment process may be formed to be less than the flow rates of the first gas used in each of the first surface treatment process and the second surface treatment process.
제1 표면 처리 공정은 제1 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함하고, 제2 표면 처리 공정은 제2 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함하며, 제3 표면 처리 공정은 제3 표면 처리 가스를 플라즈마 상태로 변환하는 공정을 포함할 수 있다.The first surface treatment process may include a process of converting a first surface treatment gas into a plasma state, the second surface treatment process may include a process of converting a second surface treatment gas into a plasma state, and the third surface treatment process may include a process of converting a third surface treatment gas into a plasma state.
이를 자세히 설명하면, 제1 표면 처리 공정은 제1 RF 전력이 공급되어 기판(W)에 제공된 제1 표면 처리 가스가 플라즈마 상태로 변환되는 공정을 포함하고, 제2 표면 처리 공정은 제2 RF 전력이 공급되어 기판(W)에 제공된 제2 표면 처리 가스가 플라즈마 상태로 변환되는 공정을 포함하며, 제3 표면 처리 공정은 제3 RF 전력이 공급되어 기판(W)에 제공된 제3 표면 처리 가스가 플라즈마 상태로 변환되는 공정을 포함할 수 있다.To explain in more detail, the first surface treatment process may include a process in which a first RF power is supplied and a first surface treatment gas provided to the substrate (W) is converted into a plasma state, the second surface treatment process may include a process in which a second RF power is supplied and a second surface treatment gas provided to the substrate (W) is converted into a plasma state, and the third surface treatment process may include a process in which a third RF power is supplied and a third surface treatment gas provided to the substrate (W) is converted into a plasma state.
제어부(700)는 제1 내지 제3 RF 전력 중 제2 RF 전력이 가장 크게 형성되도록 할 수 있다. 표면 처리 공정의 진행 초기 및 말기에 RF 전력의 크기를 작게 형성함으로써 표면 처리 대상물의 표면의 손상이 방지될 수 있다.The control unit (700) can form the second RF power among the first to third RF powers to be the largest. By forming the RF power to be small at the beginning and end of the surface treatment process, damage to the surface of the surface treatment target can be prevented.
도 10은 표면 영역을 나타낸 도면이고, 도 11은 도 10에 도시된 표면 영역의 질소 농도를 나타낸 그래프이다.Fig. 10 is a drawing showing a surface area, and Fig. 11 is a graph showing the nitrogen concentration of the surface area shown in Fig. 10.
도 10 및 도 11을 참조하면, 표면 처리 공정이 완료된 표면 영역(900)은 제1 표면 영역(910), 제2 표면 영역(920) 및 제3 표면 영역(930)을 포함하고, 각 표면 영역(910, 920, 930)은 상이한 질소 농도를 가질 수 있다. 도 10은 공정 챔버(100)의 내측벽에 형성된 표면 영역(900)을 도시하고 있다. 제1 내지 제3 표면 영역(910, 920, 930)은 공정 챔버(100)의 표면의 깊이가 작아지는 방향으로 순차적으로 형성될 수 있다.Referring to FIGS. 10 and 11, the surface region (900) on which the surface treatment process is completed includes a first surface region (910), a second surface region (920), and a third surface region (930), and each surface region (910, 920, 930) may have a different nitrogen concentration. FIG. 10 illustrates a surface region (900) formed on an inner wall of a process chamber (100). The first to third surface regions (910, 920, 930) may be sequentially formed in a direction in which the depth of the surface of the process chamber (100) decreases.
제1 표면 처리 공정은 표면 처리 대상물의 표면에 질소(N)가 포함된 제1 표면 영역(910)을 형성하기 위한 예비 단계를 나타낸다. 이를 위하여, 제1 표면 처리 가스에 포함된 제1 가스 및 제2 가스 중 제1 가스만이 질소(N)를 포함할 수 있으며, 상대적으로 낮은 크기를 갖는 제1 RF 전력에 의해 제1 표면 처리 가스가 플라즈마 상태로 변환될 수 있다. 이에, 제1 표면 영역(910)의 질소 농도는 상대적으로 낮게 형성될 수 있다. 또한, 공정 챔버(100)의 표면의 깊이가 작아지는 방향으로 진행할수록 제1 표면 영역에서의 질소 농도는 증가할 수 있다.The first surface treatment process represents a preliminary step for forming a first surface region (910) containing nitrogen (N) on the surface of a surface treatment target. To this end, among the first gas and the second gas included in the first surface treatment gas, only the first gas may contain nitrogen (N), and the first surface treatment gas may be converted into a plasma state by first RF power having a relatively low magnitude. Accordingly, the nitrogen concentration of the first surface region (910) may be formed to be relatively low. In addition, as the depth of the surface of the process chamber (100) progresses in a direction in which it becomes smaller, the nitrogen concentration in the first surface region may increase.
제2 표면 처리 공정은 요오드와의 반응성을 감소시키기 위하여 상대적으로 높은 밀도의 질소(N)가 포함된 제2 표면 영역(920)을 형성하기 위한 단계를 나타낸다. 이를 위하여, 제2 표면 처리 가스에 포함된 제1 가스 및 제3 가스가 모두 질소(N)를 포함할 수 있으며, 제1 RF 전력에 비하여 큰 제2 RF 전력에 의해 제2 표면 처리 가스가 플라즈마 상태로 변환될 수 있다. 이에, 제2 표면 영역(920)의 질소 농도는 상대적으로 높게 형성될 수 있다. 또한, 공정 챔버(100)의 표면의 깊이가 작아지는 방향으로 진행할수록 제2 표면 영역에서의 질소 농도는 증가할 수 있다.The second surface treatment process represents a step for forming a second surface region (920) containing a relatively high density of nitrogen (N) to reduce the reactivity with iodine. To this end, both the first gas and the third gas contained in the second surface treatment gas may contain nitrogen (N), and the second surface treatment gas may be converted into a plasma state by a second RF power that is greater than the first RF power. Accordingly, the nitrogen concentration of the second surface region (920) may be formed relatively high. In addition, as the depth of the surface of the process chamber (100) progresses in a direction in which it becomes smaller, the nitrogen concentration in the second surface region may increase.
제3 표면 처리 공정은 표면 처리 대상물의 표면을 보호하는 제3 표면 영역(930)을 형성하는 단계를 나타낸다. 이를 위하여, 제3 표면 처리 가스는 질소(N)가 포함된 제1 가스만을 포함할 수 있으며, 제2 RF 전력에 비하여 작은 제3 RF 전력에 의해 제3 표면 처리 가스가 플라즈마 상태로 변환될 수 있다. 여기서, 제3 RF 전력은 제1 RF 전력과 동일할 수 있다. 이에, 제3 표면 영역(930)의 질소 농도는 제1 표면 영역(910)에 비하여 높고, 제2 표면 영역(920)에 비하여 낮게 형성될 수 있다. 또한, 제2 표면 영역 및 제3 표면 영역의 경계에서 질소 농도가 최대가 되고, 공정 챔버(100)의 표면의 깊이가 작아지는 방향으로 진행할수록 제3 표면 영역에서의 질소 농도는 감소할 수 있다. 제3 표면 영역에서의 질소 농도는 제1 표면에서의 질소 농도에 비하여 대체로 크게 형성될 수 있다.제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정은 사전에 설정된 시간동안 진행될 수 있다. 제1 표면 처리 공정은 제1 시간 동안 진행되고, 제2 표면 처리 공정은 제2 시간 동안 진행되며, 제3 표면 처리 공정은 제3 시간 동안 진행될 수 있다. 여기서, 제1 내지 제3 시간은 동일할 수 있다. 또는, 제1 시간, 제2 시간 및 제3 시간은 상이할 수 있다. 예를 들어, 제2 시간은 제1 시간 및 제3 시간에 비하여 길고, 제1 시간 및 제3 시간은 동일할 수 있다. 또는, 제3 시간은 제1 시간에 비하여 길수도 있다.The third surface treatment process represents a step of forming a third surface region (930) that protects the surface of the surface treatment target. To this end, the third surface treatment gas may include only a first gas containing nitrogen (N), and the third surface treatment gas may be converted into a plasma state by a third RF power that is smaller than the second RF power. Here, the third RF power may be the same as the first RF power. Accordingly, the nitrogen concentration of the third surface region (930) may be formed to be higher than that of the first surface region (910) and lower than that of the second surface region (920). In addition, the nitrogen concentration may be maximum at the boundary between the second surface region and the third surface region, and the nitrogen concentration in the third surface region may decrease as the depth of the surface of the process chamber (100) decreases. The nitrogen concentration in the third surface region may be formed to be generally larger than that of the first surface. The first surface treatment process, the second surface treatment process, and the third surface treatment process may be performed for a preset time. The first surface treatment process may be performed for a first time, the second surface treatment process may be performed for a second time, and the third surface treatment process may be performed for a third time. Here, the first to third times may be the same. Alternatively, the first time, the second time, and the third time may be different. For example, the second time may be longer than the first time and the third time, and the first time and the third time may be the same. Alternatively, the third time may be longer than the first time.
도 12는 표면 처리 공정의 공정 조건을 나타낸 테이블이다.Figure 12 is a table showing the process conditions of the surface treatment process.
도 12를 참조하면, 본 발명의 실험예에 따른 공정 조건 테이블(1000)은 표면 처리 가스의 종류, 표면 처리 가스의 유량, RF 전력의 크기, RF 전력의 공급 시간 및 기판 간격을 명시하고 있다.Referring to FIG. 12, a process condition table (1000) according to an experimental example of the present invention specifies the type of surface treatment gas, the flow rate of surface treatment gas, the size of RF power, the supply time of RF power, and the substrate spacing.
표면 처리 공정은 제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정을 포함한다. 제1 표면 처리 공정에서 질소 및 수소가 공정 챔버(100)의 내부 공간으로 분사되고, 제2 표면 처리 공정에서 질소 및 암모니아가 공정 챔버(100)의 내부 공간으로 분사되며, 제3 표면 처리 공정에서 질소가 공정 챔버(100)의 내부 공간으로 분사된다.The surface treatment process includes a first surface treatment process, a second surface treatment process, and a third surface treatment process. In the first surface treatment process, nitrogen and hydrogen are sprayed into the internal space of the process chamber (100), in the second surface treatment process, nitrogen and ammonia are sprayed into the internal space of the process chamber (100), and in the third surface treatment process, nitrogen is sprayed into the internal space of the process chamber (100).
RF 전력의 크기는 제1 표면 처리 공정에 비하여 제2 표면 처리 공정에서 크게 형성되고, 제2 표면 처리 공정에 비하여 제3 표면 처리 공정에서 작게 형성될 수 있다.The size of RF power can be formed larger in the second surface treatment process compared to the first surface treatment process, and smaller in the third surface treatment process compared to the second surface treatment process.
표면 처리 가스의 공급 및 표면 처리 가스의 플라즈마 변환은 기판 지지부(200)가 공정 처리 공간(SP1)으로 상승한 상태에서 수행될 수 있다.The supply of surface treatment gas and plasma conversion of the surface treatment gas can be performed while the substrate support (200) is raised to the process treatment space (SP1).
도 13은 본 발명의 실시예에 따른 기판 처리 방법을 나타낸 흐름도이다.Figure 13 is a flow chart showing a substrate processing method according to an embodiment of the present invention.
도 13을 참조하면, 본 발명의 실시예에 따른 기판 처리 방법은 표면 처리 대상물의 표면에 대한 표면 처리 공정이 수행되는 단계(S1110) 및 표면 처리 공정이 완료된 기판(W)에 대한 박막 증착 공정이 수행되는 단계(S1120)를 포함할 수 있다.Referring to FIG. 13, a substrate treatment method according to an embodiment of the present invention may include a step (S1110) in which a surface treatment process is performed on a surface of a surface treatment target and a step (S1120) in which a thin film deposition process is performed on a substrate (W) on which the surface treatment process has been completed.
표면 처리 공정은 제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정을 포함할 수 있다. 제1 표면 처리 공정, 제2 표면 처리 공정 및 제3 표면 처리 공정에 대해서는 전술하였으므로, 자세한 설명은 생략하기로 한다.The surface treatment process may include a first surface treatment process, a second surface treatment process, and a third surface treatment process. Since the first surface treatment process, the second surface treatment process, and the third surface treatment process have been described above, a detailed description thereof will be omitted.
표면 처리 공정은 박막의 증착에 이용되는 공정 물질과 공정 챔버(100)의 내부 공간에 존재하는 표면 처리 대상물 간의 결합을 방지하는 공정을 포함할 수 있다. 이를 구체적으로 설명하면, 표면 처리 공정은 기판(W)에 대한 공정을 위한 공정 처리 공간을 제공하는 공정 챔버(100)의 표면 영역의 질소 농도를 제어하는 공정을 포함할 수 있다.The surface treatment process may include a process for preventing bonding between a process material used for deposition of a thin film and a surface treatment target existing in the internal space of the process chamber (100). Specifically, the surface treatment process may include a process for controlling the nitrogen concentration in a surface area of a process chamber (100) that provides a process treatment space for a process for a substrate (W).
본 발명에서 박막 증착 공정에서 사용되는 공정 물질은 요오드(I)를 포함할 수 있는데, 표면 영역(900)은 공정 물질과의 전기 음성도 차이가 상대적으로 작게 형성되는 성분을 포함할 수 있다. 예를 들어, 표면 영역(900)은 질소(N)를 포함하여 구성될 수 있는 것으로서, 공정 물질과 표면 처리 대상물의 다른 부분 간의 전기 음성도의 차이에 비하여 공정 물질과 표면 영역(900) 간의 전기 음성도의 차이가 작게 형성될 수 있다.In the present invention, the process material used in the thin film deposition process may include iodine (I), and the surface region (900) may include a component that is formed to have a relatively small difference in electronegativity with respect to the process material. For example, the surface region (900) may be configured to include nitrogen (N), and the difference in electronegativity between the process material and the surface region (900) may be formed to be small compared to the difference in electronegativity between the process material and other parts of the surface treatment target.
작은 전기 음성도 차이로 인하여 공정 물질이 표면 영역(900)에 부착되는 것이 차단되고, 공정 물질은 공정 챔버(100)에서 용이하게 배출될 수 있다.Due to the small electronegativity difference, the process material is prevented from attaching to the surface area (900), and the process material can be easily discharged from the process chamber (100).
이상과 첨부된 도면을 참조하여 본 발명의 실시예를 설명하였지만, 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자는 본 발명이 그 기술적 사상이나 필수적인 특징을 변경하지 않고서 다른 구체적인 형태로 실시될 수 있다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다.Although the embodiments of the present invention have been described with reference to the above and the attached drawings, those skilled in the art to which the present invention pertains will understand that the present invention can be implemented in other specific forms without changing the technical idea or essential characteristics thereof. Therefore, it should be understood that the embodiments described above are exemplary in all respects and not restrictive.
Claims (10)
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| KR10-2023-0118752 | 2023-09-07 | ||
| KR1020230118752A KR20250036359A (en) | 2023-09-07 | 2023-09-07 | Apparatus and method for processing substrate |
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|---|---|---|---|---|
| KR20180058262A (en) * | 2016-11-23 | 2018-06-01 | 주식회사 원익아이피에스 | Method of depositing thin film |
| US20200013589A1 (en) * | 2018-07-05 | 2020-01-09 | Applied Materials, Inc. | Protection of aluminum process chamber components |
| KR20210062712A (en) * | 2018-10-19 | 2021-05-31 | 램 리써치 코포레이션 | IN SITU protective coating of chamber components for semiconductor processing |
| KR20220044338A (en) * | 2019-08-09 | 2022-04-07 | 어플라이드 머티어리얼스, 인코포레이티드 | Protective multi-layer coatings for processing chamber components |
| KR20230016391A (en) * | 2021-07-26 | 2023-02-02 | 주식회사 원익아이피에스 | Method of treating substrate |
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| US9576792B2 (en) | 2014-09-17 | 2017-02-21 | Asm Ip Holding B.V. | Deposition of SiN |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20180058262A (en) * | 2016-11-23 | 2018-06-01 | 주식회사 원익아이피에스 | Method of depositing thin film |
| US20200013589A1 (en) * | 2018-07-05 | 2020-01-09 | Applied Materials, Inc. | Protection of aluminum process chamber components |
| KR20210062712A (en) * | 2018-10-19 | 2021-05-31 | 램 리써치 코포레이션 | IN SITU protective coating of chamber components for semiconductor processing |
| KR20220044338A (en) * | 2019-08-09 | 2022-04-07 | 어플라이드 머티어리얼스, 인코포레이티드 | Protective multi-layer coatings for processing chamber components |
| KR20230016391A (en) * | 2021-07-26 | 2023-02-02 | 주식회사 원익아이피에스 | Method of treating substrate |
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