WO2014010630A1 - パターン形成方法及び基板処理システム - Google Patents
パターン形成方法及び基板処理システム Download PDFInfo
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- WO2014010630A1 WO2014010630A1 PCT/JP2013/068883 JP2013068883W WO2014010630A1 WO 2014010630 A1 WO2014010630 A1 WO 2014010630A1 JP 2013068883 W JP2013068883 W JP 2013068883W WO 2014010630 A1 WO2014010630 A1 WO 2014010630A1
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- 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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- C23C16/45525—Atomic layer deposition [ALD]
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- 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
- C23C16/22—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 deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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- 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
- C23C16/22—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 deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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- 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
- C23C16/455—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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
- C23C16/45527—Atomic layer deposition [ALD] characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations
- C23C16/45536—Use of plasma, radiation or electromagnetic fields
- C23C16/45542—Plasma being used non-continuously during the ALD reactions
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- H01J37/32—Gas-filled discharge tubes
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- H10P14/00—Formation of materials, e.g. in the shape of layers or pillars
- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
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- H10P14/6334—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H10P14/6336—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
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- H10P14/60—Formation of materials, e.g. in the shape of layers or pillars of insulating materials
- H10P14/63—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the formation processes
- H10P14/6326—Deposition processes
- H10P14/6328—Deposition from the gas or vapour phase
- H10P14/6334—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H10P14/6339—Deposition from the gas or vapour phase using decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition deposition by cyclic CVD, e.g. ALD, ALE or pulsed CVD
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- H10P14/66—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials
- H10P14/668—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials
- H10P14/6681—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si
- H10P14/6682—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si the compound being a silane, e.g. disilane, methylsilane or chlorosilane
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- H10P14/668—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials
- H10P14/6681—Formation of materials, e.g. in the shape of layers or pillars of insulating materials characterised by the type of materials the materials being characterised by the deposition precursor materials the precursor containing a compound comprising Si
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- H10P14/69—Inorganic materials
- H10P14/692—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses
- H10P14/6921—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses containing silicon
- H10P14/69215—Inorganic materials composed of oxides, glassy oxides or oxide-based glasses containing silicon the material being a silicon oxide, e.g. SiO2
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- H10P50/28—Dry etching; Plasma etching; Reactive-ion etching of insulating materials
- H10P50/282—Dry etching; Plasma etching; Reactive-ion etching of insulating materials of inorganic materials
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- H10W20/071—Manufacture or treatment of dielectric parts thereof
- H10W20/081—Manufacture or treatment of dielectric parts thereof by forming openings in the dielectric parts
- H10W20/089—Manufacture or treatment of dielectric parts thereof by forming openings in the dielectric parts using processes for implementing desired shapes or dispositions of the openings, e.g. double patterning
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Definitions
- the present invention relates to a pattern forming method and a substrate processing system.
- Patent Document 1 discloses that a device is formed by forming a dense dielectric layer on a device by atomic layer deposition ALD (Atomic Layer Deposition). Techniques for protection are disclosed.
- ALD Atomic Layer Deposition
- Patent Document 1 does not assume that a film forming process is performed for the purpose of repairing a pattern shape formed by etching. Therefore, in Patent Document 1, the effect of repairing the pattern shape formed by etching cannot be obtained.
- an object is to provide a pattern forming method and a substrate processing system capable of forming a pattern having a good shape on a substrate.
- a layer adsorbed on the surface of the predetermined pattern using a silicon compound gas is oxidized or nitrided by plasma generated from an oxidizing gas or a nitriding gas, and a silicon oxide film or a silicon nitride film is formed on the surface of the predetermined pattern.
- a film forming process for forming a film; A pattern forming method is provided.
- a pattern having a good shape can be formed on the substrate.
- the figure for demonstrating the pattern formation method which concerns on 1st and 2nd embodiment. 5 is a flowchart showing pattern formation processing according to the first embodiment.
- FIG. 9 is a flowchart showing pattern formation processing according to the second embodiment.
- the block diagram of the substrate processing system which concerns on 1st and 2nd embodiment.
- the block diagram of the etching apparatus which concerns on 1st and 2nd embodiment.
- the block diagram of the film-forming apparatus which concerns on 1st and 2nd embodiment.
- FIG. 1 is a diagram showing the relationship between the depth of the etched contact hole and the etching rate.
- FIG. 2 is a diagram for explaining the definition of the aspect ratio of the contact hole and the bowing shape.
- the required aspect ratio of contact holes was about 50.
- the aspect ratio AR is indicated by the hole depth h with respect to the diameter ⁇ (top CD) of the hole opening as shown in “a” of FIG.
- the aspect ratio is 50.
- FIG. 1A shows a cross-sectional shape of a hole corresponding to an etching time when a hole is formed in a silicon oxide film (SiO 2 ) by etching.
- a parallel plate etching apparatus (see FIG. 10) using a lower two frequency application in parallel plate plasma is used.
- the etching process conditions are as follows: the pressure is 2.66 Pa, the frequency of the high frequency power HF for plasma generation is 60 MHz, the power is 1200 W, the frequency of the high frequency power LF for ion attraction is 400 kHz, the power is 4500 W, and the gas type is C 4 F. 6 / C 4 F 8 / Ar / O 2 mixed gas. Under this condition, the silicon oxide film is etched using polysilicon as a mask.
- FIG. 1A numerical values of the cross-sectional shape of the hole, the hole diameter ⁇ , and the aspect ratio AR when the etching times are 60 s, 180 s,... 600 s from the left are shown. According to the experimental results, as the hole depth h increases, the hole diameter ⁇ increases and the aspect ratio AR varies.
- FIG. 1B shows the depth of the etched hole of the silicon oxide film (vertical axis) and the pattern in which the silicon oxide film is etched as the etching rate (vertical axis) with respect to the etching time ET (horizontal axis).
- the etching time ET becomes longer, and the deeper the hole, the lower the etching rate of the silicon oxide film and the harder the hole is etched. Regardless of the etching time ET, the etching rate of the mask is substantially constant, and the amount of reduction of the polysilicon mask is almost constant.
- the side wall of the hole is etched, and the CD of the hole spreads.
- a desired aspect ratio cannot be formed, and desired semiconductor device characteristics cannot be obtained.
- the top CD is ⁇ 25 nm and the hole depth is 2.5 ⁇ m
- a resist mask may be used.
- the present embodiment proposes a pattern forming method for performing a film forming process for the purpose of repairing an etching shape after the etching process.
- the etching process is performed on the silicon oxide film 26 and the silicon nitride film 27 in “(a) initial state” shown in FIG.
- the silicon oxide film 26 and the silicon nitride film 27 are etched, respectively, but the structure to be etched may be the structure of only the silicon oxide film 26 or the structure of only the silicon nitride film 27.
- these are collectively referred to as a silicon-containing film 30.
- FIG. 4 is a flowchart showing the pattern forming process according to the first embodiment. Note that a hole pattern having a diameter ⁇ of 25 nm is formed in the polysilicon mask 28 using a photolithography technique.
- step S10 an etching process is performed in step S10.
- a parallel plate etching apparatus (see FIG. 10) of the lower two frequency application type is used in parallel plate plasma.
- the etching process conditions are as follows: the pressure is 2.27 Pa, the frequency of the high frequency power HF for plasma generation is 60 MHz, the power is 1500 W, the frequency of the high frequency power LF for ion attraction is 400 kHz, the power is 7800 W, and the gas type is C 4 F. 6 / C 3 F 8 / Ar / O 2 mixed gas. Under this condition, the silicon-containing film 30 (silicon nitride film 27 and silicon oxide film 26) is etched through the polysilicon mask 28.
- a mask removal process is executed in step S12. This mask removal process is executed when the mask of the etching process is a resist mask. In other words, this step can be omitted when the etching mask is not a resist mask.
- a film forming process (ALD process) by ALD is executed in step S14.
- a microwave plasma apparatus see FIG. 11
- the film forming process (S14) is performed in the order of the gas adsorption process at step S20, the first exhaust process at step S22, the plasma process process at step S24, and the second exhaust process at step S26. Is done.
- step S20 Gas adsorption process
- BTBAS bis-tertiary-butyl-amino-silane
- Ar argon gas
- the pressure is controlled to 133 Pa
- BTBAS is supplied at 30 sccm
- argon gas (Ar) is supplied at 540 sccm.
- step S22 In the first exhaust process, the excessively adsorbed film forming gas is removed. Specifically, in the first evacuation step, the processing chamber is evacuated using an evacuation device while supplying argon gas (Ar) as a purge gas. Thereby, silicon (Si) excessively chemically adsorbed on the surface of the hole can be purged (removed). Thereby, an atomic layer of silicon (Si) is formed on the surface of the hole.
- the atomic layer here includes not only a layer of silicon (Si) atoms for one atom but also a layer for a plurality of atoms.
- the pressure is controlled to 266 Pa or more and argon gas (Ar) is supplied at 540 sccm.
- Plasma treatment process In the plasma processing step, plasma processing using microwaves is performed. Specifically, in the plasma processing step, oxygen gas (O 2 ) as a reactive gas is supplied into the processing container as a plasma processing gas together with argon gas (Ar). Further, microwaves are supplied into the processing container. The plasma process gas is ionized and dissociated by the electric field energy of the microwave, thereby generating a plasma. Oxygen radicals (O * ) in the generated plasma oxidize the atomic layer adsorbed on the surface of the hole. Thereby, a silicon oxide film (SiO 2 ) is formed on the surface of the hole.
- the pressure is controlled to 133 Pa, oxygen gas (O 2 ) is supplied at 60 sccm, and argon gas (Ar) is supplied at 540 sccm. At this time, for example, 3 kW of microwave power having a frequency of 2.45 GHz is supplied.
- oxygen gas O 2
- ozone O 3
- dinitrogen monoxide N 2 O
- nitrogen oxide N 3 O
- carbon monoxide CO
- carbon dioxide CO 2
- the atomic layer adsorbed on the surface of the hole can be oxidized by oxygen radicals (O * ) in the plasma.
- oxygen radicals O *
- gases are examples of oxidizing gases.
- it can replace with argon gas (Ar) and can also use another inert gas.
- Second exhaust process In the second exhaust process, unreacted plasma processing gas is removed. Specifically, in the second exhaust process, as in the first exhaust process, the processing chamber is exhausted using an exhaust device while supplying argon gas (Ar) as a purge gas. Thereby, the unreacted plasma processing gas is exhausted.
- Ar argon gas
- the pressure is controlled to 266 Pa or more and argon gas (Ar) is supplied at 540 sccm as in the first exhaust process.
- step S28 in FIG. 5 it is determined whether a cycle corresponding to a predetermined number of repetitions has been executed, assuming that each of steps 1 to 4 is executed once as one cycle.
- a value obtained by dividing 5 nm by a film thickness that can be formed in one cycle is the number of repetitions.
- atomic layers are stacked 30 to 40 times to form a silicon oxide film having a desired thickness.
- FIG. 6 shows the experimental results of the pattern forming method.
- the “etching process” shown on the left side of FIG. 6 uses the silicon-containing film 30 (the silicon oxide film 26 and the silicon nitride film 27) as a film to be etched, and the hole after performing the etching process (step S10) of FIG. FIG.
- the mask may be removed by executing a mask removal process (step S12).
- the “etching process + ALD process” shown on the right side of FIG. 6 uses the silicon-containing film 30 (silicon oxide film 26 and silicon nitride film 27) as a film to be etched through the polysilicon mask 28 (step S10). ) Is executed, and a vertical cross section of the hole in a state where the hole is repaired by the film forming process by ALD (step S14) is shown.
- the “etching process + ALD process” each of the above-described items 1 to 4 is performed for the number of times targeted to form 5 nm (left side) and 10 nm (right side) silicon oxide films on the side wall on one side of the hole. The case where the process cycle is repeated is shown.
- the depiction on the left shows an overall view of the hole formed in the film
- the depiction on the right shows an enlarged top view of the hole.
- FIG. 7 shows various numerical values representing the results of this experiment.
- FIG. 7 shows the results of measuring the top CD, which is the diameter of the upper part of the hole, the bowing CD, which is the diameter of the middle part of the hole, the depth h, and the aspect ratio Ar (see “b” in FIG. 2).
- the aspect ratio of the hole obtained by the “etching process + ALD process” was larger than the aspect ratio of the hole obtained by the “etching process”. This is because the hole is narrowed with respect to the depth h and the CD value is reduced by the ALD process.
- the difference between the Boeing CD obtained by the “etching process + ALD process” and the top CD is smaller than the difference between the Boeing CD obtained by the “etching process” and the top CD. That is, not only the hole was narrowed by the ALD process, but also the bowing shape was improved, and the wall surface of the hole became more vertical.
- the hole diameter and the hole shape can be repaired by depositing a dense conformal silicon oxide film on the surface of the hole.
- the thickness of the silicon oxide film deposited in the hole can be adjusted.
- a silicon nitride film may be formed instead of the silicon oxide film.
- the relationship between the film to be etched and the film laminated by ALD is that when the film to be etched is a silicon oxide film, the film by ALD may be a silicon oxide film or a silicon nitride film. A silicon oxide film is preferable.
- the ALD film may be a silicon oxide film or a silicon nitride film, but is preferably a silicon nitride film. That is, the film to be etched and the film laminated by ALD are preferably the same film.
- a microwave plasma apparatus (see FIG. 11) is used as the film forming apparatus. Also in the case of forming a silicon nitride film, basically, the steps 1 to 4 in FIG. 5 (steps S20, S22, S24, and S26) are repeatedly executed for a predetermined number of cycles. .
- the description will focus on process conditions for forming a silicon nitride film.
- the pressure is controlled to 400 Pa
- DCS is supplied at 280 sccm
- argon gas (Ar) is supplied at 900 sccm
- nitrogen gas (N 2 ) is supplied at 900 sccm.
- the pressure is controlled to 266 Pa, nitrogen gas (N 2 ) is supplied at 900 sccm, ammonia gas (NH 3 ) is supplied at 400 sccm, and argon gas (Ar) is supplied at 900 sccm.
- Plasma treatment process Next, in the plasma treatment process, nitrogen gas (N 2 ) and ammonia gas (NH 3 ) are supplied together with argon gas (Ar) as reactive gases on the surface of the hole, and microwaves are fed into the processing vessel. Supply. As a result, microwave plasma processing is performed, and a silicon nitride film (SiN) is formed on the surface of the hole.
- the silicon nitride film (SiN) is an example of the repair film 29 for repairing the hole shape shown in “(c) After ALD” in FIG.
- the pressure is controlled to 667 Pa
- nitrogen gas (N 2 ) is supplied at 900 sccm
- ammonia gas (NH 3) is supplied at 400 sccm
- argon gas (Ar) is supplied at 900 sccm.
- Nitrogen gas (N 2 ) and ammonia gas (NH 3 ) are examples of nitriding gases.
- a microwave having a frequency of 2.45 GHz and a power of 4 kW is supplied.
- Second exhaust process After the plasma treatment, unreacted plasma process gas is removed in the second exhaust process. Specifically, in the second exhaust process, as in the first exhaust process, the processing container is exhausted using an exhaust device while supplying argon gas (Ar). Thereby, the unreacted plasma processing gas is exhausted.
- argon gas Ar
- the pressure is controlled to 266 Pa as in the first evacuation step, and nitrogen gas (N 2 ), ammonia gas (NH 3), and argon gas (Ar) are supplied to the first evacuation step.
- nitrogen gas (N 2 ), ammonia gas (NH 3), and argon gas (Ar) are supplied to the first evacuation step.
- the same flow rate as in the exhaust process is supplied.
- the film forming apparatus supplies plasma together with a reactive gas such as nitrogen gas (N 2 ) or ammonia gas (NH 3 ) to the surface of the hole to nitride the surface of the hole.
- a reactive gas such as nitrogen gas (N 2 ) or ammonia gas (NH 3 ) to the surface of the hole to nitride the surface of the hole.
- the hole diameter and the hole shape can be repaired by depositing a dense conformal silicon nitride film on the surface of the hole.
- the thickness of the silicon nitride film deposited in the hole can be adjusted.
- a silicon oxide film or a silicon nitride film can be deposited on the surface of the hole, and the hole diameter and the hole shape can be restored.
- OMCTS octamethylcyclotetrasiloxane
- a precursor gas such as 2
- precursor gases that can be used include 1,3-dimethyldisiloxane (CH 3 —SiH 2 —O—SiH 2 —CH 3 ) having the structure (R x —Si—O—Si—R y ) z. ), 1,1,3,3-tetramethyldisiloxane ((CH 3 ) 2 —SiH—O—SiH— (CH 3 ) 2 ), hexamethyldisiloxane ((CH 3 ) 3 —Si—O—Si) Organic disiloxanes such as-(CH 3 ) 3 ) are included.
- cyclic organosiloxanes R x —Si—O y , where y is greater than 2, x is 1-2, and R x is CH 3 , CH 2 CH 3 or other alkyl groups).
- Cyclic organosilicon compounds that can be used can include cyclic structures having three or more silicon atoms, and the cyclic structure can further include one or more oxygen atoms.
- Commercially available cyclic organosilicon compounds contain a ring having alternating silicon and oxygen atoms with one or two alkyl groups bonded to the silicon atom.
- the cyclic organosilicon compound can include one or more of the following compounds: Hexamethylcyclotrisiloxane (—Si (CH 3 ) 2 —O—) 3 -cyclic, 1,3,5,7-tetramethylcyclotetrasiloxane (TMCTS) (— SiH (CH 3 ) —O—) 4 -cyclic, Octamethylcyclotetrasiloxane (OMCTS) (— Si (CH 3 ) 2 —O—) 4 -cyclic and 1,3,5,7,9-pentamethylcyclopentasiloxane (—SiH (CH 3 ) —O— ) Five rings.
- the above precursor gas is an example of a film forming gas containing a silicon compound.
- FIG. 8 is a flowchart showing a pattern forming process according to the second embodiment.
- the pattern formation process according to the second embodiment in addition to the steps S10, S12, and S14 of the pattern formation process according to the first embodiment shown in FIG. 4, the calculation process of the number of repetitions of the ALD process in steps S30 and S32 is performed. Executed.
- the shape of the etched hole is monitored in step S30 during or after the execution of the etching process in step S10.
- the diameter of the etched hole is calculated based on the result of the monitor, the film thickness to be deposited on the surface of the hole is calculated according to the calculated hole diameter, and the ALD for the calculated film thickness is calculated.
- the process repeat count n is calculated.
- step S14 the cycle is repeated by the number of repetitions n calculated in step S32. That is, the number of steps S28 is determined based on the number of repetitions n.
- the shape of the etched hole is monitored, and the number of repetitions of the film forming process by ALD is variably controlled according to the etching process status based on the monitoring result.
- a film thickness can be adjusted according to the variation in the shape of the actual hole at the time of etching. That is, a silicon-containing layer having a film thickness corresponding to the actual shape of the hole can be deposited on the surface of the hole. Thereby, the hole diameter and the hole shape can be repaired with higher accuracy.
- the pattern forming method according to the first and second embodiments has been described in detail above. According to the pattern forming method according to the first and second embodiments, the hole diameter and the hole shape can be repaired by a film forming process performed after etching.
- the deep hole pattern including the repair film 29 formed in the first and second embodiments is a mold for forming electrodes and capacitance.
- the repair film 29 is densely formed by the ALD method.
- the oxide film 26 and the silicon nitride film 27) are not peeled off. Therefore, the repair film 29 can be quickly removed simultaneously with the silicon-containing film 30 (silicon oxide film 26 and silicon nitride film 27) after the electrodes and capacitance are formed.
- FIG. 9 is a configuration example of the substrate processing system according to the first and second embodiments.
- the substrate processing system 200 executes steps S10, S12, and S14 of FIGS. 4 and 8 on the substrate on which the laminated film shown in “the initial state of FIG. , S32 can be executed.
- the substrate processing system 200 includes an etching apparatus 1 that performs an etching process (step S10) and a mask removing process (step S12), and a film forming apparatus 2 that performs a film forming process by ALD (step S14) after the mask removing process.
- the processing apparatuses 3 and 4 may be apparatuses that perform an etching process and a film forming process.
- Etching apparatus 1, film forming apparatus 2, and processing apparatuses 3 and 4 are provided corresponding to four sides of transfer chamber 5 having a hexagonal shape, respectively.
- Load lock chambers 6 and 7 are provided on the other two sides of the transfer chamber 5, respectively.
- a load / unload chamber 8 is provided on the opposite side of the load lock chambers 6 and 7 from the transfer chamber 5.
- ports 9, 10, 11 for attaching three FOUPs F capable of accommodating the wafers W are provided.
- the etching apparatus 1, the film forming apparatus 2, the processing apparatuses 3 and 4, and the load lock chambers 6 and 7 are connected to each hexagonal side of the transfer chamber 5 through a gate valve G.
- Each chamber communicates with the transfer chamber 5 by opening each gate valve G, and is shut off from the transfer chamber 5 by closing each gate valve G.
- a gate valve G is also provided at a portion of the load lock chambers 6 and 7 connected to the carry-in / out chamber 8.
- the load lock chambers 6 and 7 are communicated with the loading / unloading chamber 8 by opening the gate valve G, and are blocked from the loading / unloading chamber 8 by closing.
- a transfer device 12 that carries the wafer W in and out of the etching device 1, the film forming device 2, the processing devices 3 and 4, and the load lock chambers 6 and 7 is provided.
- the transfer device 12 is disposed substantially at the center of the transfer chamber 5, and has two blades 14 a and 14 b that hold the wafer W at the tip of a rotatable / extensible / retractable portion 13 that can rotate and expand / contract.
- the blades 14a and 14b are attached to the rotating / extending / contracting portion 13 so as to face opposite directions.
- the inside of the transfer chamber 5 is maintained at a predetermined degree of vacuum.
- a HEPA filter (not shown) is provided on the ceiling of the carry-in / out chamber 8. Clean air that has passed through the HEPA filter and from which organic substances, particles, and the like have been removed is supplied into the carry-in / out chamber 8 in a downflow state. For this reason, the wafer W is carried in and out in a clean air atmosphere at atmospheric pressure.
- the three ports 9, 10, 11 for attaching the hoop F of the carry-in / out chamber 8 are each provided with a shutter (not shown). These ports 9, 10, 11 have wafers W accommodated or empty hoops directly attached, and when they are attached, the shutter is released to communicate with the loading / unloading chamber 8 while preventing the entry of outside air. .
- An alignment chamber 15 is provided on the side surface of the loading / unloading chamber 8, and the wafer W is aligned.
- a transfer device 16 for loading / unloading the wafer W into / from the FOUP F and loading / unloading the wafer W into / from the load lock chambers 6 and 7 is provided.
- the transport device 16 has two articulated arms, and has a structure capable of traveling on the rail 18 along the direction in which the hoops F are arranged.
- the transfer of the wafer W is performed by placing the wafer W on the hand 17 at the tip.
- FIG. 9 shows a state where one hand 17 exists in the carry-in / out chamber 8 and the other hand is inserted into the FOUP F.
- Components of the substrate processing system 200 are connected to and controlled by a control unit 20 including a computer.
- the control unit 20 is connected to a user interface 21 including a keyboard for an operator to input commands for managing the system, a display for visualizing and displaying the operating status of the system, and the like.
- the control unit 20 further includes a control program for realizing various processes shown in FIGS. 4, 5, and 8, which are executed in the system, under the control of the control unit 20, and various configurations according to processing conditions.
- a storage unit 22 in which a program (that is, a processing recipe) for causing the unit to execute processing is stored is connected.
- the processing recipe is stored in a storage medium in the storage unit 22.
- the storage medium may be a hard disk or a portable medium such as a CDROM, DVD, or flash memory.
- the structure which transmits a recipe suitably from another apparatus via a dedicated line, for example may be sufficient.
- the processing in the substrate processing system 200 is performed, for example, by calling an arbitrary processing recipe from the storage unit 22 according to an instruction from the user interface 21 and causing the control unit 20 to execute the processing recipe.
- the control unit 20 may directly control each component unit, or may provide an individual controller for each component unit and control it via them.
- the FOUP F containing the preprocessed wafer W is loaded.
- one wafer W is taken out from the FOUP F and carried into the alignment chamber 15 by the transfer device 16 in the carry-in / out chamber 8 held in a clean air atmosphere at atmospheric pressure, and the wafer W is aligned.
- the wafer W is carried into one of the load lock chambers 6 and 7, and the inside of the load lock is evacuated.
- the wafer W in the load lock is taken out by the transfer device 12 in the transfer chamber 5, and the wafer W is loaded into the etching device 1 to perform the etching process in step S10. Mask removal processing is performed.
- the wafer W is taken out by the transfer device 12 and loaded into the film forming device 2, plasma processing is performed by the ALD method, and a repair film 29 is formed. Thereafter, the wafer W is taken out by the transfer device 12, and the wafer W is carried into one of the load lock chambers 6 and 7 by the transfer device 12, and the inside thereof is returned to atmospheric pressure. The wafer W in the load lock chamber is taken out by the transfer device 16 in the loading / unloading chamber 8 and stored in one of the FOUPs F. The above operation is performed on one lot of wafers W, and one set of processing is completed.
- FIG. 10 is a configuration example of the etching apparatus 1 that performs the etching process in step S10 of FIGS. 4 and 8 in the first and second embodiments.
- the etching apparatus 1 has a chamber C that is hermetically sealed and electrically grounded.
- the etching apparatus 1 is connected to a gas supply source 120.
- the gas supply source 120 supplies an etching gas containing a fluorocarbon (CF) -based gas as an etching gas.
- the fluorocarbon-based gas may contain hexafluoro 1,3 butadiene C 4 F 6 gas.
- the chamber C has a cylindrical shape, and is composed of, for example, aluminum whose surface is anodized, and a mounting table 102 that supports the wafer W is provided inside.
- the mounting table 102 also functions as a lower electrode.
- the mounting table 102 is supported by a conductive support table 104 and can be moved up and down by an elevating mechanism 107 via an insulating plate 103.
- the elevating mechanism 107 is disposed in the chamber C and is covered with a bellows 108 made of stainless steel.
- a bellows cover 109 is provided outside the bellows 108.
- a focus ring 105 made of, for example, single crystal silicon is provided on the outer periphery above the mounting table 102.
- a cylindrical inner wall member 103 a made of, for example, quartz is provided so as to surround the periphery of the mounting table 102 and the support table 104.
- a first high frequency power source 110a is connected to the mounting table 102 via a first matching unit 111a so that high frequency power for plasma generation at a predetermined frequency (for example, 60 MHz) is supplied from the first high frequency power source 110a. It has become.
- the mounting table 102 is connected to a second high-frequency power source 110b via a second matching unit 111b, and a high-frequency power for bias having a predetermined frequency (for example, 400 KHz) is supplied from the second high-frequency power source 110b. It is like that.
- a shower head 116 that functions as an upper electrode is provided above the mounting table 102 so as to face the mounting table 102 in parallel.
- the shower head 116 and the mounting table 102 function as a pair of electrodes. It has become.
- An electrostatic chuck 106 for electrostatically attracting the wafer W is provided on the upper surface of the mounting table 102.
- the electrostatic chuck 106 has an electrode 106a interposed between insulators 106b.
- a DC voltage source 112 is connected to the electrode 106a, and when a DC voltage is applied from the DC voltage source 112 to the electrode 106a, the wafer W is attracted by Coulomb force.
- a coolant channel 104 a is formed inside the support body 104.
- a refrigerant inlet pipe 104b and a refrigerant outlet pipe 104c are connected to the refrigerant flow path 104a.
- the wafer W is controlled to a predetermined temperature by circulating, for example, cooling water or the like as a coolant appropriately in the coolant channel 104a.
- a pipe 130 for supplying cold transfer gas (backside gas) such as helium gas (He) is provided on the back side of the wafer W.
- the shower head 116 is provided in the ceiling portion of the chamber C.
- the shower head 116 has a main body 116a and an upper top plate 116b that forms an electrode plate.
- the shower head 116 is supported on the upper part of the chamber C through an insulating member 145.
- the main body 116a is made of a conductive material, for example, aluminum whose surface is anodized, and supports the upper top plate 116b in a detachable manner at the lower portion thereof.
- a gas diffusion chamber 126a is provided inside the main body 116a, and a large number of gas flow holes 116d are formed at the bottom of the main body 116a so as to be positioned below the diffusion chamber 126a.
- the upper top plate 116b is provided with a gas introduction hole 116e that communicates with the gas flow hole 116d so as to penetrate the upper top plate 116b in the thickness direction.
- the gas supplied to the diffusion chamber 126a is introduced into the plasma processing space in the chamber C through the gas flow hole 116d and the gas introduction hole 116e in a shower shape.
- the main body 116a and the like are provided with a pipe (not shown) for circulating the refrigerant, and the shower head 116 is cooled and adjusted to a desired temperature.
- the main body 116a is formed with a gas inlet 116g for introducing gas into the diffusion chamber 126a.
- a gas supply source 120 is connected to the gas inlet 116g.
- a variable DC voltage source 152 is electrically connected to the shower head 116 via a low pass filter (LPF) 151.
- the variable DC voltage source 152 can be turned on / off by an on / off switch 153.
- the on / off switch 153 is controlled to be turned on as necessary. As a result, a predetermined DC voltage is applied to the shower head 116.
- a cylindrical grounding conductor 101a is provided so as to extend upward from the side wall of the chamber C above the height position of the shower head 116.
- the cylindrical ground conductor 101a has a top plate on the top thereof.
- An exhaust port 171 is formed at the bottom of the chamber C.
- An exhaust device 173 is connected to the exhaust port 171.
- the exhaust device 173 includes a vacuum pump, and depressurizes the inside of the chamber C to a predetermined degree of vacuum by operating the vacuum pump.
- a gate valve 175 for loading or unloading the wafer W from the loading / unloading port 174 is provided on the side wall of the chamber C by opening and closing.
- a dipole ring magnet 124 extending annularly or concentrically is disposed around the chamber C corresponding to the vertical position at the time of processing of the mounting table 102.
- a vertical RF field is formed by the first high-frequency power source 110a, and a horizontal magnetic field is formed by the dipole ring magnet 124.
- a scatterometry 190 is provided as an example of a CD measuring instrument.
- the scatterometry 190 measures the CD of the hole being etched by light wave scattering measurement.
- ellipsometry or CD-SEM can be used.
- the control unit 201 controls the entire etching apparatus 1 such as a gas flow rate in the gas supply source 120 and a pressure in the chamber C. Further, the control unit 201 inputs the CD value of the hole being etched measured by the scatterometry 190, and performs the film forming process (S20, S22, S24, S26 in FIG. 5) based on the input CD value. As one cycle, the number of repetitions or the repetition time is calculated. According to this, it is possible to variably control the number of repetitions or the repetition time of the cycle according to the measured CD value. That is, the shape of the actual hole being etched is monitored, and the number of repetitions of the film forming process is variably controlled based on the monitoring result. Thereby, a silicon-containing layer having a film thickness corresponding to the actual shape of the hole formed by etching can be deposited on the surface of the hole. Thereby, the hole diameter and the hole shape can be restored with higher accuracy.
- FIG. 11 is a configuration example of a film forming apparatus 10A that performs film forming processing by ALD in step S14 of FIGS. 4 and 8 in the first and second embodiments. More specifically, the film forming apparatus executes each step of the flowchart of FIG.
- a film forming apparatus 10A shown in FIG. 11 is a single-wafer type film forming apparatus, and has a processing head for supplying a precursor gas.
- the film forming apparatus 10A includes a processing container 12A, a mounting table 14A that holds the wafer W in the processing container 12A, and a plasma generation unit 22A that generates reactive gas plasma in the processing container 12A.
- the plasma generation unit 22A includes a microwave generator 202 that generates a microwave for plasma excitation, and a radial line slot antenna 204 for introducing the microwave into the processing vessel 12A.
- the microwave generator 202 is connected via a waveguide 206 to a mode converter 208 that converts a microwave mode.
- the mode converter 208 is connected to the radial line slot antenna 204 via a coaxial waveguide 210 having an inner waveguide 210a and an outer waveguide 210b.
- the microwave generated by the microwave generator 202 is mode-converted by the mode converter 208 and reaches the radial line slot antenna 204.
- the frequency of the microwave generated by the microwave generator 202 is, for example, 2.45 GHz.
- the radial line slot antenna 204 includes a dielectric window 212 that closes the opening 120a formed in the processing container 12A, a slot plate 214 provided immediately above the dielectric window 212, a cooling jacket 216 provided above the slot plate 214, And a dielectric plate 218 disposed between the slot plate 214 and the cooling jacket 216.
- the slot plate 214 has a substantially disc shape.
- the slot plate 214 is provided with a plurality of slot pairs including two slot holes extending in a direction orthogonal to or intersecting with each other so as to be arranged in the radial direction and the circumferential direction of the slot plate 214.
- the dielectric window 212 is provided so as to face the wafer W.
- An inner waveguide 210 a is connected to the center of the slot plate 214, and an outer waveguide 210 b is connected to the cooling jacket 216.
- the cooling jacket 216 also functions as a waveguide.
- a reactive gas supply port 120b is formed on the side wall of the processing vessel 12A.
- a reactive gas supply source 220 is connected to the supply port 120b.
- an oxidizing gas for example, oxygen (O 2 ) gas is supplied together with argon (Ar) gas or the like.
- a nitriding gas, nitrogen (N 2 ) gas or ammonia (NH 3 ) gas is supplied together with argon (Ar) gas or the like.
- the reactive gas is ionized and dissociated by the electric field energy of the microwave propagating as a surface wave on the lower surface of the dielectric window 212, thereby generating a reactive gas plasma.
- the exhaust port 120c for exhausting the gas in the processing container 12A is formed at the bottom of the processing container 12A.
- a vacuum pump 224 is connected to the exhaust port 120 c via a pressure regulator 222.
- the exhaust port 120c, the pressure regulator 222, and the vacuum pump 224 are provided as an exhaust device.
- a temperature controller 226 for adjusting the temperature of the mounting table 14A is connected to the mounting table 14A.
- the film forming apparatus 10A further includes a head part 240 in which an injection port 240a for injecting the first precursor gas, the second precursor gas, and the purge gas is formed.
- the head part 240 is connected to the driving device 244 via the support part 242.
- the driving device 244 is disposed outside the processing container 12A.
- the drive unit 244 allows the head unit 240 to move between a position facing the mounting table 14A and a retreat space 120d defined in the processing container 12A. When the head unit 240 is located in the retreat space 120d, the shutter 247 moves to isolate the retreat space 120d.
- the support part 242 defines a gas supply path for supplying gas to the injection port 240a.
- the gas supply path of the support part 242 includes a first precursor gas supply source 246, a second A precursor gas supply source 248 and a purge gas supply source 250 are connected. These supply sources 246, 248, and 250 are all gas supply sources capable of controlling the flow rate. Therefore, the first precursor gas, the second precursor gas, and the purge gas can be selectively injected from the head portion 240 onto the wafer W.
- the head portion 240 and the exhaust device described above perform the gas adsorption process using the precursor gas (step S20) and the first and second exhaust processes using the purge gas (step S22 and step S26) in FIG.
- the film forming apparatus 10A includes a control unit 256.
- the control unit 256 is connected to the microwave generator 202, the vacuum pump 224, the temperature controller 226, the driving device 244, and the gas supply sources 220, 246, 248, 250. Accordingly, the control unit 256 outputs the microwave output, the pressure in the processing container 12A, the temperature of the mounting table 14A, the movement of the head unit 240, and the reactive gas, the first precursor gas, and the second precursor gas.
- the gas flow rate and supply timing of the purge gas can be controlled. For example, when performing a gas adsorption process (step S20) and a 1st exhaust process (step S22), the head part 240 is moved on the wafer W, and each process is performed.
- step S24 the plasma processing step using the reactive gas described above
- step S26 the head portion 240 is moved again onto the wafer W to execute the second evacuation step.
- the ALD process is executed by executing these steps a predetermined number of times.
- the head unit 240 of the film forming apparatus 10A can define a small space supplied with the first precursor gas, the second precursor gas, and the purge gas between the mounting table 14A.
- reactive gas plasma can be always generated in the processing vessel 12A.
- a space for supplying the precursor gas can be reduced, and plasma can be generated in the processing container 12A at all times, so that high throughput can be realized. Can do.
- a precursor gas of BTBAS bis-tertiary-butyl-amino-silane
- BTBAS bis-tertiary-butyl-amino-silane
- DCS dichlorosilane
- silane, disilane, methylsilane H4, or PH3 gas may be used.
- purge gas argon (Ar) gas, nitrogen (N 2 ) gas or the like is used.
- the film forming process used in the pattern forming method according to the present invention may be performed by plasma CVD in addition to the film forming process by the ALD method.
- the etching process and the film forming process are separately performed by different processing apparatuses, but both the etching process and the film forming process are performed by one processing apparatus. May be.
- the target to be processed by the substrate processing system according to the present invention is not limited to a wafer but may be a substrate having a predetermined size.
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Abstract
Description
フッ化炭素(CF)系ガスを含むエッチングガスから生成されたプラズマにより、マスクを介して基板上のシリコン含有膜をエッチングし、該シリコン含有膜に所定パターンを形成するエッチング工程と、
シリコン化合物ガスを使用して前記所定パターンの表面に吸着された層を、酸化性ガス又は窒化性ガスから生成されたプラズマにより酸化又は窒化させ、前記所定パターンの表面にシリコン酸化膜又はシリコン窒化膜を成膜する成膜工程と、
を含むことを特徴とするパターン形成方法が提供される。
高いアスペクト比(Aspect Ratio:AR)の深いコンタクトホール(穴)をプラズマエッチングにより形成する場合、ホールの底部が深くなるに従いプラズマのラジカルが穴底に到達する量が減少し、エッチングレートが低下する。この現象について、図1及び図2を参照しながら説明する。図1は、エッチングされたコンタクトホールの深さとエッチングレートとの関係を示した図である。図2は、コンタクトホールのアスペクト比の定義と、ボーイング形状を説明するための図である。
第1実施形態に係るパターン形成方法では、図3の「(a)初期状態」に示したように、シリコン基板(Si)25上にシリコン酸化膜(SiO2)26、シリコン窒化膜(SiN)27、ポリシリコンマスク28が順に積層された初期状態において、図4に示したパターン形成処理を行う。図4は、第1実施形態に係るパターン形成処理を示したフローチャートである。なお、ポリシリコンマスク28には、フォトリソグラフィー技術を用いて直径φが25nmのホールのパターンが形成されている。
(エッチング処理)
図4に示したパターン形成処理が開始されると、ステップS10にてエッチング処理が実行される。この実験では、平行平板プラズマにおいて下部2周波数印加型の平行平板エッチング装置(図10参照)が用いられる。エッチングのプロセス条件は、圧力が2.27Pa、プラズマ生成用の高周波電力HFの周波数が60MHz、パワーが1500W、イオン引き込み用の高周波電力LFの周波数が400kHz、パワーが7800W、ガス種がC4F6/C3F8/Ar/O2の混合ガスである。この条件でポリシリコンマスク28を介してシリコン含有膜30(シリコン窒化膜27及びシリコン酸化膜26)をエッチングする。
次に、ステップS12にてマスク除去処理が実行される。このマスク除去処理は、エッチング処理のマスクがレジストマスクの場合、実行される。換言すれば、エッチング処理のマスクがレジストマスクでない場合、本ステップを省略することができる。
次に、ステップS14にてALDによる成膜処理(ALD処理)が実行される。ここでは、マイクロ波プラズマ装置(図11参照)が成膜装置として使用される。成膜処理(S14)は、図5に示したように、ステップS20のガス吸着工程、ステップS22の第1の排気工程、ステップS24のプラズマ処理工程、ステップS26の第2の排気工程の順に実行される。
図5に示すように、ガス吸着工程では、成膜ガスとして、前駆体(プリカーサ)ガスとしてBTBAS(bis-tertiaryl-buthyl-amino-silane)及びアルゴンガス(Ar)が供給される。これにより、BTBASに含まれるシリコン原子が穴の表面に化学的に吸着される。このガス吸着工程におけるプロセス条件の一例としては、圧力を133Paに制御し、BTBASを30sccm、アルゴンガス(Ar)を540sccmを供給する。
第1の排気工程では、余剰に吸着した成膜ガスを除去する。具体的には、第1の排気工程では、パージガスとしてアルゴンガス(Ar)を供給しながら排気装置を用いて処理容器内の排気が行われる。これにより、穴の表面に過剰に化学的に吸着したケイ素(Si)をパージ(除去)することができる。これにより、穴の表面にはケイ素(Si)の原子層が形成される。ここでいう原子層は、ケイ素(Si)の原子が1原子分だけ層になったもののみならず、複数原子分の層も含む。
プラズマ処理工程では、マイクロ波によるプラズマ処理を行う。具体的には、プラズマ処理工程では、反応性ガスとして酸素ガス(O2)がアルゴンガス(Ar)と共にプラズマ処理ガスとして処理容器内に供給される。また、マイクロ波が処理容器内に供給される。マイクロ波の電界エネルギーにより、プラズマ処理ガスは電離及び解離され、これによりプラズマが生成される。生成されたプラズマ中の酸素ラジカル(O*)により、穴の表面に吸着した原子層が酸化される。これにより、穴の表面には、シリコン酸化膜(SiO2)が成膜される。
第2の排気工程では、未反応のプラズマ処理ガスを除去する。具体的には、第2の排気工程では、第1の排気工程と同様に、パージガスとしてアルゴンガス(Ar)を供給しながら排気装置を用いて処理容器内の排気を行う。これにより、未反応のプラズマ処理ガスが排気される。
図6に上記パターン形成方法による実験結果を示す。図6の左側に示した「エッチングプロセス」は、シリコン含有膜30(シリコン酸化膜26及びシリコン窒化膜27)を被エッチング対象膜として、図4のエッチング処理(ステップS10)を実行した後の穴の断面図を示す。このとき、ポリシリコンマスク28に替えてレジストマスクが用いられる場合、マスク除去処理(ステップS12)を実行してマスクを除去してもよい。
ALDによる成膜処理(ステップS14)の変形例としては、シリコン酸化膜に替えてシリコン窒化膜を成膜してもよい。被エッチング対象膜とALDにより積層される膜との関係は、被エッチング処理膜がシリコン酸化膜の場合、ALDによる膜はシリコン酸化膜であってもよいし、シリコン窒化膜であってもよいが、シリコン酸化膜であることが好ましい。また、被エッチング処理膜がシリコン窒化膜の場合、ALDによる膜はシリコン酸化膜であってもよいし、シリコン窒化膜であってもよいが、シリコン窒化膜であることが好ましい。つまり、被エッチング処理膜とALDにより積層される膜とは同じ膜であることが好ましい。
シリコン窒化膜を成膜する場合、図5のステップS20のガス吸着工程では、穴の表面に前駆体ガスであるDCS(Dichlorosilane、ジクロロシラン)が供給される。これにより、DCSに含まれるケイ素(Si)が穴の表面に化学的に吸着される。
次に、第1の排気工程では、穴の表面に窒素ガス(N2)、アンモニアガス(NH3)及びアルゴンガス(Ar)を供給する。これにより、第1の排気工程では、穴の表面に過剰に化学的に吸着したケイ素(Si)が除去され、ケイ素(Si)の原子層が形成される。
次に、プラズマ処理工程では、穴の表面に反応性ガスとして、窒素ガス(N2)及びアンモニアガス(NH3)をアルゴンガス(Ar)と共に供給し、マイクロ波を処理容器内に供給する。これにより、マイクロ波によるプラズマ処理が行われ、穴の表面には、シリコン窒化膜(SiN)が成膜される。シリコン窒化膜(SiN)は、図3の「(c)ALD後」に示した、穴形状を修復するための修復膜29の一例である。
プラズマ処理後、第2の排気工程では、未反応のプラズマ処理ガスを除去する。具体的には、第2の排気工程では、第1の排気工程と同様に、アルゴンガス(Ar)を供給しながら排気装置を用いて処理容器内の排気を行う。これにより、未反応のプラズマ処理ガスが排気される。
ヘキサメチルシクロトリシロキサン(-Si(CH3)2-O-)3-環状、
1,3,5,7-テトラメチルシクロテトラシロキサン(TMCTS)(-SiH(CH3)-O-)4-環状、
オクタメチルシクロテトラシロキサン(OMCTS)(-Si(CH3)2-O-)4-環状、および
1,3,5,7,9-ペンタメチルシクロペンタシロキサン(-SiH(CH3)-O-)5環状。
次に、第2実施形態に係るパターン形成方法について、図8を参照しながら説明する。図8は、第2実施形態に係るパターン形成処理を示したフローチャートである。第2実施形態に係るパターン形成処理では、図4に示した第1実施形態に係るパターン形成処理のステップS10、S12、S14に加えて、ステップS30、S32のALD処理の繰り返し回数の算出処理が実行される。
次に、第1及び第2実施形態に係るパターン形成方法を実施するための基板処理システムの一例について、図9を参照しながら説明する。図9は、第1及び第2実施形態に係る基板処理システムの構成例である。基板処理システム200は、図3の「(a)の初期状態」に示した積層膜が形成された基板に、図4及び図8のステップS10、S12、S14を実行するとともに、図8のS30、S32の処理を実行可能である。
次に、基板処理システム200のエッチング装置1の内部構成の一例を、図10に基づき説明する。図10は、第1及び第2実施形態にて図4及び図8のステップS10のエッチング処理を行うエッチング装置1の構成例である。
次に、基板処理システムに含まれる成膜装置1の一例について、図11を参照しながら説明する。図11は、第1及び第2実施形態にて図4及び図8のステップS14のALDによる成膜処理を行う成膜装置10Aの構成例である。より具体的には、図5のフローチャートの各工程を実行する成膜装置である。
Claims (9)
- フッ化炭素(CF)系ガスを含むエッチングガスから生成されたプラズマにより、マスクを介して基板上のシリコン含有膜をエッチングし、該シリコン含有膜に所定パターンを形成するエッチング工程と、
シリコン化合物ガスを使用して前記所定パターンの表面に吸着された層を、酸化性ガス又は窒化性ガスから生成されたプラズマにより酸化又は窒化させ、前記所定パターンの表面にシリコン酸化膜又はシリコン窒化膜を成膜する成膜工程と、
を含むことを特徴とするパターン形成方法。 - 前記成膜工程は、
前記シリコン化合物ガスとしてシリコン含有の前駆体ガスを供給し、前記所定パターンの表面に該前駆体ガスに含まれるケイ素(Si)を吸着させる吸着工程と、
前記反応性ガスを供給し、該反応性ガスから生成されたプラズマにより、前記所定パターンの表面に吸着された層を酸化又は窒化させ、前記シリコン酸化膜又は前記シリコン窒化膜を成膜するプラズマ処理工程と、
を含むことを特徴とする請求項1に記載のパターン形成方法。 - 前記成膜工程は、
前記吸着工程後であって前記プラズマ処理工程前にパージガスを供給し、前記所定パターンの表面をパージする第1の排気工程と、
前記プラズマ処理工程後にパージガスを供給し、前記所定パターンの表面をパージする第2の排気工程と、
を更に含むことを特徴とする請求項2に記載のパターン形成方法。 - 前記成膜工程は、
該成膜工程に含まれる各工程を一回ずつ実行した場合を1サイクルとして、予め定められた繰り返し回数又は繰り返し時間、前記サイクルを繰り返し実行することを特徴とする請求項2に記載のパターン形成方法。 - 前記エッチング工程中、前記所定パターンの形状を計測する計測工程と、
前記計測工程による計測結果に基づき前記繰り返し回数又は前記繰り返し時間を算出する制御工程と、を更に含み、
前記成膜工程は、
前記制御工程により算出された前記繰り返し回数又は前記繰り返し時間、前記サイクルを繰り返し実行することを特徴とする請求項2に記載のパターン形成方法。 - 前記成膜工程は、
前記所定パターンが形成されるシリコン含有膜の種類に応じて、前記酸化性ガス又は前記窒化性ガスのいずれかから選択された反応性ガスを供給することを特徴とする請求項1に記載のパターン形成方法。 - 前記前駆体ガスは、BTBAS(bis-tertiaryl-buthyl-amino-silane)又はジクロロシラン(DCS:Dichlorosilane)であることを特徴とする請求項2に記載のパターン形成方法。
- 前記エッチング工程は、
前記所定パターンを形成した後、前記マスクを除去する工程を含むことを特徴とする請求項1に記載のパターン形成方法。 - フッ化炭素(CF)系ガスを含むエッチングガスから生成されたプラズマにより、マスクを介して基板上のシリコン含有膜をエッチングし、該シリコン含有膜に所定パターンを形成するエッチング装置と、
シリコン化合物ガスを使用して前記所定パターンの表面に吸着された層を、酸化性ガス又は窒化性ガスから生成されたプラズマにより酸化又は窒化させ、前記所定パターンの表面にシリコン酸化膜又はシリコン窒化膜を成膜する成膜装置と、
を備える基板処理システム。
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| CN113169066B (zh) * | 2018-11-30 | 2024-05-31 | 东京毅力科创株式会社 | 基片处理方法和基片处理系统 |
| CN111627809A (zh) * | 2019-02-28 | 2020-09-04 | 东京毅力科创株式会社 | 基片处理方法和基片处理装置 |
| CN111627809B (zh) * | 2019-02-28 | 2024-03-22 | 东京毅力科创株式会社 | 基片处理方法和基片处理装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20150035593A (ko) | 2015-04-06 |
| JP2014017438A (ja) | 2014-01-30 |
| TW201417170A (zh) | 2014-05-01 |
| JP6001940B2 (ja) | 2016-10-05 |
| TWI576914B (zh) | 2017-04-01 |
| US9279184B2 (en) | 2016-03-08 |
| CN104380440A (zh) | 2015-02-25 |
| US20150167163A1 (en) | 2015-06-18 |
| CN104380440B (zh) | 2016-12-07 |
| KR102080246B1 (ko) | 2020-02-21 |
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