JP2021048369A - Substrate processing method, substrate processing apparatus, and substrate processing liquid - Google Patents

Abstract

To suppress a difference in etching rate due to the size of a recess.SOLUTION: A substrate processing method includes a chemical solution supply step of supplying a chemical solution including an etchant that etches a removed portion to a substrate, and an auxiliary liquid supply step of supplying an etching auxiliary liquid including a movement accelerator to the substrate, which includes a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist with the movement of the etchant to a recess, and the chemical solution supply step and the auxiliary liquid supply step are performed continuously or simultaneously.SELECTED DRAWING: Figure 2

Description

The present invention relates to a substrate processing method, a substrate processing apparatus, and a substrate processing liquid for selectively removing a portion to be removed of a substrate to form a recess.

The manufacturing process of electronic components such as semiconductor devices and liquid crystal display devices includes an etching step of partially etching and removing a substrate to form a desired pattern. For example, in the manufacture of semiconductor devices, a silicon oxide film formed on a silicon substrate when etching the (SiO ₂₎ is HF 2 ^_- and the like chemical is used (for example, Patent Documents 1 and 2) containing etchant ..

Japanese Unexamined Patent Publication No. 9-22891 Japanese Unexamined Patent Publication No. 9-115875

There are various pattern shapes to be formed by etching. In particular, with the miniaturization of patterns and the three-dimensional structure of electronic components, in the etching process, not only the conventional size recesses with relatively wide openings are formed, but also the elongated recesses with narrow and deep openings are formed. It may be required to form. However, in the etching process using a conventional chemical solution, it is difficult to efficiently move the etchant into the elongated recess. As a result, there is a problem that the etching rate in the elongated concave portion is significantly lower than the etching rate in the conventional size concave portion, and a desired structure cannot be obtained.

The present invention has been made in view of the above problems, and an object of the present invention is to provide a substrate processing method, a substrate processing apparatus, and a substrate processing liquid capable of suppressing a difference in etching rate depending on the size of a recess.

A first aspect of the present invention is a substrate processing method for selectively removing a portion to be removed from a substrate to form a recess, in which an etchant for etching the portion to be removed and a movement assisting the movement of the etchant to the recess. The portion to be removed is etched with a substrate treatment liquid containing an accelerator to form a recess, and the movement accelerator has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion.

A second aspect of the present invention is a substrate processing method for selectively removing a portion to be removed of a substrate to form a recess, and a chemical solution supply step of supplying a chemical solution containing an etchant for etching the portion to be removed to the substrate. A chemical solution comprising an auxiliary liquid supply step of supplying an etching auxiliary liquid containing a movement accelerator to a substrate, which has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etchant to the recess. It is characterized by executing the supply process and the auxiliary liquid supply process continuously or simultaneously.

A third aspect of the present invention is a substrate processing apparatus that selectively removes a portion to be removed from a substrate to form a recess, and includes a substrate holding portion that holds the substrate and an etchant that etches the portion to be removed. A substrate treatment liquid containing a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etching to the recess is generated, and the substrate is placed on the substrate held by the substrate holding portion. It is characterized by including a processing liquid supply unit for supplying the treatment liquid.

A fourth aspect of the present invention is a substrate processing apparatus that selectively removes a portion to be removed from a substrate to form a recess, wherein a substrate holding portion that holds the substrate and an etchant that etches the portion to be removed are provided. A chemical solution containing the chemical solution, a treatment liquid supply unit that has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etchant to the recess, and a treatment liquid supply unit that generates an etching auxiliary liquid containing a movement accelerator, and a chemical liquid. The chemical solution nozzle for supplying the etching auxiliary liquid to the substrate and the auxiliary liquid nozzle for supplying the etching auxiliary liquid to the substrate are provided, and the chemical solution supply from the chemical solution nozzle and the etching auxiliary liquid supply from the auxiliary liquid nozzle can be continuously or simultaneously executed. It is a feature.

Further, a fifth aspect of the present invention is a substrate treatment liquid that selectively removes a portion to be removed from the substrate to form a recess, and assists the etching of the portion to be removed and the movement of the etchant to the recess. The migration promoter is characterized by having a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion.

According to the invention configured as described above, when the portion to be removed of the substrate is selectively removed by an etchant to form a recess, a movement promoter having a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion is provided. Assists the movement of the etchant into the recess. Therefore, the concentration of the etchant inside the recess is increased, and the etching rate can be improved.

It is a figure which shows typically an example of the etching operation performed by the substrate processing method which concerns on this invention. It is a figure which shows typically the surface-induced phase transition phenomenon which occurs in a minute region. It is a figure which shows the 1st Embodiment of the substrate processing apparatus which concerns on this invention. It is a side view of the substrate processing apparatus shown in FIG. It is a partial cross-sectional view which shows the structure of a processing unit. It is a block diagram which shows the electrical structure of the control part which controls a processing unit. It is a figure which shows the structure of the substrate processing liquid supply part. It is a figure which shows the content of the substrate processing executed by the substrate processing apparatus of FIG. It is a figure which shows the 2nd Embodiment of the substrate processing apparatus which concerns on this invention partially. It is a figure which shows the 3rd Embodiment of the substrate processing apparatus which concerns on this invention partially.

<Basic Principle of Invention and Substrate Processing Method>
As one specific example of selectively removing the removed portion of the substrate to form a recess, for example, as shown in FIG. 1, the thermal oxide film (SiO ₂ ) formed on the silicon substrate is etched and removed. There is a process.

FIG. 1 is a diagram schematically showing an example of an etching operation executed by the substrate processing method according to the present invention. In the substrates Wa and Wb shown in columns (a) and (b) in the figure, a thermal oxide film W2 is formed on the upper surface of the silicon base material W1. Further, the polysilicon layer W3 is laminated and formed on the thermal oxide film W2. The polysilicon layer W3 is provided with, for example, a plurality of through holes W4 having an inner diameter of 60 nm. When diluted hydrofluoric acid (dHF) is supplied to the surface of the substrate W configured in this way, the dilute hydrofluoric acid is supplied to the thermal oxide film W2 through the through holes W4 and is contained in the dilute hydrofluoric acid. etchant (HF 2 ^_-) by exposed areas W5 facing the through hole W4 of the thermal oxide film W2 is etched, an opening W6 (i.e. with more time, the gap between the silicon substrate W1 and the polysilicon layer W3 etchant through ^partial) (HF 2 _-) enters the silicon substrate W1 and the fine region W7 sandwiched between the polysilicon layer W3. As a result, the etching of the fine region W7 proceeds.

Here, when the size of the opening W6 (corresponding to the thickness THa and THb of the thermal oxide film W2) is relatively large, the thermal oxide film (corresponding to the thickness THa and THb of the thermal oxide film W2) is formed on the upper surface of the silicon base material W1 as shown in column (c) of the figure. It _{is possible to obtain an etching rate almost the same as when dilute hydrofluoric acid is supplied to a substrate Wc in which SiO 2} ) W2 is formed in a blanket shape, for example, a thickness of about THc = 500 nm to allow etching to proceed. For example, assuming that the amounts etched from the supply of the chemical solution to the substrates Wa to Wc until a certain period of time elapses are the etching amounts EMa to EMc, respectively.
EMa ≒ EMb ≒ EMc
Will be. Then, if (EMa / EMc) and (EMb / EMc) are defined as the blanket ratios of the substrates Wa and Wb, the blanket ratios of the substrates Wa and Wb shown in columns (a) and (b) of the same figure are "1". Indicates a value relatively close to. On the other hand, as the thermal oxide film W2 becomes thinner, the blanket ratio of the substrates Wa and Wb decreases significantly. Therefore, when the substrate W in which a plurality of circuit elements and wirings are formed in a three-dimensional structure is etched with a chemical solution, the following problems occur. That is, in the substrate W, the thickness of the thermal oxide film W2 is partially different, the size of the opening through which the etchant penetrates is often different, and the etching rate becomes non-uniform.

Therefore, the inventor of the present application conducted diligent research and obtained the following findings. The finding is that a substrate treatment solution containing a migration accelerator having a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion in the chemical solution is used, or an etching auxiliary solution containing the migration accelerator is used in combination with the chemical solution. Is beneficial. Typical examples having such a molecular structure are anionic surfactants and cationic surfactants. When the migration accelerator is supplied to the surfaces of the substrates Wa and Wb together with the etchant, for example, as shown in FIG. 2, a surface-induced phase transition phenomenon (Surface) in which ions are concentrated in pores (fine regions W7) on the order of several nm. Induced Phase Transition (SIFT) occurs. Although the mechanism of this surface-induced phase transition phenomenon is not clear, it is considered that the following behavior occurs in the etching process.

FIG. 2 is a diagram schematically showing a surface-induced phase transition phenomenon that occurs in a fine region. Each symbol in the figure is explained in the broken line brackets in the figure. The wall surfaces of the silicon base material W1 and the polysilicon layer W3 constituting the fine region W7 are hydrophobic surfaces. Therefore, the state in which the fine region W7 is filled with DIW (deionized water), which is a solvent component of the chemical solution, is unstable. In this case, as schematically shown in FIG. 2, in the fine region W7, the movement promoter having a hydrophobic portion is more likely to be concentrated, and accordingly, an anionic hydrophilic portion and a cationic hydrophilic portion are present in the fine region W7. Will be done. Further, when the ion size is large, the polarity is relatively small with respect to the entire volume, so that the number of water molecules adsorbed is small with respect to the entire volume, and the water molecules become more hydrophobic. Therefore, the larger the ion size, the easier it is to concentrate. If the cation is large, the cation tends to be concentrated preferentially, and the anion is also concentrated in an attempt to maintain electrical neutrality. As part of the etchant that is present in the chemical ^- drawn even fine regions W7, etchant in the fine region W7 (HF ₂₎ ^- increases the concentration of (HF _2). In this way, the movement accelerator assists the movement of the etchant to the fine region W7 corresponding to an example of the "recess" of the present invention, and contributes to the improvement of the etching rate in the fine region W7. The amphoteric tenside can be used as a migration promoter because it exhibits the properties of an anionic surfactant in the alkaline region and the properties of a cationic surfactant in the acidic region when dissolved in DIW. On the other hand, there is a nonionic surfactant as an example of the surfactant, but the hydrophilic portion is not ionized when dissolved in DIW. Therefore, the nonionic surfactant does not function as a movement accelerator, and no improvement in the etching rate in the fine region W7 is observed. Anionic surfactants, cationic surfactants and amphoteric surfactants that function as migration promoters are referred to as "surfactant-based surfactants" in the present specification.

Further, although it is different from the surfactant-based migration promoter, it has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion, and the above-mentioned surface-induced phase transition phenomenon is expressed to determine the etching rate in the fine region W7. There are mobility promoters that contribute to the improvement. Examples of the migration accelerator include ammonium salts and alkylammonium salts. These are referred to herein as "SIFT-based migration promoters".

The ammonium salt is composed of the ammonium ion NH ₄ ⁺ and is represented by the general formula (NH ₄ ⁺ ) _n X ^n-.
・ Ammonium fluoride NH4F (Ammonium Fluoride, cation: NH4 +, anion F-)
・ Ammonium chloride NH4Cl (Ammonium Chloride, cation: NH4 +, anion Cl-)
・ Ammonium iodide NH4I (Ammonium Iodide, cation: NH4 +, anion I-)
Halides such as, sulfides such as ammonium sulfide ((NH ₄ ) ₂ SO ₄ ), and acetates such as ammonium acetate ((CH ₃ COONH ₄ )) are included.

The alkylammonium salt is a quaternary ammonium salt represented by the _{general formula (NR 4} ⁺ ) _n X ^n- _{, a tertiary amine represented by R 3} N, and a second represented by R ₂ NH. A primary _{amine, represented by a primary amine represented by RNH 2} , (R is an alkyl or aryl group) is included, eg,
・ TetraMethylAmmonium Fluoride [(CH3) 4N] F (TetraMethylAmmonium Fluoride; TMAF, cation: [(CH3) 4N] +, anion F-)
・ TetraEthylAmmonium Fluoride [(CH3CH2CH2) 4N] F (TetraEthylAmmonium Fluoride; TEAF, cation: [(CH3CH2CH2) 4N] +, anion F-)
・ TetraButhylAmmonium Fluoride [(CH3CH2CH2CH2CH2) 4N] F (TetraButhylAmmonium Fluoride; TBAF, cation: [(CH3CH2CH2CH2CH2) 4N] +, anion F-)
・ Tetramethylammonium chloride [(CH3) 4N] Cl (TetraMethylAmmonium Chloride; TMAC, cation: [(CH3) 4N] +, anion Cl-)
・ Tetraethylammonium chloride [(CH3CH2CH2) 4N] Cl (TetraEthylAmmonium Chloride; TEAC, cation: [(CH3CH2CH2) 4N] +, anion Cl-)
・ Tetrabutylammonium chloride [(CH3CH2CH2CH2CH2) 4N] Cl (TetraButhylAmmonium Chloride; TBAC, cation: [(CH3CH2CH2CH2CH2) 4N] +, anion Cl-)
・ Tetramethylammonium iodide [(CH3) 4N] I (TetraMethylAmmonium Iodide; TMAI, cation: [(CH3) 4N] +, anion I-)
・ Tetraethylammonium iodide [(CH3CH2CH2) 4N] I (TetraEthylAmmonium Iodide; TEAI, cation: [(CH3CH2CH2) 4N] +, anion I-)
・ TetraButhyl Ammonium Iodide [(CH3CH2CH2CH2CH2) 4N] I (TetraButhylAmmonium Iodide; TBAI, cation: [(CH3CH2CH2CH2CH2) 4N] +, anion I-)
Halides such as, hydrides such as tetrabutylammonium hydrogensulfate, acetates such as tetramethylammonium acetate, hydroxides such as tetraethylammonium hydroxide, perchloric acid such as tetrabutylammonium perchlorate, etc. Is done.

Further, alcohol or acid may be added to the substrate treatment liquid or the etching auxiliary liquid containing the SIFT-based movement accelerator.

The alcohol is represented by the general formula R-OH (R is an alkyl group or an aryl group), methyl alcohol (MeOH), ethyl alcohol (EtOH), 2-propanol (PrOH), n-butyl alcohol (BuOH), tert. -Contains butyl alcohol, cyclohexanol, ethylene glycol, etc.

The acid includes hydrochloric acid, sulfuric acid, nitric acid, acetic acid, phosphoric acid, hydrogen peroxide, citric acid and the like that generate hydrogen ions (H ^{+) in the etching auxiliary liquid.}

Further, in the above, alcohol is added to the substrate treatment liquid containing the SIFT-based movement accelerator and the etching auxiliary liquid, but the alcohol has a hydrophobic portion and a hydroxyl portion (-OH group) which is a polar portion. Therefore, it can be used as a movement promoter. In the present specification, those using alcohol as a main movement promoter are referred to as "alcohol-based movement promoters".

Further, a part of the organic solvent has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion, and can be used as a movement promoter. More specifically, acetic acid (CH3COOH), ethylene glycol (OHCH2CH2OH), ethylamine (CH3CH2NH2) and the like can be used, and these are referred to as "organic solvent-based migration promoters" in the present specification.

Substrate treatment liquid containing at least one of the above-mentioned "surfactant-based migration accelerator", "SIFT-based migration accelerator", "alcohol-based migration accelerator" and "organic solvent-based migration accelerator". There are the following four modes as a specific substrate processing method using the or etching auxiliary liquid.

In the first substrate treatment method, a substrate treatment liquid in which a movement accelerator is added to a chemical liquid containing an etchant and a movement accelerator is prepared in advance, and the substrate treatment liquid is supplied to the substrate W from a single nozzle for etching treatment. To execute. Here, the specific preparation method includes a method of simply mixing the chemical solution and the etching auxiliary solution, and a method of mixing the amounts of the main components of the chemical solution and the etching auxiliary solution in appropriate amounts. In the second substrate processing method, the chemical solution is supplied from the chemical solution nozzle to the substrate W, and at the same time, the etching auxiliary solution is supplied from the auxiliary solution nozzle to the substrate W to execute the etching process. In the third substrate processing method, after the chemical solution is supplied to the substrate from the chemical solution nozzle, the etching auxiliary solution is supplied from the auxiliary solution nozzle to the substrate to which the chemical solution is supplied to execute the etching process. In the fourth substrate processing method, after the etching auxiliary liquid is supplied to the substrate from the auxiliary liquid nozzle, the chemical solution is supplied from the chemical solution nozzle to the substrate to which the etching auxiliary liquid is supplied to execute the etching process.

As described above, even when subjected to an etching treatment by any of the substrate processing method, the etchant by moving accelerator (HF 2 ^_-) is efficiently penetrate into fine regions W7, increasing the etchant concentration in the fine region W7 be able to. Therefore, the etching rate in the fine region W7 can be improved and the blanket ratio can be brought close to "1". As a result, it is possible to suppress the difference in etching rate depending on the size of the recess formed by the etching process.

<Board processing equipment>
Next, the first embodiment of the substrate processing apparatus to which the above-mentioned first substrate processing method can be applied will be described with reference to the drawings.

FIG. 3 is a diagram showing a first embodiment of the substrate processing apparatus according to the present invention. Further, FIG. 4 is a side view of the substrate processing apparatus shown in FIG. These drawings do not show the appearance of the apparatus, but are schematic views which show the internal structure of the substrate processing apparatus 100 in an easy-to-understand manner by excluding the outer wall panel and other partial configurations. The substrate processing apparatus 100 is, for example, a single-wafer type apparatus installed in a clean room and etching the substrate W to form recesses.

Here, the "board" in the present embodiment includes a semiconductor wafer, a glass substrate for a photomask, a glass substrate for a liquid crystal display, a glass substrate for plasma display, a substrate for FED (Field Emission Display), a substrate for an optical disk, and a magnetic disk. Various substrates such as substrates and substrates for photomagnetic disks can be applied. In the following, a substrate processing apparatus mainly used for processing a silicon wafer will be described as an example with reference to the drawings, but the same applies to the processing of various substrates illustrated above.

In the present embodiment, in order to thermally oxidized film provided on a silicon substrate W1 (thermal oxide film W2 shown in FIG. 1, for example) is selectively removed to form a desired concave, as an etchant (HF 2 ^_-) While using, the etchant (HF 2 ^_-) not used as a drug solution comprising, 1st substrate processing method described above, i.e. etchant (HF 2 ^_-) substrate substrate treating solution comprising a transfer-promoting agent in addition to By supplying to W, the etching rate in a fine region (reference numeral W7 in FIG. 1) is improved. More specifically, tetraethylammonium iodide (TEAI) is used as a migration promoter, and hydrochloric acid (HCl) and ethyl alcohol (EtOH) are added.

In the present specification, the pattern-forming surface (one main surface) on which the pattern is formed is referred to as "front surface Wf", and the other main surface on which the pattern on the opposite side is not formed is referred to as "back surface". Further, the surface facing downward is referred to as a "lower surface", and the surface facing upward is referred to as an "upper surface". Further, in the present specification, the "pattern-forming surface" means a surface on which an uneven pattern is formed in an arbitrary region on a substrate regardless of whether it is a flat surface, a curved surface, or an uneven shape.

As shown in FIG. 3, the substrate processing apparatus 100 includes a substrate processing unit 110 that processes the substrate W, and an indexer unit 120 that is coupled to the substrate processing unit 110. The indexer unit 120 holds a container C for accommodating the substrate W (FOUP (Front Opening Unified Pod) for accommodating a plurality of substrates W in a sealed state, SMIF (Standard Mechanical Interface) pod, OC (Open Cassette), etc.). By accessing the container holding portion 121 capable of holding a plurality of containers and the container C held by the container holding portion 121, the untreated substrate W can be taken out from the container C, or the processed substrate W can be transferred to the container C. It is equipped with an indexer robot 122 for storing and storing. A plurality of substrates W are housed in each container C in a substantially horizontal posture.

The indexer robot 122 includes a base portion 122a fixed to the device housing, an articulated arm 122b rotatably provided around the vertical axis with respect to the base portion 122a, and a hand attached to the tip of the articulated arm 122b. It is equipped with 122c. The hand 122c has a structure in which the substrate W can be placed and held on the upper surface thereof. Since an indexer robot having such an articulated arm and a hand for holding a substrate is known, detailed description thereof will be omitted.

The substrate processing unit 110 includes a substrate transfer robot 111 arranged substantially in the center in a plan view, and a plurality of processing units 1 arranged so as to surround the substrate transfer robot 111. Specifically, a plurality of (eight in this example) processing units 1 are arranged facing the space in which the substrate transfer robot 111 is arranged. The substrate transfer robot 111 randomly accesses these processing units 1 and delivers the substrate W. On the other hand, each processing unit 1 executes a predetermined processing on the substrate W. In the present embodiment, these processing units 1 have the same function. Therefore, parallel processing of a plurality of substrates W is possible.

FIG. 5 is a partial cross-sectional view showing the configuration of the processing unit. Further, FIG. 6 is a block diagram showing an electrical configuration of a control unit that controls a processing unit. In the present embodiment, the control unit 4 is provided for each processing unit 1, but a plurality of processing units 1 may be controlled by one control unit. Further, the processing unit 1 may be controlled by a control unit (not shown) that controls the entire substrate processing apparatus 100.

The processing unit 1 includes a chamber 2 having an internal space 21 and a spin chuck 3 housed in the internal space 21 of the chamber 2 and functioning as a substrate holding portion for holding the substrate W. As shown in FIGS. 3 and 4, a shutter 23 is provided on the side surface of the chamber 2. A shutter opening / closing mechanism 22 (FIG. 6) is connected to the shutter 23, and the shutter 23 is opened / closed in response to an opening / closing command from the control unit 4. More specifically, in the processing unit 1, the shutter opening / closing mechanism 22 opens the shutter 23 when the unprocessed substrate W is carried into the chamber 2, and the unprocessed substrate W is in a face-up posture by the hand of the substrate transfer robot 111. Is carried into the spin chuck 3. That is, the substrate W is placed on the spin chuck 3 with the surface Wf facing upward. Then, when the hand of the substrate transfer robot 111 retracts from the chamber 2 after the substrate is carried in, the shutter opening / closing mechanism 22 closes the shutter 23. Then, in the internal space 21 of the chamber 2, the substrate treatment liquid, DIW, and nitrogen gas are supplied to the surface Wf of the substrate W as described later, and the desired substrate treatment is executed in a room temperature environment. Further, after the substrate processing is completed, the shutter opening / closing mechanism 22 opens the shutter 23 again, and the hand of the substrate transfer robot 111 carries out the processed substrate W from the spin chuck 3. As described above, in the present embodiment, the internal space 21 of the chamber 2 functions as a processing space for performing substrate processing while maintaining the room temperature environment. In addition, in this specification, "room temperature" means that it is in a temperature range of 5 ° C. to 35 ° C.

The spin chuck 3 is connected to a plurality of chuck pins 31 that grip the substrate W, a spin base 32 that supports the plurality of chuck pins 31 and is formed in a disk shape along the horizontal direction, and a spin base 32. A central shaft 33 rotatably provided around a rotation axis C1 parallel to a surface normal extending from the surface center of the substrate W, and a substrate rotation drive mechanism 34 for rotating the central shaft 33 around the rotation axis C1 by a motor are provided. ing. The plurality of chuck pins 31 are provided on the peripheral edge of the upper surface of the spin base 32. In this embodiment, the chuck pins 31 are arranged at equal intervals in the circumferential direction. Then, when the motor of the substrate rotation drive mechanism 34 operates in response to the rotation command from the control unit 4 while the substrate W mounted on the spin chuck 3 is gripped by the chuck pin 31, the substrate W moves around the rotation axis C1. Rotate. Further, in the state where the substrate W is rotated in this way, the substrate treatment liquid, DIW, and nitrogen gas are sequentially applied to the surface Wf of the substrate W from the nozzle provided in the atmosphere blocking mechanism 5 in response to the supply command from the control unit 4. Be supplied.

The atmosphere blocking mechanism 5 has a blocking plate 51, an upper spin shaft 52 rotatably provided on the blocking plate 51, and a nozzle 53 penetrating the central portion of the blocking plate 51 in the vertical direction. The blocking plate 51 is finished in a disk shape having a diameter substantially the same as or larger than that of the substrate W. The blocking plate 51 is arranged so as to face the upper surface of the substrate W held by the spin chuck 3 at intervals. Therefore, the lower surface of the blocking plate 51 functions as a circular substrate facing surface 51a facing the entire surface Wf of the substrate W. Further, a cylindrical through hole 51b that vertically penetrates the blocking plate 51 is formed in the central portion of the substrate facing surface 51a.

The upper spin shaft 52 is rotatably provided around a rotation axis (an axis corresponding to the rotation axis C1 of the substrate W) extending vertically through the center of the blocking plate 51. The upper spin shaft 52 has a cylindrical shape. The inner peripheral surface of the upper spin shaft 52 is formed as a cylindrical surface centered on the rotation axis. The internal space of the upper spin shaft 52 communicates with the through hole 51b of the blocking plate 51. The upper spin shaft 52 is rotatably supported by a support arm 54 extending horizontally above the blocking plate 51.

The nozzle 53 is arranged above the spin chuck 3. The nozzle 53 is supported by the support arm 54 in a non-rotatable state with respect to the support arm 54. Further, the nozzle 53 can be moved up and down integrally with the blocking plate 51, the upper spin shaft 52, and the support arm 54. A discharge port 53a is provided at the lower end of the nozzle 53 and faces the central portion of the surface Wf of the substrate W held by the spin chuck 3.

A cutoff plate rotation drive mechanism 55 (FIG. 6) having a configuration including an electric motor and the like is coupled to the cutoff plate 51. The cutoff plate rotation drive mechanism 55 rotates the cutoff plate 51 and the upper spin shaft 52 around the rotation axis C1 with respect to the support arm 54 in response to a rotation command from the control unit 4. Further, a blocking plate elevating drive mechanism 56 is coupled to the support arm 54. The blocking plate elevating drive mechanism 56 moves the blocking plate 51, the upper spin shaft 52, and the nozzle 53 up and down integrally with the support arm 54 in the vertical direction Z in response to an elevating command from the control unit 4. More specifically, the blocking plate elevating drive mechanism 56 substantially shields the space above the surface Wf from the surrounding atmosphere in the vicinity of the surface Wf of the substrate W whose substrate facing surface 51a is held by the spin chuck 3. It is moved up and down between the cutoff position (position shown in FIG. 3) and the retracted position (not shown) that is retracted above the cutoff position.

A processing liquid supply control unit 61, a DIW supply control unit 62, and a gas supply control unit 63 are connected to the upper end portion of the nozzle 53.

The processing liquid supply control unit 61 has a processing liquid pipe 611 connected to the nozzle 53 and a valve 612 inserted in the processing liquid pipe 611. The treatment liquid pipe 611 is connected to a treatment liquid supply unit 400 that functions as a supply source for the substrate treatment liquid.

FIG. 7 is a diagram showing a configuration of a substrate processing liquid supply unit. The treatment liquid supply unit 400 has a fluid box FB and a cabinet CC.

The cabinet CC has an explosion-proof non-measurement area 401 without explosion-proof measures and an explosion-proof measures area 402 with explosion-proof measures. In the explosion-proof non-measurement area 401, a tank 403 is arranged. Four supply pipes are connected to the tank 403. Tetraethylammonium iodide (TEAI), DIW, hydrofluoric acid (HF) and hydrochloric acid (HCl) can be supplied to the tank 403 via these four supply pipes, respectively. Therefore, when tetraethylammonium iodide, DIW, hydrofluoric acid, and hydrochloric acid are supplied to the tank 403 in appropriate amounts in response to a command from the control unit 4, the components of the substrate treatment liquid excluding ethanol (EtOH) are contained in the tank 403. An intermediate mixture for producing a substrate treatment solution is obtained. Further, the tank 403 for storing the intermediate mixed liquid is connected to the first individual flow path 412 of the mixing valve 409 provided in the fluid box FB by the first individual pipe 404. Therefore, when the pump 405 inserted in the first individual pipe 404 operates in response to a command from the control unit 4, the intermediate mixed liquid in the tank 403 is sent to the mixing valve 409.

On the other hand, in the explosion-proof area 402, a tank 406 for storing ethanol is arranged. The tank 406 is connected to the second individual flow path 413 of the mixing valve 409 by the second individual pipe 407. Therefore, when the pump 408 inserted in the second individual pipe 407 operates in response to a command from the control unit 4, the ethanol in the tank 406 is sent to the mixing valve 409.

The fluid box FB mixes the intermediate mixture and ethanol with the mixing valve 409 to generate a substrate treatment liquid, and supplies the substrate treatment liquid to the nozzle 53 via the treatment liquid pipe 611 extending in the fluid box FB. It is possible. In the fluid box FB, a valve 612 is attached to the processing liquid pipe 611 so that the supply / stop of the supply of the substrate processing liquid can be switched.

The intermediate mixture in the tank 403 is sent to the mixing valve 409 by the pump 405 as described above. The flow rate of the intermediate mixed liquid sent from the tank 403 to the mixing valve 409 can be changed by the first electric valve 410 that opens and closes the inside of the first individual pipe 404. Similarly, the ethanol in the tank 406 is sent to the mixing valve 409 by the pump 408. The flow rate of ethanol sent from the tank 406 to the mixing valve 409 can be changed by the second electric valve 411 that opens and closes the inside of the second individual pipe 407.

In the present embodiment, both the first electric valve 410 and the second electric valve 411 are electric needle valves. Here, at least one of the first electric valve 410 and the second electric valve 411 may be an electric valve other than the electric needle valve. Since the configuration of the electric needle valve is well known, detailed description thereof will be omitted, but the opening / closing and opening degree of the electric valves 410 and 411 are controlled by the control unit 4.

As shown in FIG. 7, the mixing valve 409 includes, in addition to the first individual flow path 412 and the second individual flow path 413, a first check valve 420 that prevents backflow of liquid in the first individual flow path 412. It has a second check valve 421 that prevents backflow of liquid in the second individual flow path 413, and an assembly flow path 414 that is connected to the downstream ends of the first individual flow path 412 and the second individual flow path 413. There is. Therefore, when both the first electric valve 410 and the second electric valve 411 are opened by the control unit 4, the intermediate mixed solution and ethanol are mixed with each other while flowing downstream in the collecting flow path 414 of the mixing valve 409. Thus, the intermediate liquid mixture and ethanol are mixed, an etchant (HF 2 ^_-), substrate treating solution, including tetraethylammonium iodide which functions as a transfer-promoting agent (TEAI) is generated.

The collecting flow path 414 of the mixing valve 409 is connected to the processing liquid pipe 611. Further, in the processing liquid pipe 611, as shown in FIG. 7, an in-line mixer 415 for stirring the processing liquid is inserted on the upstream side of the valve 642. The in-line mixer 415 has a pipe 415p inserted in the processing liquid pipe 611. Further, a stirring fin 415f is arranged in the pipe 415p. The stirring fin 415f has a twisted structure around an axis extending in the flow direction of the liquid. Therefore, the in-line mixer 415 functions as a static mixer. That is, in the processing liquid supply unit 400, the intermediate mixed liquid and ethanol supplied from the tank 403 and the tank 406 are mixed by the mixing valve 409, and then further mixed by the in-line mixer 415. Thus, the intermediate liquid mixture and ethanol are mixed, an etchant (HF 2 ^_-), substrate treating solution, including tetraethylammonium iodide which functions as a transfer-promoting agent (TEAI) is generated.

The treatment liquid supply unit 400 includes a branch pipe 416 branched from the treatment liquid pipe 611. The upstream end of the branch pipe 416 is connected to the treatment liquid pipe 611. A part of the treatment liquid in the treatment liquid pipe 611 passes through the upstream end of the branch pipe 416 and is supplied to the nozzle 53. On the other hand, the remaining treatment liquid in the treatment liquid pipe 611 flows into the branch pipe 416 from the upstream end of the branch pipe 416. The downstream end of the branch pipe 416 is connected to the tank 403. The downstream end of the branch pipe 416 may be connected to a treatment liquid pipe 611 provided in another processing unit 1 or may be connected to a drainage device (not shown).

The treatment liquid supply unit 400 may include a flow rate adjusting valve 418 that changes the flow rate of the substrate treatment liquid flowing from the treatment liquid pipe 611 to the branch pipe 416. The opening degree of the flow rate adjusting valve 418 can be adjusted by the control unit 4. Therefore, the flow rate of the substrate processing liquid flowing from the processing liquid pipe 611 to the branch pipe 416 is changed according to the opening degree of the flow rate adjusting valve 418. The processing liquid supply unit 400 may include an orifice plate having a hole having a diameter smaller than the inner diameter of the branch pipe 416 instead of the flow rate adjusting valve 418. In this case, the treatment liquid flows from the treatment liquid pipe 611 to the branch pipe 416 at a flow rate corresponding to the area of the hole of the orifice plate.

The treatment liquid supply unit 400 includes a solution concentration meter 417 for measuring the concentrations of various components in the substrate treatment liquid. In FIG. 7, the solution concentration meter 417 is inserted in the branch pipe 416. However, the arrangement position of the solution concentration meter 417 is not limited to this, and is arbitrary as long as it is downstream of the mixing valve 409. For example, the solution concentration meter 417 may be arranged upstream or downstream of the in-line mixer 415, or may be arranged in the nozzle 53. Alternatively, the concentration of the substrate treatment liquid discharged from the nozzle 53 may be measured by the solution concentration meter 417. Further, in the present embodiment, although not shown in FIG. 7, a densitometer (not shown) for measuring the concentration of ethanol is arranged in the cabinet CC, and the degree of evaporation of ethanol in the cabinet CC is detected. It is possible.

The control unit 4 detects the evaporation condition of ethanol based on the detected value of the solution concentration meter 417, and changes the ratio of ethanol to the intermediate mixed solution. Specifically, the control unit 4 changes the opening degree of at least one of the first electric valve 410 and the second electric valve 411 based on the detected value of the solution concentration meter 417. As a result, the proportion of ethanol contained in the substrate treatment liquid is increased or decreased, and the etching rate is adjusted.

The explanation will be continued by returning to FIG. The DIW supply control unit 62 has a DIW supply pipe 621 connected to the nozzle 53 and a valve 652 that opens and closes the DIW supply pipe 651. The DIW supply pipe 651 is connected to the DIW supply source. When the valve 622 is opened in response to the opening / closing command from the control unit 4, DIW is supplied to the nozzle 53 as a rinsing liquid, and is discharged from the discharge port 53a toward the center of the surface of the substrate W.

The gas supply control unit 63 has a gas supply pipe 651 connected to the nozzle 53 and a valve 652 that opens and closes the gas supply pipe 651. The gas supply pipe 651 is connected to the gas supply source. In the present embodiment, dehumidified nitrogen gas is used as the gas, and when the valve 652 is opened in response to the opening / closing command from the control unit 4, nitrogen gas is supplied to the nozzle 53 and the substrate W is supplied from the discharge port 53a. It is sprayed toward the center of the surface of. In addition to nitrogen gas, an inert gas such as dehumidified argon gas may be used as the gas.

In the processing unit 1, an exhaust tub 80 is provided so as to surround the spin chuck 3. Further, a plurality of cups 81 and 82 (first cup 81 and second cup 82) arranged between the spin chuck 3 and the exhaust tub 80, and a plurality of guards 84 for receiving the processing liquid scattered around the substrate W. ~ 86 (1st guard 84 to 3rd guard 86) are provided. Further, guard elevating drive mechanisms 87 to 89 (first to third guard elevating drive mechanisms 87 to 89) are connected to guards 84 to 86, respectively. The guard elevating drive mechanisms 87 to 89 independently elevate and elevate the guards 84 to 86 in response to an elevating command from the control unit 4, respectively. Note that the first guard elevating drive mechanism 87 is not shown in FIG.

The control unit 4 has an arithmetic unit such as a CPU, a fixed memory device, a storage unit such as a hard disk drive, and an input / output unit. The storage unit stores the program executed by the arithmetic unit. Then, the control unit 4 controls each unit of the device according to the above program to execute the substrate processing shown in FIG. 8 using the substrate treatment liquid containing not only the etchant but also the movement accelerator.

FIG. 8 is a diagram showing the contents of the substrate processing executed by the substrate processing apparatus of FIG. The processing target in the substrate processing apparatus 100 is, for example, a substrate W in which a thin film-like thermal oxide film W2 is formed on a silicon base material W1 as shown in columns (a) and (b) of FIG. 1, and is thermally oxidized. A part of the film W2 is removed by etching to form a recess (fine region W7) extending in the horizontal direction.

Before the unprocessed substrate W is carried into the processing unit 1, the control unit 4 gives a command to each unit of the device to set the processing unit 1 in the initial state. That is, the shutter 23 (FIGS. 3 and 4) is closed by the shutter opening / closing mechanism 22. The spin chuck 3 is positioned and stopped at a position suitable for loading the substrate W by the substrate rotation drive mechanism 34, and the chuck pin 31 is opened by a chuck opening / closing mechanism (not shown). The cutoff plate 51 is positioned at the retracted position by the cutoff plate elevating drive mechanism 56, and the rotation of the cutoff plate 51 by the cutoff plate rotation drive mechanism 55 is stopped. The guards 84 to 86 are all moved downward and positioned. Further, the valves 612, 622 and 632 are all closed.

When the unprocessed substrate W is conveyed by the substrate transfer robot 111, the shutter 23 opens. The substrate W is carried into the internal space 21 of the chamber 2 by the substrate transfer robot 111 in accordance with the opening of the shutter 23, and is delivered to the spin chuck 3 with the surface Wf facing upward. Then, the chuck pin 31 is closed, and the substrate W is held by the spin chuck 3 (step S1: loading of the substrate).

Following the loading of the substrate W, the substrate transfer robot 111 retracts out of the chamber 2, and after the shutter 23 is closed again, the control unit 4 controls the motor of the substrate rotation drive mechanism 34 to rotate the spin chuck 3. The speed (rotational speed) is increased to a predetermined processing speed (within a range of about 10 to 3000 rpm, for example, 800 to 1200 rpm) and maintained at that processing speed. Further, the control unit 4 controls the blocking plate elevating drive mechanism 56 to lower the blocking plate 51 from the retracted position and arrange the blocking plate 51 at the blocking position (step S2). Further, the control unit 4 controls the guard elevating drive mechanisms 87 to 89 to raise the first guard 84 to the third guard 86 to the upper position, so that the first guard 84 faces the peripheral end surface of the substrate W.

When the rotation of the substrate W reaches the processing speed, the control unit 4 then opens the valve 622. As a result, DIW is discharged from the discharge port 53a of the nozzle 53 and supplied to the surface Wf of the substrate W. On the surface Wf of the substrate W, the DIW receives centrifugal force due to the rotation of the substrate W and moves to the peripheral edge of the substrate W. As a result, a so-called cover rinsing process is performed in which the entire surface Wf of the substrate W is covered with DIW (step S3). The cover rinse is not an essential step, and the cover rinse may not be performed and the etching process (step S4) described below may be performed immediately.

In step S4, the control unit 4 closes the valve 612 and opens the valve 622. As a result, the liquid discharged from the discharge port 53a of the nozzle 53 changes from the DIW to the substrate processing liquid, and the substrate processing liquid is supplied to the surface Wf of the substrate W. On the surface Wf of the substrate W, the substrate processing liquid receives centrifugal force due to the rotation of the substrate W and moves to the peripheral edge of the substrate W. As a result, the entire surface Wf of the substrate W is etched by the substrate treatment liquid. In this case, the substrate treating solution, the etchant is an etching species of the thermal oxide film W2 (Figure 1) ^- include tetraethylammonium iodide which functions as a transfer-promoting agent with (TEAI) and ethanol (EtOH) is (HF ₂₎ ing. In addition, it contains hydrochloric acid (HCl), which is an additional source of hydrogen ions (H ^+).

The etching treatment with the substrate treatment liquid is continued for a predetermined etching time, during which the substrate treatment liquid discharged from the peripheral portion of the substrate W is received by the inner wall of the first guard 84, and a drainage route (not shown) is omitted. It is sent to the waste liquid treatment equipment outside the machine along. When the etching time elapses, the control unit 4 closes the valve 612 and stops the discharge of the substrate processing liquid from the nozzle 53.

Following the etching process, a rinsing process with a rinsing solution (DIW) is executed (step S5). In this DIW rinse, the control unit 4 opens the valve 622 while maintaining the positions of the first guard 84 to the third guard 86. As a result, DIW is supplied as a rinse solution from the discharge port 53a of the nozzle 53 to the central portion of the surface Wf of the substrate W that has undergone the chemical solution cleaning treatment. Then, the DIW receives the centrifugal force due to the rotation of the substrate W and moves to the peripheral edge of the substrate W. As a result, the substrate treatment liquid adhering to the substrate W is washed away by the DIW. At this time, the DIW discharged from the peripheral edge of the substrate W is discharged from the peripheral edge of the substrate W to the side of the substrate W and sent to the waste liquid treatment facility outside the machine in the same manner as the substrate treatment liquid. This DIW rinse is continued for a predetermined rinse time, after which the control unit 4 closes the valve 622 and stops the discharge of DIW from the nozzle 53.

After the completion of the DIW rinse, the control unit 4 increases the rotation speed of the substrate W to perform spin drying (step S6). In the present embodiment, in parallel with spin drying, the control unit 4 opens the valve 632 and blows the dried nitrogen gas from the nozzle 53 onto the surface Wf of the substrate W during spin drying. This promotes the drying of the substrate W.

After the spin drying is continued for a predetermined time, the control unit 4 controls the motor of the substrate rotation drive mechanism 34 to stop the rotation of the spin chuck 3 and close the valve 632 to stop the blowing of nitrogen gas (step). S7). Further, the control unit 4 controls the cutoff plate rotation drive mechanism 55 to stop the rotation of the cutoff plate 51, and controls the cutoff plate elevating drive mechanism 56 to raise the cutoff plate 51 from the cutoff position to the retracted position. Position. Further, the control unit 4 controls the third guard elevating drive mechanism 89 to lower the third guard 86 to the third guard 86, and retracts all the guards 86 to 88 downward from the peripheral end surface of the substrate W.

After that, the control unit 4 controls the shutter opening / closing mechanism 22 to open the shutters 23 (FIGS. 3 and 4), and then the substrate transfer robot 111 enters the internal space of the chamber 2 and is held by the chuck pin 31. The released processed substrate W is carried out of the chamber 2 (step S8). When the transfer of the substrate W is completed and the substrate transfer robot 111 separates from the processing unit 1, the control unit 4 controls the shutter opening / closing mechanism 22 to close the shutter 23.

As described above, in the present embodiment, the etching process (step S4) is performed using the substrate processing liquid. Therefore, as shown in FIG. 2, tetraethylammonium iodide and ethanol assist the movement of the etchant to the fine region W7, and the etching rate can be improved. Furthermore, an etchant as in the prior art (HF 2 ^_-) present in the hydrogen ion (H ⁺⁾ substrate treating solution than when etching is performed only by a chemical solution containing, which also contributes to the improvement of etching rate. By these actions, the blanket ratio can be brought close to "1". As a result, it is possible to suppress the difference in etching rate depending on the size of the recess formed by the etching process. This point will be described in detail in later examples.

The present invention is not limited to the above-described embodiment, and various modifications other than those described above can be made without departing from the spirit of the present invention. For example, in the above embodiment, the intermediate mixed solution (= TEAI + DIW + HF + HCl) and ethanol are mixed to generate the substrate treatment liquid, but the mode of producing the substrate treatment liquid may be changed. For example, ethanol may be supplied to the tank 403 to generate a substrate treatment solution in a single tank 403. Further, a mixed solution in which an intermediate mixed solution (= TEAI + DIW + HF + HCl) and ethanol is mixed in advance at another place may be generated as a substrate processing solution and transferred to a tank or the like for supplying the substrate processing solution of the substrate processing apparatus. .. Further, for example, as shown in FIG. 9, a chemical solution (= HF + DIW) is generated in one tank 431, and an etching auxiliary solution (= TEAI + DIW + EtOH + HCl) is generated in the other tank 432, and both are mixed by a mixing valve 409 to form a substrate. A treatment liquid may be produced (second embodiment). Reference numeral 433 in FIG. 9 is a drainage device.

Further, in the above embodiment, the substrate processing liquid is generated immediately before being supplied to the substrate W, and is supplied to the substrate W from the nozzle 53 for etching. However, the substrate processing liquid passes through the heating unit before being supplied. It may be configured to adjust to a temperature suitable for the etching process.

Further, in the above embodiment, the present invention is applied to the so-called single-wafer type substrate processing apparatus 100 in which the substrate processing liquid is supplied to the substrate W held by the spin chuck 3 to perform the etching process, but the so-called batch is used. The present invention may be applied to the substrate processing apparatus of the type. That is, the etching process may be performed by immersing the substrate holding portion holding the plurality of substrates W held in the substrate holding portion in the substrate processing liquid stored in the processing tank.

Further, instead of supplying the substrate treatment solution to the substrate W, the chemical solution and the etching auxiliary liquid may be directly supplied to the substrate W to execute the etching process (third embodiment). For example, as shown in FIG. 10, a chemical solution nozzle 53b for supplying a chemical solution and an auxiliary solution nozzle 53c for supplying an etching auxiliary solution are provided, and the chemical solution stored in the tank 431 is supplied from the chemical solution nozzle 53b to the substrate W to supply the chemical solution nozzle 53b to the substrate W and tank 432. The etching auxiliary liquid stored in the auxiliary liquid nozzle 53c may be supplied to the substrate W from the auxiliary liquid nozzle 53c. Here, the supply of the chemical solution to the substrate W corresponds to the "chemical solution supply step" of the present invention, and the supply of the etching auxiliary liquid to the substrate W corresponds to the "auxiliary liquid supply step" of the present invention. In addition, there are the following three combinations regarding the supply timing of the chemical solution and the etching auxiliary solution. That is, the chemical solution and the etching auxiliary solution are simultaneously supplied to the substrate W (corresponding to the second substrate processing method described above). After the chemical solution is supplied to the substrate W, the etching auxiliary liquid is supplied to the substrate W to which the chemical solution is supplied (corresponding to the third substrate processing method described above). After the etching auxiliary liquid is supplied to the substrate W, the chemical solution is supplied to the substrate W to which the etching auxiliary liquid is supplied (corresponding to the fourth substrate processing method described above).

_{Further, in the above embodiment, the silicon oxide film (SiO 2} ) is etched as an example of the "removed portion" of the present invention, but other silicon nitride film (SiN), titanium nitride film (TiN) and the like are ". The present invention can also be applied to a substrate processing technique for forming recesses by etching a part of a silicon nitride film as a "removed portion" and a substrate processing liquid.

Further, the composition of the etching auxiliary liquid is not limited to the above, and the etching auxiliary liquid described in the above-mentioned "Basic Principle of the Invention and Substrate Treatment Method" can be used. Specific examples and effects thereof will be described in detail in the next examples.

Hereinafter, preferred embodiments of the present invention will be described in more detail with reference to Examples. However, the present invention is not limited by the following examples. Therefore, it is of course possible to make appropriate changes within the scope of the above-mentioned purpose, and all of them are included in the technical scope of the present invention.

<Surfactant-based migration promoter>
A substrate treatment solution composed of dilute hydrofluoric acid (a mixture of HF and DIW at (1: 5)) and 1 mM (where M = 1 mol / L) with respect to dilute hydrofluoric acid at the blending ratios shown in Table 1. ) Was mixed as a movement accelerator to produce a substrate treatment solution. In addition, "SDS" and "CTAC" in the same table are
SDS: sodium dodecyl sulfate
CTAC: Setrimonium chloride (N-Hexadecyltrimethylammonium chloride)
Means.

Then, each substrate treatment liquid is supplied to the substrate W having the structure shown in FIG. 1, and the thickness etched in 1 minute, that is, the result of measuring the etching amounts EMca to EMc is the "etching amount". Further, (EMa / EMc) and (EMb / EMc) are the blanket ratios of the substrate W shown in columns (a) and (b) of FIG. 1, respectively. The same applies to Tables 2 to 5 described later.

As is clear from Table 1, although it is a surfactant, in Comparative Example 2 containing a nonionic surfactant (polyoxyalkylene alkyl ether), an improvement in the etching rate was not observed, but rather a decrease in the etching rate was caused. It does not function as an etching agent. On the other hand, Example 1 containing an anionic surfactant (SDS), Example 2 containing a cationic surfactant (CTAC), and other surfactants such as n-octeltrimethylammonium chloride and trimethylstearylammonium chloride. In Examples 3 to 9, each of Example 3 to Example 9 containing hexacosanyltrimethylammonium chloride, choline acetate, aqueous choline, lauryldimethylaminoacetic acid, and dodecyldimethyl (3-sulfopropyl) ammonium hydroxide intramolecular salt, the transfer of the surfactant system. The presence of the accelerator can increase the etching rate in the fine region (recess) W7 and bring the blanket ratio closer to "1". That is, it is possible to suppress the difference in etching rate depending on the size of the recess.

<SIFT-based migration promoter>
A 1 mM SIFT-based migration promoter (hereinafter referred to as "SIFT agent") is mixed with dilute hydrofluoric acid prepared by mixing HF and DIW at a mixing ratio shown in Table 2 (1: 5). A substrate treatment liquid was produced.

Then, each substrate treatment liquid was supplied to the substrate W having the structure shown in FIG. 1, the amount of etching etched in 1 minute was measured, and the blanket ratio was obtained from them, which are summarized in Table 2.

As is clear from the table, in Examples 10 to 17 containing the SIFT agent, the etching rate in the fine region (recess) W7 can be increased by the presence of the SIFT agent, and the blanket ratio can be brought close to "1". .. That is, it is possible to suppress the difference in etching rate depending on the size of the recess.

Further, a substrate treatment solution to which 170 mL of ethanol (EtOH) was added in addition to the SIFT agent (Examples 18 to 22), and a substrate treatment solution to which 100 mL of hydrochloric acid (HCl) was added in addition to the SIFT agent (Examples 23 to 22). Example 27) and a substrate treatment solution (Examples 28 to 32) to which 170 mL of ethanol (EtOH) and 100 mL of hydrochloric acid (HCl) were added in addition to the SIFT agent were produced.

Then, each substrate treatment liquid was supplied to the substrate W having the structure shown in FIG. 1, the amount of etching etched in 1 minute was measured, and the blanket ratio was obtained from them, which are summarized in Table 3.

As is clear from the table, the etching rate in the fine region (recess) W7 can be increased by adding ethanol or hydrochloric acid, and the blanket ratio can be brought close to "1". That is, it is possible to suppress the difference in etching rate depending on the size of the recess.

<Alcohol-based migration promoter>
A substrate treatment solution was produced in which hydrofluoric acid (HF), an alcohol-based migration accelerator (hereinafter, simply referred to as “alcohol”) and DIW were mixed at the blending ratios shown in Table 4. Here, methyl alcohol (MeOH), ethyl alcohol (EtOH), 2-propanol (PrOH), and n-butyl alcohol (BuOH) are used as alcohols. In addition, the values in parentheses in the same table indicate the mixing ratio.

Then, each substrate treatment liquid was supplied to the substrate W having the structure shown in FIG. 1, the amount of etching etched in 1 minute was measured, and the blanket ratio was obtained from them, which are summarized in Table 4.

As is clear from the table, in Examples 33 to 44 containing alcohol, the etching rate in the fine region (recess) W7 can be increased by the presence of alcohol, and the blanket ratio can be brought close to “1”. That is, it is possible to suppress the difference in etching rate depending on the size of the recess.

<Organic solvent-based migration promoter>
A substrate treatment solution was produced in which hydrofluoric acid (HF), an organic solvent-based migration accelerator (hereinafter, simply referred to as “organic solvent”) and DIW were mixed at the blending ratios shown in Table 5. Here, acetic acid (CH3COOH) and ethylene glycol (OHCH2CH2OH) are used as organic solvents. In addition, the values in parentheses in the same table indicate the mixing ratio.

Then, each substrate treatment liquid was supplied to the substrate W having the structure shown in FIG. 1, the amount of etching etched in 1 minute was measured, and the blanket ratio was obtained from them, which are summarized in Table 5.

As is clear from the table, in Examples 45 to 52 containing the organic solvent, the etching rate in the fine region (recess) W7 can be increased by the presence of the organic solvent, and the blanket ratio can be brought close to “1”. .. That is, it is possible to suppress the difference in etching rate depending on the size of the recess.

The present invention can be applied to a general substrate processing technique for selectively removing a portion to be removed of a substrate to form a concave portion and a general substrate treatment liquid used for the technique.

3 ... Spin chuck (board holding part)
53b ... Chemical solution nozzle 53c ... Auxiliary solution nozzle 100 ... Substrate processing device 400 ... Processing liquid supply section W ... Substrate W2 ... Thermal oxide film (removed section)
W7 ... Fine region (recess)

Claims (8)

A substrate processing method in which a portion to be removed of a substrate is selectively removed to form a recess.
The recess is formed by etching the portion to be removed with a substrate treatment liquid containing an etchant for etching the portion to be removed and a movement accelerator for assisting the movement of the etchant into the recess.
A substrate treatment method, wherein the migration accelerator has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion. A substrate processing method in which a portion to be removed of a substrate is selectively removed to form a recess.
A chemical solution supply step of supplying a chemical solution containing an etchant for etching the removed portion to the substrate, and a chemical solution supply step.
The present invention includes an auxiliary liquid supply step of supplying an etching auxiliary liquid containing a movement accelerator to the substrate, which has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etchant into the recess. ,
A substrate processing method comprising executing the chemical solution supply step and the auxiliary liquid supply step continuously or simultaneously. The substrate processing method according to claim 2.
In the chemical solution supply step, the chemical solution is supplied from the chemical solution nozzle to the substrate, and the chemical solution is supplied to the substrate.
In the auxiliary liquid supply step, a substrate processing method in which the etching auxiliary liquid is supplied to the substrate from the auxiliary liquid nozzle at the same time as the chemical solution supply step. The substrate processing method according to claim 2.
In the chemical solution supply step, the chemical solution is supplied from the chemical solution nozzle to the substrate.
In the auxiliary liquid supply step, a substrate processing method in which the etching auxiliary liquid is supplied to the substrate from the auxiliary liquid nozzle to the substrate to which the chemical liquid is supplied from the chemical liquid nozzle. The substrate processing method according to claim 2.
In the auxiliary liquid supply step, the etching auxiliary liquid is supplied to the substrate from the auxiliary liquid nozzle.
In the chemical solution supply step, a substrate processing method in which the chemical solution is supplied from the chemical solution nozzle to the substrate to which the etching auxiliary solution is supplied from the auxiliary solution nozzle. A substrate processing device that selectively removes a portion to be removed from a substrate to form a recess.
A substrate holding portion that holds the substrate and
A substrate treatment liquid containing an etchant for etching the removed portion and a movement accelerator having a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etchant to the recess is generated. A substrate processing apparatus including a processing liquid supply unit that supplies the substrate processing liquid to the substrate held by the substrate holding unit. A substrate processing device that selectively removes a portion to be removed from a substrate to form a recess.
A substrate holding portion that holds the substrate and
An etching aid containing a movement accelerator, which has a chemical solution containing an etchant for etching the removed portion and an hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion to assist the movement of the etchant into the recess. The processing liquid supply unit that generates the liquid and
A chemical solution nozzle that supplies the chemical solution to the substrate,
An auxiliary liquid nozzle for supplying the etching auxiliary liquid to the substrate is provided.
A substrate processing apparatus characterized in that the supply of the chemical solution from the chemical solution nozzle and the supply of the etching auxiliary solution from the auxiliary liquid nozzle are continuously or simultaneously executed. A substrate treatment liquid that selectively removes a portion to be removed from a substrate to form a recess.
An etchant that etches the part to be removed and
A movement promoter that assists the movement of the etchant into the recess is provided.
The substrate treatment liquid, wherein the migration accelerator has a hydrophobic portion and an anionic hydrophilic portion or a cationic hydrophilic portion.

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