US20010023701A1 - Remover for a ruthenium containing metal and use thereof - Google Patents
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- US20010023701A1 US20010023701A1 US09/788,555 US78855501A US2001023701A1 US 20010023701 A1 US20010023701 A1 US 20010023701A1 US 78855501 A US78855501 A US 78855501A US 2001023701 A1 US2001023701 A1 US 2001023701A1
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F1/00—Etching metallic material by chemical means
- C23F1/10—Etching compositions
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/3213—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
- H01L21/32133—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
- H01L21/32134—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by liquid etching only
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F1/00—Etching metallic material by chemical means
- C23F1/10—Etching compositions
- C23F1/14—Aqueous compositions
- C23F1/16—Acidic compositions
- C23F1/30—Acidic compositions for etching other metallic material
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S134/00—Cleaning and liquid contact with solids
- Y10S134/902—Semiconductor wafer
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Abstract
This invention provides a remover comprising (a) a cerium (IV) nitrate salt and (b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid.
Description
- 1. Field of the invention
- This invention relates to a remover for a ruthenium containing metal which is effective for removing an undesired ruthenium containing metal adhering to, for example, a semiconductor substrate and the use thereof.
- 2. Description of the related Art
- Recently, a high dielectric-constant film such as Ta2O5 has been used in place of a conventional silicon oxide or nitride film as a capacitance film for a DRAM or FeRAM. Such a high dielectric-constant film permits us to ensure a required accumulated capacitance in a small occupied area and to improve a degree of memory-cell integration.
- When using such a high dielectric-constant film and polysilicon as an electrode material sandwiching a capacitance film, oxygen is liberated from the high dielectric-constant film during heating a semiconductor device to oxidize the electrode material. There, therefore, exists a dielectric film (silicon oxide film) having a lower dielectric constant than the high dielectric-constant film between the electrode materials, leading to reduction in a capacitance. Thus, when using a high dielectric-constant film, it is important to select a material which does not become an insulating film due to oxidation as an electrode material sandwiching a capacitance film. It is because once a part of an electrode becomes an insulating film by oxidation, it constitutes a part of a capacitance film, resulting in a reduced capacitance. Ruthenium has recently attracted attention as an electrode material meeting the above requirement. Ruthenium is preferable because it retains conductivity even after oxidation, thus does not cause capacitance reduction and is inexpensive.
- However, forming an electrode using ruthenium may lead to peeling of a ruthenium containing metal such as ruthenium and ruthenium oxide adhering to the end face or the rear face of a silicon substrate. The peeled metal may adhere to a device forming area or may cause cross contamination between devices or wafers via a carrying system. Recently, a procedure such as forming an electrode film within a narrow hole has been frequently employed for reducing an occupied area for a capacitor. It requires even forming of a thin ruthenium film, so that it is often essential to use CVD exhibiting good coverage as a deposition method, where adhesion of the ruthenium containing metal to the end and/or the rear faces of the silicon substrate becomes more prominent.
- A ruthenium containing metal is known as a so-called lifetime killer to a semiconductor device. In particular, it may cause a variety of problems; for example, it adversely affects device operation due to reduction in carrier mobility and varying a threshold voltage of a transistor with time. A ruthenium containing metal is diffused at a higher rate in a silicon substrate than platinum also known as a lifetime killer. A trace amount of the ruthenium containing metal remaining on the silicon substrate surface may give prominent adverse affects on device properties. As described above, an undesired ruthenium containing metal remaining on a silicon substrate surface may deteriorate reliability of a device.
- Therefore, when using ruthenium as an electrode material, it is important to remove an undesired ruthenium containing metal by treatment with an etchant. There have been, however, no enchants capable of dissolving and removing a ruthenium containing metal. For example, aqua regia used for forming a platinum electrode may not be used as a remover for a ruthenium containing metal due to its insufficient dissolving ability.
- For effectively removing a ruthenium containing metal, a remover for ruthenium must not only dissolve the ruthenium containing metal but also effectively preventing the dissolved ruthenium containing metal from re-adhering to a silicon substrate.
- In the light of the above situation, an objective of this invention is to provide a remover for a ruthenium containing metal which can adequately dissolve and remove a ruthenium containing metal such as ruthenium and ruthenium oxide and can satisfactorily prevent re-adhesion of the dissolved ruthenium containing metal, and the use thereof.
- This invention provides a remover for a ruthenium containing metal, comprising (a) a cerium (IV) nitrate salt and (b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid.
- The remover of this invention exhibits prominent performance of removing a ruthenium containing metal owing to synergism in the combination of components (a) and (b) and can satisfactorily prevent re-adhesion of the dissolved ruthenium containing metal.
- This remover may be used for washing a substrate to which a ruthenium containing metal adheres or for etching a ruthenium film formed on a substrate.
- The remover of this invention is particularly suitable for removing ruthenium adhering to a semiconductor device (by washing or etching). As described above, ruthenium is known as a so-called lifetime killer to a semiconductor device. It may give serious damage to device performance when remaining on the surface of the semiconductor device. The remover according to this invention may efficiently remove a ruthenium containing metal and prevent re-adhesion so that it is suitable for removing the ruthenium containing metal on such a semiconductor substrate.
- The remover of this invention is particularly effective when used for washing a semiconductor substrate in which a ruthenium containing metal adheres to an area other than a device forming area. For example, it may be significantly effective when used for removing by washing a ruthenium containing metal adhering to an area other than a device forming area after depositing a ruthenium film in the device forming area on the semiconductor substrate. In such washing, the ruthenium containing metal adhering the area other than the device forming area is mainly made of ruthenium oxide. The remover of this invention may exhibit good performance of removal and re-adhesion for not only ruthenium but also ruthenium oxide. Thus, it may be suitably used for the above washing. For such washing, a particularly higher level of performance is required for preventing re-adhesion of the dissolved and removed ruthenium containing metal in comparison with, for example, etching. The remover of this invention exhibiting excellent performance of preventing re-adhesion may be suitably used in the above washing. The term “an area other than a device forming area” includes end and rear faces of a semiconductor substrate and also peripheral areas in the device forming area.
- As described above, the remover of this invention is characterized in that a cerium (IV) nitrate salt is combined with a particular acid.
- For a composition in which a cerium (IV) nitrate salt and an acid is combined, JP-B 7-7757 and JP-A 11-131263 have described that used as an etchant for preparing a chrome mask. When preparing the chrome mask, it is necessary to etch a chromium film such that its cross section becomes tapered. It is known that such a taper shape may be suitably formed by conducting wet etching using a composition having the above combination after forming a resist mask on a chromium film because chromium is dissolved by the action of a cerium (IV) nitrate salt while nitric acid peels the resist mask and the chromium film.
- These publications have, however, described etching chromium and there are no description for action to a ruthenium containing metal.
- As described above, it has been unknown that a combination of a cerium (IV) nitrate salt and a particular acid exhibits excellent performance in removing a ruthenium containing metal and may effectively prevent re-adhesion of the removed ruthenium containing metal. This invention is based on the observation.
- This invention also provides method of using a remover for a ruthenium containing metal wherein a substrate is washed with a liquid containing at least one of hydrofluoric acid, nitric acid, perchloric acid and oxalic acid for removing the residual remover after removing with the above remover.
- This process may allow us to effectively remove a residual remover, leading to washing with higher cleanliness.
- This invention also provides a process for removing a ruthenium containing metal comprising the steps of depositing a ruthenium film in a device forming area on a semiconductor substrate; and spraying a remover containing (a) a cerium (IV) nitrate salt and (b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid on a given area on the semiconductor substrate while rotating the substantially horizontal semiconductor substrate to remove a ruthenium containing metal adhering to an area other than the device forming area.
- The removing process may more effectively remove a ruthenium containing metal.
- FIG. 1 shows an appearance of a silicon substrate after depositing a ruthenium film.
- FIG. 2 shows another appearance of a silicon substrate after depositing a ruthenium film.
- Component (a) in this invention is a cerium (IV) nitrate salt. Examples of a cerium (IV) nitrate salt include cerium (IV) ammonium nitrate and cerium (IV) potassium nitrate. Cerium (IV) ammonium nitrate is preferable because it less influences device performance.
- Component (b) in this invention is at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid. In other words, these acids may be used alone or in combination as appropriate. Synergism in a combination of such an acid and component (a) provides prominent effect for removing a ruthenium containing metal.
- In this invention, the content of component (a) is preferably 5 wt % or more, more preferably 10 wt % or more, for adequately dissolving and removing a ruthenium containing metal and preventing re-adhesion of the removed ruthenium containing metal. The upper limit of the content is preferably 35 wt % or less, more preferably 30 wt % or less, for effectively preventing precipitation of compound (a).
- In this invention, the content of component (b) is preferably 1 wt % or more, more preferably 5 wt % or more, for adequately dissolving and removing a ruthenium containing metal and preventing re-adhesion of the removed ruthenium containing metal. There are no particular restrictions to an upper limit of the content, but it may be, for example, 30 wt % or less.
- A remover in this invention exhibits higher performance for removing a ruthenium containing metal and for re-adhesion prevention by means of synergism provided by a combination of the above components (a) and (b). It is difficult to adequately remove a ruthenium containing metal with component (a) or (b) alone.
- Besides the above components (a) and (b), a remover in this invention usually contains water as component (c), which may enhance performance of the components (a) and (b) for removing a ruthenium containing metal. The content of component (c) is for example 35 to 94 wt %.
- The remover of this invention may contain a variety of additives such as a surfactant and a water-soluble organic solvent, which may be miscible with water and other components in this invention.
- A preferable embodiment of a remover in this invention may be one consisting of the above (a), (b) or (c) alone or that to which a small amount of, for example, additive is added.
- There will be described treatment using a remover for removing a ruthenium containing metal adhering to an area other than a device forming area on a silicon substrate. FIG. 1 shows a substrate after depositing a ruthenium film where a
silicon substrate 1 is placed on asubstrate platform 5. When forming aruthenium film 2 by CVD, ruthenium adheres to the end and the rear faces of thesilicon substrate 1. A part of theruthenium film 2 then becomes ruthenium oxide due to oxidation. If the semiconductor substrate to which a ruthenium containing metal such as ruthenium oxide and ruthenium adheres is fed to a carrying system, it may cause cross contamination of a deposition apparatus. Furthermore, a ruthenium containing metal tends to adversely affect device properties. For avoiding such a problem, treatment with a remover is effective. - When forming a
ruthenium film 2′ after forming an insulatingfilm 3 as illustrated in FIG. 2, theruthenium film 2′ again adheres to the end and the rear faces of thesilicon substrate 1. Thus, treatment with the remover of this invention is effective. - It is desirable to avoid adhesion of the remover to the device forming area during conducting a removing process of this invention. For example, a removing procedure may be conducted by spin washing where only the end and the rear faces are in contact with the remover while introducing nitrogen gas to the device forming surface.
- In this invention, examples of a semiconductor substrate include a silicon substrate, a semiconductor substrate made of a III-V group compound such as GaAs, InP and GaN, and a semiconductor substrate made of a II-VI group compound such as ZnSe. Among these, this invention is particularly suitable for treating a silicon substrate because this invention exhibits good performance for removing a ruthenium containing metal and is thus prominently effective when being applied to a silicon substrate where deterioration in device performance due to diffusion of ruthenium in the substrate is significant.
- A silicon substrate on which ruthenium was deposited to a thickness of 100 nm was cut to give an about 2 cm×2 cm chip as a sample. The sample was immersed in a remover consisting of an oxidizing agent, an acid and water. Tables 1 to 7 show compositions of a remover. A content of each component is given in wt % to the whole remover. The balance is water. A temperature of the remover was varied in three steps of 40° C., 50° C. and 60° C. After leaving the sample in the remover until the ruthenium film substantially disappeared, the sample was removed, washed with running water for 1 min and dried with nitrogen blow. A dissolution rate for ruthenium was determined from the time taken until the ruthenium film disappeared. The results are shown in Tables 1 to 7, where a dissolution rate is given in Å/min and “CAN” means cerium (IV) ammonium nitrate.
- The results in the tables indicate that effect for removing ruthenium is prominent when a cerium (IV) nitrate salt is combined with a particular acid.
TABLE 1 No.1 No.2 No.3 No.4 Oxidizing CAN 10 10 10 10 agent Acid Nitric 0 5 10 30 acid Dissolution 40° C. — — — — rate 50° C. — — — — Å/min 60° C. — 30 27 28 -
TABLE 2 No.5 No.6 No.7 No.8 No.9 Oxidizing CAN 20 20 20 20 20 agent Acid Nitric 0 5 10 20 30 acid Dissolution 40° C. 370 100 — — 44 rate 50° C. 280 320 — — 95 Å/min 60° C. 230 470 105 158 146 -
TABLE 3 No.10 No.11 No.12 No.13 Oxidizing CAN 30 30 30 30 agent Acid Nitric 0 5 10 20 acid Dissolution 40° C. 430 500 258 172 rate 50° C. 750 650 380 254 Å/min 60° C. 960 950 522 316 -
TABLE 4 No.14 No.15 No.16 No.17 No.18 Oxidizing CAN 20 30 30 30 30 agent Acid Perchloric 5 5 acid Hydrochloric 5 acid Sulfuric 5 acid Phosphoric 1 acid Dissolu- 40° C. 95 630 — — — tion rate 50° C. 380 860 — — — Å/min 60° C. 500 950 — — — -
TABLE 5 No.19 No.20 Oxidizing Cerium 20 20 agent sulfate Acid Nitric acid 5 Sulfuric acid 5 Dissolution 40° C. <10 <10 rate 50° C. <10 <10 Å/min 60° C. <10 <10 -
TABLE 6 No.21 No.22 No.23 No.24 Oxidizing Cerium sulfate 8 8 agent Ferric nitrate 20 Sodium bromate 20 Acid Nitric acid 5 5 10 Sulfuric acid 8 Dissolution 40° C. 0 0 <10 <10 rate 50° C. 0 0 <10 <10 Å/min 60° C. 0 0 <10 <10 -
TABLE 7 No.25 No.26 Oxidizing CAN 30 20 agent Acid Nitric acid 5 Perchloric acid 5 Acetic acid 5 Dissolution 40° C. 540 430 rate 50° C. 820 800 Å/min 60° C. 900 920 - On a silicon substrate was deposited ruthenium oxide to a thickness of 100 nm and was then formed a resist mask having an opening. The substrate was cut to give an about 2 cm×2 cm chip as a sample. The sample was immersed in a remover consisting of an oxidizing agent, an acid and water. Table 8 shows the composition of the remover. A content of each component is given in wt % to the whole remover. The balance is water. A temperature of the remover was varied in three steps of 40° C., 50° C. and 60° C. After leaving the sample in the remover for a given period, the sample was removed, washed with running water for 1 min and dried with nitrogen blow. A dissolution rate for ruthenium oxide was determined from an immersion time and a reduced film thickness. The results are shown in Tables 8, where a dissolution rate is given in Å/min.
- The results in the table indicate that effect for removing ruthenium oxide is prominent when a cerium (IV) nitrate salt is combined with a particular acid.
TABLE 8 No.27 No.28 No.29 No.30 No.31 Oxidizing CAN 20 30 30 30 20 agent Acid Nitric acid 5 5 10 5 Perchloric 5 acid Acetic 5 acid Disolution 40° C. <10 <10 <10 <10 <10 rate 50° C. <10 150 280 350 130 Å/min 60° C. 370 640 540 590 400 - A silicon substrate on which ruthenium was deposited to a thickness of 100 nm was cut to give an about 2 cm×2 cm chip as a sample. The sample was immersed in a remover consisting of an oxidizing agent, an acid and water, where the remover was not stirred or stirred with a stirrer. Table 9 shows the composition of the remover. A content of each component is given in wt % to the whole remover. The balance is water. A temperature of the remover was varied in three steps of 25° C., 30° C. and 40° C. After leaving the sample in the remover until the ruthenium film substantially disappeared, the sample was removed, washed with running water for 1 min and dried with nitrogen blow. A dissolution rate for ruthenium was determined from the time taken until the ruthenium film disappeared. The results are shown in Table 9, where a dissolution rate is given in Å/min. The results indicate that stirring can accelerate dissolution of ruthenium. It may be, therefore, expected that spin washing utilizing physical action can provide more rapid removal than immersing.
TABLE 9 Oxidiz- ing agent Acid Stirring 25° C. 30° C. 40° C. No.1 CAN Nitric No 100 100 30 (10) acid (5) Yes 800 850 1000 No.2 CAN Nitric No 50 70 100 (10) acid (10) Yes 480 550 600 No.3 CAN Nitric No 100 320 470 (20) acid (5) Yes 1200 1350 1700 No.4 CAN Nitric No 100 110 150 (20) acid (10) Yes 480 630 960 - A silicon substrate was immersed in a washing, i.e., an aqueous solution of 30 wt % of cerium (IV) ammonium nitrate and 10 wt % of nitric acid, at 40° C. for 5 min. The substrate was removed and determined for an amount of adhering cerium, which was 2.0×1013 atoms/cm2.
- The substrate was immersed in a washing shown in Table 10, removed, washed with running water for 1 min, dried by nitrogen blow and then determined for an amount of adhering cerium. The results are shown in Table 10. A content of each component is given in wt % to the whole washing. The balance is water. An amount of adhering cerium was determined by total-reflection X-ray fluorescence spectroscopy. The results shown in the table indicate that a washing containing hydrofluoric acid and nitric acid is particularly effective in removing the residual cerium.
TABLE 10 No.1 No.2 No.3 No.4 No.5 Washing Hydrofluoric acid 0.5 0.5 Nitric acid 5 5 Perchloric acid 5 Oxalic acid 0.34 Residual cerium (× 1010 atoms/cm2) 62 80 146 0.8 70 - As described above, a remover of this invention in which a cerium (IV) nitrate salt is combined with a particular acid can adequately dissolve and remove a ruthenium containing metal and can effectively prevent re-adhesion of the removed ruthenium containing metal.
- This application is based on Japanese patent application NO.2000-46150 filed on Feb. 23, 2000, the content of which is incorporated hereinto by reference.
Claims (14)
1. A remover for a ruthenium containing metal, comprising (a) a cerium (IV) nitrate salt and (b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid.
2. The remover as claimed in used for removing a ruthenium containing metal adhering to a semiconductor substrate.
claim 1
3. The remover as claimed in used for washing a semiconductor device in which a ruthenium containing metal adheres to an area other than a device forming area.
claim 1
4. The remover as claimed in wherein the semiconductor substrate is a silicon substrate.
claim 2
5. The remover as claimed in wherein the semiconductor substrate is a silicon substrate.
claim 3
6. The remover as claimed in comprising 5 to 35 % by mass of component (a) and 1 to 30 % by mass of component (b).
claim 1
7. The remover as claimed in comprising 5 to 35 % by mass of component (a) and 1 to 30 % by mass of component (b).
claim 2
8. The remover as claimed in comprising 5 to 35 % by mass of component (a) and 1 to 30 % by mass of component (b).
claim 3
9. A method of removing a ruthenium containing metal adhering to a semiconductor substrate with a remover, the remover comprising:
(a) a cerium (IV) nitrate salt and
(b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid.
10. A method of removing a ruthenium containing metal adhering to an area other than a device forming area on a semiconductor substrate with a remover, the remover comprising:
(a) a cerium (IV) nitrate salt and
(b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid.
11. A method of using a remover for a ruthenium containing metal wherein after removing with the remover as claimed in , a substrate is washed with a liquid containing at least one of hydrofluoric acid, nitric acid, perchloric acid and oxalic acid for removing the remover residue.
claim 1
12. A method of using a remover for a ruthenium containing metal wherein after removing with the remover as claimed in , a substrate is washed with a liquid containing at least one of hydrofluoric acid, nitric acid, perchloric acid and oxalic acid for removing the remover residue.
claim 2
13. A method of using a remover for a ruthenium containing metal wherein after removing with the remover as claimed in , a substrate is washed with a liquid containing at least one of hydrofluoric acid, nitric acid, perchloric acid and oxalic acid for removing the remover residue.
claim 3
14. A process for removing a ruthenium containing metal comprising the steps of depositing a ruthenium film in a device forming area on a semiconductor substrate; and spraying a remover containing (a) a cerium (IV) nitrate salt and (b) at least one acid selected from the group consisting of nitric acid, perchloric acid and acetic acid on a given area on the semiconductor substrate while rotating the substantially horizontal semiconductor substrate to remove a ruthenium containing metal adhering to an area other than the device forming area.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US10/123,197 US6468357B1 (en) | 2000-02-23 | 2002-04-17 | Remover for a ruthenium containing metal and use thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000046150A JP4510979B2 (en) | 2000-02-23 | 2000-02-23 | Method for using ruthenium or ruthenium oxide removing liquid and method for removing ruthenium or ruthenium oxide |
JP2000-046150 | 2000-02-23 |
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US10/123,197 Division US6468357B1 (en) | 2000-02-23 | 2002-04-17 | Remover for a ruthenium containing metal and use thereof |
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US20010023701A1 true US20010023701A1 (en) | 2001-09-27 |
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US09/788,555 Abandoned US20010023701A1 (en) | 2000-02-23 | 2001-02-21 | Remover for a ruthenium containing metal and use thereof |
US10/123,197 Expired - Lifetime US6468357B1 (en) | 2000-02-23 | 2002-04-17 | Remover for a ruthenium containing metal and use thereof |
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US10/123,197 Expired - Lifetime US6468357B1 (en) | 2000-02-23 | 2002-04-17 | Remover for a ruthenium containing metal and use thereof |
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US (2) | US20010023701A1 (en) |
EP (1) | EP1130636B1 (en) |
JP (1) | JP4510979B2 (en) |
KR (1) | KR100416889B1 (en) |
CN (2) | CN100491594C (en) |
DE (1) | DE60113170T2 (en) |
TW (1) | TW527440B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020056697A1 (en) * | 1998-09-03 | 2002-05-16 | Westmoreland Donald L. | Ruthenium and ruthenium dioxide removal method and material |
US6468357B1 (en) * | 2000-02-23 | 2002-10-22 | Nec Corporation | Remover for a ruthenium containing metal and use thereof |
US6537461B1 (en) * | 2000-04-24 | 2003-03-25 | Hitachi, Ltd. | Process for treating solid surface and substrate surface |
US20030119319A1 (en) * | 2001-12-21 | 2003-06-26 | Micron Technology, Inc. | Methods for planarization of group VIII metal-containing surfaces using complexing agents |
US20030119316A1 (en) * | 2001-12-21 | 2003-06-26 | Micron Technology, Inc. | Methods for planarization of group VIII metal-containing surfaces using oxidizing agents |
US20030119321A1 (en) * | 2001-12-21 | 2003-06-26 | Micron Technology, Inc. | Methods for planarization of Group VIII metal-containing surfaces using oxidizing gases |
US20040157458A1 (en) * | 2001-12-21 | 2004-08-12 | Micron Technology, Inc. | Methods for planarization of metal-containing surfaces using halogens and halides salts |
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Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4113486A (en) * | 1973-10-22 | 1978-09-12 | Fuji Photo Film Co., Ltd. | Method for producing a photomask |
JPS5177404A (en) * | 1974-12-26 | 1976-07-05 | Fuji Photo Film Co Ltd | |
US4080246A (en) | 1976-06-29 | 1978-03-21 | Gaf Corporation | Novel etching composition and method for using same |
EP0182306B1 (en) * | 1984-11-17 | 1991-07-24 | Daikin Industries, Limited | Etchant composition |
JPS62133087A (en) * | 1985-12-05 | 1987-06-16 | Nippon Engeruharudo Kk | Removing agent for substance sticking to noble metal |
JPH077757B2 (en) | 1987-09-28 | 1995-01-30 | 三菱電機株式会社 | Chromium film patterning method |
US4976810A (en) * | 1990-03-06 | 1990-12-11 | Kabushiki Kaisha Toshiba | Method of forming pattern and apparatus for implementing the same |
US5118356A (en) * | 1990-11-19 | 1992-06-02 | Eastman Kodak Company | Process for cleaning a photographic processing device |
KR100239417B1 (en) * | 1996-12-03 | 2000-01-15 | 김영환 | Capacitor of semiconductor device amd manufacturing method thereof |
JP3366238B2 (en) | 1997-10-27 | 2003-01-14 | 鹿児島日本電気株式会社 | Chromium film etching method |
US6143192A (en) * | 1998-09-03 | 2000-11-07 | Micron Technology, Inc. | Ruthenium and ruthenium dioxide removal method and material |
JP4510979B2 (en) * | 2000-02-23 | 2010-07-28 | ルネサスエレクトロニクス株式会社 | Method for using ruthenium or ruthenium oxide removing liquid and method for removing ruthenium or ruthenium oxide |
JP3645144B2 (en) * | 2000-02-24 | 2005-05-11 | Necエレクトロニクス株式会社 | Manufacturing method of semiconductor device |
-
2000
- 2000-02-23 JP JP2000046150A patent/JP4510979B2/en not_active Expired - Lifetime
-
2001
- 2001-02-20 EP EP01104044A patent/EP1130636B1/en not_active Expired - Lifetime
- 2001-02-20 DE DE60113170T patent/DE60113170T2/en not_active Expired - Lifetime
- 2001-02-21 US US09/788,555 patent/US20010023701A1/en not_active Abandoned
- 2001-02-22 TW TW090104111A patent/TW527440B/en not_active IP Right Cessation
- 2001-02-23 CN CNB011042524A patent/CN100491594C/en not_active Expired - Lifetime
- 2001-02-23 KR KR10-2001-0009123A patent/KR100416889B1/en active IP Right Grant
- 2001-02-23 CN CN2009101325743A patent/CN101538716B/en not_active Expired - Lifetime
-
2002
- 2002-04-17 US US10/123,197 patent/US6468357B1/en not_active Expired - Lifetime
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US7327034B2 (en) | 2001-12-21 | 2008-02-05 | Micron Technology, Inc. | Compositions for planarization of metal-containing surfaces using halogens and halide salts |
US7442652B2 (en) | 2002-02-04 | 2008-10-28 | Nec Electronics Corporation | Method for removing contamination and method for fabricating semiconductor device |
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US11732365B2 (en) | 2018-11-14 | 2023-08-22 | Kanto Kagaku Kabushiki Kaisha | Composition for removing ruthenium |
Also Published As
Publication number | Publication date |
---|---|
EP1130636B1 (en) | 2005-09-07 |
EP1130636A2 (en) | 2001-09-05 |
KR100416889B1 (en) | 2004-02-05 |
US6468357B1 (en) | 2002-10-22 |
CN1311351A (en) | 2001-09-05 |
TW527440B (en) | 2003-04-11 |
EP1130636A3 (en) | 2003-07-23 |
DE60113170D1 (en) | 2005-10-13 |
CN100491594C (en) | 2009-05-27 |
CN101538716B (en) | 2011-02-09 |
JP4510979B2 (en) | 2010-07-28 |
CN101538716A (en) | 2009-09-23 |
KR20010085498A (en) | 2001-09-07 |
DE60113170T2 (en) | 2006-07-13 |
JP2001234373A (en) | 2001-08-31 |
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