US20010005638A1 - Method for removing photoresist layer - Google Patents
Method for removing photoresist layer Download PDFInfo
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- US20010005638A1 US20010005638A1 US09/792,570 US79257001A US2001005638A1 US 20010005638 A1 US20010005638 A1 US 20010005638A1 US 79257001 A US79257001 A US 79257001A US 2001005638 A1 US2001005638 A1 US 2001005638A1
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- photoresist
- layer
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- hydrogen
- polymers
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- 229920002120 photoresistant polymer Polymers 0.000 title claims abstract description 53
- 238000000034 method Methods 0.000 title claims abstract description 33
- 239000007789 gas Substances 0.000 claims abstract description 43
- 229920000642 polymer Polymers 0.000 claims abstract description 34
- 238000001020 plasma etching Methods 0.000 claims abstract description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000001301 oxygen Substances 0.000 claims abstract description 11
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
- 238000011065 in-situ storage Methods 0.000 claims abstract description 10
- 230000000149 penetrating effect Effects 0.000 claims abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 3
- 230000004907 flux Effects 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims description 2
- 229910052734 helium Inorganic materials 0.000 claims description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 2
- 238000005530 etching Methods 0.000 abstract description 13
- 239000000758 substrate Substances 0.000 abstract description 8
- 235000012431 wafers Nutrition 0.000 description 13
- 230000008901 benefit Effects 0.000 description 3
- 238000010849 ion bombardment Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Images
Classifications
-
- 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 potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table 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
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31127—Etching organic layers
- H01L21/31133—Etching organic layers by chemical means
- H01L21/31138—Etching organic layers by chemical means by dry-etching
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/427—Stripping or agents therefor using plasma means only
-
- 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 potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table 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
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31105—Etching inorganic layers
- H01L21/31111—Etching inorganic layers by chemical means
- H01L21/31116—Etching inorganic layers by chemical means by dry-etching
Definitions
- the present invention relates to a method for removing a photoresist layer and polymers layer in the fabrication of a semiconductor device. More particularly, the present invention relates to a high-density plasma method using mixing gases as source for removing a photoresist layer and polymers layer generated during plasma etching process.
- photoresist layers are widely used in patterning processes.
- the photoresist layer and the sidewall polymers generated during plasma etching step needs to be removed for subsequent processes.
- the residue affects subsequent processes and debases the quality of the device. Accordingly, it is important to avoid leaving any photoresist/polymers layer residue when the photoresist/polymers layer is removed.
- integrated circuit patterns transferred on wafers comprises steps of coating a photoresist layer over the wafer.
- the photoresist layer is sensitive to light and resistant to etching.
- the image of the master mask is replicated on the photoresist layer by an exposure system to form a patterned photoresist layer.
- An etching step is performed to form the predetermined pattern on the wafer by using the patterned photoresist layer as an etching mask layer.
- high-density plasma HDP is usually used to perform an anisotropic etching step, and during the etching step, heavy sidewall polymers are deposited to meet etching requirements (e.g. etching selectivity to substrate and profile control etc.).
- the patterned photoresist layer and sidewall polymer layers are stripped away in-situ.
- some undesirable residues are generated and accumulated on the surface of the photoresist layer and/or the sidewall of the opening formed by etching.
- the residues cannot be removed easily by oxygen plasma and leave on the wafer to affect the subsequent processes.
- the main residues include the following:
- Silicon-containing polymer is generated while performing the etching step.
- the polymers on the sidewall of the opening are generated during etching from the gasses such as C 4 H 8 , CH 2 F 2 , and C 3 H 2 F 6 .
- FIG. 1A is schematic, cross-sectional view of the conventional HDP oxide etcher for removing a photoresist/polymers layer by plasma.
- FIGS. 1B through 1C are schematic, cross-sectional views of the conventional plasma method for removing a photoresist layer.
- a bias is applied on a wafer 114 to enhance the ion bombardment of plasma for removing a photoresist layer 104 (as shown in FIG. 1B).
- an in-situ oxygen plasma etching step is used to remove the photoresist/polymers layer 104 .
- an in-situ oxygen plasma etching step is used to remove the photoresist/polymers layer 104 .
- the residual polymers 106 are generated on the top surface of the photoresist layer 104 , it is difficult to strip away the photoresist layer 104 completely.
- this invention provides a method for removing photoresist/polymers layer without any residues by using an additional gas mixed with oxygen as a source for in-situ plasma etching.
- the present method comprises the steps of providing a wafer having an oxide layer, a photoresist layer, an opening penetrating through the photoresist layer and the oxide layer.
- An in-situ plasma-etching step is performed by using a mixing gases containing oxygen as a source of plasma to remove the photoresist layer.
- the gases for mixing with oxygen as a source for plasma etching is selected from the group consisting of nitrogen, hydrogen-containing gas, the combinations thereof and the likes.
- FIG. 1A is a schematic, cross-sectional view of a conventional HDP oxide etcher for removing a photoresist layer by plasma;
- FIGS. 1B through 1C are schematic, cross-sectional views of the conventional plasma method for removing a photoresist layer.
- FIGS. 2A through 2B are schematic, cross-sectional views of the plasma method using a mixed gas as source for removing the photoresist/polymers layer in a preferred embodiment according to the present invention.
- an in-situ plasma etching step using an additional gas mixed with oxygen (O 2 /additional gas) are performed to strip away the photoresist/polymers layer 204 .
- O 2 /additional gas an additional gas mixed with oxygen
- the plasma using the O 2 /additional gas as source can efficiently strip away the photoresist/polymers layer 204 .
- the examples of O 2 /additional gas include O 2 /N 2 , O 2 /hydrogen-containing gases or O 2 /N 2 /hydrogen-containing gases.
- the preferred volume ratio of gas N 2 to O 2 /N 2 is about 1%-50%.
- the preferred volume ratio of hydrogen-containing gases to O 2 /hydrogen-containing gases is about 1%-30%.
- the preferred volume ratio of hydrogen-containing gases to O 2 /N 2 /hydrogen-containing gases and that of N 2 gas to O 2 /N 2 / hydrogen-containing gases are respectively about 1%-30% and 1%-50%.
- the hydrogen-containing gas can be CH 2 F 2 , CH 3 F, C 2 H 2 F 4 and C 3 H 2 F 6 , for example.
- the condition for practicing the method in accordance with the present invention can be varied to optimize for operation.
- the conditions for stripping away the photoresist/polymers layer 204 are such as a mixing gas flux of about 100 to 3000 standard cubic centimeter per minute (sccm), a mixing gas pressure of about 20 millitorr to 1 torr, an electrical power for generating plasma of about 1000 to 3000 W, a bias power on a wafer (not shown) of about 0 to 300 W, the wafer temperature of about ⁇ 20°C. to 400°C. and a pressure of helium used as a background gas of about 1 to 100 torr.
- a mixing gas flux of about 100 to 3000 standard cubic centimeter per minute (sccm)
- a mixing gas pressure of about 20 millitorr to 1 torr
- an electrical power for generating plasma of about 1000 to 3000 W
- a bias power on a wafer not shown
- the wafer temperature of about ⁇ 20°C. to 400°C
- the plasma using mixed gas as source has a high ability to remove the photoresist/polymers layer 204 , and the bias power applied on the wafer can be reduced, and even eliminated. Accordingly, the bombardment of the plasma to the photoresist/polymers layer 204 is moderate, and the substrate 200 and oxide layer 202 , which are in the opening 208 , do not suffer plasma damage. Therefore, the problems encountered in the conventional method, such as loss of the substrate 200 and oxide layer 202 and loss of control over the critical dimension of the opening 208 can be overcome.
- the present invention provides a method for stripping away the photoresist/polymers layer without residues, and the bias power applied on the wafer can be reduced or even eliminated.
- the problems such as loss of the substrate and oxide layer and loss of control over the critical dimension of the opening can be overcome.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Inorganic Chemistry (AREA)
- Plasma & Fusion (AREA)
- Drying Of Semiconductors (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Abstract
A method described for removing a photoresist/polymers layer on a substrate. The method comprises the steps of providing a wafer having an oxide layer, a photoresist/polymers layer, an opening penetrating through the photoresist/polymers layer and the oxide layer, and the sidewall polymer on the surface of photoresist layer and the oxide layer. An in-situ plasma-etching step using an additional gas mixed with oxygen as source is performed to remove the photoresist/polymers layer without residues, no damages to substrate and oxide and no changes on the critical dimension of the opening during etching step.
Description
- 1. Field of the Invention
- The present invention relates to a method for removing a photoresist layer and polymers layer in the fabrication of a semiconductor device. More particularly, the present invention relates to a high-density plasma method using mixing gases as source for removing a photoresist layer and polymers layer generated during plasma etching process.
- 2. Description of the Related Art
- In the fabrication procedure of a metal oxide semiconductor (MOS), photoresist layers are widely used in patterning processes. However, after an etching step is performed, the photoresist layer and the sidewall polymers generated during plasma etching step needs to be removed for subsequent processes. When the photoresist/polymers layer is not removed completely, the residue affects subsequent processes and debases the quality of the device. Accordingly, it is important to avoid leaving any photoresist/polymers layer residue when the photoresist/polymers layer is removed.
- In the conventional photolithography method, integrated circuit patterns transferred on wafers comprises steps of coating a photoresist layer over the wafer. The photoresist layer is sensitive to light and resistant to etching. The image of the master mask is replicated on the photoresist layer by an exposure system to form a patterned photoresist layer. An etching step is performed to form the predetermined pattern on the wafer by using the patterned photoresist layer as an etching mask layer. At present, high-density plasma (HDP) is usually used to perform an anisotropic etching step, and during the etching step, heavy sidewall polymers are deposited to meet etching requirements (e.g. etching selectivity to substrate and profile control etc.). Following the oxide plasma etching, the patterned photoresist layer and sidewall polymer layers are stripped away in-situ. However, during high-density plasma etching, some undesirable residues are generated and accumulated on the surface of the photoresist layer and/or the sidewall of the opening formed by etching. The residues cannot be removed easily by oxygen plasma and leave on the wafer to affect the subsequent processes. The main residues include the following:
- 1. Cross-linking polymer generated by ultraviolet irradiation is generated on the top surface of the photoresist layer;
- 2. Silicon-containing polymer is generated while performing the etching step; and
- 3. The polymers on the sidewall of the opening are generated during etching from the gasses such as C 4H8, CH2F2, and C3H2F6.
- The residues often cannot be cleaned by solvents and result in contamination and defects in the following subsequent process. Recently, in order to avoid photoresist residues as mentioned above left on the wafer, a bias is applied to the wafer to enhance the ion bombardment when the oxygen (O 2) plasma is performed to remove the photoresist layer.
- FIG. 1A is schematic, cross-sectional view of the conventional HDP oxide etcher for removing a photoresist/polymers layer by plasma. FIGS. 1B through 1C are schematic, cross-sectional views of the conventional plasma method for removing a photoresist layer.
- As shown in FIG. 1A, a bias is applied on a
wafer 114 to enhance the ion bombardment of plasma for removing a photoresist layer 104 (as shown in FIG. 1B). - As shown in FIG. 1B, after an
opening 108 is formed, an in-situ oxygen plasma etching step is used to remove the photoresist/polymers layer 104. As theresidual polymers 106 are generated on the top surface of thephotoresist layer 104, it is difficult to strip away thephotoresist layer 104 completely. - As shown in FIG. 1C, since the ion bombardment of the oxygen plasma is enhanced, the
substrate 100 and anoxide layer 102 underneath thephotoresist layer 104 are attacked by the plasma. Accordingly, it is desirable to develop a new method to solve the problems such as the loss of substrate and oxide and an inability to control the critical dimension of the opening during in-situ oxygen plasma etching step. - It is therefore an objective of the present invention to provide a method for removing a photoresist layer and polymers on the wafer surface without any photoresist residues left.
- It is an another objective of the present invention to provide a method for removing a photoresist layer as well as controlling the critical dimension of the openings formed during etching.
- To achieve these and other advantages and in accordance with the purpose of the present invention, as embodied and broadly described herein, this invention provides a method for removing photoresist/polymers layer without any residues by using an additional gas mixed with oxygen as a source for in-situ plasma etching. The present method comprises the steps of providing a wafer having an oxide layer, a photoresist layer, an opening penetrating through the photoresist layer and the oxide layer. An in-situ plasma-etching step is performed by using a mixing gases containing oxygen as a source of plasma to remove the photoresist layer.
- In a preferred embodiment of the present invention, the gases for mixing with oxygen as a source for plasma etching is selected from the group consisting of nitrogen, hydrogen-containing gas, the combinations thereof and the likes.
- It is to be understood that both the foregoing general description and the following detailed description are exemplary, and are intended to provide further explanation of the invention as claimed.
- The accompanying drawings are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification. The drawings illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention. In the drawings,
- FIG. 1A is a schematic, cross-sectional view of a conventional HDP oxide etcher for removing a photoresist layer by plasma;
- FIGS. 1B through 1C are schematic, cross-sectional views of the conventional plasma method for removing a photoresist layer; and
- FIGS. 2A through 2B are schematic, cross-sectional views of the plasma method using a mixed gas as source for removing the photoresist/polymers layer in a preferred embodiment according to the present invention.
- Reference will now be made in detail to the present preferred embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers are used in the drawings and the description to refer to the same or like parts.
- As shown in FIG. 2A, after the
opening 208 is formed, an in-situ plasma etching step using an additional gas mixed with oxygen (O2/additional gas) are performed to strip away the photoresist/polymers layer 204. Although thepolymer 206 is formed on the top surface of the photoresist/polymers layer 204 and the sidewall of theopening 208, the plasma using the O2/additional gas as source can efficiently strip away the photoresist/polymers layer 204. The examples of O2/additional gas include O2/N2, O2/hydrogen-containing gases or O2/N2/hydrogen-containing gases. The preferred volume ratio of gas N2 to O2/N2 is about 1%-50%. The preferred volume ratio of hydrogen-containing gases to O2/hydrogen-containing gases is about 1%-30%. The preferred volume ratio of hydrogen-containing gases to O2/N2/hydrogen-containing gases and that of N2 gas to O2/N2/ hydrogen-containing gases are respectively about 1%-30% and 1%-50%. The hydrogen-containing gas can be CH2F2, CH3F, C2H2F4 and C3H2F6, for example. - The condition for practicing the method in accordance with the present invention can be varied to optimize for operation. In the preferred embodiment, the conditions for stripping away the photoresist/
polymers layer 204 are such as a mixing gas flux of about 100 to 3000 standard cubic centimeter per minute (sccm), a mixing gas pressure of about 20 millitorr to 1 torr, an electrical power for generating plasma of about 1000 to 3000 W, a bias power on a wafer (not shown) of about 0 to 300 W, the wafer temperature of about −20°C. to 400°C. and a pressure of helium used as a background gas of about 1 to 100 torr. - As shown in FIG. 2B, the plasma using mixed gas as source has a high ability to remove the photoresist/
polymers layer 204, and the bias power applied on the wafer can be reduced, and even eliminated. Accordingly, the bombardment of the plasma to the photoresist/polymers layer 204 is moderate, and thesubstrate 200 andoxide layer 202, which are in theopening 208, do not suffer plasma damage. Therefore, the problems encountered in the conventional method, such as loss of thesubstrate 200 andoxide layer 202 and loss of control over the critical dimension of theopening 208 can be overcome. - Altogether, the advantages and benefit achieved by the present invention include the following:
- 1. The present invention provides a method for stripping away the photoresist/polymers layer without residues, and the bias power applied on the wafer can be reduced or even eliminated. The problems such as loss of the substrate and oxide layer and loss of control over the critical dimension of the opening can be overcome.
- 2. The method of the present invention can be practiced on the conventional devices, thus the present invention is ready to be implemented on current plant lines.
- It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the present invention without departing from the scope or spirit of the invention. In view of the foregoing, it is intended that the present invention cover modifications and variations of this invention provided they fall within the scope of the following claims and their equivalents.
Claims (8)
1. A method for removing photoresist on a wafer having an oxide layer, a photoresist/polymers layer, an opening penetrating through the photoresist/polymers layer and the oxide layer, the method comprising the steps of:
performing an in-situ plasma etching step using an additional gas mixed with oxygen as a source to remove the photoresist/polymers layer.
2. The method of , wherein the additional gas is selected from the group consisting of N2, hydrogen( H2)-containing gas and the combination thereof.
claim 1
3. The method of , wherein when the additional gas is N2, the ratio of N2 to the O2/N2 mixing gas is about 1%-50%.
claim 2
4. The method of , wherein when the additional gas is the hydrogen-containing gas, the ratio of hydrogen-containing gas to the O2/hydrogen-containing mixing gas is about 1%-30%.
claim 2
5. The method of , wherein the hydrogen-containing gas is selected from a group consisting of CH2F2, CH3F, C2H2F4, C3H2F6 and the combinations thereof.
claim 4
6. The method of , wherein when the additional gas is the combination of N2 and hydrogen-containing gas, the ratios of hydrogen containing gases and N2to the O2/N2/hydrogen-containing mixing gas are respectively about 1%-30% and 1%-50%.
claim 2
7. The method of , wherein the hydrogen-containing gas is selected from a group consisting of CH2F2, CH3F, C2H2F4, C3H2F6 and the combinations thereof.
claim 6
8. The method of , wherein the step of removing the photoresist/polymers layer is performed under the conditions of:
claim 1
a flux of about 100-3000 sccm for the mixing gas;
a pressure of about 20 millitorr to 1 torr for the mixing gas;
a power of about 1000 to 3000 W for the in-situ plasma etching step;
a bias power on a wafer of about 0 to 300 W for the in-situ plasma etching step;
a wafer temperature of about −20 to 400 centigrade for removing the photoresist/polymers layer; and
a pressure of about 1 to 100 torr for the helium background gas.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/792,570 US20010005638A1 (en) | 1998-12-15 | 2001-02-23 | Method for removing photoresist layer |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/212,727 US6218084B1 (en) | 1998-12-15 | 1998-12-15 | Method for removing photoresist layer |
| US09/792,570 US20010005638A1 (en) | 1998-12-15 | 2001-02-23 | Method for removing photoresist layer |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/212,727 Continuation US6218084B1 (en) | 1998-12-15 | 1998-12-15 | Method for removing photoresist layer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20010005638A1 true US20010005638A1 (en) | 2001-06-28 |
Family
ID=22792200
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/212,727 Expired - Lifetime US6218084B1 (en) | 1998-12-15 | 1998-12-15 | Method for removing photoresist layer |
| US09/792,570 Abandoned US20010005638A1 (en) | 1998-12-15 | 2001-02-23 | Method for removing photoresist layer |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/212,727 Expired - Lifetime US6218084B1 (en) | 1998-12-15 | 1998-12-15 | Method for removing photoresist layer |
Country Status (1)
| Country | Link |
|---|---|
| US (2) | US6218084B1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060105576A1 (en) * | 2004-11-18 | 2006-05-18 | International Business Machines Corporation | High ion energy and reative species partial pressure plasma ash process |
| US20080254637A1 (en) * | 2007-04-11 | 2008-10-16 | Micron Technology, Inc. | Methods for removing photoresist defects and a source gas for same |
| CN103903964A (en) * | 2014-04-14 | 2014-07-02 | 中国科学院微电子研究所 | Method for passivating film masked by etching glue by using fluorine-based gas |
| US20210358761A1 (en) * | 2018-09-26 | 2021-11-18 | Tokyo Electron Limited | Etching method, method of removing etching residue, and storage medium |
| US12500091B2 (en) * | 2018-09-26 | 2025-12-16 | Tokyo Electron Limited | Etching method, method of removing etching residue, and storage medium |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030015496A1 (en) * | 1999-07-22 | 2003-01-23 | Sujit Sharan | Plasma etching process |
| US6328905B1 (en) * | 1999-08-12 | 2001-12-11 | Advanced Micro Devices, Inc. | Residue removal by CO2 water rinse in conjunction with post metal etch plasma strip |
| JP4382926B2 (en) * | 1999-09-29 | 2009-12-16 | 東京エレクトロン株式会社 | Plasma processing method |
| US7179751B2 (en) * | 2001-10-11 | 2007-02-20 | Texas Instruments Incorporated | Hydrogen plasma photoresist strip and polymeric residue cleanup process for low dielectric constant materials |
| TWI226059B (en) * | 2001-06-11 | 2005-01-01 | Sony Corp | Method for manufacturing master disk for optical recording medium having pits and projections, stamper, and optical recording medium |
| US6569778B2 (en) * | 2001-06-28 | 2003-05-27 | Hynix Semiconductor Inc. | Method for forming fine pattern in semiconductor device |
| US7125496B2 (en) * | 2001-06-28 | 2006-10-24 | Hynix Semiconductor Inc. | Etching method using photoresist etch barrier |
| US6846746B2 (en) * | 2002-05-01 | 2005-01-25 | Applied Materials, Inc. | Method of smoothing a trench sidewall after a deep trench silicon etch process |
| KR100591129B1 (en) * | 2004-12-15 | 2006-06-19 | 동부일렉트로닉스 주식회사 | Photoresist removing device and method for removing semiconductor device with copper wiring |
| CN106229289A (en) * | 2016-07-28 | 2016-12-14 | 上海华力微电子有限公司 | A kind of forming method of pair of active area shallow trench |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100194789B1 (en) * | 1995-12-16 | 1999-06-15 | 김영환 | Polymer removal method of semiconductor device |
| US5908319A (en) * | 1996-04-24 | 1999-06-01 | Ulvac Technologies, Inc. | Cleaning and stripping of photoresist from surfaces of semiconductor wafers |
| JPH1167626A (en) * | 1997-08-12 | 1999-03-09 | Hitachi Ltd | Resist removal method and apparatus |
-
1998
- 1998-12-15 US US09/212,727 patent/US6218084B1/en not_active Expired - Lifetime
-
2001
- 2001-02-23 US US09/792,570 patent/US20010005638A1/en not_active Abandoned
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060105576A1 (en) * | 2004-11-18 | 2006-05-18 | International Business Machines Corporation | High ion energy and reative species partial pressure plasma ash process |
| US7253116B2 (en) * | 2004-11-18 | 2007-08-07 | International Business Machines Corporation | High ion energy and reative species partial pressure plasma ash process |
| US20080254637A1 (en) * | 2007-04-11 | 2008-10-16 | Micron Technology, Inc. | Methods for removing photoresist defects and a source gas for same |
| US8372754B2 (en) * | 2007-04-11 | 2013-02-12 | Micron Technology, Inc. | Methods for removing photoresist defects and a method for processing a semiconductor device structure |
| CN103903964A (en) * | 2014-04-14 | 2014-07-02 | 中国科学院微电子研究所 | Method for passivating film masked by etching glue by using fluorine-based gas |
| US20210358761A1 (en) * | 2018-09-26 | 2021-11-18 | Tokyo Electron Limited | Etching method, method of removing etching residue, and storage medium |
| US12500091B2 (en) * | 2018-09-26 | 2025-12-16 | Tokyo Electron Limited | Etching method, method of removing etching residue, and storage medium |
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| US6218084B1 (en) | 2001-04-17 |
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