US20100326954A1 - Method of etching a multi-layer - Google Patents
Method of etching a multi-layer Download PDFInfo
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- US20100326954A1 US20100326954A1 US12/492,152 US49215209A US2010326954A1 US 20100326954 A1 US20100326954 A1 US 20100326954A1 US 49215209 A US49215209 A US 49215209A US 2010326954 A1 US2010326954 A1 US 2010326954A1
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- etching
- layer
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- chlorine
- aluminum layer
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- 238000005530 etching Methods 0.000 title claims abstract description 101
- 238000000034 method Methods 0.000 title claims abstract description 76
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 60
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 60
- 230000008569 process Effects 0.000 claims abstract description 37
- 239000000460 chlorine Substances 0.000 claims abstract description 31
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 11
- 239000000758 substrate Substances 0.000 claims abstract description 9
- 239000004065 semiconductor Substances 0.000 claims abstract description 7
- 238000002161 passivation Methods 0.000 claims description 28
- 229910015844 BCl3 Inorganic materials 0.000 claims description 20
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 claims description 20
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 13
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000010410 layer Substances 0.000 abstract description 116
- 239000011247 coating layer Substances 0.000 abstract description 4
- 239000007789 gas Substances 0.000 description 38
- 229920000642 polymer Polymers 0.000 description 18
- 238000005260 corrosion Methods 0.000 description 12
- 230000007797 corrosion Effects 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 8
- 238000010586 diagram Methods 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 229920002120 photoresistant polymer Polymers 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000001020 plasma etching Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HIVGXUNKSAJJDN-UHFFFAOYSA-N [Si].[P] Chemical compound [Si].[P] HIVGXUNKSAJJDN-UHFFFAOYSA-N 0.000 description 1
- MXSJNBRAMXILSE-UHFFFAOYSA-N [Si].[P].[B] Chemical compound [Si].[P].[B] MXSJNBRAMXILSE-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- JRBRVDCKNXZZGH-UHFFFAOYSA-N alumane;copper Chemical compound [AlH3].[Cu] JRBRVDCKNXZZGH-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000010295 mobile communication Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- C23F4/00—Processes for removing metallic material from surfaces, not provided for in group C23F1/00 or C23F3/00
-
- 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
- H01L21/3205—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
- H01L21/32135—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 vapour etching only
- H01L21/32136—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 vapour etching only using plasmas
Definitions
- the present invention relates to a method of etching a multi-layer, especially to a method that can prevent excess polymer residue on the sidewall and the corrosion of the aluminum layer.
- IC integrated circuits
- a conventional method of forming a patterned aluminum layer is to deposit a photoresist layer on the aluminum layer, and then performing a photo-etching-process (PEP) with a patterned photo mask, then transferring the pattern of the photoresist layer onto the aluminum layer.
- PEP photo-etching-process
- FIG. 1 illustrating a cross sectional schematic diagram of a conventional method of forming a patterned aluminum layer.
- a semiconductor substrate (not shown) is provided and a dielectric layer 10 , a barrier layer 12 , an aluminum layer 14 , an anti-reflection coating (ARC) layer 16 and a photoresist layer 22 are disposed in series thereon.
- the barrier layer 12 is an optional structure and may include Ti/TiN or TaN.
- the barrier layer 12 is usually used in a conventional via plug forming process to cover the external layer of the via plug or to increase its adhesion.
- the ARC layer 16 is used to reduce the reflection phenomenon during the exposure process.
- the etching gas recipes usually include chlorine gas, BCl 3 N 2 , CHF 3 or hydrocarbon.
- the chlorine gas and BCl 3 are used as the etching gas to anisotropically etch the ARC layer 16 and the aluminum layer 14 when they are transferred to radical by the plasma in the etching chamber.
- a passivation gas is used to produce polymer on the sidewall to obtain a good sidewall protection.
- BCl 3 can not only function as an etching gas but also has passivation effect. It has therefore been widely used in various anisotropic etching processes. However, using BCl 3 may also bring some shortcomings such as excess loose polymer residue formed on the sidewall and thus the corrosion of the aluminum layer or other shortcomings. As shown in FIG. 1 , it is known that BCl 3 has passivation effect, but if BCl 3 and other passivation substances are used at the same time, excess polymer residue 24 is formed on the sidewall which is not compact. And because of the excess loose polymer residue 24 on the sidewall, lots of Cl plasma generated by the plasma is easily attached onto the polymer residue 24 and reacted with the aluminum layer 14 in the sidewall. Please refer to FIG.
- FIG. 2 illustrating a schematic diagram of a conventional aluminum corrosion reaction formed by the Cl plasma .
- AlCl x a gaseous and aqueous intermediate product AlCl x is produced.
- Al(OH) x aluminum hydroxide
- HCl (g)+(aq) gaseous and aqueous hydrochloric acid
- Formed aqueous hydrochloric acid then soon reacts with the aluminum layer 14 and regenerates with AlCl x .
- the present invention provides a method of etching a multi-layer, especially a method that can reduce the phenomenon of excess polymer residue and can produce more compact polymer residue so as to prevent the corrosion of aluminum layer in the multi-layer.
- a method of etching a multi-layer comprises an aluminum layer disposed on a semiconductor substrate and an anti-reflection coating layer disposed on the aluminum layer.
- the method comprises: performing a first etching process to etch the anti-reflection coating layer by providing a first etching gas, wherein the first etching gas comprises a chlorine-containing substance; then performing a second etching process to etch the aluminum layer by providing a second etching gas, wherein the second etching gas does not comprise a chlorine-containing compound.
- a method of anisotropically etching an aluminum layer comprises: providing an etching gas to etch the aluminum layer, wherein the etching gas comprises a chlorine-containing substance, but does not comprise a chlorine-containing compound.
- the method of etching a multi-layer in the present invention excludes chlorine-containing compound as an etching gas, not only providing a more simple process but also reducing the phenomenon of excess polymer residue and corrosion of aluminum layer, and leading to a better etching result.
- FIG. 1 illustrates a cross sectional schematic diagram of a conventional method of forming a patterned aluminum layer.
- FIG. 2 illustrates a schematic diagram of a conventional aluminum corrosion reaction formed by the Cl plasma .
- FIG. 3 illustrates a flow chart of etching a multi-layer in the present invention.
- FIG. 4 to FIG. 7 illustrate the structure schematic diagrams of each step of etching a multi-layer in the present invention.
- FIG. 3 illustrating a flow chart of etching a multi-layer in the present invention.
- the method of etching a multi-layer in the present invention comprises:
- Step 100 providing a multi-layer disposed on a semiconductor substrate, wherein the multi-layer comprises at least an aluminum layer and an anti-reflection coating (ARC) layer disposed on the aluminum layer.
- ARC anti-reflection coating
- Step 102 utilizing a patterned mask to perform a first etching process to etch the ARC layer by providing a first etching gas and a first passivation gas, wherein the first etching gas comprises a chlorine-containing substance.
- Step 104 after step 102 , performing a second etching process to etch the aluminum layer by providing a second etching gas and a second passivation gas, wherein the second etching gas does not comprise a chlorine-containing compound.
- Step 106 after etching the aluminum layer, performing an over etching process to etch a barrier layer disposed under the aluminum layer.
- FIG. 4 to FIG. 7 illustrating the structure schematic diagrams of each step of etching a multi-layer in the present invention.
- a multi-layer on a semiconductor substrate 108 is provided.
- the multi-layer in series includes a dielectric layer 110 , a barrier layer 112 , an aluminum layer 114 , an ARC layer 116 and a mask layer 122 .
- the dielectric layer 110 includes SiO 2 , SiN, SiC, tetraethoxysilane (TEOS), undoped silicon glass (USG), phosphorus silicon glass (PSG), boron phosphorus silicon glass (BPSG), other low-k dielectric material or the combination of above groups.
- TEOS tetraethoxysilane
- USG undoped silicon glass
- PSG phosphorus silicon glass
- BPSG boron phosphorus silicon glass
- the barrier layer 112 includes Ti/TiN, TaN, other suitable material or the combination of above groups.
- the aluminum layer 114 may include conventional metal aluminum or aluminum alloy such as copper-aluminum alloy.
- the ARC layer 116 includes Ti/TiN or other suitable material.
- the ARC layer 116 may include a mono-layer structure or a double-layer structure, for example, a bottom ARC layer and a top ARC layer.
- the bottom ARC layer includes TiN.
- the top ARC layer may include the same material as the bottom ARC layer or include different materials, such as an organic anti-reflection material, or inorganic anti-refection material like silicon oxynitride (SiON).
- the mask layer 122 includes a patterned structure, such as a photoresist, wherein the pattern of the mask layer 122 will be transferred to the ARC layer 116 and the aluminum layer 114 in the subsequent etching steps.
- a first etching process is provided to etch the ARC layer 116 but less to etch the aluminum layer 114 .
- step 102 is performed, most ARC layer 116 is etched away and even a small part of the aluminum layer 114 is consumed. In some circumstance, a small part of the ARC layer 116 may still be retained on the substrate 108 .
- a first etching gas 126 and a first passivation gas are provided therefore.
- the first etching gas 126 includes various kinds of chlorine-containing substance but does not include a chlorine-containing compound, for instance, using only chlorine gas but not using BCl 3 .
- the first etching gas 126 used to etch the ARC layer 116 but less to etch the aluminum layer 114 may also include all chlorine-containing substances, which means using the chlorine gas and various kinds of chlorine-containing compounds at the same time, for example, using chlorine gas and BCl 3 at the same time.
- the first passivation gas includes hydrocarbon or other suitable material, in the preferred embodiment of the present invention, the first passivation gas is ethylene (C 2 H 4 ).
- the first etching process is carried out in a plasma etching chamber.
- Table 1 provides a preferred etching recipe and operation condition when the first etching gas 126 is chlorine gas.
- the first etching process is performed under a condition as follows: a pressure between 12 and 18 mTorr, a RF power between 1200 and 1600 W, a bias power between 250 W and 350 W, a period between 120 and 180 seconds, a flow rate of chlorine gas between 150 and 210 sccm (standard cubic centimeter per minute) and a flow rate of ethylene between 120 and 180 sccm.
- the reaction time of the first etching process may be adjusted depending on the material or thickness of the ARC layer 116 . It can be longer or short and is not limited to Table 1.
- a second etching process to etch the aluminum layer 114 is provided.
- a second etching gas 128 and a second passivation gas are provided.
- the second etching gas 128 in the present invention includes a chlorine-containing substance but does not include a chlorine-containing compound, for example, using only chlorine-containing substance such as chlorine gas but avoiding conventional chlorine-containing compound such as BCl 3 .
- the second passivation gas includes hydrocarbon or other suitable material, in the preferred embodiment of the present invention, the second passivation gas is C 2 H 4 .
- the second etching process can also be carried out in-situ in the plasma etching chamber.
- the second etching process is performed under a condition as follows: a pressure between 8 and 12 mTorr, a RF power between 1300 and 1700 W, a bias power between 250 W and 350 W, a flow rate of the first etching gas between 120 and 180 sccm and a flow rate of the first passivation gas between 120 and 180 sccm.
- the reaction time of the second etching process is determined by the end point detection. When the thickness of the aluminum layer 114 or other metal layer is changed, the reaction time of the second etching process is adjusted as well.
- the time listed in Table 1 provides one embodiment and the etching method of the present invention should not be limited thereto.
- step 106 an over etching process is in-situ provided.
- a third etching gas 130 is provided to etch the barrier layer 112 and some remained aluminum layer 114 on the substrate 108 .
- a part of the dielectric layer 110 may be consumed in the third etching process to make sure the aluminum layer 114 and the barrier layer 112 being etched away completely.
- the etching recipe and operation condition are shown in Table 1, which is not described in detail.
- BCl 3 is usually used as an etching and a passivation gas in conventional arts, which may results in excess polymer residue formed on the sidewall of the patterned aluminum layer and thus brings to the serious etching and even corrosion of the aluminum layer.
- the present invention therefore provides an etching method that avoids using chlorine-containing compound such as BCl 3 as an etching gas, and in combination with a passivation gas such as hydrocarbon.
- BCl 3 produces sidewall polymer by bombarding the mask layer, but the formed sidewall polymer is usually not compact.
- hydrocarbon has longer polymer chains and thus more condensed structure ([C—H]x), it can completely replace the passivation function of BCl 3 .
- the sidewall protection is not reduced with the removal of BCl 3 .
- removing BCl 3 can avoid corrosion of the aluminum layer caused by too much Cl plasma trapped in the polymer residue.
- the method of etching a multi-layer in the present invention not only provides a simpler process by removing chlorine-containing compound as an etching gas, but also can reduce the phenomenon of excess polymer residue and corrosion of aluminum layer, leading to a better etching result.
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Abstract
A method of etching a multi-layer is provided. The multi-layer includes an aluminum layer disposed on a semiconductor substrate and an anti-reflection coating layer disposed on the aluminum layer. The method includes: performing a first etching process to etch the anti-reflection coating layer by providing a first etching gas, wherein the first etching gas includes a chlorine-containing substance; then performing a second etching process to etch the aluminum layer by providing a second etching gas, wherein the second etching gas does not include a chlorine-containing compound.
Description
- 1. Field of the Invention
- The present invention relates to a method of etching a multi-layer, especially to a method that can prevent excess polymer residue on the sidewall and the corrosion of the aluminum layer.
- 2. Description of the Prior Art
- In modern society, the micro-processor system comprised of integrated circuits (IC) is a ubiquitous device, being utilized in such diverse fields as automatic control electronics, mobile communication devices and personal computers.
- To connect various active or passive components on the semiconductor substrate, metal aluminum or its alloy is usually used as a conducting wire. By some patterning processes, a complex interconnection system is gradually formed. A conventional method of forming a patterned aluminum layer is to deposit a photoresist layer on the aluminum layer, and then performing a photo-etching-process (PEP) with a patterned photo mask, then transferring the pattern of the photoresist layer onto the aluminum layer.
- Please refer to
FIG. 1 , illustrating a cross sectional schematic diagram of a conventional method of forming a patterned aluminum layer. As shown inFIG. 1 , a semiconductor substrate (not shown) is provided and adielectric layer 10, abarrier layer 12, analuminum layer 14, an anti-reflection coating (ARC)layer 16 and aphotoresist layer 22 are disposed in series thereon. Thebarrier layer 12 is an optional structure and may include Ti/TiN or TaN. Thebarrier layer 12 is usually used in a conventional via plug forming process to cover the external layer of the via plug or to increase its adhesion. TheARC layer 16 is used to reduce the reflection phenomenon during the exposure process. - Due to the different materials of each layer in the multi-layer, it is necessary to use different etching gas recipes to accurately remove the
ARC layer 16 and thealuminum layer 14. The etching gas recipes usually include chlorine gas, BCl3 N2, CHF3 or hydrocarbon. The chlorine gas and BCl3 are used as the etching gas to anisotropically etch theARC layer 16 and thealuminum layer 14 when they are transferred to radical by the plasma in the etching chamber. In order to maintain the good directionality, a passivation gas is used to produce polymer on the sidewall to obtain a good sidewall protection. - It is known that BCl3 can not only function as an etching gas but also has passivation effect. It has therefore been widely used in various anisotropic etching processes. However, using BCl3 may also bring some shortcomings such as excess loose polymer residue formed on the sidewall and thus the corrosion of the aluminum layer or other shortcomings. As shown in
FIG. 1 , it is known that BCl3 has passivation effect, but if BCl3 and other passivation substances are used at the same time,excess polymer residue 24 is formed on the sidewall which is not compact. And because of the excessloose polymer residue 24 on the sidewall, lots of Clplasma generated by the plasma is easily attached onto thepolymer residue 24 and reacted with thealuminum layer 14 in the sidewall. Please refer toFIG. 2 , illustrating a schematic diagram of a conventional aluminum corrosion reaction formed by the Clplasma. Please refer toFIG. 2 . When the aluminum (Al(s)) in thealuminum layer 14 reacts with the Cl radical (Clplasma), a gaseous and aqueous intermediate product AlClx is produced. If the aqueous AlClx comes in contact with water (H2O), it will produce aluminum hydroxide (Al(OH)x) and gaseous and aqueous hydrochloric acid (HCl(g)+(aq)). Formed aqueous hydrochloric acid then soon reacts with thealuminum layer 14 and regenerates with AlClx. So the cycle re-entries the foregoing and continues to cycle indefinitely, making thealuminum layer 14 being etched seriously and leading to the phenomenon of aluminum layer corrosion. Although the action can be avoided by blocking of H2O, but it will further increase the burden of the controlling factors required in the etching process, making it become a complex process. - As a result, a simple etching process to etch the aluminum layer and the ARC layer that can prevent excess polymer residue production and corrosion of aluminum layer is still needed.
- The present invention provides a method of etching a multi-layer, especially a method that can reduce the phenomenon of excess polymer residue and can produce more compact polymer residue so as to prevent the corrosion of aluminum layer in the multi-layer.
- According to the present invention, a method of etching a multi-layer is provided. The multi-layer comprises an aluminum layer disposed on a semiconductor substrate and an anti-reflection coating layer disposed on the aluminum layer. The method comprises: performing a first etching process to etch the anti-reflection coating layer by providing a first etching gas, wherein the first etching gas comprises a chlorine-containing substance; then performing a second etching process to etch the aluminum layer by providing a second etching gas, wherein the second etching gas does not comprise a chlorine-containing compound.
- According to the present invention, a method of anisotropically etching an aluminum layer is provided. The method comprises: providing an etching gas to etch the aluminum layer, wherein the etching gas comprises a chlorine-containing substance, but does not comprise a chlorine-containing compound.
- The method of etching a multi-layer in the present invention excludes chlorine-containing compound as an etching gas, not only providing a more simple process but also reducing the phenomenon of excess polymer residue and corrosion of aluminum layer, and leading to a better etching result.
- These and other objectives of the present invention will no doubt become obvious to those of ordinary skill in the art after reading the following detailed description of the preferred embodiment that is illustrated in the various figures and drawings.
-
FIG. 1 illustrates a cross sectional schematic diagram of a conventional method of forming a patterned aluminum layer. -
FIG. 2 illustrates a schematic diagram of a conventional aluminum corrosion reaction formed by the Clplasma. -
FIG. 3 illustrates a flow chart of etching a multi-layer in the present invention. -
FIG. 4 toFIG. 7 illustrate the structure schematic diagrams of each step of etching a multi-layer in the present invention. - Please refer to
FIG. 3 , illustrating a flow chart of etching a multi-layer in the present invention. As shown inFIG. 3 , the method of etching a multi-layer in the present invention comprises: - Step 100: providing a multi-layer disposed on a semiconductor substrate, wherein the multi-layer comprises at least an aluminum layer and an anti-reflection coating (ARC) layer disposed on the aluminum layer.
- Step 102: utilizing a patterned mask to perform a first etching process to etch the ARC layer by providing a first etching gas and a first passivation gas, wherein the first etching gas comprises a chlorine-containing substance.
- Step 104: after
step 102, performing a second etching process to etch the aluminum layer by providing a second etching gas and a second passivation gas, wherein the second etching gas does not comprise a chlorine-containing compound. - Step 106: after etching the aluminum layer, performing an over etching process to etch a barrier layer disposed under the aluminum layer.
- For more detailed descriptions of each step, please refer to
FIG. 4 toFIG. 7 , illustrating the structure schematic diagrams of each step of etching a multi-layer in the present invention. As shown inFIG. 4 andstep 100, a multi-layer on asemiconductor substrate 108 is provided. The multi-layer in series includes adielectric layer 110, abarrier layer 112, analuminum layer 114, anARC layer 116 and amask layer 122. Thedielectric layer 110 includes SiO2, SiN, SiC, tetraethoxysilane (TEOS), undoped silicon glass (USG), phosphorus silicon glass (PSG), boron phosphorus silicon glass (BPSG), other low-k dielectric material or the combination of above groups. Thebarrier layer 112 includes Ti/TiN, TaN, other suitable material or the combination of above groups. Thealuminum layer 114 may include conventional metal aluminum or aluminum alloy such as copper-aluminum alloy. TheARC layer 116 includes Ti/TiN or other suitable material. TheARC layer 116 may include a mono-layer structure or a double-layer structure, for example, a bottom ARC layer and a top ARC layer. The bottom ARC layer includes TiN. The top ARC layer may include the same material as the bottom ARC layer or include different materials, such as an organic anti-reflection material, or inorganic anti-refection material like silicon oxynitride (SiON). Themask layer 122 includes a patterned structure, such as a photoresist, wherein the pattern of themask layer 122 will be transferred to theARC layer 116 and thealuminum layer 114 in the subsequent etching steps. - Please refer to
FIG. 5 andstep 102. A first etching process is provided to etch theARC layer 116 but less to etch thealuminum layer 114. Afterstep 102 is performed,most ARC layer 116 is etched away and even a small part of thealuminum layer 114 is consumed. In some circumstance, a small part of theARC layer 116 may still be retained on thesubstrate 108. Afirst etching gas 126 and a first passivation gas are provided therefore. Thefirst etching gas 126 includes various kinds of chlorine-containing substance but does not include a chlorine-containing compound, for instance, using only chlorine gas but not using BCl3. In another embodiment of the present invention, thefirst etching gas 126 used to etch theARC layer 116 but less to etch thealuminum layer 114 may also include all chlorine-containing substances, which means using the chlorine gas and various kinds of chlorine-containing compounds at the same time, for example, using chlorine gas and BCl3 at the same time. The first passivation gas includes hydrocarbon or other suitable material, in the preferred embodiment of the present invention, the first passivation gas is ethylene (C2H4). - The first etching process is carried out in a plasma etching chamber. Table 1 provides a preferred etching recipe and operation condition when the
first etching gas 126 is chlorine gas. As shown in Table 1, the first etching process is performed under a condition as follows: a pressure between 12 and 18 mTorr, a RF power between 1200 and 1600 W, a bias power between 250 W and 350 W, a period between 120 and 180 seconds, a flow rate of chlorine gas between 150 and 210 sccm (standard cubic centimeter per minute) and a flow rate of ethylene between 120 and 180 sccm. The reaction time of the first etching process may be adjusted depending on the material or thickness of theARC layer 116. It can be longer or short and is not limited to Table 1. -
TABLE 1 Step Step 102 Step 104Step 106First etching Second etching Over etching process process process Time (sec) 150 End point 120 detection (max = 400) RF power (W) 1400 1500 1200 Bias power (W) 300 300 1500 Pressure (mTorr) 15 10 8 BCl3 (sccm) 0 0 100 Cl2 (sccm) 180 150 100 C2H4 (sccm) 150 150 150 - Please refer to
FIG. 6 and step 104. After etching theARC layer 116, a second etching process to etch thealuminum layer 114 is provided. Asecond etching gas 128 and a second passivation gas are provided. In order to avoid forming excess polymer residue that results in serious etching and corrosion of thealuminum layer 114 by using BCl3 in conventional arts, thesecond etching gas 128 in the present invention includes a chlorine-containing substance but does not include a chlorine-containing compound, for example, using only chlorine-containing substance such as chlorine gas but avoiding conventional chlorine-containing compound such as BCl3. The second passivation gas includes hydrocarbon or other suitable material, in the preferred embodiment of the present invention, the second passivation gas is C2H4. The second etching process can also be carried out in-situ in the plasma etching chamber. Referring to Table 1, the second etching process is performed under a condition as follows: a pressure between 8 and 12 mTorr, a RF power between 1300 and 1700 W, a bias power between 250 W and 350 W, a flow rate of the first etching gas between 120 and 180 sccm and a flow rate of the first passivation gas between 120 and 180 sccm. It is noted that the reaction time of the second etching process is determined by the end point detection. When the thickness of thealuminum layer 114 or other metal layer is changed, the reaction time of the second etching process is adjusted as well. The time listed in Table 1 provides one embodiment and the etching method of the present invention should not be limited thereto. - When finishing
step 102 and step 104, the pattern of themask layer 122 has been transferred to thealuminum layer 114, forming a patternedaluminum layer 114. Referring toFIG. 7 , as shown instep 106, an over etching process is in-situ provided. Athird etching gas 130 is provided to etch thebarrier layer 112 and some remainedaluminum layer 114 on thesubstrate 108. A part of thedielectric layer 110 may be consumed in the third etching process to make sure thealuminum layer 114 and thebarrier layer 112 being etched away completely. The etching recipe and operation condition are shown in Table 1, which is not described in detail. Afterstep 106, the polymer residue is flushed by argon gas and themask layer 122 is removed, the patternedaluminum layer 114 is thus completed. - As described above, BCl3 is usually used as an etching and a passivation gas in conventional arts, which may results in excess polymer residue formed on the sidewall of the patterned aluminum layer and thus brings to the serious etching and even corrosion of the aluminum layer. The present invention therefore provides an etching method that avoids using chlorine-containing compound such as BCl3 as an etching gas, and in combination with a passivation gas such as hydrocarbon. In conventional arts, BCl3 produces sidewall polymer by bombarding the mask layer, but the formed sidewall polymer is usually not compact. In contrast, hydrocarbon has longer polymer chains and thus more condensed structure ([C—H]x), it can completely replace the passivation function of BCl3. The sidewall protection is not reduced with the removal of BCl3. On the contrary, removing BCl3 can avoid corrosion of the aluminum layer caused by too much Clplasma trapped in the polymer residue. As a result, the method of etching a multi-layer in the present invention not only provides a simpler process by removing chlorine-containing compound as an etching gas, but also can reduce the phenomenon of excess polymer residue and corrosion of aluminum layer, leading to a better etching result.
- Those skilled in the art will readily observe that numerous modifications and alterations of the device and method may be made while retaining the teachings of the invention.
Claims (20)
1. A method of etching a multi-layer, the multi-layer comprising an aluminum layer disposed on a semiconductor substrate and an anti-reflection coating (ARC) layer disposed on the aluminum layer, the method comprising:
performing a first etching process to etch the ARC layer by providing a first etching gas, wherein the first etching gas comprises a chlorine-containing substance; and
performing a second etching process to etch the aluminum layer by providing a second etching gas, wherein the second etching gas does not comprise a chlorine-containing compound.
2. The method as in claim 1 , wherein the chlorine-containing compound comprises BCl3.
3. The method as in claim 1 , wherein the second etching gas comprises chlorine gas.
4. The method as in claim 1 , wherein the first etching gas comprises chlorine gas and BCl3.
5. The method as in claim 1 , wherein the first etching gas comprises chlorine gas.
6. The method as in claim 1 , wherein the first etching process further comprises providing a first passivation gas.
7. The method as in claim 6 , wherein the first passivation gas comprises hydrocarbon.
8. The method as in claim 6 , wherein the first passivation gas comprises ethylene (C2H4).
9. The method as in claim 1 , wherein the second etching process further comprises providing a second passivation gas.
10. The method as in claim 9 , wherein the second passivation gas comprises hydrocarbon.
11. The method as in claim 9 , wherein the second passivation gas comprises ethylene.
12. The method as in claim 6 , wherein the first etching process is performed under a condition as follows: a pressure between 12 and 18 mTorr, a RF power between 1200 and 1600 W, a bias power between 250 W and 350 W, a period between 120 and 180 seconds, a flow rate of the first etching gas between 150 and 210 sccm and a flow rate of the first passivation gas between 120 and 180 sccm.
13. The method as in claim 9 , wherein the second etching process is performed under a condition as follows: a pressure between 8 and 12 mTorr, a RF power between 1300 and 1700 W, a bias power between 250 W and 350 W, a flow rate of the second etching gas between 120 and 180 sccm and a flow rate of the second passivation gas between 120 and 180 sccm.
14. A method of anisotropically etching an aluminum layer, comprising: providing an etching gas to etch the aluminum layer, wherein the etching gas comprises a chlorine-containing substance, but does not comprise a chlorine-containing compound.
15. The method as in claim 14 , wherein the chlorine-containing compound comprises BCl3.
16. The method as in claim 14 , wherein the etching gas comprises chlorine gas.
17. The method as in claim 14 , further comprising providing a passivation gas.
18. The method as in claim 17 , wherein the passivation gas comprises hydrocarbon.
19. The method as in claim 17 , wherein the passivation gas comprises ethylene.
20. The method as in claim 17 , wherein the etching process is performed under a condition as follows: a pressure between 8 and 12 mTorr, a RF power between 1300 and 1700 W, a bias power between 250 W and 350 W, a flow rate of the etching gas between 120 and 180 sccm and a flow rate of the passivation gas between 120 and 180 sccm.
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US20110306215A1 (en) * | 2010-06-14 | 2011-12-15 | Applied Materials, Inc. | Methods of processing substrates having metal materials |
US20140045338A1 (en) * | 2011-02-08 | 2014-02-13 | Tokyo Electron Limited | Plasma etching method |
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US20020016071A1 (en) * | 1999-03-24 | 2002-02-07 | Shao-Wen Hsia | Method and apparatus for high-resolution in-situ plasma etching of inorganic and metal films |
US7270761B2 (en) * | 2002-10-18 | 2007-09-18 | Appleid Materials, Inc | Fluorine free integrated process for etching aluminum including chamber dry clean |
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US6309979B1 (en) * | 1996-12-18 | 2001-10-30 | Lam Research Corporation | Methods for reducing plasma-induced charging damage |
US6146542A (en) * | 1998-01-09 | 2000-11-14 | Hyundia Electronics Industries Co., Ltd. | Dry etching method of multilayer film |
US20020016071A1 (en) * | 1999-03-24 | 2002-02-07 | Shao-Wen Hsia | Method and apparatus for high-resolution in-situ plasma etching of inorganic and metal films |
US7270761B2 (en) * | 2002-10-18 | 2007-09-18 | Appleid Materials, Inc | Fluorine free integrated process for etching aluminum including chamber dry clean |
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US20110306215A1 (en) * | 2010-06-14 | 2011-12-15 | Applied Materials, Inc. | Methods of processing substrates having metal materials |
US8435419B2 (en) * | 2010-06-14 | 2013-05-07 | Applied Materials, Inc. | Methods of processing substrates having metal materials |
US20140045338A1 (en) * | 2011-02-08 | 2014-02-13 | Tokyo Electron Limited | Plasma etching method |
KR20140051128A (en) * | 2011-02-08 | 2014-04-30 | 도쿄엘렉트론가부시키가이샤 | Plasma etching method |
US8975191B2 (en) * | 2011-02-08 | 2015-03-10 | Tokyo Electron Limited | Plasma etching method |
KR101894613B1 (en) | 2011-02-08 | 2018-10-04 | 도쿄엘렉트론가부시키가이샤 | Plasma etching method |
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