US20040154929A1 - Electroless copper plating of electronic device components - Google Patents
Electroless copper plating of electronic device components Download PDFInfo
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- US20040154929A1 US20040154929A1 US10/669,633 US66963303A US2004154929A1 US 20040154929 A1 US20040154929 A1 US 20040154929A1 US 66963303 A US66963303 A US 66963303A US 2004154929 A1 US2004154929 A1 US 2004154929A1
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- Prior art keywords
- copper
- substrate
- electroless
- ions
- composition
- Prior art date
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- 239000010949 copper Substances 0.000 title claims abstract description 63
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 60
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 59
- 238000007747 plating Methods 0.000 title abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 42
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000000758 substrate Substances 0.000 claims abstract description 22
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000008139 complexing agent Substances 0.000 claims abstract description 8
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 238000007772 electroless plating Methods 0.000 claims description 16
- -1 Cu++ ions Chemical class 0.000 claims description 13
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 3
- 239000003638 chemical reducing agent Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001913 cyanates Chemical class 0.000 claims description 2
- 229910001385 heavy metal Inorganic materials 0.000 claims description 2
- 150000003222 pyridines Chemical class 0.000 claims description 2
- 229910001431 copper ion Inorganic materials 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 239000000463 material Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000002861 polymer material Substances 0.000 claims 1
- 239000002210 silicon-based material Substances 0.000 claims 1
- 230000008021 deposition Effects 0.000 abstract description 14
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- 238000000576 coating method Methods 0.000 abstract description 9
- 230000009467 reduction Effects 0.000 abstract description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 abstract description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 abstract description 4
- 239000000654 additive Substances 0.000 abstract description 4
- 229940071826 hydroxyethyl cellulose Drugs 0.000 abstract description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 abstract description 4
- 230000004913 activation Effects 0.000 abstract description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 2
- 230000000977 initiatory effect Effects 0.000 abstract description 2
- 239000006259 organic additive Substances 0.000 abstract description 2
- 229920000620 organic polymer Polymers 0.000 abstract description 2
- 229920001983 poloxamer Polymers 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- 229920000151 polyglycol Polymers 0.000 abstract description 2
- 239000010695 polyglycol Substances 0.000 abstract description 2
- 229920005862 polyol Polymers 0.000 abstract description 2
- 150000003077 polyols Chemical class 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 14
- 238000000151 deposition Methods 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 238000009713 electroplating Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 235000012431 wafers Nutrition 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- 229910000990 Ni alloy Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 239000005297 pyrex Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 241000036313 Cupressus torulosa Species 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000454 electroless metal deposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000013532 laser treatment Methods 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
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
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/31—Coating with metals
- C23C18/38—Coating with copper
- C23C18/40—Coating with copper using reducing agents
- C23C18/405—Formaldehyde
Definitions
- This invention relates to the manufacture of metal components, such as lines, vias, and trenches, utilized in the production of semiconductor devices and Printed Circuit Boards (PCBs), and more particularly, to an improved method and composition for applying electroless copper.
- Electrolytic reduction deposits high quality metal.
- the present invention provides a method and composition that improve the deposition plating rate of electroless copper.
- the invention presents embodiments comprising using elevated plating temperatures, coupled with suitably designed bath compositions, to preserve the electroless bath stability, required to improve the deposition plating rate of electroless copper.
- the present invention also provides a method and composition that improves the quality of electroless copper coatings or films, without lowering the rate of deposition, by combining elevated interfacial substrate or solution temperatures with suitably engineered solution chemistry.
- the electroless bath composition comprises suitable individual Cu ++ and Cu + complexing agent(s), or a combination of complexing agents, surfactants, organic polymer additives, and the like, many of which can be adapted from the prior art, and suitably optimized.
- potential organic additive types or surfactants can be Polyoxes; Pluronics; Polyols; Polyglycols. Carbowaxes; Hydroxy ethyl cellulose (HEC), carboxy acetylenic, or fluocarbon acetylenic surfactants.
- the method and composition of the present invention enable the production of electroless copper coatings with improved adhesion to the substrate. This is achieved by selecting activation systems that result in copper initiation at moderate rates.
- An electroless copper composition assists, in that it too, ensures slow initial copper reduction at the substrate-solution interface.
- an electroless copper composition especially designed for slow “take-off” of the initial copper layer.
- This composition may differ from the electroless copper composition, designed to give the desired copper thickness.
- the initial metal films can be very thin, often no more than a few Angstroms thick, optimizable through routine experimentation
- the method of the invention affords electroless plating on non-conducting substrates without the use of precious metal sensitization. Examples of similar methods and compositions are disclosed in Israeli pending applications # 150364, 150577 and 150940.
- the present invention provides a method and composition that improve the deposition plating rate of electroless copper.
- the invention presents embodiments comprising using elevated plating temperatures at the substrate-solution interface. This is coupled with suitably designed bath compositions, to preserve the electroless bath stability, required to improve the deposition plating rate of electroless copper. Elevated plating temperatures can be attained by heating the electroless copper plating bath, by heating the substrate to the desired temperature (exemplified to some extent in US Pat. 2002/0086102), or by a combination of the two approaches.
- the electroless plating solution When choosing to heat the substrate, it is recommended to dispense the electroless plating solution onto the substrate by using spraying or splashing techniques. In the latter case, the electroless plating solution should be stored in a storage vessel and recirculated, as is done in well-known processes involving photoresist developing solutions. A technique known as puddle development is used. This embodiment offers several advantages, some of which are listed below:
- the wafer to be plated can be spun during deposition. This is similar to techniques widely practiced in wafer lithography, which result in interfacial solution movement, contributing to improved adhesion and plate quality.
- the wafer can be heated selectively using thermal laser treatment, resulting in selective plating, as a potential means of achieving a desired copper pattern.
- Interfacial substrate-solution plating temperatures can be well over the boiling temperature of the electroless composition.
- a preferred composition disclosed by the present invention comprises the following:
- a complexor or a combination of complexors that afford superior bath stability at elevated temperatures. They will not form an overly “tight” or strong complex that would negatively impact the rate of copper deposition. For example, EDTA strongly complexes cupric copper, but it tends to diminish the rate of deposition. On the other hand, Rochelle salt tends to give high plating speeds, but fragile electroless solution stability.
- An optional embodiment of this patent comprises therefore, a blend of complexors, to balance bath stability and, rate considerations.
- Stabilizers monovalent copper (Cu+) complexors. Generally, these are other than thio derivatives and the like, which tend to result in stressed deposits, and can negatively impact Cu film quality. Desirable additives will comprise derivatives of pyridine (i.e. bipyridine), cyanides (i.e. alkali metal cyanides), cyanates, heavy metal cyanide complexes (i.e. ferrocyanides), and the like, many of which can found in the prior art literature and optimized through trial-and error experimentation.
- pyridine i.e. bipyridine
- cyanides i.e. alkali metal cyanides
- cyanates cyanates
- heavy metal cyanide complexes i.e. ferrocyanides
- electroless copper compositions of this invention can advantageously contain relatively high concentrations of stabilizing additives, such as bipyridine, significantly above levels or concentrations disclosed in the prior art. The reason perhaps lies in combining elevated operating temperatures with suitable electroless bath compositions, as suggested in this invention.
- the embodiment of the present invention that focuses on improving plate quality will comprise:
- Annealing of the as-plated deposit to relieve stresses.
- overheating is not an issue. They are known to undergo very high temperature processes without causing major defects. Although the risk of copper migration exists, the present invention minimizes it.
- the sample Prior to being immersed in the Micro-Via composition, the sample was immersed for 5 min. in a working solution of 9072*, then transferred without a water rinse to the Micro-Via composition.
- the sample was made of double-sided copper-epoxy, containing interconnecting holes.
- step a Prior to step a, the sample was contacted with Metex 9221-S*, Metex 9275*, and Metex G-3*. Water rinsing following each process step.
- Plating time in the Micro-Via was approximately 6-7 hours, with 2-ml formaldehyde added every 2 hours to one liter of Micro-Via.
- Formaldehyde was increased by 10 g/l.
- a Pyrex glass plate was processed as in EXAMPLE 1, except:
- electroless copper it encompasses other electroless metal depositions, such as electroless nickel, cobalt, alloys of nickel or copper, and the like.
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Abstract
A method and composition for improving the deposition plating rate of electroless copper. The invention presents embodiments comprising using elevated plating temperatures at the substrate-solution interface. This is coupled with suitably designed bath compositions, to preserve the electroless bath stability, required to improve the deposition plating rate of electroless copper. In one embodiment, the electroless bath composition comprises suitable individual Cu++ and Cu+ complexing agent(s), or a combination of complexing agents, surfactants, organic polymer additives, and the like, adapted and suitably optimized. For example, potential organic additive types or surfactants can be Polyoxes; Pluronics; Polyols; Polyglycols; Carbowaxes; Hydroxy ethyl cellulose (HEC), carboxy acetylenic, or fluocarbon acetylenic surfactants. The method and composition of the present invention enable the production of electroless copper coatings with improved adhesion to the substrate. This is achieved by selecting activation systems that result in copper initiation at moderate rates. An electroless copper composition assists, in that it too, ensures slow initial copper reduction at the substrate-solution interface.
Description
- This invention relates to the manufacture of metal components, such as lines, vias, and trenches, utilized in the production of semiconductor devices and Printed Circuit Boards (PCBs), and more particularly, to an improved method and composition for applying electroless copper.
- US Pat. 2002/0011416 A1 (Landau), U.S. Pat. No. 6,319,831 (Tsai) and U.S. Pat. No. 6,180,523 (Lee) are indicative of the prior art.
- Copper has increasingly gained prominence as the preferred metal in prior art interconnect technology, due to its low cost and superior conductivity. Hence, the recent technological focus in the semiconductor devices and Printed Circuit Boards production industries on developing manufacturing techniques and compositions to improve the current state-of-the art for applying electroless copper plating.
- Today, the reduction or deposition of copper metal from solution, is performed either by electrolytic or electroless plating. Currently, the industry favors electrolytic plating (electroplating) over electroless plating. To understand this preferrence, consider some of the salient advantages and disadvantages of each process, as listed below:
- Advantages of electroplating:
- 1. Relatively low production cost per unit weight of plated copper, since the reduction process of Cu ++ to Cuo (copper metal) is performed using low cost electrical current.
- 2. Electrolytic reduction deposits high quality metal.
- 3. Higher rate of deposition, typically 20-25 micron films achievable in one hour or less, enabling higher throughput.
- 4. Lower waste generation rate.
- Disadvantages of electroplating:
- 1. High capital investment and equipment maintenance cost.
- 2. Stringent process window.
- 3. Limited deposit-application capability, resulting in a lack of uniformity in the deposited copper film thickness. Especially problematic, in view of the increasing trend towards plating high aspect-ratio geometries, of vias, microvias, trenches and other metal components.
- Advantages of electroless plating:
- 1. Low capital investment and control instrumentation cost.
- 2. Low equipment maintenance and installation cost.
- 3. Excellent thickness uniformity of plated Cu film. This feature is of special significance when plating high aspect-ratio geometries.
- Disadvantages of electroless plating:
- 1. Lower rate of deposition, typically 20 hours or more, to deposit a 20-25 micron film, resulting in low production throughput.
- 2. Higher plating cost per unit weight of plated copper, due to the use of additional chemicals, as opposed to inexpensive electrochemical reduction that uses electrical current.
- 3. Inferior plate quality that can result in functional device failure, as for example, when the components are subjected to thermal stress.
- 4. Low copper-to-substrate adhesion.
- 5. Greater waste generation rate than in electroplating.
- The most attractive feature of electroless plating is its inherent deposited plate thickness uniformity. Its most problematic attributes are its low rate of deposition and its inferior functional plate quality. If the aforementioned problematic attributes were minimized or eliminated, electroless plating would most probably supplant electroplating as the preferred plating process for the production of semiconductor devices and Printed Circuit Boards.
- Accordingly, it is a principal object of the present invention to overcome the above-mentioned problems and provide an improved method and composition for applying electroless copper, that will enable electroless copper plating to become a preferred alternative to electroplating, for the fabrication of electronic devices.
- The present invention provides a method and composition that improve the deposition plating rate of electroless copper. To achieve this, the invention presents embodiments comprising using elevated plating temperatures, coupled with suitably designed bath compositions, to preserve the electroless bath stability, required to improve the deposition plating rate of electroless copper.
- The present invention also provides a method and composition that improves the quality of electroless copper coatings or films, without lowering the rate of deposition, by combining elevated interfacial substrate or solution temperatures with suitably engineered solution chemistry. In one embodiment the electroless bath composition comprises suitable individual Cu ++ and Cu+ complexing agent(s), or a combination of complexing agents, surfactants, organic polymer additives, and the like, many of which can be adapted from the prior art, and suitably optimized. For example, potential organic additive types or surfactants can be Polyoxes; Pluronics; Polyols; Polyglycols. Carbowaxes; Hydroxy ethyl cellulose (HEC), carboxy acetylenic, or fluocarbon acetylenic surfactants.
- The method and composition of the present invention enable the production of electroless copper coatings with improved adhesion to the substrate. This is achieved by selecting activation systems that result in copper initiation at moderate rates. An electroless copper composition assists, in that it too, ensures slow initial copper reduction at the substrate-solution interface.
- In some instances it may be beneficial to expose the surface to be plated to an electroless copper composition especially designed for slow “take-off” of the initial copper layer. This composition may differ from the electroless copper composition, designed to give the desired copper thickness.
- In many instances it may be advisable to deposit an initial film, immediately adjacent to the substrate-to be-plated, prior to plating electroless copper. This initial film deposit helps achieve improved adhesion, but more importantly, helps reduce copper migration. Potential candidates for “non-copper” films are electroless nickel, cobalt, gold, and alloys of copper or nickel. U.S. Pat. No. 4,482,596 to Gulla, discloses one such method and composition that plates electroless nickel or copper coatings. Others can be found in the prior art literature.
- The initial metal films can be very thin, often no more than a few Angstroms thick, optimizable through routine experimentation
- The method of the invention affords electroless plating on non-conducting substrates without the use of precious metal sensitization. Examples of similar methods and compositions are disclosed in Israeli pending applications # 150364, 150577 and 150940.
- The present invention provides a method and composition that improve the deposition plating rate of electroless copper. The invention presents embodiments comprising using elevated plating temperatures at the substrate-solution interface. This is coupled with suitably designed bath compositions, to preserve the electroless bath stability, required to improve the deposition plating rate of electroless copper. Elevated plating temperatures can be attained by heating the electroless copper plating bath, by heating the substrate to the desired temperature (exemplified to some extent in US Pat. 2002/0086102), or by a combination of the two approaches.
- When choosing to heat the substrate, it is recommended to dispense the electroless plating solution onto the substrate by using spraying or splashing techniques. In the latter case, the electroless plating solution should be stored in a storage vessel and recirculated, as is done in well-known processes involving photoresist developing solutions. A technique known as puddle development is used. This embodiment offers several advantages, some of which are listed below:
- Avoiding excessively high temperature electroless baths that may lead to their decomposition.
- The wafer to be plated can be spun during deposition. This is similar to techniques widely practiced in wafer lithography, which result in interfacial solution movement, contributing to improved adhesion and plate quality.
- The wafer can be heated selectively using thermal laser treatment, resulting in selective plating, as a potential means of achieving a desired copper pattern.
- Interfacial substrate-solution plating temperatures can be well over the boiling temperature of the electroless composition.
- The above embodiment, wherein the substrate to be metallized, i.e. the wafer, is kept “hot”, via contact with a heat source, or via radiant heat such as IR, thermal laser, microwave, and induction current, during electroless plating, coupled with “accommodating”, tailor-made electroless copper chemistries, offers new possibilities for process improvements to those skilled in the art of electroless plating.
- A preferred composition disclosed by the present invention comprises the following:
- A complexor or a combination of complexors, that afford superior bath stability at elevated temperatures. They will not form an overly “tight” or strong complex that would negatively impact the rate of copper deposition. For example, EDTA strongly complexes cupric copper, but it tends to diminish the rate of deposition. On the other hand, Rochelle salt tends to give high plating speeds, but fragile electroless solution stability. An optional embodiment of this patent comprises therefore, a blend of complexors, to balance bath stability and, rate considerations.
- In choosing the desired complexor blend, one can be guided by the stability constant of copper complexors listed in appropriate handbooks.
- High reducer or copper ratios, again to favor rate.
- Stabilizers, monovalent copper (Cu+) complexors. Generally, these are other than thio derivatives and the like, which tend to result in stressed deposits, and can negatively impact Cu film quality. Desirable additives will comprise derivatives of pyridine (i.e. bipyridine), cyanides (i.e. alkali metal cyanides), cyanates, heavy metal cyanide complexes (i.e. ferrocyanides), and the like, many of which can found in the prior art literature and optimized through trial-and error experimentation.
- It was discovered that electroless copper compositions of this invention can advantageously contain relatively high concentrations of stabilizing additives, such as bipyridine, significantly above levels or concentrations disclosed in the prior art. The reason perhaps lies in combining elevated operating temperatures with suitable electroless bath compositions, as suggested in this invention.
- The embodiment of the present invention that focuses on improving plate quality will comprise:
- Annealing of the as-plated deposit, to relieve stresses. In choosing suitable annealing time or temperature conditions, one needs to guard against “overheating”, that may lead to degradation of the workpiece, as for example, glass or epoxy laminates of PCBs. In the case of silica wafers, “overheating” is not an issue. They are known to undergo very high temperature processes without causing major defects. Although the risk of copper migration exists, the present invention minimizes it.
- The capabilities of the present invention are further illustrated in the following examples:
- Notes:
- 1. The sign (*) denotes, throughout this disclosure, products supplied in Israel by MacDermid Israed Ltd. and used in accordance to supplier's instructions.
- 2. The sample was exposed to the above process steps by immersion.
- 3. Following each process step, the sample was rinsed with water,
- A 3″×3″ copper clad glass-epoxy pane, from which the copper has been etched away, was processed according to the following procedure:
- a. Metex Conditioner 90*
- b. Water rinse.
- c. Metex G-3*
- d. Mactivate 10*
- e. Metex 9071*
- f. Aqueous solution of Na 3PO4, 5 min., RT.
- g. Immerse for 2 hours, 70 deg.C, with intermittent work agitation in the following electroless copper solution, hereinafter referred to as “Micro-Via” composition.
Component Concentration CuSO4, 5 H2O 15 g/l EDTA 25 g/l Quadrol 6 g/l Formaldehyde 37% 33 g/l NaOH 13 g/l Bipyridine 100 ppm NaCN 18 ppm Petro Ag 10 ppm - h. Water rinse
- i. Dry
- Upon examination, the sample displayed a pink copper coating, with good adhesion (no apparent blisters or lifting of the deposit). Coating thickness was measured to be 8 microns thick.
- Same as EXAMPLE 1, except:
- Prior to being immersed in the Micro-Via composition, the sample was immersed for 5 min. in a working solution of 9072*, then transferred without a water rinse to the Micro-Via composition.
- After two hours in the Micro-Via, the sample was water-rinsed and dried. The copper coating showed blistering or lifting from the substrate. Coating thickness was about 8 microns.
- Same process steps as in EXAMPLE 1, except:
- The sample was made of double-sided copper-epoxy, containing interconnecting holes.
- Prior to step a, the sample was contacted with Metex 9221-S*, Metex 9275*, and Metex G-3*. Water rinsing following each process step.
- Plating time in the Micro-Via was approximately 6-7 hours, with 2-ml formaldehyde added every 2 hours to one liter of Micro-Via.
- After rinsing with water and drying, copper thickness in the holes was approximately 20 microns. After baking for approximately 24 hours in an air-circulating oven at approximately 150 deg C., no lifting of the plate from the substrate was observed. It was then exposed to the industry-accepted solder shock test. Metallurgical examination of the holes showed reasonable copper plate integrity and adhesion.
- Same as EXAMPLE 1, except;
- Formaldehyde was increased by 10 g/l.
- 50 μl sodium carbonate was added and dissolved
- After plating for 1 hour, no lifting of the deposit was observed, and thickness was determined as 3 microns.
- Same as EXAMPLE 4, except:
- Sodium carbonate was increased to 100 g/l.
- After plating for one hour, thickness was measured at 4.5 micron, and the copper coating showed some lifting.
- A Pyrex glass plate was processed as in EXAMPLE 1, except:
- After Mactivate 10* it was heated on a hot plate to a temperature estimated at over 200 deg. C.
- Then about 100 cc of Macudep 22* solution (made up with 20% of Macudep* concentrate A, 20% concentrate B, and the balance DI water) was dispensed onto it.
- After about 5 sec., a copious pink-colored copper layer covered the Pyrex plate.
- Having described the invention with regard to certain specific embodiments, it is to be understood that the description is not meant as a limitation since further modifications may now suggest themselves to those skilled in the art, and it is intended to cover such modifications, as fall within the scope of the appended claims, namely combining elevated substrate temperature with suitably optimized electroless solution chemistry.
- Also, while the invention has been described in terms of electroless copper, it encompasses other electroless metal depositions, such as electroless nickel, cobalt, alloys of nickel or copper, and the like.
Claims (19)
1. A composition for electroless plating of copper on a substrate, comprising copper ions, a complexing agent for Cu++ ions, a complexing agent for Cu+ ions, a reducing agent capable of reducing copper ions to metallic copper and hydroxide ions to a pH of at least 10.
2. A composition for electroless plating of copper on a substrate, comprising copper ions, a mixture of complexing agents for Cu++ ions, a mixture of complexing agents for Cu+ ions, a reducing agent capable of reducing copper ions to metallic copper and hydroxide ions to a pH of at least 10.
3. A composition according to claim 1 , wherein said agent that forms a complex with Cu++ ions is selected from a group consisting of EDTA, Quadrol and mixtures thereof.
4. A composition according to claim 1 , wherein said agent that forms a complex with Cu+ ions is selected from a group consisting of derivatives of pyridine, alkali metal cyanides, cyanates and heavy metal cyanide complexes.
5. A composition according to claim 4 , comprising at least 10 ppm of said agent that forms a complex with Cu+ ions.
6. A composition according to claim 4 , comprising at least 20 ppm of bipyridine.
7. A composition according to claim 1 , further comprising at least one surfactant.
8. An improved method for electroless plating of copper on a substrate using an electroless composition according to claim 1 .
9. An improved method for electroless plating of copper on a substrate using an electroless composition according to claim 2 .
10. A method according to claim 8 , further comprising heating the substrate to a temperature above the operating temperature of the electroless plating bath.
11. A method according to claim 10 , wherein at least part of the surface of said substrate is non-metallic.
12. A method according to claim 8 , wherein the substrate is flat.
13. A method according to claim 9 , wherein the substrate is flat.
14. A method according to claim 8 , wherein the substrate is made of
material selected from a group consisting of copper-clad polymer and silicon material.
15. A method according to claim 14 , wherein the substrate comprises vias and trenches.
16. An article manufactured by the method of claim 8 .
17. An article manufactured by the method of claim 9 .
18. An article manufactured by the method of claim 10 .
19. An article manufactured by the method of claim 11.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL15349802A IL153498A0 (en) | 2002-12-17 | 2002-12-17 | Electroless copper metallization of electronic devices |
| IL153498 | 2002-12-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040154929A1 true US20040154929A1 (en) | 2004-08-12 |
Family
ID=29798374
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/669,633 Abandoned US20040154929A1 (en) | 2002-12-17 | 2003-09-25 | Electroless copper plating of electronic device components |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20040154929A1 (en) |
| IL (1) | IL153498A0 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060194431A1 (en) * | 2005-02-28 | 2006-08-31 | Markus Nopper | Technique for metal deposition by electroless plating using an activation scheme including a substrate heating process |
| CN102534583A (en) * | 2010-12-08 | 2012-07-04 | 比亚迪股份有限公司 | Chemical copper-plating solution and chemical copper-plating method |
| WO2014154702A1 (en) * | 2013-03-27 | 2014-10-02 | Atotech Deutschland Gmbh | Electroless copper plating solution |
| US20160053379A1 (en) * | 2013-03-27 | 2016-02-25 | Atotech Deutschland Gmbh | Electroless copper plating solution |
| EP3578683A1 (en) * | 2018-06-08 | 2019-12-11 | ATOTECH Deutschland GmbH | Electroless copper or copper alloy plating bath and method for plating |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4199623A (en) * | 1974-11-01 | 1980-04-22 | Kollmorgen Technologies Corporation | Process for sensitizing articles for metallization and resulting articles |
| US4908242A (en) * | 1986-10-31 | 1990-03-13 | Kollmorgen Corporation | Method of consistently producing a copper deposit on a substrate by electroless deposition which deposit is essentially free of fissures |
-
2002
- 2002-12-17 IL IL15349802A patent/IL153498A0/en unknown
-
2003
- 2003-09-25 US US10/669,633 patent/US20040154929A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4199623A (en) * | 1974-11-01 | 1980-04-22 | Kollmorgen Technologies Corporation | Process for sensitizing articles for metallization and resulting articles |
| US4908242A (en) * | 1986-10-31 | 1990-03-13 | Kollmorgen Corporation | Method of consistently producing a copper deposit on a substrate by electroless deposition which deposit is essentially free of fissures |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060194431A1 (en) * | 2005-02-28 | 2006-08-31 | Markus Nopper | Technique for metal deposition by electroless plating using an activation scheme including a substrate heating process |
| US7560381B2 (en) * | 2005-02-28 | 2009-07-14 | Advanced Micro Devices, Inc. | Technique for metal deposition by electroless plating using an activation scheme including a substrate heating process |
| CN102534583A (en) * | 2010-12-08 | 2012-07-04 | 比亚迪股份有限公司 | Chemical copper-plating solution and chemical copper-plating method |
| WO2014154702A1 (en) * | 2013-03-27 | 2014-10-02 | Atotech Deutschland Gmbh | Electroless copper plating solution |
| US20160053379A1 (en) * | 2013-03-27 | 2016-02-25 | Atotech Deutschland Gmbh | Electroless copper plating solution |
| US9650718B2 (en) * | 2013-03-27 | 2017-05-16 | Atotech Deutschland Gmbh | Electroless copper plating solution |
| EP3578683A1 (en) * | 2018-06-08 | 2019-12-11 | ATOTECH Deutschland GmbH | Electroless copper or copper alloy plating bath and method for plating |
| WO2019234085A1 (en) | 2018-06-08 | 2019-12-12 | Atotech Deutschland Gmbh | Electroless copper or copper alloy plating bath and method for plating |
| US11396706B2 (en) | 2018-06-08 | 2022-07-26 | Atotech Deutschland Gmbh | Electroless copper or copper alloy plating bath and method for plating |
Also Published As
| Publication number | Publication date |
|---|---|
| IL153498A0 (en) | 2003-07-06 |
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