WO2003002782A1 - Method of making a nickel-coated copper substrate and thin film composite containing the same - Google Patents

Method of making a nickel-coated copper substrate and thin film composite containing the same Download PDF

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Publication number
WO2003002782A1
WO2003002782A1 PCT/IB2001/001201 IB0101201W WO03002782A1 WO 2003002782 A1 WO2003002782 A1 WO 2003002782A1 IB 0101201 W IB0101201 W IB 0101201W WO 03002782 A1 WO03002782 A1 WO 03002782A1
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Prior art keywords
nickel
copper substrate
coated copper
thin film
substrate
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PCT/IB2001/001201
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French (fr)
Inventor
Mark Farrell
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Energenius, Inc.
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Publication date
Application filed by Energenius, Inc. filed Critical Energenius, Inc.
Priority to CNB018118968A priority Critical patent/CN1318646C/en
Priority to JP2003508744A priority patent/JP2004530584A/en
Priority to EP01945555A priority patent/EP1399602A1/en
Priority to PCT/IB2001/001201 priority patent/WO2003002782A1/en
Publication of WO2003002782A1 publication Critical patent/WO2003002782A1/en

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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • C23C14/16Metallic material, boron or silicon on metallic substrates or on substrates of boron or silicon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/08Oxides
    • C23C14/088Oxides of the type ABO3 with A representing alkali, alkaline earth metal or Pb and B representing a refractory or rare earth metal
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5806Thermal treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/322Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
    • C23C28/3455Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer with a refractory ceramic layer, e.g. refractory metal oxide, ZrO2, rare earth oxides or a thermal barrier system comprising at least one refractory oxide layer

Definitions

  • This invention relates to a method of making a nickel-coated copper substrate for use in a thin film composite and thin film composites containing such nickel-coated copper substrates.
  • Energy storage devices made of thin film composites have been found to be useful in electronic and optoelectronic applications, such as ferroelectric memory devices, pyroelectronic sensor devices, waveguide modulators, and acoustic sensors.
  • thin film composites are used in a variety of semiconductor integrated circuit devices such as analog circuits, rf circuits, and dynamic random access memories (DRAM's).
  • the composites are usually composed of a substrate, a dielectric, and an electrode; the dielectric being between the substrate and the electrode.
  • Substrates are commonly composed of copper, silicon, fused silica, platinum-coated silicon, alumina, sapphire, platinum-coated sapphire, or a single crystal SrTiO substrate.
  • Copper is often preferred as a substrate in light of its ready availability.
  • thin film composites having copper substrates often evidence thermal migration and outgassing.
  • Thermal migration is the migration of copper ions into the dielectric and of ions in the dielectric into the substrate at elevated temperatures.
  • Outgassing occurs when gaseous copper atoms escape from the substrate into either the dielectric or the oven in which deposition of the dielectric occurs.
  • a copper substrate which eliminates these drawbacks is desired.
  • the invention relates to a method of preparing a copper substrate having nickel deposited thereon.
  • the invention relates to thin film composites containing such nickel-coated copper substrates.
  • the nickel-coated substrate is prepared by depositing nickel onto the copper and then annealing the resulting substrate.
  • the copper may be a foil. After annealing, a dielectric may be deposited onto the substrate by methods known in the art such as by sol-gel or vacuum deposition techniques.
  • FIG. 1 is a graph depicting optimum temperatures and durations for annealing the nickel-coated substrate in accordance with the process of the invention
  • FIG. 2 is an internal structure of a nickel-coated copper substrate pre-annealed at
  • FIG. 3 is an internal structure of a nickel-coated copper substrate pre-annealed at
  • FIGS. 4 and 5 are internal structures of a nickel-coated copper substrate pre- annealed at a temperature of 800° C for 20 minutes using a scanning electron microscope.
  • FIG. 6 is an internal structure of a nickel-coated copper substrate pre-annealed at a temperature of 500° C for 90 minutes using a scanning electron microscope.
  • FIG. 7 is an internal structure of a nickel-coated copper substrate pre-annealed at a temperature of 650° C for 30 minutes using a scanning electron microscope.
  • FIG. 8 depicts a thin film composite in accordance with the invention having a copper substrate coated on its top and bottom surfaces with nickel, a dielectric, an optional barrier or buffer layer, and a top electrode.
  • FIG. 9 depicts a thin film composite in accordance with the invention having a copper substrate completely enveloped by nickel.
  • the thin film composites in accordance with the invention contain a nickel-coated copper substrate and a dielectric.
  • the substrate is prepared by depositing nickel onto copper.
  • the nickel may be deposited on one or both sides of the copper substrate.
  • the nickel encapsulates the copper substrate.
  • the nickel-deposited copper substrate is then annealed at a temperature between approximately 400°C and 820°C, preferably approximately 800°C.
  • the optimum temperature between approximately 400°C and 820°C, preferably approximately 800°C.
  • duration of annealing varies with the annealing temperature. For example, annealing at 400°C desirably lasts for about 120 minutes, while annealing at 800°C desirably lasts for about 20 minutes.
  • FIG. 1 illustrates the optimum annealing temperatures and time durations wherein the most preferred temperature and time durations are those points on the line. Less acceptable results causing flawed substrates occur with increasing distance from the line. Flawed substrates include those exhibiting an unacceptable dielectric constant, high voltage leakage, or delamination.
  • the thickness of the substrate is between about 20 to about 50 microns.
  • the thickness of the Ni on the side contiguous to the dielectric is between from about 0.10 microns to about 2.0 microns.
  • the thickness of the Ni on the bottommost surface of the substrate is between 0.1 to about 10 microns.
  • the nickel may be applied to the copper substrate by sputtering or by other means known in the art.
  • the pre-annealing and nickel deposition steps preferably occur in an atmosphere free of oxygen, such as in a gaseous atmosphere of argon or nitrogen.
  • Pre- annealing refers to annealing prior to the deposition of dielectric material.
  • Deposition of the dielectric on the nickel-coated copper substrate generally requires a low processing temperature to minimize interdiffusion and reaction between the foil and the dielectric.
  • Such dielectrics may further be applied to the substrate by sol- gel (where the deposition occurs at room temperature and thus the annealed nickel-coated copper substrate is cooled to room temperature) or vacuum deposition (including sputtering, electron beam evaporation, and other techniques) where the annealed product is cooled to the temperature at which the deposition occurs.
  • sol- gel where the deposition occurs at room temperature and thus the annealed nickel-coated copper substrate is cooled to room temperature
  • vacuum deposition including sputtering, electron beam evaporation, and other techniques
  • the dielectric is applied at elevated temperature of between 300 about 400° C. Deposition of the dielectric may occur in a single step or in multiple steps.
  • the thickness of the dielectric varies depending on the amount of voltage desired of the resulting end product, such as capacitor. The higher the voltage is to be applied, the thicker the dielectric will likely be. A fairly typical thickness for the dielectric is about 600 nm.
  • the dielectric is a lead zirconate titanate, PZT, of the formula Pb a L b Zr x Ti y O 7 wherein L is a lanthanide metal, preferably La or Nb, x and y are independently between from about 0.35 to about 0.65, z is from about 2.5 to about 5.0, a is from about 0.95 to about 1.25 and b is from about 0.02 to about 0.10.
  • Such dielectrics may be prepared by using, as starting materials, lead acetate [Pb(CIl 3 COO) 2 H 2 O)], zirconium n-propoxide [Zr(O-nC 3 H 7 ) ], titanium isopropoxide [Ti(O-iC 3 Fl 7 ) ] and lanthanum isopropoxide [La(O-iC 3 H 7 ) 3 ] or niobium ethoxide [Nb(OC 2 II 5 ) 5 ].
  • lead acetate Pb(CIl 3 COO) 2 H 2 O)
  • Zr(O-nC 3 H 7 ) zirconium n-propoxide
  • Ti(O-iC 3 Fl 7 ) titanium isopropoxide
  • La(O-iC 3 H 7 ) 3 lanthanum isopropoxide
  • Nb(OC 2 II 5 ) 5 niobium ethoxide
  • Zirconium n-propoxide and titanium isopropoxide in 2-methoxyethanol may then be admixed with the resulting product which is at room temperature, then refluxed at 110°C for about 2 to 3 hours under vacuum from which polymer precursors, such as those of the formula Pb(Zr 0 . 5 Ti 0 . 48 )O 3 , may be obtained.
  • the 0.3 M stock solutions may be obtained by dilution with toluene and adding appropriate formamade for protecting from crack and 10 mol% excess Pb for loss of lead oxide during the final annealing processing.
  • barium titanate dielectrics especially those of the formula Ba a Ti t ,O c wherein a and b are independently between 0.75 and 1.25 and c is 2.5 to about 5.0 as well as those of the formula M a B b Ti c O d wherein a is about 0.01 to about 0.1, b is about 0.75 to about 1.25, c is about 0.75 to about 1.25 and d is about 2.5 to about 5.0 and M is a non-reactive elctroconductive metal.
  • M are gold, copper, intermetallic compounds such as Ni 3 Al, Ru and InSn.
  • Such barium dielectrics are discussed in PCT WO/98/07167, published on February 19, 1998, herein incorporated by reference.
  • the product is annealed at between 500° and 600° C for
  • the annealing temperature at this stage may be shorter if higher temperatures are used. Annealing is terminated when the desired result is achieved.
  • the pre-annealing step should occur at a higher temperature than the annealing temperature for deposition of the dielectric onto the substrate; the latter being referred to as a "post- annealing" step. If the pre-annealing step is at a temperature lower temperature than the post-annealing step, then pre-annealing may proceed at a longer time, generally longer than 20 minutes
  • FIG. 3 shows the desirable results obtained at
  • the substrate had a dielectric constant
  • FIGS. 4 and 5 show the desirable results obtained when the
  • FIG. 6 is a scanning electromicrograph of a pre-
  • FIG. 7 is a scanning electromicrograph of a pre-annealed
  • 2-4 and 6-7 was 0.1270 microns and between 0.3556 to 0.5080 microns on the bottommost surface of the substrate (not contiguous with any dielectric).
  • the thickness of the copper foil for all thin film composites of FIGS. 2-7 is about 34 microns.
  • FIG. 8 refers to an embodiment of the invention wherein the illustrated thin film composite contains a nickel-coated copper substrate comprising copper substrate 10 coated with nickel 20, dielectric 50, and, optionally, top electrode 60.
  • the nickel coating may either envelope the copper substrate completely or partially. Alternatively, the copper substrate on only two sides.
  • FIG. 8 further demonstrates use of a barrier or buffer layer 30 which is applied to the nickel-coated substrate before deposition of the dielectric.
  • the purpose of the barrier layers, generally composed of a noble metal, and the buffer layer, composed of glass, is to prevent atomic migration between the substrate and dielectric.
  • the thin film composites of the invention may further contain a top or electroconductive layer.
  • the top electrode may consist of any electrically conductive metal such as aluminum, gold, platinum, or others known in the art.
  • the thin film composites which are displayed in FIGS. 2-7 had Al as the top electrode.
  • FIG. 9 depicts a thin film composite wherein the copper substrate 10 is completely enveloped by nickel 20.
  • this thin film composite may further contain a barrier or buffer layer 30, dielectric 20, and electrode 60.

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Abstract

The invention relates to a process of preparing a copper/nickel substrate by annealing nickel-coated copper. After the nickel deposition step, a dielectric, such as lead zirconate titanate (PZT), may be deposited onto the substrate by methods known in the art such as sol-gel or vacuum deposition. This invention further relates to thin film composites. These composites comprise a pre-annealed nickel-coated copper substrate and a dielectric such as PZT.

Description

TITLE: METHOD OF MAKING A NICKEL-COATED COPPER
SUBSTRATE AND THIN FILM COMPOSITE CONTAINING THE SAME
SPECIFICATION
Field of the Invention
This invention relates to a method of making a nickel-coated copper substrate for use in a thin film composite and thin film composites containing such nickel-coated copper substrates.
Background of the Invention
In the past years, there have been extended efforts in the development of high capacitance electrochemical energy storage devices, especially capacitors and batteries, for use in reduced volumetric areas. Both capacitors and batteries store energy by the separation of positive and negative charges. The need to store greater amounts of energy in a smaller package continues to drive new research.
Energy storage devices made of thin film composites have been found to be useful in electronic and optoelectronic applications, such as ferroelectric memory devices, pyroelectronic sensor devices, waveguide modulators, and acoustic sensors. For example, thin film composites are used in a variety of semiconductor integrated circuit devices such as analog circuits, rf circuits, and dynamic random access memories (DRAM's). The composites are usually composed of a substrate, a dielectric, and an electrode; the dielectric being between the substrate and the electrode. Substrates are commonly composed of copper, silicon, fused silica, platinum-coated silicon, alumina, sapphire, platinum-coated sapphire, or a single crystal SrTiO substrate.
Copper is often preferred as a substrate in light of its ready availability. Unfortunately, however, thin film composites having copper substrates often evidence thermal migration and outgassing. Thermal migration is the migration of copper ions into the dielectric and of ions in the dielectric into the substrate at elevated temperatures. Outgassing occurs when gaseous copper atoms escape from the substrate into either the dielectric or the oven in which deposition of the dielectric occurs. A copper substrate which eliminates these drawbacks is desired.
Summary of the Invention
The invention relates to a method of preparing a copper substrate having nickel deposited thereon. In addition, the invention relates to thin film composites containing such nickel-coated copper substrates. The nickel-coated substrate is prepared by depositing nickel onto the copper and then annealing the resulting substrate. The copper may be a foil. After annealing, a dielectric may be deposited onto the substrate by methods known in the art such as by sol-gel or vacuum deposition techniques.
Brief Description of the Drawings
FIG. 1 is a graph depicting optimum temperatures and durations for annealing the nickel-coated substrate in accordance with the process of the invention
FIG. 2 is an internal structure of a nickel-coated copper substrate pre-annealed at
a temperature of 400° C for 120 minutes using a scanning electron microscope.
FIG. 3 is an internal structure of a nickel-coated copper substrate pre-annealed at
a temperature of 900° C for 5 minutes using a scanning electron microscope.
FIGS. 4 and 5 are internal structures of a nickel-coated copper substrate pre- annealed at a temperature of 800° C for 20 minutes using a scanning electron microscope.
FIG. 6 is an internal structure of a nickel-coated copper substrate pre-annealed at a temperature of 500° C for 90 minutes using a scanning electron microscope.
FIG. 7 is an internal structure of a nickel-coated copper substrate pre-annealed at a temperature of 650° C for 30 minutes using a scanning electron microscope.
FIG. 8 depicts a thin film composite in accordance with the invention having a copper substrate coated on its top and bottom surfaces with nickel, a dielectric, an optional barrier or buffer layer, and a top electrode.
FIG. 9 depicts a thin film composite in accordance with the invention having a copper substrate completely enveloped by nickel.
Detailed Description of the Preferred Embodiments
The thin film composites in accordance with the invention contain a nickel-coated copper substrate and a dielectric. The substrate is prepared by depositing nickel onto copper. The nickel may be deposited on one or both sides of the copper substrate. In a preferred embodiment, the nickel encapsulates the copper substrate.
The nickel-deposited copper substrate is then annealed at a temperature between approximately 400°C and 820°C, preferably approximately 800°C. The optimum
duration of annealing varies with the annealing temperature. For example, annealing at 400°C desirably lasts for about 120 minutes, while annealing at 800°C desirably lasts for about 20 minutes. FIG. 1 illustrates the optimum annealing temperatures and time durations wherein the most preferred temperature and time durations are those points on the line. Less acceptable results causing flawed substrates occur with increasing distance from the line. Flawed substrates include those exhibiting an unacceptable dielectric constant, high voltage leakage, or delamination.
Typically, the thickness of the substrate (prior to the nickel deposition) is between about 20 to about 50 microns. The thickness of the Ni on the side contiguous to the dielectric is between from about 0.10 microns to about 2.0 microns. The thickness of the Ni on the bottommost surface of the substrate (when no dielectric is contiguous therewith) is between 0.1 to about 10 microns.
The nickel may be applied to the copper substrate by sputtering or by other means known in the art. The pre-annealing and nickel deposition steps preferably occur in an atmosphere free of oxygen, such as in a gaseous atmosphere of argon or nitrogen. (Pre- annealing, as used herein, refers to annealing prior to the deposition of dielectric material.) Deposition of the dielectric on the nickel-coated copper substrate generally requires a low processing temperature to minimize interdiffusion and reaction between the foil and the dielectric. Such dielectrics may further be applied to the substrate by sol- gel (where the deposition occurs at room temperature and thus the annealed nickel-coated copper substrate is cooled to room temperature) or vacuum deposition (including sputtering, electron beam evaporation, and other techniques) where the annealed product is cooled to the temperature at which the deposition occurs. In the latter, for instance, when vacuum deposition is used, the dielectric is applied at elevated temperature of between 300 about 400° C. Deposition of the dielectric may occur in a single step or in multiple steps. The thickness of the dielectric varies depending on the amount of voltage desired of the resulting end product, such as capacitor. The higher the voltage is to be applied, the thicker the dielectric will likely be. A fairly typical thickness for the dielectric is about 600 nm.
In a preferred embodiment, the dielectric is a lead zirconate titanate, PZT, of the formula PbaLbZrxTiyO7 wherein L is a lanthanide metal, preferably La or Nb, x and y are independently between from about 0.35 to about 0.65, z is from about 2.5 to about 5.0, a is from about 0.95 to about 1.25 and b is from about 0.02 to about 0.10. Such dielectrics may be prepared by using, as starting materials, lead acetate [Pb(CIl3COO)2H2O)], zirconium n-propoxide [Zr(O-nC3H7) ], titanium isopropoxide [Ti(O-iC3Fl7) ] and lanthanum isopropoxide [La(O-iC3H7)3] or niobium ethoxide [Nb(OC2II5)5]. In a preferred method, such dielectrics may be prepared by dissolving lead acetate trihydrate in 2-methoxyethanol and dehydrating the composition at 1 10°C under vacuum to obtain lead acetate. Zirconium n-propoxide and titanium isopropoxide in 2-methoxyethanol may then be admixed with the resulting product which is at room temperature, then refluxed at 110°C for about 2 to 3 hours under vacuum from which polymer precursors, such as those of the formula Pb(Zr0.5 Ti0.48)O3, may be obtained. Finally, the 0.3 M stock solutions may be obtained by dilution with toluene and adding appropriate formamade for protecting from crack and 10 mol% excess Pb for loss of lead oxide during the final annealing processing.
While conventional dielectrics known in the art may be used, further desirable results are obtained by using the barium titanate dielectrics, especially those of the formula BaaTit,Oc wherein a and b are independently between 0.75 and 1.25 and c is 2.5 to about 5.0 as well as those of the formula MaBbTicOd wherein a is about 0.01 to about 0.1, b is about 0.75 to about 1.25, c is about 0.75 to about 1.25 and d is about 2.5 to about 5.0 and M is a non-reactive elctroconductive metal. Preferred as M are gold, copper, intermetallic compounds such as Ni3Al, Ru and InSn. Such barium dielectrics are discussed in PCT WO/98/07167, published on February 19, 1998, herein incorporated by reference.
Following deposition, the product is annealed at between 500° and 600° C for
about 20 minutes. The annealing temperature at this stage may be shorter if higher temperatures are used. Annealing is terminated when the desired result is achieved. The pre-annealing step should occur at a higher temperature than the annealing temperature for deposition of the dielectric onto the substrate; the latter being referred to as a "post- annealing" step. If the pre-annealing step is at a temperature lower temperature than the post-annealing step, then pre-annealing may proceed at a longer time, generally longer than 20 minutes
As set forth in FIG. 2, smooth laminated surface is obtained for the resulting
substrate pre-annealed at a temperature of 400° C for 120 minutes. A dielectric constant
of 86 was measured and a Tg δ (%) of 14. FIG. 3 shows the desirable results obtained at
pre-annealing conditions of 900° C for 5 minutes. The substrate had a dielectric constant
of 1 10 and a Tg δ (%) of 7. FIGS. 4 and 5 show the desirable results obtained when the
pre-annealing is conducted at 800° C for 20 minutes. Measured dielectric constants were 75 and 113, respectively. FIGS. 6 and 7 demonstrate less desirable pre-annealing conditions than the preceding FIGS. FIG. 6 is a scanning electromicrograph of a pre-
annealed substrate at 500° for 90 minutes. The resulting substrate was rough and exhibited delamination. FIG. 7 is a scanning electromicrograph of a pre-annealed
substrate at 650° C at 30 minutes. The resulting substrate was rough. All of the substrates in FIGS. 2-7 were obtained in an Ar atmosphere and all employed PZT as the dielectric which was deposited onto the substrate by spin-coating. The thickness of the Cu is about 33 to 35.6 microns. The tests were conducted wherein the thickness of the Ni on the uppermost surface contiguous to the dielectric in FIG. 5 was 1.78 microns. The thickness of Ni on the bottommost surface of the substrate (not contiguous with any dielectric) was between 6.35 to 7.62 microns. The thickness of the Ni on the uppermost surface contiguous to the dielectric in FIGS. 2-4 and 6-7 was 0.1270 microns and between 0.3556 to 0.5080 microns on the bottommost surface of the substrate (not contiguous with any dielectric). The thickness of the copper foil for all thin film composites of FIGS. 2-7 is about 34 microns.
FIG. 8 refers to an embodiment of the invention wherein the illustrated thin film composite contains a nickel-coated copper substrate comprising copper substrate 10 coated with nickel 20, dielectric 50, and, optionally, top electrode 60. The nickel coating may either envelope the copper substrate completely or partially. Alternatively, the copper substrate on only two sides. FIG. 8 further demonstrates use of a barrier or buffer layer 30 which is applied to the nickel-coated substrate before deposition of the dielectric. The purpose of the barrier layers, generally composed of a noble metal, and the buffer layer, composed of glass, is to prevent atomic migration between the substrate and dielectric.
Lastly, the thin film composites of the invention may further contain a top or electroconductive layer. The top electrode may consist of any electrically conductive metal such as aluminum, gold, platinum, or others known in the art. The thin film composites which are displayed in FIGS. 2-7 had Al as the top electrode.
FIG. 9 depicts a thin film composite wherein the copper substrate 10 is completely enveloped by nickel 20. In addition, this thin film composite may further contain a barrier or buffer layer 30, dielectric 20, and electrode 60.
Various modifications may be made in the nature, composition, operation and arrangement of the various elements, steps and procedures described herein without departing from the spirit and scope of the invention as defined in the following claims.

Claims

CLAIMSWhat is claimed is:
1. A thin film composite comprising:
(a) a nickel-coated copper substrate; and
(b) a dielectric layer on the nickel-coated copper substrate.
2. The thin film composite of Claim 1, wherein both top and bottom surfaces of the nickel-coated copper substrate are coated with the dielectric layer.
3. The thin film composite of Claim 2, wherein the copper of the nickel-coated copper substrate is encapsulated by nickel.
4. The thin film composite of Claim 3, wherein the dielectric is BaaTibOc, wherein a and b are independently from about 0.75 and to about 1.25 and c ranges from about 2.5 to about 5.0.
5. The thin film composite of Claim 3, wherein the dielectric is PbaLbZrxTiyOz, wherein L is a lanthanide metal, x and y independently range between about 0.35 to about 0.65, z is from about 2.5 to about 5.0, a is from about 0.95 to 1.25 and b is from about 0.02 to about 0.10.
6. The thin film composite of Claim 1, wherein a barrier or buffer layer is between the nickel-coated copper substrate and the dielectric layer.
7. The thin film composite of Claim 1 , further comprising an electroconductive layer such that the dielectric is between the electroconductive layer and nickel-coated copper substrate.
8. The thin film composite of Claim 6, wherein the barrier layer comprises a noble metal.
9. The thin film composite of Claim 6, wherein the buffer layer comprises glass.
10. The thin film composite of claim 6, further comprising an electroconductive layer such that the dielectric is between the barrier or buffer layer and nickel-coated substrate.
11. The thin film composite of Claim 2, wherein a bottom barrier or buffer layer is between the dielectric and the bottom surface of the substrate and a top barrier or buffer layer is between the uppermost dielectric and the top surface of the substrate.
12. The thin film composite of Claim 11, wherein the nickel-coated copper substrate is encapsulated by nickel.
13. A method of manufacturing a copper substrate for a thin film composite comprising:
(a) depositing nickel onto a copper substrate to render a nickel-coated copper substrate; and
(b) annealing the nickel-coated copper substrate.
14. The method of Claim 13, wherein the nickel-coated copper substrate is annealed
at a temperature between about 400°C and about 820°C.
15. The method of Claim 13, wherein the nickel-coated copper substrate is encapsulated by nickel.
16. The method of Claim 13, wherein the nickel-coated copper substrate is annealed at a temperature and for a time as set forth in FIG. 1.
17. The method of Claim 14, wherein the nickel-coated copper substrate is annealed
at a temperature of between about 650° to about 800° C.
18. The method of Claim 16, wherein the nickel-coated copper substrate is annealed at a temperature of about 400°C for about 120 minutes.
19. The method of Claim 14, wherein the nickel-coated copper substrate is annealed
at a temperature of about 800°C for about 20 minutes.
20. A method of manufacturing a thin film composite comprising:
(a) depositing nickel onto a copper substrate to render a nickel-coated copper substrate;
(b) annealing the nickel-coated copper substrate at a temperature of about
400° to about 800°C for a time sufficient to render a nickel-coated copper substrate; and
(c) depositing a dielectric on the nickel-coated copper substrate.
21. The method of Claim 20, wherein the nickel-coated copper substrate is annealed at a temperature and for a time as set forth in FIG. 1.
22. The method of Claim 20, further comprising depositing onto the dielectric layer an electroconductive layer.
23. The method of Claim 20, wherein subsequent to step (a), a barrier or buffer layer is coated onto the nickel-coated copper substrate.
24. The method of Claim 20, wherein the nickel-coated copper substrate is a copper substrate encapsulated by nickel.
PCT/IB2001/001201 2001-06-28 2001-06-28 Method of making a nickel-coated copper substrate and thin film composite containing the same WO2003002782A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CNB018118968A CN1318646C (en) 2001-06-28 2001-06-28 Method of making nickel-coated copper substrate and thin film composite containing same
JP2003508744A JP2004530584A (en) 2001-06-28 2001-06-28 Method for producing nickel-coated copper substrate and thin film composite including the substrate
EP01945555A EP1399602A1 (en) 2001-06-28 2001-06-28 Method of making a nickel-coated copper substrate and thin film composite containing the same
PCT/IB2001/001201 WO2003002782A1 (en) 2001-06-28 2001-06-28 Method of making a nickel-coated copper substrate and thin film composite containing the same

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JP4670612B2 (en) * 2005-11-30 2011-04-13 Tdk株式会社 Dielectric element and manufacturing method thereof
CN101250705B (en) * 2008-04-01 2010-10-06 西南交通大学 Method for manufacturing nickel-cuprum metallic baseband layer of highly oriented double-shaft texture
CN103177871B (en) * 2013-03-01 2016-02-17 溧阳华晶电子材料有限公司 A kind of film capacitor with composite base plate
CN107634002A (en) * 2017-09-26 2018-01-26 深圳市华星光电技术有限公司 Thin film transistor (TFT) and preparation method thereof

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JP2004530584A (en) 2004-10-07
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CN1466634A (en) 2004-01-07

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