WO2017108939A1 - Thick-film paste mediated ceramics bonded with metal or metal hybrid foils - Google Patents

Thick-film paste mediated ceramics bonded with metal or metal hybrid foils Download PDF

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Publication number
WO2017108939A1
WO2017108939A1 PCT/EP2016/082161 EP2016082161W WO2017108939A1 WO 2017108939 A1 WO2017108939 A1 WO 2017108939A1 EP 2016082161 W EP2016082161 W EP 2016082161W WO 2017108939 A1 WO2017108939 A1 WO 2017108939A1
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Prior art keywords
thick
metal
film paste
ceramic substrate
metal foil
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Ceased
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PCT/EP2016/082161
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French (fr)
Inventor
Paul GUNDEL
Anton MIRIC
Melanie BAWOHL
Gabriel ZIER
Kai Herbst
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Heraeus Deutschland GmbH and Co KG
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Heraeus Deutschland GmbH and Co KG
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Priority to JP2018519934A priority Critical patent/JP2019509237A/en
Priority to KR1020187009873A priority patent/KR20180093877A/en
Priority to US16/064,564 priority patent/US20190002359A1/en
Priority to EP16819915.6A priority patent/EP3341345B1/en
Priority to CN201680074736.0A priority patent/CN108473379A/en
Publication of WO2017108939A1 publication Critical patent/WO2017108939A1/en
Anticipated expiration legal-status Critical
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Definitions

  • the present invention relates to a process for preparing a ceramic substrate bonded with a metal foil via a thick-film layer. Moreover, the present invention relates to a metal-ceramic- substrate provided with a specific thick-film layer between the ceramic substrate and the metal foil and the use of a thick-film paste for bonding a metal foil onto a ceramic substrate.
  • this object is solved by a process for preparing a structured metal-ceramic substrate, characterized by the following process steps:
  • a metal- ceramic substrate comprising
  • the present invention it has been found out that based on the thick-film tech- nology it is possible to provide a substrate for use in the field of power electronics in which a metal foil is bonded via a thick-film paste of a metal onto a ceramic substrate (such as Al 2 O 3 ceramic, AIN ceramic or Si 3 N 4 ceramic).
  • a ceramic substrate such as Al 2 O 3 ceramic, AIN ceramic or Si 3 N 4 ceramic.
  • the thick-film paste is applied onto the ceramic substrate in the first process step.
  • the thick-film paste can be applied onto the ceramic substrate discontinuously such that the thick-film paste is only applied on those parts of the ceramic substrate, which correspond to an intended electronic circuit of the final metal- ceramic substrate.
  • the metal foil may be applied, thereafter, continuously over the whole thick-film layer of the ceramic substrate. After that, the metal foil is bonded with the ceramic substrate and then structured, for example by etching.
  • the metal foil may also be applied discontinuously over the thick-film layer only on those parts of the ceramic substrate on which the thick-film paste is applied.
  • the thick-film paste is applied continuously onto the ceramic substrate.
  • the metal foil may be applied continuously over the whole thick-film layer of the ceramic substrate and the metal foil and the thick-film layer are structured, for example, by etching after bonding.
  • the metal foil may also be applied discontinuously only on those parts of the ceramic substrate which correspond to an intended electronic circuit of the final metal- ceramic substrate.
  • the thick-film layer is structured, for example, by etching after bonding.
  • the thick-film paste may be air- dried prior to applying the metal foil onto the thick-film layer.
  • the thick-film paste may also be sintered prior to applying the metal foil.
  • Such a sintering process can be carried out by a temperature of below 1025 °C.
  • the sintering process is carried out by a tempera- ture in the range of from 300 to 1025 °C, more preferably in the range of from 600 to 1025 °C, more preferably in the range of from 900 to 1025 °C, more preferably in the range of from 900 to less then 1025 °C, more preferably in the range of from 900 to 1000 °C.
  • This tempera- ture for the sintering process does in particular not provide a bonding of the thick-film paste and the substrate via a DCB process, but provides almost a continuously coating on the ce- ramic substrate by the known thick-film technology. Accordingly, this process step of sinter- ing distinguishes the process according to the present invention from, for example, the pro- cess described in DE 10 2010 025 313 A in which the mixture of the metal and the oxide of the metal is bonded to the ceramic substrate at a higher temperature and under DCB condi- tions.
  • the thick-film paste may also be air-dried and sintered prior to applying the metal foil onto the thick-film layer.
  • the sintering conditions are as de- scribed above.
  • the sintering process of the applied thick-film paste is usually carried out under an inert at- mosphere, such as a nitrogen atmosphere.
  • the modified claimed process comprises the following process steps:
  • the thick-film paste may be coated onto the metal foil substrate by screen printing.
  • the thick-film paste may be air-dried prior to applying the metal foil onto the ceramic.
  • the metal foil and the thick-film paste are structured by etching before or after bonding the metal foil onto the ceramic sub- strate via the thick-film layer.
  • the thick-film paste may be applied onto the substrate or the metal foil by multilayer printing. If a process step of multilayer coating is applied and the thick-film paste is applied onto a substrate, the first coating of the multilayer coating may be provided with lines for contacts.
  • the bonding steps (1.3) and/or (2.3) are carried out by firing.
  • the firing is carried out at a temperature of between 750 and 1100 °C, more preferably of between 800 and 1085 °C.
  • the metal foil is bonded via the thick-film paste to the substrate basically not by applying the DCB process since the metal foil is in contact with the layer provided by the thick-film paste and not with the substrate.
  • the metal foil may be oxidized before bonding to the ceramic substrate via the thick-film lay- er in both embodiments of the processes according to the present invention.
  • the metal foil is not oxidized before bonding to the ceramic substrate via the thick-film layer.
  • the thick- film layer may be oxidized before bonding of the metal foil onto the ceramic substrate.
  • the thick-film layer is not oxidized before bonding of the metal foil onto the ceramic substrate.
  • the process steps (1.3) and/or (2.3) of bonding the metal foil onto the ceramic substrate pro- vided with the thick-film layer may be carried out under pressure.
  • the metal foil is preferably a copper foil.
  • the ceramic may be selected from the group con- sisting of an Al 2 O 3 ceramic, an AIN ceramic and a Si 3 N 4 ceramic.
  • Thick-film paste In the following, the thick-film paste, which can be used in the process according to both em- bodiments of the present invention, is described in more detail:
  • the thick-film paste used in the process according to the present invention may comprise copper as a metal and optionally Bi 2 O 3 .
  • the thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper, more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably 0 to 50 wt.-% Bi 2 O 3 , more preferably 1 to 20 wt.-% Bi 2 O 3 , most preferably 2 to 15 wt.-% Bi 2 O 3 , each based on the total weight of the thick-film paste.
  • the copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 ⁇ m, more preferably of between 1 and 10 ⁇ m, most preferably of between 2 and 7 ⁇ m.
  • the Bi 2 O 3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 ⁇ m, more preferably of less than 20 ⁇ m, most preferably of less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise copper and a glass component.
  • the amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably 40 to less than 92 wt.-% copper, more preferably in an amount of from 70 to less than 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt- %, of the glass component, each based on the total weight of the thick-film paste.
  • the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 ⁇ m, more preferably of between 1 and 10 ⁇ m, most preferably of between 2 and 7 ⁇ m.
  • the glass component particles may have a median diameter (dso) of less than 100 ⁇ m, more preferably less than 20 ⁇ m, most preferably less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise - besides the glass component and Bi 2 O 3 - further components, selected from the group con- sisting of PbO, Te0 2 , Bi 2 O 3 , ZnO, B 2 O 3 , Al 2 O 3 , Ti0 2 , CaO, K 2 0, MgO, Na 2 0, Zr0 2 , and Li 2 0.
  • the layer thickness is preferably of from 5 to 150 ⁇ m, more preferably of from 20 to 125 ⁇ m, most preferably of from 30 to 100 ⁇ m.
  • the amount of copper oxide in the thick- film paste is less than 2 wt.-%, more preferably less than 1.9 wt.-%, more preferably less than 1.8 wt.-%, more preferably less than 1.5 wt.-%.
  • the present invention relates to a metal-ceramic substrate, comprising (a) a ceramic substrate and, provided thereon, (b) a metal-containing thick-film layer, and, provided thereon,
  • the metal foil and/or the metal-containing thick-film layer may be structured.
  • the thick-film layer provided onto the ceramic substrate, comprises preferably copper as a metal and optionally Bi 2 O 3 .
  • the thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper.more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably 0 to 50 wt.-% Bi 2 O 3 , more preferably 1 to 20 wt.-% Bi 2 O 3 , most preferably 2 to 15 wt.-% Bi 2 O 3 , each based on the total weight of the thick-film paste.
  • the copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 ⁇ m, more preferably of between 1 and 10 ⁇ m, most preferably of between 2 and 7 ⁇ m.
  • the Bi 2 O 3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 ⁇ m, more preferably of less than 20 ⁇ m, most preferably of less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise copper and a glass component.
  • the amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably in an amount of from 70 to 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt- %, of the glass component, each based on the total weight of the thick-film paste.
  • the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 ⁇ m, more preferably of between 1 and 10 ⁇ m, most preferably of between 2 and 7 ⁇ m.
  • the glass component particles have may have a median diameter (d50) of less than 100 ⁇ m, more preferably less than 20 ⁇ m, most preferably less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise - besides the glass component and Bi 2 O 3 - further components, selected from the group consisting of PbO, Te0 2 , Bi 2 O 3 , ZnO, B 2 O 3 , AI2O3, Ti0 2 , CaO, K 2 0, MgO, Na 2 0, Zr0 2 , and Li 2 0.
  • the layer thickness of the thick-film paste is preferably 10 to 150 ⁇ , more preferably 20 to 125 ⁇ , most preferably 30 to 100 ⁇ m.
  • the metal foil is preferably a copper foil.
  • the ceramic may be selected from the group con- sisting of an AI2O3 ceramic, an AIN ceramic and a Si 3 N 4 ceramic.
  • the metal-ceramic substrate according to the present invention may preferably be prepared according to the above-mentioned process.
  • the present invention relates to the use of the above-mentioned thick-film paste for preparing a metal-ceramic substrate as intermediate layer between a ceramic sub- strate and a metal foil.
  • the above-mentioned thick-film is used in order to avoid the delami- nation of the resulting system of a substrate and a metal foil during operation by thermal cy- cles.
  • the thick-film layer provided onto the ceramic substrate, comprises preferably copper as a metal and optionally Bi 2 O 3 .
  • the thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper, more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably 0 to 50 wt.-% Bi 2 O 3 , more preferably 1 to 20 wt.-% B12O3, most preferably 2 to 15 wt.-% Bi 2 O 3 , each based on the total weight of the thick-film paste.
  • the copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 ⁇ m, more preferably of between 1 and 10 ⁇ m, most preferably of between 2 and 7 ⁇ .
  • the Bi 2 O 3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 ⁇ m, more preferably of less than 20 ⁇ m, most preferably of less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise copper and a glass component.
  • the amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably in an amount of from 70 to 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
  • the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt.- %, of the glass component, each based on the total weight of the thick-film paste.
  • the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 ⁇ , more preferably of between 1 and 10 ⁇ , most preferably of between 2 and 7 ⁇ m.
  • the glass component particles have may have a median diameter (dso) of less than 100 ⁇ m, more preferably less than 20 ⁇ m, most preferably less than 10 ⁇ m.
  • the metal-containing thick-film paste may comprise - besides the glass component and Bi 2 O 3 - further components, selected from the group consisting of PbO, Te0 2 , Bi 2 O 3 , ZnO, B 2 O 3) Al 2 O 3 , Ti0 2l CaO, K 2 0, MgO, IMa 2 0, Zr0 2 , and L
  • the layer thickness of the thick-film paste is preferably 10 to 150 ⁇ m, more preferably 20 to 125 ⁇ m, most preferably 30 to 100 ⁇ m.
  • the metal foil is preferably a copper foil.
  • a thick-film paste material is prepared starting from the following glass composition (in wt. %):
  • a ceramic metal substrate was prepared by printing the pastes on a Al 2 O 3 ceramic substrate in a thickness of 40 ⁇ .
  • the pastes were dried in an oven at 110 °C for 10 min and sintered at 950 °C for 10 minutes before a Cu foil with a thick- ness of 300 ⁇ m was applied onto the dried pastes and the composite was fired in an oven at 1040 °C for 150 min.
  • a ceramic metal substrate was prepared starting from the same ceramic substrate and the same Cu foil as for the examples with pastes, but using a standard DCB process with a bonding temperature of 1063 °C for 240 min.
  • the finished metal ceramic substrates have been subject to thermal cycles (15 min at -40 °C, 15 sec. transfer time, 15 min at +150 °C).
  • the test results can be seen in the following table.

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  • Organic Chemistry (AREA)
  • Parts Printed On Printed Circuit Boards (AREA)
  • Manufacturing Of Printed Wiring (AREA)
  • Laminated Bodies (AREA)
  • Ceramic Products (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)

Abstract

Described is a process for preparing a ceramic substrate bonded with a metal foil. Moreover, described is a metal-ceramic-substrate provided with a thick-film layer and the use of a thick-film paste for bonding a metal foil onto a ceramic substrate.

Description

Thick-film paste mediated ceramics bonded with metal or metal hybrid foils
Description
The present invention relates to a process for preparing a ceramic substrate bonded with a metal foil via a thick-film layer. Moreover, the present invention relates to a metal-ceramic- substrate provided with a specific thick-film layer between the ceramic substrate and the metal foil and the use of a thick-film paste for bonding a metal foil onto a ceramic substrate.
In the field of power microelectronics applications in automotive, in particular for electric ve- hicles or hybrid vehicles, the use of electronic circuits with a high current carrying capacity and high durability are a high demand. For this purpose, the use of a highly conductive mate- rial with a high current carrying capacity, such as copper, is necessary. At the same time, the respective material should have a high capacity of heat dissipation (heat removal). Moreover, it is necessary that the respective material allow a suitable connection via a bond wire, has a good solderability, and should have the possibility of an oxidation protection by currentless plattings. In the DBC technology, a copper foil is bonded onto a ceramic substrate with a eutectic melt. This process technology suffers from some disadvantages, such as a high amount of rejects, the creation of cavities between the ceramic substrate and the copper foil and the relatively low resistance against temperature changes (which leads to a delamination after some ther- mic cycles). A respective technology is described, for example, in DE 10 2010 025 313 A in which a mixture of the metal and an oxide of this metal is applied on a ceramic substrate which is then bonded via a DCB process.On the other hand, substrates, which are prepared based on the thick print technology, are also known. These substrates have the disad- vantage of high production costs and low electronic and thermal conductivity caused by the porosity of the sintered layers. Starting from this prior art situation, the present invention has the object to provide a metal- ceramic substrate which avoids the above-mentioned disadvantages.
In a first aspect, this object is solved by a process for preparing a structured metal-ceramic substrate, characterized by the following process steps:
(1.1) applying of a thick-film paste onto a ceramic substrate; (1.2) applying of a metal foil onto the thick-film layer of the ceramic substrate; and
(1.3) bonding of the metal foil with the ceramic substrate via the thick-film layer.
In a second aspect of the present invention, the underlying object is solved by a metal- ceramic substrate, comprising
(a) a ceramic substrate and, provided thereon,
(b) a metal-containing thick-film layer, and, provided thereon; (c) a metal foil.
According to the present invention, it has been found out that based on the thick-film tech- nology it is possible to provide a substrate for use in the field of power electronics in which a metal foil is bonded via a thick-film paste of a metal onto a ceramic substrate (such as Al2O3 ceramic, AIN ceramic or Si3N4 ceramic). The resulting metal-ceramic-substrates have a high conductivity and durability and can be produced with reduced costs.
At first, the above-mentioned process for preparing a structured metal-ceramic substrate is described. Thereby, the process according to the present invention can be carried out in two embodiments: First embodiment of the claimed process
In the process according to the first embodiment of the present invention, the thick-film paste is applied onto the ceramic substrate in the first process step.
First aspect: Discontinuous application of the thick-film paste
In a first aspect of the claimed process, the thick-film paste can be applied onto the ceramic substrate discontinuously such that the thick-film paste is only applied on those parts of the ceramic substrate, which correspond to an intended electronic circuit of the final metal- ceramic substrate.
In this first aspect, the metal foil may be applied, thereafter, continuously over the whole thick-film layer of the ceramic substrate. After that, the metal foil is bonded with the ceramic substrate and then structured, for example by etching.
In this first aspect, the metal foil may also be applied discontinuously over the thick-film layer only on those parts of the ceramic substrate on which the thick-film paste is applied.
Second aspect: Continuous application of the thick-film paste
In a further second aspect of the process according to the present invention, the thick-film paste is applied continuously onto the ceramic substrate.
In this second aspect, the metal foil may be applied continuously over the whole thick-film layer of the ceramic substrate and the metal foil and the thick-film layer are structured, for example, by etching after bonding.
In this second aspect, the metal foil may also be applied discontinuously only on those parts of the ceramic substrate which correspond to an intended electronic circuit of the final metal- ceramic substrate. In this case, the thick-film layer is structured, for example, by etching after bonding.
After applying the thick-film paste onto the ceramic substrate, the thick-film paste may be air- dried prior to applying the metal foil onto the thick-film layer. After applying the thick-film paste onto the ceramic substrate, the thick-film paste may also be sintered prior to applying the metal foil. Such a sintering process can be carried out by a temperature of below 1025 °C. Preferably, the sintering process is carried out by a tempera- ture in the range of from 300 to 1025 °C, more preferably in the range of from 600 to 1025 °C, more preferably in the range of from 900 to 1025 °C, more preferably in the range of from 900 to less then 1025 °C, more preferably in the range of from 900 to 1000 °C. This tempera- ture for the sintering process does in particular not provide a bonding of the thick-film paste and the substrate via a DCB process, but provides almost a continuously coating on the ce- ramic substrate by the known thick-film technology. Accordingly, this process step of sinter- ing distinguishes the process according to the present invention from, for example, the pro- cess described in DE 10 2010 025 313 A in which the mixture of the metal and the oxide of the metal is bonded to the ceramic substrate at a higher temperature and under DCB condi- tions. Such DCB conditions (in particular the required temperature) are not applied doing the sintering process in the process according to the present invention.After applying the thick- film paste onto the ceramic substrate, the thick-film paste may also be air-dried and sintered prior to applying the metal foil onto the thick-film layer. The sintering conditions are as de- scribed above.
The sintering process of the applied thick-film paste is usually carried out under an inert at- mosphere, such as a nitrogen atmosphere. Second embodiment of the claimed process
In a further modified process for preparing a structured metal-ceramic substrate according to the second embodiment of the present invention, the modified claimed process comprises the following process steps:
(2.1 ) applying of a thick-film paste onto a metal foil; (2.2) applying of a ceramic substrate onto the thick-film layer of the metal foil; and
(2.3) bonding the metal foil with the ceramic substrate via the thick-film layer.
In this modified process, the thick-film paste may be coated onto the metal foil substrate by screen printing.
After applying the thick-film paste onto the metal foil, the thick-film paste may be air-dried prior to applying the metal foil onto the ceramic.
In the modified process according to the present invention, the metal foil and the thick-film paste are structured by etching before or after bonding the metal foil onto the ceramic sub- strate via the thick-film layer.
The following explanations are given for both embodiments of the claimed process: The thick-film paste may be applied onto the substrate or the metal foil by multilayer printing. If a process step of multilayer coating is applied and the thick-film paste is applied onto a substrate, the first coating of the multilayer coating may be provided with lines for contacts.
In both processes for preparing a structured metal-ceramic substrate, i.e. the normal process and the modified process, the bonding steps (1.3) and/or (2.3) are carried out by firing. Usu- ally, the firing is carried out at a temperature of between 750 and 1100 °C, more preferably of between 800 and 1085 °C. In these bonding steps the metal foil is bonded via the thick-film paste to the substrate basically not by applying the DCB process since the metal foil is in contact with the layer provided by the thick-film paste and not with the substrate. The metal foil may be oxidized before bonding to the ceramic substrate via the thick-film lay- er in both embodiments of the processes according to the present invention. In another em- bodiment of the present invention the metal foil is not oxidized before bonding to the ceramic substrate via the thick-film layer.
In a further modification of the claimed processes according to both embodiments, the thick- film layer may be oxidized before bonding of the metal foil onto the ceramic substrate. In an- other embodiment of the present invention the thick-film layer is not oxidized before bonding of the metal foil onto the ceramic substrate.
The process steps (1.3) and/or (2.3) of bonding the metal foil onto the ceramic substrate pro- vided with the thick-film layer may be carried out under pressure. In both embodiments according to the present invention, the metal foil is preferably a copper foil.
In a further aspect of the present invention, the ceramic may be selected from the group con- sisting of an Al2O3 ceramic, an AIN ceramic and a Si3N4 ceramic.
Thick-film paste In the following, the thick-film paste, which can be used in the process according to both em- bodiments of the present invention, is described in more detail:
The thick-film paste used in the process according to the present invention (either in the normal process or in the modified process) may comprise copper as a metal and optionally Bi2O3.
The thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper, more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
The thick-film paste comprises preferably 0 to 50 wt.-% Bi2O3, more preferably 1 to 20 wt.-% Bi2O3, most preferably 2 to 15 wt.-% Bi2O3, each based on the total weight of the thick-film paste. The copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 μm, more preferably of between 1 and 10 μm, most preferably of between 2 and 7 μm.
The Bi2O3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 μm, more preferably of less than 20 μm, most preferably of less than 10 μm.
In a further embodiment of the present invention, the metal-containing thick-film paste may comprise copper and a glass component.
The amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably 40 to less than 92 wt.-% copper, more preferably in an amount of from 70 to less than 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
In the case of use of a glass component in the thick-film paste, the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt- %, of the glass component, each based on the total weight of the thick-film paste.
In the case of use of a glass component in the thick-film paste, the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 μm, more preferably of between 1 and 10 μm, most preferably of between 2 and 7 μm.
In the case of use of a glass component in the thick-film paste, the glass component particles may have a median diameter (dso) of less than 100 μm, more preferably less than 20 μm, most preferably less than 10 μm.
The metal-containing thick-film paste, preferably on the basis of copper, may comprise - besides the glass component and Bi2O3 - further components, selected from the group con- sisting of PbO, Te02, Bi2O3, ZnO, B2O3, Al2O3, Ti02, CaO, K20, MgO, Na20, Zr02, and Li20.
After applying the thick-film paste either onto the ceramic substrate or onto the metal foil, the layer thickness is preferably of from 5 to 150 μm, more preferably of from 20 to 125 μm, most preferably of from 30 to 100 μm. In a preferred embodiment of the present invention, the amount of copper oxide in the thick- film paste is less than 2 wt.-%, more preferably less than 1.9 wt.-%, more preferably less than 1.8 wt.-%, more preferably less than 1.5 wt.-%.
Metal-ceramic substrate
In a further aspect, the present invention relates to a metal-ceramic substrate, comprising (a) a ceramic substrate and, provided thereon, (b) a metal-containing thick-film layer, and, provided thereon,
(c) a metal foil.
The metal foil and/or the metal-containing thick-film layer may be structured.
The thick-film layer, provided onto the ceramic substrate, comprises preferably copper as a metal and optionally Bi2O3.
The thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper.more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
The thick-film paste comprises preferably 0 to 50 wt.-% Bi2O3, more preferably 1 to 20 wt.-% Bi2O3, most preferably 2 to 15 wt.-% Bi2O3, each based on the total weight of the thick-film paste.
The copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 μm, more preferably of between 1 and 10 μm, most preferably of between 2 and 7 μm. The Bi2O3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 μm, more preferably of less than 20 μm, most preferably of less than 10 μm.
In a further embodiment of the present invention, the metal-containing thick-film paste may comprise copper and a glass component. The amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably in an amount of from 70 to 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
In the case of use of a glass component in the thick-film paste, the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt- %, of the glass component, each based on the total weight of the thick-film paste.
In the case of use of a glass component in the thick-film paste, the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 μm, more preferably of between 1 and 10 μm, most preferably of between 2 and 7 μm.
In the case of use of a glass component in the thick-film paste, the glass component particles have may have a median diameter (d50) of less than 100 μm, more preferably less than 20 μm, most preferably less than 10 μm. The metal-containing thick-film paste may comprise - besides the glass component and Bi2O3 - further components, selected from the group consisting of PbO, Te02, Bi2O3, ZnO, B2O3, AI2O3, Ti02, CaO, K20, MgO, Na20, Zr02, and Li20.
The layer thickness of the thick-film paste is preferably 10 to 150 μητι, more preferably 20 to 125 μητι, most preferably 30 to 100 μm.
The metal foil is preferably a copper foil.
In a further aspect of the present invention, the ceramic may be selected from the group con- sisting of an AI2O3 ceramic, an AIN ceramic and a Si3N4 ceramic.
The metal-ceramic substrate according to the present invention may preferably be prepared according to the above-mentioned process.
In a further aspect, the present invention relates to the use of the above-mentioned thick-film paste for preparing a metal-ceramic substrate as intermediate layer between a ceramic sub- strate and a metal foil. The above-mentioned thick-film is used in order to avoid the delami- nation of the resulting system of a substrate and a metal foil during operation by thermal cy- cles.
The thick-film layer, provided onto the ceramic substrate, comprises preferably copper as a metal and optionally Bi2O3.
The thick-film paste comprises preferably 40 to 92 wt.-% copper, more preferably 40 to less than 92 wt.-% copper, more preferably 70 to less than 92 wt.-% copper, most preferably 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste.
The thick-film paste comprises preferably 0 to 50 wt.-% Bi2O3, more preferably 1 to 20 wt.-% B12O3, most preferably 2 to 15 wt.-% Bi2O3, each based on the total weight of the thick-film paste.
The copper particles used in the thick-film paste have a median diameter (dso) preferably of between 0.1 to 20 μm, more preferably of between 1 and 10 μm, most preferably of between 2 and 7 μιτι.
The Bi2O3 particles used optionally in the thick-film paste have a median diameter (dso) pref- erably of less than 100 μm, more preferably of less than 20 μm, most preferably of less than 10 μm. In a further embodiment of the present invention, the metal-containing thick-film paste may comprise copper and a glass component.
The amount of copper in the thick-film paste in case of a simultaneous use of a glass com- ponent might be as defined above, i.e. preferably in an amount of from 40 to 92 wt.-%, more preferably in an amount of from 70 to 92 wt.-% copper, most preferably in an amount of from 75 to 90 wt.-% copper, each based on the total weight of the thick-film paste. In the case of use of a glass component in the thick-film paste, the thick-film paste comprises preferably of from 0 to 50 wt.-%, more preferably 1 to 20 wt.-%, most preferably 2 to 15 wt.- %, of the glass component, each based on the total weight of the thick-film paste.
In the case of use of a glass component in the thick-film paste, the copper particles may have the same median diameter (dso) as already mentioned above, i.e. preferably of between 0.1 to 20 μητι, more preferably of between 1 and 10 μητι, most preferably of between 2 and 7 μm.
In the case of use of a glass component in the thick-film paste, the glass component particles have may have a median diameter (dso) of less than 100 μm, more preferably less than 20 μm, most preferably less than 10 μm.
The metal-containing thick-film paste may comprise - besides the glass component and Bi2O3 - further components, selected from the group consisting of PbO, Te02, Bi2O3, ZnO, B2O3) Al2O3, Ti02l CaO, K20, MgO, IMa20, Zr02, and L|20.
The layer thickness of the thick-film paste is preferably 10 to 150 μm, more preferably 20 to 125 μm, most preferably 30 to 100 μm.
The metal foil is preferably a copper foil.
The present invention is described in more detail with regard to the following examples:
A thick-film paste material is prepared starting from the following glass composition (in wt. %):
Figure imgf000009_0001
Vehicle formulation
Figure imgf000009_0002
Paste formulation
Figure imgf000010_0001
Starting from these paste formulations, a ceramic metal substrate was prepared by printing the pastes on a Al2O3 ceramic substrate in a thickness of 40 μιτι. The pastes were dried in an oven at 110 °C for 10 min and sintered at 950 °C for 10 minutes before a Cu foil with a thick- ness of 300 μm was applied onto the dried pastes and the composite was fired in an oven at 1040 °C for 150 min.
For comparison, a ceramic metal substrate was prepared starting from the same ceramic substrate and the same Cu foil as for the examples with pastes, but using a standard DCB process with a bonding temperature of 1063 °C for 240 min.
The finished metal ceramic substrates have been subject to thermal cycles (15 min at -40 °C, 15 sec. transfer time, 15 min at +150 °C). The test results can be seen in the following table.
Figure imgf000010_0002

Claims

1 . A process for preparing a structured metal-ceramic substrate, characterized by the following process steps:
(1.1) applying of a thick-film paste onto a ceramic substrate;
(1.2) applying of a metal foil onto the thick-film layer of the ceramic substrate; and
(1.3) bonding of the metal foil with the ceramic substrate via the thick-film layer. 2. A process for preparing a structured metal-ceramic substrate, characterized by the following process steps:
(2.1) applying of a thick-film paste onto a metal foil;
(2.
2) applying of a ceramic substrate onto the thick-film layer of the metal foil; and
(2.3) bonding the metal foil with the ceramic substrate via the thick-film layer.
3. The process according to claim 1 or 2, characterized in that the thick-film paste is applied continuously or discontinuously.
4. The process according to any one of claims 1 to 3, characterized in that the metal foil is applied continuously or discontinuously.
5. The process according to any one of claims 1 to 4, characterized in that the thick-film paste is coated onto the metal foil or the ceramic substrate by screen printing.
6. The process according to any one of claims 1 to 5, characterized in that the metal foil and/or the thick-film layer is oxidized before bonding to the ceramic substrate.
7. The process according to any one of claims 1 to 6, characterized in that the thick-film paste is applied onto the substrate or metal foil by multilayer printing.
8. The process according to claims 1 and 3 to 7, characterized in that the thick-film paste is applied onto the substrate by multilayer coating and a first coating of this mul- tilayer coating is provided with lines for contacts.
9. The process according to any of claims 1 to 8, characterized in that the thick-film paste comprises copper as a metal and optionally Bi2O3.
10. The process according to any of claims 1 to 8, characterized in that the thick-film paste comprises copper as a metal and optionally a glass material.
11. The process according to claim 9 or 10, characterized in that the thick-film paste comprises copper in an amount of from 40 to 92 wt.-%, more preferably 70 to 92 wt.- %, most preferably 75 to 90 wt.-%, each based on the total weight of the thick-film paste.
12. A metal-ceramic substrate, comprising
(a) a ceramic substrate and, provided thereon,
(b) a metal-containing thick-film layer, and, provided thereon;
(c) a metal foil.
13. The metal-ceramic substrate according to claim 12, characterized in that the thick-film layer and/or the metal foil is structured.
14. Use of a thick-film paste for preparing a metal-ceramic substrate as intermediate layer between a ceramic substrate and a metal foil.
15. The use according to claims 14, characterized in that the thick-film paste comprises copper as a metal and optionally Bi2O3.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018210786A1 (en) 2017-05-16 2018-11-22 Heraeus Deutschland GmbH & Co. KG Ceramic-metal substrate with low amorphous phase
EP3595002A1 (en) 2018-07-12 2020-01-15 Heraeus Deutschland GmbH & Co KG Metal-ceramic substrate with a film formed for direct cooling as substrate bottom
JP2020072207A (en) * 2018-07-31 2020-05-07 國家中山科學研究院 A method to increase the adhesive strength between the ceramic mounting plate and the thick film circuit
DE102019108594A1 (en) * 2019-04-02 2020-10-08 Rogers Germany Gmbh Process for the production of a metal-ceramic substrate and such a metal-ceramic substrate.

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102020120188B4 (en) * 2020-07-30 2024-08-01 Rogers Germany Gmbh Method for producing a carrier substrate and a carrier substrate produced by such a method
EP4112587A1 (en) * 2021-06-29 2023-01-04 Heraeus Deutschland GmbH & Co. KG Method for producing a metal-ceramic substrate though rapid heating
KR102873713B1 (en) * 2022-11-18 2025-10-20 한국광기술원 Insulator Composition and Method for Fabricating Insulation Layer on Metal Substrate using Thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4172919A (en) * 1977-04-22 1979-10-30 E. I. Du Pont De Nemours And Company Copper conductor compositions containing copper oxide and Bi2 O3
US4323483A (en) * 1979-11-08 1982-04-06 E. I. Du Pont De Nemours And Company Mixed oxide bonded copper conductor compositions
DE102010025313A1 (en) * 2010-06-28 2011-12-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Process for producing a structured, electrically conductive layer on a ceramic carrier
US20120107631A1 (en) * 2010-11-02 2012-05-03 Industrial Technology Research Institute Bonding material, method, and structure

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4775414A (en) * 1986-06-26 1988-10-04 Showa Denko Kabushiki Kaisha Inorganic adhesive
DE69031039T2 (en) * 1990-04-16 1997-11-06 Denki Kagaku Kogyo Kk CERAMIC PCB
US5766305A (en) * 1992-10-21 1998-06-16 Tokin Corporation Metal powder composition for metallization and a metallized substrate
JPH11236270A (en) * 1998-02-25 1999-08-31 Kyocera Corp Silicon nitride substrate and method of manufacturing the same
US6362531B1 (en) * 2000-05-04 2002-03-26 International Business Machines Corporation Recessed bond pad
US6873529B2 (en) * 2002-02-26 2005-03-29 Kyocera Corporation High frequency module
JP4345054B2 (en) * 2003-10-09 2009-10-14 日立金属株式会社 Brazing material for ceramic substrate, ceramic circuit board using the same, and power semiconductor module
US9780011B2 (en) * 2011-06-30 2017-10-03 Hitachi Metals, Ltd. Brazing material, brazing material paste, ceramic circuit substrate, ceramic master circuit substrate, and power semiconductor module
US9799421B2 (en) * 2013-06-07 2017-10-24 Heraeus Precious Metals North America Conshohocken Llc Thick print copper pastes for aluminum nitride substrates
CN104496513B (en) * 2014-11-13 2017-10-17 孝感市汉达电子元件有限责任公司 A kind of ceramic discharge tube process for sealing

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4172919A (en) * 1977-04-22 1979-10-30 E. I. Du Pont De Nemours And Company Copper conductor compositions containing copper oxide and Bi2 O3
US4323483A (en) * 1979-11-08 1982-04-06 E. I. Du Pont De Nemours And Company Mixed oxide bonded copper conductor compositions
DE102010025313A1 (en) * 2010-06-28 2011-12-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Process for producing a structured, electrically conductive layer on a ceramic carrier
US20120107631A1 (en) * 2010-11-02 2012-05-03 Industrial Technology Research Institute Bonding material, method, and structure

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018210786A1 (en) 2017-05-16 2018-11-22 Heraeus Deutschland GmbH & Co. KG Ceramic-metal substrate with low amorphous phase
US11430741B2 (en) 2017-05-16 2022-08-30 Heraeus Deutschland GmbH & Co. KG Ceramic-metal substrate with low amorphous phase
EP4212497A1 (en) 2017-05-16 2023-07-19 Heraeus Deutschland GmbH & Co. KG Ceramic-metal substrate with low amorphous phase
EP3595002A1 (en) 2018-07-12 2020-01-15 Heraeus Deutschland GmbH & Co KG Metal-ceramic substrate with a film formed for direct cooling as substrate bottom
WO2020011905A1 (en) 2018-07-12 2020-01-16 Heraeus Deutschland GmbH & Co. KG Metal-ceramic substrate comprising a foil as a bottom substrate face, said foil being shaped for direct cooling
JP2020072207A (en) * 2018-07-31 2020-05-07 國家中山科學研究院 A method to increase the adhesive strength between the ceramic mounting plate and the thick film circuit
DE102019108594A1 (en) * 2019-04-02 2020-10-08 Rogers Germany Gmbh Process for the production of a metal-ceramic substrate and such a metal-ceramic substrate.

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