WO1998039784A9 - Ceramic multilayer printed circuit boards with embedded passive components - Google Patents
Ceramic multilayer printed circuit boards with embedded passive componentsInfo
- Publication number
- WO1998039784A9 WO1998039784A9 PCT/US1998/003270 US9803270W WO9839784A9 WO 1998039784 A9 WO1998039784 A9 WO 1998039784A9 US 9803270 W US9803270 W US 9803270W WO 9839784 A9 WO9839784 A9 WO 9839784A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- green tape
- layers
- glass
- capacitor
- layer
- Prior art date
Links
- 239000000919 ceramic Substances 0.000 title claims description 49
- 239000003990 capacitor Substances 0.000 claims abstract description 125
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 229910052751 metal Inorganic materials 0.000 claims abstract description 31
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- 239000011521 glass Substances 0.000 claims description 166
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 58
- 229910052709 silver Inorganic materials 0.000 claims description 56
- 239000004332 silver Substances 0.000 claims description 56
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- 229910002113 barium titanate Inorganic materials 0.000 claims description 39
- 229910000833 kovar Inorganic materials 0.000 claims description 27
- JRPBQTZRNDNNOP-UHFFFAOYSA-N Barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 claims description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052904 quartz Inorganic materials 0.000 claims description 11
- 229910052906 cristobalite Inorganic materials 0.000 claims description 9
- 229910052839 forsterite Inorganic materials 0.000 claims description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 8
- 229910052681 coesite Inorganic materials 0.000 claims description 8
- 229910052878 cordierite Inorganic materials 0.000 claims description 8
- YEXPOXQUZXUXJW-UHFFFAOYSA-N lead(II) oxide Inorganic materials [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims description 8
- ZBSCCQXBYNSKPV-UHFFFAOYSA-N oxolead;oxomagnesium;2,4,5-trioxa-1$l^{5},3$l^{5}-diniobabicyclo[1.1.1]pentane 1,3-dioxide Chemical compound [Mg]=O.[Pb]=O.[Pb]=O.[Pb]=O.O1[Nb]2(=O)O[Nb]1(=O)O2 ZBSCCQXBYNSKPV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052682 stishovite Inorganic materials 0.000 claims description 8
- 229910052905 tridymite Inorganic materials 0.000 claims description 8
- VKJLWXGJGDEGSO-UHFFFAOYSA-N barium(2+);oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[O-2].[Ti+4].[Ba+2] VKJLWXGJGDEGSO-UHFFFAOYSA-N 0.000 claims description 7
- -1 copper-nickel Chemical compound 0.000 claims description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 5
- ROZSPJBPUVWBHW-UHFFFAOYSA-N [Ru]=O Chemical compound [Ru]=O ROZSPJBPUVWBHW-UHFFFAOYSA-N 0.000 claims description 4
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- 229920005989 resin Polymers 0.000 description 17
- 239000002270 dispersing agent Substances 0.000 description 15
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 14
- 239000002245 particle Substances 0.000 description 11
- 210000003622 mature neutrocyte Anatomy 0.000 description 10
- 239000002241 glass-ceramic Substances 0.000 description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- WUOACPNHFRMFPN-UHFFFAOYSA-N Terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 7
- 229940116411 Terpineol Drugs 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 7
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
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- 239000001856 Ethyl cellulose Substances 0.000 description 5
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 5
- 238000010344 co-firing Methods 0.000 description 5
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- 229910052763 palladium Inorganic materials 0.000 description 5
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- 238000007792 addition Methods 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 239000003989 dielectric material Substances 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
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- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
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- 229910001929 titanium oxide Inorganic materials 0.000 description 3
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
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- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium monoxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
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- 229910052788 barium Inorganic materials 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium(0) Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- BOGASOWHESMEKT-UHFFFAOYSA-N barium;oxotin Chemical compound [Ba].[Sn]=O BOGASOWHESMEKT-UHFFFAOYSA-N 0.000 description 1
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- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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Definitions
- This invention relates to multilayer, ceramic, supported printed circuit boards that have low shrinkage in two dimensions on firing. More particularly this invention relates to metal supported, multilayer, ceramic printed circuit boards that incorporate co- fired passive components.
- Ceramic compositions of crystallizing glasses are known which, when mixed with non-crystallizing glasses, form green tape compositions which can be adhered to metal core support substrates, such as copper/nickel clad or plated kovar plates.
- Kovar is a Fe/Co/Ni alloy commercially available from Carpenter Technology. One such alloy includes 53.8 weight percent of iron, 29 weight percent of nickel, 17 weight percent of cobalt and 0.2 weight percent of manganese. These alloys display a sharp change in their coefficient of expansion at certain temperatures. They are available with a 1 mil thick coating of copper and a 1 mil thick coating of nickel on both sides of the kovar core. They have a thermal coefficient of expansion (TCE) of 5.8 ppm/°C (RT to 300°C) and a thermal conductivity (z or thickness direction) of 21.8 Watt/m°K.
- TCE thermal coefficient of expansion
- a bonding glass generally a CaO-Al 2 0 3 -ZnO-B 2 0 3 glass.
- the bonding glasses can be screen printed onto the support substrate by making a printable ink of the bonding glass powder mixed with an organic binder and a solvent .
- the bonding glass is generally applied to a thickness of 40-70 microns on the support substrate.
- the bonding glass is then dried and densified by heating at 700-800°C.
- about 6% by weight of copper powder can be added to the bonding glass .
- Low firing temperature green tapes adhered to a metal core support board having a bonding glass thereon as dexcribed above are made from a mixture of crystallizing and non-crystallizing glasses.
- Suitable crystallizing glasses for example contain 20-
- these glasses have a TCE matched to kovar, and they have low dielectric loss properties; however, they have a low crystallization temperature which inhibits densification of the glass on firing.
- these glasses can be mixed with a lead-based, non-crystallizing glass.
- these non-crystallizing glasses contain from 30-80% by weight of PbO; 15-50% by weight of Si0 2 ; up to 10% by weight of Al 2 0 3 ; up to 15% by weight of B 2 0 3 ; and up to 10% by weight of ZnO.
- the TCE is lowered and the dielectric loss properties are increased.
- the lateral shrinkage (x and y) is still higher than desirable as well.
- oxide fillers such as quartz, alumina, forsterite and the like, reduces the lateral shrinkage on firing, and thus these filler- modified ceramics have desirable dielectric properties, low shrinkage during firing and a TCE matched to kovar.
- Green tape compositions useful herein are formed by mixing suitable glass powders, including crystallizing glasses, generally of the ZnO-MgO-B 2 0 3 -Si0 2 type, with non- crystallizing glasses and oxide fillers with an organic vehicle, generally including resin, solvent, dispersants and the like, and casting the resultant slurry into a thin tape, known as green tape .
- suitable glass powders including crystallizing glasses, generally of the ZnO-MgO-B 2 0 3 -Si0 2 type, with non- crystallizing glasses and oxide fillers with an organic vehicle, generally including resin, solvent, dispersants and the like, and casting the resultant slurry into a thin tape, known as green tape .
- Conductive inks can be screen printed onto the green tapes to form circuit patterns.
- Several of the green tapes can be aligned and stacked and laminated under pressure. Via holes punched in the green tapes and filled with conductive inks, e.g., mixtures of a conductive metal powder, an organic vehicle and a glass, generally the same glass as that used to make the green tape, provide a conductive path between the circuit patterns on different green tape layers.
- conductive inks e.g., mixtures of a conductive metal powder, an organic vehicle and a glass, generally the same glass as that used to make the green tape, provide a conductive path between the circuit patterns on different green tape layers.
- These laminated green tape stacks are then aligned with a support substrate coated with a bonding glass, and co- laminated, also under pressure. Since shrinkage occurs mainly in the thickness (z) dimension during firing, the circuitry is not disturbed during firing and close tolerances can be maintained.
- Ceramics are compatible with low melt temperature conductive inks, such as silver- based inks, used to form the electrically connected circuits on the various layers and to form bond pads and the like.
- conductive inks such as silver- based inks
- the ceramic circuit boards as described hereinabove have low dielectric loss properties and are useful for use with microwave/digital packaging.
- multilayer ceramic circuit boards are to include passive components, such as resistors or capacitors
- passive components such as resistors or capacitors
- solder or epoxy type adhesives to adhere the components to the multilayer ceramic.
- the addition of these components increases the number of steps needed to make these circuit boards, i.e., the components must be aligned and adhered to the ceramic multilayer board, and connected to a source of power.
- the multilayer boards have to be large. Thus the costs of making such boards is high.
- passive components such as capacitors, resistors and RF components
- passive components can be embedded in green tape stacks made of suitable glasses on a support substrate that prevents shrinkage in the x and y dimensions.
- Suitable capacitor or resistor inks and conductive layers can be screen printed onto green tapes, embedded between other green tapes, laminated and fired at fairly low temperatures, i.e., 850-900°C, without de-laminating from the support and without shrinkage in the x and y dimensions so as to produce printed circuit boards with close tolerances that have embedded components therein.
- Capacitor inks can be made from barium titanate, titanium oxide and lead magnesium niobate dielectrics, which, when combined with appropriate glasses, sinter at low temperatures.
- the capacitor inks can be screen printed onto ceramic green tapes and connected to a silver conductor layer by means of vias in the green tape that are filled with appropriate conductive inks. After printing the passive component precursor inks and other circuitry on the green tapes, multiple green tapes are aligned, laminated together and co-fired in air at a temperature of about 850-900°C.
- Capacitors can be made in a wide range of dielectric constants .
- Shunt capacitors can also be made by using a ground plane metal as the bottom capacitor plate.
- the capacitors are located one or more layers from the top of the stack.
- Capacitors can be terminated by screen printing a conductive layer over and under the printed capacitor dielectric ink.
- Thick film resistor inks can be made based on ruthenium oxide (Ru0 2 ) and appropriate glasses that sinter at low temperatures, together with suitable organic vehicles.
- the resistor inks are screen printed onto green tapes that are aligned and stacked on a support, and fired to produce embedded resistors having a wide range of resistor values and thermal coefficient of resistance (TCR) values.
- TCR thermal coefficient of resistance
- a small amount of barium titanate can be added.
- the resistors are connected to a source of power with a conductive layer screen printed on top of the green tape stack.
- the multiple green tape layers are aligned, laminated together, applied to a metal support substrate via a bonding glass, and co-fired in air at temperatures of from about 780-900°C to form printed circuit boards having embedded resistors therein that are stable and reliable.
- Fig. 1 is a graph of dielectric constant versus capacitor size for low dielectric constant inks.
- Fig. 2 is a cross sectional view of one embodiment of a buried capacitor of the invention.
- Fig. 3 is a graph of dielectric constant versus capacitor size for capacitors of the invention.
- Fig. 4 is a graph of temperature coefficient of capacitance versus capacitor size for capacitors of the invention.
- Fig. 5 is a graph of dielectric constant versus capacitor size for capacitors of the invention.
- Fig. 6 is a graph of resistor area versus resistance and TCR for resistors having a first size.
- Fig. 7 is a graph of resistor area versus resistance and TCR for resistors having a second size.
- Fig. 8 is a cross sectional view of a multilayer ceramic circuit board of the invention having buried silver layers .
- Fig. 9 is a cross sectional view of a multilayer ceramic circuit board of the invention having RF filters embedded in the layers.
- capacitor inks based on barium titanate and titanium oxide powders. These powders sinter at high temperatures, about 1100-1300°C, and thus they must be modified by combining them with low melting glasses so that the barium titanate/glass or titanium oxide/glass compositions will sinter at lower temperatures of about 850- 900°C, and to adjust the dielectric constant (K) and to minimize the temperature coefficient of capacitance (TCC) .
- Barium titanate is commercially available from the Degussa Company under the trade name AD302L, (designated below as D) and a mixture of barium titanate and barium tin oxide from the Ferro Corporation under the trade name YL12000 (designated below as F) .
- the properties of these powders are set forth below in Table I, wherein K is the dielectric constant, the dielectric loss is Tan ⁇ and the temperature is in degrees Centigrade. Particle size is given as average particle size in microns ( ⁇ m) .
- a suitable titanium oxide, #4162-01, is available from
- the barium titanate or titanium oxide powder was mixed with various low firing temperature glasses.
- the compositions of suitable glasses, in weight percent, is given below in Table II.
- the capacitor inks can be screen printed onto green tapes formulated for co-firing onto metal, particularly kovar, support substrates.
- the primary crystallizing glass used is made from a mixture of the following oxides: 29.4% of ZnO, 24.5% of MgO, 19.6% of B 2 0 3 , 24.5% of Si0 2 and 2.0% of Co 3 0 4 , all % by weight.
- Typical green tape compositions are given below in Table IV. TABLE IV
- the capacitor inks were screen printed onto the above green tapes in square capacitor patterns 1.27, 2.54 and 5.08 mm in size. Three four-layer green tapes were made with the capacitor ink layer one layer from the top of the stack. The green tapes were laminated at 278 psi and co-laminated to a kovar substrate at 347 psi. A silver-based powder or silver flake-based conductor ink was buried to make a buried co- fired capacitor. Suitable conductor ink compositions are set forth in Table V.
- the resultant laminated stack was fired at 850°C.
- the capacitance and dielectric loss (tan ⁇ ) were measured at lOKHz.
- the dielectric constant for each capacitor was calculated from the measurement of capacitance (C) in pF, the area (A) of the capacitor in square centimeters and the thickness (t) in centimeters in accordance with the equation
- BaTi0 3 -based capacitor inks using a silver powder conductor layer. Green tape and capacitor layers were laminated at 280 psi and fired at 850°C. The glass is given in volume %.
- the above capacitor compositions were tailored to promote sintering at low temperatures with a minimum dilution of the dielectric constant and to contain less than
- a barium titanate-based capacitor formulation also includes a substantial amount of a TCC modifier, SrZr0 3 .
- Table X illustrates compositions of two such suitable I 7
- capacitor inks given in % by weight.
- a silver-based ink made from 83.78% silver powder
- the green tape stacks were laminated at 1670 psi and co- laminated to a kovar substrate at 1100 psi and the whole fired at 865°C.
- the dielectric constant (K) and TCC at two temperatures are given below in Table XI .
- a capacitor ink having a low TCC and a low dielectric constant can also be made using titanium oxide (Ti0 2 ) as the dielectric.
- Ti0 2 titanium oxide
- a dielectric ink was made using 42.1% of Ti0 2 powder, 29.6% of glass 2, 1.4% of Hypermer PS2 dispersant and 26.9% of a mixture of 20% of Elvacite resin in terpineol solvent .
- the dielectric ink was applied to a green tape at least one layer below the top of the stack, and a termination layer applied thereunder using a conductor ink, and the stack laminated and fired as above.
- the TCC and dielectric constant K are given in Table XII below.
- a barrier layer can be used to block the diffusion of the ceramics into the capacitors during co-firing. This barrier layer can be of a more effective silver metal composition, or of a different dielectric material.
- a BaTi0 3 based capacitor ink can be used as a barrier material when a very low melting glass, lower melting than the glass used in the green tape layers, is used.
- This barrier glass densifies and crystallizes at a lower temperature than that required for the green tape glasses to soften significantly.
- the barrier glass blocks the diffusion of the green tape glasses into the capacitor.
- the barrier is printed as a pad larger than the capacitor, both below the bottom conductor pad and above the top conductor pad, as shown in Fig. 2.
- a three layer capacitor 12 having a two layer top and bottom conductor layers 14 and 15 respectively is sandwiched between two top and bottom two-layer barrier layers 16 and 17 respectively.
- the buried capacitor is in turn laminated to top and bottom green tape layers 18 and 19 respec ively .
- a barrier layer was printed as a pad 19x19mm, centered about a capacitor 5.08 x 5.08mm made from a PMN ink including 74.16% of PMN. Silver powder was used to make the conductor ink.
- Various layers were employed to determine how many barium titanate barrier layers were required to obtain a high dielectric constant capacitor on a kovar supported multilayer circuit board. Controls without the barrier layers were also tested. The test results are given below in Table XIV wherein the number of prints refers to the number of screen prints used for each layer. TABLE XIV
- the dielectric constant was much higher than when no barrier layer, or a thin barrier layer, was used. Buried capacitors having a high dielectric constant were achieved however using a double metallization print, and a double barrier layer print . By increasing the number of barrier prints to three on either side of the conductive layers, dielectric constant (K) values above 3000 were obtained. However, while high dielectric constant capacitors can be made via the above process, several extra printing steps are required, 22. ' ' _ ' "
- the barrier thickness must be about 16-20 microns to be effective.
- the top green tape layer is subject to tearing and care must be taken to prevent that. Further, the large number of screen printing steps required (up to eleven as described above) adds to the costs of the process.
- the silver flake while it results in a high dielectric constant capacitor, forms a structure that becomes too dense during firing, and leads to tears in the overlying green tapes.
- the use of a mixture of silver powder and silver flake although a compromise in terms of dielectric constant, does not tear the top green tape layer nor do these structures have outgassing or bubbling problems.
- a plurality of buried PMN-based capacitors on kovar substrates were made using silver powder, silver flake and a mixed silver powder and silver flake conductor layer. The layers were laminated at 1670 psi and fired at 865°C. The test results are summarized below in Table XV.
- Insulation Resistance (IR) of the first capacitor of 5.08mm size was 3.8xl0 10 ohms.
- IR of the second capacitor of 5.08mm size using silver flake was 6.0xl0 10 ohms.
- the IR of the first capacitor using the mixed silver and the same size was l.OxlO 10 ohms.
- the dielectric constant of the PMN capacitors exhibit a large size dependence; i.e., the dielectric constant increases with increasing capacitor size, and TCC also increases (becomes more negative) with increasing capacitor size. It is believed this is a result of dilution of the capacitor dielectric by the surrounding low dielectric constant ceramic. Large capacitors have less dilution effect than small capacitors. This is shown in Table XVI below, and schematically in Figs 3 and 4, graphs of dielectric constant and TCC versus capacitor size, respectively. In Table XV the capacitors are based on PMN with mixed silver powder-silver flake inks.
- Fig. 5 is a graph of dielectric constant versus capacitor size using a mixed silver conductor, illustrates the differences in the size dependence of barium titanate- based capacitors and PMN-based capacitors.
- barium titanate-based buried capacitors will be more consistent and have lower TCC as compared to PMN-based capacitors .
- the buried capacitors of the invention have been subject to the HHBT reliability test (85°C/85%RH/50VDC) for over 1000 hours with no degradation of the capacitance, dielectric loss or insulation resistance (IR) of the buried capacitors .
- the above co- fired multilayer ceramic circuit boards having buried capacitors of the invention are useful in various applications, such as cellular telephones.
- Resistor inks with resistor values of from 300 ohm/sq to 100 Kohms/sq and a TCR of ⁇ +200 ppm/°C over a temperature range of room temperature to 125°C also can be made in accordance with the invention.
- the target properties for a particular cellular telephone application are 1 Kohm/sq and a TCR less than or equal to 200 ppm/°C over the room temperature to 125°C range.
- the resistor inks are made from a fine particle size, high surface area Ru0 2 powder having the characteristics as summarized in Table XVII.
- the Ru0 2 is mixed with one or more glasses to reduce the firing temperature of the conductor powder. Glasses 1 and 3 as set forth above are suitable. A TCR modifier such as BaTi0 3 can also be added.
- the above glasses are mixed with the Ru0 2 powder, optional modifier and a suitable organic vehicle to- form a screen printable composition that can be fired at low temperatures, similar to the firing temperature of the green tape stacks they will be applied to.
- the resistor ink powder generally contains 17.33 to 24.8% by weight of Ru0 2 , 74.3- 81.7% by weight of glass 1 and 0.99 to 1.10% by weight of barium titanate.
- the preferred compositions contain 19.8 to 23.14% by weight of Ru0 2 , 75.87 to 79.21% by weight of glass 1 and 0.99 to 1.1% by weight of BaTi0 2 .
- Resistor inks were screen printed onto a green tape incorporated into a laminated green tape stack in various patterns (1/2 squares and squares) in sizes from 0.508 x 0.508 to 2.032 x 4.064 mm.
- Green tape compositions suitable for use herein include the following ingredients, summarized in Table XVIII. The median particle size of the glass and filler materials are given in microns.
- a suitable silver ink composition includes 83.78% by weight of silver powder, 0.65 weight % of glass 3, 1.22 weight% of a dispersant, 0.88 weight % of ethyl cellulose resin, 0.80 of Elvacite 2045 resin (available from Monsanto Company) , and a mixed solvent of 3.32 weight % of texanol, 6.81 weight % of terpineol and 2.54 weight % of butyl carbitol .
- the green tape stacks were laminated together and placed on a kovar support substrate and co-fired in air at 850-900°C.
- the resistors were printed and buried one layer below the top surface of the ceramic stack. After co-firing, the resistors were then connected to the outside by printing with a silver-palladium or gold conductor ink and post-fired at 700-750°C in air.
- Table XIX below summarizes the Ru0 2 -glass compositions and the properties of the fired resistors.
- Table XIX summarizes the Ru0 2 -glass compositions and the properties of the fired resistors.
- the compositions are given in weight %, and TCR was measured from room temperature to 125°C.
- a short term overload test (STOL) was also performed.
- the above resistor compositions were admixed with an organic vehicle to form an ink composition, using a dispersant (1.44% by weight), ethyl cellulose Resin N300
- the resistor ink was adjusted to about 38 volume % solids. In order to maximize circuit density, it is desirable to print small size resistors such as patterns of 0.508 x
- Suitable resistor ink compositions made from the above powder mixtures are shown below in Table XXI . TABLE -XXI
- resistor ink compositions 1 and 2 are given below in Tables XXIII and XXIV respectively. TCR was measured at room temperature and at 125°C. TABLE XXIII
- Figs. 6 and 7 are graphs of resistance versus resistor area for (1) square resistors and for (1/2) resistors respectively.
- Test 1 was for 1000 hours at 85°C/85%RH
- Test 2 consisted of cycling over 200 times between -55 and 125°C.
- Test 3 applied 15.5 Watts/cm 2 of power to the resistor at 70°C for 1000 hours.
- the resistors passed these tests.
- Resistor ink 1 was used to make a 510 ohm buried resistor 1.016 x 2.032 mm in size in a receiver board designed for operation at 1 GHz.
- a resistance value of 510 ohms ⁇ 10% was obtained after post firing, providing the dried ink thickness was maintained at between 18 and 25 microns .
- the ceramic printed circuit boards of the invention are also useful for incorporating or embedding other components, such as RF filters.
- other components such as RF filters.
- thick multilayer stacks that are over 2 mm in thickness after firing are made.
- the large number of green tape layers after firing preclude close control of the shrinkage in the x and y dimensions, and, in addition, the multilayer stack tends to de-laminate from the metal support substrate when fired.
- Useful prior art glasses used to make one type- of green tape are made from zinc-magnesium-borosilicate crystallizing glasses as described above.
- a suitable crystallizing glass is glass 3 above to which 2.0% by weight of Co 3 0 4 coloring agent is added.
- This glass is mixed with 9.6% by weight of a non- crystallizing lead-based glass of the lead-zinc-aluminum silicate system.
- An exemplary glass contains 42.0% by weight of PbO; 10.0% by weight of Al 2 0 3 , 38.8% by weight of Si0 2 and 10.0% by weight of ZnO.
- oxide fillers such as alumina, cordierite, quartz, cristoballite, forsterite and willemite, which serve to control the shrinkage and to further modify the TCE.
- oxide fillers such as alumina, cordierite, quartz, cristoballite, forsterite and willemite
- the desired dielectric properties, shrinkage characteristics and TCE matched to kovar can all be achieved.
- minor amounts of filler oxides e.g., 1.5-2% by weight of cordierite and 9.5-10.0% by weight of forsterite, produce excellent ceramics for the present applications.
- these glasses have major amounts of glass and minor amounts of oxide fillers ( ⁇ 15%) . These glasses have excellent dielectric properties at microwave frequencies, such as 1 GHz. These ceramics are referred to hereinafter as Type I glass-ceramics.
- a second type of glass-ceramic is made from the same zinc-magnesium-borosilicate glasses but they include increased amounts, over about 25% by weight, of oxide fillers. These glasses have lower shrinkage than the Type 1 glass-ceramics, and are referred to hereinafter as Type 2 glass-ceramics .
- Type 2 glass-ceramics The following Table XXV sets forth examples of different ceramic compositions useful to make the second type of green tape layers .
- Ceramic 1 2. 3_ 4. Composition —-- . ⁇ — ⁇ —--- ⁇ - ⁇ --- ⁇ - ⁇ -- ⁇ ---- ⁇ ..-—.- ⁇ - ⁇ ——
- Green tapes are made by formulating the Type 1 and
- Type 2 glass-ceramics with a resin binder together with plasticizer, dispersants and solvents in known manner, to form a thick slurry A typical glass-ceramic composition for use herein has a crystallizing glass particle size of about
- the resultant slurry is cast to form a green tape about 0.15-0.20 mm thick, and the green tape is dried.
- the two types of green tape using minor and major amounts of amounts of oxide fillers respectively, are then interleaved.
- Silver or other metal patterns are screen printed on the green tapes to form circuit patterns.
- circuit patterns are printed between two green tapes of Type 1, to form a hermetic ceramic, since the Type 2 (high filler content) glass-ceramics tend to become more porous on firing than the Type 1 glass-ceramics.
- a co-firable conductive metal-based thick film conductor ink based on the glass compositions of the invention can be made with a conductive metal powder, such as silver powder, mixed with a small amount of the glasses disclosed above, together with known dispersants, resins and solvents to form a screen printable conductor ink.
- Top conductor inks can be made in like fashion using silver- palladium powder, or a gold powder. Via fill inks to connect circuit patterns on various green tape layers together can also be made with silver powder, in known manner.
- the green tape stack is then suitably laminated at a pressure of about 1.174 kg/mm 2 at about 93°C for four minutes, and co-laminated with the prepared metal support substrate at a pressure of about 1.3-1.4kg/mm 2 .
- the multilayer stack on the kovar support is fired in a belt furnace at a belt speed of 0.4 inch/min to a peak temperature of 850-900°C.
- the organic materials are vaporized, and the low melting glazing glass softens, adhering the multilayer ceramic stack to the metal core .
- the metal core aids in limiting the shrinkage of the overlying green tapes in the x and y directions.
- a conductive ink may be applied to the top of the fired multilayer stack, as to form bond pads, inductors, microstrip interconnects and the like, in known manner .
- Example 1 The invention will be further described in the following Examples, but the invention is not meant to be limited to the details described therein. In the Examples, percent is by weight .
- Example 1 Example 1
- Type 1 green tape A
- C,D a silver-based ink applied thereto
- B Type 2 green tape
- Type I green tape Eleven layers of Type I green tape, having metallized planes on three of the layers, were interleaved with Type 2 green tapes, as shown in Fig. 8.
- Fig. 8 illustrates the Type 1 green tapes as A, Type 2 green tapes as B, C designates embedded RF filters, and D illustrates silver patterning.
- the green tapes were interleaved and stacked, laminated, co- laminated to a kovar support and fired. The fired stack was 2.40 mm thick.
- Type 2 green tape were interleaved and stacked, laminated and fired.
- the resultant stack was 2.20 mm thick.
- Type 1 (A) green tape having embedded filters (C) on one layer and ground planes (D) on two layers, as shown in Fig. 9, and 8 layers of Type 2 green tape (B) were interleaved and stacked, laminated and fired to form a stack 2.52 mm in thickness.
- Example 4 23 layers, of Example 4 5.39 0.0018 11.6 GHz
- interleaved layers 5.24 0.0019 12.2 GHz
- interleaved green tape layers can be stacked to produce thick fired metal supported multilayer circuit boards that shrink in only one dimension.
Abstract
Passive components such as capacitors, resistors, and RF filters can be made by screen printing suitable inks onto green tapes, completed with conductive layers (14, 15) below and above the component ink layers. The resultant green tape stack is then fired to form embedded capacitors. By laminating the green tape stack onto metal support board substrate, shrinkage in the x and y dimensions is limited and the components can maintain close tolerances. When many green tape layers are to be stacked, improved shrinkage is obtained when green tapes having a moderate amount of oxide fillers, e.g., less than about 15 % by weight of the green tape composition, are interleaved with green tape having higher amounts, e.g., above 25 % by weight, of oxide fillers.
Description
CERAMIC MULTILAYER PRINTED CIRCUIT BOARDS WITH EMBEDDED PASSIVE COMPONENTS
This invention relates to multilayer, ceramic, supported printed circuit boards that have low shrinkage in two dimensions on firing. More particularly this invention relates to metal supported, multilayer, ceramic printed circuit boards that incorporate co- fired passive components.
BACKGROUND OF THE INVENTION
Ceramic compositions of crystallizing glasses are known which, when mixed with non-crystallizing glasses, form green tape compositions which can be adhered to metal core support substrates, such as copper/nickel clad or plated kovar plates. Kovar is a Fe/Co/Ni alloy commercially available from Carpenter Technology. One such alloy includes 53.8 weight percent of iron, 29 weight percent of nickel, 17 weight percent of cobalt and 0.2 weight percent of manganese. These alloys display a sharp change in their coefficient of expansion at certain temperatures. They are available with a 1 mil thick coating of copper and a 1 mil thick coating of nickel on both sides of the kovar core. They have a thermal coefficient of expansion (TCE) of 5.8 ppm/°C (RT to 300°C) and a thermal conductivity (z or thickness direction) of 21.8 Watt/m°K.
To use these kovar plates as support substrates for printed circuit boards, they are heat treated in air to oxidize the nickel coating and then glazed with a bonding glass, generally a CaO-Al203-ZnO-B203 glass. The bonding glasses can be screen printed onto the support substrate by making a printable ink of the bonding glass powder mixed
with an organic binder and a solvent . The bonding glass is generally applied to a thickness of 40-70 microns on the support substrate. The bonding glass is then dried and densified by heating at 700-800°C. To improve the adhesion of the bonding glass to a kovar support, about 6% by weight of copper powder can be added to the bonding glass . These kovar support substrates prepared as above are used herein and, when co-laminated to low firing temperature green tape compositions, they prevent shrinkage of the ceramic layers in the x and y dimensions during firing.
Low firing temperature green tapes adhered to a metal core support board having a bonding glass thereon as dexcribed above are made from a mixture of crystallizing and non-crystallizing glasses. Suitable crystallizing glasses for example contain 20-
55% by weight of ZnO; 20-28% by weight of MgO; 10-35% by weight of B203; and 10-40% by weight of Si02. These glasses have a TCE matched to kovar, and they have low dielectric loss properties; however, they have a low crystallization temperature which inhibits densification of the glass on firing. Thus these glasses can be mixed with a lead-based, non-crystallizing glass. Suitably, these non-crystallizing glasses contain from 30-80% by weight of PbO; 15-50% by weight of Si02; up to 10% by weight of Al203; up to 15% by weight of B203; and up to 10% by weight of ZnO.
However, when the crystallizing glasses are mixed with lead-based, non-crystallizing glasses, the TCE is lowered and the dielectric loss properties are increased. The
lateral shrinkage (x and y) is still higher than desirable as well. The addition of minor amounts of oxide fillers, such as quartz, alumina, forsterite and the like, reduces the lateral shrinkage on firing, and thus these filler- modified ceramics have desirable dielectric properties, low shrinkage during firing and a TCE matched to kovar.
Green tape compositions useful herein are formed by mixing suitable glass powders, including crystallizing glasses, generally of the ZnO-MgO-B203-Si02 type, with non- crystallizing glasses and oxide fillers with an organic vehicle, generally including resin, solvent, dispersants and the like, and casting the resultant slurry into a thin tape, known as green tape .
Conductive inks can be screen printed onto the green tapes to form circuit patterns. Several of the green tapes can be aligned and stacked and laminated under pressure. Via holes punched in the green tapes and filled with conductive inks, e.g., mixtures of a conductive metal powder, an organic vehicle and a glass, generally the same glass as that used to make the green tape, provide a conductive path between the circuit patterns on different green tape layers. These laminated green tape stacks are then aligned with a support substrate coated with a bonding glass, and co- laminated, also under pressure. Since shrinkage occurs mainly in the thickness (z) dimension during firing, the circuitry is not disturbed during firing and close tolerances can be maintained. These ceramics are compatible with low melt temperature conductive inks, such as silver-
based inks, used to form the electrically connected circuits on the various layers and to form bond pads and the like. Thus the ceramic circuit boards as described hereinabove have low dielectric loss properties and are useful for use with microwave/digital packaging.
Up to the present time, when multilayer ceramic circuit boards are to include passive components, such as resistors or capacitors, discrete components have been mounted to the top of the fired boards, using solder or epoxy type adhesives, to adhere the components to the multilayer ceramic. The addition of these components increases the number of steps needed to make these circuit boards, i.e., the components must be aligned and adhered to the ceramic multilayer board, and connected to a source of power. Further, in order to accommodate a number of discrete devices, the multilayer boards have to be large. Thus the costs of making such boards is high.
It would be advantageous to be able to screen print passive components onto particular green tapes of multilayer, low temperature co-fired ceramic circuit boards because the packing density can be increased, reducing the size and cost of the packaging, and the number of processing steps required can be reduced. Using the recently developed low firing temperature glasses and a metal support board that reduce shrinkage in the x and y dimensions, screen printing of such components to tight tolerances, and high precision placement, become feasible. Further, because fewer interconnects need to be made, reliability would also be
improved .
However, it is difficult to maintain reduced shrinkage during firing and to prevent de-lamination of the green tape stacks from the support substrate when a plurality of green tapes are aligned and fired with components therebetween.
SUMMARY OF THE INVENTION We have found that passive components, such as capacitors, resistors and RF components, can be embedded in green tape stacks made of suitable glasses on a support substrate that prevents shrinkage in the x and y dimensions. Suitable capacitor or resistor inks and conductive layers can be screen printed onto green tapes, embedded between other green tapes, laminated and fired at fairly low temperatures, i.e., 850-900°C, without de-laminating from the support and without shrinkage in the x and y dimensions so as to produce printed circuit boards with close tolerances that have embedded components therein.
Capacitor inks can be made from barium titanate, titanium oxide and lead magnesium niobate dielectrics, which, when combined with appropriate glasses, sinter at low temperatures. The capacitor inks can be screen printed onto ceramic green tapes and connected to a silver conductor layer by means of vias in the green tape that are filled with appropriate conductive inks. After printing the passive component precursor inks and other circuitry on the green tapes, multiple green tapes are aligned, laminated together and co-fired in air at a temperature of about 850-900°C. Capacitors can be made in a wide range of dielectric
constants .
Shunt capacitors can also be made by using a ground plane metal as the bottom capacitor plate. The capacitors are located one or more layers from the top of the stack. Capacitors can be terminated by screen printing a conductive layer over and under the printed capacitor dielectric ink.
Thick film resistor inks can be made based on ruthenium oxide (Ru02) and appropriate glasses that sinter at low temperatures, together with suitable organic vehicles. The resistor inks are screen printed onto green tapes that are aligned and stacked on a support, and fired to produce embedded resistors having a wide range of resistor values and thermal coefficient of resistance (TCR) values. To adjust the TCR values, a small amount of barium titanate can be added. The resistors are connected to a source of power with a conductive layer screen printed on top of the green tape stack. After printing the resistors and other circuitry, the multiple green tape layers are aligned, laminated together, applied to a metal support substrate via a bonding glass, and co-fired in air at temperatures of from about 780-900°C to form printed circuit boards having embedded resistors therein that are stable and reliable.
When many green tape layers are to be stacked to produce a fired stack about 2 mm in thickness or higher, we have found that de-lamination and shrinkage problems still occur. Thus we have further found that by interleaving green tape layers including low dielectric loss glasses that are mixed with minor amounts of oxide fillers with green tape
layers from the same glasses but now including greater amounts of oxide fillers, many more layers of green tapes can be stacked, laminated and fired with no shrinkage in the x and y directions, and with no de-lamination from a metal support substrate. These thick multilayer metal supported circuit board stacks are particularly useful when RF components are to be embedded in the stacks.
BRIEF DESCRIPTION OF THE DRAWING Fig. 1 is a graph of dielectric constant versus capacitor size for low dielectric constant inks.
Fig. 2 is a cross sectional view of one embodiment of a buried capacitor of the invention.
Fig. 3 is a graph of dielectric constant versus capacitor size for capacitors of the invention. Fig. 4 is a graph of temperature coefficient of capacitance versus capacitor size for capacitors of the invention.
Fig. 5 is a graph of dielectric constant versus capacitor size for capacitors of the invention. Fig. 6 is a graph of resistor area versus resistance and TCR for resistors having a first size.
Fig. 7 is a graph of resistor area versus resistance and TCR for resistors having a second size.
Fig. 8 is a cross sectional view of a multilayer ceramic circuit board of the invention having buried silver layers .
Fig. 9 is a cross sectional view of a multilayer ceramic circuit board of the invention having RF filters
embedded in the layers.
DETAILED DESCRIPTION OF THE INVENTION The formulation of various capacitor inks, methods of formation and test results of embedded capacitors having differing dielectric constant and TCC will be discussed first .
We have discovered low dielectric constant, i.e., K = about 50, capacitor inks based on barium titanate and titanium oxide powders. These powders sinter at high temperatures, about 1100-1300°C, and thus they must be modified by combining them with low melting glasses so that the barium titanate/glass or titanium oxide/glass compositions will sinter at lower temperatures of about 850- 900°C, and to adjust the dielectric constant (K) and to minimize the temperature coefficient of capacitance (TCC) . Barium titanate is commercially available from the Degussa Company under the trade name AD302L, (designated below as D) and a mixture of barium titanate and barium tin oxide from the Ferro Corporation under the trade name YL12000 (designated below as F) . The properties of these powders are set forth below in Table I, wherein K is the dielectric constant, the dielectric loss is Tanδ and the temperature is in degrees Centigrade. Particle size is given as average particle size in microns (μm) .
TABLE I
CompoFirinq Av . Part . sition K Tanδ TCC,% T,°C Size, urn
F 12000 0.022 -80* 1200 1.0 D 3200 <0.02 _ 9** 1140 0.6
* RT to 125°C * *** 8855°C
A suitable titanium oxide, #4162-01, is available from
Mallincrodt Baker Co.
Prior to making capacitor ink compositions, the barium titanate or titanium oxide powder was mixed with various low firing temperature glasses. The compositions of suitable glasses, in weight percent, is given below in Table II.
TABLE II
Oxide Glass 1 Glass 2 Glass 3 Glass 4* Glass 5 Glass 6
Al-O, 6.00 10.10 1.0 1.82
BaO <2.0
B203 39.00 19.60 >5.0 5.0 8.18
Bi203 23.0
CaO 5.0
CdO 36.0
MgO 24.50
PbO 50.00 >70.0 25.0 68.82
Si02 39.90 24.50 < 2.0 5.0 2.23
Ti02 9.09
ZnO 50.00 29.40 >12.0 5.0 9.09
Zr02 2.73
Particle 11- 5-7 10-12 5.0 5.0 4.0
Size, μm 13
* Commercially available glass as SCC-11 from Sem Com, Inc., Toledo, OH Representative low dielectric constant capacitor inks were made from barium titanate powder admixed with various glasses and glass mixtures, together with conventional dispersants, resin and solvent, and screen printed onto
green tapes. The ink compositions are summarized in Table III below wherein the glass compositions are as shown in Table II.
TABLE III
BaTiO, Wt % Glass# Wt % Dispersant Resin Solvent
Tvpe Wt % Wt% Wt %
F 62.29 1 7.14 1.43 4.07 23.07
F 66.09 1 8.25 1.52 4.84 19.38
F 64.89 2 9.8 1.49 4.76 19.05
D 65.62 1 13.52 1.57 4.83 14.48
D 59.99 1 3.08 1.44 4.45 21.04
D 62.27 2 12.15 1.54 4.41 17.83
D 60.86 2 15.34 1.52 4.46 17.82
D 60.10 3 14.84 1.50 4.71 18.85
D 57.05 2 15.35 1.54 4.46 17.84
SrZr03 3.76
D 59.15 2 15.38 1.54 4.47 17.89
SrTi03 1.57
D 58.88 2 15.33 1.53 4.48 17.85
SrZr03 1.94
D 62.25 2 14.04 1.56 4.43 17.73
D 63.61 2 12.79 1.53 4.41 17.66
The capacitor inks can be screen printed onto green tapes formulated for co-firing onto metal, particularly kovar, support substrates. The primary crystallizing glass used is made from a mixture of the following oxides: 29.4% of ZnO, 24.5% of MgO, 19.6% of B203, 24.5% of Si02 and 2.0% of Co304, all % by weight. Typical green tape compositions are given below in Table IV.
TABLE IV
Additive Function Amount , wt% Amount , wt% Green tape 1 Green tape 2
Glass Primary 57.34 57.29
Crystallizing
Glass
Glass P121 Secondary 6.98 7.03
Crystallizing
Glass
Forsterite2 Ceramic 7.27 4.42 Powder Filler
Cordierite3 Ceramic 1.09 3.44 Powder Filler
Hypermer PS24 Dispersant 0.58 0.58
Butvar B985 Binder 2.04 2.04
Santicizer Plasticizer 1.36 1.36 1606
Methyl ethyl Solvent 11.67 11.67 Ketone
Anhydrous Solvent 11.67 11.67 Ethanol
1 Glass composition (wt% ) 10 . 0% Al203 , 42 . 0% PbO , 38 . 0 % Si02 ,
10 . 0% ZnO
2 3-5μm median particle size
3 2-3μm median particle size Registered trademark of ICI Americas, Inc.
5 Registered trademark of Monsanto Co.
6 Registered trademark of Monsanto Co.
The capacitor inks were screen printed onto the above green tapes in square capacitor patterns 1.27, 2.54 and 5.08 mm in size. Three four-layer green tapes were made with the capacitor ink layer one layer from the top of the stack. The green tapes were laminated at 278 psi and co-laminated to a kovar substrate at 347 psi. A silver-based powder or silver flake-based conductor ink was buried to make a buried co-
fired capacitor. Suitable conductor ink compositions are set forth in Table V.
TABLE V
Component Ink 1 Ink 2 Ink 3 Ink 4
Silver Powder1 83.78 20.11
Silver-Palladium
Powder1 84.93
Silver Flake1 80.97 60.30
Glass 3 0.65
Dispersant 1.22 1.32 0.53 1.21
Resin2 0.88 0.86 0.46 0.46
Resin3 1.85 1.84
Resin4 0.80 0.79
TTeexxaannooll SSoollvveenntt 33..2222 3.25
Terpineol Solvent 6.81 6.73 6.48 6.44
Butyl Carbitol 2.54 2.12 9.71 9.66
1 Available from Degussa Corporation, So. Plainfield, NJ 2 Ethyl Cellulose Resin N300 of Aqualon Corporation
3 Ethyl cellulose Resin N14
4 Elvacite 2045
The resultant laminated stack was fired at 850°C. The capacitance and dielectric loss (tanδ) were measured at lOKHz. The dielectric constant for each capacitor was calculated from the measurement of capacitance (C) in pF, the area (A) of the capacitor in square centimeters and the thickness (t) in centimeters in accordance with the equation
K = Ct A£r wherein εo is a constant = 0.0885pF/cm. These capacitor inks were suitable for operation at high frequency (1GHz) . The capacitor sizes and property measurements are given below in Table VI, wherein the thickness is for the fired capacitor, capacitance is measured as pF/mm2, dielectric loss is given as tanδ, K is the dielectric constant, and TCC is given in ppm/°C from room temperature (RT) to 125°C. In Table VI, the
glass is given in volume % except as otherwise noted.
TABLE VI
Capacitor Size ,mm Thick, pF/mm2 Tanδ K TCC
Composition μm
F + 13.4 :% 1.27 32 23.0 0.010 83 -115
Glass 1 5.08 32 18.9 0.011 68 515
F + 15% 1.27 32 22.1 0.007 80 582
Glass 1 5.08 10.6 0.012 74.5 689
F + 15% 1.27 30 10.5 0.007 36 878
Glass 2 5.07 9.3 0.008 31.4
D + 25% 1.27 32 16.1 0.002 59
Glass 1 5.08 14.9 0.002 56
D + 26% 1.27 32 13.5 0.003 48.5 -1136
Glass 1 5.08 10.7 0.001 38.4 37
D + 20% 1.27 33 30.4 0.007 114 -264
Glass 2
D + 25% 1.27 32 15.3 0.002 55 -560
Glass 2 5.08 12.7 0.004 46 -342
D + 30% 1.27 30 13.3 0.002 45 -918
Glass 3 5.08 9.8 0.002 33 34
D + 25% 1.27 29 40.5 0.009 131 61
Glass 2 + 5.08 38.6 0.008 125 360
6.6Wt% SrZr03
D + 25% 1.27 34 14.8 0.003 57 -756
Glass 2 + 5.08 10.9 0.003 42 193
2.7Wt% SrZr03
D + 25% 1.27 31 20.7 0.005 72.: 3 -119 glass 2 + 5.08 15.7 0.005 55 579
3.3Wt% SrZrO,
Additional low dielectric constant capacitor inks made of barium titanate were screen printed to form capacitors of various sizes, laminated at 1670 psi, terminated with a silver ink layer, co-laminated to kovar at 1740 psi, and fired at 865°C. Several screen printings were applied to produce a minimum thickness of the fired capacitor. The
composition, size and fired properties are summarized below in Table VII, wherein the glass is given in volume %.
TABLE VII
Composition Thick Size pF/mm2 K Tanδ TCC μm mm
25% Glass 2 39 1.27 15.7 71 0.004 -127
2.54 13.0 56 0.004 201
5.08 12.6 55 0.004 348
25% Glass 2 + 32 1.27 22.7 84 0.007 70
3.3wT% SrZr03 2.54 20.0 71 0.006 313
5.08 20.5 74 0.006 453
23% Glass 2* 32 1.27 19.7 71 0.003 -118
2.54 16.2 58 0.003 185
5.08 15.2 55 0.003 296
21% Glass 2 35 1.27 25.0 99 0.004 -69
2.54 22.4 89 0.004 242
5.08 22.1 90 0.004 365
30% Glass 2 35 1.27 14.8 59 0.002 271
2.54 12.9 51 0.003 360
5.08 12.6 50 0.004 411
* IR was measured to be 1.4 x 1012 ohms.
It is apparent that there is a size dependence of capacitance per unit area and dielectric constant for buried capacitors and TCC values. In general, dielectric constant decreases with an increase in capacitor size, as shown in Fig. 1, whereas TCC shows more positive capacitance. The smaller the capacitor, the higher the capacitance, which may be due to fringing capacitance effects and to interaction between capacitors and the surrounding ceramic layers.
Designing high dielectric constant buried co-fired capacitors (K = 1500) however, is a much more difficult problem. Since the capacitor dielectric materials have a high sintering temperature, the low firing temperature used
with the present green tapes results in a porous dielectric; the mixture of barium titanate with a low firing temperature glass dilutes the dielectric constant; the surrounding low dielectric constant glass-ceramics diffuse into the capacitor, resulting in further dilution effects; and the diffusion of silver metal into the capacitor also dilutes the dielectric constant . Thus the resultant buried capacitors based on barium titanate were limited to K values of no more than 700, as shown in Tables VIII and IX. Table VIII summarizes capacitor properties for buried
BaTi03 -based capacitor inks using a silver powder conductor layer. Green tape and capacitor layers were laminated at 280 psi and fired at 850°C. The glass is given in volume %.
TABLE VIII Composition Thick, m Size, mm pF/mm2 K Tanδ TCC
7.5 vol% 29 1.27 123.4 404 0. .005
Glass 4* 2.54 120.22 394 0. .007
5.08 107.5 352
Same 29 1.27 221.3 725 0. .008 259
2.54 193.6 634 0, .007 313
5.08 187.9 615 0, .007 305 The above capacitors were made with a capacitor dielectric ink applied above and below the conductor pads as a barrier,
7.5 vol% 29 1.27 167.4 549 0.008 335 Glass 4** 2.54 151.3 496 0.008 423
5.08 154.1 505 0.008 433
7.5 vol% 26 1.27 150.0 441 0.014
PbTi03/ 5.08 131.2 385 0.013
Bi203 8.8 vol% 32 1.27 158.7 574 0.009 625 Glass 5** 5.08 160.0 586 0.010 550
* using the silver powder as the conductor
** using silver-palladium powder as the conductor
The following capacitors were made, as summarized in Table IX, by laminating green tape and capacitors at 1670 psi and firing at 865°C. The silver conductor used was silver flake. The glass is given as volume %.
TABLE IX Composition Thick, urn Size, mm pF/mm2 K Tanδ TCC 7.5% Glass 4* 27.4 1. .27 215.9 668 0. .007 104
2. .54 197.9 612 0. .007 56
5. .08 214.5 664 0. .007 -173
8.8% Glass 5** 27.2 1, .27 223.2 686 0. .010 166
2, .54 220.2 677 0, .010 39
5. .08 222.4 600 0, .010 -130 7 . 5% PbTi03/ 25 . 6 1 .27 198.7 575 0, .010
Bi203 2 .54 ' 186.5 540 0, .010
5 .08 183.6 531 0. .009
* IR was 4 . 7xl 010 ohms * * IR was 5 . 1xl 010 ohms
The above capacitor compositions were tailored to promote sintering at low temperatures with a minimum dilution of the dielectric constant and to contain less than
10 volume percent of low melting oxides or glass additives made from PbO, B203, ZnO, CdO or PbTi03, materials that are soluble in the BaTi03 perovskite lattice structure. These represent fired compositions having a maximum dielectric constant of about 700.
When a low TCC is required, i.e., less than 60 ppm/°C at a temperature range of either between room temperature to -
25°C or room temperature to 85°C , a barium titanate-based capacitor formulation also includes a substantial amount of a TCC modifier, SrZr03.
Table X illustrates compositions of two such suitable
I 7
capacitor inks, given in % by weight.
TABLE X
Composition Ink 1 Ink 2
BaTi03 47.7 37.5
SrZr03 15.9 30.6
Glass 2 12.4 1.5
Glass 4 6.8
Hypermer PS2 1.5 1.5
Elvacite/solvent 22.5 22.1
A silver-based ink made from 83.78% silver powder,
0.65% glass 3 filler, 4.2% of a mixture of 15% ethylcellulose in a texanol solvent, 7.61% of 13% Elvacite resin in terpineol solvent, 1.22% of Hypermer PS2 and 2.54% of butyl carbitol solvent . The bottom electrode was screen printed as a single layer, the dielectric layer was screen printed in three layers, and the top electrode singly printed.
The green tape stacks were laminated at 1670 psi and co- laminated to a kovar substrate at 1100 psi and the whole fired at 865°C. The dielectric constant (K) and TCC at two temperatures are given below in Table XI .
TABLE XI TCC
Dielectric Size , mil RT to 85°C RT to -25°C K
1 200 -47.8 -430.4 77.8
100 12.0 -441.6 84.5
50 13.8 -356.7 97.0
2 200 -335.3 -73.5 75.6
100 -388.2 -28.6 77.6
50 -440.0 18.3 88.6
A capacitor ink having a low TCC and a low dielectric constant can also be made using titanium oxide (Ti02) as the dielectric. A dielectric ink was made using 42.1% of Ti02
powder, 29.6% of glass 2, 1.4% of Hypermer PS2 dispersant and 26.9% of a mixture of 20% of Elvacite resin in terpineol solvent .
The dielectric ink was applied to a green tape at least one layer below the top of the stack, and a termination layer applied thereunder using a conductor ink, and the stack laminated and fired as above. The TCC and dielectric constant K are given in Table XII below.
TABLE XII TCC
Size , mm RT to 85°C RT to - 25°C K
1 . 27 68 . 6 32 . 4 25.7
2 . 54 14 . 6 55 . 4 18.5
55..0088 33..00 6699..88 15.7
In order to achieve higher dielectric constants for buried co-fired capacitors (K>1000) , we have found that lead-magnesium-niobate-based (PMN) compositions must be used. Suitable high dielectric constant capacitor ink compositions based on PMN are summarized below in Table
XIII, wherein % is by weight.
TABLE XIII
%PMN Additives % Dispersant Resin Solvent
75.02 Glass 4 5.33 1.65 3.33 13.32
BaTi03 1.35
76.88 Glass 4 3.97 1.61 3.31 13.32
BaTi03 1.01
74.16 PbTi03 6.01 1.65 3.28 13.11
PbO 1.60
MgO 0.20
74.93 Glass 5 5.49 1.65 3.32 13.27
BaTi02 1.35
74.93 Glass 6 5.12 1.65 3.32 13.27
PbTi03 1.72
74.70 Glass 5 5.48 1.64 3.29 13.15
PbTiO, 1.74
Using the above lead-magnesium-niobate-based capacitor inks and co-firing on alumina support substrates, produced K values of over 2000 with a silver powder conductor ink. However, when buried in green tape laminates on kovar support substrates, the K values were dramatically lowered to about 30-50 due to the dilution effects discussed above. In order to obtain high dielectric constant capacitors on kovar, a barrier layer can be used to block the diffusion of the ceramics into the capacitors during co-firing. This barrier layer can be of a more effective silver metal composition, or of a different dielectric material.
We have found that a BaTi03 based capacitor ink can be used as a barrier material when a very low melting glass, lower melting than the glass used in the green tape layers, is used. This barrier glass densifies and crystallizes at a
lower temperature than that required for the green tape glasses to soften significantly. Thus the barrier glass blocks the diffusion of the green tape glasses into the capacitor. In such case the barrier is printed as a pad larger than the capacitor, both below the bottom conductor pad and above the top conductor pad, as shown in Fig. 2. In Fig. 2, a three layer capacitor 12 having a two layer top and bottom conductor layers 14 and 15 respectively is sandwiched between two top and bottom two-layer barrier layers 16 and 17 respectively. The buried capacitor is in turn laminated to top and bottom green tape layers 18 and 19 respec ively .
Using a capacitor ink including Glass 6 and 71.07 percent of BaTi03, as described above, a barrier layer was printed as a pad 19x19mm, centered about a capacitor 5.08 x 5.08mm made from a PMN ink including 74.16% of PMN. Silver powder was used to make the conductor ink. Various layers were employed to determine how many barium titanate barrier layers were required to obtain a high dielectric constant capacitor on a kovar supported multilayer circuit board. Controls without the barrier layers were also tested. The test results are given below in Table XIV wherein the number of prints refers to the number of screen prints used for each layer.
TABLE XIV
Dielec- tric
Function #Prints Thick pF/mm2 K Tanδ TCC IR xlO10 ohms
Barrier 3 24 Conductor 1 Capacitor 3 55 181.3 1132 0.017
Control 1 58 5.1 34
Barrier 3 24-48 Conductor 2 10 Capacitor 3 36 751.6 3058 0.038 -19.6
Control 2 35 208.0 823 0.022 -9.5
Barrier 1 10
Conductor 2 11
Capacitor 3 46 91.6 493 0.009 -17.5 8.3
Control 3 53 128.2 689 0.022 -8.5 6.4
Barrier 2 32
Conductor 2 11
Capacitor 36 360.0 1463 0.033 -21.5 2.3
Control 4 31 219.0 766
Thus when a minimum thickness barrier layer is present, the dielectric constant was much higher than when no barrier layer, or a thin barrier layer, was used. Buried capacitors having a high dielectric constant were achieved however using a double metallization print, and a double barrier layer print . By increasing the number of barrier prints to three on either side of the conductive layers, dielectric constant (K) values above 3000 were obtained. However, while high dielectric constant capacitors can be made via the above process, several extra printing steps are required,
22. ' ' _ ' "
and the barrier thickness must be about 16-20 microns to be effective.
Further, due to the thickness of the several barrier layers, conductive layers and capacitor layers, the top green tape layer is subject to tearing and care must be taken to prevent that. Further, the large number of screen printing steps required (up to eleven as described above) adds to the costs of the process.
Thus a modified buried conductor ink was sought that would be a more effective barrier, one that would require fewer printing steps and have a reduced thickness that would not subject the top green tape layer to tearing.
We have further found that a mixture of silver flake and silver powder as the conductive layer makes very effective barrier layers, better than using either silver flake or silver powder alone. Silver powder inks produce low dielectric constant capacitors. Silver flake alone formed a very effective barrier layer (K=3600) but it resulted in tearing of the overlying green tape layer during lamination or firing. Thus a mixture of 75% by weight of silver flake and 25% by weight of silver powder, although not as effective a barrier as silver flake alone, resulted in high dielectric constant capacitors. However, outgassing of capacitors is a problem during firing. If the silver metal seals the capacitor too well, the gases formed from the additive (PbO containing) materials cannot escape. Thus the silver flake, while it results in a high dielectric constant capacitor, forms a structure that becomes too dense during
firing, and leads to tears in the overlying green tapes. Thus the use of a mixture of silver powder and silver flake, although a compromise in terms of dielectric constant, does not tear the top green tape layer nor do these structures have outgassing or bubbling problems.
A plurality of buried PMN-based capacitors on kovar substrates were made using silver powder, silver flake and a mixed silver powder and silver flake conductor layer. The layers were laminated at 1670 psi and fired at 865°C. The test results are summarized below in Table XV.
TABLE XV
Silver #Prints/ Size pF/mm2 K Tanδ TCC Type thick urn mm powder 2/10-11 31 1.27 14. 6 51 0.001 -2.0 μm 2.54 27. 7 97 0.010
5.08 112. 6 394 0.018 -6.9 powder 2/l3μm 35 1.27 60. 9 246 0.009 11.4
2.54 230 908 0.021 -16.5
5.08 482. 5 1581 0.045 -27.6 flake 2/10μm 29 1.27 447 716 0.027 -21.7
2.54 716 2346 0.037 -27.6
5.08 1066 3601 0.040 -30.1 flake l/5μm 21 1.27 383 928 0.018 -30.8
2.54 841 1967 0.027 -38.1
5.08 1050 2498 0.026 -41.9 mixed l/6μm 29 1.27 228 748 0.023 -30.8
2.54 477 1564 0.033 -39.8
5.08 706 2313 0.045 -44.7 mixed 2bott/6.5 29 1.27 624 2043 0.025 -42.7 1 top/3.2 2.54 931 3052 0.037 -49.1 μm 5.08 1005 3295 0.048 -51.8
Insulation Resistance (IR) of the first capacitor of 5.08mm size was 3.8xl010 ohms. IR of the second capacitor of 5.08mm size using silver flake was 6.0xl010 ohms. The IR of
the first capacitor using the mixed silver and the same size was l.OxlO10 ohms.
The above buried capacitors made with the mixture of silver flake and silver powder as the conductor layer, required fewer printing steps and fired without any problems with bubbling or outgassing. No tearing of the overlying green tape layer was noted.
The dielectric constant of the PMN capacitors exhibit a large size dependence; i.e., the dielectric constant increases with increasing capacitor size, and TCC also increases (becomes more negative) with increasing capacitor size. It is believed this is a result of dilution of the capacitor dielectric by the surrounding low dielectric constant ceramic. Large capacitors have less dilution effect than small capacitors. This is shown in Table XVI below, and schematically in Figs 3 and 4, graphs of dielectric constant and TCC versus capacitor size, respectively. In Table XV the capacitors are based on PMN with mixed silver powder-silver flake inks.
TABLE XVI
Capacitor Fired Size pF/mm2 K Tanδ TCC IR
Compositn Thk, μm mm % xlO10
10% glass 4 22. 4 1.27 205 518 0.015 -45. ,5
+ BaTi03 2.54 496 1259 0.018 -55. ,6
5.08 728 1844 0.019 -59. .7 1
7.5% glass ; 4 1 31 1.27 7116 400 0.011 -38. .4
+ BaTi03 2.54 334 1154 0.017 -50. .3
5.08 607 2098 0.022 -57, .3
10% glass 5 24 1.27 173 456 0.007 -37, .6
+ BaTi03 2.54 508 1367 0.008 -47 .3
5.08 821 2209 0.009 -52 .9 1.5
10% glass 6 30 1.27 227 484 0.014 -24 .2
+ BaTi03 2.54 253 870 0.016 -33 .6
5.08 372 1279 0.018 -38 .4
10% glass 6 25 1.27 68 196 0.011 -18 .1
+ PbTi03 2.54 216 620 0.016 -24 .8
5.08 329 944 0.019 -27 .1
Intermediate range (K=500-700) barium titanate-based buried capacitors fabricated with the same mixed silver flake/powder conductor layers which were also laminated at
1670 psi and fired at 865°C are not as size dependent. Fig. 5, which is a graph of dielectric constant versus capacitor size using a mixed silver conductor, illustrates the differences in the size dependence of barium titanate- based capacitors and PMN-based capacitors. Thus, for applications requiring intermediate dielectric constant values, barium titanate-based buried capacitors will be more consistent and have lower TCC as compared to PMN-based capacitors .
The buried capacitors of the invention, buried one or two tape layers below the top of the stack, have been
subject to the HHBT reliability test (85°C/85%RH/50VDC) for over 1000 hours with no degradation of the capacitance, dielectric loss or insulation resistance (IR) of the buried capacitors . The above co- fired multilayer ceramic circuit boards having buried capacitors of the invention are useful in various applications, such as cellular telephones.
The formulation of various resistor inks, method of formation of embedded resistors and test results will be discussed below.
Resistor inks with resistor values of from 300 ohm/sq to 100 Kohms/sq and a TCR of <+200 ppm/°C over a temperature range of room temperature to 125°C, also can be made in accordance with the invention. The target properties for a particular cellular telephone application are 1 Kohm/sq and a TCR less than or equal to 200 ppm/°C over the room temperature to 125°C range.
The resistor inks are made from a fine particle size, high surface area Ru02 powder having the characteristics as summarized in Table XVII.
TABLE XVII
Property Specification
Particle size, microns 0.15 - 0.45 Surface Area (m2/g) 15 - 25 Purity - Wt% Ru 73-76
The Ru02 is mixed with one or more glasses to reduce the firing temperature of the conductor powder. Glasses 1 and 3 as set forth above are suitable. A TCR modifier such as BaTi03 can also be added.
The above glasses are mixed with the Ru02 powder, optional modifier and a suitable organic vehicle to- form a screen printable composition that can be fired at low temperatures, similar to the firing temperature of the green tape stacks they will be applied to. The resistor ink powder generally contains 17.33 to 24.8% by weight of Ru02, 74.3- 81.7% by weight of glass 1 and 0.99 to 1.10% by weight of barium titanate. The preferred compositions contain 19.8 to 23.14% by weight of Ru02, 75.87 to 79.21% by weight of glass 1 and 0.99 to 1.1% by weight of BaTi02.
Resistor inks were screen printed onto a green tape incorporated into a laminated green tape stack in various patterns (1/2 squares and squares) in sizes from 0.508 x 0.508 to 2.032 x 4.064 mm. Green tape compositions suitable for use herein include the following ingredients, summarized in Table XVIII. The median particle size of the glass and filler materials are given in microns.
TABLE XVIII
Material Function Comp . 1 Comp . 2
Glass 2 Crystallizing 57.34 57.29 glass
P12 glass* Non-crystall- 6.98 7.03 izing glass Forsterite Ceramic filler 7.27 4.42
Cordierite Ceramic filler 1.09 3.44
Hypermer P321 Dispersant 0.58 0.58
Butvar B982 Binder 2.04 2.04
Santicizer 1603 Plasticizer 1.36 1.36 Methyl ethyl ketone Solvent 11.67 11.67
Anhydrous ethanol Solvent 11.67 11.67
1) Registered Trademark if ICI America Inc 2) Registered Trademark of Monsanto Co. 3) Registered Trademark of Monsanto Co.
The resistors were terminated with a silver conductor ink which was also screen printed. A suitable silver ink composition includes 83.78% by weight of silver powder, 0.65 weight % of glass 3, 1.22 weight% of a dispersant, 0.88 weight % of ethyl cellulose resin, 0.80 of Elvacite 2045 resin (available from Monsanto Company) , and a mixed solvent of 3.32 weight % of texanol, 6.81 weight % of terpineol and 2.54 weight % of butyl carbitol . The green tape stacks were laminated together and placed on a kovar support substrate and co-fired in air at 850-900°C. The resistors were printed and buried one layer below the top surface of the ceramic stack. After co-firing, the resistors were then connected to the outside by printing
with a silver-palladium or gold conductor ink and post-fired at 700-750°C in air.
Table XIX below summarizes the Ru02-glass compositions and the properties of the fired resistors. In Table XIX the compositions are given in weight %, and TCR was measured from room temperature to 125°C. A short term overload test (STOL) was also performed.
TABLE XIX Composition R(KΩ/sσ) TCR, STOL ppm/°C
15% Ru02 99.9 -80 85% glass 3
22.5% Ru02 5.08 -111 200V/5sec/ 75.5% glass 3 0.06% ΔR 2.0% BaTiO,
22.8% Ru02 4.00 28 76.2% glass 3 2.0% BaTi03
24.75% Ru02 0.86 209 40V/5sec/ 74.26% glass 3 4.5% ΔR 0.99% BaTi03
21.5% Ru02 1.01 •20 77.6% glass 1 0.9% BaTiO,
21.6% Ru02 0.46 153 150V/5sec/ 77.9% glass 1 1.1% ΔR 0.5% BaTiO,
18% Ru02 0.52 262 82% glass 1
10% Ru02 22.9 44 90% glass 1
24.8% Ru02 0.54 25 74.3% glass 1 0.99% BaTiO,
18.9% Ru02 0.94 117 80.6% glass 1 0.5% BaTiO,
Thus the use of glass 3 was effective to form high value resistors of over 2 Kohms/sq. The glass 1 compositions were chosen for further development of a 1 Kohm/sq resistor.
The above resistor compositions were admixed with an organic vehicle to form an ink composition, using a dispersant (1.44% by weight), ethyl cellulose Resin N300
(0.10% by weight), Elvacite resin 2045 (3.9% by weight) and
25.18% of a mixed solvent of terpineol and butyl carbitol .
The resistor ink was adjusted to about 38 volume % solids. In order to maximize circuit density, it is desirable to print small size resistors such as patterns of 0.508 x
1.016 to 1.016 to 2.032 mm to obtain a 510 ohm resistor.
Various resistor inks were made having varying ratios of solids to adjust the resistance and TCR values while keeping the volume % constant at 38%, and maintaining the dispersant concentration constant at 2 weight % of the total powder weight. The powder components of useful resistor inks are summarized below in Table XX.
TABLE XX Material Composition, Wt% Preferred composition, Wt%
Ru02 17.33-24.8 19.8-23.14
Glass 1 74.3-81.7 75.87-79.21 BaTi03 0.99-1.10 0.99-1.1
Suitable resistor ink compositions made from the above powder mixtures are shown below in Table XXI .
TABLE -XXI
Material Function Ink Compositions, Wt%
Ru02 Conductor 16.70 14.42 14.93 glass 1 Sintering aid 54.73 57.59 56.15
BaTi03 TCR Control 0.71 0.72
Hypermer PS2 Dispersant 1.43 1.44 1.45
15% Elvacite Binder/solvent 25.12 25.84 25.38 2045/terpineol
7.5% ethyl Binder/solvent 1.31 1.32 1.30 cellulose N300 in butyl carbi tol/terpineol
After screen printing resistors on one layer of 4-5 layer laminated green tapes as above which had been co-fired onto kovar at 850-900°C, a top surface conductor ink made from silver-palladium or gold was applied and post fired at 750°C. The resistance was measured at DC or low frequency (lOKHz) and the TCR was calculated from the resistance measured at room temperature and at 125°C. The results are shown below in Table XXII.
TABLE XXII -
Ink Size Thick Area TCR, CO -fired mm μm (sq) R(KΩ) ppm/°C
2 0.51x1.02 18. ,3 0.496 0.438 91
1.02x2.03 18. ,7 0.496 0.501 10
1.52x3.05 14. ,3 0.496 0.563 -18
3 0.51x1.02 18. ,0 0.506 0.434 58
1.02x2.03 16. .0 0.502 0.504 1
1.52x2.03 14, .5 0.505 0.543 -46
2 0.51x1.02 19, .2 0.461 0.412 62
1.02x2.03 19 .3 0.487 0.503 -59
1.52C3.05 13, .1 0.490 0.617 -64
Ink Size TCR, post fired mm R(KΩ) ppm°C R(KΩ/sσ)
2 0.51x1.02 0.472 85 0.952
1.02x2.03 0.536 9 1.080
1.52x3.05 0.598 -34 1.206
3 0.51x1.02 0.471 75 0.931
1.02x2.03 0.542 -9 1.080
1.52x3.05 0.582 -34 1.154
2 0.51x1.02 0.442 58 0.959
1.02x2.03 0.540 -54 1.109
1.52x3.05 0.660 -82 1.347
It is apparent that resistance values increase after post firing at 750°C by an average of 7.3%. In addition, resistor values increase with increasing resistor size. This increase in resistance value with increasing size is due to dilution of the resistor by the silver terminating conductor layer during co-firing, which decreases sheet resistance for smaller size resistors. Additional resistors from resistor ink compositions 1 and 2 are given below in Tables XXIII and XXIV respectively. TCR was measured at room temperature and at 125°C.
TABLE XXIII
Size, mm Area, mm2 Resistance (ohms) Postfired TCR
Cofired Postfired ppm/°C
(1) Square Resistors:
0.51x0.52 0.258 721 778 -43.4
1.02x1.02 1.032 922 1003 -94.6 1.52x1.52 2.323 976 1064 -111
(2) 1/2 Resistors:
0.51x1.02 0.516 459 496 -55 1.02x2.03 1.065 498 541 -92
1.52x3.05 4.645 511 557 -108
2.03x4.06 8.258 534 582 -118
The print thickness of the 1/2 sq 1.02x2.03 mm resistor was 18.6 microns. TABLE XXIV
Size, mm Area, mm2 Resistance (ohms) Postfired TCR Thick
Co- Postfired ppm/°C (μm fired (1) Square Resistors:
0.51x0, .51 0.258 957 1022 -2
1.02x1, .02 1.032 1086 1172 -55
1.52X1, .52 2.323 1109 1200 -74
(1/2) Square Resistors:
0.51x1, .02 0.516 525 563 -9 15.3
1.02x2, .03 2.065 547 591 53 15.2
1.52x3, .05 4.645 562 608 66 13.8
2 2..0033x>4, .06 8.258 566 612 70
The data for resistors of the resistor ink composition 1 is plotted in Figs. 6 and 7 which are graphs of resistance versus resistor area for (1) square resistors and for (1/2) resistors respectively.
The above resistors were also subjected to reliability testing. Test 1 was for 1000 hours at 85°C/85%RH, Test 2 consisted of cycling over 200 times between -55 and 125°C.
Test 3 applied 15.5 Watts/cm2 of power to the resistor at 70°C for 1000 hours. The resistors passed these tests. Resistor ink 1 was used to make a 510 ohm buried resistor 1.016 x 2.032 mm in size in a receiver board designed for operation at 1 GHz. A resistance value of 510 ohms ±10% was obtained after post firing, providing the dried ink thickness was maintained at between 18 and 25 microns .
The ceramic printed circuit boards of the invention are also useful for incorporating or embedding other components, such as RF filters. In such case, thick multilayer stacks that are over 2 mm in thickness after firing are made. However, the large number of green tape layers after firing preclude close control of the shrinkage in the x and y dimensions, and, in addition, the multilayer stack tends to de-laminate from the metal support substrate when fired.
Thus a method had to be developed that would be able to control shrinkage and prevent de-lamination from a metal support substrate over many thicknesses of green tape. We have found that by interleaving green tape layers made from the prior art low dielectric loss glasses mixed with minor amounts of oxide fillers together with green tape layers made from the same glasses but including greater amounts of oxide fillers, many more layers of green tapes can be stacked, laminated and fired with no shrinkage in the x, y directions and no de-lamination from the metal support. These thick multilayer metal supported circuit board stacks are particularly useful when RF components are to be
embedded in the stacks .
Useful prior art glasses used to make one type- of green tape are made from zinc-magnesium-borosilicate crystallizing glasses as described above. A suitable crystallizing glass is glass 3 above to which 2.0% by weight of Co304 coloring agent is added.
This glass is mixed with 9.6% by weight of a non- crystallizing lead-based glass of the lead-zinc-aluminum silicate system. An exemplary glass contains 42.0% by weight of PbO; 10.0% by weight of Al203, 38.8% by weight of Si02 and 10.0% by weight of ZnO.
These crystallizing-non-crystallizing glass mixtures are combined with oxide fillers, such as alumina, cordierite, quartz, cristoballite, forsterite and willemite, which serve to control the shrinkage and to further modify the TCE. With the addition of a second oxide filler, the desired dielectric properties, shrinkage characteristics and TCE matched to kovar can all be achieved. For example minor amounts of filler oxides, e.g., 1.5-2% by weight of cordierite and 9.5-10.0% by weight of forsterite, produce excellent ceramics for the present applications.
Thus these glasses have major amounts of glass and minor amounts of oxide fillers (<15%) . These glasses have excellent dielectric properties at microwave frequencies, such as 1 GHz. These ceramics are referred to hereinafter as Type I glass-ceramics.
A second type of glass-ceramic is made from the same zinc-magnesium-borosilicate glasses but they include
increased amounts, over about 25% by weight, of oxide fillers. These glasses have lower shrinkage than the Type 1 glass-ceramics, and are referred to hereinafter as Type 2 glass-ceramics . The following Table XXV sets forth examples of different ceramic compositions useful to make the second type of green tape layers .
TABLE XXV
Ceramic 1 2. 3_ 4. Composition —-- .^—^—---^-^---^-^--^----^..-—.-^^-^——
Crystallizing glass 50.0 50.0 57.94 66.85
Non-crystallizing glass 6.1 6.1 7.04 8.15
Forsterite 30.0 21.95 30.44 21.70
Cordierite 13.9 21.95 4.57 3.30
Vol. % Glass 50.9 49.1 61.9 72.4
Vol. % Filler 49.1 50.9 38.1 27.6 Thus these ceramics include major amounts of filler, e.g., about 25-50% by weight.
Green tapes are made by formulating the Type 1 and
Type 2 glass-ceramics with a resin binder together with plasticizer, dispersants and solvents in known manner, to form a thick slurry. A typical glass-ceramic composition for use herein has a crystallizing glass particle size of about
10-12.5 microns, a non-crystallizing glass particle size of about 6.5-8 microns, forsterite having a particle size of about 3-5 microns, and cordierite having a particle size of about 2-3 microns. Table XXVI below sets forth a suitable ceramic green tape formulation in percent by weight.
TABLE XXVI
Composition Function Type 1 Type 2 Glass/ Glass/ Ceramic Ceramic Green Green Tape Tape
Primary Glass 57.34 31.2-36.4
Secondary Glass 6.98 3.8-4.4 Forsterite powder FFiilllleerr 7.27 13.7-16.0 Cordierite powder Filler 1.09 13.7-16.0 Hypermer® PS2 Dispersant 0.58 0.56-0.79 Butvar® B98 Binder 2.04 2.13-2.87 Santicizer® 160 Plasticizer 1.36 1.42-1.91 Methyl ethyl ketor Solvent 11.67 11.58-16.06 Anhydrous ethanol SSoollvveenntt 11.67 11.58-16.06
The resultant slurry is cast to form a green tape about 0.15-0.20 mm thick, and the green tape is dried.
The two types of green tape using minor and major amounts of amounts of oxide fillers respectively, are then interleaved. Silver or other metal patterns are screen printed on the green tapes to form circuit patterns. Preferably circuit patterns are printed between two green tapes of Type 1, to form a hermetic ceramic, since the Type 2 (high filler content) glass-ceramics tend to become more porous on firing than the Type 1 glass-ceramics.
In order to provide various conductor patterns on the green tapes, a co-firable conductive metal-based thick film conductor ink based on the glass compositions of the invention can be made with a conductive metal powder, such as silver powder, mixed with a small amount of the glasses
disclosed above, together with known dispersants, resins and solvents to form a screen printable conductor ink. Top conductor inks can be made in like fashion using silver- palladium powder, or a gold powder. Via fill inks to connect circuit patterns on various green tape layers together can also be made with silver powder, in known manner.
The green tape stack is then suitably laminated at a pressure of about 1.174 kg/mm2 at about 93°C for four minutes, and co-laminated with the prepared metal support substrate at a pressure of about 1.3-1.4kg/mm2. After laminating and co-laminating, the multilayer stack on the kovar support is fired in a belt furnace at a belt speed of 0.4 inch/min to a peak temperature of 850-900°C. During firing the organic materials are vaporized, and the low melting glazing glass softens, adhering the multilayer ceramic stack to the metal core . The metal core aids in limiting the shrinkage of the overlying green tapes in the x and y directions. Thus almost all of the shrinkage occurs in the z direction, perpendicular to the metal support. The presence of the interleaved Type 2 glass-ceramics, which have low shrinkage, also serves to constrain the shrinkage of the multilayer stack in the x and y directions.
After firing, a conductive ink may be applied to the top of the fired multilayer stack, as to form bond pads, inductors, microstrip interconnects and the like, in known manner .
The invention will be further described in the following Examples, but the invention is not meant to be
limited to the details described therein. In the Examples, percent is by weight . Example 1
Eleven layers of Type 1 green tape (A) , three of which had a silver-based ink applied thereto (C,D) , and 7 layers of Type 2 green tape (B) were interleaved as shown in Fig. 1. The green tape stack was then laminated and placed over a kovar support substrate, and co-laminated. The stack was fired. The shrinkage was 17.0% in the z direction, but only
0.96% in the x direction and 0.61% in the y direction. The total stack after firing was 2.50 mm thick. Example 2
Eleven layers of Type I green tape, having metallized planes on three of the layers, were interleaved with Type 2 green tapes, as shown in Fig. 8. Fig. 8 illustrates the Type 1 green tapes as A, Type 2 green tapes as B, C designates embedded RF filters, and D illustrates silver patterning. The green tapes were interleaved and stacked, laminated, co- laminated to a kovar support and fired. The fired stack was 2.40 mm thick.
The shrinkage was 17.0% in the z direction, 0.64% in the x direction and 0.60% in the y direction. Example 3 Eleven layers of Type 1 green tape and 7 layers of
Type 2 green tape were interleaved and stacked, laminated and fired. The resultant stack was 2.20 mm thick.
The shrinkage was about 17% in the z direction, 0.83%
in the x direction and 0.98% in the y direction. Example 4
Fifteen layers of Type 1 (A) green tape having embedded filters (C) on one layer and ground planes (D) on two layers, as shown in Fig. 9, and 8 layers of Type 2 green tape (B) were interleaved and stacked, laminated and fired to form a stack 2.52 mm in thickness.
The shrinkage was about 17% in the z direction, 0.35% in the x direction and 0.85% in the y direction. The physical properties of the resultant multilayer tapes alone. The results are given below in Table XXVII.
TABLE XXVII
Property Type I tape Interleaved with alone* Type 2 tape **
TCE (25-300°C) 6.3 ppm/°C *
7.7 ppm/°C **
(π-cm) >1.0 x 1012 Chemical Durability pass Buried Conductor Resistance 3.6mΩ/square Via conductor Resistance 0.72 mΩ/via
* on kovar
** ceramic alone
Example 5
Properties of various Type I and Type 2 green tape stacks were fired at 865°C and their properties measured. The results are summarized below in Table XXVIII
TABLE XXVIII
Sample Stack Fired Density £ Tanδ Frequency 5 layers Type 1 3.14 g/cc 6.41 0.0023 15.6 GHz 5 layers Type 2 2.01 g/cc 3.64 0.0017 17.9 GHz
23 layers, of Example 4 5.39 0.0018 11.6 GHz
20 interleaved layers 5.24 0.0019 12.2 GHz Thus the interleaved green tape layers can be stacked to produce thick fired metal supported multilayer circuit boards that shrink in only one dimension.
Although the invention has been described in terms of specific embodiments, it will be clear to those skilled in
the art that variations in the glass compositions, the amounts of oxide fillers, the metal support, the number of green tape layers, the types of capacitors and capacitor inks, resistors and resistor inks and conductors and conductor inks and the like can be made and are meant to be included herein. The invention is only to be limited by the appended claims.
Claims
1. A supported ceramic circuit board having an embedded component therein comprising a) a laminated green tape stack on a kovar support; b) a screen printed component screen printed onto a green tape layer from an ink comprising a dielectric and a low melt temperature glass, c) a conductor layer below said screen printed component and d) an overlying green tape layer.
2. A supported ceramic circuit board having embedded components comprising: a) a laminated green tape stack on a kovar support; b) a buried screen printed capacitor made from a dielectric selected from the group consisting of barium titanate, titanium oxide and lead-magnesium-niobate; c) a silver conductor layer printed below and above the capacitor; and d) an overlying green tape layer.
3. A supported ceramic circuit board according to claim 2 wherein said capacitor is sandwiched between silver barrier layers, said barrier layer comprised of a mixture of silver powder and silver flake.
4. A supported ceramic circuit board according to claim 2 wherein said dielectric is lead-magnesium-niobate, and said capacitor is sandwiched between silver or barium titanate barrier layers, said capacitors having a high dielectric constant over 700.
5. A green tape stack which, when fired, is at least two millimeters thick comprising alternating green tape layers of a first type comprising a mixture of crystallizing and non-crystallizing glasses together with at least 5% up to 15% by weight of an oxide filler, with green tape layers of a second type comprising a mixture of crystallizing and non-crystallizing glasses together with a higher percent by weight of an oxide filler than the first type, onto a metal support substrate.
6. A green tape stack according to claim 5 wherein said non- crystallizing glass is made from PbO, Al203 and Si02.
7. A green tape stack according to claim 5 wherein said oxide filler is selected from the group consisting of alumina, cordierite, quartz, cristobalite, forsterite and willemite.
8. A green tape stack according to claim 5 wherein said metal support substrate is a copper-nickel clad or plated kovar support .
9. A green tape stack according to claim 5 wherein a conductive layer is screen printed between one or more green tape layers of the first type.
10. A green tape stack according to claim 9 wherein said conductive layer is a silver-based layer.
11. A green tape stack according to claim 9 wherein a conductive layer is screen printed onto the top surface of the stack.
12. A fired green tape stack according to claim 5.
13. A fired green tape according to claim 5 wherein an RF component is embedded in the green tape stack.
14. A multilayer ceramic green tape structure comprising a plurality of low firing temperature green tapes that do not shrink in the x and y dimensions during firing having circuit patterns thereon mounted on a metal support substrate, a capacitor screen printed on a green tape layer one or more layers below the top of the stack, and a conductor layer screen printed above and below the capacitor.
15. A multilayer ceramic green tape structure according to claim 14 wherein said capacitor layer is made from barium titanate, titanium oxide or lead-magnesium-niobate.
16. A multilayer ceramic green tape structure according to claim 14 wherein the conductor layer is of silver.
17. A multilayer ceramic green tape structure according to claim 14 wherein said capacitor is sandwiched between two barium titanate barrier layers having a thickness sufficient to prevent diffusion of the green tape glasses into the capacitor during firing.
18. A method of forming embedded components in a multilayer ceramic circuit board on a metal support substrate ~ comprising a) forming a component precursor ink of a precursor compound, a low firing temperature glass and an organic vehicle; b) screen printing a bottom conductor layer; c) screen pringing the component precursor ink over the bottom conductor layer; d) covering said screened component precursor ink layer with one or two layers of green tape; e) screen printing a top conductor layer; f) aligning and laminating said layers together, and g) firing said laminated layers.
19. A method of forming embedded capacitors in a multilayer ceramic circuit board on a metal support substrate comprising a) forming a capacitor ink from a mixture of a dielectric selected from the group consisting of barium titanate, titanium oxide and lead-magnesium-niobate, a low firing temperature glass and an organic vehicle; b) screen printing a bottom conductor layer; c) screen printing capacitors over the bottom conductor layer; d) screen printing a top conductor layer; e) covering said capacitors with one or more layers of green tape; f) aligning and laminating said layers together, and g) firing said laminated layers.
20. A capacitor ink comprising a dielectric selected from the group consisting of barium titanate, titanium oxide and lead-magnesium niobate, a low firing temperature glass and an organic vehicle.
21. A resistor ink composition comprising ruthenium oxide, a low firing temperature glass in sufficient amount to reduce the firing temperature of the mixture within the range 850- 900┬░C and an organic vehicle.
22. A resistor ink composition according to claim 2t) further ┬╗ including a TCR modifier of barium titanate.
23. A ceramic multilayer printed circuit board including embedded resistors comprising a screen printed resistor layer of ruthenium oxide and a low firing temperature glass covered with one or two layers of green tape, said layer printed onto a green tape stack laminated to a metal support board and a conductor layer underlying said resistor layer.
24. A ceramic multilayer printed circuit board according to claim 22 wherein said metal support board is of kovar.
25. A method of making embedded resistors comprising a) forming a resistor ink comprising ruthenium oxide mixed with a sufficient amount of a low firing temperature glass so that the mixture has a firing temperature between about 850-900┬░C together with an organic vehicle; b) screen printing the ink on a green tape stack to deposit resistors thereon; c) covering said resistor layer with one or two green tape layers; and d) terminating the resistors with an underlying first conductive layer, e) laminating the resultant green tape stack; f) firing said stack to a temperature of from about 850-900┬░C, g) coating the top surface of the fired stack with a second conductive layer, and h) post firing said fired multilayers.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53854898A JP3944791B2 (en) | 1997-03-06 | 1998-03-03 | Ceramic multilayer printed circuit board |
EP98910019A EP1016106A4 (en) | 1997-03-06 | 1998-03-03 | Ceramic multilayer printed circuit boards with embedded passive components |
KR10-1999-7008082A KR100516043B1 (en) | 1997-03-06 | 1998-03-03 | Ceramic multilayer printed circuit boards with embedded passive components |
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81283297A | 1997-03-06 | 1997-03-06 | |
US08/812,172 US5866240A (en) | 1997-03-06 | 1997-03-06 | Thick ceramic on metal multilayer circuit board |
US08/812,832 | 1997-03-06 | ||
US08/812,172 | 1997-03-06 | ||
US08/812,151 | 1997-03-06 | ||
US08/812,151 US5953203A (en) | 1997-03-06 | 1997-03-06 | Multilayer ceramic circuit boards including embedded capacitors |
US09/031,745 | 1998-02-27 | ||
US09/031,745 US6055151A (en) | 1997-03-06 | 1998-02-27 | Multilayer ceramic circuit boards including embedded components |
Publications (2)
Publication Number | Publication Date |
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WO1998039784A1 WO1998039784A1 (en) | 1998-09-11 |
WO1998039784A9 true WO1998039784A9 (en) | 1999-02-18 |
Family
ID=27487928
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1998/003270 WO1998039784A1 (en) | 1997-03-06 | 1998-03-03 | Ceramic multilayer printed circuit boards with embedded passive components |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1016106A4 (en) |
JP (2) | JP3944791B2 (en) |
KR (2) | KR100546471B1 (en) |
TW (1) | TW405330B (en) |
WO (1) | WO1998039784A1 (en) |
Families Citing this family (14)
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JP3944791B2 (en) * | 1997-03-06 | 2007-07-18 | ラミナ セラミクス, インコーポレイテッド | Ceramic multilayer printed circuit board |
US6191934B1 (en) * | 1998-10-02 | 2001-02-20 | Sarnoff Corporation & Co., Ltd. | High dielectric constant embedded capacitors |
US6300267B1 (en) * | 1998-11-05 | 2001-10-09 | Sarnoff Corporation | High dielectric constant buried capacitors with extended operating temperature ranges |
US6349456B1 (en) * | 1998-12-31 | 2002-02-26 | Motorola, Inc. | Method of manufacturing photodefined integral capacitor with self-aligned dielectric and electrodes |
US6317023B1 (en) | 1999-10-15 | 2001-11-13 | E. I. Du Pont De Nemours And Company | Method to embed passive components |
US6455930B1 (en) * | 1999-12-13 | 2002-09-24 | Lamina Ceramics, Inc. | Integrated heat sinking packages using low temperature co-fired ceramic metal circuit board technology |
US6970362B1 (en) | 2000-07-31 | 2005-11-29 | Intel Corporation | Electronic assemblies and systems comprising interposer with embedded capacitors |
US6775150B1 (en) | 2000-08-30 | 2004-08-10 | Intel Corporation | Electronic assembly comprising ceramic/organic hybrid substrate with embedded capacitors and methods of manufacture |
EP1263002A3 (en) * | 2001-05-17 | 2004-01-02 | Shipley Company LLC | Resistors |
EP1353542B1 (en) | 2001-12-25 | 2018-05-16 | Ngk Spark Plug Co., Ltd | Process for production of multilayered wiring board |
US6860000B2 (en) | 2002-02-15 | 2005-03-01 | E.I. Du Pont De Nemours And Company | Method to embed thick film components |
US6893710B2 (en) | 2003-04-18 | 2005-05-17 | Yageo Corporation | Multilayer ceramic composition |
KR20050019214A (en) | 2003-08-18 | 2005-03-03 | 한국과학기술원 | Polymer/ceramic composite paste for embedded capacitor and method for fabricating capacitor using the same |
JP5402776B2 (en) * | 2010-03-30 | 2014-01-29 | 株式会社村田製作所 | Manufacturing method of metal base substrate |
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US3968412A (en) * | 1973-07-27 | 1976-07-06 | General Electric Company | Thick film capacitor |
US4061584A (en) * | 1974-12-13 | 1977-12-06 | General Electric Company | High dielectric constant ink for thick film capacitors |
US4415624A (en) * | 1981-07-06 | 1983-11-15 | Rca Corporation | Air-fireable thick film inks |
JPS5817651A (en) * | 1981-07-24 | 1983-02-01 | Hitachi Ltd | Multilayer circuit board and its manufacture |
GB2162167B (en) * | 1984-06-01 | 1988-01-20 | Narumi China Corp | Ceramic substrate material |
US5148005A (en) * | 1984-07-10 | 1992-09-15 | Raychem Corporation | Composite circuit protection devices |
JPH0725174B2 (en) * | 1985-10-18 | 1995-03-22 | 富士ゼロックス株式会社 | Method for manufacturing thick film type thermal head |
GB2182033A (en) * | 1985-10-24 | 1987-05-07 | Stc Plc | Dielectric compositions |
JPS62113758A (en) * | 1985-10-25 | 1987-05-25 | 株式会社住友金属セラミックス | Low temperature burnt ceramics |
US5166658A (en) * | 1987-09-30 | 1992-11-24 | Raychem Corporation | Electrical device comprising conductive polymers |
US4961999A (en) * | 1988-07-21 | 1990-10-09 | E. I. Du Pont De Nemours And Company | Thermistor composition |
JP3019541B2 (en) * | 1990-11-22 | 2000-03-13 | 株式会社村田製作所 | Wiring board with built-in capacitor and method of manufacturing the same |
US5256469A (en) * | 1991-12-18 | 1993-10-26 | General Electric Company | Multi-layered, co-fired, ceramic-on-metal circuit board for microelectronic packaging |
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-
1998
- 1998-03-03 JP JP53854898A patent/JP3944791B2/en not_active Expired - Fee Related
- 1998-03-03 WO PCT/US1998/003270 patent/WO1998039784A1/en active Search and Examination
- 1998-03-03 KR KR1020057006663A patent/KR100546471B1/en not_active IP Right Cessation
- 1998-03-03 EP EP98910019A patent/EP1016106A4/en not_active Withdrawn
- 1998-03-03 KR KR10-1999-7008082A patent/KR100516043B1/en not_active IP Right Cessation
- 1998-03-06 TW TW087103293A patent/TW405330B/en not_active IP Right Cessation
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2005
- 2005-12-21 JP JP2005368893A patent/JP2006165585A/en active Pending
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