U.S. patent application number 10/864309 was filed with the patent office on 2005-12-15 for copper termination inks containing lead free and cadmium free glasses for capacitors.
This patent application is currently assigned to Ferro Corporation. Invention is credited to Khadilkar, Chandrashekhar S., Kumar, Umesh, Sridharan, Srinivasan.
Application Number | 20050276002 10/864309 |
Document ID | / |
Family ID | 35460285 |
Filed Date | 2005-12-15 |
United States Patent
Application |
20050276002 |
Kind Code |
A1 |
Sridharan, Srinivasan ; et
al. |
December 15, 2005 |
COPPER TERMINATION INKS CONTAINING LEAD FREE AND CADMIUM FREE
GLASSES FOR CAPACITORS
Abstract
Lead-free and cadmium-free glass composition that is
particularly suitable for use in conductive ink applications. The
invention includes a capacitor comprising a copper termination, the
copper termination is made by firing an ink including a glass
component, the glass component may comprise up to about 65 mole %
ZnO, up to about 51 mole % SrO, about 0.1 to about 61 mole %
B.sub.2O.sub.3, up to about 17 mole % Al.sub.2O.sub.3, about 0.1 to
about 63 mole % SiO.sub.2, up to about 40 mole % BaO+CaO, and up to
about 20 mole % MgO.
Inventors: |
Sridharan, Srinivasan;
(Strongsville, OH) ; Kumar, Umesh; (Carlsbad,
OH) ; Khadilkar, Chandrashekhar S.; (Broadview
Heights, OH) |
Correspondence
Address: |
RANKIN, HILL, PORTER & CLARK, LLP
925 EUCLID AVENUE, SUITE 700
CLEVELAND
OH
44115-1405
US
|
Assignee: |
Ferro Corporation
Cleveland
OH
|
Family ID: |
35460285 |
Appl. No.: |
10/864309 |
Filed: |
June 9, 2004 |
Current U.S.
Class: |
361/321.1 |
Current CPC
Class: |
C03C 8/14 20130101; C03C
8/18 20130101; H01G 4/2325 20130101; C03C 8/04 20130101; C03C 8/16
20130101; C03C 3/066 20130101 |
Class at
Publication: |
361/321.1 |
International
Class: |
H01G 004/06 |
Claims
1. A capacitor comprising a copper termination, said copper
termination made by firing a lead-free and cadmium-free ink
including a glass component, said glass component comprising: a. up
to about 65 mole % ZnO; b. about 0.1 to about 61 mole %
B.sub.2O.sub.3; c. about 0.1 to about 63 mole % SiO.sub.2; and d.
wherein the ratio of B.sub.2O.sub.3 to SiO.sub.2 is from about 0.7
to about 5
2. The capacitor of claim 1 wherein the glass component comprises:
a. up to about 51 mole % SrO; b. up to about 17 mole %
Al.sub.2O.sub.3; c. up to about 40 mole % BaO+CaO; and d. up to
about 20 mole % MgO.
3. The capacitor of claim 2 wherein the molar ratio of
B.sub.2O.sub.3 to SiO.sub.2 in the glass component is about 0.7 to
about 3.
4. The capacitor of claim 2 wherein the glass component comprises
about 5 to about 60 mole % B.sub.2O.sub.3+SiO.sub.2.
5. The capacitor of claim 4 wherein the glass component excludes
alkali oxides.
6. The capacitor of claim 1 wherein the glass component comprises:
a. about 20 to about 60 mole % ZnO, b. up to about 49 mole % SrO,
c. about 0.1 to about 61 mole % B.sub.2O.sub.3, d. about 0.1 to
about 17 mole % Al.sub.2O.sub.3, e. about 0.1 to about 63 mole %
SiO.sub.2, f. up to about 40 mole % BaO+CaO. g. up to about 20 mole
% MgO, h. wherein the ratio of B.sub.2O.sub.3 to SiO.sub.2 is from
about 0.7 to about 3.
7. The capacitor of claim 6 wherein the glass component comprises
about 5 to about 60 mole % B.sub.2O.sub.3+SiO.sub.2.
8. The capacitor of claim 6 wherein the glass component comprises
about 25 to about 35 mole % BaO+CaO.
9. The capacitor of claim 6 wherein the glass component comprises
about 5 to about 15 mole % MgO.
10. The capacitor of claim 6 wherein the glass component further
comprises about 0.1 to about 30 mole % CuO.
11. The capacitor of claim 8 further comprising 2-15 mole %
Li.sub.2O+Na.sub.2O+K.sub.2O+Rb.sub.2O+Cs.sub.2O+Fr.sub.2O.
12. The capacitor of claim 1 wherein the glass component comprises:
a. about 0.1 to about 65 mole % ZnO, b. about 0.1 to about 51 mole
% SrO, c. about 0.1 to about 61 mole % B.sub.2O.sub.3, d. about 0.1
to about 17 mole % Al.sub.2O.sub.3, e. about 0.1 to about 63 mole %
SiO.sub.2, f. about 0.1 to about 40 mole % BaO+CaO, g. about 0.1 to
about 20 mole % MgO.
13. The capacitor of claim 1 wherein the glass component comprises:
a. about 10 to about 56 mole % ZnO, b. about 0.1 to about 49 mole %
SrO, c. about 15 to about 35 mole % B.sub.2O.sub.3, d. about 0.1 to
about 17 mole % Al.sub.2O.sub.3, e. about 1 to about 35 mole %
SiO.sub.2, f. about 0.1 to about 35 mole % BaO+CaO, g. about 0.1 to
about 15 mol % MgO, h. wherein the ratio of B.sub.2O.sub.3 to
SiO.sub.2 is from about 0.8 to about 4 i. wherein the ink has a
viscosity of about 20,000 to about 30,000 centipoise.
14. The capacitor of claim 1 wherein the glass component comprises:
a. about 40 to about 60 mole % ZnO, b. 0 mole % SrO, c. about 20 to
about 30 mole % B.sub.2O.sub.3, d. about 0.2 to about 15 mole %
Al.sub.2O.sub.3, e. about 10 to about 25 mole % SiO.sub.2, f. about
1 to about 15 mole % MgO, g. wherein the glass component excludes
alkali oxides, h. wherein the molar ratio of B.sub.2O.sub.3 to
SiO.sub.2 is from about 1.0 to about 1.8, i. wherein the ink has a
viscosity of about 15,000 to about 35,000 centipoise.
15. A lead-free and cadmium-free ink for forming a conductive
copper pathway, said ink including a glass component and a metal
component, said glass component comprising: a. up to about 65 mole
% ZnO, b. about 0.1 to about 61 mole % B.sub.2O.sub.3, c. about 0.1
to about 63 mole % SiO.sub.2, d. wherein the molar ratio of
B.sub.2O.sub.3 to SiO.sub.2 is about 0.7 to about 5 e. wherein the
ink has a viscosity of about 15,000 to about 35,000 centipoise, and
f. wherein said ink comprises by weight from about 1 to about 22
percent by weight of said glass component.
16. The ink of claim 15, wherein the glass component further
comprises: a. about 0.1 to about 20 mole % MgO, and the molar ratio
of B.sub.2O.sub.3 to SiO.sub.2 is about 0.7 to about 4, and b. said
ink comprises from about 55 to about 85 percent by weight of said
metal component.
17. The ink of claim 15, wherein the glass component further
comprises BaO and CaO, wherein the total of BaO+CaO is about 0.1 to
about 40 mole %.
18. The ink of claim 15, wherein the glass component further
comprises: a. about 0.1 to about 51 mole % SrO, b. about 0.1 to
about 17 mole % Al.sub.2O.sub.3.
19. The ink of claim 18, wherein the glass component further
comprises: a. about 1 to about 17 mole % Al.sub.2O.sub.3, b. about
0.1 to about 20 mole % CuO.
20. The capacitor of claim 18 wherein the glass component
comprises: a. about 45 to about 65 mole % ZnO, b. about 10 to about
35 mole % B.sub.2O.sub.3, c. about 1 to about 20 mole % SiO.sub.2,
d. about 0.1 to about 20 mole % MgO, e. about 0.1 to about 5 mole %
Al.sub.2O.sub.3. f. wherein the molar ratio of B.sub.2O.sub.3 to
SiO.sub.2 is about 0.7 to about 2.5.
21. The ink of claim 15 wherein said glass component further
comprises: a. about 0.1 to about 20 mole %
CO.sub.3O.sub.4+MnO.sub.2, and b. about 0.1 to about 17 mole %
La.sub.2O.sub.3+Y.sub.2O.sub.3+Ga.sub.2O.sub.3.
22. A process for making a multilayer ceramic chip capacitor having
end terminations comprising: a. forming a green chip by stacking
alternating layers of a dielectric material and a conductive
electrode material, b. firing the green chip to form a multilayer
ceramic chip capacitor body, c. applying a conductive lead-free and
cadmium-free ink to the ceramic chip capacitor body, said ink
comprising a glass component, said glass component comprising: i.
up to about 65 mole % ZnO, ii. about 0.1 to about 61 mole %
B.sub.2O.sub.3, iii. about 0.1 to about 63 mole % SiO.sub.2, iv.
wherein the ratio of B.sub.2O.sub.3 to SiO.sub.2 is from about 0.7
to about 5, and v. wherein the ink has a viscosity of about 15,000
to about 35,000 centipoise; and, d. post-firing the chip and
forming the conductive end terminations.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to lead-free and cadmium-free
copper termination inks containing reduction resistant lead-free
and cadmium-free glasses for use in producing electronic
capacitors.
BACKGROUND OF THE INVENTION
[0002] Capacitors are electrical components that have the
capability of storing electrical energy. This energy is stored in
an electrostatic field that is created by electrical charges
accumulating on conducting plates placed across an electrical
potential and separated by an insulating medium such as ceramics,
for example barium titanate (BaTiO.sub.3), magnesium titanate
(MgTiO.sub.3). These ceramic capacitors are used in various
applications such as in temperature compensation, in
semiconductors, and in applications requiring various dielectric
constants, for example Low K class I ceramics and Higher K class II
ceramics.
[0003] A conventional structure for ceramic capacitors is a
structure of multiple layers in which dielectric layers of ceramic
are interleaved with conductive electrodes. Alternating conductive
electrodes are electrically connected, resulting in a device having
two effective electrodes with a capacitance many times the
capacitance of the single dielectric layer, packed in a relatively
very small volume. These multilayer ceramic capacitors (MLCCs) are
the most reliable component for high energy density storage banks.
This type of capacitor has been developed to meet demands for
high-density ceramic capacitors.
[0004] MLCCs consist of a plurality of interleaved and staggered
layers of an electrically conductive film of metal known as
electrodes, formed by the deposition (usually by screen printing or
the like) of a thick film paste or ink, and electrically insulating
layers of a dielectric ceramic oxide, formed by laying a cast
dielectric tape or by casting a dielectric slurry over the dried
electrode. Such capacitors are well known in the art. U.S. Pat. No.
2,389,420, for example, describes the structure, manufacture and
properties of monolithic multilayer ceramic capacitors formed using
cast dielectric green (unfired) tape.
[0005] In a typical MLCC the end termination provides the vital
electrical path between the inner electrodes and components
exterior to the capacitor. A typical end termination is made by
post firing an end termination ink on a pre fired MLCC structure. A
typical end termination ink comprises metal particles and glass
particles dispersed in an organic medium. Despite its relatively
small proportion in an end termination ink, glass plays a major
role in providing adhesion to the capacitor body, providing thermal
expansion matching between the end termination and the capacitor
body to avoid cracking at the interface, ensuring good metal
densification, allowing a wider firing window, and preventing
penetration of plating solution into the termination during
subsequent processing.
[0006] Multi-layered ceramic capacitors incorporate multiple
printed layers of electrode plates and ceramic sheets. These
capacitors are more compact and have better temperature
characteristics than single-layered ceramic capacitors. Air fired
conventional multi-layered ceramic capacitors are, however, rather
expensive because their electrode plates use precious metals, such
as silver, gold, platinum, palladium and alloys thereof. Therefore
MLCCs with base metal electrodes have been developed. However these
have to be fired in atmospheres containing very little O.sub.2,
such as N.sub.2 atmosphere with less than 10 ppm oxygen.
Development of novel reduction resistant end termination inks in
general, reduction resistant Pb free and Cd free glasses for use in
termination ink in particular, is the subject of this present
invention.
SUMMARY OF THE INVENTION
[0007] The present invention provides a lead-free and cadmium-free
copper containing termination ink for use in producing a multilayer
capacitor. The ink includes a glass component. The glass component
contains at least one glass frit. At least one of the glass frits
is partially crystallizing to maintain a high viscosity to prevent
a defect called glassing which will interfere with proper solder
wetting and adhesion. In general, the present invention comprises a
termination ink having a metal component and a glass component. The
metal component comprises copper. The glass component comprises up
to about 65 mole % ZnO, up to about 51 mole % SrO, about 0.1 to
about 61 mole % B.sub.2O.sub.3, up to about 17 mole %
Al.sub.2O.sub.3, about 0.1 to about 63 mole % SiO.sub.2, up to
about 40 mole % BaO+CaO, up to about 20 mole % MgO, and the molar
ratio of B.sub.2O.sub.3 to SiO.sub.2 is from about 0.7 to about 5.
The copper termination ink for dipping will have a viscosity of
about 15,000 to about 35,000 centipoise, when measured using
Brookfield HAT type SC4 14/5R viscometer and spindle assembly.
[0008] New conductive materials, including termination inks, are
continually being sought in the MLCC industry which provide
improved adhesion to substrates, improved chemical resistance to
plating solutions, a wider processing window, and better metal
sintering. The termination inks of the present invention provide
such desired characteristics. The invention further provides a
novel capacitor made using the inventive termination ink and a
method of fusing such end termination inks.
[0009] The copper termination inks of the present invention upon
firing exhibit superior adhesion to BaTiO.sub.3 and display good
compatibility with base metal electrodes. The foregoing and other
features of the invention are hereinafter more fully described and
particularly pointed out in the claims, the following description
setting forth in detail certain illustrative embodiments of the
invention, these being indicative, however, of but a few of the
various ways in which the principles of the present invention may
be employed.
BRIEF DESCRIPTION OF THE DRAWINGS
[0010] FIG. 1 is an elevational cross-sectional view of a
multilayer ceramic chip capacitor according to the invention.
DETAILED DESCRIPTION OF THE INVENTION
[0011] The present invention provides a termination ink comprising
a metal component, a glass component and a binder component. The
invention further provides a capacitor made using the termination
ink disclosed herein.
[0012] In the description and accompanying claims, all
compositional percentages relating to the glass component are in
mole %, and ratios are molar ratios. A statement that a composition
contains, for example, "about 15 to about 35 mole % BaO+CaO" means
that with respect only to the BaO and CaO in the composition, the
combined total of BaO and CaO is about 15 to about 35 mole % of the
total composition on a molar basis. For example, 10 mole % CaO and
25 mole % BaO. All compositional percentages relating to the
composition of the termination ink are in weight percent (wt
%).
[0013] The glass component of the present invention is lead-free
and cadmium-free. As used throughout the instant specification and
the appended claims, the phrases "lead-free" and "cadmium-free"
mean that no lead, PbO, or lead-containing glasses, cadmium, CdO,
or cadmium containing glasses have been intentionally added to the
composition. While trace elements could be present from
contaminants of raw materials, with respect to the overall
inorganic portion of the ink, the content of Pb will be less than
200 ppm and similarly, the Cd content will be less than 200 ppm.
The glass frit or frits of the present invention may include ZnO,
SrO, SiO.sub.2, B.sub.2O.sub.3 Bi.sub.2O.sub.3, Al.sub.2O.sub.3,
BaO, CaO, MgO, CuO, SnO.sub.2, CeO.sub.2, MnO.sub.2,
CO.sub.3O.sub.4 as well as alkali oxides such as Li.sub.2O,
Na.sub.2O, K.sub.2O, Rb.sub.2O, Cs.sub.2O and Fr.sub.2O. It is
possible and sometimes desirable to practice the invention wherein
the glass component excludes alkali oxides.
[0014] It will be appreciated that the glass component according to
the invention can comprise one glass frit, or it can comprise a
mixture of several glass frits, including non-crystallizing glass
frits, or a mixture of glass frits and inorganic oxides such as
SiO.sub.2, ZnO, B.sub.2O.sub.3, CO.sub.3O.sub.4, and others, so as
to provide the desired glass composition. The glass frit or frits
of the glass component may be prepared utilizing conventional glass
melting techniques. A conventional ceramic refractory, fused
silica, or platinum crucible may be used to prepare the glass frit.
Typically, a mixture of selected raw materials designed to give the
desired glass composition are smelted at temperatures of from about
1000.degree. C. to about 1550.degree. C. for about 60 minutes. The
molten glass formed in the crucible is then converted to glass
flakes or cullets using water-cooled steel rollers or quenching in
a tank of water. Pouring onto cold steel rolls results in thin
flakes suitable for milling. These flakes or cullets are then
milled to a suitable particle size distribution (e.g., average
particle size of about 1 to about 6 microns). It will be
appreciated that a coarser particle size of 40-50 microns can be
used in dip coating and spraying applications. It will be further
appreciated that the production the glass frit is not per se
critical and any of the various techniques well known to those
skilled in the art can be employed.
[0015] In general the termination inks are applied and fired on a
prefired MLCC pieces (i.e., used on a post fired basis). Typical
firing temperatures of the inventive inks and glasses are from
about 750.degree. C. to about 900.degree. C., preferably from about
780.degree. C. to about 850.degree. C., and more preferably from
about 800.degree. C. to about 830.degree. C.
[0016] The metal component comprises copper metal. Copper metal
typically is provided in the form of at least one powder or flake.
Copper powders may have particle sizes ranging from about 0.1
micron to about 40 microns. In particular, more than one size range
of copper particles may be used. For example, a first, finer,
copper powder may have a size distribution of d10=0.1-0.3 microns,
d50=0.6-1.1 microns and d90=1.5-3.5 microns. A second, coarser,
copper powder may have a size distribution range of d10=2-5
microns; d50=3-8 microns; and d90=15-25 microns. Commercially
available copper powders suitable herein include Cu 10K-1 and Cu8ED
from the Ferro Corporation of Cleveland, Ohio, and Cu 1050Y and Cu
MA-CF-E from the Mitsui Mining and Smelting Co, Ltd, of Tokyo,
Japan. It will be appreciated that sinter aids such as cobalt may
be included with the metal component.
[0017] The organic binder is usually an organic resin mixed with a
suitable vehicle. The vehicle generally includes one or more
solvents. The vehicle preferably comprises a solvent and a resin.
Optionally, the vehicle may also comprise a thixotrope and a
wetting agent in order to facilitate the application of the ink to
the capacitor. Any essentially inert binder can be used in the
practice of the present invention, including various organic
liquids, with or without thickening and/or stabilizing agents
and/or other common additives. Exemplary of the organic liquids
which can be used are the aliphatic alcohols, esters of such
alcohols, for example, the acetates and propionates. Terpenes also
may be used, such as pine oil, alpha terpineol, and beta terpineol.
Suitable terpenes include those available from Hercules Corporation
under the Terpineol.RTM. trademark, including for example
Terpineol.RTM. Prime 318. Also suitable are solutions of acrylic
resins such as the polymethacrylates of lower alcohols, or
solutions of ethyl cellulose in solvents such as pine oil, the
monobutyl either of ethylene glycol monoacetate, and carbinol
kerosene, dibutyl phthalate, hexylene glycol,
2,4,4-trimethyl-1,3-pentanediol monoisobutylrate,
N-methyl-2-pyrrolidone, ethyl hydroxyethyl cellulose, wood rosin,
mixtures of ethyl cellulose and phenolic resins, and the monobutyl
ether of ethylene glycol monoacetate or mixtures thereof.
Additionally, solvents sold under the Dowanol.RTM. or Carbitol.RTM.
trademarks, commercially available from the Dow Chemical Company,
Midland Mich., may be used. Such Dowanol.RTM. solvents suitable in
the practice of the present invention include propylene glycol,
methyl ether, dipropylene glycol methyl ether, tripropylene glycol
methyl ether, propylene glycol methyl ether acetate, dipropylene
glycol methyl ether acetate, propylene glycol n-propyl ether,
dipropylene glycol n-propyl ether, and the like. Suitable solvents
sold under the Carbitol.RTM. trademark include butyl carbitol
(diethylene glycol monobutyl ether), butyl carbitol acetate
(diethylene glycol monobutyl ether acetate) and the like. Various
combinations of these and other solvents may be formulated to
obtain the desired viscosity and volatility requirements for each
application.
[0018] Examples of potential suitable thixotropic agents include
organic based thixotropes such as, for example, ethyl cellulose,
hydrogenated castor oil, silicates and derivatives thereof.
[0019] Examples of potential suitable wetting agents (i.e.,
surfactants) include fatty acid esters, for example,
N-tallow-1,3-diaminopropane di-oleate, N-tallow trimethylene
diamine diacetate, N-coco trimethylene diamine, beta diamines,
N-oleyl trimethylene diamine, N-tallow trimethylene diamine, and/or
N-tallow trimethylene diamine di-oleate.
[0020] The glass compositions of the present invention provide
superior adhesion to common capacitor substrates, including
BaTiO.sub.3, as well as good copper densification. Applicants also
believe that the inks of the present invention may be used with
other capacitor substrates, such as those made with
Nd.sub.2Ti.sub.2O.sub.7 and MgTiO.sub.3. Further, they allow a
wider firing window with no blistering or glassing effect. It is
believed that the presence of ZnO promotes adhesion of the
termination ink to BaTiO.sub.3 substrates due to the formation of
zinc titanates at the interface. The ratio of B.sub.2O.sub.3 to
SiO.sub.2 is believed to play a role in copper densification, with
a ratio over 0.7 and preferably over 1.0 providing adequate or
superior copper densification. Desirable properties of a
termination include a wide processing window (firing temperatures),
good adhesion to BaTiO.sub.3 (and other typical dielectric
components), good chemical resistance to plating solutions, as well
as good solder wetting, as well as good copper densification. As is
known in the art, a termination is sometimes known as an external
electrode.
[0021] A method of providing good adhesion at the interface
includes reactive bonding. In reactive bonding fluid glass spreads
on and reacts with a BaTiO.sub.3 substrate, forming
thermodynamically stable crystals at the interface. These crystals
can be, for example, titanates, silicates, or aluminates. Reactions
between the substrate and the crystals to form such beneficial
reactive phases are believed to lead to an overall lowering of the
total free energy of the system, which can lead to increased
adhesion. Of course, mechanical interlocking between termination
glass and substrate may also be involved.
[0022] In addition to the glass component, the metal component, and
the binder, various conventional fillers or expansion modifiers may
be included in the ink. Examples of such fillers or expansion
modifiers include zinc silicates, magnesium silicates, barium
silicates, calcium silicates, barium aluminum silicates, zirconium
silicates, barium magnesium silicates, zirconia, alumina, silica,
titania and mixtures of the foregoing.
[0023] In order to produce a termination ink, the copper powder
(one or more) and the glass component (one or more glass frits
and/or crystalline additives), together with a binder, solvent, and
wetting agent, are batched and homogenized in a mixer. In general,
a Hobart mixer is used. After homogenization, the ink is milled in
a 3-roll mill. After multiple passes, the homogeneity of the ink
will be tested by a Fineness of Grind measurement (FOG
measurement).
[0024] A first embodiment of the present invention is an ink
including a glass component, the glass component comprising up to
about 65 mole % ZnO, up to about 51 mole % SrO, about 0.1 to about
61 mole % B.sub.2O.sub.3, up to about 17 mole % Al.sub.2O.sub.3,
about 0.1 to about 63 mole % SiO.sub.2, up to about 40 mole %
BaO+CaO, up to about 20 mole % MgO, and the molar ratio of
B.sub.2O.sub.3 to SiO.sub.2 is from about 0.7 to about 5.
[0025] Variations of this embodiment of the inventive glass
component may include a ZnO content from about 10 to about 60 mole
%. The total of B.sub.2O.sub.3 and SiO.sub.2 of the glass component
may be about 5 to about 60 mole %. In another variation, the ratio
of B.sub.2O.sub.3 to SiO.sub.2 is about 0.7 to about 3.0. In
another variation, the glass component excludes alkali oxides such
as Li.sub.2O, Na.sub.2O, K.sub.2O, Rb.sub.2O, Cs.sub.2O and
Fr.sub.2O.
[0026] In another embodiment of the invention the glass component
comprises from about 20 to about 60 mole % ZnO, up to about 49 mole
% SrO, from about 0.1 to about 61 mole % B.sub.2O.sub.3, from about
0.1 to about 17 mole % Al.sub.2O.sub.3, from about 0.1 to about 63
mole % SiO.sub.2, from about 0.1 to about 40 mole % BaO+CaO, and up
to about 20 mole % MgO, wherein the ratio of B.sub.2O.sub.3 to
SiO.sub.2 is from about 0.7 to about 3. Variations of this
embodiment of the glass component may have a total content of
B.sub.2O.sub.3 and SiO.sub.2 from about 5 to about 60 mole % of the
glass component. Another variation may have a total content of BaO
and CaO of from about 25 to about 35 mole %. Yet another variation
of this embodiment may further comprise from about 0.1 to about 30
mole % CuO. The MgO content may be instead about 5 to about 15 mole
%. In another variation, the glass component may contain any of
Li.sub.2O, Na.sub.2O, K.sub.2O, Rb.sub.2O, Cs.sub.2O and Fr.sub.2O
or any combination thereof in an amount from about 2% to about 15
mole % of the composition.
[0027] Another embodiment of the present invention provides a glass
component comprising: about 0.1 to about 65 mole % ZnO, about 0.1
to about 51 mole % SrO, about 0.1 to about 61 mole %
B.sub.2O.sub.3, about 0.1 to about 17 mole % Al.sub.2O.sub.3, about
0.1 to about 63 mole % SiO.sub.2, about 0.1 to about 40 mole %
BaO+CaO, and about 0.1 to about 20 mole % MgO. The molar ratio of
B.sub.2O.sub.3 to SiO.sub.2 may be from about 0.7 to about 5, and
the termination ink in a green, unfired state, may have viscosity
of about 15,000 to 35,000 centipoise when measured using Brookfield
HAT type SC4 14/5R viscometer and spindle assembly. Preferably this
viscosity is about 20,000 to about 30,000 centipoise. More
preferably, this viscosity is about 22,000 centipoise to about
28,000 centipoise.
[0028] The ZnO content of this embodiment may be instead from about
10 to about 56 mole % or from about 40 to about 60 mole %. The SrO
content of the glass component may instead be from about 0.1% to
about 49 mole %, or from about 20 to about 45 mole %. The SrO
content may also be zero. The B.sub.2O.sub.3 content of the glass
component may be instead from about 15 to about 35 mole %, or from
about 20 to about 30 mole %. A further possible limitation on
amounts of B.sub.2O.sub.3 and SiO.sub.2 in this embodiment may be
that the total of B.sub.2O.sub.3+SiO.sub.2 is from about 30% to
about 60 mole %. The Al.sub.2O.sub.3 content of this embodiment may
instead be about 0.1 to about 15 mole %, from about 0.2 to about 5
mole %, or from about 0.3% to about 1 mole %. The total of CaO and
BaO taken together in this embodiment may instead be about 0.1 to
about 35 mole %, or from about 25 to about 35 mole %. The MgO
content of this embodiment may instead be about 0.1% or 1% to about
15 mole %, or from about 5 to about 11 mole %. This embodiment may
further comprise CuO, up to 30 mole %, or from about 0.1 to about
25 mole %.
[0029] The molar ratio of B.sub.2O.sub.3 to SiO.sub.2 in this
embodiment may be from about 0.7 to about 3, from about 0.7 to
about 2, from about 1 to about 3, or from about 1.3 to about
1.8.
[0030] Another embodiment is an ink including a glass component,
the glass component comprising about 0.1 to about 51 mole % SrO,
about 0.1 to about 61 mole % B.sub.2O.sub.3, about 0.1 to about 63
mole % SiO.sub.2, about 0.1 to about 17 mole % Al.sub.2O.sub.3, and
about 0.1 to about 20 mole % CuO. The glass component may also
include about 20 to about 40 mole % SrO, about 10 to about 30 mole
% B.sub.2O.sub.3, about 10 to about 25 mole % SiO.sub.2, about 7 to
about 17 mole % Al.sub.2O.sub.3 about 10 to about 25 mole % CuO,
wherein the molar ratio of B.sub.2O.sub.3 to SiO.sub.2 is about 0.7
to about 2.
[0031] Yet another embodiment is an ink including a glass
component, the glass component comprising about 0.1 to about 20
mole % CO.sub.3O.sub.4+MnO.sub.2, about 0.1 to about 49 mole % SrO,
about 0.1 to about 61 mole % B.sub.2O.sub.3, about 0.1 to about 17
mole % La.sub.2O.sub.3+Y.sub.2O.sub.3+Ga.sub.2O.sub.3, about 0.1 to
about 63 mole % SiO.sub.2, about 0.1 to about 40 mole % BaO+CaO, up
to about 20 mole % MgO. The molar ratio of B.sub.2O.sub.3 to
SiO.sub.2 is from about 0.7 to about 5, and the ink has a viscosity
of about 15,000 to about 35,000 centipoise.
[0032] Where two glasses are used, the primary glass is used for
adhesion without glassing, and the second glass is used to improve
the durability and/or thermal expansion matching of the glass
component, and such second glass preferably has a low content of
zinc, or preferably no zinc at all. An ink composition of the
present invention includes one or more copper powders, at least one
glass frit, a binder, organic additives and a solvent. The ink
comprises about 55-85 wt % of the copper powder, about 1-22 wt % of
one or more glass frits, about 1-10 wt % of a binder, about 0.1 to
3% of additives and about 5 to 25 wt % of a solvent. Preferably,
the ink comprises from about 70 to about 80 wt % of the one or more
copper powders, from about 2 to about 15 wt % of one or more glass
frits, from about 2 to about 6 wt % of a binder, from about 0.5 to
about 2 wt % of additives, and from about 5 to about 20 wt % of a
solvent.
[0033] A further embodiment of the present invention is a
capacitor, to include multilayer ceramic capacitors (MLCCs),
including terminations made incorporating the inventive termination
inks as discussed hereinabove. Also envisioned within the practice
of the present invention is a method of making multilayer ceramic
chip capacitor having end terminations comprising: forming a green
chip by stacking alternating layers of a dielectric material and a
conductive electrode material, firing the green chip to form a
multilayer ceramic chip capacitor, dipping the terminations of the
capacitor in a conductive paste comprising copper and an ink
including a glass component, post-firing the chip to sinter the end
terminations. Any glass component disclosed herein may be used in
the method of making a multilayer chip capacitor.
[0034] The configuration of multilayer ceramic capacitors is well
known in the art. With reference to FIG. 1, an exemplary structure
of a multilayer ceramic chip capacitor 1 is shown. End terminations
4 of the capacitor 1 are disposed on side surfaces of the capacitor
chip 10 and in electrical connection with internal electrode layers
3. The capacitor chip 10 has a plurality of alternately stacked
dielectric layers 2. The shape of the capacitor chip 10 is not
critical although it is often rectangular shaped. Also, the size is
not critical and the chip may have appropriate dimensions in
accordance with a particular application, typically in the range of
1.0 to 7.0 mm.times.0.5 to 5.0 mm.times.0.5 to 2.0 mm. The internal
electrode layers 3 are stacked such that at opposite ends they are
alternately exposed at opposite side surfaces of the chip 10. That
is, the internal electrode layers 3 of one group are exposed at one
side surface of the chip 10 and the internal electrode layers 3 of
another group are exposed at the opposite side surface of the chip
10. One end termination 4 is applied to one side chip of the
capacitor chip 10 in electrical contact with the internal electrode
layers 3 of the one group, and the other end termination 4 is
applied to the opposite side surface of the chip 10 in electrical
contact with the internal electrode layers 3 of the other group.
The dielectric layers are formed of one or more dielectric
materials which may contain barium titanate (BaTiO.sub.3) and other
oxides such as neodymium titanate (Nd.sub.2Ti.sub.2O.sub.7) and
magnesium titanate (MgTiO.sub.3) as major components, while
manganese oxide, yttrium oxide, holmium oxide, calcium carbonate,
silicon oxide, boron oxide, aluminum oxide, magnesium oxide, and
calcium oxide may be present as minor components. Other compounds
may be contained in the dielectric material provided that the other
compound does not adversely affect dielectric properties.
[0035] Each dielectric layer preferably has a thickness of up to
about 50 .mu.m, more preferably up to about 20 .mu.m. The lower
limit of thickness is about 0.5 .mu.m, preferably about 2 .mu.m.
The present invention is effectively applicable to multilayer
ceramic chip capacitors having such thin dielectric layers for
minimizing a change of their capacitance with time. The number of
dielectric layers stacked is generally from about 2 to about 600,
although embodiments having more than 600 layers are possible.
[0036] The conductor that forms the internal electrode layers 3 is
not critical, although a base metal preferably is used since the
dielectric material of the dielectric layers 2 has anti-reducing
properties. Typical base metals are nickel and nickel alloys. The
thickness of the internal electrode layers may be suitably
determined in accordance with a particular purpose and application
although its upper limit is typically about 5 .mu.m, and more
preferably about 2.5 .mu.m, and its lower limit is typically about
0.5 .mu.m, and more preferably about 1 .mu.m.
[0037] An ink or slurry for forming the dielectric layers can be
obtained by mixing a raw dielectric material with an organic
vehicle. The raw dielectric material may be a mixture of oxides and
composite oxides. The organic vehicle is a binder in an organic
solvent. The binder used herein is not critical and may be suitably
selected from conventional binders such as those disclosed
hereinabove with reference to the inks of the present
invention.
[0038] Terminations 4 are formed by applying the inventive
termination ink across the ends of a prefired MLCC. The termination
ink may be applied by dipping or brushing, as known in the art. The
thickness of the termination may be suitably determined in
accordance with a particular purpose and application although it
generally ranges from about 1 .mu.m to about 100 .mu.m. Certain
applications require the termination thickness to be about 10 .mu.m
to about 50 .mu.m, or from about 20 .mu.m to about 40 .mu.m.
[0039] The multilayer ceramic chip capacitor of the present
invention generally is fabricated by forming a green chip by
conventional tape casting, printing and sheeting methods using
slurries or pastes, firing the chip, and printing or transferring
terminations thereto followed by a second firing. The termination
inks are typically fired at temperatures lower than the initial
firing to sinter the capacitor as a whole. The initial firing of
the capacitor body generally occurs at a temperature of from about
7500 to about 1350.degree. C., and the firing of the body with the
ink applied generally occurs at a temperature of from about
650.degree. to about 900.degree. C. Further details on the
manufacturing procedures used to make a MLCC may be found in U.S.
Pat. No. 6,185,087 to Park et al. the disclosure of which is hereby
incorporated by reference.
[0040] The following examples are intended only to illustrate the
invention and should not be construed as imposing limitations upon
the claims.
EXAMPLES
[0041] Glass frits A through H having the following compositions by
mole percent, were each prepared using conventional glass melting
techniques. The compositions of the glasses made are found in table
1. The glass transition temperature (Tg), coefficient of thermal
expansion (CTE), and compositional ratios (mole B.sub.203/mole
SiO.sub.2) are found in Table 2.
[0042] Termination inks AA through HH having the compositions as
listed in Table 3 were prepared by standard ink preparation
procedures. The inks have a viscosity of about 15,000 centipoise to
about 35,000 centipoise. The copper powders used herein are
commercially available from the Ferro Corporation. Copper powder Cu
I has a D50 particle size of about 0.8 micron, Copper powder Cu II
has a D50 particle size of about 4 to 6 microns, and Copper powder
Cu III is a flaked powder having a D50 particle size of about 4 to
6 microns. BaTiO.sub.3 capacitors of case size 1206 were terminated
with these pastes and fired at different firing temperatures.
[0043] The optimum firing range (i.e., processing window) for each
termination ink was determined based on having acceptable
properties for copper densification, nickel engross depth,
adhesion, and no glassing. After firing a capacitor, the end
termination is plated with nickel. In order to find the amount of
Ni engross the capacitor is mounted in a cross section and
polished. The depth of nickel engross is measured and should not
exceed 10% of the thickness of the end termination. Further, on a
1206 capacitor, the peel strength of the end termination must be
greater than 1.5 pounds. With respect to glassing, no glass beads
or blistering should appear. The optimum firing temperature is
taken as that temperature which is 10.degree. C. below the
temperature at which glass beads or blisters (glassing defects) are
evident. If glassing is evident at 820.degree. C. and not
810.degree. C., then 810.degree. C. is the upper limit of the
processing window. The lower limit of this window is that
temperature which is 10.degree. C. above the minimum temperature at
which sufficient copper densification, as measured by cross
sectional microscopy and adhesion, as measured by a peel strength
of at least 1.5 pounds, is achieved. Copper densification should be
at least about 90% or above. The nickel engross should also be no
greater than 10% at the lower temperature limit. The optimum firing
temperatures thus obtained are listed in Table 3, which indicates a
firing window of about 10.degree. C. to about 30.degree. C. for the
inventive copper termination inks.
1TABLE 1 Representative lead-free and cadmium-free glasses for
copper termination inks Constituent (Mole Percent) Glass SrO ZnO
B.sub.2O.sub.3 SiO.sub.2 MgO Al.sub.2O.sub.3 BaO CuO A 0 59.1 25.9
15.0 0 0 0 0 B 0 56.0 21.7 13.2 9.3 0.2 0 0 C 0 20.0 30.0 20.0 0 0
30.0 0 D 30.0 25.5 21.8 13.2 9.3 0.2 0 0 E 30.0 10.0 30.0 20.0 10.0
0 0 0 F 16.4 27.8 21.2 15.1 4.7 6.4 0 8.5 G 32.8 0 20.8 17.0 0 12.5
0 17.1 H 48.5 8.4 4.3 23.4 0 5.4 0 10.0
[0044]
2TABLE 2 Properties of glasses in Table 1 Glass Coefficient of
Transition thermal Temperature, expansion Molar ratio of Total mole
% Glass .degree. C. (.times.10.sup.-7)/.degree. C.
B.sub.2O.sub.3/SiO.sub.2 B.sub.2O.sub.3 + SiO.sub.2 A 556 44 1.7
40.9 B 560 48 1.6 34.9 C 515 102.4 1.5 50.0 D 529 103.1 1.7 35.0 E
592 85 1.5 50.0 F 525 66 1.4 36.3 G 550 90 1.2 37.8 H 581 102.8 0.2
27.7
[0045]
3TABLE 3 Compositional analysis of inventive inks and optimum
firing range Terpineol Glass Acrylic prime Optimum Glass used Cu I
Cu II Cu III amount resin Surfactant 318 firing Ink (Table 1)
Weight % range, .degree. C. AA A 29.9 20.5 18.7 6.5 4.5 0.8 19.1
810-820 AB B 29.9 20.5 18.7 6.5 4.5 0.8 19.1 810-820 AC C 29.9 20.5
18.7 6.5 4.5 0.8 19.1 800-810 AD D 39.6 29.5 -0- 6.5 4.5 0.8 19.1
790-820 AE E 39.6 29.5 -0- 6.5 4.5 0.8 19.1 800-810 AF F 39.6 29.5
-0- 6.5 4.5 0.8 19.1 800-825 AG G 29.9 20.5 18.7 6.5 4.5 0.8 19.1
800-810 AH H 29.9 20.5 18.7 6.5 4.5 0.8 19.1 800-810
[0046] It will be appreciated that an ink made in accordance with
the present invention may also be used to form conductive pathways
on various electronic devices. Thus, use of the present ink is not
intended to be limited to capacitor devices alone.
[0047] Additional advantages and modifications will readily occur
to those skilled in the art. Therefore, the invention in its
broader aspects is not limited to the specific details and
illustrative examples shown and described herein. Accordingly,
various modifications may be made without departing from the spirit
or scope of the general inventive concept as defined by the
appended claims and their equivalents.
* * * * *