USPatent applicationPatented

Dielectric ceramic composition and laminated ceramic electronic component

Granted 10 Jun 2014 · 1 office action

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Abstract

A dielectric ceramic composition that contains, as its main constituent, (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 (in the formula, 0≦x+y≦0.2, 0≦z+w≦0.1), and contains CuO and Bi 2 O 3 , and the dielectric ceramic composition has a feature that the total content of the CuO and Bi 2 O 3 is 10 parts by weight or more with respect to 100 parts by weight of the main constituent, and the molar ratio CuO/(CuO+Bi 2 O 3 ) is 0.5 or less.

Description

7 parts
›CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of International application No. PCT/JP2011/061253, filed May 17, 2011, which claims priority to Japanese Patent Application No. 2010-143270, filed Jun. 24, 2010, the entire contents of each of which are incorporated herein by reference.

›TECHNICAL FIELD

The present invention relates to a dielectric ceramic composition for use in a laminated ceramic electronic component typified by a laminated ceramic capacitor.

›BACKGROUND ART

First, with reference to the FIGURE, a laminated ceramic capacitor 1 will be described as a typical example of a laminated ceramic electronic component according to this invention.

The laminated ceramic capacitor 1 includes a laminated body 2 configured with the use of a plurality of dielectric ceramic layers 3 stacked and a plurality of internal electrodes 4 and 5 formed along the specific interfaces between the dielectric ceramic layers 3 .

First and second external electrodes 8 and 9 are formed in different positions from each other on the outer surface of the laminated body 2 . The laminated ceramic capacitor 1 shown in the FIGURE has the first and second external electrodes 8 and 9 formed respectively on respective end surfaces 6 and 7 of the laminated body 5 opposed to each other. The internal electrodes 4 and 5 include the plurality of first internal electrodes 4 electrically connected to the first external electrode 8 and the plurality of second internal electrodes 5 electrically connected to the second external electrode 9 , and these first and second internal electrodes 4 and 5 are arranged alternately with respect to the stacking direction. If necessary, first plating layers 10 , 11 and second plating layers 12 , 13 are formed on the surfaces of the external electrodes 8 and 9 .

In particular, the reduction in size is required for laminated ceramic capacitors, and an approach in which dielectric ceramic green sheets and internal electrode layers are stacked and then subjected to firing at the same time is thus adopted in the production process. For the internal electrodes of the laminated ceramic capacitors, base metals such as Ni are used for reduction in cost.

In recent years, with the further progress in layer thickness reduction for dielectric ceramic layers, the layer thickness reduction for internal electrodes has been also accelerated. However, the reduction in layer thickness for internal electrodes has a problem that the coverage of the internal electrodes is likely to be decreased by spherically agglomerated metal particles, thus creating a need for firing at lower temperatures.

In addition, the demand of various characteristics for laminated ceramic electronic components has also created a need to use a wide variety of metals such as Ag and Cu as metals for internal electrodes. This reason has also created a need for firing at lower temperatures.

Thus, there has been a need for ceramic materials which are able to be fired at low temperatures, and exhibit excellent dielectric characteristics.

For example, Patent Document 1 discloses a barium titanate based dielectric ceramic composition which is suitable for multilayer substrates and laminated ceramic capacitors, and states that the composition is able to be fired at 1000° C. or less.

In addition, Patent Document 2 discloses a barium titanate based dielectric ceramic composition which is suitable for laminated ceramic substrates, and states that the composition is able to be fired at 1000° C. or less.

Patent Document 1: Japanese Patent Application Laid-Open No. 2007-290940

Patent Document 2: Japanese Patent Application Laid-Open No. 2009-132606

›SUMMARY OF THE INVENTION

However, the dielectric ceramic composition in Patent Document 1 has a dielectric constant on the order of 1500 at the highest, and thus has the problem of being difficult to respond to recent laminated ceramic capacitors which have been progressed in reduction in size and increase in capacitance.

In addition, likewise, the dielectric ceramic composition in Patent Document 2 also has a dielectric constant on the order of 1500 at the highest, and thus has the problem of being difficult to respond to recent laminated ceramic capacitors which have been progressed in reduction in size and increase in capacitance.

Therefore, an object of the present invention is to provide a dielectric ceramic composition which is able to be adequately fired at low temperatures, and exhibits favorable dielectric characteristics.

More specifically, a dielectric ceramic composition according to the present invention contains, as its main constituent, (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 (in the formula, 0≦x+y≦0.2, 0≦z+w≦0.1), and contains CuO and Bi 2 O 3 , and the dielectric ceramic composition has a feature that the total content of the CuO and Bi 2 O 3 is 10 parts by weight or more with respect to 100 parts by weight of the main constituent, and the molar ratio CuO/(CuO+Bi 2 O 3 ) is 0.5 or less. Preferably, the molar ratio CuO/(CuO+Bi 2 O 3 ) is 0.05 or more and 0.3 or less.

In addition, the present invention is also directed to a laminated ceramic electronic component including: a laminated body including a plurality of stacked ceramic layers and a plurality of internal electrodes formed along the specific interfaces between the ceramic layers; and an external electrode formed on the outer surface of the laminated body, and the component has a feature that the ceramic layers contain the dielectric ceramic composition according to the present invention.

According to the present invention, dielectric ceramic compositions can be provided which are able to be adequately fired at low temperatures, and exhibit favorable dielectric characteristics, and thus, the present invention can contribute considerably to the reduction in size and the increase in performance for laminated ceramic electronic components.

›BRIEF EXPLANATION OF THE DRAWING

The FIGURE is a diagram schematically illustrating an example of a laminated ceramic capacitor as an example of a laminated ceramic electronic component according to the present invention.

›DETAILED DESCRIPTION OF THE INVENTION

The dielectric ceramic composition according to the present invention contains a barium titanate based compound as its main constituent, and contains CuO and Bi 2 O 3 . In this case, when the total content of CuO and Bi 2 O 3 is 10 parts by weight or more with respect to 100 parts by weight of the main constituent, and when the molar ratio CuO/(CuO+Bi 2 O 3 ) is 0.5 or less, a balance is achieved between sintering at lower temperatures and a higher dielectric constant.

In addition, while the total content of CuO and Bi 2 O 3 is not to be considered to have a particularly limited upper limit, the dielectric constant is increased particularly at 20 parts by weight or less.

The main constituent of the dielectric ceramic composition according to the present invention is based on a barium titanate which may have some of Ba substituted with Ca and/or Sr, and some of Ti substituted with Zr and/or Hf. However, when the substitution total x+y at the Ba site is greater than 0.2, or when the substitution total z+w at the Ti site is greater than 0.1, the sintering at lower temperatures will be affected adversely. This is considered to be because the contents of the substitution elements have some influence on the stability of a liquid phase formed by the coexistence of CuO and Bi 2 O 3 .

When sintering at even lower temperatures is desired, the molar ratio CuO/(CuO+Bi 2 O 3 ) may be set to 0.05 or more and 0.3 or less. In this case, the liquid phase described above contributes to sintering at lower temperatures more effectively.

It is to be noted that while the molar ratio between the Ba site (Ba 1-x-y Ca x Sr y ) and the Ti site (Ti 1-z-w Zr z Hf w ) in the main constituent basically has a numerical number close to 1, the molar ratio can be controlled in the range of 0.97 or more and 1.05 or less to such an extent that no damage is caused to the object of the present invention.

In addition, rare-earth elements, Mg, Mn, V, Al, Ni, Co, Zn, and the like may be contained as accessory constituents in the present invention, to such an extent that no damage is caused to the object of the present invention.

Next, an example of a method will be described for producing the dielectric ceramic composition according to the present invention.

First, oxide or carbonate powders of Ba, Ca, Sr, Ti, Zr, and Hf are prepared as starting raw materials for the main constituent. These powders of the starting raw materials are weighed, and mixed and ground in a liquid with the use of media. After drying, the mixed powder obtained is subjected to a heat treatment, thereby providing a (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 powder as the main constituent. While this method is generally referred to as a solid-phase synthesis method, wet synthesis methods may be used as other method, such as a hydrothermal synthesis, a hydrolysis method, and an oxalic acid method.

Next, predetermined amounts of CuO powder and Bi 2 O 3 powder are added to this main constituent powder. The Cu source and Bi source are not to be considered limited to oxide powders, unless the object of the present invention is impaired. Then, these powders are mixed in the liquid, and subjected to drying to obtain a ceramic raw material powder as a final raw material.

Subsequent steps will be described with reference to an example of a laminated ceramic capacitor as an example of the laminated ceramic electronic component according to the present invention.

The above-described ceramic raw material powder is prepared. This ceramic raw material powder is mixed with an organic binder component in a solvent, if necessary, thereby providing a ceramic slurry. This ceramic slurry is subjected to sheet forming to obtain ceramic green sheets.

Next, conductor films to serve as internal electrodes are formed on the ceramic green sheets. There are several methods for this formation, and a method is simple in which a paste including metal particles and an organic vehicle is applied by screen printing into a desired pattern. The other methods include a method of transferring metal foil, and a method of forming conductor films while masking by a vacuum thin-film formation method.

In this way, the multiple layers of ceramic green sheets and internal electrode layers are stacked, and subjected to pressure bonding, thereby providing an unfired raw laminated body.

This raw laminated body is subjected to firing at a predetermined temperature in a predetermined atmosphere in a firing furnace, thereby providing a ceramic laminated body including a ceramic sintered body.

The laminated ceramic capacitor is completed by forming an external electrode on sections of the ceramic laminated body which have the internal electrodes extracted thereto. Examples of the method for forming the external electrode include a method of applying and firing a paste containing glass frit and metal particles such as Cu or Ag. Furthermore, a plating layer such as Ni and Sn is formed on the surface of the external electrode, if necessary.

It is to be noted that the laminated ceramic electronic component according to the present invention is able to be applied to not only laminated ceramic capacitors, but also various electronic components such as ceramic multilayer substrates.

›EXAMPLE

First, powders of BaCO 3 , CaCO 3 , SrCO 3 , TiO 2 , ZrO 2 , and HfO 2 were prepared as starting raw materials. These powders were weighed to satisfy the x, y, z, and w of (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 as shown for samples 1 to 83 in Tables 1 and 2, and mixed for 24 hours in water in a ball mill.

After the mixing, and then drying, this blended powder was subjected to a heat treatment under the condition of 1000° C. for 2 hours. In this way, a main constituent powder of (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 was obtained.

Next, a CuO powder and a Bi 2 O 3 powder were prepared, weighed for the total content of CuO and Bi 2 O 3 and the molar ratio CuO/(CuO+Bi 2 O 3 ) as shown in Tables 1 and 2, and added to the main constituent powder. This powder was mixed for 24 hours in water in a ball mill, and dried to provide a ceramic raw material powder.

This ceramic raw material powder was dispersed in an organic solvent including ethanol and toluene, and mixed with the addition of a polyvinyl butyral based organic binder to provide a ceramic slurry. This ceramic slurry was subjected to sheet forming to obtain ceramic green sheets.

Next, on the ceramic green sheets, an Ag internal electrode layer was formed by a sputtering method. The ceramic green sheets with the Ag internal electrode layers formed were stacked so as to alternate the sides to which the Ag internal electrode layers were extracted, and subjected to pressure bonding to obtain a raw laminated body.

This raw laminated body was heated at 270° C. in the atmosphere to remove the binder therefrom. After this, firing was carried out at 800° C. for 1 minute in the atmosphere. In the same way, firing was also carried out at 850° C. An Ag paste containing an epoxy resin was applied onto both end surfaces of the laminated body obtained, and subjected to curing at 180° C. in the atmosphere, thereby providing external electrodes connected to internal electrodes.

The laminated ceramic capacitor obtained in the way described above was 3.2 mm in length, 1.6 mm in width, and 1.6 mm in thickness, and had a ceramic layer thickness of 4.8 μm, an overlap area of 2.9 μm 2 between the internal electrodes, and 100 as the effective number of layers.

The electrostatic capacitance was measured for the obtained samples subjected to firing at 800° C. and firing at 850° C. with the use of an automatic bridge measuring instrument. The value of the dielectric constant calculated from this electrostatic capacitance was shown in Tables 1 and 2.

Samples 1 to 56 in Table 1 containing BaTiO 3 as its main constituent are intended to study the effects of varying the contents of CuO and Bi 2 O 3 .

Samples 57 to 83 in Table 2 are further intended to study the effects of element substitutions at the Ba site and Ti site of the main constituent.

From the results in Tables 1 and 2, favorable dielectric constants were achieved even in the case of sintering even at the low temperature of 850° C., for the samples containing, as their main constituent, (Ba 1-x-y Ca x Sr y )(Ti 1-z-w Zr z Hf w )O 3 (in the formula, 0≦x+y≦0.2, 0≦z+w≦0.1), in which the total content of CuO and Bi 2 O 3 is 10 parts by weight or more with respect to 100 parts by weight of the main constituent, and the molar ratio CuO/(CuO+Bi 2 O 3 ) is 0.5 or less. In addition, favorable dielectric constants are achieved even in the case of sintering even at the low temperature of 800° C., for the samples in which the molar ratio CuO/(CuO+Bi 2 O 3 ) satisfies 0.05 or more and 0.3 or less.

The dielectric ceramic composition according to the present invention is able to be applied to laminated ceramic electronic components, in particular, laminated ceramic capacitors and ceramic multilayer substrates, and intended to make contributions to reduction in layer thickness and reduction in size for the laminated ceramic electronic components.

›Tables in the description — 3
TABLE 1
The Total ContentMolar RatioDielectricDielectric
Sampleof CuO and Bi2O3CuO/(CuO +ConstantConstant
Numberxyzw(parts by weight)Bi2O3)(Firing at 850° C.)(Firing at 800° C.)
1000080.6InsufficientInsufficient
SinteringSintering
2000090.6InsufficientInsufficient
SinteringSintering
30000100.6InsufficientInsufficient
SinteringSintering
40000110.6InsufficientInsufficient
SinteringSintering
50000120.6InsufficientInsufficient
SinteringSintering
60000150.6InsufficientInsufficient
SinteringSintering
70000200.6InsufficientInsufficient
SinteringSintering
8000080.5InsufficientInsufficient
SinteringSintering
9000090.5InsufficientInsufficient
SinteringSintering
100000100.52250Insufficient
Sintering
110000110.52200Insufficient
Sintering
120000120.52210Insufficient
Sintering
130000150.52170Insufficient
Sintering
140000200.52140Insufficient
Sintering
15000080.4InsufficientInsufficient
SinteringSintering
16000090.4InsufficientInsufficient
SinteringSintering
170000100.42150Insufficient
Sintering
180000110.42150Insufficient
Sintering
190000120.42070Insufficient
Sintering
200000150.42050Insufficient
Sintering
210000200.42050Insufficient
Sintering
22000080.3InsufficientInsufficient
SinteringSintering
23000090.3InsufficientInsufficient
SinteringSintering
240000100.320802090
250000110.321002070
260000120.320502030
270000150.320001950
280000200.319801930
29000080.2InsufficientInsufficient
SinteringSintering
30000090.2InsufficientInsufficient
SinteringSintering
310000100.220402010
320000110.219801950
330000120.219201920
340000150.219001870
350000200.219301850
36000080.1InsufficientInsufficient
SinteringSintering
37000090.1InsufficientInsufficient
SinteringSintering
380000100.121302070
390000110.121002050
400000120.120602060
410000150.120101980
420000200.120001900
43000080.05InsufficientInsufficient
SinteringSintering
44000090.05InsufficientInsufficient
SinteringSintering
450000100.0522002160
460000110.0521502140
470000120.0521302100
480000150.0521102100
490000200.0520802050
50000080InsufficientInsufficient
SinteringSintering
51000090InsufficientInsufficient
SinteringSintering
520000100InsufficientInsufficient
SinteringSintering
530000110InsufficientInsufficient
SinteringSintering
540000120InsufficientInsufficient
SinteringSintering
550000150InsufficientInsufficient
SinteringSintering
560000200InsufficientInsufficient
SinteringSintering
TABLE 2 — Molar
The Total ContentRatioDielectricDielectric
Sampleof CuO and Bi2O3CuO/(CuO +ConstantConstant
Numberxyzw(parts by weight)Bi2O3)(Firing at 850° C.)(Firing at 800° C.)
570.05000100.120802090
580.05000110.121002100
590.05000120.120502030
600.05000150.120802050
610.05000200.121301990
620.25000200.1InsufficientInsufficient
SinteringSintering
630.25000100.1InsufficientInsufficient
SinteringSintering
64000.10090.1InsufficientInsufficient
SinteringSintering
65000.100100.123102260
66000.100110.122602250
67000.100120.122902270
68000.100150.122002190
69000.100200.121802150
7000.020090.1InsufficientInsufficient
SinteringSintering
7100.2500100.1InsufficientInsufficient
SinteringSintering
7200.0200100.121602150
7300.0200110.121002070
7400.0200120.120902100
7500.0200150.120702050
7600.0200200.120502020
7700.2500200.1InsufficientInsufficient
SinteringSintering
780.04000.0390.1InsufficientInsufficient
SinteringSintering
790.04000.03100.121602100
800.04000.03110.121702130
810.04000.03120.120902070
820.04000.03150.121002050
830.04000.03200.120802030
DESCRIPTION OF REFERENCE SYMBOLS
1laminated ceramic capacitor
2laminated body
3dielectric ceramic layer
4, 5internal electrode
6, 7end surface
8, 9external electrode
10, 11first plating layer
12, 13second plating layer

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IPC · International Patent Classification
Section C — Chemistry; metallurgy
  • C04B35/468
Section H — Electricity
  • H01G4/06
USPC · US Patent Classification
501/138501/139361/321.4

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