WO2006068245A1 - 積層型圧電セラミック部品、及び積層型圧電セラミック部品の製造方法 - Google Patents
積層型圧電セラミック部品、及び積層型圧電セラミック部品の製造方法 Download PDFInfo
- Publication number
- WO2006068245A1 WO2006068245A1 PCT/JP2005/023666 JP2005023666W WO2006068245A1 WO 2006068245 A1 WO2006068245 A1 WO 2006068245A1 JP 2005023666 W JP2005023666 W JP 2005023666W WO 2006068245 A1 WO2006068245 A1 WO 2006068245A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ceramic
- internal electrode
- electrode layer
- multilayer piezoelectric
- layer
- Prior art date
Links
- 239000000919 ceramic Substances 0.000 title claims abstract description 280
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 239000000843 powder Substances 0.000 claims abstract description 97
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000001301 oxygen Substances 0.000 claims abstract description 48
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 48
- 239000002184 metal Substances 0.000 claims abstract description 46
- 229910052751 metal Inorganic materials 0.000 claims abstract description 46
- 238000010304 firing Methods 0.000 claims abstract description 34
- 239000000463 material Substances 0.000 claims description 31
- 230000005684 electric field Effects 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 16
- 239000011800 void material Substances 0.000 claims description 10
- 238000006073 displacement reaction Methods 0.000 abstract description 74
- 239000007787 solid Substances 0.000 abstract description 10
- 229910010293 ceramic material Inorganic materials 0.000 abstract description 6
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 183
- 238000000034 method Methods 0.000 description 32
- 230000007423 decrease Effects 0.000 description 18
- 239000002994 raw material Substances 0.000 description 12
- 238000005245 sintering Methods 0.000 description 10
- 239000011230 binding agent Substances 0.000 description 9
- 239000010408 film Substances 0.000 description 7
- 230000005764 inhibitory process Effects 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 230000010287 polarization Effects 0.000 description 5
- 229910018054 Ni-Cu Inorganic materials 0.000 description 4
- 229910018481 Ni—Cu Inorganic materials 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000001878 scanning electron micrograph Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- 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 2
- 239000011324 bead Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000010191 image analysis Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 101001012040 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Immunomodulating metalloprotease Proteins 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000007847 structural defect Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/80—Constructional details
- H10N30/87—Electrodes or interconnections, e.g. leads or terminals
- H10N30/871—Single-layered electrodes of multilayer piezoelectric or electrostrictive devices, e.g. internal electrodes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/05—Manufacture of multilayered piezoelectric or electrostrictive devices, or parts thereof, e.g. by stacking piezoelectric bodies and electrodes
- H10N30/053—Manufacture of multilayered piezoelectric or electrostrictive devices, or parts thereof, e.g. by stacking piezoelectric bodies and electrodes by integrally sintering piezoelectric or electrostrictive bodies and electrodes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/06—Forming electrodes or interconnections, e.g. leads or terminals
- H10N30/067—Forming single-layered electrodes of multilayered piezoelectric or electrostrictive parts
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/80—Constructional details
- H10N30/87—Electrodes or interconnections, e.g. leads or terminals
- H10N30/877—Conductive materials
Definitions
- Multilayer piezoelectric ceramic component and method of manufacturing multilayer piezoelectric ceramic component are described.
- the present invention relates to a laminated piezoelectric ceramic component such as a laminated piezoelectric actuator laminated piezoelectric sounding body and a method for manufacturing the laminated piezoelectric ceramic component.
- this type of multilayer piezoelectric ceramic component has piezoelectric ceramic layers 101a ⁇ :! Olg and internal electrode layers 102a ⁇ 102f laminated alternately.
- the external electrodes 104a and 104b are formed on the end face of the ceramic body 103.
- the ceramic layer 101b when an electric field is applied, the ceramic layer 101b :: the force by which the Olf expands and contracts If the thickness of the internal electrode layers 102a-102f is thick, ⁇ :! Olf is restrained by the internal electrode layers 102a to 102f, so that the expansion and contraction of the ceramic layers 101b to 101f is inhibited. That is, as the internal electrode layers 102a to 102f are thinner, the ceramic layers 101b to! Olf are easily expanded and contracted, and the displacement amount is increased.
- the ratio of the total area of the through holes formed in the internal electrode to the total area of the internal electrode is 40 to 0%, and the same or similar composition as the ceramic layer A multilayer electronic component in which an internal electrode is formed using a paste containing 10 to 30% by weight of a ceramic material has been proposed (Patent Document 1).
- Patent Document 1 a film thickness is obtained by forming an internal electrode using a ceramic material having the same or similar composition as the ceramic layer, that is, using a paste containing 10 to 30% by weight of a ceramic co-material.
- the coverage is increased to 60 to 100% to increase the electrode area, thereby avoiding a decrease in capacitance, We are trying to avoid as much as possible the occurrence of structural defects after firing by suppressing the shrinkage of the extreme layers.
- the negative electrode of the internal electrode contains Ag element
- the positive electrode does not contain Ag element
- the internal electrode has a thickness of 1 to 3 / im
- the coverage is 50 to 99.
- Patent Document 2 A multilayered piezoelectric element controlled to% is also proposed (Patent Document 2).
- Patent Document 2 the coverage is controlled to 50 to 99%, thereby suppressing the occurrence of migration and delamination and improving reliability.
- the internal electrode layer is made of a metal material mainly composed of Pd, Z, or Pt, and has a plurality of holes penetrating in the stacking direction, and a piezoelectric ceramic is formed in the hole.
- a multilayer piezoelectric actuator is proposed which is made of the same material as the plate and is provided with a common material for connecting the respective piezoelectric ceramic plates facing each other via internal electrodes (Patent Document).
- Patent Document 3 a non-electrode part in which a through hole having a minimum inner diameter of 1Z2 or less is provided with respect to the thickness of the ceramic layer, the through hole is filled with a ceramic co-material, and a through hole is further formed.
- Patent Document 1 Japanese Patent Application Laid-Open No. 2002-164248
- Patent Document 2 JP 2001-250994 A
- Patent Document 3 Japanese Patent Laid-Open No. 63-142875
- Patent Document 1 when the technique of Patent Document 1 is applied to the multilayer piezoelectric ceramic component, the size of the non-conductive portion in which the electrode in the internal electrode layer is not formed simply by controlling the coverage. There is a problem in that variations occur in the voltage and the potential drop due to the non-conductive portion becomes large, and therefore a desired large displacement cannot be obtained.
- Patent Document 2 suppresses the occurrence of migration and delamination by controlling the coverage to 50 to 99%.
- a multilayer piezoelectric ceramic component is used. When applied to, simply controlling the coverage ratio causes variations in the size of the non-conductive part or increases the potential drop due to the non-conductive part. There was a problem that the amount could not be obtained.
- Patent Document 3 although a through hole having a minimum inner diameter dimension of 1/2 or less is provided with respect to the thickness of the ceramic layer, a potential drop occurs only by this, so that a desired large displacement amount can be obtained.
- the ratio between the non-electrode part (non-conductive part) and the electrode part (conductive part) is 1: 1 or less, sufficient coverage cannot be obtained, and the internal electrode layer and the ceramic layer There was a problem that interfacial delamination might occur.
- the present invention has been made in view of such circumstances, and even if the internal electrode layer is a thin layer, the multilayer piezoelectric ceramic component having a large amount of displacement and excellent bonding strength, and It is an object of the present invention to provide a method for manufacturing the multilayer piezoelectric ceramic component.
- a potential drop is defined by the product of an electric field and a piezoelectric constant as a result of a non-conductive part such as a through hole being formed in the internal electrode layer, resulting in a potential drop due to the non-conductive part.
- a non-conductive part such as a through hole being formed in the internal electrode layer
- the non-conductive portion increases structurally, and the potential drop at the non-conductive portion becomes significant.
- Residual stress is a phenomenon in which the stress remains due to the difference between the thermal expansion coefficient of the ceramic layer and the thermal expansion coefficient of the internal electrode layer, and the displacement of the ceramic layer is suppressed.
- Displacement inhibiting force means that when a voltage is applied, the ceramic layer expands and contracts. However, since the ceramic layer is sandwiched between internal electrode layers, the displacement of the ceramic layer is reduced. This phenomenon is hindered by the internal electrode layer.
- the present inventors have investigated the above three factors that hinder the improvement of the displacement, that is, the potential drop.
- the ratio of the average diameter X to the thickness y of the ceramic layer when the cross-sectional area of the non-conductive part of the internal electrode layer was converted to a circle x / y is controlled between 0.08 and 0.33
- the ratio z / y between the thickness z of the internal electrode layer and the thickness y of the ceramic layer is controlled between 0.04 and 0.40
- the internal electrode By controlling the coverage of the ceramic layer to 60 to 95%, it is possible to reduce residual stress and displacement inhibition force while minimizing the decrease in displacement due to potential drop. It was found that even when the electrode layer is a thin layer, it is possible to obtain a laminated piezoelectric ceramic component capable of improving both the displacement and the reliability.
- the multilayer piezoelectric ceramic component according to the present invention is a multilayer piezoelectric ceramic component in which ceramic layers and internal electrode layers are alternately stacked.
- the internal electrode layer comprises a conductive part and a non-conductive part, and the ratio xZy between the average diameter X and the thickness y of the ceramic layer when the cross-sectional area of the non-conductive part is converted into a circle is 0.08 to And the ratio z / y of the thickness z of the internal electrode layer to the thickness y of the ceramic layer is 0.04-0.40, and the internal electrode layer to the ceramic layer It is characterized by a coverage of 60-95%.
- the internal electrode layer is made of a conductive paste containing a metal powder and a ceramic powder as a solid content as described later. Since it is formed by use, the non-conductive portion has a void portion and a ceramic portion filled with ceramic powder.
- the amount of displacement in the nonconductive part is further improved by reducing the porosity in the nonconductive part to 60% or more. I found that I can plan.
- the non-conductive portion is composed of a void portion and a ceramic portion filled with ceramic powder, and the void portion is 60% of the non-conductive portion. It is characterized by occupying the above.
- the multilayer piezoelectric ceramic component can obtain a desired large displacement even when relatively inexpensive Ag is used as the main component of the conductive part material of the internal electrode layer. And it was found that the reliability can be improved.
- the conductive part is composed mainly of Ag. Do this as a special number.
- this multilayer piezoelectric ceramic component can obtain a larger amount of displacement at a high electric field that is 1/10 or more of the coercive electric field of the ceramic layer.
- the multilayer piezoelectric ceramic component of the present invention has a coercive field of 1Z of the ceramic layer.
- It is characterized by being driven by 10 or more electric fields.
- the inventors of the present invention have made ceramic powder having a specific surface area 5 to 20 times that of metal powder so that the content thereof is 20 to 50% by weight based on the total amount of metal powder and ceramic powder.
- a conductive paste is applied to the surface of a ceramic liner sheet to form a predetermined conductive pattern to be an internal electrode layer, and the conductive After laminating ceramic green sheets with patterns, they are sandwiched between ceramic green sheets without conductive patterns and pressed to form a laminate, and then subjected to firing treatment to form the ceramic body.
- the ceramic paste having a specific surface area that is 5 to 20 times that of the metal powder is formed by laminating the laminated piezoelectric ceramic component formed on the end face of the ceramic body and forming an external electrode. And the ceramic powder content is adjusted to 20 to 50% by weight based on the total amount of the metal powder and the ceramic powder.
- the firing treatment, the oxygen concentration is characterized by performing in an oxygen atmosphere at 0.:! ⁇ 15 vol%.
- the ceramic powder contained in the conductive paste diffuses also to the ceramic green sheet side during firing, from the viewpoint of preventing characteristic fluctuations, at least the main component has the same component composition as the ceramic green sheet. It is preferred to use the material that it has.
- the method for producing a multilayer piezoelectric ceramic component of the present invention is characterized in that at least a main component of the ceramic powder has the same component composition as the ceramic green sheet.
- the internal electrode layer includes a mixture of a conductive portion and a non-conductive portion.
- the ratio x / y of the average diameter X and the thickness y of the ceramic layer when the cross-sectional area of the non-conductive portion is converted into a circle is 0.08 to 0.33, and
- the ratio z / y between the thickness z of the electrode layer and the thickness y of the ceramic layer is 0.04 to 0.40, and the coverage of the internal electrode layer on the ceramic layer is 60 to 95%.
- the non-conductive portion is composed of a void portion and a ceramic portion filled with ceramic powder, and the void portion occupies 60% or more of the non-conductive portion. Residual stress and displacement hindrance can be effectively reduced, and the displacement and bonding strength can be further improved.
- the conductive portion is mainly composed of Ag
- a multilayer piezoelectric ceramic component that achieves both the amount of displacement and the bonding strength even when relatively inexpensive Ag is the main component. Can be obtained.
- the present multilayer piezoelectric ceramic component can obtain a larger displacement when driven by an electric field of 1/10 or more of the coercive electric field of the ceramic layer.
- the conductive paste contains a metal powder and a ceramic powder having a specific surface area 5 to 20 times that of the metal powder.
- the content of the ceramic powder is adjusted to 20 to 50% by weight with respect to the total amount of the metal powder and the ceramic powder, and the firing treatment is performed in an oxygen atmosphere having an oxygen concentration of 0.1 to 15% by volume. Therefore, the fine ceramic powder is effectively diffused into the ceramic green sheet during sintering, and the diffusion of metal components in the internal electrode layer into the ceramic green sheet can be suppressed. It is possible to form a minute non-conductive portion.
- firing in a low oxygen concentration atmosphere suppresses the sintering of through-holes that can be formed in the internal electrode layer, so that minute voids are distributed substantially uniformly in the internal electrode layer. As a result, the coverage is lowered and the displacement can be improved.
- the amount of conductive paste used can be reduced by reducing the coverage of the internal electrodes and making it thinner, the cost can be reduced.
- the ceramic powder has at least the same component composition as that of the ceramic green sheet, even if the ceramic powder diffuses to the ceramic green sheet side during firing, fluctuations in characteristics can be prevented.
- FIG. 1 is a cross-sectional view showing an embodiment of a multilayer piezoelectric ceramic component according to the present invention.
- FIG. 2 is an enlarged cross-sectional view of part B in FIG.
- FIG. 3 is a diagram showing an example of an SEM image of an embodiment of the present invention.
- FIG. 4 is a diagram showing an example of a conventional SEM image.
- FIG. 5 is a cross-sectional view showing a conventional example of a multilayer piezoelectric ceramic component.
- FIG. 1 is a cross-sectional view showing an embodiment of a multilayer piezoelectric actuator as a multilayer piezoelectric ceramic component according to the present invention.
- the multilayer piezoelectric actuator includes a ceramic layer 1 (la to lg) and internal electrodes. Layers 2 (2a to 2f) are alternately stacked to form the piezoelectric ceramic body 3, and from the upper surface or the lower surface of the piezoelectric ceramic body 3 to the end surface, a conductive material such as Ag having an L-shaped cross section is formed.
- the external electrode 4 (4a, 4b) is formed.
- each of the internal electrodes 2a, 2c, 2e is electrically connected to one external electrode 4b
- one end of each of the internal electrodes 2b, 2d, 2f is the other external electrode 4 It is electrically connected to a.
- the polarization direction of the laminated piezoelectric actuator is perpendicular to the inner electrode 2 surface, and each layer is polarized in opposite directions. When a voltage is applied between the external electrode 4a and the external electrode 4b, it is displaced in the longitudinal direction indicated by the arrow A by the piezoelectric lateral effect.
- FIG. 2 is an enlarged cross-sectional view of a portion B in FIG.
- a part of the internal electrode layers 2b to 2d is enlarged, but the other parts have the same structure.
- the internal electrode layer 2 (2b to 2d) includes a conductive part 5 formed by sintering metal powder and a non-conductive part 6 in which no metal powder exists, and the non-conductive part 6 further includes: It has a ceramic portion 6a in which ceramic powder having at least the same main component as the ceramic layer 1 (lb ⁇ : le) is present, and a void portion 6b in which no solid is present.
- the gap 6b does not necessarily have to penetrate.
- ceramic powder may be included in a part of the gap 6b.
- the ceramic part 6a may be present in a part of the internal electrode layer 2 that does not necessarily need to straddle the internal electrode layer 2.
- the ratio x / y between the average diameter X and the thickness y of the ceramic layer 1 when the cross-sectional area of the non-conductive portion 6 is converted into a circle is 0.08-0.33.
- the covering ratio of the internal electrode layer 2 to the ceramic layer 1 is controlled to be 60 to 95%, thereby reducing the size of the non-conductive part 6 and reducing the non-conductive part. It is possible to suppress a decrease in the amount of displacement due to a potential drop at 6 and to reduce the coverage of the internal electrode layer 2 by providing a large number of minute non-conductive portions 6. As a result, it is possible to reduce the residual stress and the displacement inhibiting force due to the internal electrode layer 2, and to improve the displacement amount and the bonding strength of the laminated piezoelectric actuator.
- the ratio x / y has a correlation with the potential drop, and when the ratio x / y is small, the average diameter X is relatively small with respect to the thickness of the ceramic layer 1, and therefore the potential drop is small and the displacement is small. Will improve. On the other hand, when the ratio xZy is increased, the average diameter X is relatively increased with respect to the thickness of the ceramic layer 1, so that the potential drop is increased and the displacement is decreased. When the coverage is less than 60%, the non-conductive portion 6 increases excessively, leading to a decrease in the amount of displacement due to a large potential drop, and the bonding between the ceramic layer 1 and the internal electrode layer 2. The strength also decreases and the field Surface peeling tends to occur.
- the covering ratio exceeds 95%, the covering ratio becomes excessive, and the displacement inhibiting force that restrains the expansion and contraction motion of the ceramic layer 1 by the internal electrode layer 2 increases, leading to a decrease in the amount of displacement. Further, there is a risk that the bonding strength is reduced due to residual stress resulting from the difference between the thermal expansion coefficient of the ceramic layer 1 and the thermal expansion coefficient of the internal electrode layer 2 during co-sintering.
- the ratio x / y is less than 0.08, the average diameter X of the non-conductive portion 6 becomes small, so that the coverage becomes difficult to control the coverage, so that the inside of the ceramic layer 1 is increased.
- the displacement inhibition force to the electrode layer 2 is increased and the displacement amount is reduced.
- the ratio x / y exceeds 0.33, the average diameter X of the non-conductive portion 6 increases, so that the potential drop due to the non-conductive portion 6 increases, and a desired large displacement amount is obtained. Can not be.
- the ratio is controlled so that the ratio x / y force SO.08-0.33 of the average diameter X of the non-conductive portion 6 to the ceramic layer y is SO.08-0.33.
- the ratio z / y between the thickness z of the internal electrode layer 2 and the thickness y of the ceramic layer 1 is preferably 0.04 to 0.40.
- the ratio z / y is preferably set to 0.04 or more.
- the ratio zZy is preferably 0.04 to 0.40.
- the thickness z of the internal electrode layer 2 is reduced, the residual stress and the displacement-inhibiting force due to the internal electrode layer 2 are reduced. Therefore, it is desirable that the thickness z of the internal electrode layer 2 be as thin as possible.
- the thickness z is preferably controlled to be in the range of 1 to 2.4 ⁇ m.
- the gap 6b formed in the internal electrode layer 2 is 60 in the non-conductive part 6 (the ceramic part 6a and the gap 6b). It is preferable to occupy / o or more. That is, by forming the internal electrode layer 2 using a conductive paste containing finer ceramic powder than the metal powder, the ceramic powder is dispersed in the ceramic layer 1 during co-sintering, thereby The bonding strength between the ceramic layer 1 and the internal electrode layer 2 can be improved. However, if the ratio of the gap 6b in the non-conductive part 6 is less than 60%, a large number of ceramic parts 6a are formed in the internal electrode layer 2, which increases the bonding strength and reduces the displacement. There is a risk of inviting. Therefore, the gap 6b preferably occupies 60% or more of the non-conductive portion 6.
- the conductive part 5 can contain Ag as a main component, for example, Ag_Pd containing 70 wt% or more of Ag.
- the covering rate generally decreases and the bonding strength tends to decrease, but the structure of the internal electrode layer 2 is improved.
- the multilayer piezoelectric actuator can be obtained with a larger displacement by being driven by a high electric field that is 1/10 or more of the coercive electric field of the ceramic layer 1. This is because the amount of displacement increases as the drive electric field increases, and the effect of reducing residual stress and displacement inhibition force by the internal electrode layer 2 loaded on the ceramic layer 1 appears more prominently.
- an organic binder plasticizer is added to the ceramic raw material powder prepared in this manner, and wet mixing is performed to form a slurry, which is then formed using a doctor blade method or the like. To produce a ceramic green sheet.
- a conductive paste is produced as follows. [0065] First, an organic vehicle in which an organic binder is dissolved in an organic solvent is produced. In the next stage, a metal powder having a predetermined specific surface area (for example:! To 3 m 2 / g) is prepared, the metal powder is mixed with the organic vehicle, kneaded with a three-roll mill or the like, and the metal is thereby mixed. Get a paste.
- a ceramic raw material having at least the same component as the ceramic raw material powder is prepared, and the ceramic raw material is put into a forced stirring device such as a bead stirrer-type pulverizer and pulverized.
- a ceramic powder (ceramic co-material) having a specific surface area S2 of 5 to 20 times the specific surface area S1 of the metal powder is produced.
- the ceramic powder and the organic vehicle are mixed, and the ceramic powder is sufficiently dispersed in the organic vehicle using a forced stirring device such as the bead stirring mill, thereby obtaining a ceramic paste. .
- the reason why the specific surface area S2 of the ceramic powder is set to 5 to 20 times the specific surface area S1 of the metal powder as described above is as follows.
- the specific surface area S2 of the ceramic powder is set to 5 to 20 times the specific surface area S1 of the metal powder.
- the metal paste and the ceramic paste are kneaded with a three-roll mill or the like so that the content of the ceramic powder in the solid content (metal powder and ceramic powder) is 20 to 50 wt%. Thereby, a conductive paste is produced.
- the ceramic powder can be effectively diffused to the ceramic green sheet side.
- the content of the ceramic powder was set to 20 to 50% by weight because when the content of the ceramic powder was less than 3 ⁇ 40% by weight, the diameter of the non-conductive part in the internal electrode layer was increased and the coverage was increased. It becomes difficult to secure a coverage of 60% or more. On the other hand, if the content exceeds 50% by weight, the ceramic powder that has not diffused into the ceramic layer 1 forms the ceramic portion 6a, resulting in an excessively high bonding strength, which may lead to a decrease in displacement. It is.
- the ceramic powder contained in the conductive paste uses a ceramic raw material having at least a main component having the same composition as the ceramic material forming the ceramic green sheet.
- Force S the main components do not necessarily have the same composition.
- the ceramic powder contained in the conductive paste diffuses to the ceramic layer side during firing, at least the main component is the same composition as the ceramic material forming the ceramic green sheet from the viewpoint of preventing characteristic fluctuations. It is more preferable to use a ceramic raw material having components.
- a piezoelectric ceramic body 3 in which ceramic layers 1 and internal electrode layers 2 are alternately laminated is formed by firing at a predetermined temperature (for example, 950 to 1100 ° C) in an oxygen concentration atmosphere of ⁇ 15% by volume. To do.
- the reason why the firing atmosphere is the low oxygen atmosphere is as follows.
- the oxygen concentration was set to 0.1 to 15% by volume.
- the coverage ratio tends to decrease, and the control of the void 6b is difficult.
- the oxygen concentration exceeds 15% by volume, the firing atmosphere becomes close to the atmosphere, and the void 6b is easily blocked by sintering, so that the desired internal electrode layer 2 described above is formed. This is because the displacement cannot be improved, and the joint strength cannot be improved.
- the same conductive paste for external electrodes made of Ag or the like is applied to a predetermined region of the end face of the piezoelectric ceramic body 3, and a baking process is performed at a predetermined temperature (for example, 750 ° C to 850 ° C). Then, the external electrodes 4a and 4b are formed, and further subjected to a predetermined polarization process, whereby a laminated piezoelectric actuator is manufactured.
- the external electrodes 4a and 4b may be formed by a thin film forming method such as a sputtering method or a vacuum evaporation method as long as the adhesion is good.
- the ceramic powder having a specific surface area S 2 that is 5 to 20 times the specific surface area S1 of the metal powder is contained in an amount of 20 to 50% by weight based on the solid content (metal powder and ceramic powder).
- the internal electrode layer 2 is formed in a state where the non-conductive portion 6 is scattered in the conductive portion 5 and the average diameter X of the non-conductive portion 6 and the thickness of the ceramic layer 2 because the firing process is performed in the atmosphere.
- the ratio X / y to y is 0.08 to 0.33, the coverage of the internal electrode layer 2 is 60 to 95%, and the thickness z of the internal electrode layer 2 and the thickness y of the ceramic layer 1 are The ratio z / y is 0.04 to 0.40, and the internal electrode layer is formed so that the gap 6b occupies 60% or more in the non-conductive part 6.
- a metal paste and a ceramic paste are kneaded to produce a conductive paste. After mixing a predetermined amount of the metal powder and the ceramic co-material, the mixture is kneaded with the organic vehicle. Make a conductive paste.
- the multilayer piezoelectric actuator is described as an example of the multilayer piezoelectric ceramic component.
- the multilayer piezoelectric actuator is suitable for multilayer piezoelectric sounding bodies and multilayer piezoelectric sensors that require high piezoelectric constants.
- the laminated structure, element shape, displacement and force direction, polarization direction, and voltage application direction are not limited to the above embodiment.
- an oxide such as Pb 2 O is used as the ceramic raw material.
- the weighed material is put into a ball mill containing a grinding medium such as Ginoleconia and mixed and ground for 24 hours. Thereafter, the obtained mixed powder was calcined at a temperature of 900 ° C. to obtain a calcined product. Then, after that, a solvent and a dispersant are added to the calcined product, and wet pulverized again with a ball mill for 24 hours, and a composition formula of 0.25Pb (Ni Nb) 0 -0. 35PbZrO _0.40PbTiO
- an ethyl cellulose resin as an organic binder and a polycarboxylate solution as a dispersant are added, and a slurry is prepared using water as a solvent.
- a slurry is prepared using water as a solvent.
- the green sheet was molded so that the thickness y of the sintered ceramic layer was 20 ⁇ m or 40 ⁇ m.
- the conductive paste for internal electrodes is screened on the ceramic green sheet while adjusting the thickness of the coating film so that the thickness z of the internal electrode layer after sintering becomes: 3 to 3 zm.
- Printed a predetermined number of these screen-printed ceramic green sheets were laminated, sandwiched between ceramic green sheets that were not screen-printed, and pressed to produce a laminate.
- these laminates are accommodated in an alumina sheath and subjected to a binder removal treatment, followed by a firing atmosphere having a firing temperature of 960 ° C to 1040 ° C and an oxygen concentration of 0.3 to 21% by volume.
- the ceramic body was cut into 3 mm length and 13 mm width and subjected to sputtering treatment using Ni-Cu as a target, and a Ni-Cu film was formed on both sides of the ceramic body from the top and bottom sides. Further, sputtering was performed using Ag as a target to form an Ag film on the Ni—Cu film, thereby forming an external electrode having a two-layer structure of the Ni—Cu film and the Ag film.
- the tensile strength X is obtained when the metal pieces are bonded to both main surfaces of the multilayer piezoelectric element, and the metal pieces are pulled with a tensile tester, and the joint surface between the ceramic layer and the internal electrode layer is peeled off. The value was determined. In this example, the bonding strength between the internal electrode layer and the ceramic layer was evaluated by the tensile strength.
- the ratio x / y and the ratio zZy were calculated by calculating the average diameter X when the internal electrode coverage and the cross-sectional area of the non-conductive portion were converted into a circle by image analysis.
- Table 1 shows the fabrication conditions of the multilayer piezoelectric elements of sample numbers 1 to 24, and Table 2 shows the measurement results.
- Sample No. 10 has a large ratio xZy of 0.41 and a large non-conductive part average diameter x of 16.5 ⁇ m, which decreases the coverage force to S45%. Therefore, the piezoelectric constant I d I is as low as 315pC / N
- sample numbers 2 to 5, 7 to 9, and 11 have a ratio x / y of 0.08 to 0.33 and a coverage force of 3 ⁇ 40 to 94%. Is as large as 338 ⁇ 362pC / N, sample number
- Tensile strength X is also 8.5 to 9.8 MPa, sample number 11 is the same as sample number 1 and tensile strength X. Sample numbers 2 to 5 and 7 to 9 are 1 against sample number 1. 2-21. It increased by 2%, and it was found that the bonding strength was improved.
- Sample Nos. 12 to 24 are cases where the thickness y of the ceramic layer is 20 / im.
- Sample No. 12 is a conventional example in which the ceramic electrode material is not contained in the internal electrode layer and the firing treatment is performed in an air atmosphere having an oxygen concentration of 21 volume%.
- the displacement amount and bonding strength of each sample number can be evaluated.
- Sample No. 17 has a large ratio x / y of 0.65, and the average diameter x of the non-conductive portion is 13.
- the piezoelectric constant I d I is as low as 313pCZN, and the tensile strength X is 8.4MPa.
- the bonding strength is lowered by 4.5%. This is because the ratio of the specific surface area S2 of the ceramic co-material to the specific surface area S1 of the metal powder is small, and the average particle size of the ceramic co-material is large. As a result, the diameter of the non-conductive part of the internal electrode layer was enlarged as described above, and the coverage was lowered, leading to deterioration of various characteristics.
- Sample No. 20 has a large ratio xZy of 0.73 and a large non-conductive part average diameter x of 14.7 ⁇ m. As a result, the coverage ratio decreased to 48%, which caused the piezoelectric constant I d I to be as low as 309 pC / N.
- Sample No. 23 has a large ratio xZy of 0.85 and a large non-conductive part average diameter x of 17.0 ⁇ m, which reduces the coverage to 41%. I force 3 ⁇ 495pC / N and low
- Sample number 12 increased by 2.9 ⁇ : 13.3%, indicating that the displacement was improved.
- Tensile strength X is 8.8-10.8MPa.
- Sample No. 24 has the same tensile strength X as Sample No. 12, but Sample Nos. 13-: 16, 18, 19, 21, and 22 The sample number 12 increased 1.:! ⁇ 22.7%, indicating that the bonding strength was improved.
- the increase rate of the piezoelectric constant is within the range of coverage of 60 to 90%.
- ⁇ I d I is greatly increased to 5.8-13.3%, and the coverage is reduced in the range of 75 to 95%.
- Fig. 3 is an SEM image of Sample No. 19 (Example of the present invention), and the non-conductive portion appears black.
- Figure 4 shows the SEM image of sample number 12 (conventional example).
- the ceramic layer is completely covered with the internal electrode layer, whereas in the embodiment of the present invention shown in FIG. 3, the non-conductive portion is exposed and distributed uniformly. Therefore, the structure of the internal electrode (coverage and average diameter X of the non-conductive part) was obtained by using a conductive paste containing ceramic co-material and firing it in a low oxygen concentration atmosphere. It was found that can be controlled.
- Ag / Pd weight ratio Ag / Pd is blended to 7/3 or 8/2, and ceramic co-material is blended so as to be 0% by weight or 30% by weight based on the total solid content. Except that, [Example 1] and A conductive paste for internal electrodes was produced by the same method 'procedure.
- the conductive paste for internal electrodes was screen-printed on the ceramic green sheet so that the thickness z of the sintered internal electrode layer was 2.4 ⁇ ⁇ ⁇ ⁇ ⁇ , and then [Example 1 ]
- a layered product was produced by the same method and procedure. Next, these laminates are accommodated in alumina pods and subjected to binder removal treatment, and then the firing temperature is 1000 ° C or 1040 ° C and the oxygen concentration is 0.5% by volume or 21% by volume.
- a ceramic body having a ceramic layer thickness y of 6 to 100 xm and a total thickness of 0.:! To 0.6 mm is obtained.
- the laminated piezoelectric elements of sample numbers 31 to 41 were produced.
- Table 3 shows the fabrication conditions of the multilayer piezoelectric elements of sample numbers 31 to 41, and Table 4 shows the measurement results.
- sample numbers 31, 33, 35, 37 and 39 marked with * are different when the thickness y of the ceramic layer is in the range of 6 to 100 ⁇ m.
- This is a metal powder containing 7/3 of Ag / Pd that does not contain ceramic co-material, and is fired at a temperature of 1040 ° C in an air atmosphere (oxygen concentration: 21% by volume). Show.
- Sample numbers 32, 34, 36, 38 and 40 are examples of the present invention corresponding to the above-described conventional example, and the internal electrode layer contains 30% by weight of ceramic co-material, and the metal powder is made of Ag. It shows the case where it is blended so that / Pd is 8/2 and calcined at a temperature of 1 000 ° C in a low oxygen concentration atmosphere with an oxygen concentration of 0.5 vol%.
- the example of the present invention contains 30% by weight of the ceramic co-material in the internal electrode layer, and the oxygen concentration is 0. Since it is fired in an atmosphere with a low oxygen concentration of 5% by volume, the ratio xZy is 0.08 to 0.33 and the coverage is reduced to 80 to 94%.
- Piezoelectric constant I d I is 0.9-8
- Sample No. 41 contains 30% by weight of ceramic co-material in the internal electrode layer and is fired in a low oxygen concentration atmosphere with an oxygen concentration of 0.5% by volume. Is 0.38 and exceeds 0.33. Therefore, even if the coverage is as large as 97%, the average diameter X of the non-conductive portion is large, and the potential drop due to the non-conductive portion is large. Piezoelectric constant I d I is 2
- Ag / Pd weight ratio Ag / Pd is blended to 7/3 or 9/1, and ceramic co-material is blended so as to be 0% by weight or 40% by weight based on the total solid content.
- a conductive paste for internal electrodes was prepared in the same manner as in [Example 1] except for the above.
- Example 1 the internal electrode conductive paste was screen-printed on the ceramic green sheet so that the thickness z of the internal electrode layer after sintering was 2 / im or 3 ⁇ , and then [actual A laminate was produced by the same method and procedure as in Example 1. Next, these laminates are accommodated in an alumina sheath and subjected to binder removal treatment, and then the firing temperature is 960 ° C or 1040 ° C and the oxygen concentration is 0.5% by volume or 21% by volume. A ceramic body having a thickness y of 20 xm and a total thickness of 0.:! To 0.6 mm was produced by firing treatment in a firing atmosphere for 8 hours. After that, [Example 1] and The same method ⁇ Procedures were used to produce laminated piezoelectric elements of sample numbers 5:! -60.
- Table 5 shows the fabrication conditions of multilayer piezoelectric elements of sample numbers 5:! -60, and Table 6 shows the measurement results.
- Sample numbers 51, 53, 55, 57 and 59 marked with * in Tables 5 and 6 have different driving electric fields in the range of:! To 1 000 V / mm. This is a metal powder containing 7/3 of Ag / Pd that does not contain bismuth and is fired at 1040 ° C in an air atmosphere (oxygen concentration: 21% by volume). Yes.
- Sample numbers 52, 54, 56, 58 and 60 are examples of the present invention corresponding to the above-described conventional example, the internal electrode layer contains 40% by weight of ceramic co-material, and the metal powder is This shows a case where Ag / Pd is blended in 9/1 and calcined at a temperature of 960 ° C in a low oxygen concentration atmosphere with an oxygen concentration of 0.5% by volume.
- the example of the present invention contains 40% by weight of the ceramic co-material in the internal electrode layer, and the oxygen concentration is 0. Since the firing is performed in an atmosphere with a low oxygen concentration of 5% by volume, the ratio xZy is 0.30 and the coverage is reduced to 82%.
- the piezoelectric constant I d I is 2 for each conventional example. 9-10. 7% increase
- the coercive electric field of the ceramic layer used in this example is 1000 V / mm.
- increased significantly from 5.0 to 10.7%.
- the weight ratio of Ag to Pd Ag / Pd is blended to 7/3 or 8/2, and the ceramic co-material is blended so as to be 0% by weight or 25% by weight based on the total solid content.
- a conductive paste for internal electrodes was prepared in the same manner as in [Example 1] except for the above.
- the conductive paste for internal electrodes was screen-printed on the ceramic green sheet so that the thickness z of the internal electrode layer after sintering was 2.4 ⁇ , and then [Example 1 ]
- a layered product was produced by the same method and procedure.
- these laminates are accommodated in an alumina cocoon and subjected to a binder removal treatment.
- the firing temperature is 1040 ° C and the oxygen concentration is 0.1 to 21% by volume in a firing atmosphere for 8 hours.
- a ceramic body having a thickness y of 20 xm and a total thickness of 0.:! To 0.6 mm was prepared by firing treatment, and then the same method and procedure as in [Example 1]
- multilayer piezoelectric elements of sample numbers 61 to 67 were produced.
- the tensile strength X and the increase rate ⁇ ⁇ are obtained from the increase rate ⁇
- Table 7 shows the fabrication conditions of the laminated piezoelectric elements of sample numbers 61 to 67, and Table 8 shows the measurement results.
- the sample number 61 marked with * is made of metal powder in which the internal electrode layer does not contain ceramic co-material and Ag / Pd is mixed in 7/3, and the atmosphere (oxygen) Concentration: 2 1% by volume), and is fired at a temperature of 1040 ° C., showing a conventional example.
- Sample Nos. 62 to 67 contain 25% by weight of the ceramic co-material in the internal electrode layer and fired in a low oxygen concentration atmosphere with an oxygen concentration of 0.5 to 15% by volume. Therefore, the ratio X / y is 0.18-0.27, the coverage is reduced to 79-94%, and the porosity of the non-conductive part is also 62-95%, resulting in excessive formation of the ceramic part. As a result, the piezoelectric constant I d is 2.5 compared to the conventional example.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- General Electrical Machinery Utilizing Piezoelectricity, Electrostriction Or Magnetostriction (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006522157A JP4565349B2 (ja) | 2004-12-24 | 2005-12-22 | 積層型圧電セラミック部品の製造方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-372671 | 2004-12-24 | ||
JP2004372671 | 2004-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006068245A1 true WO2006068245A1 (ja) | 2006-06-29 |
Family
ID=36601842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/023666 WO2006068245A1 (ja) | 2004-12-24 | 2005-12-22 | 積層型圧電セラミック部品、及び積層型圧電セラミック部品の製造方法 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP4565349B2 (ja) |
WO (1) | WO2006068245A1 (ja) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010103301A (ja) * | 2008-10-23 | 2010-05-06 | Ngk Insulators Ltd | 圧電素子の製造方法及び圧電素子 |
JP2011091151A (ja) * | 2009-10-21 | 2011-05-06 | Taiheiyo Cement Corp | 電子部品の製造方法および電子部品 |
JP2011134943A (ja) * | 2009-12-25 | 2011-07-07 | Taiheiyo Cement Corp | 電子部品の内部電極の製造方法 |
JP2015082636A (ja) * | 2013-10-24 | 2015-04-27 | 京セラ株式会社 | 積層型電子部品 |
JP2017183541A (ja) * | 2016-03-30 | 2017-10-05 | 日本碍子株式会社 | 圧電素子 |
WO2019167805A1 (ja) * | 2018-03-02 | 2019-09-06 | Tdk株式会社 | 振動デバイス及び圧電素子 |
JP2021022723A (ja) * | 2019-07-29 | 2021-02-18 | サムソン エレクトロ−メカニックス カンパニーリミテッド. | 積層型電子部品 |
WO2021125097A1 (ja) * | 2019-12-16 | 2021-06-24 | Tdk株式会社 | 積層圧電素子 |
US20220406528A1 (en) * | 2021-06-16 | 2022-12-22 | Murata Manufacturing Co., Ltd. | Multilayer ceramic electronic component |
WO2023063007A1 (ja) * | 2021-10-12 | 2023-04-20 | 太陽誘電株式会社 | 積層型圧電素子 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001035747A (ja) * | 1999-07-21 | 2001-02-09 | Taiyo Yuden Co Ltd | 積層セラミックコンデンサ |
JP2001250994A (ja) * | 2000-03-03 | 2001-09-14 | Tdk Corp | 積層型圧電素子 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003115416A (ja) * | 2001-10-05 | 2003-04-18 | Murata Mfg Co Ltd | 導電性ペースト、積層セラミック電子部品の製造方法および積層セラミック電子部品 |
JP2004111939A (ja) * | 2002-08-29 | 2004-04-08 | Ngk Insulators Ltd | 積層型圧電素子及びその製造方法 |
JP4989019B2 (ja) * | 2003-04-28 | 2012-08-01 | 京セラ株式会社 | セラミックス基板、圧電アクチュエータ基板、圧電アクチュエータおよびこれらの製造方法 |
-
2005
- 2005-12-22 WO PCT/JP2005/023666 patent/WO2006068245A1/ja active Application Filing
- 2005-12-22 JP JP2006522157A patent/JP4565349B2/ja active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001035747A (ja) * | 1999-07-21 | 2001-02-09 | Taiyo Yuden Co Ltd | 積層セラミックコンデンサ |
JP2001250994A (ja) * | 2000-03-03 | 2001-09-14 | Tdk Corp | 積層型圧電素子 |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010103301A (ja) * | 2008-10-23 | 2010-05-06 | Ngk Insulators Ltd | 圧電素子の製造方法及び圧電素子 |
JP2011091151A (ja) * | 2009-10-21 | 2011-05-06 | Taiheiyo Cement Corp | 電子部品の製造方法および電子部品 |
JP2011134943A (ja) * | 2009-12-25 | 2011-07-07 | Taiheiyo Cement Corp | 電子部品の内部電極の製造方法 |
JP2015082636A (ja) * | 2013-10-24 | 2015-04-27 | 京セラ株式会社 | 積層型電子部品 |
JP2017183541A (ja) * | 2016-03-30 | 2017-10-05 | 日本碍子株式会社 | 圧電素子 |
JP7003741B2 (ja) | 2018-03-02 | 2022-01-21 | Tdk株式会社 | 振動デバイス及び圧電素子 |
WO2019167805A1 (ja) * | 2018-03-02 | 2019-09-06 | Tdk株式会社 | 振動デバイス及び圧電素子 |
JP2019150762A (ja) * | 2018-03-02 | 2019-09-12 | Tdk株式会社 | 振動デバイス及び圧電素子 |
CN111770797A (zh) * | 2018-03-02 | 2020-10-13 | Tdk株式会社 | 振动器件及压电元件 |
US11944999B2 (en) | 2018-03-02 | 2024-04-02 | Tdk Corporation | Vibration device and piezoelectric element |
CN111770797B (zh) * | 2018-03-02 | 2022-06-14 | Tdk株式会社 | 振动器件及压电元件 |
US11450481B2 (en) | 2019-07-29 | 2022-09-20 | Samsung Electro-Mechanics Co., Ltd. | Multilayer electronic component |
JP2021168413A (ja) * | 2019-07-29 | 2021-10-21 | サムソン エレクトロ−メカニックス カンパニーリミテッド. | 積層型電子部品 |
US11037727B2 (en) | 2019-07-29 | 2021-06-15 | Samsung Electro-Mechanics Co., Ltd. | Multilayer electronic component |
US11682521B2 (en) | 2019-07-29 | 2023-06-20 | Samsung Electro-Mechanics Co., Ltd. | Multilayer electronic component |
JP2021022723A (ja) * | 2019-07-29 | 2021-02-18 | サムソン エレクトロ−メカニックス カンパニーリミテッド. | 積層型電子部品 |
US12009150B2 (en) | 2019-07-29 | 2024-06-11 | Samsung Electro-Mechanics Co., Ltd. | Multilayer electronic component |
JP2021097105A (ja) * | 2019-12-16 | 2021-06-24 | Tdk株式会社 | 積層圧電素子 |
WO2021125097A1 (ja) * | 2019-12-16 | 2021-06-24 | Tdk株式会社 | 積層圧電素子 |
US20220406528A1 (en) * | 2021-06-16 | 2022-12-22 | Murata Manufacturing Co., Ltd. | Multilayer ceramic electronic component |
US12119182B2 (en) * | 2021-06-16 | 2024-10-15 | Murata Manufacturing Co., Ltd. | Multilayer ceramic electronic component including internal conductive layer including a plurality of holes |
WO2023063007A1 (ja) * | 2021-10-12 | 2023-04-20 | 太陽誘電株式会社 | 積層型圧電素子 |
Also Published As
Publication number | Publication date |
---|---|
JP4565349B2 (ja) | 2010-10-20 |
JPWO2006068245A1 (ja) | 2008-06-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2006068245A1 (ja) | 積層型圧電セラミック部品、及び積層型圧電セラミック部品の製造方法 | |
JP4945801B2 (ja) | 圧電素子、及び圧電素子の製造方法 | |
KR100553226B1 (ko) | 적층형 압전 부품의 제조방법 및 적층형 압전 부품 | |
JP4129931B2 (ja) | 圧電磁器組成物および積層型圧電素子 | |
JP2006188414A (ja) | 圧電磁器組成物、及び圧電セラミック電子部品 | |
JPH03181186A (ja) | 積層圧電アクチュエータ及びその製法 | |
JP4238271B2 (ja) | 圧電磁器組成物および積層型圧電素子 | |
US20070080317A1 (en) | Piezoelectric ceramic composition and laminated piezoelectric element | |
JP4930410B2 (ja) | 積層型圧電素子 | |
US20020149297A1 (en) | Piezoelectric element | |
TW201923797A (zh) | 積層陶瓷電容器及其製造方法 | |
US9598319B2 (en) | Piezoceramic multi-layer element | |
EP1717873B1 (en) | Multilayered piezoelectric element | |
JP2007103676A (ja) | 圧電磁器組成物、積層型圧電素子及びその製造方法 | |
JP2002260950A (ja) | 積層型誘電素子の製造方法,並びに電極用ペースト材料 | |
JPH10335168A (ja) | 積層セラミックコンデンサ | |
JP2007258301A (ja) | 積層型圧電素子及びその製造方法 | |
JP4485140B2 (ja) | 圧電アクチュエータおよびその製造方法 | |
US8758536B2 (en) | Method for manufacturing ceramic plates | |
KR100492813B1 (ko) | 적층형 압전 세라믹 소자의 제조방법 | |
JP2007230839A (ja) | 圧電磁器組成物、積層型圧電素子及びその製造方法 | |
JP3971779B1 (ja) | 圧電磁器組成物 | |
JP5303823B2 (ja) | 圧電素子 | |
JP5196124B2 (ja) | 圧電磁器組成物および積層型圧電素子 | |
JP4736585B2 (ja) | 圧電磁器組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KN KP KR KZ LC LK LR LS LT LU LV LY MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006522157 Country of ref document: JP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 05819722 Country of ref document: EP Kind code of ref document: A1 |