WO2002027809A1 - Element a pellicule dielectrique mince, actionneur comprenant cet element, tete a jet d'encre et enregistreur a jet d'encre - Google Patents
Element a pellicule dielectrique mince, actionneur comprenant cet element, tete a jet d'encre et enregistreur a jet d'encre Download PDFInfo
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- WO2002027809A1 WO2002027809A1 PCT/JP2001/008402 JP0108402W WO0227809A1 WO 2002027809 A1 WO2002027809 A1 WO 2002027809A1 JP 0108402 W JP0108402 W JP 0108402W WO 0227809 A1 WO0227809 A1 WO 0227809A1
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- Prior art keywords
- dielectric thin
- thin film
- substrate
- electrode
- thermal expansion
- Prior art date
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- 239000010409 thin film Substances 0.000 title claims abstract description 207
- 239000000758 substrate Substances 0.000 claims abstract description 152
- 239000013078 crystal Substances 0.000 claims abstract description 54
- 239000000463 material Substances 0.000 claims abstract description 52
- 239000010408 film Substances 0.000 claims description 79
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 49
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 21
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 16
- 235000002639 sodium chloride Nutrition 0.000 claims description 16
- 239000011780 sodium chloride Substances 0.000 claims description 16
- 229910052697 platinum Inorganic materials 0.000 claims description 14
- 239000000395 magnesium oxide Substances 0.000 claims description 13
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 13
- 229910000480 nickel oxide Inorganic materials 0.000 claims description 13
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims description 13
- 239000010931 gold Substances 0.000 claims description 12
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims description 12
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 claims description 9
- HTXDPTMKBJXEOW-UHFFFAOYSA-N dioxoiridium Chemical compound O=[Ir]=O HTXDPTMKBJXEOW-UHFFFAOYSA-N 0.000 claims description 6
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052737 gold Inorganic materials 0.000 claims description 6
- 229910000457 iridium oxide Inorganic materials 0.000 claims description 6
- 229910052763 palladium Inorganic materials 0.000 claims description 6
- 229910000428 cobalt oxide Inorganic materials 0.000 claims description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- 239000007772 electrode material Substances 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 2
- 238000006073 displacement reaction Methods 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 32
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 30
- 238000004544 sputter deposition Methods 0.000 description 21
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 15
- 239000011651 chromium Substances 0.000 description 12
- 229910052786 argon Inorganic materials 0.000 description 9
- 238000010586 diagram Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 6
- 238000000206 photolithography Methods 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 229910052741 iridium Inorganic materials 0.000 description 5
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 229910001120 nichrome Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 238000002441 X-ray diffraction Methods 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000001755 magnetron sputter deposition Methods 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 4
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 4
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 239000003989 dielectric material Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000010287 polarization Effects 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000002269 spontaneous effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- -1 and at the same time Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 229910000464 lead oxide Inorganic materials 0.000 description 2
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 2
- 239000012495 reaction gas Substances 0.000 description 2
- 239000011029 spinel Substances 0.000 description 2
- 229910052596 spinel Inorganic materials 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- UAMZXLIURMNTHD-UHFFFAOYSA-N dialuminum;magnesium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Mg+2].[Al+3].[Al+3] UAMZXLIURMNTHD-UHFFFAOYSA-N 0.000 description 1
- 238000003331 infrared imaging Methods 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- AKTIAGQCYPCKFX-FDGPNNRMSA-L magnesium;(z)-4-oxopent-2-en-2-olate Chemical compound [Mg+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O AKTIAGQCYPCKFX-FDGPNNRMSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005459 micromachining Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 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
- H10N30/85—Piezoelectric or electrostrictive active materials
- H10N30/853—Ceramic compositions
- H10N30/8548—Lead-based oxides
- H10N30/8554—Lead-zirconium titanate [PZT] based
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B12/00—Dynamic random access memory [DRAM] devices
-
- 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
-
- 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
- H10N30/07—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base
- H10N30/074—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing
- H10N30/076—Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing by vapour phase deposition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2202/00—Embodiments of or processes related to ink-jet or thermal heads
- B41J2202/01—Embodiments of or processes related to ink-jet heads
- B41J2202/03—Specific materials used
-
- 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
- the present invention relates to a dielectric thin film element used for a piezoelectric element, a pyroelectric infrared detecting element, a nonvolatile memory, an electro-optical effect element, and the like, and an actuary using a piezoelectric effect of a piezoelectric dielectric.
- the present invention relates to an ink jet head and an ink jet type recording apparatus provided with the ink jet head. Background art
- Dielectrics have been applied to various elements in the electronics field, such as piezoelectric elements, infrared sensors, light modulation elements, and memory elements. With the development of micromachining technology and the demand for miniaturization and weight reduction of various devices, various thin film devices using these dielectric materials are being put to practical use by thinning technology and fine processing technology.
- FIG. 15 shows an example of the configuration of a conventional dielectric thin film element (see I. Kanno et.al: Appl. Pys. Let. 70 (1997) pi 378-1380).
- this dielectric thin-film element is composed of a lower electrode film 9 2 made of platinum (Pt) as a first electrode on a single crystal substrate 91 made of magnesium oxide (Mg ⁇ ).
- Pt platinum
- Mg ⁇ magnesium oxide
- P b (Z r, T i) ⁇ 3 lead zirconate titanate
- piezoelectric dielectric thin film 9 3 consisting of platinum as the second electrode
- the dielectric thin film element is formed by processing a single crystal substrate 91 or the like. For example, it is applied to factories, pressure sensors, acceleration sensors, etc.
- crystal parameters such as the crystal plane and lattice constant of a dielectric thin film are greatly affected by the substrate used to form it.
- ferroelectric and is lead titanate P b T i 0 3
- the crystal orientation (1 0 0) plane is made of magnesium oxide cut to leave the surface (M G_ ⁇ ) single crystal substrate in (0 0 1) plane orientation
- c plane ((0 0 0 1) face) Sahu Aia (A 1 2 0 3) is on the substrate are reported to orientation (1 1 1) plane I have.
- This lead titanate (P b T i 0 3) is, because it greatly affected by the crystal plane of the substrate being formed.
- the substrate used to form the dielectric thin film is a single crystal substrate
- a large difference in lattice constant between the substrate and the dielectric thin film affects the crystal plane to be oriented.
- the difference in the thermal expansion coefficient of the substrate changes the internal stress of the formed dielectric thin film, and as a result, the crystal constant such as the lattice constant Parame changes overnight.
- the magnitude of the change in the film properties of the dielectric thin film obtained by the conventional configuration as shown in FIG. 15 is smaller than when the thermal expansion coefficient of the substrate is largely changed.
- the substrate used to form the dielectric thin film is a single crystal substrate
- the crystal orientation plane of the dielectric thin film greatly depends on the substrate, and the plane orientation is changed. Since it is difficult to arbitrarily control the orientation, it is also difficult to greatly change the film characteristics.
- the coefficient of thermal expansion of the dielectric thin film to be formed is significantly different from the coefficient of thermal expansion of the substrate supporting it, a large compressive or tensile stress is applied to the formed dielectric thin film. Therefore, the dielectric thin film element is warped such that it is convex upward or convex downward (see Fig. 9). For this reason, when an element is formed over a large area, the workability and operability of the element pattern forming step by fine processing using photolithography, the bonding step after processing, or the cutting step are deteriorated.
- the present invention has been made in order to solve the above-mentioned problems in the prior art, and has a dielectric thin-film element having optimal film characteristics, and a device using the same, an inkjet head, an inkjet head, and an inkjet recording device.
- the purpose is to provide a good production yield.
- a first configuration of a dielectric thin film element according to the present invention includes a substrate, a first electrode formed on the substrate, and a dielectric formed on the first electrode.
- a dielectric thin film element comprising: a thin film; and a second electrode formed on the dielectric thin film, wherein the dielectric thin film element is manufactured in a state where the substrate is heated, and has a predetermined coefficient of thermal expansion as a material of the substrate. A material is used, and the crystal orientation of the dielectric thin film is controlled by a coefficient of thermal expansion of the substrate.
- the first configuration of the dielectric thin film element various characteristics such as electric characteristics are optimized by using a material having an optimum thermal expansion coefficient as a substrate material for supporting the dielectric thin film. It is possible to realize a thin dielectric thin film element.
- an intermediate layer is interposed between the substrate and the first electrode. According to this preferred example, by arranging the intermediate layer having a predetermined plane orientation regardless of the type of the substrate, it is possible to obtain a dielectric thin film having an optimal crystal orientation reflecting the plane orientation of the intermediate layer. As a result, it becomes possible to realize a dielectric thin film element in which various characteristics such as electric characteristics are further optimized.
- the rock-salt crystal structure oxide film further has (100) plane orientation, (111) It is preferable that the compound has a plane orientation or (110) plane orientation.
- the rock-salt-type crystal structure oxide film further includes at least one selected from magnesium oxide (Mg ⁇ ), nickel oxide (Ni0), cobalt oxide (Co ⁇ ), and manganese oxide (M ⁇ ). It is preferable that the film is composed of one film. In this case, it is preferable to use a spinel-type crystal structure oxide film as the intermediate layer.
- platinum (Pt), palladium (Pd), iridium (Ir), gold (Au), iridium oxide (I R_ ⁇ 2), ruthenium oxide (Ru_ ⁇ 2) ⁇ beauty conductive nickel oxide (N I_ ⁇ ) preferably at least one is found using selected from.
- a second configuration of the dielectric thin film element includes: a substrate; a first electrode formed on the substrate; a dielectric thin film formed on the first electrode; A second electrode formed on a dielectric thin film, wherein the dielectric thin film element is manufactured in a state where the substrate is heated, wherein a coefficient of thermal expansion of the dielectric thin film material is af; When the thermal expansion coefficient is as, the relationship of 0.8 ⁇ Q! F / Q; s ⁇ l.2 is satisfied.
- the amount of warpage generated in the entire element can be neglected.
- workability and operability can be improved in a device pattern forming step by fine processing using photolithography, a bonding step after processing, or a dicing cutting step.
- the thickness of the dielectric thin film is tf
- the thickness of the substrate is ts
- 0.2 m ⁇ tf ⁇ 10 xm it is preferable that the relationship of 0.15 mm ⁇ ts ⁇ l.5 mm is satisfied.
- the amount of warpage occurring in the entire element can be further neglected, and as a result, the workability and operability can be further improved.
- the dielectric thin film material is a piezoelectric dielectric thin film material and a relationship of ai / as> l is satisfied. According to this preferred example, it is possible to realize a dielectric thin film element having better piezoelectric characteristics.
- the dielectric thin film material is a pyroelectric dielectric thin film material, and the relationship of f Zo; s ⁇ l is satisfied. Is preferred. According to this preferred example, it is possible to realize a dielectric thin film element having better pyroelectric performance.
- the dielectric thin film material contains at least lead (Pb) and titanium (Ti) as constituent components.
- an intermediate layer is interposed between the substrate and the first electrode.
- a rock salt type crystal structure oxide film as the intermediate layer.
- the rock salt type crystal structure oxide film has a (100) plane orientation, a (111) plane orientation, or a (110) plane orientation.
- the rock salt type crystal structure oxide film is made of magnesium oxide (Mg ⁇ ), nickel oxide (Ni ⁇ ), cobalt oxide (Co ⁇ ), and manganese oxide (Mn ⁇ ) are preferable. It is preferable to use a spinel crystal structure oxide film as the layer.
- the structure of the present invention according to the present invention is characterized in that the piezoelectric dielectric thin film element of the present invention is used.
- an actuator In the configuration of the ink jet head according to the present invention, an actuator, a diaphragm on which the actuator is fixed, and an ink liquid are contained, and the displacement of the actuator acts via the diaphragm.
- An ink jet head comprising a plurality of pressure chambers, wherein the actuating unit according to the present invention is used as the actuating unit.
- the configuration of the ink jet recording apparatus according to the present invention is an ink jet recording apparatus comprising: an ink jet head; and a recording medium transport means for transporting a recording medium in a direction substantially perpendicular to a width direction of the ink jet head. Further, the inkjet head of the present invention is used as the inkjet head.
- the material of the pressure chamber component formed by processing the substrate while considering the thermal expansion coefficient it is possible to control the performance of the dielectric thin film element that constitutes the actuator. .
- the thermal expansion coefficient of the material (dielectric thin film material) constituting the actuator is af
- the thermal expansion coefficient of the material of the pressure chamber component is s
- the relationship of 0. Saf ZQi sl is 0.
- FIG. 1 is a cross-sectional view showing a dielectric thin film element according to a first embodiment of the present invention
- FIG. 2 is a diagram showing an X-ray diffraction pattern of the dielectric thin film according to the first embodiment of the present invention.
- FIG. 3 shows the relationship between the coefficient of thermal expansion of the substrate and the diffraction angle 2 ° of the (11 1) plane of the dielectric thin film formed on the substrate in the dielectric thin film element according to the first embodiment of the present invention.
- FIG. 4 shows the relationship between the coefficient of thermal expansion of the substrate and the relative dielectric constant of the (111) plane-oriented dielectric thin film formed on the substrate in the dielectric thin film element according to the first embodiment of the present invention.
- FIG. 5 is a cross-sectional view showing a dielectric thin film element according to a second embodiment of the present invention.
- FIG. 6 is a diagram showing an X-ray diffraction pattern of a dielectric thin film according to the second embodiment of the present invention.
- FIG. 7 shows the relationship between the coefficient of thermal expansion of the substrate and the diffraction angle 2 ° on the (002) plane of the dielectric thin film formed on the substrate in the dielectric thin film element according to the second embodiment of the present invention.
- FIG. 8 shows the coefficient of thermal expansion of the substrate and the dielectric thin film oriented on the (01) or (100) plane formed on the substrate of the dielectric thin film element according to the second embodiment of the present invention.
- FIG. 9 shows the difference in the thermal expansion coefficient of the dielectric thin film material according to the embodiment of the present invention.
- FIG. 3 is a schematic diagram showing a mechanism of a change in crystal parameters due to a change in temperature and a state of warpage of a dielectric thin film element.
- FIG. 10 shows the relationship between the coefficient of thermal expansion of the substrate and the relative permittivity of the pyroelectric thin film (PLT dielectric thin film) formed on the substrate in the dielectric thin film element according to the third embodiment of the present invention. Diagram showing the relationship,
- FIG. 11 shows the thermal expansion coefficient of the substrate and the pyroelectric coefficient a of the pyroelectric dielectric thin film (PLT dielectric thin film) formed on the substrate in the dielectric thin film element according to the third embodiment of the present invention.
- FIG. 12 is a schematic perspective view showing the overall configuration of an ink jet recording apparatus according to a fourth embodiment of the present invention.
- FIG. 13 is a schematic perspective view showing the overall configuration of an ink jet head according to a fourth embodiment of the present invention.
- FIG. 14 is an exploded perspective view, partially broken away, showing a configuration of a main part of an ink jet head according to a fourth embodiment of the present invention.
- FIG. 15 is a sectional view showing a conventional dielectric thin film element. BEST MODE FOR CARRYING OUT THE INVENTION
- FIG. 1 is a sectional view showing a dielectric thin film element according to a first embodiment of the present invention.
- reference numeral 10 denotes a dielectric thin film element.
- the dielectric thin film element 10 is composed of a lower electrode film made of platinum (Pt) as a first electrode 12 and a lead zirconate titanate (Pt) as a dielectric thin film 13 on a substrate 11. .. b Z r 0 5 3 T i 0 4 7 0 3) ( hereinafter, referred to as "PZT") films (thermal expansion coefficient: about 6 0 X 1 0 - 7 / ⁇ ) and the second electrode 1 4 Top made of chromium (Cr) as It has a structure in which electrode films are sequentially formed.
- the substrate 11 various substrates having different thermal expansion coefficients as shown in the following (Table 1) are used.
- the dielectric thin film element 10 was manufactured as follows.
- a quartz substrate is placed as a substrate 11 in a vacuum chamber, and after evacuation, the substrate 11 is heated and maintained at a temperature of 600 ° C., and a 4-inch Pt target is used. Then, a 250 nm-thick lower electrode film (Pt electrode film) made of platinum (Pt) was formed as the first electrode 12 on the substrate 11 by the RF magnetron sputtering method.
- argon (Ar) was used as a sputtering gas, the gas pressure was maintained at 1 Pa, and high-frequency power of 100 W was applied to perform sputtering for 10 minutes.
- the substrate temperature was set to 580, and a 6-inch PZT sintered body (a 20% excess of lead oxide (PbO) was added in molar ratio) was used to obtain an RF magnetron pulse.
- a 4 zm-thick dielectric thin film (PZT dielectric thin film) 14 made of PZT was formed on the first electrode 12 by the method.
- Five Sputtering was performed for 200 minutes by applying a high-frequency power of 00 W. Then, without heating the substrate, using a 4 inch Cr target,
- An upper electrode film (Cr electrode film) of chromium (Cr) with a thickness of 10 nm was formed as a second electrode 14 on the PZT dielectric thin film 14 by the C sputtering method.
- argon (Ar) was used as a sputtering gas, the gas pressure was maintained at 0.7 Pa, 100 W of electric power was applied, and sputtering was performed for 5 minutes.
- FIG. 2 shows an X-ray diffraction pattern of the PZT dielectric thin film 14 formed on the quartz substrate via the Pt electrode film (first electrode 12). This was evaluated before forming the second electrode 14. As shown in FIG. 2, as the Pt electrode film as the first electrode 12 is oriented in the (1 1 1) plane, the PZT dielectric thin film 14 also exhibits the (1 1 1) plane orientation. Was understood. In addition, the diffraction angle 26 »indicating the peak of the (111) plane of the PZT dielectric thin film 14 was 38.12 °.
- the crystal orientation of the PZT dielectric thin film 14 is mainly based on the (111) plane orientation. Become.
- a PZT dielectric thin film was formed in the same manner as described above using the various substrates having different coefficients of thermal expansion described in (Table 1) above, and the (111) surface of the formed PZT dielectric thin film was determined by the thermal expansion coefficient of the substrate.
- Table 1 the various substrates having different coefficients of thermal expansion described in (Table 1) above
- Figure 3 shows the results.
- the larger the thermal expansion coefficient of the substrate the smaller the diffraction angle on the (111) plane of the formed PZT dielectric thin film (the larger the lattice constant). This indicates that the lattice constant of the PZT dielectric thin film changes due to the difference in the thermal expansion coefficient of the substrate. This can be explained as follows using FIG.
- the coefficient of thermal expansion of the dielectric thin film material is af
- the coefficient of thermal expansion of the substrate is Then, as shown in Fig. 9 (a), if Q! F ⁇ Q! S, the substrate shrinks more than the dielectric thin film when the temperature is returned to room temperature after the film formation is completed. A compressive stress acts on the dielectric thin film under the influence of the substrate having a larger volume, and accordingly, the lattice constant in the film thickness direction becomes larger microscopically.
- Fig. 9 (b) if af> as, when the film is returned to room temperature after completion of film formation, the dielectric thin film conversely shrinks more than the substrate. A tensile stress acts on the dielectric thin film under the influence of the substrate having a small size, and accordingly, the lattice constant in the film thickness direction decreases microscopically.
- a dielectric thin-film element was manufactured by the same method as above using various substrates having different thermal expansion coefficients from the above (Table 1), and the thermal expansion coefficient of the substrate and the relative permittivity of the formed PZT dielectric thin film were measured. And examined the relationship.
- Fig. 4 shows the results. As shown in FIG. 4, the higher the thermal expansion coefficient of the substrate, the lower the relative permittivity of the formed PZT dielectric thin film.
- the thermal expansion coefficients of the substrates different, that is, by using the substrates having different thermal expansion coefficients, the crystal orientation of the formed dielectric thin film is controlled. It is possible to change film properties such as electrical properties (relative permittivity, coercive electric field, spontaneous polarization, piezoelectric constant, pyroelectric coefficient, etc.) and optical properties (refractive index, electro-optic coefficient, etc.). Therefore, by using a material with the optimum thermal expansion coefficient as the material of the substrate for supporting the dielectric thin film, it is possible to realize a dielectric thin film element in which various characteristics such as electrical characteristics are optimized. Becomes
- the dielectric thin film 13 As the first electrode 1 2 materials, platinum (P t) other than palladium (P d), iridium (I r), gold (Au), iridium oxide (I R_ ⁇ 2), ruthenium oxide (Ru_ ⁇ 2 ) Even when conductive nickel oxide (NiO) is used, or when two or more of them are used in combination, the dielectric thin film 13 Features Similar results were obtained in which the diffraction angle and relative permittivity of the crystal orientation plane could be changed without impairing the properties.
- the thermal expansion coefficient of the dielectric thin film material is af and the thermal expansion coefficient of the substrate is as, the relationship of 0.8 ⁇ a; ⁇ / as ⁇ 1.2 is satisfied.
- the amount of warpage that occurs in the entire device can be neglected.As a result, workability and operation in the device pattern forming process by micro-processing using photolithography, the bonding process after processing, or the dicing cutting process, etc. It was found that the performance could be improved.
- the thickness of the dielectric thin film is tf and the thickness of the substrate is ts
- the relation of 0.2 m ⁇ tf ⁇ 10 wm and 0.15 mm ⁇ ts ⁇ 1.5 mm is obtained. If it is satisfied, the amount of warpage generated in the entire element can be ignored, and as a result, it has been found that the workability and operability can be further improved.
- FIG. 5 is a sectional view showing a dielectric thin-film element according to a second embodiment of the present invention.
- reference numeral 50 denotes a dielectric thin film element.
- the dielectric thin film element 50 is composed of a substrate 51, a rock salt type crystal structure oxide film such as a magnesium oxide (Mg ⁇ ) film as an intermediate layer 55, and a platinum as a first electrode 52.
- the substrate 51 various substrates having different coefficients of thermal expansion as shown in the above (Table 1) are used as in the first embodiment.
- the dielectric thin film element 50 was manufactured as follows.
- a Corning 7509 glass substrate is set as the substrate 51 in a vacuum chamber, and after evacuation, the substrate 51 is heated and held at a temperature of 400 ° C., and the substrate 51 is formed by plasma MOCVD.
- an intermediate layer 55 of about 700 nm thick consisting of an MgO film with a rock salt type crystal structure with crystal orientation on the (100) plane was formed.
- magnesium acetyl acetonate (Mg (C 5 H 7 ⁇ 2 ) 2 ) vaporized at a temperature of 215 ° C. is used as the CVD source gas, and is composed of inert nitrogen (N 2 ).
- the gas was introduced into the vacuum chamber together with the carrier gas, and at the same time, oxygen ( ⁇ 2 ) gas was introduced as the reaction gas.
- the substrate 51 on which the intermediate layer 55 is formed is placed in another vacuum chamber, and after evacuation, the substrate 51 is heated and maintained at a temperature of 600 ° C., and a 4 inch Pt target A lower electrode film (Pt electrode film) of platinum (Pt) with a thickness of 250 nm was formed as the first electrode 52 on the intermediate layer 55 by the RF magnetron sputtering method.
- argon (Ar) was used as a sputtering gas, the gas pressure was maintained at 1 Pa, and high-frequency power of 100 W was applied to perform sputtering for 10 minutes.
- the substrate temperature was set to 58 Ot, and a 6-inch PZT sintered target (lead oxide (Pb ⁇ ) was added in a molar excess of 20%) was used to produce an RF mask.
- a 4 ⁇ m-thick dielectric thin film (PZT dielectric thin film) 53 made of PZT was formed on the first electrode 52 by the magnetron sputtering method.
- Sputtering was performed for 200 minutes by applying a high-frequency power of 500 W.
- the DC electrode sputtering method is used to form a second electrode 54 on the PZT dielectric thin film 53 as a second electrode 54 made of chromium (Cr).
- a nm upper electrode film (Cr electrode film) was formed.
- argon (Ar) was used as a sputtering gas, the gas pressure was maintained at 0.7 Pa, and 100 W of power was applied to perform sputtering for 5 minutes.
- Fig. 6 shows that the above-mentioned con- nection glass substrate has a (100) plane-oriented Mg ⁇ film (intermediate layer 55) and a Pt electrode film (first electrode 52).
- 7 shows an X-ray diffraction pattern of a PZT dielectric thin film 53 formed by the above method. This was evaluated before the second electrode 54 was formed.
- the Pt electrode film as the first electrode 52 is oriented in the (100) plane,? It has been found that the dielectric thin film 53 has a (01) plane orientation.
- the diffraction angles 2 ⁇ indicating the peaks of the (001) plane and the (002) plane of the PZT dielectric thin film 53 are 21.73 ° and 44.2, respectively. It was.
- the crystal orientation of the PZT dielectric thin film 53 is mainly based on the (01) plane orientation.
- a PZT dielectric thin film was formed by the same method as above using various substrates with different coefficients of thermal expansion from the above (Table 1).
- the relationship with the diffraction angle 20 on the (002) plane of the T dielectric thin film was examined.
- Figure 7 shows the results.
- the larger the thermal expansion coefficient of the substrate the smaller the diffraction angle on the (002) plane of the formed PZT dielectric thin film (the larger the lattice constant). This indicates that the lattice constant of the PZT dielectric thin film changes due to the difference in the coefficient of thermal expansion of the substrate, as in the case of the first embodiment.
- a dielectric thin film element was prepared using the various substrates having different coefficients of thermal expansion described in (Table 1) by the same method as above, and the thermal expansion coefficient of the substrate and the relative permittivity of the formed PZT dielectric thin film were determined. The relationship was investigated.
- Figure 8 shows the results. As shown in FIG. 8, as in the case of the first embodiment, the relative permittivity of the formed PZT dielectric thin film decreases as the thermal expansion coefficient of the substrate increases.
- the thermal expansion coefficients of the substrates different, that is, by using the substrates having different thermal expansion coefficients, the crystal orientation of the formed dielectric thin film is controlled. It is possible to change film properties such as electrical properties (relative permittivity, coercive electric field, spontaneous polarization, piezoelectric constant, pyroelectric coefficient, etc.) and optical properties (refractive index, electro-optic coefficient, etc.).
- the material of the intermediate layer 55 other rock salt type crystals such as nickel oxide (Ni0), cobalt oxide (Co0), and manganese oxide (Mn ⁇ ) other than magnesium oxide (MgO) are used. Even when a structural oxide is used or when two or more of them are used in combination, in the configuration of the present invention, the crystal parameter such as the lattice constant of the dielectric thin film with respect to the thermal expansion coefficient of the substrate or the ratio thereof is determined. It was found that the film characteristics such as the dielectric constant showed exactly the same tendency.
- the rock salt type crystal structure oxide film used as the intermediate layer 55 is (111) In the case of plane orientation or (110) plane orientation, the formed PZT dielectric thin film also shows (111) plane orientation or (110) plane orientation, respectively. It was found that the crystal parameters such as the lattice constant of the body thin film and the film properties such as the relative dielectric constant showed exactly the same tendency.
- the lattice constant of the dielectric thin film with respect to the coefficient of thermal expansion of the substrate etc. It was found that the film characteristics such as the crystal parameters and specific dielectric constant of the film showed exactly the same tendency.
- the dielectric thin film 5 3 As a material of the first electrode 52 formed on the intermediate layer 55, palladium (Pd) other than platinum (Pt), iridium (Ir), gold (Au), iridium oxide (I R_ ⁇ 2), when using an oxidizing ruthenium (Ru0 2) or a conductive oxidation of nickel (N i O), or even in the case of using these on 2 or more combination, the dielectric thin film 5 3 The same tendency was obtained without deteriorating the characteristics of the film and the tendency of changes in film characteristics such as crystal parameters and relative permittivity due to differences in the thermal expansion coefficients of the substrates used.
- the thermal expansion coefficient of the dielectric thin film material is af
- the thermal expansion coefficient of the substrate is ⁇ s. If the relationship of 0.8 ⁇ «f / o! S ⁇ l. 2 is satisfied, the amount of warpage that occurs in the entire device can be neglected, and as a result, fine processing using photolithography Workability and operability can be improved in an element pattern forming step, a joining step after processing, or a dicing cutting step. Therefore, by using a large-area substrate, it becomes possible to mass-produce dielectric thin-film devices at low cost.
- the thickness of the dielectric thin film is tf and the thickness of the substrate is ts, 0.2 nm ⁇ tf ⁇ 10 ⁇ m, and 0.15 mm ⁇ ts ⁇ If the relationship of 1.5 mm is satisfied, The amount of warpage was found to be further negligible.
- a pyroelectric thin film element 50 of the present embodiment has a rock-salt type crystal structure such as a magnesium oxide (MgO) film as an intermediate layer 55 on a substrate 51.
- the substrate 51 various substrates having different coefficients of thermal expansion as shown in the above (Table 1) are used as in the second embodiment.
- the pyroelectric dielectric thin film element 50 was manufactured as follows.
- a SUS304 substrate is placed as a substrate 51 in a vacuum chamber, and after evacuation, the substrate 51 is heated and held at a temperature of 400 ° C. in the same manner as in the second embodiment. Then, an intermediate layer 55 having a thickness of about 700 nm was formed on the substrate 51 by a plasma MOCVD method.
- the intermediate layer 55 was composed of an MgO film having a rock salt type crystal structure with a (100) crystal orientation.
- the substrate 51 on which the intermediate layer 55 is formed is placed in another vacuum chamber, and after evacuation, the substrate 51 is heated and maintained at a temperature of 600 ° C., and a 4 inch Pt target A lower electrode film (Pt electrode film) made of platinum (Pt) and having a thickness of 250 nm was formed as the first electrode 52 on the intermediate layer 55 by RF magnetron sputtering.
- argon (Ar) was used as a sputtering gas, the gas pressure was maintained at 1 Pa, and high-frequency power of 100 W was applied to perform sputtering for 10 minutes.
- the substrate temperature was set to 56 Ot, and a 6-inch PLT sintered body (a 20% excess of lead oxide (Pb ⁇ ⁇ ) was added in molar ratio) was used to make the RF magnet opening.
- a 3 m-thick dielectric thin film (PLT dielectric thin film) 53 made of PLT was formed on the first electrode 52 by the method.
- a high frequency power of 350 W was applied to perform sputtering for 180 minutes.
- NiCr electrode film having a thickness of 10 nm was formed.
- argon (Ar) was used as a sputtering gas, the gas pressure was kept at 0.7 Pa, and a power of 100 W was applied to perform sputtering for 5 minutes.
- the PLT dielectric formed through the Mg ⁇ film (intermediate layer 55) is formed.
- the crystal orientation of the thin film 53 is mainly (01) plane orientation.
- a pyroelectric thin-film element was fabricated by the same method as above using various substrates with different coefficients of thermal expansion from (Table 1), and the thermal expansion coefficient of the substrate and the relative permittivity of the formed PLT dielectric thin film were measured. And examined the relationship.
- Figure 10 shows the results. You. As shown in FIG. 10, as in the second embodiment, the relative permittivity of the formed PLT dielectric thin film decreases as the thermal expansion coefficient of the substrate increases.
- a pyroelectric thin-film element was fabricated by the same method using the various substrates having different thermal expansion coefficients shown in Table 1 above, and the thermal expansion coefficient of the substrate and the temperature of the PLT dielectric thin film were measured.
- the relationship with the pyroelectric coefficient a obtained from the pyroelectric current obtained by changing the temperature was investigated. The results are shown in FIG. As shown in FIG. 11, as the thermal expansion coefficient of the substrate increases, the pyroelectric coefficient a of the PLT dielectric thin film increases.
- the pyroelectric performance can be simply represented by the ratio of the pyroelectric coefficient a to the relative permittivity ⁇ , The results show that the performance of the pyroelectric infrared sensor improves as the substrate with a higher thermal expansion coefficient is used. That is, assuming that the thermal expansion coefficient of the dielectric thin film material is f and the thermal expansion coefficient of the substrate is as, if a relationship of af / as ⁇ 1 is satisfied, a pyroelectric dielectric thin film element with good performance is obtained. Can be realized.
- the structure of the present invention provides a film such as the relative permittivity of the dielectric thin film with respect to the coefficient of thermal expansion of the substrate and the pyroelectric performance. The characteristics were found to show exactly the same tendency.
- the rock salt type crystal structure oxide film used as the intermediate layer 55 has the (111) plane orientation or the (110) plane orientation
- the PLT dielectric thin films formed are also (111) It was found that the film showed a plane orientation or (110) plane orientation, and the film properties such as the relative permittivity of the dielectric thin film and the pyroelectric performance with respect to the thermal expansion coefficient of the substrate showed exactly the same tendency.
- the material of the intermediate layer 5 5 even when using a spinel type crystal structure oxide such as magnesium aluminate (Mg A 1 2 ⁇ 4), the dielectric of the dielectric thin film to thermal expansion coefficient of the substrate It was found that the film characteristics such as efficiency and pyroelectric performance showed the same tendency.
- the dielectric thin film 5 As a material of the first electrode 52 formed on the intermediate layer 55, palladium (Pd) other than platinum (Pt), iridium (Ir), gold (Au), iridium oxide (I r ⁇ 2 ), ruthenium oxide (Ru ⁇ 2 ) or conductive nickel oxide (NiO), or a combination of two or more of them, the dielectric thin film 5
- Pd palladium
- Ir platinum
- Au gold
- I iridium oxide I r ⁇ 2
- ruthenium oxide Ru ⁇ 2
- NiO conductive nickel oxide
- the thermal expansion coefficient of the dielectric thin film material is af and the thermal expansion coefficient of the substrate is as, If the relationship of 0.8 ⁇ o; f ZQ! S ⁇ l.2 is satisfied, the amount of warpage that occurs in the entire device can be ignored, and as a result, microfabrication using photolithography Workability and operability can be improved in an element pattern forming step, a joining step after processing, or a dicing cutting step. Therefore, by using a large-area substrate, large-area dielectric thin-film elements such as a dielectric thin-film element and an infrared imaging element can be mass-produced at low cost.
- the thickness of the dielectric thin film is tf and the thickness of the substrate is ts, 0.2 (im ⁇ tf ⁇ 10 / m, and 0.15 mm ⁇ It was found that if the relationship of ts ⁇ 1.5 mm was satisfied, the amount of warpage generated in the entire device could be further ignored.
- FIG. 12 shows an ink jet recording apparatus according to a fourth embodiment of the present invention.
- FIG. 2 is a schematic perspective view showing the entire configuration of the device.
- the ink jet recording apparatus 100 of the present embodiment includes an ink jet head 101 that performs recording using the piezoelectric effect of the piezoelectric dielectric thin film, and It is possible to perform recording on the recording medium 102 by landing ink droplets ejected from the ink jet 101 on a recording medium 102 such as paper.
- the ink jet head 101 is mounted on a carriage 104 slidably mounted on a carriage shaft 103 arranged in the main scanning direction (X direction in FIG. 12).
- the ink jet recording apparatus 100 includes a plurality of rollers for moving the recording medium 102 in the sub-scanning direction Y substantially perpendicular to the width direction of the ink jet head 101 (that is, the main scanning direction X). (Recording medium transfer means) 105 is provided.
- FIG. 13 is a schematic perspective view showing an entire configuration of an ink jet head according to a fourth embodiment of the present invention
- FIG. 14 is an exploded perspective view showing a configuration of a main part thereof, partially cut away.
- A is a pressure chamber component formed by processing a silicon (Si) substrate, for example.
- the pressure chamber component A has a pressure chamber opening 1 formed therein.
- B is an actuating portion composed of the dielectric thin film element of the present invention disposed so as to cover the upper end opening surface of the pressure chamber opening 1, and C is formed so as to cover the lower end opening surface of the pressure chamber opening 1.
- the pressure chamber opening 1 of the pressure chamber component A is partitioned by the actuating portion B and the ink liquid flow channel component C located above and below the pressure chamber opening 1, thereby forming the pressure chamber 2.
- an individual electrode 3 is arranged above the pressure chamber 2.
- the ink liquid flow path component C A common liquid chamber 5 shared by the pressure chambers 2, a supply port 6 communicating the common liquid chamber 5 with the pressure chamber 2, and an ink flow path 7 through which the ink liquid in the pressure chamber 2 flows out. Is formed.
- D is a nozzle plate, and the nozzle plate D is provided with a nozzle hole 8 communicating with the ink flow path 7.
- E is an IC chip, and the IC chip E supplies a voltage to the plurality of individual electrodes 3 via the bonding wire BW.
- the performance of the dielectric thin film element constituting the actuator section B is controlled by selecting the material of the pressure chamber component A formed by processing the substrate while considering the thermal expansion coefficient thereof.
- the thermal expansion coefficient of the material (dielectric thin film material) constituting the actuator part B is af and the thermal expansion coefficient of the material of the pressure chamber parts ⁇ is o; s, af Z as> 1 If the material constituting the actuator part B and the material of the pressure chamber part A are selected so as to satisfy the relationship, the ink jet having a dielectric thin film element having better piezoelectric characteristics (in this case, printing characteristics) can be obtained. Can be realized.
- a dielectric thin film element including a dielectric thin film capable of greatly changing film characteristics such as relative permittivity is provided. Therefore, it can be used for piezoelectric elements, infrared sensors, optical switches, memory elements, etc., which are required to control and optimize the element characteristics with good yield.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Photometry And Measurement Of Optical Pulse Characteristics (AREA)
- Formation Of Insulating Films (AREA)
- Particle Formation And Scattering Control In Inkjet Printers (AREA)
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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JP2002531503A JPWO2002027809A1 (ja) | 2000-09-27 | 2001-09-26 | 誘電体薄膜素子、並びにそれを用いたアクチュエータ、インクジェットヘッド及びインクジェット式記録装置 |
EP01970233A EP1324401A1 (en) | 2000-09-27 | 2001-09-26 | Dielectric thin film element, actuator comprising it, ink jet head, and ink jet recorder. |
AU2001290283A AU2001290283A1 (en) | 2000-09-27 | 2001-09-26 | Dielectric thin film element, actuator comprising it, ink jet head, and ink jet recorder. |
KR10-2003-7004432A KR100532736B1 (ko) | 2000-09-27 | 2001-09-26 | 유전체 박막 소자 및 그것을 사용한 액추에이터, 잉크젯헤드 및 잉크젯 방식 기록 장치 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2000-293803 | 2000-09-27 | ||
JP2000293803 | 2000-09-27 |
Publications (1)
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WO2002027809A1 true WO2002027809A1 (fr) | 2002-04-04 |
Family
ID=18776526
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2001/008402 WO2002027809A1 (fr) | 2000-09-27 | 2001-09-26 | Element a pellicule dielectrique mince, actionneur comprenant cet element, tete a jet d'encre et enregistreur a jet d'encre |
Country Status (7)
Country | Link |
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US (1) | US20030189241A1 (ja) |
EP (1) | EP1324401A1 (ja) |
JP (1) | JPWO2002027809A1 (ja) |
KR (1) | KR100532736B1 (ja) |
CN (1) | CN1483225A (ja) |
AU (1) | AU2001290283A1 (ja) |
WO (1) | WO2002027809A1 (ja) |
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JP2004146640A (ja) * | 2002-10-25 | 2004-05-20 | Matsushita Electric Ind Co Ltd | 圧電体薄膜素子およびそれを用いたアクチュエータ、インクジェットヘッドならびにインクジェット記録装置 |
JP2005136115A (ja) * | 2003-10-30 | 2005-05-26 | Tdk Corp | 電子デバイス及びその製造方法 |
JP2009286120A (ja) * | 2008-04-30 | 2009-12-10 | Seiko Epson Corp | 液体噴射ヘッド及び圧電素子 |
JP2014030037A (ja) * | 2007-10-15 | 2014-02-13 | Hitachi Metals Ltd | 圧電薄膜付き基板及び圧電素子 |
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DE20202297U1 (de) * | 2001-09-07 | 2002-08-29 | Drei-S-Werk Präzisionswerkzeuge GmbH & Co Fertigungs-KG, 91126 Schwabach | Flacher Aktor oder Sensor mit interner Vorspannung |
JP5089860B2 (ja) * | 2004-12-03 | 2012-12-05 | 富士フイルム株式会社 | 圧電アクチュエータ及び液体吐出ヘッド |
JP2006245247A (ja) * | 2005-03-02 | 2006-09-14 | Seiko Epson Corp | 圧電素子及びその製造方法、液体噴射ヘッド及びその製造方法並びに液体噴射装置 |
JP4543985B2 (ja) * | 2005-03-24 | 2010-09-15 | セイコーエプソン株式会社 | ニオブ酸チタン酸ジルコン酸鉛積層体 |
DE102008055123B3 (de) * | 2008-12-23 | 2010-07-22 | Robert Bosch Gmbh | Ultraschallwandler zum Einsatz in einem fluiden Medium |
JP6329130B2 (ja) * | 2012-04-10 | 2018-05-30 | アイノビア,インコーポレイティド | 噴霧エジェクタ機構、電荷分離及び制御可能な液滴電荷を提供する装置、並びに低投与量の点眼 |
MX2014013962A (es) | 2012-05-15 | 2015-06-17 | Eyenovia Inc | Dispositivos eyectores, métodos, accionadores y circuitos para los mismos. |
US9136820B2 (en) | 2012-07-31 | 2015-09-15 | Tdk Corporation | Piezoelectric device |
WO2014088691A1 (en) * | 2012-12-03 | 2014-06-12 | Advanced Technology Materials Inc. | IN-SITU OXIDIZED NiO AS ELECTRODE SURFACE FOR HIGH k MIM DEVICE |
US9016837B2 (en) | 2013-05-14 | 2015-04-28 | Stmicroelectronics, Inc. | Ink jet printhead device with compressive stressed dielectric layer |
US9016836B2 (en) | 2013-05-14 | 2015-04-28 | Stmicroelectronics, Inc. | Ink jet printhead with polarity-changing driver for thermal resistors |
JP6467258B2 (ja) * | 2015-03-20 | 2019-02-06 | 日本碍子株式会社 | 接合体、ハニカム構造体及び接合体の製造方法 |
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- 2001-09-26 AU AU2001290283A patent/AU2001290283A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
---|---|
EP1324401A1 (en) | 2003-07-02 |
AU2001290283A1 (en) | 2002-04-08 |
KR20030048413A (ko) | 2003-06-19 |
KR100532736B1 (ko) | 2005-12-01 |
US20030189241A1 (en) | 2003-10-09 |
CN1483225A (zh) | 2004-03-17 |
JPWO2002027809A1 (ja) | 2004-02-05 |
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