WO2014024696A1 - 圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ - Google Patents
圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ Download PDFInfo
- Publication number
- WO2014024696A1 WO2014024696A1 PCT/JP2013/070208 JP2013070208W WO2014024696A1 WO 2014024696 A1 WO2014024696 A1 WO 2014024696A1 JP 2013070208 W JP2013070208 W JP 2013070208W WO 2014024696 A1 WO2014024696 A1 WO 2014024696A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- piezoelectric
- layer
- piezoelectric element
- seed layer
- crystal
- Prior art date
Links
- 239000013078 crystal Substances 0.000 claims abstract description 111
- 239000000758 substrate Substances 0.000 claims abstract description 69
- 239000012798 spherical particle Substances 0.000 claims description 42
- 239000000654 additive Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 239000002245 particle Substances 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 11
- 238000000151 deposition Methods 0.000 abstract description 6
- 239000010408 film Substances 0.000 description 48
- 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 43
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 43
- 238000004544 sputter deposition Methods 0.000 description 40
- 239000010936 titanium Substances 0.000 description 38
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 29
- 238000000034 method Methods 0.000 description 25
- 238000005259 measurement Methods 0.000 description 22
- 238000002441 X-ray diffraction Methods 0.000 description 19
- 238000006073 displacement reaction Methods 0.000 description 18
- 239000010409 thin film Substances 0.000 description 16
- 229910052774 Proactinium Inorganic materials 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
- 230000005684 electric field Effects 0.000 description 12
- 229910052719 titanium Inorganic materials 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000010030 laminating Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910052697 platinum Inorganic materials 0.000 description 8
- 238000004364 calculation method Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000010287 polarization Effects 0.000 description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005477 sputtering target Methods 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 229910052746 lanthanum Inorganic materials 0.000 description 3
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- 241000877463 Lanio Species 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 229910004121 SrRuO Inorganic materials 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000007733 ion plating Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000003980 solgel method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical group [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000005621 ferroelectricity Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 230000005616 pyroelectricity Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- 238000009279 wet oxidation reaction Methods 0.000 description 1
Images
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
- H10N30/704—Piezoelectric or electrostrictive devices based on piezoelectric or electrostrictive films or coatings
- H10N30/706—Piezoelectric or electrostrictive devices based on piezoelectric or electrostrictive films or coatings characterised by the underlying bases, e.g. substrates
- H10N30/708—Intermediate layers, e.g. barrier, adhesion or growth control buffer layers
-
- 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
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/14—Structure thereof only for on-demand ink jet heads
- B41J2/14201—Structure of print heads with piezoelectric elements
-
- 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
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/14—Structure thereof only for on-demand ink jet heads
- B41J2/14201—Structure of print heads with piezoelectric elements
- B41J2/14233—Structure of print heads with piezoelectric elements of film type, deformed by bending and disposed on a diaphragm
-
- 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
- H10N30/079—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 using intermediate layers, e.g. for growth control
-
- 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
- H10N30/20—Piezoelectric or electrostrictive devices with electrical input and mechanical output, e.g. functioning as actuators or vibrators
- H10N30/204—Piezoelectric or electrostrictive devices with electrical input and mechanical output, e.g. functioning as actuators or vibrators using bending displacement, e.g. unimorph, bimorph or multimorph cantilever or membrane benders
- H10N30/2047—Membrane type
-
- 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
-
- 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
- H10N30/01—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
Definitions
- the present invention relates to a piezoelectric element in which an electrode, a seed layer, and a piezoelectric layer are laminated in this order on a substrate, a piezoelectric device including the piezoelectric element, an inkjet head including the piezoelectric device, and an inkjet It relates to the printer.
- piezoelectric materials such as Pb (Zr, Ti) O 3 have been used as electromechanical transducers for application to drive elements and sensors.
- Such a piezoelectric body is expected to be applied to a micro electro mechanical systems (MEMS) element by being formed as a thin film on a substrate such as Si (silicon).
- MEMS micro electro mechanical systems
- the cost can be greatly reduced by manufacturing the elements at a high density on a relatively large Si wafer having a diameter of 6 inches or 8 inches, compared to single wafer manufacturing in which the elements are individually manufactured. it can.
- the piezoelectric thin film and making the device MEMS the mechanical and electrical conversion efficiency is improved, and new added value such as improved sensitivity and characteristics of the device is also created.
- a thermal sensor it is possible to increase measurement sensitivity by reducing thermal conductance due to MEMS, and in an inkjet head for a printer, high-definition patterning can be achieved by increasing the density of nozzles.
- piezoelectric thin film As a material for the piezoelectric thin film (piezoelectric thin film), a crystal made of Pb, Zr, Ti, and O called PZT (lead zirconate titanate) is often used. Since PZT exhibits a good piezoelectric effect when it has an ABO 3 type perovskite structure shown in FIG.
- the shape of the unit cell of the PZT crystal having the perovskite structure varies depending on the ratio of Ti and Zr, which are atoms entering the B site. That is, when Ti is large, the crystal lattice of PZT is tetragonal, and when Zr is large, the crystal lattice of PZT is rhombohedral.
- the piezoelectric body is deformed by applying an electric field to the piezoelectric body, or conversely, an electric field (potential difference) is generated in the piezoelectric body by deforming the piezoelectric body is referred to as a piezoelectric effect.
- FIG. 19 schematically shows the difference in piezoelectric effect due to the difference in crystal orientation of the piezoelectric body.
- the piezoelectric body Since the polarization direction P and the application direction E of the electric field are aligned, the magnitude of the electric field is completely converted into the deformation force of the piezoelectric body, and the piezoelectric body is efficiently deformed in the direction perpendicular to the substrate.
- the (100) direction which is the polarization direction P of the piezoelectric body, intersects the electric field application direction E, so that the electric field magnitude is completely converted into the deformation force of the piezoelectric body. In other words, the amount of deformation of the piezoelectric body in the direction perpendicular to the substrate is reduced.
- the piezoelectric characteristics of the piezoelectric body also change depending on the crystal orientation of the piezoelectric body, and the (100) orientation is higher than the (111) orientation.
- the orientation is preferably (100) orientation.
- crystal orientations such as (111) orientation are preferable because of fatigue characteristics and ease of processing. That is, it is desirable to form the piezoelectric thin film with the (111) orientation rather than the (100) orientation in that domain rotation hardly occurs when voltage is applied and patterning processing by etching is easy. In any case, controlling the crystal orientation of the piezoelectric thin film is important for obtaining stable characteristics.
- a chemical film formation method such as a CVD (Chemical Vapor Deposition) method, a physical method such as a sputtering method or an ion plating method, a liquid phase such as a sol-gel method, etc.
- a growth method can be used.
- a technique in which a base layer (buffer layer, seed layer) for controlling the crystallinity of the piezoelectric layer is provided between the substrate and the piezoelectric layer.
- a base layer made of PLT lead lanthanum zirconate titanate
- PLZT lead lanthanum zirconate titanate
- the PLT of the underlayer has a property that a perovskite crystal can be easily formed even on the Si substrate or the lower electrode. Therefore, by forming a piezoelectric layer on such an underlayer, the piezoelectric layer can be easily formed with a perovskite structure.
- a piezoelectric layer is composed of two layers of a first piezoelectric film and a second piezoelectric film, and a PLT as a buffer layer is provided between the substrate and the piezoelectric layer.
- PLT consists of columnar particles, and its cross-sectional diameter is 40 nm, for example.
- the cross-sectional diameter (for example, 160 nm) of the columnar particles constituting the second piezoelectric film is larger than the cross-sectional diameter (for example, 40 nm) of the columnar particles constituting the first piezoelectric film on the buffer layer side. It has become. With such a configuration, high piezoelectric characteristics are realized while improving the adhesion of the piezoelectric layer and suppressing film peeling.
- JP-A-6-290983 see claim 1, paragraphs [0008] and [0014], FIG. 1 etc.
- Japanese Patent Laying-Open No. 2005-203725 see claim 2, paragraphs [0017], [0019], [0139] to [0143], etc.
- the withstand voltage is a limit voltage that can be applied to the piezoelectric element.
- the withstand voltage exceeds the withstand voltage, dielectric breakdown occurs inside the piezoelectric thin film, and the element is destroyed. Therefore, in order to obtain a high displacement by applying a high electric field to the piezoelectric thin film, it is important to improve the withstand voltage.
- the withstand voltage is lowered, the reliability as the element is greatly lowered.
- FIG. 20 is a cross-sectional view schematically showing a schematic configuration of a conventional general piezoelectric element 100 having a seed layer.
- the piezoelectric element 100 is configured by laminating a lower electrode 102, a seed layer 103, a piezoelectric layer 104, and an upper electrode (not shown) in this order on a substrate 101.
- the seed layer 103 and the piezoelectric layer 104 are formed by sputtering, generally, the crystals grow in a columnar shape and become columnar crystals (columnar particles). This is also shown in Patent Document 2 described above, but becomes clearer with reference to FIG.
- FIG. 21 schematically shows a general growth process of the crystal 201 when the seed layer 103 of the conventional piezoelectric element 100 is formed by the sputtering method.
- crystal nuclei 201a made of the constituent material of the seed layer 103 are generated on the base layer (lower electrode 102), and the crystals 201 grow from the crystal nuclei 201a as a starting point.
- each crystal 201 grows in the film thickness direction and is formed in a columnar shape.
- the interface between adjacent columnar crystals and columnar crystallites, that is, the crystal grain boundaries 103 a extend straight in the film thickness direction of the seed layer 103. For this reason, it is considered that when a voltage is applied between the upper and lower electrodes sandwiching the piezoelectric layer 104, the crystal grain boundary 103a becomes a current leakage path, resulting in dielectric breakdown.
- a triangular wave voltage (frequency 2 kHz) varying from 0 to ⁇ 100 V is applied to the electrode, and the occurrence of film peeling or the like in the piezoelectric element at that time is examined.
- the maximum voltage (100 V in absolute value in the above example) is applied to the electrode only instantaneously (for 1/2000 seconds in the above example).
- a direct current voltage is applied to the electrode, and the direct current voltage is continuously applied for a predetermined period according to the drawing position. For this reason, when considering application to an actual device, it can not be said that the withstand voltage is sufficient just because it can withstand the application of a triangular wave voltage varying from 0 to ⁇ 100V.
- the present invention has been made to solve the above-described problems, and its purpose is to sufficiently ensure a withstand voltage in practical use even in a configuration having a seed layer between a substrate and a piezoelectric layer.
- An object of the present invention is to provide a piezoelectric element that can be improved, a piezoelectric device including the piezoelectric element, an inkjet head including the piezoelectric device, and an inkjet printer.
- a piezoelectric element is a piezoelectric element in which an electrode, a seed layer for controlling crystal orientation of a piezoelectric layer, and the piezoelectric layer are laminated in this order on a substrate,
- the seed layer is formed by laminating two or more layers made of crystals of spherical particles.
- FIG. 1 is a cross-sectional view schematically showing a schematic configuration of a piezoelectric element according to an embodiment of the present invention. It is sectional drawing which shows typically the growth process of the crystal
- 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 5 is a cross-sectional view showing a manufacturing process of the piezoelectric element of Example 1.
- FIG. 4 is a graph showing the results of XRD 2 ⁇ / ⁇ measurement for PLT constituting the seed layer of the piezoelectric element of Example 1.
- FIG. 3 is a graph showing the results of XRD 2 ⁇ / ⁇ measurement for PZT constituting the piezoelectric layer of the piezoelectric element of Example 1.
- FIG. It is a perspective view which shows the schematic structure of a piezoelectric displacement measuring meter.
- 6 is a graph showing measurement results of withstand voltage in the piezoelectric elements of Example 1 and Comparative Example 1.
- 6 is a graph showing the results of XRD 2 ⁇ / ⁇ measurement for PLT constituting the seed layer of the piezoelectric element of Example 2.
- 6 is a graph showing the results of 2RD / ⁇ measurement of XRD with respect to PZT constituting the piezoelectric layer of the piezoelectric element of Example 2.
- 6 is a graph showing the results of 2RD / ⁇ measurement of XRD with respect to PLT constituting the seed layer of the piezoelectric element of Example 3.
- 6 is a graph showing the results of XRD 2 ⁇ / ⁇ measurement for PZT constituting the piezoelectric layer of the piezoelectric element of Example 3.
- FIG. 6 is a graph showing the results of 2RD / ⁇ measurement of XRD with respect to PLT constituting the seed layer of the piezoelectric element of Comparative Example 1.
- FIG. 6 is a graph showing the result of XRD 2 ⁇ / ⁇ measurement with respect to PZT constituting the piezoelectric layer of the piezoelectric element of Comparative Example 1; It is a top view which shows the structure of the piezoelectric device provided with the piezoelectric element of this embodiment.
- FIG. 15 is a cross-sectional view taken along line A-A ′ of FIG. 14. It is sectional drawing of the inkjet head provided with the said piezoelectric device. It is a perspective view which expands and shows a part of inkjet printer provided with the said inkjet head. It is explanatory drawing which shows typically the crystal structure of PZT.
- FIG. 1 is a cross-sectional view schematically showing a schematic configuration of the piezoelectric element 10 of the present embodiment.
- the piezoelectric element 10 is configured by laminating a thermal oxide film 2, a lower electrode 3, a seed layer 4, a piezoelectric layer 5, and an upper electrode 6 in this order on a substrate 1. Note that the portion excluding the upper electrode 6 in the piezoelectric element 10, that is, the one in which up to the piezoelectric layer 5 is laminated on the substrate 1 constitutes a piezoelectric thin film substrate.
- the substrate 1 is composed of a semiconductor substrate made of a single crystal Si (silicon) or a SOI (Silicon on Insulator) substrate having a thickness of about 300 to 500 ⁇ m, for example.
- the thermal oxide film 2 is made of, for example, SiO 2 (silicon oxide) having a thickness of about 0.1 ⁇ m, and is formed for the purpose of protecting and insulating the substrate 1.
- the lower electrode 3 is formed by laminating a Ti (titanium) layer and a Pt (platinum) layer.
- the Ti layer is formed in order to improve the adhesion between the thermal oxide film 2 and the Pt layer.
- the thickness of the Ti layer is, for example, about 0.02 ⁇ m, and the thickness of the Pt layer is, for example, about 0.1 ⁇ m.
- the seed 4 is a layer for controlling the crystallinity of the piezoelectric layer 5 and is also called a buffer layer.
- the seed layer 4 is made of, for example, PLT (lead lanthanum titanate), and details thereof will be described later.
- the piezoelectric layer 5 is made of PZT (lead zirconate titanate) which is a solid solution of PTO (PbTiO 3 ; lead titanate) and PZO (PbZrO 3 ; lead zirconate).
- PZT lead zirconate titanate
- the thickness of PZT varies depending on the application, it is generally 1 ⁇ m or less for memory and sensor applications, and generally 3 to 5 ⁇ m for actuators, for example.
- the Ti / Zr ratio of the piezoelectric layer 5 is set to be the ratio (48/52 to 47/53) constituting the composition phase boundary (MPB) described above or a ratio close thereto. .
- the upper electrode 6 is located on the opposite side of the piezoelectric layer 5 from the lower electrode 3 and is formed by laminating a Ti layer and a Pt layer.
- the Ti layer is formed in order to improve the adhesion between the piezoelectric layer 5 and the Pt layer.
- the thickness of the Ti layer is, for example, about 0.02 ⁇ m, and the thickness of the Pt layer is, for example, about 0.1 to 0.2 ⁇ m.
- the above-described lower electrode 3, seed layer 4, piezoelectric layer 5 and upper electrode 6 are formed by sputtering.
- the seed layer 4 is formed by laminating two or more layers made of crystals 4a of spherical particles.
- the “spherical” of the spherical particles means a shape that is not the same cross-sectional shape that extends in one direction, such as “columnar”, and includes not only a perfect spherical shape. Further, a shape obtained by deforming a sphere, a cross-sectional elliptical shape, a polyhedral shape other than a columnar shape, a shape combining a flat surface and a curved surface, a shape having irregularities, and the like are also included.
- the expression “spherical” is interpreted in this way, but in the drawings, for convenience, the spherical particles are illustrated in a completely spherical shape.
- the particle diameter (cross-sectional diameter) of the spherical particles is, for example, about 10 nm to 50 nm, which is ten times or more the lattice constant (about 0.4 nm) of PLT. That is, each unit crystal of PLT gathers to form one spherical particle (crystal 4a).
- the seed layer is usually grown with a columnar crystal as described above.
- the seed layer 4 can be formed by growing the crystal 4a of the spherical particles as described above by devising the film forming conditions such as the substrate temperature and the sputtering pressure. This will be described in more detail below.
- FIG. 2 schematically shows the growth process of the crystal 4a when the seed layer 4 is formed by sputtering.
- the film formation conditions are set so that the kinetic energy of particles (target material component) repelled from the target becomes high, and the crystal nucleus 4a 1 It is easy to generate.
- growth of crystals 4a STARTING FROM crystal nuclei 4a 1 would be the generation of new crystal nuclei 4a 1 is made almost parallel, underlying crystal 4a is grown columnar Before (after the formation of spherical particles), the upper crystal 4a can be grown starting from the crystal nucleus 4a 1 that has entered the gap between the lower crystal 4a and the crystal 4a.
- the upper crystal nucleus 4a 1 is smaller than the crystal 4a and tends to enter the gap between the lower crystal 4a and the crystal 4a. Therefore, the upper crystal nucleus 4a 1 is located directly above the spherical particles constituting the lower crystal 4a. Spherical particles constituting the crystal 4a are not formed. That is, the spherical particles are positioned in a direction perpendicular to the film thickness direction of the seed layer 4 between the upper layer and the lower layer constituting the seed layer 4. In FIG.
- the seed layer 4 has a three-layer structure including the crystal shown in a hemispherical shape in the lowermost layer. As is apparent from this figure, a deformed shape having different sizes in the film thickness direction and the substrate surface direction is also included in the spherical crystal.
- the positions of the spherical particles are shifted between the upper layer and the lower layer of the seed layer 4 so that the adjacent spherical particles and spherical layers are spherical.
- the interface (grain boundary) between the particles can be connected in a network. Thereby, it is possible to avoid the formation of a crystal grain boundary that extends straight in the film thickness direction of the seed layer 4, that is, a current leakage path.
- the withstand voltage in practical use that is, the withstand voltage when a predetermined DC voltage is continuously applied when a device such as an inkjet head is applied, is sufficiently improved. And the reliability of the element can be improved.
- the specific value of withstand voltage it shows in the subsequent Examples.
- the upper layer spherical particles constituting the seed layer 4 are positioned in a direction perpendicular to the film thickness direction from directly above the spherical particles in the layer immediately below the seed layer 4, the crystal grain boundaries are surely formed in a mesh shape. A leak path that extends straight in the film thickness direction of the seed layer 4 is not reliably formed. Thereby, the withstand voltage in actual use can be improved reliably.
- the withstand voltage of the piezoelectric element 10 is improved, a high voltage can be applied between the upper electrode 6 and the lower electrode 3 to greatly displace the piezoelectric layer 5, and a piezoelectric having high piezoelectric characteristics.
- the element 10 can be realized.
- FIG. 3A to 3D are cross-sectional views showing the manufacturing process of the piezoelectric element 10 of this embodiment.
- a thermal oxide film 2 made of SiO 2 having a thickness of about 100 nm is formed on a substrate 1 made of a single crystal Si wafer having a thickness of about 400 ⁇ m.
- the substrate 1 may be a standard substrate having a thickness of 300 ⁇ m to 725 ⁇ m and a diameter of 3 inches to 8 inches.
- the thermal oxide film 2 can be formed by exposing the substrate 1 to a high temperature of about 1200 ° C. in an oxygen atmosphere using a wet oxidation furnace.
- a Ti layer (adhesion layer) having a thickness of about 10 nm and a Pt layer having a thickness of about 100 nm are sequentially formed on the thermal oxide film 2 by a sputtering method.
- the sputtering conditions of Ti at this time are Ar flow rate: 20 sccm, pressure: 0.9 Pa, RF power applied to the target: 100 W, substrate temperature: 400 ° C.
- the sputtering conditions for Pt are Ar flow rate: 20 sccm, pressure: 0.8 Pa, RF power applied to the target: 150 W, substrate temperature: 400 ° C.
- a PLT layer having a thickness of about 100 nm is formed on the Pt layer of the lower electrode 3 by sputtering to form a seed layer 4.
- the sputtering conditions of PLT at this time are Ar flow rate: 30 sccm, O 2 flow rate: 0.6 sccm, pressure: 0.5 Pa, RF power applied to the target: 150 W, substrate temperature: 600 ° C.
- the Ti, Pt, and PLT films are formed using a ternary sputtering apparatus having three targets of Ti, Pt, and PLT in the chamber. For this reason, the laminated structure of the PLT / Pt / Ti / Si substrate can be continuously formed in-situ (in situ) without taking out the vacuum (see FIGS. 3B and 3C).
- FIG. 4 shows the result of 2RD / ⁇ measurement of XRD (X-ray diffraction) for the PLT constituting the seed layer 4 of Example 1.
- the intensity (diffraction intensity, reflection intensity) on the vertical axis in FIG. 4 is shown in an arbitrary unit (Arbitary Unit) corresponding to the count rate (cps; count per second) of X-rays per second.
- the method of expressing the intensity on the vertical axis is the same in the drawings showing other XRD measurement results.
- the seed layer 4 made of PLT is strongly oriented in the (100) plane or (001) plane of the perovskite.
- the crystal structure of PLT is almost cubic (suspected cubic), and the (100) plane and the (001) plane are almost equivalent. Expressed as a surface.
- the peak intensities in each plane orientation of the perovskite crystal obtained from X-ray diffraction are (100), (110), and (111), respectively, and the degree of orientation of the (100) plane is (100) / ⁇ (100 ) + (110) + (111) ⁇ ⁇ 100.
- the orientation degree was 99%. That is, in PLT, the ratio of crystals oriented in the (100) plane or (001) plane of the perovskite was 90% or more of the whole.
- the PLT crystal grain size is about 40 nm
- the PLT seed layer 4 is composed of two layers of crystals 4a made of spherical particles.
- PZT was formed to about 4 ⁇ m on the seed layer 4 made of PLT in the sputtering apparatus, and the piezoelectric layer 5 was formed.
- the sputtering conditions of PZT at this time were Ar flow rate: 30 sccm, O 2 flow rate: 0.6 sccm, pressure: 0.5 Pa, substrate temperature: 600 ° C., RF power applied to the target: 500 W.
- the method for forming the piezoelectric layer 5 is not limited to the sputtering method, but other physical film forming methods such as a pulse laser deposition (PLD) method and an ion plating method, MOCVD (Metal Organic Chemical Vapor Deposition); A chemical film formation method such as a vapor phase growth method) or a sol-gel method may be used.
- PLD pulse laser deposition
- MOCVD Metal Organic Chemical Vapor Deposition
- a chemical film formation method such as a vapor phase growth method) or a sol-gel method may be used.
- a sputtering target having a molar ratio of Zr to Ti (Zr / Ti ratio) of 52/48 was used.
- Pb contained in the target is likely to be re-evaporated during high-temperature film formation, and the formed thin film tends to be Pb-deficient. Therefore, it is desirable to add the Pb to the target more than the stoichiometric ratio of the perovskite crystal.
- the amount of Pb added is preferably 10 to 30% higher than the stoichiometric ratio, although it depends on the film formation temperature.
- FIG. 5 shows the XRD 2 ⁇ / ⁇ measurement results for PZT constituting the piezoelectric layer 5 of Example 1.
- the degree of orientation of the (100) plane of PZT was calculated from the peak intensities shown in FIG. 5 using the same method (calculation formula) as in PLT. As a result, the degree of orientation was 99%.
- the crystal structure of PZT is cubic when the Zr / Ti ratio completely matches the ratio constituting MPB, and the (100) plane and (001) plane can be considered equivalent. Therefore, it can be said that the calculation result of the degree of orientation described above indicates that in PZT, the ratio of crystals oriented in the (100) plane or (001) plane of the perovskite is 90% or more of the whole.
- the piezoelectric layer 5 is sequentially sputtered on the piezoelectric layer 5 to form the upper electrode 6 (see FIG. 1), and the piezoelectric element 10 is completed. Separated and taken out, the piezoelectric displacement was measured by the cantilever method using the piezoelectric displacement measuring instrument shown in FIG. 6, and the piezoelectric constant d 31 was obtained. As a result, the value of the piezoelectric constant d 31 was ⁇ 170 pm / V.
- the end of the piezoelectric element 10 is clamped by the fixed portion 11 so that the movable length of the cantilever is 10 mm, and a cantilever structure is formed.
- a maximum voltage of 0 V was applied to 6 and a minimum voltage of ⁇ 20 V was applied to the lower electrode 3 at a frequency of 500 Hz, and the displacement of the end of the piezoelectric element 10 was observed with a laser Doppler vibrometer 13. Then, the piezoelectric constant d 31 was obtained from the obtained piezoelectric displacement by a known method.
- the withstand voltage of the piezoelectric element 10 was measured by IV measurement using a semiconductor device analyzer B1500A manufactured by Agilent Technologies. As a result, the withstand voltage was + 88V with a positive bias and -89V with a negative bias.
- the positive bias refers to a state in which a positive voltage is continuously applied to the upper electrode 6 (not periodically) with the lower electrode 3 grounded, and the negative bias refers to the lower electrode 3 grounded. In this state, a negative voltage is applied continuously (not periodically) to the upper electrode 6.
- FIG. 7 shows the measurement results of withstand voltage in Example 1.
- Example 2 In this example, after forming the thermal oxide film 2 on the substrate 1 as in Example 1, a Ti layer (adhesion layer) having a thickness of about 6 nm and a Pt having a thickness of about 100 nm are formed on the thermal oxide film 2.
- the lower electrode 3 was formed by sequentially depositing the layers by sputtering.
- the sputtering conditions of Ti at this time are Ar flow rate: 20 sccm, pressure: 0.7 Pa, RF power applied to the target: 90 W, substrate temperature: 400 ° C.
- the sputtering conditions for Pt are Ar flow rate: 20 sccm, pressure: 0.4 Pa, RF power applied to the target: 150 W, substrate temperature: 400 ° C.
- a PLT layer having a thickness of about 150 nm was formed on the Pt layer of the lower electrode 3 by sputtering to form a seed layer 4.
- the sputtering conditions of PLT at this time are Ar flow rate: 30 sccm, O 2 flow rate: 0.5 sccm, pressure: 0.5 Pa, RF power applied to the target: 150 W, substrate temperature: 640 ° C.
- FIG. 8 shows the result of XRD 2 ⁇ / ⁇ measurement for the PLT constituting the seed layer 4 of Example 2.
- the seed layer 4 made of PLT is strongly oriented in the (100) plane or (001) plane of the perovskite.
- the orientation degree was 95%. That is, also in the PLT of this example, the ratio of crystals oriented in the (100) plane or (001) plane of the perovskite was 90% or more of the whole.
- the PLT crystal grain size was about 50 nm
- the seed layer 4 made of PLT had a structure in which three layers of crystals 4a made of spherical particles were laminated.
- a sputtering apparatus about 4 ⁇ m of PZT was formed on the seed layer 4 made of PLT, and the piezoelectric layer 5 was formed.
- the sputtering conditions of PZT at this time were Ar flow rate: 30 sccm, O 2 flow rate: 0.6 sccm, pressure: 0.5 Pa, substrate temperature: 600 ° C., RF power applied to the target: 500 W.
- FIG. 9 shows the XRD 2 ⁇ / ⁇ measurement results for PZT constituting the piezoelectric layer 5 of Example 2.
- the degree of orientation of the (100) plane of PZT was calculated from the peak intensities in FIG. 9 using the same method (calculation formula) as in PLT, and the degree of orientation was 99%.
- the (100) plane and the (001) plane are almost the same. It is considered equivalent (crystal structure is close to cubic). Therefore, it can be said that the calculation result of the degree of orientation described above indicates that in PZT, the ratio of crystals oriented in the (100) plane or (001) plane of the perovskite is 90% or more of the whole.
- the piezoelectric displacement is measured by a cantilever method using a piezoelectric displacement meter, as in Example 1.
- the piezoelectric constant d 31 was determined. As a result, the value of the piezoelectric constant d 31 was ⁇ 150 pm / V. Further, as with Example 1, the withstand voltage of the piezoelectric element 10 was measured, and as a result, the withstand voltage was +96 V with a positive bias and ⁇ 84 V with a negative bias. That is, in this example, the piezoelectric constant d 31 was slightly lower than that in Example 1, but the withstand voltage was the same as that in Example 1.
- Example 3 In this example, after forming the thermal oxide film 2 on the substrate 1 as in Example 1, a Ti layer (adhesion layer) having a thickness of about 6 nm and a Pt having a thickness of about 100 nm are formed on the thermal oxide film 2.
- the lower electrode 3 was formed by sequentially depositing the layers by sputtering.
- the sputtering conditions of Ti at this time are Ar flow rate: 20 sccm, pressure: 0.8 Pa, RF power applied to the target: 90 W, substrate temperature: 550 ° C.
- the sputtering conditions for Pt are Ar flow rate: 20 sccm, pressure: 0.4 Pa, RF power applied to the target: 150 W, substrate temperature: 550 ° C.
- a PLT layer having a thickness of about 150 nm was formed on the Pt layer of the lower electrode 3 by sputtering to form a seed layer 4.
- the sputtering conditions of PLT at this time are Ar flow rate: 30 sccm, O 2 flow rate: 0.5 sccm, pressure: 0.5 Pa, RF power applied to the target: 150 W, substrate temperature: 690 ° C.
- FIG. 10 shows the XRD 2 ⁇ / ⁇ measurement results for the PLT constituting the seed layer 4 of Example 3.
- the seed layer 4 made of PLT is strongly oriented in the (111) plane of the perovskite.
- the degree of orientation of the (111) plane is expressed by (111) / ⁇ (100) + (110) + (111) ⁇ ⁇ 100, from the peak intensities in FIG.
- the degree of orientation was 95%. That is, in the PLT of this example, the ratio of crystals oriented in the (111) plane of the perovskite was 90% or more of the whole.
- the particle diameter of the PLT crystal was about 40 nm, and the seed layer 4 made of PLT had a structure in which two layers of crystals 4a made of spherical particles were laminated.
- a sputtering apparatus about 4 ⁇ m of PZT was formed on the seed layer 4 made of PLT, and the piezoelectric layer 5 was formed.
- the sputtering conditions of PZT at this time were Ar flow rate: 30 sccm, O 2 flow rate: 0.6 sccm, pressure: 0.5 Pa, substrate temperature: 600 ° C., RF power applied to the target: 500 W.
- FIG. 11 shows the XRD 2 ⁇ / ⁇ measurement results for PZT constituting the piezoelectric layer 5 of Example 3.
- the degree of orientation of the (111) plane of PZT was calculated from the peak intensities in FIG. 11 using the same method (calculation formula) as in PLT, and the degree of orientation was 99%. That is, in the PZT of Example 3, the ratio of crystals oriented in the (111) plane of the perovskite was 90% or more of the whole.
- the piezoelectric displacement is measured by a cantilever method using a piezoelectric displacement meter, as in Example 1.
- the piezoelectric constant d 31 was determined. As a result, the value of the piezoelectric constant d 31 was ⁇ 120 pm / V. Further, as with Example 1, the withstand voltage of the piezoelectric element 10 was measured, and as a result, the withstand voltage was +90 V with a positive bias and ⁇ 86 V with a negative bias. That is, in this example, PZT is preferentially oriented in the (111) plane. As a result, the piezoelectric constant d 31 is lower than those in Examples 1 and 2, but the withstand voltage is equal to that in Examples 1 and 2. Obtained.
- the thermal oxide film 2 is formed on the substrate 1 in the same manner as in Example 1, and then a Ti layer (adhesion layer) having a thickness of about 20 nm and a Pt having a thickness of about 100 nm are formed on the thermal oxide film 2.
- the lower electrode 3 was formed by sequentially depositing the layers by sputtering.
- the sputtering conditions of Ti at this time are Ar flow rate: 20 sccm, pressure: 0.3 Pa, RF power applied to the target: 90 W, substrate temperature: 550 ° C.
- the sputtering conditions for Pt are Ar flow rate: 20 sccm, pressure: 0.4 Pa, RF power applied to the target: 150 W, substrate temperature: 550 ° C.
- a PLT layer having a thickness of about 150 nm was formed on the Pt layer of the lower electrode 3 by sputtering to form a seed layer 4.
- the sputtering conditions of PLT at this time are Ar flow rate: 18 sccm, O 2 flow rate: 0.5 sccm, pressure: 0.5 Pa, RF power applied to the target: 150 W, substrate temperature: 680 ° C.
- FIG. 12 shows the result of 2RD / ⁇ measurement of XRD for the PLT constituting the seed layer 4 of Comparative Example 1.
- the degree of orientation of the (100) plane of PLT was calculated from the peak intensities in FIG. 12 in the same manner as in Example 1. As a result, the degree of orientation was 64%. Further, from observation by SEM, it was found that the PLT crystal grain size was about 80 nm, and the seed layer 4 made of PLT was composed of columnar particles in which the crystal grew in the film thickness direction.
- a sputtering apparatus about 4 ⁇ m of PZT was formed on the seed layer 4 made of PLT, and the piezoelectric layer 5 was formed.
- the sputtering conditions of PZT at this time were Ar flow rate: 30 sccm, O 2 flow rate: 0.3 sccm, pressure: 0.3 Pa, substrate temperature: 650 ° C., RF power applied to the target: 500 W.
- FIG. 13 shows the XRD 2 ⁇ / ⁇ measurement results for PZT constituting the piezoelectric layer 5 of Comparative Example 1.
- the degree of orientation of the (100) plane of PZT was calculated from the peak intensities shown in FIG. 13 using the same method (calculation formula) as in PLT. As a result, the degree of orientation was 95%.
- Example 1 the piezoelectric displacement is measured by a cantilever method using a piezoelectric displacement meter, as in Example 1.
- the piezoelectric constant d 31 was determined.
- the value of the piezoelectric constant d 31 was ⁇ 156 pm / V.
- the withstand voltage of the piezoelectric element 10 was measured, and as a result, the withstand voltage was +56 V with a positive bias and ⁇ 61 V with a negative bias. That is, in Comparative Example 1, a sufficient value as the withstand voltage was not obtained as in Examples 1 to 3.
- the withstand voltage measurement results in Comparative Example 1 are also shown in FIG.
- the seed layer 4 is composed of two or more layers made of spherical particle crystals as in Examples 1 to 3, and the seed layer 4 is composed of columnar particle crystals as in Comparative Example 1.
- the withstand voltage can be greatly improved, and thereby the reliability of the piezoelectric element 10 can be sufficiently improved.
- PZT which is a general piezoelectric material
- the withstand voltage can be sufficiently improved.
- the crystal constituting the seed layer 4 has a perovskite structure, and 90% or more of the crystals are oriented in the (100) plane or the (001) plane.
- a piezoelectric layer 5 having a perovskite structure and preferentially oriented in the (100) plane or the (001) plane can be formed on 4.
- the piezoelectric layer 5 in this way, it is possible to obtain a higher piezoelectric constant d 31 compared to the configuration in which the crystals of the piezoelectric layer 5 are preferentially oriented on the (111) plane, and the efficiency when applying a voltage A large amount of displacement can be obtained by deforming the piezoelectric layer 5 well.
- the seed layer 4 is composed of PLT (having a perovskite crystal structure), it becomes easy to form the piezoelectric layer 5 on the seed layer 4 with a perovskite crystal structure, A piezoelectric layer 5 having high piezoelectric characteristics can be realized.
- Example 1 to 3 the example in which the seed layer 4 is formed by stacking two or three crystals 4a made of spherical particles has been described. However, the seed layer 4 is formed by stacking four or more layers. However, since the crystal grain boundary (leak path) that extends straight in the film thickness direction is not formed, it is the same as in Examples 1 to 3, and therefore the withstand voltage can be sufficiently improved.
- [Application examples of piezoelectric elements] 14 is a plan view showing a configuration of a piezoelectric device 20 in which the piezoelectric element 10 manufactured in the present embodiment is applied to a diaphragm (diaphragm), and FIG. 15 is a cross-sectional view taken along the line AA ′ in FIG. It is.
- the piezoelectric device 20 is driven by utilizing the d 31 deformation (the electric field direction and the polarization direction are the same and the deformation (extension / contraction) is perpendicular to them) of the piezoelectric layer 5.
- the piezoelectric device 20 is configured by forming an opening in the substrate 1 of the piezoelectric element 10. More specifically, the substrate 1 is configured by bonding two Si substrates 21 and 22, and an opening 1 a having a circular cross section is formed in one Si substrate 22 (support substrate). In the Si substrate 21, a portion located above the opening 1a (a portion serving as the upper wall of the opening 1a) constitutes the diaphragm 1b.
- the substrate 1 may be composed of a single Si substrate, and an opening may be formed by removing a portion in the thickness direction of the Si substrate, and a portion remaining above the opening may be a diaphragm. .
- the piezoelectric layer 5 is arranged in a two-dimensional staggered pattern in a necessary region of the substrate 1.
- the lower electrode 3 and the upper electrode 6 are connected to an external control circuit by wiring not shown.
- the piezoelectric layer 5 may be drawn from above the opening 1a to above the side wall of the opening 1a in order to draw out the upper electrode 6. That is, the piezoelectric layer 5 only needs to be positioned at least above the opening 1a.
- the piezoelectric layer 5 By applying an electrical signal from the control circuit to the lower electrode 3 and the upper electrode 6 sandwiching the predetermined piezoelectric layer 5, only the predetermined piezoelectric layer 5 can be driven. That is, when a predetermined electric field is applied to the upper and lower electrodes of the piezoelectric layer 5, the piezoelectric layer 5 expands and contracts in the left-right direction, and the piezoelectric layer 5 and the diaphragm 1b are bent up and down by the bimetal effect. Therefore, if the opening 1a of the substrate 1 is filled with a gas or a liquid, the piezoelectric device 20 can be used as a pump, which is suitable for an inkjet head, for example. Therefore, the piezoelectric element 10 of the present embodiment described above is very effective as a device capable of improving the withstand voltage when the piezoelectric device 20 is used.
- the deformation amount of the piezoelectric layer 5 can be detected by detecting the charge amount of the predetermined piezoelectric layer 5 through the lower electrode 3 and the upper electrode 6. That is, when the piezoelectric layer 5 is vibrated by sound waves or ultrasonic waves, an electric field is generated between the upper and lower electrodes due to an effect opposite to the above. By detecting the magnitude of the electric field and the frequency of the detection signal at this time, The piezoelectric device 20 can also be used as a sensor (ultrasonic sensor).
- the piezoelectric element 10 is replaced with a device such as an infrared sensor (thermal sensor) or a nonvolatile storage memory. It can also be used as
- FIG. 16 is a cross-sectional view of the inkjet head 30 including the piezoelectric device 20.
- the inkjet head 30 is configured by joining (for example, anodic bonding) a nozzle plate 25 to a substrate 1 of a piezoelectric device 20 via a glass plate (not shown).
- the nozzle plate 25 has a nozzle opening 25a, and the opening 1a formed in the substrate 1 communicates with the outside through the nozzle opening 25a.
- the opening 1a is connected to an ink supply path (not shown), and functions as a pressure chamber that stores ink supplied from the ink supply path.
- FIG. 17 is an enlarged perspective view showing a part of the inkjet printer 40 including the inkjet head 30 described above.
- the ink jet printer 40 has a carriage 32 that can move in the left-right direction (B direction in the figure) in a housing 31 that is partially open.
- inkjet heads 30 corresponding to each of a plurality of colors (for example, four colors of yellow, magenta, cyan, and black) are mounted in a line.
- a recording medium not shown
- the carriage 32 is moved left and right to eject ink of each color from the corresponding inkjet head 30, thereby recording the recording medium.
- a color image can be formed thereon.
- the electrode layer constituting the lower electrode 3 is not limited to Pt used in the present embodiment, and other metal such as Au, Ir, IrO 2 , RuO 2 , LaNiO 3 , SrRuO 3 , or metal oxide Products, and combinations thereof can also be used.
- the material constituting the seed layer 4 is not limited to the PLT of the present embodiment, and oxides such as LaNiO 3 , SrRuO 3 , and PbTiO 3 can also be used.
- the material constituting the piezoelectric layer 5 is not limited to the PZT of the present embodiment, but is obtained by adding impurities such as La, Nb, and Sr to PZT, BaTiO 3 , LiTaO 3 , Pb (Mg, Nb ) O 3 , Pb (Ni, Nb) O 3 , PbTiO 3, or other oxides or combinations thereof can also be used.
- the piezoelectric element described above is a piezoelectric element in which an electrode, a seed layer for controlling the crystal orientation of the piezoelectric layer, and the piezoelectric layer are stacked in this order on a substrate. Is formed by laminating two or more layers made of crystals of spherical particles.
- the crystal particles constituting the seed layer are not columnar particles but spherical particles, when two or more layers composed of such spherical particles are laminated, the second spherical particle is replaced with the first spherical particle.
- the upper layer spherical particles can be positioned at positions shifted from the spherical particles in the layer immediately below, similarly in the third and subsequent layers.
- the interface between the adjacent spherical particles and the spherical particles (grain boundary) can be connected in a substantially network shape, and a voltage that extends straight along the grain boundary in the film thickness direction of the seed layer. It is possible to avoid the formation of a leak path during application. As a result, even in the configuration in which the seed layer is provided, the withstand voltage in actual use (when the device is applied) can be sufficiently improved, and the reliability of the element can be improved.
- the spherical particles in the upper layer are shifted from a position directly above the spherical particles in the layer immediately below in a direction perpendicular to the film thickness direction.
- the crystal grain boundaries are surely connected in a network, and a leak path that extends straight in the film thickness direction of the seed layer is not formed reliably, so that the withstand voltage in actual use can be reliably improved.
- the crystal constituting the seed layer preferably has a perovskite structure, and 90% or more of the crystal is preferably oriented in the (100) plane or the (001) plane.
- the piezoelectric layer formed on the seed layer can be preferentially oriented to the (100) plane or the (001) plane with a perovskite structure in a manner that follows the crystal orientation of the seed layer.
- the crystal constituting the piezoelectric layer has a perovskite structure, and 90% or more of the crystal is preferably oriented in the (100) plane or the (001) plane.
- the piezoelectric characteristics can be improved by efficiently deforming the piezoelectric layer when a voltage is applied, compared to a configuration in which the crystals of the piezoelectric layer are oriented in the (111) plane.
- the seed layer may be PLT. Since PLT has a perovskite crystal structure, it is easy to form a piezoelectric layer with a perovskite crystal structure on which a high piezoelectric characteristic can be obtained on a seed layer made of PLT.
- the piezoelectric layer may be composed of PZT or PZT with an additive added.
- the piezoelectric layer is made of such a material, the withstand voltage in practical use can be improved.
- the above-described piezoelectric element may further include an upper electrode formed on the side opposite to the lower electrode with respect to the piezoelectric layer when the electrode is a lower electrode.
- the piezoelectric device described above includes the piezoelectric element having the above-described configuration, and an opening is formed in the substrate of the piezoelectric element, and the piezoelectric layer is located at least above the opening. It may be a configuration.
- the opening is filled with a liquid (for example, ink) or gas
- a voltage is applied to the upper electrode and the lower electrode to deform the piezoelectric layer, and pressure is applied to the liquid in the opening, so that the liquid etc. Can be discharged to the outside. Therefore, in this case, it is possible to realize a piezoelectric device that functions as a pump (including an inkjet head) and has a sufficiently improved withstand voltage.
- a piezoelectric device that functions as an ultrasonic sensor can be obtained. It can also be realized.
- the “spherical shape” of the spherical particles in each of the above explanations means a shape that is not a shape extending in one direction with the same cross-sectional shape as “columnar”. That is, it is interpreted that not only a perfect spherical shape but also a deformed shape of a sphere, an elliptical cross-sectional shape, a polyhedral shape other than a columnar shape, a shape combining a plane and a curved surface, a shape having irregularities, and the like are included.
- the crystal particles constituting the seed layer are spherical particles, and by laminating two or more layers, the spherical particles are shifted from each other in the upper and lower layers, and the seed layer is aligned along the crystal grain boundary. It is possible to avoid the formation of a leak path that extends straight in the film thickness direction. As a result, even with the configuration in which the seed layer is provided, the withstand voltage when the device is applied can be sufficiently improved, and the reliability of the element can be improved.
- the piezoelectric element of the present invention can be used for various devices such as an inkjet head, an ultrasonic sensor, an infrared sensor, and a nonvolatile memory, and an inkjet printer.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Particle Formation And Scattering Control In Inkjet Printers (AREA)
- Physical Vapour Deposition (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
Description
図1は、本実施形態の圧電素子10の概略の構成を模式的に示す断面図である。この圧電素子10は、基板1上に、熱酸化膜2と、下部電極3と、シード層4と、圧電体層5と、上部電極6とをこの順で積層して構成されている。なお、圧電素子10において上部電極6を除いた部分、つまり、基板1上に圧電体層5までを積層したものは、圧電薄膜基板を構成している。
次に、上記したシード層4の詳細について説明する。図1に示すように、シード層4は、球状粒子の結晶4aからなる層を2層以上積層して構成されている。ここで、本出願において球状粒子の「球状」とは、「柱状」のように同じ断面形状で一方向に伸びた形状ではない形状を意味しており、これには、完全な球状のみならず、球を変形させた形状、断面楕円形状、柱状以外の多面体形状、その他平面と曲面とを組み合わせた形状、凹凸を有する形状なども含まれるものとする。以下、「球状」の表現は、このように解釈するものとするが、図面では、便宜的に、球状粒子を完全な球状で図示する。
図3A~図3Dは、本実施例の圧電素子10の製造工程を示す断面図である。まず、図3Aに示すように、厚さ400μm程度の単結晶Siウェハからなる基板1に、例えば厚さ100nm程度のSiO2からなる熱酸化膜2を形成する。なお、基板1としては、厚さが300μm~725μm、直径が3インチ~8インチなどの標準的なものでよい。また、熱酸化膜2は、ウェット酸化用熱炉を用い、基板1を酸素雰囲気中で1200℃程度の高温にさらすことで形成可能である。
本実施例では、実施例1と同様に基板1上に熱酸化膜2を形成した後、熱酸化膜2上に、厚さ6nm程度のTi層(密着層)と、厚さ100nm程度のPt層とを順にスパッタ法で成膜し、下部電極3を形成した。このときのTiのスパッタ条件は、Ar流量;20sccm、圧力;0.7Pa、ターゲットに印加するRFパワー;90W、基板温度;400℃である。Ptのスパッタ条件は、Ar流量;20sccm、圧力;0.4Pa、ターゲットに印加するRFパワー;150W、基板温度;400℃である。
本実施例では、実施例1と同様に基板1上に熱酸化膜2を形成した後、熱酸化膜2上に、厚さ6nm程度のTi層(密着層)と、厚さ100nm程度のPt層とを順にスパッタ法で成膜し、下部電極3を形成した。このときのTiのスパッタ条件は、Ar流量;20sccm、圧力;0.8Pa、ターゲットに印加するRFパワー;90W、基板温度;550℃である。Ptのスパッタ条件は、Ar流量;20sccm、圧力;0.4Pa、ターゲットに印加するRFパワー;150W、基板温度;550℃である。
本比較例では、実施例1と同様に基板1上に熱酸化膜2を形成した後、熱酸化膜2上に、厚さ20nm程度のTi層(密着層)と、厚さ100nm程度のPt層とを順にスパッタ法で成膜し、下部電極3を形成した。このときのTiのスパッタ条件は、Ar流量;20sccm、圧力;0.3Pa、ターゲットに印加するRFパワー;90W、基板温度;550℃である。Ptのスパッタ条件は、Ar流量;20sccm、圧力;0.4Pa、ターゲットに印加するRFパワー;150W、基板温度;550℃である。
図14は、本実施形態で作製した圧電素子10をダイヤフラム(振動板)に応用した圧電デバイス20の構成を示す平面図であり、図15は、図14のA-A’線矢視断面図である。なお、ここでは、圧電体層5のd31変形(電界方向と分極方向とが同一で、変形(伸縮)がそれらに垂直)を利用して圧電デバイス20を駆動するものとする。
下部電極3を構成する電極層は、本実施形態で用いたPtに限定されるわけではなく、その他にも、Au、Ir、IrO2、RuO2、LaNiO3、SrRuO3等の金属または金属酸化物、およびこれらの組み合わせを用いることもできる。
1a 開口部
3 下部電極
4 シード層
4a 結晶
5 圧電体層
6 上部電極
10 圧電素子
20 圧電デバイス
30 インクジェットヘッド
40 インクジェットプリンタ
Claims (10)
- 基板上に、電極と、圧電体層の結晶配向性を制御するためのシード層と、前記圧電体層とをこの順で積層した圧電素子であって、
前記シード層は、球状粒子の結晶からなる層を2層以上積層して構成されていることを特徴とする圧電素子。 - 前記シード層において、上層の球状粒子は、その直下の層の球状粒子の真上から、膜厚方向に垂直な方向にずれて位置していることを特徴とする請求項1に記載の圧電素子。
- 前記シード層を構成する前記結晶は、ペロブスカイト型構造であり、その90%以上が(100)面または(001)面に配向していることを特徴とする請求項1または2に記載の圧電素子。
- 前記圧電体層を構成する結晶は、ペロブスカイト型構造であり、その90%以上が(100)面または(001)面に配向していることを特徴とする請求項3に記載の圧電素子。
- 前記シード層は、PLTであることを特徴とする請求項1から4のいずれかに記載の圧電素子。
- 前記圧電体層は、PZT、またはPZTに添加物を加えたもので構成されていることを特徴とする請求項1から5のいずれかに記載の圧電素子。
- 前記電極を下部電極とすると、
前記圧電体層に対して前記下部電極とは反対側に形成される上部電極をさらに備えていることを特徴とする請求項1から6のいずれかに記載の圧電素子。 - 請求項1から7のいずれかに記載の圧電素子を備え、
前記圧電素子の前記基板には開口部が形成されており、
前記圧電体層は、少なくとも前記開口部の上方に位置していることを特徴とする圧電デバイス。 - 前記開口部と外部とを連通するノズル開口を備え、請求項8に記載の圧電素子を用いて前記開口部内のインクを前記ノズル開口から吐出するよう構成されている、インクジェットヘッド。
- 請求項9に記載のインクジェットヘッドを備えたインクジェットプリンタ。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013549082A JP5472549B1 (ja) | 2012-08-10 | 2013-07-25 | 圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ |
EP13827424.6A EP2889927B1 (en) | 2012-08-10 | 2013-07-25 | Piezoelectric element, piezoelectric device, ink-jet head, and ink-jet printer |
US14/419,389 US9318687B2 (en) | 2012-08-10 | 2013-07-25 | Piezoelectric element, piezoelectric device, ink-jet head, and ink-jet printer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012-178777 | 2012-08-10 | ||
JP2012178777 | 2012-08-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2014024696A1 true WO2014024696A1 (ja) | 2014-02-13 |
Family
ID=50067929
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2013/070208 WO2014024696A1 (ja) | 2012-08-10 | 2013-07-25 | 圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ |
Country Status (4)
Country | Link |
---|---|
US (1) | US9318687B2 (ja) |
EP (1) | EP2889927B1 (ja) |
JP (1) | JP5472549B1 (ja) |
WO (1) | WO2014024696A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016052776A (ja) * | 2014-07-28 | 2016-04-14 | ローム株式会社 | 圧電体膜、圧電素子、およびインクジェットヘッド |
JPWO2015194452A1 (ja) * | 2014-06-20 | 2017-04-20 | 株式会社アルバック | 多層膜及びその製造方法 |
EP3306687A4 (en) * | 2015-05-25 | 2018-05-30 | Konica Minolta, Inc. | Piezoelectric thin film, piezoelectric actuator, inkjet head, inkjet printer, and method for manufacturing piezoelectric actuator |
JP2019047114A (ja) * | 2017-09-06 | 2019-03-22 | ローム株式会社 | 圧電素子 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014024695A1 (ja) * | 2012-08-08 | 2014-02-13 | コニカミノルタ株式会社 | 圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ |
US9887344B2 (en) * | 2014-07-01 | 2018-02-06 | Seiko Epson Corporation | Piezoelectric element, piezoelectric actuator device, liquid ejecting head, liquid ejecting apparatus, and ultrasonic measuring apparatus |
JP6721856B2 (ja) * | 2015-08-07 | 2020-07-15 | セイコーエプソン株式会社 | 圧電素子の製造方法 |
JP7415489B2 (ja) * | 2019-11-29 | 2024-01-17 | セイコーエプソン株式会社 | 圧電アクチュエーターおよびその製造方法 |
JP2022057129A (ja) * | 2020-09-30 | 2022-04-11 | 株式会社リコー | アクチュエータ、液体吐出ヘッド及び液体吐出装置 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06290983A (ja) | 1993-04-06 | 1994-10-18 | Matsushita Electric Ind Co Ltd | 誘電体薄膜及びその製造方法 |
JP2005203725A (ja) | 2003-12-16 | 2005-07-28 | Matsushita Electric Ind Co Ltd | 圧電素子及びその製造方法、並びにその圧電素子を備えたインクジェットヘッド、インクジェット式記録装置及び角速度センサ |
JP2008042069A (ja) * | 2006-08-09 | 2008-02-21 | Matsushita Electric Ind Co Ltd | 圧電体素子とその製造方法 |
WO2012020638A1 (ja) * | 2010-08-12 | 2012-02-16 | 株式会社村田製作所 | 圧電薄膜素子の製造方法、圧電薄膜素子及び圧電薄膜素子用部材 |
JP2012119347A (ja) * | 2010-11-29 | 2012-06-21 | Konica Minolta Holdings Inc | 圧電モジュール、圧電デバイスおよび圧電モジュールの製造方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3520403B2 (ja) * | 1998-01-23 | 2004-04-19 | セイコーエプソン株式会社 | 圧電体薄膜素子、アクチュエータ、インクジェット式記録ヘッド、及びインクジェット式記録装置 |
JP3379479B2 (ja) * | 1998-07-01 | 2003-02-24 | セイコーエプソン株式会社 | 機能性薄膜、圧電体素子、インクジェット式記録ヘッド、プリンタ、圧電体素子の製造方法およびインクジェット式記録ヘッドの製造方法、 |
CN100533798C (zh) * | 2004-02-27 | 2009-08-26 | 佳能株式会社 | 压电薄膜制造方法 |
JP2010021375A (ja) * | 2008-07-10 | 2010-01-28 | Seiko Epson Corp | 液体噴射ヘッド及び液体噴射装置並びに圧電素子 |
JP5615591B2 (ja) * | 2009-07-16 | 2014-10-29 | 日本碍子株式会社 | 結晶粒子の製造方法及び結晶配向セラミックスの製造方法 |
-
2013
- 2013-07-25 EP EP13827424.6A patent/EP2889927B1/en active Active
- 2013-07-25 WO PCT/JP2013/070208 patent/WO2014024696A1/ja active Application Filing
- 2013-07-25 JP JP2013549082A patent/JP5472549B1/ja active Active
- 2013-07-25 US US14/419,389 patent/US9318687B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06290983A (ja) | 1993-04-06 | 1994-10-18 | Matsushita Electric Ind Co Ltd | 誘電体薄膜及びその製造方法 |
JP2005203725A (ja) | 2003-12-16 | 2005-07-28 | Matsushita Electric Ind Co Ltd | 圧電素子及びその製造方法、並びにその圧電素子を備えたインクジェットヘッド、インクジェット式記録装置及び角速度センサ |
JP2008042069A (ja) * | 2006-08-09 | 2008-02-21 | Matsushita Electric Ind Co Ltd | 圧電体素子とその製造方法 |
WO2012020638A1 (ja) * | 2010-08-12 | 2012-02-16 | 株式会社村田製作所 | 圧電薄膜素子の製造方法、圧電薄膜素子及び圧電薄膜素子用部材 |
JP2012119347A (ja) * | 2010-11-29 | 2012-06-21 | Konica Minolta Holdings Inc | 圧電モジュール、圧電デバイスおよび圧電モジュールの製造方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2889927A4 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2015194452A1 (ja) * | 2014-06-20 | 2017-04-20 | 株式会社アルバック | 多層膜及びその製造方法 |
US9985196B2 (en) | 2014-06-20 | 2018-05-29 | Ulvac, Inc. | Multi-layered film and method of manufacturing the same |
JP2016052776A (ja) * | 2014-07-28 | 2016-04-14 | ローム株式会社 | 圧電体膜、圧電素子、およびインクジェットヘッド |
EP3306687A4 (en) * | 2015-05-25 | 2018-05-30 | Konica Minolta, Inc. | Piezoelectric thin film, piezoelectric actuator, inkjet head, inkjet printer, and method for manufacturing piezoelectric actuator |
US10369787B2 (en) | 2015-05-25 | 2019-08-06 | Konica Minolta, Inc. | Piezoelectric thin film, piezoelectric actuator, inkjet head, inkjet printer, and method for manufacturing piezoelectric actuator |
JP2019047114A (ja) * | 2017-09-06 | 2019-03-22 | ローム株式会社 | 圧電素子 |
JP7107782B2 (ja) | 2017-09-06 | 2022-07-27 | ローム株式会社 | 圧電素子 |
Also Published As
Publication number | Publication date |
---|---|
JP5472549B1 (ja) | 2014-04-16 |
JPWO2014024696A1 (ja) | 2016-07-25 |
EP2889927A4 (en) | 2016-04-06 |
US9318687B2 (en) | 2016-04-19 |
EP2889927A1 (en) | 2015-07-01 |
US20150214465A1 (en) | 2015-07-30 |
EP2889927B1 (en) | 2019-04-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5472549B1 (ja) | 圧電素子、圧電デバイス、インクジェットヘッドおよびインクジェットプリンタ | |
US9136459B2 (en) | Piezoelectric device and method of manufacturing piezoelectric device | |
US8864288B2 (en) | Piezoelectric device, method of manufacturing piezoelectric device, and liquid ejection head | |
KR100978145B1 (ko) | 에피택셜 산화물막, 압전막, 압전막 소자, 압전막 소자를이용한 액체 토출 헤드 및 액체 토출 장치 | |
JP6699662B2 (ja) | 圧電薄膜、圧電アクチュエータ、インクジェットヘッド、インクジェットプリンタおよび圧電アクチュエータの製造方法 | |
JP2005333108A (ja) | 圧電素子、インクジェットヘッド、角速度センサ及びインクジェット式記録装置 | |
JPWO2017082049A1 (ja) | インクジェットヘッドおよびその製造方法、ならびにインクジェット記録装置 | |
JP2008041921A (ja) | 圧電薄膜素子およびその製造方法、ならびにインクジェットヘッドおよびインクジェット式記録装置 | |
JP2019522902A (ja) | 優先電界駆動方向における圧電薄膜素子の分極 | |
JP6281629B2 (ja) | 圧電薄膜付き基板、圧電アクチュエータ、インクジェットヘッド、インクジェットプリンタおよび強誘電体薄膜の製造方法 | |
WO2012165110A1 (ja) | 強誘電体膜およびそれを備えた圧電素子 | |
JP5194463B2 (ja) | 圧電体薄膜素子の製造方法 | |
JP6481686B2 (ja) | 強誘電体薄膜、圧電薄膜付き基板、圧電アクチュエータ、インクジェットヘッドおよびインクジェットプリンタ | |
US9853203B2 (en) | Piezoelectric element with underlying layer to control crystallinity of a piezoelectric layer, and piezoelectric device, inkjet head, and inkjet printer including such piezoelectric element | |
JP5835460B2 (ja) | 圧電薄膜、圧電素子、インクジェットヘッド、インクジェットプリンタおよび圧電薄膜の製造方法 | |
JP2008028285A (ja) | 圧電体薄膜素子、インクジェットヘッドおよびインクジェット式記録装置 | |
JP5354876B2 (ja) | 圧電体の製造方法、圧電体素子及び液体吐出ヘッド | |
JP5861404B2 (ja) | 圧電素子およびその製造方法 | |
JP2007335489A (ja) | 圧電体薄膜素子、薄膜アクチュエータ、インクジェットヘッドおよびインクジェット式記録装置 | |
JP6468881B2 (ja) | 圧電薄膜、圧電薄膜の製造方法、圧電薄膜付き基板、圧電アクチュエータ、圧電センサ、インクジェットヘッドおよびインクジェットプリンタ | |
JP2016072568A (ja) | 電気機械変換素子及び液滴吐出ヘッド |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2013549082 Country of ref document: JP Kind code of ref document: A |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13827424 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2013827424 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14419389 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |