WO1991014028A1 - High temperature superconducting films on aluminum oxide substrates - Google Patents

High temperature superconducting films on aluminum oxide substrates Download PDF

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Publication number
WO1991014028A1
WO1991014028A1 PCT/US1991/001788 US9101788W WO9114028A1 WO 1991014028 A1 WO1991014028 A1 WO 1991014028A1 US 9101788 W US9101788 W US 9101788W WO 9114028 A1 WO9114028 A1 WO 9114028A1
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WIPO (PCT)
Prior art keywords
film
substrate
buffer layer
films
structure according
Prior art date
Application number
PCT/US1991/001788
Other languages
French (fr)
Inventor
Nathan Newman
Kookrin Char
Original Assignee
Conductus, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US07/495,568 external-priority patent/US5132282A/en
Priority claimed from US07/565,691 external-priority patent/US5130294A/en
Application filed by Conductus, Inc. filed Critical Conductus, Inc.
Priority to EP91907776A priority Critical patent/EP0610175A1/en
Publication of WO1991014028A1 publication Critical patent/WO1991014028A1/en

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    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B23/00Single-crystal growth by condensing evaporated or sublimed materials
    • C30B23/02Epitaxial-layer growth
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B25/00Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
    • C30B25/02Epitaxial-layer growth
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/16Oxides
    • C30B29/22Complex oxides
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/16Oxides
    • C30B29/22Complex oxides
    • C30B29/225Complex oxides based on rare earth copper oxides, e.g. high T-superconductors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N60/00Superconducting devices
    • H10N60/01Manufacture or treatment
    • H10N60/0268Manufacture or treatment of devices comprising copper oxide
    • H10N60/0296Processes for depositing or forming superconductor layers
    • H10N60/0576Processes for depositing or forming superconductor layers characterised by the substrate
    • H10N60/0632Intermediate layers, e.g. for growth control

Definitions

  • This invention relates to high critical temperature superconducting (HTSC) films and, more particularly, this invention relates to the preparation of HTSC films on sap ⁇ phire (aluminum oxide) substrates by the use of stable, epitaxial buffer layers.
  • HTSC high critical temperature superconducting
  • HTSC metal cuprate materials cannot readily be produced in bulk with geometries and properties suitable for microwave devices.
  • devices based on the HTSC materials are fabri ⁇ cated by formation of thin films on substrates by tech ⁇ niques similar to those used to fabricate semiconductor devices.
  • the HTSC film must be grown on a substrate having low dielectric losses at high frequencies.
  • Sapphire Al 2 0 3
  • Sapphire would appear to be an excellent substrate since it has a very low dielectric loss and is a strong, low cost, highly crystalline material available commercially in large sizes. Sapphire would be a good substrate for bolometer
  • substrate materials that provide epi ⁇ taxial growth of thin HTSC films with high superconducting transition temperatures and low rf surface resistance, such as strontium titanate (SrTi0 3 ) , calcium titanate (CaTi0 3 ) , lanthanum alu inate (LaAlO-) , magnesium oxide (MgO) and yttria stabilized zirconia (YSZ) .
  • strontium titanate SrTi0 3
  • CaTi0 3 calcium titanate
  • LaAlO- lanthanum alu inate
  • MgO magnesium oxide
  • YSZ yttria stabilized zirconia
  • thick substrat ⁇ es of some of these materials e.g. strontium or calcium titanate, exhibit too high an rf loss or do not have high enough strength to act as a substrate for large area micro ⁇ wave devices.
  • Some of these materials are only available in small sizes and/or at very high cost.
  • thin epitaxial films of these materials ex- hibit a low dielectric loss and would be useful as a buffer layer between the HTSC film and the sapphire substrate if they provided an epitaxial surface for the HTSC film and were stable and non-reactive with the HTSC film and the substrate.
  • the HTSC film did not have sufficient orientation and there were too many random grains.
  • Morris et al. [3] formed an MgO buffer layer by sputter deposition at 5.5 to 7 Pa (about 40-50 m Torr) a fairly low pressure.
  • the resulting YBCO film grown on the epitaxial MgO has high normal state resistance and a broad superconducting transition.
  • the invention provides a HTSC buffer layered structure on sapphire that is stable and suitable for microwave en ⁇ vironments or for use in the fabrication of bolometers.
  • the layered structure with a thin SrTi0 3 or CaTi0 3 buffer layer has a sharp transition and good thermal response, making it suitable for bolometer applications.
  • the HTSC film can be grown over a wide temperature range without the HTSC reacting with the sapphire substrate or the buffer reacting with the substrate or the HTSC film.
  • the layered structures of the invention provides the highest microwave performance of any sapphire supported HTSC film reported to date. Others have reported surface resistance measuring on a par with copper.
  • the layered sapphire supported HTSC structure of the invention exhibits rf surface resistance 2 to 3 times better than copper at 10 GHz and 77 K and much better than copper at lower temperatures.
  • the YBCO films grown on the buffer layer exhibit low normal state resist- ance and a narrow superconducting transition.
  • the buffer layer in the HTSC structure of the inven ⁇ tion is grown in a high pressure process such as laser ab ⁇ lation, sputtering or metallo-organic compound vapor depo- sition (MOCVD) .
  • MOCVD metallo-organic compound vapor depo- sition
  • Talvacchio et al. [2] used electron beam deposition of the MgO film.
  • Electron beam epitaxial depo ⁇ sition is conducted at relatively high vacuum, about 10 "5 Torr.
  • the low partial pressure of oxygen is believed to result in an oxygen deficient buffer layer film. These films are chemically active and react with water which de ⁇ grades the quality of the overlying HTSC film.
  • the buffer layer in the process of the invention is deposited at high ⁇ er pressure which results in inert buffer layers with good epitaxial qualities.
  • the SrTi0 3 and CaTi0 3 buffer layers are excellent intermediate substrates for forming high per ⁇ formance, stable HTSC
  • Figure 1 is a schematic drawing of a layered HTSC-Buf- fer-Sapphire structure produced according to the process of this invention
  • Figure 2 is a series of curves showing Surface Resis ⁇ tance, R s of epitaxial YBa 2 Cu 3 0 7 films as a function of tem ⁇ perature at 10 GHz;
  • Figure 3 is a series of plots of Surface Resistance, R s vs. frequency with Cu data at 77 K and Nb data at 7.7 K;
  • Figure 4(a) is a c-axis scan of the YBa 2 Cu 3 0 7 film
  • Figure 4(b) is a ⁇ -axis scan of the [103] peak of the YBa 2 Cu 3 0 7 film
  • Figure 5(a) is the mutual inductance response of the YBa 2 Cu 3 0 7 film at 1 A;
  • Figure 5(b) is the mutual inductance response of the YBa 2 Cu 3 0 7 film at 100 mA.
  • Figure 6 is a graph of surface resistivity, R s versus temperature.
  • the layered structure 10 is composed of a sapphire base or substrate 12, a thin buffer layer 14 and a HTSC layer 16.
  • the buffer layer 14 and the HTSC layer 16 may be laid down in a pattern to form a de- vice by use of a mask formed by conventional lithographic techniques or by use of shutters or shields.
  • Sapphire substrates are commercially available in high purity and in a variety of thicknesses and shapes.
  • the support need only have sufficient thickness such as 0.1 millimeters to provide a mechanically strong substrate.
  • Substrates having thicknesses above 1.0 millimeters would usually not be utilized since they add cost and weight to the device without providing any other benefit.
  • the buffer layer is an epitaxial layer having suffi- cient thickness such that the growth of HTSC film is influ ⁇ enced solely by the buffer layer and not by the sapphire substrate.
  • the buffer layer can have a minimum thickness of a monolayer or less. However, it is preferred that the buffer layer cover the sapphire surface and any anomalies on the surface and suitably has a thickness of at least 50 Angstroms. Thicknesses above about 3000 Angstroms are un ⁇ necessary and may interfere with the microwave device.
  • the buffer can be formed from crystalline materials having a close epitaxial match to the HTSC material such as stron- tiu .
  • Stron ⁇ tium titanate and calcium titanate are preferred since it appears that they form the best HTSC films.
  • the thin layer of buffer is formed by deposition in a chamber having a high percentage, usually from 10 to 100% of oxygen.
  • the pres ⁇ sure in the chamber is higher than practiced in the elec- tron beam deposition process and in other deposition pro ⁇ Deposition.
  • the pressure in the chamber is at least 40 m Torr and can be as high as 10 Torr, usually about 100 to 500 m Torr.
  • the buffer layer may be formed by a variety of vapor deposition techniques such as on- or off-axis sputtering, metallo-organic vapor deposition (MOCVD) or laser ablation. Laser ablation is preferred since it appears to pro ⁇ vide a buffer layer that provides the highest quality HTSC films. This may be due to several factors.
  • Laser ablation is conducted at a fairly high pressure.
  • the deposition chamber contains from 20 to 100% oxygen at a pressure typi ⁇ cally from 100 Torr up to several Torr.
  • the higher oxy ⁇ gen pressure could provide a more stable, more perfect crystalline epitaxial layer.
  • Laser ablation generates its own plasma.
  • the charged ionic species may assemble into a more ordered crystal form.
  • the laser is pulsed during las ⁇ er ablation. During the non-pulsed period the growing crystal can relax to allow the metal and oxygen atoms to assume their positions in the crystal lattice of strontium titanate or calcium titanate.
  • the HTSC film is preferably grown by off-axis sputter ⁇ ing, laser ablation or MOCVD. Any of these procedures can be used to form the buffer layer.
  • a common chamber can be used to form the buffer layer and HTSC film by two consecu- tive laser-ablation depositions or two consecutive off-axis sputtering depositions.
  • the sapphire substrate or the buffer layer coated sapphire substrate is placed on a heat ⁇ ed substrate holder in a sputtering chamber at an angle of at least 40°, usually 90°, from the sputtering source.
  • the substrate is heated to a temperature of from about 650 K to 800 K.
  • the chamber contains from 10-50% of an oxidizing gas such as oxygen or nitrous oxide.
  • the vapor source is a composite ceramic in the correct stoichiometric ratio for the film such as a Y_,Ba 2 Cu 3 alloy or a SrTi0 3 crystal or pressed powder source.
  • Deposition is usually conducted over several hours at a high pressure between 100 and 500 Torr.
  • a post deposition treatment in oxygen at a tempera ⁇ ture from 400 K to 600 K can be conducted in case of the HTSC film.
  • the films of high critical temperature (T c ) supercon- ducting materials (HTSC) prepared in the present invention are mixed metal cuprates or mixed metal bismuthates having a T c above about 30 K, usually above 70 K which belong to four families: the rare earth cuprates, the thallium-based cuprates, the bismuth-based cuprates and the alkaline earth bismuthates.
  • the HTSC materials have an ordered lattice and are usually crystalline ceramics of the general formula
  • M 1 is a Group IIIA metal, Group IIIB metal, Group VB or a rare earth metal
  • M 2 is a Group IIA metal
  • x, y, z and n are integers.
  • the ratio of y:x is about 2:1 and the ratio of z:x is at least 3 usually from 3:1 to 6:1.
  • the oxygen is present in an amount to satisfy valency of the metals and n is usually no more than 20, typically about 5-15.
  • M 1 can be a Group IIIA metal such as Yttrium (Y) or lanthanum (La) , a Group IIIB metal such as Thallium (Tl) , or Group VB metal such as Bismuth (Bi) or a rare earth met ⁇ al such as Erbium (Er) , Cerium (Ce) , Praseodymium (Pr) , Samarium (Sm) , Europium (Eu) , Gadolinium (Gd) , Terbium (Tb) , Dysprosium (Dy) , Holmium (Ho) , Ytterbium(Yb) , Lute- tiu (Lu) or combinations of these metals.
  • M 2 is a Group IIA metal such as strontium, barium, calcium or mixtures thereof.
  • Both laser ablation and off-axis sputtering techniques were utilized in growing low surface resistance "123" films on A1 2 0 3 with SrTi0 3 buffer layers.
  • laser ablation about 1.8 Joule/cm 2 energy density of 248 nm wave ⁇ length pulsed excimer laser beam was focused on a SrTi0 3 or an "123" pellet.
  • Other deposition parameters were 200 m Torr of oxygen pressure and 750 C substrate temperature.
  • two sputtering guns were mounted face to face and the substrates were glued on a heater that faces perpendicular to the both SrTi0 3 and "123" targets.
  • Oxygen pressure of 40 m Torr and Argon pressure of 160 m Torr were used at the substrate temperature of 740 C.
  • Figure 2 shows the temperature dependence of surface resistance R s of the "123" films grown on SrTi0 3 buffer lay ⁇ ers on Al 2 0 3 (1102) substrates.
  • the circles denote the data on a pair of films made by laser ablation and the crosses represent the data on films grown by the off-axis sputter ⁇ ing technique. They have a residual resistance of about 65 ⁇ at low temperature and about 800 ⁇ at 77 K at 10 GHz.
  • the actual resonance frequency (w) was about 11 GHz and the usual R hinder(w) ⁇ w 2 relation was used to scale back to 10 GHz.
  • These surface resistance values are compared to those of Cu at 77 K and Nb at 7.7 K in Figure 3.
  • the resistance range 65 to 200 ⁇ between 10 K and 50 K is lower than the
  • Nb 7.7 K value at 10 GHz The 800 ⁇ at 77 K is also at least a factor 10 better than that of Cu at 77 K.
  • x-ray diffraction data of a c-axis scan and a ⁇ scan of the (103) peak are shown in Figures. 4a and 4b.
  • the c-axis scan shows that the samples are well aligned in the c-axis direction.
  • the existence of (200) peaks means that there are some a-axis oriented grains in the sample.
  • a SEM (Scanning Electron Microscope) image reveals that these a-axis oriented grains reside on the surface mostly as isolated grains.
  • the rocking curve of the (005) peak is about 2.4 degree wide, which is not much different from the epitaxial "123" films on bare sap ⁇ phire.
  • the big diff rence in microstructure between epitaxial "123" thin films with SrTi0 3 buffer layer and films without SrTi0 3 buffer layer can be found in the ⁇ -scan of (103) peak in Figure 4b.
  • the sharp peaks every 90 degree means that the a-axis and b-axis are also aligned in the sapphire plane (1102).
  • the full width at half maximum, ⁇ , of the peaks in the ⁇ -scan is about 3.8 degree.
  • ⁇ of good epitaxial films on MgO, SrTi0 3 is about 1.5 de- gree.
  • these peaks do not have the shoulders.
  • the "123" films with a SrTi0 3 buffer layer have better in-plane epitaxy than those without a SrTi0 3 buffer layer. It is known that the I-V characteristics of the grain boundary of two misaligned grains have Josephson junction behavior. It was further found by a weakly coupled grain model that these grain boundaries lead to higher surface resistance as well as longer penetration depth. Improved in-plane epitaxy can be interpreted as reduction of grain boundaries, which results in lower surface resistance.
  • Strontium titanate has some reactivity with the compo ⁇ nents of the growing HTSC film limiting the temperature that can be used during growth of the HTSC film to about 760°C. High quality HTSC film can be grown at higher tem ⁇ perature.
  • strontium titanate has a lattice spacing of about 3.92 Angstroms which is close to the approximate 3.9 Angstroms lattice spacing of YBa 2 Cu 3 0 7 . x , it is far from the lattice spacing of sapphire (about 3.5 Angstroms). This lattice mismatch can cause some grains to grow in undesired directions.
  • Strontium titanate buffers are usually deposited in a thickness of at least 100 Angstroms which increases micro- wave losses and is not conducive to the formation of the smoothest HTSC films.
  • the calcium titanate can be a bulk substrate or a thin buf- fer film or a substrate of different composition such as silicon or sapphire.
  • Calcium titanate has a lattice spacing of about 3.82 Angstroms which is intermediate to the lattice spacing of YBa 2 Cu 3 0 7 . ⁇ ( ⁇ 3.9 Angstroms) and sapphire ( ⁇ 3.5 Angstroms). Calcium titanate films can be grown with less strain. Thinner films have less dislocations and crystal defects. Epitaxial films of calcium titanate which are 100 Angstroms in thickness or less provide excellent substrates for grow ⁇ ing thin HTSC films. Thinner buffer films provide lower microwave losses.
  • the deposition temper ⁇ ature can be substantially higher, e.g. about 800°C which contributes to the quality and performance of the HTSC film.
  • Preliminary measurements indicate that the critical current density of the HTSC film are about 2 times better than comparable films grown on strontium titanate buffer films on sapphire.
  • Figure 6 illustrates the data from 3 different meas ⁇ urements of the surface resistance of 500 Angstrom thick 123 YBCO films grown on 100 Angstrom thick CaTi ⁇ 3 buffer layers. The surface resistivity was scaled to 10 GHz.

Abstract

High temperature superconducting layered structures for use in microwave applications are fabricated by depositing a thin film of epitaxial buffer (14) such as strontium titanate or calcium titanate by a deposition process such as laser ablation on a low loss sapphire substrate (12) followed by depositing an in-situ grown film of high temperature superconductor (16) such as Y1Ba2Cu3O7 on the buffer layer. The YBCO film has low surface resistance and a narrow transition temperature.

Description

DESCRIPTION
HIGH TEMPERATURE SUPERCONDUCTING FILMS ON ALUMINUM OXIDE SUBSTRATES
Cross Reference To Related Applications
This application is a continuation-in-part of Serial Number 494,730 filed March 16, 1990, Serial Number 495,568 filed March 16, 1990 and Serial Number 565,691 filed August 13, 1990.
Technical Field
This invention relates to high critical temperature superconducting (HTSC) films and, more particularly, this invention relates to the preparation of HTSC films on sap¬ phire (aluminum oxide) substrates by the use of stable, epitaxial buffer layers.
Background of the Invention The recent discovery of high critical temperature superconducting materials has created interest in the use of these materials in microwave devices. The HTSC metal cuprate materials cannot readily be produced in bulk with geometries and properties suitable for microwave devices. Presently, devices based on the HTSC materials are fabri¬ cated by formation of thin films on substrates by tech¬ niques similar to those used to fabricate semiconductor devices. To be useful in a microwave device the HTSC film must be grown on a substrate having low dielectric losses at high frequencies.
Silicon, a readily used substrate for semiconductor devices, cannot be used with the HTSC cuprate materials since at the temperature prevalent during deposition the cuprate reactants readily react with silicon. Sapphire (Al203) would appear to be an excellent substrate since it has a very low dielectric loss and is a strong, low cost, highly crystalline material available commercially in large sizes. Sapphire would be a good substrate for bolometer
(infrared detector) applications since thin films of sap- phire have low heat capacity. Epitaxial films of a HTSC material such as YBa2Cu307 can be grown on sapphire substrat¬ es. However, the optimum window of substrate temperatures during film deposition is relatively narrow [4], At high temperatures above about 700 K, the YBa2Cu307 thin film reacts with the sapphire, especially the Ba atoms. At low temperature, below about 650 K, it is very difficult to produce thin YBa2Cu307 films having good epitaxy.
There are other substrate materials that provide epi¬ taxial growth of thin HTSC films with high superconducting transition temperatures and low rf surface resistance, such as strontium titanate (SrTi03) , calcium titanate (CaTi03) , lanthanum alu inate (LaAlO-) , magnesium oxide (MgO) and yttria stabilized zirconia (YSZ) . However, thick substrat¬ es of some of these materials, e.g. strontium or calcium titanate, exhibit too high an rf loss or do not have high enough strength to act as a substrate for large area micro¬ wave devices. Some of these materials are only available in small sizes and/or at very high cost.
However, thin epitaxial films of these materials ex- hibit a low dielectric loss and would be useful as a buffer layer between the HTSC film and the sapphire substrate if they provided an epitaxial surface for the HTSC film and were stable and non-reactive with the HTSC film and the substrate.
List of References
1. Multilayer YBa2Cu3Oχ - SrTi03 - YBa2Cu3Oχ Films For Insulating Crossovers, Kingston et al., Applied Phys¬ ics Letters, January 8, 1990.
I . YBa2Cu30_ Films Grown on Epitaxial MgO Buffer Layers on Sapphire, Talvacchio et al., Proceedings M2S-HTSC, Stanford, July 1989, Physica. 3. The Sputter Deposition and Characterization of Epitax¬ ial Magnesium Oxide Thin Films and Their Use as a Sap¬ phire/ YBCO Buffer Layer, Morris et al., Proc. M.A.S. Vol 169, 1990. 4. Properties of Epitaxial YBa2Cu307 Thin Films on A1203 {1012}, Char et al., Appl. Phys. Lett. 56(8) 19 Feb 1990, p.785-787. Statement of the Prior Art
Kingston et al. [1] disclose the use of SrTi03 as an insulating layer between two YB2Cu3Oχ films, one of which was deposited on an MgO substrate. MgO is not the best sub¬ strate for microwave applications due to its high dielec¬ tric loss. MgO does not provide a fully compatible lattice match with HTSC films such as YBa2Cu307 and polished MgO surfaces degrade in air with humidity. Talvacchio et al. [2] grew YBa2Cu307 films on epitaxial MgO buffer layers on sapphire. This layered structure failed as a microwave device since the MgO was excessively moisture sensitive. The HTSC film did not have sufficient orientation and there were too many random grains. Morris et al. [3] formed an MgO buffer layer by sputter deposition at 5.5 to 7 Pa (about 40-50 m Torr) a fairly low pressure. The resulting YBCO film grown on the epitaxial MgO has high normal state resistance and a broad superconducting transition.
Statement of the Invention
The invention provides a HTSC buffer layered structure on sapphire that is stable and suitable for microwave en¬ vironments or for use in the fabrication of bolometers. The layered structure with a thin SrTi03 or CaTi03 buffer layer has a sharp transition and good thermal response, making it suitable for bolometer applications. The HTSC film can be grown over a wide temperature range without the HTSC reacting with the sapphire substrate or the buffer reacting with the substrate or the HTSC film. The layered structures of the invention provides the highest microwave performance of any sapphire supported HTSC film reported to date. Others have reported surface resistance measuring on a par with copper. The layered sapphire supported HTSC structure of the invention exhibits rf surface resistance 2 to 3 times better than copper at 10 GHz and 77 K and much better than copper at lower temperatures. The YBCO films grown on the buffer layer exhibit low normal state resist- ance and a narrow superconducting transition.
The buffer layer in the HTSC structure of the inven¬ tion is grown in a high pressure process such as laser ab¬ lation, sputtering or metallo-organic compound vapor depo- sition (MOCVD) . Talvacchio et al. [2] used electron beam deposition of the MgO film. Electron beam epitaxial depo¬ sition is conducted at relatively high vacuum, about 10"5 Torr. The low partial pressure of oxygen is believed to result in an oxygen deficient buffer layer film. These films are chemically active and react with water which de¬ grades the quality of the overlying HTSC film. The buffer layer in the process of the invention is deposited at high¬ er pressure which results in inert buffer layers with good epitaxial qualities. The SrTi03 and CaTi03 buffer layers are excellent intermediate substrates for forming high per¬ formance, stable HTSC films.
These and many other objects and attendant advantages of the invention will become apparent as the invention be¬ comes better understood by reference to the following and detailed descriptions when considered in conjunction with the accompanying drawings.
Brief Description of the Drawings
Figure 1 is a schematic drawing of a layered HTSC-Buf- fer-Sapphire structure produced according to the process of this invention;
Figure 2 is a series of curves showing Surface Resis¬ tance, Rs of epitaxial YBa2Cu307 films as a function of tem¬ perature at 10 GHz; Figure 3 is a series of plots of Surface Resistance, Rs vs. frequency with Cu data at 77 K and Nb data at 7.7 K;
Figure 4(a) is a c-axis scan of the YBa2Cu307 film;
Figure 4(b) is a ø-axis scan of the [103] peak of the YBa2Cu307 film; Figure 5(a) is the mutual inductance response of the YBa2Cu307 film at 1 A;
Figure 5(b) is the mutual inductance response of the YBa2Cu307 film at 100 mA; and
Figure 6 is a graph of surface resistivity, Rs versus temperature.
Detailed Description of the Invention
Referring now to Figure 1, the layered structure 10 is composed of a sapphire base or substrate 12, a thin buffer layer 14 and a HTSC layer 16. The buffer layer 14 and the HTSC layer 16 may be laid down in a pattern to form a de- vice by use of a mask formed by conventional lithographic techniques or by use of shutters or shields.
Sapphire substrates are commercially available in high purity and in a variety of thicknesses and shapes. The support need only have sufficient thickness such as 0.1 millimeters to provide a mechanically strong substrate. Substrates having thicknesses above 1.0 millimeters would usually not be utilized since they add cost and weight to the device without providing any other benefit.
The buffer layer is an epitaxial layer having suffi- cient thickness such that the growth of HTSC film is influ¬ enced solely by the buffer layer and not by the sapphire substrate. The buffer layer can have a minimum thickness of a monolayer or less. However, it is preferred that the buffer layer cover the sapphire surface and any anomalies on the surface and suitably has a thickness of at least 50 Angstroms. Thicknesses above about 3000 Angstroms are un¬ necessary and may interfere with the microwave device. The buffer can be formed from crystalline materials having a close epitaxial match to the HTSC material such as stron- tiu . titanate, calcium titanate, lanthanum alu inate, mag¬ nesium oxide or yttrium stabilized zirconia (YSZ) . Stron¬ tium titanate and calcium titanate are preferred since it appears that they form the best HTSC films.
In the process of the invention, the thin layer of buffer is formed by deposition in a chamber having a high percentage, usually from 10 to 100% of oxygen. The pres¬ sure in the chamber is higher than practiced in the elec- tron beam deposition process and in other deposition pro¬ cesses. The pressure in the chamber is at least 40 m Torr and can be as high as 10 Torr, usually about 100 to 500 m Torr. The buffer layer may be formed by a variety of vapor deposition techniques such as on- or off-axis sputtering, metallo-organic vapor deposition (MOCVD) or laser ablation. Laser ablation is preferred since it appears to pro¬ vide a buffer layer that provides the highest quality HTSC films. This may be due to several factors. Laser ablation is conducted at a fairly high pressure. The deposition chamber contains from 20 to 100% oxygen at a pressure typi¬ cally from 100 Torr up to several Torr. The higher oxy¬ gen pressure could provide a more stable, more perfect crystalline epitaxial layer. Laser ablation generates its own plasma. The charged ionic species may assemble into a more ordered crystal form. The laser is pulsed during las¬ er ablation. During the non-pulsed period the growing crystal can relax to allow the metal and oxygen atoms to assume their positions in the crystal lattice of strontium titanate or calcium titanate.
The HTSC film is preferably grown by off-axis sputter¬ ing, laser ablation or MOCVD. Any of these procedures can be used to form the buffer layer. A common chamber can be used to form the buffer layer and HTSC film by two consecu- tive laser-ablation depositions or two consecutive off-axis sputtering depositions.
In off-axis sputtering the sapphire substrate or the buffer layer coated sapphire substrate is placed on a heat¬ ed substrate holder in a sputtering chamber at an angle of at least 40°, usually 90°, from the sputtering source. The substrate is heated to a temperature of from about 650 K to 800 K. The chamber contains from 10-50% of an oxidizing gas such as oxygen or nitrous oxide. The vapor source is a composite ceramic in the correct stoichiometric ratio for the film such as a Y_,Ba2Cu3 alloy or a SrTi03 crystal or pressed powder source. Deposition is usually conducted over several hours at a high pressure between 100 and 500 Torr. A post deposition treatment in oxygen at a tempera¬ ture from 400 K to 600 K can be conducted in case of the HTSC film.
The films of high critical temperature (Tc) supercon- ducting materials (HTSC) prepared in the present invention are mixed metal cuprates or mixed metal bismuthates having a Tc above about 30 K, usually above 70 K which belong to four families: the rare earth cuprates, the thallium-based cuprates, the bismuth-based cuprates and the alkaline earth bismuthates. The HTSC materials have an ordered lattice and are usually crystalline ceramics of the general formula
M"x1My2CuzOn where M1 is a Group IIIA metal, Group IIIB metal, Group VB or a rare earth metal, M2 is a Group IIA metal and x, y, z and n are integers. Usually the ratio of y:x is about 2:1 and the ratio of z:x is at least 3 usually from 3:1 to 6:1. The oxygen is present in an amount to satisfy valency of the metals and n is usually no more than 20, typically about 5-15. M1 can be a Group IIIA metal such as Yttrium (Y) or lanthanum (La) , a Group IIIB metal such as Thallium (Tl) , or Group VB metal such as Bismuth (Bi) or a rare earth met¬ al such as Erbium (Er) , Cerium (Ce) , Praseodymium (Pr) , Samarium (Sm) , Europium (Eu) , Gadolinium (Gd) , Terbium (Tb) , Dysprosium (Dy) , Holmium (Ho) , Ytterbium(Yb) , Lute- tiu (Lu) or combinations of these metals. M2 is a Group IIA metal such as strontium, barium, calcium or mixtures thereof.
The examples of practice of the invention will be di- rected to the YBaCuO materials of the general formula Y.,Ba2
Cu307, but the invention is equally applicable to other HTSC materials of the cuprate family or bismuthate family such as the bismuth cuprate of the general formula BiSrCaCuO or the thallium cuprate of the general formula TlBaCaCuO. The invention will now be illustrated by specific ex¬ amples. 500 Angstrom thick films of YBa2Cu307 (123) were grown on 500 Angstrom thick buffer layers of SrTiO- or CaTi03. The structural and electrical properties are char¬ acterized by x-ray diffraction data, SEM images and AC mu¬ tual inductance responses.
Both laser ablation and off-axis sputtering techniques were utilized in growing low surface resistance "123" films on A1203 with SrTi03 buffer layers. In the case of laser ablation about 1.8 Joule/cm2 energy density of 248 nm wave¬ length pulsed excimer laser beam was focused on a SrTi03 or an "123" pellet. Other deposition parameters were 200 m Torr of oxygen pressure and 750 C substrate temperature. In the case of off-axis sputtering two sputtering guns were mounted face to face and the substrates were glued on a heater that faces perpendicular to the both SrTi03 and "123" targets. Oxygen pressure of 40 m Torr and Argon pressure of 160 m Torr were used at the substrate temperature of 740 C.
In order to measure surface resistance at microwave frequency a parallel plate resonator was formed by sand¬ wiching two 1 cm by 1 cm "123" thin films face to face with a 12.5 thick Teflon dielectric in between. This resona¬ tor generates a series of transverse electromagnetic modes. The advantage of this method is that the current and field distribution can be calculated and the relation between the measured Q factor and the surface resistance Rs can be de- duced in a straightforward fashion. This method has been successfully used to measure 20μΩ for Nb films at 4.2 K at 10 GHz. The resolution of this method is about 5 μΩat 10 GHz.
Figure 2 shows the temperature dependence of surface resistance Rs of the "123" films grown on SrTi03 buffer lay¬ ers on Al203(1102) substrates. The circles denote the data on a pair of films made by laser ablation and the crosses represent the data on films grown by the off-axis sputter¬ ing technique. They have a residual resistance of about 65 μΩ at low temperature and about 800 μΩ at 77 K at 10 GHz. The actual resonance frequency (w) was about 11 GHz and the usual R„(w)∞ w2 relation was used to scale back to 10 GHz. These surface resistance values are compared to those of Cu at 77 K and Nb at 7.7 K in Figure 3. The resistance range 65 to 200 μΩ between 10 K and 50 K is lower than the
Nb 7.7 K value at 10 GHz. The 800 μΩ at 77 K is also at least a factor 10 better than that of Cu at 77 K.
For structural information x-ray diffraction data of a c-axis scan and a ø scan of the (103) peak are shown in Figures. 4a and 4b. The c-axis scan shows that the samples are well aligned in the c-axis direction. The existence of (200) peaks means that there are some a-axis oriented grains in the sample. A SEM (Scanning Electron Microscope) image reveals that these a-axis oriented grains reside on the surface mostly as isolated grains. The rocking curve of the (005) peak is about 2.4 degree wide, which is not much different from the epitaxial "123" films on bare sap¬ phire.
The big diff rence in microstructure between epitaxial "123" thin films with SrTi03 buffer layer and films without SrTi03 buffer layer can be found in the ø-scan of (103) peak in Figure 4b. The sharp peaks every 90 degree means that the a-axis and b-axis are also aligned in the sapphire plane (1102). The full width at half maximum, φ, of the peaks in the ø-scan is about 3.8 degree. In comparison, ø of good epitaxial films on MgO, SrTi03 is about 1.5 de- gree. However, unlike the data of the "123" thin films on bare sapphire [4] , these peaks do not have the shoulders. In other words, the "123" films with a SrTi03 buffer layer have better in-plane epitaxy than those without a SrTi03 buffer layer. It is known that the I-V characteristics of the grain boundary of two misaligned grains have Josephson junction behavior. It was further found by a weakly coupled grain model that these grain boundaries lead to higher surface resistance as well as longer penetration depth. Improved in-plane epitaxy can be interpreted as reduction of grain boundaries, which results in lower surface resistance.
The mutual inductance response of a film as a function of temperature is shown in Figures 5a and 5b. It was mea¬ sured at 1 kHz with a maximum magnetic field- of 0.6 Gauss on the film surface. The 86.5 K, where the mutual induc¬ tance transition starts, is in good agreement with the tem- perature where the dc resistivity goes to zero.
Low surface resistance 65 μΩ at 4.2 K and 800 μΩ at 77 K at 10 GHz were exhibited by the epitaxial YBa2Cu307 films on 500 A thick buffer layers of SrTi03 on A1203 {1102} sub¬ strates. Improved microwave surface resistance data are believed to be the results of better in-plane epitaxy due to the presence of the SrTi03 buffer layer.
Strontium titanate has some reactivity with the compo¬ nents of the growing HTSC film limiting the temperature that can be used during growth of the HTSC film to about 760°C. High quality HTSC film can be grown at higher tem¬ perature.
Though strontium titanate has a lattice spacing of about 3.92 Angstroms which is close to the approximate 3.9 Angstroms lattice spacing of YBa2Cu307.x, it is far from the lattice spacing of sapphire (about 3.5 Angstroms). This lattice mismatch can cause some grains to grow in undesired directions.
Strontium titanate buffers are usually deposited in a thickness of at least 100 Angstroms which increases micro- wave losses and is not conducive to the formation of the smoothest HTSC films.
Higher quality HTSC thin films are produced in accor¬ dance with the invention on calcium titanate substrates. The calcium titanate can be a bulk substrate or a thin buf- fer film or a substrate of different composition such as silicon or sapphire.
Calcium titanate has a lattice spacing of about 3.82 Angstroms which is intermediate to the lattice spacing of YBa2Cu307.χ (~ 3.9 Angstroms) and sapphire (~ 3.5 Angstroms). Calcium titanate films can be grown with less strain. Thinner films have less dislocations and crystal defects. Epitaxial films of calcium titanate which are 100 Angstroms in thickness or less provide excellent substrates for grow¬ ing thin HTSC films. Thinner buffer films provide lower microwave losses.
Furthermore, since calcium titanate is less reactive with the ions forming the HTSC film, the deposition temper¬ ature can be substantially higher, e.g. about 800°C which contributes to the quality and performance of the HTSC film. Preliminary measurements indicate that the critical current density of the HTSC film are about 2 times better than comparable films grown on strontium titanate buffer films on sapphire.
Figure 6 illustrates the data from 3 different meas¬ urements of the surface resistance of 500 Angstrom thick 123 YBCO films grown on 100 Angstrom thick CaTiθ3 buffer layers. The surface resistivity was scaled to 10 GHz.
In a measurement of x-ray scattering, it was found that the full width at half maximum, ø, of the peaks in the ø-scan is about 3.8 degree. In comparison, ø of good epi¬ taxial films on MgO or SrTi03 is about 1.5 degree. However, unlike the data of the "123" thin films on bar sapphire [4], these peaks do not have the shoulders. In other words, the "123" films with a CaTi03 or SrTi03 buffer layer have better in-plane epitaxy than those without a CaTi03 or SrTi03 buffer layer. It is known that the I-V characteristics of the grain boundary of two misaligned grains have Josephson junction behavior. It was further found by a weakly coupled grain model that these grain boundaries lead to higher surface resistance as well as longer penetration depth. Improved in-plane epitaxy can be interpreted as reduction of grain boundaries, which results in lower surface resistance.
The mutual inductance response of a film as a function of temperature was measured at 1 kHz with a maximum magnet¬ ic field of 0.6 Gauss on the film surface. At 86.5 K, the temperature where the mutual inductance transition starts, is in good agreement with the temperature where the dc re¬ sistivity goes to zero. Improved microwave surface resistance data and criti¬ cal current density are believed to be the results of bet¬ ter in-plane epitaxy due to the use of the CaTi03 buffer layer. It is to be realized that only preferred embodiments of the invention have been described and that numerous sub¬ stitutions, modifications and alterations are permissible without departing from the spirit and scope of the inven¬ tion as defined in the following claims.

Claims

WHAT IS CLAIMED IS:
1. A superconducting structure comprising: a sapphire substrate; a thin buffer layer of strontium titanate or cal¬ cium titanate deposited on a surface of the substrate; and a thin film of high temperature superconductor deposited on a surface of the buffer layer.
2. A structure according to claim 1 in which the film is in the form of a pattern.
3. A structure according to claim 2 in which the buffer layer has a thickness of at least 50 Angstroms.
4. A structure according to claim 3 in which the film has a thickness of at least 100 Angstroms.
5. A structure according to claim 4 in which the superconductor is a mixed metal cuprate or bismuthate.
6. A structure according to claim 5 in which the superconductor is Y1Ba2Cu307.
7. A superconducting structure comprising a thin film of high temperature superconductor deposited on the surface of calcium titanate.
8. A structure according to claim 7 in which the calcium titanate is a bulk substrate.
9. A structure according to claim 7 in which the calcium titanate is a thin buffer deposited on a substrate.
10. A structure according to claim 9 in which the substrate has low dielectric loss.
11. A structure according to claim 10 in which the substrate is sapphire.
12. A method of fabricating a high temperature super¬ conducting device comprising the steps of: depositing an epitaxial buffer layer of strontium titanate or calcium titanate on a sapphire substrate; and growing a film of high temperature superconductor on the surface of the buffer layer.
13. A method according to claim 12 in which the depo¬ sition is effected by laser ablation or off-axis sputter¬ ing.
14. A method according to claim 12 in which the depo¬ sition is conducted in an oxidizing atmospher at a pressure of at least 40 m Torr.
15. A method according to claim 12 in which the superconductor is a mixed metal cuprate or bismuthate.
16. A method according to claim 15 in which the superconductor is Y1Ba2Cu307.
17. A device produced by the method of claim 12.
18. A device according to claim 17 in which the buf¬ fer is strontium titanate or calcium titanate, the sub¬ strate is sapphire and the film is Y_,Ba2Cu307.
PCT/US1991/001788 1990-03-16 1991-03-18 High temperature superconducting films on aluminum oxide substrates WO1991014028A1 (en)

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US07/495,568 US5132282A (en) 1990-03-16 1990-03-16 High temperature superconductor-strontium titanate sapphire structures
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US495,568 1990-03-16
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EP0610175A1 (en) 1994-08-17
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