JPH0469984A - superconducting element - Google Patents
superconducting elementInfo
- Publication number
- JPH0469984A JPH0469984A JP2182105A JP18210590A JPH0469984A JP H0469984 A JPH0469984 A JP H0469984A JP 2182105 A JP2182105 A JP 2182105A JP 18210590 A JP18210590 A JP 18210590A JP H0469984 A JPH0469984 A JP H0469984A
- Authority
- JP
- Japan
- Prior art keywords
- microfabrication
- superconducting
- deposited
- film
- thin film
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 239000010409 thin film Substances 0.000 claims abstract description 16
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 6
- 238000011065 in-situ storage Methods 0.000 claims description 5
- 239000010408 film Substances 0.000 abstract description 16
- 239000000758 substrate Substances 0.000 abstract description 13
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 abstract description 3
- 150000002500 ions Chemical class 0.000 abstract description 3
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052788 barium Inorganic materials 0.000 abstract description 2
- 150000002739 metals Chemical class 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 229910052727 yttrium Inorganic materials 0.000 abstract description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 230000010354 integration Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 description 10
- 239000013078 crystal Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000001451 molecular beam epitaxy Methods 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 239000002887 superconductor Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000005669 field effect Effects 0.000 description 3
- 238000005468 ion implantation Methods 0.000 description 3
- 239000010955 niobium Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000000059 patterning Methods 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- -1 niobium ions Chemical class 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910021478 group 5 element Inorganic materials 0.000 description 1
- 238000010329 laser etching Methods 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Landscapes
- Superconductor Devices And Manufacturing Methods Thereof (AREA)
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、超伝導素子に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to superconducting devices.
高集積化した超伝導素子を作製するためには半導体素子
と同様に必ずといってよいほど微細加工技術が必要とな
る。In order to fabricate highly integrated superconducting devices, microfabrication technology is almost always required, just as in the case of semiconductor devices.
従来の酸化物超伝導素子作製のだめの微細加工は、成膜
と微細加工が独立して行なわれている。In the conventional microfabrication process for producing oxide superconducting elements, film formation and microfabrication are performed independently.
すなわち−層成膜することに成膜竣から取り出して微細
加工している。例えば「電子情報通信学会技術研究報告
」、第88巻 第146号、1988年 47〜52頁
に記載されているような酸化物超伝導トランジスタの作
製では超伝導薄膜を形成し成膜室から取り出して微細加
工して、その上にソース及びドレイン電極型成のためA
gを蒸着し再び取り出して微細加工する。さらに、ゲー
ト電極形成のためAlを蒸着し取り出して微細加工して
いる。That is, after the layer is formed, the film is taken out from the completed film and subjected to microfabrication. For example, in the fabrication of oxide superconducting transistors as described in "IEICE Technical Research Report", Vol. 88, No. 146, 1988, pages 47-52, a superconducting thin film is formed and removed from the film forming chamber. microfabricated using A, and then A for forming source and drain electrodes on top of it.
g is vapor-deposited, taken out again, and microfabricated. Further, to form a gate electrode, Al is deposited and taken out for fine processing.
また、酸化物超伝導薄膜−層の微細加工技術は超伝導薄
膜形成後成膜室から膜を外に取り出し、例えば「JAp
ANEsEJOURNAL OF A、PPL工EDF
HYS工O3J、第26巻 第9号、1987年L15
55〜L1534頁に記載されているような燐酸(H,
P 04−)溶液を用いたウェット・プロセス、あるい
は「JAPANKSE JOURNAL 0FAPPL
工ED PEYSICsJ、第27巻 第8号、198
8年 L1521〜L1525頁に記載さレテいるよう
なイオンビームエツチング(以下よりEと略記する。)
によるドライプロセスにより微細加工されている。ウェ
ットプロセスではH5po4の他に塩酸(HC工)、硝
酸(uNp3)、硫酸(HzSO+) 溶液等が用い
られており、ドライプロセスではよりEのほかにイオン
注入。In addition, microfabrication technology for oxide superconducting thin film layers involves taking the film out of the deposition chamber after forming the superconducting thin film, for example, "JAp
ANEsEJOURNAL OF A, PPL Engineering EDF
HYS Engineering O3J, Volume 26, No. 9, 1987 L15
Phosphoric acid (H,
P 04-) Wet process using solution or “JAPANKSE JOURNAL 0FAPPL
Engineering ED PEYSICsJ, Volume 27, No. 8, 198
Ion beam etching as described on pages L1521 to L1525 (hereinafter abbreviated as E)
Microfabricated using a dry process. In the wet process, in addition to H5po4, hydrochloric acid (HC engineering), nitric acid (uNp3), sulfuric acid (HzSO+) solutions, etc. are used, and in the dry process, in addition to E, ion implantation is used.
レーザーエツチング、反応性イオンエツチング(R工E
)、集束イオンビームエツチング(VよりE)等が用い
られている。Laser etching, reactive ion etching (RE
), focused ion beam etching (from V to E), etc. are used.
しかしながら前述のよ5な従来の酸化物超伝導電子作製
のための微細加工は、−層ごと成膜しその度取り出して
行なうので工程が複雑になる。さらに大気にさらすこと
により膜の表面が汚染されると同時に、酸化物超伝導体
は水分に敏感でありわずかな水分によっても特性が劣化
してしまい、特に微細加工後は表面積も増大するのでそ
の影響は著しい。従って、再現性及び歩留まりが悪(な
るという問題点を有する。However, in the conventional microfabrication for fabricating oxide superconducting electrons as described above, each layer is deposited and removed each time, making the process complicated. Furthermore, exposure to the atmosphere contaminates the surface of the film, and at the same time, oxide superconductors are sensitive to moisture, and even a small amount of moisture can cause their properties to deteriorate, especially after microfabrication, as the surface area increases. The impact is significant. Therefore, there is a problem that reproducibility and yield are poor.
酸化物超伝導薄膜の微細加工について見ると、イオン注
入及びFよりEは前述の他の方法と違いパターニング・
マスクを必要としないので、レジストによる膜表面への
汚染が無い点で有利であるまた、F工EE、イオン注入
においてはサブミクロンオーダーの微細化が可能であり
、高集積化した素子を帰ることが出来る。しかし、レジ
ストによる汚染が防げても成膜後大気にさらし微細加工
する場合、上述したように大気により表面が汚染され水
分により特性が劣化する恐れがある。従って安定した再
現性および歩留まりを得るという点で問題がある。Regarding microfabrication of oxide superconducting thin films, unlike the other methods mentioned above, ion implantation and F to E require patterning and
Since it does not require a mask, it is advantageous in that there is no contamination of the film surface by the resist.Furthermore, it is possible to miniaturize to the submicron order in F/EE and ion implantation, making it possible to return highly integrated elements. I can do it. However, even if contamination by the resist can be prevented, if the film is exposed to the atmosphere for microfabrication after film formation, the surface may be contaminated by the atmosphere and the characteristics may deteriorate due to moisture, as described above. Therefore, there is a problem in obtaining stable reproducibility and yield.
そこで本発明はこのような従来の問題点を解決するもの
で、その目的とするところは薄膜形成後膜を大気にさら
すことなくその場微細加工し、これを繰り返すことによ
って歩留まりを向上させさらに再現性のよい高集積化し
た酸化物超伝導素子を提供することにある。Therefore, the present invention is intended to solve these conventional problems.The purpose of the present invention is to perform microfabrication on the spot after forming a thin film without exposing it to the atmosphere, and to repeat this process to improve yield and further reproducibility. The object of the present invention is to provide a highly integrated oxide superconducting element with good performance.
本発明の超伝導素子は、酸化物超伝導薄膜を大気にさら
すことな(連続的にその場微細加工して作製する超伝導
素子において、その場微細加工は超高真空状態で行なう
集束イオンビームによることを特徴とする。The superconducting element of the present invention does not expose the oxide superconducting thin film to the atmosphere (in a superconducting element manufactured by continuous in-situ microfabrication, the in-situ microfabrication is performed using a focused ion beam in an ultra-high vacuum state). It is characterized by
以下本発明の実施例について説明する。 Examples of the present invention will be described below.
第1図は、本発明の一実施例である薄膜作製装置と微細
加工装置を搬送路50を介して複合化した装置を示す図
である。薄膜作製装置としては分子線エピタキシー(以
下MBEと略記する。)1を用い、微細加工装置として
はパターニング・マスク無しの集束イオンビーム装置2
を用いる。これは、レジストを使用しない清浄なプロセ
スであるからMBKのような高真空結晶成長技術との複
合化が容易である。また、各々の装置について真空ポン
プ3が備えられておりロードロック方式によりMBE装
置とFよりE装置を隔離し別々に真空引きすることがで
き、搬送路も真空状態に保つことが出来る。FIG. 1 is a diagram showing an apparatus in which a thin film production apparatus and a microfabrication apparatus are combined via a conveyance path 50, which is an embodiment of the present invention. Molecular beam epitaxy (hereinafter abbreviated as MBE) 1 is used as a thin film production device, and a focused ion beam device 2 without a patterning mask is used as a microfabrication device.
Use. Since this is a clean process that does not use a resist, it can be easily combined with high vacuum crystal growth techniques such as MBK. Further, each device is equipped with a vacuum pump 3, and the E device can be isolated from the MBE device and F by a load lock system and evacuated separately, and the conveyance path can also be kept in a vacuum state.
第2図にこの装置を用いて作製した一実施例であるソー
ス16とドレイン電極17を酸化物超伝導体にした超伝
導電界効果トランジスタ(以下5UFETと略記する。FIG. 2 shows an example of a superconducting field effect transistor (hereinafter abbreviated as 5UFET) in which the source 16 and drain electrode 17 are made of oxide superconductors, which is an example fabricated using this apparatus.
)の断面図を示す。第6図にその作製工程を示す。結晶
基板15は半導体であり、かつ酸化物超伝導体がエピタ
キシャル成長し易いものでなげればならない。チタン酸
ストロンチウムは酸化物超伝導体がエピタキシャル成長
し易く、ニオブ(Hb)などのV属元素を添加すること
によりn型の半導体になることが知られている。そこで
結晶基板として5rTiO,の単結晶(i oo)を用
いニオブイオン(Nb+)を注入し拡散させ半導体化さ
せる。酸化物超伝導体としては琳結晶が得やすいY B
a2 C! u30 yを用いる。) is shown. FIG. 6 shows the manufacturing process. The crystal substrate 15 must be a semiconductor and one on which an oxide superconductor can easily grow epitaxially. It is known that strontium titanate is easily epitaxially grown as an oxide superconductor, and can be turned into an n-type semiconductor by adding a group V element such as niobium (Hb). Therefore, a single crystal (IOO) of 5rTiO is used as a crystal substrate, and niobium ions (Nb+) are implanted and diffused to convert it into a semiconductor. As an oxide superconductor, Rin crystal is easily obtained YB
a2 C! Use u30y.
まず第5図(α)においてMBmチャンバー中で超伝導
薄膜20を形成する。この時、チャンバー中の初期真空
度は10−1°Torr 代である。蒸着物質として
イツトリウム(y) 1o 、バリウム(Ea)111
鋼(cu)12の金属をそれぞれ用いに−(1!eLL
により三元同時蒸着する。チャンバー中は高真空状態で
あるから酸素を効率よ(膜中に入れるため、Et?プラ
ズマ8により活性な酸素を基板付近に供給する。この時
、膜厚は1000又とする。得られる超伝導薄膜の表面
は非常になめらかであり、C軸方向にエピタキシャル成
長している。First, in FIG. 5(α), a superconducting thin film 20 is formed in an MBm chamber. At this time, the initial degree of vacuum in the chamber is around 10-1 Torr. Yttrium (y) 1o and barium (Ea) 111 as vapor deposition substances
Steel (cu) 12 metals are used for each -(1! eLL
Three-dimensional simultaneous vapor deposition is performed. Since the inside of the chamber is in a high vacuum state, oxygen is efficiently introduced into the film (in order to enter the film, active oxygen is supplied near the substrate by Et? plasma 8. At this time, the film thickness is 1000 mm). The surface of the thin film is very smooth and is grown epitaxially in the C-axis direction.
続いてMEEチャンバー中と同じ(らいの圧力まで真空
引きしであるFよりE装置中2にパルプ7を開は超伝導
薄膜を移し第5図(b)の形状に微細加工する。ここで
予めF工EE装置を真空引きしてお(ことにより、成膜
と微細加工を独立して行なう場合より時間が短縮できる
。移動は先端が基板ホルダーを挾めるような構造にしで
ある搬送用バー31を用い基板ホルダーごと行な′う。Next, the pulp 7 is evacuated to the same pressure as in the MEE chamber. The FE equipment is evacuated (this saves time compared to performing film formation and microfabrication separately. For movement, use a transport bar whose tip is structured to hold the substrate holder). 31 for each substrate holder.
この時基板を基板ホルダーごと裏返す。基板ホルダーは
MBE装置、F工EE装置両方に共通であり、かつ基板
が挾み込めるような構造にし裏返しても基板は落ちない
。搬送後はパルプ7を閉じる。At this time, turn over the board together with the board holder. The substrate holder is common to both the MBE device and the FEE device, and has a structure that allows the substrate to be held therein, so that the substrate will not fall out even if it is turned over. After conveyance, the pulp 7 is closed.
超伝導薄膜の微細加工はビームエネルギーが160Ke
VのAu+イオンを用い、ソース及びドレインの電極は
それぞれ10μm角の大きさにする当然パターニング−
貴スクは用いない。高真空中プロセスであるからAu+
イオンは安定に動作し長時間使える。The beam energy for microfabrication of superconducting thin films is 160Ke.
Using Au+ ions of V, the source and drain electrodes are each 10 μm square in size. Naturally, patterning is carried out.
I don't use your credit card. Since it is a high vacuum process, Au+
Ion operates stably and can be used for a long time.
微細加工終了後再びパルプ7を開は基板を裏返しMBI
IC装置中に戻す。第5図(C)に示すよりなA10y
isの絶縁層を形成する。まずメタルマスク21を基板
直下に導入し、K−Cellを用いてA19を5ooi
蒸着する。マスクと基板の回転速度は同じにする。分子
線は平行に飛ぶので他の部分への回り込みはほとんど無
い。これを酸素プラズマ中で充分酸化させてAl0yの
絶縁層を得る。次に第5図Cd)において図のような形
状にゲート電極19としてK −Oe 11を用いてA
gl 5を蒸着する。この時、膜厚は1000又とする
。なお、蒸着前に真空中でメタルマスク22はゲート電
極形成用に交換しである。After the microfabrication is completed, open the pulp 7 again and turn the substrate over for MBI.
Return it to the IC device. A10y shown in Figure 5(C)
Form an insulating layer of is. First, a metal mask 21 is introduced directly under the substrate, and A19 is placed in a 50mm increments using K-Cell.
Deposit. The rotation speed of the mask and substrate should be the same. Since the molecular beams fly in parallel, there is almost no wraparound to other parts. This is sufficiently oxidized in oxygen plasma to obtain an Al0y insulating layer. Next, in FIG. 5Cd), K-Oe 11 is used as the gate electrode 19 in the shape shown in the figure.
Deposit gl 5. At this time, the film thickness is 1000 mm. Note that before vapor deposition, the metal mask 22 was replaced in vacuum for forming the gate electrode.
上記の方法で作製した場合、従来の歩留りは50%位で
あったのに対して80%という高(・歩留まりで再現性
よ(SUFETを得ることができたさらなるFよりEに
よる微細化は可能であり素子の大きさを数μmに高集積
化させることも可能である。なお、ここに挙げた実施例
ばあ(までも一実施例に過ぎず、5UFETの他SQU
より。When fabricated using the above method, the conventional yield was about 50%, but the yield was as high as 80%. Therefore, it is possible to highly integrate the device size to several μm.The example mentioned here is just one example, and other than 5UFET and SQU
Than.
弱結合型ジョセフソン接合素子、超伝導配線等様々の超
伝導素子に応用することもできる。It can also be applied to various superconducting devices such as weakly coupled Josephson junction devices and superconducting wiring.
以上述べたように本発明によれば、薄膜形成後大気にさ
らす事なく連続的にその場微細加工することにより歩留
まりを向上させ再現性よ(高集積化させた超伝導素子を
提供することができるという効果を有する。また、成膜
と微細加工を・独立して行なう場合よりも時間が短縮で
きる。As described above, according to the present invention, by continuously performing in-situ microfabrication after forming a thin film without exposing it to the atmosphere, yield can be improved and reproducibility can be improved (highly integrated superconducting elements can be provided). In addition, the time can be reduced compared to when film formation and microfabrication are performed independently.
第1図は、本発明の超伝導素子を作製するための一実施
例である薄膜作製装置と微細加工装置を搬送路を介して
複合化した装置を示す図。
第2図は、本発明の一実施例である超伝導電界効果トラ
ンジスタの断面図。
第3図は、第2図の超伝導電界効果トランジスタの作製
工程を示す図。
1・・・・・・・・・MBE装置
2・・・・・・・・・FよりE装置
3・・・・・・・・・真空ポンプ
4・・・・・・・・・結晶基板
5・・・・・・・・・メタルマスク
6・・・・・・・・・シャッター
7・・・・・・・・・パルプ
8・・・・・・・・・RFプラズマ
9・・・・・・・・・A1とに−Cθ1110・・・・
・・・・・Yとに一0el111・・・・・・・・・B
aとK −Oe ’l 112・・・・・・・・・Ou
とK −Os 1115・・・・・・・・・A、 gと
K −Oe 1114・・・・・・・・・イオン源
5・・・・・・・・・半導体化させたS r T i
0゜6・・・・・・・・・ソース電極
7・・・・・・・・・ドレイン電極
8・・・・・・・・・A10y絶縁層
9・・・・・・・・・Alゲート電極
0・・・・・・・・・酸化物超伝導薄膜1・・・・・・
・・・絶縁層用メタルマスク2・・・・・・・・・ゲー
ト電極用メタルマスク0・・・・・・・・・搬送路
1・・・・・・・・・搬送用バー
出願人 セイコーエプソン株式会社
代理人 弁理士 鈴木喜三部(他1名)゛う
か
第
図
叢7図
2/。
/ \FIG. 1 is a diagram showing an apparatus in which a thin film production apparatus and a microfabrication apparatus are combined via a conveyance path, which is an embodiment for producing a superconducting element of the present invention. FIG. 2 is a sectional view of a superconducting field effect transistor that is an embodiment of the present invention. FIG. 3 is a diagram showing the manufacturing process of the superconducting field effect transistor shown in FIG. 2. 1......MBE device 2...F to E device 3...Vacuum pump 4...Crystal substrate 5...Metal mask 6...Shutter 7...Pulp 8...RF plasma 9... ...A1 and -Cθ1110...
・・・・・・Ytoniichi0el111・・・・・・・・・B
a and K -Oe 'l 112・・・・・・・・・Ou
and K -Os 1115...A, g and K -Oe 1114... Ion source 5... S r T made into a semiconductor i
0゜6......Source electrode 7...Drain electrode 8...A10y Insulating layer 9...Al Gate electrode 0... Oxide superconducting thin film 1...
・・・Metal mask for insulating layer 2・・・・・・Metal mask for gate electrode 0・・・・・・Transport path 1・・・・・・Transport bar Applicant Seiko Epson Co., Ltd. Agent Patent Attorney Kizobe Suzuki (and 1 other person) Figure 7 Figure 2/. / \
Claims (1)
続的にその場微細加工して作製する超伝導素子において
、その場微細加工は超高真空状態で行なう集束イオンビ
ームによることを特徴とする超伝導素子。A superconducting device manufactured by continuous in-situ microfabrication of an oxide superconducting thin film without exposing it to the atmosphere, characterized in that the in-situ microfabrication is performed using a focused ion beam in an ultra-high vacuum state. superconducting element.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2182105A JPH0469984A (en) | 1990-07-10 | 1990-07-10 | superconducting element |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2182105A JPH0469984A (en) | 1990-07-10 | 1990-07-10 | superconducting element |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0469984A true JPH0469984A (en) | 1992-03-05 |
Family
ID=16112427
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2182105A Pending JPH0469984A (en) | 1990-07-10 | 1990-07-10 | superconducting element |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0469984A (en) |
-
1990
- 1990-07-10 JP JP2182105A patent/JPH0469984A/en active Pending
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