JPH05335640A - Superconductive element - Google Patents

Superconductive element

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Publication number
JPH05335640A
JPH05335640A JP4138332A JP13833292A JPH05335640A JP H05335640 A JPH05335640 A JP H05335640A JP 4138332 A JP4138332 A JP 4138332A JP 13833292 A JP13833292 A JP 13833292A JP H05335640 A JPH05335640 A JP H05335640A
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JP
Japan
Prior art keywords
superconducting
voltage
oxide semiconductor
electrode
current
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.)
Granted
Application number
JP4138332A
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Japanese (ja)
Other versions
JP2515947B2 (en
Inventor
Mitsuo Suga
三雄 須賀
Juichi Nishino
壽一 西野
Masahiko Hiratani
正彦 平谷
Tokumi Fukazawa
徳海 深沢
Shoichi Akamatsu
正一 赤松
Akira Tsukamoto
塚本  晃
Yoshinobu Taruya
良信 樽谷
Kazumasa Takagi
一正 高木
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Hitachi Ltd
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Hitachi Ltd
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Publication of JPH05335640A publication Critical patent/JPH05335640A/en
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Publication of JP2515947B2 publication Critical patent/JP2515947B2/en
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Abstract

PURPOSE:To provide a superconductive element which can be manufactured easily and has improved amplification characteristics or switching characteristics. CONSTITUTION:Substances 3 and 4 in non-superconductive state are allowed to contact a copper oxide semiconductor 2 and a groove with a width of 1mum or less is provided between the substances 3 and 4 in non-conductive state thus inducing superconductivity within the oxide. By adding an insulation film 5 and a gate electrode 6 to the structure, an element which is controlled by electric field can also be obtained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は超電導スイッチング素子
等、超電導エレクトロニクスの分野に関わり、特にデジ
タル回路、アナログ回路の分野に応用される超電導素子
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the field of superconducting electronics such as superconducting switching elements, and more particularly to superconducting elements applied to the fields of digital circuits and analog circuits.

【0002】[0002]

【従来の技術】酸化物系の材料を用いた超電導素子とし
ては、酸化物超電導体の結晶粒界を弱結合部とした超電
導素子、および2層の酸化物超電導薄膜を貴金属で接続
した超電導素子が得られている。さらには、アプライド
・フィジックス・レターズ55巻2032頁(1989
年)に弱結合部としてYBa2Cu3yと結晶学的に同系
統のPrBa2Cu3yを用い、YBa2Cu3y薄膜によっ
て挟んだ構造が、すなわち、YBa2Cu3y−PrBa2
u3y−YBa2Cu3yの積層構造が記載されている。こ
の構造が、弱結合特性を有していることがマイクロ波照
射時の電流−電圧特性により示された。また、組成の異
なるBaBi1-xPbx3-yを積層する事により誘起される
超電導を電界で制御する超電導素子が特開平1−205
578に記載されている。
2. Description of the Related Art Superconducting elements using oxide-based materials include a superconducting element in which crystal grain boundaries of an oxide superconductor are weakly bonded, and a superconducting element in which two layers of oxide superconducting thin films are connected by a noble metal. Has been obtained. Furthermore, Applied Physics Letters, Vol. 55, p. 2032 (1989)
YBa 2 Cu 3 O y crystallographically similar PrBa 2 Cu 3 O y as a weakly bonded portion, and a structure sandwiched between YBa 2 Cu 3 O y thin films is YBa 2 Cu 3 O. y- PrBa 2 C
u 3 layered structure of O y -YBa 2 Cu 3 O y is described. It was shown by the current-voltage characteristics during microwave irradiation that this structure has weak coupling characteristics. Further, a superconducting element for controlling superconductivity induced by stacking BaBi 1-x Pb x O 3-y having different compositions by an electric field is disclosed in JP-A-1-205.
578.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、上記従
来技術は、YBa2Cu3y−PrBa2Cu3y−YBa2Cu
3yの積層構造あるいは組成の異なるBaBi1-xPbx
3-yの積層構造が必要であるため、これらの積層構造の
作製が難く、積層構造は素子性能の劣化につながる格子
欠陥および元素の拡散等を含み易い。また、BaBi1-x
Pbx3-yの積層により誘起された超電導を電界を用い
てコントロールする素子においては、キャリア濃度の高
い層を通して誘起される超電導性をコントロールするた
めに電界効果が小さく増幅特性あるいはスイッチング特
性が悪い。
However, according to the above-mentioned conventional technique, YBa 2 Cu 3 O y -PrBa 2 Cu 3 O y -YBa 2 Cu is used.
BaO 1-x Pb x O with different laminated structure or composition of 3 O y
Since a 3-y laminated structure is required, it is difficult to manufacture these laminated structures, and the laminated structures are likely to include lattice defects and element diffusion that lead to deterioration of device performance. Also, BaBi 1-x
In an element in which superconductivity induced by stacking Pb x O 3-y is controlled by using an electric field, the electric field effect is small and the amplification characteristic or switching characteristic is small in order to control the superconductivity induced through a layer having a high carrier concentration. bad.

【0004】本発明の目的は、層状ペロブスカイト構造
を持つ酸化物半導体に特有な性質を用いて、単層の酸化
物半導体に複雑な結晶構造を有さない物質を接触させる
ことにより酸化物半導体内に誘起される超電導性を用い
て、作製が難しい積層構造を必要としない超電導素子を
提供すること、および、誘起された超電導を電界により
コントロールする事により良好な増幅特性あるいはスイ
ッチング特性を有する素子を提供することにある。
It is an object of the present invention to utilize a property peculiar to an oxide semiconductor having a layered perovskite structure to bring a substance not having a complicated crystal structure into contact with a single-layer oxide semiconductor, so that To provide a superconducting element that does not require a layered structure that is difficult to fabricate by using superconductivity induced by the electric field, and to control the induced superconductivity by an electric field to obtain an element having good amplification characteristics or switching characteristics. To provide.

【0005】[0005]

【課題を解決するための手段】上記目的は、図2に示す
ように、酸化物半導体R1+xBa2-xCu3y(RはPrを
除く希土類元素,0.3<x<0.8,6<y<8)、
酸化物半導体Pr1+xBa2-xCu3y(0≦x≦0.5,
6<y<8)、酸化物半導体Y1-xPrxBa2Cu3
y(0.6≦x≦1,6<y<8)、酸化物半導体Bi2
Sr2Ca1-xxCu2y(Rは希土類元素、0.6≦x≦
1.0,8<y<8.5)、および、RBa2Cu3
y(RはYまたは希土類元素,6.0<y<6.4)の
いずれか8に、非超電導状態の物質9,10を接触さ
せ、かつ、酸化物半導体8に接触した非超電導状態の物
質9,10の間に幅1μm以下の溝をもうけることによ
り達成される。
As shown in FIG. 2, the above object is to achieve the oxide semiconductor R 1 + x Ba 2-x Cu 3 O y (R is a rare earth element other than Pr, 0.3 <x < 0.8, 6 <y <8),
Oxide semiconductor Pr 1 + x Ba 2-x Cu 3 O y (0 ≦ x ≦ 0.5,
6 <y <8), oxide semiconductor Y 1-x Pr x Ba 2 Cu 3 O
y (0.6≤x≤1, 6 <y <8), oxide semiconductor Bi 2
Sr 2 Ca 1-x R x Cu 2 O y (R is a rare earth element, 0.6 ≦ x ≦
1.0, 8 <y <8.5), and RBa 2 Cu 3 O
y (where R is Y or a rare earth element, 6.0 <y <6.4) is brought into contact with the non-superconducting substances 9 and 10, and the non-superconducting state in contact with the oxide semiconductor 8 This is achieved by providing a groove having a width of 1 μm or less between the substances 9 and 10.

【0006】[0006]

【作用】酸化物半導体R1+xBa2-xCu3y(RはPrを
除く希土類元素,0.3<x<0.8,6<y<8)、
酸化物半導体Pr1+xBa2-xCu3y(0≦x≦0.5,
6<y<8)、酸化物半導体Y1-xPrxBa2Cu3
y(0.6≦x≦1,6<y<8)、酸化物半導体Bi2
Sr2Ca1-xxCu2y(Rは希土類元素、0.6≦x≦
1.0,8<y<8.5)、および、RBa2Cu3
y(RはYまたは希土類元素,6.0<y<6.4)の
いずれか8に、非超電導状態の物質9,10を接触さ
せ、かつ、酸化物半導体8に接触した非超電導状態の物
質9,10の間に幅1μm以下の溝をもうけた構成によ
って、上記酸化物半導体8の電子状態は、非超電導状態
の物質9,10と上記酸化物半導体8の界面近傍におい
て非超電導状態の物質9,10の影響を受ける。これ
は、上記酸化物半導体8のキャリア密度と非超電導状態
の物質9,10のキャリア密度が異なるため、および、
両物質の真空準位が異なるために生じる。その結果、上
記酸化物半導体8と非超電導状態の物質9,10との界
面近傍に於て、フェルミ準位が移動するために電荷移動
型ギャップが壊れる。ゆえに、酸化物半導体8は、界面
近傍に於て超電導性を示すようになる。また、酸化物半
導体8においては、アプライドフィジックスレターズ5
8(1991)2707頁に示されたように、超電導状
態となる距離が0.4μmにもおよぶので、0.1〜0.
4μm間隔を隔てた2つの非超電導状態の物質間に、誘
起された超電導により超電導電流が流れる。このため、
上記構成により良好な弱結合特性が得られる。さらに、
酸化物半導体内部の動きうるキャリアの密度は低い(1
19個/cm3程度)ので、電界により誘起された超電
導のコントロールを行なう場合電界による効果が大き
い。このため、良好な素子性能が得られる。
[Function] Oxide semiconductor R 1 + x Ba 2-x Cu 3 O y (R is a rare earth element other than Pr, 0.3 <x <0.8, 6 <y <8),
Oxide semiconductor Pr 1 + x Ba 2-x Cu 3 O y (0 ≦ x ≦ 0.5,
6 <y <8), oxide semiconductor Y 1-x Pr x Ba 2 Cu 3 O
y (0.6≤x≤1, 6 <y <8), oxide semiconductor Bi 2
Sr 2 Ca 1-x R x Cu 2 O y (R is a rare earth element, 0.6 ≦ x ≦
1.0, 8 <y <8.5), and RBa 2 Cu 3 O
y (where R is Y or a rare earth element, 6.0 <y <6.4) is brought into contact with the non-superconducting substances 9 and 10, and the non-superconducting state in contact with the oxide semiconductor 8 Due to the structure in which a groove having a width of 1 μm or less is provided between the substances 9 and 10, the electronic state of the oxide semiconductor 8 is in the non-superconducting state near the interface between the non-superconducting substances 9 and 10 and the oxide semiconductor 8. It is affected by substances 9 and 10. This is because the carrier densities of the oxide semiconductor 8 and the non-superconducting substances 9 and 10 are different, and
It occurs because the vacuum levels of both substances are different. As a result, the Fermi level moves near the interface between the oxide semiconductor 8 and the substances 9 and 10 in the non-superconducting state, so that the charge transfer type gap is broken. Therefore, the oxide semiconductor 8 becomes superconducting near the interface. In the oxide semiconductor 8, the applied physics letters 5
8 (1991) 2707, the superconducting state distance is as long as 0.4 μm, so 0.1 to 0.1.
The superconducting current flows between the two non-superconducting substances separated by 4 μm due to the induced superconductivity. For this reason,
With the above structure, good weak coupling characteristics can be obtained. further,
The density of mobile carriers inside the oxide semiconductor is low (1
0 about 19 / cm 3), so the effect of the electric field is large when performing the induced control superconducting by an electric field. Therefore, good device performance can be obtained.

【0007】[0007]

【実施例】〈実施例1〉以下、本発明を電界効果型超電
導三端子素子の例を用いて説明する。
EXAMPLES Example 1 Hereinafter, the present invention will be described using an example of a field effect superconducting three-terminal element.

【0008】本素子の構造を、図1に示す。SrTiO3
(110)面方位単結晶基板1上に形成したLa1.5Ba
1.5Cu3y半導体薄膜2の上にAu電極(ソース)3、
Au電極(ドレイン)4を形成し、3,4間に寸法0.1
μmのギャップを形成した。その後、CaF2絶縁膜6を
設け、Au電極(ゲート)7を形成する。
The structure of this device is shown in FIG. SrTiO 3
La 1.5 Ba formed on the (110) plane-oriented single crystal substrate 1
On the Cu 3 O y semiconductor thin film 2, an Au electrode (source) 3,
An Au electrode (drain) 4 is formed, and the dimension between 3 and 4 is 0.1.
A μm gap was formed. Then, a CaF 2 insulating film 6 is provided and an Au electrode (gate) 7 is formed.

【0009】La1.5Ba1.5Cu3y薄膜は、マイクロ波
酸素プラズマを用いた反応性蒸着装置によって成膜を行
なった。雰囲気ガスは純酸素ガスとし、全圧力は8×1
0-5torrとした。原料は、それぞれ金属状態のLa,Ba,
Cuを用い、クヌードセンセルを用いて蒸発させた。酸
化力を高めるために、2.45GHz、120Wのマイ
クロ波を照射した。膜形成時の基板温度は450℃とし
た。この様な条件で形成したLa1.5Ba1.5Cu3y薄膜
2は、(110)面が基板面と垂直な方向の結晶性を有
する。Au電極およびCaF2絶縁膜の形成にも反応性蒸
着装置を用いたが、それぞれ真空中でマイクロ波を照射
せずに成膜を行なった。また、Auは、電子銃蒸着装置
を用いて蒸発させた。
The La 1.5 Ba 1.5 Cu 3 O y thin film was formed by a reactive vapor deposition system using microwave oxygen plasma. The atmosphere gas is pure oxygen gas, and the total pressure is 8 × 1.
Was 0- 5 torr. The raw materials are La, Ba, and
It was evaporated using Cu and a Knudsen cell. In order to increase the oxidizing power, microwave of 2.45 GHz and 120 W was applied. The substrate temperature during film formation was 450 ° C. The La 1.5 Ba 1.5 Cu 3 O y thin film 2 formed under such conditions has crystallinity in which the (110) plane is perpendicular to the substrate surface. A reactive vapor deposition apparatus was also used for forming the Au electrode and the CaF 2 insulating film, but the film was formed in a vacuum without irradiation with microwaves. Au was evaporated using an electron gun vapor deposition device.

【0010】超電導素子の作製行程は以下の通りとし
た。すなわち、La1.5Ba1.5Cu3y薄膜2をSrTiO3
の(110)面方位単結晶基板1上に形成した。膜厚は
100nmとした。この上に、マスク蒸着法によりバー状
のAu薄膜を形成した。Au薄膜の膜厚は30nmで、大き
さは0.2×5mmとした。この上に電子線用レジストを
塗布した後、電子線描画装置で0.2mmの辺に平行にAu
電極の中央に0.1μmの線状のパターンを描いた。反
応性イオンビームエッチング法でレジストパターンを基
にAu薄膜に溝状のパターンを形成し、それぞれAu電極
(ソース)3およびAu電極(ドレイン)4とした。こ
の溝状のチャネル5上にCaF2絶縁膜6を形成し、ゲー
ト絶縁膜とした。ゲート絶縁膜の上にAuを蒸着し、Au
電極(ゲート)7とした。
The manufacturing process of the superconducting device was as follows. That is, the La 1.5 Ba 1.5 Cu 3 O y thin film 2 is replaced with SrTiO 3
It was formed on the (110) plane-oriented single crystal substrate 1. The film thickness was 100 nm. A bar-shaped Au thin film was formed on this by a mask vapor deposition method. The Au thin film had a thickness of 30 nm and a size of 0.2 × 5 mm. After coating the electron beam resist on it, Au was made parallel to the side of 0.2 mm by the electron beam drawing device.
A 0.1 μm linear pattern was drawn in the center of the electrode. A groove-shaped pattern was formed on the Au thin film based on the resist pattern by the reactive ion beam etching method to form Au electrode (source) 3 and Au electrode (drain) 4, respectively. A CaF 2 insulating film 6 was formed on this groove-shaped channel 5 to form a gate insulating film. Au is vapor-deposited on the gate insulating film,
The electrode (gate) 7 was used.

【0011】この超電導素子の60Kにおけるソース、
ドレイン間の電流−電圧特性においては、約1.0mA
の超電導電流が流れ、これ以上のバイアス電流に対して
電圧が発生する。さらにゲートに対して200mVの電
圧を印加した場合、超電導電流は0.2mAに減少し、
これ以上のバイアス電流で電圧が発生する。以上のごと
く、本超電導素子は、三端子素子としての基本特性を有
する。また、LaのかわりにPr以外の希土類元素を用い
て素子を作製した場合も同様の特性が得られた。この場
合、Eu以外の希土類元素はクヌードセンセルの代わり
に電子銃蒸着装置を用いて蒸発させた。さらに、Auの
かわりにAg,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,I
n,Al,V,Ta,Wを用いた素子も作製したが、この場合
にも同様の特性が得られた。
The source of this superconducting element at 60K,
The current-voltage characteristics between the drains are about 1.0 mA.
Of superconducting current flows, and a voltage is generated for a bias current higher than this. Furthermore, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.2 mA,
A voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Similar characteristics were also obtained when a device was manufactured by using a rare earth element other than Pr instead of La. In this case, rare earth elements other than Eu were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, I
An element using n, Al, V, Ta and W was also manufactured, but similar characteristics were obtained in this case as well.

【0012】〈実施例2〉実施例1と同じ薄膜構造にお
いて、Au電極(ソース)3とAu電極(ドレイン)4の
間の距離のみを変更し、線の幅を0.5μmとした。作
製工程等は、実施例1と同じである。この超電導素子の
30Kにおけるソース、ドレイン間の電流−電圧特性に
おいては、約0.8mAの超電導電流が流れ、これ以上
のバイアス電流に対して電圧が発生する。さらにゲート
に対して200mVの電圧を印加した場合、超電導電流
は0.15Aに減少し、これ以上のバイアス電流で電圧
が発生する。以上のごとく、本超電導素子は、三端子素
子としての基本特性を有する。また、LaのかわりにPr
を除く希土類元素を用いて素子を作製した場合も同様の
特性が得られた。この場合、Eu以外の希土類元素はク
ヌードセンセルの代わりに電子銃蒸着装置を用いて蒸発
させた。さらに、AuのかわりにAg,Bi,Sb,PbBi,P
b,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も
作製したが、この場合にも同様の特性が得られた。
Example 2 In the same thin film structure as in Example 1, only the distance between the Au electrode (source) 3 and the Au electrode (drain) 4 was changed, and the line width was set to 0.5 μm. The manufacturing process and the like are the same as in Example 1. In the current-voltage characteristic between the source and the drain at 30 K of this superconducting element, a superconducting current of about 0.8 mA flows, and a voltage is generated for a bias current higher than this. Furthermore, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.15 A, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of La, Pr
Similar characteristics were obtained when devices were manufactured using rare earth elements other than. In this case, rare earth elements other than Eu were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Furthermore, instead of Au, Ag, Bi, Sb, PbBi, P
An element using b, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0013】〈実施例3〉実施例1と同じ薄膜構造にお
いて、Au電極(ソース)3とAu電極(ドレイン)4の
間の距離のみを変更し、線の幅を1μmとした。作製工
程等は、実施例1と同じである。この超電導素子の4.
2Kにおけるソース、ドレイン間の電流−電圧特性にお
いては、約0.2mAの超電導電流が流れ、これ以上の
バイアス電流に対して電圧が発生する。さらにゲートに
対して200mVの電圧を印加した場合、超電導電流は
0.01mAに減少し、これ以上のバイアス電流で電圧
が発生する。以上のごとく、本超電導素子は、三端子素
子としての基本特性を有する。また、LaのかわりにPr
を除く希土類元素を用いて素子を作製した場合も同様の
特性が得られた。この場合、Eu以外の希土類元素はク
ヌードセンセルの代わりに電子銃蒸着装置を用いて蒸発
させた。さらに、AuのかわりにAg,Bi,Sb,PbBi,P
b,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も
作製したが、この場合にも同様の特性が得られた。
Example 3 In the same thin film structure as in Example 1, only the distance between the Au electrode (source) 3 and the Au electrode (drain) 4 was changed, and the line width was set to 1 μm. The manufacturing process and the like are the same as in Example 1. 4. of this superconducting element
In the current-voltage characteristic between the source and drain at 2K, a superconducting current of about 0.2 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.01 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of La, Pr
Similar characteristics were obtained when devices were manufactured using rare earth elements other than. In this case, rare earth elements other than Eu were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Furthermore, instead of Au, Ag, Bi, Sb, PbBi, P
An element using b, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0014】〈実施例4〉実施例1と同じ薄膜構造にお
いて、酸化物半導体の組成のみを変更し、La1.3Ba1.7
Cu3yを用いた。作製工程等は、実施例1と同じであ
る。この超電導素子の60Kにおけるソース、ドレイン
間の電流−電圧特性においては、約1.3mAの超電導
電流が流れ、これ以上のバイアス電流に対して電圧が発
生する。さらにゲートに対して200mVの電圧を印加
した場合、超電導電流は0.3mAに減少し、これ以上
のバイアス電流で電圧が発生する。以上のごとく、本超
電導素子は、三端子素子としての基本特性を有する。ま
た、LaのかわりにPrを除く希土類元素を用いて素子を
作製した場合も同様の特性が得られた。この場合、Eu
以外の希土類元素はクヌードセンセルの代わりに電子銃
蒸着装置を用いて蒸発させた。さらに、Auのかわりに
Ag,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,In,Al,V,
Ta,Wを用いた素子も作製したが、この場合にも同様の
特性が得られた。
<Embodiment 4> In the same thin film structure as in Embodiment 1, only the composition of the oxide semiconductor was changed to obtain La 1.3 Ba 1.7.
Cu 3 O y was used. The manufacturing process and the like are the same as in Example 1. In the current-voltage characteristic between the source and the drain at 60 K of this superconducting element, a superconducting current of about 1.3 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current is reduced to 0.3 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Similar characteristics were also obtained when a device was manufactured by using a rare earth element except Pr instead of La. In this case, Eu
Other rare earth elements were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, In, Al, V,
An element using Ta and W was also manufactured, but similar characteristics were obtained in this case as well.

【0015】〈実施例5〉実施例1と同じ薄膜構造にお
いて、酸化物半導体の組成のみを変更し、La1.7Ba1.3
Cu3yを用いた。作製工程等は、実施例1と同じであ
る。この超電導素子の60Kにおけるソース、ドレイン
間の電流−電圧特性においては、約0.8mAの超電導
電流が流れ、これ以上のバイアス電流に対して電圧が発
生する。さらにゲートに対して200mVの電圧を印加
した場合、超電導電流は0.1mAに減少し、これ以上
のバイアス電流で電圧が発生する。以上のごとく、本超
電導素子は、三端子素子としての基本特性を有する。こ
の場合、Eu以外の希土類元素はクヌードセンセルの代
わりに電子銃蒸着装置を用いて蒸発させた。さらに、A
uのかわりにAg,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,
In,Al,V,Ta,Wを用いた素子も作製したが、この場
合にも同様の特性が得られた。
<Embodiment 5> In the same thin film structure as in Embodiment 1, only the composition of the oxide semiconductor was changed to obtain La 1.7 Ba 1.3.
Cu 3 O y was used. The manufacturing process and the like are the same as in Example 1. In the current-voltage characteristics between the source and the drain at 60 K of this superconducting element, a superconducting current of about 0.8 mA flows, and a voltage is generated for a bias current higher than this. Furthermore, when a voltage of 200 mV is applied to the gate, the superconducting current is reduced to 0.1 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. In this case, rare earth elements other than Eu were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Furthermore, A
Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, instead of u
A device using In, Al, V, Ta and W was also manufactured, but similar characteristics were obtained in this case as well.

【0016】〈実施例6〉実施例1と同じ薄膜構造にお
いて、酸化物半導体のみを変更し、Pr1.5Ba1.5Cu3y
を用いた。ただし、半導体薄膜の原料としてそれぞれ金
属状態のPr,Ba,Cuを用い、Prは電子銃蒸着装置を用
いて蒸発させた。その他の作製工程は、実施例1と同じ
である。
[0016] In the same film structure as <Example 6> Example 1, changing only the oxide semiconductor, Pr 1.5 Ba 1.5 Cu 3 O y
Was used. However, Pr, Ba, and Cu in a metallic state were used as raw materials for the semiconductor thin film, and Pr was evaporated by using an electron gun vapor deposition apparatus. The other manufacturing steps are the same as in the first embodiment.

【0017】この超電導素子の60Kにおけるソース、
ドレイン間の電流−電圧特性においては、約0.5mA
の超電導電流が流れ、これ以上のバイアス電流に対して
電圧が発生する。さらにゲートに対して200mVの電
圧を印加した場合、超電導電流は0.05mAに減少
し、これ以上のバイアス電流で電圧が発生する。以上の
ごとく、本超電導素子は、三端子素子としての基本特性
を有する。また、AuのかわりにAg,Bi,Sb,PbBi,P
b,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も
作製したが、この場合にも同様の特性が得られた。
The source of this superconducting element at 60K,
The current-voltage characteristics between the drains are about 0.5 mA.
Of superconducting current flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current is reduced to 0.05 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of Au, Ag, Bi, Sb, PbBi, P
An element using b, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0018】〈実施例7〉実施例6と同じ薄膜構造にお
いて、酸化物半導体の組成のみを変更し、Pr1.1Ba1.9
Cu3yを用いた。この超電導素子の60Kにおけるソ
ース、ドレイン間の電流−電圧特性においては、約0.
7mAの超電導電流が流れ、これ以上のバイアス電流に
対して電圧が発生する。さらにゲートに対して200m
Vの電圧を印加した場合、超電導電流は0.1mAに減
少し、これ以上のバイアス電流で電圧が発生する。以上
のごとく、本超電導素子は、三端子素子としての基本特
性を有する。また、AuのかわりにAg,Bi,Sb,PbBi,
Pb,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子
も作製したが、この場合にも同様の特性が得られた。
<Embodiment 7> In the same thin film structure as in Embodiment 6, only the composition of the oxide semiconductor was changed to obtain Pr 1.1 Ba 1.9.
Cu 3 O y was used. The current-voltage characteristics between the source and drain at 60 K of this superconducting element are about 0.
A superconducting current of 7 mA flows, and a voltage is generated for a bias current higher than this. 200m to the gate
When a voltage of V is applied, the superconducting current decreases to 0.1 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of Au, Ag, Bi, Sb, PbBi,
A device using Pb, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0019】〈実施例8〉実施例6と同じ薄膜構造にお
いて、酸化物半導体のみを変更し、PrBa2Cu3yを用
いた。ただし、半導体薄膜の原料としてそれぞれ金属状
態のPr,Ba,Cuを用い、Prは電子銃蒸着装置を用いて
蒸発させた。
Example 8 In the same thin film structure as in Example 6, only the oxide semiconductor was changed and PrBa 2 Cu 3 O y was used. However, Pr, Ba, and Cu in a metallic state were used as raw materials for the semiconductor thin film, and Pr was evaporated by using an electron gun vapor deposition apparatus.

【0020】この超電導素子の60Kにおけるソース、
ドレイン間の電流−電圧特性においては、約0.8mA
の超電導電流が流れ、これ以上のバイアス電流に対して
電圧が発生する。さらにゲートに対して200mVの電
圧を印加した場合、超電導電流は0.15mAに減少
し、これ以上のバイアス電流で電圧が発生する。以上の
ごとく、本超電導素子は、三端子素子としての基本特性
を有する。また、AuのかわりにAg,Bi,Sb,PbBi,P
b,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も
作製したが、この場合にも同様の特性が得られた。
The source of this superconducting element at 60K,
The current-voltage characteristic between the drains is about 0.8 mA.
Of superconducting current flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.15 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of Au, Ag, Bi, Sb, PbBi, P
An element using b, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0021】〈実施例9〉実施例1と同じ薄膜構造にお
いて、酸化物半導体のみを変更し、Y0.4Pr0.6Ba2Cu
3yを用いた。ただし、半導体薄膜の原料としてそれぞ
れ金属状態のY,Pr,Ba,Cuを用い、Y,Prは電子銃蒸
着装置を用いて蒸発させた。
<Embodiment 9> In the same thin film structure as in Embodiment 1, only the oxide semiconductor is changed to Y 0.4 Pr 0.6 Ba 2 Cu.
3 O y was used. However, Y, Pr, Ba, and Cu in a metallic state were used as raw materials for the semiconductor thin film, and Y and Pr were vaporized by using an electron gun vapor deposition apparatus.

【0022】この超電導素子の60Kにおけるソース、
ドレイン間の電流−電圧特性においては、約2.0mA
の超電導電流が流れ、これ以上のバイアス電流に対して
電圧が発生する。さらにゲートに対して200mVの電
圧を印加した場合、超電導電流は0.4mAに減少し、
これ以上のバイアス電流で電圧が発生する。以上のごと
く、本超電導素子は、三端子素子としての基本特性を有
する。また、AuのかわりにAg,Bi,Sb,PbBi,Pb,S
n,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も作製
したが、この場合にも同様の特性が得られた。
The source of this superconducting element at 60K,
About 2.0 mA in current-voltage characteristics between drains
Of superconducting current flows, and a voltage is generated for a bias current higher than this. Furthermore, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.4 mA,
A voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, instead of Au, Ag, Bi, Sb, PbBi, Pb, S
A device using n, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0023】〈実施例10〉実施例9と同じ薄膜構造に
おいて、Au電極(ソース)3とAu電極(ドレイン)4
の間の距離のみを変更し、線の幅を0.5μmとした。
作製工程等は、実施例9と同じである。この超電導素子
の30Kにおけるソース、ドレイン間の電流−電圧特性
においては、約1.2mAの超電導電流が流れ、これ以
上のバイアス電流に対して電圧が発生する。さらにゲー
トに対して200mVの電圧を印加した場合、超電導電
流は0.2mAに減少し、これ以上のバイアス電流で電
圧が発生する。以上のごとく、本超電導素子は、三端子
素子としての基本特性を有する。また、Auのかわりに
Ag,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,In,Al,V,
Ta,Wを用いた素子も作製したが、この場合にも同様の
特性が得られた。
<Embodiment 10> In the same thin film structure as in Embodiment 9, an Au electrode (source) 3 and an Au electrode (drain) 4 are used.
Only the distance between them was changed, and the line width was set to 0.5 μm.
The manufacturing process and the like are the same as in Example 9. In the current-voltage characteristic between the source and the drain at 30 K of this superconducting element, a superconducting current of about 1.2 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current is reduced to 0.2 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, In, Al, V,
An element using Ta and W was also manufactured, but similar characteristics were obtained in this case as well.

【0024】〈実施例11〉実施例9と同じ薄膜構造に
おいて、Au電極(ソース)3とAu電極(ドレイン)4
の間の距離のみを変更し、線の幅を1μmとした。作製
工程等は、実施例9と同じである。この超電導素子の
4.2Kにおけるソース、ドレイン間の電流−電圧特性
においては、約0.5mAの超電導電流が流れ、これ以
上のバイアス電流に対して電圧が発生する。さらにゲー
トに対して200mVの電圧を印加した場合、超電導電
流は0.01mAに減少し、これ以上のバイアス電流で
電圧が発生する。以上のごとく、本超電導素子は、三端
子素子としての基本特性を有する。また、Auのかわり
にAg,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,In,Al,
V,Ta,Wを用いた素子も作製したが、この場合にも同
様の特性が得られた。
<Embodiment 11> In the same thin film structure as that of Embodiment 9, an Au electrode (source) 3 and an Au electrode (drain) 4 are provided.
Only the distance between them was changed, and the line width was set to 1 μm. The manufacturing process and the like are the same as in Example 9. In the current-voltage characteristic between the source and drain at 4.2K of this superconducting element, a superconducting current of about 0.5 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.01 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, In, Al,
An element using V, Ta, and W was also manufactured, but similar characteristics were obtained in this case as well.

【0025】〈実施例12〉実施例1と同じ薄膜構造に
おいて、酸化物半導体のみを変更し、Bi2Sr2NdYCu
3Oyを用いた。ただし、半導体薄膜の原料としてそれぞ
れ金属状態のBi,Sr,Nd,Cuを用い、Yは電子銃蒸着
装置を用いて蒸発させ、他の原料はクヌードセンセルを
用いて蒸発させた。他の工程は、実施例1に記したのと
同様である。 この超電導素子の50Kにおけるソー
ス、ドレイン間の電流−電圧特性においては、約1.0
mAの超電導電流が流れ、これ以上のバイアス電流に対
して電圧が発生する。さらにゲートに対して100mV
の電圧を印加した場合、超電導電流は0.2mAに減少
し、これ以上のバイアス電流で電圧が発生する。以上の
ごとく、本超電導素子は、三端子素子としての基本特性
を有する。また、NdのかわりにYあるいは他の希土類
元素を用いた場合にも同様の特性が得られた。この場
合、Eu以外の希土類元素およびYはクヌードセンセル
の代わりに電子銃蒸着装置を用いて蒸発させた。さら
に、AuのかわりにAg,Bi,Sb,PbBi,Pb,Sn,Zn,G
a,Nb,In,Al,V,Ta,Wを用いた素子も作製したが、
この場合にも同様の特性が得られた。
<Embodiment 12> In the same thin film structure as in Embodiment 1, only the oxide semiconductor is changed, and Bi 2 Sr 2 NdYCu is used.
3 Oy was used. However, Bi, Sr, Nd, and Cu in the metallic state were used as the raw materials of the semiconductor thin film, Y was evaporated using the electron gun vapor deposition apparatus, and the other raw materials were evaporated using the Knudsen cell. Other steps are similar to those described in Example 1. The current-voltage characteristics between the source and drain at 50 K of this superconducting device are about 1.0.
A superconducting current of mA flows, and a voltage is generated for a bias current higher than this. Furthermore, 100 mV to the gate
When the voltage of 1 is applied, the superconducting current is reduced to 0.2 mA, and the voltage is generated by the bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Similar characteristics were also obtained when Y or another rare earth element was used instead of Nd. In this case, rare earth elements other than Eu and Y were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, G
An element using a, Nb, In, Al, V, Ta, W was also manufactured,
Similar characteristics were obtained in this case as well.

【0026】〈実施例13〉実施例12と同じ薄膜構造
において、酸化物半導体の組成のみを変更し、Bi2Sr2
Ca0.4Nd0.6YCu3yを用いた。この超電導素子の6
0Kにおけるソース、ドレイン間の電流−電圧特性にお
いては、約1.8mAの超電導電流が流れ、これ以上の
バイアス電流に対して電圧が発生する。さらにゲートに
対して200mVの電圧を印加した場合、超電導電流は
0.3mAに減少し、これ以上のバイアス電流で電圧が
発生する。以上のごとく、本超電導素子は、三端子素子
としての基本特性を有する。また、NdのかわりにYあ
るいは他の希土類元素を用いた場合にも同様の特性が得
られた。この場合、Eu以外の希土類元素およびYはク
ヌードセンセルの代わりに電子銃蒸着装置を用いて蒸発
させた。さらに、AuのかわりにAg,Bi,Sb,PbBi,P
b,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを用いた素子も
作製したが、この場合にも同様の特性が得られた。
<Embodiment 13> In the same thin film structure as that of Embodiment 12, only the composition of the oxide semiconductor is changed, and Bi 2 Sr 2 is added.
Ca 0.4 Nd 0.6 YCu 3 O y was used. 6 of this superconducting element
In the current-voltage characteristic between the source and the drain at 0K, a superconducting current of about 1.8 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current is reduced to 0.3 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Similar characteristics were also obtained when Y or another rare earth element was used instead of Nd. In this case, rare earth elements other than Eu and Y were evaporated using an electron gun vapor deposition device instead of the Knudsen cell. Furthermore, instead of Au, Ag, Bi, Sb, PbBi, P
An element using b, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0027】〈実施例14〉実施例12と同じ薄膜構造
において、Au電極(ソース)3とAu電極(ドレイン)
4の間の距離のみを変更し、線の幅を0.5μmとし
た。作製工程等は、実施例12と同じである。この超電
導素子の60Kにおけるソース、ドレイン間の電流−電
圧特性においては、約0.3mAの超電導電流が流れ、
これ以上のバイアス電流に対して電圧が発生する。さら
にゲートに対して200mVの電圧を印加した場合、超
電導電流は0.01mAに減少し、これ以上のバイアス
電流で電圧が発生する。以上のごとく、本超電導素子
は、三端子素子としての基本特性を有する。また、Au
のかわりにAg,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,
In,Al,V,Ta,Wを用いた素子も作製したが、この場
合にも同様の特性が得られた。
<Embodiment 14> In the same thin film structure as that of Embodiment 12, an Au electrode (source) 3 and an Au electrode (drain).
Only the distance between 4 was changed and the line width was 0.5 μm. The manufacturing process and the like are the same as in Example 12. In the current-voltage characteristics between the source and drain at 60K of this superconducting element, a superconducting current of about 0.3 mA flows,
A voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.01 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Also, Au
Instead of Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb,
A device using In, Al, V, Ta and W was also manufactured, but similar characteristics were obtained in this case as well.

【0028】〈実施例15〉実施例12と同じ薄膜構造
において、Au電極(ソース)3とAu電極(ドレイン)
4の間の距離のみを変更し、線の幅を1μmとした。作
製工程等は、実施例12と同じである。この超電導素子
の25Kにおけるソース、ドレイン間の電流−電圧特性
においては、約0.2mAの超電導電流が流れ、これ以
上のバイアス電流に対して電圧が発生する。さらにゲー
トに対して200mVの電圧を印加した場合、超電導電
流は0.01mAに減少し、これ以上のバイアス電流で
電圧が発生する。以上のごとく、本超電導素子は、三端
子素子としての基本特性を有する。また、Auのかわり
にAg,Bi,Sb,PbBi,Pb,Sn,Zn,Ga,Nb,In,Al,
V,Ta,Wを用いた素子も作製したが、この場合にも同
様の特性が得られた。
<Embodiment 15> In the same thin film structure as that of Embodiment 12, an Au electrode (source) 3 and an Au electrode (drain).
Only the distance between 4 was changed and the line width was 1 μm. The manufacturing process and the like are the same as in Example 12. In the current-voltage characteristics between the source and drain at 25K of this superconducting element, a superconducting current of about 0.2 mA flows, and a voltage is generated for a bias current higher than this. Further, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.01 mA, and a voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Further, instead of Au, Ag, Bi, Sb, PbBi, Pb, Sn, Zn, Ga, Nb, In, Al,
An element using V, Ta, and W was also manufactured, but similar characteristics were obtained in this case as well.

【0029】〈実施例16〉実施例1と同じ薄膜構造に
おいて、酸化物半導体のみを変更し、YBa2Cu36+y
を用いた。ただし、半導体薄膜の原料としてそれぞれ金
属状態のY,Ba,Cuを用い、Yは電子銃蒸着装置を用い
て蒸発させた。また、酸化物薄膜を形成した後、チェー
ンサイトの酸素を十分に欠損させるために、Ar中、4
50℃で6時間アニールした。他の工程はすべて実施例
1で記したのと同様である。
<Example 16> In the same thin film structure as in Example 1, only the oxide semiconductor was changed, and YBa 2 Cu 3 O 6 + y was added.
Was used. However, Y, Ba, and Cu in a metallic state were used as raw materials of the semiconductor thin film, and Y was evaporated by using an electron gun vapor deposition apparatus. Moreover, after forming the oxide thin film, in order to make oxygen in the chain site sufficiently deficient, in Ar, 4
Annealed at 50 ° C. for 6 hours. All other steps are similar to those described in Example 1.

【0030】この超電導素子の30Kにおけるソース、
ドレイン間の電流−電圧特性においては、約0.9mA
の超電導電流が流れ、これ以上のバイアス電流に対して
電圧が発生する。さらにゲートに対して200mVの電
圧を印加した場合、超電導電流は0.1mAに減少し、
これ以上のバイアス電流で電圧が発生する。以上のごと
く、本超電導素子は、三端子素子としての基本特性を有
する。また、Yのかわりに希土類元素を用いた場合も同
様の特性が得られた。さらに、AuのかわりにAg,Bi,
Sb,PbBi,Pb,Sn,Zn,Ga,Nb,In,Al,V,Ta,Wを
用いた素子も作製したが、この場合にも同様の特性が得
られた。
The source of this superconducting element at 30K,
The current-voltage characteristic between the drains is about 0.9 mA.
Of superconducting current flows, and a voltage is generated for a bias current higher than this. Furthermore, when a voltage of 200 mV is applied to the gate, the superconducting current decreases to 0.1 mA,
A voltage is generated with a bias current higher than this. As described above, the present superconducting element has the basic characteristics as a three-terminal element. Similar characteristics were also obtained when a rare earth element was used instead of Y. Furthermore, instead of Au, Ag, Bi,
An element using Sb, PbBi, Pb, Sn, Zn, Ga, Nb, In, Al, V, Ta, W was also manufactured, but similar characteristics were obtained in this case as well.

【0031】なお、実施例における薄膜形成法は反応性
蒸着法であったが、レーザーアブレーション法、スパッ
タリング法、MOVPE法など、他の成膜法が適用可能
であることは言うまでもない。また、本実施例において
は、SrTiO3を基板として用いたが、MgO、LaAlO
3等他の基板の上に作製できることは言うまでもない。
さらに、本実施例においては三端子素子に関して記した
が、三端子素子の構成要素である弱結合素子等他の超電
導素子を作製できることは言うまでもない。
Although the thin film forming method in the examples is the reactive vapor deposition method, it goes without saying that other film forming methods such as the laser ablation method, the sputtering method and the MOVPE method can be applied. In this embodiment, SrTiO 3 was used as the substrate, but MgO and LaAlO 3 were used.
Needless to say, it can be formed on another substrate such as 3 .
Further, although the description has been made regarding the three-terminal element in the present embodiment, it is needless to say that another superconducting element such as a weak coupling element which is a constituent element of the three-terminal element can be manufactured.

【0032】[0032]

【発明の効果】実施例の項において述べたごとく、本発
明にかかる構造の素子は以下の効果を有する。
As described in the embodiments, the device having the structure according to the present invention has the following effects.

【0033】(1)酸化物半導体に結晶構造の単純な非
超電導物質を接触させ、かつ、非超電導物質間の距離を
1μm以下とすることにより、酸化物半導体に誘起され
る超電導性を用いて動作する素子なので、複雑な積層構
造が必要でなくなり、素子の作製が単純になる。
(1) The superconductivity induced in the oxide semiconductor is used by bringing the oxide semiconductor into contact with a simple non-superconducting substance having a crystal structure and setting the distance between the non-superconducting substances to 1 μm or less. Since it is a device that operates, a complicated laminated structure is not required, and the device can be simply manufactured.

【0034】(2)酸化物半導体以外は室温で形成する
ことが出来るため、界面近傍における拡散が少なくなり
素子性能が向上する。
(2) Since elements other than oxide semiconductors can be formed at room temperature, diffusion near the interface is reduced and device performance is improved.

【0035】(3)超電導染みだしのコントロールを行
なうために、電界による効果が大きく、良好な素子性能
を有する。
(3) Since the superconducting exudate is controlled, the effect of the electric field is great and the device has good device performance.

【0036】(4)上記超電導素子を用いた超電導論理
回路、記憶回路を構成することが出来る。
(4) A superconducting logic circuit and a memory circuit using the above superconducting element can be constructed.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の一実施例を示す構成図である。FIG. 1 is a configuration diagram showing an embodiment of the present invention.

【図2】超電導の誘起及び超電導染みだしに関する原理
実験を行なうための配置図である。
FIG. 2 is a layout drawing for conducting a principle experiment on superconducting induction and superconducting exudation.

【符号の説明】[Explanation of symbols]

1.SrTiO3基板 2.La1.5Ba1.5Cu3y薄膜 3.Au電極(ソース) 4.Au電極(ドレイン) 5.チャネル 6.CaF2絶縁膜 7.Au電極(ゲート) 8.酸化物半導体 9.非超電導状態の物質 10.非超電導状態の物質1. SrTiO 3 substrate 2. La 1.5 Ba 1.5 Cu 3 O y thin film 3. Au electrode (source) 4. Au electrode (drain) 5. Channel 6. CaF 2 insulating film 7. Au electrode (gate) 8. Oxide semiconductor 9. Non-superconducting substance 10. Non-superconducting substance

───────────────────────────────────────────────────── フロントページの続き (72)発明者 深沢 徳海 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 (72)発明者 赤松 正一 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 (72)発明者 塚本 晃 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 (72)発明者 樽谷 良信 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 (72)発明者 高木 一正 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Tokumi Fukasawa 1-280 Higashi Koikeku, Kokubunji City, Tokyo Inside the Central Research Laboratory, Hitachi, Ltd. (72) Shoichi Akamatsu 1-280 Higashi Koikeku, Kokubunji, Tokyo Hitachi Central Research Laboratory (72) Inventor Akira Tsukamoto 1-280 Higashi Koigokubo, Kokubunji, Tokyo Hitachi Central Research Institute Co., Ltd. (72) Yoshinobu Tarutani 1-280 Higashi Koikeku, Kokubunji, Tokyo Hitachi Central Research Co., Ltd. In-house (72) Inventor Kazumasa Takagi 1-280, Higashi-Kengokubo, Kokubunji-shi, Tokyo Inside Central Research Laboratory, Hitachi, Ltd.

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】銅を含んだ酸化物半導体と、上記酸化物半
導体上に、互いに対抗するように設けた第1、第2の非
超電導状態の電極を備えたことを特徴とする超電導素
子。
1. A superconducting element comprising: an oxide semiconductor containing copper; and first and second non-superconducting electrodes provided on the oxide semiconductor so as to oppose each other.
【請求項2】特許請求の範囲第1項において、上記非超
電導状態の電極は、低温においても超電導状態にならな
い非超電導物質であることを特徴とする超電導素子。
2. The superconducting element according to claim 1, wherein the electrode in the non-superconducting state is a non-superconducting substance which does not enter the superconducting state even at a low temperature.
【請求項3】特許請求の範囲第1項において、上記非超
電導状態の電極は、低温において超電導状態となる超電
導物質であり、かつ、上記超電導物質の超電導転移温度
以上の温度で動作することを特徴とする超電導素子。
3. The electrode according to claim 1, wherein the non-superconducting state electrode is a superconducting substance which is in a superconducting state at a low temperature, and which operates at a temperature equal to or higher than the superconducting transition temperature of the superconducting substance. Characteristic superconducting element.
【請求項4】特許請求の範囲第1項において、上記非超
電導状態の電極は、少なくともAu,Ag,Bi,Sb,Pb,
Sn,Zn,Ga,Nb,In,Al,V,Ta,Wから選ばれた一つ
の物質を含むことを特徴とする超電導素子。
4. The electrode according to claim 1, wherein the non-superconducting electrode is at least Au, Ag, Bi, Sb, Pb,
A superconducting device comprising one substance selected from Sn, Zn, Ga, Nb, In, Al, V, Ta and W.
【請求項5】特許請求の範囲第2項において、上記非超
電導物質は、少なくともAu,Ag,Bi,Sbから選ばれた
一つの物質を含むことを特徴とする超電導素子。
5. The superconducting device according to claim 2, wherein the non-superconducting substance contains at least one substance selected from Au, Ag, Bi and Sb.
【請求項6】特許請求の範囲第3項において、上記超電
導物質は、少なくともPbBi,Pb,Sn,Zn,Ga,Nb,I
n,Al,V,Ta,Wから選ばれた一つの物質を含むことを
特徴とする超電導素子
6. The superconducting material according to claim 3, wherein the superconducting material is at least PbBi, Pb, Sn, Zn, Ga, Nb, I.
Superconducting device containing one substance selected from n, Al, V, Ta and W
【請求項7】特許請求の範囲第1項において、上記銅を
含んだ酸化物半導体はCu-O2面を有することを特徴と
する超電導素子。
7. The superconducting element according to claim 1, wherein the oxide semiconductor containing copper has a Cu—O 2 plane.
【請求項8】特許請求項目の範囲第1項において、上記
銅を含んだ酸化物半導体は、R1+xBa2-xCu3y(Rは
Prを除く希土類元素,0.3<x<0.8,6<y<
8)、Pr1+xBa2-xCu3y(0≦x≦0.5,6<y<
8)、Y1-xPrxBa2Cu3y(0.6<x≦1,6<y
<8)、Bi2Sr2Ca1-xxCu2y(Rは希土類元素、
0.6≦x≦1.0,8<y<8.5)、および、RBa
2Cu3y(RはYまたは希土類元素,6.0<y<6.
4)のいずれかであることを特徴とする超電導素子。
8. The oxide semiconductor containing copper according to claim 1 , wherein R 1 + x Ba 2-x Cu 3 O y (R is a rare earth element other than Pr, 0.3 < x <0.8, 6 <y <
8), Pr 1 + x Ba 2-x Cu 3 O y (0 ≦ x ≦ 0.5, 6 <y <
8), Y 1-x Pr x Ba 2 Cu 3 O y (0.6 <x ≦ 1,6 <y
<8), Bi 2 Sr 2 Ca 1-x R x Cu 2 O y (R is a rare earth element,
0.6 ≦ x ≦ 1.0, 8 <y <8.5), and RBa
2 Cu 3 O y (R is Y or a rare earth element, 6.0 <y <6.
4) A superconducting element which is any one of 4).
JP4138332A 1992-05-29 1992-05-29 Superconducting element Expired - Fee Related JP2515947B2 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100669702B1 (en) * 2003-11-29 2007-01-16 삼성에스디아이 주식회사 TFT and Flat panel display therewith
JP2014082357A (en) * 2012-10-17 2014-05-08 Semiconductor Energy Lab Co Ltd Semiconductor device

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63313877A (en) * 1987-06-17 1988-12-21 Toshiba Corp Superconducting transistor
JPH01276680A (en) * 1988-04-27 1989-11-07 Sony Corp Superconducting transistor
JPH03228382A (en) * 1990-02-02 1991-10-09 Hitachi Ltd Superconducting switching element

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63313877A (en) * 1987-06-17 1988-12-21 Toshiba Corp Superconducting transistor
JPH01276680A (en) * 1988-04-27 1989-11-07 Sony Corp Superconducting transistor
JPH03228382A (en) * 1990-02-02 1991-10-09 Hitachi Ltd Superconducting switching element

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100669702B1 (en) * 2003-11-29 2007-01-16 삼성에스디아이 주식회사 TFT and Flat panel display therewith
JP2014082357A (en) * 2012-10-17 2014-05-08 Semiconductor Energy Lab Co Ltd Semiconductor device

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