JPH0335571A - Tunnel element - Google Patents

Tunnel element

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Publication number
JPH0335571A
JPH0335571A JP1171431A JP17143189A JPH0335571A JP H0335571 A JPH0335571 A JP H0335571A JP 1171431 A JP1171431 A JP 1171431A JP 17143189 A JP17143189 A JP 17143189A JP H0335571 A JPH0335571 A JP H0335571A
Authority
JP
Japan
Prior art keywords
superconducting
film
film formation
tunnel
tunnel element
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
Application number
JP1171431A
Other languages
Japanese (ja)
Inventor
Eiji Natori
栄治 名取
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Seiko Epson Corp
Original Assignee
Seiko Epson Corp
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
Application filed by Seiko Epson Corp filed Critical Seiko Epson Corp
Priority to JP1171431A priority Critical patent/JPH0335571A/en
Publication of JPH0335571A publication Critical patent/JPH0335571A/en
Pending legal-status Critical Current

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  • Superconductor Devices And Manufacturing Methods Thereof (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明はジョセフソン素子、超伝導ベーストランジスタ
、準粒子トンネル効果素子、などトンネルバリアを必要
とする超伝導デバイスをこ関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to superconducting devices that require a tunnel barrier, such as Josephson devices, superconducting base transistors, and quasi-particle tunnel effect devices.

[従来の技術] ジョセフソン素子で説明する0周知の様をこジョセフソ
ン素子は点接触型、結晶粒界型、サンドイッチ型の3種
類あるが集積化を図るをこ◆よりンドイッチ型、即ちト
ンネルバリアを形成するタイプ番こする必要がある。こ
のサンドイッチ型には超伝導材料にコヒーレンス長さの
長いNbを、トンネルバリアに酸化アルミなどを用いて
いた。またトンネルバリアは蒸着法やスパッタ法により
形成していた。
[Prior art] There are three types of Josephson elements: a point contact type, a grain boundary type, and a sandwich type. It is necessary to rub the type number to form a barrier. This sandwich type used Nb, which has a long coherence length, as the superconducting material and aluminum oxide as the tunnel barrier. Further, the tunnel barrier was formed by a vapor deposition method or a sputtering method.

[発明が解決しようとする課題] しかし臨界温度が液体窒素を大幅に越え使い易くなると
共にエネルギーギャップが大きく半導体との融合や高速
スイッチ化が図れると考えられている酸化物超伝導材料
のサンドイッチ型デバイスはまだ完成していない。その
原因は酸化物超伝導材料のコヒーレンス長さがNbに比
べ1/10以下と極端に短いためである。コヒーレンス
長さが短いためトンネルバリアの厚みも薄くする必要が
あり蒸着法やスパッタ法などにより絶縁膜等を形成して
トンネルバリアとする方法はNb系でも高度な成膜技術
を必要としたのに更に薄くするため膜厚の制御やピンホ
ールの抑制が非常に困難となる。
[Problem to be solved by the invention] However, the sandwich type of oxide superconducting material has a critical temperature far exceeding that of liquid nitrogen, making it easier to use, and has a large energy gap, making it possible to integrate it with semiconductors and achieve high-speed switching. The device is not yet complete. The reason for this is that the coherence length of the oxide superconducting material is extremely short, 1/10 or less, compared to Nb. Because the coherence length is short, it is necessary to reduce the thickness of the tunnel barrier, and the method of forming an insulating film or the like using vapor deposition or sputtering to form a tunnel barrier requires advanced film formation technology even for Nb-based materials. In order to make the film even thinner, it becomes extremely difficult to control the film thickness and suppress pinholes.

今後超伝導材料の臨界温度はより高くなるものと思われ
るが臨界温度が高くなるに従いコヒーレンス長さはより
短くなるため更に上記点は大きな問題となる。
It is thought that the critical temperature of superconducting materials will become higher in the future, but as the critical temperature increases, the coherence length will become shorter, so the above point will become an even bigger problem.

本発明はこの様な問題を解決するものであり、高臨界温
度で使い安く高速スイッチ化が図れ且半導体との融合が
可能等、超伝導材料の持つ特性を引き出したトンネル素
子を容易に得んとするものである。
The present invention solves these problems and makes it possible to easily obtain a tunnel element that brings out the characteristics of superconducting materials, such as being easy to use at high critical temperatures, achieving high-speed switching, and being able to be integrated with semiconductors. That is.

[課題を解決するための手段] 上記の問題を解決するため本発明のトンネル素子は1)
超伝導電極の表面部を不活性ガス雰囲気中でプラズマ処
理し、その表面部を絶縁層または半導体層に変えた後そ
の上にもう一方の超伝導または金属電極を形成して成る
ことを特徴とする。
[Means for Solving the Problems] In order to solve the above problems, the tunnel element of the present invention has the following features: 1)
It is characterized by subjecting the surface of a superconducting electrode to plasma treatment in an inert gas atmosphere to transform that surface into an insulating layer or a semiconductor layer, and then forming another superconducting or metal electrode thereon. do.

[実施例] 以下実施例に従い本発明を説明する。[Example] The present invention will be explained below with reference to Examples.

先ず最初に第1図に示すように単結晶SrTiO3基板
1上に反応蒸着法によりHo1Ba2Cu30Y膜(以
後下部電極2とする〉を250nm形成する。
First, as shown in FIG. 1, a 250 nm thick Ho1Ba2Cu30Y film (hereinafter referred to as the lower electrode 2) is formed on a single crystal SrTiO3 substrate 1 by a reactive vapor deposition method.

成膜は蒸発原料にそれぞれHo、Ba、Cuの金属を用
い、蒸発はBaのみ電子ビーム、他の金属はKnuds
enセルにより行なった。条件は初期真空度2*10−
’Torr、成膜中真空度3〜9*10−’Torr、
基板温度560〜650℃、成膜速度20〜35nm/
minであり、酸素の供給はマイクロ* (ECR)で
活性化した酸素プラズマを基板部に成膜中に照射して行
う。この工程で得られた下部電極2はX線回折、RHE
ED分析、4端子法抵抗測定によるとエピタキシャル成
長した89〜91にの超伝導膜であった。
Film formation uses Ho, Ba, and Cu metals as evaporation raw materials, with Ba being evaporated by electron beam and other metals being evaporated by Knuds.
This was done using an en cell. Conditions are initial vacuum level 2*10-
'Torr, degree of vacuum during film formation 3-9*10-'Torr,
Substrate temperature 560-650°C, film formation rate 20-35 nm/
The supply of oxygen is performed by irradiating the substrate with oxygen plasma activated by micro* (ECR) during film formation. The lower electrode 2 obtained in this step is subjected to X-ray diffraction, RHE
According to ED analysis and 4-terminal resistance measurement, it was an epitaxially grown superconducting film of 89 to 91.

次に下部電極2の一部をレジストによりマスキングした
後プラズマリアクターを用い下部電極2の表面をプラズ
マ処理する。プラズマ処理によりプラズマに晒された部
分は還元されるとともに構造を一部破壊され半導体層か
絶縁層3になる。この層の厚さはプラズマ処理の出力を
抑えた状態では処理時間の設定で自由に精度良く変えら
れる。
Next, after masking a part of the lower electrode 2 with a resist, the surface of the lower electrode 2 is subjected to plasma treatment using a plasma reactor. During the plasma treatment, the portion exposed to the plasma is reduced and the structure is partially destroyed to become a semiconductor layer or an insulating layer 3. The thickness of this layer can be freely and accurately changed by setting the processing time when the plasma processing output is suppressed.

尚使用するガスはヘリウムやアルゴン等不活性ガスある
。塩素ガスやフッ素系ガス等エツチング力の強いガスは
超伝導部の還元や構造破壊を高精度に制御出来ないため
好ましくない。
The gas used is an inert gas such as helium or argon. Gases with strong etching power, such as chlorine gas or fluorine-based gases, are not preferred because reduction and structural destruction of the superconducting portion cannot be controlled with high precision.

次にメタルマスクをした後絶縁層3上にAuを電子ビー
ム蒸着により厚さ、成膜速度それぞれ6nm、6nm/
minで成膜し中間層4を形成する。この中間層4は後
に形成するHo1Ba2Cu30Y膜を成膜する過程で
絶縁層3が酸化し超伝導体に戻らないよう防止する為の
ものである。後工程に於て可逆変化を起こさない超伝導
材料を用いる場合はこの中間層4は必要ない。
Next, after applying a metal mask, Au was deposited on the insulating layer 3 by electron beam evaporation to a thickness of 6 nm and a deposition rate of 6 nm/6 nm, respectively.
The intermediate layer 4 is formed by forming a film at a speed of min. This intermediate layer 4 is provided to prevent the insulating layer 3 from being oxidized and returning to a superconductor during the process of forming the Ho1Ba2Cu30Y film to be formed later. This intermediate layer 4 is not necessary when using a superconducting material that does not cause reversible changes in subsequent steps.

次に下部電極2と同様に反応蒸着法によりHo1Ba2
Cu30Y膜(以後上部電極5とする)を1100n形
成する。
Next, as with the lower electrode 2, Ho1Ba2 was formed using the reactive vapor deposition method.
A Cu30Y film (hereinafter referred to as upper electrode 5) having a thickness of 1100 nm is formed.

条件は初期真空度2*10−”Torr、成膜中真空度
7〜9110−’Torr、  基板温度560℃、成
膜速度20〜25nm/minであり、酸素の供給はマ
イクロ波(ECR)で活性化した酸素プラズマを成膜中
に照射して行う、また成膜後はチャンバー内に酸素を圧
力2Torrまで導入し560℃で30分ホールドした
後徐冷した。
The conditions were an initial vacuum level of 2*10-'Torr, a vacuum level during film formation of 7 to 9110-'Torr, a substrate temperature of 560°C, and a film formation rate of 20 to 25 nm/min. Oxygen was supplied by microwave (ECR). This was carried out by irradiating activated oxygen plasma during film formation, and after film formation, oxygen was introduced into the chamber to a pressure of 2 Torr, held at 560° C. for 30 minutes, and then slowly cooled.

この様にして得られた素子のI −V、特性とマイクロ
波照射特性を調べた。
The I-V characteristics and microwave irradiation characteristics of the device thus obtained were investigated.

その結果I−V特性では超伝導ジョセフソン電流がマイ
クロ波照射特性ではシャピロステップ(VSTEP= 
n−f −h/ 2 eを満足していた。ここでfはマ
イクロ波周波数、n=o、  ±1.±2゜±3・・・
 hはブランク定数、eは電気素量である。)が見られ
ジョセフソン素子となっていることが確認された。
As a result, the superconducting Josephson current in the IV characteristic is the Shapiro step (VSTEP=
n-f-h/2e was satisfied. where f is the microwave frequency, n=o, ±1. ±2゜±3...
h is a blank constant, and e is an elementary charge. ) was observed, confirming that it was a Josephson element.

尚ここではジョセフソン素子で説明したが超伝導ベース
トランジスタ、準粒子トンネル効果素子等トンネルバリ
アを形成するものであれば効果は同じであり何等差し支
えない。
Although the Josephson device has been explained here, any device that forms a tunnel barrier, such as a superconducting base transistor or a quasi-particle tunneling effect device, will have the same effect and there is no problem.

[発明の効果] 以上述べたように本発明によれば精度良くトンネルバリ
アを形成できるためコヒーレンス長さの短い超伝導材料
を用いても容易にトンネル素子を得られる。そのため超
伝導材料の持つ高臨界温度で使い安く、高速スイッチ化
が図れ且半導体との融合が可能等の有効な特性を引き出
すことが出来
[Effects of the Invention] As described above, according to the present invention, a tunnel barrier can be formed with high precision, so a tunnel element can be easily obtained even if a superconducting material with a short coherence length is used. Therefore, it is possible to bring out the effective properties of superconducting materials, such as their high critical temperature, ease of use, high-speed switching, and compatibility with semiconductors.

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

第1図は絶縁層形成までの膜の断面図。 第2図はトンネル素子の断面図。 1・・・基板 2・・・下部電極 3・・・絶縁層 4・・・中間層 5・・・上部電極 以上 FIG. 1 is a cross-sectional view of the film up to the formation of the insulating layer. FIG. 2 is a cross-sectional view of the tunnel element. 1... Board 2...Lower electrode 3...Insulating layer 4...middle class 5...Top electrode that's all

Claims (1)

【特許請求の範囲】[Claims] (1)超伝導電極の表面部を不活性ガス雰囲気中でプラ
ズマ処理し、その表面部を絶縁層または半導体層に変え
た後その上にもう一方の超伝導または金属電極を形成し
て成ることを特徴とするトンネル素子。
(1) The surface of a superconducting electrode is subjected to plasma treatment in an inert gas atmosphere to transform that surface into an insulating or semiconductor layer, and then another superconducting or metal electrode is formed on top of that. A tunnel element characterized by:
JP1171431A 1989-07-03 1989-07-03 Tunnel element Pending JPH0335571A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1171431A JPH0335571A (en) 1989-07-03 1989-07-03 Tunnel element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1171431A JPH0335571A (en) 1989-07-03 1989-07-03 Tunnel element

Publications (1)

Publication Number Publication Date
JPH0335571A true JPH0335571A (en) 1991-02-15

Family

ID=15923000

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1171431A Pending JPH0335571A (en) 1989-07-03 1989-07-03 Tunnel element

Country Status (1)

Country Link
JP (1) JPH0335571A (en)

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