JP2913996B2 - Iodine-inserted oxide superconductor and method for producing the same - Google Patents

Iodine-inserted oxide superconductor and method for producing the same

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Publication number
JP2913996B2
JP2913996B2 JP4100202A JP10020292A JP2913996B2 JP 2913996 B2 JP2913996 B2 JP 2913996B2 JP 4100202 A JP4100202 A JP 4100202A JP 10020292 A JP10020292 A JP 10020292A JP 2913996 B2 JP2913996 B2 JP 2913996B2
Authority
JP
Japan
Prior art keywords
iodine
thallium
oxide superconductor
based oxide
producing
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.)
Expired - Fee Related
Application number
JP4100202A
Other languages
Japanese (ja)
Other versions
JPH05279037A (en
Inventor
祐一 島川
隆志 眞子
佳実 久保
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.)
NEC Corp
Original Assignee
Nippon Electric Co Ltd
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 Nippon Electric Co Ltd filed Critical Nippon Electric Co Ltd
Priority to JP4100202A priority Critical patent/JP2913996B2/en
Publication of JPH05279037A publication Critical patent/JPH05279037A/en
Application granted granted Critical
Publication of JP2913996B2 publication Critical patent/JP2913996B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E40/00Technologies for an efficient electrical power generation, transmission or distribution
    • Y02E40/60Superconducting electric elements or equipment; Power systems integrating superconducting elements or equipment

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  • Inorganic Compounds Of Heavy Metals (AREA)
  • Superconductors And Manufacturing Methods Therefor (AREA)

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、各種の超伝導応用装置
や超伝導素子に使用される酸化物超伝導材料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oxide superconducting material used for various superconducting devices and superconducting elements.

【0002】[0002]

【従来の技術】現在、超伝導材料としては、すでに金属
・合金系超伝導材料、化合物超伝導材料などが実用化さ
れている。超伝導材料は超伝導磁石用のコイルやジョセ
フソン素子などのエレクトロニクスデバイスなどを作る
のに用いられ、特にジョセフソン接合の高感度性、高精
度性、低雑音性を利用したSQUIDや精密計測への応
用の他、ジョセフソン接合の高速応答性と低消費電力に
着目した電子計算機への応用が期待されている。超伝導
材料の応用を考えた場合、その超伝導転移温度(Tc)
は、できるだけ高いことが望まれる。金属・合金系超伝
導材料、化合物超伝導材料は、冷媒として高価で希少な
液体ヘリウムを用いなければならず、このことがこれら
の超伝導体の広い分野への応用を妨げる一因となってい
る。この点では銅酸化物系超伝導体は、従来の超伝導体
よりもはるかに優れており、30KのTcをもつLa−
Ba−Cu−O系酸化物超伝導体の発見以来、90K級
のBa−Y−Cu−O系、110K級のBi−Sr−C
a−Cu−O系、120K級のTl−Ba−Ca−Cu
−O系などが相次いで発見されてきた。液体窒素温度を
はるかに越えたTcをもつ材料の発見は、実用材料とし
ての期待をますます高めている。
2. Description of the Related Art At present, as a superconducting material, a metal / alloy superconducting material, a compound superconducting material and the like have already been put to practical use. Superconducting materials are used to make coils for superconducting magnets and electronic devices such as Josephson devices, especially for SQUIDs and precision measurements that utilize the high sensitivity, high accuracy, and low noise of Josephson junctions. In addition to the application of, it is expected to be applied to electronic computers that focus on the high-speed response and low power consumption of Josephson junctions. Considering the application of superconducting material, its superconducting transition temperature (Tc)
Should be as high as possible. Metallic / alloy-based superconducting materials and compound superconducting materials must use expensive and rare liquid helium as a refrigerant, which is one of the factors that hinders the application of these superconductors to a wide range of fields. I have. In this respect, the copper oxide-based superconductor is far superior to the conventional superconductor, and has a La-Tc of 30 K.
Since the discovery of Ba-Cu-O-based oxide superconductor, 90K-class Ba-Y-Cu-O-based and 110K-class Bi-Sr-C
a-Cu-O system, Tl-Ba-Ca-Cu of 120K class
-O system and the like have been discovered one after another. The discovery of a material having a Tc far above the temperature of liquid nitrogen has further increased expectations for a practical material.

【0003】[0003]

【発明が解決しようとする課題】タリウム系超伝導体は
現在のところ最も高いTcをもち、実用化への期待が最
も高い物質である。しかしその応用に際しては、高いT
cの他に高い臨界電流密度(Jc)、高い臨界磁場(B
c)をもつことが望ましい。一般に酸化物超伝導体はT
cが高い場合でもJc,Bcが低いため、大電流での応
用や強磁場下での使用が限られていた。本発明はこのよ
うな従来の事情に鑑み、高いTcをもつタリウム系酸化
物超伝導体を用いて、さらに高いJcを併せもつ超伝導
体とその製造方法を提供することを目的とする。
The thallium-based superconductor has the highest Tc at present and is a substance expected to be put to practical use. However, in its application, high T
c, high critical current density (Jc), high critical magnetic field (B
It is desirable to have c). Generally, the oxide superconductor is T
Even when c is high, Jc and Bc are low, so that application in a large current and use under a strong magnetic field have been limited. In view of such a conventional situation, an object of the present invention is to provide a superconductor having an even higher Jc and a method of manufacturing the same using a thallium-based oxide superconductor having a high Tc.

【0004】[0004]

【課題を解決するための手段】本発明は、ITl2Ba2
Can-1Cun4+2n(式中、nは1,2,3または4で
ある。)で表されることを特徴とするヨウ素挿入タリウ
ム系酸化物超伝導体である。またその製造方法は、固体
ヨウ素とTl2Ba2Can-1Cun4+2n(式中、nは
1,2,3または4である。)で表されるタリウム系酸
化物超伝導体を混合し、熱処理するか、Tl2Ba2Ca
n-1Cun4+2n(式中、nは1,2,3または4であ
る。)で表されるタリウム系酸化物超伝導体をヨウ素を
溶解した有機溶媒に浸すか、あるいはTl2Ba2Ca
n-1Cun4+2n(式中、nは1,2,3または4であ
る。)で表されるタリウム系酸化物超伝導体を昇華した
ヨウ素気体中に入れることを特徴とする。
SUMMARY OF THE INVENTION The present invention provides an ITl 2 Ba 2
(In the formula, n 1, 2, 3 or 4.) Ca n-1 Cu n O 4 + 2n iodine inserted thallium based oxide superconductor, characterized by being represented by. The manufacturing method of a solid (wherein, n 1, 2, 3 or 4.) Iodine and Tl 2 Ba 2 Ca n-1 Cu n O 4 + 2n thallium based oxide superconductor represented by The body is mixed and heat treated or Tl 2 Ba 2 Ca
n-1 Cu n O 4 + 2n ( wherein, n 1, 2, 3 or 4.) or immersed in an organic solvent prepared by dissolving iodine thallium based oxide superconductor represented by, or Tl 2 Ba 2 Ca
(In the formula, n 1, 2, 3 or 4 in which.) n-1 Cu n O 4 + 2n , characterized in that placed in the iodine in the gas sublimed thallium-based oxide represented by superconductors .

【0005】[0005]

【作用】Tl2Ba2Can-1Cun4+2n(n=1,2,
3,4)は、n=1,2,3,4の各化合物で最高のT
cが85K,110K,125K,115Kとなる。こ
の各化合物はセラミックスの場合、77KでのJcは、
各々100A/cm2,450A/cm2,600A/c
2,500A/cm2である。しかるにタリウム系酸化
物、Tl2Ba2Can-1Cun4+2n(n=1,2,3,
4)を固体ヨウ素と混合し300℃で5時間熱処理した
ものは、粉末X線回折により解析した結果、ITl2
2Can-1Cun4+2n(n=1,2,3,4)で表さ
れ、タリウムと酸素の面の間にヨウ素が挿入された化合
物であることが確認され、さらにTcはほとんど変化し
ないが、Jcは各々170A/cm2,650A/c
2,900A/cm2,700A/cm2となることが
確認された。ヨウ素挿入タリウム系酸化物超伝導体の合
成においては、タリウム系酸化物をヨウ素を溶解したア
ルコール溶液に浸した場合、及び昇華したヨウ素気体中
に入れた場合にも粉末X線回折から同様の化合物が得ら
れ、固体ヨウ素から合成した場合と同程度の高いJcを
持つことが確認された。
[Action] Tl 2 Ba 2 Ca n-1 Cu n O 4 + 2n (n = 1,2,
3,4) is the highest T for each compound with n = 1,2,3,4.
c becomes 85K, 110K, 125K, and 115K. When these compounds are ceramics, Jc at 77K is
100 A / cm 2 , 450 A / cm 2 , 600 A / c respectively
m 2 , 500 A / cm 2 . However thallium-based oxide, Tl 2 Ba 2 Ca n- 1 Cu n O 4 + 2n (n = 1,2,3,
4) a material obtained by heat treatment for 5 hours at mixing 300 ° C. and solid iodine, the results of the analysis by powder X-ray diffraction, ITL 2 B
a 2 is represented by Ca n-1 Cu n O 4 + 2n (n = 1,2,3,4), it is confirmed a compound in which iodine is inserted between the surface of the thallium and oxygen, further Tc Changes little, but Jc is 170 A / cm 2 and 650 A / c, respectively.
m 2 , 900 A / cm 2 and 700 A / cm 2 were confirmed. In the synthesis of an iodine-inserted thallium-based oxide superconductor, the same compound is obtained from powder X-ray diffraction when the thallium-based oxide is immersed in an alcohol solution in which iodine is dissolved, and when the thallium-based oxide is placed in a sublimated iodine gas. Was obtained, and it was confirmed that the compound had a high Jc comparable to that of the case of synthesis from solid iodine.

【0006】[0006]

【実施例】以下、本発明の実施例について、Tl2Ba2
Ca2Cu310を例にとって具体的に説明する。 実施例1 通常の酸化物合成方法に従って合成したTl2Ba2Ca
2Cu310粉末にI2をITl2Ba2Ca2Cu310
比になるように秤量したものを混合し、これを石英ガラ
スに封入した後、300℃、5時間熱処理を行うことに
よりヨウ素挿入タリウム系超伝導体を得た(固体法)。
EXAMPLES Examples of the present invention will now be described with reference to Tl 2 Ba 2.
A specific description will be given using Ca 2 Cu 3 O 10 as an example. Example 1 Tl 2 Ba 2 Ca synthesized according to an ordinary oxide synthesis method
A mixture of 2 Cu 3 O 10 powder and a mixture of I 2 weighed so as to have a ratio of ITl 2 Ba 2 Ca 2 Cu 3 O 10 is mixed and sealed in quartz glass, followed by heat treatment at 300 ° C. for 5 hours. Thus, an iodine-inserted thallium-based superconductor was obtained (solid method).

【0007】実施例2 Tl2Ba2Ca2Cu310粉末または単結晶を、ヨウ素
を溶かしたアルコール溶液中に24時間浸すことにより
ヨウ素挿入タリウム系超伝導体を得た(液体法)。
Example 2 A Tl 2 Ba 2 Ca 2 Cu 3 O 10 powder or single crystal was immersed in an alcohol solution of iodine for 24 hours to obtain an iodine-inserted thallium-based superconductor (liquid method).

【0008】実施例3 Tl2Ba2Ca2Cu310粉末または単結晶を一方の端
に、反対側の端にI2を入れ、石英ガラス中に真空封入
し、I2側を熱することで昇華したヨウ素気体を発生さ
せることによりヨウ素挿入タリウム系超伝導体を得た
(気体法)。
Example 3 Tl 2 Ba 2 Ca 2 Cu 3 O 10 powder or single crystal is put at one end and I 2 is put at the other end, vacuum sealed in quartz glass, and the I 2 side is heated. As a result, an iodine-inserted thallium-based superconductor was obtained by generating sublimated iodine gas (gas method).

【0009】合成試料の確認は粉末X線回折、4軸単結
晶X線回折により行った。超伝導特性の評価は、SQU
IDマグネットメーターを用いた帯磁率測定と通常の直
流4端子法により行った。Jcは直流4端子法を用い
て、77K、0磁場において電圧端子間に0.1μV以
上の電圧が生じた時の電流により求めた。表1〜表4に
Tl2Ba2Can-1Cun4+2n(n=1,2,3,4)
各化合物のヨウ素挿入反応を施す前後のTc、Jcを示
す。ヨウ素挿入タリウム系超伝導体はヨウ素を挿入して
いない粉末および単結晶タリウム超伝導体と比較してT
cはほとんど変化しないが、高いJcをもつことが確認
される。
The synthesis sample was confirmed by powder X-ray diffraction and 4-axis single crystal X-ray diffraction. Evaluation of superconducting properties is based on SKU
The magnetic susceptibility was measured using an ID magnetometer and a normal DC four-terminal method was used. Jc was determined by a DC four-terminal method using a current when a voltage of 0.1 μV or more was generated between the voltage terminals at 77 K and zero magnetic field. Table 1 to Table 4 Tl 2 Ba 2 Ca n- 1 Cu n O 4 + 2n (n = 1,2,3,4)
The Tc and Jc before and after performing the iodine insertion reaction of each compound are shown. The iodine-inserted thallium-based superconductor has a T
Although c hardly changes, it is confirmed that it has a high Jc.

【0010】[0010]

【表1】 [Table 1]

【0011】[0011]

【表2】 [Table 2]

【0012】[0012]

【表3】 [Table 3]

【0013】[0013]

【表4】 [Table 4]

【0014】[0014]

【発明の効果】以上説明したように、本発明のヨウ素挿
入タリウム系超伝導体は高いTc、Jcをもつ材料とし
て、工業利用にとって極めて有用なものである。
As described above, the iodine-inserted thallium-based superconductor of the present invention is extremely useful for industrial use as a material having high Tc and Jc.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) C01G 15/00 C01G 1/00 H01B 12/00 ZAA CA(STN) REGISTRY(STN)──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 6 , DB name) C01G 15/00 C01G 1/00 H01B 12/00 ZAA CA (STN) REGISTRY (STN)

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ITl2Ba2Can-1Cun4+2n(式
中、nは1,2,3または4である。)で表されること
を特徴とするヨウ素挿入タリウム系酸化物超伝導体。
[Claim 1] ITL (wherein, n 1, 2, 3 or 4.) 2 Ba 2 Ca n -1 Cu n O 4 + 2n iodine inserted thallium-based oxide, which is characterized by being represented by Superconductor.
【請求項2】 請求項1記載の化合物の製造方法であっ
て、固体ヨウ素とTl2Ba2Can-1Cun4+2n(式
中、nは1,2,3または4である。)で表されるタリ
ウム系酸化物超伝導体を混合し、熱処理することを特徴
とするヨウ素挿入タリウム系酸化物超伝導体の製造方
法。
2. A method for producing a compound according to claim 1, solid iodine and Tl 2 Ba 2 Ca n-1 Cu n O 4 + 2n ( wherein, n is 1, 2, 3 or 4 A method for producing an iodine-inserted thallium-based oxide superconductor, comprising mixing and heat-treating the thallium-based oxide superconductor represented by the formula (1).
【請求項3】 請求項1記載の化合物の製造方法であっ
て、Tl2Ba2Can-1Cun4+2n(式中、nは1,
2,3または4である。)で表されるタリウム系酸化物
超伝導体をヨウ素を溶解した有機溶媒に浸すことを特徴
とするヨウ素挿入タリウム系酸化物超伝導体の製造方
法。
3. A process according to claim 1 a process for the preparation of a compound according, Tl 2 Ba 2 Ca n- 1 Cu n O 4 + 2n ( wherein, n 1,
2, 3 or 4. A method for producing an iodine-inserted thallium-based oxide superconductor, comprising immersing the thallium-based oxide superconductor represented by the formula (1) in an organic solvent in which iodine is dissolved.
【請求項4】 請求項1記載の化合物の製造方法であっ
て、Tl2Ba2Can-1Cun4+2n(式中、nは1,
2,3または4である。)で表されるタリウム系酸化物
超伝導体を昇華したヨウ素気体中に入れることを特徴と
するヨウ素挿入タリウム系酸化物超伝導体の製造方法。
4. The method of claim 1 a process for the preparation of a compound according, Tl 2 Ba 2 Ca n- 1 Cu n O 4 + 2n ( wherein, n 1,
2, 3 or 4. A method for producing an iodine-inserted thallium-based oxide superconductor, comprising placing the thallium-based oxide superconductor represented by the formula (1) in sublimated iodine gas.
JP4100202A 1992-03-27 1992-03-27 Iodine-inserted oxide superconductor and method for producing the same Expired - Fee Related JP2913996B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4100202A JP2913996B2 (en) 1992-03-27 1992-03-27 Iodine-inserted oxide superconductor and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4100202A JP2913996B2 (en) 1992-03-27 1992-03-27 Iodine-inserted oxide superconductor and method for producing the same

Publications (2)

Publication Number Publication Date
JPH05279037A JPH05279037A (en) 1993-10-26
JP2913996B2 true JP2913996B2 (en) 1999-06-28

Family

ID=14267723

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Country Status (1)

Country Link
JP (1) JP2913996B2 (en)

Also Published As

Publication number Publication date
JPH05279037A (en) 1993-10-26

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