JPH03257022A - Compound having structure of cubic type represented by ag7tas6 and its production - Google Patents

Compound having structure of cubic type represented by ag7tas6 and its production

Info

Publication number
JPH03257022A
JPH03257022A JP5242390A JP5242390A JPH03257022A JP H03257022 A JPH03257022 A JP H03257022A JP 5242390 A JP5242390 A JP 5242390A JP 5242390 A JP5242390 A JP 5242390A JP H03257022 A JPH03257022 A JP H03257022A
Authority
JP
Japan
Prior art keywords
compound
starting material
tantalum
ag7tas6
raw material
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
JP5242390A
Other languages
Japanese (ja)
Other versions
JPH0725551B2 (en
Inventor
Hiroaki Wada
和田 弘昭
Norihiko Ishii
紀彦 石井
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.)
National Institute for Research in Inorganic Material
Original Assignee
National Institute for Research in Inorganic Material
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 National Institute for Research in Inorganic Material filed Critical National Institute for Research in Inorganic Material
Priority to JP2052423A priority Critical patent/JPH0725551B2/en
Publication of JPH03257022A publication Critical patent/JPH03257022A/en
Publication of JPH0725551B2 publication Critical patent/JPH0725551B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

PURPOSE:To obtain Ag7TaS6 as a compd. useful for a semiconductor, an electronic material, an ionic conductor, etc., by heating a green compact contg. starting material for Ag, starting material for Ta and starting material for S in a prescribed ratio at a prescribed temp. in vacuum. CONSTITUTION:Metallic Ag or Ag2S as starting material for Ag is mixed with Ta or TaS2 as starting material for Ta and S or TaS2 as starting material for S in 7:1:6 atomic ratio of Ag:Ta:S. A green compact of the resulting powdery mixture is put in an alumina crucible and heated at 500-600 deg.C in an evacuated and sealed quartz tube.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はAg−Ta−5累代合物に係り、特に半導体電
子材料並びにイオン伝導体などとして有用な新規化合物
及びその製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to Ag-Ta-5 historical compounds, and particularly to novel compounds useful as semiconductor electronic materials and ion conductors, and methods for producing the same.

(従来の技術及び解決しようとする課題)従来、Ag−
Ta−8系では、三元系化合物として900℃以下の温
度で合成される六方晶系のAg、gTaS2や、菱面体
晶系のAg1/3TaS2の存在が知られている。
(Prior art and problems to be solved) Conventionally, Ag-
In the Ta-8 system, the existence of hexagonal Ag and gTaS2, which are synthesized at temperatures of 900° C. or lower, and rhombohedral Ag1/3 TaS2, which are synthesized at temperatures of 900° C. or lower, are known as ternary compounds.

しかしながら、Ag−Ta−5系の相関係については、
殆ど報告がなく、立方晶系の三元系化合物の存在につい
ては全く知られていなかった。
However, regarding the phase relationship of Ag-Ta-5 system,
There have been almost no reports, and the existence of cubic ternary compounds was completely unknown.

本発明は、かSる事情に鑑みて、Ag−Ta−8系で立
方晶系の新規な三元系化合物を得る技術を提供すること
を目的とするものである。
In view of the above circumstances, the present invention aims to provide a technique for obtaining a novel cubic system ternary compound based on Ag-Ta-8.

(課題を解決するための手段) 前記目的を達成するため、本発明者は1石英封管法によ
り500〜600℃の温度範囲で、新規なAg−Ta−
8系の三元系化合物を見い出すべく研究を重ねた結果、
ここに、立方晶系の新規化合物を発見したものである。
(Means for Solving the Problem) In order to achieve the above object, the present inventor has developed a novel Ag-Ta-
As a result of repeated research to find 8-series ternary compounds,
Here, we discovered a new compound with a cubic crystal system.

すなわち、本発明に係る新規化合物は、化学式A gt
 T a S sで示される立方晶系の構造を有する化
金物である。
That is, the novel compound according to the present invention has the chemical formula A gt
It is a metal compound having a cubic crystal structure represented by T a S s.

また、その製造法は、銀原料として金属銀又は硫化銀と
、タンタル原料としてタンタル又は二硫化タンタルと、
硫黄原料として硫黄、二硫化タンタル又は硫化銀とを、
AgとTaとSの割合が原子比で7対1対6の割合で混
合し、該混合粉末を加圧して圧粉体とし、これをアルミ
ナルツボに入れ真空引きした石英封管中で500〜60
0℃の温度に加熱することを特徴とするものである。
In addition, the manufacturing method uses metallic silver or silver sulfide as a silver raw material, tantalum or tantalum disulfide as a tantalum raw material,
Sulfur, tantalum disulfide or silver sulfide as the sulfur raw material,
Ag, Ta, and S are mixed at an atomic ratio of 7:1:6, the mixed powder is pressed to form a green compact, and this is placed in an alumina crucible and heated in a evacuated quartz sealed tube to 60
It is characterized by heating to a temperature of 0°C.

以下に本発明を更に詳述する。The present invention will be explained in further detail below.

(作用) 本発明に係る化学式Ag7TaS6で示される化合物は
、硫黄が立方密充填し、金属原子がその間隙にある六配
位位置などを占める極めて等方的な横通を有する立方晶
系の物質である。
(Function) The compound represented by the chemical formula Ag7TaS6 according to the present invention is a cubic crystal substance with extremely isotropic cross-contact, in which sulfur is cubically densely packed and metal atoms occupy hexacoordination positions in the gaps. It is.

立方晶系としての格子定数は、 a=10.5139±0.0003(人)V=1162
.23f0.09(人3)で、空間群はF43m(No
、216)である。
The lattice constant as a cubic system is a=10.5139±0.0003 (person) V=1162
.. 23f0.09 (3 people), space group F43m (No.
, 216).

この化合物についての面指数(hkQ)、面間隔d(人
)(但し、doは実測値、dcは計算値)及び粉末X線
回折強度I(%)(但し、■。は実測強度)を示すと、
第1表のとおりである。
The planar index (hkQ), interplanar spacing d (person) (however, do is the measured value, dc is the calculated value) and powder X-ray diffraction intensity I (%) (however, ■. is the measured intensity) for this compound are shown. and,
As shown in Table 1.

【以下余白1 筑1男 A i−T a S cの粉末X線回折データこの新規
化合物は、以下の方法により製造することができる。
[Margin 1 below: Powder X-ray diffraction data of Chikuichio A i-T a Sc This new compound can be produced by the following method.

すなわち、まず、銀原料として金属銀又は硫化銀と、タ
ンタル原料としてタンタル又は二硫化タンタルと、硫黄
原料として硫黄、二硫化タンタル又は硫化銀とを、Ag
とTaとSの割合が原子比で7対1対6の割合で混合す
る。この混合粉末を加圧して圧粉体とし、これをアルミ
ナルツボに入れ真空引きした石英封管中で500〜60
0℃の温度に加熱する方法である。
That is, first, metal silver or silver sulfide as a silver raw material, tantalum or tantalum disulfide as a tantalum raw material, and sulfur, tantalum disulfide, or silver sulfide as a sulfur raw material, Ag
and Ta and S are mixed in an atomic ratio of 7:1:6. This mixed powder was pressurized to form a green compact, which was then placed in an aluminium crucible and placed in a evacuated quartz sealed tube.
This is a method of heating to a temperature of 0°C.

この方法の場合、出発原料は、市販のものをそのまま使
用してもよいが、得られる化合物を半導体電子材料とし
て用いる場合には、不純物の含まないできるだけ純度の
高いものを用いるのが望ましい、また、製造時には同相
化学反応促進のため、粒径は小さい方が良く、数μm以
下であることが望ましい。
In the case of this method, commercially available starting materials may be used as they are, but if the resulting compound is to be used as a semiconductor electronic material, it is desirable to use one that does not contain impurities and is as pure as possible. In order to promote in-phase chemical reactions during production, the smaller the particle size, the better, and desirably several μm or less.

原料は、そのまま、望ましくは不活性気体雰囲気中で充
分に混合し、加圧成形して圧粉体とする。
The raw materials are thoroughly mixed as they are, preferably in an inert gas atmosphere, and then pressure-molded to form a green compact.

加圧条件は特に限定するものではないが、1〜2ton
/cm”の静水圧であることが望ましい。
Pressurization conditions are not particularly limited, but 1 to 2 tons
A hydrostatic pressure of /cm'' is desirable.

原料の混合割合は、AgとTaとSの割合が原子比で7
対1対6の割合であることが必要であり、この割合から
組成がずれると、目的とする化合物の単一相を得ること
ができない。
The mixing ratio of the raw materials is such that the atomic ratio of Ag, Ta, and S is 7.
The ratio needs to be 1:6, and if the composition deviates from this ratio, a single phase of the target compound cannot be obtained.

次いで、該圧粉体をアルミナルツボに入れ、真空引きし
た石英封管中で加熱するが、その焼成温度は500〜6
00℃であることが必要である。
Next, the green compact is placed in an alumina crucible and heated in a evacuated quartz sealed tube at a firing temperature of 500 to 600℃.
It is necessary that the temperature is 00°C.

加熱時間は特に制限しないが、500℃で3〜4日が望
ましく、それ以上の加熱は試料と器壁との反応によりタ
ンタル酸化物の生成が進行するため、好ましくない。
Although the heating time is not particularly limited, it is preferably 3 to 4 days at 500° C.; heating longer than that is not preferred because tantalum oxide will be produced due to the reaction between the sample and the vessel wall.

加熱終了後は、石英封管を水中に急冷する。得られる化
学式Ag7TaS6を有する化合物粉末は黒色であり、
粉末X線回折法によって立方晶系の結晶構造を有するこ
とが判明した。
After heating, the quartz sealed tube is rapidly cooled in water. The resulting compound powder having the chemical formula Ag7TaS6 is black;
It was found by powder X-ray diffraction that it had a cubic crystal structure.

次に本発明の実施例を示す。Next, examples of the present invention will be shown.

(実施例) 純度99.9%以上の硫化銀(Ag、S)粉末と、純度
99.96%以上の二硫化タンタル(TaS2)粉末と
、純度99.9999%以上の硫黄(S)粉末とを、A
gとTaとSの原子比が7対1対6の割合となるように
グローブボックス中で秤量し、めのう乳鉢内で約10分
間混合し、該混合粉末を加圧して圧粉体を得た。
(Example) Silver sulfide (Ag, S) powder with a purity of 99.9% or more, tantalum disulfide (TaS2) powder with a purity of 99.96% or more, and sulfur (S) powder with a purity of 99.9999% or more. A, A
The mixture was weighed in a glove box so that the atomic ratio of g, Ta, and S was 7:1:6, mixed in an agate mortar for about 10 minutes, and the mixed powder was pressed to obtain a green compact. .

次いで、これをアルミナルツボに入れ、透明石英管中に
真空封入し、500℃に設定された横型管状電気炉内に
入れ、4日間加熱し、その後、石英管を取り出し、水中
に急冷した。
Next, this was placed in an alumina crucible, vacuum sealed in a transparent quartz tube, placed in a horizontal tubular electric furnace set at 500° C., heated for 4 days, and then the quartz tube was taken out and quenched in water.

得られた試料は、Ag、Tag、単一相であり、粉末X
線回折法により各反射の面間隔d。及び回折強度工。を
測定した結果、第1表に示すとおりであった。
The obtained sample was Ag, Tag, single phase, powder
The interplanar spacing d of each reflection was determined by the line diffraction method. and diffraction intensity engineering. The results of the measurements were as shown in Table 1.

また、立方晶系としての格子定数は次のとおりであった
Moreover, the lattice constants as a cubic system were as follows.

a=10.5139±0.0003(人)V=1162
.23±0.09C人3)上記の格子定数、及び第1表
に示した各面指数(hkfi)より計算した面間隔dc
(人)は、実測の面間隔d、(人)と極めてよく一致し
た。
a=10.5139±0.0003 (person) V=1162
.. 23±0.09C person 3) Surface spacing dc calculated from the above lattice constant and each surface index (hkfi) shown in Table 1
(person) was in extremely good agreement with the actually measured surface spacing d, (person).

(発明の効果) 以上説明したように、本発明によれば、化学式Ag7T
ag、で示される立方晶系の構造を有する新規なAg−
Ta−8累代合物を提供でき、特に半導体電子材料並び
にイオン伝導体などとして有用であり、その効果は大き
い。
(Effects of the Invention) As explained above, according to the present invention, the chemical formula Ag7T
A novel Ag-
It is possible to provide Ta-8 grade compounds, which are particularly useful as semiconductor electronic materials and ion conductors, and have great effects.

Claims (2)

【特許請求の範囲】[Claims] (1)化学式Ag_7TaS_6で示される立方晶系の
構造を有する化合物。
(1) A compound having a cubic structure represented by the chemical formula Ag_7TaS_6.
(2)銀原料として金属銀又は硫化銀と、タンタル原料
としてタンタル又は二硫化タンタルと、硫黄原料として
硫黄、二硫化タンタル又は硫化銀とを、AgとTaとS
の割合が原子比で7対1対6となるように混合し、該混
合粉末を加圧して圧粉体とし、これをアルミナルツボに
入れ真空引きした石英封管中で500〜600℃の温度
に加熱することを特徴とするAg_7TaS_6で示さ
れる立方晶系の構造を有する化合物の製造法。
(2) Metallic silver or silver sulfide as a silver raw material, tantalum or tantalum disulfide as a tantalum raw material, and sulfur, tantalum disulfide or silver sulfide as a sulfur raw material, Ag, Ta and S
The mixed powder was mixed in an atomic ratio of 7:1:6, and the mixed powder was pressed to form a green compact, which was then placed in an alumina crucible and heated at a temperature of 500 to 600°C in a evacuated quartz sealed tube. 1. A method for producing a compound having a cubic structure represented by Ag_7TaS_6, which comprises heating the compound to .
JP2052423A 1990-03-02 1990-03-02 Compound having a cubic system structure represented by Ag (7), TaS (6) and method for producing the same Expired - Lifetime JPH0725551B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2052423A JPH0725551B2 (en) 1990-03-02 1990-03-02 Compound having a cubic system structure represented by Ag (7), TaS (6) and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2052423A JPH0725551B2 (en) 1990-03-02 1990-03-02 Compound having a cubic system structure represented by Ag (7), TaS (6) and method for producing the same

Publications (2)

Publication Number Publication Date
JPH03257022A true JPH03257022A (en) 1991-11-15
JPH0725551B2 JPH0725551B2 (en) 1995-03-22

Family

ID=12914374

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2052423A Expired - Lifetime JPH0725551B2 (en) 1990-03-02 1990-03-02 Compound having a cubic system structure represented by Ag (7), TaS (6) and method for producing the same

Country Status (1)

Country Link
JP (1) JPH0725551B2 (en)

Also Published As

Publication number Publication date
JPH0725551B2 (en) 1995-03-22

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