JPH11171545A - Cu2hfs3 and production thereof - Google Patents
Cu2hfs3 and production thereofInfo
- Publication number
- JPH11171545A JPH11171545A JP9363481A JP36348197A JPH11171545A JP H11171545 A JPH11171545 A JP H11171545A JP 9363481 A JP9363481 A JP 9363481A JP 36348197 A JP36348197 A JP 36348197A JP H11171545 A JPH11171545 A JP H11171545A
- Authority
- JP
- Japan
- Prior art keywords
- hfs
- compound
- producing
- powder
- mixed
- 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
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】この出願の発明は、Cu2 H
fS3 とその製造方法に関するものである。さらに詳し
くは、この出願の発明は、半導体材料や二次電池正極材
料等として有用な新規化合物であるCu2 HfS3 とそ
の製造方法に関するものである。BACKGROUND OF THE INVENTION The invention of this application is based on Cu 2 H
fS 3 and a manufacturing method thereof. More specifically, the invention of this application relates to Cu 2 HfS 3 which is a novel compound useful as a semiconductor material, a cathode material for a secondary battery, and the like, and a method for producing the same.
【0002】[0002]
【従来の技術とその課題】従来、Cu−Hf−S系にお
ける三元系化合物の相関関係については、立方晶系のス
ピネル相Cux HfS2 を除いては全く報告されていな
かった。Cu−Hf−S系三元化合物は、半導体材料や
導電性材料、さらには二次電池正極材料等としての特性
を持つものと期待されてはいるが、実際に、この三元系
化合物はこれまでのところほとんど検討されておらず、
前記の公知例を除いては今後の手がかりが得られていな
いのが実情である。 2. Description of the Related Art Hitherto, there has been no report on the correlation between ternary compounds in a Cu-Hf-S system except for a cubic spinel phase Cu x HfS 2 . Although the Cu-Hf-S ternary compound is expected to have properties as a semiconductor material, a conductive material, and further as a secondary battery positive electrode material, the ternary compound is actually So far little has been considered,
Except for the above-mentioned known examples, no clues have been obtained in the future.
【0003】そこで、この出願の発明は、従来の技術状
況の限界を克服し、今後の半導体材料等の展開が期待さ
れるCu−Hf−S系において得られる新規な化合物と
その製造方法を提供することを目的としている。Accordingly, the invention of this application overcomes the limitations of the conventional technical situation and provides a novel compound obtained in a Cu-Hf-S system, which is expected to develop semiconductor materials in the future, and a method for producing the same. It is intended to be.
【0004】[0004]
【課題を解決するための手段】この出願の発明は、上記
の課題を解決するものとして、Cu2 HfS3 で示され
る三方晶系の構造を有する化合物(請求項1)を提供す
る。また、この発明は、金属CuとHfとHfS2 、C
uSまたはSを、Cu:Hf:Sが原子比で実質的に
2:1:3の割合で混合し、当該混合粉末を加圧して圧
粉体とし、これを真空引きした封管中で加熱することに
よって焼結体を生成することを特徴とするCu2 HfS
3 の製造方法(請求項2)を提供する。Means for Solving the Problems The present invention provides a compound having a trigonal structure represented by Cu 2 HfS 3 (Claim 1) to solve the above problems. In addition, the present invention provides a method for producing a metal Cu, Hf and HfS 2 ,
uS or S is mixed at an atomic ratio of Cu: Hf: S of substantially 2: 1: 3, and the mixed powder is pressed to form a green compact, which is heated in a vacuum-evacuated sealed tube. Cu 2 HfS characterized by producing a sintered body by performing
A third manufacturing method (claim 2) is provided.
【0005】さらにこの発明は、加熱温度が600〜1
300℃であること(請求項3)、加熱時間が2日以上
であること(請求項4)等の態様をも提供する。Further, according to the present invention, the heating temperature is from 600 to 1
Embodiments such as 300 ° C. (Claim 3) and a heating time of 2 days or more (Claim 4) are also provided.
【0006】[0006]
【発明の実施の形態】この発明のCu2 HfS3 で示さ
れる化合物は、Hfが硫黄格子の六配位位置を、またC
uが四配位と三配位位置を3:1の割合で占める層状構
造物質である。三方晶系としての格子定数は、a=6.
456±0.001(Å)、c=12.188±0.0
02(Å)、V=439.9±0.2(Å3 )であり、
空間群はP31c(No.163)である。BEST MODE FOR CARRYING OUT THE INVENTION The compound represented by Cu 2 HfS 3 according to the present invention has a structure in which Hf is located at the 6-coordinate position of the sulfur lattice, and
u is a layered structure material occupying the tetracoordinate and tricoordinate positions at a ratio of 3: 1. The lattice constant of the trigonal system is a = 6.
456 ± 0.001 (Å), c = 12.188 ± 0.0
02 (Å), V = 439.9 ± 0.2 (Å 3 ),
The space group is P31c (No. 163).
【0007】また、この発明のCu2 HfS3 で示され
る化合物の製造方法については、出発原料は市販品をそ
のまま用いても良いが、半導体材料または二次電池用正
極材料として当該化合物を用いる場合には、不純物を含
まない、できるだけ純度の高い出発原料を用いることが
望ましい。さらに、熱処理の過程においては、反応を促
進させるため、粉体の粒径はできるだけ小さくするこ
と、空気中での酸化を避けるために、閉じた系でこれら
の処理を行うことが望ましい。加熱終了後は、石英封管
を水中に入れて急冷するのが適当である。In the method for producing the compound represented by Cu 2 HfS 3 of the present invention, a commercially available product may be used as a starting material as it is, but when the compound is used as a semiconductor material or a cathode material for a secondary battery. It is desirable to use a starting material having as high a purity as possible without containing impurities. Further, in the process of heat treatment, it is desirable to reduce the particle size of the powder as much as possible to promote the reaction, and to perform these treatments in a closed system in order to avoid oxidation in the air. After the heating is completed, it is appropriate to put the quartz sealed tube in water and rapidly cool it.
【0008】この発明の方法によって得られた化合物C
u2 HfS3 の粉末は黒色であり、粉末および単結晶X
線回析法によって三方晶系の結晶構造を有することが確
認されている。その構成および作用効果の特徴につい
て、さらに詳しく以下の実施例に沿って説明する。もち
ろんこの発明は以下の例によって限定されるものではな
い。Compound C obtained by the method of the present invention
The powder of u 2 HfS 3 is black, and the powder and single crystal X
It has been confirmed by a line diffraction method that it has a trigonal crystal structure. The configuration and the features of the operation and effect will be described in more detail with reference to the following embodiments. Of course, the present invention is not limited by the following examples.
【0009】[0009]
【実施例】純度99.9%以上のCu粉末と純度99.
7%以上のHfS2 粉末と純度99.9999%以上の
S粉末を、Cu:Hf:Sの原子比が2:1:3の割合
に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5分間混合し、当該混合粉末を加圧して圧粉体を生
成した。EXAMPLE A Cu powder having a purity of 99.9% or more and a purity of 99.9% or more were obtained.
7% or more of HfS 2 powder and 99.9999% or more of S powder are weighed in a glove box so that the atomic ratio of Cu: Hf: S becomes 2: 1: 3, and in an agate mortar. After mixing for 5 minutes, the mixed powder was pressed to form a green compact.
【0010】次に、これを透明石英管中に真空封入し、
600℃に設定された横型管状電気炉で1日間加熱し、
さらに800℃で2日間加熱し、その後、石英管を取り
出して水中で急冷した。得られたCu2 HfS3 相化合
物の面指数(hkl)、面間隔(d(Å))(do は実
測値、dO は計算値)および粉末X線回析強度(I
(%))(Io は実測強度)を粉末X線回析法によって
計測した。その結果を表1に示した。Next, this is vacuum-sealed in a transparent quartz tube,
Heated in a horizontal tubular electric furnace set at 600 ° C for 1 day,
After further heating at 800 ° C. for 2 days, the quartz tube was taken out and quenched in water. Plane index (hkl), plane spacing (d (Å)) (d o is a measured value, d o is a calculated value), and powder X-ray diffraction intensity (I) of the obtained Cu 2 HfS 3 phase compound
(%)) (I o is the measured intensity) was measured by the powder X-ray diffraction method. The results are shown in Table 1.
【0011】[0011]
【表1】また、前者の三方晶系としての格子定数は、a
=6.456±0.001(Å)、c=12.188±
0.002(Å)、V=439.9±0.2(Å3 )で
あった。これらの格子定数および表1に示した各面指数
(hkl)より計算した面間隔d(Å))は、実測の面
間隔(do (Å))と極めて一致した。The lattice constant of the former trigonal system is a
= 6.456 ± 0.001 (Å), c = 12.188 ±
0.002 (Å), V = 439.9 ± 0.2 (Å 3 ). The plane spacing d (Å) calculated from these lattice constants and each plane index (hkl) shown in Table 1 was extremely consistent with the measured plane spacing (d o (Å)).
【0012】さらに、四端子法によって、室温から液体
窒素温度における電気抵抗値を測定したところ、この発
明の化合物であるCu2 HfS3 は半導体であり、室温
で20Ω/cmの値を示した。Further, when the electric resistance at room temperature to liquid nitrogen temperature was measured by the four-terminal method, Cu 2 HfS 3 , a compound of the present invention, was a semiconductor and exhibited a value of 20 Ω / cm at room temperature.
【0013】[0013]
【発明の効果】以上詳しく説明したように、この発明に
よって、Cu2 HfS3 で示される三方晶系の構造を有
する新規な化合物およびその製造方法を提供する。この
Cu2 HfS3 は、半導体材料や二次電池用正極材料と
して有用である。As described above in detail, the present invention provides a novel compound having a trigonal structure represented by Cu 2 HfS 3 and a method for producing the same. This Cu 2 HfS 3 is useful as a semiconductor material or a cathode material for a secondary battery.
Claims (4)
造を有する化合物。1. A compound having a trigonal structure represented by Cu 2 HfS 3 .
はSを、Cu:Hf:Sが原子比で実質的に2:1:3
の割合となるように混合し、混合粉末を加圧して圧粉体
とし、これを真空引きした封管中で加熱することによっ
て焼結体を生成することを特徴とする請求項1のCu2
HfS3 の製造方法。2. Metal Cu and Hf and HfS 2 , CuS or S, Cu: Hf: S in an atomic ratio of substantially 2: 1: 3.
Were mixed so that the ratio of the green compact powder mixture under pressure, Cu 2 according to claim 1, characterized in that to produce a sintered body by which the heating in vacuum were sealed tube
Method of manufacturing a HfS 3.
求項2のCu2 HfS3 の製造方法。 3. The method for producing Cu 2 HfS 3 according to claim 2, wherein the heating temperature is 600 to 1300 ° C.
し3のCu2 HfS3 の製造方法。4. The method for producing Cu 2 HfS 3 according to claim 2, wherein the heating time is 2 days or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9363481A JP3049311B2 (en) | 1997-12-16 | 1997-12-16 | Cu2HfS3 and its manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9363481A JP3049311B2 (en) | 1997-12-16 | 1997-12-16 | Cu2HfS3 and its manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH11171545A true JPH11171545A (en) | 1999-06-29 |
JP3049311B2 JP3049311B2 (en) | 2000-06-05 |
Family
ID=18479426
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9363481A Expired - Lifetime JP3049311B2 (en) | 1997-12-16 | 1997-12-16 | Cu2HfS3 and its manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3049311B2 (en) |
-
1997
- 1997-12-16 JP JP9363481A patent/JP3049311B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3049311B2 (en) | 2000-06-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS63239117A (en) | Compound having lamellar structure of hexagonal system expressed in ingazn2o5 and its production | |
Rao et al. | Microwave preparation of oxide bronzes | |
JP3049311B2 (en) | Cu2HfS3 and its manufacturing method | |
Abdon et al. | Stabilization of Metal-Rich Compounds by Polar-Intermetallic Bonding. Synthesis, Structure, and Bonding in Hf5MTe3 (M= Fe, Co) | |
WO1994022620A1 (en) | Synthesis of highly phase pure bscco superconductors | |
KR101316720B1 (en) | P-type fe-sb thermoelectric material doped with yb and the manufacturing method of the same | |
JP2564537B2 (en) | Black phosphorus-silicon crystal | |
Nesterenko et al. | Extending interstitial tetrelides into carbides: Synthesis and crystal and electronic structures-of RE 2 Co 2 AlC (RE= La, Pr, Nd) | |
CN112593288A (en) | Quasi-one-dimensional superconducting material Li0.9Mo6O17Method for producing single crystal | |
JP2526416B2 (en) | Compound having an orthorhombic structure represented by Ag2HfS3 and method for producing the same | |
JP2958445B2 (en) | Compound having a cubic structure represented by Li5Ag2Hf3S8 and method for producing the same | |
JPS61222910A (en) | Production of copper selenide | |
JP2526415B2 (en) | Ag4Hf3S8 cubic structure compound and method for producing the same | |
JP2730672B2 (en) | Ag-Ti-S ternary compound and method for producing the same | |
JP2849704B2 (en) | Bismuth-vanadium oxide compound for oxide ion conductor and method for producing the same | |
JPH0725552B2 (en) | Compound having an orthorhombic structure represented by AgTaS (3) below and method for producing the same | |
JP4320398B2 (en) | Composite oxide, method for producing composite oxide, temperature sensor material for resistance thermometer, and resistance thermometer | |
JPH0375225A (en) | Compound having monoclinic system structure expressed by cu2ta5s8 and production thereof | |
JPH0210873B2 (en) | ||
JP2001270712A (en) | Silicon-containing gadolinium polyboride and method for producing the same | |
JPH0725551B2 (en) | Compound having a cubic system structure represented by Ag (7), TaS (6) and method for producing the same | |
JPH0623045B2 (en) | Ta-S compound and method for producing the same | |
JP3937005B2 (en) | Method for synthesizing metal oxides | |
JPH0393664A (en) | Production of oxide superconductor | |
JPH0495351A (en) | Lithium ion conductive solid electrolyte |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
EXPY | Cancellation because of completion of term |