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22205-45-4 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 22205-45-4 differently. You can refer to the following data:
1. Copper(I) sulfide, Cu2S, [22205-45-4], MW 159.15, is naturally occurring as the blue or gray mineral chalcocite, [21112-20-9]. Copper(I) sulfide or copper glance is insoluble in water but decomposes in nitric acid and concentrated sulfuric acid. Copper(I) sulfide is prepared by heating mixtures of copper and sulfur in a hydrogen atmosphere or by precipitation of a copper(II) ammine salt solution with hydrogen sulfide or alkali sulfides. It is used in lubricants, solar cells, semiconductors, and luminous paints.
2. Black powder or lumps.Soluble in nitric acid and ammonium hydroxide; insoluble in water. Occurs as the mineral chalcocite.

Physical Properties

Dark-blue or black orthogonal crystals; insoluble in water; slightly soluble in hydrochloric acid; decomposed by nitric acid and concentrated sulfuric acid; moderately soluble in ammonium hydroxide; dissolves in potassium cyanide solutions.

Uses

Different sources of media describe the Uses of 22205-45-4 differently. You can refer to the following data:
1. Copper(I) sulfide is used in luminous paints; antifouling paints; in solidlubricant mixtures; in solar cells; in electrodes; and as a catalyst. The compound occurs in nature as the mineral chalcocite (copper glance) with varying colors.
2. Antifouling paints, solar cells, electrodes, solid lubricants, luminous paints, catalyst.
3. Copper(I) sulfide is used in luminous paints, electrodes and in solar cells. It is also used for grain mounts, XRD and in microprobe standards for the identification of unknown minerals. It acts as a precursor for the preparation of copper(I) oxide and copper metal. Further, it acts as a catalyst.

Preparation

Copper(I) sulfide is available in nature as the mineral chalcocite. It also may be made by heating copper(II) sulfide with hydrogen, in the presence of small amounts of sulfur. Alternatively, copper(I) sulfide may be prepared by heating copper with hydrogen sulfide and hydrogen; or by heating the metal with sulfur in an atmosphere of carbon dioxide and methanol vapor.

Reactions

When heated in air, copper(I) sulfide oxidizes forming copper(II) oxide, and sulfur dioxide: Cu2S + 2O2→ 2CuO + SO2 Heating in the absence of air produces copper(II) sulfide and copper: Cu2S→ CuS + Cu When heated with nitric acid, copper(I) sulfide decomposes forming copper nitrate and hydrogen sulfide. The compound dissolves in aqueous solutions containing cyanide ions forming soluble copper-cyanide complexes. Copper(I) sulfide reacts with polysulfide anions in aqueous solutions forming soluble copper polysulfides.

Definition

Different sources of media describe the Definition of 22205-45-4 differently. You can refer to the following data:
1. ChEBI: A copper sulfide in which the metal is in the +1 oxidation state.
2. Copper glance: A mineral form ofcopper(I) sulphide,Cu2S.

General Description

Copper sulfide shows metal-like electrical conductivity, chemical-sensing capability and suitable characteristics for absorption of solar energy. Cu63 NMR, X ray photoelectron spectroscopy,2 copper sulfide CuS was studied in detail. Copper sulfide is a monovalent and oxidation state was determined to be 2.2

Check Digit Verification of cas no

The CAS Registry Mumber 22205-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,0 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22205-45:
(7*2)+(6*2)+(5*2)+(4*0)+(3*5)+(2*4)+(1*5)=64
64 % 10 = 4
So 22205-45-4 is a valid CAS Registry Number.
InChI:InChI=1/2Cu.H2S/h;;1H2/q2*+1;-2

22205-45-4 Well-known Company Product Price

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  • (Code)Product description
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  • Packaging
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  • Detail
  • Alfa Aesar

  • (14718)  Copper(I) sulfide, 99.5% (metals basis)   

  • 22205-45-4

  • 50g

  • 604.0CNY

  • Detail
  • Alfa Aesar

  • (14718)  Copper(I) sulfide, 99.5% (metals basis)   

  • 22205-45-4

  • 250g

  • 2727.0CNY

  • Detail
  • Alfa Aesar

  • (14718)  Copper(I) sulfide, 99.5% (metals basis)   

  • 22205-45-4

  • 1kg

  • 9770.0CNY

  • Detail
  • Alfa Aesar

  • (42532)  Chalcocite, naturally occurring mineral, grains, approximately, 0.06-0.19in   

  • 22205-45-4

  • 1g

  • 122.0CNY

  • Detail
  • Alfa Aesar

  • (42532)  Chalcocite, naturally occurring mineral, grains, approximately, 0.06-0.19in   

  • 22205-45-4

  • 5g

  • 422.0CNY

  • Detail
  • Alfa Aesar

  • (42532)  Chalcocite, naturally occurring mineral, grains, approximately, 0.06-0.19in   

  • 22205-45-4

  • 25g

  • 1793.0CNY

  • Detail
  • Aldrich

  • (510653)  Copper(I)sulfide  anhydrous, powder, 99.99% trace metals basis

  • 22205-45-4

  • 510653-5G

  • 1,261.26CNY

  • Detail
  • Aldrich

  • (342459)  Copper(I)sulfide  powder, −325 mesh

  • 22205-45-4

  • 342459-250G

  • 2,733.12CNY

  • Detail
  • Aldrich

  • (342459)  Copper(I)sulfide  powder, −325 mesh

  • 22205-45-4

  • 342459-1KG

  • 8,856.90CNY

  • Detail

22205-45-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name copper(I) sulfide

1.2 Other means of identification

Product number -
Other names copper stearate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22205-45-4 SDS

22205-45-4Synthetic route

Cu2Pt4S8

Cu2Pt4S8

A

sulfur
10544-50-0

sulfur

B

platinum(II) sulfide

platinum(II) sulfide

C

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
decompn. under argon at about 800 K;A 100%
B 100%
C 100%
pyrite

pyrite

copper(II) sulfate
7758-99-8

copper(II) sulfate

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

iron(II) sulfate

iron(II) sulfate

Conditions
ConditionsYield
In water byproducts: H2SO4; pptn. of Cu2S (99.3%) and formation of FeSO4 and H2SO4 by reaction of 5%ic CuSO4- soln. with FeS2 at 200 °C in presence of quartz; quartz prevents formation of Fe2O3, Cu2O and CuS as by-products; formation of CuS with higher per cent FeS2;;A 99.3%
B n/a
In water byproducts: H2SO4; pptn. of Cu2S (99.3%) and formation of FeSO4 and H2SO4 by reaction of 5%ic CuSO4- soln. with FeS2 at 200 °C in presence of quartz; quartz prevents formation of Fe2O3, Cu2O and CuS as by-products; formation of CuS with higher per cent FeS2;;A 99.3%
B n/a
copper diacetate
142-71-2

copper diacetate

thiourea
17356-08-0

thiourea

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In water for 1h; Sonication;91%
In ethanol Cu acatate and thiourea dissolved in abs.EtOH, stirred for 10 min, dip coated onto glass substrate, heated at 200°C for 10 min (several cycles), heated at 200°C for 60 min;
water
7732-18-5

water

copper(l) chloride

copper(l) chloride

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
With hydrogen sulfide In neat (no solvent) on passing over H2O-vapor at about 450°C in presence of excess H2S;;
carbon oxide sulfide
463-58-1

carbon oxide sulfide

copper(l) chloride

copper(l) chloride

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
In hydrogenchloride complete decompn.;;
In hydrogenchloride complete decompn.;;
Conditions
ConditionsYield
In water quick react. with powdered Cu;
In water slow react. at room temp., fast react. on boiling;;
In water slow react. at room temp., fast react. on boiling;;
In neat (no solvent) heating in vac. to about 110°C;;
copper(II) nitrate

copper(II) nitrate

sodium thiosulfate

sodium thiosulfate

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In water electroless thin film deposition from copper(II)/S2O3(2-) soln. (molar ratio Cu(II)/S2O3(2-)=1:2), pH ca. 5 (acetic acid), bath temp. 50°C;; rinsed with water, air dried; Rutherford back scattering anal., scanning electron microscopy, X-ray diffraction;
copper(II) chloride pentahydrate

copper(II) chloride pentahydrate

sodium thiosulfate

sodium thiosulfate

N,N-dimethylthiourea
534-13-4

N,N-dimethylthiourea

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In water aq. soln. of CuCl2*5H2O, dimethylthiourea and Na2S2O3 prepd. in deionized H2O, mixed, pH=2.3 at 70 °C, deposition time 3.5 h;
copper(II) ion

copper(II) ion

sodium thiosulfate

sodium thiosulfate

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

copper(II) sulfide

copper(II) sulfide

C

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
In water on boiling, excess Na2S2O3; product ratio depending on react. time, Na2S2O3 concn., acidity of soln.;;
In water on boiling, excess Na2S2O3; product ratio depending on react. time, Na2S2O3 concn., acidity of soln.;;
copper(II) ion

copper(II) ion

sodium thiosulfate

sodium thiosulfate

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
In water on boiling, excess Na2S2O3;;A >99
B n/a
In water on boiling, excess Na2S2O3;;A >99
B n/a
copper(II) sulfate
7758-99-8

copper(II) sulfate

sodium thiosulfate

sodium thiosulfate

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

copper(II) sulfide

copper(II) sulfide

C

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
In water heating with excess Na2S2O3 in a closed tube to 140-200°C;;
In water heating with excess Na2S2O3 in a closed tube to 140-200°C;;
copper(II) sulfate
7758-99-8

copper(II) sulfate

sodium thiosulfate

sodium thiosulfate

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In water electroless thin film deposition from copper(II)/S2O3(2-) soln. (molar ratio Cu(II)/S2O3(2-)=1:2), pH ca. 5 (acetic acid), bath temp. 50°C;; film rinsed with water, air dried; Rutherford back scattering anal., scanning electron microscopy, X-ray diffraction;
sodium thiosulfate

sodium thiosulfate

copper dichloride

copper dichloride

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In melt on melting;;
In melt on melting;;
copper(I) oxide

copper(I) oxide

sodium thiosulfate

sodium thiosulfate

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In not given sol. in Na2S2O3 soln; on heating pptn. of Cu2O and Cu2S;;
In not given sol. in Na2S2O3 soln; on heating pptn. of Cu2O and Cu2S;;
Conditions
ConditionsYield
In neat (no solvent) at elevated temperature with pure CS2-vapor or in mixture with CO2 or N2;;
In neat (no solvent) with CS2 vapor or with CS2 vapor with CO2 or N2 at elevated temp.;;
In neat (no solvent) with CS2 vapor or with CS2 vapor with CO2 or N2 at elevated temp.;;
In neat (no solvent) with CS2 contg. CO2 at elevated temp., heating to 860°C in vac.;; 99.8% Cu2S;;
In neat (no solvent) with CS2 contg. CO2 at elevated temp., heating to 860°C in vac.;; 99.8% Cu2S;;
iron sulfide

iron sulfide

silica copper(I) oxide

silica copper(I) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In neat (no solvent) byproducts: FeSiO3; at 1800°C;;
In neat (no solvent) byproducts: FeSiO3; at 1800°C;;
copper(I) oxide

copper(I) oxide

iron sulfide

iron sulfide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
In melt
barium sulfide

barium sulfide

copper(l) chloride

copper(l) chloride

copper(I) sulfide
22205-45-4

copper(I) sulfide

copper(I) bromide
7787-70-4

copper(I) bromide

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
With H2S In acetonitrile
cadmium(II) sulphide

cadmium(II) sulphide

copper(II) sulfate
7758-99-8

copper(II) sulfate

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

digenite

digenite

C

Cu1.90S

Cu1.90S

Conditions
ConditionsYield
With potassium nitrate In melt Cd-salt subjecting to electrostimulated ion exchange in melt of K-salt, residue treatment in melt of Cu-salt, according to V. A. Fedorov et al.,Phys. Status Solidi A 139 (1993) 9;
copper(l) chloride

copper(l) chloride

A

copper(I) sulfide
22205-45-4

copper(I) sulfide

B

copper dichloride

copper dichloride

Conditions
ConditionsYield
With sulfur dioxide In hydrogenchloride in dild- HCl-soln.;;
With SO2 In hydrogenchloride in dild- HCl-soln.;;
copper(l) chloride

copper(l) chloride

copper(I) sulfide
22205-45-4

copper(I) sulfide

Conditions
ConditionsYield
With sodium dithionite In water
With hydrogen sulfide In hydrogenchloride pptn.;;
With hydrogenchloride; sulfur dioxide In hydrogenchloride 5 - 15 wt.-% HCl soln.;;
copper(I) sulfide
22205-45-4

copper(I) sulfide

copper(I) oxide

copper(I) oxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) at 700°C, O2-N2-mixtures with 10 or 0% O2, 72 or 28min.;;98%
With O2 In neat (no solvent) at 700°C, O2-N2-mixtures with 10 or 0% O2, 72 or 28min.;;98%
With oxygen byproducts: SO2; heat of the reaction is given;
copper(I) sulfide
22205-45-4

copper(I) sulfide

sulfur
7704-34-9

sulfur

hydrazine
302-01-2

hydrazine

NH2NH3(1+)*NH2NH2*Cu7S4(1-)=N4H9Cu7S4

NH2NH3(1+)*NH2NH2*Cu7S4(1-)=N4H9Cu7S4

Conditions
ConditionsYield
In neat (no solvent) in inert atm. Cu2S and S were stirred at room temp. with hydrazine in sealed vial for 90 h; soln. was filtered and evapd. under N2 flow; elem. anal.;89%
for 48h;
calcium(II) sulfide

calcium(II) sulfide

copper(I) sulfide
22205-45-4

copper(I) sulfide

erbium(III) sulfide

erbium(III) sulfide

potassium bromide
7558-02-3

potassium bromide

KCaEr2CuS5

KCaEr2CuS5

Conditions
ConditionsYield
In melt (N2); mixt. of Cu2S, Er2S3, CaS (molar ratio = 1:2:3) and excess of KBr flux heated at 1000°C in Al2O3-crucible placed in evacuated silica tube for 180 h, slow cooling to 700°C over 90 h; washing with water at room temp.;65%
gadolinium

gadolinium

copper(I) sulfide
22205-45-4

copper(I) sulfide

sulfur
7704-34-9

sulfur

Cu2Gd0.67S2

Cu2Gd0.67S2

Conditions
ConditionsYield
With iodine In neat (no solvent, solid phase) Cu2S, Gd, S and I2 were kept for 2 wks under temp. gradient from 1173 Kto 1073 K;60%
copper(I) sulfide
22205-45-4

copper(I) sulfide

A

copper(I) oxide

copper(I) oxide

B

copper(II) sulfate
7758-99-8

copper(II) sulfate

Conditions
ConditionsYield
With oxygen In neat (no solvent) byproducts: SO2; at 500°C, O2-N2-mixtures with up to 60% O2;;A 50%
B n/a
With O2 In neat (no solvent) byproducts: SO2; at 500°C, O2-N2-mixtures with up to 60% O2;;A 50%
B n/a
With oxygen byproducts: SO2; over 500°C;
silver sulfide

silver sulfide

copper(I) sulfide
22205-45-4

copper(I) sulfide

stromeyerite

stromeyerite

Conditions
ConditionsYield
at room temp.; 48h;;45%
at room temp.; 24h;;24%
at room temp.; 12h;;15%
copper(I) sulfide
22205-45-4

copper(I) sulfide

A

sulfur
7704-34-9

sulfur

B

copper(l) chloride

copper(l) chloride

Conditions
ConditionsYield
With chlorine In neat (no solvent) at 100-300°C;;A n/a
B 30%
With iron(III) chloride byproducts: FeCl2;
With chlorine In neat (no solvent) at 400°C;;A n/a
B >99
calcium(II) sulfide

calcium(II) sulfide

copper(I) sulfide
22205-45-4

copper(I) sulfide

uranium(IV) sulfide

uranium(IV) sulfide

potassium bromide
7558-02-3

potassium bromide

KCuUS3

KCuUS3

Conditions
ConditionsYield
In neat (no solvent, solid phase) US2, Cu2S mixed, loaded in silica tube, sealed under 1E-4 Torr, heated at 1273 K for 10 d, mixed with CaS and KBr, ground, sealed, heated to 1123 K in 60 h, kept at 1123 K for 240 h, slowly cooled at 3 K/h to 853 K; washed with H2O, dried with acetone;10%
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

sodium chloride
7647-14-5

sodium chloride

copper dichloride

copper dichloride

Conditions
ConditionsYield
byproducts: Na2SO4; information about the react. eqs. in detail;
byproducts: Na2SO4; information about the react. eqs. in detail;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

copper(II) oxide

copper(II) oxide

Sulfate
14808-79-8

Sulfate

Conditions
ConditionsYield
With chlorine; sulfur increased SO4(2-) prodn. between 100 and 300°C; SO4(2-) detn. in aq. extract;
With chlorine between 100 and 300°C almost entirely SO4(2-) prodn.; SO4(2-) detn. in aq. extract;
With chlorine between 100 and 300°C almost entirely SO4(2-) prodn.; SO4(2-) detn. in aq. extract;
With chlorine; sulfur increased SO4(2-) prodn. between 100 and 300°C; SO4(2-) detn. in aq. extract;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

copper(II) sulfate
7758-99-8

copper(II) sulfate

Sulfate
14808-79-8

Sulfate

Conditions
ConditionsYield
With chlorine between 100 and 300°C, react. at 300°C also; SO4(2-) detn. in aq. extract;
With chlorine between 100 and 300°C, react. at 300°C also; SO4(2-) detn. in aq. extract;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

A

copper(I) oxide

copper(I) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

iron(III) sulfate

iron(III) sulfate

D

copper(II) ferrite

copper(II) ferrite

E

copper(II) oxide

copper(II) oxide

Conditions
ConditionsYield
With air byproducts: SO2, SO3; mixing of Fe2O3 and Cu2S (1:1) mech. before roasting; information about the react. eqs. in detail, about dependence on temp. from 300 till 550°C and about the effect of Fe2O3; further products;
With air byproducts: SO2, SO3; mixing of Fe2O3 and Cu2S (1:1) mech. before roasting; information about the react. eqs. in detail, about dependence on temp. from 300 till 550°C and about the effect of Fe2O3; further products;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

A

copper(I) oxide

copper(I) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

copper(II) ferrite

copper(II) ferrite

D

copper(II) oxide

copper(II) oxide

Conditions
ConditionsYield
byproducts: SO2, SO3; at roasting of Cu2S in presence of Fe2O3;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

sulfur dioxide
7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In neat (no solvent) Kinetics; kinetics and statics described;; generation of SO2;;
manganese(III) oxide

manganese(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

manganese oxide

manganese oxide

Conditions
ConditionsYield
In neat (no solvent) byproducts: Cu, SO2; react. at 700 °C;;
In neat (no solvent) byproducts: Cu, SO2; react. at 700 °C;;
Conditions
ConditionsYield
With NH3; C In ammonia aq. NH3; Cu2S nanowires on copper grids with or without carbon coating washed with HCl for ca. 20 min, then by H2O and then immersed into aq. NH3 for 2 h; samples of Cu(OH)2 nanobelts washed with H2O, dried (air);
Conditions
ConditionsYield
In neat (no solvent) byproducts: SO2, H2; at light red heat;;
In neat (no solvent) byproducts: SO2, H2; at light red heat;;
In neat (no solvent) byproducts: H2S, H2, sulphur; weak react. at red heat, violent react. at white heat;;
copper(I) sulfide
22205-45-4

copper(I) sulfide

water
7732-18-5

water

copper(I) oxide

copper(I) oxide

Conditions
ConditionsYield
In neat (no solvent) on heating;;
In neat (no solvent) on heating;;

22205-45-4Relevant articles and documents

Synthesis and the crystal structure of CeCuS2

Komatsuzaki,Takase,Smura,Takahashi,Takano,Sekizawa,Clarke

, p. 586 - 588 (2006)

Single phase of CeCuS2 has been prepared by the mixture of CeO2 and Cu2S at 1000 ° C in CS2/Ar atmosphere. All X-ray diffraction peaks of CeCuS2 are indexed on the basis of the monoclinic system (space group: P21c) the same as LaCuS 2 and NdCuS2. The lattice parameters obtained by Rietveld analysis are a=0.6573(1) nm, b=0.7256(1) nm, c=0.6875(1) nm, and β=98.566(1)°.

CuS nanostructures prepared by a hydrothermal method

Huang, Qing-Li,Chen, Hu,Zhang, Yong Cai,Le Wu, Chang

, p. 6382 - 6387 (2011)

Without using any surfactant or template, novel CuS three-dimensional (3D) structures consisting of nanosheets were successfully synthesized via a convenient one-step hydrothermal approach. X-ray diffraction pattern showed that the as-prepared product was pure hexagonal phase CuS. Scanning electron microscopy and high-resolution transmission electron microscopy images revealed that the as-prepared product comprised 3D microspheres (about 1-3 μm in diameter), which were further constructed with randomly oriented, single-crystalline CuS nanosheets (about 20 nm in thickness). The UV-vis absorption spectrum of the as-synthesized CuS 3D microspheres displayed an optical absorption minimum near 672 nm. Besides, the thermal stability of the as-synthesized CuS 3D microspheres was also studied.

Synergistic Effect of Chemical Substitution and Insertion on the Thermoelectric Performance of Cu26V2Ge6S32Colusite

Shimizu, Yuta,Suekuni, Koichiro,Saito, Hikaru,Lemoine, Pierric,Guilmeau, Emmanuel,Raveau, Bernard,Chetty, Raju,Ohta, Michihiro,Takabatake, Toshiro,Ohtaki, Michitaka

, p. 11364 - 11373 (2021)

Copper-based sulfides are promising materials for thermoelectric applications, which can convert waste heat into electricity. This study reports the enhanced thermoelectric performance of Cu26V2Ge6S32 colusite via substitution of antimony (Sb) for germanium (Ge) and introduction of copper (Cu) as an interstitial atom. The crystal structure of the solid solutions and Cu-rich compounds were analyzed by powder X-ray diffraction and scanning transmission electron microscopy. Both chemical approaches decrease the hole carrier concentration, which leads to a reduction in the electronic thermal conductivity while keeping the thermoelectric power factor at a high value. Furthermore, the interstitial Cu atoms act as phonon scatterers, thereby decreasing the lattice thermal conductivity. The combined effects increase the dimensionless thermoelectric figure of merit ZT from 0.3 (Cu26V2Ge6S32) to 0.8 (Cu29V2Ge5SbS32) at 673 K.

Anderson, C. T.

, p. 476 - 483 (1931)

Field emission from crystalline copper sulphide nanowire arrays

Chen, Jun,Deng,Xu,Wang, Suhua,Wen, Xiaogang,Yang, Shihe,Yang, Chunlei,Wang, Jiannong,Ge, Weikun

, p. 3620 - 3622 (2002)

Straight crystalline copper sulphide (Cu2S) nanowire arrays have been grown by using a simple gas-solid reaction at room temperature. These were demonstrated to exhibit semiconductor properties. Field emission was observed at a field of ~6MV/m, and its current-field characteristics deviate from Fowler-Nordheim theory, i.e., showing a nonlinear Fowler-Nordheim plot. The uniform emission from the whole arrays was observed using transparent anode technique, and their variation with applied field was recorded. The emission from individual nanowires was also studied using a field emission microscope, and was found to consist of a number of spatially resolved diffuse spots. Finally, stable emission current at different levels and over time was recorded. These findings indicate that semiconductor nanowires as cold cathode have a potential future, worthy of further comprehensive investigation. The technical importance of using semiconductor nanowires as cold cathode emitter is given.

Nagard, N. Le,Katty, A.,Collin, G.,Gorochov, O.,Willig, A.

, p. 267 - 278 (1979)

Hydrothermal synthesis of transition-metal sulfide dendrites or microspheres with functional imidazolium salt

Li, Kangfeng,Wang, Qiaojian,Cheng, Xianyi,Lv, Tianxi,Ying, Taokai

, p. L31-L35 (2010)

A series of transition-metal sulfide (PbS, CdS, ZnS, CoS, Cu2S) compounds were successfully synthesized through a facile hydrothermal method using 1-butyl-3-methlyimidazole thiocyanate ([BMIM][SCN]) as both sulfur source and capping ligand. The resultant products were characterized by X-ray powder diffraction (XRD) measurements in order to determine the crystalline phase of the products. The structural and morphological features of the samples were investigated by scanning electron microscopy (SEM), which showed that the morphologies of PbS and CdS were novel hierarchical dendrites, but rough exterior microspheres of ZnS, CoS and Cu2S. A possible reaction process was simply discussed in the end.

Feigl

, p. 32 - 43 (1927)

Sauer, E.,Steiner, D.

, p. 41 - 46 (1935)

Mokrushin, S. G.,Dem'yanova, N. M.

, p. 261 - 267 (1935)

Svensson, B.

, p. 120 - 128 (1932)

Compounds with layered structures in the systems CuGa5S8/CuIn5S8 and AgGa5S8/AgIn5S8

Haeuseler,Elitok,Memo,Arzani

, p. 1204 - 1208 (2001)

The title systems have been investigated by single crystal and powder X-ray diffraction methods on quenched samples. In the system AgGaxIn5-xS8 spinel type phases are formed up to x A compound crystallising with a hexagonal layered structure is obtained for 2 a single crystal of composition AgGa3In2S8: space group P63mc, Z = 2, a = 380.80 and c = 3076.4 pm. The structure is isotypic to the Zn2In2S5 (II a) type. The sample AgGa4InS8 crystallises in a Wurtzite like structure with a = 377.25 and c = 616.1 pm. In the system CuGaxIn5-xS8 a new compound with layered structure has been detected for 1 ≤ x ≤ 2 which crystallises hexagonally with a = 380.28 and c = 3073.4 pm (x = 2). For the spinel CuIn5S8 an exchange of In by Ga is not detected. Wiley-VCH Verlag GmbH, 2001.

Controllable synthesis of Cu-based nanocrystals in ODA solvent

Wang, Dingsheng,Li, Yadong

, p. 3604 - 3606 (2011)

We exploited a solution-based route for preparation of Cu, Cu2O, Cu3N, and Cu2S nanocrystals, that is, direct thermal decomposition of copper salts (Cu(NO3)2, CuSO4) in octadecylamine (ODA) solvent, which is a novel and ingenious chemical process.

Hahn

, p. 134 - 137 (1924)

Achievement of extra-high thermoelectric performance in doped copper (I) sulfide

Li, Guihui,Lou, Shiyun,Nkemeni, Darrin Sime,Yang, Zhe,Zhou, Shaomin

, (2021)

The development of nontoxic and inexpensive thermoelectric copper (I) sulfide (Cu2S)-based materials could enable an increase in the application of thermoelectric materials in the domain of energy conversion. By using melt quenching, mechanical alloying and spark plasma sintering, we successfully prepared doped and undoped Cu2S with excellent thermoelectric properties. Owing to the increase of carrier concentration, the electrical conductivity of the dopants enhanced from 2.0 × 104 S/m to 1.0 × 105 S/m, with the highest value acquired for Mn doped Cu2S of about 1.0 × 105 S/m at 350 K. Besides, Cu1.8Sn0.1Mn0.1S, Cu1.9Mn0.1S, and Cu1.9Sn0.1S followed an increasing variation in Seebeck coefficient with final values of 325 μV K?1, 322 μV K?1, and 294 μV K?1 at 800 K, respectively. The maximum power factor of 3.24 mW m?1 K?2 is obtained for Cu1.9Mn0.1S at 650 K, which is about 40 times greater than undoped Cu2S (0.08 mW m?1 K?2). At the same time, a peak ZT of 1.63 is attained at 700 K for Cu1.9Mn0.1S, which is about 18 times enhanced over undoped Cu2S (0.09).

Mobile copper ions as heat carriers in polymorphous copper sulfide superionic conductors

Liang, Xin

, (2017)

Liquid-like mobile Cu+ ions are generally considered as phonon scatters in copper chalcogenide superionic conductors, but this is recently disproved by a neutron spectroscopy study on lattice dynamics of Cu2Se compound [Voneshen et al., Phys. Rev. Lett. 17, 118 (2017)]. In this work, we provide a different perspective by investigating the thermal transport of three transformable polymorphs of Cu2S compounds with varying Cu+ content. We show that the disordered and mobile Cu+ ions are not the primary factor for suppressing the heat transport. A notable dependence of thermal conductivity on Cu+ content is observed. By correlating the electrically deducted thermal conductivity with the ion motion behavior for β-Cu2S superionic phase, we reveal that these fast ionic species Cu+ are heat carriers instead, which make an appreciable contribution to thermal conduction.

The phase diagrams of M2X-SiX2 (M is Cu, Ag; X is S, Se)

Venkatraman, Mahadevan,Blachnik, Roger,Schlieper, Andreas

, p. 13 - 20 (1995)

The phase diagrams of Cu2S-SiS2, Ag2S-SiS2 and Ag2Se-SiSe2 were investigated by DTA and X-ray methods. The system Cu2S-SiS2 contains two compounds: Cu2SiS3 and Cu8SiS6. The compound Cu6Si2S7 does not exist. The phasediagram of Ag2S-SiS2 is characterized by the presence of two ternary co mpounds: Ag8SiS6 and Ag10Si3S11. The Ag2Se-SiSe2 system contains only Ag8SiSe6, which forms a eutectic on either side. The stability range and the X-ray diffraction data of the compounds are presented.

Formation of CuS submicrotubes with quadrate cross section

Yan,Huang,Jia,Luo

, p. 1360 - 1365 (2009)

CuS submicrotubes with quadrate cross section were synthesized by two simple steps: (i) preparation of copper-thiourea (Tu) complex; and (ii) subsequent reaction of the as-prepared complex with Na2S solution. Copper-Tu complex was characterized

Fabrication and SERS properties of Ag/Cu2S composite micro-nanostructures over Cu foil

Song, Wei,Wang, Jinjie,Mao, Zhu,Xu, Weiqing,Zhao, Bing

, p. 1247 - 1250 (2011)

A new kind of Ag/Cu2S composite micro/nanostructures has been prepared via a convenient galvanic reduction method. SEM images of these micro/nanostructures showed that Ag nanoparticles with the size of around 50-100 nm were well deposited on the surface of Cu2S micro/nanostructures. The SEM images also indicated that the Ag nanoparticles were preferentially grown on the big polygonal Cu2S microstructures, which could be explained by a localization of the electrons on the surface of the polygonal Cu2S microstructures after the electron transfer step. Owing to the introduction of Ag nanoparticles on the surface of Cu2S micro/nanostructures, the resulting Ag/Cu2S composite micro-nanostructures could be used as a versatile substrate for surface enhanced Raman scattering.

The phase equilibria in the quasi-ternary Cu2S-CdS-SnS2 system

Piskach,Parasyuk,Olekseyuk

, p. 142 - 152 (1998)

The phase equilibria in the quasi-ternary system Cu2S-CdS-SnS2 has been investigated using differential thermal, X-ray phase, microstructural and energy-dispersive X-ray analyses. The projection of the liquid surface and the isotherm

Baskerville, C.

, p. 942 - 947 (1896)

Synthesis, crystal structure, and properties of novel perovskite oxychalcogenides, Ca2CuFeO3Ch (Ch = S, Se)

Charkin,Sadakov,Omel'Yanovskii,Kazakov

, p. 2012 - 2016 (2010)

Two new perovskite oxychalcogenides, Ca2CuFeO3S and Ca2CuFeO3Se, have been synthesized in evacuated quartz tubes. They crystallize in P4/nmm space group with lattice parameters a = 3.8271(1), c = 14.9485(2) and a = 3.8605(1), c = 15.3030(2) for Ca 2CuFeO3S and Ca2CuFeO3Se, respectively. They appear to be the first layered chalcogenide perovskites involving calcium and are structural analogs of the corresponding Sr and Ba compounds. The new compounds exhibit semiconducting properties with energy gap decreasing from the oxysulfide to the oxyselenide. Possibility of introducing Ca2+ into structures of known layered oxychalcogenides and oxypnictides is discussed.

Ultrahigh Thermoelectric Performance in Mosaic Crystals

He, Ying,Lu, Ping,Shi, Xun,Xu, Fangfang,Zhang, Tiansong,Snyder, Gerald Jeffrey,Uher, Ctirad,Chen, Lidong

, p. 3639 - 3644 (2015)

Successful research strategies to enhance the dimensionless figure of merit zT above 2 rely on either bulk nanomaterials or on single crystals. A new physical mechanism of nanoscale mosaicity is shown that goes beyond the approaches in single crystals or conventional nanomaterials. A zT value of 2.1 at 1000 K in bulk nanomaterials is achieved.

Photoelectrochemistry of pure and core/sheath nanowire arrays of Cu 2S directly grown on copper electrodes

Tang, Shangfeng,Wen, Xiaogang,Zhang, Weixin,Yang, Shihe

, p. G220-G226 (2005)

Photoelectrochemistry (PEC) of straight and isolated Cu2S nanowires arrayed on a copper foil is studied. A cathodic photocurrent is observed, which increases with the increasing negative bias of the film electrode, conforming to the p-type semiconducting nature of Cu2S. PEC studies on the core/sheath nanowires of Cu2S (Cu2S nanowires coaled with other nanoparticles such as CdS, polypyrrole, and Au) have revealed distinctly different characteristics. Cu2S/CdS nanowires exhibit a slightly higher photocurrent response due to the charge transfer between the p-type Cu2S core and n-type CdS sheath, whereas the photocurrent response obtained for Cu2S/PPy nanowires is generally an order of magnitude smaller than that for pure Cu2S nanowires under the same bias voltage. For Cu2S/Au nanowires, however. Au nanoparticles can readily accept the photogenerated electrons from the conduction band of Cu2S; this redirects the electron transfer pathway and results in the anodic photocurrent response. On the basis of these findings, different photocurrent generation mechanisms are proposed.

Divers, E.,Shimidzu, T.

, p. 636 - 639 (1885)

Mixed-metal thiophosphate CuCd3PS6: An infrared nonlinear optical material activated by its three-in-one tetrahedra-stacking architecture

Guo, Yangwu,Li, Chunxiao,Li, Zhuang,Lin, Zheshuai,Wu, Yicheng,Xing, Wenhao,Yao, Jiyong,Zhang, Shengzi

supporting information, p. 5020 - 5024 (2020/04/28)

Novel mixed-metal thiophosphate CuCd3PS6 has been firstly discovered and fully characterized. Careful experimental and theoretical investigations demonstrate that CuCd3PS6 is a benign infrared nonlinear optical material with a moderate second harmonic generation response of 0.9 × AgGaS2 at 41-74 μm, a large laser damage threshold of 4.1 × AgGaS2, a wide band gap of 2.24 eV and a low melting point of 603 °C. Moreover, first principles calculations indicate that CuCd3PS6's intriguing nonlinear optical performance is activated by its three-in-one tetrahedra-stacking architecture.

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