Copper(II) Phthalocyanine CAS#147-14-8

  • High Efficiency: CuPc achieves power conversion efficiency of around 1%, with potential improvements to 4% when doped with pentacene.

  • Effective Electron Donor: Acts as a strong electron donor when paired with fullerene-C60 or PCBM in organic photovoltaics.

  • Improved Performance: Doping with pentacene enhances the efficiency, demonstrating versatility in OPV applications.

  • Compatible with Organic Solar Cells: CuPc’s use in vacuum-deposited OPVs supports flexible, cost-effective solar cell designs.


Product Details

Copper(II) phthalocyanine, or CuPc, has been utilized as an electron donor in combination with fullerene-C60 or phenyl-C61-butyric acid methyl ester (PCBM) in vacuum-deposited organic photovoltaics (OPV). Initial power conversion efficiency of around 1% has been achieved, with a significant enhancement to 4% when a pentacene-doped CuPc layer is used.

Copper(II) Phthalocyanine#147-14-8

 

Copper(II) phthalocyanine Chemical Properties

Melting point 

600°C (dec.)

Density 

1.62[at 20℃]

Storage temp

Inert atmosphere,Room Temperature

Solubility 

insoluble in H2O, ethanol; soluble in concHSO 4

Colour Index 

74160

Form 

Fine Crystalline Powder

Color 

Dark blue

Odor

odorless

Water Solubility 

<0.1 g/100 mL at 20 ºC

λmax

602nm(CHCl3)(lit.)

Hydrolytic Sensitivity

4: no reaction with water under neutral conditions

Merck 

14,2520

BRN 

4121848

Exposure limits

ACGIH: TWA 1 mg/m3
NIOSH: IDLH 100 mg/m3; TWA 1 mg/m3

InChIKey

XCJYREBRNVKWGJ-UHFFFAOYSA-N

LogP

-1 at 23℃

NIST Chemistry Reference

Copper phthalocyanine(147-14-8)

EPA Substance Registry System

C.I. Pigment Blue 15 (147-14-8)

Absorption

λmax 678 nm (DMF)

 

 

Safety Information

Safety Statements 

22-24/25

WGK Germany 

-

RTECS 

GL8510000

TSCA 

Yes

HS Code 

32041300

Hazardous Substances Data

147-14-8(Hazardous Substances Data)

Toxicity

LD50 intraperitoneal in rat: > 3gm/kg

 Copper(II) Phthalocyanine#147-14-8

Product Usage

Copper(II) phthalocyanine plays a key role in the study of photosensitizer chemistry, particularly for uniform polymerization, luminescence chemistry, and spectrophotometric analysis, as well as in organic synthesis and polymerization. This pigment is widely used in products such as enamels, linoleum, inks, plastics, and rubber items. Additionally, photoisomerizable phthalocyanines are utilized in rewritable CD or DVD printing.

Copper(II) Phthalocyanine#147-14-8

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