Accéder au contenu
Merck
Toutes les photos(2)

Key Documents

546682

Sigma-Aldrich

Copper(II) phthalocyanine

Dye content >99 %

Synonyme(s) :

CuPc

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Formule empirique (notation de Hill):
C32H16CuN8
Numéro CAS:
Poids moléculaire :
576.07
Numéro C.I. (Colour Index):
74160
Numéro Beilstein :
4121848
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Composition

Dye content, >99%

Niveau de qualité

λmax

678 nm

Performance des dispositifs OLED

ITO/CuPc/NPD/Alq3/C60/Mg:Ag

  • Color: green
  • Max. Luminance: 17200 Cd/m2

ITO/CuPc/NPD/Alq3/LiF/Al
  • Color: red
  • Max. Luminance: 2000 Cd/m2
  • Turn-On Voltage: 7.5 V

ITO/CuPc/NPD/CBP:FIrpic (6%)/BAlq3/LiF/Al
  • Color: blue
  • Max. EQE: 4.5 %

Performance des dispositifs OPV

ITO/CuPc/PTCDA/In

  • Short-circuit current density (Jsc): 53.1 mA/cm2
  • Open-circuit voltage (Voc): 0.57 V
  • Fill Factor (FF): 0.61
  • Power Conversion Efficiency (PCE): 4.2 %

ITO/PEDOT:PSS/CuPc/C60/BCP/Al
  • Short-circuit current density (Jsc): 18.8 mA/cm2
  • Open-circuit voltage (Voc): 0.58 V
  • Fill Factor (FF): 0.52
  • Power Conversion Efficiency (PCE): 3.6 %

Chaîne SMILES 

c1ccc2c(c1)C3=NC4=[N@@H]5C(=Nc6n7c(N=C8c9ccccc9C%10=[N@@H]8[Cu]57N3C2=N%10)c%11ccccc6%11)c%12ccccc4%12

InChI

1S/C32H16N8.Cu/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;/h1-16H;/q-2;+2

Clé InChI

XCJYREBRNVKWGJ-UHFFFAOYSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Application


  • A facile molecularly engineered copper (II) phthalocyanine as hole transport material for planar perovskite solar cells with enhanced performance and stability: This study introduces a modified copper(II) phthalocyanine that enhances the performance and stability of perovskite solar cells (Yang et al., 2017).

  • Dopant-free methoxy substituted copper (II) phthalocyanine for highly efficient and stable perovskite solar cells: Discusses the synthesis and application of a methoxy-substituted copper(II) phthalocyanine, improving the efficiency and stability of perovskite solar cells (Ding et al., 2020).

  • Highly efficient dye-sensitized solar cells based on metal-free and copper (II) phthalocyanine bearing 2-phenylphenoxy moiety: Examines novel phthalocyanines for use in dye-sensitized solar cells, focusing on their synthesis and photophysical properties (Ali et al., 2016).

  • Operando HERFD-XANES and surface sensitive Delta mu analyses identify the structural evolution of copper (II) phthalocyanine for electroreduction of CO2: This research uses advanced spectroscopic techniques to explore the structural changes in copper(II) phthalocyanine during CO2 electroreduction (Mei et al., 2022).

  • New dye sensitized photocatalysts: Copper (II)-phthalocyanine/TiO2 nanocomposite for water remediation: Studies a copper(II) phthalocyanine-TiO2 composite as a photocatalyst for water remediation, showing its effectiveness in degrading pollutants under light irradiation (Albay et al., 2016).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number

Vous ne trouvez pas la bonne version ?

Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Yu Li Huang et al.
Langmuir : the ACS journal of surfaces and colloids, 26(5), 3329-3334 (2010-02-24)
The self-assembly of the binary molecular system comprising copper(II) phthalocyanine (CuPc) and copper-hexadecafluoro-phthalocyanine (F(16)CuPc) on graphite has been investigated by in situ low-temperature scanning tunneling microscopy (LT-STM). The adsorption of this binary molecular system on graphite results in the formation
Medhat A Shaibat et al.
The journal of physical chemistry. B, 114(13), 4400-4406 (2010-03-17)
Cu(II)(phthalocyanine) (CuPc) is broadly utilized as an archetypal molecular semiconductor and is the most widely used blue printing pigment. CuPc crystallizes in six different forms; the chemical and physical properties are substantially modulated by its molecular packing among these polymorphs.
Masaya Hirade et al.
ACS applied materials & interfaces, 3(1), 80-83 (2011-01-05)
To enhance the performance of organic photovoltaic (OPV) cells, preparation of organic nanometer-sized pillar arrays is fascinating because a significantly large area of a donor/acceptor heterointerface having continuous conduction path to both anode and cathode electrodes can be realized. In
Jia Liu et al.
Journal of the American Chemical Society, 133(51), 21010-21015 (2011-11-24)
The bottom-up fabrication of surface hierarchical nanostructures is of great importance for the development of molecular nanostructures for chiral molecular recognition and enantioselective catalysis. Herein, we report the construction of a series of 2D chiral hierarchical structures by trinary molecular
A Mugarza et al.
Physical review letters, 105(11), 115702-115702 (2010-09-28)
We study the electronic mechanisms underlying the induction and propagation of chirality in achiral molecules deposited on surfaces. Combined scanning tunneling microscopy and ab initio electronic structure calculations of Cu-phthalocyanines adsorbed on Ag(100) reveal the formation of chiral molecular orbitals

Articles

The conductivity of organic semiconductors can be increased, and the barriers to charge-carrier injection from other materials can be reduced, by the use of highly reducing or oxidizing species to n- or p-dope, respectively, the semiconductor.

Professor Shinar (Iowa State University, USA) summarizes the developments of a variety of sensor configurations based on organic and hybrid electronics, as low-cost, disposable, non-invasive, wearable bioelectronics for healthcare.

While dye sensitization as the basis for color photography has been accepted for a very long time,1 attempts to use this principle for the conversion of solar light to electricity generally had resulted only in very low photocurrents, below 100 nA/cm2.2

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique