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Sigma-Aldrich

5,5′′′′′-Dihexyl-2,2′:5′,2′′:5′′,2′′′:5′′′,2′′′′:5′′′′,2′′′′′-Sexithiophen

electron donor for OPV devices

Synonym(e):

α,ω-Dihexylsexithiophen, DH-6T

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About This Item

Empirische Formel (Hill-System):
C36H38S6
CAS-Nummer:
151271-43-1
Molekulargewicht:
663.08
MDL-Nummer:
MFCD06411295
UNSPSC-Code:
12352103
PubChem Substanz-ID:
24882543
NACRES:
NA.23

Form

solid

mp (Schmelzpunkt)

280 °C (dec.) (lit.)

Löslichkeit

chlorobenzene: soluble (soluble)
chloroform: slightly soluble
methylene chloride: slightly soluble

Energie der Orbitale

HOMO 5.2 eV 
LUMO 2.9 eV 

Leistung von OPV-Bauelementen

ITO/DH6T/PC61BM/Al

  • Short-circuit current density (Jsc): 0.027 mA/cm2
  • Open-circuit voltage (Voc): 0.18 V
  • Fill Factor (FF): 0.33
  • Power Conversion Efficiency (PCE): 0.002 %

ITO/PEDOT:PSS/DH6T/PC61BM/Al
  • Short-circuit current density (Jsc): 0.04 mA/cm2
  • Open-circuit voltage (Voc): 0.24 V
  • Fill Factor (FF): 0.36
  • Power Conversion Efficiency (PCE): 0.004 %

ITO/PEDOT:PSS/DH6T:PC61BM (1:1)/Al
  • Short-circuit current density (Jsc): 0.097 mA/cm2
  • Open-circuit voltage (Voc): 0.36 V
  • Fill Factor (FF): 0.24
  • Power Conversion Efficiency (PCE): 0.01 %

Halbleitereigenschaften

P-type (mobility=0.13 cm2/V·s)

SMILES String

CCCCCCc1ccc(s1)-c2ccc(s2)-c3ccc(s3)-c4ccc(s4)-c5ccc(s5)-c6ccc(CCCCCC)s6

InChI

1S/C36H38S6/c1-3-5-7-9-11-25-13-15-27(37-25)29-17-19-31(39-29)33-21-23-35(41-33)36-24-22-34(42-36)32-20-18-30(40-32)28-16-14-26(38-28)12-10-8-6-4-2/h13-24H,3-12H2,1-2H3

InChIKey

QCMASTUHHXPVGT-UHFFFAOYSA-N

Allgemeine Beschreibung

5,5′′′′′-Dihexyl-2,2′:5′,2′′:5′′,2′′′:5′′′,2′′′′:5′′′′,2′′′′′-sexithiophene (DH6T) is an alkyl substituted oligothiophene that can be used as an organic semiconductor. It has a field mobility of 1 cm2/Vs that makes it a suitable active layered material in electronic and optoelectronic applications.

Anwendung

DH6T can be used as a p-type donor molecule for the fabrication of organic electronic devices such as organic field effect transistors (OFETs), thin film transistors (TFTs) and organic solar cells (OSCs).

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Photovoltaic performance of organic solar cells based on DH6T/PCBM thin film active layers
Muhammad FF and Sulaiman K
Thin Solid Films, 519(15), 5230-5233 (2011)
Relationship between molecular structure and electrical performance of oligothiophene organic thin film transistors
Halik M, et al.
Advanced Materials, 15(11), 917-922 (2003)
High Hole Mobility and Thickness-Dependent Crystal Structure in alpha, omega-Dihexylsexithiophene Single-Monolayer Field-Effect Transistors
Mannebach EM, et al.
Advances in Functional Materials, 23(5), 554-564 (2013)
All organic near ultraviolet photodetectors based on bulk hetero-junction of P3HT and DH6T
Shalu C, et al.
Semiconductor Science and Technology, 33(9), 095021-095021 (2018)
Photovoltaic performance of organic solar cells based on DH6T/PCBM thin film active layers
Muhammad, F. F.; et al.
Thin Solid Films, 519, 5230-5233 (2011)
Alle zugehörigen Dokumente anzeigen

Artikel

Self-Assembled Nanodielectrics (SANDs) for Unconventional Electronics

Review the potential of self-assembled multilayer gate dielectric films fabricated from silane precursors for organic, inorganic, and transparent TFT and for TFT circuitry and OLED displays.

Synthetic Strategy for Large Scale Production of Oligothiophenes

Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.

Optoelectronic Devices with DPP-containing Molecules

Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

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