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Merck

510823

Sigma-Aldrich

Poly(3-hexylthiophen-2,5-diyl)

regiorandom

Synonym(e):

P3HT

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About This Item

Lineare Formel:
(C10H14S)n
CAS-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352103
NACRES:
NA.23

Farbe

red

mp (Schmelzpunkt)

238 °C

Löslichkeit

chloroform, methylene chloride, toluene, and THF: soluble

Fluoreszenz

λex 420 nm; λem 551 nm in chloroform

Leistung von OPV-Bauelementen

ITO/NiO/P3HT/PC61BM/LiF/Al

  • Short-circuit current density (Jsc): 11.3 mA/cm2
  • Open-circuit voltage (Voc): 0.64 V
  • Fill Factor (FF): 0.69
  • Power Conversion Efficiency (PCE): 5.16 %

ITO/PEDOT:PSS/P3HT:PC61BM (1:08)/Al
  • Short-circuit current density (Jsc): 9.5 mA/cm2
  • Open-circuit voltage (Voc): 0.63 V
  • Fill Factor (FF): 0.68
  • Power Conversion Efficiency (PCE): 5 %

Allgemeine Beschreibung

1:1 (head-to-head):(head-to-tail) linkages of regioisomers
Poly(3-hexylthiophene-2,5-diyl) (P3HT) is a poly(alkylthiophene) based semiconducting polymer that is hydrophobic at the neutral state and has π-π conjugation as a backbone. It′s hole mobility is in the range of 10-3-10-1cm2V-1s-1 and it can be mainly used in the development of organic electronic based devices.

Anwendung

This material has solid state properties.
P3HT is a conducting polymer that can be used in the fabrication of a variety of devices which include solar cells, field effect transistors (FETs), light emitting diodes (LEDs) and photovoltaic cells.

Verpackung

Packaged in glass bottles

Rechtliche Hinweise

Product of Rieke® Metals, Inc.

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Kunden haben sich ebenfalls angesehen

Block copolymer containing poly (3-hexylthiophene) and poly (4-vinylpyridine): Synthesis and its interaction with CdSe quantum dots for hybrid organic applications
Palaniappan K, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 49(8), 1802-1808 (2011)
Effect of the end group of regioregular poly (3-hexylthiophene) polymers on the performance of polymer/fullerene solar cells
Kim Y, et al.
The Journal of Physical Chemistry C, 111(23), 8137-8141 (2007)
Effect of doping of zinc oxide on the hole mobility of poly (3-hexylthiophene) in hybrid transistors
Hammer MS, et al.
Organic Electronics, 11(9), 1569-1577 (2010)
Morphological stabilization of polymer photovoltaic cells by using cross-linkable poly (3-(5-hexenyl) thiophene).
Miyanishi S, et al.
Macromolecules, 42(5), 1610-1618 (2009)
Lei Yang et al.
Physical chemistry chemical physics : PCCP, 14(2), 779-789 (2011-11-26)
Two hole conductor materials, spiro-OMeTAD and P3HT, were compared in solid-state dye-sensitized solar cells. Two organic dyes containing one anchor unit (D35) or two anchor units (M3) were used in the comparison. Absorbed photon to current conversion efficiency close to

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