Skip to Content
Merck
All Photos(1)

Documents

510823

Sigma-Aldrich

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

regiorandom

Synonym(s):

P3HT

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(C10H14S)n
CAS Number:
156074-98-5
MDL number:
MFCD00217686
UNSPSC Code:
12352103
NACRES:
NA.23

color

red

mp

238 °C

solubility

chloroform, methylene chloride, toluene, and THF: soluble

fluorescence

λex 420 nm; λem 551 nm in chloroform

OPV Device Performance

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 %

Related Categories

General description

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.

Application

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.
This material has solid state properties.

Packaging

Packaged in glass bottles

Legal Information

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
View All Related Papers

Articles

PCBM-Based n-Type Semiconductors

PCBM-based n-type semiconductors - Find p- and n-type organic semiconductors available with PCBM library & properties.

Conducting Polymer Device Applications

The application of conducting polymers at the interface with biology is an exciting new trend in organic electronics research.

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.

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

See All

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service