Skip to Content
Merck

510823

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

greener alternative

regioregular

Synonym(s):

P3HT

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

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

SMILES string

[s]1c(c(cc1Br)CCCCCC)Br

InChI key

NSYFIAVPXHGRSH-UHFFFAOYSA-N

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

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 %

greener alternative category

Enabling

Quality Level

100

Related Categories

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.

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.
We are committed to bringing you Greener Alternative Products, which belongs to one of the four categories of greener alternatives. This enabling product has been enhanced for energy efficiency. Click here for more information.

Legal Information

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

Packaging

Packaged in glass bottles

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCX7666
MKCW2761
MKCT9383
MKCR8745
MKCQ0537

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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)
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 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

Nanoparticle Zinc Oxide ET Layers for Org. Photodet.

Progress in solution-processed functional materials leads to thin-film optoelectronic devices for industrial and consumer electronics.

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

Novel Graphene‑Based Nanostructures Production, Functionalization, and Engineering

PCBM-Based n-Type Semiconductors

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

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.

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