Order Code: M991
Not in stock

Luminosyn™ PDPP3T is now available featuring:

  • High purity and good solubility - PDPP3T is purified by soxhlet extraction with methanol, hexane and chlorobenzene under argon atmosphere -polymer at its pure best
  • Batch-specific GPC data - so you have confidence in what you are ordering and GPC data is always convenient for your thesis and publications
  • Larger quantity orders - so you can plan your experiments with polymer from the same batch


    Batch Quantity Price
    M991 100 mg £196.00
    M991 250 mg £388.00
    M991 500 mg £698.00
    M991 1 g £1230.00
    M991 5 g / 10 g* Please enquire

     *for 5 - 10 grams order quantity, the lead time is 4-6 weeks.


    Batch details

    Batch Mw Mn PDI Stock Info
    M991 66,759 31,505 2.12 In stock


    General Information

    Full name Poly{2,2′-[(2,5-bis(2-hexyldecyl)-3,6-dioxo-2,3,5,6- tetrahydropyrrolo[3,4-c ]pyrrole-1,4-diyl)dithiophene]- 5,5′-diyl-alt-thiophen-2,5-diyl}
    Synonyms PDPP3T, DPP3T
    Chemical formula (C50H72N2O2S3)n
    CAS number 1198291-01-8
    HOMO / LUMO HOMO = -5.17 eV, LUMO = -3.61 eV [1]
    Solubility Toluene, chloroform, chlorobenzene, dichlorobenzene
    Classification / Family Pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic Photovoltaics, Polymer Solar Cells, OFETs


    pdpp3t chemical strucutre
    Chemical structure and product image of PDPP3T; Chemical formula:(C50H72N2O2S3)n; CAS# 1198291-01-8.



    PDPP3T is used as active layer material for OPV devices with 6.71% PCE reported when a solvent mixture of DCB/Chloroform/DIO was used.

    Being electron rich, PDPP3T is also used as an effective spiro-OMeTAD replacement hole-transport layer material for perovskite solar cells [1], as well as in organic field-effect transistors [2, 3] and printed electronics.


    Literature and Reviews

    1. Solution processed pristine PDPP3T polymer as hole transport layer for efficient perovskite solar cells with slower degradation, A. Dubey et al., Sol. Energ. Mat. Sol. Cells 145, 193–199 (2016);DOI: 10.1016/j.solmat.2015.10.008.
    2. Optimization of charge carrier transport balance for performance improvement of PDPP3T-based polymer solar cells prepared using a hot solution, J. Wang et al., Phys. Chem. Chem. Phys. 17, 9835--9840 (2015); DOI: 10.1039/c5cp00963d.
    3. Effects of 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane doping on diketopyrrolopyrrole-based, low crystalline, high mobility polymeric semiconductor, S. Yoon et al., Appl. Phys. Lett. 107, 133302 (2015); doi: 10.1063/1.4932530.

    To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.