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英國ossila材料PDPP3T OPV材料DPP3T CAS:1198291-01-8

產(chǎn)品簡介:英國ossila材料PDPP3T OPV材料DPP3T CAS:1198291-01-8
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只用于動物實驗研究等

英國ossila材料PDPP3T  OPV材料DPP3T CAS:1198291-01-8

PDPP3T is now available featuring:

  • High purity and good solubility (PDPP3T is purified by soxhlet extraction with methanol, hexane and chlorobenzene under argon atmosphere)
  • 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 details

BatchMwMnPDIStock Info
M99166,75931,5052.12In stock

 

General Information

Full namePoly{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}
SynonymsPDPP3T, DPP3T
Chemical formula(C50H72N2O2S3)n
CAS number1198291-01-8
HOMO / LUMOHOMO = -5.17 eV, LUMO = -3.61 eV [1]
SolubilityToluene, chloroform, chlorobenzene, dichlorobenzene
Classification / FamilyPyrrolo[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

英國ossila材料PDPP3T  OPV材料DPP3T CAS:1198291-01-8

Applications

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.

英國ossila材料PDPP3T  OPV材料DPP3T CAS:1198291-01-8

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.
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