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產(chǎn)品詳情

  • 產(chǎn)品名稱：PDPP3T

  • 產(chǎn)品型號(hào)：PDPP3T
  • 產(chǎn)品廠商：Ossila
  • 產(chǎn)品價(jià)格：0
  • 折扣價(jià)格：0
  • 產(chǎn)品文檔：
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簡(jiǎn)單介紹：
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.
詳情介紹：

Batch details

Batch Mw Mn PDI
M991 66,759 31,505 2.12

 

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.

 

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.

 

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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