隻用於(yu) 動物實驗研究等 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)
- 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)
Pricing 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 |
 Chemical structure and product image of PDPP3T; Chemical formula:(C50H72N2O2S3)n; CAS# 1198291-01-8.
ApplicationsPDPP3T 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- 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.
- 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.
- 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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