PBDTTPD, Poly[(5,6-dihydro-5-octyl-4,6-dioxo-4H-thieno[3,4-c]pyrrole-1,3-diyl)[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl], is one of the polymer semiconductors that gives high device performance in OPV solar cells.
The thieno[3,4-c]pyrrole-4,6-dione (TPD) unit offers a planar structure which is beneficial for electron delocalization to promote intrachain and interchain interactions. It also has a strong electron-withdrawing effect, leading to relatively low HOMO and LUMO energy levels for the resulting polymer semiconductors.
It has been demonstrated that linear n-octyl (rather than the branched ethyl-hexyl side chain on the acceptor moiety) enables a stronger electronic coupling with fullerene when PBDTTPD is built into OPV devices .
Luminosyn™ PBDTTPD is now available.
PBDTTPD is purified by soxhlet extraction with methanol, hexane and chloroform under argon atmosphere
Batch-specific GPC data
Have confidence in what you are ordering; batch-specific GPC data for your thesis or publications
Large quantity orders
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|Full name||Poly[(5,6-dihydro-5-octyl-4,6-dioxo-4H-thieno[3,4-c]pyrrole-1,3-diyl)[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl ]]|
|Molecular weight||See Batch Details table above|
|HOMO / LUMO||HOMO = - 5.56 eV, LUMO = - 3.75 eV; Eg = 1.81 eV |
|Suggesting solvents||Chloroform, chlorobenzene, dichlorobenzene|
|Classification / Family||Benzodithiophene, BDT, Thienopyrrole, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic photovoltaics, All-polymer solar cells, OFETs|
|M2053A1||5 g / 10 g*||Please enquire|
*for 5 - 10 grams order quantity, the lead time is 4-6 weeks.
Literature and Reviews
- A Thieno[3,4-c]pyrrole-4,6-dione-Based Copolymer for Efficient Solar Cells, Y. Zou et al., J. Am. Chem. Soc., 132 (15), 5330–5331 (2010); DOI: 10.1021/ja101888b.
- Improving the long-term stability of PBDTTPD polymer solar cells through material purification aimed at removing organic impurities, W. R. Mateker et al., Energy Environ. Sci., 6, 2529–2537 (2013); DOI: 10.1039/c3ee41328d.
- Effect of Polymer Side Chains on Charge Generation and Disorder in PBDTTPD Solar Cells, I. Constantinou et al., ACS Appl. Mater. Interfaces, 7 (48), 26999–27005 (2015); DOI: 10.1021/acsami.5b09497.n2200.
- Efficient charge generation by relaxed charge-transfer states at organic interfaces, K. Vandewa et al., Nat. Mater., 13, 63-68 (2014); DOI:10.1038/NMAT3807.
To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.