| Identification | Back Directory | [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]] | [CAS]
1223479-75-1 | [Synonyms]
PBDT(EH)-TPD(Oct)
4,5-b']dithiophene-2,6-diyl]]
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
Poly{4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b :4,5-b' ]dithiophene-2,6-diyl-alt-(1,3-(5-octyl-4H-thieno[3,4-c ]pyrrole-4,6(5H )-dione))} | [Molecular Formula]
(C40H53NO4S3)n | [MOL File]
1223479-75-1.mol |
| Hazard Information | Back Directory | [Description]
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. | [Uses]
Use in organic high efficiency photovoltaic cells (PCE 6.8%) and field effect transistors. | [General Description]
PBDT(EH)-TPD(Oct) is a conducting polymer with benzothiophene as the electron donor and thieno[3,4-c]pyrrole-4,6-dione as the electron withdrawing units. It can be used to form a π-conjugating system for the development of a variety of high performance electrochemical devices. |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H302 | [Hazard Codes ]
Xn | [Risk Statements ]
22 | [WGK Germany ]
3 | [Storage Class]
13 - Non Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral |
| Questions And Answer | Back Directory | [Classification]
Benzodithiophene, BDT, Thienopyrrole, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic photovoltaics, Polymer solar cells, OFETs.
| [Applications]
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.
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