|Molecular weight||963.42 g/mol|
|Classification / Family||Indacenodithiophene (IDT), Monomer and inermediates, ITIC, None-fullerene acceptors (NFAs), NFA-OSCs, printing electronics|
|Purity||>98% (by NMR)|
|Melting point||No data available|
IDTB6-2CHO, 4,4,9,9-Tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2,7-dicarbaldehyde, is a derivative of indacenodithiophene (IDT) with extended conjugation to the hexylphenyl side chains. IDT derivatives are electron rich and used as building blocks for the synthesis of non-fullerene acceptors (NFAs) that are employed in highly efficient organic solar cells devices.
Fused IDT core of IDTB6-2CHO is believed to have the function of facilitating π-electron delocalization and improving intermolecular π–π stacking, thus to promote the intrinsic charge carrier mobility.
Literature and Reviews
- The Crucial Role of End Group Planarity for Fused-Ring Electron Acceptors in Organic Solar Cells, J. Rech et al., Mater. Chem. Front., 2019,3, 1642-1652 (2019); DOI: 10.1039/C9QM00314B.
- An Alkylated Indacenodithieno[3,2-b]thiophene-Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses, Z. Fei et al., Adv.Mater.2018, 30, 1705209 (2018); DOI: 10.1002/adma.201705209.
- Achievement of High Voc of 1.02 V for P3HT-Based Organic Solar Cell Using a Benzotriazole-Containing Non-Fullerene Acceptor, B. Xiao et al., Adv. Energy Mater., 1602269 (2017); DOI: 10.1002/aenm.201602269.
- Extension of indacenodithiophene backbone conjugation enables efficient asymmetric A–D-A type non-fullerene acceptors, J. Song et al., J. Mater. Chem. A, 6, 18847-18852 (2018); DOI:10. 1039/C8TA07334A.
To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.