Related Experiment Video
Updated: Jan 26, 2026

Layer-by-layer Synthesis and Transfer of Freestanding Conjugated Microporous Polymer Nanomembranes
Published on: December 15, 2015
Synthesis of Polythiophene⁻Fullerene Hybrid Additives as Potential Compatibilizers of BHJ Active Layers
Sofia Kakogianni1, Aikaterini K Andreopoulou2,3, Joannis K Kallitsis4,5
1Department of Chemistry, University of Patras, University Campus, GR26504 Patras, Greece. skakogianni@upatras.gr.
Abstract:
Perfluorophenyl functionalities have been introduced as side chain substituents onto regioregular poly(3-hexyl thiophene) (rr-P3HT), under various percentages. These functional groups were then converted to azides which were used to create polymeric hybrid materials with fullerene species, either C60 or C70. The P3HT⁻fullerene hybrids thus formed were thereafter evaluated as potential compatibilizers of BHJ active layers comprising P3HT and fullerene based acceptors. Therefore, a systematic investigation of the optical and morphological properties of the purified polymer⁻fullerene hybrid materials was performed, via different complementary techniques. Additionally, P3HT:PC70BM blends containing various percentages of the herein synthesized hybrid material comprising rr-P3HT and C70 were investigated via Transmission Electron Microscopy (TEM) in an effort to understand the effect of the hybrids as additives on the morphology and nanophase separation of this typically used active layer blend for OPVs.
Related Concept Videos
Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)
Conjugate addition results in a thermodynamically stable product. The reaction retains the stronger C=O bond at the expense of the weaker C=C π bond. The process is slow as the β carbon is less electrophilic than the carbonyl carbon.
Direct addition products are...
Thermodynamics: Chemical Potential and Activity
The thermodynamic equilibrium constant is more accurately defined in terms of activity rather than concentration.
Hybrid Zones
Conjugate Addition of Enolates: Michael Addition
Hybridization of Atomic Orbitals I
Hybridization of Atomic Orbitals II

