Abstract
The morphology development of polymer-based blends, such as those used in organic photovoltaic (OPV) systems, typically arrests in a state away from equilibrium-how far from equilibrium this is will depend on the materials chemistry and the selected assembly parameters/environment. As a consequence, small changes during the blend assembly alter the solid-structure development from solution and, in turn, the final device performance. Comparing an open-cage ketolactam fullerene with the prototypical[6,6]-phenyl-C61-butyric acid methyl ester in blends with poly[2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT), we demonstrate that experimentally established, non-equilibrium temperature/composition phase diagrams can be useful beyond rationalization of optimum blend composition for OPV device performance. Indeed, they can be exploited as tools for rapid, qualitative structure-property mapping, providing insights into why apparent similar donor:acceptor blends display different optoelectronic processes resulting from changes in the phase-morphology formation induced by the different chemistries of the fullerenes.
| Original language | English |
|---|---|
| Pages (from-to) | 16304-16312 |
| Number of pages | 9 |
| Journal | Journal of Materials Chemistry C |
| Volume | 9 |
| Issue number | 45 |
| DOIs | |
| State | Published - 7 Dec 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
All Science Journal Classification (ASJC) codes
- General Chemistry
- Materials Chemistry
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