Structuring of Thin-Film Polymer Mixtures upon Solvent Evaporation

Published in Macromolecules, 2016

Cite: C. Schaefer, J.J. Michels, P. van der Schoot. "Structuring of Thin-Film Polymer Mixtures upon Solvent Evaporation." Macromolecules. 49, 6858–6870 (2016) https://pubs.acs.org/doi/abs/10.1021/acs.macromol.6b00537

Organic solar cells consists of a thin film of about 100 nanometers thickness (a ten thousandth of a millimeter), which consists of an intercalated structure of electricity conducting polymers and a fullerene molecules. The layer thickness and internal structure are formed by starting from a solution and removing the solvent in a controlled way. Small changes in the solvent quality and the evaporation conditions lead to enormous variations in the final structure in a way that is poorly understood. Various mechanisms were identified (uniform liquid-liquid phase separation (LLPS), stratified LLPS, polymer precipitation by liquid-solid phase separation [LSPS]). However, controlling which mechanism, and how structures emerge within each mechanism, are subject to trial-and-error experimentation. In this work, I investigated structure formation within the class of uniform LLPS.

For a refinement on this work, see Phys Rev Lett 2018 and Soft Matter 2019; for stratified LLPS, see my research in Schaefer et al, Macromolecules 2017, and for my work on LSPS see my contribution in van Franeker et al, JACS 2015.

Current status: The insights into each of the mechanisms mentioned above has significantly improved, however, the crossovers from one mechanism to the other remain poorly understood. In the meanwhile, new challenges have emerged following the development of ternary organic solar cells, where several phase-separation mechanisms occur simultaneously; see my work in collaboration with the group of Prof. Harald Ade for more info.